中国可持续发展能力建设中人力资源开发研究

人力资源的开发是可持续发展能力建设的重要组成部分 ,也是国家财富存量的决定性因素。它涉及教育、培训、科技、扶贫、就业与劳动力转移、体制改革和国际合作等众多领域 ,直接影响到一个国家的可持续性。本文从实现国家可持续发展的目标出发 ,阐述了人力资源理论研究的进展 ,分析了中国人力资源能力建设的现状 ,并提出了相应的对策。     

Accounting for Cadmium: Tracking Emissions of Cadmium From the Global Economy

This paper examines the flow of cadmium through the global economy, with the aim of quantifying emissions of cadmium into the environment as a result of anthropogenic activities. First, a materials balance methodology is presented as the most appropriate means of assessing cadmium emissions from a wide range of anthropogenic sources. This is then applied to the best available data, from a variety of sources, to arrive at estimated flows of cadmium. Results are presented for 10 geo-political world regions and for a range of economic activities including non-ferrous metals production, iron and steel production, combustion of fossil fuels, fertilizer manufacture and use, cement production and the manufacture, use and disposal of cadmium containing products. Initially, this analysis partitions the total flow of cadmium into three major categories: atmospheric emissions, water-borne effluents and solid or bulked waste arisings. the paper then suggests a probable further partition of the initial emissions into different environmental media.     

Heavy-metal ion complexation by particulate matter in the leachate of solid waste: a multi-method approach

The metal ion binding characteristics of particulate matter obtained from column experiments on the anaerobic digestion of solid waste were studied using a titrimetric approach. The experimental set-up allowed us to study the dynamics of particle bound ligand concentrations during digestion processes typically found in landfills.We developed a continuous titration method by simultaneously using a Cd-sensitive and pH electrode and combining metal and acid/base titrations. This technique allows for a more precise determination of pK_a-log K_M pairs for each ligand than metal titrations alone. The results were compared with titration methods using differential pulse anodic stripping voltammetry (DPASV) and atomic absorption spectroscopy (AAS) with longer equilibration times in order to further characterize ligand properties such as reaction kinetics, the electrochemical lability of the respective complex during DPASV, the distinction between metal adsorption to particulate matter and metal complexation by soluble ligands adhered to particles, reversibility of the binding process by competition studies, and resistance against purging with nitrogen gas.The properties of seven major metal binding ligands were identified and assignments to the most likely functional groups were made. The most important ligand properties are for ligand A: pK_a ≈ 9.2, log K_cd ≈ 7.0 fast reaction kinetics (mercapto groups); ligand B: pK_a = 4.8, log K_Cd ≈ 6.0, slow reaction kinetics (chelates with 3 or 4 carboxylic groups); ligand C: pK_a ≈ 6.0, log K_Cd ≈ 13.0, irreversible metal binding at basic pH-values (uptake inside bacterial cells); ligand D: pK_a = 7.7, log K_Cd = 4.0, runs parallel to N content of particulate matter with digestion time (primary amines neighboring oxo groups); ligand E: pK_a ≈ 12.0, log K_Cd = 9.0, runs parallel to P content of particulate matter (phosphate); ligand F:pK_a > 9.0, log K_{Cdf = pKa + 0.4}, runs parallel to N content of particulate matter (primary amines neighboring SH groups); and ligand G: pK_a ≤ 4.8, log K_Pb ≈ 4.3, strong Pb²⁺ ligand, even at low pH-values.Metal ions were found to be irreversibly bound by ligand C at low heavy-metal concentratins, whereas at higher concentrations the binding is reversible and can be predicted using the mass of the digestion process (methanogenic phase). All other ligands have their concentration maximum in the transition phase between acetogenic and methanogenic phase.     

多种材料对水中氨氮的吸附特性

针对黑臭水体中氨氮难以去除的问题,选取沸石、麦饭石、硅藻土、膨润土和活性炭这5种材料,通过实验考察所选材料对水中氨氮的吸附性能.结果表明,准二级动力学方程更加适用于5种材料的数据拟合,得出最大吸附量分别为2. 067 3、0. 998 2、0. 758 0、1. 748 6和1. 016 0 mg·g~(-1),且接近实验值,因此化学吸附是主要的吸附方式;采用Langmuir和Freundlich等温方程对数据进行拟合,得出硅藻土更适合Langmuir等温方程,属于单层吸附,其他4种材料则更加适合Freundlich等温方程为多层分子吸附,且5种材料的吸附都为有利吸附;通过投加量实验得知,沸石、硅藻土、膨润土和活性炭对氨氮去除率随投加量增加而升高,最大去除率分别为100%、10. 46%、49. 25%和16. 87%,而麦饭石先升高后降低,投加量为0. 4g时,取得最大值为48. 85%;在p H为4～10,沸石和麦饭石吸附量先增加后减少,而硅藻土、膨润土和活性炭的吸附量缓慢升高; 5种材料氨氮解吸量随初始浓度升高而升高.     

In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal

Potassium tungstophosphate is supported on BEA zeolite by in situ synthesis for glyphosate removal. Spectroscopic measurements identified hydrogen bonding as a primal interaction of potassium salt and BEA zeolite. Composites are evaluated for glyphosate herbicide removal and adsorption process is analyzed using two isotherm models. Obtained adsorption capacities for all prepared composites lay between 45.2 and 92.2?mg of glyphosate per gram of investigated composite. Suspension acidity revealed that glyphosate is adsorbed mainly in the zwitter-ion form at the composite surface while the amount of potassium salt in the composites is crucial for the adsorption application. Exceptional adsorption behavior is postulated to come from a high degree of homogeneity among surface active sites which is confirmed by different experimental methods. Temperature programmed desorption of glyphosate coupled with mass spectrometer detected one broad, high-temperature peak which represents overlapped desorption processes from active sights of similar strength. Introduction of potassium tungstophosphate affects active sites present in BEA zeolite for glyphosate desorption and significantly increases the amount of adsorbed pesticide in comparison to BEA zeolite. Supporting of potassium tungstophosphate on BEA zeolite via in situ synthesis procedure enables the formation of highly efficient adsorbents and revealed their perspective environmental application.     

废电路板非金属材料再生木塑产品环境安全性评价

为了评价废电路板非金属材料再生产品使用过程中的环境安全性问题,本文针对非金属材料再生产品的特性,参考相关评价标准,结合目前现有的环境危害评价方法和人体健康风险评价,构建了再生产品在使用过程中环境安全性评价模型.收集A、B两种再生木塑产品进行评价试验,评估其对环境和人体健康的潜在风险和危害.结果显示在不考虑水体稀释作用情况下,两种再生木塑产品对I类地表水均存在极度或重度污染的可能,对于其他类地表水环境风险较小,应避免在源头水等区域使用;对于地下水,产品B污染指数大于1,具有一定的环境风险;但是考虑在稀释情况下（5%）,两种再生产品对于地下水的污染指数均小于1;两种再生木塑产品的非致癌风险指数分别为0.03和0.41,均小于1,对人体健康的危害作用不明显.本文可为非金属材料再生木塑产品环境安全性管理提供评价标准和参考,有利于促进废弃电器电子产品资源化和无害化技术的发展．     

稻田镉污染原位钝化修复及磷积累与迁移特征

选择苏南某镉（Cd）污染稻田,研究钙镁磷肥和钙铝水滑石2种钝化修复材料对Cd污染土壤原位钝化修复的效果,并且探讨含磷钝化剂的使用对水土环境磷累积与迁移特征的影响.结果表明：施用2种钝化剂后均能有效降低土壤中有效态Cd的含量,且随着钝化时间的推移,有效态Cd含量均呈现稳定缓慢降低的趋势,在施加钝化剂16周后达到最低,不同处理的钝化效果依次为：1500kg/hm²钙镁磷肥>6000kg/hm²钙铝水滑石>750kg/hm²钙镁磷肥,各处理有效态Cd比施加前分别降低了54.5%、50.3%以及46.9%.各处理在不同阶段的土壤pH值与有效态Cd含量呈显著负相关.施用钙镁磷肥作为钝化剂会加快土壤中磷的累积,且随着施用量的增加60~90cm深度渗漏水中总磷和溶解性磷酸盐含量有明显升高趋势.     

MOFs材料在废水污染物吸附治理中的应用研究进展

介绍了国内外MOFs材料吸附去除废水中各种污染物的研究进展,主要针对重金属离子(Hg²⁺、U⁶⁺、Cr⁶⁺、Cd²⁺、Pb²⁺、Co²⁺、Sb⁵⁺、Sr²⁺)及类金属离子(As³⁺、As⁵⁺)、有机污染物(染料分子、芳香化合物)等的去除,分析了MOFs及改性MOFs材料对废水中污染物的吸附性能;展望了MOFs材料在废水污染物吸附治理中的应用前景,提出高稳定性及具有催化性质的MOFs材料是用于废水中污染物吸附治理的理想材料。     

含能材料生产系统排产中的瓶颈设备识别方法研究

目的 识别含能材料生产车间中的瓶颈设备,对生产系统作出预警,为排产方案制定以及实际生产工作提供指导,改善生产系统的加工效率.方法 针对传统瓶颈设备识别方法评价指标单一、识别过程复杂的问题,研究一种基于灵敏度分析和逼近理想解排序法(TOPSIS)融合的瓶颈设备识别方法.该算法首先确定作业指标与设备加工量关系的灵敏度矩阵,然后运用逼近理想解排序法,计算设备的综合瓶颈指数,通过比较各设备的综合瓶颈指数,识别出瓶颈设备.结果 采用含能材料生产车间实际数据进行仿真实验,可以在生产系统运行之前识别出系统中的瓶颈设备.结论 通过与其他方法进行对比分析,验证了研究的方法的有效性和优越性.     

成都市区高层建筑电磁环境现状调查分析

由于城镇化进程的需要,越来越多的高层建筑出现在城市里,承担了我们的工作、居家、休闲娱乐的功能。随着公众环境意识逐步增强,高层建筑的电磁环境现状已成为公众关注的焦点。本文针对成都市区的高层建筑的电磁环境现状进行了调查分析。