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Cp8400

Manufactured by Agilent Technologies
Sourced in United States

The CP8400 is a compact and versatile benchtop centrifuge designed for general laboratory applications. It features a maximum speed of 8,400 rpm and a maximum relative centrifugal force (RCF) of 9,400 x g. The CP8400 accommodates a variety of rotor options to handle different sample tube sizes and volumes.

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5 protocols using cp8400

1

Determination of Residual Solvents in Samples

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Example 1

The content of residual organic solvent is evaluated by gas chromatography according to the following protocol:

Sample Preparation Protocols

Extraction with dichloromethane by sonication for 20 minutes:

    • Sw=20 mg-50 mg of sample
    • 0.9 ml dichloromethane
    • 0.1 ml of internal standard (pentadecane) dissolved in dichloromethane.

GC operating conditions: Varian 3800 with CP8400 autosampler

    • Column: BPX35 L=32 m; ID=0.25 mm; Film=1 μm
    • Flow rate (constant mode)=1.3 ml/min
    • FID detector temperature: 300° C.
    • Injector temperature 1177: 250° C.
    • Split ratio=25
    • Oven temperature program: 40° C. (2 min)→280° C. (2 min) at 8° C./min
    • Injection mode: autosampler
    • Injection volume=1 μl
    • Carrier gas: helium

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2

Determination of Residual Solvents by GC

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Example 1

The content of residual organic solvent is evaluated by gas chromatography according to the following protocol:

Sample Preparation Protocols

Extraction with dichloromethane by sonication for 20 minutes:

    • Sw=20 mg-50 mg of sample
    • 0.9 ml dichloromethane
    • 0.1 ml of internal standard (pentadecane) dissolved in dichloromethane.

GC Operating Conditions:

Varian 3800 with CP8400 autosampler

    • Column: BPX35 L=32 m; ID=0.25 mm; Film=1 μm
    • Flow rate (constant mode)=1.3 ml/min
    • FID detector temperature: 300° C.
    • Injector temperature 1177: 250° C.
    • Split ratio=25
    • Oven temperature program: 40° C. (2 min)→280° C. (2 min) at 8° C./min
    • Injection mode: autosampler
    • Injection volume=1 μl
    • Carrier gas: helium

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3

Quantifying Methane and Carbon Dioxide Fluxes

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Gas sampling was performed with floating chambers adapted from field static chamber (Environment Agency, 2010 ) in which the gaseous matrix volume was sampled in triplicate, in intervals of 5, 10, and 15 min, stored at room temperature, and transported to the laboratory. The CH4 and CO2 concentrations were determined in mg m2 h–1, through Gas Chromatography–Flame Ionization Detector (GC-FID, Varian CP 8400, United States) (Yuesi and Yinghong, 2003 (link)), and converted to gas flow rate express in mg m–2 d–1, calculated from emission rates of the compounds in the static chamber, from the rate of change in the species concentration determined by GC-FID and with sampling intervals in the chamber using the first Fick’s law, as follows (Venterea, 2010 (link)):
Where: F is the flow of gases on the water surface (mg m–2 d–1); ρ is the specific mass of the air according to the temperature during the sampling (mg m–3); V is the internal volume of the chamber (m3); A is the surface area of the chamber exposed to water (m2); and (dC/dt) is the concentration gradient of the target species as a function of sampling intervals. The estimated CH4 flow rate limit of detection was 120 mg m–2 d–1.
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4

Gas Chromatographic Analysis of Fatty Acids

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Extraction of FA was performed according to the boron trifluoride method described by Yurchenko et al. (2016) . Fatty acid methyl esters were analyzed on a Varian 3900 gas chromatograph equipped with a flame ionization detector and autosampler CP-8400. Chromatographic separation of FAME was performed using a Supelco ionic liquid column SLB-IL111 (100m × 0.25 mm i.d., 0.20 µm film thickness). Tridecanoic acid methyl ester (C13:0) as internal standard and CRM47885 standard mixture as external standard were used. A more detailed method description has been described by Yurchenko et al. (2018) (link).
The following sums and indices were calculated: SFA, MUFA, PUFA, atherogenic index, desaturase index (DI), and ratio of n-6 and n-3 FA (n-6/n-3). The atherogenic index was calculated as has been proposed by Ulbricht and Southgate (1991) (link) as follows: atherogenic index = (C12:0 + 4 × C14:0 + C16:0)/(MUFA + n-6 + n-3), and n-6/n-3 as n-6/n-3 = (C18: 2n -6 + C20: 2n -6 + C18: 3n -6)/C18: 3n -3. The DI was defined as follows: product of desaturase/substrate of desaturase and calculated for 3 pairs of FA (DI14 = C14:1 cis-5/C14:0; DI16 = C16:1 cis-7/C16:0; DI18 = C18:1 cis-9/C18:0).
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5

GC-MS Analysis of Volatile Compounds

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Volatile compounds were analyzed in a GC (Varian 3800) equipped with an MS detector (Saturn 2200), an automatic sampler (CP-8400) and an autoinjector (CP-8410). The separation was performed on a phenomenex ZB-WAX (30 m × 0.32 mm × 0.50 µm film thickness). The injector temperature was 250 °C and helium was the carrier gas at a flow rate of 1.0 mL/min. The oven programme started at 40 °C (held for 10 min), increased to 100 °C at 15 °C/min (held for 5 min) and finally to 250 °C at 15 °C/ min and held at that temperature for 5 min. The MS was operated in electron ionization mode (70 eV) and scanning was programmed for a m/z range of 29-300. Identification of volatile compounds was achieved by comparison with reference standard, matched spectra from the NIST 2.0 library and fragmentation patterns for compounds reported in the literature. For quantitation of volatiles, stock solutions of standards were dissolved in dichloromethane, and thereafter working concentrations were prepared by diluting to appropriate levels in a model wine solution containing 10 % ethanol, 3.0 g/L malic acid and the pH adjusted to 3.0 with NaOH.
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