2013
DOI: 10.2116/analsci.29.213
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Separation of Parabens on a Zirconia-Based Stationary Phase in Superheated Water Chromatography

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Cited by 15 publications
(5 citation statements)
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References 26 publications
(30 reference statements)
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“…Subcritical water acts like a weak polar organic solvent when heated [9][10][11][12]. When subcritical water is used as the mobile phase to achieve chromatographic separation, the process is termed as subcritical water chromatography, and has been found to be a very promising technique [12][13][14][15][16][17][18][19][20][21][22][23]. Advantages of subcritical water chromatography include the elimination of hazardous organic solvents required to separate solutes and its relatively fast analysis time [9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…Subcritical water acts like a weak polar organic solvent when heated [9][10][11][12]. When subcritical water is used as the mobile phase to achieve chromatographic separation, the process is termed as subcritical water chromatography, and has been found to be a very promising technique [12][13][14][15][16][17][18][19][20][21][22][23]. Advantages of subcritical water chromatography include the elimination of hazardous organic solvents required to separate solutes and its relatively fast analysis time [9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…As mentioned above, SBWC should be applicable to substances with a broad polarity range, mainly due to decreased water polarity with increased temperature. A wide number of low molecular weight compounds has been already separated in SHWC including alcohols [31, 5257], aldehydes [58], aliphatic aromatic ketones [59], alkanols [28, 53, 54, 6063], alkyl and aromatic hydrocarbons, chlorinated hydrocarbons, benzenes/benzene derivatives [52, 56, 57, 6471], amino acids [72–74], anilines [44, 65, 74, 75], aromatic acids [59], ketones [59, 76, 77], barbiturates [46, 78, 79], benzoates [80], caffeine derivatives [31, 66, 81, 82], carbohydrates [59, 72, 73, 80, 83], carboxylic acids [72, 84], chlorophenols [85], diethyl phthalates [68, 80], flavones [86], drugs and pharmaceuticals [87–92], nucleobases [80], parabens [46, 78, 80, 82, 93], phenols [31, 44, 46, 57, 65, 67, 74, 75, 84, 89, 9496], phosphonic acids [73], polychlorinated biphenyls [97], polycyclic aromatic hydrocarbons [67, 80, 97], polyethylene glycols [98], phenylthiohydantoin–amino acids [99–101], pyridines [44, 75], steroids [99, 102104], sulphonamides [105, 106], triazine herbicides [107], triazole fungicides [108], and water‐soluble vitamins [...…”
Section: Subcritical Water Separationsmentioning
confidence: 99%
“…Several applications of SHWC in pharmaceutical analysis have been reported in the literature [ 78 , 79 , 80 , 81 , 82 , 83 ]. As examples, Fields et al [ 82 ] showed that the replacement of ACN/water mixtures with superheated water mobile phases in RP-HPLC can be successfully applied to the analysis of testosterone and several related compounds on a porous zirconia, PBD-coated column at temperatures up to 200 °C.…”
Section: Aqueous Mobile Phasesmentioning
confidence: 99%