CN105542250A - Flexible rosin-butadiene rubber material and preparation method thereof - Google Patents
Flexible rosin-butadiene rubber material and preparation method thereof Download PDFInfo
- Publication number
- CN105542250A CN105542250A CN201510941918.0A CN201510941918A CN105542250A CN 105542250 A CN105542250 A CN 105542250A CN 201510941918 A CN201510941918 A CN 201510941918A CN 105542250 A CN105542250 A CN 105542250A
- Authority
- CN
- China
- Prior art keywords
- minute
- carbon nanotube
- rosin
- mentioned
- parts
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Carbon And Carbon Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a flexible rosin-butadiene rubber material. The flexible rosin-butadiene rubber material comprises, by weight, 4-7 parts of maleated rosin, 1-3 parts of triethanolamine oleic soap, 10-17 parts of epoxidized triglyceride, 2-3 parts of potassium dihydrogen phosphate, 30-40 parts of carbon nanotubes, 50-60 parts of hydroxyl-terminated polybutadiene, 200-300 parts of n-methylpyrrolidone, 5-7 parts of boron oxide, 160-200 parts of butadiene rubber, 1.3-2 parts of sulphur, 1-2 parts of 2, 6-di-tert-butyl-4-methylphenol, 2-3 parts of xanthan gum and 0.7-1 part of magnesium chloride. Through use of rosin and xanthan gum, dispersibility of filling material particles between rubber materials is effectively improved and rubber flexibility is improved.
Description
Technical field
The present invention relates to field of rubber technology, particularly relate to a kind of pliable and tough rosin cis-1,4-polybutadiene rubber material and preparation method thereof.
Background technology
Carbon nanotube is widely used in polymkeric substance to the heat conduction of raising polymkeric substance, conduction and physicals etc. because of the structure of its uniqueness and the physical and chemical performance of excellence.But carbon nanotube itself has very high surface free energy, easily reunites, and not easily disperses in polymeric matrix, limit its application.The surface modification treatment of carbon nanotube is one of important channel of improving its dispersive ability in the polymer and then the excellent carbon nano-tube/polymer composite material of processability;
Hydroxy-terminated polybutadienes is liquid because of it at normal temperatures, and transparency is good, the low good processability of viscosity; And it and chainextender, linking agent react the cured article that can generate tridimensional network at ambient temperature or elevated temperature, this cured article has excellent mechanical property, good oil resistant and water resistance, particularly acid and alkali-resistance, wear-resisting, low temperature resistant and electrical insulation capability is better, become output in distant pawl series of fluids rubber maximum, purposes is a kind the most widely, is mainly used in the aspects such as solid propellant tackiness agent, polyurethane elastomer, material of construction, speciality coating, tackiness agent, Embedding Material, rubber and plastic and epoxy resin modification.Hydroxy-terminated polybutadienes gives its more characteristic by modification later, improves its performance, has widened the Application Areas of hydroxy-terminated polybutadienes.
Summary of the invention
The object of the invention is exactly the defect in order to make up prior art, provides a kind of pliable and tough rosin cis-1,4-polybutadiene rubber material and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of pliable and tough rosin cis-1,4-polybutadiene rubber material, it is made up of the raw material of following weight parts:
Maleated rosin 4-7, trihydroxy ethylamine oleate soap 1-3, epoxidation tri-glyceride 10-17, potassium primary phosphate 2-3, carbon nanotube 30-40, hydroxy-terminated polybutadienes 50-60, n-methyl-2-pyrrolidone 200-300, boron oxide 5-7, cis-1,4-polybutadiene rubber 160-200, sulphur 1.3-2,2,6 ditertiary butyl p cresol 1-2, xanthan gum 2-3, magnesium chloride 0.7-1.
A preparation method for described pliable and tough rosin cis-1,4-polybutadiene rubber material, comprises the following steps:
(1) above-mentioned carbon nanotube is placed in its weight 40-50 doubly, massfraction is the aqueous hydrogen peroxide solution ultrasonic disperse 30-40 minute of 0.3-0.5%, is incubated 100-120 minute, filters, vacuum-drying at 75-80 DEG C, obtains pre-treatment carbon nanotube;
(2) get sulfuric acid that volume ratio is 3-4:1, salpeter solution mixing, stir, described sulfuric acid concentration is 70-75%, concentration of nitric acid is 80-85%;
(3) pre-treatment carbon nanotube obtained above is joined in above-mentioned mixed acid solution, ultrasonic 100-110 minute at 50-60 DEG C, filtration under diminished pressure, be neutral by carbon nanotube deionized water repetitive scrubbing to the filtrate obtained, the vacuum drying oven putting into 76-80 DEG C is dried, and obtains acidifying carbon nanotube;
(4) joining in hydroxy-terminated polybutadienes by above-mentioned trihydroxy ethylamine oleate soap, stir, is fluid rubber emulsion;
(5) above-mentioned 2,6 ditertiary butyl p cresol is joined its weight 7-10 doubly, in the ethanol of 50-60%, stir, add magnesium chloride, raised temperature is 60-70 DEG C, adds aforesaid liquid rubber latex, 300-400 rev/min is stirred 10-20 minute, obtains oxidation resistance liquid body rubber emulsion;
(6) above-mentioned acidifying carbon nanotube is mixed with oxidation resistance liquid body rubber emulsion, magnetic agitation 2-3 minute, join in said n-methyl-2-pyrrolidone, ultrasonic 10-16 minute, suction filtration, by filter cake dry 20-30 minute at 100-105 DEG C, obtains hydroxyl modification acidifying carbon nanotube;
(7) mixed with boron oxide by above-mentioned hydroxyl modification acidifying carbon nanotube, ball milling is even; Being sent to concentration is in the phosphoric acid solution of 10-15%, constant temperature dipping 120-130 minute at 150-160 DEG C, discharging, and dry, send in reactor, under nitrogen protection, thermal treatment 100-120 minute at 400-450 DEG C, obtains phosphate impregnation compounded mix;
(8) joined in 10-13 times of deionized water by above-mentioned potassium primary phosphate, add xanthan gum, maleated rosin successively, insulated and stirred 4-10 minute at 60-70 DEG C, mix, stir with above-mentioned phosphate impregnation compounded mix, dehydration, obtains Preblend;
(9) by above-mentioned Preblend, cis-1,4-polybutadiene rubber mixing, plasticate 2-3 minute at 46-50 DEG C, add each raw material of residue, mixing 4-6 minute, is placed in two roller mills by the rubber unvulcanizate obtained, mixing 6-10 minute is supplemented at 30-40 DEG C, discharging, at room temperature parks 20-25 hour by sizing material, sends in vulcanizing press, at 150-155 DEG C, carry out sulfuration, to obtain final product;
The preparation method of described a kind of pliable and tough rosin cis-1,4-polybutadiene rubber material, the weight of described mixed acid solution is 18-20 times of pre-treatment carbon nanotubes.
Advantage of the present invention is:
First the present invention carries out Carboxylation process to carbon nanotube, then react with hydroxy-terminated polybutadienes, the intensity of sizing material can be strengthened, this is due to the hydroxyl reaction in the carboxyl of carbon nano tube surface and hydroxy-terminated polybutadienes, carbon nano tube surface is connected by covalent linkage with hydroxy-terminated polybutadienes molecular chain, thus improve its dispersiveness in the base, and enhance the bounding force of itself and rubber matrix, make it in rubber matrix, show better reinforcing effect;
Then the carboxylic acid carbon nanotube after hydroxy-terminated polybutadienes process is mixed with boron oxide, use phosphate impregnation compounded mix, the pyrogenous origin product P 4O10 of phosphoric acid is phosphorus oxygen glass structure, introduce B2O3 in the melt, [BPO4] structural unit can be formed, glass structure is made to change rack-like into by chain, these rack-like structures are cross-linked with each other, strengthen network structure, strengthen the bonding strength with matrix, one deck coating can be covered at matrix surface, covering surfaces hole more effectively, confining surface active site, effective prevention oxidizing gas enters intrinsic silicon by micropore or crackle, effectively raise physical strength and the antioxidant property of finished product,
The present invention adopts rosin, xanthan gum etc., effectively raise the dispersiveness of filler grain between elastomeric material, the modification snappiness of rubber.
Embodiment
A kind of pliable and tough rosin cis-1,4-polybutadiene rubber material, it is made up of the raw material of following weight parts:
Maleated rosin 4, trihydroxy ethylamine oleate soap 1, epoxidation tri-glyceride 10, potassium primary phosphate 2, carbon nanotube 30, hydroxy-terminated polybutadienes 50, n methyl-2-pyrrolidone 200, boron oxide 5, cis-1,4-polybutadiene rubber 160, sulphur 1.3,2,6 ditertbutylparacresol 1, xanthan gum 2, magnesium chloride 0.7.
A preparation method for described pliable and tough rosin cis-1,4-polybutadiene rubber material, comprises the following steps:
(1) above-mentioned carbon nanotube is placed in its weight 40 times, massfraction be 0.3% aqueous hydrogen peroxide solution ultrasonic disperse 30 minutes, at 75 DEG C, be incubated 100 minutes, filter, vacuum-drying, obtain pre-treatment carbon nanotube;
(2) get sulfuric acid that volume ratio is 3:1, salpeter solution mixing, stir, described sulfuric acid concentration is 70%, concentration of nitric acid is 80%;
(3) pre-treatment carbon nanotube obtained above is joined in above-mentioned mixed acid solution, at 50 DEG C ultrasonic 100 minutes, carbon nanotube deionized water repetitive scrubbing to the filtrate obtained was neutral by filtration under diminished pressure, the vacuum drying oven putting into 76 DEG C is dried, and obtains acidifying carbon nanotube;
(4) joining in hydroxy-terminated polybutadienes by above-mentioned trihydroxy ethylamine oleate soap, stir, is fluid rubber emulsion;
(5) above-mentioned 2,6 ditertbutylparacresols are joined its weight 7 times, 50% ethanol in, stir, add magnesium chloride, raised temperature is 60 DEG C, adds aforesaid liquid rubber latex, 300 revs/min stir 10 minutes, obtain oxidation resistance liquid body rubber emulsion;
(6) above-mentioned acidifying carbon nanotube is mixed with oxidation resistance liquid body rubber emulsion, magnetic agitation 2 minutes, join in said n methyl-2-pyrrolidone, ultrasonic 10 minutes, suction filtration, by filter cake at 100 DEG C dry 20 minutes, obtain hydroxyl modification acidifying carbon nanotube;
(7) mixed with boron oxide by above-mentioned hydroxyl modification acidifying carbon nanotube, ball milling is even; Being sent to concentration is in the phosphoric acid solution of 10%, and at 150 DEG C, constant temperature floods 120 minutes, discharging, dry, and send in reactor, under nitrogen protection, at 400 DEG C, thermal treatment 100 minutes, obtains phosphate impregnation compounded mix;
(8) joined in 10 times of deionized waters by above-mentioned potassium primary phosphate, add xanthan gum, maleated rosin successively, insulated and stirred 4 minutes at 60 DEG C, mixes with above-mentioned phosphate impregnation compounded mix, stirs, and dehydration, obtains Preblend;
(9) by above-mentioned Preblend, cis-1,4-polybutadiene rubber mixing, plasticate at 46 DEG C 2 minutes, add each raw material of residue, mixing 4 minutes, the rubber unvulcanizate obtained is placed in two roller mills, supplement mixing 6 minutes at 30 DEG C, discharging, at room temperature parks 20 hours by sizing material, sends in vulcanizing press, at 150 DEG C, carry out sulfuration, to obtain final product;
The preparation method of described a kind of pliable and tough rosin cis-1,4-polybutadiene rubber material, the weight of described mixed acid solution is 18 times of pre-treatment carbon nanotubes.
Stretch breaking strength (MPa): 18.7;
Surely modulus 100%(MPa is stretched): 2.7;
Mooney viscosity: 63;
70 DEG C × 70h air oven aging test:
Tensile strength at yield reduced rate: 4.3%, elongation at break reduced rate: 8.5%.
Claims (3)
1. a pliable and tough rosin cis-1,4-polybutadiene rubber material, it is characterized in that, it is made up of the raw material of following weight parts:
Maleated rosin 4-7, trihydroxy ethylamine oleate soap 1-3, epoxidation tri-glyceride 10-17, potassium primary phosphate 2-3, carbon nanotube 30-40, hydroxy-terminated polybutadienes 50-60, n-methyl-2-pyrrolidone 200-300, boron oxide 5-7, cis-1,4-polybutadiene rubber 160-200, sulphur 1.3-2,2,6 ditertiary butyl p cresol 1-2, xanthan gum 2-3, magnesium chloride 0.7-1.
2. a preparation method for pliable and tough rosin cis-1,4-polybutadiene rubber material as claimed in claim 1, is characterized in that, comprise the following steps:
(1) above-mentioned carbon nanotube is placed in its weight 40-50 doubly, massfraction is the aqueous hydrogen peroxide solution ultrasonic disperse 30-40 minute of 0.3-0.5%, is incubated 100-120 minute, filters, vacuum-drying at 75-80 DEG C, obtains pre-treatment carbon nanotube;
(2) get sulfuric acid that volume ratio is 3-4:1, salpeter solution mixing, stir, described sulfuric acid concentration is 70-75%, concentration of nitric acid is 80-85%;
(3) pre-treatment carbon nanotube obtained above is joined in above-mentioned mixed acid solution, ultrasonic 100-110 minute at 50-60 DEG C, filtration under diminished pressure, be neutral by carbon nanotube deionized water repetitive scrubbing to the filtrate obtained, the vacuum drying oven putting into 76-80 DEG C is dried, and obtains acidifying carbon nanotube;
(4) joining in hydroxy-terminated polybutadienes by above-mentioned trihydroxy ethylamine oleate soap, stir, is fluid rubber emulsion;
(5) above-mentioned 2,6 ditertiary butyl p cresol is joined its weight 7-10 doubly, in the ethanol of 50-60%, stir, add magnesium chloride, raised temperature is 60-70 DEG C, adds aforesaid liquid rubber latex, 300-400 rev/min is stirred 10-20 minute, obtains oxidation resistance liquid body rubber emulsion;
(6) above-mentioned acidifying carbon nanotube is mixed with oxidation resistance liquid body rubber emulsion, magnetic agitation 2-3 minute, join in said n-methyl-2-pyrrolidone, ultrasonic 10-16 minute, suction filtration, by filter cake dry 20-30 minute at 100-105 DEG C, obtains hydroxyl modification acidifying carbon nanotube;
(7) mixed with boron oxide by above-mentioned hydroxyl modification acidifying carbon nanotube, ball milling is even; Being sent to concentration is in the phosphoric acid solution of 10-15%, constant temperature dipping 120-130 minute at 150-160 DEG C, discharging, and dry, send in reactor, under nitrogen protection, thermal treatment 100-120 minute at 400-450 DEG C, obtains phosphate impregnation compounded mix;
(8) joined in 10-13 times of deionized water by above-mentioned potassium primary phosphate, add xanthan gum, maleated rosin successively, insulated and stirred 4-10 minute at 60-70 DEG C, mix, stir with above-mentioned phosphate impregnation compounded mix, dehydration, obtains Preblend;
(9) by above-mentioned Preblend, cis-1,4-polybutadiene rubber mixing, plasticate 2-3 minute at 46-50 DEG C, add each raw material of residue, mixing 4-6 minute, is placed in two roller mills by the rubber unvulcanizate obtained, mixing 6-10 minute is supplemented at 30-40 DEG C, discharging, at room temperature parks 20-25 hour by sizing material, sends in vulcanizing press, at 150-155 DEG C, carry out sulfuration, to obtain final product.
3. the preparation method of a kind of pliable and tough rosin cis-1,4-polybutadiene rubber material according to claim 2, is characterized in that, the weight of described mixed acid solution is 18-20 times of pre-treatment carbon nanotubes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510941918.0A CN105542250A (en) | 2015-12-16 | 2015-12-16 | Flexible rosin-butadiene rubber material and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510941918.0A CN105542250A (en) | 2015-12-16 | 2015-12-16 | Flexible rosin-butadiene rubber material and preparation method thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105542250A true CN105542250A (en) | 2016-05-04 |
Family
ID=55821833
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510941918.0A Pending CN105542250A (en) | 2015-12-16 | 2015-12-16 | Flexible rosin-butadiene rubber material and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105542250A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110862482A (en) * | 2018-08-27 | 2020-03-06 | 中国石油天然气股份有限公司 | Polymerization terminator for rubber synthesis |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102532621A (en) * | 2010-12-24 | 2012-07-04 | 福建省莆田市华丰鞋业有限公司 | Light modified rubber foaming undersole material prescription and processing technology |
| CN103589006A (en) * | 2013-10-29 | 2014-02-19 | 绿宝电缆（集团）有限公司 | High-elasticity cold-resistant modified cis-1, 4-polybutadiene rubber cable material |
| CN103694505A (en) * | 2013-12-24 | 2014-04-02 | 苏州华东橡胶工业有限公司 | Compound carbon nanotube and rubber material and preparation method thereof |
-
2015
- 2015-12-16 CN CN201510941918.0A patent/CN105542250A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102532621A (en) * | 2010-12-24 | 2012-07-04 | 福建省莆田市华丰鞋业有限公司 | Light modified rubber foaming undersole material prescription and processing technology |
| CN103589006A (en) * | 2013-10-29 | 2014-02-19 | 绿宝电缆（集团）有限公司 | High-elasticity cold-resistant modified cis-1, 4-polybutadiene rubber cable material |
| CN103694505A (en) * | 2013-12-24 | 2014-04-02 | 苏州华东橡胶工业有限公司 | Compound carbon nanotube and rubber material and preparation method thereof |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110862482A (en) * | 2018-08-27 | 2020-03-06 | 中国石油天然气股份有限公司 | Polymerization terminator for rubber synthesis |
| CN110862482B (en) * | 2018-08-27 | 2022-08-05 | 中国石油天然气股份有限公司 | Polymerization terminator for rubber synthesis |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103772743A (en) | Nano composite material, preparation method thereof, vulcanized rubber, and applications of vulcanized rubber | |
| CN103408948B (en) | A kind of rubber combination and application thereof | |
| CN102532673B (en) | Reinforcing method for ethylene-vinyl acetate copolymer | |
| CN103102543B (en) | A kind of thermoplastic elastomer electric wire and cable material and preparation method thereof | |
| CN101260238A (en) | Electric silicon rubber | |
| CN105524307A (en) | Nylon blended rubber material and preparation method thereof | |
| CN105985552A (en) | Lanthanum-oxide-modified rubber cable material | |
| CN106519363A (en) | Hydrogenated nitrile-butadiene rubber composition | |
| CN104710693A (en) | Low-temperature-resistant door/window sealing strip and preparation method thereof | |
| CN105542250A (en) | Flexible rosin-butadiene rubber material and preparation method thereof | |
| CN111978611B (en) | High-strength conductive self-healing rubber composite material and preparation method thereof | |
| CN105482180A (en) | Anti-corrosive butadiene rubber material and preparation method thereof | |
| CN105440350A (en) | Ageing resistant butadiene rubber material and preparation method thereof | |
| CN106366387B (en) | A kind of preparation method of epoxy natural rubber organic/inorganic hybridization material | |
| CN105440346A (en) | Lubricating butadiene rubber material and preparation method thereof | |
| CN105482179A (en) | Cis-polybutadiene rubber material and preparation method thereof | |
| CN108949064A (en) | A kind of high foaming rate automobile PVC foam primary coat glue and preparation method thereof | |
| CN105440353A (en) | Zirconium-based hard butadiene rubber material and preparation method thereof | |
| CN105462001A (en) | Hydrophobic butadiene rubber material and preparation method thereof | |
| CN105482178A (en) | Macromolecular butadiene rubber material and preparation method thereof | |
| CN105440348A (en) | Phosphatized butadiene rubber material and preparation method thereof | |
| CN105440351A (en) | High strength butadiene rubber material and preparation method thereof | |
| CN105440347A (en) | Cross-linked butadiene rubber material and preparation method thereof | |
| CN105440349A (en) | Inorganic salt reinforced butadiene rubber material and preparation method thereof | |
| CN105440343A (en) | Carbon nanotube modified butadiene rubber material and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160504 |