NO147989B - ALKENYL-AROMATIC THERMOPLASTIC FOAM, AND PROCEDURE FOR THE PREPARATION OF SUCH - Google Patents
ALKENYL-AROMATIC THERMOPLASTIC FOAM, AND PROCEDURE FOR THE PREPARATION OF SUCH Download PDFInfo
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- NO147989B NO147989B NO770347A NO770347A NO147989B NO 147989 B NO147989 B NO 147989B NO 770347 A NO770347 A NO 770347A NO 770347 A NO770347 A NO 770347A NO 147989 B NO147989 B NO 147989B
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- Prior art keywords
- blowing agent
- permeability
- methyl
- atoms
- mixture
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- 239000006260 foam Substances 0.000 title claims description 23
- 229920001169 thermoplastic Polymers 0.000 title claims description 5
- 238000000034 method Methods 0.000 title description 9
- 239000004416 thermosoftening plastic Substances 0.000 title description 2
- 239000004604 Blowing Agent Substances 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 17
- 239000003995 emulsifying agent Substances 0.000 claims description 15
- 230000035699 permeability Effects 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 229930195733 hydrocarbon Natural products 0.000 claims description 7
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims description 5
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 5
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims description 5
- 229960003750 ethyl chloride Drugs 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Chemical group 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 claims description 4
- 125000004773 chlorofluoromethyl group Chemical group [H]C(F)(Cl)* 0.000 claims description 4
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 4
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000011737 fluorine Chemical group 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 238000009413 insulation Methods 0.000 description 6
- 239000004088 foaming agent Substances 0.000 description 5
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 229940051271 1,1-difluoroethane Drugs 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- -1 alkenyl aromatic compounds Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical compound CC(F)(F)Cl BHNZEZWIUMJCGF-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 229940050176 methyl chloride Drugs 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 1
- KDWQLICBSFIDRM-UHFFFAOYSA-N 1,1,1-trifluoropropane Chemical compound CCC(F)(F)F KDWQLICBSFIDRM-UHFFFAOYSA-N 0.000 description 1
- AUTSLLHNWAZVLE-UHFFFAOYSA-N 1,1,2,2,3-pentabromo-3-chlorocyclohexane Chemical compound ClC1(Br)CCCC(Br)(Br)C1(Br)Br AUTSLLHNWAZVLE-UHFFFAOYSA-N 0.000 description 1
- WXGNWUVNYMJENI-UHFFFAOYSA-N 1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)F WXGNWUVNYMJENI-UHFFFAOYSA-N 0.000 description 1
- WGZYQOSEVSXDNI-UHFFFAOYSA-N 1,1,2-trifluoroethane Chemical compound FCC(F)F WGZYQOSEVSXDNI-UHFFFAOYSA-N 0.000 description 1
- BOUGCJDAQLKBQH-UHFFFAOYSA-N 1-chloro-1,2,2,2-tetrafluoroethane Chemical compound FC(Cl)C(F)(F)F BOUGCJDAQLKBQH-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- CYXIKYKBLDZZNW-UHFFFAOYSA-N 2-Chloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)CCl CYXIKYKBLDZZNW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000007630 basic procedure Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 1
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 1
- 229960004065 perflutren Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
- C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
Oppfinnelsen vedrører et alkenyl-aromatisk, termoplastisk polymer-skumlegeme for isolasjonsformål, bestående av en rektangulær plate med en minste tverrsnittsdimensjon på 6,35 mm og et minste tverrsnittsareal pa 51,6 cm , hvilken plate inneholder et flertall lukkede, ikke-forbundne gassformig fluorert hydrokar-bonholdige celler med en gjennomsnittlig størrelse på 0,1-1,2 mm, og er av ensartet cellestruktur og uten diskontinuiteter, fremstilt ved ekstrudering av en blanding av varmemyknet polymer og en esemiddelblanding omfattende fluorklormetan, metylklorid, etylklorid, klordifluormetan eller 1,1-difluoretan som høypermeabilitets-esemiddel sammen med et annet, fluorert hydroakarbon-esemiddel. Dette skumlegeme er karakterisert ved at de gassholdige celler inneholder et eller flere lavpermeabilitets-esemidler med formel The invention relates to an alkenyl aromatic thermoplastic polymer foam body for insulation purposes, consisting of a rectangular plate having a minimum cross-sectional dimension of 6.35 mm and a minimum cross-sectional area of 51.6 cm, which plate contains a plurality of closed, non-connected gaseous fluorinated hydrocarbon-containing cells with an average size of 0.1-1.2 mm, and are of uniform cell structure and without discontinuities, produced by extrusion of a mixture of heat-softened polymer and a blowing agent mixture comprising fluorochloromethane, methyl chloride, ethyl chloride, chlorodifluoromethane or 1, 1-difluoroethane as a high-permeability blowing agent together with another, fluorinated hydrocarbon blowing agent. This foam body is characterized by the fact that the gas-containing cells contain one or more low-permeability foaming agents with formula
hvor er metyl, etyl, klormetyl, difluormetyl, klorfluormetyl, fluormetyl eller trifluormetyl, og R2 er hydrogen eller klor, fluor, metyl eller trifluormetyl, idet esemidlet ikke inneholder mer enn 3 C-atomer, og idet esemidlet utgjøres av en forbindelse eifled 3 C-atomer hvis det som halogen inneholder bare 2 fluoratomer. Oppfinnelsen vedrører også en fremgangsmåte for fremstilling av et polymer-skumlegeme som ovenfor angitt, hvorved en esemiddelblanding av fluorklormetan, metylklorid, etylklorid, klordifluormetan eller 1,1-difluoretan som høypermeabilitets-esemiddel sammen med et annet, fluorert hydrokarbon-esemiddel injiseres i en varmemyknet polymerstrøm og blandes med denne, hvoretter blandingen ekstruderes gjennom en dyse. Denne fremgangsmåte er karakterisert ved at det som det annet esemiddel, som injiseres sammen med høypermeabilitets-esemidlet, anvendes et eller flere lavpermeabilitets-esemidler med formel where is methyl, ethyl, chloromethyl, difluoromethyl, chlorofluoromethyl, fluoromethyl or trifluoromethyl, and R2 is hydrogen or chlorine, fluorine, methyl or trifluoromethyl, the emulsifying agent does not contain more than 3 C atoms, and the emulsifying agent is made up of a compound with more than 3 C -atoms if, as a halogen, it contains only 2 fluorine atoms. The invention also relates to a method for producing a polymer foam body as stated above, whereby a blowing agent mixture of fluorochloromethane, methyl chloride, ethyl chloride, chlorodifluoromethane or 1,1-difluoroethane as a high permeability blowing agent together with another, fluorinated hydrocarbon blowing agent is injected into a heat-softened polymer stream and mixed with it, after which the mixture is extruded through a die. This method is characterized in that one or more low-permeability emulsifiers with the formula are used as the second emulsifier, which is injected together with the high-permeability emulsifier
hvor R-^ er metyl, etyl, klormetyl, dif luormetyl, klorf luormetyl, fluormetyl eller trifluormetyl, og R2 er hydrogen eller klor, fluor, metyl eller trifluormetyl, idet esemidlet ikke inneholder mer enn 3 C-atomer, og idet esemidlet utgjøres av en forbindelse med 3 C-atomer hvis det som halogen inneholder bare 2 fluor-atomer. where R-^ is methyl, ethyl, chloromethyl, difluoromethyl, chlorofluoromethyl, fluoromethyl or trifluoromethyl, and R2 is hydrogen or chlorine, fluorine, methyl or trifluoromethyl, the evaporating agent does not contain more than 3 C atoms, and the evaporating agent consists of a compound with 3 C atoms if it contains only 2 fluorine atoms as a halogen.
Cellestørrelsen måles som gjennomsnittlig cellediameter tvers over den minste tverrsnittsdimensjon av legemet (dvs. f. Cell size is measured as the average cell diameter across the smallest cross-sectional dimension of the body (i.e.
eks. med ASTM-metode D2842-69), og det avlange legeme har et e.g. with ASTM Method D2842-69), and the oblong body has a
tverrsnittsareal på minst 51,6 cm<2> og har en minste tverrsnittsdimensjon på minst 6,35 mm, skumlegemet har en vanndamp-gjennom-trengelighet som ikke er mer enn 3,02 metriske perm cm og målt med ASTM-metode C355-64 "Procedures for Desiccant Method", en tett-het på 16-80 g/l med den ytterligere begrensning at cellene inneholder et lavpermeabilitets-esemiddel som har en permeabilitet gjennom den alkenylaromatiske harpikspolymer på ikke mer enn 0,017 x permeabiliteten av nitrogen gjennom legemet,og en varmeledningsevne på 0,07 ± 20 % BTU-in/h/f t2 /°f(0 ,24* 1 CT^^O^calcm/s cm2oc)> cross-sectional area of at least 51.6 cm<2> and having a minimum cross-sectional dimension of at least 6.35 mm, the foam body having a water vapor permeability of not more than 3.02 metric perm cm and measured by ASTM Method C355-64 "Procedures for Desiccant Method", a density of 16-80 g/l with the additional limitation that the cells contain a low permeability desiccant having a permeability through the alkenyl aromatic resin polymer of no more than 0.017 x the permeability of nitrogen through the body, and a thermal conductivity of 0.07 ± 20% BTU-in/h/f t2 /°f(0 .24* 1 CT^^O^calcm/s cm2oc)>
Én av hovedanvendelsene for styrenpolymerskum er på varmeisolasjonsområdet. Et styrenpolymerskum for varmeisolasjon har ønskelig relativt små celler og utmerket dimensjonsstabilitet. Det er også sterkt ønskelig at isolasjonsverdien for skummet opp-rettholdes i så lang tid som mulig. Ut fra et prosess-standpunkt har det vært ønskelig med visse halogenholdige forbindelser, f. One of the main uses for styrene polymer foam is in the area of thermal insulation. A styrene polymer foam for thermal insulation desirably has relatively small cells and excellent dimensional stability. It is also highly desirable that the insulation value of the foam is maintained for as long as possible. From a process standpoint, it has been desirable to use certain halogen-containing compounds, e.g.
eks. diklordifluormetan, ved fremstilling av ekstruderte styrenpolymerskum. Det antas for tiden at slike forbindelser, når de frigjøres til atmosfæren, kan redusere effektiviteten til ozonsjiktet som et solarskjold, og det derfor ønskelig at fluorerte og/eller klorerte forbindelser som eventuelt kan redusere effektiviteten til ozonsjiktet generelt elimineres fra anvendelser hvor de til slutt frigjøres til atmosfæren. e.g. dichlorodifluoromethane, in the production of extruded styrene polymer foam. It is currently believed that such compounds, when released into the atmosphere, can reduce the effectiveness of the ozone layer as a solar shield, and it is therefore desirable that fluorinated and/or chlorinated compounds which may possibly reduce the effectiveness of the ozone layer are generally eliminated from applications where they are eventually released to the atmosphere.
BRD-utl.skrift 1 544 753 beskriver basisfremgangsmåten BRD publication 1 544 753 describes the basic procedure
for fremstilling av ekstruderte stokker eller planker av termo-plastskum med lukkede celler, hvorved det anvendes blandede esemidler med bestemte damptransmisjonshastigheter. for the production of extruded logs or planks of closed-cell thermo-plastic foam, whereby mixed blowing agents with specific vapor transmission rates are used.
US-patentskrift 3 900 433 beskriver ikke-cellulære sty-renpolymerperler - oppskummet på stedet - som er impregnert med en esemiddelblanding som inneholder 0,5-20 vekt% av et impregne-ringshjelpemiddel, f.eks. metylklorid eller klorfluormetan. US Patent 3,900,433 describes non-cellular styrene polymer beads - foamed in place - which are impregnated with a blowing agent mixture containing 0.5-20% by weight of an impregnation aid, e.g. methyl chloride or chlorofluoromethane.
Ingen av de ovennevnte publikasjoner åpenbarer eller foreslår et dimensjonsstabilt skumprodukt med stort tverrsnitt fremstilt med en blanding av miljømessig mer akseptable esemidler og som er spesielt nyttig for varmeisolasjon i boliger og industri-bygninger, rørledninger, tanker osv., slik produktet i henhold til foreliggende oppfinnelse er. Videre beskriver ingen av de an-gitte publikasjoner en slik esemiddelblanding som anvendes i forbindelse med foreliggende oppfinnelse. None of the above-mentioned publications discloses or suggests a dimensionally stable foam product with a large cross-section made with a mixture of environmentally more acceptable foaming agents and which is particularly useful for thermal insulation in residential and industrial buildings, pipelines, tanks, etc., such as the product according to the present invention is. Furthermore, none of the specified publications describes such a spray agent mixture which is used in connection with the present invention.
Flyktige, fluide esemidler som anvendes ved fremgangsmåten i henhold til oppfinnelsen er altså en blanding av høyperme-abilitets-esemiddel og lavpermeabilitets-esemiddel. Enten høy-permeabilitets-esemidlet og/eller lavpermeabilitets-esemidlet kan være en blanding av ett eller flere egnede esemidler.. Lavpermeabilitets-esemidlet i blandingen av esemidler som anvendes for fremstilling av skum i overensstemmelse med oppfinnelsen, utgjør fordelaktig 30-70 vekt% av esemiddelblandingen. Volatile, fluid blowing agents used in the method according to the invention are therefore a mixture of high-permeability blowing agents and low-permeability blowing agents. Either the high-permeability blowing agent and/or the low-permeability blowing agent can be a mixture of one or more suitable blowing agents. The low-permeability blowing agent in the mixture of blowing agents used for the production of foam in accordance with the invention advantageously constitutes 30-70% by weight of the foaming agent mixture.
Lavpermeabilitets-esemidler som går inn under ovennevnte begrensninger er: 1,1,1-trif luorpropan, 2 ,2^-dif luorpropan; 1,1,2,2-tetrafluoretan; 1,1,1,2-tetrafluor-2-kloretan; 1,1,1-trifluor-2-kloretan; pentafluoretan; 1,1,2-trifluoretan; 1,1,1-trifluoretan; oktafluorpropan; og 1,1-difluor-l-kloretan og bland-inger derav. Alle de foran nevnte forbindelser har den nødvendi-ge permeabilitetsverdi og varmeledningsevne. Low permeability emulsifiers that fall under the above limitations are: 1,1,1-trifluoropropane, 2,2^-difluoropropane; 1,1,2,2-tetrafluoroethane; 1,1,1,2-tetrafluoro-2-chloroethane; 1,1,1-trifluoro-2-chloroethane; pentafluoroethane; 1,1,2-trifluoroethane; 1,1,1-trifluoroethane; octafluoropropane; and 1,1-difluoro-1-chloroethane and mixtures thereof. All the compounds mentioned above have the necessary permeability value and thermal conductivity.
Betegnelsen "alkenyl-aromatisk termoplastisk polymer" refererer til en fast polymer av én eller flere polymeriserbare alkenyl-aromatiske forbindelser. Polymeren eller kopolymeren om-fatter i kjemisk kombinert form minst 70 vekt% av minst én alke-nylaromatisk forbindelse med den generelle formel The term "alkenyl aromatic thermoplastic polymer" refers to a solid polymer of one or more polymerizable alkenyl aromatic compounds. The polymer or copolymer comprises in chemically combined form at least 70% by weight of at least one alkenylaromatic compound with the general formula
hvor Ar representerer et aromatisk hydrokarbonradikal eller et aromatisk halogenhydrokarbonradikal av benzenrekken, og R er hydrogen eller metyl. Eksempler på slike alkenylaromatiske poly-merer er de faste homopolymerer av styren, a-metylstyren, o-metylstyren, m-metylstyren, p-metylstyren, ar-etylstyren, ar-vinyl-xylen, ar-klorstyren eller ar-bromstyren; og de faste kopolyme-rer av to eller flere av slike alkenylaromatiske forbindelser med små mengder av andre lett polymeriserbare olefiniske forbindelser, f.eks. metylmetakrylat, akrylnitril, maleinsyreanhydrid, citrakonsyreanhydrid, itakonsyreanhydrid, akrylsyre og gummifor-sterkede (enten naturlig eller syntetisk) styrenpolymerer. where Ar represents an aromatic hydrocarbon radical or an aromatic halogen hydrocarbon radical of the benzene series, and R is hydrogen or methyl. Examples of such alkenyl aromatic polymers are the solid homopolymers of styrene, α-methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, ar-ethylstyrene, ar-vinyl-xylene, ar-chlorostyrene or ar-bromostyrene; and the solid copolymers of two or more of such alkenylaromatic compounds with small amounts of other easily polymerizable olefinic compounds, e.g. methyl methacrylate, acrylonitrile, maleic anhydride, citraconic anhydride, itaconic anhydride, acrylic acid and rubber-reinforced (either natural or synthetic) styrene polymers.
Fremstillingen av alkenylaromatiske polymerskumlegemer The production of alkenyl aromatic polymer foam bodies
i overensstemmelse med oppfinnelsen gjøres mest bekvemt på kjent måte, hvorved det flyktige, fluide esemiddel injiseres inn i en varmemyknet polymerstrøm i en ekstruder. Fra ekstruderen føres den varmemyknede gel til en roterende mikser hvor en pigget rotor er innelukket i et hus som har en pigget innvendig over-flate som griper inn mellom piggene på rotoren. Den varmemyknede gel fra ekstruderen mates til innløpsenden i mikseren og kommer ut fra utløpsenden, idet strømmen går i generelt aksial retning. in accordance with the invention is most conveniently done in a known manner, whereby the volatile, fluid blowing agent is injected into a heat-softened polymer stream in an extruder. From the extruder, the heat-softened gel is fed to a rotary mixer where a spiked rotor is enclosed in a housing that has a spiked inner surface that engages between the spikes on the rotor. The heat-softened gel from the extruder is fed to the inlet end of the mixer and comes out from the outlet end, the flow being in a generally axial direction.
Fra mikseren passerer gelen gjennom kjølere og fra kjølerne til From the mixer, the gel passes through coolers and from the coolers to
en dyse som ekstruderer en generelt rektangulær plate. a die that extrudes a generally rectangular plate.
Ved fremgangsmåten i overensstemmelse med oppfinnelsen er det ofte ønskelig å tilsette et kjernedannelsesmiddel, f.eks. talk, kalsiumsilikat eller indigo,for reduksjon av cellestørrelsen. In the method according to the invention, it is often desirable to add a nucleating agent, e.g. talc, calcium silicate or indigo, for reduction of cell size.
Et flertall av skum ble fremstilt ved blanding av poly-styren som inneholder flammehemmende middel som er et monoklorpen-tabromcykloheksan av kommersiell renhet, bariumstearat, magnesiumoksyd og et kjernedannelsesmiddel. Blandingen ble matet til en ekstruderingsenhet, et esemiddel ble sprøytet inn i ekstruderhuset kontinuerlig, og polystyrenskum ble ekstrudert som en rektangulær plate med en tverrsnittsdimensjon på ca. 2,54 cm x 2,54 cm. Skumdannelsestemperaturene var fra 112 til 118°C. Alle konsentra-sjoner som er angitt som deler eller deler pr. 100 (pph) er vekt-deler pr. 100 deler polystyrenharpiks. Matehastighetene, esemiddelblandingen og de fysikalske egenskaper er gjengitt i de følgende tabeller. Densiteten er vist i gram/liter, cellestørrel-sen i mm, og under esemiddel er det vist vekt% og komponent i esemidlet . A majority of foams were made by mixing polystyrene containing a commercial grade monochloropentabromocyclohexane flame retardant, barium stearate, magnesium oxide and a nucleating agent. The mixture was fed to an extrusion unit, a blowing agent was injected into the extruder housing continuously, and polystyrene foam was extruded as a rectangular plate with a cross-sectional dimension of approx. 2.54cm x 2.54cm. The foaming temperatures were from 112 to 118°C. All concentrations stated as parts or parts per 100 (pph) is parts by weight per 100 parts polystyrene resin. The feed rates, the blowing agent mixture and the physical properties are given in the following tables. The density is shown in grams/litre, the cell size in mm, and under the foaming agent the weight % and component of the foaming agent are shown.
De skum som ble fremstilt og er vist i tabellene, inneholdt 3 deler pr. 100 av det flammehemmende middel, 0,075 del pr. 100 bariumstearat, 0,03 del pr." 100 magnesiumoksyd. Enhetene for den målte K-faktor er BTU-in/h/ft /°F og er bestemt på prøver som ble oppskivet fra ekstrudatet på en slik mjkte at alle over-flater av den rektangulære prøve er blitt oppskivet fra den opp-rinnelige ekstruderte plate for tilveiebringelse av kuttede celler på hver av overflatene. Aldring av prøvene foregikk ved romtemperatur, ca. 20 - 25°C. I kolonnen "beregnet K-faktor" er det beregnet verdier for K-faktoren for skummet etter 5 år ved omgivelsestemperaturer i luft, og den uendelig aldrede K-faktor. Hvis man kjenner densiteten, cellestørrelsen, esemiddelnivået, esemiddelsammensetningen, K-faktoren, permeabiliteten for ese-middelet, den første K-faktor ved ekstrudering, kan K-faktoren ved et hvert tidspunkt i fremtiden lett beregnes med høy grad The foams that were produced and are shown in the tables contained 3 parts per 100 of the flame retardant, 0.075 part per 100 barium stearate, 0.03 part per 100 magnesium oxide. The units of the measured K factor are BTU-in/h/ft /°F and are determined on samples sliced from the extrudate to such a thickness that all surfaces of the rectangular sample has been sliced from the rollable extruded plate to provide cut cells on each of the surfaces. Aging of the samples took place at room temperature, approximately 20 - 25°C. In the column "calculated K-factor" it is calculated values for the K-factor for the foam after 5 years at ambient temperatures in air, and the infinitely aged K-factor If one knows the density, cell size, blowing agent level, blowing agent composition, K-factor, permeability to the blowing agent, the first K-factor at extrusion, the K-factor at any point in the future can easily be calculated to a high degree
av nøyaktighet. K-faktoren under uendelig aldringsverdi er den K-faktor som skummet ville ha hvis esemidlet i cellene ble fullstendig erstattet med luft. De ekstruderinger som er vist i forsøk 7 og 8 i tabellen gir ikke et skum innen oppfinnelsens of accuracy. The K-factor below infinite aging value is the K-factor that the foam would have if the blowing agent in the cells were completely replaced by air. The extrusions shown in experiments 7 and 8 in the table do not produce a foam within the scope of the invention
ramme, men er bare for sammenlikningsformål. Hvis cellestørrelsen og K-faktoren betraktes, så er det innlysende at for hvilket som helst av esemiddelsystemene vil K-faktoren være desto lavere jo mindre cellestørrelsen er. Det skal også bemerkes av de første 6 linjer i tabellen at langtids-isolasjonsverdien er betydelig forbedret ved anvendelse av lavpermeabilitets-esemiddel i tilknytning til et med høy permeabilitet. Enheten for permeabilitet er cm 3 /mil/100 in 2 /dag/atm. = cm 3 /0,0254 mm/645cm 2/dag/atm. Permeabiliteten for metylklorid = 980; 1,1-difluoretan= 8,4; klordifluormetan=19; etylklorid=84; luft=110; klorfluormetan= 329; og 1,1-difluor-l-kloretan=0,07. frame, but is only for comparison purposes. If the cell size and the K-factor are considered, then it is obvious that for any of the emulsifier systems the K-factor will be the lower the smaller the cell size. It should also be noted from the first 6 lines in the table that the long-term insulation value is significantly improved by using a low-permeability sealant in conjunction with a high-permeability one. The unit of permeability is cm 3 /mil/100 in 2 /day/atm. = cm 3 /0.0254 mm/645cm 2/day/atm. The permeability to methyl chloride = 980; 1,1-difluoroethane= 8.4; chlorodifluoromethane=19; ethyl chloride=84; air=110; chlorofluoromethane= 329; and 1,1-difluoro-1-chloroethane=0.07.
Omregningsfaktor for uttrykket BTU-in/h/ft<2>/°F er Conversion factor for the expression BTU-in/h/ft<2>/°F is
3,4448 x 10~<4> (cal.-cm/sek. cm2 Qc) . 3.4448 x 10~<4> (cal.-cm/sec. cm2 Qc) .
Tabell II viser dimensjonsstabiliteten for forskjellige skum fra tabell I. Table II shows the dimensional stability of different foams from Table I.
Skum i overenstemmelse med oppfinnelsen har en Foam in accordance with the invention has a
K-verdi etter fem års aldring ved omgivelsetemperatur i luft på K-value after five years of aging at ambient temperature in air on
minst 1,0 x 10 cal. mindre enn K-verdien for det samme skum hvor esemidlet er erstattet med luft. at least 1.0 x 10 cal. less than the K value for the same foam where the blowing agent has been replaced with air.
Claims (2)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US65469076A | 1976-02-03 | 1976-02-03 |
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NO770347L NO770347L (en) | 1977-08-04 |
NO147989B true NO147989B (en) | 1983-04-11 |
NO147989C NO147989C (en) | 1983-07-20 |
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NO770347A NO147989C (en) | 1976-02-03 | 1977-02-02 | ALKENYL-AROMATIC THERMOPLASTIC FOAM, AND PROCEDURE FOR THE PREPARATION OF SUCH |
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JP (1) | JPS5295773A (en) |
AU (1) | AU507080B2 (en) |
BE (1) | BE850971A (en) |
BR (1) | BR7700611A (en) |
CA (1) | CA1086450A (en) |
CH (1) | CH633816A5 (en) |
DE (1) | DE2704278C2 (en) |
DK (1) | DK154776C (en) |
ES (1) | ES455332A1 (en) |
FR (1) | FR2340342A1 (en) |
GB (1) | GB1537421A (en) |
IT (1) | IT1112146B (en) |
NL (1) | NL170297C (en) |
NO (1) | NO147989C (en) |
SE (1) | SE426072B (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2738719A1 (en) * | 1977-08-27 | 1979-03-08 | Bayer Ag | Process for the production of foamed plastics |
GB2125796B (en) * | 1982-08-23 | 1986-03-19 | Cosden Technology | Flame retarding extruded plastics foam compositions |
US4528300A (en) * | 1984-01-31 | 1985-07-09 | The Dow Chemical Company | Process for producing dimensionally stable polyolefin foams using environmentally acceptable blowing agent systems |
BR8807460A (en) * | 1987-04-15 | 1990-04-10 | Dow Chemical Co | METHOD OF EXTRUSION OF A SYNTHETIC AROMATIC RESIN FOAM BODY WITH ALKENYLES WITH CLOSED CELLS |
JPH01247434A (en) * | 1988-03-30 | 1989-10-03 | Sekisui Plastics Co Ltd | Production of flame-retarding styrene resin foam |
JP2835726B2 (en) * | 1988-05-16 | 1998-12-14 | 株式会社 ジェイエスピー | Method for producing plate-like polystyrene resin foam |
DE3829633A1 (en) * | 1988-09-01 | 1990-03-15 | Basf Ag | METHOD FOR PRODUCING FOAM PANELS WITH HIGH PRESSURE RESISTANCE AND HIGH THERMAL INSULATION |
US4912140A (en) * | 1988-09-21 | 1990-03-27 | The Dow Chemical Company | Expandable and expanded alkenyl aromatic polymer particles |
US4916166A (en) * | 1988-10-17 | 1990-04-10 | The Dow Chemical Company | Insulating alkenyl aromatic polymer foam |
RU2073693C1 (en) * | 1988-10-17 | 1997-02-20 | Дзе Дау Кемикал Компани | Method for production of frothed polystyrene |
ES2083978T3 (en) * | 1989-02-01 | 1996-05-01 | Asahi Glass Co Ltd | AZEOTROPIC MIXTURE OR SIMILAR TO AN AZEOTROPIC MIXTURE BASED ON HYDROGENATED, CHLORINATED AND FLUORATED HYDROCARBONS. |
US5320683A (en) * | 1989-02-06 | 1994-06-14 | Asahi Glass Company Ltd. | Azeotropic or azeotropic-like composition of hydrochlorofluoropropane |
US5120481A (en) * | 1989-02-28 | 1992-06-09 | U.C. Industries, Inc. | Process for preparing extruded foam bodies |
DE3930594A1 (en) * | 1989-09-13 | 1991-03-14 | Gefinex Jackon Gmbh | Moulded foam prods., esp. of polystyrene foam - by extrusion, using mixt. of above 30 wt. per cent 1,1-di:fluoro-1-chloro-ethane and water and-or nitrogen as blowing agent |
US5011866A (en) * | 1989-11-08 | 1991-04-30 | The Dow Chemical Company | Insulating alkenyl aromatic polymer foam |
DE3939986A1 (en) * | 1989-12-02 | 1991-06-06 | Gefinex Gmbh | Prodn. of foams of polystyrene or polyethylene - using chloro:di:fluoro:methane contg. ammonium bi:carbonate or other ammonium cpd. as blowing agent |
US4956395A (en) * | 1990-01-18 | 1990-09-11 | Amoco Corporation | Styrenic foam blowing agent composition |
US6121337A (en) * | 1990-03-23 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Compositions containing 1,1,2,2-tetrafluoroethane (HFC-134) for closed-cell polymer foam production |
US5106882A (en) * | 1991-05-28 | 1992-04-21 | The Dow Chemical Company | Insulating alkenyl aromatic polymer foam |
JPH0553140U (en) * | 1991-12-20 | 1993-07-13 | 星和電機株式会社 | Waterproof retainer for cable connection |
WO1999031170A1 (en) | 1997-12-18 | 1999-06-24 | The Dow Chemical Company | Foams comprising hfc-134 and a low solubility co-blowing agent and a process for making |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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GB886811A (en) * | 1957-11-29 | 1962-01-10 | Dow Chemical Co | Method of making a latent-foaming polymeric composition |
US3287477A (en) * | 1964-11-12 | 1966-11-22 | Koppers Co Inc | Process and apparatus for extruding a foamed plastic |
CA975500A (en) * | 1969-02-06 | 1975-09-30 | Joseph G. Spitzer | Structures such as applicator pads for cleaning and other purposes, propellant compositions for forming the same, and process |
CH572269A5 (en) * | 1972-07-20 | 1976-01-30 | Bbc Brown Boveri & Cie |
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1977
- 1977-01-14 CA CA269,739A patent/CA1086450A/en not_active Expired
- 1977-01-25 ES ES455332A patent/ES455332A1/en not_active Expired
- 1977-01-27 NL NLAANVRAGE7700842,A patent/NL170297C/en not_active IP Right Cessation
- 1977-01-31 IT IT47858/77A patent/IT1112146B/en active
- 1977-01-31 GB GB3907/77A patent/GB1537421A/en not_active Expired
- 1977-02-01 CH CH120377A patent/CH633816A5/en not_active IP Right Cessation
- 1977-02-01 BE BE174560A patent/BE850971A/en not_active IP Right Cessation
- 1977-02-01 BR BR7700611A patent/BR7700611A/en unknown
- 1977-02-02 NO NO770347A patent/NO147989C/en unknown
- 1977-02-02 DE DE2704278A patent/DE2704278C2/en not_active Expired
- 1977-02-02 SE SE7701144A patent/SE426072B/en not_active IP Right Cessation
- 1977-02-02 JP JP1058877A patent/JPS5295773A/en active Granted
- 1977-02-02 DK DK044477A patent/DK154776C/en active
- 1977-02-02 AU AU21876/77A patent/AU507080B2/en not_active Expired
- 1977-02-02 FR FR7702924A patent/FR2340342A1/en active Granted
Also Published As
Publication number | Publication date |
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NO147989C (en) | 1983-07-20 |
NO770347L (en) | 1977-08-04 |
JPS577175B2 (en) | 1982-02-09 |
DK154776B (en) | 1988-12-19 |
IT1112146B (en) | 1986-01-13 |
CH633816A5 (en) | 1982-12-31 |
ES455332A1 (en) | 1978-05-16 |
SE7701144L (en) | 1977-08-04 |
AU2187677A (en) | 1978-08-10 |
DK154776C (en) | 1989-05-16 |
CA1086450A (en) | 1980-09-23 |
DE2704278C2 (en) | 1983-08-04 |
BR7700611A (en) | 1977-08-16 |
FR2340342A1 (en) | 1977-09-02 |
DE2704278A1 (en) | 1977-08-04 |
GB1537421A (en) | 1978-12-29 |
NL170297C (en) | 1982-10-18 |
JPS5295773A (en) | 1977-08-11 |
NL170297B (en) | 1982-05-17 |
AU507080B2 (en) | 1980-01-31 |
FR2340342B1 (en) | 1983-07-01 |
NL7700842A (en) | 1977-08-05 |
DK44477A (en) | 1977-08-04 |
BE850971A (en) | 1977-08-01 |
SE426072B (en) | 1982-12-06 |
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