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81.
Achour Terbouche Chafia Ait Ramdane-Terbouche Didier Hauchar Safia Djebbar 《环境科学学报(英文版)》2011,23(7):1095-1103
The adsorption capacities of new humic acids isolated from Yakouren forest (YHA) and Sahara (Tamenrasset: THA) soils (Algeria)
and commercial humic acid (PFHA) on polyaniline emeraldine base (PEB) were studied at pH 6.6. Also the adsorption of heavy
metals such as Cd2+, Zn2+ and Ni2+ on humic acid-polyaniline systems (HA-PEB) was investigated at the same conditions. HA-PEB
compounds were characterized by scanning electron microscopy (SEM), infrared spectrometry and cavity microelectrode. In addition,
batch adsorption and cavity microelectrode were used in the adsorption study of Cd2+, Zn2+ and Ni2+ on HA-PEB. To develop biocaptors
of polluting metals using a cavity microelectrode modified by HA-PEB systems, the adsorption kinetic and adsorption capacity were
investigated. The SEM analysis showed that the presence of humic acid affected the PEB surface and caused the formation of a
granular morphology. The maximum adsorption capacities (qmax) of PFHA, THA and YHA determined by adsorption isotherms were
91.31, 132.1 and 151.0 mg/g, respectively. Batch adsorption results showed that qmax of Cd2+, Zn2+ and Ni2+ on HA-PEB followed
the order: THA-PEB > YHA-PEB > PFHA-PEB. The voltammograms obtained with HA-PEB modified cavity microelectrode showed
the appearance of new redox couples reflecting the adsorption of HA on PEB. Metal-humic acid-polyaniline voltammograms were
characterized by appearance of oxidation-reduction couples or reduction wave corresponding to metal. Finally, the result may be
exploited to develop a biocaptor based on the cavity microelectrode amended by THA-PEB and YHA-PEB. 相似文献
82.
83.
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. 相似文献
84.
Xiuying Zhao Xinming Wang Xiang Ding Quanfu He Zhou Zhang Tengyu Liu Xiaoxin Fu Bo Gao Yunpeng Wang Yanli Zhang Xuejiao Deng Dui Wu 《环境科学学报(英文版)》2014,26(1):110-121
Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary. 相似文献
85.
在不同燃烧条件下对6种麦草进行焚烧,并利用GC/MS对麦秸和烟尘中的正构脂肪酸进行了测定.结果表明,烟尘中含有碳数C8~C32的正构脂肪酸.在明火烟尘中,正构脂肪酸总含量分布于1 509.3~10 543.7 mg·kg-1之间,平均值为5 871.2mg·kg-1.其轻(C8~C16)、重(C17~C32)正构脂肪酸含量之比(L/H)为0.8~5.3,平均值为2.8;C14/C16、C28/C16、C30/C16等比值的平均值分别为16.5%、14.1%、11.4%.正构脂肪酸呈双峰式分布,其主峰碳数是C16,次峰碳数是C28或C30,且具有显著的偶碳数优势.其碳优势指数(CPI)和平均碳链长度(ACL)的平均值分别为19.8和18.2.在闷烧烟尘中,正构脂肪酸的总含量为5 799.3~37 244 mg·kg-1,平均值为15 838.6 mg·kg-1.其L/H值介于1.2~5.6之间,平均为4.2;C14/C16、C28/C16、C30/C16的平均值分别为12.7%、10.1%、6.0%.闷烧烟尘中正构脂肪酸的分布模式与明火烟尘的类似,其CPI和ACL的平均值分别为24.7和17.7.总之,虽然两类烟尘和麦秸中的正构脂肪酸均具有类似的分布模式和偶碳数优势,但三者在组成上仍然存在明显的差别.这有助于识别大气气溶胶中麦秸及其燃烧排放的正构脂肪酸. 相似文献
86.
提高污泥碱性发酵挥发酸积累的新方法 总被引:4,自引:2,他引:2
为了加大剩余污泥在碱性条件下的水解酸化程度,本研究尝试了两种新的能促进污泥碱性发酵产酸的方式,分别是向批式的污泥碱性发酵系统中投加未灭菌发酵污泥和投加灭菌发酵污泥,结合温度的影响(10℃和35℃)分别考察了这两种方式对污泥水解酸化效果的影响.结果表明,中温有利于水解酶和产酸菌作用的发挥,增大了污泥的水解酸化程度,体系内有明显的挥发酸(VFAs)积累.35℃条件下,两种方式都在很大程度上促进了新鲜污泥的水解酸化程度,经灭菌后的发酵污泥的投加较等量的未灭菌的发酵污泥的投加效果更为显著.前者的水解速率是后者的2倍,发酵末期酸积累量为后者的1.5倍,且前者在较长的发酵时间内VFAs含量维持恒定.分析两种方式能促进污泥水解酸化的原因得到:未灭菌发酵污泥的投加是向系统中引入了一定量的产酸菌,灭菌发酵污泥的投加引入了大量的较易水解的有机底物.水解产物的增加能在更大程度上影响产酸的效果.因此,中温条件下向污泥碱性发酵系统中投加经灭菌处理后的发酵污泥是提高剩余污泥发酵产酸量更为有效的方式. 相似文献
87.
滴水湖及其水体交换区沉积物和土壤中PAHs的分布及生态风险评价 总被引:4,自引:3,他引:1
采用GC-MS联用技术分析了滴水湖及其水体交换区23个表层沉积物和土壤中16种多环芳烃(PAHs)的含量,探讨其分布特征及来源并对其生态风险进行评价.结果表明,滴水湖沉积物中16种PAHs含量范围是11.49~157.09 ng·g-1,平均含量为66.60 ng·g-1,湖区沉积物中PAHs含量比入湖区低,但比出湖区高.湖区外的沉积物和土壤中PAHs组成主要以中、高分子量PAHs(4环、5~6环)为主,而湖区内表层沉积物中PAHs组成则以低分子量PAHs(2~3环)和高分子量PAHs(5~6环)为主.通过特征化合物分子比值法、主成分分析及多元线性回归模型判源,表明湖区外沉积物和土壤中PAHs来源主要为燃烧源,而湖区内沉积物中PAHs来源为燃烧源和石油类产品泄漏的混合来源.生态风险评价显示,滴水湖及其水体交换区沉积物和土壤中PAHs生态风险较低. 相似文献
88.
不同碳源在污水处理过程中的变化规律研究 总被引:4,自引:4,他引:0
通过对A2/O污水处理工艺长期的分析监测,探明了城市污水处理厂原水中有机物不同生物降解性及碳源赋存形态比例.原水中大部分有机物以颗粒态存在,占进水有机物的61%.原水中快速、慢速、难生物降解有机物比例分别为15.8%、54.2%和30%,快速生物降解有机物主要以溶解态存在,慢速生物降解有机物则主要以颗粒态存在.通过快速、慢速生物降解有机物的沿程监测分析,明确了两种碳源在污水处理过程中的变化规律,厌氧池与缺氧池内均存在微生物水解发酵引起的慢速生物降解有机物的转化作用,其中厌氧反应池的转化效率最高.分析计算了污水处理过程中不同碳源的转化,明确了快慢速有机物在各单元的转化和利用情况,结果指出,2 h内慢速生物降解有机物在厌氧池与好氧池转化率分别为33%和20%.从脂肪酸的种类及含量来说,厌氧池与缺氧池的脂肪酸的种类及含量均高于原水. 相似文献
89.
利用液液萃取法和气相色谱-质谱方法对佛山境内高明河水环境多环芳烃(PAHs)进行了测定,并对PAHs的分布特征与通量进行了初步研究.结果表明高明河水环境中16种优控PAHs的浓度范围在41.6~375.6 ng/l之间,从上游到下游总体呈递增的趋势,其下游浓度偏高可能与荷城街道较为密集的工业和人口分布有关.高明河水环境PAHs的总含量高于欧美一些低污染水域,但低于国内一些主要河流.高明河PAHs年通量约为333.8 kg. 相似文献
90.
岩溶地下河水中多环芳烃、脂肪酸分布特征及来源分析 总被引:2,自引:1,他引:1
为探究重庆青木关岩溶地下河水中多环芳烃(PAHs)和脂肪酸的含量组成、分布特征、来源及污染水平,2013年雨季和旱季分别于地下河中进行水样采集,并利用气相色谱-质谱联用仪(GC-MS)对水样中PAHs和脂肪酸的组分进行定量分析.结果表明,青木关地下河水中PAHs和脂肪酸的含量范围分别为77.3~702 ng·L~(-1)和3 302~45 254 ng·L~(-1).组成上,PAHs以2~3环为主,其比例高于90%,脂肪酸碳数范围为C10~C28,以饱和直链脂肪酸为主,其次为单不饱和脂肪酸.分布特征上,雨季:地下河水中各采样点PAHs的含量差异较小,脂肪酸的含量在入口、出露处和出口呈现依次降低的趋势,其中出露处和出口脂肪酸的含量较为接近;旱季:地下河水中PAHs含量在入口、出露处和出口呈现先降后升的趋势,脂肪酸含量在各采样点较为接近.总体上,地下河水中PAHs和脂肪酸的含量都表现为雨季显著高于旱季.来源分析表明,青木关地下河水中PAHs主要来源于该河流域煤和木材、农作物秸秆等生物质的燃烧;脂肪酸主要来自该河流域内硅藻、绿藻等水生藻类和细菌,其中以水生藻类的贡献占主导.地下河水受到PAHs中轻度污染,相对于旱季,雨季污染更严重. 相似文献