Ru/γ-Al_2O_3和Ru/AC催化剂的制备及其对氨氧化反应的催化性能

分别以γ-Al_2O_3和活性炭(AC)为载体,采用浸渍法制备了Ru质量分数均为2.0%的Ru/γ-Al_2O_3和Ru/AC催化剂,并用X射线衍射仪和透射电子显微镜等方法对催化剂结构进行了表征.实验结果表明:Ru/AC中Ru沉积在AC表面,分散度较低;而Ru/γ-Al_2O_3中Ru进入到γ-Al_2O_3内部,形成了一种高度分散体系.Ru/γ-Al_2O_3对氨的催化活性高于Ru/AC,氨在Ru/γ-Al_2O_3和Ru/AC上的起活温度分别为200 ℃和266 ℃,T_(90)(氨去除率达90%时的反应温度)分别为267℃和320 ℃.随混合气体空速增大,Ru/γ-Al_2O_3催化剂的T_(90)逐渐升高,气体空速分别为3 600,4 800,5 400 h~(-1)时,T_(90)分别为235,266,303 ℃.随反应前混合气体中氨质量分数增加,氨的去除率降低.     

pH敏感性β-环糊精微球的制备及其吸附性能

采用反相微悬浮乳液聚合技术制备了β-环糊精(β-CD)微球,用丁二酸酐对β-CD微球进行化学改性,制备了pH敏感性β-CD(pH-β-CD)微球.通过傅里叶红外光谱仪和扫描电子显微镜对微球的结构、粒径和形貌进行了表征.探讨了亚甲基蓝模拟染料废水pH、吸附时间和微球加入量对亚甲基蓝吸附性能的影响.实验结果表明,在亚甲基蓝模拟染料废水pH为10.0、吸附时间为90 min的条件下,当pH-β-CD微球加入量为50 mg时,pH-β-CD微球吸附量为16.1 mg/g;当pH-β-CD微球加入量为250 mg时,pH-β-CD微球对亚甲基蓝的脱色率达96.2%.     

Study on Biodegradable Starch/OMMT Nanocomposites for Packaging Applications

The thermoplastic starch (TPS) and nanocomposite(TPS/OMMT) was prepared with 15% carbamide, 15% ethanolamine and different contents of organic activated montmorillonite (OMMT) by twin-screw extruder with a 130 °C barrel temperature. Fourier transforms infrared spectroscopy and wide angle X-ray diffraction shown that the alkylamine in dodecyl benzyl dimethyl ammonium bromide could react with MMT via cation exchange reaction. After treated, the d(001)space distance of MMT increased from 1.5 to 1.7 nm. Scanning electron microscope revealed that the lower contents of OMMT could disperse well in the matrixes of TPS. The carbamide, ethanolamine and the OMMT could destroy the crystallization behavior of starch, but only the OMMT restrained this behavior for long-term storing. Mechanical properties investigation indicated that the tensile strength and modulus of TPS/OMMT nanocomposites were better than those of TPS, while the elongation at break was descended with the increasing of OMMT contents. When the content of OMMT was 4%, the tensile strength and modulus of TPS was improved from 4.2 and 42 MPa to 6.0 and 76 MPa, respectively.     

Modification of Fe–Mn mixed oxide COS removal sorbent by rare-earth oxides addition

In order to develop highly active sorbent for COS removal, Fe–Mn mixed oxides doped with CeO₂, La₂O₃ or Sm₂O₃ were studied. The effects of these promoters on the structural properties of Fe–Mn oxides were investigated by XRD, BET, TPR and TEM techniques. XRD results revealed that the degree of crystallinity of Fe–Mn oxide phase decreased due to the addition of rare-earth oxides. Doping with CeO₂, La₂O₃ or Sm₂O₃ led to an increase in BET surface area of the sample. TPR studies showed that the reactivity of the reduction of doped samples increased in the temperature range of 300–450 °C. In addition, the desulfurization test was performed at 325 °C with a gas hourly space velocity of 1000 h⁻¹. It was found that the addition of 3% La₂O₃ greatly improved the absorption sulfur capacity of the sorbent, while the sorbent doped 3% CeO₂ achieved a sufficiently high purifying degree before breakthrough.     

Removal of Cr(VI) from simulative contaminated groundwater by iron metal

The Cr(VI) removal from simulative contaminated groundwater using zero-valent iron (Fe⁰) filings, Fe⁰ powder and nanoscale Fe⁰ in batch experimental mode was studied. Cr(VI) is a primary pollutant of some soils and groundwater. Zero-valent iron, an important natural reductant, could transform Cr(VI) to Cr(III) which is much less toxic and immobile. The Cr(VI) removal percentage was 87% at a metal to solution ratio of 6 g l⁻¹ for commercial iron powder (200 mesh) in 120 min, and 100% Cr(VI) was removed when the metal to solution ratio was 10 g l⁻¹. The results demonstrates that the Cr(VI) removal percentage was affected apparently by pH, the amount of Fe powder and the reaction temperature. The Cr(VI) removal percentage with nanoscale Fe⁰ was much higher than those with Fe⁰ filings or Fe⁰ powder at the same reaction time. Electrochemical analysis of the reaction process led to the conclusion that the Cr(VI) trended to form Cr(III) hydroxide under the reaction conditions. The kinetics analysis showed that Cr(VI) reduction by Fe⁰ could be described as a pseudo-first-order kinetics model.     

废水污染物排放总量控制监测技术路线及要求

从中国污染物宏观控制目标出发,阐述了中国实施废水污染物排放总量控制监测的技术路线、监测项目以及相关技术要求。对污染物排放总量控制监测分析方法的应用、采样及测流等有关技术问题,提出了见解。以１９９８年污染源调查统计资料为例,提出了污染物排放总量控制监测方案及有关监测质量的保证措施。     

实验室环境温度下电导率测定计算的改进

对原电导率温度校正公式进行了改进,改进后的校正公式在实验室环境温度（11－30℃）下较适用。     

浅谈TOC与CODCr的关系

介绍了TOC和CODCr的含义,比较了TOC与CODCr测定方法、使用仪器的不同和各自的优缺点,并从理论上和实际水样测定中论述了TOC和CODCr的相关性。对于不同的废水,TOC 与CODCr的相关性不一样,必须先实验求出二者之间的关系。     

Land desertification monitoring and assessment in Yulin of Northwest China using remote sensing and geographic information systems (GIS)

The objective of this study is to develop techniques for assessing and analysing land desertification in Yulin of Northwest China, as a typical monitoring region through the use of remotely sensed data and geographic information systems (GIS). The methodology included the use of Landsat TM data from 1987, 1996 and 2006, supplemented by aerial photos in 1960, topographic maps, field work and use of other existing data. From this, land cover, the Normalised Difference Vegetation Index (NDVI), farmland, woodland and grassland maps at 1:100,000 were prepared for land desertification monitoring in the area. In the study, all data was entered into a GIS using ILWIS software to perform land desertification monitoring. The results indicate that land desertification in the area has been developing rapidly during the past 40 years. Although land desertification has to some extent been controlled in the area by planting grasses and trees, the issue of land desertification is still serious. The study also demonstrates an example of why the integration of remote sensing with GIS is critical for the monitoring of environmental changes in arid and semi-arid regions, e.g. in land desertification monitoring in the Yulin pilot area. However, land desertification monitoring using remote sensing and GIS still needs to be continued and also refined for the purpose of long-term monitoring and the management of fragile ecosystems in the area.     

紫外分光光度法在水中阴离子表面活性剂标准样品研制中的应用

研究了阴离子表面活性剂水溶液的紫外吸收特性,并将研究结果用于阴离子表面活性剂水质标样的稳定性,均匀性和定值工作,简化了操作手续,获得了准确的分析结果。