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1.
The possibilities of pressurized liquid extraction (PLE) have been novelty tested to assist the cytosol preparation from wet mussel soft tissue before the determination of metals bound to metallothionein-like proteins (MLPs). Results obtained after PLE were compared with those obtained after a classical blending procedure for mussel cytosolic preparation. Isoforms MLP-1 (retention time of 4.1 min) and MLP-2 (retention time of 7.4 min) were separated by anion exchange high-performance liquid chromatography (HPLC) and the concentrations of Ba, Cu, Mn, Sr and Zn bound to MLP isoforms were directly measured by inductively coupled plasma-atomic emission spectrometry (ICP-OES) as a multi-element detector. The optimized PLE-assisted mussel cytosol preparation has consisted of one extraction cycle at room temperature and 1500 psi for 2 min. Since separation between the solid mussel residue and the extract (cytosol) is performed by the PLE system, the cytosol preparation method is faster than conventional cytosol preparation methods by cutting/blending using Ultraturrax or Stomacher devices.  相似文献   

2.
Eva María Seco-Gesto 《Talanta》2007,72(3):1178-1185
Studies on the application of a short microwave irradiation cycle and the use of diluted acids to extract trace elements from raft mussel samples were developed. Multi-element determinations (Al, Ba, Cd, Cr, Cu, Fe, Mn, Pb, Sn, V and Zn) were carried out by inductively coupled plasma-optical emission spectrometry (ICP-OES). Parameters such as acid/oxidizing reagents (diluted nitric acid, hydrochloric acid and hydrogen peroxide) concentrations, acid/oxidizing solution volume, temperature, ramp time and hold time for the microwave heating were simultaneously studied by using an experimental design approach. The optimum conditions have showed the sample pre-treatment of 10 mussel samples to less than 3.0 min when a microwave power of 600 W and a controlled temperature of 65 °C were used. This time (hold time plus ramp time) is quite shorter than those reported for conventional microwave-assisted acid digestion procedures. Since temperature inside the reactor is not high, the venting time can be shorted to 15 min. In addition, the concentration of acid/oxidizing reagents needed to complete the acid leaching (2.5 M, 3.0 M and 0.5 % (m/v) for nitric acid, hydrochloric acid and hydrogen peroxide, respectively) is lower than the required concentration for a conventional microwave-assisted acid digestion (concentrated acids). The proposed method has showed a good repeatability of the overall method, and relative standard deviations between 11 and 2% were reached for 12 replicate microwave-assisted acid leaching and ICP-OES measurements. The method was finally validated by analyzing TORT-1 and GBW-08571 certified reference materials and it was successfully applied to fast multi-element determinations in several raft mussel samples.  相似文献   

3.
A new method using diluted reagents (nitric and hydrochloric acids and oxygen peroxide) and ultrasound energy to assist metals acid leaching with from edible seaweed was optimized. The method uses a first sonication at high temperature with hydrochloric acid as a previous stage to an ultrasound-assisted acid leaching with 7 ml of an acid solution containing nitric acid, hydrochloric acid and hydrogen peroxide at concentrations of 3.7, 3.0 and 3.0 M, respectively. Optimum conditions for the first sonication step were ultrasound energy at 17 kHz, sonication temperature at 65 °C, an acid volume of 2 ml, an hydrochloric acid concentration of 6.0 M and a sonication time of 10 min. It has been found that the first sonication stage at high temperature with hydrochloric acid is necessary to obtain quantitative recoveries for As, Ba, Fe and V. Otherwise quantitative recoveries were reached for the other elements investigated (Ca, K, Na, Mg, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The repeatability of the ultrasound-assisted acid leaching method was around 10% for all elements. Adequate limit of detection and limit of quantification were reached by using inductively coupled plasma-optical emission spectrometry (ICP-OES) for measurements. The method resulted accurate after analysing several seaweed certified reference materials (IAEA-140/TM, NIES-03 and NIES-09). The method was finally applied to the multi-element determination in edible seaweed samples.  相似文献   

4.
Separation and quantification of six arsenic species have been performed in cod, tuna and mussel samples by high performance liquid chromatography (HPLC) using inductively coupled plasma-optical emission spectrometry (ICP-OES) and hydride generation-quartz furnace atomic absorption spectrometry (HG-QFAAS) as detection techniques. It has been shown that arsenic extraction with a water-methanol (11) mixture is sufficiently quantitative for the cod and tuna, in which arsenic is mainly present as arsenobetaine (about 90% of total As extracted). In contrast, only 60% of the element is extracted from the mussels and the chromatograms obtained reveal the presence of an unknown compound. Detection limits are in the g ml–1 range for the HPLC-ICP-OES technique (quantification of arsenobetaine and arsenocholine) and in the ng ml–1 range for the HPLC-HG-QFAAS system (quantification of arsenite, arsenate, monomethylarsonic and dimethylarsinic acids).  相似文献   

5.
Several complementary separation mechanisms (size-exclusion chromatography, SEC; fast protein liquid chromatography, FPLC; reverse-phase chromatography, RPC) have been coupled to inductively coupled plasma mass spectrometry (ICP-MS) detection to investigate the speciation of Cd, Se, Cu and Zn in mussel hepatopancreas. SEC with double-focusing (DF) ICP-MS detection was used first for speciation analysis of those four trace elements, both in uncontaminated mussels and in mussels exposed to Cd (500 μg l−1) or to Cd+Se (500 μg l−1 of each element). Observed SEC results indicated that Se does not seem to significantly bind to metallothionein-like proteins (MLPs) ‘in vivo’. Total cytosolic Cd and MLPs content were lower in Cd+Se exposed mussels than those exposed to Cd only. For each treatment, 50 μl of the SEC peak fraction containing the MLPs was used to perform fast protein liquid chromatography coupled ‘on-line’ with a quadrupole (Q) ICP-MS. 82Se and 114Cd isotopes were simultaneously monitored. Four and five Cd/MLPs isoforms were then detected in mussels exposed to only Cd and Cd+Se, respectively. In contrast, no signs of Se/MLP isoforms were found for both treatments. Subsequently, the bulk of MLPs eluting from the FPLC system were isolated and lyophilizated. A 50-μl aliquot of such reconstituted lyophilisate was then injected into a Vydac C8 Reverse-Phase column directly connected to the Q-ICP-MS. Results confirmed the presence of one more Cd/MLP peak in those mussels exposed to Cd+Se. However, the number of Cd/MLP peaks detected decreased to three and four in only Cd and Cd+Se exposed animals, respectively. These results tend to indicate that Se, which does not trigger the biosynthesis of MLPs, could probably orient such synthesis towards the generation of a new Cd/MLP isoform in mussels submitted to both elements. The possible interrelation/complementation between Se and MLP against Cd toxicity is discussed.  相似文献   

6.
The objective of this research was to determine the differences between farmed and wild rainbow trout in terms of heavy metal and trace element accumulation in edible tissues. The samples were analyzed for As, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Se, Sr and Zn by inductively coupled plasma-optical emission spectrometry (ICP-OES); and for Hg by cold vapor atomic absorption spectrometry (CVAAS). The results were expressed as μg/g of dry weight. With the exception of Ba and Sr, liver had significantly higher heavy metal and trace element concentrations compared to the muscle in farmed or wild fish. Higher levels of Ba, Cr, Fe, Mn and Zn, as well as lower levels of Cu and Sr were found in tissues of wild rainbow trout compared to its farmed relative. Levels of Cd in 41.6% of farmed fish samples and 45.8% of wild fish samples exceeded the European Commission regulation. Regarding the Pb, concentrations in 50% of farmed fish samples and 62.5% of wild ones were above the European Commission limit. However, levels of Hg and As in all of the examined samples were lower than the legislated limits. The differences in heavy metal and trace element accumulation observed between farmed and wild fish were probably related to the differences in their environmental conditions and dietary element concentrations.  相似文献   

7.
Rezić I  Zeiner M  Steffan I 《Talanta》2011,83(3):865-871
A simple, robust and reliable analytical procedure for the determination of 28 selected elements, namely Al, As, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, K, Hg, Mg, Mn, Mo, Na, Ni, Pb, Sc, Si, Se, Sn, Sm, Sr, Tl, V, and Zn in textile materials by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave digestion of samples was optimized and validated in this work. The total amount of elements present in textile samples was determined after microwave digestion of materials in 7 mol/L nitric acid within the optimal working program: 5 min at 150 °C (power 250 W), 15 min 180 °C (300 W) and 20 min at the maximum temperature of 200 °C (350 W). For the quality control reasons, which were ascertained by analysis of the certified cotton trace elements reference material IAEA-V9, the ICP-OES method was optimized through several parameters: by comparing Meinhard and Gemcone Low Flow nebulizers efficiency, ranging nebulizer gas flows from 0.6 to 1.0 L/min, ranging sample flows from 0.8 to 1.2 mL/min, testing RF power from 1200 to 1400 W, detecting data acquisition time (read time) from 0 to 527 s, ranging washing (delay) time from 0 to 408 s, as well as by checking the occurring interferences for the optimal line selection. Validation included determination of linearity, selectivity, accuracy, reproducibility, precision and limits of detection calculated for all 28 selected elements of interest. The developed analytical procedure was successfully applied on textile fibers (cotton, flax and hemp) as well as on standard knitted textile sample materials (cotton and wool).  相似文献   

8.
A method has been developed for the separation and determination of a set of 11 impurities from chromium matrices using oxalate form of Amberlite IRA 93. Due to slower kinetics of formation of the anionic complex, Cr(III) passed in the effluent while impurities forming strong complexes rapidly are retained on the exchanger. The adsorption of impurities of interest is found to be uniform in pH range 2-6. The adsorbed impurities are eluted with 2 mol l−1 HNO3 and determined by inductively coupled plasma-optical emission spectrometer (ICP-OES). The percentage recoveries of Al, Bi, Cd, Co, Cu, Fe, Mn, Ni, Pb, Ga and Zn are in the range 88-101% and separation of matrix is >99.9%. The method has been applied for the analysis of two samples namely CrCl3·6H2O and Cr. The R.S.D. of the method is 5-6% at >10 μg g−1 level and ∼15% at <1 μg g−1 level. The process blank values are in the range sub-μg g−1 and detection limits are in ng g−1 range.  相似文献   

9.
Pressurized liquid extraction (PLE), commonly used for organic compounds extraction, has been applied for trace element leaching from marine biological material in order to determine major and trace elements (Al, As, Cd, Co, Cu, Fe, Hg, Li, Mn, Pb, Se, Sr, V and Zn). The released elements by formic acid PLE have been evaluated by inductively coupled plasma-optical emission spectrometry (ICP-OES). Different variables, such as formic acid concentration, extraction temperature, static time, extraction steps, pressure, mean particle size and diatomaceous earth (DE) mass/sample mass ratio were simultaneously studied by applying an experimental design approach (Plackett-Burman design (PBD) and central composite design (CCD)). Results showed that the extraction temperature was statistically significant (confidence interval of 95%) for most of the elements (high metal releasing was achieved at high temperatures). In addition, formic acid concentration was also statistically significant (confidence interval of 95%) for metals such as Cd and Cu. Most of the metals can be extracted using the same PLE operating conditions (formic acid concentration of 1.0 M, extraction temperature at 125 °C, static time of 5 min, one extraction step, extraction pressure at 500 psi and DE mass/sample mass ratio of 2). Taking in mind PLE requirements at the optimised operating conditions (125 °C), a time of 6 min is needed to pre-heat the cell. Therefore, the PLE assisted multi-element leaching is completed after 12 min. Analytical performances, such as limits of detection and quantification, repeatability of the over-all procedure and accuracy, by analysing GBW-08571, DORM-2, DOLT-3 and TORT-2 certified reference materials, were finally assessed.  相似文献   

10.
Two different approaches were used to improve the capabilities of solid sampling (SS) electrothermal vaporization (ETV) coupled to inductively coupled plasma optical emission spectrometry (ICP-OES) for the direct analysis of powdered rice. Firstly, a cooling step immediately before and after the vaporization step in the ETV temperature program resulted in a much sharper analyte signal peak. Secondly, point-by-point internal standardization with an Ar emission line significantly improved the linearity of calibration curves obtained with an increasing amount of rice flour certified reference material (CRM). Under the optimized conditions, detection limits ranged from 0.01 to 6 ng g−1 in the solid, depending on the element and wavelength selected. The method was validated through the quantitative analysis of corn bran and wheat flour CRMs. Application of the method to the multi-elemental analysis of 4-mg aliquots of real organic long grain rice (white and brown) also gave results for Al, As, Co, Cu, Fe, Mg, Se, Pb and Zn in agreement with those obtained by inductively coupled plasma mass spectrometry following acid digestion of 0.2-g aliquots. As the analysis takes roughly 5 min per sample (2.5 min for grinding, 0.5–1 min for weighing a 4-mg aliquot and 87 s for the ETV program), this approach shows great promise for fast screening of food samples.  相似文献   

11.
Mineral content and botanical origin of Spanish honeys   总被引:2,自引:0,他引:2  
Eleven elements (Zn, P, B, Mn, Mg, Cu, Ca, Ba, Sr, Na and K) were determined by inductively plasma coupled spectrometry in 40 honey samples from different places of Spain and four different botanical origins: Eucalyptus (Eucalyptus sp.), Heather (Erica sp.), Orange-blossom (Citrus sinensis) and Rosemary (Rosmarinus officinalis). K, Ca and P show the higher levels with average concentrations ranged between 434.1-1935 mg kg−1 for K; 42.59-341.0 mg kg−1 for Ca and 51.17-154.3 mg kg−1 for P. Levels of Cu (0.531-2.117 mg kg−1), Ba (0.106-1.264 mg kg−1) and Sr (0.257-1.462 mg kg−1) are the lowest in all honey samples. Zn (1.332-7.825 mg kg−1), Mn (0.133-9.471 mg kg−1), Mg (13.26-74.38 mg kg−1) and Na (11.69-218.5 mg kg−1) concentrations were found strongly dependent on the kind of botanical origin.Results were submitted to pattern recognition procedures, unsupervised methods such as cluster and principal components analysis and supervised learning methods like linear discriminant analysis in order to evaluate the existence of data patterns and the possibility of differentiation of Spanish honeys from different botanical origins according to their mineral content. Cluster analysis shows four clusters corresponding to the four botanical origins of honey and PCA explained 71% of the variance with the first two PC variables. The best-grouped honeys were those from heather; eucalyptus honeys formed a more dispersed group and finally orange-blossom and rosemary honeys formed a less distinguishable group.  相似文献   

12.
A simple, rapid and efficient dispersive liquid–liquid microextraction based on the solidification of floating organic drop (DLLME–SFO) method, followed by inductively coupled plasma-optical emission spectrometry (ICP-OES) was developed for the simultaneous preconcentration and determination of heavy metals in water samples. One variable at a time method was applied to select the type of extraction and disperser solvents. Then, an orthogonal array design (OAD) with OA16 (45) matrix was employed to study the effects of different parameters on the extraction efficiency. Under the best experimental conditions (extraction solvent: 140 μL of 1-undecanol; disperser solvent: 2.0 mL of acetone; ligand to metal mole ratio: 20; pH: 6 and without salt addition), the enhancement factor ranged from 57 to 96. The calibration graphs were linear in the range of 0.5–250 μg L−1 for Mn, 1.25–250 μg L−1 for Cr, Co and Cu with correlation coefficient (r) better than 0.990. The detection limits were between 0.1 and 0.3 μg L−1. Finally, the developed method was successfully applied to extraction and determination of the mentioned metal ions in the tap, sea and mineral water samples and satisfactory results were obtained.  相似文献   

13.
A new, simple, fast and automated method based on acetic acid-pressurized liquid extraction (PLE) has been developed for the simultaneous extraction of major and trace elements (As, Ca, Cd, Co, Cr, K, Mg, Mn, Na, Pb, Sr and Zn) from edible seaweeds. The target elements have been simultaneously determined by inductively coupled plasma-optical emission spectrometry (ICP-OES). The influence of several extraction parameters (e.g. acetic acid concentration, extraction temperature, extraction time, pressure, number of cycles, particle size and diatomaceous earth (DE) mass/sample mass ratio) on the efficiency of metal leaching has been evaluated. The results showed that metal extraction efficiency depends on the mass ratio of the dispersing agent mass and the sample. The optimized procedure consisted of the following conditions: acetic acid (0.75 M) as an extracting solution, 5 min of extraction time, one extraction cycle at room temperature at a pressure of 10.3 MPa and addition of a dispersing agent (at a ratio of 5:1 over the sample mass). The leaching procedure was completed after 7 min (5 min extraction time plus 1 min purge time plus 1 min end relief time). Limits of detection and quantification and repeatability of the over all procedure have been assessed. Method validation was performed analysing two seaweed reference materials (NIES-03 Chlorella Kessleri and NIES-09 Sargasso). The developed extraction method has been applied to red (Dulse and Nori), green (Sea Lettuce) and brown (Kombu, Wakame and Sea Spaghetti) edible seaweeds.  相似文献   

14.
This study investigated the content of macronutrients (Ca, K, Mg, Na, P, and S), trace elements (Ba, Be, Co, Cr, Cu, Fe, Ga, Li, Mn, Ni, Rb, Se, Sr, V, and Zn), and trace toxic elements (As, Cd, In, Pb, and Tl) in chili powder from Korea, China, and Vietnam. For the analyses, inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma-optical emission spectroscopy (ICP-OES) were used. In addition, near-infrared (NIR) spectroscopy was used to differentiate functional groups based on the chemical constituents. For the validation of the applied analytical methods, good linearity (coefficients of determination, 0.9443–0.99997), and relative standard deviations below 4% were obtained. The contents of the toxic elements were below the provisional tolerable weekly intake values. Linear discriminant analysis using elemental contents and NIR data was performed to establish and authenticate the geographical origin of chili powder, which confirmed the reliability of the obtained results.  相似文献   

15.
A simple and fast method for the determination of As, Ba, Cd, Co, Cu, Fe, Ga, Mn, Mo, Ni, Pb, Rb, Se, Sr, Tl, U, V and Zn in biological samples by inductively coupled plasma mass spectrometry (ICP-MS), after sample solubilization with formic acid and introduction by a microconcentric nebulizer, is proposed. The sample is mixed with formic acid, kept at 90 °C for one hour and then diluted with nitric acid aqueous solution to a 50% v/v formic acid and 1% v/v nitric acid final concentrations. The final sample solution flow rate for introduction into the plasma was 30 μL min−1. The optimized and adopted nebulizer gas flow rate was 0.7 L min−1 and RF power was 800 W. These conditions are very different than those normally used when a conventional nebulizer is employed. Rodhium was used as internal standard. External calibration against aqueous standard solutions, without formic acid, could be used for quantification, except for As, Se and Zn. However, external calibration with 50% formic acid allows the determination of all analytes with high accuracy and it is recommended. The detection limits were between 0.0005 (Tl) and 0.22 mg kg−1 (Fe) and the precision expressed by the relative standard deviations (RSD) were between 0.2% (Sr) and 3.5% (Ga). Accuracy was validated by the analysis of four certified reference biological materials of animal tissues, comparing the results by linear regressions and by the t-test at a 95% confidence level. The recommended procedure avoids plasma instability and carbon deposit on the cones.  相似文献   

16.
A robust microwave-assisted acid digestion procedure followed by inductively coupled plasma-mass spectrometry (ICP-MS) was developed to quantify rare earth elements (REEs) in fluidized-bed catalytic cracking (FCC) catalysts and atmospheric fine particulate matter (PM2.5). High temperature (200 °C), high pressure (200 psig), acid digestion (HNO3, HF and H3BO3) with 20 min dwell time effectively solubilized REEs from six fresh catalysts, a spent catalyst and PM2.5. This method was also employed to measure 27 non-REEs including Na, Mg, Al, Si, K, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Zr, Mo, Cd, Cs, Ba, Pb and U. Complete extraction of several REEs (Y, La, Ce, Pr, Nd, Tb, Dy and Er) required HF indicating that they were closely associated with the aluminosilicate structure of the zeolite FCC catalysts. Internal standardization using 115In quantitatively corrected non-spectral interferences in the catalyst digestate matrix. Inter-laboratory comparison using ICP-optical emission spectroscopy (ICP-OES) and instrumental neutron activation analysis (INAA) demonstrated the applicability of the newly developed analytical method for accurate analysis of REEs in FCC catalysts. The method developed for FCC catalysts was also successfully implemented to measure trace to ultra-trace concentrations of La, Ce, Pr, Nd, Sm, Gd, Eu and Dy in ambient PM2.5 in an industrial area of Houston, TX.  相似文献   

17.
Silica gel-bound amines phase modified with p-dimethylaminobenzaldehyde (p-DMABD) was prepared based on chemical immobilization technique. The product (SG-p-DMABD) was used as an adsorbent for the solid-phase extraction (SPE) Cr(III), Cu(II), Ni(II), Pb(II) and Zn(II) prior to their determination by inductively coupled plasma optical emission spectrometry (ICP-OES). The uptake behaviors of SG-p-DMABD for extracting these metal ions were studied using batch and column procedures. For the batch method, the optimum pH range for Cr(III) and Ni(II) extraction was ≥ 3, for Cu(II), Pb(II) and Zn(II) extraction it was ≥ 4. For simultaneous enrichment and determination of all the metals on the newly designed adsorbent, the pH value if 4.0 was selected. All the metal ions can be desorbed with 2.0 mL of 0.5 mol L− 1 of HCl. The results indicate that SG-p-DMABD has rapid adsorption kinetics using the batch method. The adsorption capacity for these metal ions is in the range of 0.40-1.15 mmol g− 1, with a high enrichment factor of 125. The presence of commonly coexisting ions does not affect the sorption capacities. The detection limits of the method were found to be 1.10, 0.69, 0.99, 1.10 and 6.50 μg L− 1 for Cr(III), Cu(II), Ni(II), Pb(II) and Zn(II), respectively. The relative standard deviation (RSD) of the method under optimum conditions was 5.0% (n = 8) for all metal ions. The method was applied to the preconcentration of Cr(III), Cu(II), Ni(II), Pb(II) and Zn(II) from the certified reference material (GBW 08301, river sediment) and water samples with satisfactory results.  相似文献   

18.
In this paper, multivariate optimization was applied for the development of an ultrasound-assisted multielemental extraction procedure for analysis of bean samples by inductively coupled plasma optical emission spectrometry. For this procedure, powdered samples were treated with an acid mixture and submitted to ultrasound energy for extracting the target elements (Ba, Ca, Cu, Fe, K, Mg, Mn, Sr and Zn). Centroid simplex mixture design was used for optimize the acid proportions (nitric, acetic and chloride acid) and Box Behnken design was applied for optimize the process variables (particle size, final concentration of extracting solution and sonication time) after mixture optimization. Iron had not presented quantitative extractions and it was excluded from final samples analysis. The developed method presents the follow limits of quantification in μg g− 1: Ba (0.90); Ca (5.2); Cu (4.0); K (0.90); Mg (1.4); Mn (0.22); Sr (0.25) and Zn (4.0). Accuracy was accessed by comparison of determined concentration with the values obtained by the microwave digestion procedure. The proposed method was applied toward the determination of elemental composition in bean samples collected in the country zone from Jequié city located on the Bahia State, Brazil. The trace elements content ranged from 0.21 to 3.04, 3.84 to 10.8, 0.60 to 5.23, 31.0 to 46.5 and 10.8 to 19.6 μg g− 1 Ba, Cu, Sr, Zn, Mn, respectively. The major elements content ranged from 0.0418 to 0.0877, 0.109 to 0.153 and 1.30 to 1.56% (w/w) Ca, Mg and K, respectively.  相似文献   

19.
采用电感耦合等离子体质谱(ICP-MS)与等离子体光谱(ICP-OES)联机同时测定多金属结核样品中常量、微量、痕量元素。样品经高压密封溶样弹消解后,一次气动雾化进样,ICP-OES测定常量和微量元素,ICP-MS测定微量和痕量元素。详细探讨了不同浓度范围元素的测定方式、元素分析信号的采集模式、多原子离子干扰的校正因子。采用ICP-MS与ICP-OES二种方式同时测定Co、Cu、Ni、Zn、V、Ba、Sr,分析结果表明具有较好的一致性。所建立的ICP-MS与ICP-OES联机检测技术用于多金属结核标准样品的分析(Nod-A-1,GSPN-1,GSPN-2,GSPN-3),分析结果与推荐值符合,相对标准偏差小于10%。  相似文献   

20.
Closed-vessel microwave digestion of nine standard reference plant materials (NIST, BCR, IAEA) and a laboratory standard of plant material with different Si contents assisted by HNO3 + H2O2 (procedure A), HNO3 + H2O2 + HF + H3BO3 (procedure B) and HNO3 + H2O2 + HBF4 (procedure C) were used to determine the recovery of 36 elements by ICP-MS: Ag, Al, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, Ge, In, La, Li, Mn, Mo, Nd, Ni, Pb, Pr, Rb, Sb, Se, Sn, Sr, Th, Tl, U, V, W, Y, Zn. Additions of HF + H3BO3 and HBF4 in procedures B and C exceeded by 10% (B1, C1) and 100% (B2, C2) the equivalent concentrations of Si in the samples determined by ICP-OES. Most recoveries of certified elements (e.g., Al*, Cu, Mo*, Rb*, Sb*, Th) decreased significantly (*p ≤ 0.05) with increasing Si content in plant reference materials digested by procedure A, while the recoveries from procedures B and C decreased insignificantly only for Mo and Sb. Digestions B and C gave significantly higher recoveries of Al, Sb, W and REEs, which were tighter to the reference values of these elements. A similar effect was found for Cu, Fe, Li, Ni, Sn, Th, Tl, V, Zn, Ba, Rb and Sr recoveries in samples with Si contents exceeding 2000 μg g−1. If the Si content in plant samples is less than 10 mg g−1, digestion of 0.5 g of plant samples through 0.05 mL of HF and 0.5 mL of 4% H3BO3 or 0.1 mL of HBF4 is recommended to get satisfactory results for most of the elements. For materials with Si content exceeding 10 mg g−1 the weight of the sample for digestion should be reduced to 0.25 g. However, the operation of potential interferences should be taken into account and eliminated through correction equations and adequate dilution of the samples.  相似文献   

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