KR20000029670A - 엄격한탄성중합체적용을위한저브롬이소부틸렌-공-4-브로모메틸스티렌조성물 - Google Patents
엄격한탄성중합체적용을위한저브롬이소부틸렌-공-4-브로모메틸스티렌조성물 Download PDFInfo
- Publication number
- KR20000029670A KR20000029670A KR1019997000748A KR19997000748A KR20000029670A KR 20000029670 A KR20000029670 A KR 20000029670A KR 1019997000748 A KR1019997000748 A KR 1019997000748A KR 19997000748 A KR19997000748 A KR 19997000748A KR 20000029670 A KR20000029670 A KR 20000029670A
- Authority
- KR
- South Korea
- Prior art keywords
- bromomethylstyrene
- isobutylene
- poly
- phr
- sulfided
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims description 28
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 title claims description 10
- 229910052794 bromium Inorganic materials 0.000 title claims description 10
- 229920001971 elastomer Polymers 0.000 title description 16
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 title description 9
- 239000000806 elastomer Substances 0.000 title description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000011787 zinc oxide Substances 0.000 claims abstract description 25
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 claims abstract description 21
- 150000004763 sulfides Chemical class 0.000 claims abstract description 14
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims abstract description 11
- 235000019345 sodium thiosulphate Nutrition 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims description 13
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 claims description 9
- 235000021355 Stearic acid Nutrition 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 8
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 8
- 239000008117 stearic acid Substances 0.000 claims description 8
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 7
- RUROFEVDCUGKHD-UHFFFAOYSA-N 3-bromoprop-1-enylbenzene Chemical compound BrCC=CC1=CC=CC=C1 RUROFEVDCUGKHD-UHFFFAOYSA-N 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- VTPQLJUADNBKRM-UHFFFAOYSA-N 1-(bromomethyl)-4-ethenylbenzene Chemical compound BrCC1=CC=C(C=C)C=C1 VTPQLJUADNBKRM-UHFFFAOYSA-N 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 229920005555 halobutyl Polymers 0.000 abstract description 4
- 125000004968 halobutyl group Chemical group 0.000 abstract description 4
- 230000002829 reductive effect Effects 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 description 20
- 239000005060 rubber Substances 0.000 description 10
- 230000032683 aging Effects 0.000 description 6
- 239000004594 Masterbatch (MB) Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 239000012188 paraffin wax Substances 0.000 description 5
- 101100398918 Arabidopsis thaliana IPMS2 gene Proteins 0.000 description 4
- 101100018850 Luffa aegyptiaca IMS1 gene Proteins 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000005486 sulfidation Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 2
- QXYKBSYRGILOTK-UHFFFAOYSA-L disodium;1,6-bis(sulfonatosulfanyl)hexane Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCCCCCCSS([O-])(=O)=O QXYKBSYRGILOTK-UHFFFAOYSA-L 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- -1 ozones Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000013037 reversible inhibitor Substances 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- CPGFMWPQXUXQRX-UHFFFAOYSA-N 3-amino-3-(4-fluorophenyl)propanoic acid Chemical compound OC(=O)CC(N)C1=CC=C(F)C=C1 CPGFMWPQXUXQRX-UHFFFAOYSA-N 0.000 description 1
- LLQHSBBZNDXTIV-UHFFFAOYSA-N 6-[5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-4,5-dihydro-1,2-oxazol-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC1CC(=NO1)C1=CC2=C(NC(O2)=O)C=C1 LLQHSBBZNDXTIV-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 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
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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/18—Introducing halogen atoms or halogen-containing groups
- C08F8/20—Halogenation
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
- Y10T428/2975—Tubular or cellular
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
Abstract
Description
중합체 | PMS 함량(몰%) | Br-PMS 함량(몰%) | 무니 점도 |
BIMS1 | 2.17* | 0.33** | 39 |
BIMS2 | 2.12* | 0.38** | 45* |
BIMS3 | 2.0* | 0.49* | 43 |
BIMS4 | 2.04 | 0.24 | 48 |
BIMS5 | 2.17 | 0.17 | 47 |
BIMS6 | 2.22 | 0.23 | 45 |
IMS1 | 2.62 | 0 | 49 |
*보통값, 실제값은 측정되지 않음**FTIR에 의해 측정됨 |
실시예 | 1 | 2 | 3 | 4 |
조성물(phr) | ||||
BIMS1 | 100 | - | - | - |
BIMS2 | - | 100 | - | - |
BIMS3 | - | - | 100 | 70 |
IMS1 | - | - | - | 30 |
N330 블랙 | 55 | 55 | 55 | 55 |
광유 | 7 | 7 | 7 | 7 |
파라핀 왁스 | 2 | 2 | 2 | 2 |
ZnO | 2 | 2 | 2 | 2 |
DURALINK HTS | 1.6 | 1.6 | 1.6 | 1.6 |
DHT4A2 | 0.25 | 0.25 | 0.25 | 0.25 |
ODR@190℃, 1o원호, 60분 | ||||
MH(dNm) | 31.69 | 27.2 | 31.63 | 11.76 |
ML(dNm) | 5.87 | 5.92 | 5.88 | 5.86 |
Ts2(분) | 3.29 | 2.67 | 3.07 | 5.85 |
Tc(90)(분) | 22.56 | 18.34 | 22.26 | 31.34 |
장력 특성(오븐 노화이전) | ||||
파열 강도(MPa) | 11.14 | 12.78 | 12.62 | 9.82 |
파열신율(%) | 343 | 355 | 258 | 243 |
100% 모듈러스(MPa) | 2.35 | 2.52 | 3.3 | 3.3 |
200% 모듈러스(MPa) | 5.98 | 6.62 | 8.83 | 8.28 |
300% 모듈러스(MPa) | 9.83 | 11.15 | - | - |
장력 고정성(E%) | 6.25 | 3.44 | - | - |
장력 특성(48시간 오븐 노화이후 @177℃) | ||||
파열 강도(MPa) | 8.56 | 11.82 | 14.55 | 9.46 |
파열신율(%) | 433 | 411 | 277 | 294 |
100% 모듈러스(MPa) | 1.99 | 2.46 | 3.83 | 2.94 |
200% 모듈러스(MPa) | 4.08 | 5.38 | 10.04 | 6.68 |
300% 모듈러스(MPa) | 6.33 | 8.92 | - | - |
장력 고정성(E%) | 13.5 | 7.5 | - | - |
실시예 | 5 | 6 | 7 |
조성물(phr) | |||
BIMS4 | 100 | - | - |
BIMS5 | - | 100 | 100 |
N330블랙 | 55 | 55 | 55 |
광유 | 7 | 7 | 7 |
파라핀 왁스 | 2 | 2 | 2 |
ZnO | 2 | 2 | 3 |
Duralink HTS | 1.6 | 1.6 | 1.5 |
스테아르산 | - | - | 0.6 |
ODR @190℃, 1o원호, 고평부 MH | |||
MH(dNm) | 25.8 | 21.0 | 17.9 |
ML(dNm) | 6.3 | 5.6 | 5.7 |
Ts2(분) | 3.3 | 6.8 | 2.5 |
Tc(90)(분) | 23.4 | 120 | 15.6 |
실온에서 장력 특성(비노화됨) | |||
파열강도(MPa) | 16.0 | 12.5 | 12.4 |
파열신율(%) | 405 | 558 | 557 |
300% 장력 고정성(E%) | 1.3 | 18.8 | 8 |
장력 특성(비노화됨)@150℃ | |||
파열강도(MPa) | 6.2 | 5.8 | 4.1 |
파열신율(%) | 386 | 317 | 375 |
200% 고온 장력 고정성(E%) | 16.0 | 24 | 40 |
실시예 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 |
조성물(phr) | ||||||||
BIMS6 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 |
B234블랙 | 55 | 55 | 55 | 55 | 55 | 55 | 55 | 55 |
광유 | 5 | 5 | 5 | 5 | 5 | 5 | 5 | 5 |
파리핀 왁스 | 5 | 5 | 5 | 5 | 5 | 5 | 5 | 5 |
ZnO | 3 | 1 | 2 | 1 | 1 | 1 | 3 | 3 |
Duralink HTS | 1.5 | - | - | - | - | - | - | - |
스테아르산 | 0.25 | 2 | - | 2 | 2 | 2 | 0.5 | 0.5 |
스테아르산아연 | - | 1 | 3 | - | - | - | - | - |
ZDEDC | - | - | - | 1.5 | - | - | - | - |
TMTD | - | - | - | - | 0.2 | - | - | - |
DPTTS(Sulfads) | - | - | - | - | - | 1 | - | - |
MBTS | - | - | - | - | - | - | 1.2 | 1.2 |
DHT4A2 | - | - | - | - | - | - | 1.1 | - |
황 | - | - | - | - | - | - | 0.75 | 0.75 |
수지SP1045 | - | - | - | - | - | - | 7 | 7 |
ODR@190℃ 1o원호, 60분 | ||||||||
MH-ML(dNm) | 17.2 | 6.5 | 5.9 | 4.5 | 9.6 | 8.6 | 3.3 | 6.1 |
Ts2(분) | 3.2 | 1.9 | 2.0 | 1.3 | 1.5 | 1.4 | 7 | 2.6 |
Tc(90)(분) | 29.8 | 5.7 | 6.0 | 3.3 | 6.8 | 4.4 | 11.3 | 5.0 |
의견:경화 곡선경화된 중합체 | 안정F | RS/T | RS/T | -SEF | RSEF | RSEF | RSEF/B | RSEF/B |
색인:R=약간 가역F= 견고함S/T=부드럽고 점착성SEF=반견고함B=발포됨 |
Claims (22)
- 폴리(이소부틸렌-공-4-브로모메틸스티렌)(0.1 내지 0.45몰%의 벤질 브롬을 포함한다) 및 경화 패키지를 포함하는 황화가능한 혼합물.
- 제 1 항에 있어서,경화 패키지가 1,6-헥사메틸렌-비스(티오황산나트륨), 산화아연, 선택적으로 촉진제 및 선택적으로 지연제를 포함하는 황화가능한 혼합물.
- 제 1 항의 혼합물을 황화시킴으로서 얻어지는 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌).
- 제 2 항의 혼합물을 황화시킴으로서 얻어지는 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌).
- 제 3 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 경화조직.
- 제 4 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 경화조직.
- 제 3 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 승온에서 유용한 호스.
- 제 4 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 승온에서 유용한 호스.
- 제 3 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 개스킷.
- 제 4 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 개스킷.
- 제 3 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 약학적 스토퍼.
- 제 4 항의 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 포함하는 약학적 스토퍼.
- 필수적으로 벤질 브롬이 없는 정도로 황화된 폴리(이소부틸렌-공-4-브로모메틸스티렌)의 황화물.
- 제 13 항에 있어서,폴리(이소부틸렌-공-4-브로모메틸스티렌)이 0.1 내지 0.45몰%의 4-브로모메틸스티렌을 포함하는 황화물.
- 폴리(이소부틸렌-공-4-메틸스티렌)을 브롬화시켜 0.1 내지 0.45몰%의 벤질 브롬을 함유하는 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 얻는 단계;경화 패키지와 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 배합하는 단계; 및배합된 혼합물을 가열하여 폴리(이소부틸렌-공-4-브로모메틸스티렌)을 황화시키는 단계를 포함하는 폴리(이소부틸렌-공-4-메틸스티렌)을 황화시키는 방법.
- 제 2 항에 있어서,경화 패키지가 1,6-헥사메틸렌-비스(티오황산나트륨) 0.2 내지 6phr, 산화아연 0.1 내지 6phr, 지방산 또는 지방산 금속염 0 내지 8phr 및 지연제 0 내지 8phr을 포함하는 발명.
- 제 15 항에 있어서,경화 패키지가 1,6-헥사메틸렌-비스(티오황산나트륨) 0.5 내지 5phr, 산화아연 2 내지 4phr, 스테아르산 0 내지 2phr 및 지연제 0 내지 2phr을 포함하는 발명.
- 제 16 항에 있어서,경화 패키지가 1,6-헥사메틸렌-비스(티오황산나트륨) 2 내지 4phr, 산화아연 2 내지 4phr, 스테아르산 0 내지 2phr 및 지연제 0 내지 2phr을 포함하는 발명.
- 제 17 항에 있어서,경화 패키지가 1,6-헥사메틸렌-비스(티오황산나트륨) 0.5 내지 5phr, 산화아연 2 내지 4phr, 스테아르산 0 내지 2phr 및 지연제 0 내지 2phr을 포함하는 발명.
- 0.1 내지 0.45몰%의 벤질 브롬을 포함하고, 총 브로모메틸스티렌 및 메틸스티렌 함량이 2몰% 미만인 폴리(이소부틸렌-공-4-브로모메틸스티렌-공-4-메틸스티렌).
- 제 20 항에 있어서,브로모메틸스티렌 및 메틸스티렌 총 함량이 0.2 내지 1몰%인 공중합체.
- 0.1 내지 0.45몰%의 브롬 치환된 파라-알킬스티렌 및 2몰% 미만의 총 치환되고 비치환된 파라-알킬스티렌을 포함하는 C4-C7의 이소올레핀 및 파라-알킬스티렌의 브롬화된 상호중합체.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8/691,109 | 1996-08-01 | ||
US08/691,109 US5698640A (en) | 1996-08-01 | 1996-08-01 | Low bromine isobutylene-co-4-bromomethylstyrene compositions for severe duty elastomer applications |
Publications (1)
Publication Number | Publication Date |
---|---|
KR20000029670A true KR20000029670A (ko) | 2000-05-25 |
Family
ID=24775194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019997000748A Ceased KR20000029670A (ko) | 1996-08-01 | 1997-07-28 | 엄격한탄성중합체적용을위한저브롬이소부틸렌-공-4-브로모메틸스티렌조성물 |
Country Status (13)
Country | Link |
---|---|
US (1) | US5698640A (ko) |
EP (1) | EP0915932A2 (ko) |
JP (1) | JP2001506286A (ko) |
KR (1) | KR20000029670A (ko) |
CN (1) | CN1226269A (ko) |
AT (1) | AT410093B (ko) |
BR (1) | BR9711610A (ko) |
CA (1) | CA2259167A1 (ko) |
CZ (1) | CZ432898A3 (ko) |
EA (1) | EA199900155A1 (ko) |
HU (1) | HUP9904493A3 (ko) |
PL (1) | PL331386A1 (ko) |
WO (1) | WO1998005713A2 (ko) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6448322B1 (en) * | 1997-03-06 | 2002-09-10 | Exxon Mobil Chemical Patents Inc. | Stabilization of halogenated rubber |
US6060549A (en) * | 1997-05-20 | 2000-05-09 | Exxon Chemical Patents, Inc. | Rubber toughened thermoplastic resin nano composites |
US6809137B2 (en) * | 1998-06-08 | 2004-10-26 | Bridgestone Corporation | Rubber composition and pneumatic tire using said rubber composition |
JP4521074B2 (ja) * | 1998-06-08 | 2010-08-11 | 株式会社ブリヂストン | ゴム組成物及びそれを用いた空気入りタイヤ |
CA2282900C (en) | 1999-09-20 | 2011-02-01 | Bayer Inc. | Halogenated terpolymers of isobutylene, diolefin monomer and styrenic monomer |
DE60019806T2 (de) | 1999-12-28 | 2006-01-19 | Exxonmobil Chemical Patents Inc., Baytown | Innenreifen mit verbesserten hitzeresistenten eigenschaften |
US7328733B2 (en) * | 1999-12-28 | 2008-02-12 | Exxonmobil Chemical Patents Inc. | Inner tube compositions having improved heat resistance characteristics |
BR0114751A (pt) * | 2000-10-18 | 2004-02-10 | Exxonmobil Chem Patents Inc | Composição elastomérica |
US7425591B2 (en) * | 2001-10-16 | 2008-09-16 | Exxonmobil Chemical Patents Inc | Elastomeric composition |
AU2002233323A1 (en) * | 2001-02-09 | 2002-08-28 | Sensomotoric Instruments Gmbh | Multidimensional eye tracking and position measurement system |
WO2002098927A1 (en) | 2001-06-04 | 2002-12-12 | Exxonmobil Chemical Patents Inc. | Cured robber components for use with pharmaceutical devices |
US7338688B2 (en) * | 2001-06-04 | 2008-03-04 | Exxonmobil Chemical Patents Inc. | Protective pipe and tank linings |
CN100551955C (zh) | 2001-06-08 | 2009-10-21 | 埃克森美孚化学专利公司 | 低渗透性纳米复合材料 |
JP5002112B2 (ja) | 2001-06-13 | 2012-08-15 | エクソンモービル・ケミカル・パテンツ・インク | 低透過性ナノ複合物 |
US6939921B2 (en) * | 2001-10-16 | 2005-09-06 | Exxonmobil Chemical Patents Inc. | Colorable elastomeric composition |
US20040030036A1 (en) * | 2001-10-16 | 2004-02-12 | Waddell Walter H. | Elastomeric composition |
AU2002362122A1 (en) * | 2001-12-10 | 2003-06-23 | Exxonmobil Chemical Patents Inc. | Elastomeric compositions |
AU2002353093A1 (en) * | 2001-12-10 | 2003-07-09 | Exxonmobil Chemical Patents Inc. | Elastomeric compositions |
JP2005511829A (ja) * | 2001-12-10 | 2005-04-28 | エクソンモービル・ケミカル・パテンツ・インク | ハロゲン化イソオレフィン系ターポリマー |
US7060757B2 (en) * | 2003-02-06 | 2006-06-13 | Bridgestone Corporation | Rubber composition and pneumatic tire using the same |
US7605205B2 (en) * | 2005-11-07 | 2009-10-20 | Exxonmobil Chemical Patents, Inc. | Nanocomposite compositions and processes for making the same |
JP2009518502A (ja) * | 2005-12-05 | 2009-05-07 | エクソンモービル・ケミカル・パテンツ・インク | エラストマー性組成物の加工助剤 |
JP5421525B2 (ja) * | 2007-10-19 | 2014-02-19 | 住友ゴム工業株式会社 | ブラダー用ゴム組成物およびそれを用いたタイヤ加硫用ブラダー |
US7923491B2 (en) * | 2008-08-08 | 2011-04-12 | Exxonmobil Chemical Patents Inc. | Graphite nanocomposites |
RU2012110485A (ru) * | 2009-09-10 | 2013-09-27 | Эксонмобил Кемикэл Пейтентс Инк. | Эластомерные сополимеры, сополимерные композиции и их применение в изделиях |
US8415431B2 (en) | 2010-08-05 | 2013-04-09 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomeric compositions |
JP7143604B2 (ja) * | 2018-03-22 | 2022-09-29 | 住友ゴム工業株式会社 | 加硫ブラダー用ゴム組成物及び加硫ブラダー |
WO2020005422A1 (en) * | 2018-06-27 | 2020-01-02 | Exxonmobil Chemical Patents Inc. | Brominated isobutylene paramethyl-styrene elastomer curing bladders |
JP2021095445A (ja) * | 2019-12-13 | 2021-06-24 | Toyo Tire株式会社 | インナーライナー用ゴム組成物、及びそれを用いた空気入りタイヤ |
CN114106477B (zh) * | 2020-09-01 | 2023-07-21 | 中国石油化工股份有限公司 | 用于丁基橡胶封口塞的橡胶基体、组合物、硫化胶及其制备方法 |
WO2023121918A1 (en) | 2021-12-21 | 2023-06-29 | Exxonmobil Chemical Patents Inc. | Compositions, vulcanizates, and cure processes |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5162445A (en) * | 1988-05-27 | 1992-11-10 | Exxon Chemical Patents Inc. | Para-alkylstyrene/isoolefin copolymers and functionalized copolymers thereof |
US5013793A (en) * | 1990-07-26 | 1991-05-07 | Exxon Chemical Patents Inc. | Dynamically cured thermoplastic olefin polymers and process for producing the same |
US5246778A (en) * | 1990-05-14 | 1993-09-21 | Exxon Chemical Patents Inc. | Hose composition |
US5063268A (en) * | 1990-06-08 | 1991-11-05 | Exxon Chemical Patents Inc. | Composition for tire treads (E-235) |
DE69412399T2 (de) * | 1993-09-10 | 1999-01-21 | R.T. Vanderbilt Co., Inc., Norwalk, Conn. | Härtersystem für halogenierte Elastomere |
US5512638A (en) * | 1994-05-03 | 1996-04-30 | Exxon Chemical Patents Inc. | Curing systems for compositions containing halogenated copolymers of isobutylene and para-methylstrene |
US5538218A (en) * | 1994-09-28 | 1996-07-23 | The Goodyear Tire & Rubber Company | Tire curing bladder with improved release from the tire innerliner |
US6207764B1 (en) * | 1995-04-26 | 2001-03-27 | Monsanto Company | Halogenated elastomer compositions |
-
1996
- 1996-08-01 US US08/691,109 patent/US5698640A/en not_active Expired - Fee Related
-
1997
- 1997-07-28 AT AT0908697A patent/AT410093B/de not_active IP Right Cessation
- 1997-07-28 JP JP50805598A patent/JP2001506286A/ja active Pending
- 1997-07-28 HU HU9904493A patent/HUP9904493A3/hu unknown
- 1997-07-28 WO PCT/US1997/013474 patent/WO1998005713A2/en not_active Application Discontinuation
- 1997-07-28 EA EA199900155A patent/EA199900155A1/ru unknown
- 1997-07-28 CZ CZ984328A patent/CZ432898A3/cs unknown
- 1997-07-28 KR KR1019997000748A patent/KR20000029670A/ko not_active Ceased
- 1997-07-28 EP EP97937073A patent/EP0915932A2/en not_active Withdrawn
- 1997-07-28 BR BR9711610A patent/BR9711610A/pt unknown
- 1997-07-28 CA CA002259167A patent/CA2259167A1/en not_active Abandoned
- 1997-07-28 CN CN97196826A patent/CN1226269A/zh active Pending
- 1997-07-28 PL PL97331386A patent/PL331386A1/xx unknown
Also Published As
Publication number | Publication date |
---|---|
CA2259167A1 (en) | 1998-02-12 |
WO1998005713A2 (en) | 1998-02-12 |
HUP9904493A2 (hu) | 2000-05-28 |
AT410093B (de) | 2003-01-27 |
BR9711610A (pt) | 1999-08-24 |
WO1998005713A3 (en) | 1998-03-19 |
EA199900155A1 (ru) | 1999-08-26 |
EP0915932A2 (en) | 1999-05-19 |
ATA908697A (de) | 2002-06-15 |
HUP9904493A3 (en) | 2000-09-28 |
CN1226269A (zh) | 1999-08-18 |
CZ432898A3 (cs) | 1999-03-17 |
JP2001506286A (ja) | 2001-05-15 |
US5698640A (en) | 1997-12-16 |
PL331386A1 (en) | 1999-07-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR20000029670A (ko) | 엄격한탄성중합체적용을위한저브롬이소부틸렌-공-4-브로모메틸스티렌조성물 | |
EP1181332B1 (en) | Isobutylene based elastomer blends having improved strength, elasticity, and reduced permeability | |
EP0540617B1 (en) | Composition for tire carcass | |
JP2004511638A (ja) | エラストマー配合物 | |
EP1335950A2 (en) | Elastomeric composition | |
US5922153A (en) | Tire innerliner composition | |
EP0655080A1 (en) | Hose composition | |
CA2089179C (en) | Tire sidewall composition | |
CA2395434C (en) | Inner tube compositions having improved heat resistance characteristics | |
JP2004501231A (ja) | イソブチレン系エラストマーブレンド | |
US7328733B2 (en) | Inner tube compositions having improved heat resistance characteristics | |
AT410667B (de) | Bromierte interpolymere von c4- bis c7-isoolefin und p-alkylstyrol | |
MXPA99001101A (en) | Low bromine isobutylene-co | |
CA2258472A1 (en) | Curing of butyl rubber | |
EP1264856A1 (en) | Isobutylene based elastomer blends having improved strength, elasticity, and reduced permeability | |
KR20020092471A (ko) | 이소부틸렌계 탄성중합체 블렌드 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0105 | International application |
Patent event date: 19990129 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20020725 Comment text: Request for Examination of Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20050125 Patent event code: PE09021S01D |
|
E601 | Decision to refuse application | ||
PE0601 | Decision on rejection of patent |
Patent event date: 20050331 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20050125 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |