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1.
An on‐line solid phase extraction method for the preconcentration and determination of Cu(II) by flame atomic absorption spectrometry has been described. The procedure is based on the retention of Cu(II) ions at pH 6.0 on a minicolumn packed with Amberlite XAD‐1180 resin impregnated with chrome azurol S. After preconcentration, Cu(II) ions adsorbed on the impregnated resin were eluted by 1 mol L?1 HNO3 solution. Several parameters, such as pH, type of eluent, flow rates of sample and eluent solutions, amount of resin were evaluated. At optimized conditions, for 3.5 min of preconcentration time, the system achieved a detection limit of 1.0 µg L?1, and a relative standard deviation of 1.2% at 0.2 µg mL?1 copper. An enrichment factor of 56‐fold was obtained with respect to the copper determination. The proposed method was successfully validated by the analysis of standard reference material (TMDA 54.4 lake water) and recovery studies. The method was applied to the preconcentration of Cu(II) in natural water samples. 相似文献
2.
Manish Yadav Nitin Kumar Singh Bhupendra Kumar Soni Kusum Soni Pawan Kumar Singh 《洁净——土壤、空气、水》2023,51(1):2200059
In this study, three approaches namely parallel, sequential, and multiple linear regression are applied to analyze the local air quality improvements during the COVID-19 lockdowns. In the present work, the authors have analyzed the monitoring data of the following primary air pollutants: particulate matter (PM10 and PM2.5), nitrogen dioxide (NO2), sulfur dioxide (SO2), and carbon monoxide (CO). During the lockdown period, the first phase has most noticeable impact on airquality evidenced by the parallel approach, and it has reflected a significant reduction in concentration levels of PM10 (27%), PM2.5 (19%), NO2 (74%), SO2 (36%), and CO (47%), respectively. In the sequential approach, a reduction in pollution levels is also observed for different pollutants, however, these results are biased due to rainfall in that period. In the multiple linear regression approach, the concentrations of primary air pollutants are selected, and set as target variables to predict their expected values during the city's lockdown period.The obtained results suggest that if a 21-days lockdown is implemented, then a reduction of 42 µg m−3 in PM10, 23 µg m−3 in PM2.5, 14 µg m−3 in NO2, 2 µg m−3 in SO2, and 0.7 mg m−3 in CO can be achieved. 相似文献
3.
Jing‐Wen Zhang Yu‐Kun Wang Hai‐Ying Du Xin Du Jing‐Jun Ma Jing‐Ci Li 《洁净——土壤、空气、水》2011,39(12):1095-1098
A new method for determining lead (Pb) content was developed by dispersive liquid–liquid microextraction based on the solidification of floating organic droplets followed by flame atomic absorption spectrometry. Under optimum conditions, the calibration graph was linear within the Pb content range of 8.43–400 µg L?1 with a detection limit of 2.53 µg L?1. The relative standard deviation for 10 replicate measurements of 20 and 400 µg L?1 of Pb were 3.41 and 2.78%, respectively. The proposed method was assessed through the analysis of certified reference water and recovery experiments. 相似文献
4.
The present paper proposes the application of multiwalled carbon nanotubes (MWCNTs) as a solid adsorbent for selective separation/preconcentration of silver(I) in water samples prior to flame atomic absorption spectrometry. The procedure is based on the solid phase extraction of Ag(I)–2‐mercaptobenzothiazole chelate on MWCNTs. The elution step is carried out with 5 mL of 2 mol L?1 HNO3 in acetone solution at a flow rate of 1.0 mL min?1. The influences of the various analytical parameters including pH of the solution, eluent type, sample volume, flow rates of eluent, matrix ions were investigated for optimization of the presented procedure. Tests of addition/recovery for analyte ion in real samples were performed with satisfactory results. Preconcentration factor and limit of detection for Ag(I) were 160 and 0.21 µg L?1, respectively. The synthesized MWCNT exhibited excellent stability in eluent solution and its adsorption capacity was 5.4 mg of silver per gram of sorbent. The proposed method was successfully applied to trace silver determination in a variety of environmental water samples. 相似文献
5.
The Huancané II moraines deposited by the Quelccaya Ice Cap in southern Peru were selected by the CRONUS-Earth Project as a primary site for evaluating cosmogenic-nuclide scaling methods and for calibrating production rates. The CRONUS-Earth Project is an effort to improve the state of the art for applications of cosmogenic nuclides to earth-surface chronology and processes. The Huancané II moraines are situated in the southern Peruvian Andes at about 4850 m and ∼13.9°S, 70.9°W. They are favorable for cosmogenic-nuclide calibration because of their low-latitude and high-elevation setting, because their age is very well constrained to 12.3 ± 0.1 ka by 34 radiocarbon ages on peat bracketing the moraines, and because boulder coverage by snow or soil is thought to be very unlikely. However, boulder-surface erosion by granular disintegration is observed and a ∼4% correction was applied to measured concentrations to compensate. Samples from 10 boulders were analyzed for 10Be, 26Al, and 36Cl. Interlaboratory bias at the ∼5% level was the largest contributor to variability of the 10Be samples, which were prepared by three laboratories (the other two nuclides were only prepared by one laboratory). Other than this issue, variability for all three nuclides was very low, with standard deviations of the analyses only slightly larger than the analytical uncertainties. The site production rates (corrected for topographic shielding, erosion, and radionuclide decay) at the mean site elevation of 4857 m were 45.5 ± 1.6 atoms 10Be (g quartz)−1 yr−1, 303 ± 15 atoms 26Al (g quartz)−1 yr−1, and 1690 ± 100 atoms 36Cl (g K)−1 yr−1. The nuclide data from this site, along with data from other primary sites, were used to calibrate the production rates of these three nuclides using seven global scaling methods. The traditional Lal formulation and the new Lifton-Sato-Dunai calibrations yield average ages for the Huancané samples that are in excellent-to-good agreement with the radiocarbon age control (within 0.7% for 10Be and 36Cl and 6% for 26Al). However, all of the neutron-monitor-based methods yielded ages that were too young by about 20%. The nuclide production ratios at this site are 6.74 ± 0.34 for 26Al/10Be in quartz and 37.8 ± 2.3 (atoms 36Cl (g K)−1) (atom 10Be (g SiO2)−1)−1 for 36Cl/10Be, in sanidine and quartz, respectively. 相似文献
6.
Thermokarst lakes play a key role in the hydrological and biogeochemical cycles of permafrost regions. Current knowledge regarding the changes caused by permafrost degradation to the hydrochemistry of lakes in the Qinghai-Tibet Plateau (QTP) is limited. To address this gap, a systematic investigation of thermokarst lake water, suprapermafrost water, ground ice, and precipitation was conducted in the hinterland of the QTP. The thermokarst lake water in the QTP was identified to be of the Na-HCO3-Cl type. The mean concentrations of HCO3− and Na+ were 281.8 mg L−1 (146.0–546.2 mg L−1) and 73.3 mg L−1 (9.2–345.8 mg L−1), respectively. The concentrations of Li+, NH4+, K+, F−, NO2−, and NO3− were relatively low. Freeze-out fractionation concentrated the dissolved solids within the lake water during winter, which was deeply deepened on lake depth and lake ice thickness. Owing to solute enrichment, the ground ice was characterized by high salinity. Conversely, repeated replenishment via precipitation led to lower solute concentrations in the ground ice near the permafrost table compared to that within the permafrost. Although lower solute concentration existed in precipitation, the soil leaching and saline ground ice melting processes enhanced the solute load in suprapermafrost water, which is considered an important water and solute resource in thermokarst lakes. The influencing mechanism of permafrost degradation on thermokarst lake hydrochemistry is presumably linked to: (1) the liberation of soluble materials sequestered in ground ice; (2) the increase of solutes in suprapermafrost water and soil pore water; and (3) the changes in lake morphometry. These results have major implications on the understanding of the effects of ground ice melting on ecosystem functions, biogeochemical processes, and energy balance in a rapidly changing climate. 相似文献
7.
Heavy liquid density separation is commonly utilised in isolating specific minerals from bulk sediment for luminescence dating. K-feldspars are commonly separated from other minerals by isolating the <2.58 g cm−3 fraction which yields infrared stimulated luminescence (IRSL) signals conducive to dating. However, initial measurements of the IRSL and thermoluminescence (TL) signals from the <2.58 g cm−3 fraction of alluvial fan sediments from the Hajar Mountains, northern Oman, were atypical of K-feldspar luminescence signals reported in the literature. In this study, three different density separates (<2.58 g cm−3, 2.58–2.54 g cm−3 and <2.565 g cm−3) were trialled to attempt to isolate pure K-feldspar samples for dating, to measure K-feldspar IRSL signals which are not contaminated with inputs from other feldspar, quartz and/or heavy mineral signals. The mineralogy of these separates was explored using microscopy, X-ray diffraction and mass spectrometry. We found that despite more refined heavy liquid density separation, the proportions of K-feldspar in these separates had a maximum of 40% by weight, remaining significantly contaminated by other minerals. IRSL and TL signals were atypical of K-feldspar for all density separates and it is likely that there is a contribution of signal from IR-sensitive contaminants, such as muscovite. This highlights the importance of investigating the mineralogy of samples for luminescence dating, especially in regions where little prior work has been undertaken. 相似文献
8.
《Limnologica》2017
The study analyses the long-term biophysical and demographic changes in Dal lake, located in the heart of Srinagar city, Kashmir India, using a repository of historical, remote sensing, socio-economic and water quality data supported by the extensive field observations. The lake faces multiple pressures from the unplanned urbanization, high population growth, nutrient load from intensive agriculture and tourism. The data showed that the lake has shrunk from 31 km2 in 1859–24 km2 in 2013. Significant changes were observed in the land use and land cover (LULC) within the lake (1859–2013) and in the vicinity of the lake (1962–2013). Analysis of the demographic data indicates that the human population within the lake has shown more than double the national growth rate. Additionally, 7 important water quality parameters from 82 well distributed sites across the lake were analyzed and compared with the past data to determine the historical changes in the water quality from 1971 to 2014. The changes in the LULC and demography have adversely affected the pollution status of this pristine lake. Ortho-phosphate phosphorous concentration has increased from 16.75 μg L−1 in 1977–45.78 μg L−1 in 2014 and that of the nitrate-nitrogen from 365 μg L−1 to 557 μg L−1, indicating nutrient enrichment of the lake over the years. Built-up area within the lake has increased 40 times since 1859, which, together with the changes in the population and settlements, have led to the high discharge of untreated nutrient-rich sewage into the lake. Similarly the expansion of floating gardens within the lake and agriculture lands in the catchment has contributed to the increased nutrient load into the lake due to the increasing use of fertilizers. The information about the existing land cover, demography and water quality was integrated and analyzed in GIS environment to identify the trophic status of the lake. The analysis indicated that 32% of the lake falls under sever degradation, 48% under medium degradation while as 20% of the lake waters are relatively clean. It is believed that the results provide improved knowledge and insights about the lake health and causal factors of its degradation necessary for effectively restoring its ecological and hydrological functionality. 相似文献
9.
Interest in preconcentration techniques for the determination of metals at ultratrace levels still continues increasingly because of some disadvantages of flameless atomic absorption spectrometry and the high costs of other sensitive methods in compared to flame atomic absorption spectrometry (FAAS). Among preconcentration techniques, solid‐phase extraction is the most popular because of a number of advantages. In this work, thiol‐containing sulfonamide resin was synthesized, characterized, and applied as a new sorption material for solid phase extraction and determination of lead in natural water samples. The optimization of experimental conditions was performed using the parameters including pH, contact time, and volumes of initial and elution solutions. After preconcentration procedure, FAAS was used for determinations. The synthesized resin exhibits the superiority in compared to the other adsorption reagents because of the fact that there is no necessity of any complexing reagent as well as high sorption capacity. Consequently, 280‐fold improvement in the sensitivity of analytical scheme was achieved by combining the slotted tube atom trap‐atomic absorption spectrometry (STAT‐FAAS) and the developed preconcentration method. The limit of detection was found to be 0.15 ng mL?1. The Pb2+ concentrations in the studied water samples were found to be in the range of 0.9–6.7 ng mL?1. 相似文献
10.
To constrain the depth-dependence of in situ 14C production we measured the cosmogenic 14C concentration of quartz separates along a quartzite core from the Leymon High site in northwest Spain. A total of 16 quartz samples were measured over a depth range of 1–1545 cm (3–4017 g cm−2). The obtained 14C profile was modeled using a neutron production rate, exponentially decreasing with depth, and a fast and negative muon production parameterized as a function of the local muon flux as derived by (Heisinger et al., 2002a, 2002b). This model yields a total negative muon capture probability of 1.72 (+0.22/−0.56) × 10−2 and a fast muon reaction cross section of 0 (+11.8/−0.00) μb. Rescaled to sea level high latitude using a Lal/Stone scaling scheme, these estimates yield a surface muon production rate of 3.31 (+0.43/−1.07) and 0 (+0.42/−0.00) at·g−1 yr−1 for negative muon capture and fast muons, respectively. This is the first muon production estimate for in situ 14C from a natural setting and is within uncertainty of the previous experimental estimates. The present contribution also provides new long-term blank and standard (PP-4, CRONUS-A & CRONUS-N) in situ 14C data from the ETH Zürich 14C extraction line. 相似文献
11.
The inactivation of Fusarium solani in water was assessed by solar driven Fenton-like processes using three different iron salts: ferric acetylacetonate (Fe(acac)3), ferric chloride (FeCl3) and ferrous sulfate (FeSO4). The experimental conditions tested were [Fe] ≈ 5 mg L−1, [H2O2] ≈ 10 mg L−1 and [Fe] ≈ 10 mg L−1; [H2O2] ≈ 20 mg L−1 mild and high, respectively, and pH 3.0 and 5.0, under solar radiation. The highest inactivation rates were observed at high reaction conditions for the three iron salts tested at pH 5.0 with less than 3.0 kJ L−1 of accumulate energy (QUV) to achieve over 99.9% of F. solani inactivation. Fe(acac)3 was the best iron salt to accomplishing F. solani inactivation. The modified Fermi equation was used to fix the experimental inactivation, data showed it was helpful for modeling the process, adequately describing dose–response curves. Inactivation process using FeSO4 at pH 3.0 was modeled fairly with r2 = 0.98 and 0.99 (mild and high concentration, respectively). Fe(acac)3, FeCl3 and FeSO4 at high concentration (i.e. [Fe] ≈ 10 mg L−1; [H2O2] ≈ 20 mg L−1) and pH 5.0 showed the highest fitting values (r2 = 0.99). Iron salt type showed a remarkable influence on the Fenton-like inactivation process. 相似文献
12.
The coprecipitation method is widely used for the preconcentration of trace metal ions prior to their determination by flame atomic absorption spectrometry (FAAS). A simple and sensitive method based on coprecipitation of Fe(III) and Ni(II) ions with Cu(II)‐4‐(2‐pyridylazo)‐resorcinol was developed. The analytical parameters including pH, amount of copper (II), amount of reagent, sample volume, etc., were examined. It was found that the metal ions studied were quantitatively coprecipitated in the pH range of 5.0–6.5. The detection limits (DL) (n = 10, 3s/b) were found to be 0.68 µg L?1 for Fe(III) and 0.43 µg L?1 for Ni(II) and the relative standard deviations (RSD) were ≤4.0%. The proposed method was validated by the analysis of three certified reference materials (TMDA 54.4 fortified lake water, SRM 1568a rice flour, and GBW07605 tea) and recovery tests. The method was successfully applied to sea water, lake water, and various food samples. 相似文献
13.
The identification of the center acting as electron source for the well-known 110 °C thermoluminescence (TL) peak of quartz is of fundamental importance for practical applications in dating and dosimetry. This TL peak was studied in parallel with the electron paramagnetic resonance (EPR) signal of the [GeO4]− center on natural colourless quartz irradiated at room temperature. Immediately after irradiation, the signals of the 110 °C TL peak and of [GeO4]− center decay exponentially in the same way, yielding a lifetime of 50.4 ± 0.9 min at room temperature. Besides, we acquired the isothermal decay curves for the 110 °C TL peak and [GeO4]− center at different temperatures (the samples were held at the selected temperature in the range of 260–308 K). The lifetimes extracted by the isothermal decays were plotted as a function of reciprocal temperature, revealing again the same behavior of the 110 °C TL peak and [GeO4]− center, both characterized by activation energies very close of 0.76 ± 0.07 eV and 0.77 ± 0.07 eV, respectively. All results of the present work clearly show the role of electron source of [GeO4]− center in the emission mechanism of the 110 °C TL peak in quartz. 相似文献
14.
15.
The on- and off-site effects of soil erosion in many environments are well known, but there is still limited understanding of the soil loss fluxes in downstream direction due, among other factors, to scarce and poor quality. A four year study to (i) evaluate water and sediment fluxes at different spatio-temporal scales and (ii) interpret the results in terms of processes involved and the controlling factors, was conducted in Thukela basin, South Africa. Five hierarchically nested catchments; namely microcatchment (0.23 km2), subcatchment (1.20 km2), catchment (9.75 km2), sub-basin (253 km2) and basin (29,038 km2), were used in addition to fifteen (1 m2) microplots and ten (10 m2) plots on five locations within the microcatchment. The results showed 19% decrease of unit-area runoff (q) from 3.1 L m−2 day−1 at microplot to 2.5 L m−2 day−1 at plot scale followed by steeper (56%) decrease at microcatchment scale. The q decreased in downstream direction to very low level (q ≤ 0.26 L m−2 day−1). The changes in q were accompanied by initial 1% increase of soil loss (SL) from 18.8 g m−2 day−1 at microplot to 19.1 g m−2 day−1 at plot scale. The SL also decreased sharply (by 39 fold) to 0.50 g m−2 day−1 at microcatchment scale, followed by further decrease in downstream direction. The decrease of q with spatial scale was attributed to infiltration losses, while initial increase of SL signified greater competence of sheet than splash erosion. The decrease of SL beyond the plot scale was attributed to redistribution of the soil on the hillslope and deposition on the stream channel upstream of the microcatchment outlet. Therefore, erosion control strategies focussing on the recovery of vegetation on the slope and stabilisation of gullies are recommended. 相似文献
16.
A total number of 46 local earthquakes (2.0≤ML≤4.0) recorded in the period 2000–2011 by the Egyptian seismographic network (ENSN) were used to estimate the total (Qt−1), intrinsic (Qi−1) and scattering attenuation (Qsc−1) in Cairo metropolitan area, Egypt. The multiple lapse time window analysis (MLTWA) under the assumption of multiple isotropic scattering with uniform distribution of scatters was firstly applied to estimate the pair of Le−1, the extinction length inverse, and B0, the seismic albedo, in the frequency range 3–24 Hz. To take into account the effect of a depth-dependent earth model, the obtained values of B0 and Le−1 were corrected for an earth structure characterized by a transparent upper mantle and a heterogeneous crust. The estimated values of Qt−1, Qsc−1 and Qi−1 exhibited frequency dependences. The average frequency-dependent relationships of attenuation characteristics estimated for the region are found to be: Qt−1=(0.015±0.008)f (−1.02±0.02), Qsc−1=(0.006±0.001)f (−1.01±0.02), and Qi−1=(0.009±0.008)f (−1.03±0.02); showing a predominance of intrinsic absorption over scattering attenuation. This finding implies that the pore-fluid contents may have great effect on the attenuation mechanism in the upper crust where the River Nile is passing through the study area. The obtained results are comparable with those obtained in other tectonic regions. 相似文献
17.
Trace metal clean sampling and analysis techniques were used to examine the temporal patterns of Hg, Cu, and Zn concentrations in shallow ground water, and the relationships between metal concentrations in ground water and in a hydrologically connected river. Hg, Cu, and Zn concentrations in ground water ranged from 0.07 to 4.6 ng L−1, 0.07 to 3.10 μg L−1, and 0.17 to 2.18 μg L−1, respectively. There was no apparent seasonal pattern in any of the metal concentrations. Filtrable Hg, Cu, and Zn concentrations in the North Branch of the Milwaukee River ranged from below the detection limit to 2.65 ng Hg L−1,0.51 to 4.30 μg Cu L−1, and 0.34 to 2.33 μg Zn L−1. Thus, metal concentrations in ground water were sufficiently high to account for a substantial fraction of the filtrable trace metal concentration in the river. Metal concentrations in the soil ranged from 8 to 86 ng Hg g−1, 10 to 39 μg Cu g−1, and 15 to 84 μg Zn g−1. Distribution coefficients, KD, in the aquifer were 7900,22,000, and 23,000 L kg−1 for Hg, Cu, and Zn, respectively. These values were three to 40 times smaller than KD values observed in the Milwaukee River for suspended particulate matter. 相似文献
18.
This work presents a solid phase extraction (SPE) method for simultaneous preconcentration of trace elements in water samples prior to their ICP-OES determination. Dowex 50W-x8 and Chelex-100 resins were used as SPE sorbent materials for preconcentration of trace Cd, Co, Cr, Cu, Fe, Ni, Pb and Zn. The optimum sample pH, eluent concentration and sample flow rates were found to 6, 3.0 mol L−1 and 3.0 mL min−1, respectively. In terms of multi-element preconcentration capabilities, Dowex 50W-x8 appeared to be a better sorbent. The recoveries for all the tested analytes were >95%. However, Chelex-100 showed a better performance in terms of recovery (>95%) towards Cu, Fe and Zn. Under optimized conditions using Dowex 50W-x8, the relative standard deviations for different metals were <3%. The limits of detection and limits of quantification ranged from 0.01–0.39 μg L−1 and 0.05–0.1.3 μg L−1, respectively. The accuracy of the preconcentration method was confirmed by spike recovery test and the analysis of certified reference materials. The SPE method was applied for preconcentration of the analyte ions in tap water, bottled water and wastewater samples. 相似文献
19.
Günay Erpul Donald Gabriels Melis Özge Pınar Çağlar Sagun Wim Cornelis 《地球表面变化过程与地形》2021,46(14):2870-2883
The effects of wind-driven rain (WDR) on sand detachment were studied under various raindrop obliquities. Results suggested a significant reduction in compressive stress on sand surfaces for a two-dimensional experimental set-up in a wind tunnel. During experiments, sand particles in splash cups were exposed to both wind-free rain (WFR) and WDR driven by horizontal winds of 6.4, 8.9 and 12.8 m s−1 and rainfall intensities of 50, 60, 75 and 90-mm h−1 to assess the sand detachment rate (D, in g m−2 s−1). The effects of sand moisture state (dry and wet) on the detachment of different-sized particles (0.20–0.50 and 0.50–2.00 mm, respectively) were also tested. Factorial analysis of variance showed that shear and compressive stress components evaluated by horizontal and vertical kinetic energy flux terms (KEx and KEy, respectively, in J m−2 s−1) along with their vector sum (KEr, in J m−2 s−1) explained the variation in D. Neither sand size nor sand moisture was statistically significant alone although binary interactions of KEr, KEx and KEy with the sand size and three-way interaction of KEx, sand size and moisture were statistically significant. These results can be explained by size-dependent variation in sand compressibility and surface friction related to the total stress field developed by a given partition of shear and compressive stresses of wind-driven oblique raindrops (KEx/KEy). Further analysis of the variation of the unit sand detachment rate (Du = D/KEr = g J−1) with rain inclination (α, in degrees) better revealed the effect of WDR obliquity on Du that further changed with sand size class and moisture state. Finally, the difference in the resulting stress field differentiable by the oblique raindrop trajectories of the experiment over sand surface significantly affected the non-cohesive particle detachment rates, to some extent interacted with size-dependent compressibility and interface shear strength of sand grains. 相似文献
20.
A simple and reliable method for rapid and selective extraction and determination of trace levels of Ni2+ and Mn2+ was developed by ionic liquid (IL) based dispersive liquid–liquid microextraction coupled to flame atomic absorption spectrometry (FAAS) detection. The proposed method was successfully applied to the preconcentration and determination of nickel and manganese in soil, vegetable, and water samples. After preconcentration, the settled IL‐phase was dissolved in 100 µL of ethanol and aspirated into the FAAS using a home‐made microsample introduction system. Injection of 50 µL of each analyte into an air–acetylene flame provided very sensitive spike‐like and reproducible signals. Effective parameters such as pH, amount of IL, volume of the disperser solvent, concentration of the chelating agent, and effect of salt concentration were inspected by a (25‐1) fractional factorial design to identify the most important parameters and their interactions. Under optimum conditions, preconcentration of 10 mL sample solution permitted the detection of 0.93 µg L?1 Ni2+ and 0.52 µg L?1 Mn2+ with enrichment factors 77.2 and 82.6 for Ni2+ and Mn2+, respectively. The accuracy of the procedure was evaluated by analysis of a certified reference material (CRM TMDW‐500, drinking water). 相似文献