玉裂废水粘度对二氧化锰臭氧催化氧化处理特性的影响

通过FT-IR和GC—MS检测分析,表明了压裂废水中有机物主要以苯环结构为主的芳香类化合物和其他杂环化合物,苯环及杂环上的主要官能团包括酮、酯、羧酸、醛、酚、氨基等。同时,压裂废水中的粘度为常规水粘度的2～3倍。针对压裂废水高粘度和高COD污染水质特征,实验研究了压裂废水二氧化锰臭氧催化氧化处理特性以及粘度对处理效果的影响,研究结果表明,在粘度较高（2．2×10-3 Pa·s）压裂废水中,投加的化学药剂很难扩散,羟基自由基·OH的利用效率较低,处理效果较差。通过投加过硫酸钾（5g／L）降粘后,可在很大程度上提高二氧化锰臭氧催化氧化的处理效果。通过对压裂废水中有机物分子量分布、FT-IR分析以及GC—MS分析可知,二氧化锰臭氧催化氧化处理压裂废水是通过激发羟基自由基,破坏水中有机物极性和有机物化学构造,将复杂长链有机物转变为简单有机物,其出水COD可达到国家污水综合排放标准中的二级排放标准。     

添加VT菌剂和有机物料腐熟齐对堆肥的影响

通过在高温好氧堆肥中分别添加VT菌剂和有机物料腐熟剂,研究接种3％o的VT菌剂和有机物料腐熟剂促进堆肥的作用效果。结果表明,接种VT菌剂的处理与空白和接种有机物料腐熟剂的处理相比,堆肥初期升温更快;高温期更长;堆肥结束时,C／N降低的多,NO3-N增加的多,NH4-N挥发的少,接种VT菌剂和VT有机物料腐熟剂都可促进有机质的充分降解,缩短堆肥时间,加快堆肥腐熟,提高堆肥肥力。     

压裂废水粘度对二氧化锰臭氧催化氧化处理特性的影响

通过FT-IR和GC-MS检测分析,表明了压裂废水中有机物主要以苯环结构为主的芳香类化合物和其他杂环化合物,苯环及杂环上的主要官能团包括酮、酯、羧酸、醛、酚、氨基等。同时,压裂废水中的粘度为常规水粘度的2~3倍。针对压裂废水高粘度和高COD污染水质特征,实验研究了压裂废水二氧化锰臭氧催化氧化处理特性以及粘度对处理效果的影响,研究结果表明,在粘度较高(2.2×10^-3Pa·s)压裂废水中,投加的化学药剂很难扩散,羟基自由基·OH的利用效率较低,处理效果较差。通过投加过硫酸钾(5 g/L)降粘后,可在很大程度上提高二氧化锰臭氧催化氧化的处理效果。通过对压裂废水中有机物分子量分布、FT-IR分析以及GC-MS分析可知,二氧化锰臭氧催化氧化处理压裂废水是通过激发羟基自由基,破坏水中有机物极性和有机物化学构造,将复杂长链有机物转变为简单有机物,其出水COD可达到国家污水综合排放标准中的二级排放标准。     

污泥淤砂分离器再分离溢流污泥

研究了污泥淤砂分离器对分离原污泥所得的溢流污泥进行再分离时,分离器的分离效果和分离分流污泥的性质。实验结果表明,污泥淤砂分离器对溢流污泥进行再分离时,分离器的除砂效率为34.5%,分离度为1.60,与分离原污泥时相比,分离器的分离性能降低;分离得到的溢流污泥MLVSS/MLSS比值为0.406,仅比进料污泥增加了2.2%,未能进一步提高溢流污泥MLVSS/MLSS比值;分离得到的底流污泥浓度MLSS为16.81 g/L,仅为原污泥浓度的1.4倍,底流污泥SVI、CST分别为45.7 mL/g和1.37 s·L/g SS,与原污泥相比仅分别减小了9.3%和2.7%,溢流污泥再分离,会降低底流污泥的浓缩效果,降低底流污泥沉降性能、脱水性能的提高幅度,不利于底流污泥的处理处置。     

排口比对污泥淤砂分离器分离效能的影响

污泥淤砂分离器是一种能够使活性污泥中污泥有机质与淤砂分离的设备。为了实现污泥淤砂分离器的结构优化,重点探讨了污泥淤砂分离器最重要的结构参数-排口比K(底流口直径Du与溢流口直径Do之比)对污泥淤砂分离器分离效能的影响。实验结果表明,在排口比从0.32增加到1.0的过程中,分离器处理能力Qi基本保持不变,分流比S、分离效率η和底流污泥ρ(MLVSS)/ρ(MLSS)分别从0.084、24.7%和0.21增加到0.338、41.1%和0.33.4;污泥有机质富集率FMLVSS和淤砂富集率FMLISS分别从1.95和1.35减小到1.22和1.12。富集除砂所需要的K和分离器获得较高的除砂效率η时所需K不一致。污泥淤砂分离器排口比K设计为0.4~0.6时,能够获得较高的分离效率,并实现淤砂的富集排放。     

Enhanced excess sludge hydrolysis and acidification in an activated sludge side-stream reactor process with single-stage sludge alkaline treatment: a pilot scale study

A pilot-scale side-stream reactor process with single-stage sludge alkaline treatment was employed to systematically investigate characteristics of excess sludge hydrolysis and acidification with alkaline treatment and evaluate feasibility of recovering a carbon source (C-source) from excess sludge to enhance nutrient removal at ambient temperature. The resulting C-source and volatile fatty acid specific yields reached 349.19 mg chemical oxygen demand (COD)/g volatile suspended solids (VSS) d⁻¹ and 121.3 mg COD/g VSS d⁻¹, respectively, the process had excellent C-source recovery potential. The propionic-to-acetic acid ratio of the recovered C-source was 3.0 times that in the influent, which beneficially enhanced biological phosphorus removal. Large populations and varieties of hydrolytic acid producing bacteria cooperated with alkaline treatment to accelerate sludge hydrolysis and acidification. Physicochemical characteristics indicated that recovered C-source was derived primarily from extracellular polymeric substances hydrolysis rather than from cells disruption during alkaline treatment. This study showed that excess sludge as carbon source was successfully recycled by alkaline treatment in the process.

     

A comparative study of metal pollution and potential eco-risk in the sediment of Chaohu Lake (China) based on total concentration and chemical speciation

Total and extractable concentrations of Cu, Pb, and Zn were determined in surface sediments of west Chaohu Lake (China) by HCl-HNO₃-HF-HClO₄ digestion and an optimized BCR sequential extraction procedure, respectively. The metal pollution was evaluated by the enrichment factor approach, and the potential eco-risk was evaluated by the sediment quality guideline (SQG) and risk assessment code (RAC) assessments. The results indicated that both total and extractable metal concentrations were highly variable and were affected by sediment properties, even though the sediments were predominantly composed of <63-μm particles (>89 %). Enrichment factors of the metals based on the total and extractable concentrations all showed higher values in the northern lake area and decreasing values towards the south. This distribution indicated an input of anthropogenic metals via the Nanfei River. Anthropogenic Cu, Pb, and Zn in surface sediments showed comparable values for each metal based on the total and extractable concentrations, suggesting that anthropogenic Cu, Pb, and Zn resided predominantly in the extractable fractions. Sediment Cu had low eco-risk, and Pb and Zn had medium eco-risk by the SQG assessment, whereas the eco-risk rankings of Cu, Pb, and Zn were medium, low, and low–high, respectively, by the RAC assessment. Referencing to the labile (dilute acid soluble) metal concentrations, we deduced that the eco-risk of Cu may be largely overestimated by the RAC assessment, and the eco-risk of Pb may be largely overestimated by the SQG assessment. Overall, sediments Cu and Pb may pose low eco-risk, and Zn may pose low–high eco-risk.     

海藻酸钠-刺槐豆胶复合凝胶珠吸附孔雀绿简

以刺槐豆胶、海藻酸钠为材料制备复合凝胶珠,利用红外光谱、热重分析对其进行表征,探讨孔雀绿浓度、吸附时间及pH对复合凝胶珠吸附孔雀绿的影响。红外光谱和热重分析表明,复合凝胶珠制备成功且热稳定性介于刺槐豆胶和海藻酸钠之间。复合凝胶珠对孔雀绿的吸附在5 h后达到平衡,pH=6为最佳吸附pH,相同条件下复合凝胶珠对孔雀绿的吸附作用优于活性炭,其对孔雀绿的吸附行为符合Freundlich吸附等温方程和颗粒内扩散模型。海藻酸钠-刺槐豆胶复合凝胶珠有望成为新的处理印染废水的吸附剂。