WO2018130188A1 - Composite de caoutchouc, procédé de traitement, courroie en caoutchouc et rouleau en caoutchouc utilisant le composite, et procédé de fabrication - Google Patents
Composite de caoutchouc, procédé de traitement, courroie en caoutchouc et rouleau en caoutchouc utilisant le composite, et procédé de fabrication Download PDFInfo
- Publication number
- WO2018130188A1 WO2018130188A1 PCT/CN2018/072353 CN2018072353W WO2018130188A1 WO 2018130188 A1 WO2018130188 A1 WO 2018130188A1 CN 2018072353 W CN2018072353 W CN 2018072353W WO 2018130188 A1 WO2018130188 A1 WO 2018130188A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- rubber
- parts
- vulcanization
- rubber composition
- mixing
- Prior art date
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- 239000005060 rubber Substances 0.000 title claims abstract description 254
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- 150000001875 compounds Chemical class 0.000 claims description 40
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 27
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- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 238000001308 synthesis method Methods 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- DNZZPKYSGRTNGK-PQZOIKATSA-N (1z,4z)-cycloocta-1,4-diene Chemical compound C1C\C=C/C\C=C/C1 DNZZPKYSGRTNGK-PQZOIKATSA-N 0.000 description 1
- HGTUJZTUQFXBIH-UHFFFAOYSA-N (2,3-dimethyl-3-phenylbutan-2-yl)benzene Chemical group C=1C=CC=CC=1C(C)(C)C(C)(C)C1=CC=CC=C1 HGTUJZTUQFXBIH-UHFFFAOYSA-N 0.000 description 1
- SFTGRPFSYZGXQW-GQCTYLIASA-N (4e)-3-methylhexa-1,4-diene Chemical compound C\C=C\C(C)C=C SFTGRPFSYZGXQW-GQCTYLIASA-N 0.000 description 1
- JBVMSEMQJGGOFR-FNORWQNLSA-N (4e)-4-methylhexa-1,4-diene Chemical compound C\C=C(/C)CC=C JBVMSEMQJGGOFR-FNORWQNLSA-N 0.000 description 1
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- RCJMVGJKROQDCB-UHFFFAOYSA-N 1,3-dimethyl-1,3-butadiene Natural products CC=CC(C)=C RCJMVGJKROQDCB-UHFFFAOYSA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- AXWJKQDGIVWVEW-UHFFFAOYSA-N 2-(dimethylamino)butanedioic acid Chemical compound CN(C)C(C(O)=O)CC(O)=O AXWJKQDGIVWVEW-UHFFFAOYSA-N 0.000 description 1
- RCBGGJURENJHKV-UHFFFAOYSA-N 2-methylhept-1-ene Chemical compound CCCCCC(C)=C RCBGGJURENJHKV-UHFFFAOYSA-N 0.000 description 1
- DRWYRROCDFQZQF-UHFFFAOYSA-N 2-methylpenta-1,4-diene Chemical compound CC(=C)CC=C DRWYRROCDFQZQF-UHFFFAOYSA-N 0.000 description 1
- QDMFTFWKTYXBIW-UHFFFAOYSA-N 3-Methyl-1-heptene Chemical compound CCCCC(C)C=C QDMFTFWKTYXBIW-UHFFFAOYSA-N 0.000 description 1
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
- WNEYWVBECXCQRT-UHFFFAOYSA-N 5-methylhept-1-ene Chemical compound CCC(C)CCC=C WNEYWVBECXCQRT-UHFFFAOYSA-N 0.000 description 1
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920000034 Plastomer Polymers 0.000 description 1
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 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
- 150000001723 carbon free-radicals Chemical group 0.000 description 1
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000002431 foraging effect Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000006713 insertion reaction Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920002215 polytrimethylene terephthalate Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000011112 process operation Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 238000010059 sulfur vulcanization Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 150000005671 trienes Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000002759 woven fabric 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
-
- 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
Definitions
- Cross-linking performance includes factors such as crosslink density and cross-linking rate, which is the specific performance of the cross-linking ability of the rubber matrix during processing.
- the vinyl copolymer refers to a copolymer of ethylene and a branched ⁇ -olefin, and has a secondary branched structure, wherein the branched ⁇ -olefin may be selected from the group consisting of isobutylene and 3-methyl-1- Butylene, 4-methyl-1-pentene, 3-methyl-1-pentene, 2-methyl-1-heptene, 3-methyl-1-heptene, 4-methyl-1- The heptene, 5-methyl-1-heptene, 6-methyl-1-heptene, and the like, the comonomer may also contain a common linear alpha-olefin.
- a further preferred technical solution for the branched polyethylene is a branching degree of 80 to 105 branches/1000 carbons, a weight average molecular weight of 250,000 to 400,000, and a Mooney viscosity of ML (1+4) of 125 ° C of 40 ⁇ . 95.
- a further technical solution is that the amount of carbon black is from 30 to 60 parts by weight based on 100 parts by weight of the rubber base.
- the above-mentioned carrier core wire is subjected to a bonding treatment to improve the adhesion property of the carrier core wire to the rubber, and the bonding can be performed by dipping the carrier core wire into a treatment solution such as resorcinol formaldehyde latex (PFL impregnation liquid) and heating and drying. .
- a treatment solution such as resorcinol formaldehyde latex (PFL impregnation liquid) and heating and drying.
- the branched polyethylene used was numbered PER-7.
- Rubber mixing set the temperature of the mixer to 90 ° C, the rotor speed is 50 rpm, add 100 parts of EPDM rubber, pre-press and knead for 90 seconds; add 6 parts of zinc oxide, 1 part of stearin Acid, 2 parts of antioxidant RD, kneaded for 1 minute; then add 45 parts of carbon black N330, 5 parts of paraffin oil SUNPAR2280 and 5 parts of coumarone resin in the compound, mix for 3 minutes; then add 20 parts of length 1mm Nylon staple fiber, kneaded for 2 minutes; finally add 4 parts of cross-linking agent dicumyl peroxide (DCP) and 1.5 parts of cross-linking agent triallyl isocyanurate (TAIC), mixing for 2 minutes After the rubber is glued, the rubber compound is thinly passed on the open mill with a roll temperature of 80 ° C, and is thinned 7 times at a roll gap of 0.5 mm to fully orient the short fibers, and the roll gap is obtained to obtain a
- the above rubber mixture is placed in a screw extruder for hot refining, and then supplied to a calender for calendering to be used.
- a calender for calendering to be used.
- the thickness of the film is controlled at 4.5 to 12 mm, and it is kept warm after use.
- the aramid staple fibers in the rubber compound are longitudinally aligned.
- a high temperature resistant rubber roller using the rubber composition provided by the invention comprising the following steps:
- the rubber substrate used in Example 22 was 100 parts of PER-12, and the rubber substrate used in Example 23 was 50 parts of PER-12 and 50 parts of ethylene propylene diene monomer (ML (1+4) 125 ° C was 60, and the ethylene content was 68. %, ENB content 4.8%), the rubber substrate used in Comparative Example 3 was 100 parts of the ethylene propylene diene rubber used in Example 23. The rest of the formula is consistent.
- Example 22 has the shortest Tc90, which is about 25% shorter than that of Comparative Example 3, and the MH-ML values are very close, indicating that the branched polyethylene used in this embodiment can be superior to the conventional ternary in cross-linking ability.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
La présente invention concerne un composite de caoutchouc comprenant, en termes de parties en poids : 100 parties d'un substrat en caoutchouc, de 1,5 à 9 parties d'un agent de réticulation, et de 5 à 60 parties de fibres courtes, et comprenant également des constituants auxiliaires. Le substrat en caoutchouc comprend : du polyéthylène ramifié, dont la teneur a est telle que : 0 < a ≤ 100 parties, du caoutchouc monomère d'éthylène-propylène et du caoutchouc monomère de diène-éthylène-propylène, dont la teneur b est telle que : 0 ≤ b < 100 parties. Le composite de caoutchouc est destiné à être utilisé dans la fabrication d'une courroie de transmission, d'une courroie transporteuse, d'un rouleau en caoutchouc et d'un tube en caoutchouc.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/477,525 US12129370B2 (en) | 2017-01-13 | 2018-01-12 | Rubber composition, processing method thereof, and rubber belt and rubber roller using the same |
JP2019559140A JP7118450B2 (ja) | 2017-01-13 | 2018-01-12 | ゴム組成物および加工方法、並びにそれを用いたゴムベルト、ゴムローラおよび製造方法 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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CN201710024698.4 | 2017-01-13 | ||
CN201710024698 | 2017-01-13 | ||
CN201810020822.4A CN108314849B (zh) | 2017-01-13 | 2018-01-10 | 橡胶组合物及加工方法,及应用其的胶带、胶辊及生产方法 |
CN201810020822.4 | 2018-01-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2018130188A1 true WO2018130188A1 (fr) | 2018-07-19 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2018/072353 WO2018130188A1 (fr) | 2017-01-13 | 2018-01-12 | Composite de caoutchouc, procédé de traitement, courroie en caoutchouc et rouleau en caoutchouc utilisant le composite, et procédé de fabrication |
Country Status (1)
Country | Link |
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WO (1) | WO2018130188A1 (fr) |
Cited By (10)
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CN109296700A (zh) * | 2018-11-29 | 2019-02-01 | 浙江奋飞橡塑制品有限公司 | E型联组带 |
CN110049381A (zh) * | 2019-04-26 | 2019-07-23 | 王铁军 | 一种基站 |
CN110529668A (zh) * | 2019-08-28 | 2019-12-03 | 福州森百德机电科技有限公司 | 水泥复合管及其制备方法 |
CN113458046A (zh) * | 2021-03-23 | 2021-10-01 | 德清县强业舰船装备有限公司 | 一种抗拉伸气垫船用橡胶生产设备及其制备方法 |
CN113524738A (zh) * | 2021-07-16 | 2021-10-22 | 成都盛帮密封件股份有限公司 | 一种用于热压罐成型复合材料时未硫化橡胶板的加工方法 |
CN114425823A (zh) * | 2022-04-07 | 2022-05-03 | 山东万达宝通轮胎有限公司 | 一种橡胶混炼方法、混炼胶及应用 |
CN114921009A (zh) * | 2021-07-30 | 2022-08-19 | 集瑞泽管业(江苏)有限公司 | 一种防结垢免清洗辐照交联聚乙烯材料、管材及其制备 |
CN115073856A (zh) * | 2022-07-21 | 2022-09-20 | 中国兵器装备集团西南技术工程研究所 | 一种三元乙丙橡胶及其制备方法 |
CN115160720A (zh) * | 2021-08-09 | 2022-10-11 | 西诺瑞特新材料(上海)有限公司 | 一种用于高分子片材热熔压敏胶的流变性橡胶及其制备方法 |
CN116285038A (zh) * | 2023-03-21 | 2023-06-23 | 马鞍山宏力橡胶制品有限公司 | 一种回转支承丁腈密封圈胶料及该胶料的应用 |
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Cited By (15)
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CN109296700B (zh) * | 2018-11-29 | 2023-07-14 | 浙江奋飞橡塑制品有限公司 | E型联组带 |
CN109296700A (zh) * | 2018-11-29 | 2019-02-01 | 浙江奋飞橡塑制品有限公司 | E型联组带 |
CN110049381A (zh) * | 2019-04-26 | 2019-07-23 | 王铁军 | 一种基站 |
CN110049381B (zh) * | 2019-04-26 | 2021-12-03 | 王铁军 | 一种基站 |
CN110529668A (zh) * | 2019-08-28 | 2019-12-03 | 福州森百德机电科技有限公司 | 水泥复合管及其制备方法 |
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CN113524738A (zh) * | 2021-07-16 | 2021-10-22 | 成都盛帮密封件股份有限公司 | 一种用于热压罐成型复合材料时未硫化橡胶板的加工方法 |
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CN115160720A (zh) * | 2021-08-09 | 2022-10-11 | 西诺瑞特新材料(上海)有限公司 | 一种用于高分子片材热熔压敏胶的流变性橡胶及其制备方法 |
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