Evaluation of Sludge Digester Effluent as Feeding Solution for the Enrichment of Anammox Bacteria

The aim of this study is to evaluate the feasibility of sludge digester effluent as feeding solution to enrich anaerobic ammonium oxidation (anammox) bacteria. The performance of the two parallel pilot scale‐upflow packed bed anammox reactors (UPBAn1 and UPBAn2) are examined in terms of the enrichment of anammox bacteria. The control experiment is set up conducting synthetic wastewater as feeding solution in the UPBAn1 reactor whereas, the sludge digester effluent is fed to the nitritation reactor and then the partially nitrated digester effluent to the UPBAn2 reactor. Anammox activities are evaluated by mass balances based on ammonium (NH₄⁺), nitrite (NO₂^?), and nitrate (NO₃^?) analysis and NRR. Microbial community of anammox bacteria is analyzed using real‐time polymerase chain reaction (PCR). The results demonstrate that UPBAn 1 and UPBAn2 reactors are successfully enriched on days 64 and 40 with NRRs of 19.54 and 19.43 g N m^?3 per day, respectively. This study reveals that both synthetic wastewater and digester effluent are suitable for the enrichment of anammox bacteria; however, digester effluent as feeding solution for enrichment of anammox bacteria based on the ease of process control and process stability is more advisable.     

沉水植物氧化塘对污水厂尾水深度净化效果与机制的小试研究

室外采用玻璃缸装置研究了抚仙湖常见的9种沉水植物氧化塘对澄江县污水厂尾水营养盐的去除效果及机制.结果表明:氧化塘中沉水植物的光合作用导致水体较高的DO和pH值,从而提高氧化塘总氮和总磷的去除率,但沉水植物叶片的腐烂分解则提高了水体氮磷的含量.沉水植物氧化塘对总氮和总磷的去除率分别介于19.44%-64.71%和28.13%-98.33%.沉水植物的直接吸收对总氮和总磷量去除的贡献比较低,占氧化塘总氮和总磷量的0.26%-1.54%和0.47%-1.77%.沉水植物氧化塘内DO、pH变化,促进了氮的降解及氧化还原分解,使其对氮的去除占氧化塘总氮量的30.71%-65.25%,而磷的去除则主要通过化学沉淀及基质吸附,占氧化塘总磷量的73.37%-93.34%.最终,选出蓖齿眼子菜、苦草、黑藻、金鱼藻和光叶眼子菜对氧化塘中氮磷具有较高的去除率.     

煤矿酸性矿井水主动式生物修复中铁的行为与归宿

酸性条件下Fe(II)的生物氧化过程可以被有效应用于煤矿酸性矿井水修复中,但是Fe行为与归宿的不确定性增加了应用难度。本研究通过对某煤矿酸性矿井水场地发生的生物地球化学过程进行监测,富集培养场地沉积物嗜酸微生物群落,进行室内恒化生物反应器连续流实验,探究微生物作用下Fe及其他金属离子的行为与归宿。研究表明,Fe的形态转化是场地和反应器中最主要的生物地球化学过程。当pH<2.7时,反应更倾向于产生溶解性Fe(III);当2.7相似文献   

南海东北部冷泉区沉积物中有机质来源的生物标志物分析与环境指示意义

Multi-biomarker indexes were analyzed for two piston cores from potential cold seep areas of the South China Sea off southwestern Taiwan. Total organic carbon(TOC) normalized terrestrial(n-alkanes) and marine(brassicasterol, dinosterol, alkenones and iso-GDGTs) biomarker contents and ratios(TMBR, 1/Pmar-aq, BIT) were used to evaluate the contributions of terrestrial and marine organic matter(TOM and MOM respectively) to the sedimentary organic matter, indicating that MOM dominated the organic sources in Core MD052911 and the sedimentary organic matter in Core ORI-_(86)0-22 was mainly derived from terrestrial inputs, and different morphologies were the likely reason for TOM percentage differences. BIT results suggested that river-transported terrestrial soil organic matter was not a major source of TOM of sedimentary organic matter around these settings.Diagnostic biomarkers for methane-oxidizing archaea(MOA) were only detected in one sample at 172 cm depth of Core ORI-_(86)0-22, with abnormally high iso-GDGTs content and Methane Index(MI) value(0.94). These results indicated high anaerobic oxidation of methane(AOM) activities at or around 172 cm in Core ORI-_(86)0-22.However in Core MD052911, MOA biomarkers were not detected and MI values were lower(0.19–0.38), indicated insignificant contributions of iso-GDGTs from methanotrophic archaea and the absence of significant AOM activities. Biomarker results thus indicated that the discontinuous upward methane seepage and insufficient methane flux could not induce high AOM activities in our sampling sites. In addition, the different patterns of TEX_(86) and U_(37)~(K′) temperature in two cores suggested that AOM activities affected TEX_(86)37 temperature estimates with lower values in Core ORI-_(86)0-22, but not significantly on TEX_(86) temperature estimates in Core MD052911.     

孔道结构化合物(H3NCH2CH2NH3)3[(VO)4(PO4)2(HPO4)4]的钒氧化态与热稳定性关系研究

热处理脱除有机模板易导致VPO体系孔道结构化合物结构破坏,从而阻碍此类材料的实际应用。以孔道结构化合物(H3NCH2CH2NH3)3[(VO)4 (PO4 )2 (HPO4 )4 ](简称V2P3 en)为研究对象,利用热分析(DSC TG)、动态原位高温X 射线衍射(XRD)及多功能X 射线光电子能谱(XPS)等方法,研究了该化合物在不同气氛热处理过程中模板脱除及结构演化规律,重点探讨了钒氧化态的变化对结构稳定性的影响。结果表明,加热过程中随着有机模板的分解脱除,形成较强的还原环境,骨架中的部分钒被还原(V4+→V3+),使原有的配位环境([VⅣO5]三角双锥、[VⅣO6]畸变八面体)与钒的氧化态不符而导致结构重组。因此,钒氧化态的变化是影响热稳定性的重要因素之一。     

甲烷流体活动与沉积物中碳、氮同位素组成响应——南海东北部海洋IV号地区研究

南海东沙群岛东北部海洋IV号地区GC16站重力柱状沉积物中的有机碳、总氮,以及自生碳酸盐岩矿物的无机碳同位素组成分析结果表明,甲烷流体活动区硫酸盐甲烷转换带(SMTZ—sulfate methane transition zone)是重要的生物地球化学界面,该带内沉积物中有机碳、氮与无机碳同位素组成变化明显。GC16站SMTZ上界面以下的沉积物中有机碳、氮同位素组成分别比其上的沉积物负偏1.4‰PDB和0.93‰,反映该带内甲烷缺氧氧化作用(AOM—anaerobic oxidation of methane)与氨氧化作用发育。无机碳同位素组成表明SMTZ界面之下沉积物中的自生碳酸盐岩矿物为以微生物为媒介的甲烷驱动成因,地质历史时期(至柱状沉积物底部沉积时期)曾发生过2次较强烈的CH₄流体活动;目前该区甲烷流体活动较弱,甲烷流体影响深度与SMTZ上界面一致,未能到达海底。     

光助Fenton氧化法去除水中两种氯乙酸及其动力学研究

以二氯乙酸和三氯乙酸为目标污染物,研究了光助Fenton氧化去除水中卤乙酸的可行性及影响因素,并对其动力学进行了初步研究.结果表明,影响光助Fenton氧化的因素很多,氙灯功率500 W、H2O2和Fe2+投加量分别为5.0和1.0 mmol·L-1、pH=4.0反应60 min是所考察范围内的最佳降解条件,浓度为100 μg·L-1的二氯乙酸和三氯乙酸的降解率分别为90.32％、87.77％;在实际水质pH=7.0时,相同浓度的二氯乙酸和三氯乙酸的降解率分别为75.34％、68.80％.紫外辐射与Fenton氧化对二氯乙酸和三氯乙酸的降解具有协同效应.光助Fenton氧化对二氯乙酸和三氯乙酸的降解符合一级反应动力学,表观活化能分别为30.11、31.09 kJ·mo1-1,受温度影响不大.