一种生物处理酸性矿山废水的工艺

该发明涉及一种含硫酸盐酸性废水生物处理并回收单质硫的工艺，其特征在于是一种利用污水厂污泥酸性发酵产物为硫酸盐还原菌的碳源处理酸性硫酸盐废水并回收单质硫的工艺：厌氧生物反应器中硫酸盐还原菌（SRB）将SO4^2-生物还原为H2S或S2-；好氧生物膜反应器中无色硫细菌（CSB）将H2S或S2-生物氧化为单质硫；慢砂滤池过滤、刮砂，采用萃取设备充分溶锯砂滤料中的单质硫，     

煤化工废水中硫酸盐还原菌的分离及鉴定

从煤化工废水和厌氧污泥中分离出2株高效的硫酸盐还原菌,通过革兰氏染色、扫描电子显微镜观察其形态,通过16S r DNA序列分析法鉴定其种属,并研究其生长特性和硫酸盐还原性能。实验结果表明:菌株SRB-1为革兰氏阴性柠檬酸杆菌;菌株SRB-2为革兰氏阳性丁酸梭菌;两种菌株在最佳条件下培养4 d,菌液菌量均可达到1×106个/m L的水平;在SO2-4质量浓度为1 360 mg/L的条件下,两种菌株的SO2-4去除率分别达到93%和95%。     

荷兰的烟气生物脱硫工艺

烟气中的SO2通过水膜除尘器或吸收塔溶解于水并转化为亚硫酸盐、硫酸盐；在厌氧环境及有外加碳源的条件下，硫酸盐还原菌(SRB)将亚硫酸盐、硫酸盐还原成硫化物；然后再在好氧的条件下通过好氧微生物的作用将硫化物转化为单质硫，从而将硫从系统中去除。可以将烟气生物脱硫过程划分为两个阶段，即SO2的吸收过程和含硫吸收液的生物脱硫过程。     

钛白废水中硫酸盐生物还原影响因素的研究

在厌氧序批式反应器中,采用硫酸盐还原菌(SRB)对钛白废水中硫酸盐生物还原的影响因素及厌氧序批式反应器的运行条件进行了研究。研究结果表明,模拟废水的SO24-去除效果比实际钛白废水的SO24-去除效果好。SRB还原实际钛白废水中SO24-的最佳运行条件为:进水SO24-质量浓度不超过2000m g/L、反应温度(35±1)℃、pH6.5~8.0、CODρ/(SO24-)2.0~3.0、HRT24h、反应器运行周期8h(进水0.5h,反应6.0h,沉淀1.0h,出水0.5h)、循环间歇搅拌(搅拌1.5h,搅拌停止2.0h)方式。在此条件下SO24-去除率可达90%。     

SO42-/TiO2-WO3光催化氧化邻硝基苯酚

研究了用H2SO4溶液浸渍处理TiO2-WO3，制备SO4^2-／TiO2-WO3催化剂的方法；考察了该催化剂对邻硝基苯酚的光催化氧化性能。TiO2-WO3的最佳处理工艺条件：H2SO4浓度为0．2mol/L，WO3加入量为3％，于550℃焙烧3h。实验结果表明，反应30min后SO4^2-／TiO2-WO3催化剂可使邻硝基苯酚降解97％；邻硝基苯酚的光催化氧化降解过程遵循一级动力学规律。     

与酸雨相关的对流层光化学过程及其影响因素

以对流层为范围，叙述了光化学过程在酸雨形成中的作用，介绍了臭氧和自由基的源与汇，其对于表征大气氧化性以及SO2、NOx向H2SO4、硫酸盐、HNO3、硝酸盐的转化具有重要意义，同时讨论了相关的光化学过程及其影响因素。     

厌氧消化中硫酸盐毒性的控制

探讨了厌氧消化中硫酸盐还原菌与产甲烷菌对分子氢的两种竞争作用及硫酸盐的致毒机制，归纳分析了目前对含硫酸盐有机废水厌氧处理可能采用的几种毒性控制对策及其存在问题。     

污泥生物制酸的影响因素

用城市污水厂污泥作嗜酸菌来源及培养基，通过添加能量物质、提供适当的生长条件，使污泥中的嗜酸菌大量繁殖富集，污泥pH下降，所产酸液可用于沥滤废旧干电池中的重金属。实验结果表明，以FeSO4·7H2O作能量物质时，其最适加入量为6～8g／L；在前5d内污泥pH下降较快，其值低于以单质硫作能量物质的试样，但最终污泥pH很难降至2．0以下；污泥初始pH对污泥酸化速率有一定的影响，即使在污泥pH高达8．0甚至10．0的情况下，嗜酸菌依然能够缓慢生长，逐渐使污泥pH下降；污泥初始pH为4．0时，污泥中嗜酸菌的活性最高，污泥pH下降最快，SO4^2-的产生量最大。     

低温湿式空气氧化法处理废碱液的研究

对采用低温湿式空气氧化法处理炼油和乙烯废碱液进行了研究。考察了停留时间对废碱液中硫化物的氧化、氧化产物的形态、COD和酚去除率的影响，反应温度对废碱液中污染物氧化反应的影响。试验结果表明，废碱液的脱臭效果很好，S^2-的氧化产物以S2O3^2-和SO4^2-2种形式共存；酚、COD的去除率及S^2-的氧化反应停留时间影响小，受反应温度影响明显；废碱液的S^2-的酚浓度相当时，COD去除率一 般低于40％， 废碱液的S^2-浓度远大于酚浓度时，废碱液的COD去除率为40％－70％；废碱液中酚的质量浓度大于20000mg/L时才有回收价值。     

磁性铁矿石对CO还原SO2的催化活性

采用磁性强弱不同的铁矿石以及制备的Fe3O4作为催化剂,催化CO还原SO2。实验结果表明:在3种催化剂中弱磁性铁矿石对CO还原SO2的催化活性最好;当反应温度为700℃时,在弱磁性铁矿石催化作用下的SO2转化率达84.3%。该方法既可以有效去除炼油厂催化裂化再生装置排放的SO2,同时又利用了低品位的磁性铁矿石,实现了SO2的治理和资源的综合利用。     

Treatment of acid lignite mine flooding water by means of microbial sulfate reduction

During and after mining activities acidic waters containing high amounts of heavy metals and sulfate often occur. In addition to precipitation processes, water purification is also possible with the help of sulfate-reducing bacteria (SRB). A mixed culture of SRB was adapted to methanol as a cheap carbon source. In order to receive high sulfate-reduction rates immobilization on porous materials proved to be advantageous. Continuous laboratory experiments based on immobilized SRB were carried out with original water from a lignite mining site reaching sulfate-reducing rates up to 132 mg SO4(2-)/(1 h). Based on these results a process for the treatment of such waters was designed. Heavy metals are removed by recycling sulfide containing effluent, excess sulfide can be oxidized to elemental sulfur by addition of hydrogen peroxide. The plant with a 3.9 m3 bioreactor with immobilized SRB was constructed at the mine site. This pilot plant was operated successfully for some months. The removal of heavy metals was close to 100%, the pH of the acidic water increased from 3.0 to 6.9. The sulfate-reducing rate again reached 134 mg SO4(2-)/(1 h). The production of sulfur from the excess sulfide is possible.     

A novel additive for the reduction of acid gases and NO(x) in municipal waste incinerator flue gas.

The reduction of SO2, HCl, and NO(x) concentrations using calcium magnesium acetate (CMA) as a novel sorbent in a simulated municipal waste incinerator flue gas was investigated. The reduction of individual SO2, HCl, and NO(x) concentrations was tested at 850 degrees C and it was found that CMA could reduce the SO2 concentration by 74%, HCl concentration by 64%, or NO(x) concentration by 94%. It was observed that individual SO2 or HCl capture increased with increasing initial oxygen concentration in the reacting gas or increasing sorbent input. NO(x) reduction decreased with increasing initial oxygen concentration in the reacting gas. The simultaneous reduction of SO2, HCl, and NO(x) concentrations by CMA was also investigated. It was found that CMA could simultaneously capture 60% SO2 and 61% HCl and reduce NO(x) concentrations by 26%, when the initial oxygen concentration in the reacting gas was 4%. During the simultaneous reduction of SO2, HCl, and NO(x), it was noted that as the initial oxygen concentration in the reacting gas increased, the efficiency of SO2 capture increased too, but the efficiency of HCl capture and the efficiency of NO(x) destruction decreased.     

Treatment of exhaust fluorescent lamps to recover yttrium: experimental and process analyses

The paper deals with recovery of yttrium from fluorescent powder coming from dismantling of spent fluorescent tubes. Metals are leached by using different acids (nitric, hydrochloric and sulphuric) and ammonia in different leaching tests. These tests show that ammonia is not suitable to recover yttrium, whereas HNO(3) produces toxic vapours. A full factorial design is carried out with HCl and H(2)SO(4) to evaluate the influence of operating factors. HCl and H(2)SO(4) leaching systems give similar results in terms of yttrium extraction yield, but the last one allows to reduce calcium extraction with subsequent advantage during recovery of yttrium compounds in the downstream. The greatest extraction of yttrium is obtained by 20% w/v S/L ratio, 4N H(2)SO(4) concentration and 90°C. Yttrium and calcium yields are nearly 85% and 5%, respectively. The analysis of variance shows that acid concentration alone and interaction between acid and pulp density have a significant positive effect on yttrium solubilization for both HCl and H(2)SO(4) medium. Two models are empirically developed to estimate yttrium and calcium concentration during leaching. Precipitation tests demonstrate that at least the stoichiometric amount of oxalic acid is necessary to recover yttrium efficiently and a pure yttrium oxalate n-hydrate can be produced (99% grade). The process is economically feasible if other components of the fluorescent lamps (glass, ferrous and non-ferrous scraps) are recovered after the equipment dismantling and valorized, besides the cost that is usually paid to recycling companies for collection, treatment or final disposal of such fluorescent powders.     

赖氨酸废水的处理和氨回收

对赖氨酸浓废水调 p H沉淀处理后的澄清水进行预处理 :先加入石灰乳 ,搅拌、沉淀 ,SO42 -从 2 0 0 0 0 m g/ L 左右降至 130 0 mg/ L 左右 ,去除率为 94%左右 ,然后进行空气吹脱 ,NH3- N从 5 0 0 0 mg/ L左右降至 80 m g/ L左右 ,去除率 >98%。吹脱出水经厌氧生化处理后 ,再进行空气吹脱 ,NH3- N从 70 0 mg/ L 左右降至 85 mg/ L 左右 ,去除率 >86 %。再吹脱出水与稀废水混合后进行好氧生化和 A/ O、O系统处理 ,出水的 COD<10 0 m g/ L,BOD5<2 0 mg/ L,SS<70 mg/ L,NH3- N<2 5 m g/ L。对浓废水与石灰乳混合后搅拌过程中及两次空气吹脱过程中挥发的 NH3进行回收 ,将其与 H2 SO4反应 ,生成的 (NH4) 2 SO4回用于生产     

磁化水抑垢的研究

通过静态试验研究了Ｃａ＾２＋、Ｍｇ＾２＋的总浓度、碱度、ＰＨ、ＳＯ＾２－４对磁水抑垢效果的影响,得出了应用磁化水抑垢的适宜条件,为磁水器的实际应用提供了依据。     

Adsorption of SO2 and NO from incineration flue gas onto activated carbon fibers

Activated carbon fibers (ACFs) were used to remove SO(2) and NO from incineration flue gas. Three types of ACFs in their origin state and after pretreatment with HNO(3), NaOH, and KOH were investigated. The removal efficiencies of SO(2) and NO were determined experimentally at defined SO(2) and NO concentrations and at temperatures of 150, 200 and 260 degrees C. Experimental results indicated that the removal efficiencies of SO(2) and NO using the original ACFs were <56% and <27%, respectively. All ACFs modified with HNO(3), NaOH, and KOH solution could increase the removal efficiencies of SO(2) and NO. The mesopore volumes and functional groups of ACFs are important in determining the removal of SO(2) and NO. When the mesopore volumes of the ACFs are insufficient for removing SO(2) and NO, the functional groups on the ACFs are not important in determining the removal of SO(2) and NO. On the contrary, the effects of the functional groups on the removal of SO(2) and NO are more important than the mesopore volumes as the amount of mesopores on the ACFs is sufficient to remove SO(2) and NO. Moreover, the removal efficiencies of SO(2) and NO were greatest at 200 degrees C. When the inlet concentration of SO(2) increased to 600ppm, the removal efficiency of SO(2) increased slightly and the removal efficiency of NO decreased.     

活性炭填料塔FeSO4液相催化氧化脱硫

对活性炭及瓷拉西环两种填料用自来水进行脱硫对比实验，证明无论是等宏观表面积还是等填料层高度，活性炭填料的脱硫率均高于瓷拉西环。在活性炭填料塔中进行了FeSO4液相催化氧化脱硫实验，考察了液气比、空塔气速、吸收温度及SO2进口浓度对脱硫率的影响。综合实验结果表明，连续运行500min时，脱硫率及吸收液pH分别稳定在93．5％以上及4．6左右，且两者的变化趋势基本一致。     

Geochemistry of Iron and Sulfur in the Zone of Microbial Sulfate Reduction in Mine Tailings

The cycling of iron and sulfur in mine tailings depends on various chemical and microbial reactions. The present study was undertaken in order to assess the role played by populations of sulfate-reducing bacteria (SRB) on the fate of Fe and SO₄ ^2- in Cu–Zn and Au tailings. Samples were taken along a 50-cm deep profile at all sites and analyzed for SRB populations, solid-phase mineralogy and porewater geochemistry. Results indicated that the Cu–Zn tailings were highly oxidized near the surface, as shown by the very low pH, high redox potential, large concentrations of soluble Cu, Zn and sulfate in the porewaters, and the depletion of pyrite. On the other hand, Au tailings were more pH neutral, slightly anoxic, and showed low concentrations of Fe and SO₄ ^2- in the porewaters and very little pyrite oxidation. SRB populations in the Cu–Zn tailings increased with depth, just below the oxic/anoxic interface and were linked to a decline of sulfate and DOC concentrations around the same depths. However, large concentrations of dissolved Fe were also observed around the same depth intervals. Our results suggest that SRB could be involved in sulfate reduction in the Cu–Zn tailings, because the solubility of sulfate was not controlled by the precipitation of sulfate-rich minerals. However, the presence of soluble Fe in the reduced portion of the tailings was also indicative of the presence of iron reducing bacteria (IRB). These bacteria were not enumerated in the present study, but their co-occurrence with SRB has been reported in the past in similar mining environments. The decline of sulfate and the release of soluble iron into the porewaters were also paralleled by a pH increase and the generation of alkalinity. In the Au tailings, SRB populations were generally constant throughout the depth profile and could not be ascribed to sulfate reduction in the porewaters. The solubilities of sulfate and iron in these tailings were partially controlled by jarosite and Fe-oxide minerals. It is then clear that SRB populations could be recovered from various mining sites, but their activity cannot be ascertained based on microbial enumeration and geochemical data.     

湿法烟气脱硫石膏制备硫酸铵

采用湿法烟气脱硫石膏为原料,与( NH4)2CO3反应,制备(NH4)2SO4.通过X射线衍射仪表征可知:脱硫石膏的主要成分为CaSO4,反应后CaSO4中的Ca2+大部分以CaCO3形式存在于固体沉淀物中,CaCO3粉末平均粒径为80 nm;而原先CaSO4中的不溶性SO2-4则与NH+4结合生成(NH4)2SO4,...