陇东黄土高原地区石油污泥原位修复过程中土壤主要肥力指标动态变化分析

为了分析陇东黄土高原地区石油污泥在原位修复过程中土壤主要肥力指标的变化情况,对长庆油田第二采油厂的石油污泥进行为期105 d的原位修复,采用常规方法测定了土壤有机质、pH、总石油烃含量(TPHs)、含盐率、碱解氮、速效磷、速效钾、土壤脲酶、脱氢酶、多酚氧化酶、过氧化氢酶等土壤肥力指标;通过PCR-DGGE技术分析了土壤微生物群落的功能多样性,并采用主成分分析法对供试石油污泥的土壤肥力进行评价.结果显示:随着原位修复的时间的延长,土壤碱解氮、速效磷含量呈显著增加趋势;有机质、pH、含盐率、TPHs含量显著降低,而速效钾含量呈逐步增加趋势.土壤脲酶及脱氢酶活性增加,多酚氧化酶及过氧化氢酶活性降低.土壤微生物群落遗传多样性结果显示,ShannonWiener多样性指数、Patrick丰富度指数及Pielou均匀度指数均呈增加的趋势.经过105 d的原位修复土壤肥力显著提升,各阶段土壤肥力得分为105 d80 d60 d45 d25 d.上述实验结果有助于掌握石油污泥原位修复中土壤肥力动态变化趋势,并为土壤石油烃污染的综合治理提供基础依据和数据参考.     

同步短程硝化-厌氧氨氧化-短程反硝化颗粒污泥培育过程及其性能

本研究以低碳氮比废水为基质,厌氧氨氧化污泥优配普通活性污泥为接种物,在新型气升式内循环反应器中培育同步短程硝化-厌氧氨氧化-短程反硝化颗粒污泥.结果表明,经过225 d的连续运行可培育成熟稳定的颗粒污泥,其总氮去除率高达91.4%.相较于絮状污泥,颗粒污泥中厌氧氨氧化活性显著增加,并且厌氧氨氧化活性在4个脱氮过程中活性最大,其次是短程硝化,且短程反硝化比活性是亚硝酸盐还原比活性的2.1倍.高通量测序结果表明,颗粒污泥中短程硝化和厌氧氨氧化的优势菌分别为Nitrosomonas和Candidatus_Brocadia,并相较于絮状污泥,它们的丰度分别增加至0.70%和0.57%.Thauera可能是颗粒污泥中潜在的短程反硝化优势菌,其丰度达到0.26%.RT-qPCR分析结果表明,相比接种阶段,短程硝化的功能基因amoA和hao转录水平分别增加了3.5和1.5倍,厌氧氨氧化功能基因hzsA转录水平增加了2.1倍,短程反硝化过程中napA和narG转录水平增加的倍数之和是nirK和nirS的倍数之和的4.8倍.本研究结果将为处理低碳氮比废水提供新的思路.     

盐分对粉壤土氮转化的影响

采用室内恒温通气培养法,以北京地区耕作层典型粉壤土为对象,研究盐分对土壤氮素矿化和硝化的影响.实验设置了4个不同盐分〔以ρ（NaCl）计,分别为20,30,50和80 mg/L〕处理和对照处理,并在硝化实验的土壤中加入一定量的（NH₄）₂SO₄,分别在30 ℃恒温培养箱中进行为期105 d（矿化）和49 d（硝化）的培养实验.结果表明:在初期的培养中,低盐分有利于土壤氮素转化,ρ（NaCl）为20 mg/L的处理分别比对照处理的累积矿化量和累积硝化量多18.21%和1.87%;而在长期培养过程中,高盐分不利于土壤氮素转化,且ρ（NaCl）越高抑制越明显,其对土壤氮素矿化和硝化的抑制率达到67.92%和62.58%;土壤矿化势和硝化势随w（NaCl）分别呈指数递减,矿化速率常数和硝化速率常数与土壤中w（NaCl）为二次函数关系.      

多级A／O膜生物反应器污泥活性研究

采用一种新型的多级A／O膜生物反应器处理污水,对该工艺的污泥活性进行了研究。结果表明,VSS／SS在实验过程中呈较弱的下降趋势,多级A／O池曝气室污泥比硝化速率逐室下降,但各缺氧室污泥比反硝化速率基本一致;污泥释磷、聚磷过程在30 min和1 h内基本完成,反硝化聚磷试验表明污泥中存在DPB的富集,反硝化作用是反硝化细菌与DPB共同作用的结果。     

SBR法交替缺氧好氧模式下短程硝化效率的优化

采用SBR法以实际生活污水为研究对象,通过交替缺氧好氧的运行模式实现了短程硝化的快速启动.在不同的缺/好氧时间比条件下考察了短程硝化的启动时间、污染物处理效果以及氨利用速率的变化.结果表明,在缺氧/好氧时间比为1:1和2:1条件下,分别用了31,55d使得两系统的亚硝酸盐积累率达到90%,短程状态稳定.氨氮去除率达到95%以上,COD出水在50mg/L以下,总氮去除率提高20%,污染物的去除效率有所提高.由全程到短程的转变期间,系统氨利用速率分别提高了67.5%和89.8%,同时提高了短程硝化的效率.期间,污泥沉降性较好,污泥容积指数稳定在60~80mL/g.     

芬顿污泥制备磁性生物炭回用于对硝基苯酚的去除及机制

芬顿/絮凝组合工艺在处理难降解有机物废水时会产生大量的芬顿污泥,会提高废水处理成本,同时也会对环境构成威胁,迫切需要开发一种绿色可持续的方法实现芬顿污泥资源化利用.该研究通过将处理PNP(对硝基苯酚)废水产生的芬顿污泥和污水厂生化污泥共热解,原位制备具有高催化活性的MBC(磁性生物炭),并作为多相芬顿催化剂用于去除PNP,实现“以废治废”.结果表明：当芬顿污泥和生化污泥质量比为1∶1、热解温度为800℃时,制备得到的MBC-800-3催化性能最佳;合适的混合比例可有效避免颗粒聚集,高温形成缺陷结构和多种铁相,为MBC-800-3提供了丰富的反应活性位点;当废水初始pH为3、H₂O₂浓度为60 mmol/L、MBC-800-3投加量为0.4 g/L时,PNP和TOC(总有机碳)的去除率均最高,在催化反应100 min时分别达到98%和62%;酸性条件下,MBC活化H₂O₂产生·OH和·O₂-催化降解废水的有机物,其中,·OH作为主要活性物种,其来源包括均相芬顿反应和非均芬顿相反应...     

Interactive effect of dissolved organic matter and phenanthrene on soil enzymatic activities

The investigation of dissolved organic matter (DOM) on urease, catalase and polyphenol oxidase activity in a phenanthrene (Phe)-contaminated soil was conducted under laboratory incubation conditions. Values of soil enzymatic activity depended mainly on incubation time. In the initial 16 days, urease activity increased, and was followed by a decrease. In the initial 8 days, catalase activity decreased and then increased. Variation of polyphenol oxidase activity was just the reverse of catalase activity. After 30 days of incubation, no pronounced difference among treatments with Phe, Phe and DOM, and control were detected in urease, catalase and polyphenol oxidase activity. Phe might inhibit urease and catalase, and stimulate polyphenol oxidase. DOM could improve inhibition of Phe in soil urease and catalase activity during the initial period of applying DOM. Nevertheless, DOM had no significant effect on polyphenol oxidase activity in the Phe contaminated soil. There was a negative correlation between catalase and polyphenol oxidase (r = -0.761~(***)), and catalase and urease (r = -0.554~(**)). Additionally, a positive correlation between polyphenol oxidase and urease was also detected (r = 0.701~(***)). It is implied that the formed DOM after application of organic wastes into soils may counteract the inhibition of polycyclic aromatic hydrocarbons in soil enzyme activities.     

Interactive e ect of dissolved organic matter and phenanthrene on soil enzymatic activities

The investigation of dissolved organic matter (DOM) on urease, catalase and polyphenol oxidase activity in a phenanthrene (Phe)- contaminated soil was conducted under laboratory incubation conditions. Values of soil enzymatic activity depended mainly on incubation time. In the initial 16 days, urease activity increased, and was followed by a decrease. In the initial 8 days, catalase activity decreased and then increased. Variation of polyphenol oxidase activity was just the reverse of catalase activity. After 30 days of incubation, no pronounced di erence among treatments with Phe, Phe and DOM, and control were detected in urease, catalase and polyphenol oxidase activity. Phe might inhibit urease and catalase, and stimulate polyphenol oxidase. DOM could improve inhibition of Phe in soil urease and catalase activity during the initial period of applying DOM. Nevertheless, DOM had no significant e ect on polyphenol oxidase activity in the Phe contaminated soil. There was a negative correlation between catalase and polyphenol oxidase (r = –0.761***), and catalase and urease (r = –0.554**). Additionally, a positive correlation between polyphenol oxidase and urease was also detected (r = 0.701***). It is implied that the formed DOM after application of organic wastes into soils may counteract the inhibition of polycyclic aromatic hydrocarbons in soil enzyme activities.     

Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

SBR工艺短程硝化快速启动条件的优化

以低COD/TN的实际生活污水为研究对象,采用SBR反应器,对短程硝化的启动条件进行了优化.结果表明,温度30℃、溶解氧(DO) 2.0mg/L、污泥龄为7d时,系统在实时控制条件下运行32周期,可以成功启动短程硝化.在总氮(TN)去除率>95%的情况下,亚硝酸盐积累率(NO2--N /NOx--N)>90%,随后的64d,温度恢复到常温(20~24℃),系统仍稳定运行.荧光原位杂交技术(FISH)检测表明,经过32个周期种群优化,污泥中氨氧化菌(AOB)的含量提高了38.9%,亚硝酸盐氧化菌(NOB)的含量降低了53.2%.在线动态控制DO浓度和曝气时间可以逐渐淘汰系统中的NOB,从而获得稳定的短程硝化,提高系统脱氮效率.     

Removal of organic matter and nitrogen from distillery wastewater by a combination of methane fermentation and denitrification/nitrification processes

Introduction D istillery w astew ater m ainly includes spent w ash, w hich is one of the m ost com plex, troublesom e industrial organic effluents. This kind of w astew ater has previously been treated aerobically after dilution w ith other w ash w aters.…     

利用方式对红壤硝化作用的水分效应的影响

风干过程是土壤水分丢失的过程,研究亚热带酸性土壤硝化作用对水分水平的响应,有助于分析干土效应对硝化作用影响.本试验以分别发育于第四纪红土(Quaternary red earth,Q)和红砂岩(Tertiary red sandstone,S)、利用方式为水稻(rice,R)与旱地(upland,U)的4个农田土壤的风干土为供试材料,分别加入铵态氮0和150mg·kg-1,在5个即时水分含量下室内培养35d.结果表明,土壤水分水平显著影响供试土壤的硝化作用(p0.01),但影响程度因利用方式而异.对供试条件下无外源铵输入的处理而言,旱地土壤QU和SU硝化率的极差分别为11%和8%,显著低于水稻土的硝化率极差(QR与SR分别为35%和20%).外源铵的加入增加了土壤硝化率的极差,土壤QR、QU、SR和SU硝化率的极差分别达到56%、26%、31%、26%,且随水分水平的增高,加铵有促进土壤酸化的趋势.总之,利用方式显著影响了土壤硝化作用对水分效应的响应,进而体现为干土效应的差异.     

Inhibition and recovery of nitrification in treating real coal gasification wastewater with moving bed biofilm reactor

Moving bed biofilm reactor (MBBR) was used to treat real coal gasification wastewater. Nitrification of the MBBR was inhibited almost completely during start-up period. Sudden increase of influent total NH3 concentration was the main factor inducing nitrification inhibition. Increasing DO concentration in the bulk liquid (from 2 to 3 mg/L) had little e ect on nitrification recovery. Nitrification of the MBBR recovered partially by the addition of nitrifying sludge into the reactor and almost ceased within 5 days. Nitrification ratio of the MBBR achieved 65% within 12 days by increasing dilute ratio of the influent wastewater with tap water. The ratio of nitrification decreased to 25% when influent COD concentration increased from 650 to 1000 mg/L after nitrification recovery and recovered 70% for another 4 days.     

生物膜SBR反应器中低氨氮浓度废水亚硝化启动试验研究

为建立生物膜SBR反应器处理中低氨氮浓度废水的自养脱氮系统,采用控制DO浓度、HRT和不同生物载体填料的4组小试生物膜SBR反应器,对中低氨氮浓度废水进行了单级自养脱氮工艺亚硝化阶段的启动试验研究.结果表明:接种普通好氧活性污泥和厌氧污泥,在水温30℃±2℃,氨氮浓度60～120mg/L,DO为0.8～1.0mg/L和HRT=24h条件下,运行130d可实现稳定的亚硝化,YJZH软性组合填料更适合于微生物附着.     

人为干扰对闽江河口湿地土壤硝化-反硝化潜力的影响

选择闽江河口芦苇湿地为研究对象,研究了人为干扰活动(养殖塘、污染物排放和农业活动)对湿地土壤硝化-反硝化潜力的影响.结果表明,人类干扰活动对湿地土壤硝化和反硝化潜力均具有显著影响,4种土壤的硝化潜力表现为水稻田>养殖塘>排污闸口>芦苇湿地,其最大硝化率分别为103.45%、99.38%、12.58%和4.16%,而反硝化作用的变化规律则与之相反,24d内的最大反硝化率分别为21.89%、26.95%、78.15%和88.28%,说明人类干扰和管理程度越大,土壤硝化潜力越大,反硝化潜力越弱.土壤NO3--N含量是闽江河口地区不同人为干扰方式下土壤硝化-反硝化作用差异的重要指示指标,土壤pH值与土壤硝化-反硝化作用也具有密切关系,而土壤有机质、全氮、全磷和可溶性碳含量以及电导率等则与土壤硝化-反硝化作用不具有显著的相关关系.人类干扰活动导致土壤硝化能力的提高,反硝化能力的降低,能够增加土壤氮素以硝态氮形式淋失的风险.     

Nitrification performance evaluation of activated sludge under high potassium ion stress during high-ammonia nitrogen organic wastewater treatment

The recycling reverse osmosis（RO） membrane concentrate of some high-ammonia nitrogen（NH₄⁺-N） organic wastewater to the biological unit could cause potassium ion（K⁺） accumulation, thereby affecting the removal of NH₄⁺-N by activated sludge. Thus, the effects of high K⁺ stress on activated sludge nitrification performance was studied. The results showed that the high K⁺ stress promoted the floc sludge to produce more extr...     

处理实际生活污水短程硝化好氧颗粒污泥的快速培养

以普通序批反应器(Sequencing Batch Reactor,SBR)和气提式序批反应器(Sequencing Batch Airlift Reactor,SBAR)处理低COD/TN的实际生活污水,考察了不同沉淀时间以及反应器类型对快速培养短程硝化好氧颗粒污泥(Aerobic Granular Sludge,AGS)的影响.试验结果表明,沉淀时间为15min时,SBR和SBAR系统中均为全程硝化,当将沉淀时间分别改为5min、8min后的第17d和第16d时,两个反应器中均形成AGS,并且AGS与絮状污泥共存;此时两系统均由全程硝化转化为短程硝化,出水NO2-/(NO2- NO3-)平均值分别长期维持在98.7%和85.6%左右.本试验中以沉淀时间作为选择压,快速启动了具有短程硝化功能的序批式AGS反应器.由于AGS固有结构对氧传质的限制,使亚硝酸氮氧化受阻即抑制了亚硝酸氮氧化细菌的活性,从而产生了亚硝酸氮积累现象.DO是造成本研究中出现短程硝化的主要原因,而pH值、游离氨、温度、污泥龄等因素都不是导致短程硝化的关键因素.污泥颗粒化后,两个系统中NH4 -N降解速率分别提高了2.6倍和2.4倍.     

游离氨(FA)协同曝气时间对活性污泥沉降性能的影响

采用3个序批式反应器(SBR)(R0:硝化结束时停曝气;R_(0-30):硝化结束提前30 min停曝气;R_(0+30):硝化结束延迟30 min停曝气),控制3种游离氨(FA)浓度梯度(0.5,5.1,10.1 mg/L)协同3种曝气时间(t0:硝化结束时停曝气;t0-30:硝化结束提前30 min停曝气;t0+30:硝化结束延迟30 min停曝气)的条件下,研究了FA协同曝气时间对活性污泥沉降性能的影响。结果表明:整个试验过程,在初始FA浓度相同条件下,R0和R_(0+30)系统NH+4-N平均去除率分别为98.6%和99.3%,而R_(0-30)系统NH+4-N平均去除率仅为72.3%。在较低FA浓度(0.5,5.1 mg/L)条件下,随着曝气时间增加,活性污泥的污泥沉降比(SV30)值和污泥体积指数(SVI)值均逐渐降低,污泥沉降性能趋好。在较高FA浓度(10.1 mg/L)条件下,随着运行周期的增加,污泥沉降性能逐步变好,R_(0-30)系统的SVI平均值最大,R_(0+30)系统次之,R0系统最小,其值分别为165.1,152.5,134.5 m L/g,且污泥活性f平均值大小顺序fR_(0-30)>fR0>fR_(0+30),其值分别为0.77、0.70和0.65。这表明在较高FA浓度(10.1 mg/L)条件下,曝气时间延长,导致污泥活性降低。     

强化内源反硝化脱氮及污泥减量化研究

为提高传统污水处理工艺内源反硝化脱氮效率,在系统内部实现污泥减量,设计了水解酸化/缺氧/好氧(H/A/O)生物脱氮及污泥减量化工艺.试验采用连续流处理装置,以实际生活污水为研究对象.结果表明,在进水COD(220～410 mg/L)、NH4 -N(36～58 mg/L)、总水力停留时间为11h、硝化液回流比为300%、无外加碳源和碱度条件下,COD、NH4 -N和TN的平均去除率分别超过90%、95%和75%.在缺氧段碳源充足的条件下,随着硝化液回流比的增加,系统TN平均去除率升高;当碳源不足时,随着硝化液回流比的增加,系统TN平均去除率降低.污水经水解酸化预处理后,反硝化速率大大升高.水解酸化段利用水解酸化作用对回流剩余污泥的减量达到56.2%,污水、污泥经过水解酸化处理,大大提高了系统脱氮效率.以水解酸化作为传统的城市污水及污泥处理工艺,既可有效地改善污水的可生化性,提高系统污染物平均去除率,增强污水处理系统运行的稳定性,又可实现污水、污泥一体化处理.     

一体化A/O生物膜反应器脱氮特性研究

根据传统好氧硝化和缺氧反硝化生物脱氮的工艺原理,设计并制作了一体化 A/O生物膜反应器,并就其对模拟生活污水的脱碳、脱氮处理效果进行了试验。结果表明,该一体化反应器在水力停留时间 HRT=24h时,COD的去除率达到 97%以上,硝化率和 TN的去除率分别达到92%和82%。出水NO3-N和NO2-N浓度保持在7.4mg/L和0.2mg/L左右。对各区污泥进行的硝化活性试验结果表明,该一体化反应器的缺氧区内存活有一定数量的具有硝化活性的细菌。