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Micro elemental analyzer

Manufactured by Elementar
Sourced in Germany

The Micro elemental analyzer is a laboratory instrument designed for the rapid and accurate determination of carbon, hydrogen, nitrogen, and sulfur content in a wide range of organic and inorganic materials. It provides precise elemental analysis with a high degree of reproducibility.

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3 protocols using micro elemental analyzer

1

Collagen Extraction from Bone Samples

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Bones were mechanically cleaned by abrasion with a diamond-tip burr and subsequently ~250 mg of material was removed using a diamond-tip cutting wheel. These bone samples were demineralized in 0.5 M HCl at 4°C for a period of several weeks. After demineralization, the remaining insoluble collagen was solubilized in 10−3 M HCl at 75°C for 48 h. The solution containing the soluble collagen was then filtered using a 60–90 μm filter (Elkay, Hampshire, UK) to remove insoluble particulates and then filtered using 30 kDa molecular weight cut-off centrifuge tubes (Pall Corporation, Port Washington, NY). The >30 kDa fraction was then frozen and lyophilized. Elemental and isotopic compositions of the dried collagen were determined in duplicate at the University of British Columbia using an Elementar Isoprime continuous-flow isotope ratio mass spectrometer coupled to a Vario Micro elemental analyzer (Hanau, Germany). Details on calibration, analytical accuracy and precision are presented in S2 File).
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2

Elemental Analysis for Chitosan Derivatives

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The elemental analysis was performed on an element analysis instrument (Vario Micro Elemental Analyzer, Elementar, Germany). The carbon-nitrogen ratios were used to evaluate the degree of substitution in chitosan derivatives and the degrees of substitution (DS) were calculated by the following equations: DS1=n1×MCMN×WC/Nn2×MC
DS2=MN×WC/N+n2×MC×DS1n1×MCn3×MC
DS3=n1×MC+n3×MC×DS2n1×MN×WC/Nn2×MC×DS1n2×MN×WC/Nn4×MC
DS4=n1×MN×WC/N+n2×MN×WC/N×DS3+n2×MC×DS1n1×MCn3×MC×DS2n4×MC×DS3n5×MC
where DS1, DS2, DS3, and DS4 represent the deacetylation degree of chitosan, the DS of derivative 1, the DS of derivatives 2a-2c, and the DS of derivatives 3a-3c; MC and MN are the molar mass of carbon and nitrogen, MC = 12, MN = 14; n1, n2, n3, n4, and n5 are the number of carbon of chitin, chitosan, derivative 1, derivatives 2a-2c, and derivatives 3a-3c, n1 = 8, n2 = 2, n3 = 2, n4 = 4, n5 = 1; n1 and n2 are the number of nitrogen of chitosan and derivatives 2a-2c, n1 = 1, n2 = 2; WC/N represents the mass ratio between carbon and nitrogen in chitosan derivatives.
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3

Rhodium(III) Complex Kinetics and Analysis

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NMR spectra were recorded on a 200 MHz Varian Gemini-2000 device. Chemicals shifts (δ) are reported in ppm and referenced to tetramethylsilane. Coupling constants ( J) are reported in hertz (Hz) and splitting patterns are indicated as s (singlet) and d (doublet). Elemental analyses (C, H, N) were performed by combustion and gas chromatographic analysis with an Elementar Vario MICRO elemental analyzer. pH measurements were carried out using a Mettler Delta 350 digital pH meter with a resolution ±0.01 mV, with a combination glass electrode. This electrode was calibrated using standard buffer solutions of pH 4, 7, and 9 obtained from Sigma. Kinetic measurements of the rhodium(III) complex 1 were carried out on a Perkin-Elmer Lambda 25 or 35 double-beam spectrophotometer in thermostated 1.00 cm quartz Suprasil cells. The temperature was controlled to ±0.1 °C. Varian Cary 100 spectrophotometers equipped with a thermal control unit were also used in kinetic experiments. All kinetic measurements were performed under pseudo-first-order conditions, i.e., at least a 10-fold excess of the complex was used. Fluorescence measurements were performed on a RF-1501 PC spectrofluorometer (Shimadzu, Japan).
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