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1.
The determination of trace amount nitrobenzene in wastewater on a hanging mercury drop electrode was studied. The determination conditions of pH, supporting electrolyte, accumulation potential, accumulation time, and voltammetric response were optimized. The sharp peak of the nitrobenzene was appeared at 0.05 V. The peak electric current was proportional to the concentration of nitrobenzene in the range of 1.47 × 10−5 ∼ 1.0 × 10−3 mol/l with relative standard deviations of 3.99 ∼ 8.94%. The detection limit of the nitrobenzene in water was 5 × 10−6 mol/l. The proposed method offered low limit of determination, easy operation, the use of simple instrumentation, high sensitivity and good reproducibility. It was applied to the determination of nitrobenzene in wastewater with an average recovery of 94.0% ∼ 105%. The proposed method provided fast, sensitive and sometimes real time detection of nitrobenzene.  相似文献   

2.
Facile, selective and sensitive spectrophotometric method has been developed for the determination of carbosulfan in insecticidal formulations, fortified water, food grains, agriculture wastewater and soil samples with newly synthesized reagents. The method was based on acid and alkaline hydrolysis of the carbosulfan pesticide, and the resultant hydrolysis product of carbosulfan was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λ max of 464 nm or interaction with 2,6-dibromo-4-nitroaniline to produce yellow colored product with λ max of 408 nm or coupling with 2,4,6-tribromoaniline to form red colored product has a λ max of 471 nm. Under optimal conditions, Beer’s law range for 2,6-dibromo-4-methylaniline (DBMA) was found to be 0.2–12.0 μg ml−1, 0.6–16.0 μg ml−1 for 2,6-dibromo-4-nitroaniline (DBNA) and 0.4–15.0 μg ml−1 for 2,4,6-tribromoaniline (TBA). The molar absorptivity of the color systems were found to be 3.112 × 104 l mol−1 cm−1 for DBMA, 3.214 × 104 l mol−1 cm−1 for DBNA and 3.881 × 104 l mol−1 cm−1 for TBA. Sandell’s of the color reactions are 0.013 μg cm−2 (DBMA), 0.012 μg cm−2 (DBNA) and 0.011 μg cm−2 (TBA) respectively. The effect of the non-target species on the determination of carbosulfan was studied to enhance the selectivity of the proposed methods. The formation of colored derivatives with the coupling agents is instantaneous and stable for 28, 30, and 26 h. Performance of the proposed methods were compared statistically in terms Student’s F and t-tests with the reported methods. An erratum to this article can be found at  相似文献   

3.
N-Ethyl-3-cabazolecarboxaldehydethiosemicarbazone (ECCT) is proposed as a new, sensitive and selective complexing reagent for the separation and extractive spectrophotometric determination of palladium(II) at pH: 4.0 to form a yellowish orange colored 1:1 chelate complex, which is very well extracted in to n-butanol. The absorbance was measured at a maximum wavelength, 410 nm. This method obeys Beer’s law in the concentration range 0.0–6.6 μg mL−1 and the correlation coefficient of Pd(II)-ECCT complex is 0.998, which indicates an excellent linearity between the two variables with good molar absorptivity and Sandell’s sensitivity, 1.647 × 104 l mol−1cm−1, 6.49 × 10−3 μg cm−2, respectively. The instability constant of complex calculated from Edmond’s method, 2.724 × 10−5 was in good agreement with the value calculated from Asmus’ method 2.624 × 10−5, at room temperature. The precision and accuracy of the method is checked with calculation of relative standard deviation (n = 5), 0.839. Edmond’s method was observed to be a more selective method in the presence of EDTA, oxalate and phosphate ions. The method was successfully applied for the determination of Pd(II) in water samples, synthetic mixtures and hydrogenation catalysts, employing an atomic absorption spectrometer for comparing these results.  相似文献   

4.
A sensitive adsorptive stripping voltammetric method for the determination of simeton with universal buffer solution has been described. The method was based on the adsorption accumulation of simeton at a hanging mercury drop electrode. The overall reduction process is under controlled diffusion. The adsorptive peak was observed at ?0.8 V vs SCE in acidic solution 2 < pH < 6. The peak response was characterized with respect to pH, accumulation potential, time, and scan rate. The calibration plot was found to be linear from 1.13 × 10???5 to 3.5 × 10???8 M with a limit of detection of 2.0 × 10???8 M. Finally, the method has been applied for the determination of simeton in its formulations and vegetable samples.  相似文献   

5.
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   

6.
Facile, selective and sensitive spectrophotometric method has been developed for the determination of bendiocarb in its insecticidal formulations, fortified water, food grains, agriculture wastewater and agriculture soil samples with prepared reagents. The method was based on alkaline hydrolysis of the bendiocarb pesticide, and the resultant hydrolysis product of bendiocarb was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λmaxof457 nmorcouplingwith2, 6−dibromo−4−nitroanilinetoproducearedcoloredproductwithλmax of474~nmorcouplingwith2, 4, 6−tribromoanilinetoformorangeredcoloredproducthasaλmax of465 nm.Underoptimalconditions, Beer'slawrangefor2, 6−dibromo−4−methylaniline(DBMA)wasfoundtobe0.6−−14.0~μgmL -1, 0.8−−10.0 μgmL -1 for2, 6−dibromo−4−nitroaniline(DBNA)and0.4−−10.0 μgmL -1 for2, 4, 6−tribromoaniline(TBA).Themolarabsorptivityofthecolorsystemswerefoundtobe4.126~×~104 lmol -1cm -1 forDBMA, 3.254×104 l~mol -1cm -1 forDBNAand2.812×104 lmol -1cm -1 forTBA.Sandell'softhecolorreactionsare0.018 μgcm -2(DBMA), 0.052 μgcm -2(DBNA)and0.065 μgcm -2$ (TBA) respectively. The effect of the non-target species on the determination of bendiocarb was studied. The formation of colored derivatives with the coupling agents is instantaneous and stable for 18 h, 30 h, and 12 h. Performance of the proposed methods were compared statistically in terms Student's F and t-tests with the reported methods.  相似文献   

7.
We assessed the quality and pollution status of source surface waters in Zaria, Nigeria by monitoring the nature, cause and extent of pollution in Samaru stream, Kubanni River and Kubanni dam over a period of 10 months, between March and December 2002. A total of 228 water samples was collected from 12 sites and analysed for a total of ten physicochemical and one bacteriological quality indicators, using standard methods. Aesthetic water quality impairment parameters were also observed. The mean values of most water quality parameters were significantly higher (P < 0.05) in both the stream and river than in the dam. There was no significant correlation between faecal coliform counts (FCC) and water temperature (in the range 15–33°C); pH (5.77–7.32); and turbidity (1.4–567 NTU). The high FCC ranged from 2.0 × 101 to 1.6 × 106 MPN/100 ml and exceeded the WHO standards for drinking water and water used for fresh-produce irrigation, and correlated positively (P < 0.05) with conductivity (in the range 68–1,029 μS/cm); TDS (10.0–70.0 mg/l); TSS (10.0–70.0 mg/l); Cl (7.5–181 mg/l); PO4P (0.01–0.41 mg/l); NO3N (0.6–3.8 mg/l) and BOD5 (0.1–14.9 mg/l). The main pollution sources were municipal wastewater, stormwater runoffs, the ABU sewage treatment plant, abattoir effluents and irrigation farms treated with chemical fertilisers. We conclude that these water bodies are potentially hazardous to public health and that proper sewage treatment and river quality monitoring are needed to warn against hazards to public health.  相似文献   

8.
N-ethyl-3-carbazolecarboxaldehyde-3-thio- semicarbazone (ECCT) as an new analytical reagent used for the development of a highly sensitive extractive spectrophotometric method for the determination of copper(II). The ECCT forms a greenish-yellow colored 1:1 (M:L) complex with copper(II) at pH 3.0, which is well extracted into n-butanol and shows maximum absorbance at 380nm. The color of the complex is stable for more than forty eight hours. The system obey Beer's law in the range 0.4–3.6 with 2.243 × 104lmol−1cm−1, 2.83 × 10-3μgcm−2 molar absorptivity and Sandell's sensitivity respectively. The regression coefficient is 0.412 with 0.99 correlation coefficient. The precision and accuracy of the method was checked by finding the relative standard deviation (0.422%). This developed method has been successfully employed for the determination of copper(II) in environmental and pharmaceutical samples. The method is evaluated by analyzing samples from the bureau of analyzed samples (BCS 233, 266, 216/1, 207 and 179) and by inter comparison of experimental values using AAS.  相似文献   

9.
Temporal and spatial variations in particulate organic carbon (POC) in relation to primary production, chlorophyll a, phaeophytin, plankton abundance, secondary production and suspended particulate matter (SPM) were studied monthly for 1 year from April 1996 to March 1997 in a shallow tropical coastal lagoon on the southwest coast of India. Though temporal variations in all components were significant, spatial variabilities were not statistically significant. POC values range from 200 to 5690 mg C m3 h−1, while primary production, chlorophyll a, and phaeophytin varied between 0.02 and 14.53 mg C m−3 h−1, 0.87 and 23.11 mg m−3 and 3.02 and 30.581 mg m−3, respectively. Phytoplankton and zooplankton abundance varied from 0.01 to 655.5×105 no m−3 and negligible to 7.08×105 no m−3 respectively; secondary production from 10 to 490 mg C m−3 and SPM between 0.38 and 74.43×104 mg m−3 during this study. Temporally, postmonsoon months were observed to have the highest concentrations of POC in the lagoon waters. The bulk of the POC pool in the lagoon was composed of secondary producers (72%), followed by chlorophyll a (21%), phaeophytin (7%) and suspended particulate matter of inorganic origin (< 0.1%).  相似文献   

10.
Physico-chemical characteristics of some river and hand-dug well waters used for drinking and domestic purposes in the oil rich Niger Delta area of Nigeria were assessed using standard methods. The concentrations of the parameters in the river water samples ranged in the following order: pH (5.6–6.9), temperature (26.90–28.60°C), turbidity (23–63 NTU), electrical conductivity (52–184 μs/cm), DO (5.4–7.2 mg/l), BOD (21–57 mg/l), TDS (6.0–217 mg/l), PO4 3− (0.19–1.72 mg/l), SO4 2− (25–36.8 mg/l), NO3 (20.3–28 mg/l), Fe (6.07–15.71 mg/l), Zn (0.04–0.24 mg/l), Pb (0.01–0.17 mg/l), Ni (0.01–0.13 mg/l), Vn (0.01–0.20 mg/l) and Hg (0.001–0.002 mg/l). The concentrations of these parameters in the hand-dug well water ranged in the following order: pH (5.7–6.8) temperature (26–30°C), turbidity (134–171 NTU), electrical conductivity (160–340 μs/cm), DO (5.4–6.4 mg/l), BOD (13–34 mg/l), TDS (110–190 mg/l), PO4 3− (0.84–1.84 mg/l), SO4 2− (10.6–28.1 mg/l), NO3 (11.3–23 mg/l), Fe (13.17–16.31 mg/l), Ni (0.01–0.02 mg/l), Vn (0.01–0.04 mg/l) and Hg (0.001–0.004 mg/l). The concentrations of BOD, turbidity, NO3 and Fe in the water samples were above WHO and FMENV permissible limits for safe drinking water. The results suggest that the use of such waters for drinking and domestic purposes pose a serious threat to the health of the users and calls for the intervention of government agencies.  相似文献   

11.
Abstact Aboveground biomass, aboveground litterfall, and leaf litter decomposition of five indigenous tree stands (pure stands ofPinus brutia,Pinus nigra,Cedrus libani,Juniperus excelsa, and a mixed stand ofAbies cilicica,P. nigra, andC. libani) were measured in an eastern Mediterranean evergreen needleleaf forest of Turkey. Measurements were converted to regional scale estimates of carbon (C) stocks and fluxes of forest ecosystems, based on general non-site-specific allometric relationships. Mean C stock of the conifer forests was estimated as 97.8± 79 Mg C ha−1consisting of 83.0 ± 67 Mg C ha−1in the aboveground and 14.8 ± 12 Mg C ha−1in the belowground biomass. The forest stands had mean soil organic carbon (SOC) and nitrogen (SON) stocks of 172.0 ± 25.7 Mg C ha−1and 9.2 ± 1.2 Mg N ha−1, respectively. Mean total monthly litterfall was 376.2± 191.3 kg C ha−1, ranging from 641 ± 385 kg C ha−1forPinus brutiato 286 ± 82 kg C ha−1forCedrus libani. Decomposition rate constants (k) for pine needles were 0.0016 forCedrus libani, 0.0009 forPinus nigra, 0.0006 for the mixed stand, and 0.0005 day−1forPinus brutiaand Juniperus excelsa. Estimation of components of the C budgets revealed that the forest ecosystems were net C sinks, with a mean sequestration rate of 2.0 ± 1.1 Mg C ha−1 yr−1ranging from 3.2 ± 2 Mg C ha−1forPinus brutiato 1.6 ± 0.6 Mg C ha−1forCedrus libani. Mean net ecosystem productivity (NEP) resulted in sequestration of 98.4 ± 54.1 Gg CO2 yr−1from the atmosphere when extrapolated for the entire study area of 134.2 km2(Gg = 109 g). The quantitative C data from the study revealed the significance of the conifer Mediterranean forests as C sinks  相似文献   

12.
A simple, rapid, and sensitive method involving the interaction of 2,4-dinitrophenylhydrazine with imipramine hydrochloride in presence of vanadium (V) in sulfuric acid medium has been proposed for the determination of vanadium. The purple-colored product developed showed an absorption maximum at 560 nm and was stable for 24 h. The working curve was linear over the concentration range of 0.1–2.8 μg ml − 1, with sensitivity of detection of 0.0124 μg ml − 1. Molar absorptivity and Sandell’s sensitivity were found to be 2.6 × 104 l/mol cm and 0.0039 μg cm − 1, respectively. The accuracy of the proposed method was assessed by Student’s t test and variance ratio F test, and the results were on par with the reported method. The method was successfully used in the determination of V in water, human urine, soil, and plant samples, and it was free from interference by various concomitant ions.  相似文献   

13.
Water with high nitrate concentration (NO3 ) is unfit for human consumption, especially when its concentration exceeded the threshold limit (50 mg/l) recommended by the health authorities such as the World Health Organization (WHO). In Jordan, there is a great concern for determination and monitoring organic and inorganic pollutants that may reach groundwater. Nitrate is highly mobile and present in domestic, agricultural and industrial waste in Jordan, and thus this study focused initially on nitrate as both a contaminant of concern and as an indicator of potential groundwater contamination. The present study determined the extent of nitrate contamination in groundwater in the study area and examined the likely sources of NO3 . A total of 248 groundwater samples were collected from 16 wells in different sites of Al-Hashimiya area, Zerqa Governorate, Jordan, and investigated for NO3 concentrations. Moreover, measurements of temperature, electrical conductivity and pH were carried out in the field. Analysis was carried out according to the methods described by the American Public Health Association (APHA). Results showed that there was a dramatic increasing in NO3 concentrations from the year 2001 to 2006 for some selected wells in the present study. NO3 concentration in 2006 was ranged from 10 to 330 mg/l with an average of 77 mg/l. Overall, groundwater had elevated nitrate concentration with 92% of the samples containing more than 20 mg/l NO3 , indicating the influence of human activities. This study has shown that there is a strong correlation between the nitrate concentration and the wastewater effluents as a source of pollution.  相似文献   

14.
Total selenium (Se) and water-soluble Se in soil, and Se in a shallow groundwater were hydrogeochemically researched in an alluvial fan area in Tsukui, Central Japan. The water-soluble Se was estimated at average level of 2.6 ± 1.2μg Se kg−1 dry soil (± SD, n = 25), showing less than 1% of the total Se (349–508μg Se kg−1 dry soil) in soil. The monthly Se concentration in groundwater was average 2.2μg,L−1, ranging 1.6–2.4μg,L−1 during 2001–2003. The Se in groundwater significantly decreased with increasing groundwater level after rainfall. This result indicated that Se-bearing water percolated with relatively low Se concentration through the soil layer. According to our prediction model of linear regression curve on the observation data, Se concentration in the groundwater was estimated to be increasing with the very low rate of 4.35 × 10−3μg Se L−1,yr−1. The hydrogeochemical research and the result of the prediction model showed that any explosive increase of Se will hardly occur in this groundwater without an anthropogenic Se contamination.  相似文献   

15.
A solid phase extraction method for the determination of gold(III) at trace levels by flame atomic absorption spectrometer (FAAS) was developed. The method was based on retention of gold as chloro complexes through the Amberlite XAD-2000. The effect of some analytical parameters including hydrochloric acid concentration, sample volume, sample and eluent flow rates, eluent volume, eluent concentration and interfering ions on the recovery of gold(III) was investigated. The retention of gold(III) from 1.5 mol l−1 HCl solution and the recovery of gold with 0.07 mol l−1 NH3 solution were quantitative (≥95%). The relative standard deviation (RSD) was calculated as 3.2% (n = 10). The detection limit for gold was 2 μg l−1. The accuracy was checked with the determination of gold spiked an artificial seawater and a pure copper samples.  相似文献   

16.
The effects on the growth, physiological indexes and the cadmium (Cd) accumulation in Chlorophytum comosum under Cd stress were examined by pot-planting. The results showed that the tolerance index (TI) of C. comosum were all above 100 in soil Cd concentration of 100 mg kg − 1. The O2·-_{2^{\bullet}}^{-} production rate and electrical conductivity of C. comosum were significantly positively correlated to Cd adding-concentration while the MDA content increased and had significant differences with the control. The activities of SOD, CAT, and POD all rose significantly in lower Cd concentration and the Cd threshold of them were around 10, 50 and 20 mg kg − 1, respectively. The Cd in C. comosum root and aboveground part reached 1,522 and 865·5 mg kg − 1, respectively, in Cd concentration of soil up to 200 mg kg − 1. For the advantages of high tolerance, high accumulation, and high ornamental value, C. comosum may have tremendous application value in the treatment of Cd-contaminated soils.  相似文献   

17.
基于成都双流国际机场活动水平数据,采用排放因子法和计算模型等,编制了机场大气污染物排放清单,并完成了时空分配和不确定性分析,建立了高分辨率网格化排放清单。结果表明,成都双流国际机场标准起飞着陆(LTO)循环数为2.4×10~5次/a,CO、VOCs、NO_x、PM_(10)、PM_(2.5)、SO_2排放量分别为1.2×10~3、1.3×10~2、2.1×10~3、2.8×10、2.7×10、2.5×10~2t/a,且主要由飞机发动机排放;活动水平数据仅包括LTO循环数和地面保障设备两部分;污染物排放分布和跑道类型相关性较高;排放清单活动水平数据可靠性较高,而排放因子存在一定的不确定性。  相似文献   

18.
This study monitored atmospheric pollutants during high wind speed (> 7 m s−1) at two sampling sites: Taichung Harbor (TH) and Wuci traffic (WT) during March 2004 to January 2005 in central Taiwan. The correlation coefficient (R 2) between TSP, PM2.5, PM2.5−10 particle concentration vs. wind speed at the TH and WT sampling site during high wind speed (< 7 m s−1) were also displayed in this study. In addition, the correlation coefficients between TSP, PM2.5 and PM2.5−10 of ionic species vs. high wind speed were also observed. The results indicated that the correlation coefficient order was TSP > PM2.5−10 > PM2.5 for particle at both sampling sites near Taiwan strait. In addition, the concentration of Cl, NO3 , SO4 2−, NH4 +, Mg2+, Ca2+ and Na+ were also analyzed in this study.  相似文献   

19.
Atmospheric surface aerosol radiative forcing (SARF) ΔF, forcing efficiency ΔFe and fractional forcing efficiency ΔFFe evaluated from cloud-screened narrowband spectral and thermal-offset-corrected radiometric observations during the Asia dust outbreak episodes in Gwangju, Republic of Korea are reported in this study. Columnar aerosol optical properties (aerosol optical depth (AOD), τ , Angstrom exponent α, mass concentration of fine and coarse mode particles) were also reported for the station between January 2000 and May 2001 consisting of 211cloud-free days. Results indicate that majority of the AOD were within the range 0.25–0.45 while some high aerosol events in which AODs ≥ 0.6 were observed during the severe dust episodes. For example, AOD increases from annual average value of 0.34 ± 0.13 at 501 nm to values >0.60 during the major dust events of March 27–30 and April 7–9, 2000, respectively. The α 501–870 nm which is often used as a qualitative indicator of aerosol particle size had values ranging from 0.01 to 1.77. The diurnal forcing efficiency ΔDFe at Gwangju was estimated to be −81.10 ± 5.14 W m −2/τ 501 nm and −47.09 ± 2.20 W m −2/τ 501 nm for the total solar broadband and visible band pass, respectively while the fractional diurnal forcing efficiency ΔFDFe were −15.8 ± 0.64%/τ 501 nm and −22.87 ± 1.13%/τ 501 nm for the same band passes. Analyses of the 5-day air-mass back trajectories were further developed for Gwangju in order to classify the air-mass and types of aerosol reaching the site during the Asia dust episodes.  相似文献   

20.
Trace amounts of bismuth(III) and uranium(VI) can be simultaneously determined in a single scan by adsorptive cathodic stripping voltammetry in the presence of cupferron as a complexing agent. Optimal conditions were found to be: 0.1 mol?L?1 acetate buffer (pH 5.3), 5?×?10?5?mol?L?1 cupferron, accumulation potential of ?0.25 V, and accumulation time of 30 s. The linear range of Bi(III) and U(VI) was observed over the concentration range from 2?×?10?9 to 2?×?10?7?mol?L?1 and from 1?×?10?8 to 5?×?10?7?mol?L?1, respectively. The influence of the main components of real water samples such as foreign ions and organic substances (surface active substances, humic substances) was precisely investigated. The method was applied to the simultaneous measurements of bismuth and uranium in natural water samples.  相似文献   

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