CN108659360A - A kind of preparation method of abrasive rubber - Google Patents

A kind of preparation method of abrasive rubber Download PDF

Info

Publication number
CN108659360A
CN108659360A CN201810626509.5A CN201810626509A CN108659360A CN 108659360 A CN108659360 A CN 108659360A CN 201810626509 A CN201810626509 A CN 201810626509A CN 108659360 A CN108659360 A CN 108659360A
Authority
CN
China
Prior art keywords
parts
abrasive rubber
agent
preparation
modified
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.)
Withdrawn
Application number
CN201810626509.5A
Other languages
Chinese (zh)
Inventor
裘友玖
兰梅菊
朱东东
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Foshan Ling Chao New Material Co Ltd
Original Assignee
Foshan Ling Chao New Material Co Ltd
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.)
Filing date
Publication date
Application filed by Foshan Ling Chao New Material Co Ltd filed Critical Foshan Ling Chao New Material Co Ltd
Priority to CN201810626509.5A priority Critical patent/CN108659360A/en
Publication of CN108659360A publication Critical patent/CN108659360A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/26Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
    • C08L23/28Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or compounds containing halogen
    • C08L23/283Halogenated homo- or copolymers of iso-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

The invention discloses a kind of preparation methods of abrasive rubber, belong to technical field of polymer materials.The present invention is by octadecylamine and organic solvent in mass ratio 1:10~1:20 stirring and dissolvings, obtain lysate;By graphene oxide and lysate in mass ratio 1:10~1:20 constant temperature are stirred to react, and are filtered to get modified graphene;First chlorinated scoline is plasticated, sequentially adds polymethyl methacrylate, Corvic, tackifying resin, modified graphene, modified additive, vulcanizing agent, accelerating agent, anti-aging agent and plasticizer, are kneaded, it is subsequently added into sodium bicarbonate, is vulcanized, is discharged to get abrasive rubber.Abrasive rubber provided by the invention has excellent wear-resisting property.

Description

A kind of preparation method of abrasive rubber
Technical field
The invention discloses a kind of preparation methods of abrasive rubber, belong to technical field of polymer materials.
Background technology
Rubber industry is one of important foundation industry of national economy.It is indispensable that it not only provides daily life for people The light industrys rubber product such as daily, medical, and carried to the heavy industry such as digging, traffic, building, machinery, electronics and new industry For various rubber-producing equipments or rubber components.The wear-resisting property of General Purpose Rubber is weaker, holds after product long-time use obtained Wear phenomenon easily occurs, its service life is caused to greatly shorten.
Abrasive rubber preparation process traditional at present has degasification technique, cohesion process, liquid nano technique.
It is to select multistage degassing equipment, and combine to contain intermingle with and generally use wet type degasification technique, improvement direction in method production Solvent removal process is strengthened in the measures such as reducing pressure by regulating flow, to achieve the purpose that energy-saving.In synthetic rubber production technology, nothing Salt coagulates case technique, and oneself has quickish development.It is completed in the production of butadiene-styrene rubber and uses the salt-free cohesion process of acid.It presses The mixture of this technique, rubber cement and oil extender is agglomerated in double-screw type agglomerator with sulfuric acid.Compared with traditional cohesion process, New process can save 250 kgs/tonne of glue of salt, and power content of ashes can reduce by 50% in rubber, and emulsifier content can also subtract significantly It is few.In addition there are making flocculating agent with lignin machining object, or make the salt-free cohesion work of flocculating agent etc. from matter with polysaccharide, plant egg Skill, latter of which is it is said that quite promising.Liquid nano formula avoids traditional heating and stirs rubber production technology to rubber height The destruction of strand.Different from " dry method ", various rubber chemicals can fully be merged with rubber juice in liquid.Fully fusion makes Various rubber chemicals dosages can be minimum, and rubber content is up to 90% or more.Nanometer increases the wearability of rubber, makes rubber juice Fusion in liquid is evenly.Room temperature high-frequency vulcanization formula avoids tradition heating stirring rubber production technology to rubber high score The destruction of subchain reduces the degree of aging of rubber.The inside and outside synchronous solidification of rubber, is unlikely to external cured and internal " not yet done ".Required temperature is low when the vulcanization of rubber, pressure is low, is destroyed to rubber macromolecule small.Such abrasive rubber another Distinguishing feature is can to utilize abrasive rubber offset plate arbitrary cold patch on the materials such as steel, stainless steel, cement, plank, solve The wear-resisting problem of funnel, chute, pipeline, equipment inner wall or roller.But there is also wear-resisting properties for abrasive rubber traditional at present The problem of can not further increasing, therefore also need to study it.
Invention content
The present invention solves the technical problem of:It is asked for what traditional abrasive rubber wear-resisting property can not further increase Topic, provides a kind of preparation method of abrasive rubber.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
(1)By octadecylamine and organic solvent in mass ratio 1:10~1:20 stirring and dissolvings, obtain lysate;
(2)By graphene oxide and lysate in mass ratio 1:10~1:20 constant temperature are stirred to react, and are filtered to get modified graphite Alkene;
(3)It counts in parts by weight, takes 100~120 parts of chlorinated scolines successively, 10~15 parts of polymethyl methacrylates, 8~ 10 parts of Corvics, 8~10 parts of tackifying resins, 10~20 parts of modified graphenes, 10~20 parts of modified additives, 3~5 parts Chlorinated scoline is first plasticated, is sequentially added by vulcanizing agent, 1~3 part of accelerating agent, 2~4 parts of anti-aging agents, 1~4 part of plasticizer Polymethyl methacrylate, Corvic, tackifying resin, modified graphene, modified additive, vulcanizing agent, accelerating agent are prevented Old agent and plasticizer, be kneaded, be subsequently added into the sodium bicarbonate of 0.5~0.6 times of quality of PVC resin, vulcanize, discharging to get Abrasive rubber.
Step(1)The organic solvent is dimethylbenzene, benzene, any one in absolute ethyl alcohol or chloroform.
Step(3)The tackifying resin is Petropols and terpene resin in mass ratio 1:1~1:2 mixed preparings form.
Step(3)The preparation process of the modified additive is:It will(N- amidino groups)Dodecylacrylamide and poly- second two Alcohol phosphate in mass ratio 2:1~4:1 mixing, and the paracide of 0.2~0.4 times of polyethylene glycol phosphate quality is added and gathers The ferrocene of 0.12~0.18 times of ethylene glycol phosphate quality, constant temperature are stirred to react, and discharging is to get modified additive.
Step(3)The vulcanizing agent is sulphur, any one in sulfur monochloride or benzoyl peroxide.
Step(3)The accelerating agent is Vulcanization accelerator TMTD, any one in captax or accelerating agent ZDMC.
Step(3)The anti-aging agent is antioxidant 4020, any one in anti-aging agent RD or antioxidant NBC.
Step(3)The plasticizer is dibutyl phthalate, in octyl epoxy stearate or dioctyl adipate Any one.
The beneficial effects of the invention are as follows:
The present invention is by the modified additive of addition, and first, in preparation process, molecular structure is in modified additive active ingredient Block copolymer with parents' performance, the block copolymer can be self-assembly of imitated vesicle structure, in high temperature and pressure sulfidation In, sodium bicarbonate is thermally decomposed to generate carbon dioxide, and the generation of carbon dioxide can be reacted with the amidine group in the block copolymer, And amidine group is made to become positively charged lotus, since like charges are mutually exclusive so that vesica volume expansion, on the one hand, vesica expansion increases The elasticity of system is added, on the other hand, the swelling stress of modified vesica makes system be further compacted, and increases system Consistency, to improve the wear-resisting property of system, meanwhile, in use, swelling stress makes system longitudinal stress Increase, so that the wear-resisting property of system is further promoted, secondly, expansion vesica carries charge, in friction process In, due to electrostatic interaction, electrostatic attraction is generated, vesica inflatable elastomeric acts on simultaneously with electrostatic attraction, so that system is resistance to Mill performance is further promoted.
Specific implementation mode
It will(N- amidino groups)Dodecylacrylamide and polyethylene glycol phosphate in mass ratio 2:1~4:1 is placed in No. 2 beakers In, and the paracide and polyethylene glycol phosphate matter of 0.2~0.4 times of polyethylene glycol phosphate quality is added into No. 2 beakers The ferrocene of 0.12~0.18 times of amount is stirred 30~50min to get modification under the conditions of rotating speed is 300~500r/min Additive;By octadecylamine and organic solvent in mass ratio 1:10~1:20 are placed in No. 2 beakers, in rotating speed be 300~ Under the conditions of 500r/min, 40~60min of stirring and dissolving obtains lysate;By graphene oxide and lysate in mass ratio 1:10~ 1:20 are placed in single-necked flask, are 80~85 DEG C in temperature, under the conditions of rotating speed is 400~600r/min, constant temperature is stirred to react 24 After~48min, mixed liquor is obtained, then filters mixed liquor, obtain filter residue, is then in temperature as in baking oven by filter residue Under the conditions of 105~110 DEG C, drying is to constant weight to get modified graphene;It counts in parts by weight, takes 100~120 parts of chlorinations successively Butyl rubber, 10~15 parts of polymethyl methacrylates, 8~10 parts of Corvics, 8~10 parts of tackifying resins, 10~20 Part modified graphene, 10~20 parts of modified additives, 3~5 parts of vulcanizing agents, 1~3 part of accelerating agent, 2~4 parts of anti-aging agents, 1~4 part Chlorinated scoline is first placed in mixer by plasticizer, and under the conditions of temperature is 40~80 DEG C, plasticate 10~15min, then according to It is secondary that polymethyl methacrylate, Corvic, tackifying resin, modified graphene, modified additive, sulphur is added to mixer Agent, accelerating agent, anti-aging agent and plasticizer are kneaded 5~15min under the conditions of being 130~160 DEG C in temperature, obtain mixing materials, and will Gained mixing materials are transferred in vulcanizing press, are subsequently added into the sodium bicarbonate of 0.5~0.6 times of quality of PVC resin, Yu Wen Degree is 180~200 DEG C, under the conditions of pressure is 20~30MPa, vulcanizes 45~60min, discharges to get abrasive rubber.It is described organic Solvent is dimethylbenzene, benzene, any one in absolute ethyl alcohol or chloroform.The tackifying resin is Petropols and terpenes tree Fat in mass ratio 1:1~1:2 mixed preparings form.The vulcanizing agent is sulphur, arbitrary in sulfur monochloride or benzoyl peroxide It is a kind of.The accelerating agent is Vulcanization accelerator TMTD, any one in captax or accelerating agent ZDMC.The anti-aging agent is anti-old Any one in agent 4020, anti-aging agent RD or antioxidant NBC.The plasticizer is dibutyl phthalate, and epoxy is stearic Any one in misery ester or dioctyl adipate.
It will(N- amidino groups)Dodecylacrylamide and polyethylene glycol phosphate in mass ratio 4:1 is placed in No. 2 beakers, and 0.18 times of the paracide and polyethylene glycol phosphate quality of 0.4 times of polyethylene glycol phosphate quality is added into No. 2 beakers Ferrocene is stirred 50min to get modified additive under the conditions of rotating speed is 500r/min;By octadecylamine with it is organic Solvent in mass ratio 1:20 are placed in No. 2 beakers, and under the conditions of rotating speed is 500r/min, stirring and dissolving 60min obtains lysate; By graphene oxide and lysate in mass ratio 1:20 are placed in single-necked flask, are 85 DEG C in temperature, rotating speed is 600r/min items Under part, after constant temperature is stirred to react 48min, obtains mixed liquor, then filter mixed liquor, obtain filter residue, then by filter residue as In baking oven, under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified graphene;It counts in parts by weight, takes 120 parts successively Chlorinated scoline, 15 parts of polymethyl methacrylates, 10 parts of Corvics, 10 parts of tackifying resins, 20 parts of modified graphites Alkene, 20 parts of modified additives, 5 parts of vulcanizing agents, 3 parts of accelerating agents, 4 parts of anti-aging agents, 4 parts of plasticizer first set chlorinated scoline In mixer, under the conditions of temperature is 80 DEG C, plasticate 15min, then polymethyl methacrylate is added to mixer successively, gathers Vinyl chloride resin, tackifying resin, modified graphene, modified additive, vulcanizing agent, accelerating agent, anti-aging agent and plasticizer, in temperature It is kneaded 15min under the conditions of being 160 DEG C, mixing materials is obtained, and gained mixing materials are transferred in vulcanizing press, is subsequently added into polychlorostyrene second The sodium bicarbonate that 0.6 times of olefine resin quality, in temperature be 200 DEG C, pressure be 30MPa under the conditions of, vulcanize 60min, discharging to get Abrasive rubber.The organic solvent is dimethylbenzene.The tackifying resin is Petropols and terpene resin in mass ratio 1:2 mixing It is formulated.The vulcanizing agent is sulphur.The accelerating agent is Vulcanization accelerator TMTD.The anti-aging agent is antioxidant 4020.It is described Plasticizer is dibutyl phthalate.
It will(N- amidino groups)Dodecylacrylamide and polyethylene glycol phosphate in mass ratio 4:1 is placed in No. 2 beakers, and 0.18 times of the paracide and polyethylene glycol phosphate quality of 0.4 times of polyethylene glycol phosphate quality is added into No. 2 beakers Ferrocene is stirred 50min to get modified additive under the conditions of rotating speed is 500r/min;By octadecylamine with it is organic Solvent in mass ratio 1:20 are placed in No. 2 beakers, and under the conditions of rotating speed is 500r/min, stirring and dissolving 60min obtains lysate; It counts in parts by weight, takes 120 parts of chlorinated scolines successively, 15 parts of polymethyl methacrylates, 10 parts of Corvics, 10 Part tackifying resin, 20 parts of modified additives, 5 parts of vulcanizing agents, 3 parts of accelerating agents, 4 parts of anti-aging agents, 4 parts of plasticizer, first by chlorination fourth Base rubber is placed in mixer, and under the conditions of temperature is 80 DEG C, plasticate 15min, then polymethyl is added to mixer successively Sour methyl esters, Corvic, tackifying resin, modified additive, vulcanizing agent, accelerating agent, anti-aging agent and plasticizer are in temperature It is kneaded 15min under the conditions of 160 DEG C, mixing materials is obtained, and gained mixing materials are transferred in vulcanizing press, is subsequently added into polyvinyl chloride The sodium bicarbonate that 0.6 times of resin quality is 200 DEG C in temperature, under the conditions of pressure is 30MPa, vulcanizes 60min, discharge to get resistance to Rubber milling.The organic solvent is dimethylbenzene.The tackifying resin is Petropols and terpene resin in mass ratio 1:2 mixing are matched It makes.The vulcanizing agent is sulphur.The accelerating agent is Vulcanization accelerator TMTD.The anti-aging agent is antioxidant 4020.The increasing Modeling agent is dibutyl phthalate.
By octadecylamine and organic solvent in mass ratio 1:20 are placed in No. 2 beakers, in rotating speed be 500r/min conditions Under, stirring and dissolving 60min obtains lysate;By graphene oxide and lysate in mass ratio 1:20 are placed in single-necked flask, Yu Wen Degree is 85 DEG C, under the conditions of rotating speed is 600r/min, after constant temperature is stirred to react 48min, mixed liquor is obtained, then by mixed liquor mistake Filter, obtains filter residue, and then by filter residue as in baking oven, under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified graphene; It counts in parts by weight, takes 120 parts of chlorinated scolines successively, 15 parts of polymethyl methacrylates, 10 parts of Corvics, 10 Part tackifying resin, 20 parts of modified graphenes, 5 parts of vulcanizing agents, 3 parts of accelerating agents, 4 parts of anti-aging agents, 4 parts of plasticizer, first by chlorination fourth Base rubber is placed in mixer, and under the conditions of temperature is 80 DEG C, plasticate 15min, then polymethyl is added to mixer successively Sour methyl esters, Corvic, tackifying resin, modified graphene, vulcanizing agent, accelerating agent, anti-aging agent and plasticizer are in temperature It is kneaded 15min under the conditions of 160 DEG C, mixing materials is obtained, and gained mixing materials are transferred in vulcanizing press, is subsequently added into polyvinyl chloride The sodium bicarbonate that 0.6 times of resin quality is 200 DEG C in temperature, under the conditions of pressure is 30MPa, vulcanizes 60min, discharge to get resistance to Rubber milling.The organic solvent is dimethylbenzene.The tackifying resin is Petropols and terpene resin in mass ratio 1:2 mixing are matched It makes.The vulcanizing agent is sulphur.The accelerating agent is Vulcanization accelerator TMTD.The anti-aging agent is antioxidant 4020.The increasing Modeling agent is dibutyl phthalate.
Comparative example:Hebei rubber product Co., Ltd produces abrasive rubber.
1 to 3 gained abrasive rubber of example and comparative example product are subjected to performance detection, specific detection method is as follows:
The room temperature wearability of above-mentioned abrasive rubber is detected according to GB50474, specific testing result is as shown in table 1:
Table 1:Performance detection table
Detection content Example 1 Example 2 Example 3 Comparative example
Room temperature wearability/cm3 2.1 5.1 4.8 7.5
By 1 testing result of table it is found that present invention gained abrasive rubber has excellent wear-resisting property.

Claims (8)

1. a kind of preparation method of abrasive rubber, it is characterised in that specific preparation process is as follows:
(1)By octadecylamine and organic solvent in mass ratio 1:10~1:20 stirring and dissolvings, obtain lysate;
(2)By graphene oxide and lysate in mass ratio 1:10~1:20 constant temperature are stirred to react, and are filtered to get modified graphite Alkene;
(3)It counts in parts by weight, takes 100~120 parts of chlorinated scolines successively, 10~15 parts of polymethyl methacrylates, 8~ 10 parts of Corvics, 8~10 parts of tackifying resins, 10~20 parts of modified graphenes, 10~20 parts of modified additives, 3~5 parts Chlorinated scoline is first plasticated, is sequentially added by vulcanizing agent, 1~3 part of accelerating agent, 2~4 parts of anti-aging agents, 1~4 part of plasticizer Polymethyl methacrylate, Corvic, tackifying resin, modified graphene, modified additive, vulcanizing agent, accelerating agent are prevented Old agent and plasticizer, be kneaded, be subsequently added into the sodium bicarbonate of 0.5~0.6 times of quality of PVC resin, vulcanize, discharging to get Abrasive rubber.
2. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(1)The organic solvent For dimethylbenzene, benzene, any one in absolute ethyl alcohol or chloroform.
3. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The tackifying resin For Petropols and terpene resin in mass ratio 1:1~1:2 mixed preparings form.
4. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The modified addition The preparation process of material is:It will(N- amidino groups)Dodecylacrylamide and polyethylene glycol phosphate in mass ratio 2:1~4:1 is mixed It closes, and the paracide and polyethylene glycol phosphate quality 0.12~0.18 of 0.2~0.4 times of polyethylene glycol phosphate quality is added Ferrocene again, constant temperature are stirred to react, and discharging is to get modified additive.
5. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The vulcanizing agent is Any one in sulphur, sulfur monochloride or benzoyl peroxide.
6. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The accelerating agent is Any one in Vulcanization accelerator TMTD, captax or accelerating agent ZDMC.
7. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The anti-aging agent is Any one in antioxidant 4020, anti-aging agent RD or antioxidant NBC.
8. a kind of preparation method of abrasive rubber according to claim 1, it is characterised in that:Step(3)The plasticizer is Any one in dibutyl phthalate, octyl epoxy stearate or dioctyl adipate.
CN201810626509.5A 2018-06-19 2018-06-19 A kind of preparation method of abrasive rubber Withdrawn CN108659360A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810626509.5A CN108659360A (en) 2018-06-19 2018-06-19 A kind of preparation method of abrasive rubber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810626509.5A CN108659360A (en) 2018-06-19 2018-06-19 A kind of preparation method of abrasive rubber

Publications (1)

Publication Number Publication Date
CN108659360A true CN108659360A (en) 2018-10-16

Family

ID=63774879

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810626509.5A Withdrawn CN108659360A (en) 2018-06-19 2018-06-19 A kind of preparation method of abrasive rubber

Country Status (1)

Country Link
CN (1) CN108659360A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109988367A (en) * 2019-03-11 2019-07-09 常州明华运输有限公司 A kind of preparation method of vehicle windshield wiper abrasive rubber material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109988367A (en) * 2019-03-11 2019-07-09 常州明华运输有限公司 A kind of preparation method of vehicle windshield wiper abrasive rubber material

Similar Documents

Publication Publication Date Title
CN102212233B (en) R134a refrigerant-resistant rubber material and preparation method thereof
JP2016538394A (en) Method for continuous production of rubber masterbatch and rubber masterbatch formulated by the method
CN106046453A (en) Water-swelling nitrile butadiene rubber and preparation process thereof
CN106751183A (en) A kind of energy-conserving and environment-protective material and preparation method thereof
CN1218990C (en) Preparation method of starch and polymer comosition
CN104277258B (en) A kind of preparation method of the water swelling rubber of good weatherability
CN105733220B (en) Biodegradable plastic containing biogas residue and preparation method thereof
CN108659360A (en) A kind of preparation method of abrasive rubber
US2567016A (en) Hydrocarbon rubber plasticized with a polyvinyl compound
CN110607000A (en) Graphene natural rubber oil-resistant mixed foam material and preparation method thereof
CN1304476C (en) Method for preparing tribasic ethylene propylene rubber/polypropylene thermoplastic elastomer
CN104672834A (en) High-performance low-cost PC (polycarbonate) modified material
Al-Malki et al. Study the effect of recycled tire rubber on the mechanical and rheological properties of TPV (HDPE/Recycled tire rubber)
CN110819038B (en) PVC sheet and preparation method thereof
CN110204803B (en) Light-weight rubber product and preparation method thereof
CN114907590A (en) Synthetic rubber wet masterbatch and preparation method and application thereof
CN110734593A (en) Method for preparing emulsion polymerized styrene butadiene rubber from modified graphene
CN102604313B (en) SBS (Styrene-Butadiene-Styrene) crosslinking elastomer composite material and preparation method thereof
CN112290164B (en) High-performance additive suitable for producing ultrathin lithium battery diaphragm and preparation and application thereof
CN104327438A (en) Waste HIPS/PP composite material and preparation method thereof
CN107841026A (en) A kind of preparation method of Controllable cross-linking polyethylene
CN110591261B (en) Pre-dispersed masterbatch of vulcanization crosslinking activator of acrylate rubber and preparation method thereof
CN108048062A (en) A kind of water plugging profile control agent and preparation method thereof
CN105199267A (en) Preparation method of PVC (polyvinyl chloride) material for outdoor shielding
CN110028708A (en) A kind of preparation method of wet oxidation zinc predispersed masterbatch

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
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20181016