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991.
992.
Guanghui Wang Lei Huang Rong Yu Nansheng Deng 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2008,83(5):601-608
BACKGROUND: Endocrine disruptors in the aquatic environment and their potential adverse effects are currently issues of concern. One of these endocrine disruptors is 2,2‐bis(4‐hydroxy‐3‐methylphenyl)propane (BPP). In this work the molecular recognition interaction of BPP with β‐cyclodextrin (β‐CD) was studied using IR spectroscopy and steady state fluorescence spectroscopy, and the photocatalytic degradation behaviour of BPP based on molecular recognition interaction was investigated in a TiO2/UV–visible (λmax = 365 nm) system. This might provide a new method for the treatment of some organic pollutants in wastewater. RESULTS: β‐CD reacts with BPP to form a 1:1 inclusion complex, the formation constant of which is 4.94 × 103 L mol?1. The photodegradation rate constant of BPP after molecular recognition by β‐CD showed a 1.42‐fold increase in the TiO2/UV–visible (λmax = 365 nm) system. The photodegradation of BPP depended on the concentration of β‐CD, the pH value, the gaseous medium and the initial concentration of BPP. The photodegradation efficiency of BPP with molecular recognition was higher than that without molecular recognition. After 100 min of irradiation the mineralisation efficiency of BPP after molecular recognition by β‐CD reached 94.8%, whereas the mineralisation efficiency of BPP before molecular recognition by β‐CD was only 40.6%. CONCLUSION: The photocatalytic degradation of BPP after molecular recognition by β‐CD can be enhanced in the TiO2/UV‐visible (λmax = 365 nm) system. This enhancement is dependent on the enhancement of the adsorption of BPP, the moderate inclusion depth of BPP in the β‐CD cavity and the increase in the frontier electron density of BPP after molecular recognition. Copyright © 2008 Society of Chemical Industry 相似文献
993.
疏水缔合型聚丙烯酰胺的合成与性能评价 总被引:1,自引:0,他引:1
为了提高高相对分子质量的聚丙烯酰胺的抗温抗盐性能,利用自制的两亲表面活性单体与丙烯酰胺共聚合成了疏水缔合型聚丙烯酰胺并进行室内评价。结果表明,在高温、高盐、高钙条件下,合成的疏水缔合型聚丙烯酰胺具有良好的增粘性和较强的热稳定性;克服了疏水缔合型聚合物在盐水中溶解性差的问题,可用各种矿化度的盐水和油田产出污水配制;具有良好的无机盐增粘性能和抗温性能。 相似文献
994.
针对茂名石化乙烯工业公司全密度聚乙烯装置翅片式空气冷却器存在的问题。结合生产实际要求进行了改造。将原设备换热芯由不可拆结构改为可抽芯结构。原圆形换热管更换为椭圆管。材质由SS304不锈钢更换为铜,并对改造后的空气冷却器进行了传热核算。理论和实践证明,改造是成功的。 相似文献
995.
996.
Shufang Wang Yuanhui Ma Yanji Wang Wei Xue Xinqiang Zhao 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2008,83(11):1466-1471
BACKGROUND: A single‐step conversion of nitrobenzene (NB) to p‐aminophenol (PAP) through catalytic hydrogenation is a widely used synthesis route for PAP. The main shortcoming of this route is the use of sulfuric acid for rearrangement of the phenylhydroxylamine (PHA) intermediate. In this paper, S2O82?/ZrO2 (PSZ) solid acid and Pt‐S2O82?/ZrO2 (Pt‐PSZ) bifunctional catalysts were prepared for the synthesis of PAP in non‐acid medium. RESULTS: Calcination temperature has a substantial effect on the acidity, structure and activity for PHA rearrangement of PSZ. The highest PAP yield was 33.8% over PSZ calcined at 823 K when the reaction was carried out in water at 423 K. A high PAP yield of 23.9% was achieved by a single‐step reaction of nitrobenzene over Pt‐PSZ bifunctional catalysts. CONCLUSION: PSZ solid acid exhibits high activity for PHA rearrangement. Perfect tetragonal ZrO2 and much stronger acid sites play important roles in catalytic activity. Inhibiting the hydrogenation activity by reducing the amount of Pt loading on Pt‐PSZ can improve the competition of PHA rearrangement on acid sites with hydrogenation of PHA on metal active sites, resulting in better selectivity to PAP. Copyright © 2008 Society of Chemical Industry 相似文献
997.
998.
Xinsheng Zhu Hansong Xu Jianmei Lu Juying Wang Shunhua Zhou 《Journal of Polymer Research》2008,15(4):295-300
Poly(ethylene terephthalate) (PET) is of excellent mechanical properties and melt processability and is widely used as raw
material for textile fibers. However, the flame retardant properties of PET were rather poor, and both reactive and additive
phosphorus- and halogen-containing compounds have been employed to enhance the reaction-to-fire properties while the meltdripping
behaviour during burning hasn’t been handled properly with the flame retardants. In this work, fluoropolymer was blended with
both pure PET (pPET) and reactive phosphorus-containing flame retarded copolyester (fPET), and the flame retardance and char
formation and mechanical properties of the resulted pPET and fPET blends were investigated. The tensile strengths of modified
pPET samples were worsen whereas those of modified fPET samples were improved at low concentrations. The initial thermal degradation
in nitrogen was accelerated remarkably for the two polyesters with fluoropolymer. The oxygen indices of the all modified samples
were reduced while char formation and meltdripping suppression were encouraged. The apparent melt viscosity and elasticity
for the two polyesters were gained much with antidripping agent. Therefore, fluoropolymer improved char formation of the two
polyesters based on the gaseous phase mechanism while the partial suppression of meltdripping behavior and the decrease of
mechanical properties mainly originated from the increase of melt viscosity via fibrillation for pPET. 相似文献
999.
1000.