The present paper describes the design of a new adiabatic flow calorimeter which is capable of measuring the integral Joule-Thomson effect and the isobaric enthalpy increment in the gaseous phase. The underlying principles for calorimetric measurements are discussed, and the measuring devices are de
Measurements of the isobaric enthalpy increment and the isenthalpic Joule–Thomson effect of (methane + water) and (methane + ethane + water)
✍ Scribed by C. Day; M. Stephan; L.R. Oellrich
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 260 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0021-9614
No coin nor oath required. For personal study only.
✦ Synopsis
The direct measurement of caloric properties of model systems for natural gas is of great technical interest. Therefore, integral Joule-Thomson effects and isobaric enthalpy increments have been measured for two (methane + ethane + water) compositions and three (methane + water) compositions. The flow calorimeter facility used is described. The temperature range from near mixture dew point temperature to T = 600 K and pressures up to 7 MPa is covered. Expansion took place to p = 0.17 MPa. The investigated compositions of {xC2H6 + yH2O + (1 -x -y)CH4} were (x = 0.07, y = 0.15) and (x = 0.2, y = 0.2); and of {yH2O + (1 -y)CH4} y = (0.1, 0.2, and 0.4). The measurement results have been correlated and the residual and total enthalpy functions have been derived from them.
📜 SIMILAR VOLUMES
Isobaric enthalpy increment and isenthalpic Joule᎐Thomson effect measurements on synthetic gas containing binary, or ternary mixtures of methane, ethane, propane, and nitrogen are presented. The experimental results are presented as isobaric heat capacities C and p Joule᎐Thomson coefficients . The m
## Abstract A comparison has been made between two cryogenic preconcentration ‐ high resolution gas chromatography techniques for the analysis of non‐methane hydrocarbons in ambient air, one involving treatment of air samples with magnesium perchlorate to remove water, the other involving analysis
Gas-phase densities of the systems: pure water, methane, n-hexane, n-octane, and benzene were measured at temperatures from 523.15 K to 673.15 K and at pressures up to approximately 100 MPa. Second and third virial coefficients were determined for each system, and the cross virial coefficients were
Total amounts of CH 4 emission from a Sumatra rice ®eld were in the ranges 29 . 5±48 . 2 and 43 . 0±64 . 6 g CH 4 m À2 season À1 for the plots with chemical fertilizer (CF-plot) and those with rice straw application (RS-plot), respectively. Nearly the same amounts of CH 4 were emitted in the ®rst an
The effect of changing the L C=O -. \* H on the energy of the linear hydrogen bond has been studied by ab initio calculations for one formamide-methane complex and two formamide-water complexes, which differ in the position of the second hydrogen (H2,) of the water molecule (i.e. the one not involve