基于层次分析法的矿山地质环境影响评价研究

对治理区矿山开发过程中的地质状况进行实地调研,对治理区所处的矿山地质条件及矿山环境等展开了讨论。在此基础上,运用层次分析法对矿山地质环境影响作出定量的分析评价,文中选取目标层、标准层、指标层三个层次影响因子,计算影响因子的权重,从而得出最终影响矿山地质环境影响的结果。在定性分析的基础上,将定性分析与定量分析相结合,为后续治理区矿山开发工作研究提供借鉴意义。     

炼油工业废水局部零排放技术策略

针对我国部分炼油企业含盐废水难以达标排放这一现状,从实际情况出发,提出部分废水实施零排放处理的措施。分析了炼油废水实施零排放处理诸方面的问题,并围绕"预处理—减量化—深度浓缩—分盐结晶"的技术路线进行了探讨。     

Dynamics of major air pollutants from crop residue burning in mainland China, 2000–2014

Based on satellite image data and China's Statistical Yearbooks(2000 to 2014), we estimated the total mass of crop residue burned, and the proportion of residue burned in the field vs.indoors as domestic fuel. The total emissions of various pollutants from the burning of crop residue were estimated for 2000-2014 using the emission factor method. The results indicate that the total amount of crop residue and average burned mass were 8690.9 Tg and4914.6 Tg, respectively. The total amount of emitted pollutants including CO_2, CO, NOx,VOCs, PM_(2.5), OC(organic carbon), EC(element carbon) and TC(total carbon) were 4212.4–8440.9 Tg, 192.8–579.4 Tg, 4.8–19.4 Tg, 18.6–61.3 Tg, 18.8–49.7 Tg, 6.7–31.3 Tg, 2.3–4.7 Tg, and8.5–34.1 Tg, respectively. The emissions of pollutants released from crop residue burning were found to be spatially variable, with the burning of crop residue mainly occurring in Northeast, North and South China. In addition, pollutant emissions per unit area(10 km ×10 km) were mostly concentrated in the central and eastern regions of China. Emissions of CO_2, NOx, VOCs, OC and TC were mainly from rice straw burning, while burning of corn and wheat residues contributed most to emissions of CO, PM_(2.5) and EC. The increased ratio of PM_(2.5) emissions from crop residue burning to the total emitted from industry during the study period is attributed to the implementation of strict emissions management policies in Chinese industry. This study also provides baseline data for assessment of the regional atmospheric environment.     

美国校园安全管理探析与启示

美国是世界上最早探索如何有效保障校园安全的国家之一。本文以美国校园安全为研究对象,分别从校园安全治理组织框架、法律法规体系、安全管理模式、巩固提升与持续改进4个方面进行分析,较为系统、深入地对美国校园安全管理现状进行了剖析。依据美国校园安全管理经验,结合我国校园安全管理实际情况,提出对我国校园安全管理的一些启示。     

循环冷却水高浓缩倍率处理技术在电厂的应用研究

随着淡水资源的日益紧缺,如何提高水资源的利用率以达到节约用水的目的引起更高的关注.基于河南某电厂循环冷却水浓缩倍率仅为2.0的现状,选取两种新型高效的水处理药剂(1号、2号).经试验研究确定处理效果更佳的1号药剂为选择药剂,并确定最佳投药量为8 mg/l.将1号药剂应用到实际工程中,循环水浓缩倍率提高至6.5以上,节省了大量的水资源,同时减少废水的排放量,为该电厂带来了良好的经济和环境效益,也为类似工程的建设提供一定的参考作用.     

Modeling of acute cadmium toxicity in solution to barley root elongation using biotic ligand model theory

Protons（H⁺）as well as different major and trace elements may inhibit cadmium（Cd）uptake in aquatic organisms and thus alleviate Cd toxicity.However,little is known about such interactions in soil organisms.In this study,the independent effects of the cations calcium(Ca²⁺),magnesium(Mg²⁺),potassium（K⁺）,H+and zinc(Zn²⁺)on Cd toxicity were investigated with 5-day long barley root elongation tests in nutrient solutions.The tested concentrations of selected cations and trace metal ions were based on the ranges that occur naturally in soil pore water.The toxicity of Cd decreased with increasing activity of Ca²⁺,Mg²⁺,H⁺and Zn²⁺,but not K⁺.Accordingly,conditional binding constants were obtained for the binding of Cd²⁺,Ca²⁺,Mg²⁺,H⁺,and Zn²⁺ with the binding ligand:log K_CdBL5.19,logK_CaBL2.87,logK_MgBL2.98,logK_HBL5.13 and logK_ZnBL5.42,respectively.Furthermore,it was calculated that on average 29% of the biotic ligand sites needed to be occupied by Cd to induce a 50% decrease in root elongation.Using the estimated constants,a biotic ligand model was successfully developed to predict the Cd toxicity to barley root elongation as a function of solution characteristics.The feasibility and accuracy of its application for predicting Cd toxicity in soils were discussed.     

Sorption of tylosin and sulfamethazine on solid humic acid

Tylosin(TYL) and sulfamethazine(SMT) are ionizable and polar antimicrobial compounds,which have seeped into the environment in substantial amounts via fertilizing land with manure or sewage. Sorption of TYL and SMT onto humic acid(HA) may affect their environmental fate. In this study, the sorption of TYL and SMT on HA at different conditions(pH, ionic strength) was investigated. All sorption isotherms fitted well to the Henry and Freundlich models and they were highly nonlinear with values of n between 0.5 and 0.8, which suggested that the HA had high heterogeneity. The sorption of TYL and SMT on HA decreased with increasing p H(2.0–7.5), implying that the primary sorption mechanism could be due to cation exchange interactions between TYL~+/SMT~+ species and the functional groups of HA.Increasing ionic strength resulted in a considerable reduction in the K_d values of TYL and SMT,hinting that interactions between H bonds and π–π EDA might be an important factor in the sorption of TYL and SMT on HA. Results of Fourier transform infrared(FT-IR) and ~13C-nuclear magnetic resonance(NMR) analysis further demonstrated that carboxyl groups and O-alkyl structures in the HA could interact with TYL and SMT via ionic interactions and H bonds,respectively. Overall, this work gives new insights into the mechanisms of sorption of TYL and SMT on HA and hence aids us in assessing the environmental risk of TYL and SMT under diverse conditions.     

生物表面活性剂改性对纳米铁/炭去除地下水中NO3--N的影响

纳米铁由于其反应活性强、来源广泛等优点被广泛应用在去除地下水NO-3-N污染中.利用生物表面活性剂对纳米铁进行改性可以避免采用化学表面活性剂改性对环境造成的二次污染.本研究采用鼠李糖脂、茶皂素、无患子3种生物表面活性剂对纳米铁进行改性后附着在活性炭上构成改性纳米铁/炭复合材料,通过批试验、沉降试验、迁移试验等研究生物表面活性剂对纳米铁/炭复合材料的改性作用.结果表明:鼠李糖脂、茶皂素、无患子对纳米铁/炭改性后去除NO-3-N效果最佳时的投加量分别为0.7%、1.0%、0.7%,此时对比三者改性作用,鼠李糖脂改性纳米铁/炭去除NO-3-N效果最佳,无患子改性纳米铁/炭迁移效果最佳;鼠李糖脂投加量在0.1%到1.3%范围内时,改性纳米铁/炭迁移能力随投加量的增加而增大.     

酸浸—萃取—沉淀法回收废锂离子电池中的钴

采用酸浸—萃取—沉淀法回收废锂离子电池中的钴。实验结果表明:废锂离子电池在600℃下煅烧5 h可将正极材料上的有机黏结剂与正极活性物质分离;正极活性物质在Na OH溶液浓度为2.0 mol/L、n(Na OH)∶n(铝)=2.5、碱浸温度为20℃的条件下碱浸反应1 h后,铝浸出率达99.7%;已除铝的正极活性物质在硫酸浓度为2.5 mol/L、H_2O_2质量浓度为7.25 g/L、液固比为10、酸浸温度为85℃的条件下酸浸反应120 min,钴浸出率高达98.0%;酸浸液在p H为3.5、萃取剂P507与Cyanex272体积比为1∶1的条件下,经2级萃取,钴萃取率为95.5%;采用H_2SO_4溶液反萃后在硫化钠质量浓度为8 g/L、反萃液p H为4的条件下沉淀反应10 min,钴沉淀率达99.9%。     

WO_3/Ag_3VO_4复合光催化剂的制备及其可见光催化性能

采用超声辅助沉淀法—浸渍法制备了WO3/Ag3VO4复合光催化剂,对其进行了表征,考察了其在可见光条件下对罗丹明B的催化降解性能,并对催化机理进行了探讨。表征结果显示:WO3紧密包覆在Ag3VO4颗粒的表面,并未改变Ag3VO4的晶体结构;与Ag3VO4和WO3相比,WO3/Ag3VO4的吸收带边发生了红移。实验结果表明:w(WO3)为3.5%时,WO3/Ag3VO4对罗丹明B的可见光催化降解效果最好;在光催化剂加入量0.8 g/L、初始罗丹明B质量浓度10 mg/L的条件下,于室温下光照180 min时的罗丹明B去除率达95.76%,TOC去除率达96.5%;WO3与Ag3VO4在能带间的耦合作用下形成异质结结构,很好地抑制了光生电子-空穴对的复合。