1997
DOI: 10.1016/s0021-9673(97)00788-7
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Determination of inorganic ions in oil field waters by single-column ion chromatography

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Cited by 12 publications
(4 citation statements)
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“…The anionic exchange functionality was achieved by using γ-chloropropyl triethoxy silane, hexamethyl disilazane and N,N-dimethyl benzylamine, phenyl trichlorosilane, chlorosulfonic acid and hexamethyl disilazane were used to obtain the cationic exchange functionality. A good agreement with the results obtained with other conventional methods was confirmed [16]. Typical chromatograms of a sample are in the original publication presented in Figure 2.…”
Section: Ion Chromatographic Analyses Of Sea Waters Brines and Relatsupporting
confidence: 84%
“…The anionic exchange functionality was achieved by using γ-chloropropyl triethoxy silane, hexamethyl disilazane and N,N-dimethyl benzylamine, phenyl trichlorosilane, chlorosulfonic acid and hexamethyl disilazane were used to obtain the cationic exchange functionality. A good agreement with the results obtained with other conventional methods was confirmed [16]. Typical chromatograms of a sample are in the original publication presented in Figure 2.…”
Section: Ion Chromatographic Analyses Of Sea Waters Brines and Relatsupporting
confidence: 84%
“…7 In addition, quaternary ammonium, sulfonic and zwitterionic group-functionalized polymers or silica beads were also used for analysis of ionic compounds. [8][9][10][11][12] Recently a variety of HILIC stationary phases have been developed for different purposes, such as separation of polar compounds and peptides by multi-dimensional separation techniques, [13][14][15][16][17][18][19][20] enrichment of lower abundance biological compounds by HILIC solid-phase extraction (SPE), including glycopeptides, proteins and glycoproteins, [21][22][23] as well as analysis of complicated polar samples by using HILIC-MS hyphenated technique, due to good compatibility between organic mobile phase used in HILIC with MS. 24 A common characteristic between IC and HILIC stationary phases is that both contain polar or hydrophilic groups. In IC, ion exchange occurs between charged or chargeable moieties of the stationary phase and the ionic analytes, while HILIC displayed both electrostatic interaction and partition interaction between stationary phase and analytes.…”
Section: Introductionmentioning
confidence: 99%
“…[6][7][8] The emphasis of ion chromatographic application of inorganic anions/cations determination is mostly on the following areas: environmental analysis, power plant chemistry, semiconductor industry, metal processing, pharmaceutics, biotechnology, mining, agriculture, food and beverages, electroplating, and the pulp and paper industry. [31][32][33][34][35][45][46][47][48][49][50][51] In spite of the strong competition from atomic spectrometric techniques, the IC of metal cations is now well established as a relatively cheap method with ease of automation and on-line capability; it is particularly attractive in a wide variety of routine trace analysis. 23,24,26,27,32,33 Compared with the traditional spectroscopic methods, IC offers the advantage of providing information on metal speciation, which can distinguish different metal oxidation states such as Cr(III)/Cr(VI), Fe(II)/ Fe(III), or As(III)/As(V).…”
Section: Applicationmentioning
confidence: 99%