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Ir spectroscopy grade

Manufactured by Merck Group
Sourced in Germany

IR spectroscopy grade is a type of laboratory equipment used for infrared spectroscopy analysis. It is designed to meet the specific requirements of infrared spectroscopy applications.

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4 protocols using ir spectroscopy grade

1

FTIR Analysis of Hydrogel Samples

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The crushed hydrogel samples were mixed with potassium bromide (Merck IR spectroscopy grade) in 1:100 proportions and dried at 45 °C. The mixtures were compressed to a 12 mm semitransparent disk by a pressure of 65 kN (Pressure gauge, Shimadzu) for 1 min. The FTIR spectra were recorded over the wavelength range 4,000–400 cm−1 using FTIR spectrometer (FTIR 8400 S, Shimadzu).
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2

Hydrogel Adsorption and Characterization

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Fourier transform infrared spectroscopy (FTIR) of unloaded and loaded hydrogel samples was recorded in transmission mode by using a Bomem MB 100 FTIR spectrophotometer, as KBr pellets. Before recordings, xerogels were crumbled into powder and mixed with potassium bromide (Merck IR spectroscopy grade) in the proportion of 1:100 and then compressed into a 12 mm semi-transparent disk under pressure (Pressure gage, Shimadzu). The morphology of the hydrogel samples before and after nickel adsorption was observed on a scanning electron microscope (SEM) instrument, JEOL JSM-5800. The surface topography changes before and after adsorption were observed and recorded by atomic force microscopy (AFM) in the contact mode bt using Auto Probe CP Research (TM Microscopes—Veeco Instruments, Santa Barbara, CA, USA). For an estimation of the roughness of the samples by the determination of the arithmetic average of the absolute (Ra) roughness parameters, the software SPMLab (SPMLab NT Ver. 6.0.2., Veeco Instruments, Santa Barbara, CA, USA) was used.
The ICP-OES Thermo iCAP 6500 system, equipped with the Thermo iTEVA software, a concentric nebulizer and a Cyclonic Spray Chamber, was used for the determination of the concentration of Ni2+ ions in the solution.
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3

Structural characterization of LiMnPO4 and AmMnP

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The crystalline
phases of the products were characterized via powder X-ray diffraction
(XRD; D2 PHASER, Bruker AXS K. K., Japan) using Cu Kα radiation
generated at 30 kV and 10 mA. The diffraction patterns were acquired
with steps of 0.02° (2θ) and a counting time of 1 s/step.
The structures of the converted LiMnPO4 were refined using
the Rietveld method with the RIETAN-FP program.26 (link) The molecular structure of AmMnP was analyzed via diffuse
reflectance Fourier transform infrared spectroscopy (FT-IR; IRPrestige-21,
Shimadzu Corp., Japan). The powder sample (1 mg) was mixed with dry
KBr (100 mg; IR spectroscopy grade, Merck KGaA., Germany) and filled
into the sample holder. A thermogravimetric–differential thermal
analysis (TG–DTA; TG/DTA6200, SII Inc., Japan) was carried
out in air at a heating rate of 5 °C/min. The particle morphologies
of the products were observed using a field-emission scanning electron
microscope (FE-SEM; SU-70, Hitachi Ltd., Japan). The specific surface
area of the product was estimated from N2 adsorption measurements
(3Flex, Micromeritics Ltd., Japan). Prior to each measurement, the
powder was outgassed under vacuum at 120 °C for 3 h. The specific
surface area was calculated via the Brunauer–Emmett–Teller
(BET) method.
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4

FTIR Sample Preparation Protocol

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To crush samples, pestles and mortar were used. The crushed material was blended in 1:100 proportions with potassium bromide (Merck IR spectroscopy grade) and dried at 40°C and then compressed into a semi-transparent 12 mm disc with a pressure of 60 kN (pressure gauge, Shimadzu) for 2 min. The FTIR spectrum was recorded using an FTIR spectrometer over a wavelength range of 4000–500 cm−1 (FTIR 8400S, Shimadzu) [15 ].
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