GC-MS分析鸡树条荚蒾叶化学成分

为了开发利用鸡树条荚蒾这一潜在的民间药用植物资源,采用GC-MS方法对鸡树条荚蒾叶石油醚部分的化学成分进行了分析。经毛细管色谱柱分析分离出56个峰,共确认出其中48种成分;应用色谱峰面积归一法分析各成分的相对含量,含量较高的物质有3-甲基丁酸(40.50%)、2-甲基丁酸(14.49%)、邻苯二甲酸丁基异丁基酯(10.28%)、棕榈酸(6.02%)、α-亚麻酸(4.58%)、β-谷甾醇(3.02%)等,化合物类型主要为脂肪酸、烷烃、脂肪醇、酯类、甾醇类化合物。该方法简便可靠、快速、重现性好,并为鸡树条荚艹迷叶的化学成分研究提供了参考依据。     

茂县玫瑰精油加工方法对化学成分含量的影响

本文用毛细管气相色谱-质谱-计算机联用技术,毛细管气相色谱保留指数和标准品叠加法鉴定了茂县玫瑰精油的化学成分,并对水蒸气蒸馏精油、净油、蒸馏-萃取精油、水中精油的化学成分进行了比较,说明不同加工方法对精油成分的影响是很大的。     

荠菜叶挥发性成分分析

采用水蒸气蒸馏法对荠菜叶挥发油进行了提取。通过毛细管气相色谱—质谱联用法分离并鉴定了其化学成分,用气相色谱面积归一化法测定了各成分的相对百分含量,共分离确定了其中12种化合物,所鉴定化合物的含量占全油的65.62%,主要化学成分为：L-胍基琥珀酰亚胺（21.28%）、植醇（18%）、植酮（9.6%）、油酸（4.71%）、棕榈酸（3.97%）等。     

荠菜叶挥发性成分分析

采用水蒸气蒸馏法对荠菜叶挥发油进行了提取。通过毛细管气相色谱—质谱联用法分离并鉴定了其化学成分,用气相色谱面积归一化法测定了各成分的相对百分含量,共分离确定了其中12种化合物,所鉴定化合物的含量占全油的65.62%,主要化学成分为：L-胍基琥珀酰亚胺（21.28%）、植醇（18%）、植酮（9.6%）、油酸（4.71%）、棕榈酸（3.97%）等。     

落新妇地下部分挥发油化学成分GC-MS分析

利用水蒸汽蒸馏法提取落新妇地下部分的挥发油,测得含量为0.10%;采用气相色谱-质谱联用技术(GC-MS)对落新妇的挥发性成分进行了分离鉴定,分离出57种成分,鉴定了其中50种;运用峰面积归一法确定了各成分的相对含量,检出率为87.71%.落新妇地下部分挥发油的主要成分为邻苯二甲酸二丁酯、十六甲基八环硅氧烷.     

刺异叶花椒叶挥发性成分GC—MS分析研究

采用水蒸气蒸馏法和气相-质谱联用法对刺异叶花椒叶挥发性成分进行分析和鉴定,用气相色谱面积归一化法对其主要成分含量进行测定.共鉴定出35种化合物,其峰面积相对百分含量占总挥发油的71.6%,主要为肉豆蔻醚(23.4%)、黄樟素(19.4%)、异丁香甲醚(16.5%)、罗勒烯(5.4%)等.这些化合物同样作为刺异叶花椒果皮的主要成分,但其百分含量与叶中相比有显著不同.     

树舌灵芝菌丝体不皂化物GC-MS分析

在树舌灵芝菌丝体化学成分研究中,采用乙醚抽提法获取树舌灵芝菌丝体脂溶性物质,经皂化后使用气相色谱-质谱联用技术(GC-MS)进行分析,共鉴定出19种物质,所得到的丁羟甲苯、乙酰菲、5,6-二氢麦角甾醇对树舌灵芝菌丝体化学成分研究具有较高价值.     

落新妇地下部分挥发油化学成分GC—MS分析

利用水蒸汽蒸馏法提取落新妇地下部分的挥发油,测得含量为0．10％;采用气相色谱－质谱联用技术（GC—MS）对落新妇的挥发性成分进行了分离鉴定,分离出57种成分,鉴定了其中50种;运用峰面积归一法确定了各成分的相对含量,检出率为87．71％。落新妇地下部分挥发油的主要成分为邻苯二甲酸二丁酯、十六甲基八环硅氧烷。     

树舌灵芝菌丝体不皂化物GC—MS分析

在树舌灵芝菌丝体化学成分研究中,采用乙醚抽提法获取树舌灵芝菌丝体脂溶性物质,经皂化后使用气相色谱一质谱联用技术（CC—MS）进行分析,共鉴定出19种物质,所得到的丁羟甲苯、乙酰菲、5,6-二氢麦角甾醇对树舌灵芝菌丝体化学成分研究具有较高价值。     

永瓣藤某些化学成分的研究

对永瓣藤总糖、粗脂肪、灰分、维生素C、磷、钾和各类氨基酸的含量进行了测量和分析,并对这些化学成分在不同部位的含量进行了比较。不同部位化学成分的含量存在一定的差异,除灰分外,其它化学成分含量均是叶高于茎、嫩茎高于老茎。     

Simultaneous chemical and sensory characterization of volatile organic compounds and semi-volatile organic compounds emitted from swine manure using solid phase microextraction and multidimensional gas chromatography-mass spectrometry-olfactometry

Swine manure is associated with emissions of odor, volatile organic compounds (VOCs) and other gases that can affect air quality on local and regional scales. In this research, a solid phase microextraction (SPME) and novel multidimensional gas chromatography-mass spectrometry-olfactometry (MDGC-MS-O) system were used to simultaneously identify VOCs and related odors emitted from swine manure. Gas samples were extracted from manure headspace using Carboxen/polydimethylsiloxane (PDMS) 85-microm SPME fibers. The MDGC-MS-O system was equipped with two columns in series with a system of valves allowing transfer of samples between columns (heartcutting). The heartcuts were used to maximize the isolation, separation, and identification of compounds. The odor impact of separated compounds was evaluated by a trained panelist for character and intensity. A total of 295 compounds with molecular weights ranging from 34 to 260 were identified. Seventy one compounds had a distinct odor. Nearly 68% of the compounds for which reaction rates with OH* radicals are known had an estimated atmospheric lifetime <24 h.     

Biological degradation of some organic compounds involved in the paper industry

An evaluation of the biodegradation by aerobic microorganisms was investigated for some organic compounds occurring in paper manufacturing technology. Lines of biodegradation for nine organic compounds, as a percentage removal of chemical oxygen demand (COD), were detected over seven days incubation. The results of the biodegradability test clearly revealed that some of the organic compounds under investigation were highly biodegradable while others ranked from fairly biodegradable to non-biodegradable. Significant biodegradation results were recorded as COD removal, for anti-coating ester (95.0 percent), Basoplast 200D (85.3 percent) and Basoplast PR 8050 (87.6 percent). The bleaching agent (formamidin-sulfinic acid), Ukanol BSA and Solidurit KM demonstrated moderate biodegradation with results of 62.1 percent, 76.2 percent and 69.8 percent, respectively. Poor biodegradation results for Hedifix M/35 (12.7 percent), Basazol Orange (34.9 percent) and Basazol Brown (29.0 percent) were recorded. Accordingly, appropriate precautions should be taken into consideration when applying these compounds to paper manufacturing processes.     

蜈蚣草总黄酮体外抗氧化作用的研究

通过回流法提取蜈蚣草黄酮类化合物,利用分光光度法测定总黄酮的含量,并分析了它对羟基自由基、超氧阴离子自由基的清除作用和总抗氧化能力。结果表明,蜈蚣草总黄酮含量为6.15%,且具有较好的抗氧化能力。     

Chitosan-supported palladium catalyst. IV. Influence of temperature on nitrophenol degradation and thermodynamic parameters

Glutaraldehyde cross-linked chitosan was loaded with palladium and then reduced using an in situ hydrogen generation procedure (Zn in sulfuric acid solution) to prepare a chitosan-supported palladium catalyst. This catalyst was successfully used to degrade nitrophenol in dilute solutions in the presence of sodium formate as the hydrogen donor. The influence of the initial concentration of nitrophenol and sodium formate was studied in order to determine the minimum molar ratio between these compounds required to achieve complete conversion of the nitrogenous product at two temperatures. Increasing the temperature decreased the excess of hydrogen donor required for complete conversion of nitrophenol. The temperature was also varied between 10 and 60 degrees C in order to determine the activation energy. The pseudo first-order equation was shown to fit degradation kinetics in most cases; however, for some cases it was necessary to use a variable-order equation to model the kinetics.     

Application of lime and calcium hypochlorite in the dephenolisation and discolouration of olive mill wastewater

The application of hypochlorite for the removal of soluble COD, phenolic and polyphenolic like compounds, and other organic compounds responsible for the olive mill wastewater (OOWW) colour has been experimentally studied. After the OOWW filtration on a sand column, the effluent was subjected to a fast liming under optimal conditions. Lime application reduced polyphenols, COD and SS contents to half of their initial values but an important blackening of the treated OOWW was observed, especially when adding high concentrations of lime (10% (W/V) and 15% (W/V)).A second stage of treatment was applied using calcium hypochlorite. In this stage, removal of the studied compounds reached as much as 95% at higher concentrations, and particularly the colouring of OOWW which is generally difficult to eliminate was greatly reduced. The OOWW hypochloration acted through coagulation–flocculation and a rapid oxidation of the organic matter proceeded from the first 5 min. The kinetic study of the degradation of the waste polluting compounds from liming showed that Ca(ClO)₂ reacts similarly in the elimination of organic compounds, polyphenols, SS and colouration. The analysis of the organochloride compounds generated by the reaction between hypochlorite and the organic compounds showed that DDD, DDT and the heptachlor contents exceeded the values recommended by the International and European drinking water standards.     

乳苣总黄酮的提取及抗氧化作用研究

通过乙醇回流提取乳苣中的黄酮类化合物,利用分光光度法测定总黄酮的含量,并分析了对羟基自由基的清除作用和总抗氧化能力。结果表明,乳苣中总黄酮含量为16.8%,具有较好的抗氧化能力。     

A new way to use solid-state carbon-13 nuclear magnetic resonance spectroscopy to study the sorption of organic compounds to soil organic matter

Several solid-state 13C nuclear magnetic resonance (NMR) techniques were used to characterize soil organic matter spiked with 13C-labeled organic compounds spanning a range of hydrophobicities (benzoic acid, benzophenone, naphthalene, phenanthrene, and palmitic acid). The chemical shifts of NMR resonances of the sorbed species were shifted by up to 3 ppm relative to those of the neat compounds. Sorption also resulted in increased resonance linewidth for the compounds containing a single 13C label, indicating the presence of a range of different chemical environments at the sites of sorption. On the other hand, sorption decreased the linewidth of the resonance of naphthalene, which was uniformly 13C-labeled. This was attributed to the removal of intermolecular 13C-13C dipolar coupling. Heterogeneity of the organic matter was demonstrated using the spectral editing technique proton spin relaxation editing (PSRE), which enabled the identification and quantification of charcoal-rich domains characterized by rapid rates of proton spin-lattice relaxation in the static frame (T1H), and humic domains characterized by slow rates of T1H relaxation. Furthermore it was demonstrated that the sorbed 13C-labeled molecules "inherit" the T1H "signature" of the organic matrix in their immediate vicinity. Thus PSRE on the spiked soils enabled evaluation of the relative affinity of the two domain types for the sorbate molecules. The charcoal-rich domains were shown to have a twofold to tenfold greater affinity for the organic compounds, with greater differences found for the more hydrophobic compounds.     

Sorption of polycyclic aromatic compounds to humic and fulvic acid HPLC column materials

Two different humic acids (HA) and a fulvic acid (FA) were chemically immobilized to a high performance liquid chromatography (HPLC) silica column material. The immobilization was performed by binding amino groups in HA/FA to the free aldehyde group in glutardialdehyde attached to the silica gel. The HPLC column materials were compared with a blank column material made by applying the same procedure but without immobilizing HA or FA. Also, a column was made by binding carbonyl groups in HA to amino groups attached to the silica gel. The humic substances were selected to secure appropriate variation of their structural features. The retention factors of 45 polycyclic aromatic compounds (PAC) to the four columns were determined by HPLC. The advantage of the technique is a large number of compounds can easily be studied. The binding procedure does not appear to cause a drastic selection between the HA molecules. The k' values obtained for the two Aldrich HA columns agree in general reasonably. The retention or sorption of the compounds increased with the size of the PAC and the number of lipophilic substituents, but decreased when polar substituents were present. The PAC retention was much stronger to the two HA columns than to the FA and blank column, both for hydrophobic polycyclic aromatic hydrocarbons (PAH) and the polar PAC. Other factors impacting the PAC binding may be specific interactions with HA and the ionic strength of the aqueous phase. The technique has been applied to do direct determinations of Koc.     

Contaminants of Emerging Concern in Fish from Western U.S. and Alaskan National Parks — Spatial Distribution and Health Thresholds

Remote national parks of the western U.S. and Alaska are not immune to contaminants of emerging concern. Semivolatile organic compounds (SOCs) such as pesticides and PCBs can selectively deposit from the atmosphere at higher rates in cold, high‐elevation and high‐latitude sites, potentially increasing risk to these ecosystems. In the environment, SOCs magnify up food chains and are known to increase health risks such as cancer and reproductive impairment. One hundred twenty‐eight fish in 8 national parks in Alaska and the western U.S. were analyzed for contaminant concentrations, assessed by region, and compared to human and wildlife health thresholds. SOC concentrations from an additional 133 fish from a previous study were also included, for a total of 31 water bodies sampled. PCBs, endosulfan sulfate, and p,p′‐DDE were among the most frequently detected contaminants. Concentrations of historic‐use pesticides dieldrin, p,p′‐DDE, and/or chlordanes in fish exceeded USEPA guidelines for human subsistence fish consumers and wildlife (kingfisher) health thresholds at 13 of 14 parks. Average concentrations in fish ranged from 0.6‐280 ng/g lipid (0.02‐7.3 μg/g ww). Contaminant loading was highest in fish from Alaskan and Sierra Nevada parks. Historic compounds were highest in Alaskan parks, while current‐use pesticides were higher in the Rockies and Sierra Nevada. This study provides a rigorous analysis of CECs in fish from national parks and identifies regions at potential risk.