STUDY OF TWO-PHASE BEHAVIOR OF NITRILE POLYMERS BY IN SITU HOT-STAGE IR SPECTROSCOPY

2001 ◽  
Vol 40 (1) ◽  
pp. 15-28 ◽  
Author(s):  
O. A. Andreeva ◽  
L. A. Burkova
Keyword(s):  
Ir Spectroscopy ◽  
Phase Behavior ◽  
Two Phase

Effect of Capillary Pressure on Phase Behavior in Tight Rocks and Shales

2013 ◽  
Vol 16 (03) ◽  
pp. 281-289 ◽  
Author(s):  
B.. Nojabaei ◽  
R.T.. T. Johns ◽  
L.. Chu
Keyword(s):  
Phase Behavior ◽  
Capillary Pressure ◽  
Gas Flow ◽  
Dew Point ◽  
Bakken Formation ◽  
Equilibrium Equations ◽  
Two Phase ◽  
Small Pore ◽  
The Impact

Summary Phase behavior is important in the calculation of hydrocarbons in place and in the flow of phases through the rocks. Pore sizes can be on the order of nanometers for shale and tight-rock formations. Such small pores can affect the phase behavior of in-situ oil and gas because of increased capillary pressure. Not accounting for increased capillary pressure in small pores can lead to inaccurate estimates of ultimate recovery, and of saturation pressures. In this paper, capillary pressure is coupled with phase equilibrium equations, and the resulting system of nonlinear fugacity equations is solved to present a comprehensive examination of the effect of small pores on saturation pressures and fluid densities. Binary mixtures of methane with heavier hydrocarbons and a real reservoir fluid from the Bakken shale are considered. The results show that accounting for the impact of small pore throats on pressure/volume/temperature (PVT) properties explains the inconsistent gas/oil-ratio (GOR) behavior, high flowing bottomhole pressures, and low gas-flow rate observed in the tight Bakken formation. The small pores decrease bubble-point pressures and either decrease or increase dew-point pressures, depending on which part of the two-phase envelope is examined. Large capillary pressure also decreases the oil density in situ, which affects the oil formation volume factor and ultimate reserves calculations. A good history match for wells in the middle Bakken formation is obtained only after considering a suppressed bubblepoint pressure. The results show that the change in saturation pressures, fluid densities, and viscosities is highly dependent on the values of interfacial tension (IFT) (capillary pressure) used in the calculations.

Solution Properties and Phase Behavior of Ammonium Hexylene Octyl Succinate in Water and Water-Oil System

1970 ◽  
Vol 3 (1) ◽  
Author(s):  
Md. Hamidul Kabir ◽  
Ravshan Makhkamov ◽  
Shaila Kabir
Keyword(s):  
Critical Micelle Concentration ◽  
Phase Behavior ◽  
Liquid Crystalline ◽  
Carbon Number ◽  
Phase Region ◽  
Solution Properties ◽  
Middle Phase ◽  
Two Phase ◽  
Lamellar Liquid Crystal ◽  
Drug Ingredient

The solution properties and phase behavior of ammonium hexylene octyl succinate (HOS) was investigated in water and water-oil system. The critical micelle concentration (CMC) of HOS is lower than that of anionic surfactants having same carbon number in the lipophilic part. The phase diagrams of a water/ HOS system and water/ HOS/ C10EO8/ dodecane system were also constructed. Above critical micelle concentration, the surfactant forms a normal micellar solution (Wm) at a low surfactant concentration whereas a lamellar liquid crystalline phase (La) dominates over a wide region through the formation of a two-phase region (La+W) in the binary system. The lamellar phase is arranged in the form of a biocompatible vesicle which is very significant for the drug delivery system. The surfactant tends to be hydrophilic when it is mixed with C10EO8 and a middle-phase microemulsion (D) is appeared in the water-surfactant-dodecane system where both the water and oil soluble drug ingredient can be incorporated in the form of a dispersion. Hence, mixing can tune the hydrophile-lipophile properties of the surfactant. Key words: Ammonium hexylene octyl succinate, mixed surfactant, lamellar liquid crystal, middle-phase microemulsion. Dhaka Univ. J. Pharm. Sci. Vol.3(1-2) 2004 The full text is of this article is available at the Dhaka Univ. J. Pharm. Sci. website

The Nature of Chemisorbed CO2 in Zeolite A

2019 ◽  
Author(s):  
Przemyslaw Rzepka ◽  
Zoltán Bacsik ◽  
Andrew J. Pell ◽  
Niklas Hedin ◽  
Aleksander Jaworski
Keyword(s):  
Solid State ◽  
Ir Spectroscopy ◽  
Quantum Chemical Calculations ◽  
Quantum Chemical ◽  
Surface Coverage ◽  
Gas Mixtures ◽  
Mas Nmr ◽  
Significant Fraction ◽  
Zeolite A

Formation of CO<sub>3</sub><sup>2-</sup> and HCO<sub>3</sub><sup>-</sup> species without participation of the framework oxygen atoms upon chemisorption of CO<sub>2</sub> in zeolite |Na<sub>12</sub>|-A is revealed. The transfer of O and H atoms is very likely to have proceeded via the involvement of residual H<sub>2</sub>O or acid groups. A combined study by solid-state <sup>13</sup>C MAS NMR, quantum chemical calculations, and <i>in situ</i> IR spectroscopy showed that the chemisorption mainly occurred by the formation of HCO<sub>3</sub><sup>-</sup>. However, at a low surface coverage of physisorbed and acidic CO<sub>2</sub>, a significant fraction of the HCO<sub>3</sub><sup>-</sup> was deprotonated and transformed into CO<sub>3</sub><sup>2-</sup>. We expect that similar chemisorption of CO<sub>2</sub> would occur for low-silica zeolites and other basic silicates of interest for the capture of CO<sub>2</sub> from gas mixtures.

Catalytic activity of rhodium(I) complexes containing (ω-trimethylsilylalkyl)diphenylphosphines

1980 ◽  
Vol 45 (8) ◽  
pp. 2219-2223 ◽  
Author(s):  
Marie Jakoubková ◽  
Martin Čapka
Keyword(s):  
Catalytic Activity ◽  
Nmr Spectroscopy ◽  
Ir Spectroscopy ◽  
Electron Density ◽  
Phosphorus Atom ◽  
Proton Acceptor ◽  
Trimethylsilyl Group ◽  
Kinetics Of

Kinetics of homogenous hydrogenation of 1-heptene catalysed by rhodium(I) complexes prepared in situ from μ,μ'-dichloro-bis(cyclooctenerhodium) and phosphines of the type RP(C6H5)2 (R = -CH3, -(CH2)nSi(CH3)3; n = 1-4) have been studied. The substitution of the ligands by the trimethylsilyl group was found to increase significantly the catalytic activity of the complexes. The results are discussed in relation to the electron density on the phosphorus atom determined by 31P NMR spectroscopy and to its proton acceptor ability determined by IR spectroscopy.

Phase Behavior in Aqueous Two-Phase Systems Containing Micelle-Forming Block Copolymers

1995 ◽  
Vol 28 (10) ◽  
pp. 3597-3603 ◽  
Author(s):  
Maarten Svensson ◽  
Per Linse ◽  
Folke Tjerneld
Keyword(s):  
Block Copolymers ◽  
Phase Behavior ◽  
Two Phase ◽  
Aqueous Two Phase Systems ◽  
Phase Systems

In Situ IR Spectroscopy for Following the Copolymerization of CO2and Epoxides

2014 ◽  
Vol 86 (9) ◽  
pp. 1627-1628
Author(s):  
K. Böhm ◽  
W. Leitner ◽  
T. E. Müller
Keyword(s):  
Ir Spectroscopy ◽  
In Situ Ir ◽  
In Situ Ir Spectroscopy

PHASE TRANSITION IN LAYERED PEROVSKITE LIKE MANGANATE Ca3Mn2O7 UNDER HIGH PRESSURE

2001 ◽  
Vol 15 (18) ◽  
pp. 2491-2497 ◽  
Author(s):  
J. L. ZHU ◽  
L. C. CHEN ◽  
R. C. YU ◽  
F. Y. LI ◽  
J. LIU ◽  
...  
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
Diamond Anvil Cell ◽  
The Other ◽  
Layered Perovskite ◽  
X Ray Diffraction ◽  
Two Phase ◽  
X Ray ◽  
Diamond Anvil

In situ high pressure energy dispersive X-ray diffraction measurements on layered perovskite-like manganate Ca 3 Mn 2 O 7 under pressures up to 35 GPa have been performed by using diamond anvil cell with synchrotron radiation. The results show that the structure of layered perovskite-like manganate Ca 3 Mn 2 O 7 is unstable under pressure due to the easy compression of NaCl-type blocks. The structure of Ca 3 Mn 2 O 7 underwent two phase transitions under pressures in the range of 0~35 GPa. One was at about 1.3 GPa with the crystal structure changing from tetragonal to orthorhombic. The other was at about 9.5 GPa with the crystal structure changing from orthorhombic back to another tetragonal.

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