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1515 gel permeation chromatograph

Manufactured by Waters Corporation

The 1515 gel permeation chromatograph is a laboratory instrument designed for the separation and analysis of macromolecules. It utilizes the principle of size-exclusion chromatography to separate molecules based on their size and molecular weight. The 1515 model is capable of providing accurate and reliable data for the characterization of polymers, proteins, and other large molecules.

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3 protocols using 1515 gel permeation chromatograph

1

Waterborne Alkyd Molecular Weight

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The molecular weight of the waterborne alkyd was examined by a Waters 1515 gel permeation chromatograph (GPC). Tetrahydrofuran was applied as a mobile phase at 1.0 ml min−1 of flow rate at 25°C. The molecular weights were calculated with reference to the calibration curve of standard polystyrene.
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2

Comprehensive Characterization of Synthetic Products

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All synthetic products were analyzed by 1H NMR (Bruker, 300 MHz, tetramethylsilane as internal standard at 293 K) to verify their chemical structure and composition. Spectra were recorded in CDCl3 or D2O solution [1H NMR: CDCl3, 7.26 parts per million (ppm); D2O, 4.79 ppm; for 13C NMR: CDCl3, 77.0 ppm]. Mass spectra were acquired using a Bruker microTOF-Q III instrument. Fourier transform infrared spectra were recorded using a Nicolet 6700 spectrometer with 32 scans per sample. The number-average molecular weights (Mn) and polydispersity indices of the polymers were determined by size exclusion chromatography using a Waters 1515 gel permeation chromatograph with polyethylene glycol standards.
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3

Characterization of Synthesized Copolymers

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Gel permeation chromatography (GPC 515, Waters, Milford, MA, USA) was used to determine number- and weight-average molar masses (Mn and Mw) and dispersity (Ð) of the synthesized copolymers. The analyses were carried out using a Waters 1515 gel permeation chromatograph equipped with HR 1, HR 3, and HR 4 columns, thus covering a molecular weight range of 100–500,000 g mol−1. Tetrahydrofuran was used as the eluent at a flow rate of 1.0 mL min−1, at 30 °C. A differential refractive index detector was used and average molar masses (Mn and Mw), as well as dispersity (Ð), were calculated from a calibration curve based on polystyrene (PS) standards from Polymer Laboratories.
Copolymer composition was determined using 1H NMR (Varian Mercury 300 MHz, Varian, Santa Clara, CA, USA). Copolymer samples were dissolved in deuterated chloroform and scanned 32 times at room temperature.
Chemical structures of the copolymers and modified PLA were analyzed by Fourier transform infrared spectroscopy. The FTIR spectra of samples were measured at room temperature with 32 scans at a resolution of 1 cm−1 using a Nicolet IZ10 spectrometer (Thermo Fisher Scientific, Waltham, MA, USA) over the wavenumbers ranging from 4000 to 600 cm−1.
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