过硫酸钾去除水中的TCE

以地水中的氯代烃污染物三氯乙烯(TCE)为目标污染物,以过硫酸钾溶液为氧化剂,探讨了不同条件下过硫酸钾对TCE的去除效果。实验结果表明,在40℃,过硫酸钾初始浓度为2.43 g/L条件下,反应2 h后,TCE的去除率就可达到96.8%;过硫酸钾对TCE的去除符合一级反应动力学方程,速率常数(K)为1.3364 h-1,半衰期(t1/2)为0.51 h;过硫酸钾对TCE的去除速率在pH为中性附近时最大,其后无论pH升高或降低去除速率均减小;受温度和pH影响较明显,并且反应温度越高,受pH的影响越明显;随离子强度的增加而减小;反应活化能为119.6 kJ/mol;过硫酸钾溶于水生成过硫酸根离子(S2O28-),S2O28-会进一步生成硫酸根自由基(SO4-.),在碱性条件下,SO4-.与OH-反应会进一步生成羟基自由基(.OH)。过硫酸钾对于TCE的去除主要源自SO4-.和.OH的强氧化性。     

Determination and potential importance of diterpene (kaur-16-ene) emitted from dominant coniferous trees in Japan

Reactive volatile organic compounds (VOCs) are known to affect atmospheric chemistry. Biogenic VOCs (BVOCs) have a significant impact on regional air quality due to their large emission rates and high reactivities. Diterpenes (most particularly, kaur-16-ene) were detected in all of the 205 enclosure air samples collected over multiple seasons at two different sites from Cryptomeria japonica and Chamaecyparis obtusa trees, the dominant coniferous trees in Japan,. The emission rate of kaur-16-ene, was determined to be from 0.01 to 7.1 μg dwg⁻¹ h⁻¹ (average: 0.61 μg dwg⁻¹ h⁻¹) employing branch enclosure measurements using adsorbent sampling followed by solid phase-liquid extraction techniques. The emission rate was comparable to that of monoterpenes, which is known major BVOC emissions, collected from the same branches. In addition, total emission of kaur-16-ene at 30 °C was estimated to exceed that of total anthropogenic VOC emissions.     

高铁酸钾预处理对活性污泥脱水性能的影响

通过投入不同剂量的高铁酸钾于剩余活性污泥中,研究其对污泥絮体性质和脱水性能的影响作用。污泥絮体性质的研究包括絮体粒径的变化以及污泥EPS含量的变化。脱水性能的研究包括过滤脱水性能(以CST表征)以及脱水程度(离心泥饼含固率)。实验结果表明,高铁酸钾的强氧化性可以破坏污泥絮体结构,提高污泥的机械脱水程度;但同时污泥EPS含量增加,对污泥过滤脱水性能有负面影响。高铁酸钾氧化分解生成的Fe(OH)3具有絮凝能力,可以使污泥颗粒重新絮凝;而其混凝作用可以破坏污泥细胞的稳定性,提高污泥的沉降性能。     

羧甲基壳聚糖-膨润土复合吸附剂对Cu^2＋、Ni^2＋、Cr^3＋的吸附

用羧甲基壳聚糖和膨润土制备复合吸附剂,研究了复合吸附剂在不同参数下对Cu^2＋、Ni^2＋和Cr^3＋吸附的影响。结果表明,复合吸附剂对Ni^2＋的吸附可以很快达到吸附平衡,而对Cu^2＋和Cr^3＋的吸附分别在30min和180min时达到平衡;且pH值对吸附容量的影响很显著。通过计算不同温度下的热力学参数△G、△H和△S,3种金属的△G〈0,证实这3种金属吸附都是自发过程。Cu^2＋、Ni^2＋和Cr^3＋的吸附等温线较符合Langmuir型;反应动力学都更符合准二级吸附速率方程。     

饮用水源突发性苯胺污染应急处理技术研究

分别从水样浓度、pH、反应时间、药剂投加量以及两者联用时的投加顺序等方面研究了粉末活性炭、高锰酸钾以及两者联合使用时对苯胺的去除效果.结果表明,当污染发生时,高锰酸钾和粉末活性炭联用处理技术是可行的;先投加粉末活性炭再加高锰酸钾处理比先投加高锰酸钾再投加活性炭的去除效果好;当水样pH在中性条件下,粉末活性炭和高锰酸钾联用处理技术的去除效果好;应急处理的反应时间是30 min.     

Agricultural Chemicals in the Alluvial Aquifer of a Typical County of the Arkansas Delta

Statistical methods and a Geographic Information System (GIS) were used to investigate potential indicators of ground water vulnerability to agricultural chemical contamination in a representative area of the Mississippi River alluvial aquifer. A total of 47 wells were sampled for analysis of nitrate, phosphorus, potassium, and 13 pesticides commonly-used in the area. Ten soil and hydrogeologic variables and five ground water vulnerability indices were examined to explain the variations of chemical concentrations. The results showed that no individual soil or hydrogeologic variables or their linear combinations could explain more than 25% of the variation of the chemical concentrations. A quadratic response surface model with the values of confining unit thickness, slope, soil permeability, depth to ground water, and recharge rate accounted for 62% of the variation of nitrate, 43% of P, and 83% of K, suggesting that the interactions among soil and hydrogeologic variables were significant. Observed trends of decreasing nitrate and P concentrations with increasing well depth and/or depth to ground water seemed to correlate with carbonate equilibrium in the aquifer and more reduced environment with depth. In view of uncertainties involved, it was recognized that the limitations associated with input data resolution used in GIS and the formulation of leaching indices limited their use for predicting ground water vulnerability. Misuse of pesticides could be another factor that would complicate the relationships between pesticide concentrations and the vulnerability indices.     

一个新的拓扑指数用于芳烃化合物溶解度、分配系数及生物毒性的研究

在分子拓扑理论的基础上,提出了一个新的拓扑指数Yx,并用Yx研究了芳烃化合物的溶解度、分配系数及生物毒(活）性,给出了相关方程。结果表明,新方法计算方便,物理意义明确,预测值与相应的实验值较吻合。     

固相微萃取-气相色谱/质谱联用法测定饮用水中苯类化合物

用固相微苹取(ＳＰＭＥ)－气相色谱/质谱联用法测定饮用水中苯类化合物,以１００μｍ ＰＤＭＳ(聚二甲基硅氧烷)萃取针提取、浓缩、分离与测定九种目标化合物．萃取时间经优化选定为８ｍｉｎ,而热解析时间设定为２ｍｉｎ． 本方法的相对标准偏差小于５%,线性范围宽(２０ｎｇ·ｍｌ－１－１００００ｎｇ·ｍｌ－１),多数化合物的检测限低于５μｇ·ｌ－１．饮用水样品检测显示,样品加标回收率范围在８４%至１１０%内．     

鸭绿江（丹东段）江水中未知有机污染物分析鉴定与有毒有机物名录筛选

采用美国惠普公司MC/GS联用仪,对鸭绿江（丹东段）江水中有机污染物种类、组成进行了分析鉴定,进而采用高压液相色谱法对多环芳烃类进行定量测定与评价,进行了该江段有毒有机物名录筛选,提出由27种有毒有机污染物组成的名单。     

硅酸盐细菌解钾兼拮抗活性菌株的筛选

从紫色土壤中分离筛选出具有解钾拮抗双重活性的硅酸盐细菌CS1和CS29菌株。接菌处理,其水溶性钾分别增加75％和65％,转化率达0．82％和0．72％。两株菌对革兰氏阳性的蜡样芽孢杆菌,金黄色葡萄球菌,藤黄八叠球菌等和革兰氏阴性的大肠杆菌均有较强的抑菌活性。筛选菌株中91．2％具有解钾活性,但拮抗活性菌株只占总数的11．6％,表明二性状之间无相关关系。表4参7