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排序方式: 共有253条查询结果,搜索用时 15 毫秒
21.
Haiting Zhang Huiyu Dong Craig Adams Zhimin Qiang Gang Luan Lei Wang 《环境科学学报(英文版)》2015,27(7):116-124
The chemistry associated with the disinfection of aquarium seawater is more complicated than that of freshwater, therefore limited information is available on the formation and speciation of disinfection byproducts(DBPs) in marine aquaria. In this study, the effects of organic precursors, bromide(Br-) and pre-ozonation on the formation and speciation of several typical classes of DBPs, including trihalomethanes(THM4), haloacetic acids(HAAs),iodinated trihalomethanes(I-THMs), and haloacetamides(HAc Ams), were investigated during the chlorination/chloramination of aquarium seawater. Results indicate that with an increase in dissolved organic carbon concentration from 4.5 to 9.4 mg/L, the concentrations of THM4 and HAAs increased by 3.2–7.8 times under chlorination and by 1.1–2.3 times under chloramination. An increase in Br-concentration from 3 to 68 mg/L generally enhanced the formation of THM4, I-THMs and HAc Ams and increased the bromine substitution factors of all studied DBPs as well, whereas it impacted insignificantly on the yield of HAAs. Pre-ozonation with 1 mg/L O3 dose substantially reduced the formation of all studied DBPs in the subsequent chlorination and I-THMs in the subsequent chloramination. Because chloramination produces much lower amounts of DBPs than chlorination, it tends to be more suitable for disinfection of aquarium seawater. 相似文献
22.
The hydrolysis/precipitation behaviors of Al3+, Al13 and Al30 under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl3, PACAl13 and PACAl30 were 6.5–7.5, 8.5–9.5, and 7.5–9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl3 ? PACAl30 > PACAl13. The precipitates' size increased when the dosage increased from 50 μM to 200 μM, but it decreased when the dosage increased to 800 μM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The iso-electric points of the freshly formed precipitates for AlCl3, PACAl13 and PACAl30 were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl3 hydrolysis precipitates were lower than those of PACAl13 and PACAl30 when pH > 5.0. The Zeta potential of PACAl30 hydrolysis precipitates was higher than that of PACAl13 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al–Ferron research indicated that the hydrolysis precipitates of AlCl3 were composed of amorphous Al(OH)3 precipitates, but those of PACAl13 and PACAl30 were composed of aggregates of Al13 and Al30, respectively. Al3+ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al13 and Al30 species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al–Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al–Ferron method. The chemical composition of Ala, Alb and Alc depended on coagulant and solution pH. The Alb measured in the current case was different from Keggin Al13, and the high Alb content in the AlCl3 hydrolysis precipitates could not used as testimony that most of the Al3+ was converted to highly charged Al13 species during AlCl3 coagulation. 相似文献
23.
Biological sulfate removal from acrylic fiber manufacturing wastewater using a two-stage UASB reactor 总被引:2,自引:0,他引:2
A two-stage UASB reactor was employed to remove sulfate from acrylic fiber manufacturing wastewater. Mesophilic operation (35±0.5℃) was performed with hydraulic retention time (HRT) varied between 28 and 40 hr. Mixed liquor suspended solids (MLSS) in the reactor was maintained about 8000 mg/L. The results indicated that sulfate removal was enhanced with increasing the ratio of COD/SO42-. At low COD/SO42-, the growth of the sulfate-reducing bacteria (SRB) was carbon-limited. The optimal sulfate removal efficiencies were 75% when the HRT was no less than 38 hr. Sulfidogenesis mainly happened in the sulfate-reducing stage, while methanogenesis in the methane-producing stage. Microbes in sulfate-reducing stage performed granulation better than that in methane-producing stage. Higher extracellular polymeric substances (EPS) content in sulfate-reducing stage helped to adhere and connect the flocculent sludge particles together. SRB accounted for about 31% both in sulfate-reducing stage and methane-producing stage at COD/SO42- ratio of 0.5, while it dropped dramatically from 34% in sulfate-reducing stage to 10% in methane-producing stage corresponding to the COD/SO42- ratio of 4.7. SRB and MPA were predominant in sulfate-reducing stage and methane-producing stage respectively. 相似文献
24.
Study of metabolites from the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacterial consortium enriched from mangrove sediments 总被引:3,自引:0,他引:3
The PAH metabolites produced during degradation of fluorene, phenanthrene and pyrene by a bacterial consortium enriched from mangrove sediments were analyzed using the on-fiber silylation solid-phase microextraction (SPME) combining with gas chromatography–mass spectrometry (GC–MS) method. Seventeen metabolites at trace levels were identified in different PAH degradation cultures based on the full scan mass spectra. In fluorene degradation cultures, 1-, 2-, 3- and 9-hydroxyfluorene, fluorenone, and phthalic acid were detected. In phenanthrene and pyrene degradation cultures, various common metabolites such as phenanthrene and pyrene dihydrodiols, mono-hydroxy phenanthrene, dihydroxy pyrene, lactone and 4-hydroxyphenanthrene, methyl ester, and phthalic acid were found. The detection of various common and novel metabolites demonstrates that SPME combining with GC–MS is a quick and convenient method for identification as well as monitoring the real time changes of metabolite concentrations throughout the degradation processes. The knowledge of PAH metabolic pathways and kinetics within indigenous bacterial consortium enriched from mangrove sediments contributes to enhance the bioremediation efficiency of PAH in real environment. 相似文献
25.
聚硅硫酸铁(PFSS)的混凝性能及其应用 总被引:12,自引:1,他引:12
本文研究了聚硅硫酸铁的混凝性能和稳定性,试验了它对煤矿洗煤水,矿井水,以及城市废水的混凝处理效果,结果发现,随Fe/Si摩尔比的增大,聚硅硫酸铁的混凝效果明显提高;与聚硅酸相比,聚硅硫酸具有较好的稳定性和较强的除浊脱色性能。 相似文献
26.
微絮凝 -直接过滤工艺是一种将混凝反应、沉淀截留集中在同一滤柱内同步完成的高效水处理工艺。该工艺应用于城市污水的深度处理中 ,通过絮凝剂的加入 ,具有同步去除PO3 -4 P、SS和部分COD的功能。本文研究了该工艺对二级处理出水中PO3 -4 P、SS和COD的去除效果及其规律。研究表明 :采用聚合氯化铁 (PFC)作为絮凝剂 ,当Fe/P摩尔比为 2∶1时 ,水中PO3 -4 P的去除率达 98.8% ,浓度可降至 0 .1mg/L以下 ,同时SS、COD去除率也有明显提高。与传统的混凝、沉淀除磷工艺相比 ,该工艺具有操作简单、结构紧凑、占地面积小、污泥量少等优点 ,是一种更为经济和简单的处理单元 ,适用于现有城市污水处理厂的除磷和进一步提高水质的深度处理 相似文献
27.
深床过滤机理及其在水处理中的应用研究与进展 总被引:2,自引:0,他引:2
深床过滤既有过滤功能,又具生物处理作用,具有良好的应用前景;本文阐述了深床过滤的最新研究动向,深床过滤过程的数学模型的构建方法,国内外利用深床过滤技术处理微污染水源水、城市生活污水及污水深度处理的实验研究状况. 相似文献
28.
针对零星居民点的污水处理,开发了射流曝气周期活性污泥法工艺.它是一种连续进水、周期性间歇曝气的改良型SBR工艺,也是一种时间程序和空间程序相结合的污水处理工艺,具有良好的脱氮除磷效果.试验表明,在水力负荷4 m3/d,曝气周期为每2 h曝气15 min、静置105 min的条件下,出水COD为48.8~53.5 mg/L,去除率达79.4%~80.5%;出水TN为2.81~3.98 mg/L,去除率达82.4%~89.4%;出水NH3-N为0.36~0.78 mg/L,去除率高达96.4%~98.4%;出水TP为0.63~1.18 mg/L,去除率为67.2%~78.9%,均可达到《城镇污水处理厂污染物排放标准》(GB 18918-2002)中的一级B排放标准. 相似文献
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