废纸造纸废水有机污染物的降解研究

采用同时厌氧-好氧反应器处理广东某造纸厂废纸造纸废水,平均出水浓度COD为89.70mg/L,VFA为0.89mg/L,达到了GB3544-2001《造纸工业水污染物排放标准》。同时选用GC-MS联用仪对废纸造纸废水中的有机物进行测定,共测得有机污染物89种,其中8种有机污染物被列入美国EPA环境优先控制污染物,在进水的50种有机物中,32种有机物被完全去除。通过分析有机污染物在各工艺段的分布情况,揭示其在厌氧-好氧生物处理过程中的降解与转化规律。     

GC-MS法测定水中邻苯二甲酸酯

采用气相色谱-质谱（GC-MS）联用测定水中邻苯二甲酸酯（包括邻苯二甲酸二甲酯,邻苯二甲酸二乙酯,邻苯二甲酸二正丁酯,邻苯二甲酸丁基苄基酯,邻苯二甲酸二（2-乙基己基）酯,邻苯二甲酸二正辛酯）,优化了试验条件。GC-MS选择SIM扫描方式,外标法定量,定性定量准确,线性响应良好,干扰小。邻苯二甲酸酯的方法检出限为0.002 mg/L-0.03 mg/L,平均加标回收率在94.2%-110%之间,RSD在0.4%-6.3%之间。     

底质中有机磷农药残留分析方法

有机磷农药是继有机氯农药以后被广泛应用的一类农药,它对生物体具有一定毒性,因此对有机磷农药的充分提取及检测就密切关系到人们的饮食安全。传统提取底质中有机磷的方法为索式提取或者采用有机溶剂对底质直接萃取,而文章采用亲水溶剂对底质进行萃取,并通过固相萃取技术对其进一步纯化,气相色谱一质谱法检测,对多种有机磷农药的分离度较好。     

太湖梅梁湾2008年有机污染物检测及环境影响度

利用GC-MS技术定性和定量分析2008年不同季度太湖梅梁湾水体中的半挥发性有机污染物(SVOCs),并采用多介质环境目标值(MEG)分别就人体健康影响度(ASI)和生态环境影响度(ASII)对太湖梅梁湾水质进行了评价.结果表明,2008年春、夏、秋、冬太湖梅梁湾水体中25种EPA优先控制SVOCs的总浓度分别为17.459,11.140,11.147,5.675mg/L,其中检出率较高的是邻苯二甲酸酯类物质、苯系物和PAHs;健康和生态影响度均小于1,表明对健康和生态尚属安全.     

Identification and biological activity of sex pheromone components from females of the plum moth Illiberis rotundata Jordan (Lepidoptera: Zygaenidae: Procridinae)

The plum moth, Illiberis rotundata Jordan (Lepidoptera: Zygaenidae: Procridinae), is a pest of orchards in Japan and China. Few chemical ecological studies have been directed towards the Zygaenidae and particularly the Procridinae. To investigate the sex pheromone of this species, extracts of pheromone glands from adult female I. rotundata were analyzed by coupled gas chromatography-electroantennography (GC-EAG) and coupled gas chromatography-mass spectrometry (GC-MS). Whilst GC-EAG on male moths showed an active peak, identified as 2-butyl (7Z)-dodecenoate, GC-MS also revealed the presence of the homologue 2-butyl (9Z)-tetradecenoate. Electroantennographic investigations, as well as field tests, strongly suggested the natural compounds to have the (R)-configuration at the stereogenic centre. Field results demonstrate 0.2 mg of a 1:1-mixture of (2R)-butyl (7Z)-dodecenoate and (2R)-butyl (9Z)-tetradecenoate to be a powerful lure that may be used in pest control measures against I. rotundata. The chemical structures of the new pheromone components show the same features as those of other zygaenid species: unsaturated fatty acids esterified with a short chain chiral alcohol. This is the first example of a two-component blend constituting the pheromone of a procridinid species.     

Co-pyrolysis of paper waste and mustard press cake in a semi-batch pyrolyzer—optimization and bio-oil characterization

Under the present research study, the co-pyrolysis of paper waste and mustard press cake was conducted in a 50 mm diameter and 640 mm long semi-batch pyrolyzer in the temperature range of 673 to 1173 K in nitrogen atmosphere and synergistic relationship between the pyrolysis of two feed stocks has been observed. The paper wastes were composed of local packing paper, newspaper-based food packets of grocery, and printing paper in the ratio of 6:3:1. During co-pyrolysis, response surface methodology (RSM) technique has been employed using Design Expert Version 7.0.0 to determine the collective effects of factors, namely, A: ratio of paper waste to mustard press cake and B: pyrolysis temperature, on the yield of bio-oil, energy yield, and oxygen content of bio-oil. Optimization has been done by using RSM to identify the individual sets of values of independent parameters corresponding to maximum bio-oil yield (A: 9.0:1, B: 874.75 K), energy yield (A: 8.80:1, B: 812 K), and minimum oxygen content of bio-oil (A: 2.75:1, B: 883.06 K). Bio-oil obtained at maximum energy yield condition has been characterized using the Gas chromatography–mass spectrometry (GC-MS) and Fourier transform infrared spectroscopy (FTIR) spectroscopic analyses. The array of compounds present in the bio-oil compounds has been compared with literature data available on pyro-oil obtained from similar feed stocks.     

Simultaneous determination of organochlorine pesticides and bisphenol A in edible marine biota by GC-MS

A study to assess the level of organochlorine pesticides (OCPs) and bisphenol A (BPA) in edible marine biota collected from coastal waters of Malaysia was conducted using GC-MS and SPE extraction. An analytical method was developed and validated to measure the level of 15 OCPs and BPA simultaneously from five selected marine species. It was observed that some samples had low levels of p,p′-DDE, p,p′-DDT and p,p′- DDD ranging from 0.50 ng g⁻¹ to 22.49 ng g⁻¹ dry weight (d.w) but significantly elevated level of endosulfan I was detected in a stingray sample at 2880 ng g⁻¹ d.w. BPA was detected in 31 out of 57 samples with concentration ranging from below quantification level (LOQ: 3 ng g⁻¹) to 729 ng g⁻¹ d.w. The presence of OCPs is most likely from past use although there is also indication of illegal use in recent times. The study also reveals that BPA is more widely distributed in coastal species caught off the coast of the most developed state. The potential health risk from dietary intakes of OCPs and BPA from the analysed fish species was negligible.     

GC-MS分析短梗五加化学成分

为了开发利用短梗五加这一潜在的民间药用植物资源,采用GC-MS方法对短梗五加乙醚部分化学成分进行了分析。结果表明,经毛细管色谱柱分析分离出31个成分,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3,7,11-三甲基-2,6,10-十二碳三烯-1-醇为50.21%,化合物类型主要为萜类及其衍生物。本方法简便、可靠、快速、重现性好,为短梗五加的化学成分研究提供了参考依据。     

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。     

Analysis of munitions constituents in groundwater using a field-portable GC-MS

The use of munitions constituents (MCs) at military installations can produce soil and groundwater contamination that requires periodic monitoring even after training or manufacturing activities have ceased. Traditional groundwater monitoring methods require large volumes of aqueous samples (e.g., 2-4 L) to be shipped under chain of custody, to fixed laboratories for analysis. The samples must also be packed on ice and shielded from light to minimize degradation that may occur during transport and storage. The laboratory’s turn-around time for sample analysis and reporting can be as long as 45 d. This process hinders the reporting of data to customers in a timely manner; yields data that are not necessarily representative of current site conditions owing to the lag time between sample collection and reporting; and incurs significant shipping costs for samples.The current work compares a field portable Gas Chromatograph-Mass Spectrometer (GC-MS) for analysis of MCs on-site with traditional laboratory-based analysis using High Performance Liquid Chromatography with UV absorption detection. The field method provides near real-time (within ∼1 h of sampling) concentrations of MCs in groundwater samples. Mass spectrometry provides reliable confirmation of MCs and a means to identify unknown compounds that are potential false positives for methods with UV and other non-selective detectors.