基于专业认证的高分子材料与工程实验的综合性设计实践

工程专业认证强调以学生为中心,注重培养学生解决复杂工程问题的能力,本文设计了一个综合性的高分子材料与工程实验——高温硫化甲基乙烯基硅橡胶的制备与性能测试.实验要求学生通过文献调研、小组讨论明确实验基本原理的基础上,自主设计实验方案,制备甲基乙烯基硅橡胶制品,测试硅橡胶生胶的分子量、热行为及硫化胶的基本力学性能,以科研论...     

溶胶-凝胶-硫化法制备硅橡胶吸附萃取搅拌棒

采用溶胶-凝胶-硫化法,以甲基乙烯基硅橡胶和乙烯基封端硅橡胶为原料制备了厚壁硅橡胶吸附萃取搅拌棒(stir bar for sorptive extraction,SBSE)。采用分段硫化和多阶程序升温老化防止涂层脱落和龟裂,一次涂渍涂层厚度约150~250μm,280℃下无流失,使用寿命可达150次。利用所制备涂层,结合自制热解析系统(thermal desorption system,TDS),建立了SBSE-TDS-CGC-FID测定水样中6种多环芳烃(polyaromatichydrocarbons,PAHs)的方法。方法的线性范围为0.3~1000μg/L,检出限为0.002~0.011μg/L,相对标准偏差在0.92%~6.14%之间。该方法能够满足欧盟2005/69/EC指令对多环芳烃低于10 mg/kg的检测要求。     

硅树脂/硅橡胶杂化膜的制备及性能研究

以十三氟辛基三乙氧基硅烷、四甲基二乙烯硅氧烷、乙烯基三甲氧基硅烷和正硅酸乙酯为原料,通过水解缩合制备了乙烯基含氟硅树脂。乙烯基硅橡胶和乙烯基含氟硅树脂为基质材料,含氢硅油为交联剂,硅氢加成制备了改性硅橡胶杂化膜材料。透气性能测试表明,当含氟硅树脂质量分数50.0%时,膜的成膜性和富氧性能之间达到最佳平衡点,30℃和0.01 MPa压差下,P（O2）为628 Barre,a（O2/N2）为3.36。与普通乙烯基硅橡胶交联膜比,这种有机―无机杂化膜在保持原有氧气透过系数的基础上,较好的改进了氧氮分离性能。     

交联补强硅橡胶包埋18-甲基炔诺酮的释放行为

甲基乙烯基硅橡胶;交联补强硅橡胶包埋18-甲基炔诺酮的释放行为;药物释放系统     

用库仑法分析硅橡胶中乙烯基的含量

高分子量硅橡胶中乙烯基的含量可用库仑法间接测定。样品溶解后先和标准溴溶液反应,过量的溴用标准丙烯醇溶液除去,过量的丙烯醇又用库仑法分析.硅生胶中0.2％的乙烯基测定的精密度为5.5％.硫化胶中残余的乙烯基亦可用溴溶液较长时间溶胀反应而后分析。     

在线热裂解-气质联用分析缩合型和加成型硅橡胶

用在线热裂解-气质联用技术对缩合型硅橡胶和加成型硅橡胶分别进行分析,在其裂解产物中都检测到一系列的二甲基环硅氧烷环体.比较二者的裂解产物发现:缩合型硅橡胶非常容易发生裂解反应,产生低分子量的二甲基硅氧烷环体;而加成型硅橡胶相对难以裂解,有一定量的高级二甲基硅氧烷环体产生.除此之外还检测到微量的含氢环体和含乙烯基环体.这为缩合型和加成型这两种硅橡胶分析提供实验依据.     

基于弹性统计理论的硅橡胶纳米复合材料本构关系的建立

基于考虑了悬垂链的橡胶弹性统计模型,通过引入应变放大因子,建立了硅橡胶纳米复合材料的基于微观机制的本构关系,其中利用硅橡胶分子信息(分子量M、乙烯基含量wt_(Vi)%)、乙烯基反应程度(q)估算获得本构方程中的交联点间链段分子量(Mc),网络链(network strands)体积分数(Φ)等参数,通过拟合确定了与纳米粒子相关的部分参数(初始应变放大因子X_0,极限应变放大因子X_∞,衰减因子z),对掺杂白炭黑的单组分及长短链配合硅橡胶拉伸应力-应变数据进行拟合,在采用相同X_∞,z值情形下,拟合曲线仍能与实测值符合较好(拟合的Adj.R-Square值分别为0.99576、0.99596)。基于微观物理机制的本构关系能够成为联系微观分子结构参数与宏观应力的桥梁,本文工作有望为更有针对性地改进和优化硅橡胶的性能提供依据。     

硅橡胶新硫化体系的研究

本文介绍一种硅橡胶新硫化体系,即利用Diels-Alder反应使聚硅氧烷进行交联。所用生胶为含乙烯基的高分子量聚甲基硅氧烷,所用交联剂(硫化剂),即双烯体,系含有环戊二烯基的有机硅化合物。所得弹性体的物理机械性能达到高强度硅橡胶水平。     

4,4′-(多苯基三联苯)双(有机硅烷)的合成

前文曾经报道利用四苯基环戊二烯酮为双烯体,乙烯基或烯丙基三乙氧基硅烷及其硅氧烷为亲双烯体通过Diels-Alder反应合成的多苯基芳基有机硅化合物作为硅橡胶的热     

辐射接枝医用水凝胶的研究Ⅰ.硅橡胶辐射接技N-乙烯基吡咯烷酮

采用填加SiO_2增强的甲基乙烯基硅橡胶混炼压片。通过~(60)Co-γ射线引发辐射硫化,利用共辐照方法,将N-乙烯基吡咯烷酮接枝到该硅橡胶上,制备了高纯度医用水凝胶。本文较系统地研究了接枝单体浓度、辐照剂量率、剂量、温度和接枝试片厚度等因素对接枝共聚反应的影响。建立了接枝速率与单体浓度、剂量率之间的动力学关系式:R_g=k[M]~(4/5)D~(1/2)。讨论了反应机制和接枝区域。     

双烯类液体橡胶的研发进展

液体橡胶作为合成橡胶的重要种类,是室温下能流动的橡胶材料。本文介绍了液体橡胶的性能特点及分类,着重阐述了双烯类液体橡胶即液体聚丁二烯橡胶、液体丁腈橡胶、液体异戊橡胶、液体丁苯橡胶和液体氯丁橡胶的结构特征、性能特点及主要用途,并进一步探讨了它们的研发、生产和使用情况。液体橡胶便于实现生产连续化和自动化,且加工方便,顺应时代发展的"低碳"潮流。从产品种类、牌号,应用范围等方面对今后的发展提出了建议。     

加成型液体硅橡胶的研究进展

结合加成型液体硅橡胶的硫化原理,综述了加成型液体硅橡胶导热性能、耐高温性能及粘结性能的最新研究进展,发现加入金属氮化物导热填料是提高加成型液体硅橡胶导热性能的有效途径;改善分子结构是提高加成型液体硅橡胶耐高温性能的主要途径;共混粘结促进剂是提高加成型液体硅橡胶粘结性能的重要途径。介绍了加成型液体硅橡胶的最新应用领域,提出功能化加成型液体硅橡胶,如3D个性化打印硅橡胶、人体器官硅橡胶、高折光封装硅橡胶等功能材料是未来加成型液体硅橡胶的发展方向。     

Properties of Natural Rubber/Recycled Chloroprene Rubber Blend: Effects of Blend Ratio and Matrix

The present study investigated the effects of two types of natural rubber and different blend ratios on the cure, tensile properties and morphology of natural rubber/recycled chloroprene rubber blends. The blends of natural rubber/recycled chloroprene rubber were prepared by using laboratory two-roll mill. The result showed that the cure time prolonged with the addition of recycled chloroprene rubber (rCR). Comparability, natural rubber/recycled chloroprene rubber (SMR L/rCR) blendcured rapidly than epoxidized natural rubber/recycled chloroprene rubber (ENR 50/rCR) blend. The addition of rCRalso caused a decrement in the tensile strength and elongation at break for both rubber blends. The SMR L/rCR blendsshowed higher tensile strength and elongation at break compared to those of ENR 50/rCR blends at any blend ratios.     

Effects of rubber type on the curing and physical properties of silica filled rubber compounds

As environmental regulations are getting stricter, tire industries for automobiles have shown much interest in substituting silica for conventional carbon black partially or entirely. To take full advantage of silica as fillers for rubbers, it is essential to find a reasonable rubber system that shows an excellent performance with silica reinforcement. Therefore, in this study, several different rubber compounds comprising the same amount of silica were prepared with several different rubber systems, respectively. The processability, curing characteristics, and mechanical and viscoelastic properties of the rubber compounds were investigated to analyze the performance of the rubber compounds as tire tread materials. Among the rubber compounds studied, SBR1721 compound comprising natural rubber (NR) and styrene butadiene rubber (SBR) with high styrene content was considered the most appropriate for application to tire tread materials. Copyright © 2008 John Wiley & Sons, Ltd.     

Determination of bound rubber composition of filled SBR/BR blend compounds by analysis of the unbound rubber composition and bound rubber content

Analytical method for determination of the bound rubber composition of a filled SBR/BR blend compound was developed using measurement of the bound rubber content and microstructural analysis of the unbound rubber composition. Various filled SBR/BR blend compounds with different blend ratios were prepared using SBRs with different microstructures. This method included measurement of the bound rubber content, extraction of the unbound rubber, microstructural analysis of the unbound rubber composition, and process for determination of the bound rubber composition. Composition of the unbound rubber was analyzed using liquid proton nuclear magnetic resonance spectroscopy (H-NMR) and transmission Fourier transform infrared spectroscopy (FTIR). It was found that the analytical results using H-NMR had less experimental errors than those using transmission-FTIR. The raw SBR/BR blends were also analyzed in order to evaluate level of the experimental errors. Average SBR/BR ratios of the unbound rubbers were obtained using the 1,2- and 1,4-unit contents determined by the H-NMR analysis. The bound rubber compositions were obtained using the bound rubber contents and the average unbound rubber compositions. It was found that most of the bound rubbers had higher SBR ratios than the formulation value.     

Characterization of natural rubber concerning its components and molecular weight in Taraxacum kok-saghyz Rodin using pyrolysis gas chromatography-mass spectrometry

Taraxacum kok-saghyz Rodin (TKS) has abundant natural rubber in its root and the molecular weight of its natural rubber is higher than that in Hevea brasiliensis. Thus, TKS is an excellent alternative for the commercial production of natural rubber. The content and molecular weight of natural rubber are two qualitative indicators. Efficient determination for both indicators is still a challenge. In this study, we developed a method to simultaneously determine the content and molecular weight of natural rubber in TKS with pyrolysis－gas chromatography-mass spectrometry. The content of natural rubber was quantified by internal standard method. We optimized the pyrolysis temperature and chromatographic method during content determination. The limits of detection and quantification were 0.47 and 1.56 μg, respectively. In addition, the arachidonic acid methyl ester, an unsaturated fatty acid proposed from the α-end group of natural rubber, was quantified to obtain the number of natural rubber polymers. Based on the content and the polymer number, we also quantified the molecular weight of natural rubber. Thus, the content and molecular weight of natural rubber were simultaneously determined in TKS. Our study provides a new perspective for the high throughput analysis of natural rubber.     

VARIATION OF PHYSICO-CHEMICAL PROPERTIES OF RADIATION CROSSLINKED RUBBER WITH STORAGE TIME

The effect of storage on physico-chemical properties of non-irradiated natural rubber and radiation vulcanized natural rubber （RVNR） were evaluated. The rubber films were stored under two different conditions, namely in open air and sealed polyethylene bags. The antioxidant, tris（nonylated phenyl） phosphite （TNPP） was used for preventing degradation of RVNR films. Gel content, cross-link density, tensile strength at break and 500% elongation of rubber films were measured. The results show that the retention （%） of tensile properties of rubber films with TNPP is higher than that of rubber films without antioxidants. The rubber films stored in polyethylene bags also show better retention of tensile properties than those of rubber films stored in open air.     

聚合物共混物脆韧转变性能研究 Ⅳ橡胶粒子的分布对PVC/NBR共混物脆韧转变的影响

根据作者已建立的准网络形态模型和推导出的基体层厚度计算公式，从实验上研究了橡胶粒子的分布对聚氯乙烯（ＰＶＣ）／丁氰橡胶（ＮＢＲ）共混物脆韧转变的影响．结果表明，不仅无规形态ＰＶＣ／ＮＢＲ共混物存在脆韧转变主曲线，而且准网络形态ＰＶＣ／ＮＢＲ共混物也存在脆韧转变主曲线．但是两条主曲线明显不重合，表明橡胶粒子的分布对ＰＶＣ／ＮＢＲ共混物脆韧转变有显著影响．而且准网络形态ＰＶＣ／ＮＢＲ共混物的临界基体层厚度比无规形态ＰＶＣ／ＮＢＲ共混物的临界基体层厚度大得多，表明准网络形态比无规形态明显有利于增韧．因此临界基体层厚度不仅是基体的特征参数，还是界面粘结和橡胶粒子分布的函数．     

高密度燃料HDF-1与橡胶的相容性研究

报道了在室温和70 ℃下橡胶材料G402氟硅胶、丁腈胶5171、丁腈胶4170、贮囊橡胶用合成的高密度燃料HDF-1浸泡后性能如伸长率、邵尔硬度、重量、面积体积的变化，并与采用3号喷气燃料（RP-3）实验结果进行对照。用红外光谱测定了燃料浸泡前后橡胶组成的变化。实验结果表明，G402氟硅胶和贮囊对于HDF-1和RP-3有相近的相容性，丁腈胶5171对HDF-1的相容性比对RP-3的相容性稍差，丁腈胶4170对HDF-1的相容性比对RP-3的相容性更差的结果。因此，丁腈胶5171和丁腈胶4170不能用于HDF-1储存和输送，原使用RP-3系统的橡胶密封件不能直接使用HDF-1。     

有机硅橡胶裂解产物气相色谱-质谱联用分析

以室温硅橡胶和高温硅橡胶产品的边角废料及次品作为实验原料,进行到催化和碱催化裂解,将裂解产物进行气相色谱－质谱（ＧＣ－ＭＳ）联用分析,经过质谱数据检索,确定了两种酸催化产物的组成,高温橡胶的酸催化裂解产物主要是环状化物合;室温橡胶的酸催化一妥产物中有太和链状两类化合物,该实验为硅像胶废料利用提供了依据。碱催化产物太复杂,产物利用存在困难。