2007
DOI: 10.1016/j.jbbm.2006.09.010
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Preparation of highly efficient monolithic silica capillary columns for the separations in weak cation-exchange and HILIC modes

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Cited by 42 publications
(18 citation statements)
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“…As shown in Fig. 3, trialkoxysilanes with hydrophobic organic moieties, such as N-octadecyldimethyl [3-(trimethoxy silyl)propyl]ammonium chloride [23], n-octyltriethoxysilane (C8-TES) [32][33][34][35], phenyltriethoxysilane (PTES) [36][37][38], propyltrimethoxysilane (C3-TMS) [39], MTMS [40][41][42][43][44], and other trialkoxysilanes with active organic functionalities, such as aminopropyl triethoxysilane (APTES) [45][46][47][48][49], N-(␤-aminoethyl)-␥-aminopropyl-triethoxysilane [50], N-(␤-aminoethyl)-␥-aminopropylmethyldimethoxysilane [51], 3-chloropropyltrimethoxysilane [52], 3-mercaptopropyltrime thoxysilane (MPTMS) [53], N-trimethoxysilylpropyl-N,N,Ntrimethylammonium chloride [54], allyl-trimethoxysilane [ 55,56], and vinyltrimethoxysilane (VTMS) [57] have been selected as coprecursors with tetraalkoxysilanes, TMOS, or TEOS. Additionally, bridged silanes such as 1,4-bis(triethoxysily1)benzene [58] have also been used for preparation of hybrid monoliths.…”
Section: Sol-gel Process Of Trialkoxysilanes and Tetraalkoxysilanesmentioning
confidence: 99%
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“…As shown in Fig. 3, trialkoxysilanes with hydrophobic organic moieties, such as N-octadecyldimethyl [3-(trimethoxy silyl)propyl]ammonium chloride [23], n-octyltriethoxysilane (C8-TES) [32][33][34][35], phenyltriethoxysilane (PTES) [36][37][38], propyltrimethoxysilane (C3-TMS) [39], MTMS [40][41][42][43][44], and other trialkoxysilanes with active organic functionalities, such as aminopropyl triethoxysilane (APTES) [45][46][47][48][49], N-(␤-aminoethyl)-␥-aminopropyl-triethoxysilane [50], N-(␤-aminoethyl)-␥-aminopropylmethyldimethoxysilane [51], 3-chloropropyltrimethoxysilane [52], 3-mercaptopropyltrime thoxysilane (MPTMS) [53], N-trimethoxysilylpropyl-N,N,Ntrimethylammonium chloride [54], allyl-trimethoxysilane [ 55,56], and vinyltrimethoxysilane (VTMS) [57] have been selected as coprecursors with tetraalkoxysilanes, TMOS, or TEOS. Additionally, bridged silanes such as 1,4-bis(triethoxysily1)benzene [58] have also been used for preparation of hybrid monoliths.…”
Section: Sol-gel Process Of Trialkoxysilanes and Tetraalkoxysilanesmentioning
confidence: 99%
“…As a branch of monolithic materials, hybrid monoliths not only possess the same properties of organic and silica-based monoliths such as good permeability, fast mass transfer, and ease of modification, but also have excellent features of high pH stability of organic monoliths and mechanical stability of pure silica monoliths. These qualities make the hybrid monoliths an alternative in microcolumn formats for CLC [34,41,42]. CEC has been regarded as one of the most powerful separation techniques due to the plug profile flow of mobile phase driven by the EOF in a capillary column or a microchannel of microfluidic chip, which combines the high efficiency of CE and the high selectivity of LC.…”
Section: Microscale Separationmentioning
confidence: 99%
“…The elution order was the same as that obtained by a conventional particle-packed SCX column, Inertsil CX (3.0 mm i.d., 250 mm long, GL Science). 11 The column efficiencies of 200H-pSSA and 200H-AMPS are summarized in Table 2. For these nucleic bases, the separation efficiencies of the capillary column, 200H-pSSA, and the particle-packed column, Inertsil CX, were comparable, and theoretical plate heights H were calculated as 20 -44 μm.…”
Section: Strong Cation-exchange Modementioning
confidence: 99%
“…11 In this report, the ionexchange mode was enlarged to SCX and strong-and weak anion-exchange (SAX and WAX) modes, to show the utility of the present polymer-coating method for the column functionalization and for providing much more efficient anionexchange columns.…”
mentioning
confidence: 98%
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