ライフサイエンスコーパス: desorption

1 al to initial AsEx and mainly due to abiotic desorption.

2 ediated exonuclease cleavage and full-strand desorption.

3 low energy Ar(+)-ion (11.2 eV) for physical desorption.

4 on monolayer graphene during adsorption and desorption.

5 ploying laser-induced liquid beam ionization/desorption.

6 typical for batch experiments (finite bath), desorption accelerates with increasing partition coeffic

7 Salient results suggest that: (1) As desorption/adsorption from/onto clay minerals is the maj

8 We explain increased PAH desorption after addition of toluene by competitive adso

9 affinity of oxidized LPMO could support its desorption after catalysis and allow hydrolases to acces

10 s, reflecting the combined effect of thermal desorption and advective fluid flow.

11 e evaluated for their ability to enhance PAH desorption and biodegradation in contaminated soil after

12 -associated processes, including adsorption, desorption and crowding.

13 while the second stage is controlled by gas desorption and diffusion.

14 Results from adsorption-desorption and GC headspace analyses showed that these M

15 Here we present a novel laser desorption and ionization method delivering both the PAH

16 analysis of the compounds including offline desorption and running the extract to the liquid chromat

17 mulations that model analyte movement during desorption and the "washing effect" replicate the experi

18 rimary differences between the soil moisture desorption and the adsorption processes by the fractal d

19 Temperature-programmed desorption and X-ray photoelectron spectroscopy data pro

20 likely consists of a combination of peptide desorption and/or water-mediated breakage of pore connec

21 ated soil with all surfactants increased PAH desorption, and all except R-95 substantially increased

22 Adsorption, desorption, and heterogeneous redox events of individual

23 nsfer and optimal energy barrier of hydrogen desorption, and thus promoting the proton kinetics.

24 ained with contact-less pulsed light-induced desorption, applied to different isotopes, either bosoni

25 orption, where volumetric gas absorption and desorption are measured.

26 cally, NbOFFIVE-1-Ni offers the complete CO2 desorption at 328 K under vacuum with an associated mode

27 aterials with a volumetric working capacity (desorption at 5 bar) of 203 cm(3) cm(-3) at 80 bar and 2

28 Real-time observations of adsorption/desorption at the molecular-scale elucidate exchange rea

29 Desorption atmospheric pressure photoionization (DAPPI)

30 ed in desorption electrospray ionization and desorption atmospheric pressure photoionization was exam

31 a model system to investigate the deposition/desorption behaviors of low-volatility lake ecosystem to

32 ent of hysteresis between the adsorption and desorption branches.

33 By iterative backflushing with desorption buffer MS2-loaded membranes are successfully

34 nanoparticle, 4.0min of contact time, 0.3mL desorption by acetonitrile.

35 ved through chemical adsorption and physical desorption, can be the most powerful technique due to ba

36 ectron spectroscopy, and nitrogen adsorption-desorption characterization techniques.

37 value, adsorption time, amount of adsorbent, desorption conditions (type, concentration and volume of

38 Using optimized desorption conditions, a linear correlation between IR-M

39 magnetic nanoparticles, extraction time and desorption conditions, were optimized.

40 The gas desorption could make the "hump" more profound.

41 orbents that are cycled through sorption and desorption cycles for CO2 removal from ultradilute gases

42 Five consecutive adsorption/desorption cycles were carried out, showing a consistent

43 , the successive use over various adsorption/desorption cycles with constant performance proves the h

44 nd can be subjected to 1000 humid adsorption/desorption cycles with minimal degradation.

45 ate elution, enabling consecutive adsorption/desorption cycles.

46 housand) of conducted water vapor adsorption-desorption cycles.

47 was tested for thermal and solvent-assisted desorption, demonstrating its compatibility with both ga

48 electron transfer, molecular adsorption and desorption, diffusion, and surface rearrangement.

49 up synthesis: metal and chalcogen adsorption/desorption/diffusion on substrate and grown TMD surface,

50 owever, abiotic non-reductive release of Fe (desorption, dissolution) from particulate iron-notably l

51 cal functionalities exposed, and easiness of desorption due to weaker interactions of the analyte spe

52 e model developed to simulate the adsorption-desorption dynamics during resaturation and elution.

53 Here, we used desorption electrospray ionization (DESI) mass spectrome

54 nt from direct analysis in real time (DART), desorption electrospray ionization (DESI), or low-temper

55 onization mass spectrometric techniques like desorption electrospray ionization (DESI).

56 classes using infrared matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mass spe

57 n a transient infrared matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mode, al

58 (MSI) of biological samples using nanospray desorption electrospray ionization (nano-DESI) was devel

59 hat the ambient ionization source, nanospray desorption electrospray ionization (nanoDESI), interface

60 applicability of the ion source operated in desorption electrospray ionization and desorption atmosp

61 or biotransformations in live colonies using desorption electrospray ionization coupled with ion mobi

62 ysis with mucosal metabolome profiling using desorption electrospray ionization mass spectrometry (DE

63 n water purification membranes, we have used desorption electrospray ionization mass spectrometry (DE

64 t cancer murine xenografts were subjected to desorption electrospray ionization mass spectrometry (DE

65 Here, we used desorption electrospray ionization mass spectrometry (DE

66 rm the existence and composition of the CEI, desorption electrospray ionization mass spectrometry (DE

67 id MS profile of necrotic breast cancer with Desorption Electrospray Ionization Mass Spectrometry (DE

68 prayer design and geometry on performance in desorption electrospray ionization mass spectrometry (DE

69 is of oxidation products from the surface by desorption electrospray ionization mass spectrometry (DE

70 pectrometry (AMS), high-resolution nanospray desorption electrospray ionization mass spectrometry (na

71 We applied an approach combining desorption electrospray ionization mass spectrometry ima

72 We performed desorption electrospray ionization mass spectrometry ima

73 Through desorption electrospray ionization MS imaging (DESI-MSI)

74 alyze various morphologies were tested using desorption electrospray ionization with plastic objects

75 were measured using electrospray ionization, desorption electrospray ionization, and low temperature

76 Intraoperative desorption electrospray ionization-mass spectrometry (DE

77 denocarcinoma was objectively detected using desorption electrospray ionization-mass spectrometry ima

78 Desorption electrospray ionization-mass spectrometry ima

79 Desorption electrospray mass spectrometry imaging (DESI-

80 pectrometry using an interchangeable thermal desorption/electrospray ionization source (TD-ESI) is a

81 th respect to coordination details, hydrogen desorption energies of saturated and oversaturated speci

82 Desorption ES ionization (DESI) MS has however transform

83 801 with water as an adsorbate by conducting desorption experiments with conventional differential sc

84 the products from coal combustion and thermo-desorption experiments with local Tl-rich coal pyrite.

85 ontrolled column experiment in which arsenic desorption from ferrihydrite coated sands by variable lo

86 Furthermore, AtMic60 promotes lipid desorption from membranes, likely as an initial step for

87 Cations (Na(+), Ca(2+)) decreased SDS desorption from MWCNTs due to charge screening effects.

88 ight on the microscopic mechanisms of atomic desorption from organic coatings.

89 Controlled atomic desorption from organic Poly-DiMethylSiloxane coating is

90 high detection limit allows for direct laser desorption from sherd scrapings, avoiding the need for e

91 zation and have not been achieved via direct desorption from surfaces.

92 nius' equation, and increase the rate of TCE desorption from TCE-sorbed soil.

93 thermodenuder (TD) measurements, and thermal-desorption gas-chromatography mass-spectrometry (TD-GC-M

94 ism and dynamics of molecular adsorption and desorption has to be achieved in order to advance device

95 input of 54 kJ/mol, typical for the full CO2 desorption in conventional physical adsorbents but consi

96 to investigate dynamic moisture sorption and desorption in markedly different materials, i.e., a poly

97 were chemically characterized using thermal desorption in situ derivatization coupled to a GCxGC-ToF

98 F-CIMS), operated with two different thermal desorption inlets, designed to characterize the gas and

99 from apple tissues and introduced by thermal desorption into a comprehensive two-dimensional gas chro

100 ieties based on direct matrix-assisted laser desorption-ionisation - time-of-flight mass spectrometry

101 were characterised by matrix-assisted laser-desorption/ionisation time-of-flight mass spectrometry (

102 using nanophotonic ionization based on laser desorption ionization (LDI) from a highly uniform silico

103 ycerols (TAGs) from tissue sections by laser desorption ionization (LDI) imaging mass spectrometry (I

104 NAPA) to be an effective substrate for laser desorption ionization (LDI) of small molecules for MS.

105 LDI-MS) except the phospholipids where laser desorption ionization (LDI)-MS is employed.

106 n organic matrixes for matrix-assisted laser desorption ionization (MALDI) and surface-assisted laser

107 try imaging (MSI) with matrix-assisted laser desorption ionization (MALDI) has recently advanced to a

108 d high mass resolution matrix assisted laser desorption ionization (MALDI) imaging mass spectrometry

109 Matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry

110 ll 100% agreement with matrix-assisted laser desorption ionization (MALDI) mass spectrometry-based re

111 methods, encompassing matrix-assisted laser desorption ionization (MALDI), electrospray ionization (

112 y ionization (ESI) and matrix-assisted laser desorption ionization (MALDI), typically requiring deriv

113 We present a surface assisted laser desorption ionization (SALDI) technique, coupled with fl

114 onization (MALDI) and surface-assisted laser desorption ionization (SALDI) using gold nanoparticles,

115 eroids was achieved by matrix-assisted laser desorption ionization and either Fourier transform ion c

116 mall molecule profiling and imaging by laser-desorption ionization mass spectrometry (LDI-MS), but so

117 The ionization of LS samples in desorption ionization mass spectrometry (LS DESI MS), su

118 ime the application of matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) profi

119 es a crucial factor in matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS).

120 echnical capability of matrix-assisted laser desorption ionization mass spectrometry for characteriza

121 paration of tissue for matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-M

122 % oxygen) and employed matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-M

123 igh spatial resolution matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-M

124 Utilizing matrix-assisted laser desorption ionization mass spectrometry imaging, we iden

125 matography (LC)-MS and matrix-assisted laser desorption ionization MS.

126 rospray ionization and matrix assisted laser desorption ionization show that the reaction occurs thro

127 l electrophoresis with matrix assisted laser desorption ionization tandem time-of-flight identified 2

128 finity enrichment with matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass sp

129 Matrix-assisted laser desorption ionization time-of-flight mass spectrometry s

130 blot, glycan analysis, matrix-assisted laser desorption ionization time-of-flight mass spectrometry,

131 omatography (HPLC) and matrix-assisted laser desorption ionization time-of-flight tandem mass spectro

132 d for molecular MSI is matrix-assisted laser desorption ionization, however, the presence of a matrix

133 Matrix-Assisted Laser Desorption Ionization, MALDI, has been increasingly used

134 l screening tool using matrix assisted laser desorption ionization-fourier transform-ion cyclotron re

135 ieties are analyzed by matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS) excep

136 Matrix-assisted laser/desorption ionization-mass spectrometry imaging (MALDI-M

137 e we evaluated whether matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass sp

138 y describes the use of matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass sp

139 rdsiella species using matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) methodo

140 d for downstream rapid matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) MS orga

141 Matrix-assisted desorption ionization-time of flight mass spectrometry (

142 We implemented Bruker matrix-assisted laser desorption ionization-time of flight mass spectrometry (

143 The advent of matrix-assisted laser desorption ionization-time of flight mass spectrometry (

144 g the impact of adding matrix-assisted laser desorption ionization-time of flight mass spectrometry (

145 Matrix-assisted laser desorption ionization-time of flight mass spectrometry (

146 nts, morphologies, and matrix-assisted laser desorption ionization-time of flight mass spectrometry (

147 um species (n = 28) by matrix-assisted laser desorption ionization-time of flight mass spectrometry (

148 he spectra produced by matrix-assisted laser desorption ionization-time of flight mass spectrometry (

149 linical performance of matrix-assisted laser desorption ionization-time of flight mass spectrometry (

150 estigate the impact of matrix-assisted laser desorption ionization-time of flight mass spectrometry (

151 Matrix-assisted laser desorption ionization-time of flight mass spectrometry (

152 Matrix-assisted laser desorption ionization-time of flight mass spectrometry (

153 opment and adoption of matrix-assisted laser desorption ionization-time of flight mass spectrometry (

154 of detection (LOD) by matrix-assisted laser desorption ionization-time of flight mass spectrometry (

155 The applicability of matrix-assisted laser desorption ionization-time of flight mass spectrometry (

156 In recent years, matrix-assisted laser desorption ionization-time of flight mass spectrometry (

157 heritage samples using matrix assisted laser desorption ionization-time-of-flight mass spectrometry (

158 nalysis by micropillar-matrix-assisted laser desorption ionization-time-of-flight-mass spectrometry (

159 sembled monolayers for matrix-assisted laser desorption-ionization (SAMDI) mass spectrometry.

160 gated the potential of matrix-assisted laser desorption-ionization time of flight mass spectrometry (

161 qPCR) and quantitative matrix-assisted laser desorption-ionization time-of-flight (MALDI-TOF) mass sp

162 Laser desorption-ionization time-of-flight mass spectrometry (

163 l, we developed immuno-matrix-assisted laser desorption/ionization (iMALDI) assays with automated liq

164 online single particle analyses apply laser desorption/ionization (LDI) in a bipolar mass spectromet

165 Laser desorption/ionization (LDI) was investigated as an ioniz

166 nvestigated its use in matrix-assisted laser desorption/ionization (MALDI) as a new matrix for mass s

167 Matrix-assisted laser desorption/ionization (MALDI) coupled with a time-of-fli

168 Matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry

169 Using matrix-assisted laser desorption/ionization (MALDI) imaging, we determined tha

170 spatial resolution in matrix-assisted laser desorption/ionization (MALDI) IMS experiments.

171 The use of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) suc

172 Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging

173 e sample by a modified matrix-assisted laser desorption/ionization (MALDI) method.

174 Matrix-assisted laser desorption/ionization (MALDI) MS and capillary electroph

175 ous hypoxia marker for matrix-assisted laser desorption/ionization (MALDI) MSI.

176 mulas identity) to the matrix assisted laser desorption/ionization (MALDI), while producing higher qu

177 igh-spatial resolution matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging

178 maging approach, using matrix assisted laser desorption/ionization (MALDI)-MSI and liquid extraction

179 A-ICPMS) and molecular matrix-assisted laser desorption/ionization (MALDI-)MS were used to image and

180 so coupled to off-line matrix assisted laser desorption/ionization (MALDI-TOF) mass spectrometry (MS)

181 ectrometry (GFAAS) and matrix-assisted laser desorption/ionization (MALDI-TOF-MS) for determination o

182 a nanoparticle-based, surface-assisted laser desorption/ionization (SALDI)-type mass spectrometric me

183 Ms of hTTR by means of matrix assisted laser desorption/ionization - time of flight - mass spectromet

184 nitiator mass spectrometry (NIMS) is a laser desorption/ionization analysis technique based on the va

185 e structures and large molecules that hinder desorption/ionization by trapping large molecules.

186 Matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-I

187 Matrix-assisted laser desorption/ionization imaging showed that OG applied ont

188 The method involves matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI-

189 g TATP and are comparable with other ambient desorption/ionization mass spectrometric techniques like

190 nd molecular species operating in an ambient desorption/ionization mass spectrometry (ADI-MS) mode.

191 anced high sensitivity matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS).

192 position products with matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS).

193 pose a method based on matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF MS) t

194 oss-linking coupled to matrix-assisted laser desorption/ionization mass spectrometry and CLIP-Seq seq

195 d to ~7.8nM when using matrix-assisted laser desorption/ionization mass spectrometry as the detection

196 d to 7.8nM when using matrix-assisted laser desorption/ionization mass spectrometry as the detection

197 We employed matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-M

198 er localize compounds, matrix-assisted laser desorption/ionization mass spectrometry imaging was util

199 ion in three different matrix-assisted laser desorption/ionization MSI data sets.

200 T), allowing for rapid and efficient thermal desorption/ionization of analytes previously concentrate

201 ent with a surface area restructuring-driven desorption/ionization process where signal intensity inc

202 or mass spectrometry (NIMS) is a matrix-free desorption/ionization technique with high sensitivity fo

203 A) gene sequencing and matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass sp

204 Quantitative matrix-assisted laser desorption/ionization time-of-flight (MALDI TOF) approac

205 pectroscopy (CRM), and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass sp

206 binding proteins using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass sp

207 ere screened using the Matrix-Assisted Laser Desorption/Ionization Time-of-Flight (MALDI-TOF) techniq

208 proteins directly by a matrix assisted laser desorption/ionization time-of-flight mass spectrometer.

209 rom single colonies by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (

210 mbined with subsequent matrix-assisted laser desorption/ionization time-of-flight mass spectrometry a

211 Characterization by laser desorption/ionization time-of-flight mass spectrometry,

212 icroscopy, followed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

213 UFLC and subjected to matrix assisted laser desorption/ionization time-of-flight/time-of-flight mass

214 tion was visualized by Matrix-Assisted Laser Desorption/Ionization-Imaging Mass Spectrometry (MALDI-I

215 MDA) is reported using matrix assisted laser desorption/ionization-mass spectrometry (MALDI-MS), a co

216 zymatic digestion, and matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS).

217 ed biopsy specimens by matrix-assisted laser desorption/ionization-mass spectrometry imaging (MALDI-M

218 on, as determined with matrix-assisted laser desorption/ionization-mass spectrometry, whereas species

219 Matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass sp

220 sional electrophoresis-matrix-assisted laser desorption/ionization-time of flight mass spectrometry a

221 protein sequencing and matrix-assisted laser desorption/ionization-time of flight mass spectrometry.

222 and through the use of matrix-assisted laser desorption/ionization-time-of-flight and the 16S rRNA ge

223 rospray ionization and matrix-assisted laser desorption/ionization.

224 D s of accessible pores estimated by N2 desorption is greater than that for N2 adsorption for ea

225 ith a thermal denuder, implying that thermal desorption is reproducible across very different experim

226 C shows that the pre-exponential factor for desorption is significantly smaller than that for adsorp

227 omposites are characterized by N2 adsorption-desorption isothermal analysis and thermal gravimetric a

228 We present adsorption and desorption isotherms of methane, ethane, propane, n-buta

229 the basic principles of solid-to-solution P desorption kinetics in previously unattainable detail.

230 esses and performed batch experiments on the desorption kinetics of typical wastewater pollutants (ph

231 is employed for portable laser diode thermal desorption (LDTD) at 940 nm and compared with nanosecond

232 The growth selectivity is ensured by the desorption-limited growth regime leading to the observed

233 We propose a proton-induced desorption mechanism associated with pKa of the function

234 ase of (210)Fr population is obtained with a desorption mechanism based on direct charge transfer fro

235 Three water adsorption-desorption mechanisms are common in inorganic materials:

236 ngs indicate that many commonly used thermal desorption methods might lead to inaccurate results when

237 A portable high volume desorption module prototype was also evaluated and shown

238 asurements at 25 degrees C reveal that Rb(+) desorption occurs over several tens of seconds during wh

239 iment, passive dosing of toluene resulted in desorption of 13 +/- 0.4% PAH.

240 valuated and shown to be appropriate for the desorption of analytes with a volatility equal to or les

241 lf-hydrating crossover gases while retarding desorption of and capturing free radicals formed at the

242 ecovering properties of GO by adsorption and desorption of aptamer-conjugated Qdots.

243 been proposed on the basis of adsorption and desorption of aptamers by the surface of CDs through a c

244 up to 1 muM is due to equilibrium-controlled desorption of arsenic, adsorbed to the sediment before r

245 n be explained by redox-dependent adsorption/desorption of DOC on iron minerals.

246 Infrared laser desorption of hair strands was shown to penetrate into t

247 decomposition of silicone polymers, and the desorption of rhodamine B from an alumina surface.

248 Desorption of surface ligands as a result of dilution of

249 had weak binding ability to GO, leads to the desorption of TBA-thrombin complex from electrode surfac

250 (DESI), or low-temperature plasma (LTP), the desorption of the analytes from the SPME devices in our

251 The applied heated flow-through solvent desorption of the entire spot and online solid phase ext

252 lution of anionic species generated by laser-desorption of the near-planar, fluorinated polycyclic ar

253 ectivity towards propylene because of facile desorption of the product.

254 ak sodium ion signals can be produced by the desorption of the surface of typical dry SSA particles c

255 Desorption of the Zn was minimal from both microplastics

256 consequences for U mobility: in short-term, desorption of U(VI) increases U mobility, while reductio

257 y after the exhalation was complete by rapid desorption of water molecules from the sensor surface.

258 e to characterize the enthalpy of adsorption/desorption of zeolites and MOF-801 with water as an adso

259 mination owing to nonspecific adsorption and desorption on the substrate surface.

260 us stimuli, such as heat, solvent adsorption/desorption, or electrochemical action (in systems such a

261 This desorption potential can be easily measured through an i

262 hermostatting time and temperature, vial and desorption pressure, number of extraction cycles and sal

263 The fast phase desorption process becomes unimportant for lipophilic co

264 dual chloride through an electron-stimulated desorption process.

265 and also the energy required for adsorption/desorption processes of porous material-adsorbate system

266 The rate constants of adsorption and desorption processes of resorufin were characterized fro

267 ease the energy efficiency of the adsorption-desorption processes, we propose a new operational proce

268 pressure changes, and through gas adsorption/desorption processes.

269 Here we apply thermal desorption PTR-MS for the first time to characterise the

270 types, the response time (Tc) was 3.6 h, the desorption rate constant (k-1) was 0.0046 h(-1), and the

271 o-solution distribution coefficient (Kd) and desorption rate constants (k-1) decreased whereas an inc

272 The Arrhenius plot of the adsorption/desorption rate constants measured from 9 to 55 degrees

273 ate constant (k-1) was 0.0046 h(-1), and the desorption rate was 4.71 nmol l(-1) s(-1).

274 Slow phase desorption rates are size-selective, with larger species

275 ion capacity of 183+/-18mgPGE/g resin, and a desorption ratio of 38.2+/-7.7%.

276 ze the materials, investigate the adsorption/desorption/reaction properties of the adsorbates inside

277 (4) The contaminant-trap method yielded desorption-resistant PAH fractions of typically 90-100%,

278 g was verified using the same soil with only desorption-resistant PAHs present.

279 At elevated temperatures, CO desorption results in a partial redispersion and recover

280 amount of sorbent loading, extraction time, desorption solvent and desorption time.

281 Combination of thermal desorption spectroscopy, Raman measurements, inelastic n

282 imethylsiloxane-coated stir bar with thermal desorption (TD), followed by gas chromatography coupled

283 certain compounds, probably due to the lower desorption temperature that EG Silicone and PA coatings

284 emperature but reduced to nearly zero at the desorption temperature, which prevents analyte breakthro

285 mposition of aqueous NaHCO3, essentially CO2 desorption - the key step of Na2CO3/NaHCO3 based CO2 cap

286 ility for both thermal- and solvent-assisted desorption, these new SPME probes will properly suit var

287 ur results clearly demonstrate that sorption/desorption time scales observed in batch experiments may

288 , concentration and volume of the eluent and desorption time), sample volume and interfering ions hav

289 ncluding pH, dosage of adsorbent, adsorption-desorption time, concentration and volume of elution sol

290 Matrix-assisted laser desorption time-of-flight (MALDI-ToF) mass spectrometry

291 ing, extraction time, desorption solvent and desorption time.

292 Despite the use of short extraction/desorption times (5 min/5 s), limits of quantitation bel

293 cluding: amount of adsorbent, adsorption and desorption times, type and volume of the eluent solvent

294 omeric composition by temperature programmed desorption (TPD) and molecular beams.

295 ples and coupled it to a custom-made thermal desorption unit to introduce the samples to the PTR-MS.

296 ue gas at 40 degrees C and near complete CO2 desorption upon heating to 100 degrees C, enabling a hig

297 After that, thermal desorption was applied to the PAHs to channel them into

298 01 M CaCl2), but in synthetic earthworm guts desorption was higher from microplastics (40-60%) than s

299 hange in oxygen concentration due to thermal desorption, which we used to estimate the adsorption ene

300 We combined laser desorption with REMPI spectroscopy to study organic resi