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1.
Abstract

The biotransformation of the nonylphenol isomer [ring-U-14C]-4-(3′,5′-dimethyl-3′-heptyl)-phenol (4-353-NP, consisting of two diastereomers) was studied in soybean and Agrostemma githago cell suspension cultures. With the A. githago cells, a batch two-liquid-phase system (medium/n-hexadecane 200:1, v/v) was used, in order to produce higher concentrations and amounts of 4-353-NP metabolites for their identification; 4-353-NP was applied via the n-hexadecane phase. Initial concentrations of [14C]-4-353-NP were 1 mg L?1 (soybean), and 5 and 10 mg L?1 (A. githago). After 2 (soybean) and 7 days (A. githago) of incubation, the applied 4-353-NP was transformed almost completely by both plant species to four types of products: glycosides of parent 4-353-NP, glycosides of primary 4-353-NP metabolites, nonextractable residues and unknown, possibly polymeric materials detected in the media. The latter two products emerged especially in soybean cultures. Portions of primary metabolites amounted to 19–22% (soybean) and 21–42% of applied 14C (A. githago). After liberation from their glycosides, the primary 4-353-NP metabolites formed by A. githago were isolated by HPLC and examined by GC-EIMS as trimethylsilyl derivatives. In the chromatograms, eight peaks were detected which due to their mass spectra, could be traced back to 4-353-NP. Seven of the compounds were side-chain monohydroxylated 4-353-NP metabolites, while the remaining was a (side-chain) carboxylic acid derivative. Unequivocal identification of the sites of hydroxylation/oxidation of all transformation products was not possible. The main primary metabolites produced by A. githago were supposed to be four diastereomers of 6′-hydroxy-4-353-NP (about 80% of all products identified). It was concluded that plants contribute to the environmental degradation of the xenoestrogen nonylphenol; the toxicological properties of side-chain hydroxylated nonylphenols remain to be examined.  相似文献   
2.
本文从讨论金属结合能何以具有表面化学位移的原因开始,从金属团簇的一般性质出发,论证了金属结合能自尺寸大于1nm的团簇到金属微粒再到块体金属具有连续过渡性;金属结合能与粒径R呈正相关;与1/R具线性负相关关系,认为金微粒或团簇具有1.1eV以上的结合能负位移是可能的。并指出李九玲等同志在“评<含金硫化物矿物中不可能存在负价金>”一文中引用的某些衬底材料上的金团簇呈现结合能正位移的数据是由于这些金困簇已与其衬底材料发生了键合作用造成的,它们不能作为否定金属结合能位移与粒径呈正相关的依据。同时,笔者从“化学结合金”在氰化过程中并未被氧化成正离子金判断,它不应是负价金。并由同质并能位移与粒径可具负相关关系推论,“化学结合金”应是合企硫化物矿物中可存在的少量微粒碲金矿、碲金银矿等中的正离子金。笔者强调在讨论企的价态问题时应采用Allred-Rochow电负性数据而非常用的Pauling电负性数据,并再次指出含金硫化物矿物中不可能有负价金存在。  相似文献   
3.
为研究嘉兴市城市河网区水体中多环芳烃的污染水平和来源并进行生态风险评价,采用气相色谱-质谱法(GC-MS)对环境优控多环芳烃(PAHs)进行分析检测.结果表明,枯水期和丰水期分别检测出10种和16种优控PAHs,质量浓度范围分别为77.32~283.76ng ·L-1和13.05~133.02ng ·L-1,平均质量浓度分别为143.83ng ·L-1和73.47ng ·L-1;枯水期低环(2环和3环)占比79.18%,丰水期低环占比73.60%;嘉兴市河网区水体多环芳烃污染情况与国内外其他地区相比处于较低水平;采用同分异构比值法和主成分分析法进行污染来源分析,结果表明嘉兴市枯水期和丰水期河网水体中多环芳烃污染主要来源为城市面源污染、燃烧源以及交通污染源;Kalf风险熵值法评价结果表明,枯水期:萘(Nap)、苊烯(Acy)、二氢苊(Ace)、芴(Flu)、菲(Phe)、蒽(Ant)、荧蒽(Fla)、芘(Pyr)和苯并[a]蒽(BaA)以及∑PAHs为中等生态风险水平,丰水期:萘(Nap)、苊烯(Acy)、芴(Flu)、菲(Phe)、荧蒽(Fla)、芘(Pyr)、苯并[a]蒽(BaA)、苯并[b]荧蒽(BbF)、苯并[k]荧蒽(BkF)、苯并[a]芘(BaP)、茚苯[1,2,3-cd]芘(InP)和苯并[ghi]苝(BghiP)属于中等生态风险水平,∑PAHs为低生态风险水平;总体而言,嘉兴市河网水体中PAHs生态风险呈中等水平,有关部门需采取措施降低河网水体中PAHs的生态风险.  相似文献   
4.
研究鸟嘌呤与一系列卤代烃反应的加合产物 ,利用HPLC二极管阵列检测器得到的特征紫外光谱 (UV)对加合产物样品进行了鉴定 ,然后加合产物经薄层 (TLC)分离 ,再进一步做红外 (FTIR)鉴定 ,从而得到鸟嘌呤 卤代烃氧位和氮位加合物的红外光谱表征 .研究表明 ,鸟嘌呤卤代烃的氮位加合物异构体的紫外光谱吸收峰的波长在 240~250nm之间 ,氧位加合物UV波长在 260~270nm附近 .鸟嘌呤与本文涉及的各卤代烃的加合物的红外光谱之间差别不大 :其氮位加合物在 1700cm-1处 ,均有CO的特征吸收峰 ;其氧位加合物的红外光谱亦相近 .  相似文献   
5.
pH和发酵时间对厨余垃圾发酵产乳酸及光学特性的影响   总被引:1,自引:0,他引:1  
张波  何品晶  邵立明 《环境科学》2007,28(4):881-885
通过间歇实验探讨了在中温、非灭菌条件下,pH和发酵时间对厨余垃圾发酵产乳酸及其光学特性的影响.结果表明,采用非灭菌的厨余垃圾发酵产乳酸,发酵液中还原糖浓度低,pH调节到近中性和偏碱性(pH为6~8)的各组还原糖浓度高于偏酸性组(pH=5和pH=4的对照组);在控制pH为7时,总乳酸产生速率达到0.59 g·(L·h)-1,单位挥发性固体的乳酸产量达到0.62 g·g-1;控制pH为7和8时,以有机碳表示的乳酸分别占发酵液总有机碳的78%和89%;控制pH为8时,L-乳酸是主要的异构体形式,单位挥发性固体L-乳酸产量达到0.48 g·g-1;响应面分析结果表明,发酵时间在120 h前,随着pH升高和发酵时间的延长,发酵液中L-乳酸浓度增大,120 h后则下降;pH和发酵时间对L-乳酸占总乳酸的比例有明显影响:偏酸性条件(未调pH及pH=5),发酵前120 h,该比例随发酵时间逐渐增大,L-乳酸在总乳酸中的比例达到0.9,其后,则逐渐下降;偏碱性条件下(pH=8),L-乳酸在总乳酸中的比例在整个发酵时间段内都保持在0.86以上,在发酵时间48 h时达到0.93,而在pH中性条件下,该比例在发酵后期显著下降;控制pH为8时,可以同时获得高的乳酸产量和光学纯度.  相似文献   
6.
For elucidation of the metabolism of the endocrine disruptor nonylphenol by Sphingomonas sp. strain TTNP3, the degradation of an isomer of nonylphenol, 4(2,6-dimethyl-2-heptyl)-phenol, has been studied. As in the case of 4(3,5-dimethyl-3-heptyl)-phenol, the metabolism of this nonylphenol isomer leads to the formation of the NIH-shifted product 2(2,6-dimethyl-2-heptyl)-1,4-benzenediol (NIH: National Institute of Health), but also to the alkoxy derivative 4(2,6-dimethylheptan-2-yloxy)phenol as additional metabolite. To the best of our knowledge, this is the first report describing the formation of alkoxyphenol as a degradation product of nonylphenol. Additionally, these results provide for the first time evidence for slight differences in the biodegradation of the isomers of nonylphenol.  相似文献   
7.
全氟化合物同分异构体的环境行为及毒性效应研究进展   总被引:1,自引:0,他引:1  
以全氟辛烷磺酸盐(PFOS)和全氟辛烷羧酸(PFOA)为代表的全氟化合物(PFASs)是一类新型持久性有机污染物,目前已经在全球自然环境、野生生物及人群中广泛检出,其环境与健康问题已引起人们的高度重视。传统的电氟化法生产工艺使PFASs产品存在碳链同分异构体。这些PFAS的同分异构体可能具有不同的环境行为和毒理效应。随着分析方法的逐渐成熟,目前,国外的学者已经在该研究领域进行了一些探索性的研究,并取得了一定的进展,而我国在该领域的研究相对较少。以PFOS和PFOA为例,在介绍了PFAS同分异构体的来源、命名和世界各地生产厂家的异构体组成等基本信息的基础上,还系统介绍了环境介质中PFAS同分异构体的分析方法、环境迁移转化差异及源分析研究;生物和人体的生物累积性及毒理学差异等;并对目前存在的问题进行了讨论,为今后PFAS同分异构体的环境问题研究提供相应的参考。  相似文献   
8.
Analysis of polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) has been performed using gas chromatography mass spectrometry (GC-MS). Analysis of the most toxic isomers, in particular, 2,3,7,8-substituted PCDD/PCDF in the presence of other isomers requires a special isomer specific capillary column or high performance liquid chromatography (HPLC) fractionation prior to GC-MS analysis. Commercially available long (>50 m) polar columns can separate 2,3,7,8-TCDD from other tetra isomers. However, those columns are not satisfactory for the analyses of total PCDD/PCDF in the environmental samples. Gas chromatography -high resolution mass spectrometry (GC-HRMS) and GC-MS/MS techniques are not helpful in the analysis of 2,3,7,8-TCDD unless it is separated from the other tetra isomers. The analysis of 2,3,7,8-TCDD and total PCDD and PCDF in a single GC-MS run can ease the laborious techniques presently used. In this study we have developed a new stationary phase for the GC capillary column. The capillary column developed using this new stationary phase showed unsurpassed selectivity for the separation of 2,3,7,8-TCDD from other tetra isomers. There are several advantages of the newly developed GC capillary column.  相似文献   
9.
The dechlorination of OCDD, OCDF and 1,2,3,4,7,8‐H6CDD is studies on an alumina support impregnated with activated carbon, copper chloride and potassium chloride. There is a high correlation between the isomer pattern found after dechlorination and molecular structure properties. We also found a substantial correlation between the isomer pattern and the Gibbs free energy of formation of the individual isomers. This suggests a thermodynamically controlled process.  相似文献   
10.
Abstract

Eighty male weanling rats were fed dietary levels o£ Technical X‐factor (βisomer free BHC, a by‐product obtained during the separation of lindane from Tech. BHC) at dosages of 10, 50, 250, 750, 1500 and 3000 ppm for 90 days. No overt signs of toxicity or mortality were observed at any of the dietary levels. However, a significant reduction in food consumption and growth was evident beyond 750 ppm. Pronounced hepatomegaly observed at 1500 and 3000 ppra was associated with histolo‐gical alterations such as cellular hypertrophy, cyto‐plasmic vacuolisation and focal necrosis. Adrenals showed cortical hypertrophy and highly vacuolated cytoplasm. Though a significant increase in the levels of SGOT was noted at 3000 ppra dosage, no appreciable changes were observed in the levels of SGPT and SLDH. Technical X‐factor appeared to possess low chronic toxicity compared to Tech. BHC as evidenced by the various parameters studied. The observed low chronic toxicity of X‐factor is probably due to the absence of βisomer and altered composition of delta and alpha isomers.  相似文献   
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