Trace elements determination in red and white wines using total-reflection X-ray fluorescence

Several wines produced in different regions from south of Brazil and available in markets in Rio de Janeiro were analyzed for their contents of elements such as: P, S, Cl, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Rb and Sr. Multi-element analysis was possible with simple sample preparation and subsequent analysis by total-reflection X-ray fluorescence using synchrotron radiation. The measurement was carried at the X-ray fluorescence beamline in the Synchrotron Light Source Laboratory in Campinas, Brazil. The levels of the various elements obtained were lower in the Brazilian wines than the values generally found in the literature. The present study indicates the capability of multi-element analysis for determining the contents of various elements present in wines coming from Brazil vineyards by using a simple, sensitive and precise method.     

Analysis of low Z elements on Si wafer surfaces with synchrotron radiation induced total reflection X-ray fluorescence at SSRL, Beamline 3-3: comparison of droplets with spin coated wafers

The unique properties of synchrotron radiation, such as high incident flux combined with low divergence, its linear polarization and energy tunability, make it an ideal excitation source for total reflection X-ray fluorescence (TXRF) spectroscopy in order to non-destructively detect trace impurities of transition metals on Si wafer surfaces. When used with a detector suitable for the determination of low energy radiation this technique can be extended to the detection of low-Z elements, such as Al, Na and Mg. Experiments have been performed at SSRL Beamline 3-3, a bending magnet beamline using monochromatic radiation from a double multilayer monochromator. The wafer was mounted vertically in front of the detector, which was aligned along the linear polarization vector of the incoming synchrotron radiation. This configuration allows the detector to accept a large solid angle as well as to take advantage of the reduced scattered X-ray intensity emitted in the direction of the linear polarization vector. A comparison between droplet samples and spin coated samples was done, in order to compare the capabilities of vapor phase decomposition (VPD-TXRF) with conventional SR-straight-TXRF. Detection limits in the range of 50 fg corresponding to 2E10 atoms/cm² have been obtained for Na. The spin coated samples, prepared from solutions containing an equal amount of Na, Mg and Al showed an unexpected result when performing a scan of the angle of incidence of the incoming X-rays suggesting a different adsorption behavior of the elements in a multielement solution on the wafer surface. The observation of this behavior is important because the spin coating technique is the standard method for the preparation of surface standards in semiconductor quality control. This effect could be characteristic of the Na, Mg, Al solution used, but the angle dependence of the fluorescence signal of a standard should always be investigated before using the standard for calibration of the apparatus and quantification.     

基于同步辐射X射线荧光光谱与机器学习的非靶标金属组学预测PVC纳米塑料对水稻毒性的浓度依赖性

环境中的微/纳米塑料污染引起了人们极大关注。土壤中的微/纳米塑料不可避免对植物产生影响,因此预测微/纳米塑料的植物毒性可为土壤中微/纳米塑料治理提供抓手。本文以水稻为研究对象,发展了基于同步辐射X射线荧光 (SRXRF) 光谱与机器学习的非靶标金属组学方法,以预测聚氯乙烯纳米塑料(nPVC) 对水稻的毒性。首先将水稻暴露于不同浓度(500 ppb与500 ppm) nPVC,培养35天后,收集水稻叶;其次,利用SRXRF研究暴露nPVC后水稻叶中金属组的变化;然后,利用机器学习方法区分暴露不同浓度nPVC水稻样品。对SRXRF光谱进行主成分分析 (PCA) 非监督聚类,发现500 ppm组能够良好聚类,而500 ppb组与对照组无明显差异,表明500 ppb的nPVC暴露对植物的毒性远低于500 ppm nPVC。对SRXRF全光谱,利用线性模型K近邻算法(KNN)和非线性模型支持向量机(SVM)建立预测模型,区分不同组别的准确率可达94.12%。为了提升运算速度,减少模型计算量,使用竞争性自适应加权重采样算法(CARS)挑选特征光谱建立预测模型,区分不同组别的准确率为89.51%。相对全光谱模型,特征光谱预测模型虽然预测准确率下降了4.61%,但模型输入参数减少了99.38%,因此同样具有良好潜力。本研究表明基于SRXRF和机器学习的非靶标金属组学可准确预测不同浓度nPVC对水稻金属组的干扰程度,从而反映nPVC对水稻毒性的浓度依赖性。该方法同样可用于预测其它微/纳米塑料毒性的浓度依赖性。     

A method to correct defocused element distribution maps in electron probe microanalysis

Element distribution maps obtained on electron microprobes via the beam scan method with wavelength-dispersive spectrometers reveal a defocusing effect if they are taken at sufficiently small magnification. This effect, which occurs where the Bragg condition of the spectrometer is not adequately met, can be avoided or corrected by various methods. A method is presented here to correct defocused element distribution maps with the help of corresponding maps obtained on homogeneous standards.Dedicated to Professor Dr. rer. nat. Dr. h.c. Hubertus Nickel on the occasion of his 65th birthday     

Depth profiles of Al impurities implanted in Si wafers determined by means of the high-resolution grazing emission X-ray fluorescence technique

The synchrotron radiation based high-resolution grazing emission X-ray fluorescence (GEXRF) technique was used to extract the distribution of Al ions implanted with a dose of 10¹⁶ atoms/cm² in Si wafers with energies ranging between 1 and 100 keV. The depth distributions of the implanted ions were deduced from the measured angular profiles of the Al-Kα X-ray fluorescence line with nanometer-scale precision. The experimental results were compared to theoretical predictions of the depth distributions resulting from ion implantation. A good agreement between experiment and theory was found which proved that the presented high-resolution grazing emission X-ray fluorescence technique is well suited to perform depth profiling measurements of impurities located within the extinction depth, provided the overall shape of the distribution can be assumed a priori.     

Trace elements in human cancerous and healthy tissues: A comparative study by EDXRF,TXRF, synchrotron radiation and PIXE

It is known that trace elements play an important role in a number of biological processes. These include the activation or inhibition of enzymatic reactions, competition between elements and metal proteins for binding positions and modifications in the permeability of cellular membranes. These elements may also influence carcinogenic processes, thus the knowledge of trace element concentrations in healthy and neoplastic tissues might help in diagnostic and in the etiology and development of cancer.     

Can a radioactive implant induced X-ray emission (RIXE) technique be used to in vivo measurement of heavy elements?

A radioactive implant induced X-ray emission (RIXE) technique was examined for the in vivo determination of heavy elements. By the use of⁶⁷Ga,^99mTc,¹²³I,¹²³Xe and²⁰¹Tl implant excitation sources, the excitation efficiency and X-ray attenuation were measured to reveal the potential pairs of source-heavy element of interest for in vivo elemental analysis by the RIXE technique. Detection limits for the RIXE in vivo analysis were evaluated according to Currie's criterion. Four pairs,^99mTc–Pb,²⁰¹Tl–I,¹³³Xe–Cd and¹²³I–Cd are potential.     

Development of a liquid chromatography with mass spectrometry method for the determination of gelsemine in rat plasma and tissue: Application to a pharmacokinetic and tissue distribution study

Gelsemine from Gelsemium elegans Benth is a potential anesthetic and analgesic agent with no physical dependence and opiate addiction. This study was aimed at developing an ultrafast liquid chromatography coupled to tandem mass spectrometry method to quantify gelsemine in rat plasma and tissues. Plasma and tissues were processed with acetonitrile precipitation, and dendrobine was chosen as the internal standard. Sample separation was performed on an ACQUITY HSS T3 column. The mobile phase consisted of acetonitrile and 0.1% formic acid aqueous solution. Multiple reactions monitoring mode was utilized to detect the compounds of interest. The mass spectrometer was operated in the positive ion mode for detection. The MS/MS ion transitions monitored were m/z 323.2→70.5 for gelsemine and 264.2→108.05 for dendrobine, respectively. The calibration curves were linear over the range of 1–500 ng/mL in all biological matrices. The lower limit of quantification for rats plasma and tissues was 1.0 ng/mL. The values for inter‐ and intraday precision and accuracy were well within the ranges acceptable (< 15%). It was successfully applied to the pharmacokinetic and tissue distribution studies of gelsemine after intravenous doses of 5, 2, and 0.5 mg/kg in rats. These data of gelsemine would be useful for clinical application and further development.     

Simultaneous determination of hydride forming (As, Bi, Ge, Sb, Se, Sn) and Hg and non-hydride forming (Ca, Fe, Mg, Mn, Zn) elements in sonicate slurries of analytical samples by microwave induced plasma optical emission spectrometry with dual-mode sample introduction system

A slurry sampling method for the simultaneous determination of hydride forming (As, Bi, Ge, Sb, Se, Sn) and Hg and non-hydride forming (Ca, Fe, Mg, Mn, Zn) elements, without total sample digestion has been developed using the commercial dual-mode sample introduction system (MSIS) coupled with microwave induced plasma optical emission spectrometry (MIP-OES) from biological and environmental reference materials and real samples. The main advantage of this system is its simultaneous determination of elements that form volatile vapor species and elements that do not, without any instrumental changes. Optimization of reaction, nebulization and instrumental conditions was performed to characterize the new system. Slurry concentration up to 4% m/v (particles < 100 μm) prepared in 10% HNO₃ containing 100 μL of decanol, by application of ultrasonic agitation, was used with calibration by the standard addition technique. An ultrasonic probe was used to homogenize the slurry in the quartz cup just before its introduction into the reaction/nebulization system; the multimode sample introduction system (MSIS) combines the benefits of nebulization and vapor generation in a single device. Detection limits (LOD, 3σ_blank, peak area) of 0.07, 0.29, 0.25, 0.10, 0.12, 0.14, 0.11, 0.28, 0.42, 0.02, 0.21 and 0.34 μg g^− 1 were obtained for As, Bi, Ge, Sb, Se, Sn, Hg, Ca, Fe, Mg, Mn and Zn, respectively. The relative standard deviations were ca. 10%, adequate for slurry analysis. To test the accuracy, six certified reference materials were analyzed with the analyte concentrations mostly in the μg g^− 1 level. Measured concentrations are in satisfactory agreement with certified values for the biological reference materials (LUTS-1, DOLT-2) and environmental reference materials (PACS-1, GWB 07302, NIST 2710, NBS 1633b), all adequate for slurry sampling. The method was successfully applied to the determination of the elements in real samples (coal fly ash, lake sediment, sewage). The method requires small amounts of reagents and reduces contamination and losses.     

Ecotypic differences in responses of Arabidopsis thaliana L. to elevated polychromatic UV-A and UV-B+A radiation in the natural environment: a positive correlation between UV-B+A inhibition and growth rate

The effects of supplementary ultraviolet-A (UV-A) and ultraviolet-B+A (UV-B+A) in the natural environment on the growth and morphology of various ecotypes of Arabidopsis thaliana were investigated. The ecotypes investigated were Columbia (Col-4), Landsberg erecta (Ler-0), Cvi-0, Wassilewskija, Enkheim-D, Aa-0 and Di-1. The mutant hy-4 was also used. Results varied with the radiation treatment, ecotype and parameter measured. Plants subjected to elevated UV-A were both insensitive (all parameters Cvi-0 and Col-4) and sensitive. When responses to UV-A occurred they were mostly inhibitory (all significant responses of Di-1 and Enkheim-D, most parameters of Wassilewskija, and some parameters of hy-4), however, promotive affects were observed for some parameters of Aa-0 and Ler-0. Supplementary UV-B+A inhibited all parameters of Di-1 and Enkheim-D and most parameters of Col-4, Ler-0 and hy-4, but Wassilewskija, Aa-0 and Cvi-0 were mostly insensitive. The magnitude of the UV-B+A response varied with ecotype (compare Di-1 with Ler-0). Some ecotypes were sensitive to UV-A but not UV-B+A (Aa-0), whereas others (Ler-0, Col-4) show the opposite sensitivities. A linear relationship is reported between the degree of UV-B+A inhibition of each ecotype and growth rate. The higher the growth rate the more susceptible the ecotype is to UV-B+A inhibition. This relationship holds for the majority of growth parameters measured.     

Ecotypic differences in responses of Arabidopsis thaliana L. to elevated polychromatic UV-A and UV-B+A radiation in the natural environment: a positive correlation between UV-B+A inhibition and growth rate

The effects of supplementary ultraviolet-A (UV-A) and ultraviolet-B+A (UV-B+A) in the natural environment on the growth and morphology of various ecotypes of Arabidopsis thaliana were investigated. The ecotypes investigated were Columbia (Col-4), Landsberg erecta (Ler-0), Cvi-0, Wassilewskija, Enkheim-D, Aa-0 and Di-1. The mutant hy-4 was also used. Results varied with the radiation treatment, ecotype and parameter measured. Plants subjected to elevated UV-A were both insensitive (all parameters Cvi-0 and Col-4) and sensitive. When responses to UV-A occurred they were mostly inhibitory (all significant responses of Di-1 and Enkheim-D, most parameters of Wassilewskija, and some parameters of hy-4), however, promotive affects were observed for some parameters of Aa-0 and Ler-0. Supplementary UV-B+A inhibited all parameters of Di-1 and Enkheim-D and most parameters of Col-4, Ler-0 and hy-4, but Wassilewskija, Aa-0 and Cvi-0 were mostly insensitive. The magnitude of the UV-B+A response varied with ecotype (compare Di-1 with Ler-0). Some ecotypes were sensitive to UV-A but not UV-B+A (Aa-0), whereas others (Ler-0, Col-4) show the opposite sensitivities. A linear relationship is reported between the degree of UV-B+A inhibition of each ecotype and growth rate. The higher the growth rate the more susceptible the ecotype is to UV-B+A inhibition. This relationship holds for the majority of growth parameters measured.