纳米TiO_2-Al_2O_3负载CuMnO_x对甲苯的催化燃烧

研究采用改进的溶胶-凝胶法制备了TiO2-Al2O3复合载体,并用浸渍法制备CuMnOX/TiO2-Al2O3催化剂,通过对甲苯废气催化燃烧的实验,分别考察了Cu-Mn负载量、Cu/Mn摩尔比、焙烧温度及载体对催化剂制备过程及催化剂活性的影响。实验结果表明:活性组分负载量25%,铜锰活性组分的配比Cu:Mn=1:2,焙烧温度500℃是浸渍法制备CuMnOX/TiO2-Al2O3催化剂较佳的工艺条件;XRD衍射图谱表明,500℃下铜锰尖晶石的存在是催化剂催化活性优良的主要原因;由复合载体制备的CuMnOX/TiO2-Al2O3催化剂比单一载体制备的CuMnOX/Al2O3催化剂具有更高的甲苯转化率,其T99比单一载体要低20℃以上。     

生物流化床法处理污泥回流液的影响因素研究

将生物流化床工艺与活性污泥工艺相结合,以市政污水处理厂污泥回流液为研究对像。以0.3～0.45mm活性炭颗粒为载体对生物流化床中微生物进行培养、驯化,挂膜成功后,分别对生物流化床厌氧段和好氧段进行了单因素试验,得出进水的最佳pH值介于7.0～7.5,生物流化床厌氧段的最佳水力停留时间4.4h、最佳碳源为蔗糖,;缺氧段及好氧段的最佳水力停留时间2.69h、8.06h,曝气量0.5mL/min。在最佳工艺参数条件下进行污泥回流液脱氮除磷试验得出,此工艺可使总氮浓度为150.0mg/L,总磷浓度为59.0mg/L的污泥回流液的总氮浓度降低至65.19mg/L,此时的总氮去除率为56.54%;总磷的去除率较低。试验结果表明,该工艺对处理污泥回流液中氮磷具有一定的效果。     

循环流化床干法脱硫除尘一体化工艺去除汞探讨研究

目前,由于人类污染源每年向大气排汞量日益增长,使国际上对汞排放的控制研究成为热点,本文通过理论计算及工程实例说明了循环流化床干法烟气脱硫除尘一体化工艺系统可以有效地控制燃煤电厂汞的排放。     

Effectiveness of fluidized pellet bed for removing soluble contaminants

Fluidized pellet bed (FPB) has been successfully applied in water and wastewater treatment. However, the removal mechanism of contaminants especially the soluble ones, is still unclear. This study aimed to evaluate the e ectiveness of FPB reactor for removing soluble contaminants from synthetic wastewater. By only coagulation through jar test operation with addition of polyaluminium chloride (PACl) as primary coagulant and polyacryamide (PAM) as coagulant-aid, the removals of soluble chemical oxygen demand (COD), total phosphorus (TP), and NH4 +-N were found to be only 2.2%–7.5%, 5.7%–25.5%, and 9.9%–18.5%, respectively. However, by FPB operation under the same dosage of coagulants, these values increased to 82.7%, 37.2%, and 50%, indicating that the formation of pellets in the FPB e ectively enhanced the removal of soluble contaminants. By careful comparison of the settleablility and filterability of the pollutants after coagulation, the originally soluble contaminants could be divided into three groups, namely: (1) coagulated-andsettleable, (2) coagulated-but-nonsettleable, and (3) uncoagulable. It was found that not only the first two groups but also a large part of the third group could be e ectively removed by FPB operation. However, the mechanism for the removal of the uncoagulable pollutants by FPB operation still needs further investigation.     

纳米催化剂Pd/SnO_2的制备及催化还原硝酸盐反应的调控

采用热分解法制备了SnO2载体,并用浸渍法制备了Pd/SnO2催化剂.同时,采用X射线衍射仪(XRD)、透射电镜(TEM)、扫描电镜(SEM)及BET比表面积仪等对所制载体和催化剂材料进行了分析表征.结果表明,热分解法和浸渍法都能够获得纳米材料,SnO2及Pd/SnO2的粒径均在9～10nm左右,比表面积分别达到144.99m·2g-1和147.36m·2g-1.在以甲酸为还原剂的Pd/SnO2催化还原硝酸盐体系中,在Pd与SnO2负载比为2%～7%,反应温度为20～50℃和甲酸投加量4.0～24.0mmol·L-1的条件下,催化活性为0.70～9.48mg·min-·1g-1,且催化活性随着负载比、温度和甲酸投加量的增大而增大,随着pH的升高先升后降,最佳pH为3.反应温度升高及pH降低都能够提高Pd/SnO2的选择性.甲酸-Pd/SnO2催化还原硝酸盐体系中还原反应的调控策略为:反应温度宜控制在40～50℃内,这样可同时获得较高的催化活性和选择性,温度过高对催化活性和选择性影响很小,温度过低则会同时降低催化活性和选择性;控制pH为3时,可以获得最大的催化活性及较好的选择性,pH升高会降低Pd/SnO2的催化活性和选择性,pH降低会导致催化活性迅速降低,但对选择性影响不大;甲酸与硝酸盐的物质的量比宜大于4:1,此时可以有效地抑制pH的上升,同时获得较高的催化活性和选择性,甲酸与硝酸盐的物质的量比小于4:1时,会同时降低Pd/SnO2的催化活性和选择性.     

Catalytic performance of Fe3O4-CoO/Al2O3 catalyst in ozonation of 2-(2,4-dichlorophenoxy)propionic acid, nitrobenzene and oxalic acid in water

Fe3O4-CoO/Al2O3 catalyst was prepared by incipient wetness impregnation using Fe(NO3) 3·9H2O and Co(NO3) 2·6H2O as the precursors,and its catalytic performance was investigated in ozonation of 2-(2,4-dichlorophenoxy) propionic acid(2,4-DP) ,nitrobenzene and oxalic acid.The experimental results indicated that Fe3O4-CoO/Al2O3 catalyst enabled an interesting improvement of ozonation eciency during the degradation of each organic pollutant,and the Fe3O4-CoO/Al2O3 catalytic ozonation system followed a radical-type mechanism.The kinetics of ozonation alone and Fe3O4-CoO/Al2O3 catalytic ozonation of three organic pollutants in aqueous solution were discussed under the mere consideration of direct ozone reaction and OH radical reaction to well investigate its performance.In the catalytic ozonation of 2,4-DP,the apparent reaction rate constants(k) were determined to be 1.456×10-2 min-1 for ozonation alone and 4.740×10-2 min-1 for O3/Fe3O4-CoO/Al2O3.And O3/Fe3O4-CoO/Al2O3 had a larger Rct(6.614×10-9) calculated by the relative method than O3 did(1.800×10-9) ,showing O3/Fe3O4-CoO/Al2O3 generated more hydroxyl radical.Similar results were also obtained in the catalytic ozonation of nitrobenzene and oxalic acid.The above results demonstrated that the catalytic performance of Fe3O4-CoO/Al2O3 in ozonation of studied organic substance was universal to a certain degree.     

反相流动注射催化动力学分光光度法测定海水中的痕量Cu

在弱碱性的介质中,Cu能够对H2O2氧化对苯二酚的反应起到明显的催化作用,反应产物在500 nm波长处有最大吸收峰.据此,发展了一种反相流动注射催化动力学分光光度法测定海水痕量Cu的新方法.在最佳条件下,Cu2+的浓度在0～40 μg/L具有良好的线性关系,相关系数0.9993,检出限为0.2 μg/L,回收率为98.7%～104.2%,用5 μg/L标准溶液进样的相对标准偏差为1.03%(n=10).     

臭氧及催化臭氧化降解2,4-滴丙酸动力学研究

对臭氧及催化臭氧氧化降解2,4-滴丙酸(DCPP)的效率进行了研究,并利用竞争动力学法算得了DCPP与臭氧及羟基自由基的反应速率常数,参比有机物为硝基苯(NB).结果表明,DCPP与臭氧的反应速率常数K-DCPP为(0.733±0.163)L·mol-1·s-1,与羟基自由基的kOH-DCPP为2.367×109L·mol-1·s-1.在单独臭氧和Mn(Ⅱ)催化臭氧化降解DCPP过程中,基于上述结果计算所得的速率常数与实际所测的表观反应速率常数具有较好的吻合度.以上结果对臭氧化处理含DCPP废水具有很好的理论指导意义.     

生物质热解焦油脱除方法研究进展

生物质热解焦油的产生不仅降低了热解效率,影响设备运行,更危害着人类健康。通过介绍生物质热解焦油的特性及危害、对比分析目前各种不同除焦方法(文丘里法、旋风分离法、电捕焦法、高温裂解法和催化裂解法)的特点及应用前景,得出采用多种方法组合的形式进行联合除焦可显著提高焦油脱除效率。寻找用于湿法除焦的可再生利用的有机溶剂,开发经济、高效、长寿命的催化剂将成为生物质热解焦油脱除技术开发的重点。     

流化床富氧焚烧含油污泥技术经济性分析

介绍了流化床富氧焚烧含油污泥技术的流程和优势,计算了富氧焚烧含油污泥系统主要设备的电耗和技术经济指标。流化床富氧焚烧含油污泥技术可实现烟气及其他污染物零排放,产生的蒸汽可直接供应油田生产和生活使用,产生的液态CO2可直接用于油井驱油,烟气中的SO2和NOx可转化为硫酸和硝酸。采用日处理200 t含油污泥的流化床锅炉年处理含油污泥量约73 kt,每年减少排污费7 300万元;锅炉年产蒸汽量约177 kt,每年节约蒸汽费用1 380.6万元,合计每年节约成本8 680.6万元。回收得到质量分数为40%的稀硫酸5.56 t/d,质量分数为37%的硝酸0.708 t/d,年回收CO2约99 kt。