广西不同石漠化等级下SPAC水势梯度及其环境效应

以野外观测为基础,对广西不同石漠化等级(无石漠化、轻度石漠化、中度石漠化和重度石漠化)下土壤-植被-大气连续体(Soil-Plant-Atmosphere Continuum,简称SPAC)系统中的水势日变化、气象因子日变化过程进行了研究。结果表明:随着石漠化程度的增加,大气水势降低,大气水势对不同石漠化程度的反应敏感。岩溶区石漠化等级下植物和土壤水势较低,不同石漠化条件下的植物叶水势在-7.79±0.43~-2.68±0.11 Mpa之间,土壤水势在-4.00±0~-0.08±0.04 Mpa之间,重度石漠化等级下植物处于萎蔫状态。植物在正午受到的水分亏缺程度为:重度石漠化中度石漠化无石漠化轻度石漠化。无石漠化下植物叶片水势与大气温度呈正相关关系,与大气相对湿度呈负相关关系,轻度石漠化、中度石漠化和重度石漠化下植物叶片水势与大气温度呈负相关关系,与大气相对湿度呈正相关关系。水分在SPAC系统中运移,其能量消耗主要集中在叶片-大气的过程。叶-气水势差差值大小为:中度石漠化重度石漠化轻度石漠化无石漠化。随着石漠化程度的增加,SPAC水势梯度提高,各介质层水势差的增大,提高了水分循环和能量交换的强度。     

上海市废旧荧光灯管回收体系建设的对策研究

废旧荧光灯管因含汞列入《国家危险废物名录》,若采取不当方式回收处置对环境存在污染隐患,由于多种原因大部分废旧荧光灯管未得到无害化处置,已经引起社会各界的关注和政府部门的重视。结合上海市的废旧荧光灯管产生及回收处置现状,针对法规、政策、机制方面存在的问题,通过研究提出源头控制、多渠道回收、建立豁免管理制度以及基金补贴机制等措施,为从根本上解决废旧灯管的回收难问题和探索社会源危险废物的管理提供了对策建议。     

铝——水反应制氢发展浅析

本文就各种制氢方式中铝-水反应制氢发展进行了浅析,主要分析了铝-水制氢各方法的优劣、发展过程及发展前景,讨论了铝-水反应制氢的可行性。     

增湿除湿太阳能海水淡化系统的试验研究

基于增湿-除湿原理,设计了一种新型的太阳能海水淡化装置,该装置包含太阳能空气集热器、太阳能热管集热器、横管蒸发器、竖管冷凝器以及冷却水箱。介绍了各部件的尺寸结构和工作原理,研究了影响系统产水量的各因素。结果表明:热海水温度、进口空气流量以及冷凝海水流量对产水量影响较大,而一定范围内环境温度的变化对产水量影响较小。数据显示,系统的产水率和效率分别为5.79×10-4kg/kJ和43.5%。     

Photocatalytic activity of Fe-doped CaTiO3 under UV-visible light

The photocatalytic degradation of methylene blue（MB） over Fe-doped CaTiO3 under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction（XRD）, scanning electron microscope（SEM） equipped with an energy dispersive spectrometer（EDS） system, Fourier transform infrared spectra（FT-IR）, and UV-visible diffuse reflectance spectroscopy（DRS）. The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO3 in the visible light region. The Fe-doped CaTiO3 exhibited higher photocatalytic activity than CaTiO3 for the degradation of MB.However, the photocatalytic activity of the Fe-doped CaTiO3 was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO3 prepared at500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB（10 ppm）under UV-visible light for 180 min.     

Dyes adsorption using a synthetic carboxymethyl cellulose-acrylic acid adsorbent

Removal of noxious dyes is gaining public and technological attention. Herein grafting polymerization was employed to produce a novel adsorbent using acrylic acid and carboxymethyl cellulose for dye removal. Scanning electron microscopy and Fourier-transform infrared spectroscopy verified the adsorbent formed under optimized reaction conditions. The removal ratio of adsorbent to Methyl Orange, Disperse Blue 2BLN and malachite green chloride reached to 84.2%, 79.6% and 99.9%, respectively. The greater agreement between the calculated and experimental results suggested that pseudo second-order kinetic model better represents the kinetic adsorption data. Equilibrium adsorptions of dyes were better explained by the Temkin isotherm. The results implied that this new cellulose-based absorbent had the universaiity for removal of dyes through the chemical adsorption mechanism.     

Removal of polycyclic aromatic hydrocarbons from aqueous solution by raw and modified plant residue materials as biosorbents

Removal of polycyclic aromatic hydrocarbons （PAHs）, e.g., naphthalene, acenaphthene, phenanthrene and pyrene, from aqueous solution by raw and modified plant residues was investigated to develop low cost biosorbents for organic pollutant abatement. Bamboo wood, pine wood, pine needles and pine bark were selected as plant residues, and acid hydrolysis was used as an easily modification method. The raw and modified biosorbents were characterized by elemental analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. The sorption isotherms of PAHs to raw biosorbents were apparently linear, and were dominated by a partitioning process. In comparison, the isotherms of the hydrolyzed biosorbents displayed nonlinearity, which was controlled by partitioning and the specific interaction mechanism. The sorpfion kinetic curves of PAHs to the raw and modified plant residues fit well with the pseudo second-order kinetics model. The sorption rates were faster for the raw biosorbents than the corresponding hydrolyzed biosorbents, which was attributed to the latter having more condensed domains （i.e., exposed aromatic core）. By the consumption of the amorphous cellulose component under acid hydrolysis, the sorption capability of the hydrolyzed biosorbents was notably enhanced, i.e., 6-18 fold for phenanthrene, 6-8 fold for naphthalene and pyrene and 5-8 fold for acenaphthene. The sorpfion coefficients （Kd） were negatively correlated with the polarity index [（O＋N）/C], and positively correlated with the aromaticity of the biosorbents. For a given biosorbent, a positive linear correlation between logKoc and logKow for different PAHs was observed. Interestingly, the linear plots of logKoc-logKow were parallel for different biosorbents. These observations suggest that the raw and modified plant residues have great potential as biosorbents to remove PAHs from wastewater.     

Characterization of extracellular polymeric substances in the biofilms of typical bacteria by the sulfur K-edge XANES spectroscopy

A combined approach of physicochemical extraction and sulfur K-edge X-ray absorption near-edge structure（XANES） spectroscopy was applied to characterize the extracellular polymeric substances（EPS） of typical bacterial biofilms in this study. Physicochemical analysis showed variation of the contents of DNA,polysaccharide and protein in different fractions of EPS in different mediums. The sulfur K-edge XANES analysis yielded a variety of spectra.Spectral fitting of the XANES spectra utilizing a large set of model compounds showed that there was more reduced sulfur in both LB-EPS（loosely bound EPS） and TB-EPS（tightly bound EPS） of all the biofilms in LB medium than in R2 A medium. More oxidized sulfur was identified in LB-EPS than that in TB-EPS,suggesting different niches and physiological heterogeneity in the biofilms. Our results suggested that the sulfur K-edge XANES can be a useful tool to analyze the sulfur speciation in EPS of biofilms.     

基于主成分-聚类分析模型的生态环境脆弱性分析:以平潭综合实验区为例

目前对平潭综合实验区(平潭主岛)脆弱性评价方面的研究仅有地下水系统的脆弱性研究,对生态环境方面的脆弱性研究尚未见诸文献中。针对此情况,文章首先从自然因素、人为干扰因素和环境因素3个方面构建了生态环境脆弱性指标体系,然后运用主成分-聚类分析模型对平潭综合实验区的生态环境脆弱性进行分区。脆弱性分区结论为平潭综合实验区总体为中强度脆弱,其中极强脆弱区为白青乡,强度脆弱区为北厝镇和苏澳镇,中度脆弱区为中楼乡、澳前镇和敖东镇,轻度脆弱区为平原镇、潭城镇和流水镇,微脆弱区为芦洋乡。文章从增加防护林的面积和种类、调整优化土地利用结构、开展生态功能区划和生态环境保护规划的编制工作三方面提出了降低研究区域生态环境脆弱性的对策措施。     

贫营养条件下17β-雌二醇厌氧生物降解规律研究

17β-雌二醇作为环境甾体雌激素污染的主要污染物之一,广泛分布于自然环境中。采用批次实验,研究了在贫营养条件下17β-雌二醇厌氧生物降解规律。结果表明,在贫营养条件下,厌氧污泥对17β-雌二醇的去除率达到90%(35℃,76 d),且降解作用主要集中在快速降解阶段,降解规律符合一级降解动力学模型(R2=0.95);厌氧污泥对17β-雌二醇的去除主要是通过转化为雌性效力较低的雌酮,再由雌酮转化为其他的转化产物,如17α-雌二醇;Fe(Ⅲ)对17β-雌二醇的去除和转化没有显著的影响。接种污泥的内源代谢作用产生甲烷,Fe(Ⅲ)的存在可以提高甲烷的产率,但对甲烷的总量没有显著影响。