CN103073758B - A kind of rubber combination and preparation method thereof and its cross-linked rubber - Google Patents
A kind of rubber combination and preparation method thereof and its cross-linked rubber Download PDFInfo
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Abstract
The invention provides a kind of rubber combination and preparation method thereof and its cross-linked rubber.Described rubber combination comprises uncrosslinked rubber and is dispersed in the rubber particles with crosslinking structure wherein; The rubber particles wherein with crosslinking structure is paracril particle, and median size is 50 ~ 200nm, and gel content is 60% weight or higher; Wherein uncrosslinked rubber is styrene-butadiene rubber(SBR); The weight ratio of the described rubber particles and uncrosslinked rubber with crosslinking structure is 1: 99-20: 80.Described rubber combination comprise uncrosslinked rubber latex is mixed with the component of latex of the rubber particles with crosslinking structure after coalescence and obtaining.The latex wherein with the rubber particles of crosslinking structure is the rubber latex obtained after cross-linking radiation.The cross-linked rubber rolling resistance of described rubber combination, wet and slippery performance, wear resisting property can be improved simultaneously, may be used for preparing high-performance car tread rubber.
Description
Technical field
The present invention relates to rubber materials, say further, relate to a kind of rubber combination by rubber particles modification and preparation method thereof and its cross-linked rubber.
Background technology
Automobile more and more becomes the indispensable instrument of the modern life, and automobile power used comes from oil substantially, petroleum resources are limited, and the fast development of automotive industry simultaneously also faces Carbon emission decrement pressure, how to reduce vehicle fuel consume and becomes more and more urgent.Reduce fuel oil consumption, not only can reduce automobilism cost, and the pressure of CO2 emissions and alleviation petroleum resources can be reduced.Vehicle fuel consume is except affecting by automobile design itself factor, tire drag is also one of important factor, tire drag fuel oil consumption accounts for 14 ~ 17% of vehicle fuel consume, and tire drag often reduces by 10%, usually can reduce fuel oil consumption 1 ~ 2%.Therefore, tire drag is reduced by one of important measures as reduction fuel oil consumption.
But in the research of reduction tyre stock (mainly tread rubber) rolling resistance, encounter very stubborn problem.Namely so-called " Magic triangle " problem that rolling resistance, wet and slippery performance, wear resisting property are conflicting.Simple increase tenderizer consumption, can improve the anti-slippery of tire, but its wear resistance reduces and rolling resistance increases.Improve the consumption of reinforced filling (carbon black or white carbon black), rolling resistance can be reduced to a certain extent, but make reinforced filling be difficult to be uniformly dispersed in sizing material, and anti-slippery is reduced.Strengthen the consumption of vulcanizing agent, namely improve cross-linking density, the same with the effect increasing reinforced filling consumption, reduce rolling resistance and make anti-slippery be deteriorated simultaneously.In order to realize the balance of three aspect performances, except Design of Tire Structure is optimized, also research is extensively and profoundly carried out to sizing material (based on tread rubber) formula both at home and abroad.The on the one hand rubber raw materials (as solution polymerized butadiene styrene rubber SSBR, using trans-polyisoprene TPI, butadiene-isoprene-vinylbenzene integrated rubber SIBR, high-vinyl cis-1,4-polybutadiene rubber HVBR etc.) that is suitable for of synthesis, sets about the properties-correcting agent seeking to have better over-all properties and practical formulation on the other hand.Some progress have been obtained in formulating, more representational: solution polymerized butadiene styrene rubber (SSBR) etc. are also used or reciprocal (reversion) carbon black system with carbon black and white carbon black, system feature is that main formula is substantially constant, just different on reinforced filling, easily industrially realize; Its shortcoming is that when needing to use more silane coupling agent and refine glue, machine utilization is large, and the wear resistance of cross-linked rubber is also undesirable.
The rubber gels adopting the Chemical Crosslinking Methods such as direct polymerization method or superoxide to prepare, when filling a prescription suitable, can improve the performance of cross-linked rubber.Such as, report respectively in European patent EP 405216 and German patent DE 4220563 and in rubber combination, to add chloroprene rubber gel and cis-1,4-polybutadiene rubber gel respectively to improve wear resistance and the fatigue temperature rise of cross-linked rubber, but have lost resistance to wet skidding performance.
So a lot of patent starts to adopt the rubber gels of modification to improve the performance of vulcanization of rubber glue, such as US Patent No. 6184296 uses through the suitable fourth of surface modification and styrene-butadiene rubber(SBR) gel (latex particle swelling index 4 ~ 5 in gel, particle diameter 60 ~ 450nm), the rolling resistance of natural rubber (NR) formula system cross-linked rubber is reduced, and strength property is uninfluenced.
In US Patent No. 6133364,1-chloro-4-methyl-benzene is grafted in styrene-butadiene rubber(SBR) gel surface, then uses it in NR formula system, the rolling resistance of cross-linked rubber is reduced, and anti-slippery improves.
US Patent No. 6207757 reaches the effect reducing NR formula system cross-linked rubber rolling resistance with the styrene-butadiene rubber(SBR) gel of 1-chloro-4-methyl-benzene modification, improve hauling ability and the wearing quality of tire simultaneously.
US Patent No. 6242534 in the lump for NR formula system, not only reduces the styrene-butadiene rubber(SBR) gel containing carboxyl and amino the rolling resistance of system cross-linked rubber, improves anti-slippery, and significantly improve stress at definite elongation.
European patent EP 1431075 improve styrene-butadiene rubber(SBR) (SBR) and cis-1,4-polybutadiene rubber (BR) with styrene-butadiene rubber(SBR) gel and plasticized starch and the performance of white carbon black system, result wear resistance is improved, rolling resistance reduces, and the proportion of cross-linked rubber is also less.
US Patent No. 6699935 makes modified styrene butadiene rubber formula system have low-rolling-resistance with modification by copolymerization styrene-butadiene rubber(SBR) gel and has outstanding anti-slippery and wear resistance concurrently.
The rubber gels that above-mentioned patent documentation is mentioned all adopts Chemical Crosslinking Methods to be cross-linked, this method needs to use the higher cross-linking monomer of price and energy consumption is comparatively large, and relates generally to white carbon black system and the modified styrene butadiene rubber formula system of natural rubber formulations system or styrene-butadiene rubber(SBR).And importantly must by the rubber gels obtained after crosslinked carry out modified just can reach rolling resistance, anti-slippery and wear resistance while improve.Although there is the particle diameter of report rubber gels in these patents, but when these rubber gels are distributed in cross-linked rubber, the dispersion of initial stage particle diameter can be reached, really can play the modifying function of nano-rubber gel, not report in any patent.
Summary of the invention
For the problem of prior art, an object of the present invention is to provide a kind of rubber combination.The cross-linked rubber anti-slippery of this rubber combination, rolling resistance and wear resistance are improved simultaneously, can use as excellent automobile tread rubber.
Another object of the present invention is to provide the preparation method of described rubber combination.
Another object of the present invention is to provide the cross-linked rubber of described rubber combination.
A kind of fully vulcanized powder rubber is disclosed in the international patent application WO01/40356 (priority date on December 3rd, 1999) that the applicant submitted on September 18th, the 2000 and international patent application WO01/98395 (priority date on June 15th, 2000) that the applicant submitted June 15 calendar year 2001.Propose when after employing irradiance method cross-linked rubber latex, because cross-linking radiation makes the latex particle in rubber latex (rubber particles) reach certain gel content, the particle diameter of its latex particle is fixed up, can not in drying process afterwards adhesion or coalescence.Contriver finds under study for action, and by the paracril latex after this cross-linking radiation and the mixing of uncrosslinked styrene butadiene rubber latex, coalescence obtains the rubber combination of the particle modified styrene-butadiene rubber(SBR) of a kind of crosslinked paracril altogether afterwards.Wherein due to cross-linking radiation the paracril particle with crosslinking structure between can not adhesion and coalescence, and the latex particle meeting coalescence of common uncrosslinked styrene butadiene rubber latex, in the rubber matrix that the paracril particle therefore with crosslinking structure just can obtain after uncrosslinked styrene butadiene rubber latex coalescence with the particle size dispersion of its progenitor, and the degree that is uniformly dispersed than direct by much better in fully vulcanized powder rubber and the mixing mixture obtained of rubber.The rubber combination sulfuration obtained after described two kinds of latex coalescences is finally prepared into cross-linked rubber, because the paracril particle after cross-linking radiation has crosslinking structure, do not need the sulfuration considering disperse phase, this addresses the problem the covulcanization problem of the composition of different rubber composition; The paracril particle with crosslinking structure of cross-linking radiation is still evenly dispersed in styrene-butadiene vulcanized rubber with very little initial size very much simultaneously, so the anti-slippery of the cross-linked rubber finally obtained, rolling resistance and wear resistance can obtain raising simultaneously.
Specifically, a kind of rubber combination of the present invention, comprises uncrosslinked rubber and is dispersed in the rubber particles with crosslinking structure wherein.Uncrosslinked rubber is external phase, and the rubber particles with crosslinking structure is disperse phase.The rubber particles wherein with crosslinking structure is paracril particle, and average mark shot footpath is 50 ~ 200nm, and gel content is 60% weight or higher; Wherein uncrosslinked rubber is styrene-butadiene rubber(SBR); The weight ratio of the described rubber particles and uncrosslinked rubber with crosslinking structure is 1: 99-20: 80, preferably 1: 99-10: 90, be more preferably 3: 97-8: 92.
The above rubber particles with crosslinking structure is equal phase structure.And do not carry out any graft modification, surface modification.Preferred, described in there is the paracril particle of crosslinking structure gel content be 75% weight or higher, its median size is preferably 70 ~ 200nm, more preferably 80 ~ 180nm.
The preparation of rubber combination of the present invention, be comprise uncrosslinked rubber latex is mixed with the component of latex of the rubber particles with crosslinking structure after coalescence and obtaining: the latex wherein with the rubber particles of crosslinking structure is the rubber latex obtained after cross-linking radiation.
Specifically, the preparation method of rubber combination of the present invention, comprises the following steps:
(1) by paracril latex through cross-linking radiation, make the paracril particle in latex have crosslinking structure, reach described gel content, and make the paracril particle in latex be fixed in described average particle size range;
(2) then have the rubber particles of crosslinking structure and the mass ratio range of uncrosslinked styrene-butadiene rubber(SBR) by described, isoprene-isobutylene rubber latex and the uncrosslinked styrene butadiene rubber latex of getting above-mentioned cross-linking radiation carry out being mixed to evenly;
(3) above gained mixing latex is carried out common coalescence and obtain described rubber combination.
The preparation method of above-described rubber combination, the paracril latex wherein before styrene butadiene rubber latex and non-cross-linking radiation is synthetic rubber latex common in prior art.Wherein styrene butadiene rubber latex comprises the latex obtained after breast that emulsion polymerisation process in prior art directly prepared gathers the block latex of butylbenzene prepared by styrene-butadiene latex and any existing method; Be preferably the latex of emulsion polymerized styrene butadiene rubber in prior art.Wherein the weight ratio of the solid content of paracril latex and the solid content of styrene butadiene rubber latex is 1: 99-20: 80, preferably 1: 99-10: 90, more preferably 3: 97-8: 92.
The method of cross-linking radiation rubber latex identical in the preparation method that the cross-linking radiation of paracril latex picks up from according to the fully vulcanized powder rubber disclosed in international patent application WO01/40356 (priority date on December 3rd, 1999) in the above step (1).Paracril latex after the cross-linking radiation of gained is also with the rubber latex before drying non-after irradiation in WO01/40356.
Specifically, can not crosslinking coagent be used at paracril latex, also can use crosslinking coagent.Crosslinking coagent used is selected from simple function group crosslinking coagent, two functional group's crosslinking coagents, trifunctional crosslinking coagent, four-functional group crosslinking coagent or polyfunctional group crosslinking coagent and arbitrary combination thereof.The example of described simple function group crosslinking coagent includes, but is not limited to: (methyl) Octyl acrylate, (methyl) Isooctyl acrylate monomer, (methyl) glycidyl acrylate; The example of two described functional group's crosslinking coagents includes, but is not limited to: 1,4-butyleneglycol two (methyl) acrylate, 1,6-hexylene glycol two (methyl) acrylate, Diethylene Glycol two (methyl) acrylate, triethylene glycol two (methyl) acrylate, neopentyl glycol two (methyl) acrylate, Vinylstyrene; The example of described trifunctional crosslinking coagent includes, but is not limited to: trimethylolpropane tris (methyl) acrylate, tetramethylolmethane three (methyl) acrylate; The example of described four-functional group crosslinking coagent includes, but is not limited to: tetramethylolmethane four (methyl) acrylate, ethoxyquin tetramethylolmethane four (methyl) acrylate; The example of described polyfunctional group crosslinking coagent includes, but is not limited to: Dipentaerythritol five (methyl) acrylate.In this article, " (methyl) acrylate " refers to acrylate or methacrylic ester.These crosslinking coagents can use in the mode of arbitrary combination, as long as they contribute to crosslinked under irradiation.
The add-on of the above crosslinking coagent is generally 0.1 ~ 10% weight of dry glue weight in latex.Be preferably 0.5 ~ 9% weight, be more preferably 0.7 ~ 7% weight.
The energetic ray source of described irradiation is selected from cobalt source, ultraviolet or high-energy electron accelerator, preferred cobalt source.The dosage of irradiation can be 0.1 ~ 30Mrad, preferably 0.5 ~ 20Mrad.Generally, the rubber particles gel content after irradiation dose should make rubber latex cross-linking radiation reaches 60% weight or higher, preferably 75% weight or higher, more preferably 80% weight or higher.
Thus, in the rubber combination obtained with coalescence after common uncrosslinked styrene butadiene rubber latex mixing by the paracril latex after this kind of cross-linking radiation, be dispersed in the paracril particle dispersion phase in the external phase of uncrosslinked rubber formation, also there is the characteristic of the full vulcanised nitrile powdered rubber disclosed in WO01/40356.Namely this kind has the rubber particles of crosslinking structure is that gel content reaches 60% weight or higher, and more excellent is 75% weight or higher rubber particles.Each particulate that this kind has in the paracril particle of crosslinking structure is homogeneous phase, and namely single particulate is all homogeneous on composition, does not find the phenomenon of layering, point equal uneven phase under the observation of existing microtechnique in particulate.This paracril particle with crosslinking structure is by fixing corresponding paracril latex cross-linking radiation rubber particles particle diameter, and its particle diameter is consistent with the particle diameter of the latex particle in original paracril latex.The median size of the rubber particles (latex particle) in original paracril latex is generally 50 ~ 200nm, is preferably 70 ~ 200nm, more preferably 80 ~ 180nm.The median size with the rubber particles of crosslinking structure after cross-linking radiation is also generally 50 ~ 200nm, is preferably 70 ~ 200nm, more preferably 80 ~ 180nm.Mix and coalescence owing to utilizing two kinds of latex in the method, in paracril latex after cross-linking radiation, paracril particle is cross-linked, there is certain gel content, can not in latex coalescence process adhesion or coalescence, and can be uniformly dispersed in uncrosslinked styrene-butadiene rubber(SBR), therefore, in the rubber combination finally obtained, wherein as the median size with the rubber particles of crosslinking structure of disperse phase also at 50 ~ 200nm, be preferably 70 ~ 200nm, in the scope of more preferably 80 ~ 180nm.
The present invention is total to coalescence according to described weight ratio by after the paracril latex mixing after uncrosslinked styrene butadiene rubber latex, cross-linking radiation, prepares this rubber combination.In its preparation process, the mixing equipment used at two kinds of rubber latex mixing steps is exactly conventional mixing equipment, is selected from homogenizer of the prior art, kneader etc. mechanical mixing equipment.The coalescence condition of latex and equipment just adopt latex coalescence condition conventional in existing rubber industry and equipment.
Never the rubber combination of the present invention that prepared by cross-linked rubber latex and the rubber latex mixing coalescence of the rubber particles with crosslinking structure also can containing weighting agent conventional in rubber processing.Following substances is the weighting agent suitable especially of preparation rubber unvulcanizate of the present invention and vulcanized rubber, comprises a kind of in carbon black, white carbon black, metal oxide, silicate, carbonate, vitriol, oxyhydroxide, glass fibre or glass microballon etc. or its mixture.At least one in wherein said metal oxide preferential oxidation titanium, aluminum oxide, magnesium oxide, calcium oxide, barium oxide and zinc oxide etc.Can also containing auxiliary agent conventional in the Rubber processing sulfidations such as such as linking agent, vulcanization accelerator, antioxidant, thermo-stabilizer, photostabilizer, ozone stabilizers, processing aid, softening agent, tenderizer, anti blocking agent, whipping agent, dyestuff, pigment, wax, extender, organic acid, fire retardant and coupling agent in rubber combination of the present invention.Adjuvant used consumption is conventional amount used, or adjusts according to the requirement of practical situation.
Adding of above-described various auxiliary agent just can add when two kinds of rubber latex mixing, also can be added by the common calendering process of rubber after two kinds of rubber latex mixing coalescences, equipment can adopt method conventional in rubber industry and conventional mixing facilities, can make mill, Banbury mixer, single screw extrusion machine or twin screw extruder etc.
By the cross-linked rubber of the preparation of rubber combination of the present invention, include by described mass ratio range, sulfuration styrene-butadiene rubber(SBR) matrix and be dispersed in the paracril particle with crosslinking structure wherein with described median size.
Specifically, the Micro of rubber combination of the present invention is as previously mentioned: described uncrosslinked styrene-butadiene rubber(SBR) is external phase, and the described paracril particle with crosslinking structure is disperse phase, and disperses with the fine particle size of 50 ~ 200nm.In the cross-linked rubber that this rubber combination obtains, still there is identical microtexture.
Cross-linked rubber prepared by rubber combination of the present invention, can sulfuration in the sulfur cross-linking system of routine or non-sulfur cross-linking system not by the impact of vulcanization system.The cross-linked rubber prepared of rubber combination of the present invention by the impact of sulfuration process, can compression molding, injection sulfurization, sulfurizing pot vulcanization, individual vulcanizer sulfuration, the sulfuration of congruent melting salt, fluidized bed vulcanization, microwave vulcanization and energetic ray sulfuration etc.
Prepare conventional method and conventional mixing facilities in the mixing of cross-linked rubber and sulfidation employing rubber industry by rubber combination of the present invention, mill, Banbury mixer, single screw extrusion machine or twin screw extruder etc. can be made.
Rubber combination of the present invention as solid rubber master batch, then can also obtain rubber unvulcanizate with uncrosslinked niggerhead by blending technologies such as Banbury mixer, end runner mill, screw extrusion presss.Such as, the method of irradiation is adopted to be cross-linked in paracril latex, the rubber particles in latex is made to have crosslinking structure, then by the rubber latex after cross-linking radiation with after mixing on conventional mixing equipment with uncrosslinked rubber latex, the conventional coalescence method coalescence of rubber latex is adopted to obtain solid rubber master batch.To be adopted by this solid rubber master batch in rubber industry conventional compounding process to join in uncrosslinked niggerhead again, then add that conventional rubber processing aids is mixing, obtain cross-linked rubber after sulfuration.The rubber unvulcanizate so obtained, also can ensure the dispersion situation in the particle size range that the rubber particles with crosslinking structure of cross-linking radiation reaches described in uncrosslinked rubber matrix.
Be fixed up with the particle diameter of original latex particle owing to being made the rubber particles in paracril latex by cross-linking radiation, so in the sulfidation prepared with follow-up cross-linked rubber in coalescence process, the paracril particle of cross-linking radiation with the fine particle size of 50 ~ 200nm in uncrosslinked styrene-butadiene rubber(SBR), so just have such microscopic pattern, the paracril particle with crosslinking structure just can be made to play effect, solve the covulcanization problem that different rubber exists in sulfidation simultaneously, make the cross-linked rubber anti-slippery of rubber combination of the present invention, rolling resistance and wear resistance can obtain raising simultaneously.
Say further, the vulcanized rubber prepared by rubber combination of the present invention not only has low rolling resistance and excellent resistance to wet skidding performance, has excellent wear resistance simultaneously, can use as high-performance car tread rubber.
The preparation method of rubber combination of the present invention and cross-linked rubber thereof is simple, and processing ease, processing condition are usual conditions, are easy to widespread use.
Accompanying drawing illustrates:
Fig. 1 is Micro transmission electron microscope (TEM) picture of the rubber combination cross-linked rubber that embodiment 1 obtains.
Specific implementation method:
Further describe the present invention by embodiment below, but scope of the present invention is not by the restriction of these embodiments.Scope of the present invention is determined by accompanying claims.
(1) in embodiment, experimental data following plant and instrument and measuring method measures:
(1) rolling resistance: use RSS-II rubber rolling resistance test machine (Beijing all things on earth Yifang Technology Co., Ltd.) to measure rolling power loss.
To under constant load, the garden colyliform rubbery sample of constant motion and wheel hub close contact do relative movement.The surface that rubbery sample contacts with wheel hub produces and is out of shape under pressure load, be out of shape from point of contact increase gradually to intermediate point; A little zero is gradually reduced to leaving again from intermediate point.Due to the viscous-elastic behaviour of various rubber compounding, rubbery sample start between point of contact to intermediate point deformation phases make a concerted effort by than intermediate point to the height of making a concerted effort leaving a recovery period, this power parallel with load forces is the power loss value (J/r) of rubbery sample.The rolling resistance of this rubber compounding can be characterized accordingly.
Rolling resistance index (%): be radix by the rolling resistance measurement value of gum, the percentage ratio that the measured value of other modified adhesive accounts for gum rolling resistance measurement value is rolling resistance index.
(2) wear resisting property test: according to GB/T 1689-1998, adopts WML-76 type Akron abrasion machine to measure the wear(ing)value of cross-linked rubber.
Principle is: sample and emery wheel are rubbed under certain angle of inclination and certain load effect, measure the wear volume of certain mileage.Wear volume is calculated as follows:
V-sample abrasion volume, cm
3
M
1quality before the wearing and tearing of-sample, g
M
2quality after the wearing and tearing of-sample, g
ρ-sample density, cm
3
Sample abrasion Index for Calculation:
V
s--the wear volume of standard recipe rubber.
V
t--the wear volume of modified rubber.
Wear index (%): be radix by the wear volume measured value of gum, the percentage ratio that the wear volume measured value of other modified adhesive accounts for gum measured value is wear index.
(3) dynamic properties test (measuring wet and slippery): DMTAIV (dynamic mechanical analysis instrument) test adopting Rheometric Scientific company of the U.S. to produce, test conditions is 10Hz, 0.5% strain, heat-up rate 2 DEG C/min.
The friction of sizing material on wet structure is relevant with hysteresis loss, and the tan δ at usually adopting 0 DEG C characterizes wet-sliding resistant performance.Tan δ value at 0 DEG C is larger, and the hauling ability of tire on wet road surface is better.
Anti-slippery index (%): be radix by the anti-slippery measured value tan δ of gum, the percentage ratio that the anti-slippery measured value of other modified adhesive accounts for the anti-slippery measured value of gum is anti-slippery index.
(4) mechanical property: measure by related standard requirements.
(5) mensuration of the gel content of cross-linking radiation rubber latex: after nitrile rubber is carried out cross-linking radiation according to certain condition, carry out spraying dry, obtain fully vulcanized powder rubber, then measuring the gel content of full vulcanised nitrile powdered rubber according to method disclosed in international patent application WO01/40356 (priority date on December 3rd, 1999), is exactly the gel content of paracril latex after this cross-linking radiation.
(2) used in embodiment and comparative example raw material:
Emulsion polymerized styrene butadiene rubber latex SBR1502: solid content 20wt%, combined styrene content 23wt%, mooney viscosity 50, rubber plant of Qilu Petrochemical Company produces.
The poly-butylbenzene niggerhead of breast, the trade mark: SBR1500, Nantong chemical industry company limited of China produces.
Paracril latex: the trade mark is NBR-26, Tian Yuan Chemical Co., Ltd. of Zhaodong City produces.
Carbon black: N234 Haitun Carbon Black Co., Ltd. Tianjin
Zinc oxide: commercially available
Stearic acid: commercially available
Sulphur: Linyi City Luo Zhuan chemical plant
Accelerator TBBS: the N-tertiary butyl-2-[4-morpholinodithio time yellow acid amides, chemical plant, Kingsoft, Zhengzhou
Calcium chloride: commercially available
Starch: commercially available
Glycerine: commercially available
5% PHENOL 99.8 MIN ((CARBOLIC ACID)) liquid: commercially available
Dicumyl peroxide: commercially available
(3) latex coalescence method:
According to the recipe configuration coalescence agent solution of table 1, then join in this coalescence agent solution according to the rubber latex with coalescence agent solution identical weight, stir after 15 minutes, filtration, washing, drying, obtain solid rubber (rubber).
Table 1
| Calcium chloride | Starch | Glycerine | 5%wt PHENOL 99.8 MIN ((CARBOLIC ACID)) liquid | Water |
| 8 parts | 0.8 part | 0.3 part | 2 parts | Being adjusted to coalescence agent solution gross weight is 100 parts |
Note: be parts by weight in table 1
(4) preparation of rubber unvulcanizate and the method for sulfuration:
One segment process:
Carry out in Banbury Banbury mixer (Britain Farrel Bridge Products), volume 1.57L, rotor speed 80rmin
-1; Its process is: add styrene-butadiene rubber(SBR) rubber or rubber combination of the present invention, carbon black and other auxiliary agents (sulphur, promotor, except), put down floating weight, mixing 3min.Binder removal (temperature is at 150 ~ 160 DEG C).
Two step process:
Thin-pass is gone up six times in XK-160 type mill (Shanghai rubber machinery plant product), bottom sheet afterwards after above-mentioned one section of rubber master batch being added sulphur, promotor.Then at 160 DEG C, sulfurizing time T is pressed
90sulfuration, then makes standard batten by vulcanized rubber print, carries out every Mechanics Performance Testing, and its result is as shown in table 3.The formula of rubber unvulcanizate is in table 2, and unit is parts by weight.
Embodiment 1
1, the preparation of cross-linking radiation paracril latex
Be in the paracril latex (NBR-26) of 45%wt at solid content, after adding crosslinking coagent Viscoat 295 by the 3%wt of nitrile rubber solid content, carry out cross-linking radiation, irradiation dose is 3.0Mrad, obtain the paracril latex of cross-linking radiation, the median size 100nm of the paracril particle of cross-linking radiation in latex, gel content is 91%.
2, join in uncrosslinked emulsion polymerized styrene butadiene rubber latex SBR1502 by the paracril latex after cross-linking radiation according to certain solid content ratio, the paracril latex solid content wherein after cross-linking radiation and uncrosslinked emulsion polymerized styrene butadiene rubber latex solid content weight ratio are 5: 95.After agitator high speed stirs 15 minutes, obtain solid rubber composition according to aforementioned latex coalescence method coalescence.Wherein the composition of coalescence agent solution is with table 1.
3, above-mentioned gained rubber combination being added related auxiliaries carries out mixing, obtains rubber unvulcanizate, its formula composition with weight parts in table 2, the preparation of rubber unvulcanizate and vulcanization process ditto described in.Then vulcanized rubber print is made standard batten, carry out every Mechanics Performance Testing, its result is as shown in table 3.
In addition, the observation in the Micro transmission electron microscope picture of final sample with the rubber particles deployment conditions of cross-linking result is affected in order to prevent the carbon black in the sulfurizing formula of step 3 and zinc oxide and sulphur, rubber combination step 2 obtained is by peroxide vulcanizing system sulfuration, concrete formula is: in this rubber combination, add dicumyl peroxide, with rubber combination 100 parts by weight, dicumyl peroxide is 1.5 parts.The preparation of rubber unvulcanizate and vulcanization process ditto described in, the cross-linked rubber sample obtained is cut into the thick ultrathin section(ing) being about 0.1 μm through cryoultramicrotome, then after dyeing 3 minutes in perosmic anhydride steam, make Micro transmission electron microscope (TEM) picture, in such perosmic anhydride steam under dyeing condition, the dyeing of paracril particle is more shallow, can come with the external phase styrene-butadiene rubber(SBR) difference of dark color.See accompanying drawing 1, paracril particle disperses in styrene-butadiene rubber(SBR) external phase with median size 100nm.
Embodiment 2
Only have the paracril latex solid content after described cross-linking radiation and uncrosslinked emulsion polymerized styrene butadiene rubber latex solid content weight ratio to change 7: 93 into, other is identical with embodiment 1, and the rubber unvulcanizate formula composition of concrete rubber combination lists in table 2.Cured properties is in table 3.
Comparative example 1
Change latex into simple employing emulsion polymerized styrene butadiene rubber latex SBR1502 by the two kinds of latex mixed, other is identical with embodiment 1, and the rubber unvulcanizate formula composition of concrete rubber combination lists in table 2.Cured properties is in table 3.
Table 2 comparative example and Example formulations
| Title material | Comparative example 1 | Embodiment 1 | Embodiment 2 |
| *SBR1502 | 100 | 95 | 93 |
| Cross-linking radiation paracril | - | 5 | 7 |
| 3 #Carbon black | 50 | 50 | 50 |
| Zinc oxide | 3 | 3 | 3 |
| Stearic acid | 1 | 1 | 1 |
| Sulphur | 1.75 | 1.75 | 1.75 |
| TBBS | 1 | 1 | 1 |
| Add up to | 156.75 | 156.75 | 156.75 |
The salient features of table 3 comparative example and embodiment
| Project | Comparative example 1 | Embodiment 1 | Embodiment 2 | Testing standard |
| Hardness (Shao Er A) | 70 | 71 | 71 | GB/T531.1-2008 |
| 100% stress at definite elongation/MPa | 3.24 | 4.09 | 3.7 | GB/T528-1998 |
| 300% stress at definite elongation/MPa | 18.0 | 23.0 | 20.6 | GB/T528-1998 |
| Tensile strength/MPa | 26.4 | 25.1 | 26.8 | GB/T528-1998 |
| Compression fatigue temperature rise/DEG C | 38.25 | 37.45 | 39.45 | GB/T1687-1993 |
| Rebound resilience/% | 50 | 49 | 49 | GB/T1681-2009 |
| Rolling resistance index/% | 100 | 95.5 | 99.2 | - |
| Wear index/% | 100 | 85.6 | 94.4 | GB/T1689-1998 |
| Anti-slippery index/% | 100 | 124 | 124 | - |
As can be seen from Table 3, adopt the raising that the rolling resistance index of its cross-linked rubber of rubber combination of the present invention, wear index, anti-slippery index can obtain simultaneously, its reason is exactly that the paracril particle with crosslinking structure after cross-linking radiation is dispersed in the styrene-butadiene rubber(SBR) matrix of external phase with the fine particle size of 50 ~ 200nm.This characteristic of rubber combination of the present invention is especially suitable for use as automobile tread rubber.
Claims (8)
1. a rubber combination, comprises uncrosslinked rubber and is dispersed in the rubber particles with crosslinking structure wherein; The rubber particles wherein with crosslinking structure is paracril particle, and average mark shot footpath is 50 ~ 200nm, and gel content is 60% weight or higher; Wherein uncrosslinked rubber is styrene-butadiene rubber(SBR); The weight ratio of the described rubber particles and uncrosslinked rubber with crosslinking structure is 1 ︰ 99-20 ︰ 80; Described composition comprise uncrosslinked rubber latex is mixed with the component of latex of the rubber particles with crosslinking structure after coalescence and obtaining; The latex wherein with the rubber particles of crosslinking structure is the rubber latex obtained after cross-linking radiation.
2. rubber combination according to claim 1, the rubber particles described in it is characterized in that with crosslinking structure is equal phase structure.
3. rubber combination according to claim 1, the gel content described in it is characterized in that with the rubber particles of crosslinking structure is 75% weight or higher.
4. rubber combination according to claim 1, the median size described in it is characterized in that with the rubber particles of crosslinking structure is 70 ~ 200nm.
5. rubber combination according to claim 1, the weight ratio of the rubber particles and uncrosslinked rubber described in it is characterized in that with crosslinking structure is 1 ︰ 99-10 ︰ 90.
6. rubber combination according to claim 5, the weight ratio of the rubber particles and uncrosslinked rubber described in it is characterized in that with crosslinking structure is 3 ︰ 97-8 ︰ 92.
7. a preparation method for the rubber combination according to any one of claim 1 ~ 6, comprises the following steps:
(1) by paracril latex through cross-linking radiation, make the paracril particle in latex have crosslinking structure, reach described gel content, and make the paracril particle in latex be fixed in described average particle size range;
(2) then have the rubber particles of crosslinking structure and the mass ratio range of uncrosslinked styrene-butadiene rubber(SBR) by described, paracril latex and the uncrosslinked styrene butadiene rubber latex of getting above-mentioned cross-linking radiation carry out being mixed to evenly;
(3) above gained mixing latex is carried out common coalescence and obtain described rubber combination.
8. the cross-linked rubber prepared of the rubber combination according to any one of claim 1 ~ 6, include the sulfuration styrene-butadiene rubber(SBR) matrix by described mass ratio range, and be dispersed in the paracril particle with crosslinking structure in sulfuration styrene-butadiene rubber(SBR) matrix with described median size.
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| CN201110330407.7A CN103073758B (en) | 2011-10-26 | 2011-10-26 | A kind of rubber combination and preparation method thereof and its cross-linked rubber |
| KR1020147012677A KR101748600B1 (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
| JP2014537482A JP6084623B2 (en) | 2011-10-26 | 2012-10-26 | Rubber composition, preparation method thereof and vulcanized rubber |
| SG11201401847UA SG11201401847UA (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
| US14/354,222 US9453122B2 (en) | 2011-10-26 | 2012-10-26 | Rubber composition, preparation method and vulcanized rubber thereof |
| ES12843797T ES2940461T3 (en) | 2011-10-26 | 2012-10-26 | Rubber composition and method of preparation and vulcanized rubber thereof |
| RU2014121110A RU2607581C2 (en) | 2011-10-26 | 2012-10-26 | Rubber mixture, preparation method thereof and cured rubber produced therefrom |
| PL12843797.7T PL2772512T3 (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
| PCT/CN2012/083590 WO2013060290A1 (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
| CA2853513A CA2853513C (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
| TW101139749A TWI546343B (en) | 2011-10-26 | 2012-10-26 | Rubber composition and its preparation method and vulcanized rubber |
| EP12843797.7A EP2772512B1 (en) | 2011-10-26 | 2012-10-26 | Rubber composition and preparation method and vulcanized rubber thereof |
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| CN103788388B (en) * | 2014-01-23 | 2018-01-16 | 怡维怡橡胶研究院有限公司 | It is a kind of to improve rubber elasticity and the method for thermogenesis performance |
| CN105778165A (en) * | 2014-12-16 | 2016-07-20 | 北京橡胶工业研究设计院 | Natural rubber/radiation-crosslinked nitrile-butadiene rubber composite material and preparation method therefor |
| CN108822356B (en) * | 2018-07-13 | 2020-12-15 | 浙江想能睡眠科技股份有限公司 | Rubber material suitable for mattress inflation layer with adjustable hardness and preparation method thereof |
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| EP1149867A2 (en) * | 2000-04-27 | 2001-10-31 | JSR Corporation | Crosslinked rubber particles and rubber compositions |
| CN1342183A (en) * | 1999-11-01 | 2002-03-27 | 东海橡胶工业株式会社 | Rubber vibration isolator and method for producing the same |
| CN101787148A (en) * | 2009-01-22 | 2010-07-28 | 中国科学院化学研究所 | Green tire material containing amphipathic starch derivant and preparation method thereof |
| CN102050972A (en) * | 2009-10-27 | 2011-05-11 | 中国石油化工股份有限公司 | Modified rubber composition and preparation method thereof |
| CN102050973A (en) * | 2009-10-30 | 2011-05-11 | 中国石油化工股份有限公司 | Tread rubber composite material and preparation method thereof |
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| DE10052287A1 (en) * | 2000-10-20 | 2002-04-25 | Bayer Ag | Rubber mixture for vulcanized products, e.g. inserts for run-flat tires, contains uncrosslinked, double bond-containing rubber, crosslinked rubber particles and phenolic resin or starting materials thereof |
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| CN1342183A (en) * | 1999-11-01 | 2002-03-27 | 东海橡胶工业株式会社 | Rubber vibration isolator and method for producing the same |
| EP1149867A2 (en) * | 2000-04-27 | 2001-10-31 | JSR Corporation | Crosslinked rubber particles and rubber compositions |
| CN101787148A (en) * | 2009-01-22 | 2010-07-28 | 中国科学院化学研究所 | Green tire material containing amphipathic starch derivant and preparation method thereof |
| CN102050972A (en) * | 2009-10-27 | 2011-05-11 | 中国石油化工股份有限公司 | Modified rubber composition and preparation method thereof |
| CN102050973A (en) * | 2009-10-30 | 2011-05-11 | 中国石油化工股份有限公司 | Tread rubber composite material and preparation method thereof |
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