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2001—2002年国外塑料工业进展 总被引:7,自引:0,他引:7
CHINA PLASTICS INDUSTRY Editorial Office 《塑料工业》2003,31(3):1-21,25
收集了2001年7月到2002年6月有关国外塑料工业的相关期刊资料,介绍了2001年到2002年国外塑料工业的发展情况,提供了世界各地域塑料原材料的产量及构成比,日本,美国,加拿大,德国,法国,比利时,墨西哥,芬兰,西班牙等国家的树脂产量,消费量及增长率,以及日本,西欧,北美等地区的不同品种塑料原料消费量和增长率统计,按通用热塑性树脂(聚乙烯,聚丙烯,聚苯乙烯,聚氯乙烯,ABS树脂),工程塑料(尼龙,聚碳酸酯,聚甲醛,热塑性聚酯,聚苯醚),通用热固性树脂(酚醛,聚氨酯,不饱和树脂,环氧树脂),特种工程塑料(聚苯硫醚,液晶聚合物,聚醚醚酮)不同品种的顺序,对树脂的产量,消费量及合成工艺,产品应用开发,树脂品种的延伸及应用的进一步扩展等有关技术作了详细的介绍。 相似文献
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陶瓷美术作品的艺术魅力,在于巧用艺术手法,艺术手法大致可分引用,映衬,象征,双关,拟人,夸张,借代,对比,比喻,渲染等类,巧用这些手法,能大大地增强作品的艺术感染力。 相似文献
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尿素生产不仅具有高温、高压、易燃,易爆,易中毒的化工特点,而且介质腐蚀性强,易发生泄漏,结晶堵塞,管理不好,很容易使生产装置开开停停,造成生产的极大波动,生产管理中,我们建立了健全的安全,工艺,设备,质量等方面的各类台帐,并对其分析,归纳,总结,解决了生产中多种棘手的问题,为生产的安,稳,长,优,满运行打下了基础,诸如泵进出口阀内漏,造粒机溢流尿液,冷却器列管泄漏及泵不打量等因素对生产的影响都得有效地遏制和解决。 相似文献
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橡胆虽有良好的伸缩弹性,却无理想的强度,故早已使用补强性填料和各种骨架材料加以增强,以帘线,帘布和布等形式使用的上述骨架材料大部分由连续长纤维组成,虽有强能力高,制品形状保持性好等特点,但因伸长小,在使用上受到限制,此外,加工比较复杂,而且短纤维补强的胶料,虽无大如长纤维的补强效果,但去有充分的制品形状保持性,能控制纤维的取向和胶料的定伸强度,以及加工简便等优点,故自用添加石棉的胶料制作密封胶件始,今已广泛应用来制作胶管,三角带,轮胎,胶鞋,汽车橡胶配件,圈垫,保护面罩,防弹背心,火箭件垫,查胶海绵,电磁波屏蔽材料,防静电材料和导电橡胶等产品。 相似文献
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我国精细化工中间体与催化技术的状况 总被引:1,自引:0,他引:1
我国精细化学品的分类及催化剂的应用 根据国情和国民经济发展的需要,中国将精细化学品分为农药,染料,涂料,颜料,试剂和高纯物,信息用化学品,食品和饲料添加剂,粘合剂,催化剂和各种助剂,化学药品和日用化学品。高分子聚合物中的功能高分子等11个大类。其中催化剂包括炼油,石油化工,有机化工,精细化工,合成氨,硫酸,环保用催化剂和其它催化剂;助剂包括印染助剂,塑料助剂,橡胶助剂,水处理化学品,纤维抽丝用油剂,有机抽提剂,高分子聚合物添加剂,表面活性剂,皮革化学品,农药用助剂,油田化学品,混凝土外加剂,机械和冶金用助剂,油田添加剂,炭黑,吸附剂,电子化学品,造纸化学品及玻璃防雾剂和乳胶凝固剂等其它助剂。将生产精细化学品的工业称为精细化工。 相似文献
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The effect of water on the heats of absorption from solution is shown when the water is adsorbed on the solid or dissolved in the solvent, n-heptane. The effects are examined by taking rigorous steps to exclude water and by deliberately pre-adsorbing water onto the solid or dissolving water in the solvent. The results show that water must be excluded from the solvent and many types of solid, particularly those produced in the presence of water, must be pre-treated in a carefully standardised way if calorimetry is to be used as a standard method for surface area measurement. 相似文献
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功能表面材料与流体界面相互作用对垂直降液膜流动特性的影响 总被引:1,自引:0,他引:1
通过调节水温度、添加表面活性剂以及铝合金壁面表面改性处理来改变降膜流体与固体表面之间的表面自由能差值,运用JDC-2000型精密测微仪测定垂直降液膜的厚度,研究固体表面和液体间相互作用对流体垂直降膜流动特性的影响;考察了液膜雷诺数、流体温度、添加表面活性剂、固体表面材料物理化学性质等因素对垂直壁面降液膜流动特性的影响规律。实验结果表明:改变固体表面与降液膜流体的物理化学特性,即改变固液界面的相互作用能够改变流体的降膜流动特性。降液膜平均厚度随液固表面自由能差的增大而减小。 相似文献
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介绍了万年矿选煤厂扩能改造后煤泥水系统存在处理能力不足等问题,分析了煤泥水中固体物料粒度组成、洗水浓度对跳汰作业的影响以及絮凝剂与投药量的关系,对沉淀池、洗煤储水池、压滤系统、煤泥输送管路、高频筛和浓缩机进行了相应的改造和调整,提高了煤泥系统处理能力,实现了洗水闭路循环。 相似文献
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Shuang Kun Zhang Wei Wei Liu Hui Bo Zhang Seung Kon Ryu Ri Guang Jin 《Korean Journal of Chemical Engineering》2013,30(3):746-750
Molecular weight distribution of copolyacrylonitrile, which was obtained from precipitation copolymerization without and with using dispersants in mixed solution, is studied. The contribution ratio of liquid phase polymerization and solid phase polymerization under different polymerization conditions could be worked out through the formula, which has been deduced in literature. From the calculated results, common points of each reaction system are, i) contribution ratio (r) of solid phase to liquid phase decreases with the increase of water content; thus the solid phase polymerization is gradually strengthened, which is apt to form chain of high molecular weight, ii) the higher temperature leads to higher compatibility between water and DMSO; thus the solid phase polymerization contribution would decrease, while the value of r is considerably larger. The limit molecular weight distribution of the system without dispersants in 100% water is approaching to 2; thus the corresponding r becomes larger, the molecular weight distribution ratio (Q) decreases in the system with dispersants. 相似文献
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K. W. Dillan E. D. Goddard D. A. Mckenzie 《Journal of the American Oil Chemists' Society》1980,57(7):230-237
The rate of removal of mineral oil soils from model polyester sub-strates by the roll-up mechanism shows a marked dependence
on nonionic surfactant concentration even above the critical micelle concentration (cmc). Similarly, although the solid/water
interfacial tension is observed to be constant, the equilibrium oil/water inter-facial tension in these systems consistently
decreases as the nonionic surfactant concentration is increased. The dependence of removal time and oil/water interfacial
tension on surfactant concentration above the cmc is most pronounced for nonionic surfactants having relatively high cmc.
At a given concentration, surfactants exhibiting the lowest equilibrium oil/water interfacial tension generally provide the
most effective soil removal, suggesting that the reported depen-dence of removal time on surfactant concentration is related
to the commensurate lowering of the oil/water interfacial tension. Nonyl phenol ethoxylates perform exceptionally well with
mineral oil on polyester substrates because of the combination of a low oil/water interfacial tension and high solid/water
adhesion tension. Regardless of surfactant structure, mineral oil on Teflon FEP maintains a high contact angle in the water
because the solid/oil interfacial tension is less than the solid/water interfacial tension. Oil removal in such systems occurs
only by an inefficient necking and drawing process. Oleyl alcohol displays a high contact angle in the water on both Teflon
FEP and Mylar substrates for reasons similar to that of mineral oil on Teflon FEP. Partial oil removal occurs from both substrates
in selected built systems, presumably because a low oil/ water interfacial tension promotes necking and drawing. Given sufficient
time, unremoved oils develop a liquid crystalline phase which results in slow oil removal via dispersion. Triolein soils also
possess a relatively low solid/oil interfacial tension and similarly exhibt a high contact angle (in water) on both Teflon
FEP and Mylar substrates in unbuilt surfactant systems. Builder addition lowers the oil/water interfacial tension and thereby
prompts necking and drawing action. 相似文献
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Helium diffusion studies were made on six different inorganic hydrated systems: portland cement, magnesium oxysulfate, magnesium oxychloride, tricalcium silicate, gypsum and selected molecular sieves. The helium intake versus time curves obtained after structural water was removed incrementally, starting at 11% RH, provided data that enabled an assessment of the changing character of the solid phase. Changes in solid volume and solid density were monitored as water was removed from these systems. Factors influencing physico-chemical processes such as structural collapse due to removal of interlayer or compositional water are discussed with reference to the systems studied. This comparative study also provided a further elucidation of the factors that affect the relocation of the water molecule into the structure. 相似文献
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Hydrothermal Liquefaction of Cypress: Effect of Water Amount on Structural Characteristics of the Solid Residue 下载免费PDF全文
Hydrothermal liquefaction of cypress was performed in an autoclave with various amounts of water. The obtained acid‐soluble and acid‐insoluble solid residues were characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, sugar analysis, elemental analysis, and nuclear magnetic resonance to help understand the reaction mechanisms of this process. The characteristics of solid residues were significantly affected by the water amount. Cellulose was more stable at high water amount and hemicelluloses were much more reactive than cellulose. Comparison of nuclear magnetic resonance spectra of milled wood lignin and milled solid residues indicated a significant cleavage of the side chains. The components of milled solid residues were mainly derived from decomposition and repolymerization of lignin. The decomposition of the side chains was substantial for lignin depolymerization during hydrothermal liquefaction. 相似文献
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On the Predominant Electron-Donicity of Polar Solid Surfaces 总被引:2,自引:0,他引:2
The reasons for the predominant electron-donicity of almost all solid polar surfaces and its implications are discussed in this paper. By contact angle or interfacial tension measurements, the electron-accepting as well as the electron-donating properties of polar liquids can be ascertained, through the interplay between their energies of adhesion and cohesion. For the solid-liquid interface, direct interfacial tension measurements are not possible, but indirectly, solid/liquid interfacial tensions of polar systems can be obtained by contact angle measurement. However, as the energy of cohesion of a solid does not influence the contact angle formed by a liquid drop placed upon its surface, one can only measure the solid surface'ks residual polar property, manifested by the energy of adhesion between solid and liquid. This residual polar property is of necessity the dominant component; in most cases this turns out to be its electron donicity. When, by means of contact angle measurements with polar liquids, both electron-accepting and electron-donating potentials are found on a polar solid, it is most likely still partly covered with a polar liquid: usually water. The amount of residual water of hydration of a polar solid follows from its polar (Lewis acid-base) surface tension component (γAB). The degree of orientation of the residual water of hydration on a polar solid can be expressed by the ratio of the electron-donating to electron-accepting potentials (γ⊖/γ⊕), measured on the hydrated surface. 相似文献