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1 under low temperature and pressure (even at atmospheric pressure).
2 of soil temperature, porewater salinity, and atmospheric pressure).
3 t for an increase in preterm birth risk with atmospheric pressure.
4 ed by a surface DBD-plasma reactor in air at atmospheric pressure.
5 dstock in a nitrogen gas environment at near atmospheric pressure.
6 t (288.15, 298.15, 308.15 and 318.15)K under atmospheric pressure.
7 K approaches a similar crossover line at one atmospheric pressure.
8 fibers after sintering at 1500 degrees C and atmospheric pressure.
9 tive analytical method which operates at the atmospheric pressure.
10 ration concentration at room temperature and atmospheric pressure.
11 the outer surfaces of the cell electrodes at atmospheric pressure.
12 cyclic hydrocarbons at room temperature and atmospheric pressure.
13 ctrospray process at ambient temperature and atmospheric pressure.
14 alysis was investigated in N2 environment at atmospheric pressure.
15 real-time formation of ion/ion complexes at atmospheric pressure.
16 -port interface for subsequent ionization at atmospheric pressure.
17 9) molecules cm(-3), room temperature and at atmospheric pressure.
18 temperature range of (288.15-318.15)K and at atmospheric pressure.
19 d at temperatures, T=(293.15-318.15)K and at atmospheric pressure.
20 l pyrolysis in a high temperature furnace at atmospheric pressure.
21 of concentration at 20.0-45.0 degrees C and atmospheric pressure.
22 K and pH levels between 8.50 and 9.87 under atmospheric pressure.
23 et temperature relative to laser ablation at atmospheric pressure.
24 emble for subsequent DEER data collection at atmospheric pressure.
25 he ion source and mass spectrometer inlet at atmospheric pressure.
26 r to perform MAIV from both intermediate and atmospheric pressure.
27 mperature, vapour pressure deficit, c(a) and atmospheric pressure.
28 ic methane conversions reported so far under atmospheric pressure.
29 mpared to standard conditions carried out at atmospheric pressure.
30 = 293.15, 303.15, 313.15, and 323.15) K and atmospheric pressure.
31 n of at least one invisible excited state at atmospheric pressure.
32 n of this invisible excited state present at atmospheric pressure.
33 process temperature from 40 to 60 degrees C, atmospheric pressure.
34 It operates at room temperature and atmospheric pressure.
35 duct, however, vacuum drying works under sub-atmospheric pressures.
36 y non-equilibrium plasma process operated at atmospheric pressures.
37 g measurements at different temperatures and atmospheric pressures.
38 ted to a step-by-step pressure increase from atmospheric pressure (1 bar) to 2 and 4 bar, followed by
40 emperatures of CsFn (n = 2,3,5) compounds at atmospheric pressure (218 degrees C, 150 degrees C, -15
42 g the analytical capabilities of the flowing atmospheric-pressure afterglow (FAPA) source by explorin
46 demonstrate that the MOF can be produced at atmospheric pressure, an improvement over previous repor
48 erm birth risk were found for both increased atmospheric pressure and ambient temperature exposures d
49 ed the direct detection of gas phase ions at atmospheric pressure and confirmed a limit of detection
50 cal information on the active surfaces under atmospheric pressure and in the presence of liquids by m
52 ugh direct current (DC) plasma processing at atmospheric pressure and room temperature has been demon
55 to an inlet tube cooled with dry ice linking atmospheric pressure and the first vacuum stage of a mas
56 introduced into a heated inlet tube linking atmospheric pressure and the initial vacuum stage of the
57 periments, precursor ions are dissociated at atmospheric pressure and the resulting fragment ions are
58 nanodiamonds containing NV(-) centres at sub-atmospheric pressures and show that while they burn in a
61 and aperture from ICT analysis performed at atmospheric pressure are higher than those calculated fr
62 pure nitrogen (N2) to pure oxygen (O2) in an atmospheric pressure argon plasma jet (kINPen) will chan
63 cular exclusion of propane from propylene at atmospheric pressure, as evidenced through multiple cycl
65 verall, a reducing scenario leads to a lower atmospheric pressure at the surface and to a larger atmo
66 paper reports on the development of a hybrid atmospheric pressure atomic force microscopy/mass spectr
67 sprayed protein molecules is performed under atmospheric pressure by an automated ion landing apparat
68 cles at elevated temperature under oxygen at atmospheric pressure, by using advanced in situ electron
74 on of BFRs taking profit of the potential of atmospheric pressure chemical ionization (APCI) combined
75 ainst both electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) for the
80 urate mass (HRAM) mass spectrometry (MS) and atmospheric pressure chemical ionization (APCI) MS were
83 d using hybrid quadrupole (Q) TOF MS with an atmospheric pressure chemical ionization (APCI) source i
84 The quenched products were ionized in an atmospheric pressure chemical ionization (APCI) source i
85 periments were performed using the contained atmospheric pressure chemical ionization (APCI) source t
86 e of the new technique, a comparison with an atmospheric pressure chemical ionization (APCI) source w
87 combining electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) was deve
88 ight flavonoids and two alkaloids using ESI, atmospheric pressure chemical ionization (APCI), and hea
89 nalysis probe (ASAP), and direct inlet probe-atmospheric pressure chemical ionization (DIP-APCI) anal
91 t for physical contact, a new contained nano-atmospheric pressure chemical ionization (nAPCI) source
92 ion sources (Eletrospray Ionization-ESI and Atmospheric Pressure Chemical Ionization - APCI) in LC-M
93 desorption surface sampling with subsequent atmospheric pressure chemical ionization and mass analys
94 the sampled materials into the gas phase for atmospheric pressure chemical ionization and mass spectr
95 ectrometry and on liquid chromatography with atmospheric pressure chemical ionization combined with h
97 he minimal sampling handling associated with atmospheric pressure chemical ionization for mass spectr
98 ple of the application of gas chromatography atmospheric pressure chemical ionization Fourier transfo
99 ee, hand-held ion source based on desorption atmospheric pressure chemical ionization has been develo
100 chromatography tandem mass spectrometry with atmospheric pressure chemical ionization in selected rea
102 red to the online detector; in this case, an atmospheric pressure chemical ionization interface of a
103 , we show that gas chromatography coupled to atmospheric pressure chemical ionization mass spectromet
107 then immediately transferred to a detector (atmospheric pressure chemical ionization mass spectromet
108 on mass spectrometry running in the negative atmospheric pressure chemical ionization mode (APCI-qTOF
109 infusion on efficiency and repeatability of atmospheric pressure chemical ionization of both methyl
110 for thermolytic surface sampling followed by atmospheric pressure chemical ionization of the gas phas
112 esized and subjected to fast pyrolysis in an atmospheric pressure chemical ionization source of a lin
113 of a solution of polymer into the commercial atmospheric pressure chemical ionization source on this
114 method is based on direct injection into an atmospheric pressure chemical ionization source operated
115 applied was direct liquid injection into an atmospheric pressure chemical ionization source, followe
116 l detection was performed using positive ion atmospheric pressure chemical ionization tandem mass spe
117 ry technique (gas chromatography combined to atmospheric pressure chemical ionization tandem mass spe
118 ultra-high performance liquid chromatography-atmospheric pressure chemical ionization tandem mass spe
119 ected in Montreal urban and indoor air using atmospheric pressure chemical ionization-mass spectromet
121 on with photodiode array detection (PDA) and atmospheric pressure chemical ionization-mass spectromet
126 tably, facile switching of the ion source to atmospheric-pressure chemical ionization with the exact
129 ost identical mass spectra as APCI involving atmospheric pressure conditions, the presence of many di
130 The evolution of thin film morphology during atmospheric pressure deposition has been studied utilizi
132 sues, we outline the result from coupling an atmospheric pressure, dual-gate drift tube ion mobility
134 using an ion source originally designed for atmospheric pressure-electron capture dissociation (AP-E
136 Drought Atlas, sea surface temperatures and atmospheric pressure fields, we determine that the El Ni
137 (i.e. conventional roasting), as well as at atmospheric pressure for 10 min followed by vacuum treat
138 C pressure for 15 min followed by resting at atmospheric pressure for 3h 45 min, and repeating this c
139 N-terminal domain of L9 (NTL9), and rates at atmospheric pressure for a mutant of the C-terminal doma
140 d CH4 at room temperature (30 degrees C) and atmospheric pressure for the first time by using a novel
144 (PXDD/PXDFs, X = Br and Cl) was performed by atmospheric pressure gas chromatography tandem mass spec
145 mass spectrometry data files generated by an atmospheric pressure gas chromatography-quadrupole time-
146 Lake Michigan lake trout extract analyzed by atmospheric pressure gas chromatography-quadrupole time-
147 chromatography-mass spectrometry (GC-MS) and atmospheric pressure gas chromatography-quadrupole-time
149 novel liquid drop anode (LDA) direct current atmospheric pressure glow discharge (dc-APGD) system was
151 OES) is demonstrated using a liquid sampling-atmospheric pressure glow discharge (LS-APGD) microplasm
152 te Express plate reader to a liquid sampling-atmospheric pressure glow discharge (LS-APGD) microplasm
153 ablation (LA) system to the liquid sampling-atmospheric pressure glow discharge (LS-APGD) microplasm
154 developed ionization source, liquid sampling-atmospheric pressure glow discharge (LS-APGD), for marin
156 in preparing plasma polymeric thin layers at atmospheric pressure grown on Quartz Crystal Microbalanc
157 omains on Cu foils under intrinsically safe, atmospheric pressure growth conditions, suitable for app
158 turated hydrocarbons at room temperature and atmospheric pressure has been performed in this system t
161 as to novel environmental challenges of low atmospheric pressure, high ultraviolet radiation, and un
162 d with those obtained from coffee roasted at atmospheric pressure (i.e. conventional roasting), as we
163 additional methods that ionize molecules at atmospheric pressure, (ii) ambient pressure ion mobility
164 mard transform (HT)-type signal coupled with atmospheric pressure IMMS to complex mixtures is present
165 temperatures between 20-45 degrees C and at atmospheric pressure in an aqueous designer surfactant m
166 ls were investigated at room temperature and atmospheric pressure in an indoor Teflon chamber and nov
167 OH radicals and Cl atoms at 297 +/- 3 K and atmospheric pressure in Boulder, CO (~860 mbar) of hexam
168 trimethylamine (TMA) on a silicon powder at atmospheric pressure in synthetic air and at room temper
169 o NH3 can proceed under room temperature and atmospheric pressure in water using visible light illumi
170 SIV sources by equipping the entrance of the atmospheric pressure inlet aperture with a customized co
171 n between the DART ionization source and the atmospheric pressure inlet of the mass spectrometer, the
172 on geometry by a laser beam aligned with the atmospheric pressure inlet of the mass spectrometer.
173 -stages TMIMS was coupled with two different atmospheric pressure interface mass spectrometers (MS).
174 be reactors coupled to a chemical ionization atmospheric pressure interface time-of-flight mass spect
175 on between a CI-Orbitrap and the widely used atmospheric pressure interface time-of-flight mass spect
176 )) based chemical ionization (CI) coupled to atmospheric pressure interface time-of-flight mass spect
177 and neutral clusters was studied using three Atmospheric Pressure interface-Time Of Flight (APi-TOF)
178 HOMs were detected with chemical ionization-atmospheric pressure interface-time-of-flight mass spect
180 n of solutes and mobile phase takes place at atmospheric pressure into a specifically designed region
181 form ion mobility spectrometry (FAIMS) is an atmospheric pressure ion mobility technique that separat
182 terization techniques to nanoparticles using atmospheric-pressure ion mobility-mass spectrometry (IM-
187 Permeating analytes are entrained to an atmospheric pressure ionization source for subsequent me
188 was to qualify gas chromatography coupled to atmospheric pressure ionization tandem mass spectrometry
190 ently integrates sampling/sample cleanup and atmospheric pressure ionization, making it an advantageo
192 sensitivity of gas chromatography coupled to atmospheric pressure ionization-tandem mass spectrometry
197 on that has been reported for other types of atmospheric pressure liquid extraction-based surface sam
198 cal DBDs are often operated at low power and atmospheric pressure, making a direct transfer of insigh
201 ces for direct characterization via modified atmospheric pressure-matrix assisted laser desorption/io
204 ded to increase with first-trimester average atmospheric pressure (odds ratio per 5-mbar increase = 1
205 lective hydrocarboxylation of styrenes under atmospheric pressure of CO2 has been developed using pho
206 ass environmental chamber at 298 +/- 2 K and atmospheric pressure of synthetic air using in situ FTIR
207 Treatment of Ni(0) complexes 1a-e with sub-atmospheric pressures of trifluoroethylene (TrFE) afford
208 This study investigated the effects of low atmospheric pressure on the growth of chemoorganotrophic
209 and/or liquid media at low temperatures and atmospheric pressure open new ways to form advanced func
210 e sampling throughput by facilitating stable atmospheric-pressure optical trapping of individual part
211 frequency and persistence of preinstrumental atmospheric pressure patterns using Self-Organizing Maps
214 of solvent or dopant effects as observed in atmospheric pressure photoionization (APPI) and laser io
215 ollowed by electrospray ionization (ESI) and atmospheric pressure photoionization (APPI) coupled to h
217 e used in parallel for (1)D detection, while atmospheric pressure photoionization (APPI) MS and ESI-M
218 lectrospray ionization (ESI)(+), ESI(-), and atmospheric pressure photoionization (APPI)(+)) to chara
224 ance of a new orthogonal geometry field-free atmospheric pressure photoionization (FF-APPI) source wa
225 100 mum spatial resolution in laser ablation atmospheric pressure photoionization (LAAPPI) and laser
228 range of detectable breakdown products, with atmospheric pressure photoionization in negative ionizat
229 ption electrospray ionization and desorption atmospheric pressure photoionization was examined for fo
231 ionization mechanisms are involved in DCPI: atmospheric pressure photoionization, capable of ionizin
232 sing ultra performance liquid chromatography-atmospheric pressure photoionization-high resolution mas
235 e-step, highly-efficiency, and low-cost cold atmospheric pressure plasma (CAPP)-based method for obta
236 ave previously demonstrated that non-thermal atmospheric pressure plasma (NTP) induces death of vario
237 barrier discharge (LE-DBD) is a miniaturized atmospheric pressure plasma as emission excitation sourc
239 uate the effects of micron sized non-thermal atmospheric pressure plasma inside the animal body on br
241 and then treated them with an N2 feeding gas atmospheric pressure plasma jet (APPJ) to increase their
247 ements of solvated electrons generated by an atmospheric-pressure plasma in contact with the surface
248 of LTP treatments against bacteria using an atmospheric-pressure plasma jet and show that LTP treatm
250 he inductively-coupled plasma reactor and an atmospheric-pressure plasma jet have demonstrated that t
251 thesis of a-Si:H QDs is demonstrated with an atmospheric-pressure plasma process, which allows for ac
252 wave-driven atmospheric-pressure plasma, DBD atmospheric-pressure plasma, and two other treatments: v
253 ratus: RF plasma in vacuum, microwave-driven atmospheric-pressure plasma, DBD atmospheric-pressure pl
256 i)Pr(3))(2), Cp* = C(5)Me(5)) with ethene at atmospheric pressure produces the ethene-bridged diurani
257 d components is employed to generate ions at atmospheric pressure, provide a vacuum interface, effect
258 anic solvents and water, at 60 degrees C and atmospheric pressure, provides important illustrative ex
260 iotic CO2 uptake in arid and semiarid soils: atmospheric pressure pumping, carbonate dissolution, and
261 als in the presence of gases in the mTorr to atmospheric pressure range, which brings surface science
264 tected at the surface during a period of low atmospheric pressure resulted from fractures of extremel
269 der pressure at 25-150 MPa was compared with atmospheric pressure storage (0.1 MPa) at the same tempe
270 grow only during periods of relatively high atmospheric pressure, suggesting a formation timescale o
275 nsity and isothermal compressibility data at atmospheric pressure through the Fluctuation Theory-base
276 hat all four MOFs adsorb DMMP (introduced at atmospheric pressures through a flow of helium or air) w
277 can readily occur during their transfer from atmospheric pressure to a lower pressure, which limits p
278 ergy from a volume of water transferred from atmospheric pressure to elevated pressure across a semip
280 water, and other gases are required to raise atmospheric pressure to prevent lake waters from being l
281 tube ion mobility spectrometer, operated at atmospheric pressure, to a linear ion trap mass spectrom
283 rocess that operates at room temperature and atmospheric pressure, using only water, CO2, and electri
287 ates at temperatures below the ice point and atmospheric pressure were investigated using in situ Ram
288 gligible vapor pressures (VP) is achieved at atmospheric pressure when the proximal sample is exposed
289 lene but not propane at room temperature and atmospheric pressure, whereas the isostructural SIFSIX-3
290 n contrast, FAIMS devices operate at or near atmospheric pressure, which complicated integration with
291 ng the APCI source is the soft ionization at atmospheric pressure, which results in very limited frag
292 (B) transitions to PL as pressure approaches atmospheric pressure while field enhancement and the sec
293 temperature, and negatively correlated with atmospheric pressure, while the correlation pattern was
295 e by comparing the forming gas annealing (at atmospheric pressure with a H2 partial pressure of 0.04
296 udy unravels that CrH is a superconductor at atmospheric pressure with an estimated transition temper
297 in tissue samples in a label-free manner at atmospheric pressure with only minimum sample preparatio
298 ve heating and dry distillation performed at atmospheric pressure without any added solvent or water.