DE1494167A1 - Verfahren zum Vulkanisieren von im wesentlichen gesaettigten,linearen,amorphen Polymeren oder Mischpolymeren von Alpha-Olefinen - Google Patents
Verfahren zum Vulkanisieren von im wesentlichen gesaettigten,linearen,amorphen Polymeren oder Mischpolymeren von Alpha-OlefinenInfo
- Publication number
- DE1494167A1 DE1494167A1 DE19581494167 DE1494167A DE1494167A1 DE 1494167 A1 DE1494167 A1 DE 1494167A1 DE 19581494167 DE19581494167 DE 19581494167 DE 1494167 A DE1494167 A DE 1494167A DE 1494167 A1 DE1494167 A1 DE 1494167A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- polymer
- parts
- olefins
- ethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 13
- 230000008569 process Effects 0.000 title claims description 12
- 229920001577 copolymer Polymers 0.000 title claims description 10
- 229920006125 amorphous polymer Polymers 0.000 title claims description 4
- 229920006395 saturated elastomer Polymers 0.000 title description 10
- -1 linear Polymers 0.000 title description 5
- 239000004711 α-olefin Substances 0.000 title description 2
- 229920000642 polymer Polymers 0.000 claims description 31
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 13
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 11
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 11
- 239000011976 maleic acid Substances 0.000 claims description 11
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 9
- 239000005977 Ethylene Substances 0.000 claims description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 8
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 8
- 229910044991 metal oxide Inorganic materials 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 6
- 235000021355 Stearic acid Nutrition 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 6
- 239000008117 stearic acid Substances 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
- 229910000000 metal hydroxide Inorganic materials 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 3
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- 229930016911 cinnamic acid Natural products 0.000 claims description 3
- 235000013985 cinnamic acid Nutrition 0.000 claims description 3
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims description 3
- 150000004985 diamines Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 3
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 claims description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- CYGPPWVXOWCHJB-UHFFFAOYSA-N 2-Methylbutyl 3-methylbutanoate Chemical compound CCC(C)COC(=O)CC(C)C CYGPPWVXOWCHJB-UHFFFAOYSA-N 0.000 claims description 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims description 2
- NRSMWHGLCNBZSO-UHFFFAOYSA-N 2-ethylidenebutanedioic acid Chemical compound CC=C(C(O)=O)CC(O)=O NRSMWHGLCNBZSO-UHFFFAOYSA-N 0.000 claims description 2
- 229940091181 aconitic acid Drugs 0.000 claims description 2
- NUZLRKBHOBPTQV-UHFFFAOYSA-N but-2-ene-1,2,3-tricarboxylic acid Chemical compound OC(=O)C(C)=C(C(O)=O)CC(O)=O NUZLRKBHOBPTQV-UHFFFAOYSA-N 0.000 claims description 2
- 239000006229 carbon black Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims description 2
- 229920001897 terpolymer Polymers 0.000 claims description 2
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 claims description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 52
- 239000000047 product Substances 0.000 description 27
- 239000011787 zinc oxide Substances 0.000 description 26
- 238000004073 vulcanization Methods 0.000 description 21
- 150000002978 peroxides Chemical class 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000004342 Benzoyl peroxide Substances 0.000 description 6
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 6
- 235000019400 benzoyl peroxide Nutrition 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 6
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 5
- 239000002904 solvent Substances 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 244000269722 Thea sinensis Species 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical group ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 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
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- 101150038108 Art7 gene Proteins 0.000 description 1
- 241000251730 Chondrichthyes Species 0.000 description 1
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical compound C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 101100133458 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) nit-2 gene Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 210000001109 blastomere Anatomy 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 210000002435 tendon Anatomy 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- 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
-
- 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
- C08K5/092—Polycarboxylic 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
-
- 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
- C08K5/14—Peroxides
-
- 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
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/31—Ionic cross-link
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT43057 | 1957-01-09 | ||
| IT1099757 | 1957-07-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1494167A1 true DE1494167A1 (de) | 1969-02-13 |
Family
ID=26325009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19581494167 Pending DE1494167A1 (de) | 1957-01-09 | 1958-01-07 | Verfahren zum Vulkanisieren von im wesentlichen gesaettigten,linearen,amorphen Polymeren oder Mischpolymeren von Alpha-Olefinen |
Country Status (16)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0440923A1 (en) * | 1989-12-11 | 1991-08-14 | Sumitomo Chemical Company, Limited | Polyolefin resinsompositions and process for producing same |
Families Citing this family (100)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL103723C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1960-08-11 | |||
| US3267173A (en) * | 1962-05-18 | 1966-08-16 | Allied Chem | Product and process for making a polyethylene-maleate diester graft copolymer |
| GB1123812A (en) * | 1962-06-01 | 1968-08-14 | Allied Chem | Graft copolymers, their production, and compositions containing them |
| NL296508A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-08-31 | |||
| US3489822A (en) * | 1962-08-31 | 1970-01-13 | Uniroyal Inc | Grafted terpolymer of ethylene,propylene and a non-conjugated diene |
| US3408424A (en) * | 1963-12-30 | 1968-10-29 | Monsanto Co | Process of polymerizing vinyl halide with terpolymers of 1-monoolefins and dienes |
| NL128025C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1965-02-15 | |||
| FR1481828A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1965-06-14 | 1967-08-21 | ||
| NL6613608A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1965-09-29 | 1967-03-30 | ||
| US3480580A (en) * | 1965-10-22 | 1969-11-25 | Eastman Kodak Co | Modified polymers |
| US3956230A (en) * | 1968-02-01 | 1976-05-11 | Champion International Corporation | Compatibilization of hydroxyl-containing fillers and thermoplastic polymers |
| US3483273A (en) * | 1966-03-31 | 1969-12-09 | Ppg Industries Inc | Graft copolymers of unsaturated hydrocarbon interpolymers |
| US3538191A (en) * | 1967-03-30 | 1970-11-03 | Copolymer Rubber & Chem Corp | Process for preparing improved plastic compositions and the resulting products |
| US3456038A (en) * | 1967-07-13 | 1969-07-15 | Exxon Research Engineering Co | Blends of ethylene-propylene rubber and atactic polypropylene |
| US3819765A (en) * | 1968-12-30 | 1974-06-25 | Uniroyal Inc | Graft copolymerization of alpha-monoolefin copolymer rubbers to make gum plastics |
| BE792985A (fr) * | 1971-12-20 | 1973-04-16 | Asahi Chemical Ind | Compositions de matieres thermoplastiques |
| US3873643A (en) * | 1972-12-18 | 1975-03-25 | Chemplex Co | Graft copolymers of polyolefins and cyclic acid and acid anhydride monomers |
| US3859385A (en) * | 1973-07-20 | 1975-01-07 | Eastman Kodak Co | Emulsifiable polyethylene compositions prepared from thermally degraded low molecular weight polyethylene and crotonic acid |
| US3859386A (en) * | 1973-07-20 | 1975-01-07 | Eastman Kodak Co | Emulsifiable polyolefin compositions compositions prepared from thermally degraded low molecular weight polyolefin and crotonic acid |
| AU498559B2 (en) * | 1975-06-25 | 1979-03-15 | Exxon Research And Engineering Company | Lubricating oil concentrate |
| IT1043117B (it) * | 1975-10-03 | 1980-02-20 | Snam Progetti | Resine antiurto e metodo per la loro areparazione |
| JPS58445B2 (ja) * | 1975-10-17 | 1983-01-06 | 三井化学株式会社 | 熱可塑性エラストマ−の製造方法 |
| JPS58442B2 (ja) * | 1975-12-23 | 1983-01-06 | 三井化学株式会社 | グラフトゴムノカイシツホウホウ |
| US4026967A (en) * | 1976-06-25 | 1977-05-31 | E. I. Du Pont De Nemours And Company | Process for making grafted polymeric material |
| US4112208A (en) * | 1977-07-06 | 1978-09-05 | Eastman Kodak Company | Peroxide treated substantially amorphous polyolefins useful as pressure-sensitive adhesives |
| JPS6036217B2 (ja) * | 1981-04-07 | 1985-08-19 | 東亜燃料工業株式会社 | 変性ポリエチレン組成物 |
| JPS58142901A (ja) * | 1982-02-19 | 1983-08-25 | Nippon Zeon Co Ltd | ゴムの変性方法 |
| US4412031A (en) * | 1983-02-18 | 1983-10-25 | Nippon Zeon Co., Ltd. | Modified rubber composition employing a compound containing a carboxyl and an aldehyde group |
| US4739016A (en) * | 1984-06-11 | 1988-04-19 | Uniroyal Chemical Company, Inc. | Modified ionic elastomer and blend with nylon |
| US4544702A (en) * | 1984-06-11 | 1985-10-01 | Uniroyal, Inc. | Modified ionic elastomer and blend with nylon |
| US4623564A (en) * | 1985-05-10 | 1986-11-18 | General Dynamics, Pomona Division | Method of coating packaging material with anti-static composition |
| US4749505A (en) * | 1985-07-08 | 1988-06-07 | Exxon Chemical Patents Inc. | Olefin polymer viscosity index improver additive useful in oil compositions |
| US4753997A (en) * | 1985-11-27 | 1988-06-28 | The Standard Oil Company | Process for grafting maleic anhydride or styrene-maleic anhydride onto polyolefins |
| US4866135A (en) * | 1986-10-07 | 1989-09-12 | Exxon Chemical Patents Inc. | Heterocyclic amine terminated, lactone modified, aminated viscosity modifiers of improved dispersancy |
| CA2061474C (en) | 1991-02-22 | 2002-03-26 | Kenneth Benjamin Higgins | Bitumen backed carpet tile |
| EP0503909A1 (en) * | 1991-03-14 | 1992-09-16 | Chevron Research And Technology Company | Substantially non-crosslinked maleic anhydride-modified ethylene polymers and process for preparing same |
| EP0582588B1 (en) * | 1991-03-25 | 1996-01-24 | Exxon Chemical Patents Inc. | Grafted polymers of an isomonoolefin and an alkylstyrene |
| US5346963A (en) * | 1993-04-28 | 1994-09-13 | The Dow Chemical Company | Graft-modified, substantially linear ethylene polymers and methods for their use |
| US5883188A (en) * | 1993-04-28 | 1999-03-16 | The Dow Chemical Company | Paintable olefinic interpolymer compositions |
| US5424362A (en) * | 1993-04-28 | 1995-06-13 | The Dow Chemical Company | Paintable olefinic interpolymer compositions |
| ZA976110B (en) | 1996-07-12 | 1999-01-11 | Dow Chemical Co | Elastomers processes for their manufacture and articles made from these elastomers |
| US6323285B1 (en) | 1998-01-09 | 2001-11-27 | The Dow Chemical Company | Heteromorphic polymer compositions |
| US6362280B1 (en) | 1998-04-27 | 2002-03-26 | Honeywell International Inc. | Emulsible polyolefin wax |
| US6300419B1 (en) | 1999-12-08 | 2001-10-09 | The Dow Chemical Company | Propylene polymer composition |
| US6329454B1 (en) | 1999-12-08 | 2001-12-11 | The Dow Chemical Company | Filled propylene polymer composition |
| US20040214958A1 (en) * | 2000-06-09 | 2004-10-28 | Jourdain Eric Paul | Use of chemically modified elastomeric polymers to improve adhesion properties of thermoset elastomeric polymers components |
| US6756446B2 (en) * | 2002-10-15 | 2004-06-29 | Solvay Engineered Polymers | Engineered polyolefin materials with enhanced surface durability |
| US6914094B2 (en) * | 2000-09-29 | 2005-07-05 | Solvay Engineered Polymers, Inc. | Engineered polyolefin materials with enhanced surface durability |
| US6509416B2 (en) | 2000-09-29 | 2003-01-21 | Solvay Engineered Polymers | Engineered polyolefin materials with enhanced surface durability and methods of making same |
| US6403721B1 (en) | 2000-09-29 | 2002-06-11 | Solvay Engineered Polymers | Engineered polyolefin materials with enhanced surface durability |
| US6403692B1 (en) | 2001-04-19 | 2002-06-11 | Dow Global Technologies Inc. | Filled thermoplastic composition |
| EP1412566B1 (en) * | 2001-07-17 | 2006-09-27 | Dow Global Technologies Inc. | Elastic bicomponent and biconstituent fibers, and methods of making cellulosic structures from the same |
| KR100468641B1 (ko) | 2001-10-12 | 2005-01-27 | 금호폴리켐 주식회사 | 화학적 개질에 의한 폴리올레핀 탄성체 조성물 |
| NL1020366C2 (nl) * | 2002-04-11 | 2003-10-14 | Dsm Nv | Polymeersamenstelling met verbeterde temperatuurbestendigheid. |
| MXPA05003998A (es) * | 2002-10-15 | 2005-06-22 | Dow Global Technologies Inc | Articulos que comprenden una composicion de polimero termoplastico reforzado con fibra. |
| EP1859926B1 (en) * | 2006-05-26 | 2012-04-25 | Borealis Technology Oy | Coated pipe comprising polyolefin layer with enhanced adhesion |
| US8080607B2 (en) * | 2006-08-16 | 2011-12-20 | Dow Global Technologies Llc | Polymeric material and process for forming and using same |
| ES2344966T5 (es) | 2006-09-20 | 2015-11-06 | Dow Global Technologies Llc | Módulo de dispositivo electrónico que comprende un copolímero multibloque de etileno |
| US8581094B2 (en) | 2006-09-20 | 2013-11-12 | Dow Global Technologies, Llc | Electronic device module comprising polyolefin copolymer |
| US20080115825A1 (en) | 2006-09-20 | 2008-05-22 | Patel Rajen M | Electronic Device Module Comprising an Ethylene Multi-Block Copolymer |
| US7862671B2 (en) * | 2007-01-11 | 2011-01-04 | Dow Global Technologies Inc. | Welding of a polymeric material and structures formed thereby |
| PL1985909T3 (pl) * | 2007-04-25 | 2011-08-31 | Oy Kwh Pipe Ab | Sposób i urządzenie do powlekania rur |
| CN102164971B (zh) * | 2008-08-25 | 2014-05-28 | 陶氏环球技术有限责任公司 | 使用低聚胺交联含羧基的聚合物的方法 |
| EP2181832B1 (en) | 2008-10-29 | 2012-06-27 | Oy KWH Pipe AB | Method and apparatus for coating pipes and pipe sections |
| AU2009308805B2 (en) * | 2008-10-31 | 2015-08-06 | Performance Materials Na, Inc. | Highly abrasion-resistant polyolefin pipe |
| US8728600B1 (en) | 2008-10-31 | 2014-05-20 | E I Du Pont De Nemours And Company | Highly abrasion-resistant grafted polyolefin pipe |
| KR101620308B1 (ko) | 2008-11-06 | 2016-05-12 | 다우 글로벌 테크놀로지스 엘엘씨 | 전자 디바이스 모듈용의 공압출된 다층 폴리올레핀계 백시트 |
| US7935890B2 (en) * | 2008-12-29 | 2011-05-03 | Schlumberger Technology Corporation | Gas blocking, high temperature conductor-insulation adhesive |
| BRPI1005329B1 (pt) | 2009-01-30 | 2019-06-18 | Dow Global Technologies Llc | Composição polimérica, composição de poliolefina termoplástica enchida e processo para a fabricação de um artigo moldado |
| CA2783874C (en) | 2009-12-18 | 2016-09-06 | Given Jing Chen | Halogen-free, flame retardant compositions for wire and cable applications |
| WO2011131624A1 (en) | 2010-04-20 | 2011-10-27 | Dsm Ip Assets B.V. | Polymer composition and a sealing body made of that composition |
| EP2576685A1 (en) | 2010-05-26 | 2013-04-10 | Dow Global Technologies LLC | Electronic device module comprising polyolefin copolymer with low unsaturation and optional vinyl silane |
| US20130206224A1 (en) | 2010-06-04 | 2013-08-15 | Dow Global Technologies Llc | Electronic Device Module Comprising Film of Homogeneous Polyolefin Copolymer and Adhesive Property Enhancing Graft Polymer |
| BR112012033072A2 (pt) | 2010-06-24 | 2017-01-17 | Dow Global Technologies Llc | módulo de dispositivo eletrônico compreendendo bloco ramificado de cadeia longa (lcb), ou copolímeros interconectados de etileno e opcionalmente silano |
| EP2585292A1 (en) | 2010-06-24 | 2013-05-01 | Dow Global Technologies LLC | Electronic device module comprising heterogeneous polyolefin copolymer and optionally silane |
| CN103228442A (zh) | 2010-09-21 | 2013-07-31 | 陶氏环球技术有限责任公司 | 包括乙烯-α-烯烃递变嵌段共聚物和非必要的乙烯基硅烷的电子装置模块 |
| WO2013003541A1 (en) | 2011-06-30 | 2013-01-03 | Dow Global Technologies Llc | Multilayered polyolefin-based films having a layer comprising a crystalline block copolymer composite or a block copolymer composite resin |
| WO2013003543A1 (en) | 2011-06-30 | 2013-01-03 | Dow Global Technologies Llc | Multilayered polyolefin-based films having integrated backsheet and encapsulation performance comprising a layer comprising crystalline block copolymer composite or block copolymer composite |
| EP2570195B1 (en) | 2011-09-15 | 2014-12-03 | Borealis AG | Protective polymer layer |
| JP5997282B2 (ja) | 2011-09-30 | 2016-09-28 | ダウ グローバル テクノロジーズ エルエルシー | ポリカーボネートおよびポリプロピレンの難燃性熱可塑性組成物 |
| US8841379B2 (en) | 2011-11-07 | 2014-09-23 | E I Du Pont De Nemours And Company | Method to form an aqueous dispersion of an ionomer-polyolefin blend |
| PL2657284T3 (pl) | 2012-04-27 | 2015-04-30 | Borealis Ag | Przedmieszka z dodatkami zawierająca homo- lub kopolimer c3-c5 alfa-olefiny znajdujący się w nośniku |
| EP2657283A1 (en) | 2012-04-27 | 2013-10-30 | Borealis AG | Catalyst masterbatch |
| ES2524899T3 (es) | 2012-04-27 | 2014-12-15 | Borealis Ag | Mezcla maestra de catalizador |
| PL2895328T3 (pl) | 2012-09-14 | 2017-07-31 | Dow Global Technologies Llc | Wielowarstwowe folie na bazie poliolefin |
| ES2799799T3 (es) | 2014-06-24 | 2020-12-21 | Dow Global Technologies Llc | Módulos fotovoltaicos que comprenden organoarcilla |
| KR102396054B1 (ko) | 2014-06-24 | 2022-05-10 | 다우 글로벌 테크놀로지스 엘엘씨 | 안정화된 폴리프로필렌 층을 포함하는 폴리올레핀 광전 백시트 |
| EP3053976A1 (en) | 2015-02-09 | 2016-08-10 | Borealis AG | Adhesive composition |
| EP3409739B1 (en) | 2017-05-31 | 2019-05-01 | Borealis AG | Improved adhesive polymer composition |
| US11767426B2 (en) | 2017-11-10 | 2023-09-26 | Covestro Deutschland Ag | Glass fiber filled thermoplastic composition having good mechanical properties |
| EP3707209B1 (de) | 2017-11-10 | 2021-07-21 | Covestro Intellectual Property GmbH & Co. KG | Mineralgefüllte thermoplastische zusammensetzung mit guten mechanischen eigenschaften |
| US11174410B2 (en) | 2017-11-16 | 2021-11-16 | Dow Global Technologies Llc | Method for coating a pipeline field joint |
| WO2019105659A1 (en) | 2017-11-28 | 2019-06-06 | Borealis Ag | Improved adhesive polymer composition |
| ES2929827T3 (es) | 2018-01-30 | 2022-12-01 | Borealis Ag | Agente de acoplamiento |
| US11504949B2 (en) | 2018-04-16 | 2022-11-22 | Borealis Ag | Multilayer element |
| EP3891238B1 (en) | 2018-12-03 | 2024-02-07 | Borealis AG | Adhesive polymer composition |
| EP3890032A1 (en) | 2020-03-31 | 2021-10-06 | Borealis AG | Photovoltaic module with increased resistance against potential induced degradation |
| CN115720550B (zh) | 2020-06-30 | 2025-03-28 | 博里利斯股份公司 | 具有改善的储存稳定性的聚合物组合物 |
| WO2022013054A1 (en) | 2020-07-13 | 2022-01-20 | Borealis Ag | Adhesive polyethylene composition |
| BR112023000435A2 (pt) | 2020-07-13 | 2023-01-31 | Borealis Ag | Composição de polietileno adesiva |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA499577A (en) * | 1954-01-26 | Shell Development Company | Method for polymerization and products produced thereby | |
| US2634256A (en) * | 1949-02-15 | 1953-04-07 | Standard Oil Dev Co | Modified olefin-diolefin resin |
| US2662874A (en) * | 1950-11-01 | 1953-12-15 | Goodrich Co B F | Preparation of plastic condensable synthetic rubbers and subsequent elasto-condensation thereof |
| US2724707A (en) * | 1950-11-01 | 1955-11-22 | Goodrich Co B F | Elastic synthetic rubber composition and method of making same |
| GB760104A (en) * | 1952-09-09 | 1956-10-31 | William Hays Smyers | Improved polymerization process and products |
| US2837496A (en) * | 1952-12-31 | 1958-06-03 | Hercules Powder Co Ltd | Graft copolymers and preparation thereof from polymer hydroperoxides |
| NL202827A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1954-12-16 |
-
0
- NL NL107983D patent/NL107983C/xx active
- IL IL10992D patent/IL10992A/en unknown
- DD DD20232D patent/DD20232A/xx unknown
- LU LU35689D patent/LU35689A1/xx unknown
- NO NO126663D patent/NO126663L/no unknown
- BE BE563834D patent/BE563834A/xx unknown
- PT PT34730D patent/PT34730A/pt unknown
- IT IT600723D patent/IT600723A/it unknown
- NL NL293534D patent/NL293534A/xx unknown
- IN IN62803D patent/IN62803B/en unknown
- IT IT574913D patent/IT574913A/it unknown
- NZ NZ120319D patent/NZ120319A/xx unknown
-
1957
- 1957-12-31 US US706382A patent/US3236917A/en not_active Expired - Lifetime
-
1958
- 1958-01-07 DE DE19581494167 patent/DE1494167A1/de active Pending
- 1958-01-08 IE IE1258A patent/IE23563B1/xx unknown
- 1958-01-08 GB GB768/58A patent/GB885969A/en not_active Expired
- 1958-01-08 GB GB33999/61A patent/GB885970A/en not_active Expired
- 1958-01-09 CH CH5450958A patent/CH417086A/de unknown
- 1958-01-09 FR FR1200144D patent/FR1200144A/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0440923A1 (en) * | 1989-12-11 | 1991-08-14 | Sumitomo Chemical Company, Limited | Polyolefin resinsompositions and process for producing same |
| US5587427A (en) * | 1989-12-11 | 1996-12-24 | Sumitomo Chemical Company, Limited | Resin composition and process for producing same |
Also Published As
| Publication number | Publication date |
|---|---|
| NZ120319A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| NO126663L (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| PT34730A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| IE23563L (en) | 1958-07-09 |
| NL293534A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| IT574913A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| IT600723A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| DD20232A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| IE23563B1 (en) | 1962-10-03 |
| BE563834A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| US3236917A (en) | 1966-02-22 |
| IN62803B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1957-01-09 |
| IL10992A (en) | 1900-01-01 |
| NL107983C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| CH417086A (de) | 1966-07-15 |
| GB885969A (en) | 1962-01-03 |
| LU35689A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1900-01-01 |
| GB885970A (en) | 1962-01-03 |
| FR1200144A (fr) | 1959-12-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1494167A1 (de) | Verfahren zum Vulkanisieren von im wesentlichen gesaettigten,linearen,amorphen Polymeren oder Mischpolymeren von Alpha-Olefinen | |
| DE2646480C3 (de) | Verfahren zur Herstellung von thermoplastischen Olefinelastomeren | |
| DE68920000T2 (de) | Hydrogenierter copolymerer Kautschuk, diesen Kautschuk enthaltende Kautschukzusammensetzung und aus dem Kautschuk hergestellte Kautschukprodukte. | |
| DE69506783T2 (de) | Gummimasse | |
| DE2401375C3 (de) | Verfahren zur Herstellung von Formkörpern durch Vulkanisation von halogenhaltigen Polymerisaten | |
| DE69124695T2 (de) | Innenbelagzusammensetzung eines reifens | |
| DE2459816C2 (de) | Stabile Dispersion eines Polymeren in einem Organopolysiloxan und ihre Verwendung | |
| DE1469998A1 (de) | Verfahren zur Haertung von Polymeren mit neuartigen organischen Peroxyden | |
| DE1134198B (de) | Verfahren zur Herstellung von vulkanisierten Elastomeren | |
| DE1495618A1 (de) | Vulkanisierbare Pfropfpolymere | |
| DE2039394A1 (de) | Verfahren zur Herstellung von Pfropfmischpolymerisaten | |
| DE1645348C3 (de) | Verfahren zur Herstellung von Misch polymerisaten aus Norbornenverbindungen, Äthylen und alpha Olefinen und ihre Verwendung in vulkanisierbaren Formmassen | |
| DE2233359C3 (de) | Pastöse Kautschukmischung | |
| DE3003893A1 (de) | Reaktive silylgruppen tragende homo- oder copolymere von 1,3-dienen, verfahren zu ihrer herstellung sowie deren verwendung | |
| DE3345249A1 (de) | Polymermischungen und daraus hergestellte covulkanisate | |
| DE3226081C1 (de) | Verwendung von hydrierten Butadien-Acrylnitril-Copolymerisaten zur Herstellung von Formartikeln | |
| DE2431556A1 (de) | Copolymerisat mit regelloser verteilung der monomereinheiten | |
| DE1620820C3 (de) | Verfahren zum Erzielen einer auch in der Wärme widerstandsfähigen Haftung zwischen Schichten aus verschiedenen Elastomeren | |
| DE1142060B (de) | Verfahren zum Vulkanisieren von im wesentlichen amorphen hochmolekularen Mischpolymerisaten aus ª‡-Olefinen miteinander und/oder mit AEthylen | |
| DE1908326A1 (de) | Vulkanisierbare Formmassen | |
| DE1914691A1 (de) | Vernetzbare Mischungen auf der Grundlage von Elastomeren und vernetzbaren Mischpolymeren von Vinylchlorid | |
| DE1136107B (de) | Verfahren zur Herstellung von Elastomeren | |
| DE2626319C2 (de) | Verfahren zur Herstellung von modifizierten kautschukartigen Terpolymeren | |
| DE1101763B (de) | Verfahren zur Herstellung von halogenierten Isoolefin-Polyolefin-Mischpolymerisaten | |
| DE1131399B (de) | Verfahren zur Herstellung von vulkanisierten Elastomeren aus amorphen Mischpolymeren des AEthylens mit hoeheren ª-Olefinen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| SH | Request for examination between 03.10.1968 and 22.04.1971 |