8-羟基喹啉功能化树脂HQDK-110对Hg2+的吸附性能

8-羟基喹啉对金属离子具有良好的络合性能。研究了一种8-羟基喹啉接枝DK-110的螯合型离子交换树脂HQDK-110对Hg~(2+)的吸附性能,并与DK-110树脂进行比较。考察了不同吸附时间、Hg~(2+)浓度、温度和pH值条件下两种树脂对Hg~(2+)的吸附性能和去除性能。结果表明,HQDK-110和DK-110树脂对Hg~(2+)的适宜吸附p H值为4.5左右。25℃时,HQDK-110和DK-110树脂对Hg~(2+)的吸附容量分别为2.496 mmol/g和2.290 mmol/g。HQDK-110和DK-110对Hg~(2+)的吸附过程更接近于一级动力学方程,其一级吸附动力学常数k1分别为0.009 4 min-1和0.011 8 min-1。吸附过程符合Langmuir等温吸附方程。研究表明,HQDK-110对Hg~(2+)的吸附量和去除率优于DK-110,且树脂的稳定性优于DK-110,湿态树脂比干态树脂具有更好的重复使用性能。     

喀斯特山区水库底泥养分与重金属的含量特征——以阿哈水库为例

为摸清喀斯特山区阿哈水库底泥的养分情况和重金属污染状况,评价底泥农业资源化利用潜力,根据水库地形地貌、入库河流和出库口分布等特点,采集0~100 cm深度的底泥样品12个,分析和评价了阿哈水库底泥的养分状况及重金属污染水平。结果表明:底泥的有机质、总氮、总磷和总钾平均质量比分别为92.25 g/kg、3.35 g/kg、0.76 g/kg和14.18 g/kg,对照全国第二次土壤普查有关标准,有机质和总氮处于很高水平,总磷处于中上水平,而总钾处于中下水平,各养分指标的变异系数为25.49%~41.06%,空间差异较强;底泥Cr、Cd、Pb、As、Hg、Cu和Zn的平均质量比分别为104.86 mg/kg、1.12 mg/kg、75.87 mg/kg、26.68 mg/kg、0.27 mg/kg、59.53 mg/kg和164.65mg/kg,均高于贵州省土壤重金属背景值、贵州表生沉积物背景值和全国水系沉积物平均值,各重金属元素的变异系数为31.41%~132.34%,具有很强的空间变异性;以《食用农产品产地环境质量评价标准》为评价标准,底泥重金属內梅罗综合污染水平和潜在生态危害程度均为中等,且Cd的贡献最大。综上,阿哈水库底泥养分丰富,但污染较严重,不适于耕地利用,可考虑用于园林绿地。     

矿井环境对员工不安全行为的影响研究

通过调研,将组织任务、法制监管、作业环境、安全管理及安全技能作为影响矿工不安全行为的内部环境变量,探究内部环境与煤矿员工不安全行为的内在关联。并采用PA-LV模型检验各变量的指标权重,构建有关矿井环境因子与员工不安全行为的结构方程模型。结果表明,煤矿企业内部环境易引起矿工的操作差错,直接导致矿工的不安全行为。其中,作业环境和矿工安全技能对不安全行为影响最为显著。     

分段进水生物接触氧化工艺处理河道污水的试验研究

选择滇池入湖污染负荷最高的大清河为对象,以分段进水生物接触氧化(SFBC)工艺对河道污水开展了分流处理的试验研究,已完成冬季枯水期、春季枯水期及夏季丰水期3个时期的研究.结果表明.SFBC工艺对水质变化具有很好的适应性,调整各时期的运行参数,可以使COD及TP的去除率分别稳定在50%和40%左右,但TN的去除受水温及溶解氧等的影响很大,在逐渐稳定后去除率可达到20%左右.接种活性污泥可以加快装置的启动.但总体去除效果不及来水自然驯化的污泥.随着运行时间延长以及来水带入河道底泥的影响.有无接种污泥在处理效率上的差别逐渐消失.     

滇池流域花卉蔬菜废弃物对湖泊水质影响的模拟研究

选择流域内6种代表性的蔬菜、花卉秸秆,研究其对滇池水质的影响。结果表明：在相同水平的秸秆投加量下,TN、TP负荷量在秸秆投入水中约45d和30d左右均达到最大值,花卉秸秆在水体中TN、TP的总释放量明显高于蔬菜秸秆;水体TN、TP含量与秸秆投加量均成显著正相关。花卉、蔬菜秸秆进入滇池水后的最大潜在污染负荷量分别为：花卉秸秆的TN污染负荷为54.11g/kg,TP污染负荷为23.19g/kg;蔬菜秸秆的TN污染负荷为41.16g/kg,TP污染负荷为13.56g/kg。随意弃置堆放的花卉蔬菜秸秆对滇池水体可能存在的潜在面源污染负荷TN、TP极大值分别为12815.43 t和5290.51 t。     

西藏尼玛5.6级地震房屋震害特征分析

2009年7月24日西藏尼玛发生了5.6级地震,该地震的宏观震中位于那曲地区尼玛县西南军仓乡与阿里地区错勤县磁石乡之间,极震区烈度为7度。本文对该地震进行了现场考察,分析了灾区各类房屋建筑的震害特征及其破坏原因,并对该地区房屋的防震减灾研究提出了建议。     

Removal of fluoride from water using titanium-based adsorbents

Three adsorbents including TiO₂, Ti-Ce, and Ti-La hybrid oxides were prepared to remove fluoride from aqueous solution. The Ti-Ce and Ti-La hybrid adsorbents obtained by the hydrolysis-precipitation method had much higher sorption capacity for fluoride than the TiO₂ adsorbent prepared through hydrolysis. Rare earth (Ce and La) oxides and TiO₂ exhibited a synergistic effect in the hybrid adsorbents for fluoride sorption. The sorption equilibrium of fluoride on the three adsorbents was achieved within 4 h, and the pseudo-second-order model described the sorption kinetics well. The sorption isotherms fitted the Langmuir model well, and the adsorption capacities of fluoride on the Ti-Ce and Ti-La adsorbents were about 9.6 and 15.1 mg·g⁻¹, respectively, at the equilibrium fluoride concentration of 1.0 mg·L⁻¹, much higher than the 1.7 mg·g⁻¹ on the TiO₂. The sorption capacities of fluoride on the three adsorbents decreased significantly when the solution pH increased from 3 to 9.5. The electrostatic interaction played an important role in fluoride removal by the three adsorbents, and Fourier transform infrared (FTIR) analysis indicated that the hydroxyl groups on the adsorbent surface were involved in fluoride adsorption.     

基于3S技术的河流水污染监测信息系统的构建

分析了河流水污染的特点及其影响,简要介绍了3S技术的概念及其应用,在此基础上,构建了一个基于3S技术的河流水污染监测信息系统的总体框架,并对其中的关键技术进行了说明,以期有利于我国河流水污染防治和控制技术与手段的发展。     

Noncovalent immobilization of manganese peroxidases from P. chrysosporium on carbon nanotubes

Manganese peroxidases (MnP) from Phanerochaete chrysosporium were adsorbed onto multi-walled carbon nanotubes (MWNT). Four different loadings of MnP on MWNTs were investigated, and the maximum enzyme loading of 47.5 μg/mg of MWNTs was obtained in 12 h. The adsorbed MnP showed a catalytic activity of up to 0.1 U/mg of the weight of the system of MnP/MWNTs, with 23% of its original activity retained. The AFM image of the adsorbed enzymes indicated that a layer of MnP covered the surface of the MWNTs and retained its original three-dimensional shape. Amino-based nonspecific interactions may play the dominant role in the adsorption of MnP on MWNTs.     

Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.