Kinetics of phosphate adsorption by iron oxyhydroxides in aqueous systems     

S.A. Crosby  G.E. Millward  E.I. Butler  D.R. Turner  M. Whitfield 《Estuarine, Coastal and Shelf Science》1984,19(2):257-270

The rate of uptake of phosphate onto synthetic Fe(III)- and Fe(II)-derived oxyhydroxides has been studied using reaction conditions similar to those encountered in natural waters. Kinetic analyses were carried out on the adsorption profiles and both first-order and second-order conditional rate constants were obtained. The temperature dependence of some of the rate constants was investigated and corresponding apparent activation energies calculated. Similar experiments and analyses were undertaken using Fe from natural sources and in general the conditional rate constants obtained in seawater were in agreement with the synthetic ones. The results of this study are of value when comparing the time scales of adsorption processes in natural waters with the time scales of mixing and advection.  相似文献   

Organochlorines and dioxin-like compounds in green-lipped mussels Perna viridis from Hong Kong mariculture zones     

So MK  Zhang X  Giesy JP  Fung CN  Fong HW  Zheng J  Kramer MJ  Yoo H  Lam PK 《Marine pollution bulletin》2005,51(8-12):677-687

Concentrations of persistent organic pollutants including polychlorinated biphenyls (PCBs), organochlorine (OC) pesticides and dioxin-like compounds were measured in green-lipped mussels, Perna viridis, collected from seven mariculture zones in Hong Kong between September and October in 2002 in order to evaluate the status, spatial distribution and potential sources of pollution in these areas. Concentrations ranged from 300 to 4400 ng/g lipid weight for total OCs and 170–1000 ng/g lipid weight for total PCBs (based on 28 congeners). Relatively smaller DDT concentrations in mussels compared with previous studies suggest reduced discharges of DDTs from nearby regions into Hong Kong waters. Detection of a mixture of HCH isomers in the mussels indicated that Hong Kong waters were predominantly contaminated by technical HCHs rather than lindane. Mussel samples from all sampling locations elicited significant dioxin-like activity in the H4IIE-luc bioassay. The greatest magnitude of dioxin-like response (39 pg TEQ/g wet wt.) was detected in mussels from Ma Wan in the western waters of Hong Kong, which is strongly influenced by the Pearl River discharge. Human health risk assessment was undertaken to evaluate potential risks associated with the consumption of the green-lipped mussels. Risk quotient (RQ) for dioxin-like compounds was greater than unity suggesting that adverse health effects may be associated with high mussel consumption.  相似文献   

The amino acid composition of estuarine colloidal material     

A.C. Sigleo  P.E. Hare  G.R. Helz 《Estuarine, Coastal and Shelf Science》1983,17(1):87-96

Amino acids were determined in estuarine colloidal and particulate material from near surface waters ranging from fresh to brackish water (12 g kg^?1 salinity). The hydrolizable amino acids and associated ammonia account for an average of 80% of the nitrogen present in colloidal samples, and approximately 75% of the nitrogen from particulate fractions of the same samples. The relative proportions of these amino acids are similar to those of a cultured estuarine diatom. There are no significant amounts of D amino acids, or non-protein amino acids characteristic of bacteria in sediments and soil. A single deep-water sample (25 m) shows some evidence of bottom mud resuspension by the presence of a possible aspartic acid-hydroxyproline dimer.  相似文献   

Composition and major sources of organic compounds in urban aerosols     

Xinhui Bi  Bernd R.T. Simoneit  Guoying Sheng  Shexia Ma  Jiamo Fu   《Atmospheric Research》2008,88(3-4):256-265

Total suspended particles (TSP), collected during June 2002 to July 2003 in Guangzhou, a typical economically developed city in South China, were analyzed for the organic compound compositions using gas chromatography–mass spectrometry (GC/MS). Over 140 organic compounds were detected in the aerosols and grouped into different classes including n-alkanes, hopanoids, polycyclic aromatic hydrocarbons, alkanols, fatty acids, dicarboxylic acids excluding oxalic acid, polyols/polyacids, lignin products, phytosterols, phthalates and water-soluble sugars. The total amounts of the identified organic compounds including unresolved complex mixture (UCM) ranged from 3112 ng/m³ in spring to 5116 ng/m³ in winter, comprising on seasonal average 2.8% of TSP. Primary organic compounds peaked in winter although there are no heating systems burning fuels in Guangzhou. The highest saccharide levels occurred in fall due to agricultural activities. This study demonstrated that utilization of fossil fuels, biomass burning, soil resuspension and plastic/refuse burning are the major contributors to the identified organic compounds in the urban atmosphere of South China.  相似文献   

东营凹陷北部陡坡带稠油成藏机理与油气运聚特征   总被引：6，自引：1，他引：5  

李素梅  庞雄奇  邱桂强  高永进  孙锡年 《地球科学》2004,29(4):451-456,466

东营凹陷北部陡坡带的王庄—宁海地区发现了大量稠油 ,但原油的成因及其成藏机理仍不甚了解 .在以往原油成因与油源调查基础上 ,利用非烃含氮化合物及包裹体均一化温度对该区进行油气运移方向与相对距离、成藏时间与期次的分析 .结果表明 ,东营凹陷北部带原油具有由南而北的运移分馏效应 ,反映北部陡坡带原油来自南部的利津洼陷 ;王庄—宁海地区原油总体具有由东而西的运移分馏效应 ,其东、西两侧各有一主要油气注气点 .王庄—宁海原油烃类与非烃组成与分布特征揭示该区油气具有混合聚集特征 .包裹体测试反映王庄—宁海地区油藏主要为晚期成藏 ,距今小于 5Ma ;而靠近生油中心地带包裹体具有早期成藏的记录 (± 36Ma) .  相似文献   

南海北部油气缓释环境沉积物脂类化合物组成特征     

邱红  邹立  张民生  朱超祁  贾永刚 《沉积学报》2019,37(2):416-423

认识沉积环境有机碳留存状况是阐述油气形成过程中有机碳早期成岩的关键内容。以南海珠江口盆地及其邻近海域为背景,通过研究表层沉积物中脂类化合物的形态组成,认识脂类有机碳的来源和留存状态,阐述特征脂类分子的早期成岩特征。结果表明,研究区域表层沉积物有机碳含量为0.22%～0.66%,有机碳稳定同位素分布在-20.88‰～-22.93‰之间,表现为显著的海源特征。沉积物中共检测出21种脂肪酸、6种脂肪醇、8种甾醇和植醇;总脂肪酸、脂肪醇、甾醇和植醇含量分别为12.57～40.27μg/g、5.35～8.98μg/g、0.15～3.75μg/g和0.01～3.99μg/g干重,总体表现为靠近珠江口和台湾海峡略高。脂类化合物的存在形态以游离态(FR)和碱性水解态(BH)为主,酸性水解态(AH)贡献较低;其中植醇和甾醇呈现显著的BH优势,植醇中未检出AH组分的贡献。脂类化合物主要来自于海洋现场生产,海洋微藻和细菌的相对贡献率分别为21.18%～33.78%和11.02%～15.64%,陆源高等植物贡献低于5%。来源于硫酸盐还原菌的支链脂肪酸在靠近珠江口海域高达1.79～2.62μg/g,占总脂肪酸的5.14%～6.50%,并与硫酸盐还原过程相关的古菌分布相一致。  相似文献   

Primary Product Distributions from the Reaction of OH with m-, p-Xylene, 1,2,4- and 1,3,5-Trimethylbenzene     

D. F. Smith  T. E. Kleindienst  C. D. McIver 《Journal of Atmospheric Chemistry》1999,34(3):339-364

A study was conducted to examine the OH-initiated degradation products of the four title compounds in the presence of sub-part-per-million levels of NO_x. The oxidation was conducted in a dynamic reactor to minimize the conversion of the aromatic compounds. The experiments were designed to represent reaction pathways that occur in the atmosphere at ambient NO₂ concentrations. A wide range of ring-retaining and ring-cleavage products having widely varying yields were measured during the study. For m-xylene, the major primary products observed (with molar yields) were methyl glyoxal (0.40), 4-oxo-2-pentenal (0.12), glyoxal (0.079), and m-tolualdehyde (0.049). For p-xylene, the major primary products were p-tolualdehyde (0.103), 2,5-dimethylphenol (0.13), cis-3-hexene-2,5-dione (0.176), trans-3-hexene-2,5-dione (0.045), 2-methyl-butenedial (0.071), glyoxal (0.394), and methylglyoxal (0.217). Several other reaction products were measured at yields less than 3%. The primary products for OH + 1,2,4-trimethylbenzene were found as follows: methylglyoxal (0.44), glyoxal (0.066), cis-3-hexene-2,5-dione (0.13), trans-3-hexene-2,5-dione (0.031), biacetyl (0.114), 3-methyl-3-hexene-2,5-dione (0.079), and 2-methyl-butenedial (0.045). Six other (ring retaining) products were measured at yields less than 3%. The primary products for OH + 1,3,5-trimethylbenzene were methylglyoxal (0.90), 3-methyl-5-methylidene-5(2H)-furanone (0.1), 3,5-dimethyl-3(2H)-2-furanone (0.1), 3,5-dimethyl-5(2H)-2-furanone biacetyl (0.08), and 2-methyl-4-oxo-2- pentenal (0.05). Three other products were detected at molar yields less than 5%. In some cases, the yields for the ring fragmentation products could only be based on calibrations from surrogate compounds. Yields for several of the unsaturated dicarbonyl compounds have not been reported previously while yields for methylglyoxal, glyoxal, and biacetyl are largely consistent with previous reports. Some of the primary furanone products are the identical to those reported as secondary products in aromatic systems.  相似文献   

含氮化合物的实验方法初步评价   总被引：4，自引：0，他引：4  

李素梅  张爱云 《地球化学》1999,28(4):397-404

对吡咯类含氮化合物的两种分离方法以及两步分离法中使用国产与进口试验的实验结果进行了对比与评价。结果表明,分离方法不同,所得吡咯类含氮化合物总体馏分的丰度也不同,一步分离法普遍低于两步法;不同分离方法对吡咯类化合物相对分布的影响较小。国产与进口试验性能不影响吡咯类含氮化合物的绝对丰度与相对分布的分析结果,两步分离法具备分析试剂国产化的条件。  相似文献   

Correlations between cytochrome P450, haem synthesis enzymes, and aromatic compounds in flounder (Platichthys flesus) from the Baltic Sea     

Bogovski  S.; Sergeyev  B.; Muzyka  V.; Karlova  S. 《ICES Journal of Marine Science》1999,56(2):152-156

  相似文献   

湖泊磷的核磁共振(NMR)分析——1环境标准样品的³¹P-NMR表征   总被引：1，自引：0，他引：1  

王晓钧  丁士明  蒋海青  白秀玲  范成新 《湖泊科学》2008,20(1):45-50

通过对环境标准样进行31P-NMR测试,研究了磷的化学结构与化学位移的关系.结果表明:无机正磷酸盐(PO43-)化学位移在6.412×10-6,焦磷酸盐的化学位移在-4.353×10-6;多聚磷的化学位移分布特点是:主链末端磷化学位移在-3.53×10-6至-4.40×10-6之间,中间磷在-18.159×10-6至-20.246×10-6之间,有机磷中单酯和二醑的化学位移分别在4.3540×10-6至6.3652×10-6和-0.107×10-6至2.195×10-6之间,部分二脂不稳定,会降解为单脂;膦酸盐的化学位移在18.670×10-6至21.460×10-6之间,磷酸肌酸位于-0.380×10-6,有机多聚磷中α-P的化学位移在-8.833×10-6至-9.449×10-6之间,由于偶合作用产生P峰的裂分,P峰的偶合符合核磁中n 1的规则.结构环境影响31P的化学位移值的偏移.  相似文献