JP2009191198A - Rubber composition and method for producing the same - Google Patents
Rubber composition and method for producing the same Download PDFInfo
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- JP2009191198A JP2009191198A JP2008034668A JP2008034668A JP2009191198A JP 2009191198 A JP2009191198 A JP 2009191198A JP 2008034668 A JP2008034668 A JP 2008034668A JP 2008034668 A JP2008034668 A JP 2008034668A JP 2009191198 A JP2009191198 A JP 2009191198A
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- silane coupling
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- 229920001971 elastomer Polymers 0.000 title claims abstract description 83
- 239000005060 rubber Substances 0.000 title claims abstract description 83
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 239000000835 fiber Substances 0.000 claims abstract description 44
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 28
- 229920002678 cellulose Polymers 0.000 claims abstract description 26
- 239000001913 cellulose Substances 0.000 claims abstract description 26
- 239000002121 nanofiber Substances 0.000 claims abstract description 19
- 239000002002 slurry Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000002156 mixing Methods 0.000 claims abstract description 10
- 229920000126 latex Polymers 0.000 claims abstract description 4
- 239000007788 liquid Substances 0.000 claims abstract description 4
- 150000008117 polysulfides Polymers 0.000 claims description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 125000000101 thioether group Chemical group 0.000 claims description 2
- 239000012779 reinforcing material Substances 0.000 abstract description 11
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 7
- 230000003014 reinforcing effect Effects 0.000 description 6
- -1 dimethoxymethylsilyl Chemical group 0.000 description 5
- 238000004073 vulcanization Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 239000007822 coupling agent Substances 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 239000005077 polysulfide Substances 0.000 description 4
- 229920001021 polysulfide Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000007429 general method Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- DVNPFNZTPMWRAX-UHFFFAOYSA-N 2-triethoxysilylethanethiol Chemical compound CCO[Si](CCS)(OCC)OCC DVNPFNZTPMWRAX-UHFFFAOYSA-N 0.000 description 1
- LOSLJXKHQKRRFN-UHFFFAOYSA-N 2-trimethoxysilylethanethiol Chemical compound CO[Si](OC)(OC)CCS LOSLJXKHQKRRFN-UHFFFAOYSA-N 0.000 description 1
- HFGLXKZGFFRQAR-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yltetrasulfanyl)propyl-trimethoxysilane Chemical compound C1=CC=C2SC(SSSSCCC[Si](OC)(OC)OC)=NC2=C1 HFGLXKZGFFRQAR-UHFFFAOYSA-N 0.000 description 1
- LOOUJXUUGIUEBC-UHFFFAOYSA-N 3-(dimethoxymethylsilyl)propane-1-thiol Chemical compound COC(OC)[SiH2]CCCS LOOUJXUUGIUEBC-UHFFFAOYSA-N 0.000 description 1
- DCQBZYNUSLHVJC-UHFFFAOYSA-N 3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCS DCQBZYNUSLHVJC-UHFFFAOYSA-N 0.000 description 1
- ZSFMFCWJHYPFPG-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylthiirane-2-carboxylate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C1(C)CS1 ZSFMFCWJHYPFPG-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- AKQWHIMDQYDQSR-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylthiirane-2-carboxylate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C1(C)CS1 AKQWHIMDQYDQSR-UHFFFAOYSA-N 0.000 description 1
- FYEDERFWOKZDSN-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)SSSSCCC[Si](OCC)(OCC)OCC Chemical compound C(C1=CC=CC=C1)(=O)SSSSCCC[Si](OCC)(OCC)OCC FYEDERFWOKZDSN-UHFFFAOYSA-N 0.000 description 1
- ZSBKFEOSHGFEKJ-UHFFFAOYSA-N C1=CC=C2SC(SSSSCCC[SiH2]C(OC)OC)=NC2=C1 Chemical compound C1=CC=C2SC(SSSSCCC[SiH2]C(OC)OC)=NC2=C1 ZSBKFEOSHGFEKJ-UHFFFAOYSA-N 0.000 description 1
- BBIXUOLACCULAE-UHFFFAOYSA-N CCC[S+]=C(N(C)C)SSSSC(N(C)C)=[S+]CCC Chemical compound CCC[S+]=C(N(C)C)SSSSC(N(C)C)=[S+]CCC BBIXUOLACCULAE-UHFFFAOYSA-N 0.000 description 1
- SXLPVOKGQWNWFD-UHFFFAOYSA-N CCO[Si](CC[S+]=C(N(C)C)SSSSC(N(C)C)=[S+]CC[Si](OCC)(OCC)OCC)(OCC)OCC Chemical compound CCO[Si](CC[S+]=C(N(C)C)SSSSC(N(C)C)=[S+]CC[Si](OCC)(OCC)OCC)(OCC)OCC SXLPVOKGQWNWFD-UHFFFAOYSA-N 0.000 description 1
- SKFGZHGVWONCTD-UHFFFAOYSA-N CN(C)C(SSSSC(N(C)C)=[S+]CCC[Si](OC)(OC)OC)=[S+]CCC[Si](OC)(OC)OC Chemical compound CN(C)C(SSSSC(N(C)C)=[S+]CCC[Si](OC)(OC)OC)=[S+]CCC[Si](OC)(OC)OC SKFGZHGVWONCTD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000006237 Intermediate SAF Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- GSYVJAOBRKCNOT-UHFFFAOYSA-N diethoxymethyl-[3-[3-(diethoxymethylsilyl)propyltetrasulfanyl]propyl]silane Chemical compound CCOC(OCC)[SiH2]CCCSSSSCCC[SiH2]C(OCC)OCC GSYVJAOBRKCNOT-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- ASAOXGWSIOQTDI-UHFFFAOYSA-N triethoxy-[2-(2-triethoxysilylethyltetrasulfanyl)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)CCSSSSCC[Si](OCC)(OCC)OCC ASAOXGWSIOQTDI-UHFFFAOYSA-N 0.000 description 1
- FBBATURSCRIBHN-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyldisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC FBBATURSCRIBHN-UHFFFAOYSA-N 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- KLFNHRIZTXWZHT-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltrisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSCCC[Si](OCC)(OCC)OCC KLFNHRIZTXWZHT-UHFFFAOYSA-N 0.000 description 1
- JSXKIRYGYMKWSK-UHFFFAOYSA-N trimethoxy-[2-(2-trimethoxysilylethyltetrasulfanyl)ethyl]silane Chemical compound CO[Si](OC)(OC)CCSSSSCC[Si](OC)(OC)OC JSXKIRYGYMKWSK-UHFFFAOYSA-N 0.000 description 1
- JTTSZDBCLAKKAY-UHFFFAOYSA-N trimethoxy-[3-(3-trimethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CO[Si](OC)(OC)CCCSSSSCCC[Si](OC)(OC)OC JTTSZDBCLAKKAY-UHFFFAOYSA-N 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
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Abstract
Description
本発明は、ゴム組成物及びその製造方法に関するものであり、より詳細には、充填補強材である繊維の分散性を高め、耐久性及び剛性に優れた補強ゴム及びそれを用いたタイヤ等のゴム製品を提供することのできるゴム組成物及びその製造方法に関するものである。 TECHNICAL FIELD The present invention relates to a rubber composition and a method for producing the same, and more specifically, a reinforcing rubber excellent in durability and rigidity, a tire using the same, and the like, which improves dispersibility of fibers as a filling reinforcing material. The present invention relates to a rubber composition capable of providing a rubber product and a method for producing the same.
タイヤ製品等のゴムは一般に、カーボンブラック、シリカ等の粒状無機補強材を添加して、その強度及び剛性を高めている。しかし、このような粒状無機補強材はその形状に起因する理由でその補強性能に限界が見られる。そこで、ゴムの補強材として短繊維を選択して硬度やモジュラスなどを向上させる技術が提案されている(例えば、特許文献1を参照)。また、0.5〜1000μmのアラミド短繊維を含むマスターバッチをタイヤゴムに利用することが提案されている(例えば、特許文献2)。更に、ゴムにセルロース繊維を複合化させたゴム組成物が提案されている(例えば、特許文献3を参照)。 In general, rubber such as tire products is added with a granular inorganic reinforcing material such as carbon black or silica to increase its strength and rigidity. However, such a granular inorganic reinforcing material has a limit in its reinforcing performance because of its shape. Therefore, a technique has been proposed in which short fibers are selected as a rubber reinforcing material to improve hardness, modulus, and the like (see, for example, Patent Document 1). In addition, it has been proposed to use a master batch containing aramid short fibers of 0.5 to 1000 μm for tire rubber (for example, Patent Document 2). Furthermore, a rubber composition in which cellulose fibers are combined with rubber has been proposed (see, for example, Patent Document 3).
ところで、繊維、例えばセルロース系繊維をゴム補強材とした場合、親水性のセルロースと疎水性のゴムを複合化させたものでは、補強材のゴムへの分散性が悪く十分な耐久性及び剛性を発揮できない。また繊維/ゴム界面の接着性或いは粘着性も十分ではない。このため、ゴムが機械的応力を受けた場合に、繊維の離脱、或いは剥離が起こり、十分な強度及び耐久性が得られない。
従って、本発明は、セルロース系繊維からなる補強材のゴム成分への分散性及び接着性を高めて十分な耐久性及び剛性を発揮するゴム組成物及びその製造方法を提供することにある。
By the way, when a fiber such as a cellulose-based fiber is used as a rubber reinforcing material, a composite of hydrophilic cellulose and hydrophobic rubber has a poor dispersibility in the rubber of the reinforcing material and has sufficient durability and rigidity. I can't show it. Also, the adhesiveness or tackiness at the fiber / rubber interface is not sufficient. For this reason, when the rubber is subjected to mechanical stress, separation or peeling of the fiber occurs, and sufficient strength and durability cannot be obtained.
Accordingly, it is an object of the present invention to provide a rubber composition that exhibits sufficient durability and rigidity by enhancing dispersibility and adhesiveness of a reinforcing material composed of cellulosic fibers to a rubber component, and a method for producing the same.
本発明者は、上記課題を解決するため鋭意検討したところ、セルロース系繊維として、平均繊維径がナノオーダのセルロースナノ繊維をゴムの補強材とすると共に、かかる補強材にシランカップリング剤を配合することにより、ゴム成分への分散性を高め、更に、カップリング剤をポリスルフィド構造を持ったスルフィド系シランカップリング剤とすることにより、ゴム成分との界面での接着性及び粘着性を高めることが期待できることを見出し、本発明を完成するに至った。 The present inventor has intensively studied to solve the above problems. As a cellulose-based fiber, cellulose nanofiber having an average fiber diameter of nano-order is used as a rubber reinforcing material, and a silane coupling agent is added to the reinforcing material. By increasing the dispersibility in the rubber component, and further using a sulfide-based silane coupling agent having a polysulfide structure as the coupling agent, the adhesiveness and tackiness at the interface with the rubber component can be increased. The present inventors have found that it can be expected and have completed the present invention.
即ち、本発明に係るゴム組成物及びその製造方法は、以下の(1)乃至(7)に記載される構成或いは手段を特徴とするものである。 That is, the rubber composition and the manufacturing method thereof according to the present invention are characterized by the configuration or means described in the following (1) to (7).
(1).ゴム成分中に、セルロースナノ繊維及びシランカップリング剤を含むゴム組成物。 (1). A rubber composition comprising cellulose nanofibers and a silane coupling agent in a rubber component.
(2).上記セルロースナノ繊維は、平均繊維径が1〜1000nmの範囲にあり、平均繊維長さが0.1〜100μmの範囲にある上記(1)記載のゴム組成物。
(3).上記セルロースナノ繊維はゴム成分100質量部に対して、1〜50の範囲で含まれる上記(1)又は(2)記載のゴム組成物。
(4).上記シランカップリング剤は、セルロースナノ繊維に対して0.05〜20質量%の範囲で含まれる上記(1)〜(3)に記載のゴム組成物。
(5).上記シランカップリング剤は、硫黄数Xが2〜10のポリスルフィド構造を有するスルフィド系シランカップリング剤である上記(1)〜(4)に記載のゴム組成物。
(2). The said cellulose nanofiber is a rubber composition of the said (1) description whose average fiber diameter exists in the range of 1-1000 nm, and whose average fiber length exists in the range of 0.1-100 micrometers.
(3). The said cellulose nanofiber is a rubber composition of the said (1) or (2) description contained in the range of 1-50 with respect to 100 mass parts of rubber components.
(4). The said silane coupling agent is a rubber composition as described in said (1)-(3) contained in 0.05-20 mass% with respect to a cellulose nanofiber.
(5). The rubber composition according to (1) to (4), wherein the silane coupling agent is a sulfide-based silane coupling agent having a polysulfide structure having a sulfur number X of 2 to 10.
(6).上記(1)〜(5)に記載のゴム組成物の製造方法において、ゴムラテックスと、水に分散させた上記繊維のスラリーとを混合した後、混合液を乾燥して水を除去して得ることを特徴とするゴム組成物の製造方法。
(7).上記スラリーに上記シランカップリング剤を添加する上記(6)記載のゴム組成物の製造方法。
(6). In the method for producing a rubber composition according to the above (1) to (5), after mixing a rubber latex and a slurry of the fiber dispersed in water, the mixture is dried to remove water. A process for producing a rubber composition, characterized in that
(7). The method for producing a rubber composition according to (6), wherein the silane coupling agent is added to the slurry.
本発明のゴム組成物は、親水性であるセルロースナノ繊維と疎水性であるゴム成分とをシランカップリング剤を介することで分散性を良好にすることが可能となるため、補強性が向上する。また、シランカップリング剤が硫黄を含有すると、カップリング剤内の硫黄部分でも架橋することが可能となるため、繊維とゴムの接着性が向上し、強度を増大させることができる。 In the rubber composition of the present invention, it becomes possible to improve the dispersibility by allowing the cellulose nanofibers that are hydrophilic and the rubber component that is hydrophobic to pass through a silane coupling agent, so that the reinforcing property is improved. . Further, when the silane coupling agent contains sulfur, it is possible to crosslink even the sulfur portion in the coupling agent, so that the adhesion between the fiber and the rubber is improved and the strength can be increased.
以下、本発明に係る好ましい実施するための最良形態を詳述する。尚、本発明は以下の実施形態及び実施例に限るものではない。
本発明に係るゴム組成物は、ゴム成分に、平均繊維径がナノオーダのセルロースナノ繊維及びシランカップリング剤を含む。
BEST MODE FOR CARRYING OUT THE INVENTION Preferred embodiments for carrying out the present invention will be described in detail below. Note that the present invention is not limited to the following embodiments and examples.
The rubber composition according to the present invention contains cellulose nanofibers having an average fiber diameter of nano-order and a silane coupling agent in the rubber component.
本発明に係るゴム組成物のゴム成分は特に限定されないが、タイヤ製品等に使用することができるものとしては、例えば、以下のゴム成分を挙げることができる。
ゴム組成物のゴム成分は大別して、天然ゴム、及び合成ゴムから選択され、両者を混合使用しても良い。合成ゴムは、特に制限はなく、公知のものの中から目的に応じて適宜選択することができ、ジエン系ゴムが好ましく、スチレン−ブタジエン共重合体(SBR)、ポリイソプレン(IR)、ポリブタジエン(BR)、アクリロニトリル−ブタジエンゴム、クロロプレンゴム、及びブチルゴム等がある。
The rubber component of the rubber composition according to the present invention is not particularly limited, but examples of those that can be used for tire products include the following rubber components.
The rubber component of the rubber composition is roughly classified and selected from natural rubber and synthetic rubber, and both may be used in combination. The synthetic rubber is not particularly limited and can be appropriately selected from known ones according to the purpose. A diene rubber is preferable, and a styrene-butadiene copolymer (SBR), polyisoprene (IR), polybutadiene (BR) is used. ), Acrylonitrile-butadiene rubber, chloroprene rubber, and butyl rubber.
本発明に係るゴム組成物に配合されるセルロースナノ繊維は、平均繊維径が1〜1000nmの範囲で、平均繊維長さが0.1〜100μmの範囲であることが好ましい。特に、セルロースナノ繊維の平均繊維径が1〜500nmの範囲で、平均繊維長さが5〜50μmの範囲であることが更に好ましい。平均繊維粒径及び平均繊維長さが上記範囲未満の場合はその分散性が低下し、また上記範囲を超えると補強性能が低下する。
ここで、平均繊維径及び平均繊維長さは、繊維をエチレングリコール溶液中に分散させ、細孔電気抵抗法(コールター原理法)により計測する。
また、上記セルロースナノ繊維はゴム成分100質量部に対して、1〜50質量部の範囲、特に、3〜20質量部の範囲で含まれることが好ましい。繊維の量が少ないと補強効果が十分でなく、逆に多いとゴムの加工性が悪くなってくる。
The cellulose nanofibers blended in the rubber composition according to the present invention preferably have an average fiber diameter in the range of 1 to 1000 nm and an average fiber length in the range of 0.1 to 100 μm. In particular, the average fiber diameter of cellulose nanofibers is more preferably in the range of 1 to 500 nm, and the average fiber length is more preferably in the range of 5 to 50 μm. When the average fiber particle size and the average fiber length are less than the above ranges, the dispersibility decreases, and when the average fiber particle sizes and average fiber lengths exceed the above ranges, the reinforcing performance decreases.
Here, the average fiber diameter and the average fiber length are measured by a pore electrical resistance method (Coulter principle method) by dispersing fibers in an ethylene glycol solution.
Moreover, it is preferable that the said cellulose nanofiber is contained in the range of 1-50 mass parts with respect to 100 mass parts of rubber components, especially the range of 3-20 mass parts. If the amount of fiber is small, the reinforcing effect is not sufficient, and if the amount is large, the processability of rubber becomes worse.
本発明のゴム組成物に配合されるシランカップリング剤は、それ自体公知なものが挙げられ、例えばビス(3−トリエトキシシリルプロピル)テトラスルフィド、ビス(3−トリエトキシシリルプロピル)トリスルフィド、ビス(3−トリエトキシシリルプロピル)ジスルフィド、ビス(2−トリエトキシシリルエチル)テトラスルフィド、ビス(3−トリメトキシシリルプロピル)テトラスルフィド、ビス(2−トリメトキシシリルエチル)テトラスルフィド、3−メルカプトプロピルトリメトキシシラン、3−メルカプトプロピルトリエトキシシラン、2−メルカプトエチルトリメトキシシラン、2−メルカプトエチルトリエトキシシラン、3−トリメトキシシリルプロピル−N,N−ジメチルチオカルバモイルテトラスルフィド、3−トリエトキシシリルプロピル−N,N−ジメチルチオカルバモイルテトラスルフィド、2−トリエトキシシリルエチル−N,N−ジメチルチオカルバモイルテトラスルフィド、3−トリメトキシシリルプロピルベンゾチアゾリルテトラスルフィド、3−トリエトキシシリルプロピルベンゾリルテトラスルフィド、3−トリエトキシシリルプロピルメタクリレートモノスルフィド、3−トリメトキシシリルプロピルメタクリレートモノスルフィド、ビス(3−ジエトキシメチルシリルプロピル)テトラスルフィド、3−メルカプトプロピルジメトキシメチルシラン、ジメトキシメチルシリルプロピル−N,N−ジメチルチオカルバモイルテトラスルフィド、ジメトキシメチルシリルプロピルベンゾチアゾリルテトラスルフィド等が挙げられる。 Examples of the silane coupling agent blended in the rubber composition of the present invention include those known per se, such as bis (3-triethoxysilylpropyl) tetrasulfide, bis (3-triethoxysilylpropyl) trisulfide, Bis (3-triethoxysilylpropyl) disulfide, bis (2-triethoxysilylethyl) tetrasulfide, bis (3-trimethoxysilylpropyl) tetrasulfide, bis (2-trimethoxysilylethyl) tetrasulfide, 3-mercapto Propyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltrimethoxysilane, 2-mercaptoethyltriethoxysilane, 3-trimethoxysilylpropyl-N, N-dimethylthiocarbamoyl tetrasulfide, 3-to Riethoxysilylpropyl-N, N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilylethyl-N, N-dimethylthiocarbamoyl tetrasulfide, 3-trimethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilyl Propyl benzoyl tetrasulfide, 3-triethoxysilylpropyl methacrylate monosulfide, 3-trimethoxysilylpropyl methacrylate monosulfide, bis (3-diethoxymethylsilylpropyl) tetrasulfide, 3-mercaptopropyldimethoxymethylsilane, dimethoxymethylsilyl Examples thereof include propyl-N, N-dimethylthiocarbamoyl tetrasulfide and dimethoxymethylsilylpropylbenzothiazolyl tetrasulfide.
上記シランカップリング剤は、セルロースナノ繊維に対して0.05〜50質量%の範囲、特に、1〜20質量%の範囲で含まれることが好ましい。シランカップリング剤の量が少ないと、配合効果が十分でなくなる。また、過剰量では、大幅な性能向上は認められず、コストが上昇する。 It is preferable that the said silane coupling agent is contained in the range of 0.05-50 mass% with respect to a cellulose nanofiber, especially 1-20 mass%. When the amount of the silane coupling agent is small, the blending effect is not sufficient. On the other hand, if the amount is excessive, no significant performance improvement is observed and the cost increases.
本発明にあっては、特に、上述のシランカップリング剤の中では、硫黄数Xが2〜10のポリスルフィド構造を有するスルフィド系シランカップリング剤が好ましい。
例えば、ビス−トリエトキシシリルアルキルポリスルフィドにあっては、ポリスルフィドの硫黄数Xは、2〜10個、更に好ましいは3〜7個である。また、アルキル鎖は、2〜4の範囲が好ましい。例えば、ビス−(3−トリエトキシシリルプロピルポリスルフィドを一般式(1)で表すと、以下のように表される。
In the present invention, a sulfide-based silane coupling agent having a polysulfide structure having a sulfur number X of 2 to 10 is particularly preferable among the above-described silane coupling agents.
For example, in a bis-triethoxysilylalkyl polysulfide, the polysulfide has a sulfur number X of 2 to 10, more preferably 3 to 7. The alkyl chain is preferably in the range of 2-4. For example, bis- (3-triethoxysilylpropyl polysulfide is represented by the following general formula (1).
このような以下のポリスルフィド構造を有するスルフィド系シランカップリング剤を配合すると、図1で示すセルロース構造分子の−OHが図2に示すようにシランカップリング結合すると共に、カップリング剤内の硫黄部分でもゴム成分と架橋することが可能となるため、繊維とゴムの接着性、密着性が向上し、強度を増大させることができる。 When such a sulfide-based silane coupling agent having the following polysulfide structure is blended, -OH of the cellulose structure molecule shown in FIG. 1 binds to a silane coupling as shown in FIG. 2, and a sulfur moiety in the coupling agent. However, since it becomes possible to crosslink with the rubber component, the adhesion and adhesion between the fiber and the rubber are improved, and the strength can be increased.
次に、本発明においてゴム組成物を製造するには、先ず、上記繊維を水に分散させた後に、叩解させ、オリフィスを通過させ、適宜機械的せん断を加えて、高圧ホモジナイザーなどで分散させてスラリー化する。実際には各種繊維径の繊維が市販されており、本発明ではこれらを水中にスラリー化して用いる。かかる場合のスラリーにおける上記繊維の濃度は製造操作上、水100質量部に対して、0.1〜3質量部の範囲であることが好ましい。また本発明のシランカップリング剤、特に、スルフィド系シランカップリング剤は、上記スラリーを固化させた後にインテグラルブレンド法により、ゴム混練時に直接添加することが好ましく、混練のせん断混合によりカップリング剤のシリル基部分をセルロースの−OH基と反応させ、更にゴム−セルロース界面の化学結合を促進させる方法が望ましい。 Next, in order to produce a rubber composition in the present invention, first, the fibers are dispersed in water and then beaten, passed through an orifice, appropriately mechanically sheared, and dispersed with a high-pressure homogenizer or the like. Slurry. Actually, fibers having various fiber diameters are commercially available, and in the present invention, these are used after being slurried in water. In this case, the concentration of the fiber in the slurry is preferably in the range of 0.1 to 3 parts by mass with respect to 100 parts by mass of water in terms of manufacturing operation. Further, the silane coupling agent of the present invention, in particular, the sulfide-based silane coupling agent is preferably added directly at the time of rubber kneading by the integral blending method after solidifying the slurry, and the coupling agent by kneading shear mixing. A method of reacting the silyl group portion of the silyl group with the —OH group of cellulose and further promoting chemical bonding at the rubber-cellulose interface is desirable.
本発明に従ってゴムラテックス及び繊維、シランカップリング剤のスラリーを混合する方法には特に限定はなく、例えばホモジナイザー、ロータリー撹拌装置、電磁撹拌装置、プロペラ式撹拌装置等の一般的方法によることができる。
本発明において、混合液から水を除去するのには、例えば、オーブン乾燥、凍結乾燥、噴露乾燥などの一般的方法によることができる。
本発明における上記混合液の固形分濃度には特に限定はないが、40質量%以下であるのが好ましく、更に5〜15質量部の範囲にあるのが好ましい。この固形分濃度が40質量%を超えると、混合液の粘度が高くなり過ぎ、繊維の分散性が低下する。
The method of mixing the slurry of rubber latex, fiber, and silane coupling agent according to the present invention is not particularly limited, and for example, a general method such as a homogenizer, a rotary stirrer, an electromagnetic stirrer, or a propeller stirrer can be used.
In the present invention, water can be removed from the mixed solution by a general method such as oven drying, freeze drying, or spray drying.
Although there is no limitation in particular in solid content concentration of the said liquid mixture in this invention, it is preferable that it is 40 mass% or less, and it is preferable that it exists in the range of 5-15 mass parts. When this solid content concentration exceeds 40 mass%, the viscosity of a liquid mixture will become high too much and the dispersibility of a fiber will fall.
本発明のゴム組成物は、上記の配合成分の他に、ゴム工業で通常使用されている種々の成分を含むことができる。例えば、種々の成分として、充填剤(例えば、シリカ等の補強性充填剤;並びに炭酸カルシウム及び炭酸カルシウムなどの無機充填剤);加硫促進剤;老化防止剤;酸化亜鉛;ステアリン酸;軟化剤;及びオゾン劣化防止剤等の添加剤を挙げることができる。なお、加硫促進剤として、M(2−メルカプトベンゾチアゾール)、DM(ジベンゾチアジルジスルフィド)及びCZ(N−シクロヘキシル−2−ベンゾチアジルスルフェンアミド)等のチアゾール系加硫促進剤;TT(テトラメチルチウラムスルフィド)等のチウラム系加硫促進剤;並びにDPG(ジフェニルグアニジン)等のグアニジン系の加硫促進剤等を挙げることができる。 The rubber composition of the present invention can contain various components usually used in the rubber industry in addition to the above-described compounding components. For example, as various components, fillers (for example, reinforcing fillers such as silica; and inorganic fillers such as calcium carbonate and calcium carbonate); vulcanization accelerators; anti-aging agents; zinc oxide; stearic acid; And additives such as an ozone degradation inhibitor. As vulcanization accelerators, thiazole vulcanization accelerators such as M (2-mercaptobenzothiazole), DM (dibenzothiazyl disulfide) and CZ (N-cyclohexyl-2-benzothiazylsulfenamide); TT And thiuram vulcanization accelerators such as (tetramethylthiuram sulfide); and guanidine vulcanization accelerators such as DPG (diphenylguanidine).
具体的には、ゴム組成物はゴム成分100質量部に対して硫黄を7.0質量部以下に配合することができる。特に、3.0〜7.0質量部の範囲、更に好ましくは4.0〜6.0質量部の範囲である。ゴム組成物はゴム成分100質量部に対して有機酸コバルト塩を1.0質量部以下に配合することができる。特に、0.05〜1.0質量部の範囲、更に好ましくは0.3〜〜0.8質量部の範囲である。上記コバルト有機酸塩としては、ナフテン酸コバルト、ロジン酸コバルト、或いは炭素数が5乃至20程度の直鎖状或いは分岐鎖のモノカルボン酸コバルト塩等を挙げることができる。
またゴム組成物に、上記ゴム成分100質量部に対してカーボンブラックが40質量部以上、更には40乃至100質量部、特に、50乃至100質量部配合させることが好ましい。カーボンブラックは、通常ゴム業界で用いられるものから適宜選択することができ、例えば、SRF、GPF、FER、HAF、ISAF等を挙げることができるが、中でもGPF、HAFが物性とコストのバランスの面から好ましい。
Specifically, the rubber composition can contain 7.0 parts by mass or less of sulfur with respect to 100 parts by mass of the rubber component. In particular, it is the range of 3.0-7.0 mass parts, More preferably, it is the range of 4.0-6.0 mass parts. In the rubber composition, the organic acid cobalt salt can be blended in an amount of 1.0 part by mass or less based on 100 parts by mass of the rubber component. In particular, it is the range of 0.05-1.0 mass part, More preferably, it is the range of 0.3-0.8 mass part. Examples of the cobalt organic acid salt include cobalt naphthenate, cobalt rosinate, or a linear or branched monocarboxylic acid cobalt salt having about 5 to 20 carbon atoms.
Further, it is preferable to add 40 parts by mass or more, more preferably 40 to 100 parts by mass, particularly 50 to 100 parts by mass of carbon black to 100 parts by mass of the rubber component in the rubber composition. Carbon black can be appropriately selected from those usually used in the rubber industry, and examples thereof include SRF, GPF, FER, HAF, ISAF, etc. Among them, GPF and HAF are in terms of balance between physical properties and cost. To preferred.
以上の如く構成されるゴム組成物にあっては、セルロースナノ繊維の配合により、スラリーでの分散性が均一となり、シランカップリング剤の配合によって、ゴムへの分散性が高まる。特にポリスルフィド構造を含むシランカップリング剤の配合では分散性及びゴムへの親和性、接着性が高まり、補強性が一層向上することができる。 In the rubber composition configured as described above, dispersibility in the slurry becomes uniform by blending cellulose nanofibers, and dispersibility in rubber is enhanced by blending the silane coupling agent. In particular, when a silane coupling agent containing a polysulfide structure is blended, dispersibility, affinity to rubber, and adhesion are enhanced, and the reinforcing property can be further improved.
次に、実施例、比較例により、本発明を更に詳細に説明するが、本発明はこれらに制約されるものではない。 Next, although an Example and a comparative example demonstrate this invention further in detail, this invention is not restrict | limited to these.
天然ゴムラテックス(固形分濃度:60質量%)200g、セルロース繊維スラリー(ダイセル化学社製「セリッシュ」:平均繊維径100nm、平均繊維長45μm、固形分濃度:5質量%)300g、水1000g、及び下記表1のポリスルフィドシランを、高速混合ホモジナイザー中で毎秒3000回転で5分間混合し、セルロース・天然ゴム混合溶液を得た。
これをバットに展開し、温度100℃オーブン中にて乾燥固化させ、セルロース繊維複合天然ゴムを得た(繊維複合ゴム)。
繊維複合ゴムのゴム成分100質量部に対して、下記の表1に示す構成により、ラボ混練機により通常の混練を行い、得られた混合物を加圧プレス加硫し、厚さ2mmのゴムシートを得た。
評価試験
ゴムシートを所定のダンベルを打ち抜いき、ASTM D412に準じた加硫ゴムの引張り試験を行い、300%モジュラスと破断強度を測定した。測定値は、比較例1の値を100として、それぞれの実施例の値をそのインデックス表示としたものである。
200 g of natural rubber latex (solid content concentration: 60% by mass), 300 g of cellulose fiber slurry (“Serish” manufactured by Daicel Chemical Industries, Ltd .: average fiber diameter: 100 nm, average fiber length: 45 μm, solid content concentration: 5% by mass), 1000 g of water, and Polysulfide silanes shown in Table 1 below were mixed in a high-speed mixing homogenizer at 3000 rpm for 5 minutes to obtain a cellulose / natural rubber mixed solution.
This was developed on a vat and dried and solidified in an oven at a temperature of 100 ° C. to obtain a cellulose fiber composite natural rubber (fiber composite rubber).
With respect to 100 parts by mass of the rubber component of the fiber composite rubber, a normal kneading is performed by a laboratory kneader according to the configuration shown in Table 1 below, the resulting mixture is pressure-press vulcanized, and a rubber sheet having a thickness of 2 mm Got.
Evaluation Test A predetermined dumbbell was punched out of the rubber sheet, and a vulcanized rubber tensile test was performed according to ASTM D412 to measure 300% modulus and breaking strength. The measured values are values in Comparative Example 1 set to 100, and the values in each Example are displayed as indexes.
表中の注1;ダイセル化学社製のセリッシュ KY100G、注2;旭カーボン社製のファーネスブラックHAF、注3;大内新興化学社製のノクセラーDM、注4;大内新興化学社製のノクセラーNS、注5:デグザ社製のSi−69。
本発明のゴム組成物は、セルロース系繊維からなる補強材のゴム成分への分散性及び接着性を高めて十分な耐久性及び剛性を発揮する産業上の利用可能性の高いものである。 The rubber composition of the present invention has high industrial applicability to enhance the dispersibility and adhesiveness of a reinforcing material composed of cellulosic fibers to a rubber component and to exhibit sufficient durability and rigidity.
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