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21.
黄子龙  曾立民  董华斌  李梅  朱彤 《环境科学》2016,37(4):1188-1198
利用单颗粒气溶胶飞行时间质谱(SPAMS)于2013年6月30日~7月8日对华北地区乡村站点曲周大气单颗粒粒径及其化学组成进行了在线测量,共采集到同时含有正负离子谱图的颗粒230 152个,其粒径主要集中在0.2~2.0μm.结果表明,该地区的大气颗粒物主要分为8类:元素碳(EC,55.5%)、有机碳(OC,10.7%)、钠,钾等碱金属颗粒(alkalis,17.4%)、其他金属颗粒(other metals,1.7%)、富铁颗粒(Fe-rich,6.3%)、富铅颗粒物(Pb-rich,3.1%)、沙尘颗粒(dust,4.8%),other颗粒(0.8%),观测得到的8类气溶胶颗粒中绝大部分包含46NO-2、62NO-3、80SO-3、96SO-4、97HSO-4等二次组分离子,说明这些颗粒都经历了不同的老化过程或与二次组分进行了不同程度的混合.从气溶胶类型的谱分布看,各类型颗粒数浓度峰值基本出现在700~800 nm之间,dust、Fe颗粒主要集中在粗粒径段,EC颗粒子类研究表明随着表面不断吸附NH+4、NO-3、SO2-4等二次组分,EC颗粒逐步演化成老化程度较低的NO-3吸附型EC(ECN)和严重老化的SO2-4吸附型EC(ECS)混合态,两者日变化呈现明显的负相关性,也可能随着二次有机物在EC表面吸附,形成OC/EC混合态.  相似文献   
22.
苯甲地那铵是一种广泛使用的苦味剂,近年来被发现在欧洲水体中普遍存在。建立灵敏可靠的环境样品前处理分析方法对评价其环境行为具有重要意义。通过优化关键前处理过程参数,建立了水中苯甲地那铵的固相萃取-超高效液相色谱串联质谱分析方法,系统考察了该方法的准确度、精密度、基质效应、检出限以及线性范围。研究表明:当调节水样pH至8以上,采用混合型阳离子交换小柱(200 mg, 3 mL)富集水样,采用含体积分数2%甲酸的甲醇溶液洗脱时,该方法可获得最佳回收率;纯水和环境水样中加标回收率分别为97%~105%和89%~119%,相对标准偏差小于7%;基质效应均在24%以内;方法检出限为0.07 ng/L,线性范围为0.01~50μg/L。该方法可用于环境水体中苯甲地那铵的痕量检测。  相似文献   
23.
杨静 《中国环境监测》2021,37(1):156-164
为测定污染土壤中的6种低残留喹诺酮类抗生素(氧氟沙星、培氟沙星、恩诺沙星、环丙沙星、诺氟沙星、恶喹酸),全面优化了一种联合加速溶剂萃取(ASE)、固相萃取(SPE)和高效液相色谱/三重四级杆质谱(HPLC/MSMS)3种检测技术的分析方法.样品采用甲醇和0.1 mol/L EDTA-McIlvaine缓冲液(1∶1)进...  相似文献   
24.
In this work, water and sediment samples were collected from three different stations located along the Sakarya river between May and September 2003. Lead, copper, chromium, zinc, nickel and cadmium concentrations were determined by using solvent extraction and flame atomic absorption spectrometric method. The results show that differences based upon sampling times, regions, sediment and water samples were observed. The mean levels of copper, nickel, chromium, lead, cadmium, zinc for sediment samples are; 4.630 μg g−1, 13.520 μg g−1, 8.780 μg g−1, 2.550 μg g−1, 9.990 μg g−1 and for water samples are; 0.851 μg g−1, 1.050 μg g−1, 0.027 μg g−1, 1.786 μg g−1, 0.236 μg g−1, 0.173 μg g−1, respectively.  相似文献   
25.
The activity concentrations of soil samples collected from thirty different locations of Malwa region of Punjab were determined by using HPGe detector based on high-resolution gamma spectrometry system. The range of activity concentrations of 226Ra, 232Th and 40K in the soil from the studied areas varies from 18.37 Bq kg−1 (Sangrur) to 53.11 Bq kg−1 (Sitoguno), 57.28 Bq kg−1 (Dhanola) to 148.28 Bq kg−1 (Sitoguno) and 211.13 Bq kg−1 (Sunam) to 413.27 Bq kg−1 (Virk Khera) with overall mean values of 35 Bq kg−1, 80 Bq kg−1and 317 Bq kg−1 respectively. The absorbed dose rate calculated from activity concentration of 226Ra, 232Th and 40K ranges between 8.47 and 24.48, 35.68 and 92.38, and 8.74 and 17.11 nGy h−1, respectively. The total absorbed dose in the study area ranges from 58.08 nGy h−1 to 130.85 nGy h−1 with an average value of 79.11 nGy h−1. The calculated values of external hazard index (Hex) for the soil samples of the study area range from 0.35 to 0.79. Since these values are lower than unity, therefore, according to the Radiation Protection 112 (European Commission. Radiation Protection 112 1999) report, soil from these regions is safe and can be used as a construction material without posing any significant radiological threat to population.  相似文献   
26.
Cadmium and lead were determined simultaneously in seawater by differential pulse stripping voltammetry (DPSV) preceded by adsoptive collection of complexes with 8-hydroxyquinoline (oxine) on to a hanging mercury drop electrode (HMDE). In preliminary experiments the optimal analytical condition for oxine concentration was found to be 2.10−5 M, at pH 7.7, the accumulation potential was −1.1 V, and the initial scannig potential was −0.8 V. The peak potentials were found −0.652 V for Cd and −0.463 V for Pb At the 60 s accumalation time. The limit of detection (LOD) and limit of quantitatification (LOQ) were found to be by voltammetry as 0.588 and 1.959 μg l−1 (RSD, 5.50%) for Cd and 0.931 and 3.104 μg l−1 (RSD, 4.10%) for Pb at 60 s stirred accumulation time respectively. In these conditions the most of the seawater samples are amenable for direct voltammetric determination of cadmium and lead using a HMDE. An adsorptive stripping mechanism of the electrode reaction was proposed. For the comparison, seawater samples were also analysed by ICP-atomic emission spectrometry method (ICP-AES). The applied voltammetric technique was validated and good recoveries were obtained.  相似文献   
27.
长江沉积物中痕量氯代酚类化合物的测定   总被引:12,自引:0,他引:12  
本文利用同位素稀释质谱法对长江南京段沉积物中18种氯代酚进行了分离鉴定,结果表明,沉积物中CPs的含量以五氯苯酚为主,  相似文献   
28.
建立了土壤和沉积物中8种多溴联苯醚(PBDEs,BDE-28、BDE-47、BDE-99、BDE-100、BDE-153、BDE-154、BDE-183和BDE-209)加速溶剂同时萃取和净化-气相色谱-三重四极杆串联质谱(ASE-GC-MS-MS)的分析方法。通过优化加速溶剂萃取与弗罗里硅土在线净化和串联质谱多反应监测模式的条件,较好地去除基质干扰,并提高了三重四极杆串联质谱定性的准确性及定量的灵敏性。该方法采用改进的色谱柱能同时分析包括高溴代联苯醚BDE-209在内的8种PBDEs,其浓度范围为1~100 ng/mL(BDE-209为10~1 000 ng/mL),线性良好,线性回归系数均大于0.997。方法检出限为0.004~0.1 ng/g,方法回收率为75%~110%,方法精密度为2.4%~15.6%。适于批量处理土壤和沉积物中含有多组分痕量PBDEs的样品。  相似文献   
29.
The free living nematode Caenorhabditis elegans is a proven model organism for lipid metabolism research. Total lipids of C. elegans were extracted using chloroform and methanol in 2:1 ratio (v/v). Fatty acids composition of the extracted total lipids was converted to their corresponding fatty acids methyl esters (FAMEs) and analyzed by gas chromatography/accurate mass quadrupole time of flight mass spectrometry using both electron ionization and chemical ionization techniques. Twenty-eight fatty acids consisting of 12 to 22 carbon atoms were identified, 65% of them were unsaturated. Fatty acids containing 12 to17 carbons were mostly saturated with stearic acid (18:0) as the major constituent. Several branched-chain fatty acids were identified. Methyl-14-methylhexadecanoate (iso- 17:0) was the major identified branched fatty acid. This is the first report to detect the intact molecular parent ions of the identified fatty acids in C. elegans using chemical ionization compared to electron ionization which produced fragmentations of the FAMEs.  相似文献   
30.
The aim of this study was to determine the level of 26 polycyclic aromatic hydrocarbons (PAHs) at parking garages and to provide the necessary annual information based on occupational inhalation exposure and non-occupational inhalation exposure, which carry risks for the environment. For this purpose, 22 samples were collected continuously from both gas and particulates phase PAHs from two parking garages at Konya City Center, Turkey. The exposure-based risk of these samples was evaluated using concentrations of the carcinogenic PAH compounds. None of the 26 PAHs measured had values exceeding the recommended exposure limits (RELs) standard values for inhalation rate recommended by the World Health Organization (WHO). Exposure levels of gas and particulate PAHs for the occupational group and the public (children and adults who spend time in shopping centers) were found to be 0.07–28.24 μgm?3 and 0.05–5.753 μgm?3, respectively, representing levels two to four times higher than those at the control site. Maximum daily inhalation of B[a]Py was estimated at 1.33 ngd?1 for exposure of the public and as 274 ngd?1 for the occupational group. It is believed that traffic makes a substantial contribution to the PAH profile, which had relatively high concentrations of naphthalene (Napth) and coronene (Coro). Highly carcinogenic dibenzo(a,l)pyrene (B[al]Pyre) was found in the ambient air at two parking garages. Napth and phenanthrene (Phen) were the main compounds found in nearly all the tested samples. In this study, benzo[e]pyrene (B[e]Py) was used as a reference for PAHs because its concentration is stable and does not change seasonally. Considering the importance of these compounds in relation to human health, the aim of this work was to characterize and quantify the more toxic PAHs in parking garages. Conducting PAH sampling and their chemical analysis is very costly and labor intensive. This study produced data that can be a powerful tool for environmental forensics.  相似文献   
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