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Db 5 capillary column

Manufactured by Hewlett-Packard
Sourced in United States

The DB-5 capillary column is a type of gas chromatography (GC) column used for the separation and analysis of a wide range of chemical compounds. It is a fused silica column coated with a 5% phenyl-methylpolysiloxane stationary phase, which provides a balance of polarity and selectivity for a variety of analytes. The DB-5 column is commonly used in various analytical applications, such as environmental analysis, food testing, and pharmaceutical research, where the separation and identification of complex mixtures are required.

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4 protocols using db 5 capillary column

1

GC-FID and GC-MS Analysis of Oil Samples

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Oil sample analysis was achieved on an Hp-6890 gas chromatograph equipped with an FID and a DB-5 capillary column, 30 m × 0.25 mm, 0.25 μm film thickness, temperature was programmed as follows: 60 °C −240 °C at 4 °C/ min. The carrier gas was N2 at a flow of 2.0 ml/min; injector port and detector temperature were 250 °C and 300 °C, respectively. The sample was injected by splitting and the split ratio was 1:10.
GC/MS analysis was done on a Hewlett-Packard 6890 /5972 system with a DB-5 capillary column (30 m × 0.25 mm; 0.25 μm film thickness). The operating conditions were the same conditions as described above but the carrier gas was He. Mass spectra were taken at 70 eV. Scan mass range was from 40–400 m/z at a sampling rate of 1.0 scan/s. Quantitative data were obtained from the electronic integration of the FID peak areas. The components of the oil were known by their retention time, retention indices, relative to C9-C28 n-alkanes, computer matching with the WILEY275.L library, as well as by comparison of their mass spectra with data already available in the literature (10 ). The percentage of composition of the identified compounds was computed from the GC peaks areas without any correction factors and was calculated relatively.
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2

Quantitative Analysis of Fruit Odor

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For quantitative analyses, 0.1 μg of octadecane was added as an internal standard to each of the eluted fruit odor samples collected by dynamic headspace adsorption (see above). All samples were analyzed with an HP5890 Series II gas chromatograph (Hewlett-Packard, Palo Alto, CA, USA), equipped with a DB5 capillary column (30 m × 0.25 mm i.d.) that used hydrogen as the carrier gas (2 ml min−1 constant flow). One microliter of each sample was injected splitless at 40°C. After 1 min, the split valve was opened and the temperature increased by 4°C min−1 until reaching a temperature of 300°C. GC/MS analyses were carried out on an HP 6890 Series GC connected to an HP 5973 mass selective detector (Hewlett-Packard) fitted with a BPX5 fused-silica column (25 m, 0.22 mm i.d., 0.25 μm film thick, SGE). Mass spectra (70 eV) were recorded in full scan mode. Retention indices were calculated from a homolog series of n-alkanes. Structural assignments were based on comparison of analytical data obtained with natural products and data reported in the literature [6 (link), 26 (link), 34 ], and those of synthetic reference compounds. Structures of identified candidate compounds were verified by co-injection.
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3

GC-MS Analysis of Organic Compounds

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All samples were analyzed using an Hewlett Packard 6890 (HP 6890) gas chromatography system equipped with an HP 5972 mass selective detector (MSD) operating in selective ion monitoring mode using a DB-5 capillary column (30 m × 0.25 mm × 0.25 μm). Splitless injection of 1.0 μL of sample was conducted using an autosampler. The GC oven temperatures were programmed to increase from 80 to 180 °C at a rate of 10 °C/min, then to 220 °C at a rate of 2 °C/min, and finally to 290 °C at a rate of 8 °C/min.
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4

GC-FID Analysis of Organic Compounds

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A Hewlett-Packard 5890A gas chromatograph equipped with a flame ionization detector and a DB-5 capillary column (30 m in length, 0.25 mm in diameter (i.d.) ) was used. Additionally, a split injection of 25:1 was used. Helium at a flow rate of 30 cm/s was used as a carrier gas. The oven temperature was programmed to increase from 130 to 240℃ at 4℃/min. The injector and detector temperatures were 270℃ and 280℃, respectively. The peak area was integrated with a Hewlett-Packard HP3396 series II integrator.
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