2001
DOI: 10.1016/s0376-7388(01)00452-5
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Mixed-gas permeation of syngas components in poly(dimethylsiloxane) and poly(1-trimethylsilyl-1-propyne) at elevated temperatures

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Cited by 211 publications
(92 citation statements)
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“…Because the transport of common gases (N 2 , O 2 , H 2 ) in PDMS is well understood, 2-23 this polymer will serve as a valuable baseline material to compare with novel candidate polymers to be tested later. Figure 2-15 presents the permeability coefficients of syngas components at room temperature in PDMS as a function of the gas critical temperature, T C (Merkel et al, 2001). Frequently, in a solubilityselective polymer such as PDMS, there is a strong correlation between the logarithm of gas permeability and T C Van Amerongen, 1964).…”
Section: Characterization Of a Baseline Solubility Selective Polymer:mentioning
confidence: 99%
“…Because the transport of common gases (N 2 , O 2 , H 2 ) in PDMS is well understood, 2-23 this polymer will serve as a valuable baseline material to compare with novel candidate polymers to be tested later. Figure 2-15 presents the permeability coefficients of syngas components at room temperature in PDMS as a function of the gas critical temperature, T C (Merkel et al, 2001). Frequently, in a solubilityselective polymer such as PDMS, there is a strong correlation between the logarithm of gas permeability and T C Van Amerongen, 1964).…”
Section: Characterization Of a Baseline Solubility Selective Polymer:mentioning
confidence: 99%
“…The test gas pressure was 30 psi and temperatures were varied from 20˚C to 70˚C. Dry mixed gas experiments have been carried out using a method previously described in the literature [1][2][3][4][5][6][7][8]. In the mixed gas procedure, permeation is determined analytically by gas chromatography.…”
Section: Appendicesmentioning
confidence: 99%
“…After stirring for about 2 h at room temperature, the resulting homogeneous mixture was crystallized under static hydrothermal conditions at 373 K in a Teflon lined autoclave for 96 h. The molar composition of the initial gel mixture was 1.0:0.58:0.50:60 TEOS/CTAB/NaOH/H2O. The solid product was obtained by filtration, washed with deionized water, dried in vacuum oven at 353 K and calcined in air at 833 K for 10 hwith 1 K/min of heating rate to remove the CTAB.This method results the unmodified version of MCM-48 nanoparticles [25]. As shown in Figure 1, surface modification of MCM-48 particles was performed this way: Before removing CTAB, sylilation of MCM-48 with dimethylsilane was achived by immersionof MCM-48 nanoparticles into liquid dimethyldichlorosilane (DMDCS,Merck) for 72 h. Afterwards CTAB was removed by means of soxhlet extraction apparatus using 300 ml of methanol and 30 ml of aqueous HCL (10% vol).…”
Section: Experimental Synthesis and Functionalization Of Mcm-48 Nanopmentioning
confidence: 99%