Mechanism of complexation of toxic arsenate,selenate, and molybdate with hydrotalcites

Environmental Chemistry Letters - Wastewater from the uranium mining industry contains toxic arsenate (AsO43–), selenate (SeO42–), and molybdate (MoO42–) that can be removed by...     

活性炭吸附和两级Fenton氧化组合工艺处理高盐对氨基苯酚生产废水

采用活性炭吸附和两级Fenton氧化组合工艺对高盐度对氨基苯酚生产废水进行了处理实验研究。结果表明,p H值对活性炭去除有机物的影响较小。当活性炭投加量为4 g/L时,TOC去除率61%。分级加药可以有效提高Fenton氧化对有机物的去除效率。在温度为25℃、p H为3、30%H2O2投加量为3%(V/V)、Fe2+/H2O2摩尔比为0.05时,两级Fenton氧化处理后,出水TOC降至150 mg/L以下。此外,Fenton氧化后形成氢氧化铁污泥颗粒粒径为4.5μm,经过聚丙烯酰胺(PAM)絮凝之后,污泥的粒径明显增加,过滤特性改善。PAM絮凝效果依赖于溶液的p H值,当p H超过10后会失去作用,故在使用过程中需要严格控制溶液的p H值。     

基于压力响应关系法的湖泊营养物基准制定

湖泊富营养化与氮、磷及有机物含量过高密切相关,建立数字型营养物基准能够防止富营养化对水体指定用途造成影响.太湖流域是我国华东地区经济腹地,近年来流域内湖泊水质每况愈下,对其基准研究可为湖泊治理提供依据.详细介绍了压力响应关系法制定湖泊营养物基准的步骤,并将此方法运用到太湖流域营养物基准制定研究中.为满足大多数水体指定用途,研究中将该流域湖泊基本功能确定为娱乐、永生生物栖息地及饮用水,以此构建流域概念模型.选择压力变量为总氮(TN)、总磷(TP)和有机物,响应变量为叶绿素a(chl-a).用非参数分析法和线性回归法分别建立压力-响应模型,通过2种方法相互验证得到TN、TP和CODMn基准分别为0.593、0.067和4.092 mg/L.     

丙烯腈生产废水中聚合物的资源化利用

以丙烯腈生产废水中的丙烯腈低聚物为原料制备聚丙烯酰胺。通过正交实验考察了水解反应条件和交联反应条件对反应的影响。FTIR表征结果显示,丙烯腈低聚物中的氰基已完全水解为酰胺基,产物聚丙烯酰胺中含有酰胺基和羧基。实验结果表明,在自来水加入量100 m L、水解反应温度95℃、m(Na OH)∶m(丙烯腈低聚物)=2.0、水解反应时间3 h的最佳水解反应条件,交联反应温度60℃、质量分数37%~40%的甲醛加入量6 m L、交联反应时间2 h的最佳交联反应条件下,处理20 g丙烯腈低聚物,可得到产物聚丙烯酰胺14.50 g,聚丙烯酰胺的水解度为21.1%、相对分子质量为2.7×106。产品性能满足Q/SH 0046—2007《钻井液用聚丙烯酰胺技术要求》中部分水解聚丙烯酰胺的性能要求。     

A mini review of fluoride-induced apoptotic pathways

Fluorine or fluoride can have toxic effects on bone tissue and soft tissue at high concentrations. These negative effects include but not limited to cytotoxicity, immunotoxicity, blood toxicity, and oxidative damage. Apoptosis plays an important role in fluoride-induced toxicity of kidney, liver, spleen, thymus, bursa of Fabricius, cecal tonsil, and cultured cells. Here, apoptosis activated by high level of fluoride has been systematically reviewed, focusing on three pathways: mitochondrion-mediated, endoplasmic reticulum (ER) stress-mediated, and death receptor-mediated pathways. However, very limited reports are focused on the death receptor-mediated apoptosis pathways in the fluoride-induced apoptosis. Therefore, understanding and discovery of more pathways and molecular mechanisms of fluoride-induced apoptosis may contribute to designing measures for preventing fluoride toxicity.     

Study on the denitrification performance of FexLayOz/activated coke for NH3-SCR and the effect of CO escaped from activated coke at mid-high temperature on catalytic activity

Currently, activated coke is widely used in the removal of multiple pollutants from industrial flue gas. In this paper, a series of novel Fe_xLa_yO_z/AC catalysts was prepared by the incipient wetness impregnation for NH₃-SCR denitrification reaction. The introduction of Fe-La bimetal oxides significantly improved the denitrification performance of activated coke at mid-high temperature, and 4% Fe_0.3La_0.7O_1.5/AC exhibited a superior NO_x conversion efficiency of 90.1% at 400 °C. The catalysts were further characterized by BET, SEM, XRD, Raman, EPR, XPS, FTIR, NH₃-TPD, H₂-TPR, et al., whose results showed that the perovskite-type oxide of LaFeO₃ and oxygen vacancies were produced on the catalysts’ surfaces during roasting. Fe-La doping enhanced the amount of acid sites (mainly Lewis and other stronger acid sites) and the content of multifarious oxygen species, which were beneficial for NO_x removal at mid-high temperature. Moreover, it was investigated that the effect of released CO from activated coke at mid-high temperature on the NO_x removal through the lifetime test, in which it was found that a large amount of CO produced by pyrolysis of activated coke could promote the NO_x removal, and long-term escaping of CO on the activated coke carrier did not have a significant negative impact on catalytic performance. The results of the TG-IR test showed that volatile matter is released from the activated coke while TG results showed that the weight loss rate of 4% Fe_0.3La_0.7O_1.5/AC only was 0.0015~0.007%/min at 300–400 °C. Hence, 4% Fe_0.3La_0.7O_1.5/AC had excellent thermal stability and denitrification performance to be continuously used at mid-high temperature. Finally, the mechanisms were proposed on the basis of experiments and characterization results.

     

Concentrations and accumulation rates of polychlorinated biphenyls in soil along an urban–rural gradient in Shanghai

Environmental Science and Pollution Research - This study proposed an in situ soil experimental system to quantify concentration and accumulation rates of polychlorinated biphenyl (PCB) congeners...     

Recycling sewage sludge into ceramic materials: A review

Environmental Chemistry Letters - Huge amounts of unwanted sewage sludge are generated in the process of wastewater treatment, calling for methods to recycle sewage sludges into value-added...     

MCM-41分子筛负载铁铈催化降解甲基橙

采用等体积浸渍法制备了负载型有序介孔Fe-Ce/MCM-41催化剂。研究了该催化剂降解甲基橙的适宜工艺条件,并采用XPS,XRD,TEM技术对该催化剂进行了表征。实验结果表明,该催化剂Fenton氧化降解甲基橙的较适宜工艺条件为:溶液pH 5.0、甲基橙溶液初始质量浓度100 mg/L、催化剂加入量2.0 g/L、H_2O_2浓度20 mmol/L,在此适宜条件下反应120 min时,甲基橙去除率接近100%。表征结果显示:Fe-Ce/MCM-41催化剂主要由铁、铈、氧、碳4种元素组成;铁与铈的摩尔比接近3∶1;铁和铈主要以Fe_3O_4和CeO_2的形态存在于催化剂表面。     

顶空毛细柱气相色谱法测定水中七种苯系物研究

选用Elite-FFAP色谱柱,利用顶空-毛细柱气相色谱技术对水中的苯、甲苯、乙苯、对二甲苯、间二甲苯、邻二甲苯、苯乙烯七种挥发性苯系物进行同时测定,并对样品的平衡温度、保温时间、程序升温的条件控制、水中含盐量等影响因素进行了探讨,优化了检测条件,使七种挥发性苯系物得到不错的分离。样品平衡温度控制在70℃,样品平衡时间19 min,进样口温度180℃,检测器温度230℃,10 mL水样中加入4 g NaCl的条件下,分离效果最佳。