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1                                              FTIR analyses pointed to the formation of metal carboxyl
2                                              FTIR analysis of polysaccharide extracts showed dominant
3                                              FTIR and GC/MS showed fertiliser treatment resulted in t
4                                              FTIR and wide-angle X-ray scattering spectroscopy also i
5                                              FTIR results indicated incorporation of peptides into th
6                                              FTIR showed that when kafirin was dissolved in GAA its a
7                                              FTIR spectra showed minor changes in peak intensities (a
8                                              FTIR spectra suggested the possible formation of hydroge
9                                              FTIR spectroscopic imaging was used to study the tissues
10                                              FTIR spectroscopy is a common in situ reaction monitorin
11                                              FTIR studies revealed alterations in protein secondary s
12                                              FTIR-ATR combined with chemometrics analysis such as hie
13                                              FTIR-identified microplastics 50-1500 mum, including pol
14                                              FTIR/smog chamber experiments and ab initio quantum calc
15 as used to simultaneously image two acrylic, FTIR waveguide imaging elements from below, at frame rat
16 e the individual vibrational bands within an FTIR absorbance spectrum by curve fitting, which leads t
17         Fourier transform-infrared analyses (FTIR), field emission scanning electron microscopy (FESE
18 ncreased the thermal stability of VD(3), and FTIR confirmed the presence of the biopolymers and VD(3)
19 ploying cyclic voltammetry, amperometry, and FTIR with various electrolytes of varying concentrations
20 ons were determined by Congo red binding and FTIR analysis.
21                      3D fluorescence, CD and FTIR studies established significant conformational chan
22 es, including MS, ion mobility (IM), CD, and FTIR spectroscopy assays.
23 ha-linolenic acids were slightly changed and FTIR spectra showed minor variation in peak intensities
24 nce assays for amyloid fibril detection, and FTIR assays, we investigated the role of HtrA1 both in n
25               Using a combination of DFT and FTIR, we also provide a hypothesis for the chemical iden
26 ble light (6000 lx, 24 degrees C, 344 h) and FTIR spectra were recorded periodically with or without
27 n preservation (e.g., %N, microporosity, and FTIR spectroscopic analyses), but these are often destru
28                                Using NMR and FTIR spectroscopy, here we addressed how the T43I substi
29                    In addition, (1)H NMR and FTIR spectrums confirmed the presence of pectin in obtai
30 X-ray photoelectron spectroscopy, Raman, and FTIR show that the electron-deficient pyrazine sites in
31                   The combination of SEC and FTIR data showed that alpha-1,6-glycosidic bonds are mor
32 tering, zeta potential, surface tension, and FTIR spectroscopic characterization.
33 hysiological measurements and UV-visible and FTIR spectroscopy, we characterized the proton transfer
34                                      XRD and FTIR analyses were used to explain changes in protein st
35 s prepared and characterised by SEM, XRD and FTIR.
36           The setup is easily adapted to any FTIR and fiber-coupled Raman spectrometers and gas analy
37                     This has led us to apply FTIR spectroscopy to the investigation of blood samples
38                             Ninhydrin assay, FTIR, WAXD, SEM and mechanical tests documented successf
39            Attenuated total reflection (ATR)-FTIR spectroscopic imaging allows probing of a sample at
40                                          ATR-FTIR directly on fresh purees satisfactorily predicted t
41 olecular order was observed from XRD and ATR-FTIR spectra.
42 onitored using (13)C solid-state NMR and ATR-FTIR.
43  data showed strong correlations between ATR-FTIR, clinical, and lipidomic information.
44 lecular fingerprinting as dry powders by ATR-FTIR spectroscopy and Raman spectroscopy.
45 n film and then, their quantification by ATR-FTIR using a standard addition method.
46  our APXPS interpretation, complementary ATR-FTIR Kretschmann experiments on a similar model system,
47 mercial samples were tested by developed ATR-FTIR methodology and RT-PCR technique, mutually confirmi
48 success rates of 99, 81, 76, and 66% for ATR-FTIR, NIR reflectance spectroscopy, LIBS, and XRF, respe
49 th 99, 91, 97, and 70% success rates for ATR-FTIR, NIR reflectance spectroscopy, LIBS, and XRF, respe
50 using attenuated total reflectance-FTIR (ATR-FTIR) spectroscopy.
51 pectroscopy in the Kretschmann geometry (ATR-FTIR Kretschmann).
52  reflectance Fourier transform infrared (ATR-FTIR) and Raman spectra of non-extracted seed material h
53 l reflection-Fourier transform infrared (ATR-FTIR) spectroscopic method compatible with the requireme
54 l reflection fourier transform infrared (ATR-FTIR) spectroscopy and direct analysis in real time mass
55  reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and paper spray mass spectrometry (PS
56 l reflection Fourier-transform infrared (ATR-FTIR) spectroscopy combined with multivariate analysis w
57 l reflection Fourier-transform infrared (ATR-FTIR) spectroscopy in conjunction with chemometric techn
58 l reflection Fourier transform infrared (ATR-FTIR) spectroscopy ready for use in commercial FTIR spec
59  reflectance Fourier transform infrared (ATR-FTIR) spectroscopy revealed a presence of oxygen-contain
60  reflectance Fourier transform infrared (ATR-FTIR) spectroscopy to analyze urine samples collected fr
61 l Reflection Fourier-transform infrared (ATR-FTIR) spectroscopy, using chemometric approaches, includ
62 l Reflection Fourier Transform Infrared (ATR-FTIR) spectroscopy.
63 l Reflection Fourier Transform Infrared (ATR-FTIR) to detect B. bovis in red blood cells (RBCs).
64  reflectance-Fourier transform infrared (ATR-FTIR) to identify and quantify proteins in urine at low
65                              Here, macro ATR-FTIR spectroscopic imaging, along with a variable angle
66 s study was to evaluate the potential of ATR-FTIR and chemometrics to discriminate espresso coffees w
67 ed, results support the applicability of ATR-FTIR for the in situ determination of the grade of liver
68 as alteration in interrelated nuances of ATR-FTIR spectra, XRD-pattern, morphology, charge on protein
69 te, for the first time, the potential of ATR-FTIR spectroscopy combined with multivariate analysis as
70 These results reinforce the potential of ATR-FTIR spectroscopy with multivariate analysis as a new to
71 on were analyzed by expert pathologists, ATR-FTIR spectroscopy, lipid biochemical analysis, and UPLC-
72           A novel spectroelectrochemical ATR-FTIR thin-film cell was designed and applied to elucidat
73                   Infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) confirm
74 Fourier Transform infrared spectroscopy (ATR-FTIR) combined with attenuated total internal reflectanc
75 Fourier-transform infrared spectroscopy (ATR-FTIR) combined with chemometric methods were used for cl
76 Fourier transform infrared spectroscopy (ATR-FTIR) nicely agreed with interaction energies computed f
77 lectance Fourier transform spectroscopy (ATR-FTIR) was applied on fresh (NF), freeze-dried (FD) and c
78 flection Fourier transform spectroscopy (ATR-FTIR) without the need for collimated or polarised incid
79 Fourier transform infrared spectroscopy (ATR-FTIR), near-infrared (NIR) reflectance spectroscopy, las
80 Fourier transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), and energy-di
81 nd Fourier transform infra-spectroscopy (ATR-FTIR).
82 ral Binding Characterization (MBC) (TGA, ATR-FTIR and zeta Potential), while at the "macroscopic" sca
83                        Results show that ATR-FTIR captures a global picture of the lipid composition
84              Success rates indicate that ATR-FTIR, NIR reflectance spectroscopy, and LIBS coupled wit
85 correlation spectroscopy analysis of the ATR-FTIR spectra revealed that higher initial BSA concentrat
86 mparison of the results obtained by TLSE-ATR-FTIR to the results of conventional analyses carried out
87 er transform infrared spectroscopy (TLSE-ATR-FTIR).
88 ults demonstrate the advantages of using ATR-FTIR as a rapid and non-destructive tool that achieves a
89  the parasite in a cell population using ATR-FTIR for a babesiosis diagnostic.
90 ion studies: evening primrose oils using ATR-FTIR spectroscopy and ground nutmeg using NIR diffuse re
91 also extracted from MD simulations while ATR-FTIR experiments indicated strongly hindered diffusion w
92 n changes in the IR spectral bands, with ATR-FTIR in combination with Partial Least Squares-Discrimin
93 ization of TLSB was then performed with BET, FTIR, XRD, TGA, PZC, SEM, and TEM analyses.
94 with MagLev, followed by characterization by FTIR-ATR, enabled identification of fentanyl in a sample
95  prepared at each step were characterized by FTIR and SEM.
96                    They are characterized by FTIR, (1)H-NMR, and, for the first time, a comprehensive
97 lar cage structure was also characterized by FTIR, NMR, and MALDI-TOF.
98                 Man-AOP was characterized by FTIR, SEM and PXRD revealing a covalent interaction.
99 es were observed by SEM and characterized by FTIR.
100 etal-chlorophylls complexes was confirmed by FTIR spectroscopy.
101 er chains and antioxidants were confirmed by FTIR where spectra displayed a shift of the amide-III pe
102 ntent of 23.6 +/- 0.9% that was confirmed by FTIR.
103 ers were not reported, as fiber detection by FTIR imaging was not available at the time of analyses.
104 to ferulic acid and vanillin was explored by FTIR analysis.
105       Specific chemical bonds were probed by FTIR spectroscopy.
106 teraction between the raw materials shown by FTIR, justify the increase in water solubility [0.072 (0
107 lity of virgin olive oil (VOO) via mesh cell-FTIR spectroscopy monitoring.
108     Real time monitoring of VOO by mesh cell-FTIR was found to be a useful tool to follow the combine
109 X-ray absorption spectroscopy, chemisorption FTIR, operando UV/Vis and (1) H-(13) C HSQC NMR spectros
110                                     Combined FTIR and XPS analyses demonstrated that the redox activi
111                                    Combining FTIR and UV-Vis spectroscopy along with molecular dynami
112 IR) spectroscopy ready for use in commercial FTIR spectrometers.
113 posure to O(2)-lean CO oxidation conditions, FTIR spectroscopy indicates the partial deconfinement of
114 n analysis of vibrational spectroscopy data (FTIR, Raman and near-IR) highlighting a series of critic
115  surface hydrophobicity, circular dichroism, FTIR spectroscopy, and fluorescence analyses revealed pr
116 reflectance-Fourier transforms infrared (DRS-FTIR) spectral monitoring of fluoroquinolone antibiotics
117                    The advantages of the DRS-FTIR method are its simplicity, sensitivity and suitabil
118 1-102.3% from poultry eggs samples using DRS-FTIR method.
119 antibiotics in poultry egg samples using DRS-FTIR.
120 trapped in surfactant and analyzed using DRS-FTIR.
121 d non-invasive spectroscopic analyses (i.e., FTIR and Raman spectroscopy) and complimented with pyrol
122                               Isotope-edited FTIR spectroscopy, coupled with DFT calculations, enable
123 odels, underlining the advantage of dry-film FTIR measurement.
124 , we developed PLSR models based on dry-film FTIR spectroscopy for the prediction of both DH% and M(w
125 ifferent transfer technologies described for FTIR spectrochemical applications.
126 e value usually considered to be optimum for FTIR devices.
127                              SR-FTIR and FPA-FTIR measurements were performed in liver sections harve
128 microspectroscopy and focal plane array (FPA-FTIR) microspectroscopy to characterize periductal fibro
129 proving secondary structure predictions from FTIR spectra has been tested using 71 structures determi
130 aled correlations between CD values and full FTIR spectra (4000-600 cm(-1)), and different spectral r
131                                        Here, FTIR spectroelectrochemistry is coupled with density fun
132 formation of ester was confirmed by (1)HNMR, FTIR and UV spectroscopy.
133 pectral characterizations viz., proton-HNMR, FTIR, UV and LC-MS.
134 ed S,N-GQDs are characterized by XRD, HRTEM, FTIR, EDS and PL.
135 eloped to enable automated mapping, improved FTIR throughput, and lower detection size limit.
136 of different analytical techniques including FTIR, UV spectrophotometry, HPLC and LC-MS analysis.
137 PR spectra of the S2 state and flash-induced FTIR spectra of both D1-N87A and D1-N87D PSII core compl
138 ing conventional Fourier-transform infrared (FTIR) and direct absorption spectroscopy.
139                  Fourier Transform Infrared (FTIR) and proton nuclear magnetic resonance ((1)H NMR) s
140 hniques, such as Fourier-transform infrared (FTIR) and Raman spectroscopy, have been successful metho
141 y (SEM/EDS), and Fourier transform infrared (FTIR) micro-spectroscopy with automated spectral mapping
142 imetry (DSC) and Fourier Transform InfraRed (FTIR) microspectroscopy.
143 ature laboratory Fourier transform infrared (FTIR) spectrometer using partial least-squares (PLS) reg
144 ctroscopy (EIS), fourier transform infrared (FTIR) spectroscopy and atomic force microscopy (AFM) met
145 (Florida), using Fourier-transform infrared (FTIR) spectroscopy and infrared thermography.
146 characterized by Fourier transform infrared (FTIR) spectroscopy and modeled by density functional the
147 chniques such as Fourier-transform infrared (FTIR) spectroscopy are used to study interactions of lig
148 reflection (ATR)-Fourier transform infrared (FTIR) spectroscopy for the detection of brain cancer, al
149                  Fourier transform infrared (FTIR) spectroscopy has been used to directly record chem
150                  Fourier transform infrared (FTIR) spectroscopy has its own sensitivity to molecular
151 chniques such as Fourier-transform infrared (FTIR) spectroscopy have recently gained increasing clini
152 ured by means of Fourier Transform Infrared (FTIR) spectroscopy in a very broad range (from near- via
153                  Fourier transform infrared (FTIR) spectroscopy is a powerful technique that detects
154                  Fourier transform infrared (FTIR) spectroscopy is commonly employed to understand th
155 le, we conducted Fourier Transform Infrared (FTIR) spectroscopy studies which showed lipid extraction
156                  Fourier-transform infrared (FTIR) spectroscopy was applied to predict the degree of
157 ffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and thermogravimetric analysis (TGA)
158 plied, including Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (D
159 spectroscopy and Fourier Transform InfraRed (FTIR) spectroscopy, which are all techniques of relevanc
160 characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning el
161 chroism (CD) and Fourier-transform infrared (FTIR) spectroscopy.
162 were examined by Fourier transform infrared (FTIR) spectroscopy.
163  NMR titrations, Fourier transform infrared (FTIR) studies, electrospray ionization (ESI)-mass spectr
164  by the pronounced differences in the 1D-IR (FTIR), 2D-IR, and vibrational circular dichroism spectra
165                                      To make FTIR data quantitative, precalibration or offline analys
166 oteins in cutaneous trunci than in masseter (FTIR), supported by a myosin associated peak at 55.8 deg
167 rthermore, synchrotron radiation-based micro-FTIR spectra revealed that surface oxygen groups corresp
168      Micro-Fourier transform infrared (micro-FTIR) spectroscopy and Raman spectroscopy enable the rel
169 ging, X-ray fluorescence spectroscopy, micro-FTIR, and SEM-EDS.
170 sformation infrared spectroscopy/microscopy (FTIR/ muFTIR).
171 e of comparable quality to transmission mode FTIR spectra collected for pure HEs.
172                                    Moreover, FTIR showed no prominent interaction.
173 tures of the compounds were confirmed by MS, FTIR &(1)H NMR; and their properties were characterized
174 ) using micro-Fourier transform infrared (mu-FTIR) hyperspectral imaging and machine learning tools.
175 ier-transform infrared microspectroscopy (mu-FTIR), and pyrolysis-gas chromatography/mass spectrometr
176                      Therefore, mu-Raman, mu-FTIR, and pyr-GC/MS were further tested for their capabi
177  reflection and transmission modes, and nano-FTIR microscopy to study the biochemical alterations in
178                                    (1)H NMR, FTIR, and GC/MS characterization of the fluids indicated
179 ical and spectroscopic techniques ((1)H NMR, FTIR-ATR, HS-SPME/GC-MS).
180 sory attributes, confirming the potential of FTIR and chemometrics in coffee quality evaluation.
181                             The potential of FTIR spectroscopy for determination of bovine and porcin
182                    Characterization based on FTIR, XPS, XRD, Raman spectroscopy, FE-SEM, HR-TEM, AFM,
183 mometric methods (HCA, PAM, and PCA) done on FTIR spectra collected for four high explosive materials
184 ligand sphere affecting the CN(-) ligands on FTIR spectroscopy and catalysis.
185          It allows for simultaneous operando FTIR and Raman spectroscopic measurement, which provide
186 ing kansui, which was confirmed by SDS-PAGE, FTIR, and HPLC results.
187 e and after plasma treatment using SDS-PAGE, FTIR, UPLC-MS/MS and ELISA.
188 n annihilation lifetime spectroscopy (PALS), FTIR and solid-state NMR spectroscopy) to demonstrate ho
189 echanisms for osmolyte effects, we performed FTIR experiments that characterized the impact of each c
190      Bead properties (mechanical properties, FTIR fingerprint, cell release) and parameters of fermen
191 at are not equivalent in view of the protein FTIR spectra.
192 ier-transform infrared spectroscopy (STA-PTA-FTIR) was used to determine sorption capacity, reversibi
193 more sensitive than any previously published FTIR study.
194 s a convenient method to obtain quantitative FTIR data.
195 this study, we applied synchrotron radiation-FTIR (SR-FTIR) microspectroscopy and focal plane array (
196   Using a combination of experimental Raman, FTIR, UV-VIS absorption and emission data, together with
197 S, PL, fluorescence lifetime imaging, Raman, FTIR, TGA, KPFM, XPS, NMR and EPR clearly show that the
198 rties were characterized by Temperature-Ramp FTIR, DSC & CMC measurements.
199 D) analysis and Fourier transform infra-red (FTIR) spectroscopy.
200 al spectroscopy attenuated total reflectance FTIR and nonlinear vibrational spectroscopy sum frequenc
201  analysis using attenuated total reflectance-FTIR (ATR-FTIR) spectroscopy.
202        Frustrated total internal reflection (FTIR) imaging was used to perform remote optical measure
203  to deliver high-quality, spatially resolved FTIR transmission-like spectra below the diffraction lim
204                                            S-FTIR is a useful microscopy tool that can detect structu
205                                            S-FTIR measurements were carried out in macroscopic attenu
206 ased on the average spectra extracted from S-FTIR chemical images obtained from each type of the micr
207                                      Here, S-FTIR microspectroscopy was applied to observe the micros
208    Synchrotron Fourier transform infrared (S-FTIR) microspectroscopy allows the label-free examinatio
209 by synchrotron-Fourier transform infrared (S-FTIR) microspectroscopy and the cheese was softer.
210    Synchrotron-Fourier transform infrared (S-FTIR) microspectroscopy was used to investigate the effe
211 r electrophysiology, time-resolved step-scan FTIR, and Raman spectroscopy of fully dark-adapted ChR2.
212  nanocomposite was confirmed by AFM, FE-SEM, FTIR, and CLSM.
213 tensively using TEM, EDX, SAED, XRD, FE-SEM, FTIR, DIC, and electrochemical techniques.
214 (alpha-TCsNe) was characterized through SEM, FTIR and XRD techniques.
215 ed CS-PAEO-Nm was characterized through SEM, FTIR, and XRD and evaluated for improved biological acti
216 tment, all the zein preparations had similar FTIR spectra, with greater alpha-helical conformation, t
217 alyzed in detail by catalytic tests, in situ FTIR and transient studies using temporal analysis of pr
218                                      In situ FTIR showed the formation of surface nitrate species, wh
219                    Kinetic analysis, in situ FTIR, and in situ XAS measurements suggest that the AA f
220 SC), and Fourier transform infrared spectra (FTIR).
221  by Fourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) and applied
222 and Fourier-transform infrared spectroscopy (FTIR) analysis.
223 by Fourier transforms infrared spectroscopy (FTIR) and Differential Scanning calorimetry (DSC).
224     Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) were employed
225 ith Fourier-transform infrared spectroscopy (FTIR) and Optical emission spectroscopy (OES), whereas h
226 C), fourier transform infrared spectroscopy (FTIR) and UV-visible spectrophotometry.
227 ing Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS).
228 and Fourier-transform infrared spectroscopy (FTIR) are employed to characterize the synthesized NiFe(
229     Fourier transform infrared spectroscopy (FTIR) imaging with automated data analysis showed that p
230 py, Fourier transform infrared spectroscopy (FTIR) in reflection and transmission modes, and nano-FTI
231 The Fourier transform infrared spectroscopy (FTIR) showed the formation of Si-O-Si and Si-O-C covalen
232     Fourier transform infrared spectroscopy (FTIR) was applied to examine conformational changes of t
233 IC, Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM).
234 is, Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) equipped w
235 M), Fourier-Transform Infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA).
236 Fourier transform mid infrared spectroscopy (FTIR), gas chromatography/mass spectrometry (GC/MS) and
237 ourier transformation infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy
238 D), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and, energy-di
239 ing Fourier Transform Infrared Spectroscopy (FTIR), scanning electron microscopy (SEM) as well as ala
240 py, fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), atomic force
241 ing Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Dynamic Light
242  by fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffrac
243  of fourier-transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-Visible), vi
244  by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spec
245 ing Fourier transform infrared spectroscopy (FTIR).
246 ith Fourier transform infrared spectroscopy (FTIR).
247 and Fourier transform infrared spectroscopy (FTIR).
248 and Fourier-transform infrared spectroscopy (FTIR).
249 ith Fourier transform infrared spectroscopy (FTIR).
250 and Fourier-Transform Infrared spectroscopy (FTIR); releases were quantified by Inductively Coupled P
251 itu Fourier-transform-infrared-spectroscopy (FTIR) method.
252 M, atomic-force microscopy, CD spectroscopy, FTIR spectroscopy, analytical ultracentrifugation, and t
253                          Raman spectroscopy, FTIR spectroscopy and LIMS, which are high sensitivity t
254 then characterized via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light scattering and scanning
255 e, and characterized by UV-VIS spectroscopy, FTIR, TEM, DLS, and XRD.
256                                           SR-FTIR and FPA-FTIR measurements were performed in liver s
257 y, we applied synchrotron radiation-FTIR (SR-FTIR) microspectroscopy and focal plane array (FPA-FTIR)
258   Then, we use data derived from synchrotron FTIR studies of the T. rex vessels to analyse their cros
259                     Characterization by TGA, FTIR, EDX, XANES, EXAFS, and EQCM collectively provides
260              These correlations confirm that FTIR spectroscopy is a rapid and simple method for measu
261                  These results indicate that FTIR-based technology is a potential tool to detect the
262                                          The FTIR analysis additionally suggested that a synergy may
263                                          The FTIR analysis confirmed that the myrtle extract was enca
264                                          The FTIR analysis indicated the formation of hydrogen bonds
265                                          The FTIR analysis revealed that HMT and CAT increased the de
266                                          The FTIR data show that the C-O vibrations are substantially
267                                          The FTIR signals collected during the course of a reaction a
268                                          The FTIR spectra revealed the presence of aromatic amino aci
269  obtained from load cells placed beneath the FTIR imaging elements.
270                             By comparing the FTIR spectra of wild-type enzyme and two mutagenesis var
271        The anomeric bonds, identified in the FTIR and NMR spectrum, indicate that the extracts are a
272 ic amino acids were detected by means of the FTIR and py-GC-MS analyses.
273 tra were then systematically compared to the FTIR absorption spectra collected for kerogen samples is
274 monosaccharide composition together with the FTIR and NMR analyses, indicated that both fractions are
275                                    With this FTIR method we expand current options to investigate the
276 s in secondary structure, determined through FTIR, the observed behaviour was primarily attributed to
277  17 major metabolites were evaluated through FTIR and GC-MS.
278 dsorption mechanism was investigated through FTIR, EDX and SEM, which demonstrated that the introduct
279 signal to background ratio (SBR) compared to FTIR absorption techniques.
280                                  Compared to FTIR spectroscopy, novel and elaborated measurement tech
281                       Raman and transmission FTIR spectroscopic techniques have been coupled in a new
282  reflection Fourier transform infrared (uATR-FTIR) spectroscopic mapping by univariate and multivaria
283                                        Using FTIR spectro-electrochemistry on the [FeFe] hydrogenase
284 ogy and thermal property were analyzed using FTIR, EDX, XRD, TGA, VSM, and TEM.
285 0min) combinations was investigated by using FTIR spectroscopy and compared with the change in enzyme
286  PXDDA samples were then characterized using FTIR and XRD.
287                   It was characterized using FTIR, FE-SEM/EDX before and after analyte ions biosorpti
288 ization of mannan hydrolysate was done using FTIR and (13)C NMR which revealed alpha and beta form of
289 success without any sample preparation using FTIR-ATR technique.
290 nt functional moieties is also studied using FTIR analysis; while phases of the constituents are conf
291 il/water (5/95)-emulsions was determined via FTIR, analyzing the Amide I/Amide II peak intensity rati
292 re, antibody immobilization was followed via FTIR and Raman spectroscopy.
293 This nanohybrid was characterized by UV-Vis, FTIR and Raman spectroscopies, DLS, and XRD.
294 ion monitoring instrumentation (like UV-vis, FTIR, Raman, and 2D NMR benchtop spectrometers), is show
295 lyophilized extracts were characterized with FTIR and DSC analyses.
296  content, is a good choice when dealing with FTIR spectra.
297 e thoroughly characterized by TEM, SEM, XPS, FTIR, and nitrogen-adsorption surface area analysis.
298 red nanomaterials were characterized by XRD, FTIR dynamic light scattering (DLS), FESEM, HRTEM, and E
299 rized using common analytic procedures (XRD, FTIR, and MDSC).
300 nanocomposite was characterized by TEM, XRD, FTIR, XPS, TGA, BET, and CV using the redox couples [Fe(

 
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