Study on the denitrification performance of FexLayOz/activated coke for NH3-SCR and the effect of CO escaped from activated coke at mid-high temperature on catalytic activity

Currently, activated coke is widely used in the removal of multiple pollutants from industrial flue gas. In this paper, a series of novel Fe_xLa_yO_z/AC catalysts was prepared by the incipient wetness impregnation for NH₃-SCR denitrification reaction. The introduction of Fe-La bimetal oxides significantly improved the denitrification performance of activated coke at mid-high temperature, and 4% Fe_0.3La_0.7O_1.5/AC exhibited a superior NO_x conversion efficiency of 90.1% at 400 °C. The catalysts were further characterized by BET, SEM, XRD, Raman, EPR, XPS, FTIR, NH₃-TPD, H₂-TPR, et al., whose results showed that the perovskite-type oxide of LaFeO₃ and oxygen vacancies were produced on the catalysts’ surfaces during roasting. Fe-La doping enhanced the amount of acid sites (mainly Lewis and other stronger acid sites) and the content of multifarious oxygen species, which were beneficial for NO_x removal at mid-high temperature. Moreover, it was investigated that the effect of released CO from activated coke at mid-high temperature on the NO_x removal through the lifetime test, in which it was found that a large amount of CO produced by pyrolysis of activated coke could promote the NO_x removal, and long-term escaping of CO on the activated coke carrier did not have a significant negative impact on catalytic performance. The results of the TG-IR test showed that volatile matter is released from the activated coke while TG results showed that the weight loss rate of 4% Fe_0.3La_0.7O_1.5/AC only was 0.0015~0.007%/min at 300–400 °C. Hence, 4% Fe_0.3La_0.7O_1.5/AC had excellent thermal stability and denitrification performance to be continuously used at mid-high temperature. Finally, the mechanisms were proposed on the basis of experiments and characterization results.

     

CWPO体系中污泥炭催化降解头孢氨苄废水

通过加入正丁醇以共沸蒸馏法对剩余污泥进行脱水,再对污泥进行干燥、焙烧和改性得到污泥炭催化剂.将污泥炭催化剂用于催化湿式过氧化氢氧化体系,处理头孢氨苄废水.采用响应面法中的中心组合设计实验,考察反应温度、初始pH和过氧化氢投加量对TOC降解率的影响,反应温度和过氧化氢投加量具有显著交互作用.在最佳实验条件下(T=50℃、pH=3.00、H_2O_2=0.071 mol·L~(-1)),TOC去除率为59%,接近预测的TOC去除率(60%),在95%的置信区间内,说明该模型可靠.SEM、TEM、TPD-MS、XPS和FT-IR等分析结果表明污泥炭表面存在纳米尺寸片状结构,这种结构中存在酚羟基、羰基、羧基等活性官能团和醌类结构,且ICP-OES、EDAX和~(57)Fe穆斯堡尔谱等分析结果表明,污泥炭中含有不同价态的Fe,能有效地催化过氧化氢分解,将头孢氨苄转化为苯甲酸、丁二酮等小分子物质,再进一步完全氧化.     

畜禽环境中抗生素的去除及其风险评估

抗生素作为饲料添加剂广泛应用于畜禽养殖业,造成养殖环境抗生素大量蓄积,尤其是在畜禽粪便中,长期的积累不仅污染养殖场内土壤环境,残留的抗生素还会随畜禽粪便进入周边水体及农田环境,威胁农作物及人体健康。目前,国内相关研究主要集中在抗生素的降解工艺及降解规律方面,而对其去除效率的影响因素及风险评价研究相对较少。笔者综述了国内外抗生素的降解转化及去除方式等的研究进展,并概述了抗生素在畜禽环境中的生态风险评估的研究现状,为抗生素的高效去除、风险预估及畜禽粪便资源化安全利用提供理论基础和技术支撑。     

Catalytic oxidation of CO over Pt/Fe3O4 catalysts: Tuning O2 activation and CO adsorption

• Strong metal-support interaction exists on Pt/Fe₃O₄ catalysts. • Pt metal particles facilitate the formation of oxygen vacancies on Fe₃O₄. • Fe₃O₄ supports enhance the strength of CO adsorption on Pt metal particles. The self-inhibition behavior due to CO poisoning on Pt metal particles strongly impairs the performance of CO oxidation. It is an effective method to use reducible metal oxides for supporting Pt metal particles to avoid self-inhibition and to improve catalytic performance. In this work, we used in situ reductions of chloroplatinic acid on commercial Fe₃O₄ powder to prepare heterogeneous-structured Pt/Fe₃O₄ catalysts in the solution of ethylene glycol. The heterogeneous Pt/Fe₃O₄ catalysts achieved a better catalytic performance of CO oxidation compared with the Fe₃O₄ powder. The temperatures of 50% and 90% CO conversion were achieved above 260°C and 290°C at Pt/Fe₃O₄, respectively. However, they are accomplished on Fe₃O₄ at temperatures higher than 310°C. XRD, XPS, and H₂-TPR results confirmed that the metallic Pt atoms have a strong synergistic interaction with the Fe₃O₄ supports. TGA results and transient DRIFTS results proved that the Pt metal particles facilitate the release of lattice oxygen and the formation of oxygen vacancies on Fe₃O₄. The combined results of O₂-TPD and DRIFTS indicated that the activation step of oxygen molecules at surface oxygen vacancies could potentially be the rate-determining step of the catalytic CO oxidation at Pt/Fe₃O₄ catalysts. The reaction pathway involves a Pt-assisted Mars-van Krevelen (MvK) mechanism.     

N2O profiles in the enhanced CANON process via long-term N2H4 addition: minimized N2O production and the influence of exogenous N2H4 on N2O sources

Environmental Science and Pollution Research - Production of the greenhouse gas nitrous oxide (N2O) from the completely autotrophic nitrogen removal over nitrite (CANON) process is of growing...     

氯自由基介导的BDD电极选择性氧化脱氮

为实现氨氮的高效选择性转化,设计了一个氯自由基介导的电化学体系。该电化学体系以稳定性好、氧化能力强的掺硼金刚石(BDD)电极为阳极,以Pd-Cu修饰的泡沫镍材料(Pd-Cu/NF)为阴极,以氯化钠为电解质,对BDD电极选择性电催化氧化性能与机理进行了研究。结果表明:在4.0 V电压下,体系中的Cl~-原位可转NO_3~-,副产物N_2;分别探究了阴极材料、电场强度、电极间距、溶液pH和电解质种类对氨氮转化性能的影响。通过电子顺磁共振和自由基捕获实验,证实了Cl·在氨氮转化过程中发挥了重要作用。在最优条件下,可实现40 min内100%的氨氮转化率和25 mg·L~(-1)的N_2生成量,以上研究结果可为解决水体中氨氮的污染问题提供参考。     

德国铁路噪声实时监测系统研究现状

分析了德国铁路噪声在线监测的应用背景，介绍了德国铁路噪声实时监测系统的研究现状，包括测量站点的选取原则、技术结构和具体信息，列车声压级曲线时域连续变化图、单次列车通过声压级曲线图、单次列车通过参数表和等效声压级曲线图/表等测量结果的表达方法，以及无效数据的处理方式等，为我国建立铁路噪声自动监测系统提供参考。     

基于环境容量的县域农用地土壤重金属风险概率预警研究

《土壤污染防治法》的正式出台,标志着我国土壤污染防治工作由"现状治理"转向"风险预防",为此开展区域土壤重金属风险预警研究具有一定的理论与现实意义。以太湖沿岸某产粮县为研究对象,以2015年为基准年,运用重金属输入-输出通量模型和土壤环境负载容量法对研究区耕地土壤中的As、Hg、Cr、Cd、Pb 5种重金属15年(2030年)与35年(2050年)后的风险概率进行预警研究。研究结果表明:大气干湿沉降成为除As以外其他4种土壤重金属的主要来源,畜禽粪便、化肥投入与灌溉水也会在一定程度上影响土壤重金属输入;此外,研究区耕层土壤中As、Cr、Pb 3种重金属整体情况较为良好,Hg、Cd污染风险概率较高,主要分布在研究区中部的O镇、P镇。通过GIS技术与区域物质流通量模型的结合能够很好地对不同区域以及不同重金属污染类型的区域进行风险预警,这可以为土壤污染差别化管控策略的制定提供重要思路。     

基于BP神经网络的受限空间火灾联合探测方法

针对航空受限空间火灾探测高误报的问题，在现有技术成果基础上对多种火灾探测方式进行研讨，并提出1种基于BP神经网络技术的飞机机身内部受限空间火灾联合探测报警方法。该方法结合现有烟雾感应、气体传感器探测等常用火灾探测技术，以红外热成像探测为辅助手段，采用神经网络实现数据融合，对模拟实验舱火灾烟雾进行联合探测，在单一火灾探测方式基础上提高了探测准确率。     

挥发性有机废气治理技术的现状与进展

本文通过查阅文献资料,总结了当前企业挥发性有机废气产生情况、政策管理办法以及相关处理技术,并分析了未来挥发性有机废气治理政策发展趋势,旨在提高挥发性有机废气治理效率,提高空气环境质量。