Arsenic accumulation by two brake ferns growing on an arsenic mine and their potential in phytoremediation

In an area near an arsenic mine in Hunan Province of south China, soils were often found with elevated arsenic levels. A field survey was conducted to determine arsenic accumulation in 8 Cretan brake ferns (Pteris cretica) and 16 Chinese brake ferns (Pteris vittata) growing on these soils. Three factors were evaluated: arsenic concentration in above ground parts (fronds), arsenic bioaccumulation factor (BF; ratio of arsenic in fronds to soil) and arsenic translocation factor (TF; ratio of arsenic in fronds to roots). Arsenic concentrations in the fronds of Chinese brake fern were 3-704 mg kg-1, the BFs were 0.06-7.43 and the TFs were 0.17-3.98, while those in Cretan brake fern were 149-694 mg kg-1, 1.34-6.62 and 1.00-2.61, respectively. Our survey showed that both ferns were capable of arsenic accumulation under field conditions. With most of the arsenic being accumulated in the fronds, these ferns have potential for use in phytoremediation of arsenic contaminated soils.     

废纸造纸废水处理工程应用

报道了自制混凝剂产品处理废纸造纸废水的工程应用情况。经过 1年多的运行结果表明 ,当进水CODCr、悬浮物浓度分别为 972mg/L、82 5mg/L以及色度为 3 0 0倍时 ,采用该工艺处理后 ,CODCr去除率平均为 95 .7% ,SS去除率平均为 98.9% ,色度去除率平均为 99.3 % ,出水水质远低于国家一级排放标准 (GB3 5 44 - 92 ) ,并且工厂实践表明 ,对生产有显著的效益 ,从而证明该方法对于废纸造纸废水的处理是可行的。该处理工艺设备简单 ,系统运行稳定 ,操作方便 ,成本低     

填闲作物防治菜田土壤硝酸盐污染的研究进展

探讨了通过调整蔬菜生产的轮作结构 ,运用生物修复的原理 ,引入适宜的深根系填闲作物对深层土壤硝酸盐吸收利用 ,以避免硝酸盐进一步淋失 ,提高氮素的利用率的可行性。填闲作物应选择生长迅速、生物量大、氮素累积能力强的作物 ,在考虑填闲作物防治硝酸盐淋溶的同时 ,要兼顾其经济利用价值 ,并指出结合深根系的填闲作物进行合理轮作是蔬菜安全生产及可持续发展的途径之一     

富营养化湖泊底泥污染控制技术评估

回顾了我国在富营养化湖泊底泥污染控制技术方面的研究进展,并从富营养化湖泊底泥污染控制技术的运用效果、环境影响、社会影响、经济性、适用性以及与其他技术的相关性等六个方面,全面评估了破坏分层、人工曝气、化学增氧、底泥疏浚和底泥封闭等五类技术.     

Changes of copper speciation in maize rhizosphere soil

Chemical forms of copper in the rhizosphere and bulk soil of maize were investigated using rhizobox cultivation and sequential extraction techniques. The copper accumulations were also determined. The results demonstrated that there were continuous changes in copper fractionation within the maize rhizosphere. Initially, the amount of exchangeable copper increased before dropping below the initial level after 40 days or so. Carbonate associated copper followed a similar trend of change, but with a slower pace than the exchangeable copper. The increase in carbonate associated copper only become evident after 30 days, with the net loss occurring after 60 days. There were also initial increases in oxide bound copper as well as decreases in the organic matter associated copper, both followed by a turnover after 40-50 days. The accumulation of copper in the maize plant was found to be biomass dependent. The amount of accumulated copper absorbed in the plant material exceeded the initial quantity of the exchangeable copper in the soil, revealing a transformation from less bioavailable to more bioavailable fractions. During cultivation, decreases in redox potential and increases in pH, dissolved organic carbon (DOC), and microbial activity in the maize rhizosphere were observed. The change in copper speciation may result from root-induced changes in DOC, redox potential, and microbial activity in the rhizosphere.     

Characterization of atmospheric PM10 and related chemical species in southern Taiwan during the episode days

The concentrations of atmospheric PM10 on days with episodes of pollution were examined at four different sampling sites (CC, DL, LY, and HK) in southern Taiwan. The related to particulates water-soluble ionic species (Na+, K+, Mg2+, Ca2+, NH4+, Cl-, NO3-, SO4(2-)), carbonaceous species (EC and OC) and metallic species (Zn, Ni, Pb, Fe, Mn, Al, Si, V) were also analyzed. On the episode days of this study, the PM10 mass concentration ranged from 155 to 210 microgm(-3), from 150 to 208 microgm(-3), from 182 to 249 microgm(-3), and from 166 to 228 microgm(-3) at CC, DL, LY, and HK, respectively. The results indicate that the dominant water-soluble species were SO4(2-), NO3-, NH4+, and Cl- at the four sampling sites on these days. Moreover, the high sulfate and nitrate conversion values (SOR and NOR) presented herein suggest that secondary formations from SO2 to SO4(2-) and from NO2 to NO3- are present in significant quantities in the atmosphere of southern Taiwan on episode days. In particular, high SOR and NOR verified that both SO4(2-) and NO3- dominated the increase of atmospheric PM10 concentration in southern Taiwan on episode days.     

汽车尾气净化催化剂涂层改性研究

汽车尾气净化催化剂的净化转化效果及其耐久性，与催化剂涂层的涂覆量以及涂层和载体的结合强度密切相关。本文研究了几种不同类型表面活性剂对浆料固体含量、涂层涂覆量以及涂层结合强度的影响。研究结果表明，不使用表面活性剂时，30％为最佳的固体含量；在使用表面活性剂的情况下，浆料的固体含量可以提高至35％。非离子型表面活性剂有助于提高催化剂涂层涂覆量，而使用离子型表面活性剂的浆料球磨过程中产生大量泡沫，无法涂覆。使用非离子型表面活性剂的催化剂涂层的结合强度最好。     

生物活性炭法深度处理纺织废水二级出水中生物活性的研究

采用上流式曝气生物活性炭法处理碱减量印染废水二级生物处理出水，利用TTC-脱氢酶活性（DHA）法监测反应器内DHA生物活性分布。研究发现反应器内生物炭表面附着生物膜活性较高，特别是反应器上部生物碳粒同样具有较高的DHA活性，这与反应器运行一年多能够保持对COD、色度和UV等较高去除率有一定关系。还研究了活性炭吸附、反应器反冲洗对DHA活性的影响。本研究为曝气生物活性炭法有效去除印染碱减量废水中难降解有机物提供了一定的理论依据。     

Rapid degradation of butachlor in wheat rhizosphere soil

The degradative characteristics of butachlor in non-rhizosphere, wheat rhizosphere, and inoculated rhizosphere soils were measured. The rate constants for the degradation of butachlor in non-rhizosphere, rhizosphere, and inoculated rhizosphere soils were measured to be 0.0385, 0.0902, 0.1091 at 1 mg/kg, 0.0348, 0.0629, 0.2355 at 10 mg/kg, and 0.0299, 0.0386, 0.0642 at 100 mg/kg, respectively. The corresponding half-lives for butachlor in the soils were calculated to be 18.0, 7.7, 6.3 days at 1 mg/kg, 19.9, 11.0, 2.9 days at 10 mg/kg, and 23.2, 18.0, 10.8 days at 100 mg/kg, respectively. The experimental results show that the degradation of butachlor can be enhanced greatly in wheat rhizosphere, and especially in the rhizosphere inoculated with the bacterial community designated HD which is capable of degrading butachlor. It could be concluded that rhizosphere soil inoculated with microorganisms-degrading target herbicides is a useful pathway to achieve rapid degradation of the herbicides in soil.     

Wet air oxidation of a reactive dye solution using CoAlPO(4)-5 and CeO(2) catalysts

Wet air oxidation of a prepared reactive dye solution was performed to assess the efficacy of CoAlPO(4)-5 and CeO(2) as catalysts in the reaction. Via adsorption and oxidation of dye, CoAlPO(4)-5 effectively decreased American Dye Manufacturers Institute and chemical oxygen demand (COD) values in the dye solution. At a reaction temperature of 135 degrees C and an applied pressure of 1.0 MPa, color and COD removal were as high as 95% and 90%, respectively, after 2 h. Active sites on the outer surface of CoAlPO(4)-5 are responsible for adsorption and decomposition of dye while active sites in the pores dominate further destruction and oxidation of intermediate products. Since the outer surface only represents a minor part of the total surface, the color removal does not increase appreciably with loading of CoAlPO(4)-5. The CeO(2) catalyst, calcined from cerium chloride under high thermal impact (type A CeO(2)) was very effective in removing color and COD from the solution. This catalyst demonstrated near 100% color removal at temperatures above 135 degrees C and the COD removal could be above 95% at 165 degrees C. With both CoAlPO(4)-5 and CeO(2) catalysts, COD rose and then fell back during the reaction, a feature typical of a consecutive reaction. In contrast to prepared CeO(2), a commercial CeO(2) did not exhibit any catalytic ability for the removal of color and COD. The durability of both CoAlPO(4)-5 and prepared CeO(2) is considered to be fair.