NaClO2海水溶液强化烟气脱硝效果的实验研究

海水中富含多种盐类,具有一定碱性,是天然的缓冲剂,在脱硫脱硝方面具有良好的应用前景.利用不同浓度的NaClO_2溶液进行废气循环喷淋脱硝实验.结果表明,NaClO_2模拟海水溶液与NaClO_2淡水溶液都能将NO完全脱除,且当NO完全被脱除时,模拟海水溶液的持续时间比淡水溶液更长,模拟海水中所含有的少量HCO_3~-和OH~-是造成这种差异的主要原因.滴定实验结果显示0.066 mmol的HCl就可使NaClO_2淡水溶液的pH值降到7,而NaClO_2模拟海水溶液的pH值降到7需要0.114 mmol的HCl;在循环喷淋脱硝过程中NaClO_2模拟海水溶液的pH值基本维持在7以上.离子色谱检测结果显示脱硝后溶液中主要阴离子为Cl~-和NO_3~-.基于质量平衡计算结果,当NaClO_2浓度为20 mmol·L~(-1)时,在脱硝过程中淡水溶液中NaClO_2的利用率为56%,而模拟海水溶液中NaClO_2的利用率可达67.25%,提高幅度为20.1%.     

电-Fenton法降解低含盐量反渗透浓缩液中腐植酸

为研究采用碳毡-Pt电-Fenton体系处理模拟低含盐量反渗透浓缩液中的腐植酸的影响因素和降解机制,通过单因素试验,以COD_Cr去除率为评价指标,以Fe2+添加量、通氧量、电流密度、pH为考察因素,探讨了不同条件对电-Fenton体系ρ（H₂O₂）和COD_Cr去除率的影响.结果表明:采用电-Fenton法降解模拟反渗透浓缩液,较低的含盐量有助于COD_Cr的去除,与高含盐量（1 000~2 000 mg/L）相比,在低含盐量（500~1 000 mg/L）条件下COD_Cr去除率提高10%~20%;并且最佳条件下实际电流效率（GCE）达到15.6%,电化学能耗为32 kW·h/kg.最佳反应条件:通氧量为0.3 m3/L,Fe2+添加量为0.1 mmol/L,电流密度为3.5 mA/cm2,pH=3,在该条件下反应180 min时,电-Fenton体系产生的ρ（H₂O₂）为105 mg/L,可使ρ（COD_Cr）由150 mg/L降至16 mg/L,COD_Cr去除率达到90%.研究显示,较宽的pH范围（3~7）内碳毡-Pt电-Fenton体系对腐植酸的降解表现稳定,COD_Cr去除率均达到60%以上.      

钛基修饰电极催化电解去除水中硝酸盐氮的研究

利用热分解法制备CuO修饰Ti基阴极和SnO2-Sb2O5修饰Ti基阳极,组成无隔膜电解体系,以模拟废水(NO3--N 50mg/L)为对象,进行了水中NO3--N去除实验研究.结果数据表明,CuO修饰Ti基阴极对水中NO3--N的去除率随电流密度、极板间距、搅拌强度和电解时间增加而增加,在电流密度10mA/cm2、极板间距9mm、中等搅拌强度下电解150min,NO3--N催化还原去除率可达93.8%.Cl-支持电解可使NO3--N催化还原产物NH4+-N氧化为N2-N去除.在电流密度10mA/cm2、极板间距9mm、NaCl添加量600mg/L、中等搅拌强度下电解120min后,NO3--N和TN的去除率达到89.3%和86.9%,NO2--N和NH4+-N未检出.分析认为NO3--N还原机制为NOx中O被阴极表面Cu吸附固定,N—O键受氢攻击破坏,逐步还原.阳极电解Cl-生成HOCl,HOCl氧化NH4+-N成N2-N.     

IC＋A/O＋BIOFOR处理高浓度有机废水工程实例

江西某生物化工有限公司在生产乳酸的过程中产生大量高浓度有机废水,采用IC＋A/O＋BIOFOR联合工艺进行处理。当进水ρ（COD）平均为5 483 mg/L,ρ（NH3-N）平均为97.83 mg/L时,出水ρ（COD）平均为84 mg/L,去除率达98%;出水ρ（NH3-N）平均为12.07 mg/L,去除率为88%...     

亚氯酸钠溶液烟气脱硝与烟气余热回收的一体化试验

锅炉烟气中的NO_x是大气污染的重要原因之一.针对燃气锅炉NO_x超低排放的要求以及烟气中大量余热被浪费的现状,提出了烟气脱硝与余热回收一体化的新方法,通过搭建一体化试验台,分析在烟气余热回收的条件下,c[NaClO₂（亚氯酸钠）]、液气比、喷淋水温度等因素对脱硝效率以及烟气余热回收效率的影响.烟气脱硝与余热回收一体化的新方法主要体现在逆流式烟气喷淋塔中,可利用NaClO₂溶液对低φ（NO_x）的烟气脱硝并同时回收烟气余热.试验结果表明,c（NaClO₂）越高、pH越低、液气比越大,NaClO₂溶液脱硝率越高.当c（NaClO₂）为0.020 0 mol/L、喷淋水温度在30~80℃之间变化时,存在最优的喷淋水温度64℃,使脱硝率最高为36%.同时,液气比及喷淋水温度对余热回收效果影响显著,液气比越大、喷淋水温度越低,余热回收效果越好.试验结果还显示了当烟气温度为83℃、喷淋水温度为48℃、c（NaClO₂）为0.015 0~0.020 0 mol/L、液气比为13.8 L/m3时,烟气脱硝效率约为40%,同时回收了26.4 kW的烟气余热.研究显示,在逆流式烟气喷淋塔中,利用NaClO₂溶液进行烟气脱硝并同时回收烟气余热的一体化方法是可行的,可应用于工程实践.      

电解浮选用于活性污泥固液分离的研究

在装有Ti/RuO₂-IrO₂-TiO₂阳极、Ti阴极的电解浮选槽中进行了活性污泥固液分离的研究.考察了影响电解浮选性能的操作参数,这些参数包括水力停留时间、电流密度、进水SS浓度和进水pH值.研究表明,电解浮选是高效的固液分离单元,水力停留时间和电流密度是主要的影响因素.SS的去除率随着水力停留时间和电流密度的增加而增大;污泥负荷增加,SS的去除率下降;pH值影响电解产生微气泡的尺寸和污泥性质,但对SS的去除影响不大,实际应用中可以不调节pH值.进水SS约1 000mg/L时,当水力停留时间为20min,接触室电流密度为5 mA/cm²,分离区电流密度为2.5 mA/cm²,SS的去除率可达97%以上,此时的能耗为0.4～0.5(kW.h)/m³废水.电解浮选产生的浮渣含水率为95.9%,低于溶气气浮和二沉池的污泥含水率,对污泥减量化及其最终处置有较大的意义.     

铁碳催化内电解-A/O工艺处理印刷线路板综合废水

针对印刷线路板综合废水p H低,Cu、Ni、氨氮含量高等特点,采用铁碳催化内电解结合A/O组合工艺进行废水处理。最佳条件下,一级催化内电解对总铜去除率可达99.6%,由179.7 mg/L降低至0.71 mg/L;对总镍去除率为62.7%,由0.83 mg/L降至0.31 mg/L。二级催化内电解对总铜去除率达96.3%,降低至0.026 mg/L;对总镍去除率达92.6%,降低至0.023 mg/L。两级铁碳内电解对COD和TP去除率为53.3%和91.2%。经过A/O系统处理后,最终出水ρ(COD)<44 mg/L、ρ(TP)<0.21 mg/L、ρ(TN)<14 mg/L、ρ(NH+4-N)<1.6 mg/L、ρ(总铜)<0.02 mg/L、ρ(总镍)<0.016 mg/L,可达到GB 18918—2002《城镇污水处理厂污染物排放标准》一级A标准。     

工业燃煤锅炉烟气循环方式下飞灰的汞吸附特性

为探究燃煤锅炉烟气循环方式下飞灰汞的吸附特性,利用固定床汞吸附装置,对立式煤粉沉降炉不同模拟烟气循环工况条件下形成的飞灰汞吸附特性进行了研究,重点考察了烟气循环比例、煤种、关键燃烧气体组分等因素的影响.结果表明:①烟气循环工况条件下形成的飞灰汞吸附能力明显优于非烟气循环工况（空气燃烧）条件下形成的飞灰,并且随烟气循环比例的增加,飞灰汞吸附量呈逐渐增加趋势.褐煤在净烟气循环比例为60%、40%、20%的条件下形成的飞灰汞吸附量分别是非烟气循环条件下的3.0、2.3和1.6倍.②烟气循环引起燃烧气体氛围中ρ（SO₂）与ρ（NO）的变化会影响飞灰的物化特性及其汞吸附性能.随燃烧氛围中ρ（SO₂）的提高,飞灰汞吸附量先增后减.烟气循环比例为40%且燃烧气体氛围中ρ（NO）为803 mg/m3条件下,ρ（SO₂）为2 857 mg/m3时褐煤与烟煤燃烧形成的飞灰汞吸附量较高（分别为0.45和0.75 μg/g）,分别较ρ（SO₂）为1 428和4 286 mg/m3时提高了25%~300%和53%~78%.随燃烧氛围中ρ（NO）的提高,飞灰汞吸附量呈逐渐增加趋势.烟气循环比例为40%且燃烧气体氛围中ρ（SO₂）为2 857 mg/m3条件下,ρ（NO）为1 205 mg/m3时褐煤和烟煤燃烧形成的飞灰汞吸附量较高,分别较ρ（NO）为803和402 mg/m3时提高了1.2~3.6和1.1~1.6倍.③飞灰中UBC（未燃尽碳）、CaO、MgO及Fe₂O₃可促进飞灰对汞的吸附.与褐煤飞灰相比,烟煤飞灰表现出更优的汞吸附性能,与UBC、CaO、MgO及Fe₂O₃在飞灰中的含量存在一定的正相关性.研究显示,烟气循环方式下飞灰汞吸附特性发生明显变化,煤质的合理选择、烟气循环比例、循环气体成分及浓度参数的优化控制可显著改善燃煤锅炉烟气中汞的排放控制效果.      

三级生物膜工艺处理水产养殖循环水

采用三级生物膜工艺处理水产养殖循环水,并对该工艺去除模拟水产养殖循环水主要污染物的作用进行了研究.结果表明:在进水pH为7.5～8.5,温度为28～32 ℃,ρ（DO）为0.5～1.0 　mg/L,ρ（FA）为5～10 　mg/L时,水产养殖循环水的COD_Cr,NH₄+-N和TN的平均去除率分别为94.4%,91.6%和70.1%,ρ（NO₂--N）平均值小于5.2 　mg/L.说明三级生物膜工艺可用于低ρ（C）/ρ（N）比水产养殖循环水的生物处理,尤其可消除NO₂--N对水产养殖动物的潜在威胁,并达到养鱼回用标准.      

气体扩散电极制备及其对苯酚降解效果的研究

以质量比9∶1的活性炭和乙炔黑制备气体扩散电极,着重研究电流密度、pH值、曝气量等因素对H2O2产生量的影响.结果表明:pH值在较大范围内均适用;电流密度控制在50～75 mA/cm2,曝气量确定为5 L/min时,反应产生H2O2较多.另外,利用该气体扩散电极做阴极,石墨电极做阳极,以Na2SO4为电解质,研究了电解时间、电流密度、pH值、初始苯酚浓度、曝气量等因素对苯酚降解效果的影响.结果表明:在电流密度为75 mA/cm2、曝气量为5 L/min、初始pH=3的条件下,当苯酚的初始浓度为80 mg/L时,1 h后其去除率达77%.     

凹凸棒石催化氧化脱除柴油机尾气中的NOx

采用反应吸收法实验研究了天然凹凸棒石黏土、水和氢氧化钠等制备成的吸收液脱除柴油机尾气中氮氧化物(NOx)的特性.在吸收液的作用下,尾气中的NO经催化氧化和碱中和联合吸收过程而脱除.凹凸棒石黏土经稀土改性,可增强NOx的脱除效果.考察了吸收液的pH值、温度和稀土加入量等因素对NOx脱除效率的影响,并对其脱除机理进行了探讨.在最佳实验条件下,NOx脱除效率达90.6%.气相阻力为3.5kPa.     

Mass transfer in the absorption of SO2 and NOx using aqueous euchlorine scrubbing solution

Attempts have been made to generate euchlorine gas by chlorate-chloride process and to utilize it further to clean up SO2 and NOx from the flue gas in a lab scale bubbling reactor.Preliminary experiments were carried out to determine the gas and liquid phase mass transfer coefficients and their correlation equations have been established.Simultaneous removal of SO2 and NOx from the simulated flue gas using aqueous euchlorine scrubbing solution has been investigated.Euchlorine oxidized NO into NO2 completely and the later subsequently absorbed into the scrubbing solution in the form of nitrate.SO2 removal efficiency of around 100% and NOx removal efficiency of around 72 % were achieved under optimized conditions.Mass balance has been confirmed by analyzing the sulfate, nitrate, euchlorine and chloride ion using ion chromatograph/auto-titrator and comparing it with their corresponding calculated values.     

Simultaneous removing SO2 and NO by a new system containing cobalt complex

Absorption and catalytic oxidation of nitric oxide can be achieved by using cobalt（Ⅲ） ethylenediamine （Co（en）3^3＋. When simultaneous absorbing SO2 and NO, the precipitation of Co2（SO3）3 will be yielded and the NO removal will be decreased. A new catalyst system using Co（en）3^3＋ coupled with urea has been developed to simultaneous remove NO and SO2 in the flue gas. NO is absorbed and catalytically oxidized to nitrite and nitrate by Co（en）3^3＋. The dissolved oxygen in scrubbing solution from the feed stream acts as oxidant. Urea restrains the precipitation of Co2（SO3）3 by oxidizing SO3^2-to SO4^2- as COSO4 is more soluble in water. The experimental results proved that nearly all SO3^2- can be oxidized to SO4^2- and the high NO and SO2 removal could be obtained with the new system. The NO removal is influenced by gas flow rate, the concentration of Co（en）3^3＋ and urea in the absorption solution, the temperature of the scrubbing solution and the content of oxygen in the flue gas. The low gas flow rate is favorable to increase the NO removal. The experiments proved that the NO removal could be maintained at more than 95% by the system of 0.02 mol/L Co（en）3^3＋ and 1% urea at 50℃ with 10% O2 in the flue gas.     

蒸汽相变促进WFGD系统脱除PM_(2.5)的协同作用分析

蒸汽相变作为预处理措施能显著提高常规除尘设备对PM2.5细颗粒的脱除效率,但对于水汽含量低的原始燃煤烟气蒸汽耗量太大,限制了工程应用,而在燃煤电厂湿法烟气脱硫(WFGD)过程中,烟气降温增湿,再添加少量蒸汽就可以建立PM2.5凝结长大所需要的过饱和环境,进而实现WFGD系统对PM2.5的协同高效脱除。在分析蒸汽相变促进PM2.5脱除影响因素的基础上,结合湿法脱硫过程传热传质特性,定性分析了脱硫塔塔前、塔内和塔出口添加蒸汽对WFGD系统脱除PM2.5的促进作用,并提出具体工艺方案。     

煤浆催化氧化法烟气脱硫研究

基于液相催化氧化原理,以煤浆做洗涤介质进行烟气脱硫。此法起催化作用的Fe2+/Fe3+离子通过SO2、O2和煤中的黄铁矿作用而现场产生。实验过程控制模拟烟气中的SO2摩尔分率和O2浓度范围分别为760×10-6￣3200×10-6和3%￣20%。实验表明,反应温度约在40℃以上时,脱硫率即达90%以上。二氧化硫浓度增大,脱硫率呈下降趋势,与石灰/石灰石脱硫过程类似。在实验范围内,pH值和氧气浓度对脱硫率基本没有影响,实际烟气中的O2浓度完全满足催化氧化反应的需要。随烟气脱硫过程的进行,脱硫浆液中的总铁含量不断增加,说明煤中黄铁矿被不断浸出,故此法在脱除烟气中的二氧化硫的同时也降低了煤中的黄铁矿硫。     

烧结烟气湿式氨法同时脱硫脱硝实验研究

在鼓泡反应器中进行烧结烟气湿式氨法同时脱硫脱硝的实验研究,考察了添加剂/NO物质的量比、吸收液NH3-NH+4浓度和烟气性质对烧结烟气脱硫脱硝的影响。实验结果表明:随着添加剂/NO物质的量比、烟气温度和NO浓度的增加,脱硝率均呈现先增大后减小的趋势。脱硝率随着吸收液中NH3-NH+4浓度的增大而增大。随着SO2浓度的增大,脱硝率逐渐减小。在所有实验条件下,脱硫率均接近或达到100%。在最佳实验条件下,脱硝率可达61.49%。通过添加添加剂部分氧化烧结烟气,可使烧结烟气湿式氨法脱硫工艺的脱硝率提高20%~30%。     

Review on the NO removal from flue gas by oxidation methods

Due to the increasingly strict emission standards of NOx on various industries, many traditional flue gas treatment methods have been gradually improved. Except for selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) methods to remove NOx from flue gas, theoxidation method is paying more attention to NOx removal now because of the potential to simultaneously remove multiple pollutants from flue gas. This paper summarizes the efficiency, reaction conditions, effect factors, and reaction mechanism of NO oxidation from the aspects of liquid-phase oxidation, gas-phase oxidation, plasma technology, and catalytic oxidation. The effects of free radicals and active components of catalysts on NO oxidation and the combination of various oxidation methods are discussed in detail. The advantages and disadvantages of different oxidation methods are summarized, and the suggestions for future research on NO oxidation are put forward at the end. The review on the NO removal by oxidation methods can provide new ideas for future studies on the NO removal from flue gas.     

Removal of nitric oxide from simulated flue gas via denitrification in a hollow-fiber membrane bioreactor

A hollow-fiber membrane bioreactor(HMBR) was studied for its ability to treat nitric oxide(NO) from simulated flue gas. The HMBR was operated for 9 months and showed a maximum elimination capacity of 702 mg NO/(m2·day) with a removal efciency of 86%(gas residence time of 30 sec, inlet NO concentration of 2680 mg/m3, pH 8). Varying operation parameters were tested to determine the stability and response of the HMBR. Both the inlet NO concentration and gas residence time influenced the removal of NO in the HMBR. NO elimination capacity increased with an increase in inlet NO concentration or a shortening of gas residence time. Higher removal efciency of NO was obtained at a longer gas residence time or a lower inlet NO concentration. Microbial communities of the HMBR were sensitive to the variation in pH value and alkalescence corresponding to an optimum pH value of 8. In addition, NO elimination capacity and removal efciency were inversely proportional to the inlet oxygen concentration. Sulfur dioxide had no great influence on elimination capacity and removal efciency of NO. Product analysis was performed to study N2O and N2 production and confirmed that the majority of the microorganisms were denitrifying bacteria in the HMBR. Compared to other bioreactors treating NO, this study showed that the denitrifying HMBR was a good option for the removal of NO.     

Fe2+EDTA络合-铁屑还原连续脱除烟气中NO

研究了铁屑塔式反应器连续脱除烟气中NO的过程,建立了该过程的数学模型,并对其主要影响因素进行了讨论.结果表明,铁屑塔式反应器可连续稳定地脱除烟气中NO,进气NO浓度的变化对脱硝效率没有影响,脱硝效率随烟气流量的增加而下降,随脱硝溶液流量和填料层高度的增加而增加.所建模型的计算值和实测值能够很好地吻合,该模型可用于预测脱硝过程参数对脱硝效率的影响.