聚合氯化铝铁(PAFC)絮凝剂污水除磷的研究

用聚合氯化铝铁(PAFC)絮凝剂对城镇生活污水除磷处理效果进行研究,研究内容包括:PAFC用量对模拟污水和实际生活污水除磷效果的影响,污水经PAFC处理后pH值的变化情况,污水酸度对除磷效果的影响,PAFC用量对模拟污水和实际生活污水除浊效果的影响.结果表明:铝铁复合絮凝剂有良好的除磷效果,除磷处理后磷含量可低于0.5mg·l-1,能达到生活污水国家一级排放标准;污水处理后pH值较稳定;除浊效果好,除浊率可达到95%以上.     

硬木地板材料和棉花秆的变氧浓度热解燃烧表观动力学的实验研究

本文采用TG-FTIR分析方法深入研究了火场中硬木地板材料和棉花秆变氧浓度燃烧过程,深入分析了氧浓度对纤维物质燃烧表观热失重影响;通过大量的动力学参数计算得出了可燃物的表观活化能与实际氧浓度成线性关系;分析了氧浓度对木材燃烧气体产物的影响,并探索了氧浓度影响热解和燃烧的机理。     

生物除磷过程厌氧释磷的代谢机理及其动力学分析

运用充分曝气后的好氧末端活性污泥进行了厌氧释磷实验.结果表明,在厌氧释磷过程中VSS呈现出上升的趋势,而MLSS及灰分均呈现出下降的趋势.当微生物体内的糖原耗尽时,会引起厌氧吸收HAc及释磷过程的中断.得出ΔρPΔρPHB、ΔρGLYΔρPHB、ΔρPΔCOD、ΔρPHBΔCOD各比值的平均值分别为0.48、0.50、0.44、0.92.通过对厌氧吸收HAc及释磷动力学过程进行模拟,得到QHAc,max为164mg·g-1·h-1,QP,max为69.9mg·g-1·h-1,KGYL为0.005,KCOD为3mg·L-1.ΔρPΔCOD与溶液中pH呈明显的线性关系,且得到了二者之间的线性方程.     

多种进水碳源条件下侧流活性污泥工艺的脱氮除磷机制

为提高污水氮磷营养盐的去除能力和稳定性,侧流活性污泥工艺开始被应用于世界多地的污水处理项目.污水有机碳的水解代谢行为影响侧流工艺的营养盐去除机制,但目前的研究多侧重简单碳源物质.本文采用多种碳源种类(简单碳源乙酸钠,大分子碳源葡萄糖、淀粉、蛋白胨、豆油及其组合)模拟实际污水有机碳组成,以探索更复杂碳源在侧流工艺(主流一...     

嘉兴市不同天气条件下大气污染物和气溶胶化学组分的分布特征

为研究不同天气条件下大气污染物(PM_(2.5)、PM_(1.0)、SO_2、NO_2、O_3和CO)和气溶胶化学组分的污染特征,分别使用SHARP-5030监测仪、热电EMS系统、气溶胶化学成分在线监测仪(ACSM)和宽范围颗粒粒径谱仪(WPS)对嘉兴市2015年5月1~31日PM、污染气体、PM_(1.0)中化学组分和10 nm~10μm气溶胶数浓度进行了观测分析.结果表明,观测期间嘉兴市PM_(2.5)、PM_(1.0)、SO_2、NO_2、O_3和CO的平均浓度分别为52.8和37.2μg·m~(-3)、10.3μg·m~(-3)、38.1μg·m~(-3)、92.1μg·m~(-3)和1.2 mg·m~(-3).PM_(1.0)中OA、SO_2-4、NO-3、NH_4~+和Cl-的平均浓度为2.18、1.24、0.87、0.63和0.08μg·m~(-3).数浓度主要集中在爱根核模态(20~100 nm),浓度为12 411.2 cm~(-3),其次是核模态(10~20 nm),浓度为4 946.6 cm~(-3).不同天气过程中PM和污染气体的浓度分布和日变化特征不同.不同天气条件下PM_(1.0)中化学组分分布不同.雨天和晴天PM_(1.0)中化学组分浓度从大到小顺序均为OASO_2-4NO-3NH_4~+Cl-,新粒子天PM_(1.0)中化学组分浓度的顺序为OANO-3SO_2-4NH_4~+Cl-.新粒子天OA和NO-3分别是晴天的1.61和1.42倍,说明OA和NO-3是影响新粒子生成事件的主要化学成分.不同天气条件下不同模态气溶胶的日变化特征不同.     

Denitrification and phosphorus uptake by DPAOs using nitrite as an electron acceptor by step-feed strategies

Denitrifying phosphorus accumulating organisms (DPAOs) using nitrite as an electron acceptor can reduce more energy. However, nitrite has been reported to have an inhibition on denitrifying phosphorus removal. In this study, the step-feed strategy was proposed to achieve low nitrite concentration, which can avoid or relieve nitrite inhibition. The results showed that denitrification rate, phosphorus uptake rate and the ratio of the phosphorus uptaken to nitrite denitrified (anoxic P/N ratio) increased when the nitrite concentration was 15 mg·L^-1 after step-feeding nitrite. The maximum denitrification rate and phosphorus uptake rate was 12.73 mg NO2-–N·g MLSS-1?h-1 and 18.75 mg PO43-–P·g MLSS-1?h-1, respectively. These rates were higher than that using nitrate (15 mg·L^-1) as an electron acceptor. The maximum anoxic P/N ratio was 1.55 mg PO43--P?mg NO2--N-1. When the nitrite concentration increased from 15 to 20 mg NO2--N?L-1 after addition of nitrite, the anoxic phosphorus uptake was inhibited by 64.85%, and the denitrification by DPAOs was inhibited by 61.25%. Denitrification rate by DPAOs decreased gradually when nitrite (about 20 mg·L^-1) was added in the step-feed SBR. These results indicated that the step-feed strategy can be used to achieve denitrifying phosphorus removal using nitrite as an electron acceptor, and nitrite concentration should be maintained at low level (<15 mg·L^-1 in this study).     

四氮唑废水处理工艺设计

高浓度、高盐分的四氮唑生产废水通过三效蒸发浓缩,馏出液经铁炭氧微电解和混凝预处理,再采用水解酸化一接触氧化一反应二沉主体组合工艺进行处理。研究了该工艺所需构筑物和设备的设计与选型。该工艺在正常运行条件下,处理后出水pH6～9,COD 302mg／L,BOD5 108mg／L,SS30mg／L,色度36倍,水质达到GB8978--1996（污水综合排放标准》三级标准。     

Streambank Soil and Phosphorus Losses Under Different Riparian Land‐Uses in Iowa1

Abstract: Phosphorus and sediment are major nonpoint source pollutants that degrade water quality. Streambank erosion can contribute a significant percentage of the phosphorus and sediment load in streams. Riparian land‐uses can heavily influence streambank erosion. The objective of this study was to compare streambank erosion along reaches of row‐cropped fields, continuous, rotational and intensive rotational grazed pastures, pastures where cattle were fenced out of the stream, grass filters and riparian forest buffers, in three physiographic regions of Iowa. Streambank erosion was measured by surveying the extent of severely eroding banks within each riparian land‐use reach and randomly establishing pin plots on subsets of those eroding banks. Based on these measurements, streambank erosion rate, erosion activity, maximum pin plot erosion rate, percentage of streambank length with severely eroding banks, and soil and phosphorus losses per unit length of stream reach were compared among the riparian land‐uses. Riparian forest buffers had the lowest streambank erosion rate (15‐46 mm/year) and contributed the least soil (5‐18 tonne/km/year) and phosphorus (2‐6 kg/km/year) to stream channels. Riparian forest buffers were followed by grass filters (erosion rates 41‐106 mm/year, soil losses 22‐47 tonne/km/year, phosphorus losses 9‐14 kg/km/year) and pastures where cattle were fenced out of the stream (erosion rates 22‐58 mm/year, soil losses 6‐61 tonne/km/year, phosphorus losses 3‐34 kg/km/year). The streambank erosion rates for the continuous, rotational, and intensive rotational pastures were 101‐171, 104‐122, and 94‐170 mm/year, respectively. The soil losses for the continuous, rotational, and intensive rotational pastures were 197‐264, 94‐266, and 124‐153 tonne/km/year, respectively, while the phosphorus losses were 71‐123, 37‐122, and 66 kg/km/year, respectively. The only significant differences for these pasture practices were found among the percentage of severely eroding bank lengths with intensive rotational grazed pastures having the least compared to the continuous and rotational grazed pastures. Row‐cropped fields had the highest streambank erosion rates (239 mm/year) and soil losses (304 tonne/km/year) and very high phosphorus losses (108 kg/km/year).     

Estrogen equivalent concentration of 13 branched para-nonylphenols in three technical mixtures by isomer-specific determination using their synthetic standards in SIM mode with GC-MS and two new diasteromeric isomers

Thirteen isomers of branched para-nonylphenols (para-NP) in three technical mixtures were isomer-specifically determined using their synthesized standards by SIM of structurally specific ions, m/z 135, 149 or 163 with GC–MS. Of the 13 isomers, four isomers, 4-(2,4-dimethylheptan-4-yl)phenol, 4-(4-methyloctan-4-yl)phenol, 4-(3-ethyl-2-methylhexan-2-yl)phenol (3E22NP) and 4-(2,3-dimethylheptan-2-yl)phenol synthesized for their determinations were first used as standard substances. The 13 isomers in the technical mixtures individually occurred at mass percent portion of more than 2%. The total mass percent portions in the mixtures from Tokyo Chemical Industry (TCI), Aldrich, and Fluka covered with 89 ± 2%, 75 ± 4% and 77 ± 2%, respectively. The abundance of 4-(3,6-dimethylheptan-3-yl)phenol in the three mixtures was the largest with 11.1 ± 2% to 9.9 ± 0.3%, while that of 4-(2-methyloctan-2-yl)phenol was the smallest with 2.9 ± 0.3% to 3.0 ± 0.2%. Additionally, structures of four new isomers of more than 1% portion present in a technical mixture were elucidated as two pairs of diastereomeric isomers: two types of 4-(3,4-dimethylheptan-4-yl)phenol (344NP) and those of 4-(3,4-dimethylheptan-3-yl)phenol (343NP). By estrogenic assay of 13 isomers with yeast estrogen screen system, the activity of 3E22NP was the highest, while that of 4-(3-methyloctan-3-yl)phenol was the least. Their relative activities to that of 3E22NP were individually calculated. Estrogenic equivalent concentrations of the three technical mixtures were predictively evaluated. The ratio of the EEC to the conventional concentration, total mass percent portions of the 13 isomers in technical mixtures were 0.208 for TCI, 0.206 for Aldrich and 0.205 for Fluka. The predicted estrogenic activity of measured concentration of para-NP in technical mixtures was approximately 5-fold greater than the measured estrogen agonist activity.     

Prediction of Pb speciation in concentrated and dilute nutrient solutions

Despite the presence of numerous studies in the literature examining the phytotoxicity of Pb, there is a lack of precise quantitative data on limiting concentrations of Pb for plant growth. Using the PhreeqcI chemical equilibrium model, simulations were conducted to examine the speciation of Pb in concentrated and dilute nutrient solutions. Due to the higher P concentration of Hoagland's solution (1000microM), precipitation of chloropyromorphite (Pb5(PO4)3Cl) was predicted to occur at lower pH values, and at lower Pb concentrations, than for a dilute nutrient solution (2microM P). Although nutrient solutions prepared in the glasshouse were supersaturated (and Pb concentrations were substantially higher than predicted by modeling), they confirmed the importance of the P concentration in influencing the precipitation of Pb. Given the low solubility of Pb-phosphates, nutrient solutions with low P concentrations should be utilized, and plant growth should be related to measured Pb concentrations rather than to the quantity of Pb initially added.