臭氧对活性污泥特性影响研究

探讨了臭氧对于污水生物处理中活性污泥特性的影响。结果显示，随着臭氧化的进行，促进了活性污泥生物量的减少，并有一定量的生物污泥被无机化，并且污泥的活性和存活性降低了。其中臭氧投加量低于0．1gO3／g SS时污泥活性即大幅下降，而后污泥浓度才随着臭氧量的增加而显著降低。     

超声、臭氧处理石化污水厂剩余活性污泥研究

采用超声波和臭氧处理石化污水处理厂的剩余活性污泥，促进其脱水和破解。实验结果表明，小功率超声对污泥脱水效果较好，最佳超声条件为：输出电压70 V，超声时间2 min；污泥抽滤后的含水率在试验范围内随臭氧量的增加而降低，最佳臭氧剂量为0.05 g O³/g SS。经超声处理过的臭氧化污泥要比没经超声处理过的含水率低约1%。在传统的絮凝方法下，加上超声和臭氧可以使污泥含水率再降低2%以上，减少絮凝剂用量近40%；臭氧和超声联合比单独臭氧对污泥破解效果更显著，污泥可减量约25%。臭氧投量较少时，超声破解效果更明显。     

畜禽养殖废水生物处理剩余污泥臭氧减量过程中的重金属释放

采用臭氧氧化污泥减量法对畜禽养殖废水SBR中的剩余污泥进行处理。当臭氧反应时间控制在30min时，污泥的溶解比例在30％左右（以MLSS计）。上清液中一定量的SCOD溶出可为生物处理单元提供充足的碳源，同时在上清液中，TN、TP及水相重金属浓度增加有限，臭氧氧化后的污泥液回流污水处理系统后造成的N、P处理负荷较小，重金属对污泥微生物的活性抑制风险较低。若继续延长臭氧的反应时间，上清液SCOD、TN、TP以及重金属cu、Pb的释放速率明显增加，同时上清液的C／N降低，臭氧化后的污泥液回流反而不利于生物单元的脱氮处理。综合考虑TN、TP及水相重金属浓度增加的危害性，臭氧反应时间应控制在30min，臭氧实际投加量应为123．1mg O3／gSS。     

污泥臭氧氧化处理过程中活菌抗药基因丰度的消减

臭氧氧化技术是一种广泛应用的污泥减量技术,然而臭氧处理能否对污泥中的抗生素抗药基因进行有效消减还不清楚。采用单叠氮溴化丙锭(propidium monoazide,PMA)预处理结合定量PCR(qPCR)方法对污泥臭氧减量过程中不同臭氧消耗量下活性污泥活菌中的四环素、氨基糖苷和大环内酯3大类共21种抗药基因的变化进行了研究。结果表明:臭氧氧化可以有效消减活性污泥活菌中21种抗药基因的绝对丰度(每毫升污泥的抗药基因拷贝数),在臭氧消耗量0.31 g·g~(-1)(TSS)情况下抗药基因总量降低了75.44%;尽管绝对丰度下降,污泥臭氧氧化处理过程中大量抗药基因的相对丰度(抗药基因拷贝数与细菌16S rRNA基因拷贝数的比例)逐渐增加,表明臭氧处理后污泥中耐药菌占总活菌比例可能增加,具有一定的抗性传播风险;Ⅰ型整合子是抗药基因水平转移的重要遗传元件,其绝对丰度同样随着臭氧消耗量增加而降低,而相对丰度逐渐上升。     

畜禽养殖废水生物处理剩余污泥臭氧减量过程中的重金属释放简

采用臭氧氧化污泥减量法对畜禽养殖废水SBR中的剩余污泥进行处理。当臭氧反应时间控制在30 min时，污泥的溶解比例在30%左右（以 MLSS计）。上清液中一定量的SCOD溶出可为生物处理单元提供充足的碳源，同时在上清液中，TN、TP及水相重金属浓度增加有限，臭氧氧化后的污泥液回流污水处理系统后造成的N、P处理负荷较小，重金属对污泥微生物的活性抑制风险较低。若继续延长臭氧的反应时间，上清液SCOD、TN、TP以及重金属Cu、Pb的释放速率明显增加，同时上清液的C/N降低，臭氧化后的污泥液回流反而不利于生物单元的脱氮处理。综合考虑TN、TP及水相重金属浓度增加的危害性，臭氧反应时间应控制在30 min，臭氧实际投加量应为123.1 mg O₃/g SS。     

臭氧氧化污泥的试验研究

采用接触反应柱对污泥臭氧氧化过程中污泥性质的变化进行了研究。结果表明,在相同臭氧投量下,低浓度臭氧分解污泥的效率较高;在臭氧投量为0．1gO3／gss、臭氧浓度为16．8mg／L时,臭氧化使污泥溶液中的溶解性TOC从114．9mg／L增加到803．7mg／L;臭氧氧化后溶解性IC(无机碳)从2．63mg／L减少到1．02mg／L;臭氧氧化显著提高了污泥沉淀性能,氧化后污泥的SV和SVI相当于氧化前28．9％和58％。臭氧氧化使污泥的pH从初始的7．13降低到投量增加到0．44gO3／gss时的4．40。污泥臭氧化的最佳投量点为0．1gO3／gSS。     

臭氧在污泥减量技术中的应用

大量的剩余污泥已成为国内外污水处理行业亟待解决的问题,因此各种物理、化学和生物方法被应用到污泥处理中,臭氧以其独特的性质从一开始应用就备受青睐.详细地说明了臭氧在污泥减量技术中应用的背景及原理,重点介绍了臭氧对污泥性质的影响,并分别从臭氧氧化技术与传统活性污泥法组合、与AO工艺组合、与膜生物反应器(MBR)组合、与磷回收工艺组合、与SBR工艺组合等角度分析了臭氧在污泥减量技术中的应用与现状、目前存在的问题及未来的发展方向.     

壳聚糖强化生物作用的机理研究

将不同分子量的壳聚糖投加于 SBR生物反应器处理生活废水 ,通过比较处理效率、污泥活性、污泥结构等指标来探明壳聚糖强化活性污泥生物作用的机理。研究表明 ,壳聚糖虽对污泥活性有一定抑制作用 ,但能很好地改善污泥的絮体结构 ,从而提高活性污泥的处理效率 ,其中分子量越大的壳聚糖强化生物处理的效果越佳。     

耐盐活性污泥驯化及其动力学实验研究

为探讨直接生物法处理环氧氯丙烷废水的可行性,对其活性污泥驯化过程和生物降解性能进行了研究。结果表明,经过长时间的驯化,活性污泥能够适应高盐度环境。污泥驯化过程中,污泥浓度保持稳定,含盐量从0.3%增加到3%,微生物的活性和耗氧速率随之降低,COD的去除率由96%下降至75%左右。同时,对环氧氯丙烷废水的生物降解动力学进...     

脉冲弧光放电等离子体水解活性污泥

活性污泥水解对提高污泥的稳定性、缩短厌氧消化时间和增大甲烷产率具有重要意义。研究了脉冲弧光放电等离子体(PADP)水解活性污泥方法,考察水解效果、影响因素和水解后的污泥性状。结果表明:随着峰值电压、频率和电导率的增加,污泥上清液营养物质含量呈增长趋势,溶胞率(R)升高;随着放电时间的增加,R增加,氨氮物质(NH_4~+-N)先增加后降低,可证明NH_4~+-N降解率逐渐上升且最终高于其释放率;污泥在14kV、25 Hz、1600μS·cm~(-1)条件下放电150min,R增加到51.3%,NH_4~+-N、蛋白质和多糖等有机物大量释放;经过PADP处理,污泥沉降性降低,絮凝体结构改变,含固量和颗粒尺寸降低,污泥生物大量死亡,水解污泥生物由光滑、完整的表面结构变得粗糙、破裂,细胞壁(膜)受损明显,污泥发生水解。     

原位臭氧氧化污泥减量工艺的运行效能

采用ASBR/SBR原位臭氧污泥减量工艺,重点研究了原位臭氧氧化对SBR段污泥产率和出水水质的影响。两个相同的ASBR/SBR组合工艺同时运行,每隔3个周期向臭氧投加组SBR的曝气阶段原位间歇投加臭氧,臭氧投加量为0.027 g O3/g MLSS,连续运行40 d;对照组不投加臭氧作为对比。结果表明,原位臭氧氧化实现污泥减量约43.9%,臭氧投加组SBR段平均污泥产率系数为0.1447 g SS/g SCOD,而对照组为0.2580 g SS/g SCOD,投加组没有惰性污泥的累积,并且污泥沉淀性能得到改善。原位臭氧氧化对出水水质影响不大,投加组与对照组相比,臭氧投加3周期后的出水COD、NH4+-N、TN和TP平均值分别为47.8、0.76、14.1和6.4 mg/L,去除率分别下降了4%、2%、3%和7.7%,其中COD、NH4+-N和TN均能达到《城镇污水处理厂污染物排放标准》(GB18918-2002)一级A标准。     

原位臭氧氧化对活性污泥系统硝化和反硝化作用的影响研究

将厌氧序批式间歇反应器(ASBR)和序批式间歇反应器(SBR)串联组成污泥减量新工艺,着重探讨了对SBR段进行原位臭氧投加时,臭氧氧化作用对系统硝化和反硝化能力的影响,并以不投加作为对照。结果表明,将臭氧原位投加到ASBR—SBR组合工艺的SBR段,臭氧投加量为0.027g(以每克MLSS计),每隔3个周期再次投加、连续运行40d,试验组SBR段臭氧投加当期出水COD去除率为86%,比对照组下降了9百分点,但臭氧氧化细胞内大量有机物进入混合液中,为反硝化作用提供了外加碳源,对污泥反硝化能力的提高起到了一定的促进作用;试验组部分硝化细菌由于臭氧的强氧化作用而失去活性,但是随着剩余污泥量的减少,系统的污泥龄延长,有利于硝化细菌的生长,使得系统的硝化能力基本未受影响;试验组臭氧投加当期SBR段出水NO2--N平均浓度比对照组的高18.9%,但经过3个周期的运行后,其SBR段出水NO2--N平均质量浓度降低至7.57mg/L,基本与对照组持平;试验组臭氧投加当期SBR段出水NO3--N的平均浓度高于对照组,但经过3个周期的运行后,试验组出水NO3--N平均浓度低于对照组;试验组臭氧投加当期SBR段出水TN和对照组的出水TN平均去除率分别为65%和75%,但试验组再经过3个周期的运行后,出水TN平均去除率可以达到72%。可见,原位投加臭氧并未对SBR段的硝化和反硝化能力产生明显的影响。     

Enhanced sludge solubilization by microbubble ozonation

A microbubble ozonation process for enhancing sludge solubilization was proposed and its performance was evaluated in comparison to a conventional ozone bubble contactor. Microbubbles are defined as bubbles with diameters less than several tens of micrometers. Previous studies have demonstrated that microbubbles could accelerate the formation of hydroxyl radicals and hence improve the ozonation of dyestuff wastewater. The results of this study showed that microbubble ozonation was effective in increasing ozone utilization and improving sludge solubilization. For a contact time of 80 min, an ozone utilization efficiency of more than 99% was obtained using the microbubble system, while it gradually decreased from 94% to 72% for the bubble contactor. The rate of microbial inactivation was obviously faster in the microbubble system. At an ozone dose of 0.02 g O₃ g⁻¹ TSS, about 80% of microorganisms were inactivated in the microbubble system, compared with about 50% inactivation for the bubble contactor. Compared to the bubble contactor, more than two times of COD and total nitrogen, and eight times of total phosphorus content were released from the sludge into the supernatant by using the microbubble system at the same ozone dosage. The application of microbubble technology in ozonation processes may provide an effective and low cost approach for sludge reduction.     

污泥减量过程中臭氧氧化对硝化和反硝化影响的试验研究

采用AO工艺,考察了在污泥减量过程中臭氧(O3)氧化对生物系统硝化和反硝化能力的影响.结果表明,在每克SS中O3投量为0.05 g时,氧化后污泥中的CODcr由37.5 mg/L增至700mg/L,TN由4.86 mg/L增至36.6 mg/L,NH4 -N由0.353mg/L增至7.49 mg/L,NO3--N由2.19 mg/L增至5.15 mg/L.虽然氧化系统出水NH4 -N浓度略高于对照系统,但氧化系统NH4 -N的去除率大于98%,硝化能力基本没有受到O3氧化的影响.O3氧化污泥后增加的有机物作为附加的碳源循环至缺氧段,提高了反硝化的效果,当污泥氧化比例分别为10%、20%、30%时,进入缺氧段的CODCr/TN分别平均增至11.21、11.56、11.88,氧化系统的反硝化效果也随之分别提高5%、25%、37%.     

Estrogenic activity removal of 17beta-estradiol by ozonation and identification of by-products

This work investigated the degradation of a natural estrogen (17beta-estradiol) and the removal of estrogenic activity by the ozonation process in three different pHs (3, 7 and 11). A recombinant yeast assay (YES assay) was employed to determine estrogenic activity of the ozonized samples and of the by-products formed during the ozonation. Ozonation was very efficient for the removal of 17beta-estradiol in aqueous solutions. High removals (>99%) were achieved with low ozone dosages in the three different pHs. Several by-products were formed during the ozonation of 17beta-estradiol. However, only a few compounds could be identified and confirmed. Different by-products are formed at different pHs, which is probably due to different chemical pathways and different oxidants (O(3) and OH radical). The by-products formed at pH 11 were 10epsilon-17beta-dihydroxy-1, 4-estradieno-3-one (DEO) and 2-hydroxyestradiol, which were not formed in pH 3. Only testosterone could be observed in pH 3, whereas at pH 7 all three by-products were found. At pH 7 and 11 the applied ozone dosages were not enough to remove all the estrogenicity from samples, even though the 17beta-estradiol residual concentration for these two pHs was lower than at pH 3. Higher estrogenicity was detected at pH 11. An explanation to this fact may be that oxidation via OH radical forms more by-products with estrogenic activity. Probably, the formation of 2-hydroxyestradiol at pHs 7 and 11 is contributing to the residual estrogenicity of samples ozonized at these pHs. In this work, complete removal of estrogenic activity was only obtained at pH 3.     

Catalytic activity of Ru/Al2O3 for ozonation of dimethyl phthalate in aqueous solution

With dimethyl phthalate as the model pollutant and Ru/Al(2)O(3) as catalyst, this paper systemically investigates the removal of total organic carbon (TOC) of system. Our results have confirmed that Ru/Al(2)O(3) can significantly increase the effect of ozonation. TOC removal in 120 min can reach 72% while only 24% with ozone alone. The optimal catalyst preparing condition was 0.1 wt% Ru content, 600 degrees C calcination temperature, 0.5-1.0mm particle diameter, which is characterized by a high surface area and a large population of surface active sites. The contrasting experiments of ozone alone, catalyst adsorption after ozonation, and catalytic ozonation confirmed that catalytic reaction was the most important process to TOC removal in system with Ru/Al(2)O(3) as catalyst.     

Influence of ozone pre-treatment on sludge anaerobic digestion: removal of pharmaceutical and personal care products

The effect of an oxidative pre-treatment with ozone on the removal of Pharmaceutical and Personal Care Products (PPCPs) during the anaerobic digestion of sewage sludge has been investigated. Besides, the digested sludge characteristics in terms of pathogens content, dewatering properties, heavy metals content and linear alkylbenzene sulfonates (LAS) were determined. During ozonation (20mg O(3)/g TSS), about 8% of volatile solids (VS) and 60% of the chemical oxygen demand (COD) were solubilized. However, no mineralization was observed. The elimination of VS and total COD during anaerobic digestion were not affected by ozone treatment with efficiencies ranging from 60% to 65%. All PPCPs considered were removed during anaerobic treatment of sludge, with efficiencies ranging from 20% to 99%. No significant influence of ozone pre-treatment was observed on PPCPs elimination except for carbamazepine. Pathogens, heavy metals and LAS contents after conventional and pre-ozonation treatment of sewage sludge were below the legal requirements. However, the dewatering properties of sludge were deteriorated when the ozone pre-treatment was applied.