ライフサイエンスコーパス: anolyte

1 ynamically stable at low operating voltages (anolytes).

2 ontaminants compared to the rates of nitrate anolyte.

3 h m(-3) by switching from nitrate to sulfate anolyte.

4 ctrolytes that act as both the catholyte and anolyte.

5 om Ni catalyst, with 0.25 M H(2)SO(4) as the anolyte.

6 cted from overoxidation in the ammonia-based anolyte.

7 n principles for future classes of MCC-based anolytes.

8 s at BDD anodes in sulfate and inert nitrate anolytes.

9 for higher levels of degradation in certain anolytes.

10 ll testing, where a concentrated Fe-NTMPA(2) anolyte (0.67 M) is paired with a Fe-CN catholyte, demon

11 system integrates a neutral bacteria-driven anolyte, a basic electrolyte bridge, and an acidic catho

12 pparently resulted via neutralization of the anolyte acid, H2SO4, by reaction with the base mineral s

13 e/catholyte interfaces, the Na(+) ion in the anolyte actually facilitates the transport of NH4(+) ion

14 mmol) with electrolytes of 0.5 M KOH for the anolyte and 0.5 M NaCl for the catholyte with a constant

15 enhanced concentration of circa 3.2 m in the anolyte and a relatively low redox potential of 2.2 V vs

16 s arising from the pH difference between the anolyte and catholyte remained relatively constant durin

17 m, exploiting derivatized fullerenes as both anolyte and catholyte species in a series of battery cel

18 ading to relatively stable pH values in both anolyte and catholyte.

19 ng an ion-immobilized polymer electrolyte as anolyte and organic solvent as catholyte.

20 his issue may be addressed by separating the anolyte and the catholyte with a membrane that only allo

21 mpeded by a lack of electroactive compounds (anolytes and catholytes) with the necessary combination

22 These anolytes are coupled with 2,4,6-tri-(1-cyclohexyloxy-4-i

23 te concentrations, solution conductivity, or anolyte buffer capacity at applied voltages up to 1.1 V,

24 te concentrations, solution conductivity, or anolyte buffer capacity at applied voltages up to 1.1 V,

25 ve enabled the identification of a promising anolyte candidate for NRFBs and have also provided key i

26 A combination of cyclic voltammetry of anolyte candidates and independent synthesis of their co

27 nnan equilibrium at cation exchange membrane-anolyte/catholyte interfaces, the Na(+) ion in the anoly

28 fluidic flow-through configuration: a porous anolyte chamber is formed by filling a microfluidic cham

29 ate increased from 0.8 to 1.6 m(3)-H(2)/m(3)-anolyte/day for seawater and river water flow rates rang

30 Herein, we present a low potential anolyte design by using Na substituted phosphotungstic a

31 e separated effectively from the REEs in the anolyte, favoring REE extraction and allowing sustainabl

32 )2 TTz]Cl4 , as a novel two-electron storage anolyte for aqueous organic redox flow battery (AORFB) a

33 deep-eutectic-solvent is investigated as an anolyte for redox-flow batteries.

34 low-reduction potential, and high-solubility anolytes for nonaqueous redox flow batteries (NARFBs).

35 ss of metal-coordination complexes (MCCs) as anolytes for NRFBs.

36 Furthermore, separation of the pure alcohol anolyte from the aqueous catholyte minimizes competing o

37 grid storage systems, but the development of anolytes has lagged far behind that of catholytes due to

38 and corrosion nature of anthraquinone-based anolytes in reported acidic and alkaline AORFBs constitu

39 One drop of bacteria-containing anolyte into the anodic inlet and another drop of potass

40 onic diammonium salt AQDS(NH(4) )(2) , as an anolyte material for pH-neutral AORFBs with solubility o

41 CBu)(2) V, as a highly stable, high capacity anolyte material under near pH neutral conditions.

42 ess led to the identification of a promising anolyte material, N-methyl 4-acetylpyridinium tetrafluor

43 nts the use of the hybrid molecules as novel anolyte materials for nonaqueous redox-flow batteries.

44 anthraquinone molecules represent promising anolyte materials in aqueous organic redox flow batterie

45 tionary design of a series of pyridine-based anolyte materials that exhibit up to two reversible redo

46 However, soluble anolyte materials that undergo reversible redox processe

47 ic modifications to improve the stability of anolyte materials under the targeted conditions.

48 tteries based on these fluorenone derivative anolytes operate efficiently and exhibit stable long-ter

49 the system tends to acidify (or basify) the anolyte (or catholyte), their effects are buffered by a

50 rolytes that undergo redox events at as low (anolyte) or high (catholyte) potentials as possible whil

51 However, liquid anolyte permeation to the cathode causes salt precipitat

52 ver 150 h operation at 100 mA cm(-2) without anolyte replenishment.

53 When paired with methyl viologen (MV) as an anolyte, resulting FcNCl/MV and FcN2Br2/MV AORFBs were o

54 environmentally benign deep-eutectic-solvent anolytes reveals great potential towards cost-effective,

55 Near-neutral-pH RFBs employing a viologen anolyte, (SPr)(2)V, in excess with the [Fe(bpy)(3)](2+/3

56 both the anode-based biofilm (55.1%) and the anolyte suspension (87.9%) with the remaining biovolume

57 alanced electrolyte with a more concentrated anolyte than a catholyte.

58 the identification of a new pyridinium-based anolyte that undergoes 1e(-) electrochemical charge-disc

59 didate was paired with a viologen derivative anolyte to achieve a proof-of-concept all-organic flow b

60 rials on the water profile direction and the anolyte to catholyte filtrate ratio.

61 ncreased sodium ion transport (52%) from the anolyte to the catholyte rather than through a change in

62 s redox flow cell with butyl viologen as the anolyte to yield a 2.0 V battery.

63 cellent cycling stability making it an ideal anolyte toward the development of energy-dense RFBs.

64 continuously regenerated thin stillage, the anolyte was concentrated to 14 g/L acetic acid, and conv

65 with S. frigidimarina was observed when the anolyte was half-strength marine broth (1/2 MB) (0.28 mu

66 This anolyte was paired with N-(2-(2-methoxyethoxy)-ethyl)phe

67 A library of 24 potential bipyrimidine anolytes were synthesized and systematically evaluated t

68 binary solvent system to enable a long-lived anolyte which exhibited no fade over 350 cycles.

69 onia diffusion from the catholyte toward the anolyte, will help effective design and operation of bio

70 of a bromide catholyte and an ethyl viologen anolyte with the addition of tetrabutylammonium bromide.

71 vestigate the utility of phosphine oxides as anolytes with extremely negative potentials.

72 transition of oxidized catholyte (or reduced anolyte) with confinement in the pores of electrodes.