CN108203486A - A kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber - Google Patents

A kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber Download PDF

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CN108203486A
CN108203486A CN201611187533.0A CN201611187533A CN108203486A CN 108203486 A CN108203486 A CN 108203486A CN 201611187533 A CN201611187533 A CN 201611187533A CN 108203486 A CN108203486 A CN 108203486A
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environment
friendly type
preparation
type oil
parts
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殷兰
庞建勋
孙继德
王秀芝
李永茹
刘洪伟
侯军
石捷强
郭睿达
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China Petroleum and Natural Gas Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F236/00Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • C08F236/10Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • C08C1/14Coagulation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/38Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00Polymerisation catalysts
    • C08F4/40Redox systems

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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention provides a kind of preparation methods of environment-friendly type oil-extended styrene buadiene rubber, include the following steps:(1) in nitrogen atmosphere, sequentially add soft water, emulsifier, electrolyte, reducing agent, tert-dodecyl mercaptan, styrene and butadiene, when cooling the temperature to 5 DEG C~8 DEG C, initiator hydrogen peroxide is added in Meng's alkane, when conversion ratio reaches 60%, it adds in terminator D600 and terminates reaction, obtain base latex;The component that the terminator D600 is included is:N isopropylhydroxylas and tetren;(2) by base latex with after filling fat liquor blending uniformly, being added in a concentration of 0.4%~0.6% dilution heat of sulfuric acid, stirring, after cohesion, wash drying, obtain raw rubber finished product.

Description

A kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber
Technical field
The invention belongs to synthetic rubber production technical field, more particularly to a kind of improved high combinated styrene content environment-friendly type is filled Oily butadiene-styrene rubber preparation method.
Background technology
Emulsion polymerized styrene butadiene rubber is global yield highest, the high synthetic rubber kind of consumption figure maximum, is mainly used in automobile The fields such as tire, industrial conveyor, sebific duct.Oil classification whether is filled by it, emulsion polymerized styrene butadiene rubber can be divided into non-oil-filled series Product and oil-filled series of products;By the textural classification of polymer, it is 23.5% that emulsion polymerized styrene butadiene rubber, which can be divided into styrene-content, High structural type and higher combinated styrene content (31%, 35%, 40%) series of products.
With the enhancing of countries in the world environmental consciousness, some countries and regions, which are limited in rubber, uses condensed-nuclei aromatics The higher high aromatic oil of compounds content and the rubber for filling such oil.European Union is about disabling condensed ring containing excess in tire production The instruction (2005/69/EC) of the toxic rubber filling oil such as the aromatic naphtha of aromatic hydrocarbons is required in 1 day January in 2010 in tire production Middle completely forbid uses toxic rubber oil.The filling that instruction regulation puts goods on the market is oily and for manufacturing condensed ring in the filling oil of tire Aromatic hydrocarbons (PAHs) content is less than 3%;8 kinds of carcinogenic aromatic hydrocarbons total contents are less than 10mg/L.
SBR1769/1739 is the oil-extended styrene buadiene rubber of environment-friendly type, is the oil-extended styrene buadiene rubber of current usage amount maximum The upgrading products of SBR1721, the cementing conjunction styrene-content in basis is 40.0%, the low condensed ring virtue of 37.5 parts of filling in 100 parts of glue Hydrocarbon ils (or naphthenic oil), PAHs contents are less than 3% in oil product, and 8 kinds of carcinogenic aromatic hydrocarbons total contents are less than 10mg/L, are ring type fillings Aromatic naphtha (or naphthenic oil) and the butadiene-styrene rubber without nitrosamine are protected, is widely used in cross-ply, radial tyre of passenger car In light radial truck tire and other rubbers.
The production of SBR1769/1739 is divided into the production of base latex and two stages of filling of environment-friendly aromatic oil.With it is other Emulsion polymerization process is the same, and SBR1769/1739 base latex polymerization processes are also required to use terminator.In the prior art, it is newborn Most of terminator used in liquid polymerization (as being used for producing styrene butadiene rubber latex) is by dimethyl dithiocarbamate, two Alkyl hydroxylamine, sodium nitrite composition.This unfavorable conditions combined is dialkylhydroxyamines and dimethyl dithiocarbamic acid Salt is the precursor of Carcinogenic Nitrosamines, in the acidic environment of latex gel, easily forms secondary amine, secondary amine and nitrating agent such as Asia Reaction of nitrogen oxides present in sodium nitrate, air forms carcinogenic substance-nitrosamine.It is an object of the present invention to provide one effectively Terminator, the presence of no nitrosamine parent cannot also generate stability nitrosamine, meet what European Union formulated for this problem The Principles of Chemistry TRGS552, and ensure that product is stablized, it also avoids in production and mixing and other process, generates carcinogenic Object nitrosamine.
About the free-radical emulsion polymerization terminator for not generating nitrosamine, document discloses many kinds, major in the world Synthetic rubber production company begins one's study new polymerization terminator, to substitute the dimethyl dithiocarbamic acid for easily forming secondary amine Salt, dialkylhydroxyamines, to eliminate the formation of nitrosamine.
The method for having been proposed solving to form nitrosamine in United States Patent (USP) US4985326 and US5177164, the former adopts Make the method for free radical polymerization termination with the carbodithioic acid phenol acids of non-nitrous amine precursor;The latter advocates only to be used alone more For vulcanized sodium as reaction terminating agent, sodium polysulfide used is Na2S4, for 0.02-0.5phm, (phm is relative to 100 parts to dosage The addition of pure monomer), the polymer of generation is made to be free of nitrosamine.But carbodithioic acid phenol acids is expensive, more sulphur Change sodium and easily form sediment in the duct.
Isopropylhydroxyla or salt are used in US5384372, and as terminator, specific type has N- isopropylhydroxylas, second Sour isopropylhydroxyla, hydrochloric acid isopropylhydroxyla, sulfuric acid isopropylhydroxyla, addition 0.05-0.2phm, Adding Way is with passing The Adding Way of system process termination agent is identical, and the addition of its aqueous solution is reached in the polymerisation for requiring conversion ratio.It is but single Solely using isopropylhydroxyla or salt, the environmentally friendly butadiene-styrene rubber properties of product of production are than traditional handicraft butadiene-styrene rubber as terminator Difference cannot get the accreditation of tire applications client.
Invention content
The purpose of the invention is to avoid in emulsion polymerization SBR1769/1739 rubber process and product is prepared generation, Carcinogenic substance-nitrosamine is remained, after traditional low temperature emulsion polymerisation process synthesis SBR1769/1739 latex, is had using specific The terminator of effect terminates free-radical emulsion polymerization reaction, prepares SBR1769/1739 base latex, does not have nitrosamine in the process The presence of parent cannot also generate stability nitrosamine, meet European Union and be directed to the Principles of Chemistry TRGS552 that this problem is formulated, and really It protects properties of product to stablize, the tensile strength and stress at definite elongation of product are above domestic similar product.
It is an object of the present invention to emulsion polymerisation process synthesize SBR1769/1739 base latex after, using D600 for termination Agent can effectively terminate SBR1769/ using the compound of N- isopropylhydroxylas and tetren as reaction terminating agent 1739 free-radical emulsion polymerizations react, and do not generate nitrosamine.0.05~0.1 part of N- isopropylhydroxylas in D600, four ethylenes five 0.3~0.4 part of amine.
Tetren is a kind of vulcanization accelerator of low toxicity, can be compounded well with N- isopropylhydroxylas, to the poly- fourth of breast Benzene rubber has vulcanization facilitation well, can properly increase the performance of SBR1769/1739 products.
In order to achieve the above objectives, the present invention provides a kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber, including following step Suddenly:
(1) in nitrogen atmosphere, soft water, emulsifier, electrolyte, reducing agent, tert-dodecyl mercaptan, styrene are sequentially added And butadiene, when cooling the temperature to 5 DEG C~8 DEG C, initiator hydrogen peroxide is added in Meng's alkane, when the conversion ratio of monomer reaches 60% When, it adds in terminator D600 and terminates reaction, obtain base latex;The component that the terminator D600 is included is:N- isopropyl hydroxyls Amine and tetren;
(2) by base latex with after filling fat liquor blending uniformly, being added to a concentration of 0.4%~0.6% dilute sulfuric acid In solution, stirring after cohesion, washs drying, obtains raw rubber finished product.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, in step (1), the parts by weight of each polymeric component Number is preferably:
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, wherein, the terminator D600 each components Parts by weight are preferably:0.05~0.1 part of N- isopropylhydroxylas, 0.3~0.4 part of tetren.
The preparation method of oil-extended styrene buadiene rubber of the present invention, these, it is preferred to, by the N- isopropylhydroxylas and Tetren adds in stirred tank, and terminator D600 is made under agitation, and is sent to intermediate storage tank storage, intermediate storage tank bottom Portion is equipped with back-mixing pump.On this condition, N- isopropylhydroxylas and tetren can be kept to be sufficiently mixed, and keeps solution Homogeneity, so as to ensure the stable quality of final products.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, wherein, the emulsifier is preferably disproportionated pine Fragrant acid potash soap, parts by weight are preferably 4.0~5.0 parts.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, wherein, component that the electrolyte includes and Parts by weight are preferably:0.2~0.3 part of phosphoric acid, 0.3~0.5 part of potassium hydroxide, 0.03 part of tetrasodium salt of EDTA and ten 0.1~0.2 part of dialkyl benzene sulfonic acids sodium.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, wherein, component that the reducing agent includes and Parts by weight are preferably:0.01 part of ferrous sulfate, 0.03~0.05 part of rongalite and tetrasodium salt of EDTA 0.025 part.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, in step (2), the condition of stirring is preferably: Temperature 60 C~65 DEG C, time 5~10 minutes.
The preparation method of environment-friendly type oil-extended styrene buadiene rubber of the present invention, in step (2), the filling fat liquor includes Component and part be preferably:
21.5~23.5 parts of TDAE environment-friendly aromatic oils (or naphthenic oil),
11.7~12.0 parts of water,
2.8~3.0 parts of isproportionated potassium rosinate.
Technical solution of the present invention is specific as follows:
(1) first to polymeric kettle carry out vacuum, nitrogen replace, successively by soft water, emulsifier, electrolyte solution, reducing agent, Tert-dodecyl mercaptan, styrene, butadiene are added in polymeric kettle, when polymeric kettle temperature is down to 5 DEG C~8 DEG C, is added in and are caused Agent hydrogen peroxide carries out polymerization experiment, when conversion ratio reaches 60%, adds in terminator and terminate reaction, obtain to Meng's alkane SBR1769/1739 base latex;
(2) by after SBR1769/1739 base latex, with filling fat liquor blending uniformly, it is added to a concentration of 0.5% In dilution heat of sulfuric acid, stirring, at 60 DEG C~65 DEG C, the time is 5 minutes~10 minutes for temperature control, after cohesion, washs drying, obtains To raw rubber finished product.
The polymeric component and parts by weight that above-mentioned steps (1) include be:
The emulsifier be isproportionated potassium rosinate, preferably 4.0~5.0 parts of parts by weight.
The component and part that the electrolyte includes is:
The component and part that the reducing agent includes is:
0.01 part of ferrous sulfate
0.03~0.05 part of rongalite
0.025 part of tetrasodium salt of EDTA
The component and part that the terminator D600 is included is:
0.05~0.1 part of N- isopropylhydroxylas
0.3~0.4 part of tetren
The component and part that the filling fat liquor includes is:
21.5~23.5 parts of TDAE environment-friendly aromatic oils (or naphthenic oil)
11.7~12.0 parts of water
2.8~3.0 parts of isproportionated potassium rosinate.
Advantageous effect of the present invention:
In SBR1769/1739 base latex polymerisations, terminated freely using the specific effective terminator of the present invention Emulsion polymerization reacts, and finally prepares SBR1769/1739 products, and the presence of no nitrosamine parent in the process also cannot Stable nitrosamine is generated, nitrosamine specified in the oil-filled glue product of environment-friendly type does not detect, meets European Union and is formulated for this problem The Principles of Chemistry TRGS552, and properties of product are suitable with the general combinated styrene content oil-extended styrene buadiene rubber of non-environmental protection type, environmental protection 35 minutes 300% stress at definite elongations of the oil-filled glue vulcanizate of type are higher than the oil-filled glue respective performances 0.5Mpa of non-environmental protection.
Specific embodiment
The present invention is described further for the following examples, but not thereby limiting the invention.
Embodiment 1
(1) vacuum is carried out to polymeric kettle first, nitrogen is replaced.Successively by soft water, emulsifier, electrolyte solution, reducing agent, Tert-dodecyl mercaptan, styrene, butadiene are added in polymeric kettle, when polymeric kettle temperature is down to 7 DEG C, add in initiator peroxide Change hydrogen to Meng's alkane, carry out polymerization experiment, when conversion ratio reaches 60%, add in terminator D600 and terminate reaction, obtain SBR1739 Base latex;
(2) by after SBR1739 base latex, with filling fat liquor blending uniformly, it is added to a concentration of 0.5% dilute sulfuric acid In solution, stirring, at 62 DEG C, the time is 7 minutes for temperature control, after cohesion, washs drying, obtains raw rubber finished product.
The component and part that above-mentioned steps (1) emulsion polymerization includes is:
The emulsifier isproportionated potassium rosinate and its number are:4.5 part
The component and number that the electrolyte includes be:
The component and number that the reducing agent includes be:
0.01 part of ferrous sulfate
0.04 part of rongalite
0.025 part of tetrasodium salt of EDTA
The component and number that the terminator D600 is included be:
0.05 part of N- isopropylhydroxylas
0.30 part of tetren
The component and part that the filling fat liquor includes is:
22.5 parts of TDAE environment-friendly aromatic oils
11.8 parts of water
2.9 parts of isproportionated potassium rosinate
After testing, N-nitrosodimethylamine is not contained in SBR1739 samples, is environment-friendly type oil-extended styrene buadiene rubber.
Embodiment 2
(1) vacuum is carried out to polymeric kettle first, nitrogen is replaced.Successively by soft water, emulsifier, electrolyte solution, reducing agent, Tert-dodecyl mercaptan, styrene, butadiene are added in polymeric kettle, when polymeric kettle temperature is down to 5 DEG C, add in initiator peroxide Change hydrogen to Meng's alkane, carry out polymerization experiment, when conversion ratio reaches 60%, add in terminator D600 and terminate reaction, obtain SBR1739 Base latex;
(2) by after SBR1739 base latex, with filling fat liquor blending uniformly, it is added to a concentration of 0.5% dilute sulfuric acid In solution, stirring, at 60 DEG C, the time is 5 minutes for temperature control, after cohesion, washs drying, obtains raw rubber finished product.
The component and part that above-mentioned steps (1) emulsion polymerization includes is:
The emulsifier isproportionated potassium rosinate and its number are:4.0 part
The component and number that the electrolyte includes be:
The component and number that the reducing agent includes be:
0.01 part of ferrous sulfate
0.03 part of rongalite
0.025 part of tetrasodium salt of EDTA
The component and number that the D600 is included be:
0.1 part of N- isopropylhydroxylas
0.4 part of tetren
The component and part that the filling fat liquor includes is:
21.5 parts of TDAE environment-friendly aromatic oils
11.7 parts of water
2.8 parts of isproportionated potassium rosinate
After testing, N-nitrosodimethylamine is not contained in SBR1739 samples, is environment-friendly type oil-extended styrene buadiene rubber.
Embodiment 3
(1) vacuum is carried out to polymeric kettle first, nitrogen is replaced.Successively by soft water, emulsifier, electrolyte solution, reducing agent, Tert-dodecyl mercaptan, styrene, butadiene are added in polymeric kettle, when polymeric kettle temperature is down to 8 DEG C, add in initiator peroxide Change hydrogen to Meng's alkane, carry out polymerization experiment, when conversion ratio reaches 60%, add in terminator D600 and terminate reaction, obtain SBR1739 Base latex;
(2) by after SBR1739 base latex, with filling fat liquor blending uniformly, it is added to a concentration of 0.5% dilute sulfuric acid In solution, stirring, at 65 DEG C, the time is 10 minutes for temperature control, after cohesion, washs drying, obtains raw rubber finished product.
The component and part that above-mentioned steps (1) emulsion polymerization includes is:
The emulsifier isproportionated potassium rosinate and its number are:5.0 part
The component and number that the electrolyte includes be:
The component and number that the reducing agent includes be:
0.01 part of ferrous sulfate
0.05 part of rongalite
0.025 part of tetrasodium salt of EDTA
The component and number that the terminator D600 is included be:
0.07 part of N- isopropylhydroxylas
0.33 part of tetren
The component and part that the filling fat liquor includes is:
23.5 parts of TDAE environment-friendly aromatic oils
12.0 parts of water
3.0 parts of isproportionated potassium rosinate
After testing, N-nitrosodimethylamine is not contained in SBR1739 samples, is environment-friendly type oil-extended styrene buadiene rubber.
Comparative example 1
(1) vacuum is carried out to polymeric kettle first, nitrogen is replaced.Successively by soft water, emulsifier, electrolyte solution, reducing agent, Tert-dodecyl mercaptan, styrene, butadiene are added in polymeric kettle, when polymeric kettle temperature is down to 5 DEG C, add in initiator peroxide Change hydrogen to Meng's alkane, carry out polymerization experiment, when conversion ratio reaches 60%, it is whole to add in terminator sodium dimethyl dithiocarbamate It only reacts, obtains non-environmental protection SBR1739 base latex (i.e. SBR1721 base latex).
(2) it is dilute with the uniform rear addition a concentration of 0.5% of filling fat liquor blending by non-environmental protection SBR1739 base latex In sulfuric acid solution, stirring, at 60 DEG C, the time is 5 minutes for temperature control, after cohesion, washs drying, obtains raw rubber finished product.
The component and part that above-mentioned steps (1) emulsion polymerization includes is:
Mentioned emulsifier isproportionated potassium rosinate, parts by weight are 4.5 parts
The component and part that above-mentioned electrolyte includes is:
The component and part that above-mentioned reducing agent includes is:
0.01 part of ferrous sulfate
0.03 part of rongalite
0.025 part of tetrasodium salt of EDTA
The component and part that the filling fat liquor includes is:
22.5 parts of TDAE environment-friendly aromatic oils
11.8 parts of water
2.9 parts of isproportionated potassium rosinate
After testing, N-nitrosodimethylamine carcinogenic substance is contained in comparative example non-environmental protection SBR1739 samples.
1 embodiment 1 of table and the detection of 1 properties of product of comparative example
Certainly, the present invention can also have other various embodiments, without deviating from the spirit and substance of the present invention, ripe Various corresponding changes and deformation, but these corresponding changes and deformation can be made according to the present invention by knowing those skilled in the art It should all belong to the scope of protection of the present invention.

Claims (9)

1. a kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber, which is characterized in that include the following steps:
(1) in nitrogen atmosphere, soft water, emulsifier, electrolyte, reducing agent, tert-dodecyl mercaptan, styrene and fourth are sequentially added Diene when cooling the temperature to 5 DEG C~8 DEG C, adds in initiator hydrogen peroxide to Meng's alkane, when the conversion ratio of monomer reaches 60%, It adds in terminator D600 and terminates reaction, obtain base latex;The component that the terminator D600 is included is:N- isopropylhydroxylas and Tetren;
(2) by base latex with after filling fat liquor blending uniformly, being added to a concentration of 0.4%~0.6% dilution heat of sulfuric acid In, stirring after cohesion, washs drying, obtains raw rubber finished product.
2. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1, which is characterized in that in step (1), respectively The parts by weight of polymeric component are:
3. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1 or 2, which is characterized in that the termination The parts by weight of agent D600 each components are:0.05~0.1 part of N- isopropylhydroxylas, 0.3~0.4 part of tetren.
4. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 3, which is characterized in that by the N- isopropyls Base azanol and tetren add in stirred tank, and terminator D600 is made under agitation.
5. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1 or 2, which is characterized in that the emulsification Agent is isproportionated potassium rosinate, and parts by weight are 4.0~5.0 parts.
6. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1 or 2, which is characterized in that the electrolysis The component and part that matter includes is:0.2~0.3 part of phosphoric acid, 0.3~0.5 part of potassium hydroxide, tetrasodium salt of EDTA 0.03 part and 0.1~0.2 part of neopelex.
7. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1 or 2, which is characterized in that the reduction The component and part that agent includes is:0.01 part of ferrous sulfate, 0.03~0.05 part of rongalite and ethylenediamine tetraacetic 0.025 part of acetic acid tetrasodium salt.
8. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1, which is characterized in that in step (2), stir The condition mixed is:Temperature 60 C~65 DEG C, time 5~10 minutes.
9. the preparation method of environment-friendly type oil-extended styrene buadiene rubber according to claim 1, which is characterized in that in step (2), institute Stating the component and part that filling fat liquor includes is:
21.5~23.5 parts of TDAE environment-friendly aromatic oils (or naphthenic oil),
11.7~12.0 parts of water,
2.8~3.0 parts of isproportionated potassium rosinate.
CN201611187533.0A 2016-12-20 2016-12-20 A kind of preparation method of environment-friendly type oil-extended styrene buadiene rubber Pending CN108203486A (en)

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Cited By (3)

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Publication number Priority date Publication date Assignee Title
CN111518324A (en) * 2019-02-03 2020-08-11 中国石油天然气股份有限公司 Environment-friendly oil-extended styrene-butadiene rubber and preparation method thereof
CN111560096A (en) * 2019-02-14 2020-08-21 中国石油天然气股份有限公司 Preparation method of styrene butadiene rubber
CN114805686A (en) * 2021-01-19 2022-07-29 中国石油天然气股份有限公司 Oil-extended styrene-butadiene rubber and preparation method thereof

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CN105985455A (en) * 2015-02-15 2016-10-05 中国石油天然气股份有限公司 Preparation method of low-odor oil-extended styrene butadiene rubber

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CN114805686B (en) * 2021-01-19 2024-03-01 中国石油天然气股份有限公司 Oil-extended styrene butadiene rubber and preparation method thereof

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Application publication date: 20180626