磺胺二甲嘧啶在水溶液中的光化学降解

研究了4种光源(高压汞灯、氙灯、紫外灯和太阳光)下磺胺二甲嘧啶(SM2)的光化学降解(简写为光解)动力学.结果表明:(1)4种光源下,SM2的光解符合一级动力学方程,光解速率常数依次为紫外灯＞高压汞灯＞氙灯＞太阳光.(2)在相同条件下,SM2的光解速率常数随着初始浓度的增加而减小.(3)SM2在不同pH的缓冲溶液下的光...     

厌氧反应器废水资源化过程在线监测系统

为克服现行厌氧反应器状态离线分析的滞后性,充分利用资源,改进废水排放状态,研究了基于荧光光谱的废水资源化处理过程在线监测系统。系统以厌氧反应器中的关键产物色氨酸、核黄素及辅酶为主要检测组分,自动定位滤波轮并控制脉冲氙灯的闪烁次数,使用光电倍增管采集荧光信号。针对反应产物的混合体系,提出了将三维数据二维化的准三维荧光谱概念,优化获得了的3×3荧光强度矩阵,采用偏最小二乘法并优化其模型参数,实现了反应器中3种关键过程产物的实时在线检测、统计与分析,使其回收率范围达到85%至112%。     

大气二氧化硫浓度的光学测定方法

介绍了测定二氧化硫浓度的几种光学方法 ,指出了目前一些化学方法的局限性 ,特别对紫外荧光法的原理、二氧化硫的吸收光谱以及荧光光谱进行分析探讨 ,设计了实验分析系统 ,得出该方法具有操作简单、灵敏度高、可实时在线的智能化优点 ,将会成为今后研究的主导方向。     

总氮测定中的注意事项

碱性过硫酸钾消解紫外分光光度法测定总氮中，对空白值偏高的影响因素进行了实验和分析，提出了几点建议及改进措施。     

陶瓷负载Ag、Ce共掺杂TiO_2光催化剂降解甲基橙的研究

以陶瓷为载体,采用溶胶-凝胶法制备了银离子和铈离子共掺杂TiO2的负载型光催化剂——T-AC/陶瓷,研究了pH值、双氧水用量、催化剂用量、紫外灯强度、废水的初始浓度等因素对T-AC/陶瓷光催化剂降解甲基橙染料废水的影响。结果表明,当pH为2、双氧水用量为0.5 mL/100 mL、催化剂用量为3 g/L、紫外灯功率为20 W、废水初始浓度为10mg/L时,甲基橙的降解率可达85.9%,并且甲基橙的光催化降解属于一级动力学方程,T-AC/陶瓷催化剂有较高的活性和稳定性,在废水处理中具有较好的应用前景。     

陶瓷负载Ag、Ce共掺杂TiO2光催化剂降解甲基橙的研究

以陶瓷为载体,采用溶胶-凝胶法制备了银离子和铈离子共掺杂TiO2的负载型光催化剂——T-AC/陶瓷,研究了pH值、双氧水用量、催化剂用量、紫外灯强度、废水的初始浓度等因素对T-AC/陶瓷光催化剂降解甲基橙染料废水的影响。结果表明,当pH为2、双氧水用量为0.5 mL/100 mL、催化剂用量为3 g/L、紫外灯功率为20 W、废水初始浓度为10mg/L时,甲基橙的降解率可达85.9%,并且甲基橙的光催化降解属于一级动力学方程,T-AC/陶瓷催化剂有较高的活性和稳定性,在废水处理中具有较好的应用前景。     

实验室测定二氧化硫的影响因素

空气二氧化硫的测定，对实验室测定条件比较敏感，通过实验表明，显色时间、显色温度、PRA纯度、蒸馏水质量等条件，均对其校准曲线的斜率和空白值有影响，所以在实验分析过程中，必须严格把握操作条件，严格遵循操作步骤。     

2-甲基-4-氯苯氧乙酸及其脱氯产物的光化学降解

紫外消毒工艺作为废水/给水处理的重要步骤,不仅可以有效控制水中的病原体,而且可使废水或水源水中存在的一些污染物发生化学降解作用,但目前对这一作用过程的研究尚不完善。本文针对一种典型的除草剂——2-甲基-4-氯苯氧乙酸(MCPA)及其脱氯产物二甲基苯氧乙酸(MPA),研究了两者在紫外灯照射下的光化学行为,并进一步考察了波长、初始pH值、H2O2及水中其他共存物质对MCPA和MPA光降解效率的影响。研究结果表明,不同光源对MCPA的光降解速率大小为:254 nm波长紫外灯365 nm波长紫外灯可见光灯;低pH值不利于MCPA的光降解,但对MPA光降解的影响不大;在溶液中加入H2O2,会增大MCPA和MPA的光降解速率;MCPA的光降解过程符合一级动力学方程;腐殖酸(HA)会降低MCPA的光降解速率;MPA与MCPA呈现相似的光降解效应,但反应速率比MCPA略快,且在两者共存状态下会降低MCPA的光降解速率。     

真空紫外灯动态降解空气中低浓度甲醛的研究

以集中空调中处理室内可挥发性有机物（VOCs）为应用背景，搭建了试验台。实验研究了真空紫外灯（主波长254nm，185nm）降解甲醛的影响因素以及产生O3的情况。研究表明，在产生的O3浓度低于室内空气质量标准（0．16mg／m^3）的情况下，真空紫外灯也能够高效地降解空气中低浓度甲醛（〈1mg／m^3）；甲醛降解率与反应器空气流速及甲醛初始浓度成反比；降解速率与甲醛初始浓度成正比，与反应器空气的流速成反比；绝对湿度对真空紫外灯降解甲醛有一定的影响；反应器空间大小对甲醛降解影响比较显著。应用于集中空调系统净化室内空气中VOCs，取得了很好的效果。     

钙基脱硫灰在酸性条件下的稳定性研究

常温下钙基脱硫灰的稳定性主要受外界pH值的影响，其次还与所处的气氛有关。文中对空气和氮气两种气氛下灰样中亚硫酸钙在酸性条件下分解放出二氧化硫的量进行了测定，研究了常温下钙基脱硫灰的稳定性及其对环境的影响。     

Spectrophotometric determination of sulphur dioxide

Sulphur dioxide, an important industrial gas and air pollutant, is usually estimated using mercury salts. The authors have developed a method in which hazardous mercury salts are avoided. Sulphur dioxide is trapped in aqueous morpholine and mixed with the excess of dichromate solution in acidic medium. The hexavalent chromium in dichromate is reduced to trivalent chromium by sulphur dioxide and the excess of hexavalent chromium is determined with diphenylcarbazide which yields a soluble red-violet complex with an absorption maximum at 540 nm. The decrease in the absorbance values of the red-violet complex formed after reduction, when compared to that of a reagent control, is proportional to the concentration of sulphur dioxide used for reduction. Beer's law operates between 0.4 and 4 microg ml(-1) concentration of sulphur dioxide in solution.     

基于CFD的两种紫外消毒模型的比较研究

为了预测紫外反应器的消毒效率,提高模拟的准确度,对两种紫外光强模型进行了比较分析。利用CFD技术,采用数值模拟的方法,对线源和柱源两种光强模型进行了光强分布以及消毒效率的模拟,并采用生物实验进行了验证。结果表明:与柱源模型相比,线源模型在近灯管处强度高42.3%,在1.2 cm处二者趋于一致;针对同一管式紫外反应器,透光率为95%时,线源模型的模拟结果偏大,柱源结果偏小;透光率为80%时,线源及柱源模型的模拟结果都偏大,流量及模型影响较小,透光率成为主要影响因素。综合比较,柱源模型适用于小型管式紫外灯消毒数值模型的开发。     

Abiotic degradation of imazethapyr in aqueous solution

The photodegradation of imazethapyr [2-(4,5-dihydro-4-méthyl-4-(1-méthylethyl)-5-oxo-1H-imidazol-2-yl)-5-ethyl-3-pyridinecarboxylic acid] in aqueous solution in the presence of titranium dioxide (TiO2) and humic acids (HA) at different ratios of herbicide/TiO2 and herbicide/humic acids was studied at pH 7.0. Irradiation was carried out with polychromatic light using Heraeus apparatus equipped with xenon lamp to simulate sunlight having a spectral energy distribution similar to solar irradiation (>290 nm). The concentration of remaining herbicide was followed using a High Pressure Liquid Chromatograph (HPLC) equipped with UV detector at 230 nm. In pure aqueous solution imazethapyr degrades slowly and the photodegradation leads to the formation of two metabolites labelled A and B. The presence of TiO2 caused enhancement of the degradation rate. The presence of HA induced an increase of the photodegradation of the pesticide with respect to pure aqueous solution.     

Study on the indoor volatile organic compound treatment and performance assessment with TiO2/MCM-41 and TiO2/quartz photoreactor under ultraviolet irradiation

Volatile organic compounds (VOCs) are the cause of indoor air pollution and are readily emitted from furniture and cleaning agents. In Taiwan, the concentrations of indoor VOCs range roughly from 1 to 10 ppm. It is important to effectively reduce indoor VOC emissions and establish the implementation of long-term, low-cost, controlled techniques such as those found in the ultraviolet/titanium dioxide (UV/TiO2) control systems. This study evaluates the performance of a photoreactor activated by visible irradiation and packed with TiO2/quartz or TiO2/mobile catalytic material number 41 (MCM-41). The photocatalysts tested include commercial TiO2 (Degussa P-25) and synthesized TiO2 with a modified sol-gel process. The UV light had a wavelength of 365 nm and contained an 8-W, low-pressure mercury lamp. Reactants and products were analyzed quantitatively by using gas chromatography with a flame-ionization detector. It is important to understand the influence of such operational parameters, such as concentration of pollutant, temperature, and retention time of processing. The indoor concentrations of VOCs varied from 2 to 10 ppm. Additionally, the temperatures ranged from 15 to 35 degrees C and the retention time tested from 2 to 8.2 sec. The results show that quartz with TiO2 had a better photoreductive efficiency than quartz with MCM-41. The toluene degradation efficiency of 77.4% with UV/TiO2/quartz was larger than that of 54.4% with the UV/TiO2/MCM-41 system under 10-min reaction time. The degradation efficiency of the UV/TiO2 system decreased with the increasing concentrations of indoor VOCs. The toluene degradation efficiency at 2 ppm was approximately 5 times greater than that at 10 ppm. The photoreduction rate of the VOCs was also evaluated with the Langmuir-Hinshewood model and was shown to be pseudo-first-order kinetics.     

Deposition of particulate matter in diffusion tube samplers for the determination of NO2 and SO2

The applicability of tube-like diffusion samplers for the determination of ambient air concentrations of sulfur dioxide and nitrogen dioxide was evaluated. The diffusion tubes were made from polyethylene and triethanolamine was used as an absorbent. Artifacts due to the deposition of gaseous or particulate compounds to the tube walls were considered. With respect to sampling of nitrogen dioxide no interference by the tube walls could be observed. The determination of sulfur dioxide was strongly biased by the collection of particulate sulfate at the entrance part of the tube and along the tube walls. This effect leads to a large overestimation of the average air concentrations compared with fluorescence monitors.     

臭氧/紫外联合降解甲醛的试验研究

在臭氧单独作用、紫外光单独作用和UV/O₃ 3种条件下分别对甲醛进行降解试验，研究表明,臭氧和紫外在降解甲醛的试验中存在明显的协同促进作用。单独臭氧对甲醛降解效果并不显著。紫外单独作用时，对甲醛几乎没有降解作用。在UV/O₃条件下，甲醛的降解率大大提高，特别是在高浓度臭氧条件下，降解率高达63％。臭氧浓度增大，降解率增大；紫外光强度增大，降解效果提高；气体流量增大，降解率下降；湿度增大，降解率提高。对甲醛降解试验进行动力学研究，结果表明，光照强度和臭氧浓度增大，一级反应速率增大，提高臭氧浓度要比加强紫外强度更能促进甲醛的降解。     

Photocatalytic oxidation of volatile organic compounds using fluorescent visible light

Photocatalytic oxidation (PCO) of volatile organic compounds (VOCs) is a highly attractive alternative technology for purification and deodorization of indoor air. The main objectives of this study were to demonstrate that a common fluorescent visible light (FVL) lamp can be used to effectively remove by PCO low concentrations of VOCs from slightly contaminated air and to provide some fundamental and technical details on the process. The target VOC was n-butanol, which is a standard reference odorant. Its PCO was studied under a long residence time in a 3.7-L cylindrical reactor with commercial titanium dioxide (TiO2) as the reference photocatalyst and using mostly FVL for illumination. For comparison only, a UV (black) light lamp was used. The gas-phase products were detected and quantified online by gas chromatography (GC). The effects of reactor residence time, of inlet concentration, and of the relative light intensity on the efficiency of the process were also evaluated. At a high n-butanol concentration (0.1 vol %), butanal and propanal were identified as the intermediate products of the process; ethanal appeared when the initial concentration was < or = 850 ppm(v). This indicates that PCO leading to CO2 and H2O is relatively slow and proceeds in a stepwise manner. Although the efficiency of the process with an FVL lamp was significantly lower than when using a UV black light, complete PCO of low concentrations was achieved for 100 ppm(v). In a search for a material with photoactivation extended to higher wavelengths or increased photoactivity, several samples of transition metal- or silver ion-doped (2 atomic %) TiO2 as well as SrTi(1-x-)Fe(x)O3 (x = 0.1 and 0.15) perovskites were included in the study. None of these materials was more active than pure TiO2. The results of this study open new horizons in the area of in door air quality (IAQ) control.     

Ambient and Source SO2 Detector Based on a Fluorescence Method

The principle of this detector is based on the measurement of the intensity of the ultraviolet fluorescence of SO₂ produced by absorption of the Zn 2138 Å or Cd 2288 Å line. The fluorescence intensity was found to be linear from 0.1 to 500 ppm of SO₂ in air with the Zn lamp and from 0.1 to 1600 ppm with the Cd lamp. The detection limit at present is about 20 ppb. There is no detectable interference from O₃, H₂S, NO₂, CO₂, CO, or H₂, although the presence of a large concentration of CS₂ (500 times as much as SO₂) NO (500 times) or C₂H₄ (4000 times) interferes with the measurement. The presence of 2% H₂0 reduces the signal by 25%, while up to 1 % CH₄ has almost no effect.     

新型无极紫外灯的光氧化性能研究

本实验对新型无极紫外灯的发射光谱、不同波长光线在溶液中的传播、·OH和O3的生成量、活性艳红X-3B溶液的降解情况进行了测定,并与普通中压汞灯进行了比较.结果表明,无极紫外灯在紫外区光强约为相近功率的普通中压汞灯的20倍;在溶液中紫外光比可见光更易被吸收;·OH生成与溶液对短波长光子的吸收存在对应关系,本实验中无极紫外灯的最大氧化距离约为6 cm;O3的生成量随着空气曝气量或254 nm处的光强的增大呈指数增加;降解活性艳红X-3B溶液的过程符合负一级动力学关系,降解效果明显好于普通中压汞灯,并且证明了无极紫外灯与生成的臭氧在活性艳红X-3B的降解过程中存在协同作用.     

The effects of sulphur dioxide on the parasitism of the rust fungus Uromyces viciae-fabae on Vicia faba

Vicia faba cv. Aguadulce was grown in fumigation chambers ventilated with filtered air or air containing sulphur dioxide (SO(2)) at controlled concentrations, and inoculated with the rust fungus Uromyces viciae-fabae. The influence of the pollutant was rated in terms of production of uredia and dehiscent urediospores. Exposures to SO(2) levels around 70-90 nl litre(-1) enhanced uredia density. Pre-inoculation fumigations at 70-86 nl litre(-1) increased uredia density, whilst post-inoculation fumigations stimulated urediospore production. Lower concentrations increased diffusion resistance of the host plant and slightly increased uredia density. Concentrations between 100 and 130 nl litre(-1) were somewhat inhibitory for the parasite, even in the absence of any visible damage symptoms on the host. Total sulphur accumulation in leaf tissue was reduced by the presence of the fungal infection. Growing under SO(2) pollution neither decreased germination ability nor modified morphological parameters of the urediospores. However, elongation of the germination tube of spores coming from filtered air was adversely affected by the pollutant.