废弃混凝土再生利用的产业化研究

作为大规模城市化的产物,废弃混凝土引发了一系列的资源和环境问题.废弃混凝土的再生利用技术已经日趋成熟,而市场化推广却遇到成本、制度等方面的一系列难题.引入循环经济的理念,对废弃混凝土与再生混凝土进行成本比较、对产业化的困难和条件进行了剖析,并从技术、产业、经济等各方面提出了政策建议,也可为其它资源再生产业的发展提供一定的借鉴.     

论区际环境关系及其调控

区际环境关系是环境科学理论和实践研究的重要课题，随着生产力的发展，环境作为一种烯缺资源纳入人类的经济生活和社会生活中，由于存在局部环境利益的差异，不同区域的环境利益主体在追求利益最大化的驱动下，势必把环境成本转嫁与其他区域，这就促使原始的纯粹的区际自然关系发生深刻变化，新的区际环境关系发育和建立，文章认为，区际环境关系受社会经济诸多因素的影响，应从经济，法律和行政等多方面着手调控区际环境关系，建立科学，合理，公平的区际环境协作关系，以实现环境资源的集约化使用和生态环境问题的系统整治。     

模拟酸雨下土壤中稀土元素的环境化学行为和植物可利用性研究

研究了模拟酸雨对两种土壤中稀土元素的环境化学行为和植物可利用性的影响．结果表明，酸雨的酸度及淋洗量皆对稀土元素的淋溶产生影响，酸雨淋洗使土壤中稀土元素的形态含量发生了改变．由回归分析得知，有效态稀土的主要存在形态是交换态和松结有机态，实验表明，稀土的植物可利用性随模拟酸雨淋洗液的酸度增大而减小．     

Fluorescence spectroscopic studies of natural organic matter fractions

Because of the well-known molecular complexity and heterogeneity of natural organic matter (NOM), an aquatic bulk NOM was fractionated into well-defined polyphenolic-rich and carbohydrate-rich subfractions. These fractions were systematically characterized by fluorescence emission, three dimensional excitation-emission matrices, and synchronous-scan excitation spectroscopy in comparison with those of the reference International Humic Substances Society soil humic acid and Suwannee River fulvic acid. Results indicate that fluorescence spectroscopy can be useful to qualitatively differentiate not only NOM compounds from varying origins but also NOM subcomponents with varying compositions and functional properties. The polyphenolic-rich NOM-PP fraction exhibited a much more intense fluorescence and a red shift of peak position in comparison with the carbohydrate-rich NOM-CH fraction. Results also indicate that synchronous excitation spectra were able to provide improved peak resolution and structural signatures such as peak positioning, shift, and intensity among various NOM components as compared with those of the emission and excitation spectra. In particular, the synchronous spectral peak intensity and its red shift in the region of about 450-480 nm may be used to indicate the presence or absence of high molecular weight and polycondensed humic organic components, or the multicomponent nature of NOM or NOM subcomponents.     

日光/H_2O_2/草酸铁体系对垃圾渗滤液深度处理的试验研究

以草酸铁络合物/H2O2作光氧化剂,利用日光对垃圾渗滤生化出水进行了光氧化降解试验。结果表明,在溶液的初始体系pH=3.0,H2O2投加量为460mg/L,Fe3+质量浓度为20mg/L条件下,反应60min后,CODCr去除率可达80%以上;溶液初始体系的pH、H2O2和Fe3+的投加量及废水的水质对光解过程有显著影响,而且在太阳光照射下,CODCr去除率比紫外光照射下高。研究表明,在一定试验条件下,用日光/H2O2/草酸铁体系对城市垃圾渗滤液处理效果较好,可作为垃圾渗滤液的深度处理。     

水体pH和曝气方式对藻类生长的影响

利用水族箱微宇宙研究了藻类在不同pH和曝气条件下的生长和种类变化.使用天然湖水,一组试验每天调节pH,使其分别保持在8.0、8.5、9.0和9.5;另一组试验是设定不同的曝气方式,分别为不曝气、完全曝气、昼间曝气和夜间曝气,定期测定水体叶绿素a和藻类组成.pH试验结果显示,在pH 8.0～9.5范围内,pH 8.5下藻类生长状况最好,pH 9.5下生长最差,人为改变pH使其远离8.5能够抑制藻类生长.曝气试验结果显示,曝气不能抑制水体中藻类的生长,昼间曝气甚至还有明显的促进作用.     

Reaction-enhanced mass transfer and transport from non-aqueous phase liquid source zones

The objective of the following research is to theoretically quantify the enhancement of interphase mass transfer of dissolved non-aqueous phase liquid (NAPL) compounds from the non-aqueous phase to the aqueous phase and the enhancement of dispersive mass transport from a NAPL zone due to destruction of dissolved NAPL compounds. For relatively slow reaction rates, such as for permanganate and perchloroethene (PCE), local-scale mass transfer enhancement is expected to be small. Dispersive mass transport with reaction from a horizontal NAPL zone can be quantified using equations derived for a mathematically equivalent falling film reactor system. In contrast to local-scale interphase mass transfer, dispersive mass transport from NAPL zones may be significantly increased by reaction. Enhancement factors due to destruction of the NAPL compound(s) are mainly dependent on NAPL solubility and oxidant concentration and to a lesser extent on reaction rate, stoichiometry, and transverse dispersion coefficients. Higher NAPL solubility and/or lower oxidant concentration reduces the maximum expected enhancement factor. Reaction enhancement factors for mass transport from NAPL zones are expected to be in the range of 5-50 for permanganate and chlorinated solvents. Theoretical results suggest that assuming instantaneous reaction rates may be appropriate for dispersive mass transport from NAPL zones.     

Bioaccumulation of the rare earth elements lanthanum, gadolinium and yttrium in carp (Cyprinus carpio)

Widespread use of the rare earth elements (REEs) in China for agricultural purposes, together with many other applications, has resulted in a remarkable increase of REE concentrations in the environment. The comparative bioaccumulations of representative light, medium and heavy REEs in a variety of tissues of carp (Cyprinus carpio L.) were investigated for an evaluation of their impacts on aquatic animals. The fish were exposed continuously to solutions containing 0.50 mg litre(-1) of each element for 45 days at pH 6.0 and sacrificed at time intervals. Skeleton, muscle, gills and internal organs were analysed for REE contents. A method using cation-exchange resin separation and ICP-AES determination was developed for the quatification of individual REEs. The results show that carp has low ability to take up the REEs under the experimental conditions. The order of REEs under the experimental conditions. The order of maximum bioconcentration factors was mostly internal organs > gills > skeleton > muscle. Neither synergistic nor antagonistic effects of the mixed REE solutions for carp were observed. The relative distributions of different REEs in the investigated tissues exhibited similar patterns. Among the selected tissues studied, the concentration of a heavy REE (Y) was the smallest, while concentrations of a medium (Gd) and a light REE (La) showed only a slight difference.     

新型水处理活性炭选型技术

活性炭依其原料不同、生产工艺不同,而有不同的吸附性能.使用简易的活性炭选型方法,可以减少应用测试时的备选炭型,从而大大降低活性炭水处理技术的运行成本.以碘值、甲基蓝值、苯酚值和丹宁酸值4种吸附容量性能指标为依据的活性炭选型技术,可以有效地预测活性炭对于水中各种大小不同污染物的去除能力.BET测试结果证明了这4项指标数据对于活性炭孔径分布预测的准确性.2,4-二氯苯酚和腐殖酸等目标化合物的吸附容量实验结果也都验证了这4项指标的预测功用,说明这种简便的活性炭选型技术有着广泛的应用价值.     

有机粘土和粘土对p,p''''-DDE的吸附/解吸研究

采用批量平衡实验,研究阳离子表面活性剂十六烷基三甲基铵离子(HDTMA)改性的zeo-HDTMA(有机沸石)、mont-HDTMA(有机蒙脱土)和atta-HDTMA(有机凹凸棒土)及其原粘土对典型有机氯农药DDT代谢产物p,p'-DDE的吸附解吸特性.结果表明,随原粘土阳离子交换容量(CEC)的增大,有机粘土吸附量增大,且有机粘土的吸附量比原粘土大大提高;有机粘土和原粘土对p,p'-DDE的吸附能力顺序为:zeo-HDTMA＞mont-HDTMA＞atta-HDTMA≥mont(蒙脱土)＞atta(凹凸棒土)＞zeo(沸石),这一顺序与它们的有机碳质量分数大小顺序一致.原粘土对p,p'-DDE的吸附等温线符合Langmuir吸附等温方程,吸附呈单分子层形式,且存在竞争吸附;有机粘土对p,p'-DDE的吸附等温线符合Linear吸附等温方程,吸附是p,p'-DDE在有机粘土中有机相的分配所致.当CaCl2质量浓度从0增加到50 g/L时,mont-HDTMA对p,p'-DDE吸附量提高了10.3%.有机粘土和原粘土对p,p'-DDE的解吸率大小顺序为:zeo＞atta＞mont＞atta-HDTMA＞mont-HDTMA＞zeo-HDTMA,这一顺序与它们的有机碳质量分数大小顺序相反.