CN1176269A - 脂肪族聚碳酸酯丁苯橡胶的改性方法 - Google Patents
脂肪族聚碳酸酯丁苯橡胶的改性方法 Download PDFInfo
- Publication number
- CN1176269A CN1176269A CN 97114243 CN97114243A CN1176269A CN 1176269 A CN1176269 A CN 1176269A CN 97114243 CN97114243 CN 97114243 CN 97114243 A CN97114243 A CN 97114243A CN 1176269 A CN1176269 A CN 1176269A
- Authority
- CN
- China
- Prior art keywords
- aliphatic polycarbonate
- modifying
- styrene
- peroxide
- styrene rubber
- 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.)
- Granted
Links
- 125000001931 aliphatic group Chemical group 0.000 title claims abstract description 16
- 239000004417 polycarbonate Substances 0.000 title claims abstract description 16
- 229920000515 polycarbonate Polymers 0.000 title claims abstract description 16
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 title claims abstract description 8
- 238000002715 modification method Methods 0.000 title 1
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical group [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 239000005864 Sulphur Substances 0.000 claims description 5
- 235000021355 Stearic acid Nutrition 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 4
- 230000001737 promoting effect Effects 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 239000008117 stearic acid Substances 0.000 claims description 4
- 238000004073 vulcanization Methods 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 claims description 3
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 claims description 3
- 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 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 3
- 229960002447 thiram Drugs 0.000 claims description 3
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 claims description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 claims description 2
- LSEGDMYKXHVBGV-UHFFFAOYSA-N 1-butylperoxybutane;1,1,3-trimethylcyclohexane Chemical group CC1CCCC(C)(C)C1.CCCCOOCCCC LSEGDMYKXHVBGV-UHFFFAOYSA-N 0.000 claims description 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims description 2
- JFISFZKKYWLPPP-UHFFFAOYSA-N 4-sulfanyl-3h-1,3-benzothiazole-2-thione Chemical compound C1=CC=C2SC(S)=NC2=C1S JFISFZKKYWLPPP-UHFFFAOYSA-N 0.000 claims description 2
- 239000004342 Benzoyl peroxide Substances 0.000 claims description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 2
- UPIWXMRIPODGLE-UHFFFAOYSA-N butyl benzenecarboperoxoate Chemical group CCCCOOC(=O)C1=CC=CC=C1 UPIWXMRIPODGLE-UHFFFAOYSA-N 0.000 claims description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 2
- 150000004659 dithiocarbamates Chemical class 0.000 claims description 2
- 150000002632 lipids Chemical class 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical group C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 claims description 2
- 150000003557 thiazoles Chemical class 0.000 claims description 2
- KMNUDJAXRXUZQS-UHFFFAOYSA-L zinc;n-ethyl-n-phenylcarbamodithioate Chemical compound [Zn+2].CCN(C([S-])=S)C1=CC=CC=C1.CCN(C([S-])=S)C1=CC=CC=C1 KMNUDJAXRXUZQS-UHFFFAOYSA-L 0.000 claims description 2
- 150000002357 guanidines Chemical class 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 abstract description 5
- 239000000806 elastomer Substances 0.000 abstract description 4
- 230000032683 aging Effects 0.000 abstract description 3
- 229920005990 polystyrene resin Polymers 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 229960001866 silicon dioxide Drugs 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明属于丁苯橡胶的改性方法。现有技术是用高聚苯乙烯树脂改性丁苯橡胶,本发明提供一种采用脂肪族聚碳酸酯改良丁苯橡胶的方法。所得改性弹性体与原纯弹性体比较具有良好的力学性能。拉伸强度提高3倍以上,耐热空气老化性能也大幅提高。成本与纯丁苯橡胶相近,而且工艺简单,又能利用大气中丰富的二氧化碳资源,缓解化工原料的短缺状况,同时对于降低大气中二氧化碳的含量,缓解全球性的温室效应,保护生态环境具有积极的意义。
Description
本发明属于丁苯橡胶改性。
一般纯丁苯橡胶力学性能较差,而有效的补强填充剂为碳黑,由于颜色较深,限制了制品的用途。为了制造浅色制品一般可以加入二氧化硅、陶土等,但补强效果不大,加入过多二氧化硅和陶土又会影响制品的物理性能。曾有人采用其它聚合物与丁苯橡胶并用对其补强,例如用短丝纤维补强SBR(D.K.Setua,《K.G.K.》,1984,Vo137),并用体系的拉伸强度提高,但不理想,而且硬度大,伸长率低(30%);用聚乙烯改性SBR(朱玉俊等,《特种橡胶制品》,1985,Vo16),并用体系拉伸强度提高,但所得并用弹性体永久变形大,断裂伸长率较低,而且加工温度高,工艺复杂。还有采用高苯乙烯树脂改性SBR(什瓦尔茨等,《橡胶与塑料及合成树脂的并用》,石油工业出版社,1976)所得弹性体力学性能尚可,但是并用弹性体硬度高,永久变形大,加工温度也较高,而且高苯乙烯树脂价格昂贵,成本无法过关。
本发明的目的在于采用廉价的脂肪族聚碳酸酯改性丁苯橡胶。该脂肪族聚碳酸酯系由二氧化碳共聚合成。使用脂肪族聚碳酸酯还可以改善弹性体的物理机械性能和耐热老化性能。
本发明通过下述步骤实现:在100份(重量)丁苯橡胶中加入脂肪族聚碳酸酯1~100份,主交联剂0.2~50份,促进剂0.1~50份,辅助交联剂0.1~80份和活性剂0.1~20份,在90℃~200℃下加压硫化2~200分钟。所用脂肪族聚碳酸酯分子量为2000~300000,分子链含端羟基的饱和树脂,所用的主交联剂是硫磺或过氧化物,如过氧化苯甲酰,特丁基过氧化苯甲酰,过氧化二异丙苯,二特丁基过氧化物,1,1-特丁基过氧-3,3,5三甲基环己烷等,所用促进剂为次磺酰胺类,秋兰姆类,二烷基二硫代氨基甲酸盐类,噻唑类和胍类促进剂,如N-环己基-2-苯并噻唑次磺酰胺(CZ),二硫化二苯并噻唑(DM),二硫醇基苯并噻唑(M),二硫化四甲基秋兰姆(TMTD),乙基苯基二硫代氨基甲酸锌(PX),二苯胍(D)等。所用辅助交联剂是酸酐或异氰酸酯类,如丁二酸酐,顺丁烯二酸酐,四氢邻苯二甲酸酐,六氢邻苯二甲酸酐,三烯丙基异氰酸酯等,所用活性剂是金属氧化物和脂肪酸,如氧化锌和硬脂酸。本发明实施的特点是可以直接将脂肪族聚碳酸酯加到丁苯橡胶中,加工过程在常温下进行,不需要特殊加工设备。弹性体在交联剂以及物理缠结作用下,形成网状交联。交联助剂则通过与羟基反应,进一步改善交联网络的结构,从而提高弹性体的力学性能和耐热性能。
本发明提供的丁苯橡胶改性方法不但提供具有优异的耐热性能和力学性能的改性丁苯橡胶,而且本改性方法加工工艺简单,所采用的脂肪族聚碳酸酯是由二氧化碳共聚合成,改良后产品成本与纯丁苯橡胶相近。该脂肪族聚碳酸酯的广泛应用不仅可以开辟新资源,缓解化工原料的短缺状况,而且对于控制大气中二氧化碳的含量,缓解全球性的温室效应,保护生态环境具有重大意义。
实例1
将100克丁苯橡胶(苯乙烯含量23.5%)与脂肪族聚碳酸酯(分子量100000)10克用双辊混炼机混合均匀,混合温度40℃~50℃,时间5分钟,然后加入氧化锌3克,硬脂酸1克,促进剂CZ1.2克,硫磺1.8克,顺丁烯二酸酐4克,充分混合后放入模具中加压硫化,压力15MPa,温度150℃,时间30分钟。所得改性弹性体拉伸强度9.3MPa,断裂伸长率1321%,扯断永久变形52.8%,硬度32度(邵A).70℃热空气老化24hr后拉伸强度10.8MPa,断裂伸长率870%,扯断永久变形14.4%。硬度35度(邵A)实例2
将100克丁苯橡胶(苯乙烯含量23.5%)与脂肪族聚碳酸酯(分子量17000)20克用双辊混炼机混合均匀,混合温度40℃-50℃时间5分钟,然后加入氧化锌3克,硬脂酸1克,促进剂DM1.0克,促进剂D0.7克,硫磺1.8克,过氧化物DCP1.5克,充分混合后放入模具中加压硫化,压力15MPa,温度150℃,时间20分钟。所得丁苯橡胶弹性体拉伸强度6.5MPa,断裂伸长率902%,硬度39度(邵A),扯断永久变形24.8%。70℃热空气老化24hr后拉伸强度10.2MPa,断裂伸长率791%,扯断永久变形5%。硬度40度(邵A)。
Claims (6)
1、一种用脂肪族聚碳酸酯改性丁苯橡胶的方法,其特征在于100份(重量)丁苯橡胶中加入脂肪族聚碳酸酯1~100份,硫磺或过氧化物为主交联剂0.2~50份,促进剂次磺酰胺类,或秋兰姆类,或二烷基二硫代氨基甲酸盐类,或噻唑类,或胍类0.1~50份,以及辅助交联剂酸酐或异氰酸酯类0.1~80份,活性剂金属氧化物和脂肪酸0.1~20份,在90℃~200℃下加压硫化2~200分钟。
2、根据权利要求1中所述的改性方法,其特征在于所述的脂肪族聚碳酸酯是分子量为2000~300000的分子链含端羟基的饱和树脂。
3、根据权利要求1中所述的改性方法,其特征在于所述的主交联剂是硫磺,过氧化苯甲酰,特丁基过氧化苯甲酰,过氧化二异丙苯,二特丁基过氧化物,1,1-特丁基过氧-3,3,5三甲基环己烷。
4、根据权利要求1中所述的改性方法,其特征在于所述的促进剂是N-环己基-2-苯并噻唑次磺酰胺,二硫化二苯并噻唑,二硫醇基苯并噻唑,二硫化四甲基秋兰姆,乙基苯基二硫代氨基甲酸锌,二苯胍。
5、根据权利要求1中所述的改性方法,其特征在于所述的辅助交联剂是丁二酸酐,或顺丁烯二酸酐,或四氢邻苯二甲酸酐,或六氢邻苯二甲酸酐,三烯丙基异氰酸酯。
6、根据权利要求1中所述的改性方法,其特征在于所述的活性剂是氧化锌和硬脂酸。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97114243A CN1050853C (zh) | 1997-09-10 | 1997-09-10 | 脂肪族聚碳酸酯丁苯橡胶的改性方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97114243A CN1050853C (zh) | 1997-09-10 | 1997-09-10 | 脂肪族聚碳酸酯丁苯橡胶的改性方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1176269A true CN1176269A (zh) | 1998-03-18 |
CN1050853C CN1050853C (zh) | 2000-03-29 |
Family
ID=5172818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN97114243A Expired - Fee Related CN1050853C (zh) | 1997-09-10 | 1997-09-10 | 脂肪族聚碳酸酯丁苯橡胶的改性方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1050853C (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103740072A (zh) * | 2013-11-20 | 2014-04-23 | 青岛佰众化工技术有限公司 | 一种聚碳酸酯复合物 |
EP2933283A1 (en) | 2014-04-17 | 2015-10-21 | Changchun Institute Of Applied Chemistry Chinese Academy Of Sciences | Chlorinated poly(propylene carbonate) and preparation method thereof |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4444949A (en) * | 1981-02-26 | 1984-04-24 | General Electric Company | Composition of a polycarbonate, a butadiene-styrene copolymer and a (meth)acrylate interpolymer |
JPS5817153A (ja) * | 1981-07-24 | 1983-02-01 | Idemitsu Petrochem Co Ltd | ポリカ−ボネ−ト樹脂組成物 |
CA1266340A (en) * | 1986-09-16 | 1990-02-27 | Hajime Sakano | Thermoplastic resin composition |
-
1997
- 1997-09-10 CN CN97114243A patent/CN1050853C/zh not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103740072A (zh) * | 2013-11-20 | 2014-04-23 | 青岛佰众化工技术有限公司 | 一种聚碳酸酯复合物 |
EP2933283A1 (en) | 2014-04-17 | 2015-10-21 | Changchun Institute Of Applied Chemistry Chinese Academy Of Sciences | Chlorinated poly(propylene carbonate) and preparation method thereof |
US9546245B2 (en) | 2014-04-17 | 2017-01-17 | Changchun Institute Of Applied Chemistry, Chinese Academy Of Sciences | Chlorinated poly(propylene carbonate) and preparation method thereof |
US9908969B2 (en) | 2014-04-17 | 2018-03-06 | Changchun Institute Of Applied Chemistry, Chinese Academy Of Sciences | Chlorinated poly(propylene carbonate) and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1050853C (zh) | 2000-03-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100535281B1 (ko) | Sbr고무겔을함유하는고무혼합물 | |
CN105924690B (zh) | 一种耐老化改性天然橡胶复合材料 | |
CN110791029B (zh) | 一种木质素接枝溴化丁基橡胶复合材料及其制备方法 | |
US4818601A (en) | Rubber-cord composite bodies | |
CN108641150B (zh) | 一种可重复加工橡胶材料及其制备方法 | |
CA2419362A1 (en) | Rubber mixtures based on non-vulcanised rubber and vulcanised rubber particles and multifunctional isocyanates based on polyurethane | |
US6525105B1 (en) | Methods of separating vulcanized or unvulcanized rubber and separating rubber composite, rubber composition containing recovered rubber or recovered carbon black, and process for producing carbon black | |
WO2002048233A1 (de) | Gelhaltige kautschukmischungen mit multifunktionellen isocyanaten und polyolen | |
CN114163822B (zh) | 有机硅改性三元乙丙橡胶及其制备方法 | |
CN1050853C (zh) | 脂肪族聚碳酸酯丁苯橡胶的改性方法 | |
CN111560130A (zh) | 一种车用轮胎 | |
CN106916394A (zh) | 一种防滑地毯用pvc改性材料及其制备方法 | |
CN110396265B (zh) | 具有自愈合功能的橡胶组合物和硫化橡胶及其制备方法和应用 | |
CN109679232A (zh) | 一种低温下变形能快速恢复的新型橡胶 | |
Kok | The effects of compounding variables on the reversion process in the sulphur vulcanization of natural rubber | |
CN104610596A (zh) | 一种液体橡胶改性丁腈橡胶电缆材料 | |
CN1113930C (zh) | 三元乙丙橡胶的改性方法 | |
CN1239110A (zh) | 脂肪族聚碳酸酯改性丁苯橡胶的方法 | |
CN109082100B (zh) | 一种高性能发电机减震垫及其制备方法 | |
CN1247202A (zh) | 丁苯橡胶的改性方法 | |
US2610954A (en) | Oxidized alkali lignin as a rubber reinforcing agent | |
CN1032757C (zh) | 脂肪族聚碳酸酯丁腈橡胶的改性 | |
KR940018418A (ko) | 개선된 에틸렌-비닐 아세테이트 가황물 | |
US8207386B2 (en) | Rubber-like articles and rubber-like material-containing articles | |
US3364158A (en) | Method of producing lignin-reinforced rubber, using alkylene diamines |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C06 | Publication | ||
PB01 | Publication | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |