Study on heat conduction and adsorption/desorption characteristic of MIL-101/few layer graphene composite

Journal of Porous Materials - Aiming at the poor heat conduction performance of porous MIL-101 applied in adsorption cooling process, few layer graphene (FLG) was selected as a promising thermal...     

Synergistic inhibition between o-phenanthroline and chloride ion for steel corrosion in sulphuric acid

The corrosion inhibition of cold rolled steel in 0.5 M sulphuric acid in the presence of o-phenanthroline and sodium chloride (NaCl) has been investigated by using weight loss and electrochemical techniques. The experimental data suggest that the inhibition efficiency increases with increasing NaCl concentration in the presence of 0.0002 M o-phenanthroline, but decreases with increasing temperature. A synergistic effect is observed when o-phenanthroline and chloride ions are used together to prevent cold rolled steel corrosion in 0.5 M sulphuric acid. The polarization curves showed that the complex of o-phenanthroline and NaCl acts as a mixed type inhibitor. The experimental results suggested that the presence of chloride ions in the solution stabilized the adsorption of o-phenanthroline molecules on the metal surface and improved the inhibition efficiency of o-phenanthroline. The adsorption of the complex accords with the Langmuir adsorption isotherm. Some thermodynamic parameters such as adsorption heat, adsorption entropy and adsorption free energy have been calculated by employing thermodynamic equations. Kinetic parameters such as apparent activation energy and pre-exponential factor have been calculated and discussed.     

回火过程应力场计算机模拟

回火过程应力场计算机模拟林家骝，杨振枢，于震宗，段贵明（清华大学）郭剑仁，史全兴，谢克仁（内蒙古第一机器厂）ＡＳｔｕｄｙｏｆＮｕｍｅｒｉｃａｌＳｉｍｕｌａｔｉｏｎｏｆＳｔｒｅｓｓＦｉｅｌｄｄｕｒｉｎｇＴｅｍｐｅｒｉｎｇ￥ＬｉｎＪｉａｌｉｕ；ＹａｎｇＺ...     

煤焦油蒸馏的新产品-改质沥青的生产

论述了利用热缩聚方法对中温沥青进行改质处理来生产改质沥青 ,提高了沥青的软化点、β树脂含量及结焦值 ;并介绍了生产工艺的特点、主要工艺参数及产品的质量     

A rheological model for iron oxide suspensions

We have examined the rheological properties of a Co-adsorbed γ-Fe₂O₃ magnetic suspension with polyurethane (PU) as a binder and methyl ethyl ketone (MEK) or cyclohexanone (CH) as a solvent. A Haake RV20 viscometer was used to measure the suspension viscosity and the vane method was adopted to determine the fluid yield stress. A rheological model which can be viewed as a combination of the Casson model and the Bingham model is proposed to describe the suspension viscosity. The effects of temperature, particle content, and binder concentration are included in the model.     

Effects of Stearic Acid on the Injection Molding of Alumina

This research investigated the influence of stearic acid on the injection molding of alumina, by varying the concentration of stearic acid. The interaction between stearic acid and alumina was identified using transmission infrared spectroscopy, indicating stearic acid preferentially adsorbed onto the alumina powder surface. In addition to slightly modifying the intrinsic binder viscosity, stearic acid adsorbed onto the powder surface changed the flow behavior of the mixtures from dilatant flow to pseudoplastic flow at low temperatures. As a result, inhomogeneous distribution of binder in the injection-molded parts was minimized with increased stearic acid concentration. However, the possibility of forming bubbles in the mixtures arising from vaporization of stearic acid was enhanced. Additionally, the binder burnout temperature range was broadened with the increase of stearic acid concentration.     

枯草杆菌碱性磷酸酶制备的最佳工艺条件及酶促反应动力学性质的研究

以枯草杆菌为菌种液体培养制备碱性磷酸酶，研究确定了培养的最佳工艺条件，并对碱性磷酸酶的酶促反应动力学性质进行了初步探讨。结果表明，枯草杆菌制备碱性磷酸酶的最佳工艺条件为：40℃，pH值7．4振荡培养10h，酶活最高。对碱性磷酸酶的动力学性质研究表明，该酶催化底物磷酸苯二钠水解反应的最适pH值8．8，最适温度52℃，米氏常数Km值为2．94mmol／L。     

Gel formation in diimide‐hydrogenated polymers

The hydrogenation of diene‐based polymers via diimide is a very attractive alternative to the conventional catalytic hydrogenation route based on gaseous molecular hydrogen. However, serious crosslinking always accompanies it and limits the end‐use properties of the polymers. Gel formation in polymers that are hydrogenated via diimide has been investigated in detail through an inspection of all the chemical reactions involved in the process. The results indicate that hydrogen peroxide decomposition, some reactions related to oxygen, and the redox reaction between hydrogen peroxide and hydrazine are capable of generating radicals. However, radicals generated in the aqueous phase do not appear to initiate the crosslinking of diene‐based polymers in the latex form. It is proposed that the primary radicals giving rise to crosslinking are generated in the polymer phase in situ, and the step responsible for generating these organic radicals is possibly the diimide disproportionation reaction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1122–1125, 2005     

High temperature polymerization of propylene catalyzed by MgCl2‐supported Ziegler–Natta catalyst with various cocatalysts

Four cocatalysts, referred to as ethylaluminoxanes, were synthesized by the reaction between triethylaluminium (AIEt₃) and water under various molar ratios of H₂O/Al at ?78°C. Aluminoxanes were used as cocatalysts for a MgCl₂‐supported Ziegler–Natta catalyst for propylene polymerization at temperatures ranging from 70 to 100°C. When the polymerization was activated by AlEt₃, the activity as well as the molecular weight and isotacticity of the resulting polymer gradually dropped as the temperature varied from 70 to 100°C. When ethylaluminoxane was employed as the cocatalyst, good activity and high molecular weight and isotacticity were obtained at 100°C. Furthermore, when the cocatalyst varied from AlEt₃ to ethylaluminoxane, the atactic fraction and polymer fraction with moderate isotacticity decreased and the high isotactic fraction slightly increased, which indicated that the variation of the cocatalyst significantly affects the isospecificity of active sites. It was suggested that the reactivity of the Al‐Et group and the size of the cocatalyst were correlated to the performance of the Ziegler–Natta catalyst at different temperatures. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1978–1982, 2006