Numerical Simulation of Multi-Grade Separators for Multi-Phase Fluid Media Down Hole in Offshore Oilfield

2010 ◽  
Author(s):  
Yong Zhang ◽  
Yan Zhang ◽  
Minghu Jiang
Keyword(s):  
Production Efficiency ◽  
Modular Design ◽  
Maximum Diameter ◽  
Fluid Media ◽  
In Series ◽  
Oil Water ◽  
Multi Phase ◽  
Water Gas ◽  
Phase Fluid

It’s an effective method to get higher oil production efficiency during offshore petroleum production by separating some water from produced fluid and re-injecting it in some given formation using down hole separators. However some kinds of oil, water, gas and sand will enter the separator in the down hole separating system as a mixture because of the complex environment down hole. In oilfield onshore multiphase separators will be a good answer to this puzzle. But it becomes almost impossible to use multi-phase separators down hole because of the complex condition and the limitation of diameter of well bore. However multi-grade separators can be arranged in bridge or in series and some path-breaking theoretical and experimental investigation related has been done which based on modular design. This not only gives the answer to the puzzle to arrange multi-grade separators, but also bring it to be possible to separate different separating media with different separator. And this takes role of multiphase separator limited by maximum diameter down hole. Some new results are introduced in this paper about the implement method of separating gas/oil/water in different grade of separators which are arrayed in series. It shows different conditions for down hole separators simulating by CFD technique which can be a perfect reference for design of separators and separating systems.

scholarly journals Production of Fuels and Chemicals from a CO2/H2 Mixture

Reactions ◽  
2020 ◽  
Vol 1 (2) ◽  
pp. 130-146
Author(s):  
Yali Yao ◽  
Baraka Celestin Sempuga ◽  
Xinying Liu ◽  
Diane Hildebrandt
Keyword(s):  
Co2 Hydrogenation ◽  
Water Gas Shift ◽  
Liquid Fuels ◽  
Saturated Hydrocarbons ◽  
Reverse Water Gas Shift ◽  
Cu Catalyst ◽  
In Series ◽  
Fuels And Chemicals ◽  
Water Gas ◽  
Aspen Simulation

In order to explore co-production alternatives, a once-through process for CO2 hydrogenation to chemicals and liquid fuels was investigated experimentally. In this approach, two different catalysts were considered; the first was a Cu-based catalyst that hydrogenates CO2 to methanol and CO and the second a Fisher–Tropsch (FT) Co-based catalyst. The two catalysts were loaded into different reactors and were initially operated separately. The experimental results show that: (1) the Cu catalyst was very active in both the methanol synthesis and reverse-water gas shift (R-WGS) reactions and these two reactions were restricted by thermodynamic equilibrium; this was also supported by an Aspen plus simulation of an (equilibrium) Gibbs reactor. The Aspen simulation results also indicated that the reactor can be operated adiabatically under certain conditions, given that the methanol reaction is exothermic and R-WGS is endothermic. (2) the FT catalyst produced mainly CH4 and short chain saturated hydrocarbons when the feed was CO2/H2. When the two reactors were coupled in series and the presence of CO in the tail gas from the first reactor (loaded with Cu catalyst) significantly improves the FT product selectivity toward higher carbon hydrocarbons in the second reactor compared to the standalone FT reactor with only CO2/H2 in the feed.

scholarly journals New insights into the mechanisms of ultrasonic emulsification in the oil-water system and the role of gas bubbles

2021 ◽  
pp. 105501
Author(s):  
W.H. Wu ◽  
D.G. Eskin ◽  
A. Priyadarshi ◽  
T. Subroto ◽  
I. Tzanakis ◽  
...  
Keyword(s):  
Water System ◽  
Gas Bubbles ◽  
Ultrasonic Emulsification ◽  
Oil Water

scholarly journals The role of JrPPOs in the browning of walnut explants

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Shugang Zhao ◽  
Hongxia Wang ◽  
Kai Liu ◽  
Linqing Li ◽  
Jinbing Yang ◽  
...  
Keyword(s):  
Tissue Culture ◽  
Production Efficiency ◽  
Phenolic Content ◽  
Leaf Tissue ◽  
Limiting Factor ◽  
Mature Leaves ◽  
Survival Percentage ◽  
Highly Active ◽  
Young Leaves

Abstract Background Tissue culture is an effective method for the rapid breeding of seedlings and improving production efficiency, but explant browning is a key limiting factor of walnut tissue culture. Specifically, the polymerization of PPO-derived quinones that cause explant browning of walnut is not well understood. This study investigated explants of ‘Zanmei’ walnut shoot apices cultured in agar (A) or vermiculite (V) media, and the survival percentage, changes in phenolic content, POD and PPO activity, and JrPPO expression in explants were studied to determine the role of PPO in the browning of walnut explants. Results The results showed that the V media greatly reduced the death rate of explants, and 89.9 and 38.7% of the explants cultured in V media and A media survived, respectively. Compared with that of explants at 0 h, the PPO of explants cultured in A was highly active throughout the culture, but activity in those cultured in V remained low. The phenolic level of explants cultured in A increased significantly at 72 h but subsequently declined, and the content in the explants cultured in V increased to a high level only at 144 h. The POD in explants cultured in V showed high activity that did not cause browning. Gene expression assays showed that the expression of JrPPO1 was downregulated in explants cultured in both A and V. However, the expression of JrPPO2 was upregulated in explants cultured in A throughout the culture and upregulated in V at 144 h. JrPPO expression analyses in different tissues showed that JrPPO1 was highly expressed in stems, young leaves, mature leaves, catkins, pistils, and hulls, and JrPPO2 was highly expressed in mature leaves and pistils. Moreover, browning assays showed that both explants in A and leaf tissue exhibited high JrPPO2 activity. Conclusion The rapid increase in phenolic content caused the browning and death of explants. V media delayed the rapid accumulation of phenolic compounds in walnut explants in the short term, which significantly decreased explants mortality. The results suggest that JrPPO2 plays a key role in the oxidation of phenols in explants after branch injury.

scholarly journals The Role of Chromium in Iron-based High-Temperature Water-Gas Shift Catalysts under Industrial Conditions

2021 ◽  
pp. 120465
Author(s):  
M.I. Ariëns ◽  
V. Chlan ◽  
P. Novák ◽  
L.G.A. van de Water ◽  
A.I. Dugulan ◽  
...  
Keyword(s):  
High Temperature ◽  
Water Gas Shift ◽  
High Temperature Water ◽  
Iron Based ◽  
Water Gas ◽  
Temperature Water

scholarly journals Elucidating the Influence of Electric Fields toward CO2 Activation on YSZ (111)

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 271
Author(s):  
Nisa Ulumuddin ◽  
Fanglin Che ◽  
Jung-Il Yang ◽  
Su Ha ◽  
Jean-Sabin McEwen
Keyword(s):  
Electric Field ◽  
Electric Fields ◽  
Heterogeneous Catalysts ◽  
Co2 Reduction ◽  
Total Density ◽  
Reverse Water Gas Shift ◽  
High Thermodynamic Stability ◽  
Shift Reaction ◽  
Water Gas

Despite its high thermodynamic stability, the presence of a negative electric field is known to facilitate the activation of CO2 through electrostatic effects. To utilize electric fields for a reverse water gas shift reaction, it is critical to elucidate the role of an electric field on a catalyst surface toward activating a CO2 molecule. We conduct a first-principles study to gain an atomic and electronic description of adsorbed CO2 on YSZ (111) surfaces when external electric fields of +1 V/Å, 0 V/Å, and −1 V/Å are applied. We find that the application of an external electric field generally destabilizes oxide bonds, where the direction of the field affects the location of the most favorable oxygen vacancy. The direction of the field also drastically impacts how CO2 adsorbs on the surface. CO2 is bound by physisorption when a +1 V/Å field is applied, a similar interaction as to how it is adsorbed in the absence of a field. This interaction changes to chemisorption when the surface is exposed to a −1 V/Å field value, resulting in the formation of a CO3− complex. The strong interaction is reflected through a direct charge transfer and an orbital splitting within the Olatticep-states. While CO2 remains physisorbed when a +1 V/Å field value is applied, our total density of states analysis indicates that a positive field pulls the charge away from the adsorbate, resulting in a shift of its bonding and antibonding peaks to higher energies, allowing a stronger interaction with YSZ (111). Ultimately, the effect of an electric field toward CO2 adsorption is not negligible, and there is potential in utilizing electric fields to favor the thermodynamics of CO2 reduction on heterogeneous catalysts.

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