Chemiluminescence spectral analysis of styrene-butadiene and acrylonitrile-butadiene rubbers using a multichannel Fourier-transform chemiluminescence spectrometer

The chemiluminescence spectra of styrene-butadiene and acrylonitrile-butadiene rubbers isothermally heated in the range between room temperature and 200 °C were measured with a multichannel Fourier-transform chemiluminescence spectrometer. The observed spectra were analyzed by a least-squares fit using a Gaussian function to determine the peak intensity and the peak wavelength of emission bands. It was found that the peak wavelength of acrylonitrile-butadiene rubbers was slightly longer than that of styrene-butadiene rubbers due to the influence of the nitrile groups. The peak intensity of chemiluminescence from styrene-butadiene rubbers decreased with the styrene content, while that from hydrogenated acrylonitrile-butadiene rubbers increased with the iodine value. From these experimental results, it is concluded that the content of double bonds in the butadiene units in rubbers is measurable by chemiluminescence spectral analysis.     

An investigation of radiation-induced structural changes in nitrile rubber

The mechanism of radiation-induced structural changes in nitrile rubber with different acrylonitrile contents were investigated by ESR, NMR, and FTIR. To investigate new structures solid-state NMR methods had to be used due to crosslinking of the irradiated rubbers, and higher probe temperatures were used to obtain better resolution. The radicals generated on the acrylonitrile groups were found to abstract hydrogen from the adjacent butadiene units resulting in the formation of allylic radicals. These allylic radicals reacted to form intermolecular crosslinks and cyclisation. Cyclisation of the butadiene units were found to occur in the initial stages of the irradiation. Radiation yields of radicals increased with acrylonitrile content from 1.42, 1.58, to 2.42 for 18, 30, and 45% acrylonitrile rubbers. The radiation yields for intermolecular crosslinking were higher in rubbers with higher acrylonitrile contents, giving G values of 17.8, 21.3, and 24.5 for 18, 30, and 45% acrylonitrile rubbers, respectively. However, the crosslink clustering was found to be less in the rubbers with a higher acrylonitrile content. © 1996 John Wiley & Sons, Inc.     

Gasoline- and oil-proof rubbers based on cyclic α-oxides for heavy-duty rubber technical goods

The physicomechanical properties of oil- and gasoline-proof rubbers based on cyclic α-oxides (epichlorohydrin, propylene oxide) and hydrocarbon rubbers (butadiene-nitrile, chloroprene) are described. It is shown that epichlorohydrin rubbers (EKhGKs) have some advantages over butadiene-nitrile and chloroprene rubbers, particularly for operation in extreme conditions in oil drilling and gas equipment for environments with a high content of hydrogen sulfide. Examples of the application of low-molecular EKhGKs as adhesives and sealants are given.     

Diene Rubber Modification Using Thiol-Type Derivatives

Thiol-containing antioxidants such as 4-(mercaptoacetamido)-diphenylamine (MADA) undergo ready addition of-SH groups to the double bonds in diene rubbers in the presence of initiators. The reaction is a radical chain process leading to rubbers with improved thermooxidative resistance. The modification reaction has been carried out on high cis-polyisoprene and polybutadiene, and conditions under which the physicochemical properties (e.g., inherent viscosity, gel content, and microstructure) are less affected have been found. An oxygen absorption test and DSC were used as rapid methods for evaluation of thermooxidative stability of modified rubbers. The superiority of rubbers with MADA chemically attached (ranging from 1 to 4 phr) was shown by a circulating air oven test and by an extraction process which simulates the aggressive environments experienced by many rubbers under practical conditions. The results obtained show that a small degree of modification (1 phr MADA) is large enough to provide good thermooxidative stability without alteration of the molecular characteristics of the parent rubbers. At higher degrees, cistrans isomerization can occur.     

Radiation effects on polymers—IV: Straight radiation vulcanization of styrene-butadiene rubber mixes

Vulcanization of styrene-butadiene rubbers was carried out by gamma radiation in air. For unloaded unextracted rubbers, the dose required for optimum cross-linking was about 40 megaroentgens (MR). Elimination of foreign materials and stabilizers and also incorporation of filler affected the vulcanization. Loaded samples gave vulcanizates with best complex physico-mechanical properties for filler content of 50 (phr) and a dose of 30 MR. Evaluation of various fillers has shown that the best properties were obtained with HAF among the black fillers and silica in the case of white fillers.     

微波消解-原子吸收光谱法测定橡胶及其制品中镉

建立了橡胶及其制品中镉含量的快速测定方法. 样品采用微波消解, 消解溶液中的镉用火焰原子吸收光谱法测定. 方法的检出限为2.5 mg/kg, 多种代表性橡胶及其制品的镉元素回收率在101.6%～104.4%之间. 对某含镉橡胶样品的10个实验室3次平行测定的结果表明实验室内和实验室间的相对标准偏差分别1.8%和8.2%. 方法适用于各种橡胶材料中镉的快速分析.     

Synthesis of ferrocenyl-containing silicone rubbers via platinum-catalyzed Si–H self-cross-linking

Self-cross-linkable ferrocenyl-containing polymethylhydrosiloxanes were synthesized. Karstedt's catalyst and cis-[PtCl₂(BnCN)₂] were examined as cross-linking catalysts at room temperature for the reaction between Si–H groups of the ferrocenyl-containing polymethylhydrosiloxanes. Cis-[PtCl₂(BnCN)₂] is an effective catalyst that allows cross-linked ferrocenyl-containing silicones (silicone rubbers) to be obtained with no visible mechanical defects (bubbles or cracks) compared with Karstedt's catalyst. The ferrocene content of the ferrocenyl-containing silicone rubbers was found to be approximately 50 wt.% by energy-dispersive X-ray analysis. Compared with cross-linked non-modified polymethylhydrosiloxanes, the ferrocenyl-containing silicone rubbers exhibited improved tensile properties (the tensile strength increased from 0.47 to 0.75 MPa) and a 1.5–2.5 times lower cross-linking degree. The surface resistivity of the ferrocenyl-containing silicone rubbers (50 wt.% ferrocenyl units) was approximately 7 × 10⁹ Ω/□, which was 10,000 times lower than that of pure polymethylhydrosiloxane. The obtained flexible electroactive ferrocenyl-containing silicone rubbers can potentially be applied as coatings for electronic and electrostatic-sensitive devices, interfaces, and sensors.     

Experimental branching results for diene polymers by use of gel-permeation chromatography

Branching analyses in styrene–butadiene rubbers and polybutadiene rubbers have revealed large differences in branching between rubbers polymerized in different ways. The functionalities of several star-branched solution-polymerized styrene–butadiene rubbers were calculated and compared to their expected structures. Emulsion-polymerized polybutadiene rubber and a series of solution-polymerized polybutadienes made with different catalysts had different degrees of random branching, and evidence is presented indicating that the different available catalyst systems provide some latitude in making rubbers of different branching contents. Random branching analyses on a series of emulsion-polymerized styrene–butadiene rubbers revealed the dependency of branching on molecular weight and molecular weight distribution. The influence of polymerization temperature on the branching of emulsion-polymerized styrene–butadiene rubber was also studied.     

基于乘用车轮胎胎面胶粉的再生橡胶的制备及性能

通过力化学再生法制备了以废轮胎胶粉为原料的再生橡胶，研究了不同活化剂420用量对再生橡胶性能的影响，测试表明：再生橡胶含硫键断裂生成了硫自由基，随着活化剂含量的增加，再生橡胶的邵氏硬度和交联密度持续降低；拉伸强度、断裂延伸率和凝胶含量均先升高后降低，在活化剂用量为0.9 phr时，拉伸强度和断裂延伸率最大，再生橡胶的凝胶含量最大为19.7%。 微观形貌发现，废轮胎胎面胶粉的颗粒较为分散，再生橡胶的结构颗粒相互粘连，孔洞和缺陷较多，再生橡胶的门尼黏度随着活化剂含量的增加而降低。 综合来看，活化剂420的最佳含量为0.9 phr，再生橡胶各项性能最优。     

Preparation of esters of styrene sulfonic acid and their emulsion copolymerization with isoprene

Sulfonate-containing rubbers were prepared by emulsion copolymerization of isoprene and the secondary butyl ester of styrene sulfonic acid. Substantially gel-free copolymers of relatively high sulfonate content were prepared. It was shown that hydrolysis of the ester copolymers with a suitable base can lead to the formation of ionically crosslinked elastomers.     

Control of the plasticity of organosilicon rubbers by their modification with polypyrrole

Modification of organosilicon rubbers SKTN and SKTV with polypyrrole was studied. The modifying agent was synthesized directly in the rubbers containing iron trichloride acting as oxidant and catalyst, using the diffusion procedure and impregnation of organosilicon rubbers with pyrrole-2-carboxylic acid in supercritical carbon dioxide. Changes in the ductility and viscosity of the composite materials were analyzed.     

Kuhn–Mark–Houwink–Sakurada Coefficients for Determination of Molecular Parameters of cis-Polybutadiene Rubbers by Gel Permeation Chromatography

Industrial samples of polybutadiene rubbers with a high (95% or more) content of cis-1,4-units obtained on the neodymium-containing catalysts are studied by GPC and NMR spectroscopy (600 MHz). The GPC data obtained under different experimental conditions are analyzed taking into account the molecular weight calculated from NMR data. As a result, the coefficients of the Kuhn–Mark–Houwink–Sakurada equation for the solutions of cis-polybutadiene rubbers in toluene and tetrahydrofuran are refined.     

溶聚丁苯链化学结构的NMR研究

溶聚丁苯链化学结构的NMR研究;溶聚丁苯; 链化学结构; 相容性     

Flow boundary conditions for chain-end adsorbing polymer blends

Using the phenol-terminated polycarbonate blend as an example, we demonstrate that the hydrodynamic boundary conditions for a flow of an adsorbing polymer melt are extremely sensitive to the structure of the epitaxial layer. Under shear, the adsorbed parts (chain ends) of the polymer melt move along the equipotential lines of the surface potential whereas the adsorbed additives serve as the surface defects. In response to the increase of the number of the adsorbed additives the surface layer becomes thinner and solidifies. This results in a gradual transition from the slip to the no-slip boundary condition for the melt flow, with a nonmonotonic dependence of the slip length on the surface concentration of the adsorbed ends.     

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.     

Synergistic effect between POSS and fumed silica on thermal stabilities and mechanical properties of room temperature vulcanized (RTV) silicone rubbers

In this paper, both divinyl-hexa[(trimethoxysilyl)ethyl]-POSS (DVPS) and fumed silica were firstly introduced into polydimethylsiloxane (PDMS) system using as the cross-linker and the reinforcing filler respectively. And a series of novel RTV silicone rubbers synergistically enhanced by DVPS and fumed silica were prepared. The cross-linked networks in the novel RTV silicone rubbers have been studied by attenuated total reflection infrared spectroscopy, and the dispersions of POSS and fumed silica in these novel RTV silicone rubbers have been observed by means of scanning electron microscope (SEM). And thermal stabilities, thermo-oxidative stabilities and mechanical properties of these novel RTV silicone rubbers were studied by means of thermal gravimetric analysis and universal tensile testing machine, respectively. From the obtained results, it was found that synergistic effect between POSS-rich areas and fumed silica on thermal stability and mechanical property of RTV silicone rubber indeed existed. And the experimental results also exhibited that the thermal stabilities and mechanical properties of the novel RTV silicone rubbers were far better than those of the reference materials (DVPR and MTFR). The striking enhancements in thermal properties and improvements on mechanical properties of novel RTV silicone rubbers were likely attributed to the synergistic effect between POSS-rich domains and fumed silica. Meanwhile, it was found that the mechanical properties of RTV silicone rubbers prepared with a given amount of POSS cross-linker were enhanced with the increment of the loading amount of fumed silica.     

Determination of the antioxidant alurofen in synthetic rubbers by pyrolysis-gas chromatography

A pyrolysis—gas chromatographic (Py—GC) method for the determination of the antioxidant Alurofen in synthetic rubbers was developed. The Alurofen was extracted from the rubber, then pyrolysed as 873 K in continuous-mode furnace pyrolyser in 20 s. Chromatographic conditions for the separation of the pyrolysis products were established. The pyrolysis of the Alurofen at several temperatures was investigated by measuring the yields of the pyrolysis products. It was observed that 2-phenyl-2-(4-hydroxyphenyl)propane was produced in the greatest, amounts, and the effect of the pyrolysis temperature on the yield of this compound was studied. The overall Py—GC method for the determination of the Alurofen content of rubbers had a mean relative error of 2.7% and a relative standard deviation of 2.94%.     

The Effect of Hollow Corundum Microspheres on the Properties of Materials Based on Carbon-Chain Rubbers

The effect of hollow corundum microspheres on the properties of a rubber mixture based on a combination of carbon-chain rubbers was studied. Owing to the formation of a cross-linked structure of microspheres with a rubber matrix and its additional structuring with Hexol KhPI adhesion modifier, it was shown that it is possible to increase the physicomechanical characteristics and the heat and fire resistance of rubber by establishing the optimal microsphere content in it.     

双烯烃橡胶复分解-加氢制备端羧基聚烯烃

采用烯烃复分解法,以双烯烃橡胶为原料,在Grubbs II代催化剂和链转移剂(马来酸)的作用下制得相应的端羧基聚二烯烃,通过对甲苯磺酰肼/三正丙胺试剂对其进一步加氢得到端羧基聚烯烃.主要研究了反应时间、反应温度、橡胶中双键/催化剂摩尔比、橡胶中双键/链转移剂摩尔比等因素对产物分子量及分子量分布的影响.通过核磁共振氢谱(1H-NMR)和碳谱(13C-NMR)、红外光谱(FTIR)、凝胶渗透色谱仪(GPC)、热重分析(TGA)和示差扫描量热分析(DSC)对产物的结构和性能进行了测试表征.结果表明,通过调整橡胶中双键/催化剂的摩尔比或橡胶中双键/链转移剂的摩尔比可以调控产物的分子量.另外,采用该方法制得的端羧基聚丁二烯具有较高的反式1,4-结构含量,与原料相比其顺式1,4-结构含量大幅下降,从而对产物的性能产生一定影响;而以异戊橡胶为原料时并没有观察到该现象.端羧基聚二烯烃经加氢反应后转变成端羧基聚烯烃,具有更好的热稳定性.该方法合成步骤简单,产物分子量可控,为功能材料的制备提供了新的可能.     

Specific features of separate and joint mastication of natural and 1,4-cis-butadiene rubbers in the presence of dibenzoylaminodiphenyl disulfide

Variation of the molecular structure characteristics and properties of natural and 1,4-cis-polybutadiene rubbers (gel content, molecular weight, degree of branching of macromolecules, viscosity) in the course of their separate and joint mastication in the presence of dibenzoylaminodiphenyl sulfide as mastication accelerator or without it was studied.