CA2228364A1 - Amorphous, transparent sheet of a crystallisable thermoplastic having high standard viscosity - Google Patents
Amorphous, transparent sheet of a crystallisable thermoplastic having high standard viscosity Download PDFInfo
- Publication number
- CA2228364A1 CA2228364A1 CA002228364A CA2228364A CA2228364A1 CA 2228364 A1 CA2228364 A1 CA 2228364A1 CA 002228364 A CA002228364 A CA 002228364A CA 2228364 A CA2228364 A CA 2228364A CA 2228364 A1 CA2228364 A1 CA 2228364A1
- Authority
- CA
- Canada
- Prior art keywords
- sheet
- range
- polyethylene terephthalate
- measured
- accordance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229920001169 thermoplastic Polymers 0.000 title claims description 32
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 32
- 238000000034 method Methods 0.000 claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 76
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 72
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 claims description 48
- -1 polyethylene terephthalate Polymers 0.000 claims description 43
- 229960005215 dichloroacetic acid Drugs 0.000 claims description 24
- 230000005540 biological transmission Effects 0.000 claims description 20
- 238000001125 extrusion Methods 0.000 claims description 20
- 238000005259 measurement Methods 0.000 claims description 20
- 230000008018 melting Effects 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 13
- 239000000155 melt Substances 0.000 claims description 10
- 238000009499 grossing Methods 0.000 claims description 8
- 238000002425 crystallisation Methods 0.000 claims description 7
- 230000008025 crystallization Effects 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 6
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 5
- 238000005498 polishing Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- PHBCDAHASFSLMJ-UHFFFAOYSA-N 2-hydroxybenzotriazole Chemical group C1=CC=CC2=NN(O)N=C21 PHBCDAHASFSLMJ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 3
- 238000005516 engineering process Methods 0.000 claims description 3
- 150000003918 triazines Chemical class 0.000 claims description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims 5
- 239000013036 UV Light Stabilizer Substances 0.000 claims 1
- 229920001707 polybutylene terephthalate Polymers 0.000 claims 1
- 230000007547 defect Effects 0.000 description 29
- 238000002845 discoloration Methods 0.000 description 18
- 239000003381 stabilizer Substances 0.000 description 11
- 230000003287 optical effect Effects 0.000 description 9
- 230000009477 glass transition Effects 0.000 description 7
- 239000004611 light stabiliser Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 6
- 238000007493 shaping process Methods 0.000 description 5
- LEVFXWNQQSSNAC-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-hexoxyphenol Chemical compound OC1=CC(OCCCCCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 LEVFXWNQQSSNAC-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- 239000004417 polycarbonate Substances 0.000 description 4
- 229920000515 polycarbonate Polymers 0.000 description 4
- 238000006068 polycondensation reaction Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 239000011265 semifinished product Substances 0.000 description 3
- 238000003856 thermoforming Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- UXWKVPJOPVIIRU-UHFFFAOYSA-N (6-methylsulfanylpyridin-3-yl)boronic acid Chemical compound CSC1=CC=C(B(O)O)C=N1 UXWKVPJOPVIIRU-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 206010041662 Splinter Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000007539 photo-oxidation reaction Methods 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- 239000004605 External Lubricant Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007707 calorimetry Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229930195143 oxyphenol Natural products 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000006303 photolysis reaction Methods 0.000 description 1
- 230000015843 photosynthesis, light reaction Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical class OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D7/00—Producing flat articles, e.g. films or sheets
- B29D7/01—Films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C43/00—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
- B29C43/22—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor of articles of indefinite length
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C43/00—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
- B29C43/22—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor of articles of indefinite length
- B29C43/222—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor of articles of indefinite length characterised by the shape of the surface
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Moulding By Coating Moulds (AREA)
Abstract
The invention relates to a transparent, amorphous plate with a thickness in the 1 to 20 mm range, having as its main component a crystallisable thermoplast and in which the crystallisable thermoplast has a standard viscosity SV (DCE) in the 1800 to 6000 range, a process for its production and its use.
Description
WO 97/04948 *~ PCT/~P96/03089 Amorphous, transparent sheet of a crystallizable thermoplastic having high standard viscosity The invention relate~ to an amorphous, transparent sheet of El crystallizable thermoplastic having high stAn~lArd viscosity whose thickness is in the range from 1 to 20 mm. The sheet is distinguished by very good optical and mechanical properties. The invention furthermore relates to a process for the production of this sheet, and to the use of the sheet.
Amorphous, transparent sheets having a thickness of from 1 to 20 mm are well known. These two~ n~ional struc-ture!s comprise amorphous, non-crystallizable thermoplastics.~Typical examples of such thermoplastics which can be converted into sheets are, for example, polyvinyl chloride (PVC), polycarbonate (PC) and poly-~methyl methacrylate (PMMA). These semifinished products are produced on so-called extrusion lines (cf. Polymer Werkstoffe, Volume II, Technologie 1, p. 136, Georg Thieme Verlag, Stuttgart, 1984). The pulverulent or granular raw material is melted in an extruder. After extrusion, the amorphous thermoplastics can easily be shaped via polishing stacks or other shaping tools as a consec~uence of their viscosity, which continuously increases with decreasing temperature. After shaping, amorphous thermoplastics then have adec~uate stability, i.e. a high viscosity, in order to be self-supporting in the calibration die. However, they are still sufficiently soft to be shaped by the die. The melt viscosity and inherent rigidity of amorphous thermoplastics is 80 high in the calibration die that the semifinished product does not collapse in the calibration die before cooling. In the case of easily decomposed materials, for example PVC, special processing aids, for example processing stabi-lize!rs against decomposition and lubricants against excessive internal friction and thus uncontrollable warming, are necessary during extrusion. External lubricants are necessary to prevent sticking to walls and rolls.
The processing of PMMA iB carried out using, for example, a vented extruder to enable removal of moisture.
The production of transparent sheets from amorphous thermoplastics sometimes requires expensive additives, which can migrate and can cause production problems owing to evaporations and surface coatings on the semifinished product. PVC sheets can be recycled only with difficulty or using special neutralization or electrolysis process-es. PC and PMMA sheets can likewise only be recycled withdifEiculty and only with 1088 or extreme impairment of the mechanical properties.
In addition to these disadvantages, PMMA sheets also have ext~emely poor impact strength and splinter on fracture or mechanical 10A~; ng. Furthermore, PMMA sheets are readily combustible, which means that they cannot be emp:Loyed, for example, for internal applications and in exhLbitions.
P ~ ~ and PC sheets furthermore cannot be shaped when cold; PMMA sheets disintegrate to form dangerous splin-ter~, while PC sheets undergo hairline cracking and stress whitening.
EP-A-O 471 528 describes a process for shaping an article from a polyethylene terephthalate (PET) sheet. The intrinsic viscosity of the PET employed is in the range from 0.5 to 1.2. The PET ~heet is heat-treated on both ~ides in the thermofilming mold in a temperature range between the glass transition temperature and the melting point. The shaped PET sheet is removed from the mold when the degree of crystallization of the shaped PET sheet is in the region of 25 to 50%. The PET sheets disclosed in EP-i~-O 471 528 have a thickness of from 1 to 10 mm. Since the thermoformed molding produced from the PET sheet is partially crystalline and thus no longer transparent and the surface properties of the molding are determined by the thermoforming process and by the thermoforming temE~erature and mold, it is unimportant what optical properties (for example gloss, haze and light tranLsmission) the PET sheets employed have. In general, the optical properties of these sheets are poor and in need of optimization.
US-A-3,496,143 describes the vacuum thermoforming of a 3 mm thick PET sheet whose degree of crystallization is said to be in the range from 5 to 25%. However, the crystallinity of the thermoformLed molding iB greater than 25%. Again, no rec~uirements regarding optical properties are made of these PET sheets. Since the crystallinity of the sheets employed is already between 5 and 25%, these sheets are hazy and non-transparent.
The object of the present invention is to provide an amorphous, transparent sheet having a thickness of from 1 to 20 mm which has both good mechanical and optical properties.
The good optical properties include, for examLple, high light transmission, high surface gloss, extremely low haze and high clarity.
The good mechanical properties include, inter alia, high impact strength and high breAk; ng strength.
In alddition, the novel sheet should be recyclable, in particular without 1088 of the mechanical properties, and have low combustibility 80 that it can also be employed, for example, for indoor applications and in exhibitions.
This object is achieved by a transparent, amorphous sheet having a thickness in the region of 1 to 20 mm which contains, as principal constituent, a crystallizable thermoplastic, wherein the crystallizable thermoplastic has a standard viscosity SV (DCA), measured in dichloroacetic acid in accordance with DIN 53728, in the range from 1800 to 6000.
The stAn~rd viscosity SV (DCA) of the crystallizable the~moplastic, measured in dichloroacetic acid in accordance with DIN 53728, iB preferably from 2000 to 500(), particularly preferably from 2500 to 4000.
The intrinsic viscoE~ity IV (DCA) is calculated from the stAr~rd viscosity SV (DCA) as follows:
IV (DCA) = 6.67 . 10-4 SV (DCA) + 0.118 The surface gloss, measured in accordance with DIN 67530 (mealsurement angle 20~), is greater than 120, preferably grealter than 130, the light transmission, measured in accordance with ASTM D 1003, is greater than 84%, pre~erably greater than 86%, and the haze of the sheet, meaEIured in accordance with ASTM D 1003, is less than 15%, preferably less than 11%.
The transparent, amorphous sheet contains, as principal conE~tituent, a crystallizable thermoplastic. Suitable cryE~tallizable or partially crystalline thermoplastics are, for example, polyethylene terephthalate, polybuty-lene terephthalate, cycloolefin polymers and cycloolefin copolymers, preference being given to polyethylene terephthalate.
For the purposes of the invention, the term crystal-lizalble thermoplastics is taken to mean - crystallizable homopolymers, - crystallizable copolymers, - crystalliza~le compounds, - crystallizable recyclate and - other variations of crystallizable thermoplastics.
For the purposes of the present invention, the term amorphous sheet is taken to mean a sheet which is non-crystalline, although the crystallizable thenmoplastic employed preferably has a crystallinity of from 5 to 65%, particularly preferably from 25 to 65%. Non-cry~talline or essentially amorphous means that the degree of crystallinity is generally less than 5%, preferably less than 2%, particularly preferably 0%.
An amorphous sheet of this type is essentially unoriented.
Processes for the preparation of the crystallizable then~oplastics are known to the person skilled in the art.
For example, polyethylene terephthalates are usually prepared by polyco~n~ation in the melt or by a two-step polycondensation in which the first step is carried out to a mean molecular weight - correspon~; ng to a mean intrinsic viscosity IV of from about 0.5 to 0.7 - in the melt and the further con~nRation is carried out by solid-state con~enRation. The polycon~enRation is gener-ally carried out in the presence of known polyco~nRa-tion catalysts or catalyst systems. In the solid-state condensation, PET chips are wanmed at temperatures in the range of from 180 to 320~C under reduced pressure or under a protective gas until the desired molecular weight has been reached.
The preparation of polyethylene terephthalate is desc1ribed in detail in a large number of patents, such as, for example in JP-A-60-139 717, DE-C-2 429 087, DE-A-27 07 491, DE-A-23 19 089, DE-A-16 94 461, JP-63-41 528, JP-62-39 621, DE-A-41 17 825, DE-A-42 26 737, JP-60-141 715, DE-A-27 21 501 and US-A-5,296,586.
Polyethylene terephthalates having particularly high molecular weights can be prepared by polycondensation of dicarboxylic acid/diol precondensates (oligomers) at elevated temperature in a liquid heat-transfer medium in the presence of conventional polycondensation catalysts and, if desired, coco~n~able modifiers if the liquid heat:-transfer medium is inert and free from aromatic moieties and has a boiling point in the range from 200 to 320'C, the weight ratio between dicarboxylic acicL/diol/precondensate ~oligomer) employed and liquid heat:-transfer medium is in the range from 20:80 to 80:20, and the polycondensation is carried out in the boiling reaction mixture in the presence of a dispersion stabilizer.
In the case of polyethylene terephthalate, measurement of the Charpy impact strength an (measured in accordance with.ISO 179/lD) of the sheet is preferably not accompa-nied. by fracture. In addition, the Izod notched impactstrength ak (measured in accordance with ISO 180/lA) of the sheet is preferably in the range from 2.0 to 8.0 kJ/m2, particularly preferably in the range from 4.0 to 6.0 kJ/m2.
The clarity of the sheet measured at an angle of less than 2.5~ (ASTM D 1003) is preferably greater than 96%, particularly preferably greater than 97%.
Polyethylene terephthalate polymers having a cry~talline melting point Tm~ as measured by DSC (differential scan-ning calorimetry) at a heating rate of 10~C/min, of from220~ to 280~C, in particular from 220~C to 260~C, prefer-ably from 230~C to 250~C, a crystallization temperature range Tc from 75~C to 280~C, preferably from 75~C to 260~C, a glass transition temperature Tg of from 65~C to 90~C and a density, measured in accordance with DIN 53479, of from 1.30 to 1.45 g/cm3 and a crystallinity of iErom 5 to 65%, are preferred polymers as starting mate!rials for production of the novel sheet.
The bulk density, measured in accordance with DIN 53466, is preferably from 0.75 to 1.0 kg/dm3, particularly preferably from 0.80 to 0.90 kg/dm3.
The polydispersity of the polyethylene terephthalate M[~,~/Mn, measured by GPC, is usually from 1.5 to 6.0, preferably from 2.5 to 6.0, particularly preferably from 3.0 to 5Ø
In a particularly preferred embodiment, the novel sheet is E~rovided with a W light stabilizer.
The concentration i8 preferably from 0.01 to 5% by weight base!d on the weight of the crystallizable thermoplastic.
Light, in particular the ultra-violet part of sunlight, i.e. having a wavelength in the range of 280 to 400 nm, initiates degradation processes in thermoplastics, resulting not only in a change in the visual appearance as a consecfuence of color change or yellowing, but also adversely affecting the mechanical-physical properties.
The inhibition of these photooxidative degradation processes is of considerable industrial and economic importance, since otherwise the potential uses of numer-OU8 thermoplastics are drastically limited.
Polyethylene terephthalates begin to absorb W light, for example, even at below 360 ~Lm, their absorption increases considerably below 320 nm and is very pronounced at belo 300 nm. The maximum absorption is between 280 and 300 nmL.
In t:he presence of oxygen, principally chain cleavage, but no crossl;nk;ng is observed. Carbon - oY;de, carbon dioxide and carboxylic acids represent the predominant photooxidation products in terms of amount. Besides dire!ct photolysis of the ester groups, consideration must also be given to oxidation reactions, which likewise result in the formation of carbon dioxide via peroxide free radicals.
The photooxidation of polyethylene terephthalates can also result, by elimination of hydrogen in the ~-position of t:he ester groups, in hydroperoxides and decomposition proclucts thereof, and associated chain cleavage (H. Day, D. ~l. Wiles: J. Appl. Polym. Sci 16, 1972, page 203).
W tabilizers and W absorbers as light stabilizers are chemical compounds which can engage in the physical and chem~ical processes of photoinduced degradation. Carbon black and other pigments can provide partial protection from, light. However, the substances are unsuitable for transparent sheets since they result is discoloration or a color change. For transparent, amorphous sheets, the only suitable compounds are organic and organometallic compounds which impart only an extremely weak color or color change, or none at all, in the thermoplastics to be stabilized.
Examples of suitable light stabilizers or W stabilizers are 2-hydroxybenzophenones, 2-hydroxybenzotriazoles, organonickel compounds, salicylic esters, cinnamic ester derivatives, resorcinol monobenzoates, oxanilides, hydroxybenzoic esters, sterically hindered amines and triazines, preference being given to 2-hydroxybenzotriazoles and triazines.
In a particularly preferred emlbodiment, the novel trans-parent, amorphous sheet contains, as principle constitu-ents, a crystallizable polyethylene terephthalate and from 0.01 to 5.0% by weight of 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxyphenol (structure in Fig. la) or from 0.01 to 5.0% by weight of 2,2'-methylene-bis(6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol (structure in Fig. lb). In a preferred emlbodiment, it is also possible to employ mixtures of these two W stabi-lizers or mixtures of at least one of these two W
stabilizers with other W stabilizers, where the total concentration of light stabilizers is preferably from 0.01 to 5.0% by weight, based on the weight of cryE~tallizable polyethylene terephthalate.
Weat:hering tests have shown that the novel W-stabilized sheets exhibit no yellowing, no embrittlement, no 1088 of glols on the surface, no cracking on the surface and no impaLirment of the mechanical properties even after use out~ide for from 5 to 7 years.
In addition, entirely unexpectedly, good cold formability without fracture, hairline cracking and/or stress whitening was observed, meAn;ng that the novel sheet can be ahaped and bent without the action of heat.
In addition, measurements showed that the novel sheet has low combustibility and low flammability, 80 that it is suitable, for example, for internal applications and in exhibitions.
Furthermore, the novel sheet can easily be recycled without environmental pollution and without 1088 of the mechanical properties, meAning that it is suitable, for example, for use as short-term advertising hoardings or other advertising articles.
In the W-stabilized embodiment, the sheet has improved weathering resistance and increased W stability. This means that the sheets are only damLaged to an extremely small extent, or not at all, by weathering and sunlight or by other W radiation, 80 that the sheets are suitable for external applications and/or critical internal applications.
The novel transparent, amorphous sheet can be produced, for example, by extrusion in an extrusion line.
An extrusion line of this type is shown diagrammatically in E'ig. 2. It essentially comprises - an extruder (1) as plastication unit, - a sheet die (2) as shaping tool, - a polishing stack/calender (3) as calibration die, - a cooling bed (4) and/or a roller conveyor (5) for aftercooling, - a take-off roll (6), - a separating saw (7), - an edge trimming device (9), and, if desired, - a stacking unit (8).
The process comprises drying the crystallizable thermo-pla~ltic if necessary, then melting the dry polymer in the extruder, if desired together with the W stabilizer, extruding the melt through a die, calibrating, smoothing and cooling the sheet in the polishing stack and then cutting the sheet to size.
The process for the production of the novel sheet iB
described in detail below using the example of polyethy-lene! terephthalate.
The polyethylene terephthalate is preferably dried for from 4 to 6 hours at from 160 to 180~C before extrusion.
The polyethylene terephthalate is then melted in the extruder. The temperature of the PET melt is preferably in the range from 250 to 320~C, it being possible for the temp~erature of the melt to be adjusted essentially both through the temperature of the extruder and through the residence time of the melt in the extruder.
If a light stabilizer is used, this can already have been adde!d by the producer of the raw material or be metered intc, the extruder during production of the sheet.
The light stabilizer is particularly preferably added via mast:erbatch technology, where the light stabilizer is fully dispersed in a solid carrier material. Suitable carrier materials are certain resins, the crystallizable thermoplastic itself, such as for example, polyethylene terephthalate, or alternatively other polymers which are sufficiently compatible with the crystallizable thermoplastic.
It i8 important that the particle size and bulk density of the masterbatch are similar to the particle size and bulk density of the crystallizable thermoplastic, BO that a homogeneous distribution and thus homogeneous W
stabilization can take place.
The melt then leaves the extruder through a die. This die is preferably a sheet die.
The PET melted by the extruder and shaped by a sheet die is calibrated, i.e. intensively cooled and smoothed, by smoothing calender rolls. The calender rolls can be arranged, for example, in an I-, F-, L- or S-shape (see Fig. 3).
The PET material can then be cooled on a roller conveyor, cut to size in width, cut into appropriate lengths and finally stacked.
The thickness of the PET sheet is determined essentially by t:he take-off unit, which is arranged at the end of the coo:Ling zone, the chill ~moothing) rolls, which are coupled to the take-off unit with respect to speed, and the conveying rate of the extruder on the one hand and the separation between the roll~ on the other hand.
The extruders employed can be either single-screw or twin-screw extruders.
The sheet die preferably comprises a collapsible die body, the lips and the restrictor bar for flow regulation over the width. To this end, the restrictor bar can be bent by means of tension and pressure screws. The thick-ness is set by adjusting the lips. It is important toensure a uniform temperature of the PET and of the lip, since otherwise the PET melt flows out through the vari.ous flow channels in different thicknesses.
The calibration tool, ie. the smoothing calender, gives the PET melt shape and ~i ~n~ions. This is achieved by freezing at below the glass transition temperature by cooling and smoothing. Shaping should not be carried out in this state, since otherwise surface defects would form in this cooled state. For this reason, the calender rolls are preferably driven jointly. The temperature of the cale!nder rolls must be lower than the crystalline melting point in order to avoid sticking of the PET melt. The PET
melt leaves the sheet die at a temperature of from 240 to 300~C
The first smoothing/chill roll is at a temperature of from 50~C to 80~C, dep~n~;ng on the output rate and sheet thickness. The second, somewhat colder roll cools the second or other surface.
In order to obtain a uniform sheet having excellent surface properties, it is essential here that the temperature of the first smoothing/chill roll is in the range from 50 to 80~C.
While the calibration unit freezes the sheet surfaces as smoothly as possible and cools the profile until it is rigid in shape, the aftercooling device lowers the temperature of the sheet virtually to room temperature.
The aftercooling can be carried out on a roller board.
The take-off rate should be matched accurately to the calender roll speed in order to prevent defects and thickness variations.
As ;~dditional equipment, the extrusion line for the production of the sheets can also include a separating saw for cutting the sheet to length, a side trimmer, a stacking unit and a monitoring station. The side or edge trimmer is advantageous since the thickness in the edge region may under certain circumstances not be uniform. At CA 02228364 l998-0l-30 the monitoring station, the thickness and optical proper-ties of the sheet are measured.
The surprising multiplicity of excellent properties makes the novel, transparent, amorphous sheet highly suitable for a multiplicity of different uses, for example for interior room panels, for exhibitions and exhibition articles, as displays, for signs, in the lighting sector, in shop fitting and shelf construction, as advertizing articles, as menu holders, as basketball backboards, as room dividers, as information panels and as brochure and news]paper stands.
In tlle W-stabilized embodiment, the novel sheet is also suitable for external applications, such as, for example, for greenhouses, roofing systems, external clA~;ng, covers, applications in the construction sector, illuminated advertising profiles, balcony clA~;ng and roof exit doors.
The invention is described in greater detail below with reference to working examples without this representing a limitation.
The i.ndividual properties are measured in accordance with the .Eollowing stAn~Ards or by the following processes.
Measurement methods Surface gloss:
The i3urface gloss is measured at a measurement angle of 20~ :in accordance with DIN 67530. The reflector value is measured as an optical parameter for the surface of a sheet. In accordance with the stAn~A~ds ASTM-D 523-78 and IS0 2813, an angle of incidence is set at 20~. A light beam hits the planar test surface at the set angle of incidence and is reflected or scattered thereby. The light beams hitting the photoelectronic receiver are indicated as a proportional electrical quantity. The mea~~ured value is dimensionless and must be given together with the angle of incidence.
Light transmission:
The light transmission is taken to mean the ratio between the total amount of transmitted light and the amount of incident light.
The light transmission is measured using a "Hazegard plu~~" instrument in accordance with ASTM D 1003.
Haze and clarity:
Haze is the percentage of transmitted light deflected from the incident ray bundle by an average of more than 2. 5~. The clarity is measured at an angle of less than 2.5~.
The haze and clarity are measured using a "Hazegard plus"
instrument in accordance with ASTM D 1003.
Surface defects:
The surface defects are determined visually.
Charpy impact strength an:
This parameter is determined in accordance with ISO 179/lD.
Izod notched impact strength ak:
The Izod notched impact strength ak is measured in accordance with ISO 180/lA.
Den~lity:
The density is determined in accordance with DIN 53479.
SV (DCA) and IV (DCA):
The stAn~Ard viscosity SV (DCA) i8 measured in accordance with DIN 53726 in dichloroacetic acid.
The intrinsic viscosity (IV) is calculated as follows from the standard viscosity (SV):
IV (DCA) = 6.67 x 10 4 SV (DCA) + 0.118.
Thermal properties:
The thermal properties, such as crystalline melting point T~, crystallization temperature range Tc, after- or cold-cryE~tallization temperature TCN and glass transition tem~)erature Tg are measured by differential sc~nn;ng calorimetry (DSC) at a heating rate of 10~C/min.
Molecular weight and polydispersity:
The molecular weights Mw and Mn and the resultant poly-disE~ersity MW/Mn are measured by gel permeation chroma-tography (GPC).
Weat;hering (on both sides), W stability:
The W stability is tested as follows in accordance with ISO 4892 test specification:
Test. instrument : Atlas Ci 65 Weather-O-meter Test. conditions : ISO 4892, i.e. artificial weathering Expc,sure time : 1000 hours, (per side) Exposure : 0.5 W/m2, 340 nm TemF~erature : 63~C
Rela.tive atmospheric humidity : 50%
Xenon lamp : inner and outer filters made of borosilicate Exposure cycles : 102 minutes W light, then 18 minutes W light with water spraying of the samples, then a further 102 minutes W light, etc.
Color change:
The color change of the samples after artificial weather-ing is measured in accordance with DIN 5033 using a spec-trophotometer.
CA 02228364 l998-0l-30 The following symbols are used:
~L: Difference in brightness +~L: The sample i8 brighter than the standard -~L: The sample i8 darker than the standard oA: Difference in the red-green region +~A: The sample is redder than the st~n~rd -~A: The sample is greener than the st~n~rd ~B: Difference in the blue-yellow region +~B: The sample is yellower than the st~n~rd -~B: The sample i8 bluer than the st~n~rd ~E: Overall color change ~E = ~L2 + ~A2 + ~B2 The larger the numerical deviation from the st~n~rd, the grea.ter the color difference.
Nume!rical values of 5 0. 3 can be neglected and mean that there is no significant color change.
Yellow value:
The yellow value G is a deviation from colorlessness towa.rd "yellow" and is measured in accordance with DIN
6167. Yellow values of 5 5 are invisible.
The examples and comparative examples below each relate to single-layer transparent sheets of various thicknesses prod.uced on the extrusion line described.
All sheets were weathered in accordance with ISO 4892 test. specification on both sides for 1000 hours per side using the Atlas Ci 65 Weather-O-meter and subsequentl test:ed for their mechanical properties discoloration, surf.ace defects, haze and gloss.
Exa~lple 1:
The polyethylene terephthalate from which the transparent sheet is produced has a standard viscosity SV (DCA) of 3490, which corresponds to an intrinsic viscosity IV
(DC~.) of 2.45 dl/g. The moisture content is ~ 0.2% and the density (DIN 53479) is 1.35 g/cm3. The crystallinity is 19%, and the crystalline melting point, according to DSC measurements, is 243~C. The crystallization tempera-ture range Tc is between 82~C and 243~C. The polydispersity MW/Mn of the polyethylene terephthalate is 4.3, where Mw is 225070 g/mol and Mn is 52400 g/mol. The glass transition temperature is 82~C.
Before extrusion, the polyethylene terephthalate is dried in a drier for 5 hours at 170~C and then extruded in a single-screw extruder at an extrusion temperature of 292~C through a sheet die onto a smoothing calender whose rolls are arranged in an S-shape, and smoothed to give a sheet with a thickness of 3 mm. The first calender roll has a temperature of 73~C and the subsequent rolls each have a temperature of 67~C. The take-off rate and the calender roll ~peed are 6.5 m/min.
Following aftercooling, the transparent PET sheet with a thickness of 3 mm is trimmed at the edges using separating saws, cut to length and stacked.
The transparent PET sheet produced has the following property profile:
- t]hickness : 3 mm - surface glo~s, 1st side : 215 (measurement angle 20~) 2nd side : 214 - light transmission : 94%
- clarity : 100%
- haze : 0.8%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects - crystallinity : 0%
- density : 1. 33 g/cm3 Example 2 A transparent sheet is produced analogously to Example 1 using a polyethylene terephthalate with the following properties:
- S'V (DCA) : 2717 - I'V (DCA) : 1. 93 dl/g - d,ensity : 1. 38 g/cm3 - c:rystallinity : 44%
- M~v : 175640 g/mol _ ~ : 245~C
- c:rystalline melting point Tm : 49580 g/mol - c:rystallization temperature range TC : 82~ C to 245~C
- polydispersity M,V/Mn : 3. 54 - glass transition temperature : 82~C
The extrusion temperature is 280~C. The first calander roll has a temperature of 66~C and the subse~auent rolls have a temperature of 60~C. The take-off rate and the calender roll speed are 2.9 m/min.
The transparent PET Qheet produced has the following property profile:
- thickness : 6 mm - ~urface gloss, 1st side : 192 (measurement angle 20~) 2nd side : 190 - light transmis~ion : 92.1%
- clarity : 99.8%
- haze : 2.0%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc) - C~harpy impact strength an : no fracture - Izod notched impact strength ak : 4.8 kJ/m2 - cold formability : good, no defects - c:rystallinity : o%
- density : 1.33 g/cm3 Example 3:
A transparent sheet is produced analogously to Example 2.
The extrusion temperature i8 275~C. The first calender roll has a temperature of 57~C and the subsequent rolls have a temperature of 50~C. The take-off rate and the calender roll speed are 1.7 m/min.
The PET sheet produced has the following property profile:
- t:hickness : 10 mm - surface glos~, 1st side : 173 (mea~urement angle 20~) 2nd side : 171 - light transmission : 88.5%
- clarity : 99.4%
CA 02228364 l998-0l-30 - haze : 3.2%
- ~urface defects per m2 : none Cfisheyes, orange peel, bubbles, ~!tC) - C'harpy impact strength an : no fracture - I:zod notched impact strength ak : 5-0 kJ/m2 - cold formability : good, no defects - cryRtallinity : 0%
- d.ensity : 1. 33 g/cm3 Exa~lple 4:
A transparent sheet is produced analogously to Example 3 using a polyethylene terephthalate having the following proE~erties:
- SV (DCA) : 3173 - IV (DCA) : 2.23 dl/g - ~density : 1. 34 g/cm3 - crystallinity : 12%
- ~rystalline melting point Tm : 240~C
- crystallization temperature range 'Tc : 82~C to 240~C
- polydispersity MW/Mn : 3.66 - glass transition temperature : 82~C
204, 660 g/ml ~In : 55,952 g/mol The extrusion temperature is 274~C. The first calender rol:L ha~ a temperature of 50~C and the subsequent rolls have a temperature of 45~C. The take-off rate and the calender roll speed are 1.2 m/min.
- CA 02228364 l998-0l-30 The PET sheet produced has the following property profile:
- t.hickness : 15 mm - ~urface gloss, 1st side : 162 (measurement angle 20~) 2nd side : 159 - light transmission : 89.3%
- clarity : 98.9%
- haze : 5. 8%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5.1 kJ/m2 - cold formability : good, no defects - crystallinity : o%
- density : 1.33 g/cm3 Example 5:
A transparent sheet produced analogously to Example 2.
70% of polyethylene terephthalate from Example 2 are blended with 30% of this polyethylene terephthalate after recycling.
The transparent PET sheet produced has the following property profile:
- t:hickness : 6 mm - surface gloss, 1st side : 188 (measurement angle 20~) 2nd side : 186 - light transmission : 92.2%
- clarity : 99. 6%
- h.aze : 2.2%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-7 kJ/m2 - cold formability : good, no defects - crystallinity : o%
- density : 1.33 g/cm3 Exam.ple 6:
A transparent, amorphous sheet with a thickness of 3 mm which contains, as principal constituents, the polyethylene terephthalate from Example 1 and 1.0% by weight of the W stabilizer 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-hexyl)oxyphenol ( Tinuvin 1577 from Ciba-Geigy) is produced analogously to Example 1. Tinuvin 1577 has a melting point of 149~C and is thermally stable up to about 330~C.
1.0% by weight of the W stabilizer are incorporated into the polyethylene terephthalate directly by the raw-material producer.
The,~rying, extrusion and process parameters are selected as in Example 1.
The transparent PET sheet produced has the following property profile:
- thickness : 3 mm - surface gloss, 1st side : 208 (measurement angle 20~) 2nd side : 205 - light transmission : 92%
- clarity : 100%
- haze : 1.0%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects - c:rystallinity : 0%
- density : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the following properties:
- thickness : 3 mm - surface gloss, 1st side : 202 (measurement angle 20~) 2nd side : 200 - l:ight transmission : 91.7%
- c:Larity : 100%
- haze : 1.2%
- o~rerall discoloration ~E : 0.22 - dark discoloration ~L : -0.18 - red-green discoloration ~A : -0.08 - b:Lue-yellow discoloration ~B : 0.10 - surface defects (cracks, embrittlement) : none - ylellow value G : 4 - C:harpy impact strength an : no fracture - Izod notched impact strength ak : 4.1 kJ/m2 - cold formability : yood Example 7:
A transparent, amorphous sheet with a thickness of 3 mm is E~roduced analogously to Example 6. The W stabilizer 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxyphenol ( Tinuvin 1577) is metered-in in the form of a masterbatch. The masterbatch consists of 5% by weight of Tinuvin 1577 as active component and 95% by weight of the polyethylene terephthalate from Example 1.
Before the extrusion, 80% by weight of polyethylene terephthalate from Example 1 are dried for 5 hours at 170~C together with 20% by weight of the masterbatch. The extrusion and sheet production are carried out analogously to Example 1.
The transparent, amorphous PET sheet produced has the following property profile:
- t~hickness : 3 mm - surface gloss, 1st side : 204 (measurement angle 20~) 2nd side : 201 - l.ight transmission : 91.8%
- clarity : 100%
- haze : 0.9%
- surface defects : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-0 kJ/m2 - cold formability : good - crystallinity : 0%
- d.ensity : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing properties:
- thickness : 3 mm - surface glos~, 1st side : 200 (measurement angle 20~) 2nd side : 198 - light transmission : 91.7%
- clarity : 100%
- haze : 1.0%
- overall discoloration ~E : 0.24 - dark discoloration aL : -o . l9 - red-green discoloration ~A : -0.08 - blue-yellow discoloration ~B : 0.12 - surface defects (cracks, embrittlement) : none - yellow value G : 5 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-0 kJ/m2 - cold formLability : good ExamLple 8:
A transparent, amorphous sheet with a thickness of 6 mm contA;n;ng, as principal constituent, the polyethylene tere!phthalate described in Example 2 and 0.6% by weight of the W stabilizer 2,2'-methylenebis(6-(2~-bena:otriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol ( Tinuvin 360 from Ciba-Geigy), based on the weight of the polymer is produced analogously to Example 2. Tinuvin 360 has a melting point of 195~C and is thermally stable up t;o 250~C.
As i.n Example 6, 0.6% by weight of the W stabilizer are incorporated into the polyethylene terephthalate directly by t:he raw material producer.
The extrusion temperature is 280~C. The first calender roll has a temperature of 66~C and the subsecluent rolls have! a temperature of 60~C. The take-off rate and the cale!nder roll speed are 2.9 m/min.
The transparent PET sheet produced has the following property profile:
- thickness : 6 mm - surface gloss, 1st side : 187 ~measurement angle 20~) 2nd side : 185 - light transmission : 91.8%
- clarity : 99.6%
- haze : 2.5%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4- e kJ/m2 - cold formability : good, no defects - crystallinity : 0%
- density : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing properties:
- l_hickness : 6 mm - ~3urface gloss, 1st side : 182 (measurement angle 20~) 2nd side : 179 - :Light transmission : 90.9%
- clarity : 99.5%
- haze : 2.7%
- overall discoloration ~E : 0.56 - clark discoloration ~L : -0.21 - red-green discoloration A : -0.11 - blue-yellow discoloration ~B : +0.51 - çlurface defects ~cracks, embrittlement) : none - yellow value G : 6 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects Exa~lple 9:
A transparent, amorphous sheet is produced analogously to Example 8. The extrusion temperature is 275~C. The first calender roll has a temperature of 57~C and the sub-sec~lent rolls have a temperature of 50~C. The take-off rate and the calender roll speed are 1.7 m/min. The sheet is ~~tabilized as described in Example 3.
The transparent PET sheet produced has the following property profile:
- t:hickness : 10 mm - ç;urface gloss, 1st side : 168 I'measurement angle 20~) 2nd side : 167 - light transmission : 88.5%
- clarity : 99.2%
- haze : 3-95%
- ~~urface defects per m2 : none ~fisheyes, orange peel, bubbles, e!tc . ) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5.1 kJ/m2 - cold formability : good, no defects - crystallinity o%
- d.ensity : 1.33 g/cm3 Afte~r weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing propertie~~:
- thickness : 10 mm - surface gloss, 1st side : 164 (measurement angle 20~) 2nd side : 162 - light transmission : 88.2%
- clarity : 99.1%
- haze : 5.0%
- overall discoloration ~E : 0.47 - d.ark discoloration ~L : -0.18 - red-green discoloration AA : -0.09 - hlue-yellow discoloration ~B : +0.42 - ~urface defects (cracks, embrittlement) : none - yellow value G : 5 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.5 kJ/m2 - cold formability : good, no defect6 Comparative Example 1:
A transparent sheet is produced analogously to Example 1.
The polyethylene terephthalate employed has a stAn~Ard viscosity SV (DCA) of 760, which corresponds to an intrinsic viscosity IV (DCA) of 0.62 dl/g. The other properties are identical with the properties of the polyethylene terephthalate from Example 1 within the limits of measurement accuracy. The process parameters and the temperature were selected as in Example 1. As a consequence of the low viscosity, sheet production is impossible. The melt stability is inadequate, 80 that the melt collapses before cooling on the calender rolls.
Comparative Example 2:
A trensparent sheet is produced analogously to Example 2, also using the polyethylene terephthalate from Example 2.
The Eirst calender roll has a temperature of 98~C and the subsequent rolls each have a temperature of 92~C.
The sheet produced is extremely hazy. The light transmission, the clarity and the gloss are significantly reduced. The sheet exhibits surface defects and structures. The optical properties are unacceptable for a transparent application.
The sheet produced has the following property profile:
- thickness : 6 mm - surface gloss, 1st side : 95 (measurement angle 20~) 2nd side : 93 - light transmission : 74%
- clarity : 90%
- haze : 52%
- ~urface defects per m2 : bubbleR, (fisheyes, orange peel, bubbles, orange peel e!tc. ) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5-0 kJ/m2 - cold formability : good - crystallinity : approx. 8%
- density : 1. 34 g/cm3
Amorphous, transparent sheets having a thickness of from 1 to 20 mm are well known. These two~ n~ional struc-ture!s comprise amorphous, non-crystallizable thermoplastics.~Typical examples of such thermoplastics which can be converted into sheets are, for example, polyvinyl chloride (PVC), polycarbonate (PC) and poly-~methyl methacrylate (PMMA). These semifinished products are produced on so-called extrusion lines (cf. Polymer Werkstoffe, Volume II, Technologie 1, p. 136, Georg Thieme Verlag, Stuttgart, 1984). The pulverulent or granular raw material is melted in an extruder. After extrusion, the amorphous thermoplastics can easily be shaped via polishing stacks or other shaping tools as a consec~uence of their viscosity, which continuously increases with decreasing temperature. After shaping, amorphous thermoplastics then have adec~uate stability, i.e. a high viscosity, in order to be self-supporting in the calibration die. However, they are still sufficiently soft to be shaped by the die. The melt viscosity and inherent rigidity of amorphous thermoplastics is 80 high in the calibration die that the semifinished product does not collapse in the calibration die before cooling. In the case of easily decomposed materials, for example PVC, special processing aids, for example processing stabi-lize!rs against decomposition and lubricants against excessive internal friction and thus uncontrollable warming, are necessary during extrusion. External lubricants are necessary to prevent sticking to walls and rolls.
The processing of PMMA iB carried out using, for example, a vented extruder to enable removal of moisture.
The production of transparent sheets from amorphous thermoplastics sometimes requires expensive additives, which can migrate and can cause production problems owing to evaporations and surface coatings on the semifinished product. PVC sheets can be recycled only with difficulty or using special neutralization or electrolysis process-es. PC and PMMA sheets can likewise only be recycled withdifEiculty and only with 1088 or extreme impairment of the mechanical properties.
In addition to these disadvantages, PMMA sheets also have ext~emely poor impact strength and splinter on fracture or mechanical 10A~; ng. Furthermore, PMMA sheets are readily combustible, which means that they cannot be emp:Loyed, for example, for internal applications and in exhLbitions.
P ~ ~ and PC sheets furthermore cannot be shaped when cold; PMMA sheets disintegrate to form dangerous splin-ter~, while PC sheets undergo hairline cracking and stress whitening.
EP-A-O 471 528 describes a process for shaping an article from a polyethylene terephthalate (PET) sheet. The intrinsic viscosity of the PET employed is in the range from 0.5 to 1.2. The PET ~heet is heat-treated on both ~ides in the thermofilming mold in a temperature range between the glass transition temperature and the melting point. The shaped PET sheet is removed from the mold when the degree of crystallization of the shaped PET sheet is in the region of 25 to 50%. The PET sheets disclosed in EP-i~-O 471 528 have a thickness of from 1 to 10 mm. Since the thermoformed molding produced from the PET sheet is partially crystalline and thus no longer transparent and the surface properties of the molding are determined by the thermoforming process and by the thermoforming temE~erature and mold, it is unimportant what optical properties (for example gloss, haze and light tranLsmission) the PET sheets employed have. In general, the optical properties of these sheets are poor and in need of optimization.
US-A-3,496,143 describes the vacuum thermoforming of a 3 mm thick PET sheet whose degree of crystallization is said to be in the range from 5 to 25%. However, the crystallinity of the thermoformLed molding iB greater than 25%. Again, no rec~uirements regarding optical properties are made of these PET sheets. Since the crystallinity of the sheets employed is already between 5 and 25%, these sheets are hazy and non-transparent.
The object of the present invention is to provide an amorphous, transparent sheet having a thickness of from 1 to 20 mm which has both good mechanical and optical properties.
The good optical properties include, for examLple, high light transmission, high surface gloss, extremely low haze and high clarity.
The good mechanical properties include, inter alia, high impact strength and high breAk; ng strength.
In alddition, the novel sheet should be recyclable, in particular without 1088 of the mechanical properties, and have low combustibility 80 that it can also be employed, for example, for indoor applications and in exhibitions.
This object is achieved by a transparent, amorphous sheet having a thickness in the region of 1 to 20 mm which contains, as principal constituent, a crystallizable thermoplastic, wherein the crystallizable thermoplastic has a standard viscosity SV (DCA), measured in dichloroacetic acid in accordance with DIN 53728, in the range from 1800 to 6000.
The stAn~rd viscosity SV (DCA) of the crystallizable the~moplastic, measured in dichloroacetic acid in accordance with DIN 53728, iB preferably from 2000 to 500(), particularly preferably from 2500 to 4000.
The intrinsic viscoE~ity IV (DCA) is calculated from the stAr~rd viscosity SV (DCA) as follows:
IV (DCA) = 6.67 . 10-4 SV (DCA) + 0.118 The surface gloss, measured in accordance with DIN 67530 (mealsurement angle 20~), is greater than 120, preferably grealter than 130, the light transmission, measured in accordance with ASTM D 1003, is greater than 84%, pre~erably greater than 86%, and the haze of the sheet, meaEIured in accordance with ASTM D 1003, is less than 15%, preferably less than 11%.
The transparent, amorphous sheet contains, as principal conE~tituent, a crystallizable thermoplastic. Suitable cryE~tallizable or partially crystalline thermoplastics are, for example, polyethylene terephthalate, polybuty-lene terephthalate, cycloolefin polymers and cycloolefin copolymers, preference being given to polyethylene terephthalate.
For the purposes of the invention, the term crystal-lizalble thermoplastics is taken to mean - crystallizable homopolymers, - crystallizable copolymers, - crystalliza~le compounds, - crystallizable recyclate and - other variations of crystallizable thermoplastics.
For the purposes of the present invention, the term amorphous sheet is taken to mean a sheet which is non-crystalline, although the crystallizable thenmoplastic employed preferably has a crystallinity of from 5 to 65%, particularly preferably from 25 to 65%. Non-cry~talline or essentially amorphous means that the degree of crystallinity is generally less than 5%, preferably less than 2%, particularly preferably 0%.
An amorphous sheet of this type is essentially unoriented.
Processes for the preparation of the crystallizable then~oplastics are known to the person skilled in the art.
For example, polyethylene terephthalates are usually prepared by polyco~n~ation in the melt or by a two-step polycondensation in which the first step is carried out to a mean molecular weight - correspon~; ng to a mean intrinsic viscosity IV of from about 0.5 to 0.7 - in the melt and the further con~nRation is carried out by solid-state con~enRation. The polycon~enRation is gener-ally carried out in the presence of known polyco~nRa-tion catalysts or catalyst systems. In the solid-state condensation, PET chips are wanmed at temperatures in the range of from 180 to 320~C under reduced pressure or under a protective gas until the desired molecular weight has been reached.
The preparation of polyethylene terephthalate is desc1ribed in detail in a large number of patents, such as, for example in JP-A-60-139 717, DE-C-2 429 087, DE-A-27 07 491, DE-A-23 19 089, DE-A-16 94 461, JP-63-41 528, JP-62-39 621, DE-A-41 17 825, DE-A-42 26 737, JP-60-141 715, DE-A-27 21 501 and US-A-5,296,586.
Polyethylene terephthalates having particularly high molecular weights can be prepared by polycondensation of dicarboxylic acid/diol precondensates (oligomers) at elevated temperature in a liquid heat-transfer medium in the presence of conventional polycondensation catalysts and, if desired, coco~n~able modifiers if the liquid heat:-transfer medium is inert and free from aromatic moieties and has a boiling point in the range from 200 to 320'C, the weight ratio between dicarboxylic acicL/diol/precondensate ~oligomer) employed and liquid heat:-transfer medium is in the range from 20:80 to 80:20, and the polycondensation is carried out in the boiling reaction mixture in the presence of a dispersion stabilizer.
In the case of polyethylene terephthalate, measurement of the Charpy impact strength an (measured in accordance with.ISO 179/lD) of the sheet is preferably not accompa-nied. by fracture. In addition, the Izod notched impactstrength ak (measured in accordance with ISO 180/lA) of the sheet is preferably in the range from 2.0 to 8.0 kJ/m2, particularly preferably in the range from 4.0 to 6.0 kJ/m2.
The clarity of the sheet measured at an angle of less than 2.5~ (ASTM D 1003) is preferably greater than 96%, particularly preferably greater than 97%.
Polyethylene terephthalate polymers having a cry~talline melting point Tm~ as measured by DSC (differential scan-ning calorimetry) at a heating rate of 10~C/min, of from220~ to 280~C, in particular from 220~C to 260~C, prefer-ably from 230~C to 250~C, a crystallization temperature range Tc from 75~C to 280~C, preferably from 75~C to 260~C, a glass transition temperature Tg of from 65~C to 90~C and a density, measured in accordance with DIN 53479, of from 1.30 to 1.45 g/cm3 and a crystallinity of iErom 5 to 65%, are preferred polymers as starting mate!rials for production of the novel sheet.
The bulk density, measured in accordance with DIN 53466, is preferably from 0.75 to 1.0 kg/dm3, particularly preferably from 0.80 to 0.90 kg/dm3.
The polydispersity of the polyethylene terephthalate M[~,~/Mn, measured by GPC, is usually from 1.5 to 6.0, preferably from 2.5 to 6.0, particularly preferably from 3.0 to 5Ø
In a particularly preferred embodiment, the novel sheet is E~rovided with a W light stabilizer.
The concentration i8 preferably from 0.01 to 5% by weight base!d on the weight of the crystallizable thermoplastic.
Light, in particular the ultra-violet part of sunlight, i.e. having a wavelength in the range of 280 to 400 nm, initiates degradation processes in thermoplastics, resulting not only in a change in the visual appearance as a consecfuence of color change or yellowing, but also adversely affecting the mechanical-physical properties.
The inhibition of these photooxidative degradation processes is of considerable industrial and economic importance, since otherwise the potential uses of numer-OU8 thermoplastics are drastically limited.
Polyethylene terephthalates begin to absorb W light, for example, even at below 360 ~Lm, their absorption increases considerably below 320 nm and is very pronounced at belo 300 nm. The maximum absorption is between 280 and 300 nmL.
In t:he presence of oxygen, principally chain cleavage, but no crossl;nk;ng is observed. Carbon - oY;de, carbon dioxide and carboxylic acids represent the predominant photooxidation products in terms of amount. Besides dire!ct photolysis of the ester groups, consideration must also be given to oxidation reactions, which likewise result in the formation of carbon dioxide via peroxide free radicals.
The photooxidation of polyethylene terephthalates can also result, by elimination of hydrogen in the ~-position of t:he ester groups, in hydroperoxides and decomposition proclucts thereof, and associated chain cleavage (H. Day, D. ~l. Wiles: J. Appl. Polym. Sci 16, 1972, page 203).
W tabilizers and W absorbers as light stabilizers are chemical compounds which can engage in the physical and chem~ical processes of photoinduced degradation. Carbon black and other pigments can provide partial protection from, light. However, the substances are unsuitable for transparent sheets since they result is discoloration or a color change. For transparent, amorphous sheets, the only suitable compounds are organic and organometallic compounds which impart only an extremely weak color or color change, or none at all, in the thermoplastics to be stabilized.
Examples of suitable light stabilizers or W stabilizers are 2-hydroxybenzophenones, 2-hydroxybenzotriazoles, organonickel compounds, salicylic esters, cinnamic ester derivatives, resorcinol monobenzoates, oxanilides, hydroxybenzoic esters, sterically hindered amines and triazines, preference being given to 2-hydroxybenzotriazoles and triazines.
In a particularly preferred emlbodiment, the novel trans-parent, amorphous sheet contains, as principle constitu-ents, a crystallizable polyethylene terephthalate and from 0.01 to 5.0% by weight of 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxyphenol (structure in Fig. la) or from 0.01 to 5.0% by weight of 2,2'-methylene-bis(6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol (structure in Fig. lb). In a preferred emlbodiment, it is also possible to employ mixtures of these two W stabi-lizers or mixtures of at least one of these two W
stabilizers with other W stabilizers, where the total concentration of light stabilizers is preferably from 0.01 to 5.0% by weight, based on the weight of cryE~tallizable polyethylene terephthalate.
Weat:hering tests have shown that the novel W-stabilized sheets exhibit no yellowing, no embrittlement, no 1088 of glols on the surface, no cracking on the surface and no impaLirment of the mechanical properties even after use out~ide for from 5 to 7 years.
In addition, entirely unexpectedly, good cold formability without fracture, hairline cracking and/or stress whitening was observed, meAn;ng that the novel sheet can be ahaped and bent without the action of heat.
In addition, measurements showed that the novel sheet has low combustibility and low flammability, 80 that it is suitable, for example, for internal applications and in exhibitions.
Furthermore, the novel sheet can easily be recycled without environmental pollution and without 1088 of the mechanical properties, meAning that it is suitable, for example, for use as short-term advertising hoardings or other advertising articles.
In the W-stabilized embodiment, the sheet has improved weathering resistance and increased W stability. This means that the sheets are only damLaged to an extremely small extent, or not at all, by weathering and sunlight or by other W radiation, 80 that the sheets are suitable for external applications and/or critical internal applications.
The novel transparent, amorphous sheet can be produced, for example, by extrusion in an extrusion line.
An extrusion line of this type is shown diagrammatically in E'ig. 2. It essentially comprises - an extruder (1) as plastication unit, - a sheet die (2) as shaping tool, - a polishing stack/calender (3) as calibration die, - a cooling bed (4) and/or a roller conveyor (5) for aftercooling, - a take-off roll (6), - a separating saw (7), - an edge trimming device (9), and, if desired, - a stacking unit (8).
The process comprises drying the crystallizable thermo-pla~ltic if necessary, then melting the dry polymer in the extruder, if desired together with the W stabilizer, extruding the melt through a die, calibrating, smoothing and cooling the sheet in the polishing stack and then cutting the sheet to size.
The process for the production of the novel sheet iB
described in detail below using the example of polyethy-lene! terephthalate.
The polyethylene terephthalate is preferably dried for from 4 to 6 hours at from 160 to 180~C before extrusion.
The polyethylene terephthalate is then melted in the extruder. The temperature of the PET melt is preferably in the range from 250 to 320~C, it being possible for the temp~erature of the melt to be adjusted essentially both through the temperature of the extruder and through the residence time of the melt in the extruder.
If a light stabilizer is used, this can already have been adde!d by the producer of the raw material or be metered intc, the extruder during production of the sheet.
The light stabilizer is particularly preferably added via mast:erbatch technology, where the light stabilizer is fully dispersed in a solid carrier material. Suitable carrier materials are certain resins, the crystallizable thermoplastic itself, such as for example, polyethylene terephthalate, or alternatively other polymers which are sufficiently compatible with the crystallizable thermoplastic.
It i8 important that the particle size and bulk density of the masterbatch are similar to the particle size and bulk density of the crystallizable thermoplastic, BO that a homogeneous distribution and thus homogeneous W
stabilization can take place.
The melt then leaves the extruder through a die. This die is preferably a sheet die.
The PET melted by the extruder and shaped by a sheet die is calibrated, i.e. intensively cooled and smoothed, by smoothing calender rolls. The calender rolls can be arranged, for example, in an I-, F-, L- or S-shape (see Fig. 3).
The PET material can then be cooled on a roller conveyor, cut to size in width, cut into appropriate lengths and finally stacked.
The thickness of the PET sheet is determined essentially by t:he take-off unit, which is arranged at the end of the coo:Ling zone, the chill ~moothing) rolls, which are coupled to the take-off unit with respect to speed, and the conveying rate of the extruder on the one hand and the separation between the roll~ on the other hand.
The extruders employed can be either single-screw or twin-screw extruders.
The sheet die preferably comprises a collapsible die body, the lips and the restrictor bar for flow regulation over the width. To this end, the restrictor bar can be bent by means of tension and pressure screws. The thick-ness is set by adjusting the lips. It is important toensure a uniform temperature of the PET and of the lip, since otherwise the PET melt flows out through the vari.ous flow channels in different thicknesses.
The calibration tool, ie. the smoothing calender, gives the PET melt shape and ~i ~n~ions. This is achieved by freezing at below the glass transition temperature by cooling and smoothing. Shaping should not be carried out in this state, since otherwise surface defects would form in this cooled state. For this reason, the calender rolls are preferably driven jointly. The temperature of the cale!nder rolls must be lower than the crystalline melting point in order to avoid sticking of the PET melt. The PET
melt leaves the sheet die at a temperature of from 240 to 300~C
The first smoothing/chill roll is at a temperature of from 50~C to 80~C, dep~n~;ng on the output rate and sheet thickness. The second, somewhat colder roll cools the second or other surface.
In order to obtain a uniform sheet having excellent surface properties, it is essential here that the temperature of the first smoothing/chill roll is in the range from 50 to 80~C.
While the calibration unit freezes the sheet surfaces as smoothly as possible and cools the profile until it is rigid in shape, the aftercooling device lowers the temperature of the sheet virtually to room temperature.
The aftercooling can be carried out on a roller board.
The take-off rate should be matched accurately to the calender roll speed in order to prevent defects and thickness variations.
As ;~dditional equipment, the extrusion line for the production of the sheets can also include a separating saw for cutting the sheet to length, a side trimmer, a stacking unit and a monitoring station. The side or edge trimmer is advantageous since the thickness in the edge region may under certain circumstances not be uniform. At CA 02228364 l998-0l-30 the monitoring station, the thickness and optical proper-ties of the sheet are measured.
The surprising multiplicity of excellent properties makes the novel, transparent, amorphous sheet highly suitable for a multiplicity of different uses, for example for interior room panels, for exhibitions and exhibition articles, as displays, for signs, in the lighting sector, in shop fitting and shelf construction, as advertizing articles, as menu holders, as basketball backboards, as room dividers, as information panels and as brochure and news]paper stands.
In tlle W-stabilized embodiment, the novel sheet is also suitable for external applications, such as, for example, for greenhouses, roofing systems, external clA~;ng, covers, applications in the construction sector, illuminated advertising profiles, balcony clA~;ng and roof exit doors.
The invention is described in greater detail below with reference to working examples without this representing a limitation.
The i.ndividual properties are measured in accordance with the .Eollowing stAn~Ards or by the following processes.
Measurement methods Surface gloss:
The i3urface gloss is measured at a measurement angle of 20~ :in accordance with DIN 67530. The reflector value is measured as an optical parameter for the surface of a sheet. In accordance with the stAn~A~ds ASTM-D 523-78 and IS0 2813, an angle of incidence is set at 20~. A light beam hits the planar test surface at the set angle of incidence and is reflected or scattered thereby. The light beams hitting the photoelectronic receiver are indicated as a proportional electrical quantity. The mea~~ured value is dimensionless and must be given together with the angle of incidence.
Light transmission:
The light transmission is taken to mean the ratio between the total amount of transmitted light and the amount of incident light.
The light transmission is measured using a "Hazegard plu~~" instrument in accordance with ASTM D 1003.
Haze and clarity:
Haze is the percentage of transmitted light deflected from the incident ray bundle by an average of more than 2. 5~. The clarity is measured at an angle of less than 2.5~.
The haze and clarity are measured using a "Hazegard plus"
instrument in accordance with ASTM D 1003.
Surface defects:
The surface defects are determined visually.
Charpy impact strength an:
This parameter is determined in accordance with ISO 179/lD.
Izod notched impact strength ak:
The Izod notched impact strength ak is measured in accordance with ISO 180/lA.
Den~lity:
The density is determined in accordance with DIN 53479.
SV (DCA) and IV (DCA):
The stAn~Ard viscosity SV (DCA) i8 measured in accordance with DIN 53726 in dichloroacetic acid.
The intrinsic viscosity (IV) is calculated as follows from the standard viscosity (SV):
IV (DCA) = 6.67 x 10 4 SV (DCA) + 0.118.
Thermal properties:
The thermal properties, such as crystalline melting point T~, crystallization temperature range Tc, after- or cold-cryE~tallization temperature TCN and glass transition tem~)erature Tg are measured by differential sc~nn;ng calorimetry (DSC) at a heating rate of 10~C/min.
Molecular weight and polydispersity:
The molecular weights Mw and Mn and the resultant poly-disE~ersity MW/Mn are measured by gel permeation chroma-tography (GPC).
Weat;hering (on both sides), W stability:
The W stability is tested as follows in accordance with ISO 4892 test specification:
Test. instrument : Atlas Ci 65 Weather-O-meter Test. conditions : ISO 4892, i.e. artificial weathering Expc,sure time : 1000 hours, (per side) Exposure : 0.5 W/m2, 340 nm TemF~erature : 63~C
Rela.tive atmospheric humidity : 50%
Xenon lamp : inner and outer filters made of borosilicate Exposure cycles : 102 minutes W light, then 18 minutes W light with water spraying of the samples, then a further 102 minutes W light, etc.
Color change:
The color change of the samples after artificial weather-ing is measured in accordance with DIN 5033 using a spec-trophotometer.
CA 02228364 l998-0l-30 The following symbols are used:
~L: Difference in brightness +~L: The sample i8 brighter than the standard -~L: The sample i8 darker than the standard oA: Difference in the red-green region +~A: The sample is redder than the st~n~rd -~A: The sample is greener than the st~n~rd ~B: Difference in the blue-yellow region +~B: The sample is yellower than the st~n~rd -~B: The sample i8 bluer than the st~n~rd ~E: Overall color change ~E = ~L2 + ~A2 + ~B2 The larger the numerical deviation from the st~n~rd, the grea.ter the color difference.
Nume!rical values of 5 0. 3 can be neglected and mean that there is no significant color change.
Yellow value:
The yellow value G is a deviation from colorlessness towa.rd "yellow" and is measured in accordance with DIN
6167. Yellow values of 5 5 are invisible.
The examples and comparative examples below each relate to single-layer transparent sheets of various thicknesses prod.uced on the extrusion line described.
All sheets were weathered in accordance with ISO 4892 test. specification on both sides for 1000 hours per side using the Atlas Ci 65 Weather-O-meter and subsequentl test:ed for their mechanical properties discoloration, surf.ace defects, haze and gloss.
Exa~lple 1:
The polyethylene terephthalate from which the transparent sheet is produced has a standard viscosity SV (DCA) of 3490, which corresponds to an intrinsic viscosity IV
(DC~.) of 2.45 dl/g. The moisture content is ~ 0.2% and the density (DIN 53479) is 1.35 g/cm3. The crystallinity is 19%, and the crystalline melting point, according to DSC measurements, is 243~C. The crystallization tempera-ture range Tc is between 82~C and 243~C. The polydispersity MW/Mn of the polyethylene terephthalate is 4.3, where Mw is 225070 g/mol and Mn is 52400 g/mol. The glass transition temperature is 82~C.
Before extrusion, the polyethylene terephthalate is dried in a drier for 5 hours at 170~C and then extruded in a single-screw extruder at an extrusion temperature of 292~C through a sheet die onto a smoothing calender whose rolls are arranged in an S-shape, and smoothed to give a sheet with a thickness of 3 mm. The first calender roll has a temperature of 73~C and the subsequent rolls each have a temperature of 67~C. The take-off rate and the calender roll ~peed are 6.5 m/min.
Following aftercooling, the transparent PET sheet with a thickness of 3 mm is trimmed at the edges using separating saws, cut to length and stacked.
The transparent PET sheet produced has the following property profile:
- t]hickness : 3 mm - surface glo~s, 1st side : 215 (measurement angle 20~) 2nd side : 214 - light transmission : 94%
- clarity : 100%
- haze : 0.8%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects - crystallinity : 0%
- density : 1. 33 g/cm3 Example 2 A transparent sheet is produced analogously to Example 1 using a polyethylene terephthalate with the following properties:
- S'V (DCA) : 2717 - I'V (DCA) : 1. 93 dl/g - d,ensity : 1. 38 g/cm3 - c:rystallinity : 44%
- M~v : 175640 g/mol _ ~ : 245~C
- c:rystalline melting point Tm : 49580 g/mol - c:rystallization temperature range TC : 82~ C to 245~C
- polydispersity M,V/Mn : 3. 54 - glass transition temperature : 82~C
The extrusion temperature is 280~C. The first calander roll has a temperature of 66~C and the subse~auent rolls have a temperature of 60~C. The take-off rate and the calender roll speed are 2.9 m/min.
The transparent PET Qheet produced has the following property profile:
- thickness : 6 mm - ~urface gloss, 1st side : 192 (measurement angle 20~) 2nd side : 190 - light transmis~ion : 92.1%
- clarity : 99.8%
- haze : 2.0%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc) - C~harpy impact strength an : no fracture - Izod notched impact strength ak : 4.8 kJ/m2 - cold formability : good, no defects - c:rystallinity : o%
- density : 1.33 g/cm3 Example 3:
A transparent sheet is produced analogously to Example 2.
The extrusion temperature i8 275~C. The first calender roll has a temperature of 57~C and the subsequent rolls have a temperature of 50~C. The take-off rate and the calender roll speed are 1.7 m/min.
The PET sheet produced has the following property profile:
- t:hickness : 10 mm - surface glos~, 1st side : 173 (mea~urement angle 20~) 2nd side : 171 - light transmission : 88.5%
- clarity : 99.4%
CA 02228364 l998-0l-30 - haze : 3.2%
- ~urface defects per m2 : none Cfisheyes, orange peel, bubbles, ~!tC) - C'harpy impact strength an : no fracture - I:zod notched impact strength ak : 5-0 kJ/m2 - cold formability : good, no defects - cryRtallinity : 0%
- d.ensity : 1. 33 g/cm3 Exa~lple 4:
A transparent sheet is produced analogously to Example 3 using a polyethylene terephthalate having the following proE~erties:
- SV (DCA) : 3173 - IV (DCA) : 2.23 dl/g - ~density : 1. 34 g/cm3 - crystallinity : 12%
- ~rystalline melting point Tm : 240~C
- crystallization temperature range 'Tc : 82~C to 240~C
- polydispersity MW/Mn : 3.66 - glass transition temperature : 82~C
204, 660 g/ml ~In : 55,952 g/mol The extrusion temperature is 274~C. The first calender rol:L ha~ a temperature of 50~C and the subsequent rolls have a temperature of 45~C. The take-off rate and the calender roll speed are 1.2 m/min.
- CA 02228364 l998-0l-30 The PET sheet produced has the following property profile:
- t.hickness : 15 mm - ~urface gloss, 1st side : 162 (measurement angle 20~) 2nd side : 159 - light transmission : 89.3%
- clarity : 98.9%
- haze : 5. 8%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5.1 kJ/m2 - cold formability : good, no defects - crystallinity : o%
- density : 1.33 g/cm3 Example 5:
A transparent sheet produced analogously to Example 2.
70% of polyethylene terephthalate from Example 2 are blended with 30% of this polyethylene terephthalate after recycling.
The transparent PET sheet produced has the following property profile:
- t:hickness : 6 mm - surface gloss, 1st side : 188 (measurement angle 20~) 2nd side : 186 - light transmission : 92.2%
- clarity : 99. 6%
- h.aze : 2.2%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-7 kJ/m2 - cold formability : good, no defects - crystallinity : o%
- density : 1.33 g/cm3 Exam.ple 6:
A transparent, amorphous sheet with a thickness of 3 mm which contains, as principal constituents, the polyethylene terephthalate from Example 1 and 1.0% by weight of the W stabilizer 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-hexyl)oxyphenol ( Tinuvin 1577 from Ciba-Geigy) is produced analogously to Example 1. Tinuvin 1577 has a melting point of 149~C and is thermally stable up to about 330~C.
1.0% by weight of the W stabilizer are incorporated into the polyethylene terephthalate directly by the raw-material producer.
The,~rying, extrusion and process parameters are selected as in Example 1.
The transparent PET sheet produced has the following property profile:
- thickness : 3 mm - surface gloss, 1st side : 208 (measurement angle 20~) 2nd side : 205 - light transmission : 92%
- clarity : 100%
- haze : 1.0%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects - c:rystallinity : 0%
- density : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the following properties:
- thickness : 3 mm - surface gloss, 1st side : 202 (measurement angle 20~) 2nd side : 200 - l:ight transmission : 91.7%
- c:Larity : 100%
- haze : 1.2%
- o~rerall discoloration ~E : 0.22 - dark discoloration ~L : -0.18 - red-green discoloration ~A : -0.08 - b:Lue-yellow discoloration ~B : 0.10 - surface defects (cracks, embrittlement) : none - ylellow value G : 4 - C:harpy impact strength an : no fracture - Izod notched impact strength ak : 4.1 kJ/m2 - cold formability : yood Example 7:
A transparent, amorphous sheet with a thickness of 3 mm is E~roduced analogously to Example 6. The W stabilizer 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxyphenol ( Tinuvin 1577) is metered-in in the form of a masterbatch. The masterbatch consists of 5% by weight of Tinuvin 1577 as active component and 95% by weight of the polyethylene terephthalate from Example 1.
Before the extrusion, 80% by weight of polyethylene terephthalate from Example 1 are dried for 5 hours at 170~C together with 20% by weight of the masterbatch. The extrusion and sheet production are carried out analogously to Example 1.
The transparent, amorphous PET sheet produced has the following property profile:
- t~hickness : 3 mm - surface gloss, 1st side : 204 (measurement angle 20~) 2nd side : 201 - l.ight transmission : 91.8%
- clarity : 100%
- haze : 0.9%
- surface defects : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-0 kJ/m2 - cold formability : good - crystallinity : 0%
- d.ensity : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing properties:
- thickness : 3 mm - surface glos~, 1st side : 200 (measurement angle 20~) 2nd side : 198 - light transmission : 91.7%
- clarity : 100%
- haze : 1.0%
- overall discoloration ~E : 0.24 - dark discoloration aL : -o . l9 - red-green discoloration ~A : -0.08 - blue-yellow discoloration ~B : 0.12 - surface defects (cracks, embrittlement) : none - yellow value G : 5 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4-0 kJ/m2 - cold formLability : good ExamLple 8:
A transparent, amorphous sheet with a thickness of 6 mm contA;n;ng, as principal constituent, the polyethylene tere!phthalate described in Example 2 and 0.6% by weight of the W stabilizer 2,2'-methylenebis(6-(2~-bena:otriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol ( Tinuvin 360 from Ciba-Geigy), based on the weight of the polymer is produced analogously to Example 2. Tinuvin 360 has a melting point of 195~C and is thermally stable up t;o 250~C.
As i.n Example 6, 0.6% by weight of the W stabilizer are incorporated into the polyethylene terephthalate directly by t:he raw material producer.
The extrusion temperature is 280~C. The first calender roll has a temperature of 66~C and the subsecluent rolls have! a temperature of 60~C. The take-off rate and the cale!nder roll speed are 2.9 m/min.
The transparent PET sheet produced has the following property profile:
- thickness : 6 mm - surface gloss, 1st side : 187 ~measurement angle 20~) 2nd side : 185 - light transmission : 91.8%
- clarity : 99.6%
- haze : 2.5%
- surface defects per m2 : none (fisheyes, orange peel, bubbles, etc.) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4- e kJ/m2 - cold formability : good, no defects - crystallinity : 0%
- density : 1.33 g/cm3 Ater weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing properties:
- l_hickness : 6 mm - ~3urface gloss, 1st side : 182 (measurement angle 20~) 2nd side : 179 - :Light transmission : 90.9%
- clarity : 99.5%
- haze : 2.7%
- overall discoloration ~E : 0.56 - clark discoloration ~L : -0.21 - red-green discoloration A : -0.11 - blue-yellow discoloration ~B : +0.51 - çlurface defects ~cracks, embrittlement) : none - yellow value G : 6 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.6 kJ/m2 - cold formability : good, no defects Exa~lple 9:
A transparent, amorphous sheet is produced analogously to Example 8. The extrusion temperature is 275~C. The first calender roll has a temperature of 57~C and the sub-sec~lent rolls have a temperature of 50~C. The take-off rate and the calender roll speed are 1.7 m/min. The sheet is ~~tabilized as described in Example 3.
The transparent PET sheet produced has the following property profile:
- t:hickness : 10 mm - ç;urface gloss, 1st side : 168 I'measurement angle 20~) 2nd side : 167 - light transmission : 88.5%
- clarity : 99.2%
- haze : 3-95%
- ~~urface defects per m2 : none ~fisheyes, orange peel, bubbles, e!tc . ) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5.1 kJ/m2 - cold formability : good, no defects - crystallinity o%
- d.ensity : 1.33 g/cm3 Afte~r weathering for 1000 hours per side using the Atlas Ci 65 Weather-O-Meter, the PET sheet exhibits the foll.owing propertie~~:
- thickness : 10 mm - surface gloss, 1st side : 164 (measurement angle 20~) 2nd side : 162 - light transmission : 88.2%
- clarity : 99.1%
- haze : 5.0%
- overall discoloration ~E : 0.47 - d.ark discoloration ~L : -0.18 - red-green discoloration AA : -0.09 - hlue-yellow discoloration ~B : +0.42 - ~urface defects (cracks, embrittlement) : none - yellow value G : 5 - Charpy impact strength an : no fracture - Izod notched impact strength ak : 4.5 kJ/m2 - cold formability : good, no defect6 Comparative Example 1:
A transparent sheet is produced analogously to Example 1.
The polyethylene terephthalate employed has a stAn~Ard viscosity SV (DCA) of 760, which corresponds to an intrinsic viscosity IV (DCA) of 0.62 dl/g. The other properties are identical with the properties of the polyethylene terephthalate from Example 1 within the limits of measurement accuracy. The process parameters and the temperature were selected as in Example 1. As a consequence of the low viscosity, sheet production is impossible. The melt stability is inadequate, 80 that the melt collapses before cooling on the calender rolls.
Comparative Example 2:
A trensparent sheet is produced analogously to Example 2, also using the polyethylene terephthalate from Example 2.
The Eirst calender roll has a temperature of 98~C and the subsequent rolls each have a temperature of 92~C.
The sheet produced is extremely hazy. The light transmission, the clarity and the gloss are significantly reduced. The sheet exhibits surface defects and structures. The optical properties are unacceptable for a transparent application.
The sheet produced has the following property profile:
- thickness : 6 mm - surface gloss, 1st side : 95 (measurement angle 20~) 2nd side : 93 - light transmission : 74%
- clarity : 90%
- haze : 52%
- ~urface defects per m2 : bubbleR, (fisheyes, orange peel, bubbles, orange peel e!tc. ) - Charpy impact strength an : no fracture - Izod notched impact strength ak : 5-0 kJ/m2 - cold formability : good - crystallinity : approx. 8%
- density : 1. 34 g/cm3
Claims (26)
1. A transparent, amorphous sheet having a thickness in the range from 1 to 20 mm which contains, as principal constituent, a crystallizable thermoplastic, wherein a crystallizable thermoplastic has a standard viscosity SV (DCA), measured in dichloroacetic acid in accordance with DIN 53728, in the range from 1800 to 6000, with the exception of a sheet containing a crystallizable thermoplastic having a standard viscosity SV (DCA) of 1800 as principal constituent and a UV stabilizer.
2. A sheet as claimed in claim 1, wherein the standard viscosity is in the range from 2000 to 5000.
3. A sheet as claimed in claim 1, wherein the standard viscosity is in the range from 2500 to 4000.
4. A sheet as claimed in claims 1 to 3, wherein the surface gloss, measured in accordance with DIN 67530 (measurement angle 20°), is greater than 120.
5. A sheet as claimed in any one of the preceding claims, wherein the light transmission, measured in accordance with ASTM D 1003 is greater than 84%.
6. A sheet as claimed in any one of the preceding claims, wherein the haze, measured in accordance with ASTM D 1003, is less than 15%.
7. A sheet as claimed in one of the preceding claims, wherein the crystallizable thermoplastic used is selected from polyethylene terephthalate, polybutylene terephthalate, a cycloolefin polymer and a cycloolefin copolymer.
8. A sheet as claimed in claim 7, wherein the crystallizable thermoplastic used is polyethylene terephthalate.
9. A sheet as claimed in claim 8, wherein the polyethylene terephthalate contains recycled polyethylene terephthalate.
10. A sheet as claimed in claim 8 or 9, wherein the measurement of the Charpy impact strength an, measured in accordance with ISO 179/1D, is not accompanied by a fracture.
11. A sheet as claimed in any one of claims 8 to 10, wherein the Izod notched impact strength ak, measured in accordance with ISO 180/1A, is in the range from 2.0 to 8.0 kJ/m2.
12. A sheet as claimed in any one of claims 8 to 11, wherein the clarity, measured in accordance with ASTM D 1003 at an angle of less than 2.5°, is greater than 96%.
13. A sheet as claimed in any one of claims 8 to 12, wherein the polyethylene terephthalate has a crystalline melting point, measured by DSC at a heating rate of 10°C/min, in the range from 220° to 280°C.
14. A sheet as claimed in any one of claims 8 to 13, wherein the polyethylene terephthalate has a crystallization temperature, measured by DSC at a heating rate of 10°C/min, in the range from 75° to 280°C.
15. A sheet as claimed in at least one of claims 8 to 14, wherein the polyethylene terephthalate employed has a crystallinity in the range from 5 to 65%.
16. A sheet as claimed in any one of the preceding claims, which contains at least one UV light stabilizer.
17. A sheet as claimed in claim 16, wherein the concentration of the UV stabilizer is in the range from 0.01 to 5% by weight, based on the weight of the crystallizable thermoplastic.
18. A sheet as claimed in claim 16 or 17, wherein the UV
stabilizer is selected from 2-hydroxybenzotriazoles and triazines.
stabilizer is selected from 2-hydroxybenzotriazoles and triazines.
19. A process for the production of a transparent, amorphous sheet as claimed in any one of claims 1 to 18, which comprises melting the crystallizable thermoplastic in the extruder, extruding the melt through a die, calibrating, smoothing and cooling the extrudate in a polishing stack with at least two rolls, and cutting of the sheet to size, where the first roll in the polishing stack has a temperature in the range from 50 to 80°C.
20. A process as claimed in claim 19, wherein the crystallizable thermoplastic is melted in the extruder together with the UV stabilizer.
21. The process as claimed in claim 19 or 20, wherein the crystallizable thermoplastic is dried before melting in the extruder.
22. The process as claimed in claim 19 to 21, wherein the crystallizable thermoplastic is polyethylene terephthalate (PET).
23. The process as claimed in claim 22, wherein the polyethylene terephthalate is dried at from 160 to 180°C for from 4 to 6 hours before extrusion.
24. The process as claimed in claim 22 or 23, where the temperature of the PET melt is in the range from 250 to 320°C.
25. The process as claimed in any one of claims 20 to 24, wherein the UV stabilizer is added by master-batch technology.
26. The use of a transparent, amorphous sheet as claimed in any one of Claims 1 to 18 for internal and external applications.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19528336A DE19528336A1 (en) | 1995-08-02 | 1995-08-02 | Amorphous, transparent plate made of a crystallizable thermoplastic with high standard viscosity |
DE19528336.8 | 1995-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2228364A1 true CA2228364A1 (en) | 1997-02-13 |
Family
ID=7768478
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002228364A Abandoned CA2228364A1 (en) | 1995-08-02 | 1996-07-15 | Amorphous, transparent sheet of a crystallisable thermoplastic having high standard viscosity |
Country Status (16)
Country | Link |
---|---|
EP (1) | EP0842039A1 (en) |
JP (1) | JPH11510112A (en) |
KR (1) | KR19990036024A (en) |
CN (1) | CN1196698A (en) |
AU (1) | AU6699096A (en) |
BG (1) | BG102212A (en) |
BR (1) | BR9610186A (en) |
CA (1) | CA2228364A1 (en) |
CZ (1) | CZ30098A3 (en) |
DE (1) | DE19528336A1 (en) |
HU (1) | HUP9802435A2 (en) |
NO (1) | NO980393L (en) |
OA (1) | OA10662A (en) |
PL (1) | PL324868A1 (en) |
TW (1) | TW355718B (en) |
WO (1) | WO1997004948A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19535180A1 (en) * | 1995-09-22 | 1997-03-27 | Hoechst Ag | Use of thermoplastic, amorphous polyethylene terephthalate plates in refrigeration systems |
US6063495A (en) * | 1998-04-23 | 2000-05-16 | Hna Holdings, Inc. | Polyester fiber and methods for making same |
US5959066A (en) * | 1998-04-23 | 1999-09-28 | Hna Holdings, Inc. | Polyesters including isosorbide as a comonomer and methods for making same |
US6025061A (en) * | 1998-04-23 | 2000-02-15 | Hna Holdings, Inc. | Sheets formed from polyesters including isosorbide |
US5958581A (en) * | 1998-04-23 | 1999-09-28 | Hna Holdings, Inc. | Polyester film and methods for making same |
US6140422A (en) * | 1998-04-23 | 2000-10-31 | E.I. Dupont De Nemours And Company | Polyesters including isosorbide as a comonomer blended with other thermoplastic polymers |
US6063465A (en) * | 1998-04-23 | 2000-05-16 | Hna Holdings, Inc. | Polyester container and method for making same |
US6063464A (en) * | 1998-04-23 | 2000-05-16 | Hna Holdings, Inc. | Isosorbide containing polyesters and methods for making same |
US6126992A (en) * | 1998-04-23 | 2000-10-03 | E.I. Dupont De Nemours And Company | Optical articles comprising isosorbide polyesters and method for making same |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK120505B (en) * | 1964-12-03 | 1971-06-07 | Glanzstoff Ag | Process for the preparation by the vacuum deep drawing method of moldings of polyethylene terephthalate. |
CA965895A (en) * | 1969-10-09 | 1975-04-08 | Herbert F. Kuhfuss | Transparent crystalline polyester film |
CH550060A (en) * | 1972-03-01 | 1974-06-14 | Ciba Geigy Ag | PROCESS FOR MANUFACTURING POLYESTER DEEP-DRAWING MOLDED PARTS. |
US3950301A (en) * | 1974-08-01 | 1976-04-13 | General Electric Company | Light stabilized polyester resin composition |
US4230656A (en) * | 1975-10-23 | 1980-10-28 | Allied Chemical Corporation | Transparent sheets and containers formed from polycarbonate-polyester blends and formation thereof |
DE2928055A1 (en) * | 1978-07-12 | 1980-01-31 | Eastman Kodak Co | METHOD FOR IMPROVING THE RESISTANCE OF POLYESTER MOLDED BODIES TO DEGRADATION BY U.V. LIGHT |
JPS57212053A (en) * | 1981-06-23 | 1982-12-27 | Nippon Sheet Glass Co Ltd | Laminated panel |
JP2918616B2 (en) * | 1990-03-27 | 1999-07-12 | ポリプラスチックス株式会社 | Transparent polyester container and method for producing the same |
IE68430B1 (en) * | 1990-08-12 | 1996-06-12 | Polysheet Ireland Ltd | A method and apparatus for forming an article of PET material |
-
1995
- 1995-08-02 DE DE19528336A patent/DE19528336A1/en not_active Withdrawn
-
1996
- 1996-07-15 PL PL96324868A patent/PL324868A1/en unknown
- 1996-07-15 CN CN96197028A patent/CN1196698A/en active Pending
- 1996-07-15 HU HU9802435A patent/HUP9802435A2/en unknown
- 1996-07-15 CZ CZ98300A patent/CZ30098A3/en unknown
- 1996-07-15 JP JP9507164A patent/JPH11510112A/en active Pending
- 1996-07-15 CA CA002228364A patent/CA2228364A1/en not_active Abandoned
- 1996-07-15 AU AU66990/96A patent/AU6699096A/en not_active Abandoned
- 1996-07-15 WO PCT/EP1996/003089 patent/WO1997004948A1/en not_active Application Discontinuation
- 1996-07-15 BR BR9610186A patent/BR9610186A/en not_active Application Discontinuation
- 1996-07-15 EP EP96927002A patent/EP0842039A1/en not_active Withdrawn
- 1996-07-15 KR KR1019980700689A patent/KR19990036024A/en not_active Application Discontinuation
- 1996-07-30 TW TW085109483A patent/TW355718B/en active
-
1998
- 1998-01-28 BG BG102212A patent/BG102212A/en unknown
- 1998-01-29 NO NO980393A patent/NO980393L/en unknown
- 1998-02-02 OA OA9800018A patent/OA10662A/en unknown
Also Published As
Publication number | Publication date |
---|---|
OA10662A (en) | 2002-11-20 |
JPH11510112A (en) | 1999-09-07 |
DE19528336A1 (en) | 1997-02-06 |
HUP9802435A2 (en) | 1999-02-01 |
PL324868A1 (en) | 1998-06-22 |
WO1997004948A1 (en) | 1997-02-13 |
TW355718B (en) | 1999-04-11 |
AU6699096A (en) | 1997-02-26 |
EP0842039A1 (en) | 1998-05-20 |
NO980393D0 (en) | 1998-01-29 |
CZ30098A3 (en) | 1998-07-15 |
BG102212A (en) | 1998-10-30 |
NO980393L (en) | 1998-01-29 |
KR19990036024A (en) | 1999-05-25 |
CN1196698A (en) | 1998-10-21 |
BR9610186A (en) | 1999-07-06 |
MX9800940A (en) | 1998-10-31 |
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Legal Events
Date | Code | Title | Description |
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FZDE | Discontinued |