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111.
苔藓Lophozia ventricosa挥发油化学成分研究 总被引:1,自引:0,他引:1
采用水蒸气蒸馏法提取苔藓Lophozia ventricosa挥发油,用毛细管色谱法对挥发油进行了分析,采用归-化法确定各组分的相对含量,并用GC—MS联用技术对分离的化学成分进行鉴定.经计算机检索并结合文献调研,共鉴定出28个化合物,占挥发油总量的93.3%,其中含1个单萜、23个倍半萜(15个为含氧倍半萜)和1个二萜,主要成分为Maalioxide(45.6%)和Eudesma-4.(15),7(11)-dien-8-one(28.9%).图2表1参12 相似文献
112.
焦化废水中有机物在A1-A2-O系统各段的降解与转化 总被引:7,自引:0,他引:7
在厌氧酸化-缺氧-好氧(A1-A2-O)生物膜系统小试装置中处理焦化废水,以探讨有机物在各阶段的降解与转化情况。通过UV吸收光谱及GC/MS分析发现,上海焦化厂废水中的有机组分主要为:甲酚、苯酚、二甲酚等酚类化合物,及以喹啉、吲哚为代表的含氮杂环化合物,约占有机物总量的90%。经A1-A2-O生物膜系统处理后,大部分有毒有害难降解有机物得到了降解和转化。厌氧段中原有物质浓度的增加和新物质的生成,是厌氧酸化使部分有机物降解产生中间产物而造成;缺氧段使大部分有机物被完全降解或转化,还产生一些新的简单有机物,如卤代烃、酯类、醛类等;经好氧段反应后,有机物进一步降解和转化,部分被完全去除,在降解转化过程中又产生了一些中间产物和衍生物,如苯酚、羟基喹啉等。 相似文献
113.
自动固相微萃取-毛细管气相色谱法检测环境水中苯系物的研究 总被引:6,自引:0,他引:6
对自动固相微萃取(SPME)-毛细管气相色谱法测定环境水中苯系物的方法进行了研究。通过对环境水中苯系物在不同SPME条件的优化、筛选实验,建立了苯系物的自动固相微萃取-气相色谱的检测方法,该方法简便、灵敏、快捷、可靠,分离度高,准确性好。在0.001mg/L~1.00mg/L范围内有良好的线性关系,最低检测浓度为0.1lμg/L~0.41μg/L。样品测定的相对标准偏差为1.8%~3.5%,回收率为88%~108%,精密度和准确度均较好。 相似文献
114.
Breakthrough curves, on a semi-log scale, from tests in porous media with block-input of viruses, bacteria, protozoa and colloidal particles often exhibit a typical skewness: a rather slowly rising limb and a smooth transition of a declining limb to a very long tail. One-site kinetic models fail to fit the rising and declining limbs together with the tail satisfactorily. Inclusion of an equilibrium adsorption site does not seem to improve simulation results. This was encountered in the simulation of breakthrough curves from a recent field study on the removal of bacteriophages MS2 and PRD1 by passage through dune sand. In the present study, results of laboratory experiments for the study of this issue are presented. Breakthrough curves of salt and bacteriophages MS2, PRDI, and phiX174 in 1 D column experiments have been measured. One- and two-site kinetic models have been applied to fit and predict breakthrough curves from column experiments. The two-site model fitted all breakthrough curves very satisfactorily, accounting for the skewness of the rising limb as well as for the smooth transition of the declining limb to the tail of the breakthrough curve. The one-site model does not follow the curvature of the breakthrough tail, leading to an overestimation of the inactivation rate coefficient for attached viruses. Interaction with kinetic site 1 is characterized by relatively fast attachment and slow detachment, whereas attachment to and detachment from kinetic site 2 is fast. Inactivation of viruses and interaction with kinetic site 2 provide only a minor contribution to removal. Virus removal is mainly determined by the attachment to site 1. Bacteriophage phiX174 attached more than MS2 and PRD1, which can be explained by the greater electrostatic repulsion that MS2 and PRD1 experience compared to the less negatively charged phiX174. 相似文献
115.
Müller K Pelzing M Gnauk T Kappe A Teichmann U Spindler G Haferkorn S Jahn Y Herrmann H 《Chemosphere》2002,49(10):1247-1256
An increasing percentage of agricultural land in Germany is used for oil seed plants. Hence, rape has become an important agricultural plant (in Saxony 1998: 12% of the farmland) in the recent years. During flowering of rape along with intensive radiation and high temperatures, a higher production and emission of biogenic VOC was observed. The emissions of terpenes were determined and more importantly, high concentrations of organic carbonyl compounds were observed during this field experiment. All measurements of interest have been carried out during two selected days with optimal weather conditions. It is found that the origin or the mechanism of formation of different group of compounds had strong influence on the day to day variation of their concentrations. The emission flux of terpenes from flowering rape plants was determined to be 16–32 μg h−1 m−2 (30–60 ng h−1 per g dry plant––540–1080 ng h−1 per plant), in total. Limonene, -thujene and sabinene were the most important compounds (about 60% of total terpenes). For limonene and sabinene reference emission rates (MS) and temperature coefficients were determined: βlimonene=0.108 K−1 and MS=14.57 μg h−1 m−2; βsabinene=0.095 K−1 and MS=5.39 μg h−1 m−2.
The detected carbonyl compound concentrations were unexpectedly high (maximum formaldehyde concentration was 18.1 ppbv and 3.4 ppbv for butyraldehyde) for an open field. Possible reasons for these concentrations are the combination of primary emission from the plants induced by high temperature and high ozone stress, the secondary formation from biogenically and advected anthropogenically emitted VOC at high radiation intensities and furthered by the low wind speeds at this time. 相似文献
116.
Konrad Müller Matthias Pelzing Thomas Gnauk Anett Kappe Ulrich Teichmann Gerald Spindler Sylvia Haferkorn Yvonne Jahn Hartmut Herrmann 《Chemosphere》2002,49(10)
An increasing percentage of agricultural land in Germany is used for oil seed plants. Hence, rape has become an important agricultural plant (in Saxony 1998: 12% of the farmland) in the recent years. During flowering of rape along with intensive radiation and high temperatures, a higher production and emission of biogenic VOC was observed. The emissions of terpenes were determined and more importantly, high concentrations of organic carbonyl compounds were observed during this field experiment. All measurements of interest have been carried out during two selected days with optimal weather conditions. It is found that the origin or the mechanism of formation of different group of compounds had strong influence on the day to day variation of their concentrations. The emission flux of terpenes from flowering rape plants was determined to be 16–32 μg h−1 m−2 (30–60 ng h−1 per g dry plant––540–1080 ng h−1 per plant), in total. Limonene, α-thujene and sabinene were the most important compounds (about 60% of total terpenes). For limonene and sabinene reference emission rates (MS) and temperature coefficients were determined: βlimonene=0.108 K−1 and MS=14.57 μg h−1 m−2; βsabinene=0.095 K−1 and MS=5.39 μg h−1 m−2.The detected carbonyl compound concentrations were unexpectedly high (maximum formaldehyde concentration was 18.1 ppbv and 3.4 ppbv for butyraldehyde) for an open field. Possible reasons for these concentrations are the combination of primary emission from the plants induced by high temperature and high ozone stress, the secondary formation from biogenically and advected anthropogenically emitted VOC at high radiation intensities and furthered by the low wind speeds at this time. 相似文献
117.
水解酸化-缺氧法处理采油废水的污染物迁移降解试验研究 总被引:4,自引:0,他引:4
水解酸化.缺氧法对采油废水有较好的处理效果,采用GC/MS技术对水解酸化-缺氧法处理采油废水过程中污染物的迁移降解进行的研究表明:水解酸化段和缺氧段对采油废水中碳原子为C6-C9、分子量为100—140的有机物均有较好的降解能力。其中,在水解酸化段中酮类、芳烃得到较好的降解,缺氧段中酚类和醚类化合物降解明显。水解酸化-缺氧工艺对于采油废水中的甲苯和二甲苯具有较好的降解能力。 相似文献
118.
Municipal wastewater reclamation is becoming of increasing importance in the world to solve the problem of water scarcity. A better understanding of the molecular composition of effluent organic matter(Ef OM) in the treated effluents of municipal wastewater treatment plants(WWTPs) is crucial for ensuring the safety of water reuse. In this study, the molecular composition of Ef OM in the secondary effluent of a WWTP in Beijing and the reclaimed water further treated with a coagulation–sedimentation–ozonation process were characterized using a non-target Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR MS) method and compared to that of natural organic matter(NOM) in the local source water from a reservoir. It was found that the molecular composition of Ef OM in the secondary effluent and reclaimed water was dominated by CHOS formulas, while NOM in the source water was dominated by CHO formulas. The CHO formulas of the three samples had similar origins. Anthropogenic surfactants were responsible for the CHOS formulas in Ef OM of the secondary effluent and were not well removed by the coagulation-sedimentation-ozonation treatment process adopted. 相似文献
119.
120.
SPME-GC/MS法测定垃圾渗沥液中双酚A 总被引:3,自引:3,他引:0
建立了固相微萃取-气相色谱质谱联用法测定垃圾渗沥液中双酚A的方法,并用于广州大田山垃圾渗沥液中双酚A含量的测定。对影响萃取的参数进行了优化,实验选用涂层厚度为85μm聚丙烯酸酯(PA)萃取纤维,在搅拌速度为1200r/min、NaCl浓度为20%、pH2.0和室温条件下萃取60min。方法的线性范围为0.1~100μg/L,检出限为0.03μg/L,精密度为6.6%。应用本方法监测了广州大田山垃圾渗沥液中BPA的含量在生物法处理过程中的变化情况。 相似文献