氯离子对COD测定影响的探讨

研究含有高氯离子样品COD的测定,发现其中的白色沉淀为AgCl。实验结果证明,按照标准方法,当取样体积为20 mL时,按0.4 g HgSO4络合2 000 mg/L Cl-的比例投加掩蔽Cl-可以取得理想的效果。     

不同钝化剂对重金属污染土壤稳定化效应的研究

利用腐殖质、硫酸铵、石灰、过磷酸钙及其复配组合对污染土壤中的重金属进行快速钝化处理,根据稳定效率和钝化剂的钝化能力Cap值对钝化材料进行筛选,并采用BCR形态分级实验(European Communities Bureau of Referent,欧共体标准测量与检测局提取法)研究钝化前后土壤中重金属的形态变化.结果表明:1在单一钝化材料实验中,2%石灰稳定效果最好;在复配实验中,以2%腐殖质+2%石灰稳定效果最好,Pb、Cu、Cd、Zn稳定效率分别达98.49%、99.40%、95.86%、99.21%.2钝化能力Cap值顺序:石灰腐殖质+石灰硫酸铵+石灰磷肥硫酸铵+磷肥腐殖质+磷肥腐殖质硫酸铵.3BCR形态分级实验表明,腐殖质+石灰复合钝化剂对重金属的稳定化效应优于单一石灰处理.此外,当2%腐殖质先添加时Cd被活化,使Cd在随后加入的2%石灰处理下更容易转换为了稳定性较高的有机结合态和残渣态.     

超声、过硫酸钾协同去除水中诺氟沙星的效果

过硫酸钾活化可产生强氧化性硫酸根自由基(SO-4·),采用超声/过硫酸钾体系氧化降解诺氟沙星,考察了过硫酸钾浓度、诺氟沙星初始浓度、溶液初始p H值及自由基淬灭剂甲醇、叔丁醇对降解效果的影响.结果表明,超声/过硫酸钾体系能够显著降解和矿化诺氟沙星,与单独过硫酸钾、超声相比,超声/过硫酸钾对诺氟沙星的去除率分别提高了3.2和8.9倍,降解过程符合一级反应动力学.诺氟沙星的去除率随过硫酸钾浓度的增加趋于平缓.p H对诺氟沙星的降解影响较大,这是因为随p H的升高,体系中的氧化性物种由SO-4·转化为以SO-4·/HO·为主.TOC去除和大肠杆菌抗菌实验表明,反应180 min,超声/过硫酸钾能够实现49.12%的诺氟沙星矿化,且对大肠杆菌的抑菌圈直径由45 mm减小到14 mm(滤纸直径),完全去除其抗菌性.结果表明超声/过硫酸钾能够有效用于诺氟沙星废水处理.     

硫酸铁与聚合氯化铝处理城市景观水的比较实验研究

针对城市景观水的水质状况加剧恶化,本文对比在不同情况下用氯化铁及聚合氯化铝处理景观水,探讨了投加量、搅拌速度、搅拌时间、静沉时间以及pH对景观水有机物和浊度去除率的影响.结果表明:当水样pH值在6～8之间时,投加4～6mL混凝剂后,当先中速搅拌(120 r/min)2 min,最后慢速搅拌(60 r/min)搅拌10 min.此后静沉35 min,此时CODcr去除率及浊度去除率都可达到最佳情况;其中pH为8时,硫酸铁对CODcr去除率可达82％,浊度去除率率为92％;当PH为7时PAC对城市景观水CODcr的去除可达84％,浊度去除率率为96％.聚合氯化铝的处理效果优于硫酸铁,故而得出处理城市景观水时更适合选用聚合氯化铝.     

Antimony(V) removal from water by hydrated ferric oxides supported by calcite sand and polymeric anion exchanger

We fabricated and characterized two hybrid adsorbents originated from hydrated ferric oxides(HFOs) using a polymeric anion exchanger D201 and calcite as host. The resultant adsorbents(denoted as HFO-201 and IOCCS) were employed for Sb(V) removal from water. Increasing solution pH from 3 to 9 apparently weakened Sb(V) removal by both composites, while increasing temperature from 293 to 313 K only improved Sb(V) uptake by IOCCS. HFO-201 exhibited much higher capacity for Sb(V) than for IOCCS in the absence of other anions in solution. Increasing ionic strength from 0.01 to 0.1 mol/L NaNO3would result in a significant drop of the capacity of HFO-201 in the studied pH ranges; however, negligible effect was observed for IOCCS under similar conditions. Similarly, the competing chloride and sulfate pose more negative effect on Sb(V) adsorption by HFO-201 than by IOCCS, and the presence of silicate greatly decreased their adsorption simultaneously, while calcium ions were found to promote the adsorption of both adsorbents. XPS analysis further demonstrated that preferable Sb(V) adsorption by both hybrids was attributed to the inner sphere complexation of Sb(V) and HFO, and Ca(II) induced adsorption enhancement possibly resulted from the formation of HFO-Ca-Sb complexes. Column adsorption runs proved that Sb(V) in the synthetic water could be effectively removed from 30 μg/L to below 5 μg/L(the drinking water standard regulated by China), and the effective treatable volume of IOCCS was around 6 times as that of HFO-201, implying that HFO coatings onto calcite might be a more effective approach than immobilization inside D201.     

Characteristics of secondary inorganic aerosol and sulfate species in size-fractionated aerosol particles in Shanghai

Sulfate, nitrate and ammonium(SNA) are the dominant species in secondary inorganic aerosol, and are considered an important factor in regional haze formation. Size-fractionated aerosol particles for a whole year were collected to study the size distribution of SNA as well as their chemical species in Shanghai. SNA mainly accumulated in fine particles and the highest average ratio of SNA to particulate matter(PM) was observed to be 47% in the fine size fraction(0.49–0.95 μm). Higher sulfur oxidation ratio and nitrogen oxidation ratio values were observed in PM of fine size less than 0.95 μm. Ion balance calculations indicated that more secondary sulfate and nitrate would be generated in PM of fine size(0.49–0.95 μm). Sulfur K-edge X-ray absorption near-edge structure(XANES) spectra of typical samples were analyzed. Results revealed that sulfur mainly existed as sulfate with a proportion(atomic basis) more than 73% in all size of PM and even higher at 90% in fine particles. Sulfate mainly existed as(NH4)2SO4 and gypsum in PM of Shanghai. Compared to non-haze days, a dramatic increase of(NH4)2SO4 content was found in fine particles on haze days only, which suggested the promoting impact of(NH4)2SO4 on haze formation. According to the result of air mass backward trajectory analysis, more(NH4)2SO4 would be generated during the periods of air mass stagnation. Based on XANES, analysis of sulfate species in size-fractionated aerosol particles can be an effective way to evaluate the impact of sulfate aerosols on regional haze formation.     

油田回注水中硫酸盐还原原核生物的快速检测和群落结构分析

利用荧光原位杂交(Fluorescence in situ hybridization,FISH)技术,采用荧光标记的rRNA探针及其组合对胜利油田胜利采油厂回注水中硫酸盐还原原核生物(Sulfate reducing prokaryotes,SRPs,包括硫酸盐还原细菌和硫酸盐还原古菌)进行检测,分析了该回注水中SRPs群落结构.结果表明:SRPs在胜利油田回注水中具有极高的种群多样性,广泛分布于4个细菌门和1个古菌门;总数可达2.86×104个/mL,占回注水中总微生物细胞的20%左右;其中优势菌属为脱硫弧菌属(Desulfovibrio)和脱硫肠状菌属(Desulfotomaculum),分别占回注水微生物总细胞数的8.71%(±4.45%),和12.15%(±3.90%).Desulfobacterales和Syntrophobacterales这2个目中的SRPs,Thermodesulfobacteriales以及Thermodesulfovibro属的SRPs分别占样品微生物总量的7.59%(±2.92%),3.57%(±1.39%)和2.32%(±0.80%).除此之外,也检测到了占微生物总量4.29%(±1.75%)的Archaeoglobus属的SRPs,证明了古菌类SRPs是回注水中一个不容忽视的硫酸盐还原微生物种群.FISH法能够快速、准确地检测回注水中SRPs数量,解析SRPs群落结构.     

电化学间接氧化法处理H_2S气体的研究

采用填料塔对铁盐溶液吸收 H2 S的过程进行了初步研究 ,考察了气液比、填料层高度、吸收温度、Fe3+浓度、进气 H2 S浓度和 H+浓度等因素对 H2 S去除率的影响。结果表明 ,气液比、填料层高度和吸收温度对吸收效率的影响比较显著。通过正交试验选出最佳工艺条件 ,在此工艺条件下 H2 S的去除率接近 10 0 %。     

CHANGE IN LAKE TROPHIC STATE AND INTERNAL PHOSPHORUS RELEASE AFTER ALUMINUM SULFATE APPLICATION1

ABSTRACT: Recovery of eutrophic lakes after nutrient diversion may be delayed if the lake experiences significant internal phosphorus (p) loading to the water column. A maximum dose of aluminum sulfate, defined herein, was applied to the anaerobic sediments of the hypolimnia of two dimictic Ohio lakes following septic tank diversion, with the objective of attaining long term control of the release of phosphorus to the water column from these sediments. The results were compared to a similar, downstream, untreated lake. Total phosphorus concentration declined sharply after treatment and has remained so through 1980 for both lakes, a period of 5 and 6 years of control, respectively. Internal P loading from anaerobic, hypolimnetic sediments was partially controlled by the treatment but there are other important sources, perhaps in the littoral zone, in these lakes. Algal biomass is Smaller and water transparency has increased. Both lakes became mesotrophic after treatment, as described by the Carlson (1977) trophic state index, and remain in that improved condition to date. No deleterious side effects were observed, although one lake experienced a significant decrease in diversity of planktonic microcrustacea and a lakeward extension of the macrophyte community. This method appears to be an effective and lasting means of accelerating the recovery of a eutrophic lake following nutrient diversion.     

Management strategy for acidic deposition in Western and Northern Canada

The governments of British Columbia, Alberta, Saskatchewan, Manitoba, Northwest Territories, and Canada held joint consultations in 1980 to review the available information on acid rain from Western and Northern Canada. It was concluded that acid rain might become a problem in the future and, hence, a research, monitoring, and management strategy for acidic deposition was needed. An overview of the joint governments' management strategy, organization of research and monitoring programs, and accomplishments to date are discussed in this article.The authors are members of the Technical Committee for the Long Range Transport of Atmospheric Pollutants (LRTAP)/Acid Deposition in Western and Northern Canada, and represent Alberta and British Columbia, respectively.