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1 ontaminants compared to the rates of nitrate anolyte.
2 h m(-3) by switching from nitrate to sulfate anolyte.
3 n principles for future classes of MCC-based anolytes.
4 s at BDD anodes in sulfate and inert nitrate anolytes.
5 pparently resulted via neutralization of the anolyte acid, H2SO4, by reaction with the base mineral s
6 e/catholyte interfaces, the Na(+) ion in the anolyte actually facilitates the transport of NH4(+) ion
7 enhanced concentration of circa 3.2 m in the anolyte and a relatively low redox potential of 2.2 V vs
8 m, exploiting derivatized fullerenes as both anolyte and catholyte species in a series of battery cel
10 mpeded by a lack of electroactive compounds (anolytes and catholytes) with the necessary combination
11 ve enabled the identification of a promising anolyte candidate for NRFBs and have also provided key i
13 nnan equilibrium at cation exchange membrane-anolyte/catholyte interfaces, the Na(+) ion in the anoly
14 fluidic flow-through configuration: a porous anolyte chamber is formed by filling a microfluidic cham
15 ate increased from 0.8 to 1.6 m(3)-H(2)/m(3)-anolyte/day for seawater and river water flow rates rang
16 e separated effectively from the REEs in the anolyte, favoring REE extraction and allowing sustainabl
17 )2 TTz]Cl4 , as a novel two-electron storage anolyte for aqueous organic redox flow battery (AORFB) a
20 grid storage systems, but the development of anolytes has lagged far behind that of catholytes due to
22 ess led to the identification of a promising anolyte material, N-methyl 4-acetylpyridinium tetrafluor
23 tionary design of a series of pyridine-based anolyte materials that exhibit up to two reversible redo
26 the system tends to acidify (or basify) the anolyte (or catholyte), their effects are buffered by a
27 rolytes that undergo redox events at as low (anolyte) or high (catholyte) potentials as possible whil
28 When paired with methyl viologen (MV) as an anolyte, resulting FcNCl/MV and FcN2Br2/MV AORFBs were o
29 environmentally benign deep-eutectic-solvent anolytes reveals great potential towards cost-effective,
30 both the anode-based biofilm (55.1%) and the anolyte suspension (87.9%) with the remaining biovolume
31 the identification of a new pyridinium-based anolyte that undergoes 1e(-) electrochemical charge-disc
33 continuously regenerated thin stillage, the anolyte was concentrated to 14 g/L acetic acid, and conv
34 with S. frigidimarina was observed when the anolyte was half-strength marine broth (1/2 MB) (0.28 mu
35 onia diffusion from the catholyte toward the anolyte, will help effective design and operation of bio
36 of a bromide catholyte and an ethyl viologen anolyte with the addition of tetrabutylammonium bromide.
37 transition of oxidized catholyte (or reduced anolyte) with confinement in the pores of electrodes.
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