The largest database of trusted experimental protocols

Nicolet avatar 370 ft ir spectrometer

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Nicolet Avatar 370 FT-IR spectrometer is a laboratory instrument designed for the analysis of samples using Fourier Transform Infrared (FT-IR) spectroscopy. It is capable of measuring the absorption or transmission of infrared light by a sample, which can provide information about the sample's molecular structure and chemical composition.

Automatically generated - may contain errors

6 protocols using nicolet avatar 370 ft ir spectrometer

1

Synthesis and Characterization of Cyanophenol Derivatives

Check if the same lab product or an alternative is used in the 5 most similar protocols
All reagents, including benzonitrile, 2-cyanophenol, NH4Cl, 3-cyanophenol, 4-cyanophenol, DMF, anhydrous K2CO3, ethyl acetate, petroleum ether, and sodium hydroxide, were purchased from Aladdin (Shanghai, China) and were of analytical grade. Sodium azide, of an analytical grade, was purchased from Tianjin Fengchuan Chemical Reagent Technology Co., Ltd. (Tianjin, China). A total of 36–38% hydrochloric acid, acetic anhydride, methanol, butanone, dichloromethane, and acetone were analytical graded and provided by Beijing Tongguang Fine Chemicals Co., Ltd. (Beijing, China). Potassium bromide was of chromatographic grade and purchased from China National Pharmaceutical Group Chemical Reagent Co., Ltd. (Beijing, China). All reagents were used as received without further purification. Infrared (IR) spectra were acquired using a Thermo Nicolet AVA-TAR 370 FT-IR spectrometer. 1H NMR and 13C NMR analyses were performed on an Advance Bruker III 400 (400 MHz) NMR spectrometer, with TMS as the internal standard and DMSO-d6 as the solvent. UV-vis spectroscopy was carried out using a Hitachi U4150 ultraviolet spectrometer in the 200–600 nm range, with methanol were used as the solvent for sample analysis. The separation of compounds was accomplished by High-Resolution Mass Spectrometry (HRMS) utilizing a Triple Quadrupole MS instrument (Waters India Pvt Ltd., Karnataka, India).
+ Open protocol
+ Expand
2

Comprehensive Characterization of Electrospun Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Scanning electron microscope (SEM) images were taken on a Shimadzu SSX-550 field emission scanning electron microscope (Shimadzu, Co. Ltd., Kyoto, Japan) at 15.0 kV. The as-electrospun samples were dispersed in ethanol with the assistance of an ice-water ultrasonic bath at 35 kHz, and a drop of the well-dispersed sample was cast repeatedly onto a piece of silicon wafer and air-dried. A thin gold coating was utilized to avoid charging during scanning, and a thorough microscopic study was carried out. The detailed morphology and size were examined with a Hitachi H-8100 transmission electron microscope (TEM, Hitachi, Ltd., Tokyo, Japan). As for SEM measurement, the as-electrospun samples for TEM were dispersed in ethanol with the assistance of an ice-water ultrasonic bath at 35 kHz. A drop of the well-dispersed sample above was cast repeatedly onto a specimen holder and air-dried. Fourier transform infrared (FTIR) spectra were recorded on a Thermo Nicolet Avatar 370 FTIR spectrometer. UV–visible absorption spectra (UV–vis, Hitachi, Ltd., Tokyo, Japan) were collected with a Hitachi U-3900H spectrophotometer in the 300–700 nm wavelength range. X-ray photoelectron spectra (XPS) were recorded with Mg Kα radiation.
+ Open protocol
+ Expand
3

FT-IR Analysis of Protein Conjugates

Check if the same lab product or an alternative is used in the 5 most similar protocols
FT-IR spectra of PD, BSA, HSA, PD-BSA and PD-HSA conjugates were collected using a Nicolet AVATAR 370 FT-IR Spectrometer (Thermo Scientific, USA). Each sample (1 mg) was put into agate mortar and well mixed with KBr (100 mg) and lapping. The mixture was compressed tightly to obtain a similar packing thickness about 5 mm. Each spectrum was an average of 32 scans with a resolution of 4 cm1 across the wavenumbers 4000–400 cm1. Each sample was scanned three times, and the average spectrum of three measurements was to build the model. The temperature was equilibrated at 25°C and the humidity was kept at 60%.
Second Derivative (DII) and Curve Fitting (Gaussian algorithm) procedures were performed to identify the precise position and absorbance of specific bands. By using OMNIC 8.0 software (Thermo Fisher Scientific), curve fitting was conducted on spectra in the range of 1700–1600 cm1 after two points baseline linear fitted. In order to determine the underlying component bands, the number of peaks as well as their positions was identified based on DII results, resulting in the optimal reconstructed curve (residual close to zero).
+ Open protocol
+ Expand
4

Comprehensive Spectroscopic Analysis of Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Infrared spectra were recorded as KBr pellets on a Thermo Nicolet Avatar 370 FT-IR spectrometer. 1H NMR spectra were recorded on a Bruker Avance Spectrospin–500 spectrometer. UV-vis spectra were recorded on a Perkin Elmer Lambda 750 UV-vis-NIR Spectrometer. Mass spectroscopic measurements were performed by the use of positive ion matrix-assisted laser desorption ionization (MALDI–TOF) technique on a micromass M@LDI-LR mass spectrometer. The sample blended or dissolved in the matrix material was irradiated by nitrogen UV laser at 337 nm with 10 Hz pulses under high vacuum. Mass ion peaks were identified for the spectrum using the MassLynx v4.0 software.
+ Open protocol
+ Expand
5

Optimized Synthesis of Organic Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
Unless otherwise noted, reagents were obtained commercially and used without further purification. CH2Cl2 was distilled from CaH2 under a nitrogen atmosphere. THF was distilled from sodium–benzophenone under a nitrogen atmosphere. Toluene was distilled from sodium under a nitrogen atmosphere. All chemicals were purchased from Sigma-Aldrich, TCI America, or Alfa Aesar (United States) unless otherwise noted. Thin-layer chromatography (TLC) analysis of reaction mixtures was performed on Dynamic adsorbents silica gel F-254 TLC plates. Flash chromatography was carried out on Zeoprep 60 ECO silica gel. 1H and 13C NMR spectra were recorded with Varian INOVA (400, 500 MHz) spectrometers. Infrared (IR) spectra were recorded on a Thermo Nicolet Avatar 370 FT-IR spectrometer. Compound purity (≥95%)was confirmed on the basis of the integration of the area under the UV absorption curve at λ = 254 or 210 nm signals using an Agilent 1260 series HPLC system coupled with a 6120 Quadrupole mass spectrometer (column: ZORBAX Narrow Bore SB-C18 RRHT, 2.1 × 50 mm, 1.8 μm, PN 827700-902). The system was eluted at 0.5 mL/min with a gradient of water/acetonitrile with 0.1% formic acid: 0–5 min, 5–95% acetonitrile; 5–7 min, 95% acetonitrile; 7–7.25 min, 95–5% acetonitrile; 7.25–8.5 min, 5% acetonitrile.
+ Open protocol
+ Expand
6

Characterization of Reduced Graphene Oxide Sponges

Check if the same lab product or an alternative is used in the 5 most similar protocols
40 kHz ultrasonic cleaner YX‐2080 was used for dispersing graphite oxide. For drying the samples, the freeze dryer, model FD‐5010‐BT was used. The SEM images of the samples were recorded using Leo 1450VP. The FTIR spectra were obtained using Thermo Nicolet Avatar 370 FT‐IR Spectrometer scanning from 4000 to 500 cm−1. The XRD patterns were recorded using Bruker D8 Advanced diffractometer with Cu Kα radiation. The thermogravimetric analysis (TGA) was performed using BÄHR Thermal Analyzer model STA 503 to investigate the thermal stability of RW and RGO/CR‐RW sponges in the temperature range of 25–800 °C with a ramp rate of 10 °C min−1 under Ar atmosphere. The thermal images of the samples were obtained using a FLIR ONE thermal camera P/N 435‐0003‐01‐00 made. The WCA tests were measured using a commercial contact angle system of 5 V‐USB port power source equipped with a CCD camera and IrcA96 software for triplicate measurements. The volume of water droplet was 4 µL.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!