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Tensor 37 ftir spectrometer

Manufactured by Bruker
Sourced in Germany, United States

The Tensor 37 FTIR spectrometer is a high-performance Fourier Transform Infrared (FTIR) instrument designed for analytical and research applications. It features a robust and compact design, providing reliable and accurate measurements across a wide spectral range. The Tensor 37 is capable of performing various FTIR techniques, such as transmission, reflection, and attenuated total reflectance (ATR) measurements.

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45 protocols using tensor 37 ftir spectrometer

1

Identification of Plastic Items and Microplastics

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For identification of plastic items from surface sampling, a subset of 38.4% (total: 1075) of all items from field LK and 100% (total: 314) of items from field HB were analysed with a with a Tensor 37 FTIR spectrometer (BrukerOptics GmbH) combined with a Platinum-ATR-unit (BrukerOptics GmbH). Each item was measured after 16 background scans by 16 sample scans (spectral resolution: 4 cm−1 in a wavenumber range of 4000–400 cm−1). Spectra identification was carried out with the internal OPUS 7.0 (BrukerOptics GmbH) database, showing average OPUS-HIT ratios of 619.3 (LK) and 601.9 (HB). For microplastics from soil samples, a subset of 35.4% (total: 99) particles was analysed with a µFTIR spectrometer (Lumos II, BrukerOptics GmbH) with 30 background and 30 sample scans (spectral resolution: 4 cm−1 in a wavenumber range of 4000–680 cm−1). µFTIR spectra were identified using spectra correlation via OpenSpecy59 (link), resulting in an average r2 of 0.84. Each plastic item or microplastic particle, regardless of the spectrometric analysis, was classified according to its visual surface characteristics (particle type, surface form and surface degradation)60 (link). Statistical operations were performed in Microsoft Excel 2021 (Microsoft), and R (R Core Team, 2020), using RStudio (Version 3.4.1; RStudio Inc.). Spatial data analysis and processing was performed in QGIS61 .
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2

Diffuse Reflectance NIR Spectroscopy of Kernels

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The NIR spectra were collected with the bare kernels in the diffuse reflectance mode using a Bruker TENSOR 37 FTIR spectrometer (Bruker Optics, Ettlingen, Germany). A fiber bundle was used to illuminate the sample and collect the scattered light. The fiber probe was placed to contact directly with equatorial region of a kernel. Considering the differences in the internal composition of a kernel, the diffuse reflectance spectrum was obtained by averaging the three measurements around the kernel. Each spectrum was the average of 64 scans, and more scans did not reduce the signal noise significantly. The range of the raw spectra was from 12,000 to 4000 cm−1, and the data were measured with an interval of 1.929 cm−1 and a resolution of 4 cm−1, so each raw spectrum has 4148 individual data points. The work temperature was kept at 25°C and the sequence of NIR analysis for all the objects was randomly arranged.
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3

FTIR Analysis of ICA-Tocozeinolate Nanoformulation

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FTIR spectra of the optimized ICA–tocozeinolate nanosphere formula and single formula components (ICA, SDC, TPGS, and zein) were investigated at 4000–400 cm−1 using a Tensor 37, FTIR spectrometer (Bruker, Fremont, CA, USA).
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4

Characterization of Nickel-Modified ZSM-5 Zeolites

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Powder X-ray diffraction (XRD) patterns of the obtained ZSM-5 zeolite and nickel-modified ZSM-5 zeolites were carefully analyzed on a PANalyrical advance powder diffractometer in the 2θ range of 5–35° with an interval of 0.1°. Nitrogen adsorption–desorption measurements were performed at 77 K using a Micromeritics ASAP 2010 analyzer on degassed samples (10−1 mbar, 573 K, 4 h). The surface area of the examined samples was determined using the Brunauer–Emmett–Teller (BET) equation, and the pore volume and pore diameter were obtained by using the Barrett–Joyner–Halenda (BJH) method with the N2 adsorption isotherm. The crystallite size of the synthesized zeolite was observed by field emission scanning electron microscopy (SEM) on a Quanta 200F instrument, and the crystallite size was statistically analyzed by counting at least 500 crystals. Pyridine-absorbed FTIR was characterized on a Bruker Tensor 37 FTIR spectrometer. Pyridine-absorbed FTIR was determined after absorbing and desorbing pyridine at 473 and 623 K, respectively.
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5

Characterization of Synthesized Nanocomposites

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The chemical composition of the synthesized nanocomposites was studied by infrared spectroscopy while their morphology was investigated using superficial area measurements.
Fourier transform infrared (FT-IR) spectra were obtained with a Bruker Tensor 37 FT-IR spectrometer, equipped with a Deuterated Triglycine Sulfate (DTGS) detector. The spectrometer consisted of a diamond ATR cell with a circular surface of 3 mm in diameter and three internal reflections. The spectra were recorded in the range of 600–4000 cm−1 at a 4 cm−1 resolution with 64 co-added scans. The data acquisition was performed by OPUS software (version 4.2, Bruker, Ettligen, Germany).
The measurements of the superficial areas of the composites were carried out using a Quanta chrome® ASiQwinTM-Automated Gas Sorption Data analyzer (Quantachrome, Boynton Beach, FL, USA) at the Institute of Fine Chemistry and Nanochemistry at the University of Cordoba. The analysis was based on the nitrogen adsorption/desorption at −196 °C and the specific surface area values were calculated using the BET (Brunauer–Emmett–Teller) equation.
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6

ATR-FTIR Analysis of Liquid Oils

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ATR-FTIR spectra of the particles were obtained by using a Bruker Tensor 37 FT-IR Spectrometer (Bruker, Ettlingen, Germany) coupled with the ATR sampling accessory Golden Gate (Specac Ltd., Orpington, UK). Approximately 50 mg of liquid oil and encapsulates were deposited onto the diamond crystal to collect the spectra. All spectra were recorded within the wavenumber range 4000–600 cm−1 by averaging 10 scans at 4 cm−1 resolution. Measurements were performed in triplicate. Analysis of spectral data was carried out using the OPUS 4.0 data collection software program (Bruker, Ettlingen, Germany).
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7

ATR-FTIR Characterization of DBS Capsules

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A Bruker Tensor 37 FT-IR Spectrometer (Bruker, Ettlingen, Germany) was used to measure the ATR-FTIR spectra of DBS capsules. The low-temperature ATR sampling accessory Golden Gate (Specac Ltd., Orpington, UK) was used to guarantee proper contact between the diamond crystal and DBS encapsulated samples (50 mg approximately). All spectra were recorded within the wavenumber range 4000–600 cm−1 by averaging 10 scans, with a resolution of 4 cm−1. The results were normalized to the intensity of the band at 1519 cm−1 for better comparison among the different capsules. Analysis of spectral data was carried out using the OPUS 4.0 data collection software program (Bruker, Ettlingen, Germany). The measurements were performed in triplicate.
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8

FTIR Analysis of Poly(2,6-DHN) Formation

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Fourier transform infrared analysis (FTIR) was applied to evaluate the poly(2,6-DHN) formation on the carbon electrode. The FTIR spectra were acquired using a Tensor 37 FT-IR spectrometer (Bruker, Billerica, MA, USA) equipped with a Golden Gate ATR. All samples were recorded from 4000 to 400 cm−1.
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9

ATR-FTIR Spectroscopic Analysis of Samples

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A Tensor 37 FT-IR Spectrometer (Bruker, Ettlingen, Germany) coupled with the ATR sampling accessory Golden Gate (Specac Ltd., Orpington, UK) was used to study the ATR-FTIR spectra of the samples. A total of 50 mg of sample was deposited on the diamond crystal for the analysis. The spectra were acquired in the range 4000–600 cm−1, by averaging 10 scans, with a 4 cm−1 resolution. Spectral data were analyzed using the OPUS 4.0 software (Bruker, Ettlingen, Germany). Origin 8.5 (OriginLab, Northampton, MA, USA) was used for peak deconvolution using the Bigaussian fitting function.
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10

Analytical Techniques for Compound Identification

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Liquid chromatographic analyses were performed using an Agilent 1260 Infinity HPLC system (Agilent, Palo Alto, CA, USA) equipped with a binary high-pressure pump for mobile phase delivery and an autosampler. Identification and quantification of the analytes were performed on an Agilent 6420 triple quadrupole MS with electrospray source using the Agilent MassHunter Software (version B.06.00) for data analyses.
Magnetic stirrers from J.P. Selecta, S.A. (Barcelona, Spain) and a Vibramax 110 shaker from Heidolph Instruments (Schwabach, Germany) were used for the stirring during extraction and elution procedures, respectively.
Scanning electron microscope (SEM) images were obtained by using a JEOL JSM 7800F microscope (JEOL, Tokyo, Japan) at the Central Service for Research Support (SCAI) of the University of Córdoba. ATR-IR spectra were acquired with a Bruker Tensor 37 FT-IR spectrometer (Bruker Optik, GmbH, Ettlingen, Germany) equipped with a three internal reflections diamond ATR cell (Platinum ATR accessory, Bruker). Data collection and processing were done using the OPUS software package (Bruker, Ettlingen, Germany). Contact angle measurements were performed in a Ramé-hart Model 200 Standard Goniometer with DropImage Standard v2.3 equipped with an automated dispensing system at the Instituto de Ciencia Molecular (ICMol) of the University of Valencia.
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