Geochemical migration of impurity trace elements and resultant fractal distribution patterns in source rocks

1994 ◽  
Vol 26 (4) ◽  
pp. 419-435 ◽  
Author(s):  
Yongzhang Zhou ◽  
Edward H. Chown ◽  
Guangzhi Tu ◽  
Jayanta Guha ◽  
Huangzhang Lu
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
L. Zhang ◽  
Y. Wang ◽  
M.-W. Li ◽  
Q.-Z. Yin ◽  
W. Zhang

AbstractThe accumulation and spatial distribution of economically important petroleum in sedimentary basins are primarily controlled by its migration from source rocks through permeable carrier beds to reservoirs. Tracing petroleum migration entails the use of molecular indices established according to sorption capacities of polar molecules in migrating petroleum. However, little is known about molecular sorption capacities in natural migration systems, rendering these indices unreliable. Here, we present a new approach based on a novel concept of relative sorption coefficient for quantitatively assessing sorption capacities of polar molecules during natural petroleum migration. Using this approach, we discovered previously unrecognized “stripping” and “impeding” effects that significantly reduce the sorption capacities of polar compounds. These discoveries provide new insights into the behaviors of polar compounds and can easily explain why traditional molecular indices yield incorrect information about petroleum migration. In light of these new findings, we established new molecular indices for tracing petroleum migration. We demonstrate via case studies that the newly established indices, unlike traditional molecular indices, are reliable and effective in tracing petroleum migration. Our approach can be applied to diverse basins around the world to reveal distribution patterns of petroleum, which would decrease environmental risks of exploration by reducing unsuccessful wells.


2001 ◽  
Vol 65 (2) ◽  
pp. 249-276 ◽  
Author(s):  
G. Tischendorf ◽  
H.-J. Förster ◽  
B. Gottesmann

AbstractMore than 19,000 analytical data mainly from the literature were used to study statistically the distribution patterns of F and the oxides of minor and trace elements (Ti, Sn, Sc, V, Cr, Ga, Mn, Co, Ni, Zn, Sr, Ba, Rb, Cs) in trioctahedral micas of the system phlogopite-annite/siderophyllite-polylithionite (PASP), which is divided here into seven varieties, whose compositional ranges are defined by the parametermgli(= octahedral Mg minus Li). Plots of trace-element contentsvs.mglireveal that the elements form distinct groups according to the configuration of their distribution patterns. Substitution of most of these elements was established as a function ofmgli. Micas incorporate the elements in different abundances of up to four orders of magnitude between the concentration highs and lows in micas of ‘normal’ composition. Only Zn, Sr and Sc are poorly correlated tomgli. In compositional extremes, some elements (Zn, Mn, Ba, Sr, Cs, Rb) may be enriched by up to 2–3 orders of magnitude relative to their mean abundance in the respective mica variety. Mica/melt partition coefficients calculated for Variscan granites of the German Erzgebirge demonstrate that trace-element partitioning is strongly dependent on the position of the mica in the PASP system, which has to be considered in petrogenetic modelling.This review indicates that for a number of trace elements, the concentration ranges are poorly known for some of the mica varieties, as they are for particular host rocks (i.e. igneous rocks of A-type affiliation). The study should help to develop optimal analytical strategies and to provide a tool to distinguish between micas of ‘normal’ and ‘abnormal’ trace-element composition.


2011 ◽  
Vol 30 (12) ◽  
pp. 1914-1923 ◽  
Author(s):  
Lin Wang ◽  
Xuelei Zhou ◽  
Dubao Yang ◽  
Zhenyong Wang

Lead acetate (300 mg/L) and/or cadmium chloride (50 mg/L) were administered as drinking water to Sprague-Dawley rats for 9 weeks to investigate the effects of concurrent exposure to lead and cadmium on the distribution patterns of five essential trace elements. Inductively coupled plasma mass spectrometry was used to determine the concentrations of zinc, copper, manganese, selenium and iron in the urine at different exposure times, as well as their levels in the renal cortex and serum at the end of treatment. Compared with the control group, exposure to lead and/or cadmium resulted in a significant increase in the urinary excretion of these five elements during the experiment, whereas significant decreased levels of these elements were found in kidney and serum. In conclusion, increased urinary loss of antioxidant trace elements due to lead and/or cadmium exposure induced the deficiency of antioxidants in the body, which could result in further oxidative damage. Moreover, there was an obvious synergistic effect of lead combined with cadmium on the distribution patterns of these essential trace elements, which may be related to the severity of co-exposure to these two metals.


Minerals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 323 ◽  
Author(s):  
Qiang Wei ◽  
Weijiao Song

The mineralogical and chemical characteristics of the feed coals and coal combustion products (CCPs) from two power plants (Xilaifeng and Damo) that consume coals from the Wuda Coalfield, Inner Mongolia, were investigated, using XRD, SEM–EDS, XRF, and ICP-MS. The feed coals from Xilaifeng and Damo are both of high ash yield (52.93% and 48.36%, respectively), and medium and high total sulfur content (2.22% and 3.32%, respectively). The minerals in the feed coals are primarily composed of kaolinite, quartz, illite, pyrite, and, to a lesser extent, gypsum and anatase. In addition to the elevated incompatible elements (Nb, Ta, Zr, Hf and Th), Li and Hg are enriched in the feed coals from the Xilaifeng and Damo power plants, respectively. Rare earth elements and yttrium (REY) are more enriched in the feed coals from Xilaifeng (194 μg/g) than those of Damo (93.9 μg/g). The inorganic phases of CCPs from both power plants are mainly composed of amorphous phase, quartz, hematite, illite, and anhydrite. Compared with the feed coals, concentrations of most trace elements in the CCPs are elevated, and they are preferentially enriched in the fly ashes relative to the bottom ashes (*f/b > 1), especially F, As, Sr, Mo, Se, and Hg (*f/b > 2.5). Furthermore, most trace elements (Xilaifeng: excluding Li, Cr, Co, Ni, Rb, Nb and Cs; Damo: excluding Li, V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Cs and Ba) are more enriched in the (fine) fly ashes relative to the laboratory high-temperature coal ashes (HTAs). The REY barely differentiate in either the fly ash or bottom ash from Xilaifeng. In contrast, the REY in the fine and coarse fly ashes from Damo have very similar H-type distribution patterns with negative Ce and slightly positive Y anomalies. Attention should be paid to the enriched toxic elements (including F, As and Hg) in the fly ashes from both power plants due to possible adverse environmental effect.


1996 ◽  
Vol 103 (1-2) ◽  
pp. 23-37 ◽  
Author(s):  
Thierry Mongenot ◽  
Nicolas-Pierre Tribovillard ◽  
Alain Desprairies ◽  
Elisabeth Lallier-Vergès ◽  
Fatima Laggoun-Defarge

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