共查询到12条相似文献,搜索用时 62 毫秒
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生物质吸附剂处理活性艳红X-3B废水 总被引:2,自引:0,他引:2
采用城市污水处理厂二沉池的剩余活性污泥为原料,以浓度为3mol/L的ZnCl2溶液浸泡污泥,采用水蒸气为活化气和保护气,在600℃下活化污泥3h,制备出性能良好的生物质吸附剂,其碘吸附值为388.95mg/g,比表面积为447.79m^2/g,平均孔径为4.39nm,孔体积为0.31cm^3/g,微孔体积为0.09cm^3/g。实验结果表明,用该生物质吸附剂处理活性艳红X-3B废水,在废水(10mL)中活性艳红X-3B质量浓度为300mg/L、生物质吸附剂加入量为0.20g、吸附时间为30min的条件下,废水脱色率可达99.7%。活性艳红X-3B在生物质吸附剂上的吸附行为遵循Lagergren二级动力学规律,同时也可用一级吸附动力学方程描述。 相似文献
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微波无极紫外光催化-内电解协同降解活性艳红X-3B 总被引:5,自引:1,他引:4
采用微波无极紫外光源,以活性炭作为光催化剂TiO2的载体,与外加铁屑构成内电解反应,处理活性艳红X-3B模拟废水.实验结果表明,微波无极紫外光催化-内电解法对活性艳红X-3B的降解速率是微波无极紫外光催化和微波-内电解法单独作用时降解速率之和的2倍.在活性艳红X-3B模拟废水初始pH为7、空气曝气量为0.50 L/min、铁屑加入量为5 g/L、反应温度为40~45℃的最佳条件下,微波无极紫外光催化-内电解法的活性艳红X-3B模拟废水色度去除率达100%,TOC和可吸附有机卤化物的去除率分别为69.5%和81.8%. 相似文献
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用水解酸化池-膜生物反应器处理活性艳红X-3B废水 总被引:1,自引:0,他引:1
采用水解酸化池-膜生物反应器处理含活性艳红X-3B的模拟废水,研究了水力停留时间(HRT)对水解酸化池废水处理效果的影响,考察了水解酸化池-膜生物反应器对废水的处理效果及膜生物反应器中污泥沉降性能对膜污染的影响。实验结果表明:水解酸化池HRT为16h时,废水的可生化性最好,挥发性脂肪酸质量浓度与COD比值为0.5;HRT为17h时,废水脱色率达69%,而COD的去除率受HRT影响较小;膜生物反应器主要起去除废水中COD的作用;水解酸化池-膜生物反应器处理后废水的脱色率和COD去除率分别为83%和97%;膜生物反应器中活性污泥沉降性能的变化直接影响膜污染的速率。 相似文献
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以粉煤灰为原料,采用碱熔融-水热法制备了3种沸石分子筛,运用XRD、XRF、SEM和BET等手段进行了表征,并将分子筛用于吸附溶液中的氨氮,考察了影响氨氮吸附效果的主要因素、氨氮等温吸附特征和吸附动力学特征。结果表明:分子筛B(Na20.8Al23Si36O117·7.69 H2O)对氨氮的吸附效果最佳,在初始氨氮质量浓度100 mg/L、分子筛B加入量2 g/L、初始溶液pH 7、吸附温度25℃、转速150 r/min的条件下,吸附60 min后,氨氮吸附量和去除率分别为40.61 mg/g和90%;4种阳离子对氨氮吸附效果的影响顺序依次为K+>Ca2+>Na+>Mg2+;分子筛B对氨氮的吸附为单分子层吸附,具有化学吸附的特征;分子筛B吸附氨氮的的最佳工艺条件为初始溶液pH 7、吸附温度45℃、初始氨氮质量浓度40 mg/L,在该条件下,氨氮去除率为93%。 相似文献
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采用粉煤灰作为吸附混凝剂,研究了粉煤灰对废水中阴离子表面活性剂十二烷基磺酸钠(SDS)的去除及机理。分析了粉煤灰投加量、吸附时间、pH值对废水中SDS去除率的影响,探讨了最佳条件下废水中SDS去除率,研究了粉煤灰动力学特征。结果表明,在200mL浓度50mg/L的SDS溶液中,调节pH值为13,加入70 g粉煤灰,搅拌20m in后,SDS的去除率为83.3%。粉煤灰对SDS的吸附符合Freund lich吸附等温式。 相似文献
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Katsuya Nakayama Kuchar Dalibor Keisuke Sakai Mitsuhiro Kubota Hitoki Matsuda 《Journal of Material Cycles and Waste Management》2008,10(2):102-109
The present work focuses on investigation of the effective recovery of heavy metals from molten fly ash by applying chloride-induced
volatilization. In particular, the effect of unburned carbon on the chloride-induced volatilization of lead, zinc, and copper
from model and real molten fly ashes was investigated in the temperature range 873–1173 K under a N2 atmosphere. As a result, almost 100% of lead and a significant proportion of zinc were volatilized from the real molten fly
ash samples at 1173 K. In contrast, for the model fly ash, volatilization ratios of lead and zinc at 1173 K were only 85%
and 25%, respectively. Further, the results of X-ray diffraction analysis suggested that PbO in molten fly ash was converted
either to Pb2OCl2 or Pb by respective chlorination and reduction reactions. Meanwhile ZnO and CuO in the molten fly ash were reduced to Zn
and Cu by reaction with unburned carbon. Subsequently, Pb, Zn, and Pb2OCl2 were volatilized, but Cu remained in the solid residue. Finally, the volatilization ratio of zinc increased with the addition
of carbon, and more than 98% of zinc was volatilized at 1173 K from a fly ash with a carbon content of 20%. 相似文献