TiO2-蒙脱石光催化降解苯酚的实验研究

本文采用TiCl4在HCl中水解制备二氧化钛柱撑蒙脱石(TiO2-PILM)纳米材料，通过X射线衍射和BET N2比表面积分析对其进行表征，并研究其对苯酚在紫外光下的催化降解曲线，考察了苯酚的初始浓度、TiO2-PILM投放量、苯酚溶液pH值对光催化降解效果的影响。结果表明，制备的结构稳定的TiO2-PILM具有2．26nm大晶面间距和285．7m^2／g大比表面积。TiO2-PILM对苯酚有一定的光催化降解性，其过程是先吸附后降解。随苯酚初始浓度、TiO2-PILM投入量和苯酚溶液pH值的升高，TiO2-PILM对苯酚降解速率增大。在苯酚初始浓度为5mg／L、投样量为1g／L、pH为10时，TiO2-PILM对苯酚有较好的降解效果。     

天然锰钾矿氧化降解水体中苯酚实验研究

在酸性条件下进行了锰钾矿氧化降解水体中苯酚的实验研究，结果表明：室内自然光照和氧气环境不影响苯酚降解；反应溶液酸度越大，反应进行得越快；样品用量越多、粒径越小，越有利于降解反应；反应温度升高与振荡速度增大也有利于降解反应的进行；共存电解质氯化钠、氯化钙不影响降解反应，而磷酸钠与醋酸钠则不利于降解反应。当介质pH值为2、1，160～200目锰钾矿用量为10g／L，反应温度为25℃，振荡速度为200r／min，反应8h，对50mL浓度为100mg／L苯酚的降解率基本上达到100％，达到了工业排放标准。从反应产物初步推断，苯酚降解的实质是锰钾矿氧化降解作用，为处理苯酚废水增加了一种有效的方法，并拓宽了天然锰钾矿的开发应用前景。     

矿物溶解的表面化学动力学机理

本文应用表面化学理论分析了矿物在水溶液中的溶解反应动力学机理。表面化学的催化作用使矿物溶解反应的活化能显著降低。矿物溶解速率受表面吸附、表面交换反应和解吸反应等表面化学过程的控制并与溶液的pH值有关，正比于溶液αH＋值的nθ次幂。受表面吸附控制时，nθ＝1，溶解速率随pH增大而减小；受表面交换反应控制时，nθ＝0，溶解速率与pH无关；受解吸反应控制时，酸性条件下nθ为0～1内的正小数，碱性条件下nθ为-1～0之内的负小数。大多数矿物的溶解作用在酸性条件下受表面吸附和／或表面交换反应控制，在碱性条件下受解吸反应的控制。     

铁(氢)氧化物矿物对有机污染物的光催化氧化作用

对水溶液中(氢)氧化铁的光催化氧化反应的发展与机理研究进行了总结,着重对近十年来应用针铁矿／过氧化氢进行光催化氧化环境中有机物的研究进展及其环境矿物学意义作了概述和探讨。采用天然生物矿化的纳米针铁矿／过氧化氢以偶氮染料甲基橙为光解模型物进行了光催化氧化的初步研究,结果表明铁细菌形成的针铁矿具有降解生物难降解的有机污染物的能力。在甲基橙溶液初始浓度为30mg／L,铁细菌矿化的针铁矿用量2．5g／L,反应体系H2O2的初始浓度97mmol／L,pH值为6．92,15W紫外灯照射2h后,甲基橙浓度可降低33％。     

Fe/Ag催化臭氧氧化降解苯酚的研究

为研究双金属催化剂去除有机污染物的效果,采用自制Fe/Ag催化剂对模拟苯酚废水进行了臭氧催化氧化处理。通过扫描电子显微镜(SEM)、比表面积分析仪(BET)和X射线衍射(XRD)对催化剂进行表征,并考察了催化剂类型、催化剂投加量和溶液初始pH值对降解效果的影响规律。结果表明:与Fe相比,Fe/Ag比表面积减少了22.8%,在Fe/Ag/O₃与含苯酚废水的反应体系中,反应遵循臭氧直接作用和活性自由基(·OH、·O₂、H₂O₂)共同作用的机理;Fe/Ag在反应过程中体现出良好的协同作用;300 mg/L的苯酚模拟废水在pH=6.3、Fe/Ag投加量为1.00 g的最优反应条件下经60 min反应,苯酚与化学需氧量(COD)去除率比单独臭氧氧化分别提高了18.4%和29.4%。     

粤北大宝山多金属矿氧化亚铁硫杆菌对闪锌矿的生物氧化作用初步研究

利用从大宝山尾矿库酸性矿山废水培养得到的氧化亚铁硫杆菌(A.f.菌)和闪锌矿进行初始pH 2.00和pH 3.00条件下的无菌氧化、含菌含铁氧化和含菌不含铁氧化实验.通过测定实验过程溶液的阳离子、硫酸根离子含量和pH值,实验固体产物的XRD分析和反应前后闪锌矿表面的电镜扫描(SEM)对比分析,获得如下结论:①在不含铁离子的情况下,闪锌矿在pH为2.00的环境下比pH为3.00的环境下更容易被氧化;②氧化亚铁硫杆菌对闪锌矿的氧化有明显的促进作用,其氧化速率比无菌氧化速率要提高10～30倍;③铁离子存在对闪锌矿生物氧化有明显的促进作用,最高可达300倍;④氧化亚铁硫杆菌以及铁离子存在使闪锌矿的生物氧化作用最终溶液pH值明显低于无菌氧化作用的pH值;⑤闪锌矿的微生物氧化的最佳pH条件在2.0～2.4之间.闪锌矿的生物氧化过程中,细菌的直接氧化作用和间接氧化作用可能都是存在的.     

天然锰钾矿氧化降解水体中的苯胺研究

天然锰钾矿去除水体中苯胺的影响因素及其机制的研究表明，酸度是影响苯胺降解反应的主要因素，温度、振荡速度、矿物用量、矿物粒径及电介质浓度都不同程度地影响苯胺的降解；当介质pH值为3．0时，160～200目锰钾矿用量为10g／L、反应温度为25℃、振荡速度为200r／min、反应4h可以使50mL浓度为20mg／L的苯胺去除95％，达到工业废水一级排放标准；天然锰钾矿在酸性条件下具有强氧化性。可以使苯胺逐步降解为无机物质。以上结果都说明天然锰钾矿降解苯胺废水是一种经济有效的方法。     

靖宇县玄武岩区矿泉水特征组分H2SiO3成因实验——以王大山泉为例

以靖宇县典型泉岩样为实验材料,结合野外实际情况,考虑pH值和CO₂影响因素设计了矿泉水中H₂SiO₃实验,对实验结果进行了化学动力学分析,并利用matlab建立数学模型分析了矿物反应的机理。结果表明:1)仅考虑pH值的情况下:初始pH值近中性(pH=7.25)时,实验溶液中H₂SiO₃释放量较小,反应难以发生;初始pH值为碱性(pH=8.10)时,实验溶液中H₂SiO₃缓慢增加,平均释放速率为3.08 mg/(kg·d)。2)在考虑pH值和CO₂情况下:初始pH值为碱性条件时,通入CO₂能够较快促进H₂SiO₃产生,平均释放速率可由4.29 mg/(kg·d)升高为12.00 mg/(kg·d);初始pH值为弱酸性(pH=6.64)时,实验溶液中H₂SiO₃增加较快,通入CO₂,溶液中H₂SiO₃释放速率稍微增加。3)实验溶液中H₂SiO₃释放规律符合Stanford一阶反应动力学模型。靖宇县矿泉水中H₂SiO₃主要来自偏硅酸矿物(斜长石、镁橄榄石、辉石)的反应。在中性条件下,玄武岩矿物很难反应;在碱性条件时,主要是玄武岩矿物的水解,反应缓慢;在弱酸性条件下,主要是玄武岩矿物与H⁺和CO₂的反应,反应强度较大。     

二价铁活化过硫酸盐去除水中苯胺

零价铁和硝基苯反应后生成二价铁和苯胺,而苯胺也是地下水污染物。硫酸根自由基具有强氧化性,可以降解苯胺。而二价铁可以活化过硫酸盐产生硫酸根自由基,进而去除苯胺。本文研究了二价铁浓度、过硫酸盐浓度、苯胺初始浓度、体系初始pH、反应温度等因素对二价铁活化过硫酸盐去除水中苯胺处理效率的影响。结果表明:1)Fe2+活化过硫酸盐生成SO-4·能快速并有效氧化降解苯胺,对于目标浓度为1 000 mg/L的苯胺而言,Fe2+浓度为3.3 mmol/L,Na2S2O8浓度为4.4 mmol/L时,对苯胺有较佳降解效果,苯胺的降解率为86.33%。2体系对较低浓度的苯胺降解效果较好,当污染物初始浓度由1 000 mg/L降低到500 mg/L和100 mg/L时,苯胺降解率由86.33%升高为90.27%和97.16%。3初始pH对苯胺的降解率影响较大,中性条件下(pH=7左右)降解率较好,高初始pH(pH=9,11)和低初始pH条件(pH=3,5)下均低于中性条件下苯胺的降解效率。4体系的温度变化对降解率影响不明显。     

软锰矿对酸性大红GR的氧化脱色研究

本文主要研究了天然软锰矿对酸性大红GR的脱色效果,并从溶液的pH值和软锰矿的用量、粒径以及水浴温度、振荡速度方面探讨了软锰矿对其脱色效果的影响。实验表明,软锰矿可使250mL浓度为40mg/L的酸性大红溶液脱色达到95%以上,脱色效果较好,溶液pH值是影响酸性大红脱色的最主要因素,软锰矿的用量、粒径以及水浴温度、振荡速度对酸性大红脱色影响不大。软锰矿对酸性大红的高脱色率以及红外光谱分析和COD去除率表明,酸性大红在矿物界面发生了氧化还原反应,其显色基团被氧化破坏,但并不能将染料溶液全部氧化去除。软锰矿对酸性大红GR的氧化脱…     

硅烷偶联剂改性TiO2/膨胀石墨复合材料的制备及其光催化性能研究

以硅烷偶联剂黏结剂,利用溶胶-凝胶法将TiO2（P25）负载在膨胀石墨上,利用XRD、EDS以及SEM等分析技术对TiO2/膨胀石墨复合材料进行表征;以橙黄Ⅱ为目标降解物,考察了TiO2/膨胀石墨复合材料光催化性能以及重复使用性能。结果表明：随着TiO2含量的增加,TiO2/膨胀石墨复合材料的光催化效率随之增加,对橙黄Ⅱ的光催化降解符合一级反应动力学方程,TiO2负载量为15%时,反应速率常数为0.387 h-1,高于P25的反应速率常数。TiO2/膨胀石墨复合物使用4次仍保持较高的光催化活性。     

UV/H2O2法降解乙酸影响因素的研究

通过采用UV/H₂O₂法,以乙酸为研究对象,高压汞灯为光源,在温度为（35±2）℃、曝空气量为0.8 L/min的条件下,研究了UV/H₂O₂技术对500 mL浓度为8 mmol/L的乙酸溶液进行的光降解反应。考察了各种因素对UV/H₂O₂降解乙酸的影响。实验表明,H₂O₂浓度为15 mmol/L、pH值为3.4时,乙酸降解效果最佳,此时,在240 min内,乙酸、TOC和COD的去除率可分别达到98%、98%和97%,体系中乙酸完全矿化。利用UV/H₂O₂法对实际糠醛废水进行了降解,效果良好。     

Advanced approach for degradation of recalcitrant by nanophotocatalysis using nanocomposites and their future perspectives

Industrial effluents containing persistent pollutants play a significant role in environmental pollution. Classical techniques such as chlorination, coagulation, ion flotation, membrane process and sedimentation that have been used to decontaminate polluted water are incapable of efficient degradation due to the generation of secondary pollutants. Photocatalysis, an advanced oxidation process in which the photoreaction is accelerated by the irradiation of catalyst, has shown efficient degradation of recalcitrant in water system. Usage of nanoparticles as homogenous photocatalyst has become prevalent due to their improved properties such as large surface-to-volume ratio, controlled uniform particle size and its composition which enhances the degradation rate. The recombination of holes and electron pair which is considered to be the limitation in homogenous system can be overcome by nanocomposites or heterogeneous photocatalysts. This system decreases the rate of recombination, leading to effective degradation of individual pollutants because of their enhanced physicochemical and structural properties. In recent years, heterogeneous nanophotocatalytic processes employing titanium dioxide (TiO₂) and zinc oxide (ZnO) composites have gained immense research interest as an effective wastewater treatment method because of its efficacy in decomposing and mineralizing the hazardous organic and inorganic pollutants utilizing the UV and visible photons. This paper reviews about the process, synthesis and parameters influencing photocatalytic reaction and their kinetics with much emphasize on types of nanoparticles and nanocomposites and its application in wastewater treatment.     

Detoxification of toxic dyes using biosynthesized iron nanoparticles by photo-Fenton processes

Environmental contamination resulting from dyes has become a serious concern for today’s world. The textile effluents are highly colored, and the disposal of these in water bodies causes severe damage to the environment by reducing the solar light penetration which may affect the photosynthetic activity and the aquatic life in water. Further, the high water solubility of dyes also leads to surface and ground water contamination. Thus, in this study, we attempt to develop a cost-effective and eco-friendly method for removal of toxic dyes from aqueous using biosynthesized iron nanoparticles (INPs). Various complimentary instruments such as a thermogravimetric analysis, scanning electron microscopy/energy dispersive X-ray spectrometer, and X-ray diffraction were employed for identification and characterization of INPs. The biosynthesized INPs were applied as a Fenton-like catalyst for decolorization of toxic dyes solution like methylene blue, methyl orange, allura red, brilliant blue, and green S using hydrogen peroxide under solar radiation. The decolorization of the toxic dyes solution using INPs was monitored by UV–visible spectrophotometer, and the data obtained were utilized to evaluate the kinetic rate of the reactions. The kinetic data suggest that the decolorization of all studied toxic dyes solution follows first-order rate with rate constant values in the range of 13.1 × 10^?3–17.7 × 10^?3 min^?1. Therefore, such a clean method employing non-toxic plant extract in INP synthesis and the application of INPs as a Fenton-like catalyst in toxic dyes decolorization can be considered as an alternative technique to the expensive and toxic chemical methods.     

Efficiency removal of phenol, lead and cadmium by means of UV/TiO2/H2O2 processes

A variety of processes can be used in treatment of industrial wastewaters. The relatively newest of which is photo catalysis with titanium dioxide which may also be used plus hydrogen peroxide to improve the treatment rate. In this study, photo catalysis/ hydrogen peroxide processes had been employed for the removal of phenol, lead and cadmium by three different pHs of 3.5, 7 and 11. The treatment tests were also accomplished without UV irradiation. In both experiments, the variables were pH and concentrations of reagent chemicals, but the detention time was kept constant (180 min). Results indicated that the optimum efficiencies of phenol and Cd removal were 76 % and 97.7 % at pH=11, respectively, and for lead, it was 98.8% in all pHs. In other words, no pH dependency was regarded for lead treatment. These results were all obtained by simultaneous use of UV irradiation with 3 mL/L H₂O₂ and 0.8 g/L TiO₂. Finally, the best pH for treatment, when all the three contaminants are presented is considered to be at 11. These results should be regarded by all industrial treatment plants which have experienced the problem of these three special contaminants in their effluents.     

Landfill Base Liners: Assessment of Material Equivalency and Impact to Groundwater

This paper gathered available flow and transport solutions and used them for two composite liners, consisting of geomembrane (GM) overlying either a compacted clay liner (CCL) or a geosynthetic clay liner (GCL). Its aim is to provide a guiding framework for the possible choices of (a) approaches to bottom liner design, (b) respective analytical solutions to flow and transport equations, as well as (c) parameters required for each type of solution. On the basis of the obtained results, the following recommendations are made. When the goal of analysis is to determine material equivalency, leachate flow rate is an adequate key parameter for GM-CCL composite liners. For GM-GCL composite liners, it is necessary to compute contaminant concentration or mass flux, considering (a) transport through defects for inorganic contaminants and (b) diffusion and the contribution of any available attenuation layer for organic contaminants. When the goal of analysis is to assess impact to groundwater, it is advised to calculate both discharge rate and contaminant mass flux regardless of liner type. The critical parameter for the transport calculations is the retardation factor of the contaminant, for the case of CCLs, while the results for GCLs are much less sensitive to this parameter.     

Agricultural contaminants in Quaternary aquitards: A review of occurrence and fate in North America

The intensity of agriculture has increased significantly during the past 30 years, resulting in increased detection of agricultural contaminants (nutrients, pesticides, salts, trace elements, and pathogens) in groundwater. Till, glaciolacustrine, and loess deposits of Quaternary age compose the most common surficial deposits underlying agricultural areas in North America. Quaternary aquitards generally contain higher concentrations of solid organic carbon (SOC, as much as 1.4%), dissolved organic carbon (DOC, as much as 205 mg/L), and reduced sulfur (as much as 0.9%) than do aquifers. Their potential to sorb pesticides increases with the percent of older SOC, because diagenesis increases K_oc. Denitrification consistently reduces nitrate to non-detectable levels in unweathered Quaternary aquitards. Organic carbon of Quaternary age is a more labile electron donor than carbon from shale clasts. Pyrite is a more labile electron donor than carbon in many instances. Unweathered Quaternary aquitards provide a high degree of protection for underlying aquifers, due to their large reserves of SOC and reduced sulfur for sorption and denitrification, combined with their typically low hydraulic conductivity. In contrast, agricultural contaminants are common in weathered Quaternary aquitards. Lower reserves of reduced sulfur and sorptive/labile organic carbon, and a higher bulk K due to fractures, limit their ability to attenuate nitrate and pesticides. Subsurface drainage, which is common in Quaternary aquitards because of high water tables, bypasses the attenuation capacity of Quaternary aquitards and facilitates the transport of agricultural contaminants to surface water. Electronic Publication     

紫外光及日光下天然金红石光催化降解苯酚的研究

研究了山西代县天然金红石在紫外光和日光照射条件下对苯酚的光催化降解性能,考察了光照时间、pH值、苯酚初始浓度以及H2O2添加量对降解过程的影响。在紫外光照射下,酸性条件(pH=3.5)利于光催化降解,中性和碱性条件下降解效率较低;当初始浓度为60mg/L时,降解速率可达1.922mg/(L.h);H2O2作为电子捕获剂可提高苯酚降解速率,最佳投加量为2mL/L。在日光条件下,天然金红石对苯酚表现出良好的降解性能,照射7h后,降解率达87.68%,仅略低于P25型TiO2(99.72%),可在14h内完全降解。根据电子探针和X射线衍射分析结果,认为天然金红石晶格中的V、Fe等杂质可能是提高其可见光响应效果和光催化活性的主要原因。