环保促进剂用量对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响

采用环保促进剂Vulcofac ACT 55与硫化剂Diak No 1组成硫化体系,研究了Vulcofac ACT 55用量对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响。结果表明,随着Vulcofac ACT 55用量的增加,共混胶的交联密度先增大后减小,焦烧时间逐渐缩短,硫化反应速率则逐渐增大;共混硫化胶的物理机械性能、耐热老化性能、耐ASTM No 1标准油性能和热稳定性先得到改善后又变差。差示扫描量热研究结果显示,Vulcofac ACT 55用量为2份(质量,下同)时共混硫化胶的耐IRM 903标准油性能最差、玻璃化转变温度最高。动态热机械分析结果显示,Vulcofac ACT 55用量超过2份后共混硫化胶的玻璃化转变温度逐渐降低,而用量不同共混硫化胶处于高弹态时的储能模量相近。     

硫化剂对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响

为提高丙烯酸酯橡胶(ACM)/乙烯丙烯酸酯橡胶(AEM)共混胶的综合性能,采用硫化剂Diak No 1与促进剂Vulcofac ACT 55组成硫化体系,研究了硫化剂用量对ACM/AEM共混胶性能的影响。结果表明,随着Diak No 1用量的增加,共混胶焦烧时间逐渐延长,硫化反应速率逐渐减小;共混胶物理机械性能、耐热老化性能和耐IRM 903标准油性能逐渐提高,压缩永久变形性能先提高后降低。动态力学性能分析和差示扫描量热分析结果表明,随着Diak No 1用量的增加,共混胶的玻璃化转变温度逐渐升高,储能模量逐渐增大。     

炭黑对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响

考察了炭黑种类对丙烯酸酯橡胶(ACM)/乙烯丙烯酸酯橡胶(AEM)共混胶硫化特性、物理机械性能、耐油性能、动态力学性能及热稳定性等的影响。结果表明,与未加入炭黑的试样相比,加入不同种类炭黑后共混胶的最大转矩(M_H)、最小转矩(M_L)及二者之差(M_H-M_L)均显著增大,焦烧时间(t_(10))和正硫化时间(t_(90))均缩短。共混硫化胶的物理机械性能、耐油性能及热稳定性均显著增强,但压缩永久变形变差,玻璃化转变温度均升高,损耗因子峰值均下降。随着炭黑粒径的增大,共混胶的M_H、M_L和M_H-M_L逐渐减小,t_(10)和t_(90)逐渐延长,物理机械性能逐渐变差,但热稳定性及压缩永久变形逐渐升高。加入炭黑N 990的共混硫化胶的热稳定性较差。     

共混比对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响

研究了共混比对丙烯酸酯橡胶(ACM)/乙烯丙烯酸酯橡胶(AEM)共混胶硫化特性、物理机械性能、耐热老化性能、耐油性能、耐低温性能、热稳定性和动态力学性能的影响。结果表明,AEM用量的增加改善了ACM/AEM共混胶的加工安全性能、物理机械性能和热稳定性能,耐热老化性能变化不明显,耐低温性能稍有下降,ACM/AEM共混胶耐ASTM No 1标准油性能变好,耐IRM 903标准油性能变差;当ACM/AEM共混比为60/40时,共混胶的综合性能最佳,能够满足密封圈的性能要求。     

环保型增塑剂对丙烯酸酯橡胶/乙烯丙烯酸酯橡胶共混胶性能的影响

研究了环保型增塑剂RS-107、RS-700、RS-735和TegMeR?812对丙烯酸酯橡胶(ACM)/乙烯丙烯酸酯橡胶(AEM)共混胶性能的影响,结果表明,随着增塑剂的加入,ACM/AEM共混胶的转矩明显下降,不同增塑剂对共混胶硫化影响的差别不大。加入4种增塑剂均使得共混硫化胶的硬度、拉伸强度和100%定伸应力减小而扯断伸长率增大,压缩永久变形性能和热稳定性都出现了不同程度的下降,耐低温性能得以改善,提高了耐IRM 903标准油性能,但对耐ASTM No 1标准油性能的影响不大。加入增塑剂使得共混胶的玻璃化转变温度明显向低温方向偏移、储能模量减小。其中,RS-700赋予共混硫化胶最好的综合性能。     

氢化丁腈橡胶/乙烯丙烯酸酯橡胶共混胶的性能(英文)

研究了不同并用比例下氢化丁腈橡胶(HNBR)/乙烯丙烯酸酯橡胶(AEM)共混胶的物理机械性能、耐油性能、耐老化性能及动态力学性能。结果表明,HNBR和AEM具有很好的相容性,并用AEM后改善了HNBR的耐老化性能、抗压缩永久变形和低温性能。     

丙烯酸酯橡胶/乙烯丙烯酸酯橡胶并用胶性能的研究

制备丙烯酸酯橡胶(ACM)/乙烯丙烯酸酯橡胶(AEM)并用胶,并对其性能进行研究。结果表明:ACM与AEM并用能够实现共硫化;与ACM相比,ACM/AEM并用胶的拉伸强度增大,耐热空气老化性能和耐低温性能得到改善,耐油性能有所下降。当ACM/AEM并用比为60/40、炭黑N550和N774用量分别为40份、1#硫化剂用量为1.5份时,ACM/AEM并用胶的物理性能最佳。     

硫化剂HMDC和促进剂DPG对乙烯-丙烯酸酯橡胶性能的影响

研究硫化剂HMDC和促进剂DPG对乙烯-丙烯酸酯橡胶(AEM)性能的影响。结果表明:促进剂DGP用量一定(3份)时,随着硫化剂HMDC用量增大,混炼胶的硫化速率减小,硫化胶的交联密度和拉伸强度增大,耐热空气老化性能提高,耐低温性能降低;硫化剂HMDC用量一定(1份)时,随着促进剂DPG用量增大,混炼胶的硫化速率增大,硫化胶的交联密度减小,拉断伸长率和撕裂强度增大,耐热空气老化性能降低,耐低温性能提高。     

剪切速率对乙烯-丙烯酸酯橡胶/聚偏氟乙烯热塑性硫化胶性能的影响

采用动态硫化法制备了乙烯-丙烯酸酯橡胶（AEM）/聚偏氟乙烯（PVDF）热塑性硫化胶（TPV）,考察了动态硫化过程中转子剪切速率对TPV微观相态结构及性能的影响。结果表明,动态硫化过程中转子的剪切速率越快,AEM和PVDF更易发生相转变,微观相态结构更加精细,形成具有“海-岛”结构的TPV。随转子的剪切速率加快,TPV的拉伸强度和扯断伸长率均先增大后减少。当剪切速率为75 r/min时,AEM/PVDF TPV具有较好的力学性能,拉伸强度达到14.84 MPa,扯断伸长率为246%,TPV具有更加优异的耐热油和热空气老化性能。     

氯丁橡胶/丙烯酸酯橡胶共混研究

丙烯酸酯橡胶(ACM)的耐热老化性能和耐油性能较好,但力学性能较差。而氯丁橡胶(CR)的力学性能较高,耐温性能较差。两种橡胶并用可使力学性能和热老化性能有显著的提高。采用丙烯酸酯橡胶(ACM)和氯丁橡胶(CR)共混改性,通过偏光显微镜(×400)对共混物中两种橡胶的分散情况进行了分析。研究了CR/ACM共混物质量比、混炼和硫化工艺对共混物性能的影响,结果表明:当CR/ACM并用比在75/25时,采用过氧化二异丙苯、氧化锌、硫磺共硫化体系,白炭黑在混炼时分两次加入,硫化条件为165℃×10 MPa×30 min时,获得的CR/ACM共混物具有优异的力学性能和热老化性能。     

ACM/FKM并用胶的性能研究

研究了不同并用比的氟橡胶（FKM）和丙烯酸酯橡胶（ACM）并用胶的硫变特性、物理机械性能、耐老化性、热稳定性和压缩永久变形性能。实验结果表明：ACM与FKM可以很好地混合并且各自交联,从而制备综合性能优异的并用胶;并用比为30/70的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,并用胶有很好的热稳定性。     

氯化聚乙烯用量对三元乙丙橡胶/尼龙共混胶性能的影响

研究了增容剂氯化聚乙烯（CPE）的用量对三元乙丙橡胶/尼龙（EPDM/PA）硫化胶热空气老化前后和用非极性油处理后力学性能及耐磨性能、耐油性能的影响。结果表明,随着CPE用量的增大,EPDM/PA硫化胶热空气老化后拉伸强度和100%定伸应力呈上升趋势,扯断伸长率和永久变形均缓慢下降,邵尔A硬度保持不变。用非极性油处理后EPDM/PA硫化胶的拉伸强度和扯断伸长率随CPE用量的增大呈上升趋势,100%定伸应力基本不变。CPE的加入对硫化胶的拉伸强度、撕裂强度、扯断伸长率等性能有一定的提高,说明EPDM和PA两相的相容性改善,在用量为6份时硫化胶的力学性能较佳。随着CPE用量的增大,DIN磨耗呈下降趋势,耐磨性能提高;质量变化率和体积变化率略有降低,耐油性能有所提高。     

Effect of some curatives on the properties of ethylene propylene diene rubber/polyethylene blends

A series of ethylene propylene diene rubber/polyethylene (EPDM/PE) blends has been prepared containing different weight fractions of PE up to 0.66. The blends were vulcanized with a sulphur system N-cyclohexyl-2-benzthiazol sulphenamide/sulphur (CBS/S), and a non-sulphur-system dicumyl peroxide (DCUP). The concentration of the latter has been changed from 1.5 phr up to 6 phr calculated on the total weight of the blend composition. It has been found that the maximum torque obtained from rheographs for blends vulcanized with the CBS/S system decreases markedly with increasing PE concentration in comparison with those vulcanized with peroxide. The E modulus obtained from the stress–strain diagram at 110 °C showed the role played by the crosslinking of PE, the E modulus for blends vulcanized by peroxide being higher than for samples vulcanized with CBS/S. In contrast, the values of E modulus of both samples are practically the same at room temperature and attain more than 40 MPa depending on the composition. The tensile strength at room temperature strongly increases with increasing the weight fraction of PE. It has also been confirmed that the melting point of the crystalline phase of PE decreases with increasing crosslinking density of PE. The shear modulus obtained from dynamic mechanical measurements is in accordance with that obtained from static mechanical measurements. © 1999 Society of Chemical Industry     

Rheological and viscoelastic properties of multiphase acrylic rubber/fluoroelastomer/polyacrylate blends

Dynamic viscoelastic properties and dynamic mechanical properties of blends of acrylate rubber (ACM), fluoroelastomer and polyacrylate plastics have been investigated with a rheometer (ARES RDA III) at a frequency (ω) range of 0.1 to 100 rad.s^?1. The analysis of thermorheological properties revealed that the dynamic moduli and dynamic viscosity of blends varied with the composition of the ACM/FKM blend and the level and type of polyfunctional acrylates. The blends showed negative deviation of the dynamic viscosity additive rule. Higher polyfunctional acrylates induced phase separations and showed temperature dependency. It was found that the data of the blends did not follow the Cole‐Cole plot of miscibility and the plot of log G′‐log G″ of the blend showed composition dependency. The dynamic mechanical analysis exhibited lower tan δ values for blends containing higher functional acrylates. Stress relaxation measurements showed longer periods of relaxation for all blends.     

Distribution of carbon black in natural rubber/acrylic rubber blends

Distributions of carbon black in 30/70% (w/w) natural rubber (NR)/acrylic rubber (ACM) blends were investigated as a function of the carbon black content and type using a dynamic mechanical thermal analysis (DMTA) technique. Two different types of carbon black (N220 and N330) were used, and 10–50 phr carbon black was compounded to the rubber blends. From the DMTA thermograms of various blends, the weight fractions of carbon black in the NR and ACM phases were calculated. Carbon black was unevenly distributed in the rubber blend. It preferred to migrate into the NR phase, regardless of the amount of carbon black that was used. By increasing the carbon black content, the weight fraction of carbon black in the NR phase decreased whereas that in the ACM phase increased. A change in the type of carbon black from N220 to N330 significantly decreased the weight fraction of carbon black in the NR phase, but it was not sufficiently strong to affect the tensile properties and hardness of the rubber blend. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:248–256, 2006