养殖废水新型处理技术中试

针对畜禽养殖污染废水传统处理方法效率不高、噪声较大等缺点进行改进,采用"水解酸化池-塔式膜生物反应器-悬浮澄清池"工艺进行处理,结果表明:COD、氨氮去除率分别为97.5%和91%,出水水质可达GB 18596—2001《畜禽养殖污染物排放标准》。     

产甲烷抑制剂氯仿对污泥厌氧消化中同型产乙酸作用的影响

厌氧消化是城市污泥常用的资源化处理方式,添加产甲烷抑制剂得到的发酵产物乙酸相比于甲烷被认为更具附加值.同型产乙酸途径是污泥厌氧发酵产乙酸途径之一,然而产甲烷抑制剂的存在对其影响尚不明确,这对污泥厌氧发酵产酸工艺的优化和应用至关重要.本文研究了不同氯仿浓度抑制产甲烷条件下挥发性脂肪酸、气体浓度及同型产乙酸菌和总细菌数量的变化,基于乙酸的稳定性碳同位素分馏效应分析了不同温度条件下氯仿对同型产乙酸作用的影响.结果显示,0.1%和0.5%(V/V)氯仿浓度条件下最高乙酸浓度分别为24.5和22.4 mmol·L~(-1),远低于对照组的52.6 mmol·L~(-1).氯仿抑制产甲烷条件下乙酸的稳定碳同位素丰度δ~(13)C值均高于污泥有机质的δ~(13)C值,50℃时乙酸的δ~(13)C值最高,且同型产乙酸菌相对丰度也低于15和30℃条件下.可见,产甲烷抑制剂氯仿同时能够抑制同型产乙酸作用,0.5%浓度下的抑制效果高于0.1%浓度下,且50℃条件下其抑制作用强于15和30℃条件下.     

两种抗生素菌渣经SEA-CBS技术处理后的肥料特性

抗生素菌渣的环境无害化利用处置目前已成为行业和政府管理部门亟待解决的难题.为有效实现抗生素菌渣的资源化利用,开展了经SEA-CBS高效复合资源化利用技术制成的吉他霉素和螺旋霉素菌渣有机肥理化特性研究,并分析了未施肥、施加不同比例的商品肥和菌渣有机肥对苦苣生长的影响.结果表明:吉他霉素和螺旋霉素菌渣有机肥的pH分别为6.59和7.92,含水率分别为5.21%和10.60%,抗生素残留均未检出;吉他霉素菌渣有机肥中w（Cr）、w（Pb）和w（As）相对较高,分别为33.40、7.05和1.57 mg/kg,而w（Cd）（0.34 mg/kg）和w（Hg）（低于0.002 mg/kg）相对较低;两种抗生素菌渣有机肥的总养分含量均在5%以上,w（有机质）均大于80%,均符合NY 884—2012《生物有机肥》及NY 525—2012《有机肥料》中的相关限值.植株生长试验研究发现,施加1%和3%的吉他霉素菌渣有机肥时,苦苣的株高、鲜质量和干质量均优于未施肥处理,且株高均大于施入商品肥处理;施加1%螺旋霉素菌渣有机肥下苦苣生长性能优于未施肥情况.研究显示,SEA-CBS技术可有效去除菌渣中残留的抗生素,并实现抗生素菌渣的资源化利用.      

Complexes of fulvic acid on the surface of hematite, goethite, and akaganeite: FTIR observation

The present work extended our knowledge on the binding and complexation of a fulvic acid (FA) derived from leonardite and the iron oxides (hematite, goethite and akaganeite) by Fourier transform infrared spectroscopy (FTIR). As a prerequisite, the iron oxides were firstly prepared and characterized by transmission electron micrograph (TEM). All iron phases were single and well-described crystalloid. The FTIR data obtained by two different sampling preparation methods gave the consisting evidences that under our experimental conditions the interaction mechanism was to the ligand-exchange involving carboxylic functional groups of the FA and the surfaces sites of both hematite and goethite, while no complexation can be evidenced in the case of akaganeite, only surface adsorption. In general, the binding affinities of the iron oxides with the FA was in the order of hematite>goethite>akaganeite. The present method, although associated with some uncertainties, provided an opportunity to increase the knowledge in the field of the humic chemistry.     

深海热液喷口微生物对矿物元素行为的影响

介绍了生长在深海热液喷口周围的微生物的种类及其生长繁殖的能量来源;并就其参与的矿物沉积和浸出行为做了阐述;最后在目前国内外研究现状的基础上提出了今后应该研究的方向。     

厌氧颗粒污泥对五氯苯酚脱氯过程中的影响因素

在间歇培养血清瓶中,研究了厌氧颗粒污泥对五氯酚脱氯过程中的影响因素.结果表明,葡萄糖、酵母膏和蛋白胨显著提高了PCP的脱氯速率.添加甲酸、乙酸、乙醇对PCP脱氯速率有一定提高,丙酸和丁酸对脱氯速率没有影响.20%氢气的加入对PCP脱氯速率的影响显著.废水中硝酸盐和硫酸盐等电子受体的存在降低了PCP的脱氯速率.微生物抑制剂氯仿、青霉素降低了PCP脱氯速率,表明厌氧微生物尤其是甲烷菌对还原脱氯有重要影响.PCP最佳还原脱氯温度为38℃,最佳pH为7,低的氧化还原电位(<-200mV)有利于脱氯的进行.图5参13     

伊春河河水水溶性腐殖酸内源释放模型

以水溶性腐殖酸含量很高的伊春河为例，利用冬季冰封无外源输入的条件，在有产室内模拟研究的基础上，通过现场采样及测定，建立了伊春河河水水溶性腐殖酸的内源释放模型，根据同期采集样品进行的验证表明，该模型能够准确地反映河流沉积物中水溶性瘁殖酸向河水中释放的速率以及速率与流速等条件的定量关系。     

酸性媒介黄GG生物降解性能的试验研究

通过试验研究酸性媒介黄GG染料在厌氧、好氧条件下的生物降解机理、降解能力及共代谢降解效果.试验结果表明,厌氧菌能够通过葡萄糖共代谢作用很快降解酸性媒介黄GG;而好氧条件下经驯化活性污泥不能降解酸性媒介黄GG,经过较长时间驯化活性污泥能降解酸性媒介黄GG,但降解效果很差.葡萄糖浓度的升高对提高酸性媒介黄GG厌氧生物降解率有利,当葡萄糖浓度为2000 mg/L时,40mg/L酸性媒介黄GG的12和60 h厌氧生物降解率分别达到81.5%和93.5%.酸性媒介黄GG浓度对厌氧菌的生物降解能力也有影响.当葡萄糖浓度为2000 mg/L,酸性媒介黄GG(浓度为20～100 mg/L)的厌氧降解率最好,降解效率达到了94%,说明厌氧菌对酸性媒介黄GG的降解能力较好.     

Observation and analysis of atmospheric volatile organic compounds in a typical petrochemical area in Yangtze River Delta, China

Volatile organic compounds (VOCs) are a kind of important precursors for ozone photochemical formation. In this study, VOCs were measured from November 5th, 2013 to January 6th, 2014 at the Second Jinshan Industrial Area, Shanghai, China. The results showed that the measured VOCs were dominated by alkanes (41.8%), followed by aromatics (20.1%), alkenes (17.9%), and halo-hydrocarbons (12.5%). The daily trend of the VOC concentration showed a bimodal feature due to the rush-hour traffic in the morning and at nightfall. Based on the VOC concentration, a receptor model of Positive Matrix Factorization (PMF) coupled with the information related to VOC sources was applied to identify the major VOC emissions. The result showed five major VOC sources: solvent use and industrial processes were responsible for about 30% of the ambient VOCs, followed by rubber chemical industrial emissions (23%), refinery and petrochemical industrial emissions (21%), fuel evaporations (13%) and vehicular emissions (13%). The contribution of generalized industrial emissions was about 74% and significantly higher than that made by vehicle exhaust. Using a propylene-equivalent method, alkenes displayed the highest concentration, followed by aromatics and alkanes. Based on a maximum incremental reactivity (MIR) method, the average hourly ozone formation potential (OFP) of VOCs is 220.49?ppbv. The most significant source for ozone chemical formation was identified to be rubber chemical industrial emissions, following one by vehicular emission. The data shown herein may provide useful information to develop effective VOC pollution control strategies in industrialized area.     

Elimination of a pollution associated with chromic acid during the electro-deposition of Cr(III) using appropriate anodic and membrane materials in a double film bath

A method using trivalent chromium has been used to replace hexavalent chromium for the electro-deposition of chromium. Using a tri-chamber bath system various anodic materials and membranes were evaluated to minimize the production of environmentally and health damaging chromic acid. By measuring the absorbance of Cr(VI) at 640 nm, the results indicate that the use of a titanium plated ruthenium (Ti-Ru) anode produces the least amount of chromic acid byproduct compared to lead-gold alloy and graphite anodes. The concentration of Cr(VI) in the immediate vicinity of the Ti-Ru anode decreased from 0.389 mg/L to 0 during a 40-min deposition period. The use of a Nafion^TM quaternary cation exchange membrane portioning the buffer and anode selectively prevented Cr(III) from entering the anode compartment whilst allowing the migration of H⁺ to maintain overall voltaic continuity. It has been demonstrated that the use of a Ti-Ru anode with a Nafion^TM membrane can eliminate the production of chromic acid associated with the electro-deposition of chromium plate thereby preventing its health damaging exposure to plant operators and preventing discharge of Cr(VI) into the environment. Addition of a surfactant improved current efficiency by 34.7%.