Dosing low-level ferrous iron in coagulation enhances the removal of micropollutants, chlorite and chlorate during advanced water treatment

Drinking water utilities are interested in upgrading their treatment facilities to enhance micropollutant removal and byproduct control. Pre-oxidation by chlorine dioxide (ClO₂) followed by coagulation-flocculation-sedimentation and advanced oxidation processes (AOPs) is one of the promising solutions. However, the chlorite (ClO₂^–) formed from the ClO₂ pre-oxidation stage cannot be removed by the conventional coagulation process using aluminum sulfate. ClO₂^– negatively affects the post-UV/chlorine process due to its strong radical scavenging effect, and it also enhances the formation of chlorate (ClO₃^–). In this study, dosing micromolar-level ferrous iron (Fe(II)) into aluminum-based coagulants was proposed to eliminate the ClO₂^– generated from ClO₂ pre-oxidation and benefit the post-UV/chlorine process in radical production and ClO₃^– reduction. Results showed that the addition of 52.1-µmol/L FeSO₄ effectively eliminated the ClO₂^– generated from the pre-oxidation using 1.0 mg/L (14.8 µmol/L) of ClO₂. Reduction of ClO₂^– increased the degradation rate constant of a model micropollutant (carbamazepine) by 55.0% in the post-UV/chlorine process. The enhanced degradation was verified to be attributed to the increased steady-state concentrations of HO^· and ClO^· by Fe(II) addition. Moreover, Fe(II) addition also decreased the ClO₃^– formation by 53.8% in the UV/chlorine process and its impact on the formation of chloro-organic byproducts was rather minor. The findings demonstrated a promising strategy to improve the drinking water quality and safety by adding low-level Fe(II) in coagulation in an advanced drinking water treatment train.     

Evidence on the causes of the rising levels of CODMn along the middle route of the South-to-North Diversion Project in China: The role of algal dissolved organic matter

As the biggest inter-basin water transfer scheme in the world,the South-to-North Water Diversion Project（SNWD） was designed to alleviate the water crisis in North China.The main channel of the middle route of the SNWD is of great concern in terms of the drinking water quality.In this study,we tested the hypothesis that the dissolved organic matter（DOM） derived from the planktonic algae causes the rising levels of COD_Mn along the middle route by monitoring data on water quality（2015-20...     

Occurrence and fate of hormone steroids in the environment

Hormone steroids are a group of endocrine disruptors, which are excreted by humans and animals. In this paper, we briefly review the current knowledge on the fate of these steroids in the environment. Natural estrogenic steroids estrone (E1), 17beta-estradiol (E2) and estriol (E3) all have a solubility of approximately 13 mg/l, whereas synthetic steroids 17alpha-ethynylestradiol (EE2) and mestranol (MeEE2) have a solubility of 4.8 and 0.3 mg/l, respectively. These steroids have a moderate binding on sediments and are reported to degrade rapidly in soil and water. Estrogenic steroids have been detected in effluents of sewage treatment plants (STPs) in different countries at concentrations ranging up to 70 ng/l for E1, 64 ng/l for E2, 18 ng/l for E3 and 42 ng/l for EE2. E2 concentrations in river waters from Japan, Germany, Italy and the Netherlands ranged up to 27 ng/l. In addition, E2 concentrations ranging from 6 to 66 ng/l have also been measured in mantled karst aquifers in northwest Arkansas. This contamination of ground water has been associated with poultry litter and cattle manure waste applied on the land. Although hormone steroids have been detected at a number of sources worldwide, currently, there is limited data on the environmental behaviour and fate of these hormone steroids in different environmental media. Consequently, the exposure and risk associated with these chemicals are not adequately understood.     

川东平行岭谷区野生春剑伴生植物群落特征研究

为了对春剑野生种群生物多样性保护和再引入生态重建提供理论和技术基础，采用典型样地调查法，对川东平行岭谷区野生春剑伴生植物群落特征进行了研究。结果表明：野生春剑主要分布在松科与壳斗科针阔混交林、壳斗科常绿 落叶阔叶混交林和松树林植物群落，伴生植物有40科58属70种，优势种主要是乔木层的马尾松、青冈、巴山松、油松等，灌木层的杜鹃花、马桑、山茶花等，草本层的蕨类和地被层的苔藓。其中，马尾松、杜鹃花、蕨类、苔藓具有较高的重要值，可作为野生春剑栖息地的指示植物。春剑伴生植物种类具有相对的特异性和选择性，与其它群落相比，群落3、群落4和群落6物种多样性指数H′和均匀度指数E都相对较低，松科和壳斗科植物个体数量较多并占有突出地位，春剑种群的生态密度也相对较高。虽然川东平行岭谷区野生春剑的适生生境条件依然存在，但春剑种群数量总体较小，种群的生态密度在11～60株/hm2，人为破坏性的滥采，是其濒危的直接原因。加强野生春剑资源的就地保护和生境保护，突破春剑种子野生环境共生萌发技术瓶颈，积极开展春剑的“再引入”工作，是春剑保育策略的重要方向     

基于协调发展视角的区域发展差异研究

20世纪90年代以来，区域差异研究成为学术界和政府管理者关注的热点领域。长期以来学者们主要以单一经济指标或复合经济指标作为衡量因子，分析区域经济差异时空演变及差异背后的自然、社会、经济驱动机理。从可持续发展的角度看，区域发展不单是区域经济的发展，而应是社会、经济与资源环境三方面的协调。基于这一理解，从可持续协调发展入手，建立了区域发展综合评价指标体系，选取了表征社会进步、经济发展和资源环境支持3个方面的27个因素作为评价指标，分析了区域综合发展的测算方法，提出了综合发展指数和发展协调指数。在案例分析中运用所设计的测度方法对江苏省内县级行政单位的综合发展进行了评价和分析。     

Theoretical study on the reaction mechanism of ozone addition to the double bonds of keto-limonene

The reaction mechanism of ozone (O₃) addition to the double bonds of gas phase keto-limonene was investigated using ab initio methods. Two different possibilities for O₃ addition to the double bond were considered and two corresponding van derWaals complexes (Complex 1 and Complex 2) were found for 1-endo and 2-endo. The rate constants were calculated using the transition state theory at the CCSD(T)/6-31G(d) + CF//B3LYP/6-31G(d,p) level. The high-pressure limit of the total rate constant at 298 K was 3.51 × 10^-16 cm³/(molecule sec), which was in a good agreement with the experimental data.     

聚合物/表面活性剂二元体系对油水界面性质的影响

文章应用界面张力仪、Zeta电位仪和表面黏弹性仪测定了聚合物、表面活性剂及其二元复合体系的质量浓度对油水界面性质的影响,并应用透射电镜观察了采出液的液膜结构。结果表明,随着聚合物质量浓度的增加,油水界面的界面剪切黏度值和界面张力值增大,颗粒表面Zeta电位的绝对值增大;随着表面活性剂质量浓度的增加,油水界面的界面剪切黏度变化幅度很小,但界面张力显著减小,颗粒表面Zeta电位绝对值增大;聚合物与表面活性剂复合能够形成稳定的聚合体,具有较大的界面剪切黏度值,较小的界面张力和较高的Zeta电位值;体系中聚合物、表面活性剂及水中悬浮物形成了类似"晶体"结构。     

COD组分分析的实验条件及结果可靠性分析

本研究尝试用SF(OURmax/OURen)代替S(0)/X(0)来作为呼吸法确定COD组分最优实验条件的参数,从而简化测量过程且可实现自动化操作.另外由生长消耗COD与生物量的比值来判断测量结果的可靠性.结果表明,获得可靠的RBCOD组分分析结果的实验条件为:1对于易生物降解含量较高的水质(如由乙酸钠配制的污水),SF在2.8~5.3范围内,生长消耗COD与生物量比值在30%以内;2对于易生物降解和难生物降解物质适中的水质(如典型生活污水),SF应在5.8~6.4左右,生长消耗COD与生物量比值在30%以内;3而对于含有大量难生物降解物质的工业废水(垃圾渗滤液),SF在15以下,且生长消耗COD与生物量的比值在40%以内.由此可见,采用呼吸法确定COD组分,其最优条件SF范围随碳源的复杂程度的上升而上升.