CN113930064A - 一种聚氨酯用复合抗黄变剂组成物 - Google Patents
一种聚氨酯用复合抗黄变剂组成物 Download PDFInfo
- Publication number
- CN113930064A CN113930064A CN202111147890.5A CN202111147890A CN113930064A CN 113930064 A CN113930064 A CN 113930064A CN 202111147890 A CN202111147890 A CN 202111147890A CN 113930064 A CN113930064 A CN 113930064A
- Authority
- CN
- China
- Prior art keywords
- phosphite
- polyurethane
- agent composition
- composite anti
- yellowing
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- 238000004383 yellowing Methods 0.000 title claims abstract description 27
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 24
- 239000004814 polyurethane Substances 0.000 title claims abstract description 24
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 20
- 239000002131 composite material Substances 0.000 title claims abstract description 15
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 9
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000012965 benzophenone Substances 0.000 claims abstract description 7
- PXXJHWLDUBFPOL-UHFFFAOYSA-N benzamidine Chemical compound NC(=N)C1=CC=CC=C1 PXXJHWLDUBFPOL-UHFFFAOYSA-N 0.000 claims abstract description 6
- -1 4-ethoxycarbonylphenyl Chemical group 0.000 claims description 10
- 230000003078 antioxidant effect Effects 0.000 claims description 7
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims description 7
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 claims description 6
- 230000002745 absorbent Effects 0.000 claims description 5
- 239000002250 absorbent Substances 0.000 claims description 5
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 3
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 3
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 3
- NRLOQEQAWOKEJF-UHFFFAOYSA-N (6-methyl-1,1-diphenylheptyl) dihydrogen phosphite Chemical compound C=1C=CC=CC=1C(OP(O)O)(CCCCC(C)C)C1=CC=CC=C1 NRLOQEQAWOKEJF-UHFFFAOYSA-N 0.000 claims description 2
- ADRNSOYXKABLGT-UHFFFAOYSA-N 8-methylnonyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC(C)C)OC1=CC=CC=C1 ADRNSOYXKABLGT-UHFFFAOYSA-N 0.000 claims description 2
- VOTGEHHZAFEPOI-UHFFFAOYSA-N C(C)OC(=O)C1=CC=C(C=C1)N(C=NC1=CC=C(C=C1)C(=O)OCC)C1=CC=CC=C1 Chemical compound C(C)OC(=O)C1=CC=C(C=C1)N(C=NC1=CC=C(C=C1)C(=O)OCC)C1=CC=CC=C1 VOTGEHHZAFEPOI-UHFFFAOYSA-N 0.000 claims description 2
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 claims description 2
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 claims description 2
- QOQNJVLFFRMJTQ-UHFFFAOYSA-N trioctyl phosphite Chemical compound CCCCCCCCOP(OCCCCCCCC)OCCCCCCCC QOQNJVLFFRMJTQ-UHFFFAOYSA-N 0.000 claims description 2
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 claims description 2
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 claims description 2
- PEXOFOFLXOCMDX-UHFFFAOYSA-N tritridecyl phosphite Chemical compound CCCCCCCCCCCCCOP(OCCCCCCCCCCCCC)OCCCCCCCCCCCCC PEXOFOFLXOCMDX-UHFFFAOYSA-N 0.000 claims description 2
- 239000006260 foam Substances 0.000 abstract description 5
- 238000005286 illumination Methods 0.000 abstract description 5
- 239000006096 absorbing agent Substances 0.000 abstract description 4
- 230000007547 defect Effects 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229920005830 Polyurethane Foam Polymers 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000011496 polyurethane foam Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- GBRSPKXOFRTAHS-UHFFFAOYSA-N 5-(4-nitrophenyl)-1,2-oxazole-3-carboxylic acid Chemical compound O1N=C(C(=O)O)C=C1C1=CC=C([N+]([O-])=O)C=C1 GBRSPKXOFRTAHS-UHFFFAOYSA-N 0.000 description 1
- 206010051246 Photodermatosis Diseases 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000008845 photoaging Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001960 triggered effect Effects 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- 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
- C08K5/132—Phenols containing keto groups, e.g. benzophenones
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
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)
- Polyurethanes Or Polyureas (AREA)
Abstract
本发明公开了一种聚氨酯用复合抗黄变剂组成物,包含:苯甲脒类的紫外线吸收剂、二苯甲酮类紫外线吸收剂、亚磷酸酯类抗氧剂。本发明组成物添加于聚氨酯软泡中,可有效改善其光照后的黄变缺点。
Description
技术领域
本发明是关于一种聚氨酯用抗黄变剂组成物,具体涉及一种用于聚氨酯以减缓其黄变的复合抗黄变剂。
背景技术
聚氨酯材料大多以芳香族异氰酸酯为原料合成,在光、热、氧,特别是紫外线的作用下,会引发氨酯键发生分解,生成芳胺,经氧化重排后,生成醌式结构等发色基团,导致聚氨酯制品颜色发生黄变,特别是浅色聚氨酯材料黄变的状况会更加明显。脂肪族异氰酸酯为原料的聚氨酯材料虽然不会黄变,但由于其强度低、不耐溶剂、更容易降解、成本高,导致其应用不多。虽然许多工作者采用添加剂的方法改善上述问题,但仍有不足之处,单组份的抗氧剂或紫外线吸收剂无法满足聚氨酯材料抗黄变效果要求。
发明内容
本发明针对现有技术存在的不足,提供一种用于聚氨酯材料的的复合抗黄变剂组成物,其适合添加于聚氨酯材料,尤其适用添加于聚氨酯软泡、弹性体,可有效改善聚氨酯材料光照后黄变和稳定性能。
本发明所提供的复合抗黄变剂组成物包括:苯甲脒类的紫外线吸收剂、二苯甲酮类紫外线吸收剂、亚磷酸酯类抗氧剂。
本发明的复合抗黄变剂组成物中,其中苯甲脒类的紫外线剂为:N-(4-乙氧基羰基苯基)-N'-甲基-N'-苯基甲脒,N-(4-乙氧基羰基苯基)-N'-乙基-N'-苯基甲脒,N,N'-双(4-乙氧甲酰基苯基)-N-苯基甲脒,或其混合物。
本发明的复合抗黄变剂组成物中,苯甲脒类的紫外线剂的重量百分比为5%-90%。
本发明的组成物中,其中二苯甲酮类紫外线吸收剂为:2,4-二羟二苯甲酮,2-羟基-4-正辛氧基二苯甲酮,2-羟基-4-甲氧基二苯甲酮,或其混合物。
本发明的复合抗黄变剂组成物中,二苯甲酮类紫外线吸收剂的重量百分比为5%-90%。
本发明的组成物中,其中苯亚磷酸酯类抗氧剂为:亚磷酸三辛酯,亚磷酸三癸酯,亚磷酸三月桂酸酯,亚磷酸三(十三烷基)酯,亚磷酸二苯酯,亚磷酸二苯基异辛基酯,亚磷酸二苯基异癸基酯,亚磷酸三苯酯,亚磷酸三(壬基苯基)酯,亚磷酸一苯二异辛酯,亚磷酸一苯二异癸酯,或其混合物。
本发明的复合抗黄变剂组成物,亚磷酸酯类抗氧剂的重量百分比为5%-90%。
本发明的复合抗黄变剂组成物可由一般公知方法混合,例如,将三种主要成分,包括苯甲脒类的紫外线剂、二苯甲酮类紫外线吸收剂、亚磷酸酯类抗氧剂,同时以公知技术均匀混合而成。当个别成分有固体和液体形式同时存在时,较适合的混合方式是将固体混入液体的方式,并搅拌均匀,形成混合液或分散液。更佳的混合方式是将本发明组成物主要成分中的液态成分进行升温,再将固体成分混入加热的溶液中,混合后的组成物可以保温存放以减少混合物溶液中晶体析出,如果组成物溶液中有结晶现象发生,可以再次升温使组成物溶液液化。
本发明除上述紫外线吸收剂、抗氧剂,亦可并用其他添加剂,如润滑剂,乳化剂,抗静电剂,发泡剂,增塑剂等。
具体实施方式
实施例1
将10克N-(4-乙氧基羰基苯基)-N'-甲基-N'-苯基甲脒、10克亚磷酸二苯基异辛基酯混合后,搅拌升温至50℃,加入5克2-羟基-4-甲氧基二苯甲酮,充分搅拌形成均一溶液,添加入聚氨酯软泡制备配方中,添加量为聚氨酯原料的0.5%。将得到的聚氨酯泡沫塑料制品放入加速老化实验仪,50℃恒温环境下,以340nm灯管对样品持续光照24h,再以色差仪检测试样光照前后的黄变指数YI值,评价其抗黄变性能,结果见表1。
实施例2
将10克N-(4-乙氧基羰基苯基)-N’-甲基-N’-苯基甲脒、8克亚磷酸三苯酯混合后,搅拌升温至50℃,加入、2克2,4-二羟二苯甲酮,充分搅拌形成均一溶液,添加入聚氨酯软泡制备配方中,添加量为聚氨酯原料的1%。将得到的聚氨酯泡沫塑料制品放入加速老化实验仪,50℃恒温环境下,以340nm灯管对样品持续光照24h,再以色差仪检测试样光照前后的黄变指数YI值,评价其抗黄变性能,结果见表1。
实施例3
将10克N-(4-乙氧基羰基苯基)-N'-甲基-N'-苯基甲脒、5克亚磷酸一苯二异辛酯混合后,搅拌升温至50℃,加入2克2-羟基-4-正辛氧基二苯甲酮,充分搅拌形成均一溶液,添加入聚氨酯软泡制备配方中,添加量为聚氨酯原料的1.2%。将得到的聚氨酯泡沫塑料制品放入加速老化实验仪,50℃恒温环境下,以340nm灯管对样品持续光照24h,再以色差仪检测试样光照前后的黄变指数YI值,评价其抗黄变性能,结果见表1。
将回收的活性氧化铝重复使用3次,其他制备方法同实施例3,结果见表1。
表1 加速光老化试验结果
Claims (4)
1.一种聚氨酯用复合抗黄变剂组成物,该组成物包括:
(1)5-90重量份的苯甲脒类的紫外线吸收剂;
(2)5-90重量份的二苯甲酮类紫外线吸收剂;
(3)5-90重量份的亚磷酸酯类抗氧剂。
2.如权利要求1所述的复合抗黄变剂组成物中,苯甲脒类的紫外线剂为:N-(4-乙氧基羰基苯基)-N'-甲基-N'-苯基甲脒,N-(4-乙氧基羰基苯基)-N'-乙基-N'-苯基甲脒,N,N'-双(4-乙氧甲酰基苯基)-N-苯基甲脒中的一种或其混合物。
3.如权利要求1所述的复合抗黄变剂组成物中,二苯甲酮类紫外线吸收剂为:2,4-二羟二苯甲酮,2-羟基-4-正辛氧基二苯甲酮,2-羟基-4-甲氧基二苯甲酮中的一种或其混合物。
4.如权利要求1所述的复合抗黄变剂组成物中,亚磷酸酯类抗氧剂为:亚磷酸三辛酯,亚磷酸三癸酯,亚磷酸三月桂酸酯,亚磷酸三(十三烷基)酯,亚磷酸二苯酯,亚磷酸二苯基异辛基酯,亚磷酸二苯基异癸基酯,亚磷酸三苯酯,亚磷酸三(壬基苯基)酯,亚磷酸一苯二异辛酯,亚磷酸一苯二异癸酯中的一种或其混合物。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111147890.5A CN113930064A (zh) | 2021-09-29 | 2021-09-29 | 一种聚氨酯用复合抗黄变剂组成物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111147890.5A CN113930064A (zh) | 2021-09-29 | 2021-09-29 | 一种聚氨酯用复合抗黄变剂组成物 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN113930064A true CN113930064A (zh) | 2022-01-14 |
Family
ID=79277313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111147890.5A Pending CN113930064A (zh) | 2021-09-29 | 2021-09-29 | 一种聚氨酯用复合抗黄变剂组成物 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113930064A (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114481624A (zh) * | 2022-02-08 | 2022-05-13 | 东莞市中纺化工有限公司 | 一种抗黄变添加剂及其制备方法与应用 |
CN115109348A (zh) * | 2022-08-17 | 2022-09-27 | 曾荣华 | 一种耐黄变透气型塑胶跑道及制备方法 |
CN117264334A (zh) * | 2023-10-18 | 2023-12-22 | 东莞市博恩密封技术有限公司 | 一种耐热老化三元乙丙橡胶组合物及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5369140A (en) * | 1990-05-10 | 1994-11-29 | Ciba-Geigy Corporation | Radiation curable light-stablised compositions |
CN107200866A (zh) * | 2016-11-24 | 2017-09-26 | 汕头市八隅新材料有限公司 | 一种聚氨酯软泡耐黄剂 |
-
2021
- 2021-09-29 CN CN202111147890.5A patent/CN113930064A/zh active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5369140A (en) * | 1990-05-10 | 1994-11-29 | Ciba-Geigy Corporation | Radiation curable light-stablised compositions |
CN107200866A (zh) * | 2016-11-24 | 2017-09-26 | 汕头市八隅新材料有限公司 | 一种聚氨酯软泡耐黄剂 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114481624A (zh) * | 2022-02-08 | 2022-05-13 | 东莞市中纺化工有限公司 | 一种抗黄变添加剂及其制备方法与应用 |
CN114481624B (zh) * | 2022-02-08 | 2024-05-03 | 东莞市中纺化工有限公司 | 一种抗黄变添加剂及其制备方法与应用 |
CN115109348A (zh) * | 2022-08-17 | 2022-09-27 | 曾荣华 | 一种耐黄变透气型塑胶跑道及制备方法 |
CN117264334A (zh) * | 2023-10-18 | 2023-12-22 | 东莞市博恩密封技术有限公司 | 一种耐热老化三元乙丙橡胶组合物及其制备方法 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113930064A (zh) | 一种聚氨酯用复合抗黄变剂组成物 | |
CN108017766B (zh) | 一种用于防止或减轻聚氨酯软泡变红的复合抗氧剂及其应用 | |
US2476779A (en) | Stabilized aromatic isocyanates | |
CN101775204A (zh) | 用于聚氨酯纤维复合抗氧化剂 | |
DE19630903A1 (de) | Verfahren zur Farbstabilisierung von Isocyanaten mittels einer Kombination von speziellen Phosphorverbindungen mit 2,6-Di-tert.-butyl-4-methyl-phenol | |
US2748096A (en) | Rubbers stabilized by a bis (2-hydroxy-3-alpha-alkyl-cycloalkyl-5-methylphenyl)-methene or salts thereof | |
JP2010111611A (ja) | 有機ポリイソシアネート組成物 | |
US4606972A (en) | Polyamide yarn with antioxidant finish | |
DE69426262T2 (de) | Stabilisierter polyetherpolyol sowie daraus erhaltener polyurethanschaum | |
US1919301A (en) | Age resisting vulcanized rubber and antioxidant agent | |
JPS5998050A (ja) | 有機イソシアナ−ト化合物の着色防止方法 | |
US1836702A (en) | Carbazol antioxidant | |
JP2005170793A (ja) | 有機ポリイソシアネート組成物 | |
KR100257965B1 (ko) | 가황속도및내스코치성이개선된고무조성물 | |
US1916286A (en) | Rubber composition and method of preserving rubber | |
CN111320859B (zh) | 稳定聚醚的抗氧化剂 | |
RU2447119C1 (ru) | Герметик на основе полисульфидного олигомера | |
US2651622A (en) | Stabilized organic compositions | |
CN115073323A (zh) | 一种异氰酸酯稳定剂 | |
CN112760059B (zh) | 一种补胎胶水溶剂的复合稳定剂及其制备方法、常温硫化补胎胶水 | |
CN106008912A (zh) | 一种新型聚氨酯 | |
JPH0920744A (ja) | イソシアナート化合物の着色防止方法 | |
US1916287A (en) | Rubber composition and method of preserving rubber | |
US2849516A (en) | Shaped rubber compositions containing petroleum cresylic acid monosulfides | |
CN107955277B (zh) | 一种橡胶制品及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20220114 |