scholarly journals A Comparative Study of Selected Trace Element Content in Malay and Chinese Traditional Herbal Medicine (THM) Using an Inductively Coupled Plasma-Mass Spectrometer (ICP-MS)

2013 ◽  
Vol 14 (2) ◽  
pp. 3078-3093 ◽  
Author(s):  
Fairuz Rasdi ◽  
Nor Bakar ◽  
Sharifah Mohamad
Author(s):  
Mikołaj Dąbrowski ◽  
Anetta Zioła-Frankowska ◽  
Marcin Frankowski ◽  
Jacek Kaczmarczyk ◽  
Łukasz Kubaszewski

Bone metabolism and the trace element content associated with it change at each stage of degenerative disease. The aim of this study was to find out about the role of the analyzed elements in different stages of hip osteoarthritis. Elements associated with oxidative and enzymatic processes were analyzed depending on the changes in the radiological images of the hip joint. Element content analysis was performed by the inductively coupled plasma mass spectrometry analytical technique. The femoral head in severely osteoarthritic hips (KL3–4) compared to mild grade osteoarthritis (KL2) had a greater content of Cu (median 1.04 vs. 0.04), Sr (median 38.71 vs. 29.59), and Zn (median 75.12 vs. 63.21). There were no significant differences in the content of Mo, Cr, and Fe in the femoral head and neck between the groups. The Cu/Fe correlation was negative in the KL2 group (−0.47) and positive in the KL3–4 groups (0.45). Changes in the content and correlation of trace elements in the hip joint explain the changes in metabolism dependent on the severity of degenerative changes.


2014 ◽  
Vol 624 ◽  
pp. 119-123 ◽  
Author(s):  
Qi Chen ◽  
Yong Ya Wang ◽  
Fu Xi Gan

This work aims to explore the sources of raw materials of archaic serpentine jade artifacts by comparing their trace element content. The major and trace elements of serpentine jade samples from different deposits in China are determined by external-beam proton-induced X-ray emission (PIXE). Trace element concentrations are also measured by inductively coupled plasma atomic emission spectroscopy for comparison. The relationship between the trace element content and the mechanism of serpentine formation is discussed. The results indicate that Type I jade has a small amount of Ni in it and almost no Cr and Co while significant amount of Cr, Co and Ni was found in Type II jade. Thus, this could be used to distinguish the two kinds of serpentine jade formed by different mechanisms.


2020 ◽  
Vol 58 (3) ◽  
pp. 293-311 ◽  
Author(s):  
Zeinab Azadbakht ◽  
David R. Lentz

ABSTRACT Biotite grains from 22 felsic intrusions in New Brunswick were mapped in situ using a laser ablation-inductively coupled plasma-mass spectrometer (LA-ICP-MS). We investigated the extent to which biotite can retain its magmatic zoning patterns and, where zoning does exist, how it can be used to elucidate early to late stage, syn-magmatic to post-crystallization processes. Although the major element and halogen contents of the examined biotite phenocrysts are homogeneous, two-thirds of the grains display trace-element zoning for Ba, Rb, and Cs. The results also indicated that zoning is better retained in larger grains (i.e., > 500 × 500 μm) with minimal alteration and mineral inclusions. An exceptionally well-zoned Li-rich siderophyllite from the Pleasant Ridge topaz granite in southwestern New Brunswick shows Ti, Ta, Sn, W, Cs, Rb, and V (without Li or Ba) zoning. Cesium values increase from 200 to 1400 ppm from core to rim. Conversely, Sn and W values decrease toward the rim (50 to 10 and 100 to 10 ppm, respectively). Tantalum and Ti values show fewer variations but drop abruptly close to the rim of the grain (100 to 20 and 2000 to 500 ppm, respectively). These observations may indicate crystallization of mineral phases with high partition coefficients for these highly incompatible elements (except Ti) (e.g., cassiterite and rutile) followed by fractionation of a fluid phase at a later stage of magma crystallization. The preservation of zoning may indicate rapid cooling post-crystallization of the parent magma.


Minerals ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 147 ◽  
Author(s):  
Allan Pring ◽  
Benjamin Wade ◽  
Aoife McFadden ◽  
Claire E. Lenehan ◽  
Nigel J. Cook

The nature of couple substitutions of minor and trace element chemistry of expitaxial intergrowths of wurtzite and sphalerite are reported. EPMA and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses display significant differences in the bulk chemistries of the two epitaxial intergrowth samples studied. The sample from the Animas-Chocaya Mine complex of Bolivia is Fe-rich with mean Fe levels of 4.8 wt% for wurztite-2H and 2.3 wt% for the sphalerite component, while the sample from Merelani Hills, Tanzania, is Mn-rich with mean Mn levels in wurztite-4H of 9.1 wt% and for the sphalerite component 7.9 wt% In both samples studied the wurtzite polytype is dominant over sphalerite. LA-ICP-MS line scans across the boundaries between the wurtzite and sphalerite domains within the two samples show significant variation in the trace element chemistries both between and within the two coexisting polytypes. In the Merelani Hills sample the Cu+ + Ga3+ = 2Zn2+ substitution holds across both the wurztite and sphalerite zones, but its levels range from around 1200 ppm of each of Cu and Ga to above 2000 ppm in the sphalerite region. The 2Ag+ + Sn4+ = 3Zn2+ coupled substitution does not occur in the material. In the Animas sample, the Cu+ + Ga3+ = 2Zn2+ substitution does not occur, but the 2(Ag,Cu)+ + Sn4+ = 3Zn2+ substitution holds across the sample despite the obvious growth zoning, although there is considerable variation in the Ag/Cu ratio, with Ag dominant over Cu at the base of the sample and Cu dominant at the top. The levels of 2(Ag,Cu)+ + Sn4+ = 3Zn2+ vary greatly across the sample from around 200 ppm to 8000 ppm Sn, but the higher values occur in the sphalerite bands.


2016 ◽  
Vol 31 (2) ◽  
pp. 531-536 ◽  
Author(s):  
Sune G. Nielsen ◽  
Jeremy D. Owens ◽  
Tristan J. Horner

We present and verify a new method to measure vanadium isotope ratios using a Thermo Scientific Neptune multi-collector inductively-coupled plasma mass spectrometer (MC-ICP-MS) operated in medium mass resolution mode.


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