Thermo gravimetric analysis and morphological behavior of castor oil based polyurethane–polyester nonwoven fabric composites

Castor oil (CO) based polyurethane (PU)– polyester nonwoven fabric composites were fabricated by impregnating the polyester nonwoven fabric in a reactive composition containing CO and diisocyanate. Composites were fabricated with two different isocyanates such as toluene‐2, 4‐diisocyanate (TDI) and hexamethylene diisocyanate (HMDI). Thermogravimetric analysis (TGA) studies of the composites were performed to establish the thermal stability and their mode of thermal degradation. It was found that degradation of neat PU takes place in two steps and that of polyester nonwoven fabric reinforced PU composites takes place in three steps. From the TGA thermograms, a little improvement in thermal stability incase of polyester nonwoven fabric reinforced PU composites were noticed compared to unreinforced PUs. Degradation kinetic parameters were obtained for the composites using Broido, Coats and Redfern, and Horowitz and Metzger methods. Tensile fractured composite specimens were used to analyze the morphology of the composites by scanning electron microscopic technique. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Fluorinated acrylic polymers: Surface properties and XPS investigations

A series of polymers based on methylmethacrylate, butylacrylate, and ω‐perfluorooctylalkylacrylate were prepared by radical polymerization. By changing both the length of the hydrocarbon spacer, between the fluorinated chain and the ester function of the fluorinated monomer, and its concentration, the surface properties of the resulting terpolymers were greatly influenced. Polymers containing small amounts of fluorinated comonomer units had considerably reduced surface energies compared to the copolymer poly (methylmethacrylate‐co‐butylacrylate) taken as reference. The outermost surface composition has been investigated by the XPS technique, confirming the strong fluorine enrichment. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 821–827, 2006     

Influence of titanium dioxide on crystallization behavior of an ethylene–propylene copolymer

Crystallization of an ethylene–propylene copolymer (E/P) filled with diverse weight percentages of titanium dioxide (TiO₂) was performed under isothermal and nonisothermal conditions to investigate the influence of the inorganic substance on the nucleation and growth mechanisms of the matrix. The overall and radial crystallization rates of the composite materials were measured using, respectively, differential scanning calorimetry (DSC) and optical microscopy. The nucleation density of E/P spherulites as a function of composition was investigated by scanning electron microscopy (SEM), revealing a nucleating effect of TiO₂. A comparison between the spherulitic texture of specimens showed a higher fineness of the composites relative to the neat matrix, whereas no changes of surface nucleation density were appreciable among composites within the explored compositional range. The thermal behavior is discussed in the light of the enhanced thermal conductivity of polymer composites, which conciliates the crystallization kinetics of the matrix, analyzed using the Avrami equation, to optical and SEM observations. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3409–3416, 2003     

Sulfur deactivation and regeneration of Pt/BaO/Al2O3 and Pt/SrO/Al2O3 NO x storage catalysts

Transient experiments were performed to study sulfur deactivation and regeneration of Pt/BaO/Al₂O₃ and Pt/SrO/Al₂O₃ NO _x storage catalysts. It was found that the strontium-based catalysts are more easily regenerated than the barium-based catalysts and that a higher fraction of the NO _x storage sites are regenerated when H₂ is used in combination with CO₂ compared to H₂ only.     

天然橡胶/顺丁橡胶并用硫化胶的力学破坏机理

用扫描电子显微镜对天然橡胶／顺丁橡胶并用硫化胶的力学破坏机理进行了研究，结果表明试验样拉伸疲劳破坏断面具有拉伸断裂和屈挠龟裂的双重特征。白炭黑和Ｓｉ６９的加入使硫化胶的屈挠疲劳初始裂口形式发生变化。热氧老化使试样的拉伸断裂由韧性向脆性转化。     

The Mechanical Behaviour of Polyimide/Copper Laminates Part 2: Peel Energy Measurements

The mechanical peel behaviour of laminates consisting of polyimide films adhered to copper foil using a modified acrylic adhesive has been studied over a wide range of test rates and temperatures. The laminates were prepared from polyimide films which had been subjected to either a “high-thermal history” or a “low-thermal history” treatment during the production of the film. The measured peel energies of the laminates could be superimposed to give a master curve of peel energy versus the reduced rate of peel test, Ra_T, where R is the rate of peel test and a_T is the time-temperature shift factor. The appropriate shift factors were a function of the test temperature and were mainly deduced from tensile tests conducted on the bulk adhesive. The “high-thermal history” laminates gave higher peel energies and the locus of failure of the laminates was mainly by cohesive fracture through the adhesive layer. At low values of log₁₀ Ra_T, i.e. Low rates of peel and high test temperatures, the “low-thermal history” laminates also failed in the adhesive layer and possessed similar peel energies to those measured for the “high-thermal history” laminates. However, at high log₁₀ Ra_T values, the peel energies measured for the “low-thermal history” laminates were lower and showed a wider scatter. These arose from a different locus of failure occurring in these “low-thermal history” laminates when tested under these conditions. Namely, it was found that most of these laminates failed in a weak boundary layer in the outer regions of the “low-thermal history” polyimide film.     

Investigation of conductivity characteristics of nitrile butadiene rubber vulcanizates filled with semiconducting carbide ceramic

SiC‐ and B₄C‐filled NBR rubber composites were prepared with various volume fractions of filler by a conventional roll‐mill method. The morphological structures of the NBR–SiC and NBR–B₄C composites were analyzed by scanning electron microscopy. The dependence of room‐temperature volume resistivity (ρ_v) on the concentration of filler in the two systems was studied. In addition, variation in the number of current carriers (n), mobility carriers (μ), dielectric constant (ε), and dielectric loss factor (tan δ) on filler concentration in the two systems were investigated in detail. The applicability of composites as negative temperature coefficient (NTCR) linear thermistors was studied by the dependence of volume resistivity on temperature. The resistivity showed negative temperature dependence and changed linearly with temperature parallel. The conduction mechanism of the conductivity of the two composites was analyzed in terms of the computed activation energy and hopping energy. Change in volume resistivity as a function of frequency for the two systems was also investigated. Finally, the dependence of volume resistivity on applied pressure and possible real applications of these composites as transducers in pressure sensors were also studied. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2158–2165, 2007     

高压蒸汽管道保温研究

计算了不同管径和保温厚度下蒸汽管道输送高压蒸汽的热损失和温度降。结果表明:保温厚度越大,蒸汽的热损失越小、温度降越小;保温材料导热系数与蒸汽的热损失呈正比;环境温度越高,蒸汽的热损失越小;环境风速对热损失的影响不大。同时研究了保温材料选择和保温结构对节能的影响。     

Enhancement of radiation‐resistant effect in ethylene–vinyl acetate copolymers by the formation of ethylene–vinyl acetate copolymers/clay nanocomposites

Ethylene–vinyl acetate (EVA) copolymers/clay nanocomposites, prepared by using nonreactive organophilic clay and reactive organophilic clay, were characterized by X‐ray diffraction and by high‐resolution transmission electron microscopy. The influence of gamma irradiation on the structure and properties of the pure EVA and EVA/clay nanocomposites was systematically investigated. In the presence of gamma radiation, the clay can effectively restrain the increase of the storage modulus of EVA/clay nanocomposites, which was supported by dynamical mechanical analysis. Gamma irradiation had almost no effect on the thermal properties of EVA/clay nanocomposites by using nonreactive organophilic clay, but it obviously improved the thermal stability of EVA/clay nanocomposites by using reactive organophilic clay. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2532–2538, 2005     

延长生焦时间对延迟焦化装置的影响

国内焦化装置的生焦时间几乎都采用24小时，设计的焦炭塔空高较大，在装置低负荷生产时，适当延长生焦时间，不仅可降低装置的运营成本、提高焦炭质量、降低劳动强度，而且还可降低维修费用。安庆焦化成功地在一套装置上实现了48小时生焦操作，年运行200天，增效约100万元。