ライフサイエンスコーパス: Nafion

1 n events occurring in hydrophobic domains of Nafion.

2 red with the best proton conductors, such as Nafion.

3 modified with carbon nanotubes dispersed in nafion.

4 re evaluated by measuring permeation through Nafion.

5 rosulfonic acid polymer chains that comprise Nafion.

6 shed small-angle scattering data of hydrated Nafion.

7 lassy carbon working electrode modified with Nafion.

8 cess of the 1.58 g/cm3 commonly employed for Nafion.

9 for the Nafion-silica films relative to pure Nafion.

10 The film was then coated with Nafion.

11 also exceed those of biological channels and Nafion.

12 ugh ostensibly impermeable membranes such as Nafion.

13 en deposited as an ink with carbon black and Nafion.

14 PEDOT (poly(3,4-ethylenedioxythiophene) and Nafion.

15 ive way without using any glucose oxidase or nafion.

16 with cathodes prepared from TBA(+) modified Nafion.

17 he mixture of multiwall carbon nanotubes and nafion.

18 densities of commercial Nafion 117 and cast Nafion 1100 films were determined by the hydrostatic wei

19 The density of acid-pretreated Nafion 1100 was constant at 1.95 +/- 0.03 g/cm3 for all

20 f the model is appropriate for water-treated Nafion 1100.

21 cular transport in an ion-exchange membrane (Nafion, 1100 equiv wt) has been studied using a scanning

22 The densities of commercial Nafion 117 and cast Nafion 1100 films were determined by

23 ion characterizes density for the commercial Nafion 117 films.

24 The structure of Nafion 211 after reaction with H(*) or HO(*) was determi

25 ade possible by determining the structure of Nafion 211 using calibrated (19)F magic angle spinning n

26 perfluorinated sulfonated ionomer membrane, Nafion 211, is described.

27 membrane exhibits higher power density than Nafion 212 membrane, but with a comparative weight of on

28 AA to the electrode surface, a thin layer of Nafion, a cation exchange polymer, has been electrodepos

29 those at carbon fiber electrodes coated with Nafion, a perfluorinated ion-exchange material.

30 ts greater than nanotube-Nafion and graphene-Nafion actuators and continuous operation for more than

31 on for more than 5 hours is observed for TMD-Nafion actuators.

32 ls of MWCNTs and the hydrophobic backbone of Nafion allows the MWCNTs to be dispersed in Nafion, whic

33 ovement in signal was obtained compared with Nafion alone.

34 of lactate sensitive electrode made without Nafion analogue.

35 ver, when a substrate is prepared using both Nafion and a hydrophilic, high-molecular-weight polymer,

36 Thin films of a composite of nafion and carbon microparticles have been deposited on

37 tienzyme systems immobilized to solvent cast Nafion and cellulose acetate-modified Pt.

38 ric oxide sensors have been fabricated using Nafion and electropolymerized polyeugenol or o-phenylene

39 The presence of Nafion and fluoride during the electrochemical polymeriz

40 y(methylene blue)/tetrabutylammonium bromide/Nafion and glutaraldehyde (3D bioanode electrode).

41 ncy, tip displacements greater than nanotube-Nafion and graphene-Nafion actuators and continuous oper

42 fast diffusion of water and protons through Nafion and its persistence at low temperatures.

43 ruthenium(II) (Ru(bpy)3 2+) ion-exchanged in Nafion and Nafion-silica composite materials have been i

44 over 100 hours, surpassing both the baseline Nafion and platinum-containing recast Nafion membranes.

45 A Nafion and poly(3,4-ethylenedioxythiophene) (PEDOT) cont

46 Spectra are reported for thermally processed Nafion and related perfluoroalkyl ionomer materials cont

47 prototype TAML activator, carbon black, and Nafion and the subsequent use of this composition in het

48 pores filled with the ion-selective polymer Nafion) and a biological membrane (hairless mouse skin)

49 is not reversible for the chosen model film (Nafion) and sample (Ru(bpy)(3)(2+)) but it can be regene

50 th poly(3,4-ethylenedioxythiophene) (PEDOT), Nafion, and multi-walled carbon nanotubes were tested in

51 des, covered with an anionic polyelectrolyte Nafion, and their electrochemical properties were probed

52 cial and long-range structural properties of Nafion are affected by the material with which it is in

53 g, both dip-coating and electrodeposition of Nafion are associated with substantial fouling, similar

54 The side chains of Nafion are terminated by sulfonate groups with sodium co

55 glassy carbon rotating disk electrode using Nafion as a binder.

56 fabricated as a three electrode system with Nafion as a proton exchange membrane (PEM).

57 MWCNT-Polyhis/GOx) bilayers and one layer of Nafion as anti-interferent barrier.

58 hree orders of magnitude higher than that of Nafion at low humidity.

59 afion was in contact with a PtO surface, the Nafion at the Pt interface became hydrophilic.

60 tivity and fouling resistance to electrodes: Nafion, base-hydrolyzed cellulose acetate (BCA), and fib

61 dent binding ability of DAP2+ is retained in Nafion, but the selectivity is considerably different.

62 sed on selective permeation of water through Nafion can thus be enhanced by cooling the membrane.

63 iron porphyrin immobilized into a conductive Nafion/carbon powder layer is a stable cathode producing

64 s with PdHx proton conducting contacts and a Nafion channel achieve 25 ms spiking, short term depress

65 alated cation and the sulfonate sites of the Nafion characterizes density for the commercial Nafion 1

66 uL min(-1) flow rate of 6 mm i.d. pumps with Nafion coated electrodes operate daily for 5 min at 1 V

67 Two types of PEDOT:Nafion coated electrodes were then analyzed electrochemi

68 PEDOT:Nafion-coated electrodes made using 200 muM EDOT exhibit

69 PEDOT:Nafion-coated electrodes were lowered into the nucleus a

70 Nafion-coated elliptical electrodes have previously been

71 e reductase held by dialysis membrane onto a Nafion-coated glassy carbon electrode.

72 ric acids was eliminated by application of a Nafion-coated membrane.

73 oxydopamine, fast-scan cyclic voltammetry at Nafion-coated, carbon-fiber microelectrodes was used to

74 d the procedure for fabricating cylindrical, Nafion-coated, carbon-fiber microelectrodes.

75 The thickness of the Nafion coating and a diffusion coefficient (D) in the fi

76 affeine was examined at GCE without and with Nafion coating, to exclude interferences, and the sensor

77 The response time of a SiO2/ZrO2-Nafion composite (sensor 2) was short (5 s), and a small

78 ach are films of porous sol-gel SiO2 or SiO2-Nafion composite doped with low-pKa indicators.

79 ted with a cation-selective, sol-gel-derived Nafion composite film designed for the detection of a mo

80 fied with single walled carbon nanotubes and nafion composite film is delineated for the first time t

81 osensing layer was placed onto a polyaniline-Nafion composite platinum electrode and covered with a c

82 equently bonding with water, not possible in Nafion composites based on carbon nanotube and graphene.

83 od for the determination of caffeine using a Nafion covered lead film electrode.

84 Nafion crystallites (approximately 10 vol%), which form

85 Experiments suggest that Nafion degradation is caused by generation of trace radi

86 he sulphonated tetrafluoroethylene copolymer Nafion developed by DuPont in the late 1960s, with a hig

87 The Nafion doped sols were spin cast on glassy carbon electr

88 considerably higher and more stable than the Nafion dryer (81.3-94.5%).

89 grees C are conveniently reached by use of a Nafion dryer operated at approximately 0 degree C.

90 ciency of the Desolvator and frequently used Nafion dryer, the removal efficiency of the Desolvator s

91 Water vapor is removed using a heated nafion dryer.

92 Rh(III)) complex, immobilized within a MWCNT/Nafion electrode, and its integration into a molecular c

93 ilization of alcohol dehydrogenase (ADH) via Nafion entrapment, with excellent analytical characteris

94 approximately 5 microm in radius coated with Nafion-entrapped solgel-derived silica (Nafion-silica) c

95 a permanent increase in the thickness of the Nafion film and a decrease in the scattering length dens

96 vely expanded the electrode surface into the Nafion film and thereby reduced the diffusion distance o

97 The microsensors were coated with a thin Nafion film before use.

98 n the optically transparent charge-selective Nafion film coating the electrode.

99 tration of Nafion, the sensitivity of the F2/Nafion film electrodes (reagentless biosensors) to gluco

100 afion overcoat reduced the sensitivity of F1/Nafion film electrodes to NADH by >98%.

101 he uptake of aqueous Fe2+ by the bipy-loaded Nafion film is reported.

102 A Nafion film loaded with novel catalyst-free multiwalled

103 immobilizing the PtPd-MWCNTs catalysts in a Nafion film on a glassy carbon electrode.

104 y immobilizing PtM/MWCNTs nanocatalysts in a Nafion film on a glassy carbon electrode.

105 measured absorbance on sample flow rate and Nafion film thickness, and also provide calibration curv

106 tin oxide (ITO) sensor platform with a 50 nm Nafion film to preconcentrate the analytes, equimolar mi

107 The presence of the Nafion film was confirmed with environmental scanning el

108 d to characterize the structure of the MWCNT-Nafion film, followed by electrochemical characterizatio

109 ically at a platinum electrode coated with a Nafion film, while the acidification rate is measured po

110 enzyme-polymer film between an electrode and Nafion film.

111 odified with a thin iron hydroxide-decorated Nafion film.

112 e attributed to irreversible swelling of the Nafion film.

113 d optical response of the complex ion in the Nafion film.

114 n the surface of a graphite electrode with a Nafion film.

115 y)(3)(2+)] that employs ultrathin (24-50 nm) Nafion films as the charge-selective layer.

116 Electrodes modified with Nafion films containing 2,7-dimethyldiazapyrenium (DAP2+

117 ed on a glassy carbon electrode surface with Nafion films employed to sandwich the layer of biologica

118 to the dip-coating procedures employed with Nafion films that lead to nonuniform coatings at cylindr

119 Evidence of physical changes of aged Nafion films was obtained, and the results showed a perm

120 ally, the degree of bundling of the SWNTs in Nafion films was probed with the 1H-13C CP-MAS technique

121 he direct incorporation of [Ru(bpy)3]2+ into Nafion films without the need for subsequent loading.

122 are crucial for the mechanical properties of Nafion films, are elongated and parallel to the water ch

123 When immobilized in Nafion films, the turnover frequencies for the 4e(-)/4H(

124 Their accumulation is reduced by applying Nafion-films to the electrodes.

125 findings showed that electrodes treated with Nafion first, followed by o-PD, were very sensitive to N

126 The result is a Nafion-free, room-temperature fuel cell that has the hig

127 kinetics in the nanoscopic water channels of Nafion fuel cell membranes at various hydration levels a

128 ascribed to the Donnan exclusion and ensuing Nafion-gated ionic fluxes, which enhanced enzyme activit

129 The interface properties of the CNF/Nafion/GC were characterized by electrochemical impedanc

130 C electrode, the CNF/Nafion modified GC (CNF/Nafion/GC) electrode improved the sensitivity for lead d

131 Thin, free-standing films of Nafion gel and Nafion that were sufficiently clear to re

132 Preconcentration factors into Nafion gel and Nafion were 350 and 50, respectively, aft

133 tive analogue of a heart imaging agent, with Nafion gel, which is Nafion plasticized with tri-n-butyl

134 on, the well-defined cyclic voltammograms at Nafion gel-modified electrodes exhibit diffusion-control

135 The formal reduction potential at Nafion gel-modified electrodes is shifted positively com

136 hancement of approximately 4 was observed at Nafion gel-modified spectroscopic graphite over a bare e

137 ential pulse voltammetry vs concentration at Nafion gel-modified spectroscopic graphite was linear in

138 ws a more rapid uptake of the complex by the Nafion gel.

139 te possible sensor performance enhancements, Nafion giving the most satisfactory results.

140 lation of an aqueous suspension comprised of Nafion, graphite oxide, and chloroplatinic acid to form

141 ack to the hydroxamic acid by treatment with Nafion-H in 2-propanol.

142 In contrast, Ni-TMPP electrodes (with Nafion) had significantly poorer detection limits (76 +/

143 .0 x 10(-2) S cm(-1) at 115 degrees C, while Nafion has a conductivity of 3.3 x 10(-2) S cm(-1) at th

144 sparent electrode coated with a thin film of Nafion has been demonstrated for the determination of aq

145 Although Nafion has been suggested to resist fouling, both dip-co

146 of GOx, and the permselective properties of Nafion have allowed building up a sensitive, selective,

147 osely related to the segmental motion of the Nafion host matrix.

148 nce and the stability of the ensuing xerogel/Nafion hybrid film are evaluated.

149 ucting membranes are well established (e.g., Nafion), hydroxide conducting membranes (alkaline anion

150 Nafion imparts increased sensitivity for dopamine and no

151 olution of ethylenedioxythiophene (EDOT) and Nafion in acetonitrile.

152 Furthermore, the films were as effective as Nafion in the attenuation of the response to ascorbate a

153 2+) was complexed with 2,2'-bipyridyl in the Nafion in the film to form an intense red complex that w

154 new model can explain important features of Nafion, including fast diffusion of water and protons th

155 Simulations for various other models of Nafion, including Gierke's cluster and the polymer-bundl

156 the films strongly depends on the amount of Nafion incorporated into the hybrid sol.

157 It is shown that Nafion increases the sensitivity of the technique while

158 ween the enzyme activity-pH profiles and the Nafion-induced pH increase in the underlying chitosan fi

159 In addition, the effects of incorporating Nafion into the xerogel matrix on sensor performance and

160 was also strongly dependent on the amount of Nafion introduced into the composite with greater ECL ob

161 Nafion-silica films with a low content of Nafion ion-exchanged less Ru(bpy)3 2+ and exhibited tail

162 When benchmarked against the 1100 EW Nafion ionomer in glucose/air enzymatic fuel cells (EFCs

163 The structure of the Nafion ionomer used in proton-exchange membranes of H(2)

164 ving intermediates that might be formed when Nafion is exposed to H(2) (or H(+)) and O(2) in the pres

165 to benefit a wide variety of studies because Nafion is so commonly used in electroanalytical chemistr

166 ort side chain Aquivion ionomers relative to Nafion is traced to effects of ionomer ion-exchange capa

167 A nanojunction [cation-selective material (Nafion)] is patterned along the tilted concentrated chan

168 -bipyridyl)ruthenium(II), [Ru(bpy)3]2+, into Nafion Langmuir-Schaefer (LS) films is described.

169 Combination with a previously applied nafion layer did not protect the sensors against acute b

170 ic and hydrophilic domains formed within the Nafion layer when equilibrated with saturated D(2)O vapo

171 thyl viologen was allowed to absorb into the Nafion layer, which acted as a reservoir for the electro

172 rmediate chitosan layer, along with an outer Nafion layer.

173 trode modified with lead film recovered by a Nafion layer.

174 Nafion LS films (tens of nanometers thick) were formed o

175 e oxidase were deposited on the surface in a Nafion matrix to stabilize the enzyme as well as to prev

176 lute H2SO4 were sprayed onto both sides of a Nafion membrane and dried to fabricate flexible solid-st

177 uantum mechanics (QM) mechanistic studies of Nafion membrane degradation in a polymer electrolyte mem

178 A Nafion membrane diffusion scrubber (DS) is used with hem

179 A temperature-controlled high-efficiency Nafion membrane diffusion scrubber is used to collect ga

180 ss spectrometry incorporating a hollow-fiber Nafion membrane has been evaluated for the determination

181 sections joined with each other via tubular Nafion membrane insertions.

182 (working electrode) inserted into a tubular Nafion membrane is described, which confines the sample

183 in equilibrium with sorption sites within a Nafion membrane is given by log P(WN) = -3580/T + 10.01,

184 The hydrophilic Nafion membrane preferentially transports methanol and e

185 The modified Nafion membrane provided the best electrical communicati

186 high-efficiency proton transport through the Nafion membrane separator: The ohmic drop loss is only 0

187 n platinum sputtered on a filter paper and a Nafion membrane to immobilize the enzyme glucose oxidase

188 ase membrane inlet mass spectrometry using a Nafion membrane to the monitoring of a chloroform recove

189 cases tested, but the required length of the Nafion membrane was 4 times greater for the more sensiti

190 e separated by a strip of ion perm-selective Nafion membrane which plays the role of nanofluidic pote

191 To reach this goal, a solid electrolyte (Nafion membrane) is used in an electrolysis apparatus.

192 be completely retained on a cation-exchanger Nafion membrane, constituting a colorimetric sensor for

193 added as an additive to the proton exchange Nafion membrane, provide significant enhancement in powe

194 e due to insufficient permselectivity of the Nafion membrane.

195 al arrangement of an electrode and a tubular Nafion membrane.

196 parated from a porous counter electrode by a Nafion membrane.

197 nd by the water absorption properties of the Nafion membrane.

198 de in a home-made electrolyzer by means of a Nafion membrane.

199 od is demonstrated drawing on the example of Nafion membranes and a variety of metal oxides with an e

200 s as additives to enhance the performance of Nafion membranes in fuel cells.

201 es, iodide/triiodide redox electrolytes, and Nafion membranes is described.

202 The use of Nafion membranes to construct devices capable of deliver

203 characteristics similar to that observed for Nafion membranes.

204 seline Nafion and platinum-containing recast Nafion membranes.

205 a glassy carbon electrode (GCE) by chitosan-Nafion mixture and then utilized the fabricated bioelect

206 Also, the G/My-SWCNT/Nafion modified electrode demonstrated a great potential

207 Compared to a bare GC electrode, the CNF/Nafion modified GC (CNF/Nafion/GC) electrode improved th

208 n of caffeine has been developed at bare and Nafion-modified glassy carbon electrodes (GCE).

209 Using Nafion-modified microelectrodes, we present the first en

210 The immunosensor consists of (i) a Nafion-multiwall carbon nanotubes-bismuth nanocomposite

211 Nickel oxide nanoparticles modified nafion-multiwalled carbon nanotubes screen printed elect

212 Also, the electrochemical behavior of NiONPs/Nafion-MWCNTs composites in aqueous alkaline solutions o

213 voltammetric studies showed that the NiONPs/Nafion-MWCNTs film modified SPE, lowers the overpotentia

214 ze, distribution and structure of the NiONPs/Nafion-MWCNTs were characterized by transmission electro

215 The immunosensing performance of BiNPs/Nafion-MWCNTs/GCE was evaluated based on sandwich immuno

216 ilm modified glassy carbon electrodes (BiNPs/Nafion-MWCNTs/GCE) as a sensing platform and (ii) titani

217 n nanotubes screen printed electrode (NiONPs/Nafion-MWCNTs/SPE) were prepared using pulsed electrodep

218 functionalized carbon nano tubes (FCNTs) and Nafion (Naf).

219 strate the first liquid phase exfoliated WS2-Nafion nanocomposite based electro-mechanical actuators.

220 amperometric detection of ethanol on the ADH-Nafion/NiOxNPs/GC modified electrode gives linear respon

221 ensors modified with various combinations of Nafion, o-PD, or nickel(II) meso-tetrakis(3-methoxy-4-hy

222 (tetrabutyl ammonium bromide (TBAB)-modified Nafion; octyl-modified linear polyethyleneimine (C8-LPEI

223 ch showed the importance of the ratio of CNF/Nafion on electrode performance.

224 Smooth, idealized layers of Nafion on glassy carbon (GC) and Pt surfaces were used t

225 The Nafion overcoat reduced the sensitivity of F1/Nafion fil

226 When filled with Nafion perfluorinated resin, the PB-nt membrane demonstr

227 con substrate covered with a sensing film of Nafion perfluorosulfonate ionomer.

228 art imaging agent, with Nafion gel, which is Nafion plasticized with tri-n-butyl phosphate, has been

229 A composite polymeric outer membrane [Nafion + poly-(2-hydroxy-ethyl methacrylate) is used for

230 biosensors were coated with a permselective Nafion-Poly(o-phenylenediamine) layer and cross-linked t

231 ed for bulk SWNTs, H2SO4-treated SWNTs, SWNT-Nafion polymer composites, SWNT-AQ55 polymer composites,

232 f a 96-well microplate cover was coated with Nafion polymer doped with Ag(+) ions.

233 The Nafion polymer junction was creased by infiltrating poly

234 y carbon (GC) electrode that was coated with Nafion polymer was evaluated as a new electrode material

235 ical mechanisms for OH radical attack on the Nafion polymer: (1) OH attack on the S-C bond to form H(

236 uated the most commonly used membranes, i.e. nafion, polyphenylenediamine, polypyrrole, polyaniline,

237 ectrode (ITO OTE) coated with a thin film of Nafion preloaded with the ligand 2,2'-bipyridine (bipy).

238 vation energy that is comparable to those of Nafion presently used in fuel cells.

239 t, for films composed of IrOx nanoparticles, Nafion(R) and glucose oxidase (GOx), a Michaelis-Menten

240 alues, which are obtained more commonly when Nafion(R) is not present in the films, are also importan

241 However, a Nafion((R)) coated copper plating electrode shows a succ

242 A hydrophobic Nafion region was formed adjacent to a Pt film.

243 The coating of such biosensors with Nafion resulted in the current increase by up to 1000%,

244 ass and indium tin oxide (ITO) directly from Nafion-[Ru(bpy)3]2+ Langmuir films assembled at the wate

245 esol with isopropyl alcohol in scCO(2) using Nafion SAC-13 as the catalyst.

246 to graphene-supported Pt nanoparticles on a Nafion scaffold.

247 que chemical reprogramming capability of the Nafion shape memory polymer, we have developed a reconfi

248 cked phase (matrix phase) in a pre-stretched Nafion sheet.

249 which pre-cut flaps open to produce pores in Nafion sheets when humidity increases, as might occur du

250 ized with the obtained electrode (G/My-SWCNT/Nafion) showed a voltammetric signal due to a one-step r

251 I) (Ru(bpy)3 2+) ion-exchanged in Nafion and Nafion-silica composite materials have been investigated

252 [Re(I)(DMPE)3]+ and [Re(II)(DMPE)3]2+ in the Nafion-silica composite.

253 l preconcentration of [Re(I)(DMPE)3]+ by the Nafion-silica composite.

254 composite with greater ECL observed for the Nafion-silica films relative to pure Nafion.

255 Nafion-silica films with a low content of Nafion ion-exc

256 with Nafion-entrapped solgel-derived silica (Nafion-silica) composite.

257 roxide (H2O2) using a reduced graphene oxide-nafion@silver6 (rGO-Nf@Ag6) nanohybrid modified glassy c

258 The charge-selective composite film of Nafion-SiO2 was used to entrap the mediator, Ru(bipy)3(2

259 m filtering a well-dispersed carbon nanotube-Nafion solution through a laser-cut acrylic stencil onto

260 Highly exfoliated layers of WS2 mixed with Nafion solution, solution cast and doped with Li(+) was

261 A three-layer Nafion structure was formed when Nafion was in direct co

262 on of the membranes was achieved by reacting Nafion sulfonyl fluoride poly(perfluorosulfonyl fluoride

263 tric properties of hybrid membranes based on Nafion that contain a [(ZrO(2)).(Ta(2)O(5))(0.119)] "cor

264 Thin, free-standing films of Nafion gel and Nafion that were sufficiently clear to record visible sp

265 For a given hydration level of Nafion, the excited-state proton transfer and the orient

266 Nafion, the most widely used polymer for electrolyte mem

267 contrast, depending on the concentration of Nafion, the sensitivity of the F2/Nafion film electrodes

268 membrane offers a number of advantages over Nafion--the membrane widely used as a proton exchange me

269 Indentation of hydrated Nafion thin films reveals that both the in-plane diffusi

270 ptically transparent electrode coated with a Nafion thin-film (20 nm) that rapidly preconcentrated th

271 Each electrode site was coated with Nafion to attenuate the interference of anionic redox sp

272 n electrodes, which were further coated with Nafion to improve their selectivity and stability.

273 prepared using o-phenylenediamine (o-PD) and Nafion to modify the surface of 30 microns diameter carb

274 The application of Nafion to such biosensors predictably improved their sel

275 pon further modification with a thin film of Nafion (to prevent interferences from anions, especially

276 ters, differential permeation of H2O through Nafion tubing was effective in both cases tested, but th

277 nd spectral features of a receptor membrane (Nafion) upon dehydration are measured.

278 e ammonia-lyase enzyme was immobilized using nafion was characterized by attenuated total reflectance

279 However, when Nafion was in contact with a PtO surface, the Nafion at

280 three-layer Nafion structure was formed when Nafion was in direct contact with GC.

281 alled nanotubes (SWNTs) in sulfuric acid and Nafion was investigated using solid-state nuclear magnet

282 ltiwalled carbon nanotubes, carbon paste and nafion was used as electroactive support for immobilizat

283 Nafion was used as the selective cation exchange film fo

284 The effective size of the Nafion water channels at various hydration levels are es

285 Preconcentration factors into Nafion gel and Nafion were 350 and 50, respectively, after 4 h of soaki

286 Different multilayer structures of Nafion were found in contact with the Pt or GC surfaces.

287 Nafion allows the MWCNTs to be dispersed in Nafion, which was then coated as a thin film on the GC e

288 nked with glutaraldehyde while the other had Nafion with BSA cross-linked with glutaraldehyde.

289 One recording site was coated with Nafion with L-glutamate oxidase and bovine serum albumin

290 hylaminomethyl)phenethyltrimethoxysilane and Nafion with NO gas.

291 placing passive ion-exchange membranes, like Nafion, with membranes that use light to drive ion trans

292 e can be restored using the cation exchanger Nafion without significantly increasing the pH response.

293 The fabricated Nafion/XOD/TiO2-G/GCE sensor exhibited excellent electro

294 The wet [Nafion/(ZrTa)(1.042)] membrane has a conductivity of 7.0