青海省东部农业区参考作物蒸散量的变化及对气象因子的敏感性分析

使用FAO推荐的Penman-Monteith公式计算了青海省东部农业区7个气象代表站的逐日参考作物蒸散量(ET₀),运用多窗谱方法(MTM)对青海省东部代表站的ET₀的变化周期进行了分析,同时,分析了影响ET₀的主要气象要素的变化趋势,运用基于偏导数的敏感系数法分析了生长季ET₀对气温、日照时数、相对湿度、风速的敏感性,结果表明,青海省东部农业区的7个站点有比较一致的19.23~22.22 a的周期;整个东部农业区的气温(最高温度、最低温度、平均温度)呈明显的上升趋势,日照时数、风速、相对湿度则随纬度的变化而趋势不同,北纬36°以南的两个站日照时数、风速均有增加的趋势,相对湿度则减小,以北的5个站则呈相反的变化;ET₀对日照时数最为敏感,其次是气温、相对湿度和风速;敏感系数在整个生长季随气象因子的变化而变化,日照时数敏感系数呈波动状,最大值出现在4月,最小值出现在9月,气温敏感系数呈现单峰型变化,最大值出现在7月,风速敏感系数则呈单谷型变化,最小值出现在7月。     

Adsorption and movement of carbaryl in soils: A verification of cosolvent theory and comparison of batch equilibrium and soil thin layer chromatography results

Batch equilibrium and soil thin layer chromatography (TLC) techniques were used to investigate the influence of different volume fractions of organic cosolvents (acetone and methanol) on the adsorption and movement of carbaryl in four different types of Indian soils. L-shaped isotherms were obtained for both the cosolvent–water mixtures at all f _s values and were in close agreement with the Freundlich equation. Higher adsorption was observed on F.R.I. soil (FSL) followed by Alampur soil (ASL), Kalai soil (KL), and Bhoran soil (BSL) at all f _s values for both the cosolvent systems as was anticipated from the K and K _D values. The K and K _D values also confirmed that carbaryl adsorption was higher in methanol–water mixture than acetone–water mixture and decreased with increasing f _s values. The frontal R _f values obtained from soil TLC studies were inversely proportional to the K and K _D values for both the cosolvent systems. The higher K and K _D values and lower R _f values in methanol–water mixtures relative to acetone–water mixtures for all the soils indicated that acetone had a greater potential for ground water contamination compared to methanol. The adsorption data were used to evaluate the cosolvent theory for describing adsorption of carbaryl in acetone–water and methanol–water mixtures. The aqueous phase partition coefficients, K _DW (mol g^?1), normalized with respect to f _oc for carbaryl was evaluated by extrapolating f _s → 0.     

Electrochemical degradation of Acid Red I dye and its treatment by UV light

Degradation of Acid Red I (ARI) dye by electrochemical treatment and UV light irradiation was studied in this work. The effect of the current density and the concentration of NaCl and dye on the decoloration and degradation efficiency were studied and optimized. The UV irradiation was monitored by UV-Vis spectrophotometry and chemical oxygen demand. The kinetic constants for decoloration and degradation were calculated. Degradation of 86% was achieved in 160?min and the first-order kinetic constant was 0.013?min^?1. Degradation products were identified by gas chromatography/mass spectrometry. The mechanism for the degradation of ARI was proposed.     

Photocatalytic degradation of ciprofloxacin in aqueous media: a short review

The frequent detection of antibiotics such as ciprofloxacin in surface and drinking waters around the world has attracted concern from various researchers. Such presence is an indication that the decontamination of water polluted by antibiotics is beyond the conventional treatment methods. However, among the different treatment methods that have been developed in the area of water purification, heterogeneous photocatalysis using semiconductor as a mediator has been rated as an efficient and a green wastewater treatment method. This is because, the process is effective in degrading and mineralizing organic pollutants, using UV or visible light. The present review paper covers a brief survey over a range of publications in the last decade, involving photocatalytic materials that have been employed in the purification of water contaminated by ciprofloxacin.     

Determination and QSPR analysis of log Kow and log Koc for fluorine containing benzene derivatives

Octanol‐water partition coefficients (Kow) and soil organic carbon sorption coefficients (Koc) were determined for 14 fluorinated benzene derivatives. Quantitative structure‐property relationships were developed using molecular connectivity indices and quantum chemical parameters to analyze the most significant factors influencing these physico‐chemical properties of the compounds. The substitution by F in benzene derivatives has greater influence on Koc than on Kow.     

杭州无车日大气细颗粒物化学组成形成机制及光学特性

在世界无车日期间对PM2.5化学组分、光学参数及气态污染物进行同步监测,评估机动车尾气排放对杭州市细颗粒物污染及能见度的影响.结果表明:管制期间NO2、NOx、CO和PM2.5浓度分别为45.0, 50.8, 1119, 85.8μg/m3,比平日分别下降了17.5%、23.3%、20.6%和32.6%.管制期间PM2.5中OC、EC和二次无机组分浓度为8.58, 4.29, 25.95μg/m3,比管制前下降了13.8%、12.6%和15.7%,管制后则达到20.24, 10.85, 27.39μg/m3,上升了136.0%、152.7%和5.5%.管制期间较高的NO3-/PM2.5和NOR(0.15)表明PM2.5的形成更多受二次无机转化影响,管制后PM2.5中上升的OC、EC比例和较低的NOR(0.07)则说明PM2.5主要来自机动车排放的碳质组分的贡献.硫酸盐、硝酸盐、有机气溶胶和EC是最主要的消光组分,共解释了总消光系数的74.0%~89.7%.管制后,机动车排放的有机物和EC消光比例达到26.6%和24.6%,大气消光系数则达到438.7Mm-1,比管制期间上升了60.5%,表明机动车污染排放已成为影响杭州大气细颗粒物污染和能见度下降的重要因素.     

喀斯特石漠化山区苔藓多样性及水土保持研究

喀斯特石漠化已成为制约我国西南地区可持续发展的重要生态环境问题. 以云南芝云洞山区苔藓植物为研究对象,于2012年1月进行调查和样地设置,共采集样品75份,采用经典形态分类法进行鉴定,分析苔藓多样性及其对水土保持的贡献. 结果表明:苔藓植物有11科25属53种;苔藓植物种数为无石漠化区(34)＞轻度石漠化区(14)＞中度石漠化区(12)＞强度石漠化区(7),丰富度指数也为无石漠化区(2.8748)＞轻度石漠化区(0.1941)＞中度石漠化区(-1.1767)＞强度石漠化区(-1.8923). 石漠化区苔藓植物相似性指数相差较小,其中强度石漠化区与中度石漠化区的相似性指数为0.3750,强度石漠化区与轻度石漠化区为0.3077,中度石漠化区与轻度石漠化区为0.3846;而石漠化区与无石漠化区相似性指数相差较大,其中无石漠化区与强度和轻度石漠化区的相似性指数分别为0.0714和0.0952. 强度、中度和轻度石漠化区与无石漠化区均匀度指数分别为0.5900、0.5133、0.4899和0.6107. 6种优势苔藓植物(长叶纽藓、卷叶湿地藓、东亚小石藓、黑扭口藓、卵叶青藓和狭叶湿地藓)的生物量、成土量和饱和吸水量分别在0.962~9.546、1.294~40.181、8.890~82.571g/m2之间,表明可以将苔藓植物作为该类地区的先锋植物.      

水体中磺胺甲恶唑和甲氧苄氨嘧啶的自然光降解

实验研究了磺胺甲恶唑和甲氧苄氨嘧啶连续暴露于自然光下72 h,在pH值为4.0、7.0、9.0水体中的光降解行为,同时考察了黑暗条件下对照样品在不同pH条件下的稳定性.实验表明,光强、光照时间、水体pH都直接影响到磺胺甲恶唑的去除率.在自然光照环境下,不同pH溶液中的磺胺甲恶唑均易发生光降解,而黑暗对照样品去除率较小.甲氧苄氨嘧啶则比较稳定,几乎未发生降解,但黑暗对照样品在pH值为4.0和7.0的溶液中,与起始浓度相比,去除率大于10%,这可能主要与该药物在不同pH溶液中的离子形态及光照过程中的温度波动有关.     

碘铈共掺杂纳米TiO_2的制备及可见光光催化性能

采用溶胶凝胶法制备了不同原料比例碘铈共掺杂纳米TiO2催化剂,运用X射线光电子能谱（XPS）,X射线衍射（XRD）,透射电镜（TEM）等检测手段对催化剂进行了初步表征.结果表明,经过450℃煅烧处理得到的TiO2、铈掺杂TiO2以及碘铈共掺杂TiO2催化剂均为锐钛矿相,掺杂的Ce和I原子可能以I—Ce—O及O—Ti—I等键合方式进入TiO2晶格内部,此外,I-Ce离子共掺杂能有效降低TiO2表面的电子-空穴对的复合.以染料罗丹明B（Rhodamine B,RhB）和无色小分子水杨酸（Salicylic acid,SA）为降解的目标化合物,发现碘铈共掺杂的最佳物质的量之比为nCe∶nI∶nTi=0.04∶0.05∶1,即I0.05Ce0.04TiO2催化剂在可见光照射下（λ〉420 nm）降解目标化合物其光化学活性明显优于单掺铈的TiO2催化剂和未掺杂的TiO2.该催化反应涉及到空穴氧化,并伴有羟基自由基（.OH）、超氧自由基（O2.-）及H2O2等氧化物种的产生.