海藻酸钠/蒙脱石联合负载型纳米Fe0对Cu(II)的去除研究

由于蒙脱石负载型纳米Fe~0(Mt-n ZVI)在使用中易随水迁移,造成出水水质混浊和Fe~0流失.因此,本研究制备了海藻酸钠(SA)和蒙脱石(Mt)联合负载型纳米零价铁(SA/Mt-n ZVI),探究其对水中Cu(Ⅱ)的去除效果,并考察了Cu(Ⅱ)初始浓度、pH值对去除率的影响.结果表明:以2%(质量分数)SA和6%(质量分数)Mt-n ZVI条件制备的SA/Mt-n ZVI小球对Cu(Ⅱ)处理效果好,反应24 h后,SA/Mt-n ZVI小球对初始浓度为40 mg·L-1Cu(Ⅱ)的去除率达到92.11%,与游离的Mt-n ZVI颗粒相比,其活性并未降低;Cu(Ⅱ)的去除率随其初始浓度升高而降低;在pH为2~6之间,Cu(Ⅱ)去除率随pH升高而升高.SA/Mt-n ZVI小球可有效净化污水中的Cu(Ⅱ),将其重复使用3次后,对Cu(Ⅱ)的去除率仍维持在59.52%.     

不同碳源和碳氮比对一株好氧反硝化细菌脱氮性能的影响

利用间歇培养装置研究了好氧条件下丁二酸盐、乙酸盐和苹果酸盐3种不同碳源对好氧反硝化细菌X31脱氮性能的影响,并就不同碳氮比(C/N)条件下菌株X31的反硝化能力展开了研究.结果显示,不同碳源种类对菌株硝酸还原酶活性有明显影响.以丁二酸盐和乙酸盐作为碳源时,其脱氮效果均要明显好于苹果酸盐作为碳源.以乙酸盐作为碳源时菌株的反硝化速率要稍高于丁二酸盐作为碳源,其反硝化速率可以达到11.86 mg·g-1·h-1.不同碳氮比(C/N)条件下,X31菌株的好氧反硝化能力亦不相同.当C/N大于5时,脱氮率能达到90%以上.最适宜的碳氮比是5～6,在此区间能进行完全的反硝化.当C/N在1～14之间变化时,硝酸盐还原基本都发生在菌株生长的第4～10 h,整个反硝化过程中亚硝酸盐浓度一直保持在极低的水平.     

微囊藻栅藻资源竞争的动力学过程Ⅰ.光能和磷营养的半饱和参数及其生长率动态

以Ｔｉｌｍａｎ提出的“资源竞争机制学说”为依据，在单因子（光、磷）限制条件下，测定并计算铜绿微囊藻（Ｍｉｃｒｏｃｙｓｔｉｓ ａｅｒｕｇｉｎｏｓａ）和斜生栅藻（Ｓｃｅｎｅｄｅｓｍｕｓ ｏｂｌｉｑｕｕｓ）的半饱和常数，以双因子交互作用模型预测它们的生长动态。结果表明；在光强为１０．０～１７．１ｕＥ的磷浓度为３．１０～２０．０ｕｍｏｌ的范围内，微囊藻的生长率大于栅藻的生长率，说明磷的增加是微囊藻成为水华     

长期施肥农田黑土微生物量碳、氮季节性变化

研究长期不同施肥处理农田黑土微生物量碳、氮(MBC、MBN)季节性特征,于不同月份采集单施化肥(NPK)、单倍有机肥(M)、双倍有机肥(M2)、单倍有机肥与化肥配施(MNPK)和对照(CK)处理土样。结果表明:与其它处理相比,M2处理MBC、MBN季节性变化较小。MBC季节性变化规律为:4月(春耕前)各处理较高,其它月份较低,CK、NPK、MNPK的最低值出现在5月(出苗期),M和M2的最低值出现在7月(拔节期),8、9月(灌浆期和收获后)各处理略有回升。MBN变化规律为:4月NPK、M、MNPK较低,其它月份较高,4、8月CK较低,其它月份较高。所有月份各处理均值方差分析结果表明:与CK相比,NPK、M、MNPK、M2均能提高MBC和MBN,其中M、MNPK、M2对MBC的提高达到显著水平(p<0.01),M对MBN的提高达到显著水平(p<0.01),其它处理未达到显著水平。另外,长期适量施用有机肥可以提高土壤微生物对有机碳及全氮的利用率。微生物量碳与土壤基本理化指标相关性显著,能够较好地反映出土壤质量变化情况。     

用煤矸石和鼓风炉淤泥制备聚硅酸铁铝混凝剂

研究了以煤矸石和鼓风炉淤泥为原料，在常压条件下制备高效混凝剂凝剂聚硅酸铁铝的方法，确定了合理的生产工艺和操作条件，用该混凝剂处理实际废水，并与聚合硫酸铁的处理效果进行比较，结果表明，出水COD和色度去除率均提高约30%，SS去除率提高约10%，同时探讨了该混凝剂处理废水的反应机理。     

施肥及秸秆还田处理下玉米季温室气体的排放

以华北地区冬小麦-夏玉米轮作农田为研究对象,在玉米整个生长季,运用静态箱法针对正常施肥及正常施肥结合秸秆还田处理进行了为期3年N2O排放通量的连续观测,并开展了1季CO2和CH4交换通量的研究.在玉米整个生长过程中施肥阶段N2O的排放量占到了总排放量的83%—96%,表明现有化肥的使用明显导致了农田N2O排放增加.与控制地相比,施肥和耕种可导致玉米田CO2排放明显增加,且正常施肥及秸秆还田样地CO2排放主要集中在苗期至吐丝期.控制地、正常施肥样地及施肥结合秸秆还田样地CH4的累积排放量均为负值,说明旱地土壤是CH4的一个汇.秸秆还田在一定程度上增加了玉米季N2O和CO2的排放量,但对CH4的吸收有所抑制.正常施肥样地和秸秆还田样地全球净增温潜势分别为-1392.8 kg C.hm-2和-179.2 kg C.hm-2,表明华北农田在现有耕作方式下是大气温室气体的一种重要汇.     

2009年北京市苯系物污染水平和变化特征

采用Tenax-TA/吸附热解吸、光离子化气相色谱法(GC-PID)对北京市大气中苯系物(BTEX)的小时平均浓度进行了为期1年的观测.结果表明,苯、甲苯、乙苯、间/对-二甲苯和邻二甲苯的年平均浓度分别为:4.43、7.03、2.27、4.18和2.06μg.m-3.苯系物之间具有很好的同源性,其浓度存在明显的日变化和季节变化,这些变化特征与交通尾气排放、采暖期化石燃料燃烧、光化学反应活性等密切相关.苯与甲苯特征比值(B/T)的分析表明,交通尾气排放是北京市大气中苯系物的主要来源,冬季和早春采暖期化石燃料燃烧也是北京市大气中BTEX的重要来源之一.乙苯与二甲苯比值(E/X)的季节变化为:夏季>春季>秋季>冬季,与北京市大气光化学反应活性季节变化趋势相似.2009年北京夏季总苯系物的平均浓度比2004年夏季减少了2/3,表明北京市政府为改善空气质量所采取的一系列控制措施十分有效.     

不同深度处理工艺再生水中余氯衰减规律及溶解性有机物变化特性比较

考察了余氯在不同深度处理工艺再生水中的衰减规律,并利用紫外-可见吸收差光谱和三维荧光光谱对余氯衰减过程的有机物变化进行了初步解析.结果表明,再生水中的余氯衰减迅速,加氯前0.5 h内的氯消耗占8 h内氯消耗的50%以上.混凝出水水样的余氯衰减速率大于超滤出水和臭氧出水.加氯后,混凝出水和超滤出水的紫外-可见吸收差光谱在230 nm和280 nm附近出现特征峰,表明余氯衰减过程中,水中具有不饱和键和生色团的物质被破坏.臭氧出水在波长230 nm附近出现特征峰.加氯使再生水的荧光强度减弱,混凝出水中腐殖质类物质荧光强度的降低程度大于超滤出水和臭氧出水,表明该类物质可能是影响余氯衰减速率的主要物质.     

Levels, sources and health risks of carbonyls and BTEX in the ambient air of Beijing, China

The atmospheric concentrations of carbonyls and BTEX (benzene, toluene, ethylbenzene, m,p-xylene and o-xylene) were measured simultaneously at a same sampling site in Beijing from September 2008 to August 2010. The average concentrations of the total measured carbonyls during autumn, winter, spring, and summer were 37.7, 31.3, 39.7, 50.5 μg/m³, respectively, and maximal values for their diurnal variations usually happened at noontime. In contrast to carbonyls, the average concentrations of the total measured BTEX during the four seasons were 27.2, 31.9, 23.2, 19.1 μg/m³, respectively, and minimal values for their diurnal variations always occurred in the early afternoon. The average concentration for carbonyls increased about 24% from September 2008-August 2009 to September 2009-August 2010, for BTEX, increased about 15%. Integrated life time cancer risks for three carcinogens (benzene, formaldehyde and acetaldehyde) in Beijing exceeded the value of 1E-06, and the hazard quotient (HQ) of non-cancer risk of exposure to formaldehyde exceeded unity.     

Kinetic analysis of anaerobic phosphorus release during biological phosphorus removal process

Enhanced biological phosphorus removal (EBPR) is a commonly used and sustainable method for phosphorus removal from wastewater. Poly-β-hydroxybutyrate (PHB), polyphosphate, and glycogen are three kinds of intracellular storage polymers in phosphorus accumulation organisms. The variation of these polymers under different conditions has an apparent influence on anaerobic phosphorus release, which is very important for controlling the performance of EBPR. To obtain the mechanism and kinetic character of anaerobic phosphorus release, a series of batch experiments were performed using the excessively aerated sludge from the aerobic unit of the biological phosphorus removal system in this study. The results showed that the volatile suspended solid (VSS) had an increasing trend, while the mixed liquid suspended sludge (MLSS) and ashes were reduced during the anaerobic phosphorus release process. The interruption of anaerobic HAc-uptake and phosphorus-release occurs when the glycogen in the phosphorus-accumulating-organisms is exhausted. Under the condition of lower initial HAc-COD, HAc became the limiting factor after some time for anaerobic HAc uptake. Under the condition of higher initial HAc-COD, HAc uptake was stopped because of the depletion of glycogen in the microorganisms. The mean ratio of Δρ _P/Δρ _PHB, Δρ _GLY/Δρ _PHB, Δρ _P/ΔCOD, was 0.48, 0.50, 0.44, and 0.92, respectively, which was nearly the same as the theoretical value. The calibrated kinetic parameters of the HAc-uptake and phosphorus-release model were evaluated as follows: Q _HAc,max was 164 mg/(g · h), Q _P,max was 69.9 mg/(g · h), K _gly was 0.005, and KCOD was 3 mg/L. An apparently linear correlation was observed between the ratio of Δρ _P/ΔCOD and pH of the solution, and the equation between them was obtained in this study. Translated from Acta Scientiae Circumstantiae, 2005, 25(9), 1164–1169 [译自: 环境科学学报]