ライフサイエンスコーパス: inlet

1 of the mass spectrometer (MS) vacuum at the inlet.

2 pounds is possible using a direct sample gas inlet.

3 grees C to form NO2 or NO in a heated quartz inlet.

4 ion that killer whales remained in Admiralty Inlet.

5 provided by means of a standard microfluidic inlet.

6 ion of matrix interferences at the capillary inlet.

7 ss (36%) of labile GOMTK from the denuder or inlet.

8 the aerosol flow through the nebulizing gas inlet.

9 ionization (ESI)-MS with a heated capillary inlet.

10 ip and directed toward the mass spectrometer inlet.

11 e polymerase chain reaction, near the column inlet.

12 in layer of homogeneous porous medium to its inlet.

13 sure ESI source that used a heated capillary inlet.

14 sition with respect to the mass spectrometer inlet.

15 c interface can be formed near the capillary inlet.

16 sequentially position the emitters at the MS inlet.

17 e geometrical configuration of the spray and inlet.

18 lets and ions and directing it toward the MS inlet.

19 tubing through which solution flows into the inlet.

20 ered by grounding line retreat into Hercules Inlet.

21 ter passing through a temperature controlled inlet.

22 sampling and capture of the vapor on the PTV inlet.

23 le introduction through the split/splittless inlet.

24 flow rate ratio of the microfluidic chamber inlets.

25 h both front-end LC equipment and typical MS inlets.

26 surface-adsorbed acids on sampling lines and inlets.

27 (top-loading) inlets and parallel (in-line) inlets.

28 adjust the fluid column height at the fluid inlets.

29 on (250 micromx500 microm) fed by two square inlets (250 micromx250 microm).

30 When intense pressure was applied to a fluid inlet, a circular portion of the coverslip beneath the w

31 advances (e.g., a stacked ring ion guide AP inlet, a dual cell QLT), the dcQLT-orbitrap exhibited in

32 t] = 7) via satellite telemetry in Admiralty Inlet, a large fjord in the Eastern Canadian Arctic.

33 coupling along the redox gradient in Saanich Inlet-a seasonally anoxic fjord with biogeochemistry ana

34 ion geometry (at 180 degrees relative to the inlet) ablates the matrix/analyte sample deposited on th

35 sulation was carried out in a spray-drier at inlet air temperature of 160 degrees C.

36 normally closed membrane valves that have an inlet, an outlet, and a membrane-pressurization chamber

37 emical Analysis of Aerosol Online") particle inlet and a proton-transfer-reaction time-of-flight mass

38 An orthogonal ion injection inlet and a repeller plate electrode was used to direct

39 The GC, equipped with a gas inlet and a valve that transfers the H2S to a thermal co

40 mass spectrometer (PTR-TOF) using a new gas inlet and an innovative reaction chamber design.

41 ce to face with a thin spacer and feature an inlet and an outlet port.

42 rface of the metal plate are directed to the inlet and analyzed by a mass spectrometer.

43 bacteria-containing anolyte into the anodic inlet and another drop of potassium ferricyanide for cat

44 etention of larger particles near the column inlet and elution of smaller particles occurred during c

45 , and, by interacting with the enzyme at the inlet and exit of the transmembrane proton channel, in p

46 ation of N2O5 transmission efficiency on the inlet and filter system due to the accumulation of inorg

47 terized by low QD deposition near the column inlet and increasing solid-phase concentrations along th

48 table for coupling DART with ETV as a sample inlet and ionization platform for time-of-flight MS, (2)

49 ssion were sucked into the mass spectrometer inlet and mass spectra were recorded.

50 has a U-tube configuration, consisting of an inlet and outlet channel which run parallel and contain

51 for injection or sampling are located at the inlet and outlet of the cell chamber.

52 The inlet and outlet of the DFC were coupled with a Tekran M

53 asured as a function of particle size at the inlet and outlet of the scrubber.

54 onsider several configurations of fibres and inlet and outlet pipes.

55 s also appears driven by differences between inlet and outlet pressure, as well as venting and leakin

56 a fused-silica capillary which has both the inlet and outlet pressurized so that the average column

57 een gas and condensed phases at the scrubber inlet and outlet.

58 m inside diameter, 70 cm long) for the probe inlet and outlet.

59 onlinear effects), and has a very accessible inlet and outlet.

60 yer with two reference electrodes located at inlet and outlet.

61 e pelvises had transverse oval appearance in inlet and size of the female pelvis.

62 aided by inclusion of an isothermal channel inlet and thermal relaxation times in the experimental p

63 tions of blood flow in vessels with multiple inlets and outlets, constructed using an angiogenesis mo

64 mps, tubing, etc.-are vertical (top-loading) inlets and parallel (in-line) inlets.

65 Ungauged lateral inlets and sparse GW data limited the study, and argue f

66 ive communities (Grise Fiord, Kugaaruk, Pond Inlet, and Pangnirtung), where the population was <2000

67 solation membrane is placed at the reactor's inlet, and paraffin-encapsulated reagents are prestored

68 s spectrometer via a matching multicapillary inlet, and the results were compared with those obtained

69 g sample solutions in close proximity to the inlet aperture of a heated mass spectrometer inlet tube.

70 alyte in a suitable matrix be exposed to the inlet aperture of an atmospheric pressure ionization mas

71 ing the entrance of the atmospheric pressure inlet aperture with a customized cone that is sealed wit

72 essure differential at the mass spectrometer inlet aperture.

73 cell capture behavior near the affinity chip inlet area and compared the different performances of ve

74 ncy and purity; however, cell capture at the inlet area and inlet design have not been extensively de

75 Cell density near the inlet area was much higher than that in the remaining ch

76 for parallel inlet chips cell density at the inlet area was similar to that in the rest of the channe

77 significant cell capture capability near the inlet area, which led to the formation of cell blockages

78 ciated groups, and the third associated with inlet areas.

79 avoids the use of a conductance limiting ion inlet, as required by a conventional atmospheric pressur

80 The occurrence of the inlet assemblage in the western and eastern ends of the

81 drogen gas was directly injected into the GC inlet at 0.5 min intervals, using a home-built electroma

82 around the ion source and mass spectrometer inlet at atmospheric pressure.

83 After closure of the umbilical inlet at birth, portal vessels undergo a transition from

84 while cooling a short segment of the column inlet at subambient temperatures, solutes are concentrat

85 Facilitated by the use of inlet beam-type activation (i.e., trapHCD) for productio

86 oved by increasing gas conductance of the MS inlet by 4.3-fold.

87 rom the container into the mass spectrometer inlet by the pressure differential at the mass spectrome

88 indicating that the LS was carried to the MS inlet by the spray that emerged from the cone.

89 Furthermore, careful selection of the inlet capillary dimensions allowed to eliminate the firs

90 idic platforms incorporate three independent inlet channels and a microfluidic chamber with an monoli

91 the remaining channel, whereas for parallel inlet chips cell density at the inlet area was similar t

92 in a 1 L min(-1) air current with a variable inlet concentration in the range of tens of ppmv without

93 Inlet conditions were established to prevent issues with

94 A continuous atmospheric inlet consisting of a stainless steel capillary and DC i

95 gies either deep inside the cavity or at its inlet, contacting three to four consecutive GroEL apical

96 carried out in a tapered capillary with the inlet cross-section three times larger than the cross-se

97 however, cell capture at the inlet area and inlet design have not been extensively described or stud

98 Our findings show that inlet design is critical and must be considered when fab

99 erated with two different thermal desorption inlets, designed to characterize the gas and aerosol com

100 pared the different performances of vertical inlet devices and parallel inlet devices.

101 Vertical inlet devices showed significant cell capture capability

102 ances of vertical inlet devices and parallel inlet devices.

103 Plug base flow requires stronger inlet disturbance for transition.

104 When inlet disturbance is located in the core region, helical

105 When inlet disturbance is near the wall, certain quasi-spanwi

106 ventricles, 2 intracardiac devices, 1 double inlet-double outlet RV).

107 of the relative sample concentration at the inlets enables generation of gradients with varying slop

108 umn studies demonstrated that changes in the inlet end plate configuration designed to ensure uniform

109 Electrospray ionization inlet (ESII) combines positive aspects of electrospray i

110 Moreover, the optimization of the inlet flow ratio resulted in a minimized dilution factor

111 The calculation of the split ratio of the inlet flow to the two outlets is challenging because of

112 We present results utilizing a Filter Inlet for Gases and AEROsol coupled to a chemical ioniza

113 nts an expedient highly efficient separation inlet for MS, capable of separating isobaric oligosaccha

114 epts an asynchronous mixture of cells at the inlet, fractionates the cell populations according to th

115 duces or totally eliminates corrosion of the inlet frit and radically improves retention stability.

116 d from acid corrosion of the stainless steel inlet frit greatly accelerate the hydrolysis of the silo

117 We show that removing the stainless steel inlet frit, or use of a titanium frit, greatly reduces o

118 the field by addition of NO3 or N2O5 to the inlet from a portable source followed by conversion of N

119 hannels, were manipulated via changes in the inlet FTMA concentration, potentials applied to the elec

120 nced sample preparation, rapid online hot GC inlet gas phase sample derivatization, fast GC low therm

121 al split mass flow rate is determined by the inlet gas temperature and the overall heat-transfer coef

122 that heat recovery increases dramatically as inlet gas temperature rises and outlet gas temperature f

123 transfer coefficient, particularly at higher inlet gas temperatures.

124 lity of their estimates for well-to-refinery inlet gate (WTR) GHG emissions.

125 millifluidic research: Reynolds number (Re), inlet geometry, and channel height.

126 using an optimized protocol considering swab-inlet geometry, tip-sample angles and distances, rotatio

127 Moreover, the fraction of THg as MeHg at the inlet has not changed despite decadal decreases in atmos

128 at SS and TP concentrations at the reservoir inlet have declined under most discharges in recent deca

129 We found that the inlet hydrogen atoms in the hydrogen passivation serve a

130 eated between the FAIMS exit and a capillary inlet (i.d. = 0.5 mm).

131 so discuss the possibility of using vertical inlets in negative-selection separations.

132 this study we show that mangroves in desert inlets in the coasts of the Baja California have been ac

133 s of the bay is consistent with a history of inlets in these areas, even though prior to Hurricane Sa

134 es a new ionization method, droplet assisted inlet ionization (DAII), where aqueous droplets are prod

135 t observed with SAII and this electrosprayed inlet ionization (ESII) method are very similar for weak

136 ospray ionization (ESI) and solvent assisted inlet ionization (SAII) provides higher ion abundances o

137 and nonpolar compounds, and solvent assisted inlet ionization capable of ionizing larger molecules li

138 Inlet ionization is a new approach for ionizing both sma

139 The utility of solvent based inlet ionization mass spectrometry (MS) as a method for

140 81)Br obtained for these solutions with dual-inlet IRMS measurements on CH3Br gas.

141 with online EA-Cr/HTC-IRMS and offline dual-inlet IRMS.

142 The inflow at the inlet is duplicated from a fully developed flow generate

143 cule reactions, no preseparation or membrane inlet is necessary when the compounds of interest are di

144 ization inlet method, with MAIV, heating the inlet is not necessary.

145 characterized in-house by conventional dual inlet isotope ratio mass spectrometry has been analyzed

146 in the region between the glass slide and MS inlet, leading to generation of reagent ions for chemica

147 n mass spectrometer (CIMS) equipped with an "inlet-less" NO3(-) ion source.

148 Besides, the empty bed residence time and inlet load range of biofilter were set to 20 s and 21.23

149 ped a stand-alone system based on a membrane inlet mass spectrometer (MIMS) for measuring dissolved g

150 A membrane inlet mass spectrometer is mounted onto an all-electric

151 ment using [(18)O]-labeled O2 and a membrane inlet mass spectrometer to characterize Chlamydomonas re

152 2 s), the CF-MIMS (Continuous Flow Membrane Inlet Mass Spectrometer) is an innovative tool allowing

153 romatograph (GC) and an atmospheric pressure inlet mass spectrometer, was constructed.

154 oard measurements of O(2)/Ar by equilibrator inlet mass spectrometry (EIMS).

155 EIMS with the previously described membrane inlet mass spectrometry (MIMS) approach.

156 A membrane inlet mass spectrometry (MIMS) system has been used for

157 Membrane inlet mass spectrometry (MIMS) uses diffusion across a p

158 nterplay between PSII and CrCAH3 by membrane inlet mass spectrometry and x-ray crystallography.

159 Via membrane inlet mass spectrometry gas exchange, chlorophyll a fluo

160 aphy and (18)O exchange measured by membrane inlet mass spectrometry have been used to investigate st

161 Membrane inlet mass spectrometry measurements showed that CrCAH3

162 Membrane-inlet mass spectrometry measurements suggest that at lea

163 ombination of EPR and time-resolved membrane inlet mass spectrometry that the binding of ammonia pert

164 paper describes the application of membrane inlet mass spectrometry to determine the oxygen isotope

165 Here, we used membrane inlet mass spectrometry to measure the temperature respo

166 Using membrane-inlet mass spectrometry we demonstrate that acts as a mo

167 Using membrane inlet mass spectrometry, (18)O2 isotope, and various inh

168 mbrane contractors (gas-equilibrium membrane-inlet mass spectrometry, GE-MIMS).

169 Using (18)O exchange measured by membrane inlet mass spectrometry, we determined catalytic activit

170 ion of (18)O from CO(2) measured by membrane inlet mass spectrometry.

171 eviously reported matrix assisted ionization inlet method, with MAIV, heating the inlet is not necess

172 version distribution were cryotrapped at the inlet of a (4)D column, on which achiral separation allo

173 gnificant enrichment of H(+) occurs near the inlet of a charged solid-state nanopore, appreciably red

174 the radially spread pulses of ions into the inlet of a commercial MS platform (Micromass QToF2).

175 esses, the location being close to the water inlet of a drinking water supply company and their possi

176 mpled directly into the atmospheric pressure inlet of a quadrupole time-of-flight mass spectrometer a

177 an ion-selective electrode installed at the inlet of a sewage treatment plant, showed a distinctive

178 The reduced pressure at the inlet of an atmospheric pressure ionization mass spectro

179 e first, discrete sample zones flow past the inlet of an electrophoresis channel and a portion is inj

180 igh and low) has been designed to fit in the inlet of an ion mobility spectrometer (IMS).

181 tly form a spray that is directed toward the inlet of an ion-trap mass spectrometer.

182 the laser of the Raman spectroscope and the inlet of mass spectrometer.

183 oped aerosols were sampled directly into the inlet of our mass spectrometer from the vacuumed particl

184 ed urine samples were then introduced to the inlet of paper microfluidic channel, which flowed throug

185 the pressurized eluent is transferred to the inlet of the chromatographic column, along which, in a t

186 anism-containing wastewater is added into an inlet of the closed battery stack and it is transported

187 eginning part is formed and delivered to the inlet of the column at a higher-than-normal flow rate.

188 to the inlet of the mass spectrometer used for analysis.

189 ies, ejected droplets are aspirated into the inlet of the mass spectrometer, resulting in the facile

190 nization source and the atmospheric pressure inlet of the mass spectrometer, the aerosol is exposed t

191 r beam aligned with the atmospheric pressure inlet of the mass spectrometer.

192 sample relative to the DESI sprayer and the inlet of the mass spectrometer.

193 to lead to polymer membrane formation at the inlet of the micropipes thanks to capillarity.

194 directly connected to the extended capillary inlet of the MS, high ion transfer efficiency to the vac

195 mated from flow and pressure measured at the inlet of the tracheal tube and expressed as resistance (

196 body and analyte are introduced into the two inlets of a T-sensor.

197 n pumping yellow and blue solutions into the inlets of a Y-shaped device, and measuring the extent of

198 inor fully reversible reconfiguration of gas-inlets of the ion source.

199 ping was applied to the atmospheric pressure inlet on the mass spectrometer to compensate for the inc

200 n once the ions reach the vicinity of the MS inlet orifice.

201 parallel concentrators connected to a single inlet/outlet and applying it to parallel concentration a

202 topia in the cervical esophagus, also termed inlet patch (IP), varies substantially, ranging from 0.1

203 osest to the c-ring probably line the proton inlet path to an essential carboxyl group in the c-subun

204 w during transition the energy norms of such inlet perturbations grow exponentially rather than algeb

205 te microliter volumes of samples from single inlet points into arrays of detection zones (with number

206 sed into hydrodynamic jets by using a single inlet port.

207 ative to VJM, HS-2, and HS-10 with symmetric inlet ports, especially when the secondary liquid flow r

208 muaq) at high ratios of aqueous-inlet to oil-inlet pressure (AIP/OIP), yielding a linear relationship

209 the experimental measurements of the column inlet pressure and of the temperature profile along the

210 methanol and water, and operated under high inlet pressure using the retention time method.

211 Then, the column inlet pressure was increased by using capillary flow res

212 .85, 1.15, and 1.45 mL/min, corresponding to inlet pressures of 357.2, 559.5, 765.1, and 972.9 bar, r

213 EMT, BT, and TM with asymmetric inlets provided better mixing performances relative to V

214 This inlet provides extremely rapid mass detection as well as

215 rganic nitrogen (SPIN) coupled to a membrane inlet quadrupole mass spectrometer (MIMS) was developed

216 led substrates combined with online membrane inlet quadrupole mass spectrometry (MIMS).

217 enter the mass spectrometer through a heated inlet, rapid vaporization leads to the formation of mole

218 bead suspension loaded into the appropriate inlet reservoirs.

219 chieved primarily through a reduction in the inlet residence time; and (2) the development of a calib

220 sing multiplexed solvent assisted ionization inlet (SAII) mass spectrometry (MS).

221 By further miniaturizing the probe inlet, sampling with 200 ms resolution at 30 nL/min (pul

222 areas are at risk from human intervention by inlet sand mining, construction of groins and jetties th

223 ithin a 400-m stretch of natural, unmodified inlet shoreline).

224 from flats, and installation of seawalls on inlet shorelines that induce erosion of flats.

225 lectrophoresis platform composed of a single-inlet, single-outlet microchannel powered solely by volt

226 including in those experiments in which the inlet solution was first filtered via 0.45 mum.

227 ery from experiments using 0.45 mum filtered inlet solutions was only about 0.1%, and colloids of >0.

228 line tidal creek in the estuary at Murrell's Inlet, South Carolina and characterized with respect to

229 fluxes of THg and MeHg have decreased in the inlet stream and lake water apparently in response to de

230 Despite filtering office inlet supplies to remove outdoor particles, gas-phase pr

231 An aerodynamic lens-based inlet system created a well-collimated particle beam tha

232 ty spectrometry (CD-IMS) with a novel sample inlet system was designed and constructed as a detector

233 ies due to the aerodynamic particle focusing inlet system which reduces the gas phase species by a fa

234 itored mass spectrometrically via a membrane inlet system, and formaldehyde and formic acid were dete

235 In combination with an optimized inlet system, the high time and mass resolution of PTR-T

236 MCN 6000 desolvating system, or (3) an Apex inlet system.

237 patible with a wide range of chromatographic inlet systems, performs with an average, absolute bias o

238 ial source of biogenic emissions near to air inlet systems.

239 Due to the high flow rate and different inlets, TAPI data were systematically lower than the UNR

240 ot water, 40% ethanol, C18 purified), drying inlet temperature (130, 150, 170 degrees C) and amount o

241 tation of the thermometer ion using DAII was inlet temperature dependent and similar in magnitude to

242 However, higher inlet temperature is required for high-mass analytes, fo

243 Laser ablation from vacuum requires lower inlet temperature relative to laser ablation at atmosphe

244 treated by UHPH (300 MPa and 75 degrees C of inlet temperature) were studied in comparison to UHT-ste

245 The pigment matrix, inlet temperature, and carrier amount had biggest impact

246 equency, atmospheric pressure (AP) to vacuum inlet temperature, and mass analyzer ion trap conditions

247 es C) and treated at 300 MPa at 80 degrees C inlet temperature.

248 ilk was treated at 200 MPa combined with two inlet temperatures (55 or 75 degrees C) and treated at 3

249 00 and 300 MPa in combination with different inlet temperatures (Tin) (55, 65 and 75 degrees C) on th

250 tivity similar to that of ESI but, at higher inlet temperatures, appears to have the attributes of bo

251 n was addressed by using a novel slot shaped inlet that exhibited desolvation properties identical to

252 At the inlet, the M-values for all particle sizes in blood were

253 erse, posterior sagittal diameters of pelvic inlet, the plane of greatest diameter, the plane of leas

254 orbed onto the solid surface near the column inlet, thereby preventing QD attachment, whereas in the

255 s channel whereby solution is pulled from an inlet, through a channel, and into the steadily increasi

256 central channel of the h-FAPA is used as the inlet to a mass spectrometer.

257 g two different distances from the capillary inlet to a single detector.

258 e viscosity (muaq) at high ratios of aqueous-inlet to oil-inlet pressure (AIP/OIP), yielding a linear

259 ally the Deans' switch is used to switch one inlet to one of two outlets, by means of two auxiliary f

260 distance between the emitter and the heated inlet to the mass spectrometer and the voltage applied t

261 duced by the emitter array, a multicapillary inlet to the mass spectrometer was also constructed.

262 drophobic membrane, which also serves as the inlet to the mass spectrometer.

263 ways decreased with distance from the stream inlet to the swamp.

264 igh capture affinity using multiple vertical inlets to an affinity surface.

265 cell capture enhancement effects at vertical inlets to the affinity surface.

266 -filled pipette tips as fluid columns at the inlets, to introduce low speed flows to the flow focusin

267 lter filled with EAF-slag removed 37% of the inlet total P, whereas the filter filled with BOF-slag r

268 lter filled with BOF-slag removed 62% of the inlet total P.

269 spectrometer coupled with a heated flow tube inlet (TPD-CIMS) with kinetic model calculations.

270 following: (1) an overall improvement in the inlet transmission efficiencies (92 +/- 2% for NO3 and 9

271 NO3 absorption cross section rather than the inlet transmission efficiency.

272 sterior including three conjugates of pelvic inlet, transverse, posterior sagittal diameters of pelvi

273 harge separation in solution, and the hot MS inlet tube and the high velocity of gas through the tube

274 n of volatile or nonvolatile analyte into an inlet tube cooled with dry ice linking atmospheric press

275 Mass spectrometers in which a heated inlet tube is not available can be used for ionization u

276 olution is directly introduced into a heated inlet tube linking atmospheric pressure and the initial

277 lary, used with SAII, inserted into a heated inlet tube of an Orbitrap Exactive mass spectrometer (MS

278 At a low inlet tube temperature, ESII has an ionization selectivi

279 inlet aperture of a heated mass spectrometer inlet tube.

280 observed by heating rather than cooling the inlet tube.

281 nities, NPs tend to accumulate mostly at the inlet tumor vessels leaving the inner and outer vasculat

282 oxetic acid-enhanced MR images with the dual-inlet two-compartment uptake model presents a new and pr

283 In this paper, we discuss the effects of inlet type on chip fabrication, nonspecific binding, cel

284 de the entire torch, i.e., from the injector inlet up to the ionization and reaching the sampler.

285 The most common inlets-used to connect the microfluidic chip to pumps, t

286 The new inlet using center-sampling through a critical orifice r

287 This suction opens the inlet valve and is required for filling in the presence

288 transient drop in pressure downstream of the inlet valve following contraction.

289 Regardless of inlet VAM concentrations, methane was captured at almost

290 nd fluid flow that entered through a central inlet vessel, branched into an extensive capillary bed,

291 A sorption trap inlet was constructed to serve as the interface between

292 though prior to Hurricane Sandy in 2012, no inlet was present in the eastern bay in almost 200 years

293 ould be explained by the geochemistry of the inlet water.

294 The most relevant parameters of a multimode inlet were optimized to increase the injection volume up

295 rent types of electrospray ionization source inlets were converted to LSIV sources by equipping the e

296 d use), as well as increased time in coastal inlets, were important determinants of increased PCB con

297 urfaces, which were most pronounced near the inlet where larger diffusive boundary layers formed arou

298 ly caused by the hydrodynamics at the column inlet which produced a concentrated AgNP flux to the sol

299 of cephalopelvic mismatch possess a rounder inlet, which is beneficial for obstetrics.

300 he DART ion source and the mass spectrometer inlet, with the entire observed mass spectral fingerprin