NO145798B - FOOD POLYMER MIXTURE BASED ON POLYVINYL CHLORIDE - Google Patents
FOOD POLYMER MIXTURE BASED ON POLYVINYL CHLORIDE Download PDFInfo
- Publication number
- NO145798B NO145798B NO764062A NO764062A NO145798B NO 145798 B NO145798 B NO 145798B NO 764062 A NO764062 A NO 764062A NO 764062 A NO764062 A NO 764062A NO 145798 B NO145798 B NO 145798B
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- weight
- parts
- mixtures
- vinyl chloride
- density
- Prior art date
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- 229920002959 polymer blend Polymers 0.000 title claims description 7
- 239000004800 polyvinyl chloride Substances 0.000 title description 4
- 229920000915 polyvinyl chloride Polymers 0.000 title description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 14
- 239000004698 Polyethylene Substances 0.000 claims description 13
- -1 polyethylene Polymers 0.000 claims description 13
- 229920000573 polyethylene Polymers 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 11
- 239000004088 foaming agent Substances 0.000 claims description 8
- 239000000155 melt Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 28
- 239000006260 foam Substances 0.000 description 13
- 239000000314 lubricant Substances 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000004604 Blowing Agent Substances 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 3
- 235000019399 azodicarbonamide Nutrition 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- 229910052793 cadmium Inorganic materials 0.000 description 3
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920012128 methyl methacrylate acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- ISNKSXRJJVWFIL-UHFFFAOYSA-N (sulfonylamino)amine Chemical class NN=S(=O)=O ISNKSXRJJVWFIL-UHFFFAOYSA-N 0.000 description 1
- GOYVSMJIJAIOLT-UHFFFAOYSA-N 1,3-bis(4-phenylphenyl)-2,4-dihydrotriazine Chemical compound C1C=CN(C=2C=CC(=CC=2)C=2C=CC=CC=2)NN1C(C=C1)=CC=C1C1=CC=CC=C1 GOYVSMJIJAIOLT-UHFFFAOYSA-N 0.000 description 1
- NBOCQTNZUPTTEI-UHFFFAOYSA-N 4-[4-(hydrazinesulfonyl)phenoxy]benzenesulfonohydrazide Chemical compound C1=CC(S(=O)(=O)NN)=CC=C1OC1=CC=C(S(=O)(=O)NN)C=C1 NBOCQTNZUPTTEI-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004801 Chlorinated PVC Substances 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- PFBWBEXCUGKYKO-UHFFFAOYSA-N ethene;n-octadecyloctadecan-1-amine Chemical compound C=C.CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC PFBWBEXCUGKYKO-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- ALIFPGGMJDWMJH-UHFFFAOYSA-N n-phenyldiazenylaniline Chemical compound C=1C=CC=CC=1NN=NC1=CC=CC=C1 ALIFPGGMJDWMJH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 150000003751 zinc Chemical class 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
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions 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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- 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
- C08J2327/00—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 a halogen; Derivatives of such polymers
- C08J2327/02—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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
-
- 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
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Jellies, Jams, And Syrups (AREA)
- Confectionery (AREA)
- General Preparation And Processing Of Foods (AREA)
Description
Oppfinnelsen vedrører skumbare polymerblandinger på basis av homopolymerisat av vinylklorid som inneholder intet eller lite mykningsmiddel, vanlige tilsetningsstoffer, samt et van- The invention relates to foamable polymer mixtures based on homopolymer of vinyl chloride which contain no or little plasticizer, common additives, as well as a
lig esemiddel og har forbedrede skummings- og bearbeidings-egenskaper. similar foaming agent and has improved foaming and processing properties.
Polymerskum på basis av vinylkloridpolymerisater som innehol- Polymer foam based on vinyl chloride polymers containing
der lite eller intet mykningsmiddel er bl.a., kjent fra tysk utlegningsskrift nr. 2.047.969 . where little or no plasticizer is, among other things, known from German specification no. 2,047,969.
For fremstilling derav går man ut fra vinylkloridpolymerblandinger, som ved siden av kjemiske og/eller fysikalske esemid- For their production, the starting point is vinyl chloride polymer mixtures, which, in addition to chemical and/or physical esemid-
ler også kan inneholde ett eller flere andre hjelpestoffer, clay may also contain one or more other excipients,
som stabiliseringsmiddel, bearbeidelseshjelpemiddel, stoffer for forbedring av slagfasthet, glidemiddel osv.. as stabilizer, processing aid, substances for improving impact resistance, lubricant, etc.
Bearbeidingen av esemiddelholdige hårde vinylkloridpolymerisater , f.eks. ekstrudering av dem til profiler, forloper i flere henseender utilfredsstillende. Overflåtestrukturen av det således erholdte skum er ofte mangelfull og skumcellene er ofte av forskjellig storrelse. Tettheten av det skummete materiale er vanskelig å innstille og blir i mange tilfeller hoyere enn onsket. Også formbestandigheten er ved forhoyet temperatur.generelt for liten, slik at skummet etter ekstruderingen ved gjennomforingen gjennom et kalibreringsanlegg ikke kan bear-beides til et ekstrudat med konstante henholdsvis onskede dimensjoner. Dessuten er bearbeidingshjelpemidler og andre tilsetningsstoffer relativt kostbare, slik at det er ønskelig å holde mengden av slike hjelpestoffer så liten som mulig. The processing of hard vinyl chloride polymers containing blowing agents, e.g. extrusion of them into profiles is unsatisfactory in several respects. The surface structure of the foam thus obtained is often defective and the foam cells are often of different sizes. The density of the foamed material is difficult to adjust and in many cases is higher than desired. Also, the dimensional stability at elevated temperature is generally too low, so that the foam after extrusion when passing through a calibration facility cannot be processed into an extrudate with constant or desired dimensions. Furthermore, processing aids and other additives are relatively expensive, so that it is desirable to keep the amount of such aids as small as possible.
I en skumbar polymerblanding av den innledningsvis nevnte type In a foamable polymer mixture of the initially mentioned type
er det ifølge foreliggende oppfinnelse innarbeidet pr. 100 vektdeler vinylkloridpolymerisat maksimalt 4 vektdeler polyetylen med en smelteindeks på minst 0,10 dg/min. og maksimalt 2,1 dg/min.målt ifølge ASTM-D 1238. is according to the present invention incorporated per 100 parts by weight vinyl chloride polymer maximum 4 parts by weight polyethylene with a melt index of at least 0.10 dg/min. and a maximum of 2.1 dg/min. measured according to ASTM-D 1238.
De anvendbare vinylkloridpolymerisater ifolge oppfinnelsen The usable vinyl chloride polymers according to the invention
kan også tilsettes etterklorerte vinylkloridpolymerisater. De ved foreliggende oppfinnelse benyttede vinylkloridpolymerisa- post-chlorinated vinyl chloride polymers can also be added. The vinyl chloride polymers used in the present invention
ter har en K-verdi etter Fikentscher på fortrinnsvis 45-85 ter has a K-value according to Fikentscher of preferably 45-85
og spesielt fra 50-75. and especially from 50-75.
Vinylkloridpolymerisatene kan fremstilles på hvilken som helst The vinyl chloride polymers can be produced on any
i og for seg kjent måte, f.eks. ved suspensjonspolymerisasjon, emulsjonspolymerisasjon eller polymaisasjon i massen. in and of itself known way, e.g. by suspension polymerization, emulsion polymerization or polymerization in the pulp.
Overraskende nok viste det seg at ved opptak av relativt små mengder polyetylen, som svarer til det forannevnte, i vinyl-kloridpolymerblandingen erholdes vinylkloridpolymerblandinger, som lar seg forarbeide til skum med en regelmessig cellestruktur og en gunstig, relativt liten densitet. Formbestandigheten til disse skummene ved høyere temperatur er slik at s kurmiene kan kalibreres godt og ékstrudatene, særlig profiler, har en godt utseende og glatt overflatestruktur. Surprisingly, it turned out that by incorporating relatively small amounts of polyethylene, which corresponds to the aforementioned, into the vinyl chloride polymer mixture, vinyl chloride polymer mixtures are obtained, which can be processed into foam with a regular cell structure and a favorable, relatively low density. The dimensional stability of these foams at higher temperatures is such that the scurmies can be calibrated well and the extrudates, especially profiles, have a good appearance and smooth surface structure.
Vinylkloridpolymerisatskummets densitet er sterkt avhengig av art og mengde av det i blandingen opptatte esemiddel. Ved anven deise av 0,2 til maksimalt 2 vektsdeler av et kjemisk esemiddel kan det erholdes skum med en densitet på ca. 0,4 til ca. 1. The density of the vinyl chloride polymer foam is strongly dependent on the type and quantity of the foaming agent used in the mixture. By using 0.2 to a maximum of 2 parts by weight of a chemical foaming agent, foam can be obtained with a density of approx. 0.4 to approx. 1.
Ved anvendelse av relativt store esemiddelmengder kan riktig-nok skum erholdes med liten densitet, men slike blandinger eg-ner seg lite eller ikke for fremstilling av skummete ekstrudater som profiler. Esemiddelmengden kan være så stor at skummin-gen forløper temmelig heftig, hvorved det oppstår et uregel-messig skum med uensartede celler og en uensartet overflate. Derfor anvendes det ifølge oppfinnelsen fortrinnsvis maksimalt 1 vektdel esemiddel. Videre er da en nøyaktig, gjensidig avpasning av komponentene også nødvendig. Man tilstrebei: en så liten densitet som mulig og en så ensartet skumstruktur som mulig. Dette siste kravet begrenser den anvendbare esemiddelmengden. Den nøyaktige esemiddelmengden er avhengig av det anvendte esemiddel. Den gassmengde som skal utvikles av en bestemt vektmengde esemiddel betinges bl.a. av molekyl-vekten. Spaltningshastigheten spiller også en rolle. Fag-mannen kan lett bestemme den optimale mengde eksperimentelt. By using relatively large amounts of blowing agent, it is true that foam can be obtained with a low density, but such mixtures are little or not suitable for the production of foamy extrudates such as profiles. The amount of foaming agent can be so large that the foaming proceeds rather violently, resulting in an irregular foam with non-uniform cells and a non-uniform surface. Therefore, according to the invention, a maximum of 1 part by weight of foaming agent is preferably used. Furthermore, an exact, mutual matching of the components is also necessary. One strives for: as little density as possible and as uniform a foam structure as possible. This last requirement limits the amount of spray agent that can be used. The exact amount of blowing agent depends on the used blowing agent. The amount of gas that must be developed by a specific weight amount of effervescent agent depends on, among other things, of the molecular weight. The rate of cleavage also plays a role. The person skilled in the art can easily determine the optimal amount experimentally.
Selv om akumstrukturens densitet hovedsakelig bestemmes av esemiddelmengden, viser det seg likevel at densiteten også Although the density of the accumulator structure is mainly determined by the amount of foaming agent, it nevertheless turns out that the density also
kan påvirkes av bestemte tilsetningsstoffer. Således kan til-setningen av polyetylen påviselig bevirke en nedsettelse av densiteten. can be affected by certain additives. Thus, the addition of polyethylene can demonstrably cause a reduction in density.
Anvendelsen av polyetylen med en smelteindeks på mere enn The use of polyethylene with a melt index of more than
0,10 og maksimalt 2,1 byr dessuten på økonomiske fordeler i sammenligning med de hittil vanlige modifiseringsmidler, som for eksempel ABS, MBS og MABS<+>^, som er betraktelig mer kostbare og som må tilsettes i større mengder for å oppnå sammen-lignbare densiteter. Også i andre henseender viser anvendelsen av høyraolekulart polyetylen seg gunstig. Man kan som nevnt,bearbeide blandingene ifølge oppfinnelsen til skummede ekstrudater som profiler, som i tillegg til en gunstig densitet har en regelmessig cellestruktur og en godt utseende, glatt overflate. 0.10 and a maximum of 2.1 also offer economic advantages in comparison with the hitherto common modifiers, such as for example ABS, MBS and MABS<+>^, which are considerably more expensive and which must be added in larger quantities to achieve - similar densities. In other respects too, the use of high-molecular polyethylene proves beneficial. As mentioned, the mixtures according to the invention can be processed into foamed extrudates such as profiles, which in addition to a favorable density have a regular cell structure and a good-looking, smooth surface.
Formbestandigheten ved hoyere temperatur er god, slik at blandingene ifolge oppfinnelsen lar seg kalibrere godt etter eks-truder ing . The dimensional stability at higher temperatures is good, so that the mixtures according to the invention can be calibrated well after extrusion.
Egenskapene kan etter onske forbedres ytterligere idet man i blandingene opptar ett eller flere vanlige modifikasjonsmidler, som etterklorert polyvinylklorid, ABS, MBS,' MABS eller polyme-tylmetakrylat. If desired, the properties can be further improved by including one or more common modifiers in the mixtures, such as post-chlorinated polyvinyl chloride, ABS, MBS, MABS or polymethyl methacrylate.
Ved fremgangsmåten ifolge oppfinnelsen kan de enkelte komponen-ter foreligge i hvilken som helst form. Fortrinnsvis blander man dog pulverformige stoffer. Pulverblandingen kan anvendes som sådan eller etter forutgående granulering. In the method according to the invention, the individual components can be in any form. Preferably, however, powdery substances are mixed. The powder mixture can be used as such or after prior granulation.
+ ) Dette er de i praksis vanlige betegnelser for plast + ) These are the common designations for plastic in practice
på basis av akrylonitril, butadien og styren; metylmet-akrylat, butadien og styren; henh. metyImetakrylat, akryl-nitril, butadien og styren. on the basis of acrylonitrile, butadiene and styrene; methyl methacrylate, butadiene and styrene; henh. methyl methacrylate, acrylonitrile, butadiene and styrene.
Esemidlet anvendes i mengder på ca. 0,1-2 vektsdeler, fortrinnsvis i mengder på 0,2-1,5 vektdeler, pr. 100 vektdeler vinyl-klor idpolymer isat . Det kan opptas i blandingen ifolge oppfinnelsen de forskjelligste kjemiske esemidler. Egnete esemidler er nitrogenavspaltende midler, som azobisformamid, azodikarbonamid, azobisisobutyronitril, diazoaminobenzen, p.p'-oksybis-(benzensulfonylhydrazid), N,N'-dinitrosopentametylentetramin, p,p'-azobis(benzensulfonylsemikarbonamid), dietylazoisobutyrat, 1,3-bis(xenyl)triazin og 4,4'-oksibis(benzensulfonylhydrazid). The emulsifier is used in quantities of approx. 0.1-2 parts by weight, preferably in amounts of 0.2-1.5 parts by weight, per 100 parts by weight of vinyl-chlorinated polymer. A wide variety of chemical foaming agents can be included in the mixture according to the invention. Suitable elution agents are nitrogen-releasing agents, such as azobisformamide, azodicarbonamide, azobisisobutyronitrile, diazoaminobenzene, p.p'-oxybis-(benzenesulfonylhydrazide), N,N'-dinitrosopentamethylenetetramine, p,p'-azobis(benzenesulfonylsemicarbonamide), diethylazoisobutyrate, 1,3-bis (xenyl)triazine and 4,4'-oxybis(benzenesulfonylhydrazide).
Det dreier seg ved disse esemidler generelt om azo-, nitroso-eller sulfonylhydrazinforbindelser. These emulsifiers are generally azo-, nitroso- or sulfonylhydrazine compounds.
Det kan anvendes vanlige aktivatorer, såkalte initiatorer, på basis av bly, barium, kadmium eller sinksalter o.l.. Disse aktivato-rene nedsetter generelt temperaturen, hvorved esemidlet avgir gass. Common activators, so-called initiators, based on lead, barium, cadmium or zinc salts etc. can be used. These activators generally lower the temperature, whereby the blowing agent emits gas.
Videre kan man i blandingene ifolge oppfinnelsen oppta de vanlige glidemidler og glidemiddelblandinger samt andre vanlige tilsetningsstoffer. Glidemidler og glidemiddelblandinger opp- Furthermore, the mixtures according to the invention can contain the usual lubricants and lubricant mixtures as well as other usual additives. Lubricants and lubricant mixtures up-
tas i mengder på ca. 0,5-5, fortrinnsvis 1-4 vektdeler i blandingene. Egnete glidemidler henh. glidemiddelblandinger er f. taken in quantities of approx. 0.5-5, preferably 1-4 parts by weight in the mixtures. Suitable lubricants acc. lubricant mixtures are e.g.
eks. paraffin, polyetylenvokser, kalsiumstearat, etylenbis-stearylamid og andre kjente glidemidler. e.g. paraffin, polyethylene wax, calcium stearate, ethylene bis-stearylamide and other known lubricants.
Videre kan i blandingene ifolge oppfinnelsen opptas findisper-gerte uorganiske fyllstoffer og/eller pigmenter i mengder på Furthermore, finely dispersed inorganic fillers and/or pigments can be included in the mixtures according to the invention in quantities of
ca. 1-15 vektsdeler. Slike fyllstoffer eller pigmenter er f. about. 1-15 parts by weight. Such fillers or pigments are e.g.
eks. t itandioksyd, jernoksyd, kalsiumkarbonat eller t-ilicium-dloksyd. e.g. titanium dioxide, iron oxide, calcium carbonate or silicon dioxide.
Det kan videre tilsettes stabilisatorer som f.eks. vanlige blyforbindelser, barium/kadmium- og tinnforbindelser i meng- Stabilizers such as e.g. common lead compounds, barium/cadmium and tin compounds in
der på 0,5-4 vektdeler i blandingene. there of 0.5-4 parts by weight in the mixtures.
Ifølge oppfinnelsen anvendes enten ingen mykningsmidler eller løsningsmidler, eller henh. ytterst små mengder på maksimalt 5 vekt-%. According to the invention, either no plasticizers or solvents are used, or extremely small amounts of a maximum of 5% by weight.
Oppfinnelsen anskueliggjøres ytterligere gjennom de etter-følgende eksempler. The invention is further illustrated through the following examples.
EKSEMP EL 1 EXAMPLE EL 1
Det gåes ut fra en polyvinylkloridblanding hvori er opptatt et polyetylen og som deretter blir "bearbeidet til skumstruktur. The starting point is a polyvinyl chloride mixture in which a polyethylene is incorporated and which is then "processed into a foam structure.
Utgangsblandingen består av polyvinylklorid med en K-verdi The starting mixture consists of polyvinyl chloride with a K value
etter Fikentscher på 59 og inneholder pr. 100 vektsdeler polyvinylklorid : 3,5 vektsdeler av en barium/kadmium/bly-stabilisator; after Fikentscher on 59 and contains per 100 parts by weight polyvinyl chloride : 3.5 parts by weight of a barium/cadmium/lead stabilizer;
1,2 vektsdeler av et kombinert glidemiddel, bestående av 1.2 parts by weight of a combined lubricant, consisting of
av en teknisk blanding av hoyere fettsyrer,deres metall-salter og estere av hoyere alkoholer med de hoyere fett-syrer ; of a technical mixture of higher fatty acids, their metal salts and esters of higher alcohols with the higher fatty acids;
0,5 vektdeler azodikarbonamid; 0.5 parts by weight of azodicarbonamide;
5 vektdeler fint kalsiumkarbonat55 parts by weight fine calcium carbonate5
2 vektdeler titandioksyd. 2 parts by weight titanium dioxide.
I denne utgangsblandingen opptas ett i handelen tilgjengelig lavtrykkspolyetylen med en smelteindeks på 0,11 i mengder på 0,5, 1,0, 2,0, 5,0 henh. 10,0 vektdeler pr. 100 vektdeler. I figuren fremstilles densitetene til blandinger som inneholder polyetylenet med en smelteindeks på 0,11 og utgangs-blandingens densitet. Det viser seg at ved mengder på 4 vektsdeler eller mindre opptrer en nedsettelse av densiteten i sammenligning med utgangsblandingen. Blandingene ifolge oppfinnelsen gir skum med regelmessige celler og en pen overflatestruktur. A commercially available low-pressure polyethylene with a melt index of 0.11 is taken up in this starting mixture in amounts of 0.5, 1.0, 2.0, 5.0 respectively. 10.0 parts by weight per 100 parts by weight. The figure shows the densities of mixtures containing the polyethylene with a melt index of 0.11 and the density of the starting mixture. It turns out that at amounts of 4 parts by weight or less, a reduction in density occurs in comparison with the starting mixture. The mixtures according to the invention provide foam with regular cells and a neat surface structure.
EKSEMPEL 2 EXAMPLE 2
I utgangsblandingen opptas 0,5, 1,0, 2,0, 5,0 henh. 10,0 vektdeler av et lavtrykkspolyetylen med en smelteindeks på In the starting mixture, 0.5, 1.0, 2.0, 5.0 are taken up respectively. 10.0 parts by weight of a low pressure polyethylene with a melt index of
2,1 dg/min. Av denne blandingen ekstruderes små strimler, hvor-av densiteten bestemmes. 2.1 dg/min. Small strips are extruded from this mixture, from which the density is determined.
I figuren er det gjengitt densitetene av blandingene med polyetylen med en smelteindeks på 2,1 og densiteten til utgangsblandingen. Når utgangsblandingen inneholder 4 eller færre vektdeler polyetylen viser det seg at densiteten i sammenligning med densiteten til utgangsmaterialet blir mindre. De beskrevne blandingene gir skum med regelmessige celler og en pen overflatestruktur. The figure shows the densities of the mixtures with polyethylene with a melt index of 2.1 and the density of the starting mixture. When the starting mixture contains 4 or fewer parts by weight of polyethylene, it turns out that the density in comparison with the density of the starting material becomes smaller. The described mixtures produce foam with regular cells and a nice surface structure.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7513958A NL7513958A (en) | 1975-11-29 | 1975-11-29 | FOAMABLE VINYL CHLORIDE POLYMERS AND HARD FOAM STRUCTURES MANUFACTURED THEREOF. |
Publications (3)
Publication Number | Publication Date |
---|---|
NO764062L NO764062L (en) | 1977-06-01 |
NO145798B true NO145798B (en) | 1982-02-22 |
NO145798C NO145798C (en) | 1982-06-02 |
Family
ID=19824946
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO764062A NO145798C (en) | 1975-11-29 | 1976-11-26 | FOOD POLYMER MIXTURE BASED ON POLYVINYL CHLORIDE |
Country Status (9)
Country | Link |
---|---|
BE (1) | BE848689A (en) |
DE (1) | DE2653578A1 (en) |
DK (1) | DK533376A (en) |
FR (1) | FR2336443A1 (en) |
GB (1) | GB1557980A (en) |
IT (1) | IT1076846B (en) |
NL (1) | NL7513958A (en) |
NO (1) | NO145798C (en) |
SE (1) | SE416211B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6113822A (en) * | 1998-12-23 | 2000-09-05 | General Electric Company | Polyolefins as nucleating agent for foamed engineering polymers |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE332072B (en) * | 1968-04-22 | 1971-01-25 | Kema Nord Ab | |
BE792581A (en) * | 1971-12-09 | 1973-06-12 | Ici Ltd | EXPANDABLE COMPOSITIONS BASED ON VINYL CHLORIDE POLYMERS AND PROCESS FOR PREPARING THEM |
-
1975
- 1975-11-29 NL NL7513958A patent/NL7513958A/en not_active Application Discontinuation
-
1976
- 1976-11-24 BE BE172646A patent/BE848689A/en not_active IP Right Cessation
- 1976-11-25 IT IT52353/76A patent/IT1076846B/en active
- 1976-11-25 DE DE19762653578 patent/DE2653578A1/en not_active Withdrawn
- 1976-11-26 FR FR7635789A patent/FR2336443A1/en active Granted
- 1976-11-26 SE SE7613301A patent/SE416211B/en unknown
- 1976-11-26 NO NO764062A patent/NO145798C/en unknown
- 1976-11-26 DK DK533376A patent/DK533376A/en not_active Application Discontinuation
- 1976-11-26 GB GB49417/76A patent/GB1557980A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1557980A (en) | 1979-12-19 |
FR2336443A1 (en) | 1977-07-22 |
SE7613301L (en) | 1977-05-30 |
SE416211B (en) | 1980-12-08 |
IT1076846B (en) | 1985-04-27 |
BE848689A (en) | 1977-05-24 |
DE2653578A1 (en) | 1977-06-08 |
NO145798C (en) | 1982-06-02 |
FR2336443B1 (en) | 1982-11-05 |
NL7513958A (en) | 1977-06-01 |
NO764062L (en) | 1977-06-01 |
DK533376A (en) | 1977-05-30 |
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