Synthesis, crystal structure, photodegradation kinetics and photocatalytic activity of novel photocatalyst ZnBiYO4

ZnBiYO₄ was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiYO₄ were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance. ZnBiYO₄ crystallized with a tetragonal spinel structure with space group I41/A. The lattice parameters for ZnBiYO₄ were a = b = 11.176479 Å and c= 10.014323 Å. The band gap of ZnBiYO₄ was estimated to be 1.58 eV. The photocatalytic activity of ZnBiYO₄ was assessed by photodegradation of methyl orange under visible light irradiation. The results showed that ZnBiYO₄ had higher catalytic activity compared with N-doped TiO₂ under the same experimental conditions using visible light irradiation. The photocatalytic degradation of methyl orange with ZnBiYO₄ or N-doped TiO₂ as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01575 and 0.00416 min^-1 for ZnBiYO₄ and N-doped TiO₂, respectively. After visible light irradiation for 220 min with ZnBiYO₄ as catalyst, complete removal and mineralization of methyl orange were observed. The reduction of total organic carbon, formation of inorganic products, SO₄^2- and NO₃^-, and evolution of CO₂ revealed the continuous mineralization of methyl orange during the photocatalytic process. The intermediate products were identified using liquid chromatography- mass spectrometry. The ZnBiYO₄/(visible light) photocatalysis system was found to be suitable for textile industry wastewater treatment and could be used to solve other environmental chemical pollution problems.     

Pd-Fe/石墨烯多功能催化阴极降解4-氯酚机制研究

制备出Pd-Fe/石墨烯多功能催化阴极,与Ti/Ir O2/Ru O2阳极、有机涤纶滤布构成隔膜电解体系,将阴极催化加氢脱氯作用和阴阳极氧化作用耦合起来对含4-氯酚的有机废水进行降解,采用TOC仪、紫外扫描、高效液相色谱、离子色谱分析方法研究其降解效果及反应历程.结果表明,在最佳反应条件下,Pd-Fe/石墨烯催化体系阴阳极室中4-氯酚转化率分别为98.1%和95.1%,优于Pd/石墨烯催化体系阴阳极室的93.3%和91.4%.Pd-Fe/石墨烯催化体系脱氯效果高于95%,表明双金属催化剂具有更强的析氢能力.在阴阳极的协同作用下,反应120 min时4-氯酚被完全转化.通过阴极加氢脱氯作用,4-氯酚被还原成苯酚.随后苯酚在阴阳极的共同氧化作用下,被氧化生成对二苯酚、苯醌等中间产物,继而被氧化为小分子有机酸,最后被矿化为CO2和H2O,据此提出了4-氯酚降解的可能历程.     

Ag3PO4/g-C3N4复合光催化剂的制备及其可见光催化性能

采用简单的原位沉淀法合成了可见光驱动型光催化剂Ag₃PO₄/g-C₃N₄.利用X-射线衍射（XRD）、傅里叶红外光谱（FT-IR）、扫描电子显微镜（SEM）、X-射线能谱（XPS）以及紫外可见漫反射光谱（UV-Vis DRS）等表征手段对合成的样品进行了表征.与单一的Ag₃PO₄和g-C₃N₄相比,Ag₃PO₄/g-C₃N₄复合材料对左氧氟沙星表现出了更高的催化效率.根据能带分析和自由基捕获试验,提出了Ag₃PO₄/g-C₃N₄复合材料Z型异质结构的作用机制.     

Bi-FeC2O4复合催化剂活化过硫酸盐降解罗丹明B

采用溶剂热法将Bi单质附着于草酸亚铁（FeO_x）上,制备了系列Bi-FeOx复合催化剂并用于活化过硫酸盐.通过X射线衍射仪（XRD）、傅里叶变换红外光谱仪（FT-IR）、扫描电子显微镜（SEM）、X射线光电子能谱仪（XPS）等表征方法对复合催化剂的结构、形貌和元素价态进行表征.以罗丹明B（RhB）为降解对象,研究了Bi-FeOx/过硫酸盐/可见光体系中Bi单质含量、催化剂投加量、pH及过硫酸盐浓度等因素对RhB的降解影响.在最佳条件下,反应5 min后,RhB的降解率高达99.8%.Bi的引入,使得复合催化剂增强了对可见光的吸收,提高了光生电子的传输效率,从而加速了对RhB的降解.     

Enhanced bio-decolorization of 1-amino-4-bromoanthraquinone-2-sulfonic acid by Sphingomonas xenophaga with nutrient amendment

Bacterial decolorization of anthraquinone dye intermediates is a slow process under aerobic conditions. To speed up the process, in the present study, effects of various nutrients on 1-amino-4-bromoanthraquinone-2-sulfonic acid (ABAS) decolorization by Sphingomonas xenophaga QYY were investigated. The results showed that peptone, yeast extract and casamino acid amendments promoted ABAS bio-decolorization. In particular, the addition of peptone and casamino acids could improve the decolorization activity of strain QYY. Further experiments showed that L-proline had a more significant accelerating effect on ABAS decolorization compared with other amino acids. L-Proline not only supported cell growth, but also significantly increased the decolorization activity of strain QYY. Membrane proteins of strain QYY exhibited ABAS decolorization activities in the presence of L-proline or reduced nicotinamide adenine dinucleotide, while this behavior was not observed in the presence of other amino acids. Moreover, the positive correlation between L-proline concentration and the decolorization activity of membrane proteins was observed, indicating that L-proline plays an important role in ABAS decolorization. The above findings provide us not only a novel insight into bacterial ABAS decolorization, but also an L-proline-supplemented bioaugmentation strategy for enhancing ABAS bio-decolorization.     

耕作制度对川中丘陵区冬灌田CH4和N2O排放的影响

采用静态暗箱/气相色谱法连续2 a田间原位测定,研究川中丘陵区冬灌田CH₄和N₂O的排放特征和不同耕作制度对冬灌田CH₄和N₂O排放的影响.结果表明,1a只种1季中稻冬季灌水休闲的冬灌田(PF),在水稻生长期,CH₄平均排放通量为(21.44±1.77)mg·(m²·h)^-1,非水稻生长期为(3.77±0.99)mg·(m²·h)^-1,分别大大低于以前文献报道的在西南其它地方观测值;全年CH₄排放量以水稻生长期CH₄排放量为主,非水稻生长期CH₄排放量仅占全年总排放量的23.2%.冬灌田N₂O排放通量年均值为(0.051±0.008)mg·(m²·h)^-1,且主要集中在水稻生长季,非水稻生长期N₂O排放量仅占全年总排放量的8.1%.在采用水旱轮作制后,冬灌田CH₄排放量大大降低,稻-麦轮作(RW)和稻-油菜轮作(RR)全年CH₄排放量分别为PF的43.8%和40.6%.但冬灌田改为水旱轮作制后,N₂O排放量显著增大,RW和RR的N₂O年排放量分别是PF的3.7倍和4.5倍.综合考虑冬灌田在采用不同耕作制度后排放CH₄和N₂O的全球增温潜势(GWP),无论是短时间尺度还是长时间尺度,采用3种耕作制度全年所排放的CH₄和N₂O所产生的综合GWP都为:PF RW≈RR.在20a、100a和500a时间尺度上,PF分别约是RW和RR的2.6、2.1和1.7倍.冬灌田改为水旱轮作制度后能大大减少CH₄和N₂O所产生的综合GWP.     

尿素/KMnO4湿法烟气脱硫脱氮的试验研究

采用尿素和KMnO₄配制成的吸收液,在填有金属鲍尔环的柱式喷淋吸收反应器中,对模拟烟气进行湿法烟气同时脱硫脱氮研究.结果表明:采用尿素和KMn0₄配制成的吸收液可以高效地脱除模拟烟气中的SO₂和NO_x,脱硫脱氮率平均分别达到99.6%和62.5%;反应吸收液中主要含有因吸收NOx和SO₂而生成的NO₃-,NO₂-,NH₄+和SO₄2-等离子;NO₃-,NO₂-和NH₄+的生成曲线及尿素的消耗曲线均为线性,其速率常数分别为0.009 1,0.0074,0.091 6和0.950 8 mmol/(L·min).吸收反应为零级反应.      

准好氧填埋工艺氧气浓度对甲烷与二氧化碳浓度的影响研究

构建了准好氧填埋模拟装置,在其产气相对稳定期间,测定填埋装置内不同点位的ψ(O₂),ψ(CH₄)和ψ(CO₂),并用数学模型对ψ(O₂)与ψ(CH₄)和ψ(CO₂)之间的关系进行拟合.结果表明:随着ψ(O₂)的增加,上层ψ(CH₄)呈对数规律下降,而ψ(CO₂)呈线性规律下降;中层ψ(CH₄)和ψ(CO₂)均呈指数规律下降;下层ψ(CH₄)呈指数规律下降,而ψ(CO₂)先保持在34%左右波动,当ψ(O₂)大于1.8%后呈指数规律下降.上层主要为好氧带,ψ(CH₄)低于ψ(CO₂);中层主要为兼氧带,当ψ(O₂)小于5.8%时ψ(CH₄)高于ψ(CO₂),而当ψ(O₂)大于5.8%时ψ(CH₄)低于ψ(CO₂);下层主要为厌氧带,当ψ(O₂)小于2.8%时ψ(CH₄)高于ψ(CO₂),而当ψ(O₂)大于2.8%时ψ(CH₄)低于ψ(CO₂).      

DBD结构对船用LNG发动机尾气CH4氧化脱除的影响

为提高等离子体氧化CH₄的脱除效率,同时避免放电过程中副产物NO_x的生成,在模拟天然气 (LNG) 发动机排气中,研究了介质阻挡放电 (DBD) 反应器电极结构参数对CH₄脱除效率、CO₂选择性及NO_x生成的影响及其机理。结果表明：增大电极直径使得气隙中折合场强E/N提高,增加了·O和·OH自由基的生成,促进了CH₄的氧化,提高了CO₂选择性;内电极直径的增大使E/N在气隙中分布更加集中,抑制了N₂(X, v)和N自由基的生成,减少了副反应的发生。与圆杆电极相比,螺纹电极的螺牙顶部附近具有过高的电场强度,从而促进N自由基的生成并抑制·O自由基的产生,故圆杆电极比螺纹电极具有更高的CH₄脱除效率及更低的NO_x生成。电极长度过长降低了折合场强以及电子平均能量,不利于氧化性活性粒子生成,导致CH₄脱除效率和CO₂选择性降低,同时增加了N₂(X,v) ,也使得NO_x增加。本研究可为提高低温等离子体协同催化剂促进甲烷还原NO_x系统的脱除效率,降低DBD反应器能耗提高能源利用率提供参考。     

序批式活性污泥法工艺处理含盐废水动力学模型研究

为了实现含盐废水序批式活性污泥法(SBR)工艺的启动,采用逐步提高废水中NaCl浓度负荷的方法对活性污泥进行驯化,并建立有机物(COD)与NH4+-N的降解动力学模型。结果表明,经过280d的驯化和稳定运行,SBR系统可以有效降解含盐废水,COD去除率高于74%,NH4+-N平均去除率高于90%,实现了SBR工艺处理含盐废水的启动和稳定运行。含盐废水有机物(COD)降解动力学参数r0(无盐条件下的COD去除速率)为129.87mg/(L.h),KY(盐抑制常数)为7700.01mg/L;含盐废水硝化反应动力学参数Ks(饱和常数)为186.52mg/L,vmax(NH4+-N的最大比降解速率)为0.0034h-1。