IE83257B1 - Plasticizer-free moulding mass based on polyvinylchloride - Google Patents
Plasticizer-free moulding mass based on polyvinylchlorideInfo
- Publication number
- IE83257B1 IE83257B1 IE1990/3045A IE304590A IE83257B1 IE 83257 B1 IE83257 B1 IE 83257B1 IE 1990/3045 A IE1990/3045 A IE 1990/3045A IE 304590 A IE304590 A IE 304590A IE 83257 B1 IE83257 B1 IE 83257B1
- Authority
- IE
- Ireland
- Prior art keywords
- weight
- moulding compound
- parts
- oxide
- plasticiser
- Prior art date
Links
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 12
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 12
- 238000000465 moulding Methods 0.000 title description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium monoxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 48
- 239000000206 moulding compound Substances 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 31
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 30
- 239000000945 filler Substances 0.000 claims description 26
- 239000000292 calcium oxide Substances 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims description 20
- 229910000514 dolomite Inorganic materials 0.000 claims description 17
- 239000010459 dolomite Substances 0.000 claims description 17
- 229920003023 plastic Polymers 0.000 claims description 17
- 239000004033 plastic Substances 0.000 claims description 17
- 239000000395 magnesium oxide Substances 0.000 claims description 15
- BZHJMEDXRYGGRV-UHFFFAOYSA-N vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- 239000000654 additive Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- -1 polyethylenes Polymers 0.000 claims description 11
- YLUIKWVQCKSMCF-UHFFFAOYSA-N calcium;magnesium;oxygen(2-) Chemical compound [O-2].[O-2].[Mg+2].[Ca+2] YLUIKWVQCKSMCF-UHFFFAOYSA-N 0.000 claims description 10
- 239000003381 stabilizer Substances 0.000 claims description 10
- 239000011575 calcium Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 8
- 229920001519 homopolymer Polymers 0.000 claims description 8
- 229920001897 terpolymer Polymers 0.000 claims description 8
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 claims description 7
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000011780 sodium chloride Substances 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 6
- 239000003063 flame retardant Substances 0.000 claims description 6
- 239000000049 pigment Substances 0.000 claims description 6
- 150000004671 saturated fatty acids Chemical group 0.000 claims description 6
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 6
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 6
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- AQSJGOWTSHOLKH-UHFFFAOYSA-N Phosphite Chemical compound [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- YNGDWRXWKFWCJY-UHFFFAOYSA-N dihydropyridine Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 claims description 5
- 239000000975 dye Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxyl anion Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
- 239000000314 lubricant Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene (PE) Substances 0.000 claims description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 3
- 230000000996 additive Effects 0.000 claims description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 3
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 239000004604 Blowing Agent Substances 0.000 claims description 2
- 238000001746 injection moulding Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 230000003014 reinforcing Effects 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims 1
- 239000008247 solid mixture Substances 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 150000004665 fatty acids Chemical class 0.000 description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 12
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 11
- 239000004926 polymethyl methacrylate Substances 0.000 description 11
- 238000004381 surface treatment Methods 0.000 description 10
- 239000012188 paraffin wax Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 229920005862 polyol Polymers 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 7
- 239000004610 Internal Lubricant Substances 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- GUJHKKNKJWZINP-UHFFFAOYSA-N 1-phenylicosane-1,19-dione Chemical compound CC(=O)CCCCCCCCCCCCCCCCCC(=O)C1=CC=CC=C1 GUJHKKNKJWZINP-UHFFFAOYSA-N 0.000 description 5
- 229960005069 Calcium Drugs 0.000 description 5
- 229960003563 Calcium Carbonate Drugs 0.000 description 5
- 239000004605 External Lubricant Substances 0.000 description 5
- 150000001447 alkali salts Chemical class 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxystearic acid Chemical compound CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N Antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 150000007942 carboxylates Chemical class 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- MDSNZOMERYGQAQ-UHFFFAOYSA-N C=1C=CC=CC=1C(CCCCCCCCCOP([O-])[O-])C1=CC=CC=C1 Chemical compound C=1C=CC=CC=1C(CCCCCCCCCOP([O-])[O-])C1=CC=CC=C1 MDSNZOMERYGQAQ-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 3
- 229910052793 cadmium Inorganic materials 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000012170 montan wax Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- JLIDBLDQVAYHNE-IBPUIESWSA-N (s)-(+)-Abscisic acid Natural products OC(=O)\C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-IBPUIESWSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L Calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical group CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- NMAKPIATXQEXBT-UHFFFAOYSA-N didecyl phenyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OC1=CC=CC=C1 NMAKPIATXQEXBT-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 229920000578 graft polymer Polymers 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- KREXGRSOTUKPLX-UHFFFAOYSA-N octadecanoic acid;zinc Chemical compound [Zn].CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O KREXGRSOTUKPLX-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-M stearate Chemical class CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 2
- 229940113165 trimethylolpropane Drugs 0.000 description 2
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 2
- NIONDZDPPYHYKY-SNAWJCMRSA-N (2E)-hexenoic acid Chemical compound CCC\C=C\C(O)=O NIONDZDPPYHYKY-SNAWJCMRSA-N 0.000 description 1
- JUMARTCPADSKCD-HZJYTTRNSA-N (9Z,12Z)-2-aminooctadeca-9,12-dienoic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCC(N)C(O)=O JUMARTCPADSKCD-HZJYTTRNSA-N 0.000 description 1
- 239000001602 (E)-hex-3-enoic acid Substances 0.000 description 1
- JBSOOFITVPOOSY-KTKRTIGZSA-N (Z)-2-hydroxyoctadec-9-enoic acid Chemical compound CCCCCCCC\C=C/CCCCCCC(O)C(O)=O JBSOOFITVPOOSY-KTKRTIGZSA-N 0.000 description 1
- XRKBQVGBWJWJJJ-UHFFFAOYSA-N 2-aminooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(N)C(O)=O XRKBQVGBWJWJJJ-UHFFFAOYSA-N 0.000 description 1
- JGHSBPIZNUXPLA-UHFFFAOYSA-N 2-hydroxypalmitic acid Chemical compound CCCCCCCCCCCCCCC(O)C(O)=O JGHSBPIZNUXPLA-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-M 2-hydroxystearate Chemical class CCCCCCCCCCCCCCCCC(O)C([O-])=O KIHBGTRZFAVZRV-UHFFFAOYSA-M 0.000 description 1
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K Aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M Aluminium hydroxide oxide Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N Azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L Calcium hydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000004608 Heat Stabiliser Substances 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 229940088417 PRECIPITATED CALCIUM CARBONATE Drugs 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229940075582 Sorbic Acid Drugs 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N Triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L Zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- 229940053200 antiepileptics Fatty acid derivatives Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium(0) Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- PVEOYINWKBTPIZ-UHFFFAOYSA-N but-3-enoic acid Chemical compound OC(=O)CC=C PVEOYINWKBTPIZ-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- XXHDAWYDNSXJQM-ARJAWSKDSA-N cis-hex-3-enoic acid Chemical compound CC\C=C/CC(O)=O XXHDAWYDNSXJQM-ARJAWSKDSA-N 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000004021 humic acid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical compound OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- WSWCOQWTEOXDQX-UHFFFAOYSA-N sorbic acid Chemical compound CC=CC=CC(O)=O WSWCOQWTEOXDQX-UHFFFAOYSA-N 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 230000003019 stabilising Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 description 1
- XCHNVUHBTJJNPV-UHFFFAOYSA-N tridecyl phosphite Chemical compound CCCCCCCCCCCCCOP([O-])[O-] XCHNVUHBTJJNPV-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- 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
Description
PLASTICIZER—FREE MOULDING MASS BASED ON POLYVINYLCHLORIDE
SOLVAY KUNSTSTOFFE GMBH
Description
The present invention relates to a plasticiser—free
moulding compound on the basis of polyvinyl chloride,
containing a plastics material consisting of vinyl
chloride homopolymer, copolymer and/or terpolymer,
mixtures thereof or compounds therewith, having a PVC
content of more than 70% by weight, preferably more
than 85% by weight, and 15 to 0% by weight of at least
one impact-modifying polymer, selected from the group
of polyalkyl acrylates, chlorinated polyethylenes,
ethylene/vinyl acetate copolymer or ethylene/vinyl
acetate/carbon monoxide terpolymer, and other
additives, processing aids and the like. According to,
the invention, the plastics moulding compound on the
basis of polyvinyl chloride contains.certain parts by
weight of at least one co-stabiliser, surface-treatedt
alkaline earth oxide and/or partly hydrated alkaline
earth oxide and additional auxiliaries.
The invention furthermore relates to a method for
preparing the moulding compound and the use of the same
in extrusion processes.
A rigid, heat-stabilised composition on the basis of
vinyl chloride polymers, which contains as heat
stabilisers magnesium oxide and a saturated polyvalent
aliphatic alcohol, and also calcium and zinc stearate
and other processing aids and additives, is already
known from EP-B-0 001 859. These heat-stabilised
compositions are particularly suitable for the
They have the
advantage that they are free from lead and cadmium.
production of tubes and profiles.
The thermal stability and processing properties of
these compositions are however in need of improvement.
It was an object of the present invention to discover a
moulding compound having improved properties and/or
improved processing properties and a method for the
preparation of the same and/or that the moulded parts
produced from the moulding compound should have
improved properties. In particular, improved thermal
stability of the moulding material during processing
was to be achieved. Furthermore, additionally lead-
containing and cadmium-containing stabilisers were to
be avoided. when processing the moulding compound in
an extruder, the risk of corrosion occurring was to be
avoided.
It was established according to the invention that
these objects are met by a plasticiser-free moulding
compound on the basis of polyvinyl chloride, containing
a plastics material, vinyl chloride homopolymer,
copolymer and/or terpolymer, mixtures thereof or
compounds therewith, having a vinyl chloride or PVC
content of more than 70% by weight, preferably more
than-85% by weight, and 15 to 0% by weight of at least
one impact-modifying polymer, selected from the group
of polyalkyl acrylates, chlorinated polyethylenes,
ethylene/vinyl acetate copolymers or ethylene/vinyl
acetate/carbon monoxide terpolymers.
Per 100 parts by weight of this PVC mixture or of the
.vinyl chloride mixed polymer, the moulding compound
contains
a)’ 0.01 to 3 parts by weight of at least one calcium
carboxylate,
b) 0.01 to 3 parts by weight of at least one zinc
carboxylate,
c) 0.01 to 3 parts by weight of at least one organic
co-stabiliser, selected.from the group of at least
one 3-diketone, organic phosphite and/or dihydro—
pyridine, optionally pigments, dyes, lubricants,
blowing agents, flame retardants, fillers,
reinforcing fibres or other processing aids and
additives, and, according to the invention,
d) 0.01 to 5 parts by weight of at least one alkaline
earth oxide, alkaline earth hydroxide and/or
partly hydrated alkaline earth oxide, preferably
calcium oxide and/or magnesium oxide, and/or
partly hydrated calcium oxide and/or partly
hydrated magnesium oxide and/or_calcined dolomite
or partly hydrated calcined dolomite, with the
alkaline earth oxide, alkaline earth hydroxide
and/or partly hydrated alkaline earth oxide,
preferably the calcium oxide and/or magnesium
oxide, and/or the partly hydrated calcium oxide
and/or partly hydrated magnesium oxide and/or the
calcined dolomite or the partially hydrated
calcined dolomite being coated on the entire,
surface or in partial regions of the surface with
a surface—modifying treatment agent or coating
agent.
Salts of calcium and/or zinc with fatty acids and/or
derivatives thereof, preferably of fatty acids
additionally containing polar groups, with C8 to Cu,
preferably Cm to Ca, are used as calcium and/or zinc
carboxylates. Preferably C5 to Cm fatty acids,v
derivatives thereof and/or mixtures thereof, in
particular also fatty acids containing additional polar
groups, are used. Stearates, hydroxystearates,
palmitates and/or behenates or fatty acids or fatty
acid derivatives of these compounds which contain
additional polar groups, preferably hydroxyl groups,
have proved particularly suitable.
According to a preferred embodiment, the moulding
compound additionally contains
e) 0.01 to 15 parts by weight of at least one filler,
preferably at least one inorganic filler.
According to another preferred embodiment, the moulding
compound additionally contains per 100 parts by weight
of the PVC mixture or the vinyl chloride mixed polymer
f) 0.01 to 5 parts by weight of at least one external
lubricant and/or internal lubricant, and/or
g) 0.01 to 5 parts by weight of a processing aid or
‘ additive, preferably selected from the group of
polymeric alkyl methacrylates.
According to a preferred embodiment of the invention,
per 100 parts by weight of the plastics material or
plastics mixture, additionally
a)~ 0.05 to 1.5 parts by weight of at least one
calcium carboxylate,
‘b) 0.05 to 1.5 parts by weight of at least one zinc
carboxylate,
c) 0.05 to 2 parts by weight of at least one organic
co-stabiliser, selected from the group of at least
one fi—diketone, organic phosphite and/or dihydro-
pyridine,
d) 0.05 to 1 part by weight calcium oxide and/or
magnesium oxide,
e) 0.05 to 10 parts by weight of at least one filler,
preferably an inorganic filler,
f) 0.5 to.5 parts by weight of at least one pigment
and/or dye, lubricant and/or internal lubricant,
g) 0.5 to 3.5 parts by weight of a processing aid or
additive, selected from the group of polymeric
alkyl methacrylates, preferably polymethyl
methacrylate,
are contained in the moulding compound.
Preferably a benzoylstearoyl methane is used as
fl-diketone within the scope of the invention.
Preferably triphenyl phosphite, trilauryl phosphite,.
diphenyldecyl phosphite, tridecyl phosphite and/or
phenyldidecyl phosphite are added to the moulding
compound as phosphites.
According to a preferred embodiment of the invention,
up to 70% by weight (relative to 100% by weight of the
co-stabiliser used), preferably up to 50% by weight, of
the co-stabiliser, selected from the group of at least
one B—diketone, organic phosphite and/or dihydro—
The content of the
polyol should if possible be below 50% by weight,
pyridine, is replaced by a polyol.
particularly preferably below 40% by weight (relative
to 100% by weight of the co-stabiliser used), in order
to achieve improved heat stabilisation of the moulding
compound.
Preferably trimethylol propane, di—trimethylol propane,
pentaerythrite and mixtures of these polyols with each
other or with other polyols are used as polyols.
According to a further embodiment, the polyol which is
‘
used in a certain proportion as co—stabiliser is
replaced by a polyether polyol.
According to another preferred embodiment, the moulding
compound additionally contains per 100 parts by weight
of the PVC mixture or of the vinyl chloride mixed
polymer, in addition to the additives already
mentioned,
h) 0.01 to 10 parts by weight, preferably 0.5 to 5
parts by weight, of a pigment and/or dye, and/or
i) 0.05 to 4 parts by weight, preferably 0.1 to 2
parts by weight, of at least one expanding agent
and/or
j) 0.5-to 10 parts by weight, preferably 1 to 8 parts
by weight, of at least one flame retardant, or the
moulding compound consists thereof.
Organic-Chemical and/or inorganic-chemical expanding
‘agents are used as expanding agents, preferably those
which eliminate nitrogen or carbon dioxide in heat.
Preferably expanding agents from the group of
azodicarbonamides and/or sodium bicarbonates are used.
The flame retardants known for plastics materials,
preferably aluminium hydroxide and/or antimony
trioxide, are used as flame retardants.
As already mentioned, according to the invention the
calcium oxide, magnesium oxide, partly hydrated calcium
oxide, partly hydrated magnesium oxide, the calcined
dolomite and/or partly hydrated calcined dolomite is
coated with a surface—modifying treatment agent or
coating agent on its entire surface or in partial
regions of the surface, and the surface-modifying
treatment agent or coating agent is a saturated or
unsaturated fatty acid or esters, salts or derivatives
thereof.
According to a preferred embodiment of the invention,
both the filler or the filler mixture or a portion of
the filler or the filler mixture and the calcium oxide
and/or the magnesium oxide is coated with a surface-
modifying treatment agent or coating agent on its
entire surface or in partial regions, and the surface-
modifying treatment agent or coating agent is a._
saturated or unsaturated fatty acid or esters, salts or
derivatives thereof.
The surface treatment agents or coating agents are
applied in the form of a solution, dispersion, melt and
the like.
surface treatment agent or coating agent is applied in
the hot state or in the form of a melt to the alkaline
earth oxide or partly hydrated alkaline earth oxide,
According to a preferred embodiment, the
preferably to the calcium oxide, magnesium oxide,
partly hydrated calcium oxide, partly hydrated
magnesium oxide, to the calcined dolomite or the partly
hydrated, calcined dolomite. Preferably a hot mixer or
a hot mixer/cooling mixer combination is used for this
purpose.
The application of the surface treatment agent to the
filler is preferably effected in the form of a
dispersion or solution of the surface treatment agent
or coating agent.
According to a preferred embodiment of the invention,
the calcium oxide, magnesium oxide, partly hydrated
calcium oxide, partly hydrated magnesium oxide, the
calcined dolomite and/or the partly hydrated calcined
dolomite is surface—modified with a saturated or
unsaturated fatty acid which additionally bears at
least one OH group or at least one other polar group in
addition to the COOH, ester and/or COO group.
According to another preferred embodiment, the calcium
oxide and/or magnesium oxide and/or the filler or the
filler mixture or a portion of the filler or the filler
mixture which preferably contains or consists of finely
divided calcium carbonate is surface—modified with at
least one saturated or unsaturated fatty acid, esters,
salts or derivatives thereof, which additionally bears
at least one OH group or at least one other polar group
in addition to the COOH, ester and/or COO group.
Saturated and/or unsaturated monocarboxylic acids or
polycarboxylic acids, their derivatives, substituted
»compounds and/or salts which contain one or more
hydroxyl group(s), amino group(s), carbonyl group(s)
and/or ester group(s) are used as organic carboxylic
acids containing polar groups. The salts of the
monocarboxylic acids, preferably the fatty acids, or
the acids themselves are preferred.
Preferably the fatty acids, bearing additional polar
groups, with C8 to C9, preferably cm to Ca, which
consist entirely of saturated fatty acid bearing at
least one additional polar group or contain up to 20%
by weight, preferably up to 6% by weight, of an
unsaturated fatty acid containing at least one
additional polar group are used. Preferably the fatty
acids containing polar groups, preferably fatty acids
containing hydroxyl groups or fatty acids containing
amino groups, preferably hydroxystearic acid,
hydroxypalmitic acid, hydroxyoleic acid, aminostearic
acid, aminolinoleic acid and/or the alkali salts of
this compound are used for the surface treatment of the
fillers and/or of magnesium oxide and/or calcium oxide.
According to a preferred embodiment, a synthetic
surface—coated calcium carbonate is used as filler,
preferably produced by introducing carbon dioxide into
a calcium hydroxide suspension and by subsequent
surface treatment of the resulting calcium carbonate
with an alkali or ammonium salt of a saturated or
unsaturated aliphatic monocarboxylic acid or fatty acid
containing in addition to a carboxylic acid, fatty acid
or substituted fatty acid containing at least one polar
group, preferably with an alkali or ammonium salt, at
least one hydroxyl, carbonyl, amino and/or ester group.
In this case, during the surface treatment the
corresponding calcium compound of this fatty acid
containing polar groups is formed entirely or partly on
the surface of the calcium carbonate.
The surface layer formed on the surface of the
synthetic calcium carbonate after the application of-
the treatment agent preferably consists of or contains
a calcium and/or alkali salt, and also optionally
ammonium salt of at least one fatty acid with Cm to Ca,
containing at least one hydroxyl group.
According to another embodiment, a singly or multiply
unsaturated, preferably a doubly unsaturated conjugated
or non—conjugated carboxylic acid, preferably an alkali
salt thereof or an ammonium salt of a singly or doubly
unsaturated carboxylic acid, or a mixture thereof, is
used as surface treatment agent for the fillers and/or
for the calcium oxide and/or magnesium oxide (or partly
hydrated compounds thereof) as unsaturated carboxylic-
acid, in particular crotonic acid, 2—pentenoic acid,
4-pentenoic acid, 2—hexenoic acid, 3—hexenoic acid,
2,4-pentadienoic acid, 3-butenoic acid and/or 3—methyl-
crotonic acid, but.preferably sorbic acid.
- 110 to 120°C.
According to a preferred embodiment, up to 60% by
weight (relative to 100 parts by weight of the
carboxylic acids used for surface treatment),
preferably up to 40% by weight, of the singly or
multiply unsaturated carboxylic acid or carboxylic
- acids or a mixture thereof is replaced by a saturated
and/or unsaturated monocarboxylic acid with C2 - Cg
containing a polar group in addition to the carboxyl
groups and/or humic acid.
According to a preferred embodiment of the invention,
up to 60% by weight (relative to 100 parts by weight of
the modifying agent used), preferably up to 35% by
weight, of the alkyl acrylate used as modifying agent,
preferably butyl acrylate, is replaced by polymethyl
methacrylate (PMMA).
The vinyl chloride homopolymer, copolymer and/or
terpolymer contained in the moulding compound
preferably has a K value of 58 to 73. Particularly
preferably, K values of 64 to 71 are used.
The present invention furthermore relates to a.method
for producing the plasticiser-free moulding compound.
According to the method of the invention, the plastics
materials and the additives are mixed in a hot mixer at
temperatures above 35°C and are heated with a
temperature increase to temperatures between 100 and
125°C (calculated as compound temperature), preferably
Then the moulding compound is cooled in
a cooling mixer to temperatures below 40°C, preferably
below 35°C.
According to a preferred embodiment, the plastics
material or the plastics mixture and the additives
which are solid at ambient temperature (with the
exception of titanium dioxide) are pre-mixed at 35 to
50°C, preferably 37 to 45°C, in a hot mixer, the liquid
additives are admixed thereto after an increase in
temperature when a temperature of between 55 and 65°C,
preferably 57 to 62°C, is reached, and subsequently is
mixed further with a temperature increase to 100 to
125°C (calculated as compound temperature), preferably
110 to 120°C.
a cooling mixer to temperatures of below 40°C,
Then the moulding compound is cooled in
preferably below 35°C.
When using titanium dioxide as a pigment, the addition
of titanium dioxide to the plastics/additives mixture
pre-mixed in the hot mixer is effected in the range of
90 to 125°C (calculated as compound temperature),
preferably 110 to 120°C, and then the moulding compound
is cooled in a cooling mixer to temperatures below
40°C, preferably below 35°C.
According to a preferred embodiment, the alkaline earth
oxide or partly'hydrated alkaline earth oxide,
preferably calcium oxide and/or magnesium oxide, partly
hydrated calcium oxide and/or partly hydrated magnesium
oxide and/or the calcined dolomite or partly hydrated,
calcined dolomite has an average particle size of less
than 25 pm, preferably less than 5 pm. Particularly
preferably, average particle sizes of between 0.5 and
pm are used.
According to a preferred embodiment, the weight of the
modifying agent or coating agent used for surface
treatment, dependent on the particle size of the
alkaline earth oxide or partly hydrated alkaline earth
oxide, preferably of the calcium oxide, magnesium oxide
and/or partly hydrated calcium oxide and/or magnesium
oxide is 0.02 to 4.5% by weight, preferably 0.5 to 2.5%
by weight, relative to 100 parts by weight alkaline
earth oxide or partly hydrated alkaline earth oxide.
According to a preferred embodiment, the filler or the
filler mixture has an average particle size of less
than 10 um, preferably less than 1 pm.
preferred embodiment, the average particle size of the
alkaline earth oxide or partly hydrated alkaline earth
According to a
oxide used is at least twice as large as the average
particle size of the filler or filler mixture.
The present invention furthermore relates to the use of
the plasticiser-free moulding compound in extrusion or
injection-moulding processes for the production of
profiles or articles or hollow bodies, preferably
extruded window profiles or extruded tubes.
The moulded parts and profiles produced from the
plasticiser-free moulding compounds according to the
invention have a very good surface condition (a
uniform, smooth surface). The processing properties
and properties of the finished articles or of the
profiles including the subsequent treatment thereof
(such as cutting, welding, drilling, sawing, bending
and the like) is comparable with or better than those
moulded parts or profiles which are produced using
compounds containing barium, cadmium or lead.
Examgle 1
Group Parts by weight
Suspension vinyl chloride homopolymer (K value 68) 100
Polymethyl nethacrylate (PMMA) 9 1
Talcun (micronised) e 10
Benzoylstearoyl methane c 0.1
1,k-dihydropyridine c 0.2
Diphenyldecyl phosphite c 0.?
Calcium stearate a 0.8
Zinc octoate b 0.4
Calcium oxide, coated with 2% by weight hydroxystearic d 0.1
acid (relative to 100 parts by weight Cao)
Magnesium oxide, coated with 2% by weight hydroxy~ d 0.15
palmitic acid (relative to 100 parts by weight M90)
Mixture of internal and external lubricants with the f 0.75
joint use of montan waxes
Hard paraffin f 0.2
Partly oxidised hard paraffin f 0.1
Example 2
Zinc octoate
Group Parts by weight
Suspension vinyl chloride homopolymer (K value 68) 100
with 8 parts by weight modifying agent, consisting of
butyl acrylate and polymethyl methacrylate
Polymethyl methacrylate (PHMA) 9 1
Natural calciun carbonate (ground chalk) surface~ e 10
modified with stearic acid
Titaniun dioxide h 4
Benzoylstearoyl methane c 0.1
1,4-dihydropyridine c 0.1
Trilauryl phosphite c 0.5
Mixture of trimethylol propane, di-trimethylol propane c 0.5
and pentaerythrite
Calciun behenate a 0.4
Magnesiun oxide, coated with 2% by weight d 0.25
hydroxystearic acid (relative to 100 parts by weight
M90)
Mixture of internal and external lubricants with the f 0.75
joint use of montan waxes
Hard paraffin f .1
Partly oxidised hard paraffin f .1
Examgle 3
Group Parts by weight
Vinyl chloride graft polymer with 6% by weight butyl 100
acrylate
Polymethyl methacrylate (PMA) 9 1
- synthetic calciun carbonate (CCP) coated with 2% by e 5
weight hydroxystearic acid (relative to 100 parts by
weight CaCo3)
Titaniun dioxide h 4
Benzoylstearoyl methane c 0.1
1,4-dihydropyridine c 0.1
Phenyldidecyl phosphite c 0.6
Di-trimethylol propane c 0.7
Calciun stearate a 0.8
Zinc stearate 0.8
Calciun oxide, coated with 2% by weight hydroxystearic d 0.15
acid (relative to 100 parts by weight Cao)
Mixture of internal and external lubricants with the f 0.75
joint use of rnontan waxes
Hard paraffin f 0.2
Partly oxidised hard paraffin f 0.1
Example 4
Group
Parts by weight
parts by weight suspension vinyl chloride
homopolymer (K value 64) and 20 parts by weight vinyl
chloride/ethylene/vinyl acetate graft copolymer (with a
content of 10% by weight EVA)
Polymethyl methacrylate (PMHA)
Precipitated calcium carbonate having a particle size
of<0J;m
Titaniun dioxide
Benzoylstearoyl methane
,4-dihydropyridine
Diphenyldecyl phosphite
Calciun stearate
Zinc stearate
calcined dolomite (micronised) having a particle size
of < 1 um, coated with 2% by weight hydroxystearic acid
(relative to 100 parts by weight calcined dolomite)
Mixture of internal and external lubricants with the
joint use of montan waxes
Hard paraffin
Partly oxidised hard paraffin
Finely divided sodiun bicarbonate
Azodicarbonamide
Antimony trioxide
Aluminium hydroxide
O-|—IOOOl'\J
u-a
[UNIV-'-'
Groups:
I-'-D'kQl'h(DQ-GU‘!!!
\_J.
= calcium carboxylate
= zinc carboxylate
= co-stabilisers
= alkaline earth oxide
= filler
= lubricants
= processing aids
= pigments
= expanding agents
= flame retardants
Claims (9)
- A plasticiser-free moulding compound on the basis of polyvinyl chloride, containing a plastics material and, consisting of vinyl chloride homopolymer, copolymer, terpolymer, mixtures thereof or compounds therewith, having a VC or PVC content of more than 70% by weight, preferably more than 85% by weight, relative to the plastics material, and O to 15% by weight, relative to the plastics material, of an impact-modifying polymer, selected from the group of polyalkyl acrylates, chlorinated polyethylenes, ethylene/vinyl acetate copolymers or ethylene/vinyl acetate/carbon monoxide terpolymers, per 100 parts by weight of this plastics material, 0.01 to 3 parts by weight of at least one calcium carboxylate, 0.01 to 3 parts by weight of at least one zinc carboxylate, 0.01 to 3 parts by weight of at least one organic co—stabiliser, selected from the group of at least one 3-diketone, organic phosphite and/or dihydro— pyridine, and optionally pigments, dyes, lubricants, blowing agents, flame retardants, fillers, reinforcing fibres or other processing aids and additives, characterised in that 18 d) 0.01 to 5 parts by weight of at least one alkaline earth oxide, alkaline earth hydroxide and/or partly hydrated alkaline earth oxide, preferably calcium oxide and/or magnesium oxide, and/or partly hydrated calcium oxide and/or partly hydrated magnesium oxide and/or calcined dolomite or partly hydrated calcined dolomite, with the alkaline earth oxide, alkaline earth hydroxide and/or partly hydrated alkaline earth oxide, preferably the calcium oxide and/or magnesium oxide, and/or the partly hydrated calcium oxide and/or partly hydrated magnesium oxide and/or the calcined dolomite being coated on the entire surface or in partial regions of the surface with a surface-modifying treatment agent or coating agent, are contained in the plasticiser—free moulding compound.
- 2. A plasticiser—free moulding compound according to Claim 1, characterised in that it contains 0.01 to 15 parts by weight filler, preferably inorganic filler.
- 3. A plasticiser—free moulding compound according to Claim 1 and 2, characterised in that the filler or the filler mixture or a portion of the filler or of the filler mixture is coated on its surface completely or in partial regions with a surface-modifying treatment agent or coating agent.
- 4. A plasticiser—free moulding compound according to Claims 1 to 3, characterised in that the surface- modifying treatment agent or coating agent is a saturated or unsaturated fatty acid or esters, salts or derivatives thereof, which additionally contains at 19 least one OH group or at least one other polar group in addition to the COOH, ester and/or COO group.
- 5. A plasticiser-free moulding compound according to Claims 1 to 4, characterised in that the vinyl chloride homopolymer, copolymer and/or terpolymer contained in the moulding compound has an average K value of 58 to 73, preferably 64 to 71.
- 6. A method for preparing a plasticiser-free moulding compound according to Claims 1 to 5, characterised in that the plastics material(s) and the other additives are mixed in a hot mixer at temperatures above 35°C and are heated with a temperature increase to temperatures between 100 and 125°C (calculated as compound temperature), preferably 110 to 120°C, and then the moulding compound is cooled in a cooling mixer to temperatures below 40°C, preferably below 35°C.
- 7. A method according to Claim 6, characterised in that the plastics material and the solid mixture constituents (with the exception of T102) are pre-mixed at 35 to 50°C, preferably at 37 to 45°C, and the liquid additives are admixed after a temperature increase to 55 to 65°C, preferably at 57 to 62°C.
- 8. A method according to Claims 6 and 7, characterised in that the addition of T102 to the plastics material/additive mixture pre—mixed in the hot mixer is effected at temperatures of 90 to 125°C, preferably 110 to 120°C.
- 9. The use of a plasticiser-free moulding compound according to Claims 1 to 5 in extrusion or injection- moulding processes for the production of profiles or articles, preferably window profiles or extruded tubes. F. R. KELLY & CO., AGENTS FOR THE APPLICANTS.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEGERMANY23/08/1989P3927777.1 | |||
DE3927777A DE3927777A1 (en) | 1989-08-23 | 1989-08-23 | SOFTENER-FREE MOLDING MATERIAL BASED ON POLYVINYL CHLORIDE, METHOD FOR THE PRODUCTION AND USE THEREOF |
Publications (2)
Publication Number | Publication Date |
---|---|
IE83257B1 true IE83257B1 (en) | |
IE903045A1 IE903045A1 (en) | 1991-02-27 |
Family
ID=6387667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE304590A IE903045A1 (en) | 1989-08-23 | 1990-08-22 | Unplasticized polyvinyl-chloride-based moulding compound,¹process for its production and use |
Country Status (14)
Country | Link |
---|---|
US (1) | US5124373A (en) |
EP (1) | EP0422335B1 (en) |
AT (1) | ATE142238T1 (en) |
BR (1) | BR9004155A (en) |
CA (1) | CA2023155C (en) |
DD (1) | DD297176A5 (en) |
DE (2) | DE3927777A1 (en) |
DK (1) | DK0422335T3 (en) |
ES (1) | ES2093620T3 (en) |
GR (1) | GR3021266T3 (en) |
HU (1) | HU210749B (en) |
IE (1) | IE903045A1 (en) |
NO (1) | NO305129B1 (en) |
PT (1) | PT95075B (en) |
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NL9000840A (en) * | 1990-04-10 | 1991-11-01 | Wavin Bv | METHOD AND INSTALLATION FOR MANUFACTURING PLASTIC PREPARATIONS USING A HOT PVC POWDER MIXTURE AND ADDITIVES, AND A WARM BLENDER SUITABLE FOR USE IN THIS METHOD |
US5283273A (en) * | 1990-11-30 | 1994-02-01 | Ciba-Geigy Corporation | Stabilized chlorine-containing polymers |
EP0488950B1 (en) * | 1990-11-30 | 1995-09-20 | Ciba-Geigy Ag | Stabilized chlorinated polymers |
ES2078197B1 (en) * | 1992-05-19 | 1996-08-01 | Witco Corp | ELECTRIC QUALITY POLY (VINYL CHLORIDE) RESIN COMPOSITION STABILIZED WITH A LEAD-FREE STABILIZER. |
JPH08231798A (en) * | 1994-12-28 | 1996-09-10 | Showa Kako Kk | Chlorine-containing resin composition |
WO1996026333A1 (en) * | 1995-02-24 | 1996-08-29 | Anderson Carl E | Improved pvc building trim |
US5924455A (en) * | 1996-08-01 | 1999-07-20 | Certainteed Corporation | Folded PVC-based conduit and conduit liner composition |
TW461911B (en) | 1998-03-26 | 2001-11-01 | Ajinomoto Kk | Thermal stabilizer and thermally stabilized halogen-containing resin composition |
US6225402B1 (en) | 1998-09-25 | 2001-05-01 | Mcwhorter Technologies, Inc. | Aqueous based dispersions for polyolefinic substrates |
US6872776B1 (en) * | 1999-03-31 | 2005-03-29 | Kaneka Corporation | Vinyl chloride resin composition and molded object comprising the same |
WO2002006389A2 (en) * | 2000-07-14 | 2002-01-24 | Akzo Nobel N.V. | Stabiliser system comprising hydroxyacids |
DE10052662A1 (en) * | 2000-10-24 | 2002-05-08 | Horst Filipp Gmbh | Dowel with screw-in expansion screw |
WO2003016395A1 (en) * | 2001-08-16 | 2003-02-27 | Dover Chemical Corporation | Polymer dispersible polybasic metal carboxylate complexes |
DE10209698A1 (en) | 2002-03-06 | 2003-09-18 | Sachtleben Chemie Gmbh | Process for the production of coated, finely divided, inorganic solids and their use |
EP1657278A1 (en) | 2004-11-12 | 2006-05-17 | SOLVAY (Société Anonyme) | Coated particles of calcium carbonate having a high specific surface |
DE102005010242A1 (en) * | 2005-03-05 | 2006-09-07 | Rehau Ag + Co. | Improved PVC composition |
KR100722518B1 (en) | 2006-03-16 | 2007-05-28 | 경남대학교 산학협력단 | Compositions of rigid pvc foam sheet |
DE102008018872A1 (en) | 2008-04-14 | 2009-10-15 | Ika Innovative Kunststoffaufbereitung Gmbh & Co. Kg | Stabilizer system for halogen-containing polymers |
ES2370453T3 (en) * | 2008-08-26 | 2011-12-16 | Omya Development Ag | TREATED MINERAL LOAD PRODUCTS, PREPARATION PROCESS OF THE SAME AND USES OF THE SAME. |
DE102009045701A1 (en) * | 2009-10-14 | 2011-04-21 | Ika Innovative Kunststoffaufbereitung Gmbh & Co. Kg | Stabilizer combinations for halogen-containing polymers |
DE102010011191A1 (en) | 2010-03-11 | 2011-09-15 | Ika Innovative Kunststoffaufbereitung Gmbh & Co. Kg | Stabilizer mixtures for halogenated plastics by underwater granulation |
RS53276B (en) | 2011-06-20 | 2014-08-29 | Imerys Minerals Limited | Methods and compositions related to recycling polymer waste |
CN113185786B (en) * | 2021-04-13 | 2022-12-30 | 长春联塑实业有限公司 | Low-temperature weather-resistant PVC composition and preparation method and application thereof |
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US3471439A (en) * | 1966-03-10 | 1969-10-07 | Amicon Corp | Reinforcing filler |
US3969313A (en) * | 1972-06-14 | 1976-07-13 | Asahi Kasei Kogyo Kabushiki Kaisha | Thermoplastic composite compositions |
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JPS52103449A (en) * | 1976-02-27 | 1977-08-30 | Adeka Argus Chem Co Ltd | Stabilized synthetic resin compositions |
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-
1989
- 1989-08-23 DE DE3927777A patent/DE3927777A1/en not_active Ceased
-
1990
- 1990-06-12 ES ES90111046T patent/ES2093620T3/en not_active Expired - Lifetime
- 1990-06-12 DK DK90111046.0T patent/DK0422335T3/en active
- 1990-06-12 AT AT90111046T patent/ATE142238T1/en not_active IP Right Cessation
- 1990-06-12 DE DE59010482T patent/DE59010482D1/en not_active Expired - Fee Related
- 1990-06-12 EP EP90111046A patent/EP0422335B1/en not_active Expired - Lifetime
- 1990-08-02 NO NO903402A patent/NO305129B1/en unknown
- 1990-08-13 CA CA002023155A patent/CA2023155C/en not_active Expired - Fee Related
- 1990-08-16 HU HU905039A patent/HU210749B/en not_active IP Right Cessation
- 1990-08-21 DD DD90343564A patent/DD297176A5/en unknown
- 1990-08-22 PT PT95075A patent/PT95075B/en unknown
- 1990-08-22 IE IE304590A patent/IE903045A1/en not_active IP Right Cessation
- 1990-08-22 BR BR909004155A patent/BR9004155A/en not_active IP Right Cessation
- 1990-08-23 US US07/571,263 patent/US5124373A/en not_active Expired - Lifetime
-
1996
- 1996-10-04 GR GR960402618T patent/GR3021266T3/en unknown
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