共查询到17条相似文献,搜索用时 437 毫秒
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氯醚橡胶/氟橡胶共混物性能的研究 总被引:1,自引:0,他引:1
初步研究了具有不同共混比的氟橡胶(FKM)/氯醚橡胶(CO)共混物的硫化特性、物理机械性能、耐老化性能和压缩永久变形性能。结果表明:CO用量少于20份时,共混胶拉伸强度、100%定仲应力及压缩永久变形性能与纯FKM相当;当CO用量为20-40份时.共混胶拉伸强度和压缩永久变形性能均急剧下降;当用量高于40份时,趋于缓慢。FKM/CO共混胶耐老化性能保持率达到85%。 相似文献
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TCY/TMTD硫化体系对CO/ECO共混物性能的影响 总被引:1,自引:1,他引:0
研究了三聚硫氰酸(TCY)/二硫化四甲基秋兰姆(TMTD)复合硫化体系对CO/ECO共混物的力学性能、耐热老化性能和高温压缩永久变形性能的影响。结果表明:适当的TCY用量可以获得较好力学性能的CO/ECO共混胶。增加TCY用量可以显著提高共混胶的耐热老化性能和高温压缩永久变形性能;而增加TMTD用量会导致CO/ECO共混胶耐热老化性能和高温压缩永久变形性能下降;二段硫化可以降低共混胶的压缩永久变形。 相似文献
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二段硫化的均聚型/共聚型氯醚共混胶的性能 总被引:1,自引:0,他引:1
研究了二段硫化对均聚型(CO)/共聚型(ECO)氯醚共混胶的力学性能以及高温压缩永久变形的影响:结果表明,采用NA-22硫化体系硫化的CO/ECO共混胶,在合适的二段硫化条件下,可增加硫化胶的拉伸强度,但降低了其扯断伸长认;而采用TCY硫化的共混胶.二段硫化后,硫化胶的拉伸强度基本不变,扯断伸长率减小,二段硫化能明显减少CO/ECO共混胶的高温压缩永久变形,而且在一定范围内.二段硫化时间的延长有利于减少硫化胶的高温压缩永久变形。 相似文献
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硫化体系对CO/ECO共混胶压缩永久变形的影响 总被引:1,自引:0,他引:1
研究了不同硫化体系对CO/ECO共混胶的硫化特性,高温压缩交变形的影响。结果表明,采用三嗪类衍生物硫化体系的CO/ECO共混胶高温压缩永久变形较小,增加硫化剂Na-22或TCY的用量或者对胶料进行二次硫化均能减小胶料高温压缩永久变形。在适当的二次硫化条件下。加入适量的TMTD能减小Na-22硫化的共混胶高温压缩永久变形,TMTD用量过多则增大共混胶高温压缩永久变形,在TCY硫化体系中加入TMTD则使得共混胶高温压缩永久变形增加。 相似文献
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ACM/FKM并用胶的性能研究 总被引:1,自引:0,他引:1
研究了不同并用比的氟橡胶和丙烯酸酯橡胶并用胶的硫化特性、物理机械性能、耐老化性、热稳定性和压缩永久变形性能.结果表明: ACM与FKM可以很好地混合并各自交联,从而制备综合性能优异的并用胶;并用比为30/70时,ACM/FKM并用胶综合性能较佳,二段硫化后其物理机械性能和压缩永久变形性能均明显改善,且耐热空气老化性能优异;热重分析结果表明,并用胶具有很好的热稳定性. 相似文献
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在固定氟橡胶(FKM)硫化体系(双酚AF)的条件下,研究了改变氯醚橡胶(CO)硫化体系对FKM/CO共混物硫化特性以及硫化胶的物理机械性能、耐老化性能、耐油性能及热稳定性的影响。结果表明,采用促进剂NA-22/MgO体系时,FKM/CO共混物具有较好的硫化特性,硫化胶的综合物理机械性能较好,但耐老化性能仍需改善;采用促进剂TCY/MgO/CaCO3体系时需要较长的硫化时间,且焦烧性能较差;并用促进剂TMTD或促进剂DTDM后混炼胶的交联效果变差;FKM/CO共混物具有较好的热稳定性且热失重起始温度高于300℃。 相似文献
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研究了3种硫化助剂对MVQ/EPDM共混胶硫化特性、力学性能、耐热老化性能、高温压缩永久变形性能及动态力学性能的影响。结果表明,添加硫化助剂HVA—2的共混胶焦烧时间和正硫化时间均明显缩短;添加硫化助剂丁羟胶和TAIC的共混胶焦烧时间和正硫化时间均变化不大;添加硫化助剂丁羟胶的共混胶具有最好力学性能、耐热老化性能和压缩永久变形性能,其玻璃化温度也比空白样的低近3℃。 相似文献
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Mechanochemically devulcanized ground fluoroelastomer (FKM) was used as a low‐cost functional additive for the enhancement of the thermal stability of nitrile–butadiene rubber (NBR) vulcanizates. Without the use of any chemicals, the stress‐induced mechanochemical devulcanization of ground FKM was achieved through solid‐state mechanochemical milling at ambient temperature. The sol fraction of the ground FKM was increased from its original 1.4 to 19.8% after milling; this confirmed the realization of the mechanochemical devulcanization of FKM. Moreover, the oxygen‐containing polar groups on the surface of the mechanochemically milled FKM benefitted its interfacial adhesion with the polar NBR matrix. The curing characteristics and mechanical properties of the devulcanized, FKM‐filled NBR vulcanizates were investigated and compared with those of the untreated FKM‐filled NBR vulcanizates. The results show that the mechanical properties of the devulcanized FKM‐filled NBR vulcanizates were much better than those of the untreated FKM‐filled NBR vulcanizates. The presence of the reclaimed FKM significantly increased the onset degradation temperature of the NBR vulcanizates as a result of the improved polymer–filler interaction, uniform dispersion, and high thermal stability of the reclaimed FKM. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
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This article explored the possibility of using silica from fly‐ash particles as reinforcement in natural rubber/styrene–butadiene rubber (NR/SBR) vulcanizates. For a given silica content, the NR : SBR blend ratio of 1 : 1 (or 50 : 50 phr) exhibited the optimum mechanical properties for fly‐ash filled NR/SBR blend system. When using untreated silica from fly‐ash, the cure time and mechanical properties of the NR/SBR vulcanizates decreased with increasing silica content. The improvement of the mechanical properties was achieved by addition of Si69, the recommended dosage being 2.0 wt % of silica content. The optimum tensile strength of the silica filled NR/SBR vulcanizates was peaked at 10–20 phr silica contents. Most mechanical properties increased with thermal ageing. The addition of silica from fly‐ash in the NR/SBR vulcanizates was found to improve the elastic behavior, including compression set and resilience, as compared with that of commercial precipitated silica. Taking mechanical properties into account, the recommended dosage for the silica (FASi) content was 20 phr. For more effective reinforcement, the silica from fly‐ash particles had to be chemically treated with 2.0 wt % Si69. It was convincing that silica from fly‐ash particles could be used to replace commercial silica as reinforcement in NR/SBR vulcanizates for cost‐saving and environment benefits. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
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Kunio Mori Hidetoshi Hirahara Yoshiyuki Oishi Saiso Kim Kosaku Tamura Akira Iwabuchi 《应用聚合物科学杂志》1994,51(1):71-80
Fluorinated (FKM) vulcanizates were treated by immersing in an aqueous solution of triazine thiols, NaOH, and onium salts for 15–60 min at 50–95°C (W-Method). Treated FKM vulcanizates further were postcured in an air oven for 20 h at 200°C to complete the reaction. The onium salt of triazine thiols were found to be formed by a reaction among the triazine thiols, NaOH, and onium salts and to act as cross-linking agents to the surface of FKM vulcanizates. In the acetone solution of onium salts of triazine thiols, FKM vulcanizates were also treated by immersing for a few minutes at 20°C and then by heating in an air oven for 20 min at 200°C (A-Method). Triazine thiols were introduced as crosslinks onto the FKM backbone. The degree of cross-linking in the surface increased by these treatments and the depth of cross-linking reached up to about 40 μm thickness by control of treating conditions. The coefficient of friction in FKM vulcanizates decreased as a result of the surface treatment up to about 0.5 from 2.6. FKM vulcanizates decreased the tensile strength by these surface treatments because of the generation of cracks on the surface at 50% or 100% elongation. The surface treatment of FKM vulcanizates suppressed markedly the fixing between FKM vulcanizates and stainless steel at 150°C. Especially, the A-Method was very effective treating for retarding the fixing between FKM vulcanizates and metals. © 1994 John Wiley & Sons, Inc. 相似文献
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In this study we reported synergic activity of a novel secondary accelerator N‐Benzylimine aminothioformamide (BIAT) along with tetramethylthiuram disulfide (TMTD) in improving cure and mechanical properties of gum and filled mixes of Styrene‐Butadiene Rubber (SBR). The feasibility of application of BIAT in sulfur vulcanization of an ideal blend of SBR and natural rubber (NR) has also been investigated. The mechanical properties like t ensile strength, tear resistance, hardness, compression set, and abrasion loss were measured. Swelling values were also determined as a measure of crosslink densities of the vulcanizates. The binary accelerator system BIAT‐TMTD was found very effective in improving cure properties of the mixes of pure SBR and a 50/50 blend of SBR and NR.There was also found simultaneous improvement in mechanical properties of vulcanizates of both pure and blend. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献