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L. Zhou

Publications and source records attributed to L. Zhou.

4 recordsLinked to original sources

A feasibility study of geological CO2 sequestration in the Ordos Basin, China

The Shaanxi Province/Wyoming CCS Partnership (supported by DOE NETL) aims to store commercial quantities of CO2 safely and permanently in the Ordovician Majiagou Formation in the northern Ordos Basin, Shaanxi Province, China. This objective is imperative because at present, six coal-to-liquid facilities in Shaanxi Province are capturing and venting significant quantities of CO2. The Wyoming State Geological Survey and the Shaanxi Provincial Institute of Energy Resource and Chemical Engineering conducted a feasibility study to determine the potential for geological CO2 sequestration in the northern Ordos Basin near Yulin. The Shaanbei Slope of the Ordos Basin is a huge monoclinal structure with a high-priority sequestration reservoir (Majiagou Formation) that lies beneath a 2,000+ meter-thick sequence of Mesozoic rocks containing a multitude of lowpermeability lithologies. The targeted Ordovician Majiagou Formation in the location of interest is more than 700 meters thick. The carbonate reservoir is located at depths where pressures and temperatures are well above the supercritical point of CO2. The targeted reservoir contains high-salinity brines (20,000-50,000 ppm) that have little or no economic value. The targeted reservoir is continuous as inferred from well logs, and cores show that porosity ranges from 1 to 15% with average measured porosity of 8%, and that permeability ranges from 1-35 md. This paper focuses on calculations that will help evaluate the capacity estimates through the use of high-resolution multiphase numerical simulation models, as well as a more simple volumetric approach. The preliminary simulation results show that the Ordovician Majiagou Formation in the Ordos Basin has excellent potential for geological CO2 sequestration and could store the CO2 currently emitted by coal-to-liquid facilities in Shaanxi Province for hundreds of years (i.e., 9 Mt/year CO2; 450 Mt over a 50-year period at one injection site). ?? 2011 Published by Elsevier Ltd.

Conference Paper

Removal of iron interferences by solvent extraction for geochemical analysis by atomic-absorption spectrophotometry

Iron is a common interferent in the determination of many elements in geochemical samples. Two approaches for its removal have been taken. The first involves removal of iron by extraction with methyl isobutyl ketone (MIBK) from hydrochloric acid medium, leaving the analytes in the aqueous phase. The second consists of reduction of iron(III) to iron(II) by ascorbic acid to minimize its extraction into MIBK, so that the analytes may be isolated by extraction. Elements of interest can then be determined using the aqueous solution or the organic extract, as appropriate. Operating factors such as the concentration of hydrochloric acid, amounts of iron present, number of extractions, the presence or absence of a salting-out agent, and the optimum ratio of ascorbic acid to iron have been determined. These factors have general applications in geochemical analysis by atomic-absorption spectrophotometry.

Talanta

Determination of total tin in geological materials by electrothermal atomic-absorption spectrophotometry using a tungsten-impregnated graphite furnace

An electrothermal atomic-absorption spectrophotometric method is described for the determination of total tin in geological materials, with use of a tungsten-impregnated graphite furnace. The sample is decomposed by fusion with lithium metaborate and the melt is dissolved in 10% hydrochloric acid. Tin is then extracted into trioctylphosphine oxide-methyl isobutyl ketone prior to atomization. Impregnation of the furnace with a sodium tungstate solution increases the sensitivity of the determination and improves the precision of the results. The limits of determination are 0.5–20 ppm of tin in the sample. Higher tin values can be determined by dilution of the extract. Replicate analyses of eighteen geological reference samples with diverse matrices gave relative standard deviations ranging from 2.0 to 10.8% with an average of 4.6%. Average tin values for reference samples were in general agreement with, but more precise than, those reported by others. Apparent recoveries of tin added to various samples ranged from 95 to 111% with an average of 102%.

Talanta

Determination of indium in geological materials by electrothermal-atomization atomic absorption spectrometry with a tungsten-impregnated graphite furance

The sample is fused with lithium metaborate and the melt is dissolved in 15% (v/v) hydrobromic acid. Iron(III) is reduced with ascorbic acid to avoid its coextraction with indium as the bromide into methyl isobutyl ketone. Impregnation of the graphite furnace with sodium tungstate, and the presence of lithium metaborate and ascorbic acid in the reaction medium improve the sensitivity and precision. The limits of determination are 0.025–16 mg kg −1 indium in the sample. For 22 geological reference samples containing more than 0.1 mg kg −1 indium, relative standard deviations ranged from 3.0 to 8.5% (average 5.7%). Recoveries of indium added to various samples ranged from 96.7 to 105.6% (average 100.2%).

Analytica Chimica Acta