泥沙对黄河水质参数COD、高锰酸钾指数和BOD5的影响——三论黄河的COD值与高锰酸钾指数不能真实反映其污染状况

研究了黄河泥沙含量与COD、高锰酸盐指数和BOD5等水质参数间的关系,揭示了当前黄河COD和高锰酸盐指数监测与评价中存在的问题.结果表明,在上述3个描述耗氧有机物污染程度的参数中,BOD5能真实地反映黄河的有机污染状况,而COD和高锰酸盐指数,不论是用含泥沙的浑水样品测得的数值,还是用滤除掉泥沙的清水样品测得的数值,均在相当程度上夸大了黄河的水污染程度.这种夸大作用在未污染和轻污染河段尤为显著.作者认为,在使用COD和高锰酸盐指数等参数对黄河水质进行评价时,不宜使用直接测得的数值,而应使用经"泥沙有机质本底量"校正的数值.     

黄河水质COD监测问题的研究

通过研究黄河原状水样COD值与澄清水COD值的关系,得出黄河泥沙对分析结果影响太大,不能合理分析黄河水质受污染的程度,建议对黄河水质COD监测与评价采用原状水与澄清水同时进行的方案为最佳.     

黄河耗氧性有机物污染特征及泥沙对其参数测定的影响

对黄河干流1980,1992～1999年耗氧性有机物污染监测数据进行了分析,并通过对高锰酸盐指数(CODMn)与泥沙含量监测数据间的相关分析和模拟实验研究,探讨了泥沙对CODMn测定的影响.结果表明:(1)由于泥沙中腐殖质的成分之一富里酸能溶解于酸,在水样加酸处理过程中将进入水相,且富里酸能被化学氧化剂所氧化,但在自然条件下很难发生生物氧化和消耗水体的溶解氧,因此,由于泥沙的影响,CODMn夸大了耗氧性有机物的污染;(2)黄河干流河水的生化需氧量(BOD5)从上游至下游存在增加的趋势;(3)1992年干流河水的BOD5显著大于1980年的BOD5,在1992～1999年间,河水BOD5的年均值存在上升的趋势,枯水期均值存在上升的趋势,而丰水期均值的增长趋势不明显,由此表明,耗氧性有机污染物的点源排放在增加,而面源排放的增长趋势不明显,甚至存在降低的趋势;(4)黄河干流的耗氧性有机污染物主要来自点源排放,BOD5的点源与面源负荷的多年均值之比为2 81.     

解决黄河耗氧有机物评价中存在问题的方法探讨--四论黄河耗氧有机物污染评价问题

黄河水泥沙含量高,现行的BOD5、COD和高锰酸盐指数测定方法所测结果常不能真实反映其污染状况．针对上述问题提出在评价黄河水质时,不采用COD、高锰酸盐指数和BOD5的实测值,而采用经分别校正的数值,对COD和高锰酸盐指数而言,应从实测值中扣除由泥沙有机质本底量所产生的那部分数值．对BOD5而言,既可通过改进测试操作解决,也可通过乘以校正系数以恢复测量过程中受泥沙沉淀影响而降低的那部分数值．应用校正公式,通过案例研究,对校正方法的正确性进行了检验．     

煤矿排放废水的化学耗氧量(COD)的特性及其测定方法探讨

煤矿矿井水及洗煤厂排水一般不测定化学耗氧量(COD),但有时根据当地需要,对此废水要了解COD值。测定废水COD值系采用重铬酸钾氧化法,方法规定要吸取经过搅拌的均匀水样。鉴于浓硫酸介质中的重铬酸钾其氧化性特强,能够氧化大多数的有机物质,对于煤矿排放废水中的悬浮煤粒的有机质,当然也不例外,于是导致COD值大大增高。然而煤粒的有机质长期在水中仍然非常稳定,它并不消耗水中的氧,萍乡矿务局高坑煤矿在煤泥沉淀池内每年养鱼2000斤,可以说明这一问题。煤虽是有机物,但不属     

黄河兰州段耗氧有机污染物浓度统计预测模型的建立

黄河是一条多泥沙河流,流域内面源污染严重,在分析研究黄河的水环境问题时,必须考虑面源污染这个因素。建立河流污染断面耗氧有机污染物(以COD表示)浓度预测模型是河流水质规划的一     

UV-C辐照对河水溶解有机质降解及微生物可利用性的影响

从黄浦江及其上游支流采集表层水样,进行了微生物培养、UV-C辐照和微生物再培养等处理过程,测定水样ρ(DOC)(DOC为溶解有机碳)、紫外可见吸收光谱和荧光光谱,探讨河水DOM(溶解有机质)的光化学降解和微生物可利用性特征. 结果表明:不同处理过程对DOM不同组分去除的贡献率不同,黄浦江河水经微生物培养后,ρ(DOC)和CDOM(有色溶解有机质)含量〔以a₃₃₅(335nm处的吸收系数)计〕分别下降了5%~27%和5%左右,而FDOM(荧光溶解性有机质)含量(以最大荧光强度表示)稍有增加;继续经UV-C辐照24h后,ρ(DOC)和CDOM含量分别下降了7%~36%和79%~96%,而FDOM含量下降了95%以上,说明水体中大部分CDOM和FDOM可通过UV-C辐照去除,并且去除率显著高于微生物降解. UV-C辐照不仅可以降解DOM,而且可以改变DOM的微生物可利用性,其中一部分SLDOM(半活性溶解有机质)经UV-C辐照后能够再次被微生物利用,其中4%~28%的DOC和5%~14%的CDOM可再次被微生物降解.      

多沙河流COD监测方法评价及改进方法

在分析黄河泥沙特性及泥沙对水环境影响的基础上,分析以往及现有COD监测方法对黄河水的监测中存在的主要问题,在此基础上,提出了多沙河流COD监测的改进方法。在该方法中,引入泥沙非降解COD值的概念,并用试验方法建立黄河下游泥沙非降解COD值的估算公式。多沙河流COD监测改进后的方法简单易行,准确度较高,其测定结果基本能够客观地反映多沙水体受耗氧有机物污染的程度。     

水质指标COD的优缺点及其测量方法发展

COD是最常用的评价水体污染程度的综合性指标。COD指标由于测量方便,费用低,适用范围广等优点已成为我国水质监测中必测的一项指标。但在水质成分复杂,水中无机还原性污染物、难降解有机物含量高时,用COD指标来表征有机污染程度会出现很大的偏差。并且由于COD的标准测定方法易受干扰,使得COD的测定值与理论值相差较大。文章综合分析COD指标应用的局限性及其测定方法的发展。     

水中有机污染物综合指标分析述评

目前,水中有机污染物综合指标有BOD_5、COD、TOD、TOC及UVA等。一、生化需氧量(BOD_5) 多年来,沿用BOD_5这一参数作为水中有机污染物可被微生物降解的综合指标,以此掌握水质的有机污染程度,了解污水生化降解的可能性,为生化处理的构筑物设计提供基础数据,评价污水处理技术的效果。     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.