Exogenously applied oxalic acid assists in the phytoremediation of Mn by Polygonum pubescens Blume cultivated in three Mn-contaminated soils

• The OA supply significantly increased the water-extractable Mn in all soils. • All OA supply levels promoted plant growth in unexplored soil. • Low OA supply level promoted plant growth in explored and tailing soils. • OA amendment increased the Mn concentrations and total Mn in P. pubescens. • P. pubescens experienced less Mn stress in unexplored soil than in the other two soils. The current study evaluated the effects of oxalic acid (OA) application on the growth and Mn phytoremediation efficiency of Polygonum pubescens Blume cultivated in three different manganese (Mn)-contaminated soils sampled from an unexplored area (US), an explored area (ES) and a tailing area (TS) of the Ertang Mn mine, South China. The supplied levels of OA were 0 (control), 1 (low level), 3 (medium level), and 9 (high level) mmol/kg, referred to as CK, OA1, OA3 and OA9, respectively. The results revealed that the average water-extractable Mn concentrations US, ES and TS amended with OA increased by 214.13, 363.77 and 266.85%, respectively. All OA supply levels increased plant growth and Mn concentrations in US. The low OA supply level increased plant growth in ES and TS; however, contrasting results were found for the medium and high OA supply levels. Plant Mn concentrations and total Mn increased in ES and TS in response to all OA supply levels. Total Mn in the aerial parts increased by 81.18, 44.17 and 83.17% in US, ES and TS, respectively; the corresponding percentages for the whole plants were 81.53, 108.98 and 77.91%, respectively. The rate of ·O₂⁻ production and malondialdehyde (MDA) concentrations increased in response to OA amendment, especially the medium and high OA supply levels in ES and TS. In general, antioxidant enzymes might play a vital role in alleviating Mn stress in plants cultivated in US, while non-enzymatic antioxidants might be the main factor for plants cultivated in ES and TS.     

Preliminary studies on potential remediation of acid mine drainage‐impacted soils by amendment with drinking‐water treatment residuals

Mining operations result in a wide range of environmental impacts: acid mine drainage (AMD) and acid sulfate soils being among the most common. Due to their acidic pH and high soluble metal concentrations, both AMD and acid sulfate soils can severely damage the local ecosystems. Proper post‐mining management practices are necessary to control AMD‐related environmental issues. Current AMD‐impacted soil treatment technologies are rather expensive and typically not environmentally sustainable. We conducted a 60‐day bench‐scale study to evaluate the potential of a cost‐effective and environment‐friendly technology in treating AMD‐impacted soils. The metal binding and acid‐neutralizing capacity of an industrial by‐product, drinking water treatment residuals (WTRs) were used for AMD remediation. Two types of locally generated WTRs, an aluminum‐based WTR (Al‐WTR) and a lime‐based WTR (Ca‐WTR) were used. Highly acidic AMD‐impacted soil containing very high concentrations of metals and metalloids, such as iron, nickel, and arsenic, was collected from the Tab‐Simco coal mine in Carbondale, Illinois. Soil amendment using a 1:1 Al‐ and Ca‐WTR mix, applied at 5 and 10 percent rates significantly lowered the soluble and exchangeable fractions of metals in the AMD‐impacted soil, thus lowering potential metal toxicity. Soil pH increased from an extremely acidic 2.69 to a near‐neutral 6.86 standard units over the 60‐day study period. Results from this preliminary study suggest the possibility of a successful scale‐up of this innovative, cost‐effective, and environmentally sustainable technology for remediating AMD‐impacted acid sulfate soils.     

萃取法分离回收不锈钢酸洗污泥硫酸浸出液中的重金属

采用非皂化P204和皂化P204萃取剂对不锈钢酸洗污泥的硫酸浸出液进行萃取。在浸出液pH为0.80、非皂化P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取时间为5 min的条件下,Fe~(3+)萃取率达99.64%,Cr~(3+)和Ni~(2+)萃取率为3.98%和6.99%,一次萃余液pH为0.64。采用皂化P204对除Fe~(3+)后的一次萃余液进行萃取,在P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取剂皂化率为60%、一次萃余液pH为1.50、萃取时间为5 min的条件下,Ni~(2+)萃取率为93.12%,Cr~(3+)萃取率为20.69%,二次萃余液pH为2.63。     

聚硅酸钛制备及其助凝特性

采用在活化硅酸制备过程中加入适量Ti Cl4的方法,试制了一种新型无机高分子助凝剂—聚硅酸钛。研究了不同[Si]/[Ti]条件下制备的聚硅酸钛在固定p H值的水中分散物的粒径和Zeta电位随着活化时间的变化趋势,并与活化硅酸作比较。结果表明,在Si/Ti=20,活化48 h的条件下能制备出较为稳定的聚硅酸钛。与活化硅酸相比,聚硅酸钛在水中的分散物具有较大的粒径和更高的Zeta电位。通过对比制备的活化硅酸和聚硅酸钛的红外图谱发现,聚硅酸钛中有TiO-Si键,证明钛离子参与了聚合反应,新生成的化学键提高了它的聚合度和稳定性。采用硫酸铝为混凝剂,聚硅酸钛为助凝剂进行混凝除浊实验。测定了絮凝体的Zeta电位和混凝沉淀后的上清液浊度,研究了硫酸铝投加量和混凝p H对聚硅酸钛助凝效果的影响。结果表明,投加适量的聚硅酸钛助凝剂,明显提高了混凝除浊效果且拓宽了有效混凝p H值的范围。     

硫酸盐还原菌污泥固定化特性

采用玉米芯为碳源,聚乙烯醇(PVA)为包埋载体,饱和硼酸(H3BO3)为交联剂,研究了硫酸盐还原菌污泥(SRBS)、铁屑、麦饭石共固处理合成煤矿酸性废水的最优配比与机理,并分析了固定化过程中小球稳定性及活性的变化规律。实验结果表明,SRBS投加量是影响处理效果的最显著因子,当投加30%SRBS、2%铁屑、3%麦饭石时SO2-4、Mn2+去除率分别为94.13%和84.39%,溶液p H为7.03,未检测出Fe2+;随着交联时间的延长,小球膨胀率及SO2-4还原率分别呈线性与指数下降,从保持小球稳定性与活性角度考虑,可将交联时间设定为4~8 h;该法可为市政污泥的处置以及生物法处理煤矿酸性废水的工程应用提供技术参考。     

高效液相色谱-二极管阵列检测器测定邻苯二甲酸酯色谱条件优化

采用高效液相色谱-二极管阵列检测器对6种PAEs类物质进行测定,并对梯度洗脱条件、流速、检测波长等影响化合物色谱响应的关键参数进行优化。综合考虑样品测试效率、分析精度、实际样品中存在杂质干扰等因素,确定以乙腈-水为流动相进行梯度洗脱,洗脱0~11 min流动相乙腈-水梯度比例为50∶50,11 min后流动相调整为100%乙腈,各化合物均能完全分离;色谱分析流速为0.8 m L/min;PAEs的最佳吸收波长为225 nm。在优化的色谱条件下,6种PAEs的线性良好,相关系数均大于0.999 8,仪器检出限为0.08~0.12 mg/L,保留时间、峰面积的相对标准偏差分别为0.02%~0.60%、0.13%~0.86%。方法灵敏度较高,适合土壤等邻苯二甲酸酯含量较高基质样品的快速分析。     

化学环境下的应力-渗流耦合对尾 矿库稳定性影响试验

通过扫描电镜（FE-SEM）、能谱分析（EDX）、X射线衍射（XRD）、LMS-30激光粒度分析等室内试验探究了尾矿库内存在的酸、碱离子对尾矿颗粒的沉降、微观形貌、物质组成以及粒径级配的影响；建立酸、碱影响下的孔隙比与渗透系数的数学关系模型，并将建立的模型用来表征尾矿库内的应力渗-流场两场耦合机制，实现代入有限元计算软件的目的。结果表明:化学因素的存在影响着尾矿颗粒的多项性状，酸性环境下尾矿颗粒发生溶蚀，部分金属元素流失；碱性环境下尾矿颗粒间生成胶结物质，孔隙出现以含氢氧化铁为主的絮状、团簇状堵塞物，改变了渗流速度；尾矿库内浸润线高度在碱性、中性、酸性环境下依次降低，而渗流速度依次升高。     

皂素和柠檬酸复合淋洗土壤中的钍

采用振荡淋洗和土柱动态淋洗实验研究了皂素和柠檬酸复合对土壤中钍的淋洗性能。实验结果表明:将质量浓度为20 g/L的皂素与浓度为20 mmol/L的柠檬酸以体积比1∶10配制复合淋洗液对污染土壤中钍的去除效果最佳,淋洗3.0 h,钍去除率为84.98%;准一级动力学方程能更好地描述复合淋洗液对钍的淋洗动力学特征;动态淋洗实验中当复合淋洗液用量为1 600 mL时,钍的累积去除量为73.66 mg/kg;淋洗后土壤中钍的酸可提取态、氧化结合态和有机结合态含量分别减少了79.63%、38.13%和20.34%,残渣态含量变化不大;淋洗后土壤中钍的稳定性增加。     

Feasibility of honeycomb monolith supported sugar catalyst to produce biodiesel from palm fatty acid distillate (PFAD)

Carbon coated monolith was prepared by sucrose solution 65 wt.% via dip-coating method. Sulfonation of incomplete carbonized carbon coated monolith was carried out in order to synthesize solid acid catalyst. The textural structure characteristics of the solid acid catalyst demonstrated a low surface area and pore volume. Palm fatty acid distillate (PFAD), a by-product of palm oil refineries, was utilized as oil source in biodiesel production. The esterification reaction subjected to different reaction conditions was performed by using the sulfonated carbon coated monolith as heterogeneous catalyst. The sulfonation process had been performed by using vapour of concentrated H₂SO₄ that was much easier and efficient than liquid phase sulfonation. Total acidity value of carbon coated monolith was measured for unsulfonated sample (0.5 mmol/g) and sulfonated sample (4.2 mmol/g). The effect of methanol/oil ratio, catalyst amount and reaction time were examined. The maximum methyl ester content was 89% at the optimum condition, i.e. methanol/oil molar ratio (15:1), catalyst amount (2.5 wt.% with respect to PFAD), reaction time (240 min) and temperature 80 °C. The sugar catalyst supported on the honeycomb monolith showed comparable reactivity compared with the sugar catalyst powder. However, the catalyst reusability studies showed decrease in FFA% conversion from 95.3% to 68.8% after four cycles as well as the total acidity of catalyst dropped from the value 4.2 to 3.1 mmol/g during these cycles. This might be likely due to the leaching out of SO₃H group from the sulfonated carbon coated monolith surface. The leaching of active species reached a plateau state after fourth cycle.     

PW_(12)/g-C_3N_4光催化降解甲基橙

采用浸渍法制备了磷钨酸(PW12)/g-C3N4复合光催化剂,并将其用于溶液中甲基橙的光催化降解,运用IR技术对使用前后的光催化剂进行了表征。表征结果显示,PW12和g-C3N4的结构未在浸渍负载中发生改变,且PW12和g-C3N4结合牢固。实验结果表明:最佳的PW12负载量(光催化剂中PW12的质量分数)为50%;光催化降解甲基橙的优化反应条件为初始甲基橙质量浓度5 mg/L、光催化剂加入量0.6 g/L、初始溶液p H=7;在优化条件下,分别采用紫外光、模拟太阳光、可见光照射120 min后,甲基橙的降解率分别为96.59%,82.23%,42.78%;该光催化剂固载良好,使用中不易发生溶脱,稳定性好,可重复使用。