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14 protocols using nicolet nexus 670 ftir

1

FTIR Analysis of Waterborne Emulsion

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The waterborne emulsion was dropped on the potassium bromide tablets and dried under an infrared lamp, then put into a Nicolet-Nexus 670 FTIR (Thermo Fisher, Waltham, MA, USA) for analysis in the range of 4000 to 400 cm−1.
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2

ATR-FTIR Analysis of Fish Scales

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An Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR) spectroscope (Thermo Nicolet NEXUS 670 FTIR, USA) was used to obtain the FTIR data. Fish scale samples were kept on the ATR crystals in such a way that there is no air-gap between the fish scale and ATR crystal. At room temperature (22°C), 128 scans of 2 cm−1 were performed for samples with and without mucus. The data were collected and processed using Omnic software.
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3

Characterization of Colloidal Cuboids

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Colloidal cuboids and their assemblies were imaged by using a Hitachi SU-70 Schottky field emission gun SEM at an operation voltage of 10 kV. TEM images and EDS maps were taken by using a JEOL 2100 FEG TEM at an operation voltage of 200 kV. XRD patterns were recorded with a Bruker Smart1000 (Bruker AXS Inc., USA) using Cu Kα radiation. FT-IR spectral measurement was performed on a Thermo Nicolet NEXUS 670 FTIR (32 scans) with a resolution of 4 cm−1. POM images were obtained by using a Nikon Eclipse Ti-S microscope with polarizer.
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4

Characterization of Synthesized Compounds

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The melting points of the compounds were determined using an electric melting point apparatus (Toshniwal Pvt. Ltd., India) and the values were uncorrected. Thin layer chromatography (TLC) technique on silica gel-GF254 coated plates (Merck, Germany) is used for purity checking. Spots of TLC were recognized by iodine chamber. The ultraviolet (UV)-visible spectra of all the compounds were obtained at 200–400 nm using a double beam Shimadzu UV 1800 spectrophotometer at a concentration of 50 μg dissolved in methanol. The infrared (IR) spectra of synthesized compounds were recorded on a Thermo Nicolet Nexus 670-FTIR using KBr disc method with minimum forty scans. 1H-NMR spectra were obtained on Bruker UX-NMR instrument at 300 MHz, using tetramethylsilane as an internal standard and CDCl3 as a solvent, and chemical shift values were expressed in δ ppm. 13C NMR spectra were recorded on Bruker DPX at 300 Hz. The mass spectra were recorded on MASPEC (MSW/9629), and values were expressed as %relative abundance. Elemental analyses for synthesized compounds were carried over Perkin Elmer 240 CHN analyzer.
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5

Characterization of Biosynthesized Silver Nanoparticles

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The surface free biomass residue or unbound extracts of the synthesized AgNPs were removed by washing them three times with distilled water. The AgNPs were then separated from the bulk by centrifugation at 10,000 rpm for 15 minutes, dried, and ground with potassium bromide (KBr) pellets, after which their infrared spectra were recorded via FTIR. The characteristic infrared (IR) absorption spectra of the different functional groups were recorded in the frequency range of 4,000–400 cm−1 using a Thermo Nicolet Nexus 670 FT-IR (Thermo Fisher Scientific, Waltham, MA, USA). The spectra were obtained by operating the same equipment in the diffuse reflectance mode at 4 cm−1 resolution. Likewise, the FTIR spectra of the KBr encapsulated dried powder of the control plant extract was also obtained. Reference blank KBr pellets were used for background correction.17
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6

Characterization of Bioinspired Nanoparticles

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UV-Vis measurements were performed on samples using a Thermo Scientific Genesys 10S UV-Vis spectrophotometer immediately after sample collection and dilution. For these measurements, 10 μL of the nanoparticle solution was diluted with 990 μL of the synthesis solvent, and the baseline measurement was taken using the synthesis solvent for each nanoparticle type. The UV-Vis spectra were collected over the 225 to 800 nm range.
Fluorescence measurements were taken using a TECAN infinite M200 PRO fluorescence spectrometer at excitation wavelengths of 365, 465, and 680 nm with a measured emission range of 385–850 nm, 485–850 nm, and 700–850 nm, respectively. Images were also taken of undiluted 24 h time point BVNPs under a365 nm wavelength UV lamp. ζ potential measurements were taken for the 10 min and 24 h time points using a Malvern Zetasizer.
FT-IR samples were prepared by dropping 500 μL of the nanoparticle solution onto Kevley MirrIR corner frosted FT-IR slides and allowing them sit overnight, after which they were placed under vacuum until they had completely dried. FT-IR measurements were taken using a Thermo Nicolet Nexus 670 FT-IR.
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7

Analysis of Polymer Oxidation via FTIR

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Oxidation of UHMMPE fiber samples and binder resin material was measured using Fourier Transform Infrared Spectroscopy (FTIR). A Thermo Nicolet NEXUS 670 FTIR equipped with an attenuated total reflectance (ATR) accessory was used to measure the oxidation of the materials. The final spectrum of each sample represents the average of 128 individual scans with a resolution of 2 cm−1 between 650 cm−1 and 4000 cm−1 wavenumbers. A background was collected and subtracted prior to each sample run. Three replicates were prepared for each sample. Spectra analysis, including baseline correction and normalization, was performed. The spectra were baseline corrected and normalized using the peak at 1472 cm−1, which was attributed to the CH bending [43 , 44 ]. Typical standard uncertainties for spectral measurement are 2 cm−1 in wavenumber and 5 % in peak intensity. To evaluate the degree of oxidation, the overlapping peaks between 1712 cm−1 and 1735 cm−1, assigned to the oxidation products (ester and ketone groups), were deconvolved using commercial software.
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8

FTIR Analysis of Waterborne Emulsion

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The waterborne emulsion was dropped on the potassium bromide tablets and dried under an infrared lamp, then put into a Nicolet-Nexus 670 FTIR (Thermo Fisher, Waltham, MA, USA) to analyze in the range from 4000 to 400 cm−1.
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9

Characterization of Novel Compounds

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Melting points of all compounds were recorded on an Optimelt-100 automatic melting point apparatus and are uncorrected. IR (KBr) spectra were recorded with a Thermo Nicolet Nexus 670 FT-IR. The NMR spectra were obtained with a Bruker Avance III 600 spectrometer (1H: 600 MHz, 13C: 150 MHz) with tetramethylsilane as internal standard. Chemical shifts are given in values of ppm and coupling constants in hertz. LC/MS was recorded with an Agilent 1200 capillary spectrometer. Thin-layer chromatography (TLC) was performed on precoated silica gel plates (Qingdao Marine Chemical Industry Factory, Qingdao, China). Column chromatography was carried out using silica gel (200–300 mesh, Qingdao Marine Chemical Industry Factory, Qingdao, China).
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10

Synthesis and Characterization of PETN-CNH Derivatives

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Reagents were purchased from Aldrich and solvents from Fisher Scientific. Infrared spectroscopy measurements were taken using a Thermo Nicolet NEXUS 670 FT-IR, and NMR (nuclear magnetic resonance) experiments were performed on a 400 MHz Bruker Avance system. PETN–CNH3Cl (MW = 292.59 g mol–1), PETN–CNH3Br (MW = 337.04 g mol–1), and PETN–CNH2 (MW = 256.13 g mol–1) were prepared following literature procedures.19 ,20
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