活性炭阴极电化学法回收废水中Ni(Ⅱ)的研究

研究了采用活性炭阴极电化学法,回收废水中的Ni(Ⅱ)生产硫酸镍的工艺。着重探讨了电流密度、Ni(Ⅱ)的初始浓度、溶液的pH值与反应温度对Ni(Ⅱ)回收率的影响。在电流密度为0.05A/cm2,废水中Ni(Ⅱ)的含量为250 mg/L,溶液pH值为6.0、温度为30℃及反应时间为150min条件下,废水中的Ni(Ⅱ)回收率达99.2%。     

Effect of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction of NOx with C2H5OH

The influence of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction （SCR） of NOx with C2H5OH was investigated experimentally. The activity test results suggest that Ag-Pd/Al2O3 shows a small activity loss in the presence of SO2 when using C2H5OH as a reductant. In situ DRIFTS spectra show that the activity loss originates from the formation of surface sulphate species on the Ag-Pd/Al2O3. The surface sulphate species formation inhibits the formation of nitrate, whereas hardly changes the partial oxidation of C2H5OH. Compared with the NOx reduction by C3H6, an obvious suppression of the surface sulphate species formation was observed by DRIFTS experiment when using C2H5OH as a reductant. This phenomenon reveals the better catalytic performance and strong SO2 tolerance of Ag-Pd/Al2O3-C2H50H system.     

离子色谱法测定水中无机阴离子水样的预处理

本文介绍了用离子色谱法测定无机阴离子，对污染严重的水样通常采用预处理柱法。论述了预处理柱的制备、再生，测定了预处理柱对重金属及有机物的去除率及无机阴离子的回收率。     

纤维素基吸附剂——绿色、经济的水处理材料

介绍了一类基于天然纤维素的水处理用吸附剂.对纤维素修饰羧基等阴离子基团,可以用来吸附水中的重金属阳离子(如cd(2+)、Cu(2+)、Hg(2+)、Ni(2+)、Pb(2+).对纤维素修饰铝铁或胺基等成分,可以吸附水中含砷阴离子、氟离子等有害阴离子.在纤维素上修饰疏水链,可以吸附水中氯苯、染料等危害健康的有机物.     

聚硫酸铁强化混凝除锑(V)作用机制探讨

以聚硫酸铁(PFS)为絮凝剂,考察强化混凝去除饮用水源水中五价锑(Sb(V))时原水pH值、PFS投量、共存阴离子(HCO3－和PO43－)及腐殖酸(HA)等对其去除效果影响及作用机制.结果表明,原水pH值对强化混凝过程Sb(V)存在形态及PFS的水解产物有重要影响,表现为较低pH值和较高PFS投量均有利于提高Sb(V)的去除率;由于竞争吸附作用的存在,共存阴离子与HA均对Sb(V)的混凝去除产生负面效应.此外, PFS除Sb(V)过程较为符合准二级动力学模型.     

氨法烟气脱硫技术及其进展

阐述了氨法烟气脱硫技术的原理和工艺特点.介绍了Walther氨法、AMASOX氨法、GE氨法、NADS氨-肥法、电子束氨法和流光放电氨法烟气脱硫工艺,重点介绍了新型流光放电氨法烟气脱硫技术的特点及其工程应用情况.展望了氨法烟气脱硫技术的应用前景.     

高分子凝聚剂凝聚效果的评价方法与最佳添加量

在稀悬浮液体系的絮凝沉淀中,硫酸铝和微阴离子性聚合物并用时聚合物的效果及其最佳添加量,是以絮状物的沉降速度和透射光强度的变化为指标进行研究的。其结果:既定聚合物添加量时硫酸铝的最佳添加量是以絮状物形成速度及絮状物直径的最大值(Kmax及Dtmax)、沉降速度式中系数a的最大值、系数n的最小值确定。根据(9)式、(10)式或(15)式、(16)式计算得出。从水处理的经济观点考虑,认为聚合物的添加量是Kmax,Dtmax折射点(Cp-ref)以下的添加量。     

HYDROLOGICAL AND GEOCHEMICAL TRENDS AND PATTERNS IN THE UPPER RIO GRANDE, 1975 TO 19991

ABSTRACT: Hydrological and geochemical spatial patterns and temporal trends were analyzed using U.S. Geological Survey (USGS) water quality data collected from 1975 to 1999 along the uppermost 600 km of the Rio Grande in Colorado and New Mexico. Data on discharge, specific conductivity (SC), total dissolved solids (TDS), pH, Ca²⁺, Na⁺, Mg²⁺, K⁺, HCO₃^?, SO₄^2‐, Cl^?, F^?, and SiO₂ came from six USGS stations ranging from the Colorado‐New Mexico border to below Albuquerque, New Mexico. Linear regression, Kendall's S, and Seasonal Kendall's S’ were used to detect trends, and ANOVA was used to analyze spatial differences between stations. Statistically significant increasing trends occurred in SC, TDS, Ca²⁺, Na⁺, Mg²⁺, K⁺, Cl^?, and F^?in the uppermost reaches, and significant decreasing trends of SC, TDS, Ca²⁺, Mg²⁺, K⁺, HCO₃^?, and SO₄^2‐occurred at the lower stations around Albuquerque. Both fluoride concentrations and pH values increased at and below Albuquerque over the study period. Discharge data show an increasing trend across all stations. Spatially, data for dissolved substances show generally linear upstream to downstream increases in concentrations in the upper four stations, with several notable nonlinear increases at and below Albuquerque (SC, TDS, Na⁺, Cl^?). Significant increases in pH appear at and below Albuquerque, relative to upstream stations, probably due to improved sewage treatment.     

Field Intercomparison of Main Components in Air in EMEP

Within the European monitoring network (EMEP, ) several different sampling procedures for measuring the main air components have been applied. This has contributed to systematic concentration differences and a comparability problem. Since 1997 co-located experiments in 15 countries have been carried out to quantify these differences. In addition, three major measurement campaigns were organized by EMEP between 1985 and 1991. Differences among results depend on the concentration level and methods used. The decrease in SO₂ concentrations over the last twenty years has placed greater demands on the methodology. Absorbing solutions methods for SO₂, (H₂O₂ and tetrachloromercurate (TCM)) typically have higher detection limits than the reference method, which uses KOH impregnated filters. The TCM method also has problems with negative interference, especially in summertime. UV fluorescence monitors have in a few cases proven to give good results, but interferences, detection limit and poor maintenance can be problems. For NO₂, many countries are using the TGS absorption solution method, which has a higher detection limit than the reference method using NaI impregnated glass sinters. The Salzmann method gives unreliable results at concentrations below 1 μgN/m³, and even at higher concentrations the uncertainty is rather unsatisfactory. The chemiluminescence monitor with molybdenum converters tends to systematically overestimate NO₂ concentrations, possibly because zero-drift problems and the non-specific response to NO₂. Particulate sulphate measurements in general have lower bias and uncertainties than gas and other aerosol measurements.     

Effects of maize root exudates and organic acids on the desorption of phenanthrene from soils

The effects of maize root exudates and low-molecular-weight-organic anions (LMWOAs) on the desorption of phenanthrene from eight artificially contaminated soils were evaluated. A significant negative correlation was observed between the amounts of phenanthrene desorbed and the soil organic carbon (SOC) contents (P<0.01), and the influences of soil pH and clay content on phenanthrene desorption were insignificant (P>0.1). Neither maize root exudates nor oxalate and citrate anions influenced desorption of phenanthrene with the addition of NAN3. A faster phenanthrene desorption occurred without the addition of NaN3 in the presence of maize root exudates than oxalate or citrate due to the enhanced degradation by root exudates. Without the addition of NaN3, oxalate or citrate at different concentrations could inhibit phenanthrene desorption to different extents and the inhibiting effect by citrate was more significant than by oxalate. This study leads to the conclusion that maize root exudates can not enhance the desorption under abiotic condition with the addition of NaN3 and can promote the desorption of phenanthrene in soils without the addition of NAN3.