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11.
The permeability of copoly (1-trimethylsilyl-1-propyne-pentamethyldisilyl-1-propyne) membrane for twelve gases (0_2, N_2, CO_2, H_2, D_2, He, At, CH_4, C_2H_4, C_2H_6, C_3H_6 and C_3H_8) was examined. The basic laws of solution and diffusion of the gases in the membrane were expounded preliminarily. It was found that a linear relationship between logarithm of diffusion coefficient (D) and critical molar volume (V_c) of the gases. The permeation characteristics of the gases in the copoly (1-trimethylsilyl-1-propyne-pentamethyldisilyl-1-propyne) membrane was also discussed. 相似文献
12.
A series of calixcrown ethers for which the cavity size of the crown ring is varied from crown-6 to crown-7 to crown-8 were examined for the transport abilities toward alkali metal ions. These ligands were incorporated into supported liquid membranes (SLMs) and into polymer inclusion membranes (PIMs) composed of cellulose triacetate (CTA) as a support and 2-nitrophenyl octyl ether (NPOE) and tris(2-butoxyethyl) phosphate (TBEP) as a plasticizer. In both membrane systems, calixcrown-6 showed the best selectivity toward a cesium ion over other alkali metal ions. The polymeric CTA membrane showed more rapid transport rate as well as higher durability than did the SLMs. 相似文献
13.
Affinity enrichment of plasma membrane for proteomics analysis 总被引:6,自引:0,他引:6
Proteomics analysis of plasma membranes from cells exposed to different extracellular environments is potentially a powerful approach for the identification of membrane-associated proteins responding to these environments. Preparation of high concentration plasma membrane fractions with low contamination from cellular organelles is essential for such studies. Here, we describe an affinity enrichment method, which combines cell surface biotinylation with affinity enrichment by immobilized streptavidin beads, for the isolation of plasma membranes. This method results in a 400-fold enrichment of plasma membrane relative to endoplasmic reticulum, a major contaminant in standard plasma membrane preparations, and dramatically reduces contamination from other cellular organelles. The biotinylation reaction did not interfere with ligand-dependent activation of receptor tyrosine kinases or G-protein coupled receptors, suggesting cell-surface signal transduction machinery remains functional. Membrane fractions prepared by this method should provide excellent starting materials for membrane proteomics analysis such as studies of dynamic trafficking and regulation of signaling molecules or identification of disease-specific membrane markers. 相似文献
14.
The applicability of pulsed field gradient nuclear magnetic resonance spectroscopy to nanocapsule systems is demonstrated on dispersed poly-n-butylcyanoacrylate nanocapsules as a model system. Spectroscopic data are presented that allow for the structural characterization of the inner cavities, the observation of Brownian motion of the capsules and the detection of rapid molecular exchange through the capsule walls. An analytical formula is proposed that yields equilibrium populations and average residence times of a given tracer molecule, thus leading to crucial information regarding the permeability of the capsule walls. Based on these analytical methods, two varieties of nanocapsules are compared that derive from two different preparation procedures. It is found that thinner capsule walls obtained under acidic conditions of the organic phase during interfacial polymerization lead to correspondingly higher exchange rates of benzene as a tracer molecule. 相似文献
15.
Effect of solution chemistry on the surface charge of polymeric reverse osmosis and nanofiltration membranes 总被引:1,自引:0,他引:1
A streaming potential analyzer has been used to investigate the effect of solution chemistry on the surface charge of four commercial reverse osmosis and nanofiltration membranes. Zeta potentials of these membranes were analyzed for aqueous solutions of various chemical compositions over a pH range of 2 to 9. In the presence of an indifferent electrolyte (NaCl), the isoelectric points of these membranes range from 3.0 to 5.2. The curves of zeta potential versus solution pH for all membranes display a shape characteristic of amphoteric surfaces with acidic and basic functional groups. Results with salts containing divalent ions (CaCl2, Na2SO4, and MgSO4) indicate that divalent cations more readily adsorb to the membrane surface than divalent anions, especially in the higher pH range. Three sources of humic acid, Suwannee River humic acid, peat humic acid, and Aldrich humic acid, were used to investigate the effect of dissolved natural organic matter on membrane surface charge. Other solution chemistries involved in this investigation include an anionic surfactant (sodium dodecyl sulfate) and a cationic surfactant (dodecyltrimethylammonium bromide). Results show that humic substances and surfactants readily adsorb to the membrane surface and markedly influence the membrane surface charge. 相似文献
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By means of a vacuum time-lag method, gas transport properties of apolyimide based on 2, 2- bis (3, 4- decarboxyphenyl ) hexafluoropropane dianhydride (6FDA )and meta- phenylenediamine (mPDA ) have been measured as a function of upstream pres-sure and temperature. The results show that no gas-induced plasticization occurs for thispolyimide in the upstream pressure range from 1 atm to 20atm. The temperature depen-dence of P and D can be described by the Arrhenius equations. The activation energiesof permeation and diffusion were obtained for the gas/polymer pair studied and correlatedwith the size of penetrant gas. 相似文献
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19.
A new family of eight poly(urethane-amide-imide) (PUAI) block copolymers with the same hard block and different soft blocks were synthesized in two steps from a dianhydride monomer containing amide functions (4,4′-methylene-bis(trimellitic anhydride-N-phenylamide)) and α,ω-dihydroxy telechelic oligomers which varied in both chemical structure (polyethers: PEG, PTMG, PPG; polyester: PCL) and molar weight (MW ≅ 600 or 1000 g/mol). The PUAI were obtained in high yields (ranging from 81 to 98 wt%) and with reduced viscosities which varied from 0.36 to 0.84 dL/g (for C = 1 mg/mL in DMF at 25 °C). Their characterization by FTIR and 1H NMR fully confirmed their chemical structure. Their solubility was typically limited to a few wt/vol% even in strong apolar diprotic solvents like DMF and NMP. This particular feature showed the very strong physical cross-linking of their very stiff hard block and enabled to cast membranes capable of withstanding exposure to many common organic solvents. Systematic permeability experiments showed that the PUAI membranes could be used to separate the azeotropic mixture EtOH (20 wt%)/ETBE very easily, with interesting prospects for the purification of ETBE (a fuel octane enhancer used instead of lead derivatives in the European Community). An analysis in terms of structure-property relationships pointed out that the soft block molar weight and polarity were two key parameters for the optimization of selective permeability. The best compromise was obtained with the soft block PEG1000. The corresponding polymer led to performances so far outstanding for polyamideimides with a very high flux of more than 1.1 kg/h m2 for a normalized thickness of 5 μm at 50 °C and a selectivity α = 22.7 in the high range for this kind of separation. 相似文献
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