IL10992A - Vulcanized elastomers from substantially amorphous polymers and copolymers of alpha olefins and process for preparing the same - Google Patents
Vulcanized elastomers from substantially amorphous polymers and copolymers of alpha olefins and process for preparing the sameInfo
- Publication number
- IL10992A IL10992A IL10992DA IL10992A IL 10992 A IL10992 A IL 10992A IL 10992D A IL10992D A IL 10992DA IL 10992 A IL10992 A IL 10992A
- Authority
- IL
- Israel
- Prior art keywords
- parts
- elastomers
- substance
- polymeric
- weight
- Prior art date
Links
- 229920001577 copolymer Polymers 0.000 title claims description 45
- 229920001971 elastomer Polymers 0.000 title claims description 32
- 239000000806 elastomer Substances 0.000 title claims description 28
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 229920006125 amorphous polymer Polymers 0.000 title claims 3
- 239000004711 α-olefin Substances 0.000 title 1
- 229920000642 polymer Polymers 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 27
- 238000004073 vulcanization Methods 0.000 claims description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 20
- 230000008569 process Effects 0.000 claims description 20
- 239000003999 initiator Substances 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 11
- 239000011787 zinc oxide Substances 0.000 claims description 10
- 230000002378 acidificating effect Effects 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 229910044991 metal oxide Inorganic materials 0.000 claims description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000006229 carbon black Substances 0.000 claims description 7
- 150000004706 metal oxides Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 150000001336 alkenes Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 238000001704 evaporation Methods 0.000 claims description 4
- 150000002894 organic compounds Chemical class 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 239000012190 activator Substances 0.000 claims 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 229920001967 Metal rubber Polymers 0.000 claims 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims 1
- 229920005684 linear copolymer Polymers 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 150000001451 organic peroxides Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 10
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 10
- 150000008064 anhydrides Chemical class 0.000 description 10
- 235000019400 benzoyl peroxide Nutrition 0.000 description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 6
- 239000011976 maleic acid Substances 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 5
- 150000002978 peroxides Chemical class 0.000 description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- 238000007669 thermal treatment Methods 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- -1 aliphatic olefins Chemical class 0.000 description 2
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 2
- 238000010504 bond cleavage reaction Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 210000002445 nipple Anatomy 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- NGZXDRGWBULKFA-NSOVKSMOSA-N (+)-Bebeerine Chemical compound C([C@@H]1N(C)CCC=2C=C(C(=C(OC3=CC=C(C=C3)C[C@H]3C=4C=C(C(=CC=4CCN3C)OC)O3)C=21)O)OC)C1=CC=C(O)C3=C1 NGZXDRGWBULKFA-NSOVKSMOSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- QSWLSAYLEATCSH-UHFFFAOYSA-N 3-propan-2-ylfuran-2,5-dione Chemical compound CC(C)C1=CC(=O)OC1=O QSWLSAYLEATCSH-UHFFFAOYSA-N 0.000 description 1
- 235000003913 Coccoloba uvifera Nutrition 0.000 description 1
- 241001508691 Martes zibellina Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 240000008976 Pterocarpus marsupium Species 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- CHIHQLCVLOXUJW-UHFFFAOYSA-N benzoic anhydride Chemical compound C=1C=CC=CC=1C(=O)OC(=O)C1=CC=CC=C1 CHIHQLCVLOXUJW-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000007705 chemical test Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- JCYWCSGERIELPG-UHFFFAOYSA-N imes Chemical class CC1=CC(C)=CC(C)=C1N1C=CN(C=2C(=CC(C)=CC=2C)C)[C]1 JCYWCSGERIELPG-UHFFFAOYSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical group CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 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 |
|---|---|
| IL10992A true IL10992A (en) | 1900-01-01 |
Family
ID=26325009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL10992D IL10992A (en) | 1957-01-09 | Vulcanized elastomers from substantially amorphous polymers and copolymers of alpha olefins and process for preparing the same |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3236917A (pt) |
| BE (1) | BE563834A (pt) |
| CH (1) | CH417086A (pt) |
| DD (1) | DD20232A (pt) |
| DE (1) | DE1494167A1 (pt) |
| FR (1) | FR1200144A (pt) |
| GB (2) | GB885970A (pt) |
| IE (1) | IE23563B1 (pt) |
| IL (1) | IL10992A (pt) |
| IN (1) | IN62803B (pt) |
| IT (2) | IT600723A (pt) |
| LU (1) | LU35689A1 (pt) |
| NL (2) | NL293534A (pt) |
| NO (1) | NO126663L (pt) |
| NZ (1) | NZ120319A (pt) |
| PT (1) | PT34730A (pt) |
Families Citing this family (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL103723C (pt) * | 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 |
| NL126427C (pt) * | 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 (pt) * | 1965-02-15 | |||
| FR1481828A (pt) * | 1965-06-14 | 1967-08-21 | ||
| NL6613608A (pt) * | 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 |
| US3642950A (en) * | 1968-12-30 | 1972-02-15 | Uniroyal Inc | Graft copolymerization on 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 |
| US4544702A (en) * | 1984-06-11 | 1985-10-01 | Uniroyal, Inc. | Modified ionic elastomer and blend with nylon |
| US4739016A (en) * | 1984-06-11 | 1988-04-19 | Uniroyal Chemical Company, Inc. | Modified ionic elastomer and blend with nylon |
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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 |
| US2724707A (en) * | 1950-11-01 | 1955-11-22 | Goodrich Co B F | Elastic synthetic rubber composition and method of making same |
| US2662874A (en) * | 1950-11-01 | 1953-12-15 | Goodrich Co B F | Preparation of plastic condensable synthetic rubbers and subsequent elasto-condensation thereof |
| 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 |
| NL92954C (pt) * | 1954-12-16 |
-
0
- NL NL107983D patent/NL107983C/xx active
- IT IT574913D patent/IT574913A/it unknown
- NL NL293534D patent/NL293534A/xx unknown
- LU LU35689D patent/LU35689A1/xx unknown
- NZ NZ120319D patent/NZ120319A/xx unknown
- IN IN62803D patent/IN62803B/en unknown
- IT IT600723D patent/IT600723A/it unknown
- NO NO126663D patent/NO126663L/no unknown
- DD DD20232D patent/DD20232A/xx unknown
- PT PT34730D patent/PT34730A/pt unknown
- BE BE563834D patent/BE563834A/xx unknown
- IL IL10992D patent/IL10992A/en 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 GB33999/61A patent/GB885970A/en not_active Expired
- 1958-01-08 GB GB768/58A patent/GB885969A/en not_active Expired
- 1958-01-09 FR FR1200144D patent/FR1200144A/fr not_active Expired
- 1958-01-09 CH CH5450958A patent/CH417086A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PT34730A (pt) | 1900-01-01 |
| NL107983C (pt) | 1900-01-01 |
| IT574913A (pt) | 1900-01-01 |
| NZ120319A (pt) | 1900-01-01 |
| IN62803B (pt) | 1957-01-09 |
| IE23563L (en) | 1958-07-09 |
| BE563834A (pt) | 1900-01-01 |
| DD20232A (pt) | 1900-01-01 |
| IE23563B1 (en) | 1962-10-03 |
| DE1494167A1 (de) | 1969-02-13 |
| NL293534A (pt) | 1900-01-01 |
| US3236917A (en) | 1966-02-22 |
| FR1200144A (fr) | 1959-12-18 |
| GB885970A (en) | 1962-01-03 |
| IT600723A (pt) | 1900-01-01 |
| GB885969A (en) | 1962-01-03 |
| NO126663L (pt) | |
| LU35689A1 (pt) | 1900-01-01 |
| CH417086A (de) | 1966-07-15 |
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