ライフサイエンスコーパス: Nafion

1 ive way without using any glucose oxidase or nafion.

2 ter/mole H(+)) is 5-10x greater than that of Nafion.

3 he mixture of multiwall carbon nanotubes and nafion.

4 n events occurring in hydrophobic domains of Nafion.

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

6 modified with carbon nanotubes dispersed in nafion.

7 re evaluated by measuring permeation through Nafion.

8 such as those typically observed in pristine Nafion.

9 rosulfonic acid polymer chains that comprise Nafion.

10 shed small-angle scattering data of hydrated Nafion.

11 lassy carbon working electrode modified with Nafion.

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

13 ties (IEC) is >2x that of the benchmark CEM, Nafion.

14 thick layer of the proton exchange membrane Nafion.

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

16 also exceed those of biological channels and Nafion.

17 ugh ostensibly impermeable membranes such as Nafion.

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

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

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

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

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

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

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

25 ion characterizes density for the commercial Nafion 117 films.

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

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

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

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

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

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

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

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

34 ovement in signal was obtained compared with Nafion alone.

35 of lactate sensitive electrode made without Nafion analogue.

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

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

38 trode was prepared and optimized in terms of Nafion and catalyst concentrations.

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

40 uce the interference signal much better than Nafion and Chitosan.

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

42 The presence of Nafion and fluoride during the electrochemical polymeriz

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

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

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

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

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

48 for VRFB and LFP can be achieved by reducing nafion and PVDF components, respectively.

49 ct, which modulates the interactions between Nafion and PVDF in electrospun membranes.

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

51 We assessed the polymer Nafion and the crystal cryolite as optically transparent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 commercially available cobalt precursor and Nafion binder mixture coated on a glassy carbon electrod

67 Furthermore, the ADH-Nafion bonding for the S. cerevisiae strain was confirme

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

69 Six fluoroethers were detected in serum; Nafion by-product 2, PFO4DA, and PFO5DoA were detected i

70 CFRE: a perfluorinated ether sulfonic acid (Nafion byproduct 2; range: 1-110 ng/g) and two perfluori

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

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

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

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

75 rst time we takes the advantages of chitosan-Nafion (Chit-Naf) composite as a highly conductive surfa

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

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

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

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

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

81 lled carbon nanotube (SWCNT) electrode and a Nafion-coated SWCNT electrode were used, for the first t

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

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

84 we have previously shown that addition of a Nafion coating on top of the SWCNT electrode is essentia

85 Nafion coating stabilized the potential of the Ag refere

86 temporal response; therefore, we implemented Nafion coating to alleviate the electrode fouling and pr

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

88 shells wrapping the polar side chains of the Nafion component.

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

90 The so-activated 2D-Co-MOF@Nafion composite exhibits an outstanding electrocatalyti

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

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

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

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

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

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

97 the standard bore columns, thereby avoiding Nafion deformation as a source of chromatographic band b

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

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

100 a, and gamma dielectric relaxation events of Nafion domains supported on beta-PVDF.

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

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

103 Water vapor is removed using a heated nafion dryer.

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

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

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

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

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

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

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

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

112 A Nafion film loaded with novel catalyst-free multiwalled

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

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

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

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

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

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

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

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

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

122 e attributed to irreversible swelling of the Nafion film.

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

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

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

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

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

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

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

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

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

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

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

134 particles and other photoactive materials in Nafion for transient spectroscopy and time-resolved tera

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

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

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

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

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

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

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

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

143 f the bridged calix[4]arene with P(2)O(5) or Nafion-H, leading (apart from polymers) to a macrocyclic

144 .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

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

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

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

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

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

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

151 Nafion imparts increased sensitivity for dopamine and no

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

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

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

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

163 Nafion is an ideal suspension matrix because it has high

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 n, a polyelectrolyte from the same family as Nafion, is used to stabilize the mixed potential of a pl

169 pamine molecules, a cation exchange polymer, nafion, is utilized as a membrane over imprinted sites t

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

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

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

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

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

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

176 n the relaxations of beta-PVDF with those of Nafion matrix is directly correlated to the "reciprocal

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

178 s achieved on a mixed 4-styrenesulfonic acid-nafion matrix.

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

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

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

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

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

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

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

186 The hydrophilic Nafion membrane preferentially transports methanol and e

187 The modified Nafion membrane provided the best electrical communicati

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

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

190 e applied microfluidic device consisted of a Nafion membrane to induce the CP and an array of individ

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

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

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

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

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

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

197 e due to insufficient permselectivity of the Nafion membrane.

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

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

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

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

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

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

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

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

206 characteristics similar to that observed for Nafion membranes.

207 seline Nafion and platinum-containing recast Nafion membranes.

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

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

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

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

212 Electrochemical activation of a 2D-Co-MOF@Nafion-modified graphite electrode in aqueous solution i

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

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

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

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

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

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

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

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

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

222 larization phenomena of electrospun PVDF (P)/Nafion (N) blended fiber mats ([P/N(0.9)](M) and beta-[P

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

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

225 dified with graphene quantum dots (GQDs) and Nafion (NF) has been developed for the determination of

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

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

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

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

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

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

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

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

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

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

236 The Nafion polymer junction was creased by infiltrating poly

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

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

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

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

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

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

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

244 The Pt-Nafion(R) sensor was characterized morphological and ele

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

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

247 Suspensions of nanoparticles in Nafion require only small amounts of sample (<5 mg) and

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

249 es associated with the successful example of Nafion resulted in the search for alternate proton condu

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

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

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

253 passed similar microelectrodes coated with a Nafion screening layer.

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

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

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

257 or that incorporates ADH, NAD(+), Pd-NPs and Nafion showed no loss of enzyme activity after preparati

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

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

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

261 s configuration also eliminates the internal Nafion sleeve that is critical to operation for the stan

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

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

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

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

266 odel material to demonstrate the efficacy of Nafion suspensions for transient THz spectroscopy.

267 Thus, the Nafion/SWCNT electrode was further characterized and use

268 This study shows that the fabricated Nafion/SWCNT sensor has potential to be applied in clini

269 he limit of detection for oxycodone with the Nafion/SWCNT sensor was 85 nM, and the linear range was

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

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

272 Nafion, the most widely used polymer for electrolyte mem

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

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

275 uried interface is shown to be a function of Nafion thickness, with the highest activity observed for

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

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

278 with analytical purposes using a coating of Nafion, thus providing a way to develop a potentiometric

279 ifts ion transport from channel transport in Nafion to a hopping mechanism in the organic-inorganic i

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

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

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

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

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

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

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

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

288 Nafion was used as the selective cation exchange film fo

289 An electrode modified by a Ti complex in Nafion was used in the electrochemical detection of nitr

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

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

292 ng inorganic Zn-X zeolite nanoparticles with Nafion, which shifts ion transport from channel transpor

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

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

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

296 hylaminomethyl)phenethyltrimethoxysilane and Nafion with NO gas.

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

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

299 Consequently, the Zn@Nafion-Zn-X composite anode delivers high coulombic effi

300 d organic-inorganic hybrid protection layer (Nafion-Zn-X) is developed by complexing inorganic Zn-X z

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