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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

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