ライフサイエンスコーパス: atmospheric pressure

1 under low temperature and pressure (even at atmospheric pressure).

2 l variations in ice mass and air mass (i.e., atmospheric pressure).

3 tive analytical method which operates at the atmospheric pressure.

4 ration concentration at room temperature and atmospheric pressure.

5 cyclic hydrocarbons at room temperature and atmospheric pressure.

6 ctrospray process at ambient temperature and atmospheric pressure.

7 alysis was investigated in N2 environment at atmospheric pressure.

8 real-time formation of ion/ion complexes at atmospheric pressure.

9 9) molecules cm(-3), room temperature and at atmospheric pressure.

10 temperature range of (288.15-318.15)K and at atmospheric pressure.

11 d at temperatures, T=(293.15-318.15)K and at atmospheric pressure.

12 l pyrolysis in a high temperature furnace at atmospheric pressure.

13 of concentration at 20.0-45.0 degrees C and atmospheric pressure.

14 K and pH levels between 8.50 and 9.87 under atmospheric pressure.

15 et temperature relative to laser ablation at atmospheric pressure.

16 emble for subsequent DEER data collection at atmospheric pressure.

17 he ion source and mass spectrometer inlet at atmospheric pressure.

18 t for an increase in preterm birth risk with atmospheric pressure.

19 r to perform MAIV from both intermediate and atmospheric pressure.

20 ed organic aerosol particles in real time at atmospheric pressure.

21 the values for oil that had been drained at atmospheric pressure.

22 compared to similar frying with drainage at atmospheric pressure.

23 phosphorylation pathway were up-regulated at atmospheric pressure.

24 cifically on Cu{100} surface orientations at atmospheric pressure.

25 compared with the conventional method using atmospheric pressure.

26 igh yield of sequence coverage compared with atmospheric pressure.

27 e only variable considered in this study was atmospheric pressure.

28 ethod was found to be much faster than using atmospheric pressure.

29 Bi; VI = S, Se, Te) at room temperature and atmospheric pressure.

30 C-H bond of methane at room temperature and atmospheric pressure.

31 absorption peak height by 24 h of heating at atmospheric pressure.

32 uated as it equilibrates with the decreasing atmospheric pressure.

33 lt+water were determined at 298 (+/- 1)K and atmospheric pressure.

34 mass spectrometry analysis, but performed at atmospheric pressure.

35 ed by a surface DBD-plasma reactor in air at atmospheric pressure.

36 dstock in a nitrogen gas environment at near atmospheric pressure.

37 t (288.15, 298.15, 308.15 and 318.15)K under atmospheric pressure.

38 K approaches a similar crossover line at one atmospheric pressure.

39 fibers after sintering at 1500 degrees C and atmospheric pressure.

40 ures and selective adsorption at approximate atmospheric pressures.

41 duct, however, vacuum drying works under sub-atmospheric pressures.

42 ted to a step-by-step pressure increase from atmospheric pressure (1 bar) to 2 and 4 bar, followed by

43 s unaffected by magnesium perchlorate or low atmospheric pressure (10 mbar).

44 emperatures of CsFn (n = 2,3,5) compounds at atmospheric pressure (218 degrees C, 150 degrees C, -15

45 The aerosol flowing atmospheric-pressure afterglow (AeroFAPA) ion source is

46 The flowing atmospheric-pressure afterglow (FAPA) is a promising new

47 g the analytical capabilities of the flowing atmospheric-pressure afterglow (FAPA) source by explorin

48 One such ADI-MS source, the flowing atmospheric-pressure afterglow (FAPA), is capable of dir

49 Its ability to grow at atmospheric pressure allows for both easy genetic manipu

50 terglow (FAPA) is a promising new source for atmospheric-pressure, ambient desorption/ionization mass

51 The atmospheric pressure and 1000 degrees C evaporation temp

52 erm birth risk were found for both increased atmospheric pressure and ambient temperature exposures d

53 ed the direct detection of gas phase ions at atmospheric pressure and confirmed a limit of detection

54 ethod are the potential for counting ions at atmospheric pressure and for obtaining ion specific emis

55 cal information on the active surfaces under atmospheric pressure and in the presence of liquids by m

56 nds can be stably formed in the gas phase at atmospheric pressure and neutral gas temperatures <100 d

57 The experiments were performed at atmospheric pressure and over a range of temperatures (5

58 ugh direct current (DC) plasma processing at atmospheric pressure and room temperature has been demon

59 The ability of the ROMIAC to operate at atmospheric pressure and serve as a front-end analyzer t

60 under highly oxidative conditions at ambient atmospheric pressure and temperature.

61 esponse to meteorological parameters such as atmospheric pressure and temperature.

62 to an inlet tube cooled with dry ice linking atmospheric pressure and the first vacuum stage of a mas

63 introduced into a heated inlet tube linking atmospheric pressure and the initial vacuum stage of the

64 periments, precursor ions are dissociated at atmospheric pressure and the resulting fragment ions are

65 nanodiamonds containing NV(-) centres at sub-atmospheric pressures and show that while they burn in a

66 l(2), bis(imino)pyridine 6 (1 mol %), CO(2) (atmospheric pressure), and a hydride source (EtMgBr, 1.2

67 Atmospheric-pressure (AP) IM-MS offers an advantage in t

68 and aperture from ICT analysis performed at atmospheric pressure are higher than those calculated fr

69 pure nitrogen (N2) to pure oxygen (O2) in an atmospheric pressure argon plasma jet (kINPen) will chan

70 cular exclusion of propane from propylene at atmospheric pressure, as evidenced through multiple cycl

71 peseed oil under vacuum at 125 degrees C and atmospheric pressure at 165 degrees C.

72 paper reports on the development of a hybrid atmospheric pressure atomic force microscopy/mass spectr

73 d that base flipping kinetics can proceed at atmospheric pressure but with a very small propensity.

74 sprayed protein molecules is performed under atmospheric pressure by an automated ion landing apparat

75 cles at elevated temperature under oxygen at atmospheric pressure, by using advanced in situ electron

76 We introduce a new atmospheric pressure charge stripping (AP-CS) method for

77 conjunction with UV-visible spectroscopy and atmospheric pressure chemical ionisation (APCI) mass spe

78 Electrospray (ESI) and atmospheric pressure chemical ionisation (APCI) sources

79 rometry/mass spectrometry (HPLC-MS/MS) using atmospheric pressure chemical ionisation (APCI) under bo

80 e quadrupole mass spectrometry equipped with atmospheric pressure chemical ionisation (APCI).

81 pectroscopy (IT-MS), using positive polarity atmospheric pressure chemical ionisation (APCI).

82 Since the positive atmospheric pressure chemical ionisation mass spectromet

83 In this study atmospheric pressure chemical ionisation-mass spectromet

84 Negative ion atmospheric pressure chemical ionization (APCI(-)) of 23

85 ic desorption (LIAD) was recently coupled to atmospheric pressure chemical ionization (APCI) and show

86 on of BFRs taking profit of the potential of atmospheric pressure chemical ionization (APCI) combined

87 ainst both electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) for the

88 Atmospheric pressure chemical ionization (APCI) in air o

89 Atmospheric pressure chemical ionization (APCI) is used

90 Recent evidence has shown that the atmospheric pressure chemical ionization (APCI) mechanis

91 urate mass (HRAM) mass spectrometry (MS) and atmospheric pressure chemical ionization (APCI) MS were

92 Atmospheric pressure chemical ionization (APCI) offers t

93 The novel atmospheric pressure chemical ionization (APCI) source h

94 d using hybrid quadrupole (Q) TOF MS with an atmospheric pressure chemical ionization (APCI) source i

95 The quenched products were ionized in an atmospheric pressure chemical ionization (APCI) source i

96 The corona discharge atmospheric pressure chemical ionization (APCI) source w

97 e of the new technique, a comparison with an atmospheric pressure chemical ionization (APCI) source w

98 combining electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) was deve

99 onal gas chromatography (GC x GC) coupled to atmospheric pressure chemical ionization (APCI) with a h

100 In this work, the potential of atmospheric pressure chemical ionization (APCI), a softe

101 ight flavonoids and two alkaloids using ESI, atmospheric pressure chemical ionization (APCI), and hea

102 A flame-induced atmospheric pressure chemical ionization (FAPCI) source,

103 s been demonstrated by liquid chromatography atmospheric pressure chemical ionization (LC-APCI) analy

104 desorption surface sampling with subsequent atmospheric pressure chemical ionization and mass analys

105 the sampled materials into the gas phase for atmospheric pressure chemical ionization and mass spectr

106 ectrometry and on liquid chromatography with atmospheric pressure chemical ionization combined with h

107 Gas chromatography using atmospheric pressure chemical ionization coupled to mass

108 he minimal sampling handling associated with atmospheric pressure chemical ionization for mass spectr

109 ple of the application of gas chromatography atmospheric pressure chemical ionization Fourier transfo

110 ee, hand-held ion source based on desorption atmospheric pressure chemical ionization has been develo

111 chromatography tandem mass spectrometry with atmospheric pressure chemical ionization in selected rea

112 Atmospheric pressure chemical ionization in the positive

113 red to the online detector; in this case, an atmospheric pressure chemical ionization interface of a

114 erformance liquid chromatography (HPLC) with atmospheric pressure chemical ionization mass spectromet

115 serum was analyzed for 25(OH)D by using HPLC atmospheric pressure chemical ionization mass spectromet

116 ling flow injection analysis coupled with an atmospheric pressure chemical ionization mass spectromet

117 , we show that gas chromatography coupled to atmospheric pressure chemical ionization mass spectromet

118 We used atmospheric pressure chemical ionization mass spectromet

119 Direct infusion atmospheric pressure chemical ionization mass spectromet

120 In particular, atmospheric pressure chemical ionization mass spectromet

121 on mass spectrometry running in the negative atmospheric pressure chemical ionization mode (APCI-qTOF

122 infusion on efficiency and repeatability of atmospheric pressure chemical ionization of both methyl

123 for thermolytic surface sampling followed by atmospheric pressure chemical ionization of the gas phas

124 An electron emitter as a soft atmospheric pressure chemical ionization source is prese

125 of a solution of polymer into the commercial atmospheric pressure chemical ionization source on this

126 method is based on direct injection into an atmospheric pressure chemical ionization source operated

127 applied was direct liquid injection into an atmospheric pressure chemical ionization source, followe

128 l detection was performed using positive ion atmospheric pressure chemical ionization tandem mass spe

129 ry technique (gas chromatography combined to atmospheric pressure chemical ionization tandem mass spe

130 compound RDX was achieved through selective atmospheric pressure chemical ionization using nitrate r

131 molecules in laser diode thermal desorption/atmospheric pressure chemical ionization was systematica

132 e ionization (API) sources (electrospray and atmospheric pressure chemical ionization).

133 ected in Montreal urban and indoor air using atmospheric pressure chemical ionization-mass spectromet

134 on with photodiode array detection (PDA) and atmospheric pressure chemical ionization-mass spectromet

135 The potential of using atmospheric-pressure chemical ionization (APCI) coupled

136 The use of a new atmospheric-pressure chemical ionization source for gas

137 e monolayer N-doped graphene (NG) sheets via atmospheric-pressure chemical vapor deposition, yielding

138 Atmospheric pressure cold plasma has the potential to mo

139 diameters were synthesized and tested under atmospheric pressure conditions and H2 /CO=2.

140 Under the atmospheric pressure conditions of the reaction, the tot

141 sealed so that they are commonly used under atmospheric pressure conditions.

142 es; furthermore, we show that characteristic atmospheric pressure CVD hexagonal domains are grown on

143 The evolution of thin film morphology during atmospheric pressure deposition has been studied utilizi

144 Atmospheric pressure drift tube ion mobility spectrometr

145 sues, we outline the result from coupling an atmospheric pressure, dual-gate drift tube ion mobility

146 ereas the reaction was strongly dependent at atmospheric pressure (E(a)=181 kJ mol(-1)).

147 Atmospheric pressure electron capture dissociation (AP-E

148 Atmospheric pressure electron capture dissociation (AP-E

149 using an ion source originally designed for atmospheric pressure-electron capture dissociation (AP-E

150 profile in comparison with the conventional atmospheric pressure electrospray ionization (ESI)-MS wi

151 (i.e. conventional roasting), as well as at atmospheric pressure for 10 min followed by vacuum treat

152 C pressure for 15 min followed by resting at atmospheric pressure for 3h 45 min, and repeating this c

153 N-terminal domain of L9 (NTL9), and rates at atmospheric pressure for a mutant of the C-terminal doma

154 d CH4 at room temperature (30 degrees C) and atmospheric pressure for the first time by using a novel

155 n vacuum (LSIV) with operation directly from atmospheric pressure for use in mass spectrometry.

156 (low environmental pressure) or convection (atmospheric pressure) from substrates.

157 (PXDD/PXDFs, X = Br and Cl) was performed by atmospheric pressure gas chromatography tandem mass spec

158 novel liquid drop anode (LDA) direct current atmospheric pressure glow discharge (dc-APGD) system was

159 Presented here, the liquid sampling-atmospheric pressure glow discharge (LS-APGD) is assesse

160 OES) is demonstrated using a liquid sampling-atmospheric pressure glow discharge (LS-APGD) microplasm

161 A novel atmospheric pressure glow discharge generated in contact

162 150 mg/L) for 30 minutes in normothermia and atmospheric pressure (group 1), or hyperthermia (42 degr

163 group 1), or hyperthermia (42 degrees C) and atmospheric pressure (group 2), or normothermia and high

164 in preparing plasma polymeric thin layers at atmospheric pressure grown on Quartz Crystal Microbalanc

165 omains on Cu foils under intrinsically safe, atmospheric pressure growth conditions, suitable for app

166 Plasma polymerization reaction at atmospheric pressure has been used as a simple and viabl

167 An enclosed atmospheric-pressure helium-plasma ionization (HePI-MS)

168 as to novel environmental challenges of low atmospheric pressure, high ultraviolet radiation, and un

169 d with those obtained from coffee roasted at atmospheric pressure (i.e. conventional roasting), as we

170 mard transform (HT)-type signal coupled with atmospheric pressure IMMS to complex mixtures is present

171 ls were investigated at room temperature and atmospheric pressure in an indoor Teflon chamber and nov

172 trimethylamine (TMA) on a silicon powder at atmospheric pressure in synthetic air and at room temper

173 ne Sandy bears a striking correlation to the atmospheric pressure in the US state New Jersey during t

174 o NH3 can proceed under room temperature and atmospheric pressure in water using visible light illumi

175 SIV sources by equipping the entrance of the atmospheric pressure inlet aperture with a customized co

176 face between a gas chromatograph (GC) and an atmospheric pressure inlet mass spectrometer, was constr

177 n between the DART ionization source and the atmospheric pressure inlet of the mass spectrometer, the

178 on geometry by a laser beam aligned with the atmospheric pressure inlet of the mass spectrometer.

179 uadrupole ion-trap mass spectrometer with an atmospheric pressure interface is designed, built, and c

180 -stages TMIMS was coupled with two different atmospheric pressure interface mass spectrometers (MS).

181 analysis in combination with most commercial Atmospheric Pressure Interface MS (API-MS) systems.

182 be reactors coupled to a chemical ionization atmospheric pressure interface time-of-flight mass spect

183 and neutral clusters was studied using three Atmospheric Pressure interface-Time Of Flight (APi-TOF)

184 HOMs were detected with chemical ionization-atmospheric pressure interface-time-of-flight mass spect

185 that allowed with a conventional continuous atmospheric pressure interface.

186 d-held mass spectrometers with discontinuous atmospheric pressure interfaces (DAPI).

187 d-held mass spectrometers with discontinuous atmospheric pressure interfaces.

188 n of solutes and mobile phase takes place at atmospheric pressure into a specifically designed region

189 This paper describes an atmospheric pressure ion detector based on coupling a PM

190 t that has traditionally been served well by atmospheric pressure ion mobility spectrometry (IMS) sys

191 form ion mobility spectrometry (FAIMS) is an atmospheric pressure ion mobility technique that separat

192 to use positive ion monitoring mode with an atmospheric pressure ion mobility time-of-flight mass sp

193 c pressure photoionization (LAAPPI), a novel atmospheric pressure ion source for mass spectrometry.

194 APPI in negative mode if compared with other atmospheric pressure ionization (API) sources (electrosp

195 Evolved gases are forced to enter the atmospheric pressure ionization interface of the MS by a

196 The reduced pressure at the inlet of an atmospheric pressure ionization mass spectrometer suffic

197 atrix be exposed to the inlet aperture of an atmospheric pressure ionization mass spectrometer.

198 lysis time using NO(y) chemiluminescence and atmospheric pressure ionization mass spectrometry (API-M

199 Metabolic profiles of biofluids obtained by atmospheric pressure ionization mass spectrometry-based

200 red to data obtained by using other existing atmospheric pressure ionization methods.

201 Permeating analytes are entrained to an atmospheric pressure ionization source for subsequent me

202 was to qualify gas chromatography coupled to atmospheric pressure ionization tandem mass spectrometry

203 The advantage with respect to atmospheric pressure ionization techniques, normally cou

204 ently integrates sampling/sample cleanup and atmospheric pressure ionization, making it an advantageo

205 red with previous SESI ionizers coupled with atmospheric pressure ionization-mass spectrometry (API-M

206 sensitivity of gas chromatography coupled to atmospheric pressure ionization-tandem mass spectrometry

207 ry alkyl bromides and sulfonates with CO2 at atmospheric pressure is described.

208 ry, and tertiary alkyl chlorides with CO2 at atmospheric pressure is described.

209 After the return to atmospheric pressure, it is demonstrated that non-gaseou

210 In this work, we investigate the atmospheric pressure laser ionization (APLI) technique c

211 Atmospheric pressure laser ionization (APLI) was used as

212 We present atmospheric pressure laser-induced acoustic desorption c

213 Atmospheric-pressure laser ionization mass spectrometry

214 on that has been reported for other types of atmospheric pressure liquid extraction-based surface sam

215 cal DBDs are often operated at low power and atmospheric pressure, making a direct transfer of insigh

216 Atmospheric pressure matrix-assisted laser desorption/io

217 l size were performed with a high resolution atmospheric-pressure matrix-assisted laser desorption/io

218 ces for direct characterization via modified atmospheric pressure-matrix assisted laser desorption/io

219 by gaseous neutral species, by examining an atmospheric-pressure microplasma formed in different amb

220 The antimicrobial activity of atmospheric pressure non-thermal plasma has been exhaust

221 This study highlights the capacity of atmospheric pressure non-thermal plasma to modify and de

222 ded to increase with first-trimester average atmospheric pressure (odds ratio per 5-mbar increase = 1

223 lective hydrocarboxylation of styrenes under atmospheric pressure of CO2 has been developed using pho

224 ass environmental chamber at 298 +/- 2 K and atmospheric pressure of synthetic air using in situ FTIR

225 Treatment of Ni(0) complexes 1a-e with sub-atmospheric pressures of trifluoroethylene (TrFE) afford

226 frequency and persistence of preinstrumental atmospheric pressure patterns using Self-Organizing Maps

227 y controlled by interrelated, synoptic-scale atmospheric pressure patterns.

228 We present laser desorption atmospheric pressure photochemical ionization mass spect

229 of solvent or dopant effects as observed in atmospheric pressure photoionization (APPI) and laser io

230 ollowed by electrospray ionization (ESI) and atmospheric pressure photoionization (APPI) coupled to h

231 Here, we present atmospheric pressure photoionization (APPI) Fourier tran

232 e used in parallel for (1)D detection, while atmospheric pressure photoionization (APPI) MS and ESI-M

233 ethanol loss fragment ions formed within the atmospheric pressure photoionization (APPI) source, were

234 s spectrometry, as compared to ESI(+)/(-) or atmospheric pressure photoionization (APPI)(+).

235 compared to liquid chromatography (LC)-APCI/atmospheric pressure photoionization (APPI)-HRTOF-MS for

236 stionization is achieved in both cases using atmospheric pressure photoionization (APPI).

237 Desorption atmospheric pressure photoionization (DAPPI) allows surf

238 or pretreatment, on the basis of desorption atmospheric pressure photoionization (DAPPI) coupled to

239 Electrospray- and atmospheric pressure photoionization (ESI, APPI) ultrahi

240 ance of a new orthogonal geometry field-free atmospheric pressure photoionization (FF-APPI) source wa

241 The laser ablation atmospheric pressure photoionization (LAAPPI) and LDTD-A

242 In this paper we introduce laser ablation atmospheric pressure photoionization (LAAPPI), a novel a

243 Here, we used atmospheric pressure photoionization Fourier transform i

244 range of detectable breakdown products, with atmospheric pressure photoionization in negative ionizat

245 e desolvated and ionized in the gas-phase by atmospheric pressure photoionization using a 10 eV vacuu

246 ption electrospray ionization and desorption atmospheric pressure photoionization was examined for fo

247 Atmospheric pressure photoionization was selected as the

248 ionization mechanisms are involved in DCPI: atmospheric pressure photoionization, capable of ionizin

249 As in atmospheric pressure photoionization, ionization in CPI

250 sing ultra performance liquid chromatography-atmospheric pressure photoionization-high resolution mas

251 a triple quadrupole mass spectrometer using atmospheric pressure photoionization.

252 ave previously demonstrated that non-thermal atmospheric pressure plasma (NTP) induces death of vario

253 barrier discharge (LE-DBD) is a miniaturized atmospheric pressure plasma as emission excitation sourc

254 Flowing low temperature atmospheric pressure plasma devices have been used in ma

255 uate the effects of micron sized non-thermal atmospheric pressure plasma inside the animal body on br

256 and then treated them with an N2 feeding gas atmospheric pressure plasma jet (APPJ) to increase their

257 Non-thermal atmospheric pressure plasma provides a novel therapeutic

258 we present a study on the H2O2 synthesis by atmospheric pressure plasma-water interactions.

259 ements of solvated electrons generated by an atmospheric-pressure plasma in contact with the surface

260 he inductively-coupled plasma reactor and an atmospheric-pressure plasma jet have demonstrated that t

261 thesis of a-Si:H QDs is demonstrated with an atmospheric-pressure plasma process, which allows for ac

262 Cold atmospheric pressure plasmas are gaining increased inter

263 g are two known forms of naturally occurring atmospheric pressure plasmas.

264 , utilizes only electric fields, operates at atmospheric pressure, produces a continuous output of mo

265 d components is employed to generate ions at atmospheric pressure, provide a vacuum interface, effect

266 anic solvents and water, at 60 degrees C and atmospheric pressure, provides important illustrative ex

267 while H5N1 infections correlate with TEM and atmospheric pressure (PRS).

268 iotic CO2 uptake in arid and semiarid soils: atmospheric pressure pumping, carbonate dissolution, and

269 tion of proteins than prolonged digestion at atmospheric pressure ranging from 18 to 24 h.

270 ties and volatilities in different phases at atmospheric pressure remains a challenge.

271 High-resolution atmospheric-pressure scanning microprobe matrix-assisted

272 The first utilizes an atmospheric pressure solids analysis probe to rapidly de

273 replacement-ion chromatography (RIC) with an atmospheric-pressure solution-cathode glow discharge (SC

274 der pressure at 25-150 MPa was compared with atmospheric pressure storage (0.1 MPa) at the same tempe

275 grow only during periods of relatively high atmospheric pressure, suggesting a formation timescale o

276 In an atmospheric pressure surface barrier discharge the inher

277 t ionization method has been developed using atmospheric pressure thermal desorption-extractive elect

278 nsity and isothermal compressibility data at atmospheric pressure through the Fluctuation Theory-base

279 hat all four MOFs adsorb DMMP (introduced at atmospheric pressures through a flow of helium or air) w

280 ergy from a volume of water transferred from atmospheric pressure to elevated pressure across a semip

281 nd nanocrystals, with stable levitation from atmospheric pressure to high vacuum.

282 water, and other gases are required to raise atmospheric pressure to prevent lake waters from being l

283 of concentration at 20.0-45.0 degrees C and atmospheric pressure using DSA-5000 M.

284 rocess that operates at room temperature and atmospheric pressure, using only water, CO2, and electri

285 are carried out at moderate temperatures and atmospheric pressure, using potassium hydroxide as base

286 to have a large scale height (over which the atmospheric pressure varies by a factor of e).

287 The activation energy values at atmospheric pressure were 548.6kJ/mol and 324.5kJ/mol re

288 thermal plasma (NTP) at room temperature and atmospheric pressure were investigated in a corona react

289 ates at temperatures below the ice point and atmospheric pressure were investigated using in situ Ram

290 n contrast, FAIMS devices operate at or near atmospheric pressure, which complicated integration with

291 ne complex is predominant mechanistically at atmospheric pressure, which is an important step towards

292 ng the APCI source is the soft ionization at atmospheric pressure, which results in very limited frag

293 ort High--a characteristic peak in sea level atmospheric pressure--which tends to accelerate an antic

294 e by comparing the forming gas annealing (at atmospheric pressure with a H2 partial pressure of 0.04

295 udy unravels that CrH is a superconductor at atmospheric pressure with an estimated transition temper

296 in tissue samples in a label-free manner at atmospheric pressure with only minimum sample preparatio

297 es of 0.795 W cm(-2) at room temperature and atmospheric pressure, with a round-trip voltage efficien

298 ve heating and dry distillation performed at atmospheric pressure without any added solvent or water.

299 In situ atmospheric-pressure X-ray photoelectron spectroscopy (A

300 f stabilized peroxy radicals and to estimate atmospheric pressure yields.