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Db 1ms capillary column

Manufactured by Shimadzu
Sourced in Japan

The DB-1MS capillary column is a high-performance gas chromatography column designed for the separation and analysis of a wide range of organic compounds. It features a 100% dimethylpolysiloxane stationary phase, which provides excellent thermal stability and inertness for a variety of applications.

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2 protocols using db 1ms capillary column

1

Synthesis and Characterization of Fe-Exchanged Y-Zeolite

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Na ion-exchanged Y-type zeolite (Na-Y) with SiO2/Al2O3 = 5.5 was supplied by Tosoh Co. The following chemicals were used as received: FeSO4∙7H2O (Wako, > 99%), sodium nitrate (Wako, 99.0%), ethylenediaminetetraacetate acid (TCI, 98.0%), ethylenediaminetetraacetate acid disodium salt (Wako, 99.5%), sodium hydroxide (Wako, 93%), 2,2′;6′,2″-terpyridine (TCI, 98.0%), methanol (Wako, 99.8%), 30% aqueous hydrogen peroxide (Wako, 30–35.5%), benzene (Wako, 99.5%), phenol (Wako, 99.0%), catechol (Wako, 99.0%), hydroquinone (Wako, 99.0%), o-dichlorobenzene (Wako, 98.0%), and acetonitrile (Wako, 99.5%).
ICP-AES and CHN elemental analyses of all catalysts were carried out after the sample was dissolved into a HF solution. The powder XRD patterns of the catalysts were collected on a Rigaku MiniFlex II diffractometer using CuKα radiation. The Brunauer–Emmet–Teller (BET) surface area measurements were conducted to determine the specific surface areas and pore diameters of the samples by performing N2 adsorption experiments at 77 K using a BEL Japan Bellsorp-max instrument. The UV-vis spectra were recorded on a Hitachi U-4000 spectrometer for solid samples. Gas chromatography (GC, Shimadzu GC-2014) was performed using a flame ionization detector equipped with a DB-1MS capillary column (internal diameter = 0.25 mm and length = 30 m) at the nature of the non-polar liquid phase.
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2

GC-MS Analysis of Compound Identification

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Gas chromatography and mass spectrometry (GC-MS) analysis was performed at the Technological Development Park of the Universidade Federal do Ceará using a GCMS QP 5050A (Shimadzu, Kyoto, Japan) equipped with a non-polar AW Scientific DB-1 MS capillary column (50 m × 0.25 mm × 0.25 μm). The oven temperature was set at 70°C with an increase of 4°C/min until 230°C and then maintained for 15 min. The carrier gas was helium, with a constant flow rate of 1.7 mL/min. The temperature of the ionization source was maintained at 280°C, ionization energy at 70 eV, and ionization current at 0.7 kV. Mass spectra were recorded from 30 to 450 m/z. Individual components were identified by matching their 70 eV mass spectra with those of the spectrometer database by using the Wiley L-Built library and by comparing their retention indices and fragmentation patterns with those of the NIST MS library (Stein et al., 1997) and those reported in the literature (Adams, 2001) .
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