SU971106A3 - Способ получени эластичных резин - Google Patents

Способ получени эластичных резин Download PDF

Info

Publication number: SU971106A3
Authority: SU; USSR - Soviet Union
Prior art keywords: weight; parts; stearate; group; mixture
Prior art date: 1977-04-14

Application number

SU782603400A

Other languages

English (en)

Spanish (es)

Russian (ru)

Inventor

Камерон Эдвардс Дуглас

Сато Киосаку

Original Assignee

Полисар Лимитед(Фирма)

Priority date (The priority date 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 date listed.)

1977-04-14

Filing date

1978-04-13

Publication date

1982-10-30

1977-04-14 Priority claimed from CA276,216A external-priority patent/CA1100659A/en

1977-04-14 Priority claimed from CA276,224A external-priority patent/CA1094721A/en

1977-04-14 Priority claimed from CA276,217A external-priority patent/CA1096084A/en

1978-04-13 Application filed by Полисар Лимитед(Фирма) filed Critical Полисар Лимитед(Фирма)

1982-10-30 Application granted granted Critical

1982-10-30 Publication of SU971106A3 publication Critical patent/SU971106A3/ru

Links

238000000034 method Methods 0.000 title abstract description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 22
239000000377 silicon dioxide Substances 0.000 claims abstract description 11
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 6
239000000378 calcium silicate Substances 0.000 claims abstract description 5
229910052918 calcium silicate Inorganic materials 0.000 claims abstract description 5
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims abstract description 5
150000001875 compounds Chemical class 0.000 claims abstract description 4
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 13
150000001412 amines Chemical class 0.000 claims description 13
229920001971 elastomer Polymers 0.000 claims description 9
239000005060 rubber Substances 0.000 claims description 9
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
238000004073 vulcanization Methods 0.000 claims description 7
235000021355 Stearic acid Nutrition 0.000 claims description 6
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 6
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 6
239000008117 stearic acid Substances 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 5
235000012239 silicon dioxide Nutrition 0.000 claims description 5
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
229940088990 ammonium stearate Drugs 0.000 claims description 4
235000013539 calcium stearate Nutrition 0.000 claims description 4
239000008116 calcium stearate Substances 0.000 claims description 4
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 4
229940114930 potassium stearate Drugs 0.000 claims description 4
RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 claims description 3
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
229940078456 calcium stearate Drugs 0.000 claims description 3
239000000945 filler Substances 0.000 claims description 3
239000000395 magnesium oxide Substances 0.000 claims description 3
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 3
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 claims description 3
229940080350 sodium stearate Drugs 0.000 claims description 3
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 3
229940057977 zinc stearate Drugs 0.000 claims description 3
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
239000005642 Oleic acid Substances 0.000 claims description 2
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 claims description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims 1
150000004985 diamines Chemical class 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 28
229920000642 polymer Polymers 0.000 abstract description 20
239000000654 additive Substances 0.000 abstract description 3
238000001816 cooling Methods 0.000 abstract description 3
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
230000000996 additive effect Effects 0.000 abstract 1
229910052791 calcium Inorganic materials 0.000 abstract 1
239000011575 calcium Substances 0.000 abstract 1
238000010438 heat treatment Methods 0.000 abstract 1
150000004760 silicates Chemical class 0.000 abstract 1
238000002474 experimental method Methods 0.000 description 12
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 9
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 9
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 description 5
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
150000002978 peroxides Chemical class 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 3
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
238000005096 rolling process Methods 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011787 zinc oxide Substances 0.000 description 2
FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 description 1
YKGBNAGNNUEZQC-UHFFFAOYSA-N 6-methyl-n,n-bis(6-methylheptyl)heptan-1-amine Chemical compound CC(C)CCCCCN(CCCCCC(C)C)CCCCCC(C)C YKGBNAGNNUEZQC-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
239000002253 acid Substances 0.000 description 1
-1 acryponitrile Chemical compound 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
125000002704 decyl 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])* 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
210000003743 erythrocyte Anatomy 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000005098 hot rolling Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229960004889 salicylic acid Drugs 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds

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)
Tires In General (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Sealing Material Composition (AREA)

SU782603400A 1977-04-14 1978-04-13 Способ получени эластичных резин SU971106A3 (ru)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CA276,216A CA1100659A (en)	1977-04-14	1977-04-14	Vulcanizates containing siliceous fillers
CA276,224A CA1094721A (en)	1977-04-14	1977-04-14	Vulcanizates containing silica
CA276,217A CA1096084A (en)	1977-04-14	1977-04-14	Siliceous filled vulcanizates

Publications (1)

Publication Number	Publication Date
SU971106A3 true SU971106A3 (ru)	1982-10-30

Family

ID=27165027

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU782603400A SU971106A3 (ru)	1977-04-14	1978-04-13	Способ получени эластичных резин

Country Status (14)

Country	Link
JP (1)	JPS53128647A (ja)
AR (1)	AR221483A1 (ja)
AU (1)	AU521489B2 (ja)
BR (1)	BR7802236A (ja)
DE (1)	DE2816065A1 (ja)
ES (1)	ES468275A1 (ja)
FR (1)	FR2400532A1 (ja)
GB (1)	GB1601434A (ja)
IN (1)	IN147279B (ja)
MX (1)	MX149286A (ja)
NL (1)	NL7803767A (ja)
SE (1)	SE439923B (ja)
SU (1)	SU971106A3 (ja)
TR (1)	TR19890A (ja)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4357432A (en) *	1981-05-11	1982-11-02	Polysar Limited	Vulcanizates
DE3775893D1 (de) *	1986-11-11	1992-02-20	Ici Plc	Mischung aus einer carbonsaeure und einem amin.
JP3488926B2 (ja) *	1995-01-23	2004-01-19	日本ゼオン株式会社	ゴム組成物及びその製造方法
US5939493A (en) *	1997-03-11	1999-08-17	Bridgestone Corporation	Pneumatic tire
EP0864604A3 (en) *	1997-03-11	1999-01-13	Bridgestone Corporation	Rubber composition
FR2984896B1 (fr)	2011-12-21	2014-10-24	Michelin Soc Tech	Pneumatique comprenant une composition essentiellement depourvue de derive guanidique et comprenant une amine primaire

1978
- 1978-03-28 ES ES468275A patent/ES468275A1/es not_active Expired
- 1978-04-10 NL NL7803767A patent/NL7803767A/xx not_active Application Discontinuation
- 1978-04-10 AU AU34929/78A patent/AU521489B2/en not_active Expired
- 1978-04-11 FR FR7810624A patent/FR2400532A1/fr active Granted
- 1978-04-11 TR TR19890A patent/TR19890A/xx unknown
- 1978-04-11 BR BR7802236A patent/BR7802236A/pt unknown
- 1978-04-12 SE SE7804127A patent/SE439923B/sv not_active IP Right Cessation
- 1978-04-12 IN IN264/DEL/78A patent/IN147279B/en unknown
- 1978-04-13 SU SU782603400A patent/SU971106A3/ru active
- 1978-04-13 JP JP4374578A patent/JPS53128647A/ja active Pending
- 1978-04-13 AR AR271773A patent/AR221483A1/es active
- 1978-04-13 DE DE19782816065 patent/DE2816065A1/de not_active Withdrawn
- 1978-04-13 GB GB14481/78A patent/GB1601434A/en not_active Expired
- 1978-04-14 MX MX173116A patent/MX149286A/es unknown

Also Published As

Publication number	Publication date
JPS53128647A (en)	1978-11-09
MX149286A (es)	1983-10-10
GB1601434A (en)	1981-10-28
AU3492978A (en)	1979-10-18
FR2400532A1 (fr)	1979-03-16
BR7802236A (pt)	1978-12-26
SE7804127L (sv)	1978-10-15
FR2400532B1 (ja)	1982-01-29
SE439923B (sv)	1985-07-08
DE2816065A1 (de)	1978-10-26
NL7803767A (nl)	1978-10-17
TR19890A (tr)	1980-04-09
ES468275A1 (es)	1978-12-01
AU521489B2 (en)	1982-04-08
IN147279B (ja)	1980-01-12
AR221483A1 (es)	1981-02-13

Publication	Publication Date	Title
SU764612A3 (ru)	1980-09-15	Способ модификации бромбутилкаучука
DE3217546A1 (de)	1982-12-16	Verfahren zur herstellung von kautschukartigen vulkanisaten
EP3313928B1 (de)	2020-01-08	Mit amin vernetzbare kautschukzusammensetzung mit hellem füllstoff
SU971106A3 (ru)	1982-10-30	Способ получени эластичных резин
JPH03139550A (ja)	1991-06-13	エラストマー組成物
US5728794A (en)	1998-03-17	Process for the production of poly(diorganosiloxanes) with diorganyloxyorganylsilyl or triorganyloxysilyl end groups, crosslinkable mixtures containing them and use thereof
DE3213616A1 (de)	1982-12-16	Hitzehaertbare silikonkautschukmasse
JPH11503483A (ja)	1999-03-26	フリーラジカル硬化エラストマーの早期硬化防止
DE3875271T2 (de)	1993-03-11	Mit benzimidazolinonen modifizierte kautschukmischungen.
JP3833326B2 (ja)	2006-10-11	ポリアクリレートと部分水素化ニトリルゴムとの過酸化物キュア可能なブレンドおよびキュアせる生成物
DE2233359C3 (de)	1980-07-03	Pastöse Kautschukmischung
SU1037843A3 (ru)	1983-08-23	Способ получени эластичных резин
DE3523206A1 (de)	1987-01-02	Verfahren zur herstellung von poly(diorganosiloxanen) mit alkoxyendgruppen
DE2015402A1 (de)	1971-10-21	Verfahren zur Verbesserung des Vulkani sationsverhaltens und zur Hitzestabili sierung von Polyorganosiloxanelastomeren
US4150014A (en)	1979-04-17	Vulcanizates containing siliceous fillers
DE69627332T2 (de)	2004-04-08	Verbesserte phenolische vorvernetzungshemmende mittel
JPH02107657A (ja)	1990-04-19	アクリル系ゴム組成物
DE102004012353A1 (de)	2004-09-23	Fluorsilicongummi-Zusammensetzung und Dichtungsgummi-Erzeugnis daraus
RU2686035C1 (ru)	2019-04-23	Резиновая смесь на основе бутадиен-стирольного каучука с шунгитом
SU436835A1 (ru)	1974-07-25	Резинова смесь
DE2005946C3 (de)	1978-08-03	Verfahren zur Herstellung eines vulkanisierten Formkörpers
RU2096430C1 (ru)	1997-11-20	Резиновая смесь
SU1224315A1 (ru)	1986-04-15	Резинова смесь на основе бутадиен-нитрильного каучука
SU854954A1 (ru)	1981-08-15	Композици на основе бутадиеннитрильного каучука
DE1191961B (de)	1965-04-29	Verfahren zur Herstellung von elastomeren Formkoerpern