仿刺参水溶性海参皂苷的分离制备及抗真菌活性的研究

利用海洋生物资源进行天然抗真菌新药的开发,从冻干海参加工废液中提取了水溶性海参皂苷,并对其抗真菌活性进行了研究。采用大孔吸附树脂法提取水溶性海参皂苷,经Libermann Burchard反应等对提取物的性质进行鉴定后,利用管碟法对所得提取物的抗菌活性进行了测定,并利用琼脂稀释法测定了所得水溶性海参皂苷对6株供试真菌的最低抑菌浓度(MIC)。提取物在Molish反应、沉淀反应和泡沫实验中均为阳性,说明提取物中确含有皂苷类成分;在Libermann Burchard反应中,液体的颜色处在红色与紫色之间,显示提取物可能是1种三萜类皂苷。水溶性海参皂苷对6株供试真菌均具有显著的抑制作用,且在浓度为0.5~4 mg/mL的范围内,其抑菌活性与所用浓度之间呈明显的正相关性;在浓度为4 mg/mL时,水溶性海参皂苷对6株供试真菌抑制活性的大小依次为裂殖酵母菌、啤酒酵母菌、白色念珠菌、葡萄炭疽病原菌、黄瓜枯萎病原菌和黑曲霉,海参皂苷对6株真菌的MIC值依次分别为0.002,0.016,0.063,0.063,0.125,0.250 mg/mL。     

Changes in dissolved organic matter (DOM) amount and composition along nested headwater stream locations during baseflow and stormflow

Amount and composition of dissolved organic matter (DOM) were evaluated for multiple, nested stream locations in a forested watershed to investigate the role of hydrologic flow paths, wetlands and drainage scale. Sampling was performed over a 4‐year period (2008–2011) for five locations with drainage areas of 0.62, 3.5, 4.5, 12 and 79 ha. Hydrologic flow paths were characterized using an end‐member mixing model. DOM composition was determined using a suite of spectrofluorometric indices and a site‐specific parallel factor analysis model. Dissolved organic carbon (DOC), humic‐like DOM and fluorescence index were most sensitive to changes with drainage scale, whereas dissolved organic nitrogen, specific UV absorbance, Sr and protein‐like DOM were least sensitive. DOM concentrations and humic‐like DOM constituents were highest during both baseflow and stormflow for a 3.5‐ha catchment with a wetland near the catchment outlet. Whereas storm‐event concentrations of DOC and humic DOM constituents declined, the mass exports of DOC increased with increasing catchment scale. A pronounced dilution in storm‐event DOC concentration was observed at peak stream discharge for the 12‐ha drainage location, which was not as apparent at the 79‐ha scale, suggesting key differences in supply and transport of DOM. Our observations indicate that hydrologic flow paths, especially during storms, and the location and extent of wetlands in the catchment are key determinants of DOM concentration and composition. This study furthers our understanding of changes in DOM with drainage scale and the controls on DOM in headwater, forested catchments. Copyright © 2014 John Wiley & Sons, Ltd.     

喜马拉雅珠峰地区冬季大气气溶胶化学组分及光学特征

为了研究喜马拉雅山北坡冬季大气气溶胶化学组分、光学特征及来源,2017年11—12月在珠穆朗玛峰站(QOMS)共采集22个PM2.5样品.结果显示:PM2.5中包括水溶性离子(WSIs)、有机质(OM)、元素碳(EC)在内的所有检测成分,总质量浓度为(3.36±1.06)μg·m-3;有机碳(OC)、元素碳(EC)和水...     

Water-soluble organics in atmospheric particles: A critical review of the literature and application of thermodynamics to identify candidate compounds

Although organic compounds typically constitute a substantial fraction of the fine particulate matter (PM) in the atmosphere, their molecular composition remains poorly characterized. This is largely because atmospheric particles contain a myriad of diverse organic compounds, not all of which extract in a single solvent or elute through a gas chromatograph; therefore, a substantial portion typically remains unanalyzed. Most often the chemical analysis is performed on a fraction that extracts in organic solvents such as benzene, ether or hexane; consequently, information on the molecular composition of the water-soluble fraction is particularly sparse and incomplete.This paper investigates theoretically the characteristics of the water-soluble fraction by splicing together various strands of information from the literature. We identify specific compounds that are likely to contribute to the water-soluble fraction by juxtaposing observations regarding the extraction characteristics and the molecular composition of atmospheric particulate organics with compound-specific solubility and condensibility for a wide variety of organics. The results show that water-soluble organics, which constitute a substantial fraction of the total organic mass, include C2 to C7 multifunctional compounds (e.g., diacids, polyols, amino acids). The importance of diacids is already recognized; our results provide an impetus for new experiments to establish the atmospheric concentrations and sources of polyols, amino acids and other oxygenated multifunctional compounds.     

Real-Time Observation on Water-Soluble Ions of PM_(2.5)in Beijing under the Influences of Different Air Masses in Summer

To further understand the variations of water-soluble ions in PM2.5 in Beijing,the authors observed their concentrations continuously and in high temporal resolution by the system for rapid collection of fine particles and ion chromatography(RCFP-IC) during 12–18 July 2010.These results combined with those of earlier backward trajectory research are used analyzed to determine the causes of concentration changes in water-soluble ions under the influences of two kinds of air masses in summer.The results indicate that concentrations of NO3-,SO42-,and NH4+ were influenced strongly by the continental air mass than by the marine air mass.Cl- and Na+ were not changed significantly.Because the sources of K+,Mg2+,and Ca2+ are mainly concentrated on land,their concentration levels were slightly higher under the control of continental air mass than that of the marine air mass.Variations of NO2- during the observation differed from those of other ions;its concentration was significantly higher under the influence of marine air mass.Moreover,the authors obtain the diurnal variations of eight water-soluble inorganic ions including NH4+,K+,Mg2+,Ca2+,Cl-,NO2-,NO3-,and SO42-.Diurnal variations of NH4+,NO3-,and Cl- showed single peak,which appeared before noon,while SO42- showed two peaks that appeared during rush hours.Those of Mg2+,Ca2+,and K+ showed single peak that appeared in the afternoon.That of NO2- showed with a peak appearing at sunrise and a valley appearing at sunset.     

祁连山老虎沟地区夏季大气颗粒物中水溶性离子的变化特征

为了研究青藏高原东北缘老虎沟地区大气颗粒物中水溶性无机离子组分的变化特征,于2016年7月16日至8月11日共采集13个PM_2.5样品和4套粒径分级样品。研究结果显示：非沙尘期间,水溶性离子总质量浓度为2.35 μg·m^-3,主要离子SO₄^2-、Ca²⁺、NH₄⁺和NO₃^-的浓度分别为1.28、0.33、0.32和0.28 μg·m^-3,约占水溶性离子浓度总和的94%;沙尘期间,水溶性无机离子总质量浓度为12.63 μg·m^-3,是非沙尘期间浓度的5倍,主要离子SO₄^2-、Ca²⁺、Cl^-、Na⁺和NO₃^-的浓度依次为5.36、4.77、0.80、0.62和0.61 μg·m^-3,约占水溶性离子浓度总和的96%。分级样品分析结果表明,NO₃^-主要分布在粗颗粒模态,可能是前体物在粉尘表面发生非均相反应产生。在沙尘时期,SO₄^2-主要为粉尘贡献,集中分布在粗颗粒模态。在非沙尘时期,SO₄^2-在粗颗粒模态和积聚模态都有较多的分布。积聚模态的SO₄^2-主要是通过前体物与NH₃发生均相反应产生。据估算,非沙尘时期的二次反应对PM_2.5中SO₄^2-的贡献约为80%。     

世界水溶气资源分布、现状及问题

针对世界水溶气资源及国内外勘探开发现状统计结果表明,全世界水溶气资源丰富,总量达33 837×1012m3,这比常规天然气资源量(293×1012m3)高两个数量级;中国主要的含油气盆地中水溶气资源也很丰富,43个盆地的水溶气资源量的估算结果达到19×1012m3。对水溶性气藏成藏条件的分析研究认为:丰富的气源、异常高地层压力、储集层和保存条件是形成该类气藏的主要条件。根据天然气溶解的Henry经验定律、分子间隙溶解机理分析,认为溶解和脱气过程中除了考虑温度和压力变化,还存在构造震荡脱气等脱气过程。由于对不同的地层水条件下,天然气的溶解度变化的认识尚不太清晰,且富集条件及静态气藏形成条件是否能够促成动态气藏的形成,以及其他因素对气藏有何影响亦需要深入研究,对国内水溶性气藏资源需要进行系统的评价,确定气藏的有效开发技术方法,以促进水溶性天然气的勘探和开发,增加我国天然气供给的途径。     

Gas-Phase Formation of Water-Soluble Organic Compounds in the Atmosphere: A Retrosynthetic Analysis

Atmospheric particles contain a myriad of organiccompounds, including many multifunctional,water-soluble organic compounds. Many of thesecompounds are postulated to be secondary of origin. This work investigates the possible precursors ofseveral classes of multifunctional, water-solublesecondary organic compounds by analyzing the pathwaysleading to their formation, based on known gas-phasereactions. The analysis is termed `retrosynthetic'due to the backward direction of the analysis, fromproducts to precursors. Pathways for multi-functionalcompounds were generated combinatorially, consideringthe formation of one functional group at a time.Many multifunctional organic compounds with carboxylicacid, carbonyl, and hydroxy functional groups werefound to be first- or second-generation products ofcommon anthropogenic and biogenic volatile organiccompounds such as alkanes, alkenes, aromatics, andcyclic alkenes. The estimated yields of water-solubleorganic compounds from primary precursors ranged fromless than 1% to over 10%, based on stoichiometricconsiderations. The SOA formation index, whichcombines the concepts of yields and rates, was used tocompare the feasibility of the retrosyntheticpathways. Many of the candidate pathways involve theisomerization reaction of alkoxy radicals andoxygenated intermediate products such asmonocarboxylic acids and hydroxyaldehydes.     

武汉市冬季灰霾期PM2.5中水溶性无机离子的特征

2018年1月,利用颗粒物采样器采集武汉市大气PM_2.5样品并进行水溶性无机离子（F^-、Cl^-、NO₃^-、SO₄^2-、Na⁺、NH₄⁺、K⁺、Mg²⁺、Ca²⁺）的分析.结果表明,NO₃^-、SO₄^2-、NH₄⁺是PM_2.5中最主要的3种水溶性无机离子,除Mg²⁺与Ca²⁺外,PM_2.5与WSⅡs （水溶性无机离子）之间的相关性显著,且移动源贡献占主导地位.阴阳离子平衡表明武汉市冬季灰霾期PM_2.5呈中性或弱酸性.通过混合单粒子拉格朗日综合轨迹模式模拟并采用分层聚类得出了4种主要的后向气流轨迹及相应的PM_2.5和水溶性离子浓度,结果表明区域传输对此次灰霾期影响较大.     

固相萃取—高温裂解—气相色谱质谱法测定西台晶间卤水中溶解性有机质

采用3种固相萃取材料(C18、XAD-8/4和PPL)分离富集西台吉乃尔盐湖卤水中的溶解性有机物(DOM),通过总有机碳/总氮分析(TOC/TN)、紫外—可见光谱分析、元素分析、傅里叶变换红外光谱分析(FTIR)、高温裂解—气相色谱质谱联用仪(Py-GC/MS)等对富集的有机物进行表征和分析方法比较。结果表明,西台吉乃尔盐湖卤水中的溶解性有机物主要有多糖类,芳香类、含氮类有机物,烷烃烯烃类化合物。PPL,C18和XAD-8/4的回收率分别为40±2%,7±2%和16±1%,虽然C18和XAD-8/4回收率较低,但3种吸附剂都有各自的特点,C18较易吸附烷烃烯烃类有机物,XAD-8/4较易吸附芳香类有机物,PPL较易吸附含N类有机物和多糖类有机物。