株洲市工业区大气中SO2转化速率的研究

在湖南省株洲市工业区的下风向布点,同时测定大气中ＳＯ２的浓度、ＴＳＰ和＜０．２５μｍ细粒子中ＳＯ２－４的浓度．结果表明,大气中ＳＯ２浓度随着离污染源距离的增加迅速下降,和ＳＯ２相比,颗粒物中ＳＯ２－４浓度随距离的增加而降低的程度要慢得多．同步测定的ＳＯ２浓度和细粒子ＳＯ２－４浓度有显著的相关关系．根据风向、风速和新产生的细粒子中的ＳＯ２－４浓度及大气中ＳＯ２的浓度计算了株洲教育学院处ＳＯ２的转化速率,春季湿度大,ＳＯ２转化速率也大,为４．８％／ｈ,秋季湿度小,ＳＯ２的转化速率变低,为１．５％／ｈ．春季中路铺ＳＯ２转化速率为３．１％／ｈ．     

反硝化型甲烷厌氧氧化(DAMO)系统pH值耦合模型研究

对3个具有不同优势菌种反应器中厌氧氧化(DAMO)过程与pH值进行动力学耦合,结果表明,在25℃,Anammox-DAMO混培系统最大脱氮速率、硝酸盐初始抑制浓度和铵盐初始抑制浓度分别为3.95mg/(L·d),182.63,196.40mg/L;Nitrate-DAMO系统最大脱氮速率、硝酸盐初始抑制浓度分别为4.3...     

牛仔布浆染污水处理工程实践

通过实例阐述了采用混凝气浮 厌氧 接触氧化工艺处理牛仔布浆染污水的工艺流程、工艺论述、技术参数及在运行中遇到的问题 ,并得出了采用该工艺处理牛仔布浆染污水可取得良好的效果     

色拉油废水处理工程设计

色拉油废水COD、动植物油、氨、氮、磷浓度都很高。采用预处理除油 倒A2 O 接触氧化 化学除磷组合工艺处理 ,效果明显 ,出水各项指标 (特别是磷酸盐 )均能达《污水综合排放标准》(GB8978 1 996 )中的一级排放标准     

SiO2掺杂对Ru-TiO2催化剂的结构及其对丁二酸湿式氧化活性的影响

在TiO2粉末中掺杂SiO2,制备0—20%的SiO2TiO2载体.利用浸渍法在载体上负载Ru,制备Ru/SiO2TiO2催化剂.结果表明,催化剂的晶相以锐钛矿为主,晶粒尺寸为30—50nm.掺杂的SiO2主要为无定型,以5—15nm分散于催化剂中,比表面积随SiO2掺杂量的增加显著增大,但对TiO2的晶体结构无明显影响,也未形成Si—O—Ti键.Ru因粒径细化及含量过低未产生衍射峰.在300ml间歇式反应釜中,反应温度210—270℃,初始氧分压085MPa条件下,对丁二酸(74g·l-1,COD=7000mg·l-1)的催化湿式氧化结果表明,SiO2掺杂量对COD的去除率有显著影响,掺杂10%SiO2的催化剂对COD的去除率最高.在连续十次运行中,COD的去除率保持在85%左右,活性未见降低.     

新型生物脱氮技术的工艺研究

以上流式厌氧污泥床反应器（ Ｕ Ａ Ｓ Ｂ） 作为厌氧氨氧化（ａｎａｍ ｍｏｘ） 反应器,用无机盐培养液完成了反应器的启动,并稳态运行ａｎａｍ ｍｏｘ 反应器．采用生物膜反应器作为生物硝化反应器,以无机盐培养液完成反应器的启动．将硝化反应器和ａｎａｍｍｏｘ 反应器组合在一起构成新型生物脱氮系统,以硝化反应器的出水作为ａｎａｍｍｏｘ反应器的进水,同时补充相应数量的 Ｎ Ｈ４ ＋ Ｎ．整个系统的总氮容积去除率可达１ ５７７ ｍｇ Ｌ－ １ ｄ － １ ．该新型生物脱氮系统能同时去除 Ｎ Ｈ４ ＋ Ｎ 和 Ｎ Ｏ Ｘ－ Ｎ,并且对高浓度的 Ｎ Ｈ４ ＋ Ｎ 去除具有较大的潜力．     

Oxidative treatment of simulated dyehouse effluent by uv and near-UV light assisted Fenton's reagent

UV/Fenton, near-UV-visible/Fenton, dark Fenton, and H₂O₂/UV reactions have been used to treat simulated dyehouse effluents representing wastewater from the textile dyeing and rinsing process. Experiments were carried out in a lab - scale photochemical reactor using concentrations of 0.5–25 mM H₂O₂, 0.04-0.5 mM Fe²⁺-ion and different dilutions of textile wastewater. To assess the extent of mineralization, decolourization kinetics and the effect of different fight sources on treatment efficiency, DOC, optical density at 254 nm and 600 nm wavelength and residual H₂O₂ concentrations were measured during the course of the advanced oxidation reactions. Comparative evaluation of the obtained results revealed that the decolourization rate increased with applied H₂O₂ and Fe²⁺-ion dose as well as the strength of the synthetic textile wastewater. The best results were obtained by the near - UV/visible/Fenton process with a decolourization rate constant of 1.57 min⁻¹, a UV_254nm reduction of 97% and a DOC removal of 41% at relatively low doses of the H₂O₂ oxidant and Fe²⁺-ion catalyst within 60 min treatment time.     

电化学法处理含盐染料废水

研究了电化学法处理含盐染料废水的可行性及其处理效果．结果表明,电化学法对废水的色度和COD具有良好的去除效果,电解过程中余氯的产生对色度和COD的去除有决定性作用．实验确定的高浓度含盐废水电化学处理条件为：电流密度0．017A/cm²,电压10．3V,平均电导率12．35ms/cm,电解60min,色度和COD的去除率分别为85％和99．8％．电解过程无难以继续反应的中间产物生成．     

聚醚废水处理工艺研究

研究了中和混凝-厌氧十好氧-生物活性炭组合工艺,在不同工况和运行参数条件下处理聚醚废水的效果．结果表明,中和混凝能有效地降低生物处理的污泥负荷,调节pH值6．7,聚合氯化铝的投加量为l00mg/L时．聚醚废水COD去除率可达28％,当进水的COD为3000～4000mg/L时,聚醚废水经此组合工艺处理后,COD的总去除率达96％以上,出水COD值约150mg/L.     

Metabolic transformations of acquired lucibufagins by firefly “femmes fatales”

Summary. Female Photuris fireflies sequester defensive steroidal pyrones (lucibufagins) from male fireflies of the genus Photinus. Lucibufagin analyses of Photuris females and Photinus ignitus males show that the lucibufagin mixtures of predator and prey differ in their composition. Analyses of whole body extracts showed that P. ignitus males contain a mixture of eight non-glycosylated lucibufagins, composed mostly of compounds with two oxygenated positions in the steroidal A-ring (C-3, C-5). After feeding on P. ignitus males, Photuris females contain six major lucibufagins. Three of these compounds are not present in the prey, including the novel lucibufagin glycoside 5β,11α-dihydroxy-12-oxo-3β-O-β-D-xylopyranosylbufalin, and two other lucibufagins with a trioxygenated A-ring (C-2, C-3, C-5). These results indicate that Photuris females transform the sequestered lucibufagins both by glycosylation and oxidation, which could affect the systemic transportability of these compounds due to an increase in their polarity. Received 18 February 1999; accepted 19 April 1999.