Determination of haloacetic acids in hospital effuent after chlorination by ion chromatography

The ion chromatography combined solid phase extraction (SPE) method was developed for the analysis of low concentration haloacetic acids (HAAs), a class of disinfection by-products formed from chlorination of hospital wastewater. The monitored HAAs included monochloroacetic acid, monobromoacetic acid, dichloroacetic acid, dibromoacetic acid and trichloroacetic acid. The method employed a sodium hydroxide eluent at a flow rate of 0.8 mlmin, electrolytically generated gradients, and suppressed conductivity detection. To analyze the HAAs in real hospital wastewater samples, C18 pretreatment cartridge was utilized to reduce samples' turbidity. Preconcentration with SPE and matrix elimination with treatment cartridges were investigated and found to be able to obtain acceptable detection limits. Linearity, repeatability and detection limits of the above method were evaluated. The detection limits of monobromoacetic acid and dibromoacetic acid were 2.61 μgL and 1.30 μgL, respectively, and the other three acids are ranging from 0.48 to 0.82 μgL under 25-fold preconcentration. When the above optimization procedure was applied to three hospital wastewater samples with different treatment processes in Tianjin, it was found that the dichloroacetic acid was the major compound, and the growth ratios of the HAAs after disinfection by sodium hypochlorite were 91.28%, 63.61% and 79.50%, respectively.     

阴离子表面活性剂测定中不同萃取方法的比较

通过对水中阴离子表面活性剂测定中不同萃取方法的比较，从而简化操作步骤，提高了工作效率。     

环境样品中C2-C5脂肪羧酸的直接电导离子色谱法分析

叙述离子排斥色谱法分析环境样品中的C2-C5脂肪羧酸,以4%的正丁醇水溶液代替无机酸溶液作淋洗液,使分析物质得到较好地分离,尤其本底电导降低,可使用电导检测器直接检测,不需抑制,从而使灵敏度有很大提高,适合环境样品的分析.     

高氯离子低COD废水样品COD的测定方法探讨

对于氯离子含量高于2000mg/L，而COD值较低的废水样品，按硫酸汞与氯离子之比（W／W）为15：1投加硫酸汞作掩蔽剂，同时扣除空白氯离子残留的COD值，结果准确可靠，此结果扩展了标准方法的使用范围。     

祁连山东端地表及地下水水化学时空变化特征

于2016~2017年5~9月采集祁连山东端（乌鞘岭、古浪、天祝）的地表水和地下水样品进行水化学分析,综合运用统计分析、Piper三线图、Gibbs图以及离子比值等方法探究了祁连山东端地表水和地下水主要离子组成特征、来源以及时空变化.结果表明,祁连山东端地表水和地下水化学组成中优势阳离子为Ca²⁺和Na⁺,Ca²⁺的平均浓度为76.897mg/L,占比73.89%;Na⁺的浓度为16.592mg/L,占比15.94%.优势阴离子为HCO₃^-和SO₄^2-,HCO₃^-浓度190.117mg/L,占比68.71%;其次是SO₄^2-,平均值为67.565mg/L,占比为24.42%.乌鞘岭河水、地下水,天祝河水、地下水的水化学类型为HCO₃^--Ca²⁺型,古浪河水、地下水水化学类型为HCO₃^--Ca²⁺-Mg²⁺型,处于水化学易变区.不同水体离子来源于岩石风化,主要受碳酸盐与硅酸盐风化溶解共同作用控制,人类活动在一定程度上贡献了水体的离子来源.不同水体主要离子浓度的时间变化特征各不相同,整体上大部分水体的离子浓度随时间变化不明显,总体趋势较平缓.     

锂枝晶导致的锂离子电池内短路模拟研究

锂离子电池内短路是导致其热失控的主要原因之一,机械撞击、集流体边缘毛刺和锂枝晶生长等都可刺穿隔膜导致电池内短路。采用有限元数值模拟方法,对锂枝晶引起的锂离子电池内短路进行了研究,比较分析了不同锂枝晶半径、数量和中心距情况下电池的热响应特征。结果表明锂枝晶导致的电池内短路产热来源主要是正负极可逆和不可逆热。短路电流、产热功率和电池最高温度等都随锂枝晶半径的增大而增大。锂枝晶中心距增大时,短路电流和产热功率也随之变大,但由于受到电解液锂离子浓度的影响二者增加的幅度越来越小。锂枝晶中心距越大时虽然电池总产热量越大,电池平均温度更高,但由于此时短路点分布较分散,电池最高温度却较反而较小。     

Feasible conversion of solid waste bauxite tailings into highly crystalline 4A zeolite with valuable application

Bauxite tailings are a major type of solid wastes generated in the flotation process. The waste by-products caused significant environmental impact. To lessen this hazardous effect from poisonous mine tailings, a feasible and cost-effective solution was conceived and implemented. Our approach focused on reutilization of the bauxite tailings by converting it to 4A zeolite for reuse in diverse applications. Three steps were involved in the bauxite conversion: wet-chemistry, alkali fusion, and crystallization to remove impurities and to prepare porous 4A zeolite. It was found that the cubic 4A zeolite was single phase, in high purity, with high crystallinity and well-defined structure. Importantly, the 4A zeolite displayed maximum calcium ion exchange capacity averaged at 296 mg CaCO₃/g, comparable to commercially-available zeolite (310 mg CaCO₃/g) exchange capacity. Base on the optimal synthesis condition, the reaction yield of zeolite 4A from bauxite tailings achieved to about 38.43%, hence, this study will provide a new paradigm for remediation of bauxite tailings, further mitigating the environmental and health care concerns, particularly in the mainland of PR China.     

亚甲基蓝褪色催化动力学光度法测定痕量Cu~(2+)

研究了在聚乙二醇-200(PEG-200)活化下,Cu2+催化H2O2氧化亚甲基蓝的褪色反应,建立了亚甲基蓝褪色催化动力学光度法测定痕量Cu2+的方法。在25mL容量瓶中,加入1.00mL pH为11.68的氨水溶液、2.00mL H2O2溶液(质量分数15%)、1.00mL亚甲基蓝溶液(质量浓度0.20mg/mL)、3.00mL PEG-200溶液,76℃恒温反应5min后冷却,测定吸光度,根据加Cu2+溶液和不加Cu2+溶液的吸光度差值与Cu2+质量浓度绘制了工作曲线,并由试样的吸光度差值确定痕量Cu2+含量。该法的测定波长为664nm,检出限为5.4×10-6g/L,最大相对标准偏差为2.58%,回收率为97.5%~104.5%。     

用弱碱性离子交换树脂分离2-萘磺酸的研究

介绍了采用弱碱性离子交换树脂回收2－萘磺酸废水中的2－萘磺酸的试验研究。进行了pH、交换温度、共存阴离子等影响因素的条件试验及树脂再生试验,在较佳条件下,2－萘磺酸交换吸附率达98％以上,洗脱率接近100％。     

微生物絮凝剂研究进展

相对于传统絮凝剂而言,微生物絮凝剂具有絮凝范围广、絮凝活性高、安全无害、无二次污染、可为生物降解等优点。本文综述了微生物絮凝剂的发展历程,详细介绍了微生物絮凝剂的特性,分析了微生物絮凝剂的絮凝性能影响因素,指出被絮凝物质的性能、温度、pH值、金属离子、絮凝剂的浓度及附位点均对微生物的絮凝性能具有一定程度的影响。指出了当前微生物絮凝剂研究的不足及今后研究的侧重点,对开展微生物絮凝剂的研究具有重要的参考价值。