离子交换法选择性回收污泥厌氧消化液中的磷

为探讨高效选择性回收污泥厌氧消化液中磷的离子交换方法,采用静态实验和动态实验研究了4种阴离子交换树脂（D213、D202、D301和DSQ）的磷回收性能,筛选了适合富磷污泥厌氧消化液选择性磷回收的高交换容量树脂。实验结果表明,D213、D202、D301和DSQ 4种树脂对正磷浓度为70 mg/L的厌氧消化液进行动态处理时,其最大穿透体积分别为3、7、17和90 BV;DSQ树脂磷交换容量远高于其他3种树脂,达到6 860 mg P/L湿树脂,是目前报道的高磷交换容量树脂的3~4倍;DSQ树脂能有效地抵抗厌氧消化液中有机质和硫酸根等阴离子的干扰;用NaOH溶液再生DSQ树脂并回收磷,磷洗脱率超过96%,洗脱液是高浓度含磷液,可作为磷矿石的优质替代品。研究表明,DSQ树脂是一种高效选择性分离磷的树脂,适用于污泥厌氧消化液的磷回收。     

固体厌氧消化原料流变特性研究综述

厌氧消化原料的流变特性是厌氧消化工艺设计和运行的重要参数。本文从研究对象、实验操作、研究内容和结果、影响因素以及发展方向等方面对固体厌氧消化原料,特别是污泥的流变特性研究现状进行了概述。研究表明,污泥来源广泛,成分复杂,属于非牛顿流体的范畴,其流变特性受多种因素影响,其中污泥的总悬浮固体(TSS)(或混合液悬浮固体(MLSS))和温度是最主要的影响因素。大部分研究采用层流剪切实验对物料的流变特性进行表征,研究对象范围有待于扩大。尚需针对流体本构方程的改进,共消化对于原料流变特性的影响,混合液固、液相指标与流变参数的关系等方面开展研究,为利用流变参数作为工艺控制参数提供理论依据,并解决工程放大等问题。     

正交试验-硝酸微波消解-冷原子吸收法测定土壤中汞

应用硝酸微波消解土壤样品-冷原子吸收法测定土壤中的汞。通过正交试验，优化了土壤中汞的微波消解条件。并对干扰消除、方法精密度、加标回收、检出限进行了试验研究。在0～10μg／L范围内线性关系良好，方法测定下限为0．20μg／L，土壤中汞的检出限为0．005μg／g。该优化条件对汞含量为0．02—0．46μg／g的土壤样品，汞提取完全。建立了一种简便、成本低、干扰少、灵敏度高的方法。     

稀硫酸预处理对稻草厌氧消化的影响

以稻草为对象,研究了热稀硫酸预处理后对厌氧消化过程中的COD、pH、挥发性脂肪酸(VFA)、产气量及产气速率的影响。结果表明,以1.0%、1.5%和2.0%稀硫酸溶液预处理后,稻草厌氧消化系统总产气量分别提高了34%、125%和66%,甲烷产量分别提高了61.5%、215.1%和113.9%,挥发性固体(VS)去除率分别提高了15.5%、22.4%和17.6%,COD去除率分别提高了47.1%、57.4%和53.9%。浓度1.5%稀硫酸预处理对稻草厌氧消化效果最佳。     

Enclave development and ‘offshore corporate social responsibility’: Implications for oil-rich sub-Saharan Africa

This paper critically reflects on the challenges of engaging, proactively, in Corporate Social Responsibility (CSR) in oil-rich sub-Saharan Africa. Most of the region's oil production takes place in enclave-type environments offshore and in countries ruled by autocratic governments which generally exert minimal pressure on companies to embrace CSR. With companies having little sense of who to target in their local economic development policies and programs, there is always a possibility of ‘offshore CSR’ – recognized here as potentially-effective ideas for improving social welfare that linger within the enclave and never fully materialize – surfacing. The aim is to conceptualize and broaden understanding of the challenge of developing CSR programs in these settings, where there are no clear linkages to communities or local economies more generally.     

The structure of the fire fighting foam surfactant Forafac®1157 and its biological and photolytic transformation products

For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by ¹H, ¹³C and ¹⁹F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility.     

微波消解-流动注射分光光度法测定土壤中的总磷

采用热效率高的微波消解系统对土壤中的总磷进行消解,建立了微波消解-流动注射分光光度法测定土壤中总磷的方法,该方法对比HJ632-2011碱熔-钼锑抗分光光度法具有快速、简便、节约试剂等特点。本文用两种分析方法对实际土壤样品及标准样品进行定量测定,所得结果表明微波消解法能快速测定大量土壤样品的总磷。     

M3法测定土壤有效态Cd、Cr、Pb和Ni

通过M3法对耕地土壤重金属的联合测定,为土壤重金属污染监测应用提供快速联合测定的方法。用M3法测定北方耕地土壤的有效Cd、Cr、Pb和Ni,通过对M3法与其他方法进行有效重金属测定值差异性及其相关性比较,与全量的浸出率分析等探讨M3法对耕地土壤有效重金属测定的特征。结果表明,M3法在《土壤环境质量标准》(GB 15618—1995)的土壤重金属含量范围内可以测定土壤有效态重金属Cd、Cr、Pb和Ni,且呈线性极显著相关。M3法与其他方法有效Cd、Cr、Pb和Ni有较好的相关性,与DTPA法呈极显著相关;与NaNO₃法除有效Pb外,呈极显著和显著相关;与HCl法除褐土和潮土的有效Pb外,也呈极显著和显著相关。M3法的有效态Cd、Cr、Pb和Ni的测定值均为最大。M3法对4种耕地土壤有效Cd、Cr、Pb和Ni的浸出率,因土壤类型不同,有效重金属含量所占比率不同,但利用M3法测定的有效态Cd、Cr、Pb和Ni的浸出率最大。     

基于汶川8.0级强震记录的近场地震动特征分析

在汶川8.0级大地震中,国家数字强震动台网布设在龙门山断裂带及其周围地区的50多个台站获得了大于100 Gal的加速度记录。选取其中断层附近11个台站的加速度记录,分别进行了地震反应谱分析和基于正交化HHT法的能量分布特征分析,通过对竖向与水平向加速度峰值比、竖向与水平向加速度反应谱比值,以及能量分布和峰值系数的分析与比较,探讨了汶川地震的近场地震动特征。     

青海玉树7.1级地震震害特点分析及启示

根据2010年4月14日玉树7.1级地震震害现场调查资料,对其震害特点进行了全面的分析总结,阐述了震区环境及其地质构造背景,对断层效应及场地效应等也进行了分析,并归纳总结了防震减灾的经验与启示。