Determination of Pb, Cr, Ni and Mn in Tap Water of Riyadh Metropolitan City Using ICP-MS after Preconcentration with Multiwalled Carbon Nanotubes

The determination of toxic metals in water using multiwalled carbon nanotubes （MWNTs） as a solid-phase extraction adsorbent prior to their determination by inductively coupled plasma mass spectrometry （ICP-MS） has been investigated. Standard addition method was applied for the calibration using aqueous solutions. Multiwalled carbon nanotubes （MWNTs） absorb these metals at pH 8.0, HNO3 of 1.0 mol-Ll is used for complete elusion of these metals from MWNTs. Previously investigated parameters have been applied for the determination of Pb, Cr, Ni and Mn in tap water samples. Fifteen tap water samples from different locations of Riyadh metropolitan area have been determined by ICP-MS after preconcentration with MWNTs.

Determination of Fe, Cu, and Zn in Water Samples by Microcolumn Packed with Multiwalled Carbon Nanotubes as a Solid Phase Extraction Adsorbent Using ICP-MS

The heavy metals determination in tap water samples using microcolumn packed with multiwalled carbon nanotubes （MWNTs） as a solid-phase extraction adsorbent before to their determination by inductively coupled plasma mass spectrometry （ICP-MS） has been studied. Standard addition method was applied for the calibration using aqueous solutions. The metals ions absorption were achieved by multiwalled carbon nanotubes （MWNTs） at pH 8.0, and then these retained metals on MWNTs column were eluted by 1.0 mol.L^-1 HNO3. The analytical parameters for the determination ofFe, Cu, and Zn in tap water samples which have been investigated previously were applied. Fifteen tap water samples were collected from different locations of Riyadh metropolitan area and then determined the concentration ofFe, Cu, and Zn by ICP-MS after preconcentration with MWNTs. The concentration range for Fe, Cu, and Zn measured （μg/L） in water samples are 23.37-137.91, 2.12-121.36, and 14.43-202.47 respectively. The level of Fe exceeded the limits set by WHO and SASO for drinking water.

Determination of trace elements in high purity nickel by high resolution inductively coupled plasma mass spectrometry

The contents ofMg, Al, Si, Ti, Cr, Mn, Fe, Co, Cu, Ga, As, Se, Cd, Sb, Pb and Bi in high purity nickel were determined by high resolution inductively coupled plasma mass spectrometry （HR-ICP-MS）. The sample was dissolved in HNO3 and HCI by microwave digestion. Most of the spectral interferences could be avoided by measuring in the high resolution mode. The matrix effects because of the presence of excess HC1 and nickel were evaluated. Correction for matrix effects was made using Sc, Rh and T1 as internal standards. The optimum conditions for the determination were tested and discussed. The detection limits range from 0.012 to 1.76 ~tg/g depending on the type of elements. The applicability of the proposed method is also validated by the analysis of high purity nickel reference material （NIST SRM 671）. The relative standard deviation （RSD） is less than 3.3%. Results for determination of trace elements in high purity nickel were presented.

Determination of impurity elements in MnZn ferrites by inductively coupled plasma mass spectrometry

An inductively coupled plasma mass spectrometry(ICP-MS) method was developed for the determination of Na, Mg, Al,K, Ca, Ti, Cr, Co, Ni, Cu, Ga, As, Mo, Ag, Cd and Pb in MnZn ferrites. The sample was digested by HNO3+HCl with microwave digestion followed by dilution with ultrapure water, then the above 16 impurity elements in the solution were analyzed directly by ICP-MS. The impurity elements were introduced by the helium gas or hydrogen gas into the octopole reaction system(ORS) to eliminate the polyatomic interferences caused by the high salty matrixes. The matrix effect was minimized through matrix matching,and Be, Y and Rh were used as internal standard elements. The working parameters of the instrument were optimized. The results show that the method has good precision and high accuracy. The detection limits for the investigated elements are in the range of0.9-37.5 ng/L, the relative standard deviation of each element is within 1.1%-4.8%, and the recovery of each element is 90%-108%.

Accuracy of LA-ICPMS zircon U-Pb age determination:An inter-laboratory comparison

LA-ICPMS zircon U-Pb dating has been greatly advanced and widely applied in the past decade because it is a cheap and fast technique.The internal error of LA-ICPMS zircon U-Pb dating can be better than 1%,but reproducibility(accuracy)is relatively poor.In order to quantitatively assess the accuracy of this technique,zircons from two dioritic rocks,a Mesozoic dioritic microgranular enclave(FS06)and a Neoproterozoic diorite(WC09-32),were dated independently in eight laboratories using SIMS and LA-ICPMS.Results of three SIMS analyses on FS06 and WC09-2 are indistinguishable within error and give a best estimate of the crystallization age of 132.2 and 760.5 Ma(reproducibility is^1%,2RSD),respectively.Zircon U-Pb ages determined by LA-ICPMS in six laboratories vary from 128.3±1.0 to 135.0±0.9 Ma(2SE)for FS06 and from 742.9±3.1 to777.8±4.7 Ma(2SE)for WC09-32,suggesting a reproducibility of^4%(2RSD).Uncertainty produced during LA-ICPMS zircon U-Pb analyses comes from multiple sources,including uncertainty in the isotopic ratio measurements,uncertainty in the fractionation factor calculation using an external standard,uncertainty in the age determination as a result of common lead correction,age uncertainty of the external standards and uncertainty in the data reduction.Result of our study suggests that the uncertainty of LA-ICPMS zircon U-Pb dating is approximately 4%(2RSD).The uncertainty in age determination must be considered in order to interpret LA-ICPMS zircon U-Pb data rationally.