ライフサイエンスコーパス: electrolyte solution

1 fabrication until dissolved by an ultrapure electrolyte solution.

2 opy (SEM), and resistance measurements in an electrolyte solution.

3 with a contact (reference) electrode and an electrolyte solution.

4 provided for high-resolution STM imaging in electrolyte solution.

5 ate perfusion of the jejunum with a balanced electrolyte solution.

6 above by immersing them in a TPrA-containing electrolyte solution.

7 dium or water during perfusion of a balanced electrolyte solution.

8 ss polar medium than that of the surrounding electrolyte solution.

9 and LiNi(0.5)Mn(1.5)O4 (LNMO)) into the same electrolyte solution.

10 face between porous carbon electrodes and an electrolyte solution.

11 trode (NiO-RuRe) was confirmed in an aqueous electrolyte solution.

12 limited if the surface is in contact with an electrolyte solution.

13 rce by simple modification of the sustaining electrolyte solution.

14 ppropriately selecting the salt anion in the electrolyte solution.

15 urrent signals of a redox probe taken in the electrolyte solution.

16 ional reference electrode with its reference electrolyte solution.

17 ated for the first time in the absence of an electrolyte solution.

18 on on unpatterned substrates in an isotropic electrolyte solution.

19 in the whole membrane was influenced by the electrolyte solution.

20 nanopores can transiently localize DNA in an electrolyte solution.

21 is designed to modulate the properties of an electrolyte solution.

22 ing the electric field within the contacting electrolyte solution.

23 (-)] = 0.15 M, [Ca(2+)] = 0 - 75 mM) aqueous electrolyte solutions.

24 ty measurements of the interface between two electrolyte solutions.

25 ater at the Ag-water interface in NaF and KF electrolyte solutions.

26 te the photophysics and chemistry of aqueous electrolyte solutions.

27 sisted anion transfer between two immiscible electrolyte solutions.

28 ubstituted tetraphenylborate in both aqueous electrolyte solutions.

29 f Li2O2 in low-polarity and weakly solvating electrolyte solutions.

30 cles at the interface between two immiscible electrolyte solutions.

31 , perchlorate-, sulfate-, and chloride-based electrolyte solutions.

32 trends in mean activity coefficients of the electrolyte solutions.

33 ke on the role of ions in traditional dilute electrolyte solutions.

34 charged redox species as expected for dilute electrolyte solutions.

35 -supported interfaces between two immiscible electrolyte solutions.

36 ase (SCD) lyse in deoxygenated isosmotic non-electrolyte solutions.

37 whereas the water uptake was lower in 0.1 M electrolyte solutions.

38 t surface layers transferrable to fresh base electrolyte solutions.

39 balt oxide materials from phosphate-buffered electrolyte solutions.

40 ons, followed by flushing with particle-free electrolyte solutions.

41 ion increases dramatically on > 30-muM inert electrolyte solutions.

42 enzoyl peroxide as a coreactant in the above electrolyte solutions.

43 ties of the interface between two immiscible electrolyte solutions, 1,2-dichloroethane-H2O.

44 After filling the open channels with electrolyte solution, a meniscus forms at the end of the

45 efficiency of the calcium pump in background electrolyte solutions, a complexometric titration with k

46 rted ITIES (interface between two immiscible electrolyte solutions, also called a liquid/liquid (L/L)

47 serted inside a nanopipette probe containing electrolyte solution and a second electrode placed in a

48 The other barrel was filled with an electrolyte solution and Ag/AgCl electrode as part of a

49 ccelerated the redox couple diffusion in the electrolyte solution and improved charge transfer at the

50 region between the electrode surface and the electrolyte solution and is often characterized by numer

51 ion of uncompensated ohmic resistance of the electrolyte solution and of the adsorbed film, as distin

52 s a dual-barrel theta pipet probe containing electrolyte solution and quasi-reference counter electro

53 ollowing their first contact with an aqueous electrolyte solution and used these transients to determ

54 do not simply form coils in acidic or strong electrolyte solutions and elongated structures in dilute

55 se nanoparticles can be transferred to fresh electrolyte solutions and there exhibit stable ferrocene

56 NMs by allowing the membrane to separate two electrolyte solutions and using an electrode in each sol

57 fusion of shed blood, crystalloids (balanced electrolyte solution), and norepinephrine support.

58 Above the membrane, there is an electrolyte solution, and a gold counterelectrode.

59 endence of the applied potentials within the electrolyte solution, and most importantly the shift of

60 led pipet and filling the open channels with electrolyte solution, and quasi-reference counter electr

61 ally, conditioning creates free Cl(-) in the electrolyte solution, and we suggest the free Cl(-) adso

62 by placing the nanotube membrane between two electrolyte solutions, applying a transmembrane potentia

63 ractions of Mn(3+) in the aprotic nonaqueous electrolyte solution are constant over the duration of o

64 Voltammetric investigations in the electrolyte solutions are used to confirm the magnitude

65 tral tert-butyl alcohol is added to all cITP electrolyte solutions as an internal reference.

66 tion potential between two mutually miscible electrolyte solutions, as commonly described with the He

67 olutions in the pH range of 3-14, in <250 mM electrolyte solutions, at high and low temperatures (95

68 ive to electric double layer interactions in electrolyte solutions, but provides only a qualitative v

69 out electron transfer between two immiscible electrolyte solutions, but to the best of our knowledge,

70 tips in air by electrostatic discharge or in electrolyte solution by electrochemical etching.

71 mum in the surface tension of dilute aqueous electrolyte solutions by Jones and Ray in the 1930s is c

72 ween the nanochannel surface and the aqueous electrolyte solution, causing significant changes in mea

73 cycling between 3.5 and 4.5 V vs Li/Li(+) in electrolyte solution containing 1 M LiPF6 or LiClO4 in 1

74 ractive force between identical macroions in electrolyte solutions containing divalent counterions.

75 In serum-like electrolyte solutions containing physiologically relevan

76 ane (100-nm-diam pore size) hydrated with an electrolyte solution, containing a redox-active probe mo

77 l h(-1), chylous lymph) or a dextrose and/or electrolyte solution (control lymph).

78 In pH 2 citrate buffer with added NaClO4 electrolyte, solution cyclic voltammetry of these nanopa

79 Measurements were performed in aqueous electrolyte solutions depending on ionic strength and pH

80 Laplace's equation has been solved for the electrolyte solution for a range of tip geometries, enab

81 ygen-carrying blood substitute, colloid, and electrolyte solution for limited fluid resuscitation wit

82 isms for ethylene carbonate (EC) molecule in electrolyte solutions for lithium-ion batteries are comp

83 , which is contacted at its edges by aqueous electrolyte solution, has been characterized electrochem

84 Previous NO gas sensors that employ internal electrolyte solutions have been assembled using acidic i

85 Mechanisms of nucleation from electrolyte solutions have been debated for more than a

86 Electrolyte solutions having pH, pNa, or pLi values of 0

87 e range of current densities in contact with electrolyte solutions, IEDEM behave as ideally non-polar

88 ly, when sufficient voltage is applied to an electrolyte solution in which a BPE is immersed, the pot

89 simultaneously by applying a voltage to the electrolyte solution in which the BPE array is immersed.

90 These junctions may operate in gas phase or electrolyte solution (in situ).

91 from the sensor surface and the salinity of electrolyte solution, in the framework of both linear an

92 a liquid/liquid interface between immiscible electrolyte solutions, in which the ion transfer approac

93 ene and the electrochemical potential of the electrolyte solution, indicating that the n-Si/Graphene

94 electrolyte cations at the nanoparticle film/electrolyte solution interface.

95 crom) containing an electroactive species in electrolyte solution is brought to a sample electrode su

96 anowires (SiNWs) in physiologically relevant electrolyte solution is demonstrated.

97 The viscosity of a supercritical electrolyte solution is measured for the first time usin

98 approach for positioning the UME in aqueous electrolyte solution is presented using either changes o

99 o promote solution-phase discharge in stable electrolyte solutions is a central challenge for develop

100 ctions between proteins and nanoparticles in electrolyte solutions is crucial for advancing biologica

101 t across an interface between two immiscible electrolyte solutions (ITIES) and its diffusion into the

102 -supported interfaces between two immiscible electrolyte solutions (ITIES) as tips.

103 A nanoscale interface between two immiscible electrolyte solutions (ITIES) provides a unique analytic

104 t-supported interface between two immiscible electrolyte solutions (ITIES) to reveal the important io

105 t-supported interface between two immiscible electrolyte solutions (ITIES) were carried out, and the

106 nanoscale interfaces between two immiscible electrolyte solutions (ITIES).

107 ated at the interface between two immiscible electrolyte solutions (ITIES).

108 arboxylate) followed by soaking in a typical electrolyte solution leads to the new solid lithium elec

109 on (IGL-1) is an emerging extracellular-type electrolyte solution, low in viscosity, containing polye

110 to humidity prior to their first contact to electrolyte solution minimizes the initial (reproducible

111 tinum UME remains unchanged from the aqueous electrolyte solution mixed potential until approximately

112 ay of microinterfaces between two immiscible electrolyte solutions (mu-ITIES).

113 microscale interfaces between two immiscible electrolyte solutions (muITIES) were formed using glass

114 ay of microinterfaces between two immiscible electrolyte solutions (muITIES).

115 rrayed nanointerfaces between two immiscible electrolyte solutions (nanoITIES) was achieved.

116 across nanointerfaces between two immiscible electrolyte solutions (nanoITIES); (2) combined atomic f

117 rine at a ratio of 5:1 are simulated in NaCl electrolyte solutions of different concentration using t

118 nt dissolved manganese cation in LiPF6-based electrolyte solutions of Li-ion batteries with lithium m

119 emical behaviour of caffeine was examined in electrolyte solutions of phosphate buffer saline, sodium

120 on-bridged cations in the ion atmosphere for electrolyte solutions of salts with reduced activity.

121 ing pipet electrodes filled with the organic electrolyte solutions of their tetrakis(4-chlorophenyl)b

122 s a highly active electrocatalyst in aqueous electrolyte solution (overpotential of approximately 200

123 This novel design is based on the flow of electrolyte solution past a microwire electrode situated

124 The model accurately captures electrolyte solution pH and conductivity, including impo

125 tients received either a polyethylene glycol electrolyte solution preparation or a phospho-soda prepa

126 ss residual fluid than a polyethylene glycol electrolyte solution preparation.

127 ol subjects who ingested polyethylene glycol electrolyte solution prior to imaging.

128 anodic polarization using an inner alkaline electrolyte solution provides the basis for improved sel

129 pH 7 and under conditions of flowing aqueous electrolyte solutions ranging in NaCl concentrations fro

130 OM carbon, filling of the 3DOM pores with an electrolyte solution results in a nanostructured materia

131 rgo sol-gel transition in the presence of an electrolyte solution such as biological fluids and salts

132 ons of the liquid-vapor interface of aqueous electrolyte solutions suggest that ions little larger th

133 (often of the brand named Vycor) contain the electrolyte solution that forms a salt bridge between th

134 s glass plugs are widely used to contain the electrolyte solution that forms a salt bridge between th

135 d poly(vinyl chloride) (PVC) membrane and an electrolyte solution that was triggered via the oxidatio

136 y on Pt electrodes from CH(3)CN/Bu(4)NClO(4) electrolyte solutions that films comprised of 1-2 monola

137 opipette is positioned close to a surface in electrolyte solution, the direct ion current (DC), drive

138 al expectations, for charged macroions in an electrolyte solution, the entropic force is repulsive at

139 In electrolyte solutions, these silicas show the same expon

140 nsfer of charge-compensating anions from the electrolyte solution to the monolayer nanoparticle "phas

141 eposited MWNTs were then rinsed at different electrolyte solutions to induce the release of MWNTs fro

142 nstrated by switching the conductivity of an electrolyte solution up and down.

143 cts on characteristic time scale in a binary electrolyte solution using parallel plate electrode conf

144 lavage with warmed polyethylene glycol 3350/electrolyte solution via the ileostomy and postoperative

145 ition from gas-phase clusters to behavior of electrolyte solutions was clearly revealed, and the larg

146 Nine carbohydrate-electrolyte solutions were perfused at the rate of 15 mL

147 a generator-collector device submerged in an electrolyte solution, were carried out to calibrate the

148 The 2D crystalline systems form in aqueous electrolyte solution, which provides a high dielectric e

149 noise in baseline conductance upon mixing an electrolyte solution with water, and dispersion/relative

150 Electrolyte solutions with high concentrations of ions a

151 uantification of supported lipid bilayers in electrolyte solutions with nanoscale spatial resolution.

152 iquids are expected to behave as dilute weak electrolyte solutions, with typical effective dissociate

153 cles can be transferred to nanoparticle-free electrolyte solutions without desorption and ferrocene v