水中苯胺类化合物检测1—萘酚试剂盒的研制

本文提出一种能快速灵敏地检测地面水和污水中苯胺类化合物的试剂盒。该方法是以 N-氯代丁二酰亚胺氧化苯胺 ,在 p H9- 1 1的碱性介质中 〔1〕,以 1 -萘酚偶联显色。显色反应所得的蓝色化合物的最大吸收波长为 61 0 nm,在苯胺浓度为 0 .2～ 8mg/L的浓度范围内符合比尔定律 ,最低检出限为 0 .0 2 mg/L ,测定的重现性在± 5 %以内。该试剂盒用于合成水样和环境水样的分析 ,回收率在 94.9～ 98.2之间。这种试剂盒可以成功地用于合成水样和环境水样的分析     

On the oxidative coupling of methane with carbon dioxide over CeO2/ZnO nanocatalysts

The nano-CeO₂/ZnO catalysts were prepared using a novel combination of homogeneous precipitation with micro-emulsion for oxidative coupling of methane with CO₂ as an oxidant. The prepared catalysts were compared with those prepared using the conventional impregnation. The catalysts prepared in two ways were characterized with FTIR, TEM, XRD and CO₂-TPD. The effects of the reaction temperature, the amount of ZnO doped in the catalysts and the average size were investigated. The experimental investigation demonstrated that methane conversion over the nano-CeO₂/ZnO catalysts prepared by the combined technique was higher than that obtained over catalysts prepared by the conventional impregnation. A better low-temperature activity has also been achieved over the nanocatalysts. There was no clear trend between the average size of nano-CeO₂/ZnO catalysts and their catalytic performance but methane conversion increased with increasing fractal dimension of nanocatalysts.     

航空胶片显影液调整的计算机处理方法

为解决航空胶片显影液调整问题，采用了Visual Basic6.0开发了“显影液化学分析调整软件，该系统具有一定的应用价值。     

低温快烧无铅精陶釉的研制

采用高温熔融法制备了适用精陶的低温无铅熔块，并应用热膨胀分析仪、SEM等方法研究了精陶釉的光泽度、热稳定性、热膨胀系数等性能。结果表明：采用Li2O，SrO，B2O3等复合熔剂，可以制备出光泽度高，热稳定好，坯釉膨胀系数匹配，结合良好，适于低温快烧工艺的无铅精陶釉。     

Synthesis and characterization of superabsorbent hydrogels composites based on polysuccinimide

A kind of novel superabsorbent hydrogel with high swelling ratio property that could be used for the development of water absorbing resin, soil water retention agent, and chemical sand‐fixing material was synthesized in this study. The hydrogels were prepared by the crosslinking reaction of polysuccinimide (PSI). The relationships between swelling ratio and volume of solvent as well as the concentration of crosslinking agent were investigated in detail. Several composites, such as starch, carrageenan, and polyacrylamide, were added into hydrogels to enhance the swelling ratio. It was found that the swelling ratio was significantly increased, which the maximum water absorbency was enhanced 2.46 times when the composite polyacrylamide (PAM) was added compared to the control. The effects of ionic strength and sensitivity of pH on hydrogels were also studied. The modified hydrogels products with swelling ratio less sensitivity to the salinity as well as relative high swelling ration in salinity system were also obtained by adding PAM. Through the Fourier transform infrared spectroscopy (FTIR) characterizations, the crosslinking reaction mechanism and the structure of composite were proposed. In addition, the transmission electron microscopy (TEM) examinations showed that some composite materials elevated the physical crosslinked and connected channels density substantially. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 550–557, 2006     

Decane reforming reaction over Pt,Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on Y-zeolite

Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on NaY- and HY-zeolite were examined as a catalyst for producing gasoline from n-decane via simultaneous reforming and cracking. The catalysts were prepared by calcining and reducing metal-ion-exchanged Y-zeolite with O₂ and H₂ at 300°C., respectively. Thus prepared catalysts were characterized by hydrogen chemisorption and temperature programmed desorption of ammonia. Pt-Ni/NaY and Pt-Ir/NaY bimetallic catalysts offered the improved activity maintenance compared to Pt/NaY monometallic catalyst. The catalysts supported on HY-zeolite showed higher selectivity toward C₅–C₇ and skeletal isomers of C₅–C₇- and C₈–C₁₀ than those of the catalysts supported on NaY-zeolite, which is a desired characteristic for increasing octane value of gasoline these days. However, deactivation with reaction time was much more pronounced on HY-zeolite-supported catalyst. When the catalyst was prcsulfided with H,S, the stability with time on stream was enhanced and the selectivity was quite different from that of the catalyst before presulfiding. The acidity of Y-zeolite and presulfiding of catalyst greatly influenced the activny, selectivity and stability of Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on Y-zeolite in n-decane reforming reaction.     

Role of La2O3 in Pd-Supported Catalysts for Methanol Decomposition

Systems of Pd supported on various La₂O₃-modified -Al₂O₃ and CeO₂–Al₂O₃ catalysts were tested for catalytic methanol decomposition and characterized by means of XRD, BET, TPR, H₂-chemisorption and CO–FTIR. The addition of lanthanum significantly improved the selectivity of CO and H₂ for all the catalysts but showed a different influence on the catalytic activity in two systems. Methanol conversion decreased on La₂O₃-modified Pd/-Al₂O₃ catalysts, in line with the reduction of Pd dispersion, while the addition of La₂O₃ improved the dispersion of Pd and reinforced Pd–CeO₂ interaction for La₂O₃-modified Pd/CeO₂–Al₂O₃ catalysts, which resulted in a high production rate of CO and H₂. Thus, a synergistic effect between CeO₂ and La₂O₃ was observed on -Al₂O₃-supported Pd catalyst for methanol decomposition.     

电凝聚方法处理聚氯乙烯工业废水试验

对电凝聚方法处理聚氯乙烯工业废水的效果及影响因素进行了分析研究。现场运 行结果表明,该方法试验装置对聚氯乙烯废水的处理效果较好,出水水质达到综合排放 标准,对COD,BOD和TSS的去除率分别达到95％,91％和90％;对废水流量负荷的变化 具有较好的适应性,保证出水水质稳定;装置的运行成本经济实用。     

骨组织工程支架材料

寻找理想的支架材料是目前骨组织工程研究的热点。本文对用于骨组织工程支架材抖的天然生物衍生材料、聚合物类材料、陶瓷材料及其复合材料等的研究现状进行综述，分析了这些材料的优缺点，并对骨组织工程支架材料发展趋势进行了展望。     

Synthesis and properties of new polymerized monomer reactants matrix resins of pyrrolone–benzimidazole copolymers containing pyridine unit

A series of new polymerized monomer reactants (PMR) matrix resins of poly(pyrrolone‐benzimidazole)s containing a pyridine unit (PPBP) were synthesized by polycondensation of monoethyl ester of cis‐5‐norbornene‐endo‐2,3‐dicarboxylic acid, 2,6‐diphenyl ester pyridinedicarboxylic acid or 3,5‐diphenyl ester pyridinedicarboxylic acid, and diethyl ester of 4,4′‐oxydiphthalic acid with 3,3′‐diaminobenzidine in a mixing solution of anhydrous ethyl alcohol and N‐methylpyrrolidone under given temperature and pressure conditions. The resulting resin solutions showed good solubility in polar organic solvents and stability at room temperature. The corresponding PPBP matrix resin, molded powder, and molded plate were prepared by undergoing amidation, imidization, cyclization, and crosslinking reactions when the reaction temperature was increased from 80 to 350°C, successively; the crosslinking structure was formed by the reverse Diels–Alder reaction at 270–290°C under 50 MPa pressure (2.5–3.5 MPa displayed by the pressure meter). The chemical reactions and properties of the resulting PPBP were studied by means of FTIR, TGA, and DMA methods, and the results indicated that the kinds of PPBP materials retain excellent thermal stability and processability; when the initial decomposition temperature was above 620°C the T_g was at 413.5°C for 3,5‐PPBP‐20 molded plate. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3981–3990, 2004