马来酸酐接枝橡胶离聚体改性PVC的研究

试验研究以马来酸酐（MA）接枝BR部分替代NBR，通过离子交联提高BR／NBR／PVC共混物的相容性。正交试验结果表明，当接枝单体（MA）、交联剂（氧化锌）和引发剂（过氧化二异丙苯）用量分别为1．5，4和0．1份时，共混物的拉伸性能较好；红外光谱分析证明，MA已成功地接枝在BR大分子链上。     

聚烯烃离聚体原位增容PP/LLDPE共混物的研究!

用傅立叶红外光谱(FTIR)、力学性能测试等方法研究了聚烯烃离聚体原位增容聚丙烯/线性低密度聚乙烯(PP/LLDPE)共混物。结果表明:熔融状态下,在马来酸酐接枝聚丙烯/马来酸酐接枝线性低密度聚乙烯(PP-g-MAH/LLDPE-g-MAH)(质量比50/50)共混物中加入二水醋酸锌,共混物中的马来酸酐基团(羧酸基团)与Zn2+发生离子偶联反应,相界面就地产生的聚烯烃离聚体增加了两相界面黏合力,共混物力学性能提高;原位增容后共混物中的PP和LLDPE相熔点略微下降,LLDPE结晶温度向高温移动;在角频率为0.01～100.00s-1,原位增容后共混物的储能模量、损耗模量和复数黏度都高于简单共混物的,损耗正切(tanδ)低于简单共混物的;对于PP/PP-g-MAH/LLDPE/LLDPE-g-MAH四元体系,SEM显示原位增容后共混物的相界面变得模糊,相容性提高。     

PVC／NBR／BR三元共混弹性体的制备与研究

本文重点叙述了聚氯乙烯(PVC)、丁腈橡胶(NBR)、顺丁橡胶(BR)三元共混弹性体的制备与研究,通过添加顺丁胶后,三元共混体的冲击回弹性、耐磨性及耐寒性均比二元PVC/NBR共混物得以改善,但拉仲强度、断裂伸长率及耐油性降低。获得最佳综合性能的共混比为PVC:NBR:BR=30:60:10(重量比)。实验表明,PVC/NBR/BR三元共混弹性体是复相体系,有较好的相容性。     

马来酸酐接枝聚丙烯及其应用研究

为制备NBR/PP共混物的增容剂,用机械共混法研制了马来酸酐接枝聚丙烯,并将其应用于NBR/PP共混物的增容,得到了满意的效果。本文对接枝反应机理及引发剂量、马来酸酐量、接枝温度、接枝时间等对马来酸酐接枝率及接枝效率的影响作了系统研究,并给出了最佳工艺条件和应用实例。     

丁腈橡胶/三元乙丙橡胶共混胶的制备与性能

将不同质量比的丁腈橡胶(NBR)和三元乙丙橡胶(EPDM)制备共混胶,考察了增容剂碳纳米管(CNTs)和马来酸酐接枝三元乙丙橡胶(EPDM-MAH)、助交联剂三烯丙基异三聚氰酸酯(TAIC)、甲基丙烯酸锌(ZDMA)和三羟甲基丙烷三甲基丙烯酸酯(PL-500)对NBR/EPDM共混胶物理机械性能的影响,研究了共混胶的相容性。结果表明,随着EPDM用量的增加,共混胶的拉伸强度和撕裂强度均降低,邵尔A硬度提高,NRB/EPDM适宜质量比为70/30;分别加入助交联剂TAIC、PL-500、ZDMA和增容剂CNTs均可使NBR/EPDM共混胶的拉伸强度提高,加入EPDM-MAH对共混胶的拉伸强度没有影响,同时加入ZDMA和CNTs可使共混胶的相容性和综合性能提高幅度最大;分别加入ZDMA和CNTs可改善NBR与EPDM的相容性,NBR/EPDM共混胶中粒子分散均匀,界面未出现分层现象。     

马来酸酐辐照接枝三元乙丙橡胶的研究

采用辐照技术,用马来酸酐(MAH)对三元乙丙橡胶(EPDM)进行接枝改性,测定接枝物的交联度和接枝率.分析了辐照剂量、马来酸酐用量以及阻交联剂用量对接枝物交联度和接枝率的影响.同时,采用正交试验优化了试验参数.结果表明,当辐照强度为0.3 kGy/h、辐照剂量为0.15 kGy、MAH与EPDM的质量比为0.025:1以及阻交联剂的质量分数为0.02%时,接枝率达到1.35%.     

聚乙烯接枝马来酸酐／聚氯乙烯共混体系的研究

研究聚乙烯与马来酸酐单体接枝反应，探讨反应条件对接枝率的影响，通过红外光谱对接枝率结构进行表征；研究接枝物及聚氯乙烯含量对共混体系拉伸强度的影响规律，用扫描电子显微镜观察共混物中的界面形态。结果表明，低密度聚乙烯接枝马来酸酐／聚氯乙烯共混体系的相容性和力学性能均有较大提高，接枝率为10％左右，PVC含量为40%时，共混物的拉伸强度可达13．80MPa。     

NR/PVC/NBR共混物的耐油性能研究

研究用NBR改善NR/PVC共混物的耐油性能 ,通过测试所设计的各配方共混物的拉伸强度、扯断伸长率、硬度、耐磨性和耐油性等性能 ,得出NBR改性NR/PVC共混体系的最佳配比关系。最佳配方为 :PVC　 30 ;NR　10 0 ;NBR　 2 5 ;硫黄　 3;促进剂TMTD　 0 8;促进剂D　 1 5 ;促进剂DM　 1 5 ;白炭黑　 40 ;轻质碳酸钙　 30 ;氧化锌　 5 ;硬脂酸　 1 5 ;防老剂D　 2。共混物的耐油性能可达到NBR制品的要求     

硫酸盐基离聚体的形态结构、力学性能及其共混

由环氧化（苯乙烯-丁二烯-苯乙烯）三嵌段共聚物（SBS）与硫酸氢钠水溶液反应制备了新型含硫酸盐基的SBS离聚体，研究了离聚体的形态结构、力学性能、离聚体时SI玛／氯醇橡胶（CHR）共混物的增容作用以及离聚体／聚丙烯（PP）共混物的力学性能。结果表明：在透射电镜下硫酸铅基离聚体呈现黑色圆柱状或四方晶形离子微区，硬脂酸锌作为离子增塑剂能提高钠离聚体的力学性能；随着离子基含量的提高，离聚体的拉伸强度及扯断伸长率增加；少量离聚体可以提高SBS／CHR共混物的力学性能，减小共混物的吸煤油率；扫描电镜图片显示二者的相容性增加；离聚体／PP共混物在拉伸强度与组成的关系方面呈现协同效应，并且其耐甲苯性能提高。     

三元共聚尼龙/聚氯乙烯/丁腈橡胶三元共混弹性体研究

选择三元共聚尼龙（PA），聚氯乙烯（PVC）和丁腈橡胶（NBR）为主体材料，采用高温机械共混，化学交联工艺制得了PA／PVC／NBR三元共混弹性体，探讨了PA／NBR，POM／NBR，PVC／NBR，HMWPVC／NBR三元共混体系性能，重点讨论了PA／PVC／NBR共混比，不同硫化体系，有机过氧物DCP用量等因素对PA／PVC／NBR三元共混弹性体性能的影响，实验结果表明：选择适宜配方制得力学性能和耐油耐溶剂性能较好的PA／PVC／NBR三元共混弹性体，扫描电镜的实验结果证实m(PA):m(PVC):m(NBR)=10:30:60和m(PA):m(PVC):m(NBR)=30:10:60两个体系的三元共混弹性体均具有较好的相容性，且前者的相容性更好。     

The Effects of PP-g-MA on the Physical Properties and Morphology of Polypropylene (PP)/Recycled Acrylonitrile Butadiene Rubber (rNBR) Blends

Polypropylene-grafted maleic anhydride (PP-g-MA) was used to enhance the compatibility of polypropylene (PP) and recycled acrylonitrile butadiene rubber (rNBR) blends. The blends were prepared by melt mixing using a Haake Rheomix Polydrive R 600/610 mixer at 180°C. The processing torque was used to investigate the mixing process. The better mixing of compatibilized blends (PP/rNBR-MA) was evidence by the higher stabilization torque. Compared to uncomapatibilized PP/rNBR blends, tensile properties and oil resistance of compatibilized PP/rNBR were improved. SEM micrographs of tensile fractured surfaces showed better dispersion and better interfacial adhesion between the phases of compatibilized blends compared to uncompatibilized counterparts.     

氢化丁腈橡胶／超细全硫化粉末丁腈橡胶共混物的结构与性能研究

采用熔融共混工艺制备了氢化丁腈橡胶（HNBR）／超细全硫化粉末丁腈橡胶（UFPNBR）共混物,研究了共混物相态结构、动态力学性能、力学性能及老化性能,并与HNBR／NBR共混物作了对比。透射电镜观察表明：在HNBR／UFPNBR体系中,HNBR容易形成连续相,UFPNBR为分散相;在HNBR／NBR体系中容易形成双连续相结构。DMA动态力学性能分析表明：2种共混物都只有一个tanδ峰,且相容性较好。HNBR／UFPNBR共混物在玻璃化转变区的tanδ峰值逐渐降低,而HNBR／NBR体系的tanδ峰值先减小后增大。加入适量的UFPNBR能降低HNBR／UFPNBR共混物的压缩永久变形;与常规共混胶相比,HNBR／UFPNBR具有低脆性温度和良好的耐老化性能,但力学性能略低。     

Homogeneous Styrene Butadiene/Acrylonitrile Butadiene Rubber Blends

The graft copolymerization of acrylonitrile (AN) onto butadiene rubber (BR) was carried out in toluene at 80°C, using dibenzoyl-peroxide (BPO) as initiator. The synthesized poly acrylonitrile-grafted-butadiene rubber (AN-g-BR) was characterized by N% elemental analysis and Fourier-transform infrared (FT-IR) spectroscopy. Styrene butadiene rubber/acrylonitrile butadiene rubber (SBR/NBR) blends were prepared with different blend ratios in presence and absence of AN-g-BR, where the homogeneity of such blends were examined with intrinsic viscosity (η) measurements, differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). The scanning electron micrographs illustrate disappearance of the macro-scale phase separation of SBR/NBR rubber blend as a result of the incorporation of AN-g-BR into that blend. Viscosity measurements confirm homogeneity of that blend. Differential Scanning Calorimetry traces exhibit shifts in glass transition temperatures (T _g's) of SBR and NBR in their blend, indicating some degree of homogeneity. Physico-mechanical properties of the rubber blend vulcanizates with different blend ratios, in presence and absence of AN-g-BR, were investigated before and after accelerated thermal aging. The SBR/NBR (25/75) homogeneous blend possessed the best physico-mechanical properties after thermal aging, together with the best swelling behavior in motor oil. The physico-mechanical properties of SBR/NBR (25/75) filled blend with different types of inorganic fillers during thermal aging were studied.     

Comparison of Properties of Polypropylene (PP)/Virgin Acrylonitrile Butadiene Rubber (NBRv) and Polypropylene (PP)/Recycled Acrylonitrile Butadiene Rubber (NBRr) Blends

The comparison properties of polypropylene (PP)/recycled acrylonitrile butadiene rubber (NBRr) blends and polypropylene/virgin acrylonitrile butadiene rubber (NBRv) blends were investigated. The tensile properties such as tensile strength, tensile modulus and elongation at break of PP/NBRv blends are higher than PP/NBRr blends. However, PP/NBRv blends exhibit lower stabilization torque and higher swelling percentage than PP/NBRr blends. Based on SEM, a finer morphology was observed in PP/NBRv blends in comparison with the PP/NBRr blends. The thermal stability of PP/NBRr is better than that of PP/NBRv blends.     

PA6/PP/SEBS-g-MAH共混物的相容性研究

采用马来酸酐接枝(氢化苯乙烯/丁二烯/苯乙烯)共聚物(SEBS-g-MAH)作为增容剂,研究了增容剂用量对尼龙6/聚丙烯(PA6/PP)共混体系相态结构、力学性能的影响,以及在相同增容剂用量下不同PA6、PP配比对体系相形态的影响。结果表明,SEBS-g-MAH中的酸酐基团能与PA6末端的氨基发生化学反应,在PA6和PP的内表面形成PA6-SEBS接枝共聚物,明显改善了两相的界面相容性,并使共混物的力学性能得到显著提高。共混物冲击断面形貌的分析表明,共混物发生了明显的脆韧转变。     

The Behaviour of Styrene Butadiene Rubber/Acrylonitrile Butadiene Rubber Blends in the Presence of Chlorinated Hydrocarbons

The behaviour of styrene butadiene rubber/acrylonitrile butadiene rubber (SBR/NBR) blends in the environment of chlorinated hydrocarbons, such as carbon tetrachloride, chloroform and dichloromethane, in the temperature range 32–52°C has been investigated. Sulphur, dicumyl peroxide and a mixed system consisting of sulphur and peroxide were used as the vulcanising systems for the matrix. The effects of vulcanising agents, blend composition, solvents and temperature on the sorption characteristics were studied. The sulphur-vulcanised systems exhibited the highest solvent uptake and those with dicumyl peroxide as the vulcanising agent the lowest. This difference has been explained on the basis of the nature of cross links established between the polymer chains during vulcanisation. The solvent uptake increased with an increase in SBR content in the blends when carbon tetrachloride was used as the penetrant, whilst it decreased with SBR content when chloroform and dichloromethane were used as the probes. This behaviour has been explained on the basis of the polarity difference of the solvents. For a given blend system, the solvent uptake was maximum when dichloromethane was used as the solvent and minimum when carbon tetrachloride was used. This has been accounted for in terms of the difference in the size of the penetrants. The intrinsic diffusion coefficient, permeation coefficient, cross link density and interaction parameter were estimated from the sorption data. Thermodynamic parameters such as enthalpy and free energy changes were also calculated. These values indicate that the sorption process in the present systems is exothermic and is more spontaneous in sulphur-vulcanised systems. The experimental results, when compared with different theoretical diffusion models, have been found to be closer to Robeson’s and Maxwell’s models.     

Ionic elastomer blends of zinc salts of maleated natural rubber and carboxylated nitrile rubber: Effect of grafted maleic anhydride

Zinc neutralized maleated natural rubbers (Zn‐MNR) were prepared by solution grafting and neutralization with zinc acetate in one‐step. It was later used for blending with carboxylated nitrile rubber (XNBR) in the composition of 50/50 parts by weight. The effect of grafted anhydride content (1.2, 1.6, 2.0, and 2.5% wt of NR) on the tensile properties of ionic rubber blends (Zn‐MNR/XNBR) was investigated. The tensile strength of the ionic blends was found to be greater than those of pure rubbers. The modulus, tensile, and tear strength of the blends dramatically increased with increasing levels of grafted anhydride. The ionic rubber blends also possessed superior physical properties compared to those of the corresponding nonionic rubber blends (MNR/XNBR). Dynamic mechanical thermal analysis and scanning electron microscopic studies were performed to verify the process of mixing. Fourier transform infrared spectroscopic studies were carried out to characterize the nature of specific intermolecular interactions between Zn‐MNR and XNBR chain segments. The results indicated that the ion‐ion (Zn⁺ ‐COO^?) interactions between Zn‐MNR and XNBR are formed at the interface, which provides the mean of compatibilization in the ionic rubber blends. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

丁二烯橡胶（BR）9000产品质量统计与分析

通过10年对国内某合成橡胶生产厂生产的丁二烯橡胶（BR）9000每月进行1批次样品的全项目检验,将10年所检验样品的生胶性能、力学性能的数据进行统计分析;10年共对该厂的BR9000样品累计检验120批次,优等品率为93．3％,合格品率为100％;BR9000样品的挥发分质量分数、生胶门尼黏度均出现未达到优等品现象;灰分质量分数、混炼胶门尼黏度、力学性能等指标波动不大,各年的检验结果基本一致,总体来说产品质量逐步提高,产品性能趋于稳定。     

纳米氧化锌在NR/BR并用胶及SBR胶料中的应用

研究纳米氧化锌替代普通氧化锌在天然橡胶(NR)/顺丁橡胶(BR)并用胶以及丁苯橡胶(SBR)胶料中的应用。结果表明,纳米氧化锌减量10%代替普通氧化锌,NR/BR并用胶及SBR胶料的加工性能和物理性能基本不变,质量减小,成本降低。     

Fracture toughness of modified polypropylene/poly(styrene‐ran‐butadiene) blends

Fracture toughness of polypropylene (PP)/poly(styrene‐ran‐butadiene) rubber (SBR) blends as a function of concentration of maleic anhydride (MA) in the maleated polypropylene (MAPP) compatibilizer was investigated under uniaxial static and impact loading conditions. The addition of MAPP to the unmodified PP/rubber blend enhanced the tensile modulus and yield stress as well as the Charpy impact strength. The maximum values were recorded at 1.0 wt% grafted MA in the compatibilizer. V‐shaped blunt‐notched specimens exhibited typical ductile behavior and no breakage of the specimens occurred during the impact fracture tests. Sharp‐notched specimens of uncompatibilized and low‐content MA blends broke in a semibrittle manner, supported by a rapid crack propagation process. Increasing MA content in the blends led to semibrittle‐to‐ductile transition characterized by stable crack propagation. Fracture mechanics experiments, supplemented by scanning electron microscopy (SEM), were also employed to obtain a better understanding of the fracture and deformation behavior. Copyright © 2005 Society of Chemical Industry