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1 pendent reduction of acetylene (ARA) using a gas chromatograph.
2 OCs) using a semivolatile thermal-desorption gas chromatograph.
3 l a challenge due to heat-degradation in the gas chromatograph.
4 d fused silica capillary to an injector of a gas chromatograph.
5 an analytical instrument such as a liquid or gas chromatograph.
6 cetamide (BSTFA) prior to injection into the gas chromatograph.
7 4)C-labeled compounds were injected into the gas chromatograph.
8 ith a photoionization source interfaced to a gas chromatograph.
9 utput of a thermionic detector attached to a gas chromatograph.
10 n be introduced into the injection port of a gas chromatograph.
11 ucted with the detector interfaced to a fast gas chromatograph.
12 xtraction, the extract was injected into the gas chromatograph.
13 eathing air through an injection port from a gas chromatograph.
14 s of the plasma source itself connected to a gas chromatograph and a mass spectrometer using a borosi
15 he PIES detector was set up in series with a gas chromatograph and a thermal conductivity detector.
16                                            A gas chromatograph and combustion and reduction furnaces
17 inogen synthesis and degradation rates using gas chromatograph and mass spectrometry analysis.
18 pentane are first separated using a standard gas chromatograph and then introduced into a MCA flow ce
19 uction under visible light were evaluated by gas chromatograph, and the midgap states of ZnS introduc
20 ntration system for use with continuous-flow gas chromatograph combustion isotope ratio mass spectrom
21                                            A gas chromatograph-combustion (GC-C) system is described
22 ces, a headspace solid phase microextraction gas chromatograph-combustion-isotope ratio mass spectrom
23 method was developed using a two-dimensional gas chromatograph coupled to a high-resolution time-of-f
24 lend was performed through a two-dimensional gas chromatograph coupled to a mass spectrometer with ti
25 rinated biphenyls (PCBs) and pesticides in a gas chromatograph coupled to a mass spectrometer.
26 ction in isooctane, and then injected into a gas chromatograph coupled to a multicollector inductivel
27 y volatile to be separated and measured by a gas chromatograph coupled to an isotope ratio mass spect
28 otocatalytic reactions were analyzed using a gas chromatograph coupled with a mass spectrometer.
29 extraction was qualified and quantified by a gas chromatograph coupled with an electron capture detec
30 (DEHP) in packaged food prior to analysis by gas chromatograph coupled with flame ionisation detector
31 oncentrations determined by biosensor and by gas chromatograph coupled with mass spectrometer exhibit
32                        A portable ultra-fast gas-chromatograph coupled with a surface acoustic wave s
33 cal plate number, a widely-used indicator of gas chromatograph efficiency, is more than 100 times hig
34 PRBS) with a mean frequency of 0.1 Hz into a gas chromatograph equipped with a flame ionization detec
35  at 230 degrees C in the injection port of a gas chromatograph equipped with a flame ionization detec
36 e remaining gas species are analyzed using a gas chromatograph equipped with a mass spectrometer (GC-
37 esidues were detected and quantified using a gas chromatograph equipped with an electron capture dete
38 is quantified in the organic extract using a gas chromatograph equipped with both a short-path therma
39 phenation of the flow field thermal gradient gas chromatograph (FF-TG-GC) developed by HyperChrom wit
40 ry columns housed in a standard Agilent 6890 gas chromatograph fitted with a high data acquisition ra
41                  Samples are injected into a gas chromatograph fitted with a megabore capillary colum
42 L of the sedimented phase was analysed using gas chromatograph-flame ionisation detector (GC-FID) and
43 hermally desorbed in the injection port of a gas chromatograph for separation, detection, and quantit
44 the utility of a relatively simple multiplex gas chromatograph for the analysis of environmental samp
45  transient ion source, it was connected to a gas chromatograph for the mass spectrometric determinati
46  plasma (LTP) ionization interface between a gas chromatograph (GC) and an atmospheric pressure inlet
47                            The method uses a gas chromatograph (GC) coupled with a multicollector ind
48                                  A prototype gas chromatograph (GC) electron monochromator (EM) refle
49  The nitrobenzene produced was measured on a gas chromatograph (GC) equipped with a nitrogen-phosphor
50  beads, followed by loading the beads into a gas chromatograph (GC) injector insert for subsequent de
51 rface (CRI) to convert samples coming from a gas chromatograph (GC) or high-performance liquid chroma
52                            A small, portable gas chromatograph (GC) was assembled for the trace detec
53 let system coupled with a fast, miniaturized gas chromatograph (GC).
54 opment of a comprehensive, three-dimensional gas chromatograph (GC3) instrument is described.
55                                            A gas chromatograph has been coupled to a direct-current g
56        A novel comprehensive two-dimensional gas chromatograph has been developed that utilizes diffe
57                                              Gas chromatographs have been flown to both Mars and Venu
58 he Likens-Nickerson apparatus on-line with a gas chromatograph hyphenated with a mass spectrometer.
59 etic isotope effects were determined using a gas chromatograph in conjunction with a mass selective d
60 nventional extractives, known androgens, and gas chromatograph index (GCI) profiles.
61                                          The gas chromatograph-ion mobility spectrometer (GC-IMS) has
62 scribed technique in which the effluent of a gas chromatograph is continuously analysed isotopically,
63                            Effluent from the gas chromatograph is pyrolyzed by passage over a heated
64 s for analysis of trace components in air, a gas chromatograph isotope ratio mass spectrometer (GC-IR
65                                 Coupled to a gas chromatograph, labeling analysis provided enrichment
66 ort direct atmospheric measurements from the Gas Chromatograph Mass Spectrometer (GCMS), including al
67                                    By way of gas chromatograph mass spectrometry (GC-MS) analysis, th
68 ctosamine (GalNAc), and glucose (Glc), using gas chromatograph mass spectrometry (GC-MS), matrix-assi
69 aroma compounds were identified according to gas chromatograph-mass spectrometer (GC-MS), aroma extra
70 rometry (AMS) instrument with a conventional gas chromatograph-mass spectrometer (GC/MS) is described
71 thyl esterificated with BF3, and analyzed by gas chromatograph-mass spectrometer (GC/MS).
72  with a cooled injection system coupled to a gas chromatograph-mass spectrometer (ILR-CIS-GC-MS) has
73  through extraction with dichloromethane and gas chromatograph-mass spectrometer analysis.
74               We measured retinoid levels by gas chromatograph-mass spectrometer technique in plasma
75 tomated fashion and injected directly into a gas chromatograph-mass spectrometer without further work
76  et al. claims to show that the Viking GCMS (gas chromatograph-mass spectrometer) experiment, which c
77 formance liquid chromatography, 15N NMR, and gas chromatograph-mass spectrometry analyses.
78  obtained by solid-phase microextraction and gas chromatograph-mass spectrometry were analysed using
79  lipid molecular species are determined with gas chromatograph-mass spectrometry.
80 tates continuous admission of analyte into a gas chromatograph/mass spectrometer (GC/MS) for methods
81                            A next-generation gas chromatograph-molecular rotational resonance (MRR) s
82                  A prototype microfabricated gas chromatograph (muGC) adapted specifically for the ra
83 s of two identical prototype microfabricated gas chromatographs (muGC) adapted for the in situ determ
84  the use of two prototype Si-microfabricated gas chromatographs (muGC) for continuous, short-term mea
85                                   Microscale gas chromatographs (muGCs) promise in-field analysis of
86 were analyzed by solid-phase microextraction gas chromatograph-olfactometry-mass spectrometry.
87  (GC-FID) and the peaks were confirmed using gas chromatograph-positive chemical ionisation-mass spec
88 ages of PBDDs and PXDDs were studied using a gas chromatograph-quadrupole time-of-flight (GC-QTOF) ma
89 ogate compounds, which are assigned based on gas-chromatograph retention time and mass spectral signa
90 es must be volatile enough to pass through a gas chromatograph, silylated derivatization reactions ar
91 s of selected parameters calculated from the gas chromatograph spectra are in a remarkable narrow ran
92 ed a semivolatile thermal desorption aerosol gas chromatograph (SV-TAG) and filter samplers to measur
93 he ability of the thermal desorption aerosol gas chromatograph (TAG) to measure gas-to-particle-phase
94 atography using a Thermal Desorption Aerosol Gas Chromatograph (TAG) with simultaneous detection by b
95 MS responses of methoxylated (MeO-)PCBs on a gas chromatograph-tandem mass spectrometry system.
96 system programmable-temperature vaporization gas chromatograph (TDS-PTV-GC) with a mu-ECD detector.
97                         A prototype portable gas chromatograph that combines a multiadsorbent preconc
98 mperature-programmable silicon micromachined gas chromatograph that employs a standard capillary colu
99  mussels and principle component analysis of gas chromatograph time-of-flight mass spectrometer resul
100 fraction is automatically transferred to the gas chromatograph to be analysed.
101 ned plasma chip is coupled to a conventional gas chromatograph to investigate its performance as an o
102       Details of interfacing a high-pressure gas chromatograph to the internal ion source of a Fourie
103 e compound analysis devices, including micro gas chromatographs, to replace the current single-step p
104                                     A modest gas chromatograph which uses air as the carrier gas was
105                                              Gas chromatograph with a corona discharge-ion mobility s
106 olid-phase dynamic extraction coupled with a gas chromatograph with a mass spectrometer was used to d
107 simple coupling of a standard, packed-column gas chromatograph with a microcantilever array (MCA) is
108 nsitivity and precision when combined with a gas chromatograph with barrier ionization discharge (GC-
109 em quadrupole mass spectrometer coupled to a gas chromatograph with headspace autosampler (HS-GC-MS/M
110 anometalloidal compounds were detected using gas chromatograph with mass spectrometric or fluorine-in
111 (top/bottom/spontaneous) were analyzed using Gas Chromatograph with Mass-Selective Detector (GC-MSD)

 
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