Decontamination of Cr(VI) facilitated formation of persistent free radicals on rice husk derived biochar

PFRs were produced on biochar during Cr(VI) decontamination. PFRs formation on biochar was owing to the oxidization of phenolic-OH by Cr(VI). Appearance of excessive oxidant led to the consumption of PFRs on biochar. Biochar charred at high temperature possessed great performance to Cr(VI) removal. This study investigated the facilitation of Cr(VI) decontamination to the formation of persistent free radicals (PFRs) on rice husk derived biochar. It was found that Cr(VI) remediation by biochar facilitated the production of PFRs, which increased with the concentration of treated Cr(VI). However, excessive Cr(VI) would induce their decay. Biochar with high pyrolysis temperature possessed great performance to Cr(VI) removal, which was mainly originated from its reduction by biochar from Inductively Coupled Plasma Optical Emission Spectroscopy and X-ray Photoelectron Spectroscopy. And the corresponding generation of PFRs on biochar was primarily ascribed to the oxidization of phenolic hydroxyl groups by Cr(VI) from Fourier Transform Infrared Spectroscopy analysis, which was further verified by the H₂O₂ treatment experiments. The findings of this study will help to illustrate the transformation of reactive functional groups on biochar and provide a new insight into the role of biochar in environmental remediation.     

粉末活性污泥处理含铀废水的特性

以生活污水处理厂剩余活性污泥为原料,制备粉末活性污泥(PAS)作为生物吸附剂,考察p H值,PAS投加量,U(Ⅵ)初始浓度和吸附时间对PAS吸附U(Ⅵ)的影响,探讨了PAS吸附U(Ⅵ)的作用机理。实验结果表明,在U(Ⅵ)初始浓度为10 mg/L时,其最佳吸附p H值为3,去除率97.77%,吸附平衡时间120 min;吸附过程较好地拟合了准二级动力学模型(R2≈1)和Freundlich等温模型(R2≈1);X射线能谱和离子交换实验分析表明,离子交换为其主要吸附方式,参与交换的主要离子为Ca2+;红外光谱分析表明,PAS吸附U(Ⅵ)后自身结构未发生改变。以0.1 mol/L的HCl溶液作为解吸液,初次解吸率达92.83%,循环利用3次仍具有较好的吸附效果。     

含TOA微胶囊对Cr2O7^2—萃取的研究

用乙基纤维素作膜材将三辛胺（简称ＴＯＡ）微胶囊化，用于萃取酸性水溶液中的Ｃｒ２Ｏ７＾２－离子。通过搅拌法萃取实验表明，ＴＯＡ被微胶囊化后对铬离子仍具有较高的萃取速度，实验测定渗透系数为６．７８×１０＾－６ｍ／ｍｉｎ，并能有效地防止乳化现象。将微胶囊制备成填充柱对Ｃｒ２Ｏ７＾２－进行萃取实验。对外相水的流速、微胶囊粒径、柱的重复使用次数与萃取容量的关系进行了研究。当粒径为１００－２００μｍ，流速为３     

Chromium sorption on grape stalks encapsulated in calcium alginate beads

A novel sorbent based on 2% grape stalk wastes encapsulated in calcium alginate beads was investigated for the removal of Cr(VI) and Cr(III) from aqueous solutions. The sorbent proved to be efficient for chromium removal in both hexavalent and trivalent forms from aqueous solution at pH 3.0. In binary mixtures, the presence in solution of one of the forms enhances the sorption of the other which results in an increase of the amount of total chromium removed. This study suggests that the proposed sorbent can be used for the removal of chromium from wastewaters through a cost-effective and environmentally friendly process.     

微波密封消解法快速测定CODcr

标准法──重铬酸钾法测定ＣＯＤＣｒ的缺点是测定时间长，氯离子干扰大。微波密封消解法对此进行了改进。实验结果表明，该法具有消解时间短，减轻了二次污染，准确度高，精密度好等优点，可同标准回流法等效使用。     

苏州河市郊段底泥中COD_(Cr)和NH_3-N的空间分布特征

对苏州河截流区外河段(城郊段)东大盈河口—北新泾,按河道形态,支流与城镇分布等因素,沿程采集24个底泥柱样,测定其不同部位不同深度底泥中COD_(Cr)和NH_3-N含量,分析COD_(Cr)和NH_3-N在沿程和垂向上的分布特征及其成因。结果表明,底泥中污染沿程分布呈不规则波状起伏,东大盈河、蕴藻浜、盐铁塘、封浜、华漕港、新槎浦等支流口,浮泥层中COD_(Cr)含量达2万mg/kg,超过背景值2—3倍,支流口下游200m范围内均较高;黄渡小支流口、华漕港支流口浮泥层中NH_3-H含量达250mg/kg,超过背景值3倍。在垂向分布上,底泥柱样都出现峰值分布,在某些弯道及支流口出现递减分布。底泥耗氧污染程度主要与支流及其排污量有关,其次是弯道凸岸处污染物易于沉积富集。这为苏州河市郊段环境综合治理、底泥疏浚和处置提供了科学依据。     

高浓度电镀废水的处理

介绍了某自行车厂电镀车间高浓度电镀废水处理工艺的设计；结合工艺运行的调试，对设计缺陷进行了分析。     

Speciation of heavy metals in estuarine sediments in the northeast of Brazil

An analytical procedure involving a three-step sequential extraction was used to determine the chemical association of heavy metals (Zn, Cr, Mn and Fe) with the major phases (exchangable, reducible and oxidizable) in samples from a fishpond of estuarine sediments. The pond is located in the Capibaribe River estuary, within the boundaries of the city of Recife, in the State of Pernambuco in the northeast of Brazil. The total metal content was determined as well. All metals were extracted from the residual fraction at a percentage greater than 50%.     

某电厂堆灰场附近浅层地下水中Cr6+的成因及治理措施

分析了焦作某电厂堆灰场附近浅层地下水中Cr6+ 的形成原因。根据该区水文地质背景 ,提出在地下污染水羽的下游建可渗透反应墙的漏斗 -通道系统 ,用对Cr6+ 有很高去除效率的风化煤作为反应材料 ,使污染水羽流经此系统时有效去除地下水中的Cr6+ ,达到净化的目的     

紫外活化甲酸产二氧化碳阴离子自由基还原Cr (VI)的研究

研究高效还原技术是去除废水中Cr（VI）的有效手段,本研究提出了一种新颖有前景的基于紫外（UV）活化甲酸（HCOOH）产还原性二氧化碳阴离子自由基（CO₂^•;-）去除Cr（VI）的方法.通过对比UV、HCOOH、UV/HCOOH三种体系对Cr（VI）还原效率和电子自旋共振（EPR）对体系中自由基的检测研究了其活化原理和还原机制.结果表明UV能显著活化HCOOH产生CO₂^•-（α_H=19.08G,α_N=15.86G,g=2.0036）.此外,试验考察了主要影响因素对Cr（VI）去除效果的影响,包括初始Cr（VI）浓度、甲酸投加量、初始pH值、反应温度、有机污染物以及水中常见阴离子.结果显示当甲酸浓度为40mmol/L,Cr（VI）初始浓度为10mg/L,反应时间在60min内,UV/HCOOH体系对Cr（VI）的去除率能达到100%.在酸性条件下（pH≤3.5）能显著促进Cr（VI）的还原,且Cr（VI）去除效率随着初始HCOOH浓度和反应温度升高而增加.进一步研究表明,该体系下NO₃^-对Cr（VI）的还原有着显著的促进作用,而Cl^-、HCO₃^-和对硝基苯酚（pNP）则有抑制作用.不同温度下Cr（VI）去除率与时间关系的拟合结果表明,当反应时间t³;40min,UV/HCOOH体系去除Cr（VI）过程遵循准一级反应动力学,根据不同温度下对应的反应速率常数k,结合阿伦尼乌斯方程,计算求得准一级反应的活化能为15.9kJ/mol.