森林新近凋落叶溶出DOM的性质及其对菲增溶作用的影响

凋落叶作为森林凋落物的主要组成部分,其溶出的大量有机质也是森林土壤可溶性有机质（DOM）的主要来源之一。研究森林凋落叶溶出DOM对PAHs增溶作用的影响有利于合理预测及评价森林土壤中PAHs的环境行为和生态风险。本研究采集了南亚热带常绿阔叶人工林的4种常见树种--尾叶桉（Eucalyptus urophylla）、木荷（Schima superba）、大叶相思（Acacia auriculiformis）和湿地松（Pinus elliottii）的新近凋落叶为试验材料,研究其DOM含量、组成与性质,对比分析了不同凋落叶DOM对菲的増溶作用及其与DOM性质的相关关系。结果表明,4种凋落叶的可溶性有机碳（DOC）质量分数在C 11.61~36.25 mg·g-1之间,其中尾叶桉的含量最大,湿地松最小。尾叶桉和木荷DOM的主要组分是可溶性糖（SS）和可溶性酚（SP）,两者总C量占DOC的比例超过47%,而大叶相思和湿地松中SS和SP两者总量所占比例均低于30%。另外,4种凋落叶DOM的质量分数（以C计）与其电导率的线性关系图中有明显转折点,说明它们均具有表面活性剂的性质。凋落叶DOM在临界胶束浓度（CMC）之上对菲具有不同程度的増溶作用,其与菲的结合系数（logKDOC）的大小顺序为尾叶桉（3.05 L·kg-1）＞木荷（3.02 L·kg-1）＞大叶相思（2.79 L·kg-1）＞湿地松（2.54 L·kg-1）,这表明尾叶桉和木荷DOM的增溶作用明显高于大叶相思和湿地松DOM。经分析表明,logKDOC与各DOM在254、280 nm处的特征紫外吸光度值（SUV-A254、SUV-A280）及其SS、SP的相对含量均呈显著正相关（p＜0.01）,与A240/A420、A254/A400比值呈显著负相关（p＜0.01）,说明DOM的芳香化程度越高,分子量越大, SS与SP所占比例越高,其对菲的増溶效果越明显。     

Effects of salinity on soil bacterial and archaeal community in estuarine wetlands and its implications for carbon sequestration: verification in the Yellow River Delta

Soils from two typical tidal salt marshes with varied salinity in the Yellow River Delta wetland were analysed to determine possible effects of salinity on soil carbon sequestration through changes in soil microbiology. The mean soil respiration (SR) of the salt water–fresh water mixing zone (MZ) was 2.89 times higher than that of the coastal zone (CZ) (4.73 and 1.63?μmol?m^?2?s^?1, respectively, p?Pseudomonas sp. and Limnobacter sp. that might have led to its higher dehydrogenase activity and respiratory rates. Additionally, the CZ possessed more Halobacteria and Thaumarchaeota with the ability to fix CO₂ than the MZ. Significantly lower soil salinity in MZ (4.25?g?kg^?1) was suitable for β-Proteobacteria, but detrimental for Halobacteria compared with CZ (7.09?g?kg^?1, p?相似文献   

高岭土对不同污染物微滤过程的影响

本研究采用原子力显微镜(AFM)结合自制的膜探针以及Zeta电位仪通过分别测量不同有机污染物,即腐殖酸(HA)、牛血清蛋白(BSA)和海藻酸钠(SA)与微滤膜之间的粘附力以及相应污染物的Zeta电位,对高岭土在不同有机物微滤过程的影响进行了系统性研究。结果表明,高岭土对污染膜通量衰减的影响主要发生在膜过滤的初期阶段,其存在使HA污染膜的初期通量衰减幅度增加,BSA和SA污染膜的初期通量衰减幅度减缓;清洗后HA污染膜的通量恢复率降低,而BSA和SA污染膜的通量恢复率增大。而且,高岭土的存在使膜-HA之间的粘附力变大以及HA溶液的Zeta电位变小,膜-BSA、SA之间的粘附力变小以及相应污染物的Zeta电位都增大。因此,膜-污染物之间粘附力以及溶液的Zeta电位的变化可以指示膜污染的变化趋势。     

An overview of the methods used in the characterisation of natural organic matter (NOM) in relation to drinking water treatment

Natural organic matter (NOM) is found in all surface, ground and soil waters. During recent decades, reports worldwide show a continuing increase in the color and NOM of the surface water, which has an adverse affect on drinking water purification. For several practical and hygienic reasons, the presence of NOM is undesirable in drinking water. Various technologies have been proposed for NOM removal with varying degrees of success. The properties and amount of NOM, however, can significantly affect the process efficiency. In order to improve and optimise these processes, the characterisation and quantification of NOM at different purification and treatment processes stages is important. It is also important to be able to understand and predict the reactivity of NOM or its fractions in different steps of the treatment. Methods used in the characterisation of NOM include resin adsorption, size exclusion chromatography (SEC), nuclear magnetic resonance (NMR) spectroscopy, and fluorescence spectroscopy. The amount of NOM in water has been predicted with parameters including UV-Vis, total organic carbon (TOC), and specific UV-absorbance (SUVA). Recently, methods by which NOM structures can be more precisely determined have been developed; pyrolysis gas chromatography-mass spectrometry (Py-GC-MS), multidimensional NMR techniques, and Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS). The present review focuses on the methods used for characterisation and quantification of NOM in relation to drinking water treatment.     

炼焦过程挥发性有机物排放特征及其大气化学反应活性

利用不锈钢采样罐和全自动预浓缩/GC/MS系统,在58-Ⅱ型和JN43-80型焦炉顶测试了炼焦过程中挥发性有机物(VOCs)中各组分的浓度,研究了VOCs排放特征,结合OH自由基消耗速率分析了这些物质的反应活性.研究发现,在装煤时刻和炼焦过程中,58-Ⅱ型焦炉产生的总挥发性有机物(TVOCs)浓度分别为7022 μg·m-3和6266μg·m-3;JN43-80型焦炉产生的TVOCs浓度分别为4185 μg·m-3和3298μg·m-3.装煤时刻产生的TVOCs浓度明显高于炼焦过程产生的.炼焦过程(包括装煤时刻)无组织排放的VOCs,包含烯烃、烷烃、芳香烃、卤代烃以及少量的醛和酮,其中乙烯、乙烷、丙烯、苯以及甲苯等为主要成分.这些产生的VOCs反应活性各不相同,活性最大的是烯烃类物质.其活性占TVOCs反应活性比重为86.2%±2.1%;其次是芳香烃类物质,其活性比重为9.2%±3.1%;反应活性最大的5个物种分别是丙烯、乙烯、1,3-丁二烯、1-丁烯以及苯乙烯.     

溶解性有机氮乙酰胺氯化生成饮用水THMs的影响因素研究

氯化消毒可以有效杀灭细菌,但同时会产生危害人体健康的消毒副产物(DBPs).溶解性有机氮(DON)是DBPs的重要前体物,为考察DON对THMs的影响,首次选取乙酰胺(AcAm)作为前体物DON的代表物质,采用Plackett-Burman和Box-Behnken方法设计试验,考察了AcAm初始浓度、加氯量、pH、温度、溴离子浓度和反应时间等因素对三卤甲烷(THMs)生成的影响.结果表明,在AcAm生成THMs的过程中,AcAm初始浓度、pH和反应温度3个因素的影响程度较小,溴离子、有效氯和反应时间3因素的影响较大,其中溴离子的影响最为显著.溴离子浓度一定时,改变有效氯的含量,生成的THMs总量变化不大,溴离子对THMs的生成有一定的催化作用,控制溴离子的浓度是减少AcAm生成THMs的有效措施.在有效氯为8.77 mg/Ｌ、溴离子为0.77 mg/Ｌ及接触时间为6.20 h的条件下,THMs存在最大生成量为45.82 μg/L.随着反应时间的推移,溴分配系数n呈上升趋势,控制消毒反应时间,是减少THMs致癌风险的有效方法.同时探讨了AcAm生成THMs的反应路径,表述了溴离子的催化作用机制.     

Co-transport of dissolved organic matter and heavy metals in soils induced by excessive phosphorus applications

To evaluate the e ects of long-term applications of phosphorus fertilizers on mobility of dissolved organic matter (DOM) and heavy metals in agricultural soils, a sandy soil and a loamy soil were spiked with ammonium phosphate at application rates of 0, 25, 50, 100, 250, and 500 mg P per kilogram of soil. A series of 15-cm long soil columns were constructed by packing incubated soils of varying concentrations of P. The soil columns were consecutively leached by simulated rainfalls for six cycles. The contents of water extractable organic carbon in both sandy and loamy soils increased significantly with increasing rates of P applications. Relatively high rates of P applications could induce a marked increase in DOM concentrations in the leachates, the e ects were larger with the sandy soil rather than with the loamy soil. Applications of P changed the partitioning of trace metals in the soil solids and the soil solutions. The increased P application rates also seemed to elevate the leaching of Cu, Cd, and Zn from soils. The concentrations of Cu, Cd, and Zn in the leachates were positively correlated with DOM, probably due to the formation of metal-DOM complexes. In contrast, Pb concentrations in the leachates were negatively correlated with DOM, and decreased with increasing rates of P applications. The boosted leaching of DOM induced by high rates of P applications was probably due to the added phosphate ions competing for adsorption sites in the soil solids with the indigenous DOM.     

活性碳纤维改性技术研究进展

介绍了活性碳纤维(ACF)的孔结构及表面官能团,综述了国内外ACF改性技术的研究现状.ACF的改性主要包括孔结构调控和表面化学改性,表面化学改性包括氧化还原法、表面负载法、浸渍法、热处理法、远程等离子体处理法、微波辐照法等,也可将多种方法结合来对ACF进行改性,以改善和提高ACF的吸附性能.在总结现有研究的基础上,对ACF改性技术发展趋势进行了展望.     

环境中VOCs的污染现状及处理技术研究进展

综述了近十年来大气环境中挥发性有机物(VOcs)的污染现状及其主要处理技术的研究进展.介绍了目前大气环境中VOCs的主要处理技术(包括吸附、冷凝及膜分离等回收技术和燃烧、等离子体、光催化降解和生物降解等销毁技术)的适用条件、经济性、可操作性和净化效率.提出要对VOCs的吸收和生物降解的反应动力学模型、催化机制、材料的性能及微生物活性进行深入研究的建议.     

Toxicity and subcellular distribution of cadmium in wheat as affected by dissolved organic acids

We aim to investigate the effects of humic acid (HA) and citric acid (CA) on the toxicity and subcellular distribution of Cd in wheat. Results show that the toxicity and uptake of Cd decreased with increasing HA. The EC₅₀ values of Cd increased from 3.36 μmol/L to 4.96 and 7.33 μmol/L at 50 and 250 mg/L HA, respectively, but decreased to 1.39 μmol/L in the presence of CA based on free ion activity model (FIAM). HA decreased the relative subcellular distribution of Cd in the heat-denatured proteins (decreased from 54% to 33%) but increased Cd in the heat-stable proteins in root (from 25% to 50%) at 7.61 μmol/L {Cd²⁺} (free Cd activity), which resulted in decreasing Cd toxicity. However, CA increased Cd toxicity due to the increased internalization of Cd although the relative subcellular distributions of Cd exhibited a decrease in the heat-denatured proteins and increase in the granule fraction compared to the control at high-level Cd. The FIAM could not predict the toxicity of Cd in the presence of organic acids. Alternatively, the internal Cd accumulation and subcellular Cd concentration were better to describe the toxicity of Cd to wheat.