基于“四元主体模型”的矿产资源开发生态补偿主体研究

生态补偿是矿产资源开发中迫切需要研究解决的问题,其关键是解决补偿主体缺位和研究补偿主体之间的相互关系.利用“四元主体模型”对我国矿产资源开发的生态补偿主体进行了研究.四元生态补偿主体是指矿产资源开发企业、矿产输入区、各级政府和民间环境保护组织.将矿产资源开发分为三个阶段进行研究,第一阶段是以政府为主导的开发前预防性补偿阶段,第二阶段是以企业为主导的开发中即时性补偿阶段,第三阶段是开采后的修复性补偿阶段.具体分析了矿产资源开发三个阶段的四元补偿主体变化过程及其主导补偿主体和辅助补偿主体的关系.     

Monoclonal antibody produced by heterologous indirect enzyme-linked immunosorbent assay and its application for parathion residue determination in agricultural and environmental samples

A heterologous indirect enzyme-linked immunosorbent assay (ELISA) was developed, which was based on monoclonal antibody (Mab) to determine parathion residue in agricultural and environmental samples. Eight Mabs were produced by introducing the heterologous indirect ELISA into the screening procedure. It was shown that these Mabs had more broad-reactivity with twenty competitors than that of 5H7 (Mab produced by homologous screening). So it became much easier using these new Mabs to develop heterologous immunoassays. In addition, all the developed heterologous ELISAs could be used to determine parathion residue in semiquantitative or quantitative level, and their detection limitation (LOD) was around 2 ng/mL. Compared with the previous heterologous ELISA (hapten 11/5H7) with IC₅₀ of 13.3 ng/mL, a better heterologous ELISA (hapten 11/1E1) was obtained with IC₅₀ of 3.8 ng/mL, which improved the sensitivity 3.5 times. Finally, the latter was applied to parathion residue determination in spiked agricultural and environmental samples without extraction or cleanup. The average recoveries of parathion added to water, soil, cucumber, Chinese cabbage and carrot were between 80.4 % and 111.8 %. The LOD for water and soil samples was 5 ng/mL, and the LOD for cucumber, rice and corn samples was 10 ng/mL.     

环境管制与煤炭企业竞争力关系的理论研究

随着对煤炭企业环境管制的加强,环境管制与煤炭企业竞争力之间的关系成为广泛关注的热点问题之一.环境管制最根本的目的是在环境保护的基础上维护有效和公平的竞争秩序,因此必须重新构建基于环境管制的煤炭企业竞争力模型,以期提升煤炭企业的长期竞争力,并为煤炭企业的环境战略管理决策提供参考,实现经济效率和社会效益的平衡.     

河流型水源地源水有机物种类分布特性及其与消毒副产物关系

研究了不同水文期条件下长三角某典型河流型水源地源水有机物种类分布特性及其与消毒副产物关系。结果表明，该水源地源水有机污染特性呈现出丰水期>平水期>枯水期的特点，水体腐殖化程度依次降低。经树脂富集分离后水样溶解性有机物(DOM)各组分占总有机碳(DOC)的比例有所不同。丰水期：疏水性有机酸(HPO A,38%)>亲水性有机物(HPI,26%)>过渡亲水性有机酸(TPI A,16%)>疏水性有机中性物质(HPO N,12%)>过渡亲水性中性物质(TPI N,8%)；平水期：HPO A(32%)>HPO N(22%)>TPI A(20%)>HPI(18%)>TPI N(8%)；枯水期：HPO A(28%)>TPI A(24%)>HPO N(20%)>HPI(19%)>TPI N(9%)。DOM中仅HPI组分比紫外吸光度值(SUVA)低于原水，其余均高于原水，其中HPO A组分SUVA值最高，是原水的177倍。各水文期条件下，疏水性有机物（疏水性有机酸和疏水性中性物质）对三卤甲烷和卤乙酸生成的贡献，分别超过全部有机物氯化后消毒副产物生成量的60%和65%，表明疏水性有机物是最主要的消毒副产物前体物，应当作为水处理工艺重点去除的有机物组分。各水文期源水有机物特性与消毒副产物生成潜能的关系变化不大，三卤甲烷生成潜能(STHMFP)与SUVA的线性相关度较高，卤乙酸生成潜能(SHAAFP)与SUVA的线性相关度一般。因此，可用水样SUVA值间接反映三卤甲烷生成潜能，以利于在实际生产中快速监控水中消毒副产物前体物的变化趋势     

张家口地区生态可持续性评价研究

张家口市生态环境比较脆弱。经济上属于河北省落后地区，且近邻首都北京，因此它的发展不断引起人们的关注。本文选用了由加拿大生态学家Rees和Wackenagel等提出的生态足迹模型，对张家口地区进行可持续发展的定量测算。结果表明：张家口市自1990年到2000年一直处于不可持续状态，且人均生态赤字呈逐年增大的趋势。针对这种情况，本文提出全面发展精细农业、促进工业升级以及以“人”为本的区域发展对策。     

丁二烯过氧化物的生成、危害及安全性研究

综述了国内外丁二烯过氧化物研究进展，主要包括丁二烯过氧化物的危害性、成因、危险评价和热稳定性，并对今后的研究方向进行了展望。     

湖北野生食果资源特点及其开发途径

野生食果为营养丰富的食用资源植物。在深入调查的基础上，分析了湖北野生食果资源的特点，提出了野生食果资源开发的对策以及产品深加工的途径，为野生食果资源的开发利用打下了坚实的基础。     

The Effect of Hydroxyl Radical Generation on Free-Radical Activation of TMP Fibers

The purpose of this work was to study the mechanisms involved in free radical activation of thermal mechanical pulp (TMP) fibers with the ultimate goal of developing methods for bonding wood fiber without the use of traditional adhesives. The generation of hydroxyl radicals in a mediated Fenton system was studied using electron spin resonance (ESR) spin-trapping techniques and indirectly through chemiluminescence measurement. The activation of TMP fibers was also evaluated by ESR measurement of free phenoxy radical generation on solid fibers. The results indicate that low molecular weight chelators can improve Fenton reactions, thus in turn stimulating the free radical activation of TMP fibers. However, it was also shown that excessive and prolonged free radical treatment may cause the destruction of fiber phenoxy radicals. In conclusion, this study demonstrates the potential for application, but also the complexity of free radical chemistry in biological materials, especially with regard to the chelation of transition metals and the interaction between free radicals.