液体浮选法回收废旧电脑线路板中铜的研究

本文用物理及化学方法研究了废旧电脑线路板的处理回收工艺.首先通过粉碎机将线路板破碎,在不同破碎时间和转速下,对筛分后各粒级的产物作累积产率曲线,得到理想的破碎时间和转速,然后利用液体对破碎的物料进行浮选,量化分析铜与非金属的解高程度,最后通过碘量法检测浮选后铜的回收情况.实验结果表明:在R＞2000 rpm的条件下线路板粉碎120s,采用三溴甲烷作浮选液,进行液体浮选,在dp＜0.074 mm的细粒级中,主要是玻璃纤维和碳化硅等非金属物质,线路板中的铜主要富集在0.84～0.125 mm粒级中,在0.84～0.42 mm粒级中,铜的回收率可达到97.89%.     

PVC包装材料中酞酸酯增塑剂残留的ASE-GC-MS分析

针对PVC包装材料中酞酸酯（PAEs）增塑剂残留，采用加速溶剂萃取（ASE）和GC／MS联用技术分析5种PAEs（DMP，DEP，DBP，BBP，DEHP），结果表明加速溶剂萃取用于PVC包装材料中PAEs的提取，最佳温度条件为120℃，最佳循环次数为3次。方法检出限达到0．1mg／kg，回收率达到95．5％-99．8％；并且具有很好的重现性和精密度。     

关于建设(开发)项目环境影响评价报告书编制两个版本的思考

为充分发挥环境影响评价报告书的作用，提出应在环境影响报告书技术版的基础上编制一个面向领导决策者和公众的参考版。并就参考版的主要内容及编制应注意的问题进行了概述。     

Detection of Escherichia coli in wastewater based on enzyme immunoassay

This research describes a fast detection method on the basis of enzyme-linked immunosorbent assay (ELISA) for Escherichia coli in drainage of wastewater treatment plants. Optimized conditions such as the reaction format (sandwich or direct), the concentrations of diluted horseradish peroxidase (HRP)-E. coli conjugate, and anti-HPR antibody and pretreatment of E. coli were studied. Those results showed that the linear range of detection for E. coli was 10 cfu/mL-6 × 10⁴ cfu/mL. Compared with conventional methods, it is a convenient and sensitive detection method with low cost. Translated from Environmental Science, 2005, 26(5): 128–131 [译自: 环境科学]     

X射线晶体学对造岩矿物研究的应用

本文主要叙述XRD（X射线衍射）及单晶X射线回摆图在选岩矿物研究中的应用，不涉及X射线晶体结构分析。     

抚顺市空气可吸入颗粒物特征的研究

于2002年1～7月份在抚顺市区四个点位采集了环境空气中的可吸入颗粒物样品，经分析后获得了可吸入颗粒物组分的时间分布和空间分布特征，即采暖期PM10样品中有机碳（OC）、元素碳（EC）的绝对含量和相对含量均高于非采暖期，工业区PM10样品中的Fe、Zn、Pb的绝对含量和相对含量均明显高于其它点位，反映了其工业区的特点。     

Cu／A1-Ce-PILC在丙烯选择性催化还原NO反应中的失活研究

采用聚合羟基复合阳离子合成交联黏土A1-Ce-PILC，经SO4^2-改性后，以浸渍法制备了铜基交联黏土催化剂Cu／A1-Ce-PILC，并将其应用于C3H6选择性催化还原NO的反应，350℃时NO转化率达到最大值56％，700℃时下降至22％．为探究催化剂高温失活的原因，采用XPS、TPR、TGA、Py-IR和DSC对反应前后催化剂的物化性能进行了表征．结果表明，经过H2预处理活化后活性组分Cu物种以Cu^＋形式存在，而高温反应后Cu物种除以Cu^＋和Cu^2＋ 2种形式存在外，还出现了少量CuO物种；高温反应过程中A1-Ce-PILC上结构羟基和SO4^2-流失导致催化剂表面酸性减弱；此外，还存在表面积炭覆盖了部分活性中心并堵塞了催化剂孔道的现象．这三者的共同影响促进了C3H6深度氧化，抑制了NO还原，从而导致催化剂的失活．     

Carbon isotope ratios in logged and unlogged boreal forests: Examination of the potential for determining wildlife habitat use

Due to assimilation of recycled CO₂ from litter decomposition and photosynthetic changes in carbon fractionation at low light levels, the foliage at the base of a forest is often more depleted in¹³C compared to that exposed to the atmosphere in either the canopy or in open clearings. This is referred to as the canopy effect. African research has indicated that these habitat differences in foliar ¹³C can be substantial enough to affect the carbon isotope ratios of resident fauna. Previous work documenting a 30-year chronology on moose teeth from Isle Royale National Park indicated a progressive depletion in¹³C and suggested that this could be due to forest regrowth following extensive burning. The present study examined the assumption implicit in this hypothesis that foliar ¹³C varies between open and closed boreal forest sites. I found a marginal canopy effect of 2 ¹³C difference between upper canopy and ground flora for a forest in northwestern Ontario and an average difference of 1.2 in under- and mid-story vegetation between closed forests and open clear-cuts. Because of these small differences, the utility of carbon isotope analysis in quantifying temporally integrated exploitation of deforested habitats will be low for northern boreal locations. In denser forests, such as those in the tropics or western North American where the canopy effect can be expected to be much greater, ¹³C analysis may still offer some promise for determining selection by wildlife of disturbed habitats.     

Synthesis and biodegradation of poly(γ-butyrolactone-co-l-lactide)

Biodegradable polyesters were synthesized by ring-opening copolymerization of -butyrolactone (BL) and its derivatives withl-lactide (LLA). Although tetraphenyl tin was the main catalyst used, other organometallic catalysts were used as well.¹H and¹³C NMR spectra showed that poly(BL-co-LLA)s were statistical and that their number-average molecular weights were as high as 7×10⁴. The maximum BL content obtained from copolymerization BL/LLA was around 17%. TheT _m andT _g values of the copolymers showed a gradual depression with an increase in BL content. NoT _m was obtained for the copolymers containing more than 13 mol% BL. The biodegradability of the copolyesters was evaluated by enzymatic hydrolysis and nonenzymatic hydrolysis tests. The enzymatic hydrolysis was carried out at 37°C for 24 h using lipases fromRhizopus arrhizus andR. delemar. Hydrolyses by both lipases showed that an increase in BL content of the copolymer resulted in enhanced biodegradability. Nonenzymatic accelerated hydrolysis of copolymers at 70°C was found to increase proportionally to their exposure time. The hydrolysis rate of these copolymers was considerably faster than that of PLLA. The higher hydrolyzability was recorded for the BL-rich copolymers. The copolymerization of -methyl--butyrolactone (MBL) or -ethyl--butyrolactone (EBL) with LLA resulted in relatively LA-rich copolymers.     

重金属离子-二乙基二硫代氨基甲酸钠螯合体系的HPLC分析方法研究

采用二乙基二硫代氨基甲酸钠(NaDDC)为螯合剂,对Cu(Ⅱ)、Hg(Ⅱ)、Pb(Ⅱ)、Zn(Ⅱ)、Cd(Ⅱ)、Cr(Ⅵ)六种重金属离子进行了螯合萃取分离体系的方法研究,用HPLC方法建立了上述金属离子的最佳分离条件及定性定量分析方法.结果表明,用C18反相柱(5μm,150×4.6mmi.d.)和流动相(V(乙腈):V(甲醇):V(水)=55:15:30)能有效分离上述重金属离子,最低检测限在0.1～1.6ng范围内,线性范围及线性关系满足定量分析要求.