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5 s hysteresis results from the formation of a Donnan potential at high pH which shifts the ionic equil
8 electrolyte concentration consistent with a Donnan potential due to the selective partitioning of io
9 solution-diffusion model taking into account Donnan exclusion and unhindered advection due to imperfe
10 the generic non-ideal competitive adsorption-Donnan (NICA-Donnan) model in addition to adsorption to
12 y enhancement is attributed to the amplified Donnan potential from the ionization of carboxyl and ami
14 ss, two Donnan effects, osmotic pressure and Donnan equilibrium potentials, are significantly amplifi
15 l dielectric effect isolated from steric and Donnan exclusion through fitted pore dielectric constant
17 electrostatic models (Gouy-Chapman-Stern and Donnan-plus-binding) used to compute electrical potentia
19 properties of the hemichannels (also cast as Donnan potentials) will produce either an accumulation o
22 the MXene channels is primarily affected by Donnan equilibrium at the membrane-solution interface.
23 ses between phases, generating the so-called Donnan electrical potential at the solution/membrane int
25 ncentrations determined with the soil column Donnan membrane technique in a range of soils varying in
27 s study reports an innovative ligand-enabled Donnan dialysis process to recover orthophosphate (P(V))
29 effects of improved size exclusion, enhanced Donnan exclusion, and suppressed hydrophobic interaction
30 ing ion selectivity through locally enhanced Donnan effects while remaining unaffected by variations
31 paper (75-mum thickness), a cation-exchange Donnan exclusion membrane (FKL), and a silver-foil worki
33 the transmembrane Cl(-) gradient: (i) fixed 'Donnan' charges inside and outside the cell; (ii) the pr
35 ecovery efficiencies were slightly lower for Donnan dialysis with real, alum-laden WAS, namely 45.1%
36 3-8), which is contrary to expectations from Donnan theory and the observed high rejection of salts.
39 quilibrium simultaneously to establish Gibbs-Donnan equilibrium in a polyelectrolyte-directed mineral
40 d solution-diffusion model that incorporates Donnan electrostatic exclusion of ions and unhindered ad
41 xyquinoline allowed sensing through inducing Donnan osmotic pressure and tuning its lattice spacing.
42 lt-polyelectrolyte preferential interaction (Donnan) coefficient (Gamma(u)coul) per polyion charge at
44 governed by steric exclusion and interfacial Donnan exclusion as well as EDL screening along the nano
48 acidification, and that an interior-negative Donnan potential is responsible for low endosomal [Cl-]
50 Such electroanalysis, based on the Nernst-Donnan equation, has been predominantly performed using
51 f the nonideal competitive adsorption (NICA)-Donnan model for organic matter (OM) coupled with the ge
52 predicted using both WHAM/Model VII and NICA-Donnan speciation models for both traditionally and mild
53 on-ideal competitive adsorption-Donnan (NICA-Donnan) model in addition to adsorption to hydrous ferri
54 Importantly, we established new generic NICA-Donnan parameters that substantially improved model accu
57 trode and a biocompatible and nonpolarizable Donnan exclusion anion-exchanger membrane reference/coun
58 mplementary approaches: a direct approach of Donnan equilibrium dialysis read out by atomic emission
61 cellular environment and a generalization of Donnan (electrostatic) equilibrium that accounts for act
62 echnical aspects describing the influence of Donnan equilibria on neuronal chloride ion (Cl(-)) distr
64 oncentrations below or above a set value of 'Donnan' charges, and show that at any value of these fix
67 antiscaling performance by combining strong Donnan exclusion through an AEM with ionic buffering in
69 lso indicated that for all membranes tested, Donnan theory provided an appropriate theoretical framew
70 eases in salt concentration, suggesting that Donnan osmotic pressure is negligible above this thresho
78 on of this membrane is dominated by both the Donnan effect and the size exclusion of the interspaces.
79 cellular milieu are negatively charged, the Donnan potential provides an additional driving force fo
80 solutions has two principal components: the Donnan contribution and a contribution due to protein-pr
83 -established ways to indirectly estimate the Donnan potential, it has been widely reported that it ca
85 established theoretical models including the Donnan theory and the Poisson-Boltzmann cylindrical cell
88 lysis further indicated that, because of the Donnan equilibrium at cation exchange membrane-anolyte/c
89 e report the first direct measurement of the Donnan potential of an ion exchange membrane equilibrate
90 Our results highlight the dependence of the Donnan potential on external salt concentration and coun
93 y, high solution concentrations suppress the Donnan exclusion effect of the charged RED membranes, se
94 ludes the electrostatic potential due to the Donnan equilibrium, which arises from the semipermeable
95 cation of glucose signal was ascribed to the Donnan exclusion and ensuing Nafion-gated ionic fluxes,
96 hat a MDP of up to -5 mV, in addition to the Donnan potential, may be generated at high workloads, ev
98 e amount of genome packaged by utilizing the Donnan potential (through increases in the capsid radius
102 Theoretical analysis of the relaxation to Donnan equilibrium utilized for such vesicle uptake assa
103 pecies to the protein hydrogel gives rise to Donnan potentials that change the hydrogel volume causin
106 ates counter ions in the polymer network via Donnan equilibrium and creates a sizeable osmotic pressu
108 nder higher feed salinities, due to weakened Donnan exclusion within the SCEM, and strong internal io
112 sed solubilization strategy was coupled with Donnan dialysis to recover P(V) into a clean sodium chlo