Lithium extraction from salt lake brines with high magnesium/lithium ratio: a review

Environmental Chemistry Letters - The demand for lithium is growing rapidly with the increase in electric vehicles, batteries and electronic equipments. Lithium can be extracted from brines, yet...     

基于SHERPA的环境空气质量减排情景模拟评估

分析了SHERPA综合评价模型的基本原理和主要建模理念,重点介绍了其在环境空气质量减排情景模拟评估方面的作用,以及在排放源与受体关系(SRR)方面的处理方法,比较了其与欧盟常用的其他情景模拟模型的优缺点。SHERPA模型的特点是空间灵活性较好,对于任何给定地点,可以快速评估不同地区对该研究地点空气质量的影响。SHERPA模型的3个主要功能为污染物来源分析、决策支持和情景模拟。基于SHERPA模型对法国环境空气中PM_(2.5)、PM_(10)和NO_2年均浓度进行污染来源分析、决策支持分析和减排情景模拟评估,展示了模型在环境治理措施优先级筛选和政府间联合治理措施协调建议方面的功能和作用,以期为中国环境空气质量预测预报、环境质量管理措施的制定和成效评估等环境服务与管理工作提供借鉴。     

CS/PEG/PFT膜制备及对含铜废水的处理

实验将溶胶凝胶法和高分子辅助倒相法结合,制备出一种新型的壳聚糖/聚乙二醇/亚铁氰化钾钛(CS/PEG/PFT)复合膜,通过FT-IR和SEM对膜进行表征后,将其用于模拟铜废水的吸附和脱附实验,并探究出膜吸附的最佳工艺条件为:p H 5.50、实验温度55℃、实验时间2 h,该条件下,膜对铜离子最大吸附量为9.85 mg/g,去除率达到95%以上。CS/PEG/PFT膜的除铜过程符合Langmuir等温吸附方程(y=0.0597x+0.0168),线性相关度达到0.9917。     

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.     

一种新型铋基光催化剂的合成及其可见光催化性能

采用水热法合成铋基光催化剂Bi4VO8Br,通过X-射线粉末衍射、扫描电镜等手段对其进行表征.选择甲基橙为目标降解物来评价不同条件下合成的Bi4VO8Br在可见光下的光催化活性,发现pH 3、反应时间15 h、反应温度160℃为材料水热合成的最佳条件.考察了Bi4VO8Br在可见光及紫外光下对几种农药和增塑剂的光催化降解性能,显示了Bi4VO8Br对不易光解的含苯环有机物的可见光高活性.五氯酚的光催化过程影响因素优化结果表明,可见光和紫外光分别照射120 min和20 min,其降解率分别达到97％和99％,Bi4VO8Br表面上活性基团的捕获即空穴的氧化作用是主要反应原理.     

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。     

煤与瓦斯共采在错层位巷道布置中的机理研究及应用构想

为了完善现有煤与瓦斯共采技术，创新煤与瓦斯共采方法，对错层位巷道布置下的煤与瓦斯共采系统展开研究，利用相似模拟试验，分析错层位巷道布置覆岩运动情况，预测其开采围岩裂隙发育和瓦斯运移形式，提出了创新煤与瓦斯共采技术构想。研究结果表明:采空区覆岩三带高度随接续工作面的增加而增大，相邻采空区垮落矸石压实区呈现“O-L-O”形变化，多个相邻采空区覆岩出现大“O”形圈裂隙带；相邻采空区内瓦斯可实现相互运移，大“O”形圈裂隙带内赋存大量瓦斯气体；研究提出了地面钻井抽采瓦斯、走向高位瓦斯抽采巷和外错尾巷穿层钻孔3种煤与瓦斯共采技术，比传统巷道布置情况下的煤与瓦斯共采技术在安全、经济等方面更具优势。     

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.