零价铁-反硝化菌在地下水硝酸盐污染修复中的应用

综述了应用零价铁-反硝化菌复合体系去除地下水中硝酸盐氮污染的研究进展.脱氮技术主要包括物理化学法、化学还原法和生物反硝化法,但单独使用任何一种方法都无法得到令人满意的处理效果.以零价铁在水中厌氧腐蚀所释放的氯气供给微生物进行反硝化,可以同时解决这两种技术单独使用时所存在的弊端.在此复合体系中,主要反应包括产氨、析氢和反硝化,降低脱氮产物中的氨氮比例就要减少产氨反应的发生几率.此外,使用纳米铁代替零价铁和反硝化细菌复合,可以大大提高脱氮反应速率.然而,该技术的研究在国内外尚处于起步阶段,在反应机理、产物控制、条件优化等方面都存在不足,还需要深入研究.     

Organic matter and concentrated nitrogen removal by shortcut nitrification and denitrification from mature municipal landfill leachate

An UASB＋Anoxic/Oxic （A/O） system was introduced to treat a mature landfill leachate with low carbon-to-nitrogen ratio and high ammonia concentration. To make the best use of the biodegradable COD in the leaehate, the denitrifieation of NOx^--N in the reeireulation effluent from the elarifier was carried out in the UASB. The results showed that most biodegradable organic matters were removed by the denitrifieation in the UASB. The NH4^＋-N loading rate （ALR） of A/O reactor and operational temperature was 0.28- 0.60 kg NH4^＋-N/（m^3-d） and 17-29℃ during experimental period, respectively. The short-cut nitrification with nitrite accumulation efficiency of 90%-99% was stabilized during the whole experiment. The NH4^＋-N removal efficiency varied between 90% and 100%. When ALR was less than 0.45 kg NH4^＋-N/（m^3.d）, the NH4^＋-N removal efficiency was more than 98%. With the influent NH4^＋-N of 1200-1800 mg/L, the effluent NH4^＋-N was less than 15 mg/L. The shortcut nitrification and denitrifieation can save 40% carbon source, with a highly efficient denitrifieation taking place in the UASB. When the ratio of the feed COD to feed NH4^＋-N was only 2-3, the total inorganic nitrogen （TIN） removal efficiency attained 67%-80%. Besides, the sludge samples from A/O reactor were analyzed using FISH. The FISH analysis revealed that ammonia oxidation bacteria （AOB） accounted for 4% of the total eubaeterial population, whereas nitrite oxidation bacteria （NOB） accounted only for 0.2% of the total eubaeterial population.     

Effect of sulfate on the methanogenic activity of a bacterial culture from a brewery wastewater during glucose degradation

The maximum specific methanogenic activity （SMA） of a sludge originating from a brewery wastewater treatment plant on the degradation of glucose was investigated at various levels of sulfate on a specific loading basis. Batch experiments were conducted in serum bottles at pH 7 and 35℃. A comparison of the values indicates that the SMA of this mixed culture was increased and reached its highest level of 0.128 g CH4 gas COD/（g VSS.d） when biomass was in contact with sulfate at a ratio of 1：0.114 by weight.     

Effects of nitrate concentration in interstitial water on the bioremediation of simulated oil-polluted shorelines

Nutrient addition has been proved to be an effective strategy to enhance oil biodegradation in marine shorelines.To determine the optimal range of nutrient concentrations in the bioremediation of oil-polluted beaches,nitrate was added to the simulated shoreline models in the initial concentration of 1,5 and 10 mg/L.Whenever the NO3-N concentration declined to 70% of its original value, additional nutrients were supplemented to maintain a certain range.Results showed adding nutrients increased the oil biodegradation level,the counts of petroleum degrading bacteria(PDB)and heterotrophic bacteria (HB),and the promoted efficiency varied depending on the concentration of nitrate.Oil degradation level in 5 mg/L(NO_3-N)group reached as much as 84.3% accompanied with the consistently highest counts of PDB;while in 1 mg/L group oil removal efficiency was only 35.2%,and the numbers of PDB and HB were relatively low compared to the other groups supplemented with nutrients.Although counts of HB in the 10 mg/L group were remarkable,lower counts of PDB resulted in poorer oil removal efficiency (70.5%) compared to 5 mg/L group.Furthermore,it would need more NO_3-N(0.371 mg)to degrade 1 mg diesel oil in the 10 mg/L group than in the 5 mg/L group(0.197 mg).In conclusion, Nitrate concentration in 5 mg/L is superior to 1 and 10 mg/L in the enhancement of diesel oil biodegradation in simulated shorelines.     

Removal of arsenic from wastewater using iron compound: Comparing two different types of adsorbents in the context of LCA

A study was carried out in order to compare the environmental performance of two different types of adsorbents in removing arsenic (As) from wastewater. A FeCl₃-based adsorbent and a poly-Fe-based adsorbent were first synthesized and their abilities in adsorbing As from wastewater were investigated in terms of the adsorption density and the rate of adsorption. Here, it should be noted that the main material being used in the synthesis of the poly-Fe-based adsorbent was a waste product, known as polyferric sulfate or poly-Fe in short, which exits the manufacturing process of titanium dioxide.Both adsorbents were then compared in the context of life-cycle assessment (LCA). In other words, the experimental results (i.e. the value of the adsorption density and the rate of adsorption) were input into the LCA model in order to assess the environmental performance of each adsorbent in removing arsenic. An estimate for the environmental burden of each option was finally calculated as the sum of the depletion of abiotic resources (ADP), the global warming potential (GWP), the acidification potential (AP), the photo-oxidant formation potential (POCP), the eutrophication potential (EP), and the human toxicity potential (HTP). The main finding of this study was that the adsorption of arsenic by using the poly-Fe-based adsorbent is more attractive treatment option in the environmental protection point of view than the adsorption by using the FeCl₃-based adsorbent, which generates a relatively larger environmental burden.     

光合细菌强化二级流化床工艺处理焦化废水的研究

采用厌氧酸化加二级流化床组合工艺处理焦化废水。一级反应器内光合细菌与兼性厌氧菌处于共生状态,二级反应器内光合细菌与亚硝酸细菌处于共生状态。一级反应器内光合细菌有充分的小分子有机酸可降解并形成二次酸化,在二级反应器内完成进一步降解。结合反应条件：温度,pH,DO和基质浓度等,将二级反应器内硝化反应控制在亚硝化阶段,有效地保证了废水中碳源的利用。稳定运行了60 d,结果显示,出水COD和NH₃-N浓度分别为105～135 mg/L和14～20 mg/L,去除率分别稳定在90.3%～92.5%和92%～95%。TN去除率稳定在83%～86%。酚、氰化物和BOD5的去除率均在95%以上。     

硝酸盐对反硝化除磷过程的影响分析

在厌氧/缺氧间歇反应器内考察了硝酸盐进水浓度及进水方式对反硝化除磷过程的影响。结果表明：在缺氧阶段,反硝化除磷菌(DPBs)可将硝酸盐转化为亚硝酸盐,当硝酸盐浓度较低时,DPBs以亚硝酸盐为电子受体吸磷。进水COD浓度为220 mg/L,正磷浓度为6.8 mg/L,硝酸盐初始浓度为26 mg/L时,系统达到最佳脱氮除磷效果,期间亚硝酸盐浓度积累至10.71 mg/L。采用连续流投加硝酸盐的方式更利于氮磷的高效去除。     

壳聚糖衍生物-镁盐复配去除中性兰模拟废水色度的研究

研究了有机高分子絮凝剂NCTS-M对中性兰染料的絮凝性能。通过测量絮体的Zeta电位以及对絮体进行彩色电视显微扫描初步探讨了该絮凝过程的絮凝机理。结果表明,当投加量为30 mg/L,pH=6时,絮凝效果最明显,脱色率可达93.1%。其絮凝机理主要是压缩双电层以及高分子吸附架桥作用,以压缩双电层为基础。絮凝剂中镁离子在中性条件下对絮凝过程也起到了较强的助凝作用。     

聚硅酸锌铝的制备及其性能研究

以硅酸钠、硫酸锌、硫酸铝为原料,通过共聚法制备了无机高分子絮凝剂聚硅酸锌铝（PSZAS）,研究了Na₂SiO₃的摩尔浓度、活化时间、Al/Si、Zn/Si 配比及絮凝剂的投加量对絮凝效果的影响,用X-射线衍射（XRD）和电子扫描电镜（SEM）对该絮凝剂的结构及形貌进行了表征。结果表明：当硅酸钠的浓度为0.4 mol/L,硅酸活化时间为2 h,Si∶Al∶Zn=1∶1∶1.5,絮凝剂投加量为20 mL/L废水时,絮凝剂的电中和能力和吸附架桥能力最强,絮凝剂对含H-酸染料模拟废水的絮凝效果最好。     

用电解锰阳极泥和含SO_2工业尾气制备硫酸锰

以电解锰阳极泥与电解锌生产中产生的含SO_2尾气为原料,经过反应、浸出、浸出液两次净化和浓缩结晶制备硫酸锰,考察了反应时间、含SO_2尾气的流量及反应温度对Mn~(4+)转化率的影响.实验结果表明:在反应时间45 min、反应温度20～30 ℃、含SO_2尾气流量16 L/min的条件下,Mn~(4+)转化率达90%以上;尾气中SO_2利用率随尾气流量增加而降低;所得MnSO_4·H_2O产品质量达到GB1622-86<工业级硫酸锰标准>.