CA1037672A - Polyester yarn production - Google Patents
Polyester yarn productionInfo
- Publication number
- CA1037672A CA1037672A CA146,417A CA146417A CA1037672A CA 1037672 A CA1037672 A CA 1037672A CA 146417 A CA146417 A CA 146417A CA 1037672 A CA1037672 A CA 1037672A
- Authority
- CA
- Canada
- Prior art keywords
- yarn
- filaments
- denier
- quenching
- uster
- 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.)
- Expired
Links
- 229920000728 polyester Polymers 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 238000010791 quenching Methods 0.000 claims abstract description 49
- 238000000034 method Methods 0.000 claims abstract description 24
- 230000000171 quenching effect Effects 0.000 claims abstract description 21
- 238000001816 cooling Methods 0.000 claims abstract description 9
- 238000002074 melt spinning Methods 0.000 claims abstract description 3
- 238000009987 spinning Methods 0.000 claims description 34
- 229920000642 polymer Polymers 0.000 claims description 12
- 238000001125 extrusion Methods 0.000 claims description 9
- -1 polyethylene terephthalate Polymers 0.000 claims description 8
- 230000007774 longterm Effects 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 4
- 230000008018 melting Effects 0.000 claims description 4
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 4
- 230000001419 dependent effect Effects 0.000 claims description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 3
- 208000012886 Vertigo Diseases 0.000 claims 2
- 230000000704 physical effect Effects 0.000 abstract description 5
- 239000000112 cooling gas Substances 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 6
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000009977 dual effect Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- IDXQLFFTZPPEPW-UHFFFAOYSA-N C(CCCCCCC(=O)O)(=O)O.C(CCCC(=O)O)(=O)O Chemical compound C(CCCCCCC(=O)O)(=O)O.C(CCCC(=O)O)(=O)O IDXQLFFTZPPEPW-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241001282736 Oriens Species 0.000 description 1
- 101100083192 Streptomyces coeruleorubidus pacX gene Proteins 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 229960004838 phosphoric acid Drugs 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
- D01D5/088—Cooling filaments, threads or the like, leaving the spinnerettes
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/902—Reinforcing or tyre cords
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/903—Sewing threads
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/298—Physical dimension
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
ABSTRACT
A method and apparatus are disclosed for the production of a novel industrial polyester filament yarn of improved uniformity wherein a plurality of filaments are melt-spun into a heated zone coupled with controlled cooling.
The yarn produced has improved long and short term Uster uniformity and improved uniformity of physical properties, particularly breaking strength, as shown by a reduced standard deviation of breaking strength. The yarn is produced by melt spinning into a heated zone which maintains the filaments molten for intervals below the spinneret face and subsequently quenching the filaments with a radial outflow of cooling gases, thereby producting a low birefringence yarn which is capable of being drawn at high draw ratios to high tenacities.
A method and apparatus are disclosed for the production of a novel industrial polyester filament yarn of improved uniformity wherein a plurality of filaments are melt-spun into a heated zone coupled with controlled cooling.
The yarn produced has improved long and short term Uster uniformity and improved uniformity of physical properties, particularly breaking strength, as shown by a reduced standard deviation of breaking strength. The yarn is produced by melt spinning into a heated zone which maintains the filaments molten for intervals below the spinneret face and subsequently quenching the filaments with a radial outflow of cooling gases, thereby producting a low birefringence yarn which is capable of being drawn at high draw ratios to high tenacities.
Description
~3767A~
BACKGROUND OF THE INVENTION
In the production of polyester industrial yarn, often referred to as heavy denier continuous filament yarn, it has often been the practice to produce undrawn filaments of low birefringence such that high draw ratios can subsequently be utilized, thereby obtaining the highest degree of mole-cular orientation and consequently high tenacities. Such high orien~ation contributes to the high tenacity of the resulting fibers-. It was previously discovered that polyester fibers of low birefringence can be most highly ; oriented in subsequent drawing steps, but that as filament spinning speeds increase, birefringence tended to increase because of the induced orientation of the filament which occurs in the rapid takeup of the yarn. Thls results in increased pulling tensions on the yarn in the spinning column, i.e. in-creases in column draw down. To alleviate the draw down in the column, vari-ous procedures have been incorporated into the spinning, including higher extrusion pressures and means for maintaining the filaments molten for a period of time after extrusion. The filaments on quenching and drawing, while achieving high tenacities and modulus and desirable elongations, are found to be deficient in uniformity as measured in percent Uster. This results in a ~igher standard deviation for the physical properties, such as breaking strength, which is of most critical importance to industrial yarn.
This invention seeks to provide a method for producing a heavy denier industrial polyester yarn of improved uniformity of physical properties.
This invention further seeks to provide apparatus for spinning such polyester filament yarns.
This invention further seeks to provide a heavy denier industrial polyester filament yarn of high tenacity, improved long and short term percent Uster values and lower standard deviation in breaking strength.
DESCRIPTION OF THE INVENTION
In accordance with the invention, a method is provided for producing an industrial polyester filament yarn of improved uniformity comprising melt ~)37~
spinning a plurality of filaments at an extrusion temperature above the poly- -mer melting point into a heated zone maintained at a temperature of 260 - 460 degrees centigrade, maintaining said filaments in said heated zone for fila-ment travel distance of about 6 to 24 inches and hence, immediately passing said filaments about a gaseous quenching zone, directing quenching gases onto said filaments in a radial outward flow direction, said quenching gas being maintained at a temperature of about 15 to 50 degrees centigrade in a gaseous volume of about 20 to 130 standard cubic feet per minute to provide a con-trolled cooling of said filaments and taking said filaments up as a yarn of improved Uster uniformity.
According to this invention there is provided a heavy denier poly-ester filament yarn having a tenacity of more than 7.0 grams per denier, a long and short term percent Uster of less than 1.5, a tensile factor of more than 28, and a breaking strength standard deviation of less than 0.20 grams per denier as measured in yarns across a beam.
According to this invention there is further provided a method for producing an industrial polyester filament yarn of improved uniformity com-e prising melt spinning a plurality of filaments at an extrusion temperature above the polymer melting point into a heated zone maintained at a tempera-ture of about 260 to 460 degrees centigrade, and maintaining said filaments in said heated zone for a filament travel distance of about 6 to 24 inches, and hence immediately passing said filaments through a gas quenching zone, directing quenching gas onto said filaments in a radial outflow direction, said quenching gas being maintained at a temperature of 15 to 80 degrees centigrade and at a flow of 20 to 130 standard cubic feet per minute to pro-vide a controlled cooling of said filaments and taking up said filaments as a yarn of improved Uster uniformity.
The heavy denier industrial polyester filament yarn produced in accordance ~ith this invention has a denier ~ 3 ~
lQ376~Z
per filament of 3 to 20, a tenacity of more than 7.0 grams per denier, a long and short term percent Uster of less than 1.5, and more preferably a long term percent Uster of less than 1.0, a tensile factor (TEl/2) of more than 28 and a breaking strength standard deviation of less than 0.20 grams per denier as measured in yarns across a beam.
The improved uniformity of the yarn is achieved primarily through the utilization of controlled temperature conditions from immediately adjacent to the extrusion point to the cooling of the ilaments to a temperature below their second order transition temperature. The improvement is not only highly pronounced in Uster uniformity, but also in reduction in the average standard deviation of physical properties, particularly tensile strength. It is also noticeable in the reduction of both major and minor beaming defects as noted by Lindley defect counting at beaming.
DETAI LS OF T~IE INVENTION
The invention will be more ully described by reference to the drawings wherein:
FIG, 1 is a front elevational and partial schematic ~3q~
of the apparatus of the present invention showing more particularly the relationship of the extrusion heated zone and quenching apparatus in a spinning column;
FIG. 2 is a graph which illustrates the relationship between the quenching distance from the spinneret face as it relates to long term Uster values and tensile factor (TE )i FIG. 3 is a graph which relates long term Vster, elongation, tensile factor (TEl/ ) and tenacity wlth various quench gas flow rates.
Referring more particularly to FIG. 1, the schematic drawing of spinning pack 10 is representative of a standard polyester pack which includes final filtration means for the polymer and 8 spinneret with a pre-selected number of holes for the extrusion of polymer. The polymer conveyed to the pack is maintained at a spinning temperature whiah is nor-mally comfortably above the melting temperature of the poly-mer, i.e. about 257 degrees centigrade for polyethylene tere-phthalate. Thus, spinning temperatures are normally in the range of about 290 to 310 aegrees centigrade. The spinneret utilized is selected in accordance with the denier and filament count of the yarn being produced. If desired, one or more yarns can be spun from a single pack in a single column as illustrated in the drawing.
The spinning speed varies with the particular process and fiber type being spun, but generally is in the range of 2,000 to 10,000 feet per minute or more at wind up in a spin-draw process.
The molten polymer, as it is extruded from pack 10, immediately enters a heated zone which is maintained at an elevated temperature by a heated cylindrical shroud 12 which ~0376~Z
preferably is positioned adjacent to pacX lO and extends downwardly into the spinning column for a distance of about 6 to 24 inches. The shroud has an internal diameter of sufficient size to permit safe passage of the fila-ments therethrough without danger of contact with the ' heated shroud. Conveniently, leeway of one to several inches of distance is provided between the outside filament travel line and the inside diameter of the shroud. The shroud is heated preferably by internal heating means such as electrical resisters, circulating fluids or the like conventional heating means to produce an internal surface temperature on the shroud in the range of 260 degrees to 460 degrees centigrade, and more preferably 300 degrees to 360 degrees centigrade. Such shroud tempera-tures provide a heated zone of temperatures slightly less than the surface temperature, but because of heat radiated from the spinning pack and molten extrudate, a temperature near that of the shroud is readily maintained. The exact temperature utilized is primarily dependent upon the size of the shroud, distance away from the filaments, heat loss from the shroud area, filament denier, polyester type and the like considerations. The temperature selected i8 one sufficient to maintain the as-spun polymer in a molten condition as it passes through the shroud area.
Immediately adjacent to the lower section of heated shroud 12 is outflow quench stick 14. Quench stick 14 is centered among the filaments and positioned by means of positioning guide ~piece pin)16 in a central location under the pack and spinneret. The filaments are guided down the quench stick so as not to come in contact there-~Lo376r~z with, but to spread the filaments uniformly around the quench stick. Quench stick 14 is positioned by ~eans of positioning guide 16 and spacer 18, so as to conveniently position each quench stick in the same location in a plural-ity of packs and spinning columns.
The quench stick preferably extends into the area of the heated shroud so as to provide a controlled cooling immediately as the filaments exit from the shroud. As will be appreciated by those skilled in the art, the rapid passage of fibers down the spinning column creates a downward draft of convection currents which tends to carry both the heat of the shroud and the cooling effect of the quench gases downwardly along the filament path o travel. There-fore, by utilizing the preferred quench stick positioning, the most desirable control of cooling is obtained.
The quench stick is preferably made of a porous material, such as ceramic, or sintered metal in a manner which provides a predetermined, even flow of air throughout the length and circumference of the stick. Such quenching sticks are commercially available in a variety of porosities suitable cor this application.
The air flow through the quench stick afEects the quality of the yarn produced and therefore, for a given spinning process a preferred gas flow, e.g. air, results in the most desirable spinning. It has been found that the air flow as measured in standard cubic feet per minute (SCFM) is proportional to the total denier of the yarn being spun and the spinning speed with higher total deniers and higher speeds requiring higher flow rates. For instance, the air flow is in a gas volume of about 20 to 130 SCFM
1~3'76~Z
with the preferred air flow in the range of about 20 to 60 SCFM. This is more clearly illustrated in FIG 3 which . .
relates changes in yarn physical properties with changes in air flow rates for a 1000/192 industrial yarn. It will be noted from this graph that the best results for this yarn at a 5.8 draw ratio is an air flow of about 40 SCFM.
Ambient quench gas temperatures have been found to be satisfactory, although in the compression of the gas, a temperature rise is often unavoidable. Therefore, under certain climatic conditions, it may be desirable to utilize a quench gas temperature within the range of 15 to 80 degrees centigrade, and more preferably about 25 to 50 degrees centigrade.
The quench stick length and diameter are selecked in accordance with the spinning speed, filament count, total denier, air flow desired and the like parameters, so as to provide controlled cooling of the yarn in the manner des-cribed herein. In a preferred embodiment, such quench sticks are normally of a diameter of about 1-1/2 to 4 inches and a length of about 8 to 20 inches.
Upon quenching the filaments, a spin finish is applied and the filaments are drawn and taken up on a package as a finished yarn or alternatively, taken upon a package in an undrawn state. In accordance with the present invention, it is preferable to split the threadline into two or more portions and apply the finish separately to each of the portions, such as by utilizing dual finish rolls 20. It has been found that it is particularly important to insure that the as-spun filaments do not touch any portion of the splnning column or apparatus until the application of 1~376~Z
the spin finish. Therefore, the split threadline and multiple or dual finish applicators are particularly im-~portant to insure that stray filaments do not come in contact with items such as the quench stick or air supply therefor.
As is often desired in using a split th:readline quench, the yarns may be retained separately and taken up or drawn separately. Alternatively, the split threadlines can be recombined at the drawing stage and taken up as a single yarn.
While it has been described that the yarns may be taken up on a package after the ap~lication of the spin finish, it is normally most desirable in a modern poly-ester production plant to immediately thereafter draw the yarn in one or more stages under known drawing conditions and heat set and/or relax the yaxn if desired prior to ~-taking the yarn up as a finished product. In industrial yarns, with which the present invention is primarily con-cerned, yarns are normally drawn at the highest achievable draw ratio which can be successfully processed in continuous operation. Thus, draw ratios in excess of 3, and more preferably on the order of 4 to about 6.5 to 1 are preferably utilized with multi-stage drawing being the preferred method of operation. The actual total draw ratio utilized is dependent upon the as-spun birefringence which, as noted above, is preferably as low as possible so as to achieve the highest draw ratio. Thus, such drawn yarns have tenacities in excess of 7 grams per denier, and more pre-ferably in the range of 8 to 11 grams or more per denier.
Tensile factor, i.e. TEl/2, is determined by 0 multiplying the tenacity in grams per denier times the ~37~qZ
square root of thejelon~ation at break. The yarns produced in accordance with the present method have tensile factors greater than 28 and more preferably, greater than 30.
Typically, the range of tensile factor is between 28 and 40.
The yarns of the present invention are preferably high tenacity industrial yarns such as tire yarns, conveyer belt yarns, sewing threads and the like, having denier per filaments of at least 1.0 and more preferably 3.0 to 20 or more. Total drawn deniers of such yarns range from about 100 to 10,000 with most yarns having total deniers of about 500 to 3,000. All of such yarns are considered to be heavy deniers.
As has been noted above, the long, i.e. in~rt, and the short, i.e. normal, percent Uster of yarns produced in accordance with the present invention is less than 1.5, and more preferably less than 1Ø The Uster is measured in accordance with Uster Evenness Tester, Model GGPC 10, in accordance with the manufacturer's recommended procedure, with the proviso that a feed tension of 25 grams is utili~ed on the yarn and a yarn feed rate of 25 yards per minute to the tester for at least three minutes. The rotofil setting of the tester is placed at number 3 for convention-al industrial yarns.
The breaking strength standard deviation () of yarns produced in accordance with the present invention is also substantially improved over previous industrial yarn processes. Such breaklng strength standard deviation is less than 0.20 grams per denier between position-to-position yarns and most preferably, less than 0.15 grams per denier, when measured in accordance with ASTM Method ~1~37~t7~ :
D885-68. The standard deviation is calculated based upon the testing of at least lS samples of yarn from position-to-position across production machines. It is often more convenient to measure the standard deviation of the yarns across a beam and such yarns fall within the specified range.
With the improved uniformity of the yarns pro-duced in accordance with the present invention, marked improvement will be noted in major and minor defects in beaming as compared to previously produced yarns.
The preferred polyesters used in this invention are obtained from terephthalic acid via any of the known poly-merization routes, i.e. ester interchange, direct esteri~ -fication, ~HET and the like, wherein at least 75~ of the recurring structural units of the polyester are glycol terephthalate structural units. The polymers used are fiber forming and preferably of an intrinsic viscosity of at least 0.45 up to 1.00 or more as measured in 8 orthochlorophenol at 25 degrees centigrade.
As conditions for heat setting, a temperature of 120 - 300 degrees centigrade and a time of 0.01-2 secQnds may be adopted.
While polyester polymer used in the percent inven-tion preferably contains at least 75 mol percent of ethylene terephthalate units, other acid components, when used, are a dibasic acid such as phthalic acid, isophthalic acid, adipic acid, oxalic acid, sebacic acid, suberic acid glutaric acid, pimelic acid, fumaric acid and succinic acid. A polymerization degree modifier like propionic acid may be used. As alcohol components, a divalent alcohol such as polymethylene glycol ~37617Z
having 2-10 carbon atoms (trimethylene glycol and butylene glycol) and cyclohexyl dimethanol may be cited. And they may contain a small amount of the following compound as a modifier, 5-oxydimethyl isophthalate, 5-oxydimethyl hexahydroiso-phthalate, benzene-1,3,5-tricarboxylic acid, para-carbo-methoxy phenyl diethyl phosphonate,3,5~ dicarboxy phenyl diethyl phosphonate, pentaerythritol, glycerol, glucose,phos-phoric acid, triphenyl phosphate, tri-p-carbometho~y phenyl phosphate, triphenyl phosphinate, triphenyl arsenite, tri-capryl borate, sorbitol trimesic acid, diethylene glycol and the like.
The following e`xamples illustrate certain pre-ferred embodiments of the present invention. Unless other-wise indicated, all parts and percentages used herein are by weight and all temperatures are in degrees centigrade.
EXAMPLE I
Polyethylene terephthalate was produced in accord-ance with a continuous polymerization process to provide a molten polymer having an intrinsic viscosity of O.B8, as measured in the final product, which was fed directly to a spinning pack and apparatus in accordance with FIG.l.
The polymer was spun at a spinning temperature of 297 to 300 degrees centigrade at a rate of 30.9 pounds per hour. The yarn spun was 1000/192 yarn utilizing a split threadline wherein one-half the filaments were split on either side of the quench stick A spin ~inish was applied utilizing dual finish applicator rolls and the yarn recombined for drawing in a spin-draw process. The yarn was drawn to a total draw ratio of 5.8.
During the spinning of the yarn, various para-1(~376~2 meters with respect to the outflow quench system and heated shroud were changed to determine the effect on the yarn properties. In accordance with FIG.2, the distance of the initiation of outflow quench from the spinning pack was varied from 6 inches to 16 inches, and the effect on tensile factor and percent Uster (inert), i.e. long term, was measured. The spinning was carried out at a set quench air flow of 30 SCFM. ~he results are graphically illustrated in FIG. 2.
The experiments were continued in the same manner with the spinning at a rate of 30.9 pounds per hour, the outflow quench distance being approximately 10 inches from the spinning pack, quench air temperature at about 40 degrees centigrade, the pack to outflow spacer distance being three-quarters of an inch, and the shroud temperature at 320 degre~s centigrade. With these pre-set conditions, the air flow was varied from 20 SCFM to 60 SCFM to determine the effect on percent Uster (inert), tensile factor, i.e. TEl/2, percent elongation at break (E), and tenacity in grams per denier (gpd). These effects are shown graphically in FIG.3.
While variations in the noted spinning para-meters have the noted effects on the yarn quality and spinning performance, it should be noted that this Ex-ample illustrated the preferred parameters for 1000/192 ; yarn in a spin-draw process. As will be appreciated by those skilled in the art, changes in the polymer being spun, the particular denier thereof, and the like, will affect the preferred operating conditions such as 1037~qZ
by shifting the various curves in the graphs of FIGS. 2-3 to the right or left as the case may be.
Such changes in these spinning parameters to obtain the most preferred conditions for a given yarn will be readily ascertained from the guidance and exempli-fication given herein.
The process of the present invention was com-pared to standard production spinning processes which , included the use of a heated shroud at a temperature of 320 degrees centigrade, but without an outflow quench, The spinning process utilized 0.88 intrinsic viscosity polyethylene terephthalate, a spinning rate of about 31 pounds per hour, a draw-spin procedure at a total draw ratio of 6.08 to produce a 1020/192 yarn. The percent Uster of standard production yarn utilizing the heated shroud was then compared with the process of the present invention wherein the heated shroud was utilized at the same temperature but combined with the outflow quench of the air flow of 40 SCFM, a quench air temperature of about 40 degrees centigrade, and a quench distance of about 10 inches from the spinning pack. All other conditions were the same as the com-parison. The standard production yarn had a p,ercent Uster (inert) of 2.3, whereas the yarn of the present invention had a percent Uster (inert) of 0.5.
The breaking load of the yarn of the present invention was 9072 grams. Standard deviation of break-ing load in position-to-position, as measured in yarns across a beam was 0.15 grams per denier. The standard ~376~;~Z
production yarn had a breaking load of 9096 grams, with a standard deviation in breaking load in position-to-position, as measured in yarns across a beam, of 0.21 grams per denier. The number of major and minor defects in beam of these yarns was found to be signi-ficantly reduced in the yarns of the present invention compared to the standard production. .
In the same manner as Example 2, 1330/192 yarn was produced in accordance with the present invention and compared to standard production yarn which utilized a heated shroud. The percent Uster ~inert) was 0.8 for yarn of the present invention. Standard production yarn had a percent Uster (inert) of 2Ø The standard deviation of the yarn of the present invention was 0.14 grams per denier, whereas the standard deviation of standard production yarn was 0.18 as measured in yarns across the beam.
The tenacity of the yarn of the present in-vention was 8.90 and TE / was 31.3. The tenacity of standard production was 8.84 and TE / was 30.2.
BACKGROUND OF THE INVENTION
In the production of polyester industrial yarn, often referred to as heavy denier continuous filament yarn, it has often been the practice to produce undrawn filaments of low birefringence such that high draw ratios can subsequently be utilized, thereby obtaining the highest degree of mole-cular orientation and consequently high tenacities. Such high orien~ation contributes to the high tenacity of the resulting fibers-. It was previously discovered that polyester fibers of low birefringence can be most highly ; oriented in subsequent drawing steps, but that as filament spinning speeds increase, birefringence tended to increase because of the induced orientation of the filament which occurs in the rapid takeup of the yarn. Thls results in increased pulling tensions on the yarn in the spinning column, i.e. in-creases in column draw down. To alleviate the draw down in the column, vari-ous procedures have been incorporated into the spinning, including higher extrusion pressures and means for maintaining the filaments molten for a period of time after extrusion. The filaments on quenching and drawing, while achieving high tenacities and modulus and desirable elongations, are found to be deficient in uniformity as measured in percent Uster. This results in a ~igher standard deviation for the physical properties, such as breaking strength, which is of most critical importance to industrial yarn.
This invention seeks to provide a method for producing a heavy denier industrial polyester yarn of improved uniformity of physical properties.
This invention further seeks to provide apparatus for spinning such polyester filament yarns.
This invention further seeks to provide a heavy denier industrial polyester filament yarn of high tenacity, improved long and short term percent Uster values and lower standard deviation in breaking strength.
DESCRIPTION OF THE INVENTION
In accordance with the invention, a method is provided for producing an industrial polyester filament yarn of improved uniformity comprising melt ~)37~
spinning a plurality of filaments at an extrusion temperature above the poly- -mer melting point into a heated zone maintained at a temperature of 260 - 460 degrees centigrade, maintaining said filaments in said heated zone for fila-ment travel distance of about 6 to 24 inches and hence, immediately passing said filaments about a gaseous quenching zone, directing quenching gases onto said filaments in a radial outward flow direction, said quenching gas being maintained at a temperature of about 15 to 50 degrees centigrade in a gaseous volume of about 20 to 130 standard cubic feet per minute to provide a con-trolled cooling of said filaments and taking said filaments up as a yarn of improved Uster uniformity.
According to this invention there is provided a heavy denier poly-ester filament yarn having a tenacity of more than 7.0 grams per denier, a long and short term percent Uster of less than 1.5, a tensile factor of more than 28, and a breaking strength standard deviation of less than 0.20 grams per denier as measured in yarns across a beam.
According to this invention there is further provided a method for producing an industrial polyester filament yarn of improved uniformity com-e prising melt spinning a plurality of filaments at an extrusion temperature above the polymer melting point into a heated zone maintained at a tempera-ture of about 260 to 460 degrees centigrade, and maintaining said filaments in said heated zone for a filament travel distance of about 6 to 24 inches, and hence immediately passing said filaments through a gas quenching zone, directing quenching gas onto said filaments in a radial outflow direction, said quenching gas being maintained at a temperature of 15 to 80 degrees centigrade and at a flow of 20 to 130 standard cubic feet per minute to pro-vide a controlled cooling of said filaments and taking up said filaments as a yarn of improved Uster uniformity.
The heavy denier industrial polyester filament yarn produced in accordance ~ith this invention has a denier ~ 3 ~
lQ376~Z
per filament of 3 to 20, a tenacity of more than 7.0 grams per denier, a long and short term percent Uster of less than 1.5, and more preferably a long term percent Uster of less than 1.0, a tensile factor (TEl/2) of more than 28 and a breaking strength standard deviation of less than 0.20 grams per denier as measured in yarns across a beam.
The improved uniformity of the yarn is achieved primarily through the utilization of controlled temperature conditions from immediately adjacent to the extrusion point to the cooling of the ilaments to a temperature below their second order transition temperature. The improvement is not only highly pronounced in Uster uniformity, but also in reduction in the average standard deviation of physical properties, particularly tensile strength. It is also noticeable in the reduction of both major and minor beaming defects as noted by Lindley defect counting at beaming.
DETAI LS OF T~IE INVENTION
The invention will be more ully described by reference to the drawings wherein:
FIG, 1 is a front elevational and partial schematic ~3q~
of the apparatus of the present invention showing more particularly the relationship of the extrusion heated zone and quenching apparatus in a spinning column;
FIG. 2 is a graph which illustrates the relationship between the quenching distance from the spinneret face as it relates to long term Uster values and tensile factor (TE )i FIG. 3 is a graph which relates long term Vster, elongation, tensile factor (TEl/ ) and tenacity wlth various quench gas flow rates.
Referring more particularly to FIG. 1, the schematic drawing of spinning pack 10 is representative of a standard polyester pack which includes final filtration means for the polymer and 8 spinneret with a pre-selected number of holes for the extrusion of polymer. The polymer conveyed to the pack is maintained at a spinning temperature whiah is nor-mally comfortably above the melting temperature of the poly-mer, i.e. about 257 degrees centigrade for polyethylene tere-phthalate. Thus, spinning temperatures are normally in the range of about 290 to 310 aegrees centigrade. The spinneret utilized is selected in accordance with the denier and filament count of the yarn being produced. If desired, one or more yarns can be spun from a single pack in a single column as illustrated in the drawing.
The spinning speed varies with the particular process and fiber type being spun, but generally is in the range of 2,000 to 10,000 feet per minute or more at wind up in a spin-draw process.
The molten polymer, as it is extruded from pack 10, immediately enters a heated zone which is maintained at an elevated temperature by a heated cylindrical shroud 12 which ~0376~Z
preferably is positioned adjacent to pacX lO and extends downwardly into the spinning column for a distance of about 6 to 24 inches. The shroud has an internal diameter of sufficient size to permit safe passage of the fila-ments therethrough without danger of contact with the ' heated shroud. Conveniently, leeway of one to several inches of distance is provided between the outside filament travel line and the inside diameter of the shroud. The shroud is heated preferably by internal heating means such as electrical resisters, circulating fluids or the like conventional heating means to produce an internal surface temperature on the shroud in the range of 260 degrees to 460 degrees centigrade, and more preferably 300 degrees to 360 degrees centigrade. Such shroud tempera-tures provide a heated zone of temperatures slightly less than the surface temperature, but because of heat radiated from the spinning pack and molten extrudate, a temperature near that of the shroud is readily maintained. The exact temperature utilized is primarily dependent upon the size of the shroud, distance away from the filaments, heat loss from the shroud area, filament denier, polyester type and the like considerations. The temperature selected i8 one sufficient to maintain the as-spun polymer in a molten condition as it passes through the shroud area.
Immediately adjacent to the lower section of heated shroud 12 is outflow quench stick 14. Quench stick 14 is centered among the filaments and positioned by means of positioning guide ~piece pin)16 in a central location under the pack and spinneret. The filaments are guided down the quench stick so as not to come in contact there-~Lo376r~z with, but to spread the filaments uniformly around the quench stick. Quench stick 14 is positioned by ~eans of positioning guide 16 and spacer 18, so as to conveniently position each quench stick in the same location in a plural-ity of packs and spinning columns.
The quench stick preferably extends into the area of the heated shroud so as to provide a controlled cooling immediately as the filaments exit from the shroud. As will be appreciated by those skilled in the art, the rapid passage of fibers down the spinning column creates a downward draft of convection currents which tends to carry both the heat of the shroud and the cooling effect of the quench gases downwardly along the filament path o travel. There-fore, by utilizing the preferred quench stick positioning, the most desirable control of cooling is obtained.
The quench stick is preferably made of a porous material, such as ceramic, or sintered metal in a manner which provides a predetermined, even flow of air throughout the length and circumference of the stick. Such quenching sticks are commercially available in a variety of porosities suitable cor this application.
The air flow through the quench stick afEects the quality of the yarn produced and therefore, for a given spinning process a preferred gas flow, e.g. air, results in the most desirable spinning. It has been found that the air flow as measured in standard cubic feet per minute (SCFM) is proportional to the total denier of the yarn being spun and the spinning speed with higher total deniers and higher speeds requiring higher flow rates. For instance, the air flow is in a gas volume of about 20 to 130 SCFM
1~3'76~Z
with the preferred air flow in the range of about 20 to 60 SCFM. This is more clearly illustrated in FIG 3 which . .
relates changes in yarn physical properties with changes in air flow rates for a 1000/192 industrial yarn. It will be noted from this graph that the best results for this yarn at a 5.8 draw ratio is an air flow of about 40 SCFM.
Ambient quench gas temperatures have been found to be satisfactory, although in the compression of the gas, a temperature rise is often unavoidable. Therefore, under certain climatic conditions, it may be desirable to utilize a quench gas temperature within the range of 15 to 80 degrees centigrade, and more preferably about 25 to 50 degrees centigrade.
The quench stick length and diameter are selecked in accordance with the spinning speed, filament count, total denier, air flow desired and the like parameters, so as to provide controlled cooling of the yarn in the manner des-cribed herein. In a preferred embodiment, such quench sticks are normally of a diameter of about 1-1/2 to 4 inches and a length of about 8 to 20 inches.
Upon quenching the filaments, a spin finish is applied and the filaments are drawn and taken up on a package as a finished yarn or alternatively, taken upon a package in an undrawn state. In accordance with the present invention, it is preferable to split the threadline into two or more portions and apply the finish separately to each of the portions, such as by utilizing dual finish rolls 20. It has been found that it is particularly important to insure that the as-spun filaments do not touch any portion of the splnning column or apparatus until the application of 1~376~Z
the spin finish. Therefore, the split threadline and multiple or dual finish applicators are particularly im-~portant to insure that stray filaments do not come in contact with items such as the quench stick or air supply therefor.
As is often desired in using a split th:readline quench, the yarns may be retained separately and taken up or drawn separately. Alternatively, the split threadlines can be recombined at the drawing stage and taken up as a single yarn.
While it has been described that the yarns may be taken up on a package after the ap~lication of the spin finish, it is normally most desirable in a modern poly-ester production plant to immediately thereafter draw the yarn in one or more stages under known drawing conditions and heat set and/or relax the yaxn if desired prior to ~-taking the yarn up as a finished product. In industrial yarns, with which the present invention is primarily con-cerned, yarns are normally drawn at the highest achievable draw ratio which can be successfully processed in continuous operation. Thus, draw ratios in excess of 3, and more preferably on the order of 4 to about 6.5 to 1 are preferably utilized with multi-stage drawing being the preferred method of operation. The actual total draw ratio utilized is dependent upon the as-spun birefringence which, as noted above, is preferably as low as possible so as to achieve the highest draw ratio. Thus, such drawn yarns have tenacities in excess of 7 grams per denier, and more pre-ferably in the range of 8 to 11 grams or more per denier.
Tensile factor, i.e. TEl/2, is determined by 0 multiplying the tenacity in grams per denier times the ~37~qZ
square root of thejelon~ation at break. The yarns produced in accordance with the present method have tensile factors greater than 28 and more preferably, greater than 30.
Typically, the range of tensile factor is between 28 and 40.
The yarns of the present invention are preferably high tenacity industrial yarns such as tire yarns, conveyer belt yarns, sewing threads and the like, having denier per filaments of at least 1.0 and more preferably 3.0 to 20 or more. Total drawn deniers of such yarns range from about 100 to 10,000 with most yarns having total deniers of about 500 to 3,000. All of such yarns are considered to be heavy deniers.
As has been noted above, the long, i.e. in~rt, and the short, i.e. normal, percent Uster of yarns produced in accordance with the present invention is less than 1.5, and more preferably less than 1Ø The Uster is measured in accordance with Uster Evenness Tester, Model GGPC 10, in accordance with the manufacturer's recommended procedure, with the proviso that a feed tension of 25 grams is utili~ed on the yarn and a yarn feed rate of 25 yards per minute to the tester for at least three minutes. The rotofil setting of the tester is placed at number 3 for convention-al industrial yarns.
The breaking strength standard deviation () of yarns produced in accordance with the present invention is also substantially improved over previous industrial yarn processes. Such breaklng strength standard deviation is less than 0.20 grams per denier between position-to-position yarns and most preferably, less than 0.15 grams per denier, when measured in accordance with ASTM Method ~1~37~t7~ :
D885-68. The standard deviation is calculated based upon the testing of at least lS samples of yarn from position-to-position across production machines. It is often more convenient to measure the standard deviation of the yarns across a beam and such yarns fall within the specified range.
With the improved uniformity of the yarns pro-duced in accordance with the present invention, marked improvement will be noted in major and minor defects in beaming as compared to previously produced yarns.
The preferred polyesters used in this invention are obtained from terephthalic acid via any of the known poly-merization routes, i.e. ester interchange, direct esteri~ -fication, ~HET and the like, wherein at least 75~ of the recurring structural units of the polyester are glycol terephthalate structural units. The polymers used are fiber forming and preferably of an intrinsic viscosity of at least 0.45 up to 1.00 or more as measured in 8 orthochlorophenol at 25 degrees centigrade.
As conditions for heat setting, a temperature of 120 - 300 degrees centigrade and a time of 0.01-2 secQnds may be adopted.
While polyester polymer used in the percent inven-tion preferably contains at least 75 mol percent of ethylene terephthalate units, other acid components, when used, are a dibasic acid such as phthalic acid, isophthalic acid, adipic acid, oxalic acid, sebacic acid, suberic acid glutaric acid, pimelic acid, fumaric acid and succinic acid. A polymerization degree modifier like propionic acid may be used. As alcohol components, a divalent alcohol such as polymethylene glycol ~37617Z
having 2-10 carbon atoms (trimethylene glycol and butylene glycol) and cyclohexyl dimethanol may be cited. And they may contain a small amount of the following compound as a modifier, 5-oxydimethyl isophthalate, 5-oxydimethyl hexahydroiso-phthalate, benzene-1,3,5-tricarboxylic acid, para-carbo-methoxy phenyl diethyl phosphonate,3,5~ dicarboxy phenyl diethyl phosphonate, pentaerythritol, glycerol, glucose,phos-phoric acid, triphenyl phosphate, tri-p-carbometho~y phenyl phosphate, triphenyl phosphinate, triphenyl arsenite, tri-capryl borate, sorbitol trimesic acid, diethylene glycol and the like.
The following e`xamples illustrate certain pre-ferred embodiments of the present invention. Unless other-wise indicated, all parts and percentages used herein are by weight and all temperatures are in degrees centigrade.
EXAMPLE I
Polyethylene terephthalate was produced in accord-ance with a continuous polymerization process to provide a molten polymer having an intrinsic viscosity of O.B8, as measured in the final product, which was fed directly to a spinning pack and apparatus in accordance with FIG.l.
The polymer was spun at a spinning temperature of 297 to 300 degrees centigrade at a rate of 30.9 pounds per hour. The yarn spun was 1000/192 yarn utilizing a split threadline wherein one-half the filaments were split on either side of the quench stick A spin ~inish was applied utilizing dual finish applicator rolls and the yarn recombined for drawing in a spin-draw process. The yarn was drawn to a total draw ratio of 5.8.
During the spinning of the yarn, various para-1(~376~2 meters with respect to the outflow quench system and heated shroud were changed to determine the effect on the yarn properties. In accordance with FIG.2, the distance of the initiation of outflow quench from the spinning pack was varied from 6 inches to 16 inches, and the effect on tensile factor and percent Uster (inert), i.e. long term, was measured. The spinning was carried out at a set quench air flow of 30 SCFM. ~he results are graphically illustrated in FIG. 2.
The experiments were continued in the same manner with the spinning at a rate of 30.9 pounds per hour, the outflow quench distance being approximately 10 inches from the spinning pack, quench air temperature at about 40 degrees centigrade, the pack to outflow spacer distance being three-quarters of an inch, and the shroud temperature at 320 degre~s centigrade. With these pre-set conditions, the air flow was varied from 20 SCFM to 60 SCFM to determine the effect on percent Uster (inert), tensile factor, i.e. TEl/2, percent elongation at break (E), and tenacity in grams per denier (gpd). These effects are shown graphically in FIG.3.
While variations in the noted spinning para-meters have the noted effects on the yarn quality and spinning performance, it should be noted that this Ex-ample illustrated the preferred parameters for 1000/192 ; yarn in a spin-draw process. As will be appreciated by those skilled in the art, changes in the polymer being spun, the particular denier thereof, and the like, will affect the preferred operating conditions such as 1037~qZ
by shifting the various curves in the graphs of FIGS. 2-3 to the right or left as the case may be.
Such changes in these spinning parameters to obtain the most preferred conditions for a given yarn will be readily ascertained from the guidance and exempli-fication given herein.
The process of the present invention was com-pared to standard production spinning processes which , included the use of a heated shroud at a temperature of 320 degrees centigrade, but without an outflow quench, The spinning process utilized 0.88 intrinsic viscosity polyethylene terephthalate, a spinning rate of about 31 pounds per hour, a draw-spin procedure at a total draw ratio of 6.08 to produce a 1020/192 yarn. The percent Uster of standard production yarn utilizing the heated shroud was then compared with the process of the present invention wherein the heated shroud was utilized at the same temperature but combined with the outflow quench of the air flow of 40 SCFM, a quench air temperature of about 40 degrees centigrade, and a quench distance of about 10 inches from the spinning pack. All other conditions were the same as the com-parison. The standard production yarn had a p,ercent Uster (inert) of 2.3, whereas the yarn of the present invention had a percent Uster (inert) of 0.5.
The breaking load of the yarn of the present invention was 9072 grams. Standard deviation of break-ing load in position-to-position, as measured in yarns across a beam was 0.15 grams per denier. The standard ~376~;~Z
production yarn had a breaking load of 9096 grams, with a standard deviation in breaking load in position-to-position, as measured in yarns across a beam, of 0.21 grams per denier. The number of major and minor defects in beam of these yarns was found to be signi-ficantly reduced in the yarns of the present invention compared to the standard production. .
In the same manner as Example 2, 1330/192 yarn was produced in accordance with the present invention and compared to standard production yarn which utilized a heated shroud. The percent Uster ~inert) was 0.8 for yarn of the present invention. Standard production yarn had a percent Uster (inert) of 2Ø The standard deviation of the yarn of the present invention was 0.14 grams per denier, whereas the standard deviation of standard production yarn was 0.18 as measured in yarns across the beam.
The tenacity of the yarn of the present in-vention was 8.90 and TE / was 31.3. The tenacity of standard production was 8.84 and TE / was 30.2.
Claims (14)
1. A heavy denier polyester filament yarn having a tenacity of more than 7.0 grams per denier, a long and short term percent Uster of less than 1.5, a tensile factor of more than 28, and a breaking strength standard deviation of less than 0.20 grams per denier as measured in yarns across a beam.
2. The heavy denier yarn of claim 1 wherein the polyester if polyethylene terephthalate and the tenacity is greater than 8.0 grams per denier.
3. The heavy denier polyester yarn of claim 1 wherein the long term percent Uster is less than 1Ø
4. The heavy denier polyester yarn of claim 1 wherein the denier per filament is 3 to 20, the total denier is 500 to 5,000, the tenacity is 8 to 11 grams per denier and the tensile factor is more than 30.
5. A method for producing an industrial polyester filament yarn of improved uniformity comprising melt spin-ning a plurality of filaments at an extrusion temperature above the polymer melting point into a heated zone maintained at a temperature of about 260 to 460 degrees centigrade, and maintaining said filaments in said heated zone for a filament travel distance of about 6 to 24 inches, and hence immediately passing said filaments through a gas quenching zone, direct-ing quenching gas onto said filaments in a radial outflow direction, said quenching gas being maintained at a tempera-ture of 15 to 80 degrees centigrade and at a flow of 20 to 130 standard cubic feet per minute to provide a controlled cooling of said filaments and taking up said filaments as a yarn of improved Uster uniformity.
6. The method of claim 5 wherein the filaments after quenching have applied thereto a spin finish and are drawn at a draw ratio of more than 3.0 prior to being taken up on a package.
7. The method of claim 6 wherein the draw ratio is within the range of 4 to 6.5 to 1.
8. The method of claim 5 wherein the volume of quenching gas is dependent on the total denier of the yarn being spun, said gas volume being proportional to the denier.
9. The method of claim 8 wherein the quenching gas volume is about 40 standard cubic feet per minute for 1000 total denier yarn.
10. The method of claim 5 wherein the heated zone is maintained at a temperature of 300 to 360 degrees centigrade for a filament travel distance of 8 to 12 inches.
11. The method of claim 10 wherein the heated zone is immediately adjacent to the extrusion point.
12. The method of claim 5 wherein the quenching gas is at a temperature of 25 to 50 degrees centigrade.
13. The method of claim 5 wherein the filaments from a single spinning position are split around the quenching zone into at least two threadlines, separately applying finish to each threadline and taking up said threadlines as separate yarns.
14. The method of claim 5 wherein the filaments from a single spinning position are split around the quenching zone into at least two threadlines, separately applying finish to each threadline and recombining said threadlines prior to drawing into a single yarn.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US160019A US3858386A (en) | 1971-07-06 | 1971-07-06 | Polyester yarn production |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1037672A true CA1037672A (en) | 1978-09-05 |
Family
ID=22575140
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA146,417A Expired CA1037672A (en) | 1971-07-06 | 1972-07-05 | Polyester yarn production |
Country Status (4)
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US (1) | US3858386A (en) |
BR (1) | BR7204477D0 (en) |
CA (1) | CA1037672A (en) |
GB (1) | GB1382499A (en) |
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US4285646A (en) * | 1980-05-13 | 1981-08-25 | Fiber Industries, Inc. | Apparatus for quenching melt-spun filaments |
US4332764A (en) * | 1980-10-21 | 1982-06-01 | Fiber Industries, Inc. | Methods for producing melt-spun filaments |
CH667676A5 (en) * | 1985-09-18 | 1988-10-31 | Inventa Ag | DEVICE FOR COOLING AND PREPARING MELT-SPONNED SPINNING MATERIAL. |
CH673659A5 (en) * | 1987-03-05 | 1990-03-30 | Inventa Ag | |
US4988270A (en) * | 1985-09-18 | 1991-01-29 | Ems-Inventa Ag | Apparatus for cooling and conditioning melt-spun material |
FR2611748B2 (en) * | 1985-09-18 | 1990-07-27 | Inventa Ag | DEVICE FOR COOLING AND PREPARING MOLTEN YARNS |
DE3822571A1 (en) * | 1988-07-04 | 1990-02-01 | Hoechst Ag | SPINNING METHOD AND DEVICE FOR IMPLEMENTING THEREOF |
ATA53792A (en) * | 1992-03-17 | 1995-02-15 | Chemiefaser Lenzing Ag | METHOD FOR PRODUCING CELLULOSIC MOLDED BODIES, DEVICE FOR IMPLEMENTING THE METHOD AND USE OF A SPINNING DEVICE |
MY115308A (en) * | 1993-05-24 | 2003-05-31 | Tencel Ltd | Spinning cell |
AT399729B (en) * | 1993-07-01 | 1995-07-25 | Chemiefaser Lenzing Ag | METHOD FOR PRODUCING CELLULOSIC FIBERS AND DEVICE FOR IMPLEMENTING THE METHOD AND THE USE THEREOF |
AT402738B (en) * | 1993-07-28 | 1997-08-25 | Chemiefaser Lenzing Ag | SPIDER NOZZLE |
DE19821778B4 (en) * | 1998-05-14 | 2004-05-06 | Ems-Inventa Ag | Device and method for producing microfilaments of high titer uniformity from thermoplastic polymers |
DE10134003A1 (en) * | 2001-07-12 | 2003-01-23 | Neumag Gmbh & Co Kg | Device for melt spinning and cooling a filament sheet |
US20030017066A1 (en) * | 2001-07-19 | 2003-01-23 | Baxter International Inc. | Apparatus, flexible bag and method for dispensing |
US6511624B1 (en) | 2001-10-31 | 2003-01-28 | Hyosung Corporation | Process for preparing industrial polyester multifilament yarn |
US20030141611A1 (en) * | 2002-01-25 | 2003-07-31 | Giese Kenneth Charles | Adjustable shroud for spinning synthetic yarns |
WO2014118080A1 (en) | 2013-02-04 | 2014-08-07 | Nv Bekaert Sa | Quench tube for polymer fiber extrusion |
CN106757431A (en) * | 2016-11-25 | 2017-05-31 | 南通杰克拜尼服帽有限公司 | A kind of production technology of moisture-absorption and perspiration polyester filament |
CN115552062A (en) * | 2021-03-02 | 2022-12-30 | 尚科纺织企业工业及贸易公司 | protective woven fabric |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1081089A (en) * | 1963-11-19 | 1967-08-31 | Dunlop Rubber Co | Improvements in or relating to textile cord material and pneumatic tyres manufacturedtherewith |
GB1098012A (en) * | 1965-01-14 | 1968-01-03 | Chemstrand Ltd | Improvements in or relating to elastic yarns and the manufacture thereof |
US3342027A (en) * | 1965-05-04 | 1967-09-19 | Du Pont | Coalesced multifilament yarn |
US3670489A (en) * | 1969-07-28 | 1972-06-20 | Eastman Kodak Co | Textile yarn |
US3664114A (en) * | 1969-07-31 | 1972-05-23 | Eastman Kodak Co | Spun polyester strands and method for making |
-
1971
- 1971-07-06 US US160019A patent/US3858386A/en not_active Expired - Lifetime
-
1972
- 1972-07-05 CA CA146,417A patent/CA1037672A/en not_active Expired
- 1972-07-06 BR BR4477/72A patent/BR7204477D0/en unknown
- 1972-07-06 GB GB3169372A patent/GB1382499A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US3858386A (en) | 1975-01-07 |
BR7204477D0 (en) | 1973-06-07 |
GB1382499A (en) | 1975-02-05 |
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