红萍净化水产养殖水体的研究

利用红萍(Azolla)对富营养化水产养殖水体进行净化研究。结果表明,红萍能显著增加水体中的DO,增氧幅度随流量在16.88%～70.46%之间变化,随着养殖水体流经的层数增多或者处理的时间延长,红萍对水体的增氧量加大,水中DO最终趋向一个常数值K;同时,红萍对水体中的NH₃-N和TP都有明显的去除效果,NH₃-N去除率随流量在9.86%～38.90%间波动,TP的去除率则随流量的变化在5.80%～38.43%之间波动。可见,红萍是净化水质的良好材料,能有效改善水产养殖水环境。利用红萍净化水体将为解决高密度集约化水产养殖的瓶颈提供新途径,实现水产养殖用水的封闭循环利用。     

三级串联人工快渗系统处理养殖废水

人工快速渗滤系统（constructed rapid infiltration,CRI）是在传统的污水快速渗透系统上发展起来的一种新的生物处理方法。采用猪粪浸泡污水模拟实际猪场处理系统的厌氧出水,研究三级串联人工快渗系统对其污染物的去除效果。试验结果表明,三级串联系统对废水COD、NH3N的去除率稳定在81%和94.5%,出水均满足了《畜禽养殖行业污染物排放标准》（GB18596-2001）的要求,同时三级串联系统还可以有效预防系统的堵塞。     

CASS处理技术的原理和应用

介绍了CASS工艺的原理、特点、核心构筑物和设计、运行中应注意的主要问题以及常见故障的排除方法。     

论我国国际河流可持续开发利用的问题与法律对策

中国是世界上国际河流最多的国家之一,在国际河流的开发利用方面采取了一定的措施并取得了一定的成绩,但是在国际河流的可持续开发利用中仍存在不少问题,需要完善相关的国际与国内法律制度并采取其他有效的措施予以解决。从中国国际河流的概况出发,阐述对其进行可持续的开发利用在促进中国经济发展、加强民族团结以及保障国防安全等方面的重大意义,进而分析中国国际河流在可持续开发利用中存在的问题,包括立法缺失、保障措施缺位、管理机构缺乏等,最后从完善可持续开发利用的前提要素、确立可持续开发利用的基本原则、完善可持续开发利用的立法以及积极参与可持续开发利用的国际合作等方面提出解决上述问题的对策思考,以促进和保障我国国际河流可持续开发利用的实现.     

河北省海岸带土壤盐渍化研究

在当今土地资源日益短缺的年代,作为一种土地资源,盐渍化土地越来越重要,越来越受到社会的普遍关注。本文通过分层采集土样,对整个河北省海岸带的土壤盐渍化进行了研究,在借鉴国内外先进经验的基础上,提出了土壤盐渍化防治和综合利用应视各国、各地具体情况而定,并指出盐渍土未来的研究趋势应以利用新技术、探寻新的改良方法及与农业生态和环境保护研究密切线合这三个方面为主。     

提高高校档案利用的新途径

针对目前高校档案利用率不高的实际情况,为有效地提高档案利用率,充分发挥高校档案在高校发展建设、科学管理、提升教育教学水平中的作用,笔者通过多年的探索实践,提出了加大宣传力度、搞好基础建设、提高人员素质、拓展服务方式、创新服务内容等高校档案利用的新途径,与从事高校档案工作的广大同仁商榷。     

废聚碳酸酯水解法制双酚A

以1,4-二氧六环为溶剂、NaOH为催化剂,采用废聚碳酸酯(PC)常压水解法制双酚A(BPA).对反应影响因素进行了研究.实验结果表明,在反应温度为100℃、反应时间为8h、m(NaOH):m(水+溶剂)=1:33、m(溶剂):m(PC)=4:1、m(水):m(PC)=1:1的最佳反应条件下,PC水解率大于98%,BPA收率大于95%.     

利用含铬废水和含铅废水制备铬黄

利用净化后的含铬废水和含铅废水制备铬黄.采用沉淀法对废水进行净化预处理,最佳工艺条件:100mL含铬废水中加入20 g Na_2CO_3,及10 mL H_2O_2,用NaOH调节含铬废水pH为10.00;用NaOH调节含铅废水pH为2.65.将净化后的10 mL含铬废水和25 mL含铅废水混合,在55-60℃条件下反应10 min,合成的铬黄达到GB/T 3184-2008<铬酸铅颜料和钼铬酸铅颜料>的质量标准.经重金属吸附剂处理Pb~(2+)后铬黄合成滤液中的Cr~(6+)和Pb~(2+)质量浓度均达到GB8978-1996<污水综合排放标准>的指标.     

Photocatalytic mechanisms of indoleamine destruction by the quinalphos metabolite 2-hydroxyquinoxaline: a study on melatonin and its precursors serotonin and N-acetylserotonin

The redox-active quinalphos main metabolite, 2-hydroxyquinoxaline, is particularly effective under excitation by light. We have studied the photocatalytic destruction of melatonin and its precursors, because the cytoprotective indoleamine has been detected in high quantities in mammalian skin. In photooxidation reactions, in which melatonin, N-acetylserotonin and serotonin are destroyed by 2-hydroxyquinoxaline, the photocatalyst is virtually not consumed. Rates of melatonin and serotonin destruction are not changed by the singlet oxygen quencher 1,4-diazabicyclo-(2,2,2)-octane, indicating that this oxygen species is not involved in the primary reactions, so that the persistence of 2-hydroxyquinoxaline has to be explained by redox cycling. This should imply formation of an organic radical, presumably the quinoxaline-2-oxyl radical, from which 2-hydroxyquinoxaline is regenerated by electron abstraction from indolic radical scavengers. Electron donation by 2-hydroxyquinoxaline is demonstrated by reduction of the 2,2′-azino-bis-(3-ethylbenzthiazolinyl-6-sulfonic acid) cation radical under ultrasound excitation. The compound 2-hydroxyquinoxaline interacts with the specific superoxide anion scavenger Tiron. Formation of oligomeric products from melatonin and serotonin is strongly inhibited by sodium dithionite. Products from photocatalytic indolamine conversion are predominantly dimers and oligomers. No kynuramines were detected in the case of serotonin oxidation, and melatonin's otherwise prevailing oxidation product N ¹-acetyl-N ²-formyl-5-methoxykynuramine, another cytoprotective metabolite, is only formed in relatively small quantities. The proportion between products from melatonin is changed by 1,4-diazabicyclo-(2,2,2)-octane: singlet oxygen, also formed under the influence of excited 2-hydroxyquinoxaline, only affects secondary reactions.     

Corynebacterium glutamicum as an indicator for environmental cobalt and silver stress–A proteome analysis

Cobalt and silver are toxic for cells, but mechanisms of this toxicity are largely unknown. Analysis of Corynebacterium glutamicum proteome from cells grown in control and cobalt or silver enriched media was performed by two dimensional gel electrophoresis (2DE) followed by mass spectrometry. Our results indicate that the cell adapted to cobalt stress by inducing five defense mechanisms: Scavenging of free radicals, promotion of the generation of energy, reparation of DNA, reparation and biogenesis of Fe-S cluster proteins and supporting and reparation of cell wall. In response to the detoxification of Ag⁺ many proteins were up-regulated, which involved reparation of damaged DNA, minimizing the toxic effect of reactive oxygen species (ROS) and energy generation. Overexpression of proteins involved in cell wall biosynthesis (1,4-alpha-glucan branching enzyme and nucleoside-diphosphate-sugar epimerase) upon cobalt stress and induction of proteins involved in energy metabolism (2-methylcitrate dehydratase and 1, 2-methylcitrate synthase) upon silver demonstrate the potential of these enzymes as biomarkers of sub-lethal Ag⁺ and Co toxicity.