低分子量有机还原性物质与土壤的相互作用Ⅰ.低分子量有机还原性物质的化学性质

应用多学科研究手段,研究了低分子量有机还原性物质的化学性质。主要结果是,该类物质含-COOH和-C-=NOH2功能团、酚类化合物、挥发性有机酸,等电点变动在3.5～9.5。不同还原强度组份的峰电位大多分布在0.00～0.70 V,负电荷有机还原性物质可占总量的70%～80%,表观分子量小于500～1 000,在电极过程中具有明显的伏安行为。     

高锰酸钾氧化修复污染土壤中菲和芘的研究

利用人工污染土壤,研究了高锰酸钾对4种不同土壤中菲和芘的氧化修复效果。结果表明,当高锰酸钾浓度为33.33mmol·L^-1时,土壤中菲和芘的氧化去除率达到最大。高锰酸钾氧化去除率不仅与高锰酸钾浓度有关,还与土壤性质和老化时间有关。土壤有机质含量的增加会降低高锰酸钾对土壤中菲和芘的氧化去除率;随着老化时间的增加,高锰酸钾的氧化去除率逐渐降低。老化40d后,4种土壤中菲和芘的氧化去除率显著降低,菲的氧化去除率在14%～67%之间,芘的氧化去除率在61%～84%之间。高锰酸钾氧化前后,4种土壤中有机质含量下降范围为0.77%～9.21%。从土壤有机质含量来看,高锰酸钾氧化修复多环芳烃污染土壤对土壤质量影响较小,具有较好的应用前景。     

Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Suspended Particle Mater in Rainy Season from Jialing River in Chongqing

16 polycyclic aromatic hydrocarbons (PAHs) were measured by GC-MS for 13 suspended particle matter samples collected from Jialing River in Chongqing in rainy season. The results showed that the total concentrations of 16 PAHs ranged from 447.47 ng/g to 1 344.92 ng/g, with a mean value of 927.48 ng/g. The concentration of total PAHs in suspended particle matter showed the trend of“up-down-up-down”in spatial distribution in the 13 sampling sites. The predominant PAHs in suspended particle matter were 4 ring PAHs, which accounting for 41.87% of the tatal PAHs. The ratio analysis and principle factor analysis-multiple linear regression(PCA-MLR) indicated that the major source of PAHs was the engine combustion source, in which the proportion of gasoline combustion and diesel combustion were 37.79% and 29.97%, respectively. The ecological risk of PAHs was evaluated by the effects range median values (ERM) and the effects range low values (ERL). The results illustrated that Acy, Ace, Fl and DahA had certain ecological risks, while the ERL values of other12 PAHs in all suspended particle matter samples were lower than the ERL guideline value,namely, PAHs in Jialing River in Chongqing could not cause obvious ecological risk.     

酿造大麦挥发性风味物质组成分析

为给啤酒风味的稳定性研究提供借鉴,利用固相微萃取与气-质联用分析了两个优质酿造大麦品种Sabastian和Gairdner中的挥发性风味物质组成.在两个大麦品种中共分析鉴定出34种化合物,Sabastian中检出28种,Gairdner中检出32种.在Sabastian中共检出醛类化合物11种,占总质量分数的17.58％;醇类化合物7种,占总质量分数的7.32％;酮类3种,占总质量分数的13.08％;酸类化合物2种,占总质量分数的8.41％;其他类化合物5种,占总质量分数的9.54％.在Gairdner中共检出醛类化合物10种,占总质量分数的38.36％;醇类化合物9种,占总质量分数的25.36％;酮类化合物4种,占总质量分数的9.07％;酸类化合物2种,占总质量分数的6.81％;其他类型化合物7种,占总质量分数的7.77％.两个大麦品种中含量较高的成分为正己醛(Sabastian,13.56％;Gairdner,30.76％)、丙酮(Sabastian,12.82％;Gairdner,8.39％)、乙酸(Sabastian,8.00％;Gairdner,4.86％).作为大麦特征风味物质的异戊醛和2-甲基丁醛的含量在Sabastian中分别为0.51％和0.79％,在Gairdner中分别为1.93％和1.72％.     

Analysis of Volatile Compounds of Jinmudan Oolong Tea by Different Wrapping-Twisting

In this study,the volatile compounds in four kinds of Jinmudan Oolong tea were extracted and analyzed by simultaneous steam distillation and extraction （SDE） and gas chromatography-mass spectrometry （GC-MS）,respectively.The relative contents of the chemical constituents in the volatile components were quantified by peak area normalization and NIST database.A total of 93 volatile components were identified,46 for sample 1,56 for sample 2,45 for sample 3 and 30 for sample 4.Alcohols and esters were the most abundant volatiles in Jinmudan Oolong tea.Palmitic acid,nerolidol,2-phenylethanol,phytol,cis-5-ethenyltetrahydro-,α,α-5-trimethyl-2-furanmethanol,2,2,6-trimethyl-6-ethenyltetrahydro-2h-pyran-3-ol,a-farnesene,eicosane,hexadecane,indole,β-phenethyl hexanoate,β-phenethyl hexanoate,methyl palmitate,benzoic acid,2-phenylethyl ester,tetrahydro-6-（cis-2-pentenyl）-2h-pyran-2-one and cis-jasmone were in all of the samples.Nerolidol was shown to be the aroma components with the highest content in Jinmudan Oolong tea,which accounted for 26.61％,36.89％,36.89％ and 36.89％.     

Sensory properties and aromatic composition of baked snacks containing brewer's spent grain

The incorporation of brewer's spent grain (BSG) into baked snacks (crispy-slices) was investigated in terms of nutritional, sensory and aromatic properties. Wheat flour was replaced with BSG at the levels of 10, 15 and 25%. Snacks containing 10% BSG exhibited high Crispiness index (Ci), low Crispiness work (Wc) and a high number of peaks during texture analysis, indicating that the crispiness of the samples was not negatively affected. However higher levels of BSG affected the texture and the crumb structure of snacks and the results were significantly different to the 100% wheat control. Addition of BSG altered the odour profile of the snacks as shown by the volatile profiles, however sensory results indicated that BSG-containing snacks at a level of 10% were highly acceptable and highlighted the possibility of using BSG as a baking ingredient in the formulation of enhanced fibre baked snacks.     

植物提取物在烟草工业中的应用研究

卷烟调香、降焦减害是烟草行业的热点话题,目前国内外学者对植物提取物在卷烟中的应用及开发已成为研究热点。从卷烟增香保润、降低危害2个角度,分别阐述了芳香植物挥发油和中草药生物活性提取物在卷烟中的开发利用及其功效研究概况。     

不同灌溉方式对初烤烟叶内在品质的影响

[目的]研究不同灌溉方式对烤后烟叶化学成分、致香物质含量及感官评吸质量的影响。[方法]采用田间试验,设浇灌和喷灌2个处理。浇灌处理分别在团棵期(5月26日)、旺长期(6月18日)各人工根灌1次,灌水量1 kg/(株.次);喷灌处理在团棵期(5月26日)进行人工根灌1次,灌水量1 L/株。[结果]与浇灌方式相比,喷灌处理极显著提高中上部位烟叶主要致香物质,中橘三(C3F)等级烟叶主要致香物质非挥发性有机酸、挥发性有机酸、石油醚提取物、新植二烯、中性致香物质总量分别增加24.4%、32.6%、20.7%、33.8%、26.3%,上橘二(B2F)等级烟叶主要致香物质非挥发性有机酸、挥发性有机酸、石油醚提取物、新植二烯、中性致香物质总量分别增加16.3%、6.0%、6.1%、10.8%、8.1%;极显著降低中上部位烟叶烟碱含量,提高烟气协调性、醇和性及持火力。[结论]烤烟生产中,微喷灌技术是一种改善烤后烟叶内在品质的重要途径,在季节性干旱频繁烟区,烟草微喷灌溉可有效解决烟叶成熟期气候干旱导致烟叶品质下降的问题。     

土种绿茶挥发物成分及其对人体脑波的影响

[目的]对茶叶的挥发性芳香物质及其对人体脑波影响进行分析。[方法]采用顶空套袋采集法和TDS-GC/MS,分析自然状态室温下摊放4h绿茶鲜叶挥发性芳香物质成分,并使用生物反馈仪测定嗅闻茶叶挥发性芳香物质的人体脑波变化。[结果]摊放鲜叶的挥发性芳香物质以酯类和萜烯类化合物为主。香气成分能够显著增加α波的波值。嗅闻摊放鲜叶对人体具有放松身心的功效。[结论]该研究可以为茶的芳香疗法提供初步参考。     

Organic geochemical parameters for estimation of petrogenic inputs in the coastal area of Kavala City,Greece

Background, aims, and scope  Sediments and soils in coastal areas are frequently polluted by anthropogenic contaminants as the result of both riverine or terrestrial discharge and autochthonic marine emissions. In order to determine petrogenic contamination in the coastal industrial area of Kavala City in northern Greece, a combination of polycyclic aromatic hydrocarbon (PAH) and organic geochemical petroleum biomarker analyses has been performed on marine and freshwater sediments as well as soils. Materials and methods  Soils, freshwater, and marine sediments have been treated by standard extraction methods. The dried and desulphurized sample extracts have been fractionated by column chromatography, followed by addition of surrogate standards. Qualitative and quantitative data were obtained by gas chromatograph connected with a flame ionization and electron capture detector (GC-FID/ECD) and by GC linked to a mass spectrometer (GC/MS), whereas identification of compounds was based on EI⁺-mass spectra and gas chromatographic retention times. Quantitative data were obtained by integration of specific ion chromatograms. Results  The total PAH concentrations measured in the area varied highly, showing different levels from 18 up to 318,000 ng g⁻¹ dry weight (dw). Several PAH ratios, as well as the ratio of pristane (Pr) to phytane (Phyt), have been considered. Out of 39 samples, 22 revealed a specific distribution of hopane fingerprints indicating petrogenic input. Finally, in numerous samples, the ratio of 17α(H)-22,29,30-trisnorhopane (Tm) and 18α(H)-22,29,30-trisnorhopane (Ts) was calculated, as well as the ratio of 22S-17α(H),21β(H)-30 homohopane (αβC₃₁-hopane 22S) and 22R-17α(H),21β(H)-30 homohopane (αβC₃₁-hopane 22R). Discussion  Based on the specific PAH ratios, a group of samples was clearly characterized to be contaminated dominantly by combustion-derived emissions, whereas a second group of samples exhibited mixed influence from petrogenic and pyrogenic PAHs. On the other hand, the exhibition of specific hopane fingerprints in many samples indicates a direct petrogenic input. Finally, the values of the ratio of Tm/(Ts + Tm) and of αβC₃₁-hopanes 22S/(22S+22R)-isomer demonstrated an input of highly mature organic matter that has to be clearly attributed to petroleum-derived contamination, while the ratio of Pr/Phyt showed that most samples exhibited an input of organic matter. Conclusions  The coastal area of Kavala is strongly affected by anthropogenic contaminants. Petrogenic emissions were pointed out firstly by PAH analyses that separated dominantly pyrogenic contaminated sites from areas affected by both pyrogenic and petrogenic emissions. However, analyses of organic geochemical biomarkers revealed a much higher sensitivity in identifying petroleum-derived contaminations and were successfully used to differentiate several petrogenic contaminations in the marine and terrestrial samples. Recommendations and perspectives  Based on this study, it was recommended to use a complementary approach of source-specific substances to successfully characterize petrogenic emissions. Generally, a PAH-based source identification of petrogenic versus pyrogenic contaminations should be combined with petroleum biomarker analysis. PAH and biomarker ratios as well as individual biomarker fingerprints revealed a more comprehensive view on the quality and quantity of petrogenic emissions in sediments and soils.