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Perkin elmer spectrum 400 spectrometer

Manufactured by PerkinElmer
Sourced in Spain

The Perkin-Elmer Spectrum™ 400 spectrometer is a laboratory instrument designed for spectroscopic analysis. It is capable of measuring and analyzing the absorption or emission of electromagnetic radiation by samples, providing information about their molecular structure and composition.

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2 protocols using perkin elmer spectrum 400 spectrometer

1

Infrared Spectroscopy Analysis of Frankfurters

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The infrared spectra of each sample were recorded using a Perkin-Elmer SpectrumTM 400 spectrometer (Perkin Elmer Inc., Tres Cantos, Madrid, Spain) in mid-IR mode, equipped with an attenuated total reflectance (ATR) sampling device containing a diamond/ZnSe crystal according to Pintado, Herrero, Ruiz-Capillas, Triki, Carmona and Jimenez-Colmenero [24 (link)]. Measurements were performed at room temperature using approximately 25 mg of the samples (without any previous sample preparation), which were placed on the surface of the ATR crystal, and lightly pressed with a flat-tip plunger. For each type of frankfurter, 9 measurements were carried out. Sums of 3 spectra (24 accumulations) were performed, and these 3-sum spectra were analysed for each sample.
Spectra were acquired with the Spectrum software version 6.3.2 and spectral data were treated with the Grams/AI version 9.1 software (Thermo Electron Corporation, Waltham, MA, USA). The spectral region 3000–2800 cm−1 was analysed to study the lipid structural characteristics of the samples [24 (link)].
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2

Infrared Spectroscopy of Frankfurter Lipids

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Infrared spectra were recorded for each sample using a Perkin-Elmer SpectrumTM 400 spectrometer (Perkin Elmer Inc., Spain) in mid-infrared mode, equipped with an ATR sampling device (Pintado, Herrero, Ruiz-Capillas, et al., 2016) . Approximately 25 mg of each sample (with no previous preparation) was analysed and nine measurements were made per sample. A total of three sum spectra (72 accumulations) were analysed for each type of frankfurter. The 3000-2800 cm -1 spectral region was analysed to study the lipid structure. To avoid any spectral influence from water and other ingredients, the corresponding aqueous solution spectrum was appropriately subtracted using the 2125 cm -1 association band of water as an internal intensity standard (Vincent, Steer, & Levin, 1984) .
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