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991.
稀土复合热稳定剂对聚氯乙烯性能影响研究 总被引:7,自引:0,他引:7
主要以有机锡热稳定剂为对比物,研究了稀土热稳定剂对聚氯乙烯(PVC)的热稳定性及其他性能的影响。稀土热稳定剂对PVC的力学性能、加工性能都有不同程度的提高,稀土热稳定剂的热稳定性能符合PVC的加工条件要求,并研究了抗冲改性剂ACR(丙烯酸酯共聚物)对体系的影响。 相似文献
992.
993.
The objective of this work is to study the transfer of oxygen from gas to liquid phase in an electroflotation cell. The measurements
were performed in a laboratory scale cell using insoluble electrodes, titanium coated with ruthenium oxide as anode and stainless
steel as cathode. The volumetric mass transfer coefficient K
L
a, was characterized for clean tap water as liquid phase for different values of current density (J). The global coefficient
of mass transfer based on the liquid film, K
L
, and the specific interfacial area, a, were characterized. A model which relates K
L
a to current density was established. Different evaluation criteria of oxygen transfer in electroflotation process were determined
and compared with other aeration process. 相似文献
994.
995.
聚合物防老化稳定剂的协同作用机理 总被引:18,自引:0,他引:18
从聚合物热氧老化和光氧老化机理出发,介绍了不同稳定剂间的相互作用,可能产生的协同及反协同作用机理以及一些实用实例。 相似文献
996.
The N‐[3‐(dimethoxy‐methyl‐silanyl)‐propyl]‐N′‐ (9‐methyl‐3,9‐dioxo‐2,4,8,10‐tetraoxa‐3,9‐diphospha‐spiro[5.5]undec‐3‐yl)‐ethane‐1,2‐diamine/dimethoxy dimethyl silane copolymer (PSiN II), which simultaneously contains silicon, phosphorus, and nitrogen, is synthesized and incorporated into polypropylene (PP). The flame retardancy is evaluated by the limiting oxygen index value, which is enhanced to 29.5 from 17.4 with 20% total loading of PSiN II. The thermal degradation behavior of PP/PSiN II is investigated by thermogravimetric analysis under N2 and air. The PP/PSiN II sample degrades at 400°C for different amounts of time, and the process of degradation is studied by Fourier transform IR. The morphology of the char formed at 400°C for 10 min is investigated by scanning electron microscopy. The swollen inner structure, close, and smooth outer surface provide a much better barrier for the transfer of heat and mass during fire and good flame retardancy. The thermal stability of PP is improved by incorporation of PSiN II. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2487–2492, 2005 相似文献
997.
Jose Gerde Connie Hardy Walter Fehr Pamela J. White 《Journal of the American Oil Chemists' Society》2007,84(6):557-563
Two extruded-expelled physically refined soybean oils with reduced contents of linolenic acid, ultra-low- linolenic acid (ULL,
1.5%) and low-linolenic acid (LL, 2.6%), and a extruded-expelled physically refined control oil (control, 5.3% linolenic acid)
were evaluated by frying French fries in a commercial-like setting for 6 h day−1 during 23 days. The oils became darker, increased in yellow color at the beginning, and became redder and less green throughout
the process. Free fatty acids levels were not different among the oils until day 14, after which, ULL was different from the
control for the remainder of frying. The conjugated dienoic acid values were greatest in the control. Generally, ULL and LL
oils had lower percentages of polar compounds than did the control, providing a frying life 2 days longer than the control
and ~30% increase in frying time. A trained sensory panel evaluated the French fries on days 2, 5, and 6. Buttery and potato
flavors decreased, and rancid and painty flavors increased over frying time for all products. Rancid flavor was highest in
the fries from the control oil. Overall, the ULL and LL oils performed better than did the control oil and ULL tended to perform
better than the LL. 相似文献
998.
999.
Raúl Quijada Juan Luis Guevara Mehrdad Yazdani-Pedram Griselda B. Galland Daniel Ribeiro 《Polymer Bulletin》2002,49(4):273-280
Summary
1-Octadecene (C18) was polymerized by using different metallocene catalysts. The rac-Et(Ind)2ZrC12/MAO (I) and rac-Me2Si(Ind)2ZrC12/MAO (III) presented the highest activity as compared with ra-Et(2-Me-Ind)2ZrCl2/MAO (II) and Ph2C(Flu)(Cp)ZrC12/MAO (IV) catalysts. Catalyst IV produced polymers with highest molecular weights. The microstructure of the polymers was
determined by 13C-NMR spectroscopy. Catalyst systems I, II and III produced isotactic polymers while catalyst IV produced polymers with mainly
syndiotactic structures but with large amount of stereoregular error.
Received: 21 June 2002/Revised version: 4 November 2002/ Accepted: 4 November 2002 相似文献
1000.