ライフサイエンスコーパス: formic acid

1 (electrooxidation of methanol, ethanol, and formic acid).

2 d electrolyte system consisted of 100 mmol/L formic acid.

3 he Pd(0)-mediated formation of hydrogen from formic acid.

4 rotective groups were cleaved with refluxing formic acid.

5 ate and the direct overlay of organisms with formic acid.

6 t or by renewable reductants such as formate/formic acid.

7 mary secondary amine and acidified with 0.1% formic acid.

8 s such as 5-hydroxy-methylfurfural (HMF) and formic acid.

9 der mild conditions using CO(2), formate and formic acid.

10 t uses CO(2) and hydrogen to store energy in formic acid.

11 in CO stripping and the electro-oxidation of formic acid.

12 proximately equal production of methanol and formic acid.

13 of acetonitrile/water (80:20) (v/v), with 1% formic acid.

14 1-naphthylnitrenium cation is 860 ps in 88% formic acid.

15 ion was found for 50% H2O/33% 2-propanol/17% formic acid.

16 photolysis of the appropriate azides in 88% formic acid.

17 oning all plants except its host plants with formic acid.

18 may undergo rapid aromatization, as well as formic acid.

19 ontal cortex of AD brains homogenized in 70% formic acid.

20 eloped that is based on chemical cleavage by formic acid.

21 h nitrogen atom and the hydroxyl hydrogen in formic acid.

22 that enables hydrogen gas release from neat formic acid.

23 ethane, bromochloromethane, formaldehyde and formic acid.

24 in the third step, yielding an estrogen and formic acid.

25 performed on an X-Bridge C18 column with ACN-formic acid 0.1% as the mobile phase.

26 y membrane filtration and analyzed in dilute formic acid (0.5%) in negative ion mode.

27 xtraction conditions reveals that the use of formic acid (1%), in place of the more commonly used per

28 performed using acetonitrile acidified with formic acid (1%, v/v).

29 gas-phase acidity (DeltaH degrees (acid)) of formic acid (1) over methanol (2).

30 Low-temperature 1H and 13C NMR spectra of formic acid (1) showed separate signals for the E and Z

31 Formic acid-(13)C (nominally 99 at. % (13)C) was measure

32 d utilized for 13-carbon isotope analysis of formic acid-(13)C and acetic acid-(13)C, each highly enr

33 and Ea = 31 kJ/mol) and one-pot reactions of formic acid, 2-nitrophenol, and aldehydes into benzoxazo

34 pH 2.25; 500 mM acetic acid, pH 2.54; 200 mM formic acid, 200 mM acetic acid, pH 2.05; and 200 mM imi

35 oltage, and time) with standard solutions in formic acid 50 mM.

36 -1) of ferulic acid in an acetonitrile:water:formic acid 50:33:17 v/v/v mixture.

37 phase of acetonitrile-water containing 0.1% formic acid (50:50, v/v) and an optimal mobile phase flo

38 Methylene chloride/ethyl acetate/formic acid (6:10:1, v/v) as the mobile phase and 1% van

39 ved on a C(18) column with acetonitrile/5 mM formic acid (60:40, v/v) as the mobile phase followed by

40 ites was carried out with acetonitrile-water-formic acid (80:19:1, v/v/v).

41 toxic metabolite in methanol intoxication is formic acid, a mitochondrial toxin known to inhibit the

42 Various OVOCs, including acetic acid, formic acid, acetaldehyde, and acetone were observed dur

43 od was applied to measure the enrichments of formic acid, acetic acid, and propionic acid in the perf

44 t for the low isotopomer enrichment assay of formic acid, acetic acid, propionic aicd, butyric acid,

45 The optimal volumes of processed urine, formic acid/acetonitrile, and supernatant spotted onto t

46 ictet-Spengler cyclization of 13 in formalin/formic acid afforded the dibenzo[a,g]quinolizine 14 in 6

47 equent removal of the tert-butyl esters with formic acid affords a triacid that is coupled to three m

48 Moreover, although not explicitly sought, formic acid/ammonium formate is produced as an important

49 gregates are not dissociated by concentrated formic acid, an extremely effective solvent for otherwis

50 e phase consisting of acetonitrile plus 0.1% formic acid and 25 mM ammonium acetate.

51 Even formic acid and acetone, the simplest odorants possessin

52 age systems based on liquids, in particular, formic acid and alcohols, are highly attractive hydrogen

53 ent oxygenolytic cleavage of cyanide (CN) to formic acid and ammonia.

54 low temperatures by 1H and 13C NMR for both formic acid and an adduct with hexafluoroacetone, HCO2C(

55 ates of decay of the singlet nitrenes in 88% formic acid and are as follows: p-biphenylyl (taugrowth

56 e ethylenediaminetetraacetic acid (EDTA) and formic acid and are efficient in extracting dyes, but pr

57 on, by oxalate decarboxylase (OXDC), forming formic acid and carbon dioxide.

58 gradient elution with acetonitrile and 0.2% formic acid and detected on an electrospray ionization m

59 es was accomplished with mixtures of aqueous formic acid and dimethylsulfoxide with increasing concen

60 ry studies, including measurements of plasma formic acid and fomepizole, were performed.

61 t Py catalyzes the homogeneous reductions of formic acid and formaldehyde en route to formation of CH

62 At metal electrodes, formic acid and formaldehyde were observed to be interme

63 nd its two succeeding intermediates, namely, formic acid and formaldehyde, to ultimately form CH3OH.

64 redicted to undergo fragmentation to produce formic acid and formaldehyde, with regeneration of (*)OH

65 The main products are formic acid and formaldehyde.

66 hydride and proton transfer steps to reduce formic acid and formaldehyde.

67 electric field is switched on and identifies formic acid and formamide as key intermediate products o

68 was observed from cocktails containing more formic acid and from mixtures including CH3CN.

69 tandem process involving dehydrogenation of formic acid and hydrogenation of C-C multiple bonds usin

70 Tryptic digests were prepared in 50 mM formic acid and loaded onto the strong cation-exchange m

71 actions, namely, the hydrogenation of CO2 to formic acid and methanol and the reverse dehydrogenation

72 At very cathodic potentials, formic acid and methanol are formed as well.

73 talytic activity and very high stability for formic acid and methanol oxidation and the oxygen reduct

74 lower onset potentials for the oxidation of formic acid and methanol than either pure Pt or Pt-Ru na

75 higher oxidation current densities for both formic acid and methanol than pure Pt, Pt-Ru, or atomica

76 solar energy to convert CO2 to fuels (e.g., formic acid and methanol) apparently could simultaneousl

77 nonlinear gradient consisting of 0.1% (v/v) formic acid and methanol.

78 C-DAD-MS), after extraction of the dyes with formic acid and methanol.

79 yde dehydrogenase to convert formaldehyde to formic acid and monitors the creation of an NADH analog

80 foliation syndrome (XFS) were homogenized in formic acid and subjected to cyanogen bromide (CNBr) cle

81 furic anhydride (FSA), that is produced from formic acid and sulfur trioxide under supersonic jet con

82 em and its atmospherically relevant isomers: formic acid and the Criegee intermediate CH2OO.

83 itionally, acidities were calculated for the formic acid and vinyl alcohol vinylogues in which the fo

84 (70%) provided lower conductivity than 0.25% formic acid and was evaluated as low ionic-strength and

85 to both internal and terminal alkynes using formic acid and Zn as the terminal reductants has been d

86 f a mobile phase comprising water (with 0.5% formic acid) and acetonitrile (90:10, v/v) on Phenomenex

87 h a gradient system of ultrapure water (0.1% formic acid) and acetonitrile, a temperature of 35 degre

88 homogenised sample with 20 ml methanol (+1% formic acid) and measurement by LC-MS/MS multiple reacti

89 ed to rapidly convert 100% of gaseous CO2 to formic acid, and >500 mM formate was observed to accumul

90 lution, with a mobile phase of acetonitrile, formic acid, and ammonium acetate, at pH 3.6.

91 a mixture of a functionalized PDMS oligomer, formic acid, and an IL (or lithium-in-IL solution), a re

92 synthons: bromo[2-(13)C]acetic acid, [(13)C]formic acid, and elemental (77)Se.

93 tion methods, including the direct, on-plate formic acid, and ethanol/formic acid tube extraction met

94 ented using incubation with Pronase E and/or formic acid, and in each case a complete set of fluoresc

95 methods typically involved the use of HPLC, formic acid, and large amounts of expensive radiolabeled

96 cpcT mutant and wild type were cleaved with formic acid, and the products were analyzed by SDS-PAGE.

97 nanoparticle structure, slow dehydration of formic acid, and weak binding of CO on Au147@Pt surface.

98 concentration is also monitored by employing formic acid as a chemical probe, which is shown to adsor

99 ransfer hydrogenation of benzaldehydes using formic acid as a hydrogen source.

100 column using acetonitrile in water with 0.1% formic acid as a mobile phase.

101 d in proteomics: 100 A C18 sorbent with 0.1% formic acid as an ion-pairing modifier.

102 the presence of [Rh2(OAc)4] as catalyst and formic acid as reducing agent, leading to the high yield

103 transfer hydrogenation conditions employing formic acid as terminal reductant, 2-butyne couples to a

104 e analytes were collected in 21 muL of 10 mM formic acid as the acceptor phase, and the extracts were

105 nderivatized fused-silica capillary with 1 M formic acid as the background electrolyte.

106 adient of water/acetonitrile each containing formic acid as the mobile phase.

107 elution program with methanol and 0.1% (v/v) formic acid as the mobile phases was used.

108 quantify the stoichiometric accumulation of formic acid as the product of the reaction and demonstra

109 itrile and water as mobile phases (both with formic acid at 0.1%).

110 ficantly enhance the production of H(2) from formic acid at ambient temperature.

111 nd/or selective for hydrogen production from formic acid at room temperature.

112 ing, we infer a substantial emission flux of formic acid at the canopy level ( approximately 1 nmol m

113 ntration but higher pH values than the 50 mM formic acid background electrolyte.

114 Among the formic acid-based cocktails examined, the slowest rate o

115 protein detection from complex mixtures: (1) formic acid-based formulations, (2) perfluorooctanoic ac

116 d 94 (M + H)+ ions, 119 were observed from a formic acid-based matrix with no more than 10 common to

117 a user-supplemented database and an on-plate formic acid-based preparation method and compared result

118 on modes employed identical LC settings with formic-acid-based eluents in the last dimension.

119 ate in the presence of sodium metal to yield formic acid, [bis(N,N-diisopropylamino)phosphino]-beta-(

120 An ammonium formate/formic acid buffer with a methanol/water gradient was us

121 curs much more readily in low ionic strength formic acid buffers.

122 a feature consistent with its solubility in formic acid but not at neutral pH.

123 can be completely dissolved in concentrated formic acid, but a soluble protein oligomer containing t

124 for A beta40 and A beta42 extractable in 70% formic acid, by assessment of amyloid plaque formation u

125 Photochemical reduction of CO(2) (to produce formic acid) can be seen both as a method to produce a t

126 equired during the hydrogenation of CO(2) to formic acid catalyzed by ruthenium trimethylphosphine co

127 The formic acid cleavage method generated comparable or bett

128 1,4-dimethoxy-2,5-bis(2-pyridyl)benzene bis(formic acid) complex 10, and 1,4-dimethoxy-2,5-bis(2-pyr

129 the reaction could not be fully stopped with formic acid concentrations up to 0.75 mM (the maximum ty

130 Plasma formic acid concentrations were detectable in eight pati

131 osphates, however, mixtures of acidic (0.1 M formic acid-containing) acetonitrile/water (80:20) or ac

132 Our results suggest that formic acid decomposes at the surface of unbiased Pt thr

133 lysts, as demonstrated here for the cases of formic acid decomposition and formic acid electro-oxidat

134 While many catalysts exist for both formic acid dehydrogenation and carbon dioxide reduction

135 three-step extractions (TBS, detergent, and formic acid) demonstrated that the lower level of total

136 ernal standards ((13)C-labeled), addition of formic acid (denaturation agent), and dilution with wate

137 egate of expanded polyQ that is insoluble in formic acid, does not enter polyacrylamide gels, but is

138 r the cases of formic acid decomposition and formic acid electro-oxidation reactions.

139 Formic acid electrooxidation with this novel material sh

140 smenyl (vinyl-ether) containing lipids using formic acid enabled these species to be readily differen

141 the addition of a modifier (acetic acid and formic acid) enhanced the degree of preferential ionizat

142 onic strength mobile phases at low pH (e.g., formic acid), even with highly inert silica RP-HPLC colu

143 nd can generate methanol or sequester CO2 as formic acid ex vivo.

144 grees C are in the order pre-LGA < pre-HMF < formic acid, explaining why LGA is the kinetically favor

145 einase K sensitive, detergent insoluble, and formic acid extractable.

146 e evaluated BACE activity, BACE protein, and formic acid-extractable A beta levels in cohorts of youn

147 BACE activity correlated with formic acid-extractable A beta levels in transgenic mous

148 a with treatment up to 5 weeks in WT mice or formic acid-extractable brain Abeta with 3 month treatme

149 -treated mice in cortical levels of soluble, formic acid extracted, or histologically detectable beta

150 beta plaque load and biochemical analysis of formic acid-extracted Abetax-40 and Abetax-42 levels and

151 relative efficiencies of the HCl, EDTA, and formic acid extraction methods are compared by analyzing

152 ion of nucleobases and nucleobase analogs in formic acid extracts of 12 different meteorites by liqui

153 HPLC profiles of EDTA or formic acid extracts of silk dyed, for example, with pag

154 found that the widely used conditions, 0.1% formic acid (FA) and NH(4)Ac at different pH, are far fr

155 This report describes a short, on-plate formic acid (FA) extraction method for the identificatio

156 pattern toward lower-charged species and of formic acid (FA) for causing higher charging.

157 Formic acid (FA) is an attractive compound for H2 storag

158 o form H(2)SO(4) in the presence of a single formic acid (FA) molecule.

159 (L) smears, with and without a 1-mul direct formic acid (FA) overlay.

160 en at 12 mo of age in both CHAPS-soluble and formic acid (FA)-soluble brain fractions.

161 Formic acid (FA, HCO2H) receives considerable attention

162 ne phase in low-pH, volatile buffers such as formic acid, favored for mass spectrometric analysis.

163 The SECM tip, which generated a constant formic acid flux, was scanned above the array and the ox

164 ylurea and p-toluenesulfinic acid in aqueous formic acid followed by reaction of the obtained N-[(2-a

165 d by extracting using water, with or without formic acid, for 10 min at 100 degrees C.

166 uction of carbon dioxide to products such as formic acid, formaldehyde, and methanol.

167 aptobenzothiazole matrixes performed well in formic acid formulations.

168 Further, formic acid from N. fulva venom is the detoxifying agent

169 and electro-oxidation of HCOOH in the direct formic acid fuel cell.

170 and that an acid that reduces Pd(+2) salts, formic acid, functions better than other carboxylic acid

171 numerous substrates, including citric acid, formic acid, glucose 6-phosphate, capric acid, gamma-hyd

172 bably promoting the release of formaldehyde, formic acid, glycolaldehyde, glyoxal, acetic acid, glyco

173 Water/acetonitrile mixtures, to which formic acid had been added (generally, 0.1%), were emplo

174 A simple treatment method using formic acid has been found to increase the fluorescence

175 CHOO with the two simplest carboxylic acids, formic acid (HCOOH) and acetic acid (CH3 COOH), employin

176 Formic acid (HCOOH) has great potential as an in situ so

177 As a case study, the decomposition of formic acid (HCOOH) in acidic media at open circuit on P

178 Formic acid (HCOOH) is one of the most abundant carboxyl

179 oducts carbon monoxide (CO, yields >54%) and formic acid (HCOOH, yields >6%).

180 tic cycles, involving the decarboxylation of formic acid, hydration of the alkyne, and hydrogenation

181 Formic acid hydrolysis, immunoprecipitation experiments,

182 f (A) methanol:acetonitrile (8:2) - (B) 0.1% formic acid in a gradient mode.

183 gainst the toxic actions of methanol-derived formic acid in a rodent model of methanol toxicity.

184 Briefly, the samples were extracted with 1% formic acid in acetonitrile and directly analysed with H

185 Samples were extracted using 0.1% formic acid in acetonitrile:water (8:2) with the additio

186 hat are very selective for the production of formic acid in dimethylformamide (DMF)/water mixtures (F

187 ence cluster Fe(3)O(MeCOO)(6)(H(2)O)(3) with formic acid in dimethylformamide exposed to air at 110 d

188 s A (0.1% formic acid in water), and B (0.1% formic acid in methanol).

189 achieved by using 0.1% acetic acid and 0.1% formic acid in negative ionization mode.

190 T in chloroform/methanol (2:1, v/v), with 1% formic acid in the final mixture, 57 lipid entities were

191 aqueous and organic mobile phases were 0.1% formic acid in water and acetonitrile, respectively.

192 100 mm, 1.7 mum) with mobile phases of 0.1% formic acid in water and acetonitrile.

193 radient on a Kinetex XB-C18 column with 0.1% formic acid in water and acetonitrile.

194 mobile phase consisting of solvents A (0.1% formic acid in water), and B (0.1% formic acid in methan

195 surements of OVOCs, including high levels of formic acid, in the atmosphere (measured by an online hi

196 Extraction with formic acid indicated that ATP concentration did not cha

197 oom-temperature photocatalytic conversion of formic acid into either hydrogen or carbon monoxide.

198 The dissociation of formic acid into H2 and CO2 serves to demonstrate how a

199 cause the reverse reaction is also feasible, formic acid is a form of stored hydrogen.

200 Formic acid is a promising energy carrier for on-demand

201 Formic acid is considered a promising energy carrier and

202 he solubility of the polymerized material in formic acid is controlled by the degree of graft copolym

203 oxidation of acetate to a mixture of CO2 and formic acid is coupled to methanol reduction.

204 In the proposed model, formic acid is first physisorbed on bismuth and then dep

205 rage including continuous H2 production from formic acid is highlighted.

206 ining the expanded polyQ and released by the formic acid is not dissociated to monomer.

207 novel catalytic cycle for the reaction with formic acid is proposed and subjected to a variety of ex

208 n carolinus, although topically sensitive to formic acid, is able to prey on formic acid-spraying ant

209 on of CO2 into energy-dense liquids, such as formic acid, is desirable as a hydrogen carrier and a ch

210 Formic acid matrix revealed many lipoproteins and an 828

211 tiful atmospheric abundance of FA, makes the formic acid mediated hydrolysis reaction a potentially i

212 duction reaction, and oxidation reactions of formic acid, methanol and carbon monoxide) of noble meta

213 r the direct hydrogenation of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly

214 The gas-phase acidities of formic acid, methanol, vinyl alcohol (5), and their viny

215 gen-dependent reduction of carbon dioxide to formic acid offers a promising route to greenhouse gas s

216 TE), that catalyzes the reduction of CO2 and formic acid on a glassy carbon electrode.

217 The integral heat of molecular adsorption of formic acid on clean Pt(111) at 100 K is 62.5 kJ/mol at

218 d by studying the dissociative adsorption of formic acid on oxygen-presaturated (O-sat) Pt(111) to ma

219 tational results, the oxidation mechanism of formic acid on Pt(111) electrodes modified by the incorp

220 at the chemical shift value of an adsorbate (formic acid) on metal colloid catalysts measured by (13)

221 tein precipitation, only dilution with 0.1 M formic acid, one aliquot of 100 microL of serum was inje

222 ergent-insoluble fraction extracted with 70% formic acid or 6 M guanidine hydrochloride decreased mar

223 was achieved in CE separations using either formic acid or phosphate buffer.

224 ects responsible for the enhanced acidity of formic acid over methanol, accounting for between roughl

225 "score." We found that a heavy smear with a formic acid overlay (H+FA) produced optimal MALDI-TOF MS

226 A heavy smear with formic acid overlay was either superior or equivalent to

227 tly applied to a target plate, followed by a formic acid overlay.

228 n Ketjen carbon are catalytically active for formic acid oxidation in HClO(4) solution.

229 dation, benzoquinone (BQ) reduction, and the formic acid oxidation reaction (FAOR) at a Pt microelect

230 agonal (fct) structure, and further promotes formic acid oxidation reaction (FAOR).

231 atio) as a better electrocatalyst toward the formic acid oxidation than pure Pd or Pt in 0.1 M KHCO(3

232 bes and spheres (including oxygen reduction, formic acid oxidation, and methanol oxidation) were test

233 exhibited enhanced catalytic activity toward formic acid oxidation, with a current density 2.5 and 7.

234 influence the activity of a noble metal for formic acid oxidation.

235 atalytic activity and high durability toward formic acid oxidation.

236 ng methanol -5mM ammonium acetate containing formic acid (pH 3.5).

237 5 mM naphthalene trisulfonate (NTS) in 0.4 M formic acid, pH 2.0 is developed for detection of UV tra

238 ion of metabolic acidosis, the inhibition of formic acid production, the achievment of therapeutic pl

239 technology or as a cell factory dedicated to formic acid production, which is a commodity in itself a

240 equential in nature (in which the formate to formic acid protonation can be assisted by a negatively

241 Thus, extraction of textiles with EDTA or formic acid reagents can yield significantly more inform

242 ed complexes among the most promising CO2-to-formic acid reducing catalysts developed to date; addres

243 In Huntington's disease, a formic acid-resistant oligomer is present in cerebral co

244 % (R) were achieved using Meldrum's acid and formic acid, respectively.

245 sin and eluted with acidified methanol (0.1% formic acid), resulting in analyte recoveries generally

246 The addition of 1% formic acid results in low ( approximately 30%) depth of

247 umns and adding TFA as an acid modifier to a formic acid/reversed phase gradient, providing additiona

248 hich, when deleted in combination, predicted formic acid secretion in Saccharomyces cerevisiae under

249 mate dehydrogenase mutant (fdh1 fdh2), while formic acid secretion in wild-type yeast was undetectabl

250 tant strain showed the predicted increase in formic acid secretion relative to a formate dehydrogenas

251 The esters of the 16alpha-formic acid series had the highest ER affinity with litt

252 igand-capped cadmium sulfide nanocrystals in formic acid/sodium formate release up to 116+/-14 mmol H

253 changes in sodium dodecyl sulfate-soluble or formic acid-soluble Abeta pools or Abeta oligomers in Tg

254 ort that the levels of detergent-soluble and formic acid-soluble levels of Abeta and deposition are e

255 In this study we compared the formic acid-soluble proteins expressed by strains 43895O

256 meter) were formed by dispersing polyaniline/formic acid solution into acetonitrile.

257 he conductivities of aqueous acetic acid and formic acid solutions were measured from 0.1% to 100% co

258 e to the [M+H](+) ion generated using a 0.1% formic acid solvent modifier.

259 sensitive to formic acid, is able to prey on formic acid-spraying ants (Camponotus floridanus).

260 The resistance of oligomer and polymer to formic acid suggests the participation of covalent bonds

261 a lack of (18)O incorporation in the product formic acid, supporting only the Compound I pathway.

262 Formic acid suppressed ionization, as did neutral salts

263 based on extraction with acetonitrile/water/formic acid, ten-fold dilution and analysis by LC-MS/MS

264 isoning tolerance in the electrooxidation of formic acid than Pt cubes; the oxidation of CO on Pt nan

265 eport a new (13)C-tagging method using (13)C-formic acid that delivers high sensitivity, good quantit

266 ized lignin under mild conditions in aqueous formic acid that results in more than 60wt% yield of low

267 process may produce a few Tg/year of gaseous formic acid, the amount comparable to its primary source

268 otonated, this species preferentially expels formic acid through an O-O cleavage transition state.

269 zyme from Escherichia coli normally oxidizes formic acid to carbon dioxide and couples that reaction

270 emical reversibility during the oxidation of formic acid to CO(2).

271 ate, and it also intercepts the intermediate formic acid to generate dimethylformamide.

272 egral heat of the dissociative adsorption of formic acid to make monodentate formate (HCOOmon,ad) plu

273 istic studies point to the unique ability of formic acid to mediate the cyclization forming the clusi

274 as eluted with 30% acetonitrile plus 100 muM formic acid to provide sufficient hydrogen ions to ioniz

275 TasA fibers required harsh treatments (e.g., formic acid) to be depolymerized.

276 catalytically active for dehydrogenation of formic acid (TOF = 1718 h(-1) and Ea = 31 kJ/mol) and on

277 was performed under mild conditions with the formic acid/triethylamine (5:2) system as the hydrogen s

278 substituted substrates, the more established formic acid/triethylamine system gives superior results.

279 he direct, on-plate formic acid, and ethanol/formic acid tube extraction methods, were evaluated for

280 nes 25-26 were synthesized in one step using formic acid, urea, guanidine carbonate, and phenylisocya

281 er mobile phase (80:20, v/v) containing 0.1% formic acid using isocratic flow at 0.15 mL/min for 13 m

282 We report electrocatalytic oxidation of formic acid using monometallic and bimetallic dendrimer-

283 cetate and hexane in the presence/absence of formic acid, using different extraction times and temper

284 arameters at the lowest values tested (0.35% formic acid v/v, and 17.6 min).

285 ray and the oxidation current generated when formic acid was collected by active electrocatalytic spo

286 An on-plate testing method using formic acid was evaluated on the Bruker Biotyper matrix-

287 Formic acid was generated at a Hg on Au ultramicroelectr

288 of iron(III) rhodotoluate was improved when formic acid was replaced by the ion-pairing reagent hept

289 The electrochemical oxidation of formic acid was studied by the tip generation-substrate

290 tes with a solvent mixture of ethyl formate, formic acid, water, toluene 30/4/3/1.5 (v/v/v/v).

291 membrane inlet system, and formaldehyde and formic acid were detected by ESI-MS after a derivatizati

292 ation of methanol generates formaldehyde and formic acid which then condense with methanol to form di

293 analysis of the oxygen atoms of the product (formic acid), which exchange with the solvent (water) un

294 rate salt) (11) establishes that reaction of formic acid with 9 does not form an ionic pyridinium sal

295 ne of the few catalysts that reduce CO2 into formic acid with high selectivity but at high overpotent

296 ctions of acetic acid, acetic-d3 acid-d, and formic acid with the Ge(100)-2 x 1 surface have been inv

297 ng gas-phase molecules (water, methanol, and formic acid), with a slope of 1.00.

298 f photoreceptors to the cytotoxic actions of formic acid, with a partial recovery of rod-dominated re

299 roved practical to degas and electrolyze 95% formic acid (without added electrolyte) due to adequate

300 The on-plate method using formic acid yielded identification percentages similar t