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Labram hr evo

Manufactured by Horiba
Sourced in Japan, France

The Labram HR Evo is a compact and versatile Raman spectrometer designed for high-resolution Raman analysis. It features a modular design and advanced optics to deliver high-quality Raman data across a wide range of applications.

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4 protocols using labram hr evo

1

Characterization of Polymer Membrane Morphology

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Morphology of NPs was investigated using FESEM (Model: Gemini SEM 300 Brand: Carl Zeiss). Surface functionality and crystallinity were studied using FTIR (PerkinElmer Frontier MIR) and WAXD (PANalytical). Structure defects of GO were investigated using Raman spectroscopy (532 nm laser-Horiba Labram HR Evo). The blend formation of CA-PCL was investigated using FTIR (PerkinElmer Frontier MIR) and WAXD (PANalytical). The water contact angle of the membrane was measured (Kyowa, DMs-401, Japan) to gain a piece of knowledge about the hydrophilicity of the membranes. The contact angles conveyed are an average of ve measurements done at different locations on the individual membrane samples. Information regarding the mechanical stability, tensile strength, and percentage elongation of the membrane was obtained using Universal Testing Machine (UTM-Shimadzu, AG-X plus, Japan).
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2

Characterization of Catalytic Materials

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GIXRD measurements were performed on a X’PertPro MPD (Panalytical) with Cu Kα radiation (λ = 0.15406 nm). The morphology of the prepared materials was observed with TEM (H-7650, Hitachi Co., Japan). High-resolution TEM, HAADF-STEM, and EELS mapping were carried out by a JEM-ARM200F TEM/STEM (JEOL Co., Japan). The defect degree of carbon was characterized by Raman spectroscopy (LABRAM HR EVO, Horiba Co, Japan). XAFS (Co K-edge) were obtained at Beamline 11B from the Shanghai Synchrotron Radiation Facility, China. Co K-edge XANES data were collected in fluorescence mode and analyzed using the ATHENA module implemented in the IFEFFIT package43 (link). A cubic spline function was used to fit the background above the absorption edge. To amplify the EXAFS oscillations in the mid-k region, k2 weighting was applied, followed by a Fourier transform process for converting the data to a radial distribution (R) space with a k range of 2.5–12 Å−1 at the Co K edge. High-resolution X-ray absorption spectra were collected at the Catalysis and Surface Science Endstation at the BL11U Beamline in the National Synchrotron Radiation Laboratory (NSRL) in Hefei, China. SRPES measurements were conducted at the photoemission end-station at the BL10B Beamline in the NSRL in Hefei, China.
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3

Raman Spectroscopy of Cured Pork Mince

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The Raman spectra were collected using a high-resolution Raman spectrometer/microscope (Lab RAM HR EVO, Horiba Jobin Yvon S.A.S, Paris, France) with a 532 nm laser source. The measurement of the cured pork mince was done by cutting 1 mm × 10 mm × 10 mm slices from the center and placing them on a slide. The laser was first focused on the sample with a 50 × long focal length lens, and then Raman signals were acquired in the range of 400–2000 cm−1. The measurement parameters were: the resolution of 2 cm−1, exposure time of 60 s, and 5 scans for each sample. The obtained spectra were smoothed using Labspec6 analysis software with multi-point baseline correction to remove the fluorescent background. The spectra were normalized to the vibrational intensity of the phenylalanine ring at a 1003 cm−1 wave number (Pan, Guo, Li, Song, & Ren, 2017 (link)).
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4

Structural Characterization of Cu-Based Nanostructures

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A Bruker D8 Discover diffractometer equipped with Cu Kα radiation ( λ=1.5418 Å) was used, with angles between 30 and 80 ( θ--2θ ), for the crystallographic characterization of the copper-based nanostructures obtained from the annealing under hydrogen or air atmosphere. The Raman analysis was performed using a Horiba micro-Raman system, model LabRAM HR Evo, with laser power 10 mW, 405 nm excitation wavelength and CCD detector, with additional sample preparation. Deconvolution of the Raman spectrum was carried out using Voigt functions of the Fityk program (version 1.3.1). A PG Instruments spectrometer (model T80+) with a step of 0.5 nm and air as the baseline was used to obtain solid state ultraviolet visible (UV–Vis) spectra. Glass slices doped with 6 mol% of copper ions, with a thickness of 0.1 mm, were scanned before and after the annealing at 430C under H2 (g) atmosphere. The scanning electron microscopy (SEM) was performed with a JEOL JSM-6390LV scanning electron microscope. In this analysis, CuOnano@glass powder was spread on gold-coated double-sided carbon tape and analyzed using an acceleration voltage of 10 kV. The total content of copper on borophosphate glasses was determined by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) using a Thermo Scientific iCap 6000 Series Spectrometer2 (link) using the Cu emission line at 324.754 nm (axial view).
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