Prediction of In-Situ Combustion Process Variables By Use of TGA/DSC Techniques and the Effect of Sand-Grain Specific Surface Area on the Process

1985 ◽  
Vol 25 (05) ◽  
pp. 656-664 ◽  
Author(s):  
Shapour Vossoughi ◽  
Gordon W. Bartlett ◽  
Paul G. Willhite

Prediction of In-Situ Combustion Prediction of In-Situ Combustion Process Variables By Use of Process Variables By Use of TGA/DSC Techniques and the Effect of Sand-Grain Specific Surface Area on the Process Abstract This paper describes a new technique to predict the parameters that govern the performance of the in-situ combustion process. This prediction is accomplished by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) of the crude-oil combustion. The effect of surface area on the in-situ combustion-tube runs was also investigated. The crude oil studied was from Iola field, Allen County, KS. This oil has a gravity of 19.8 API [0.94 g/cm3] and a viscosity of 222 cp [0.222 Pa-s] at 100.4 F [38 C] and 98 cp [0.098 Pa-s] at 129.2 F [54 C]. Pa-s] at 100.4 F [38 C] and 98 cp [0.098 Pa-s] at 129.2 F [54 C]. At a bulk density of the combustion-tube pack of 104.26 lbm/cu ft [1.67 g/cm3], the minimum crude-oil content to support an adiabatic combustion process was estimated to be 7.1 wt%. This translates into 34.4% oil saturation for the sandpack of 37% porosity and the crude-oil gravity of 19.8 API [0.94 g/cm3]. However, the combustion front, in a sandpack of 70 mesh (specific surface area of 76 cm2/g [7.6 m2/kg]) with an oil content even greater than the required minimum oil content predicted by the present approach, did not sustain itself. Additional tube runs were performed with finer sand grains having specific surface areas of 317, 1,120 and 3,332 cm2/g [31.7, 112, and 333.2 m2/kg]. A strong, sustained combustion front was observed only in the last run-i.e., the greatest specific surface area. TGA was applied to the samples taken at 1- to 2-in. [2.54-to 5.08-cm] intervals ahead of the front to study crude-oil distribution. In the case of unsuccessful runs, the amount of the crude oil ahead of the front decreased to a level that sufficient fuel could not be laid down to sustain the front. In the self-sustained run with the greatest surface area, crude-oil content immediately ahead of the front was even higher than the original sand/oil mixture. Therefore, a minimum surface area is required to provide conditions for sufficient fuel to be laid down by the coking process. process. This finding is believed to be important in revealing the mechanism responsible for the lack of self-sustained combustion in sandpacks or porous rocks with low specific surface area. It also reveals the porous rocks with low specific surface area. It also reveals the importance of the specific surface area available to the crude oil for determining whether a self-sustained combustion could be achieved. Introduction In-situ combustion is a complex process that involves simultaneous heat and mass transfer in a multiphase environment coupled with chemical reactions of crude-oil combustion. Many studies on the thermal and fluid dynamics of the in-situ combustion process have been conducted, but little has been done to study chemical reaction kinetics and mechanisms involved in underground combustion. In a recent study, Fassihi et al. showed that the combustion of crude oil in porous media follows several consecutive reactions. They identified three groups of reactions (low-, middle-, and high-temperature reactions), and argued that the first was heterogeneous (gas/liquid), the second, homogeneous (gas phase), and the third, heterogeneous (gas/solid phase). They produced a model based on Weijdema's kinetic equation in which a simple reaction is assumed for each group of crude-oil reactions and Arrhenius-type dependency of the rate constant on temperature. This model, however, allowed only the prediction of crude-oil combustion parameters under very stringent and controlled conditions. The oxidative behavior of crude oils under varying conditions of temperature, pressure, and atmosphere may also be studied by thermal analysis. Most researchers took a qualitative approach and used thermal analysis techniques to study the thermo-oxidative behavior of crudes with specific reference to the temperatures at which each oxidation reaction occurs. Weckowska and Bogdanow, however, took a different approach to thermal analysis by investigating the thermal decomposition kinetics of the vacuum-distillation residue of crude oil. They used the kinetic model of Zsako to describe mathematically the kinetics of thermal decomposition of a Romashkino crude-oil residue. SPEJ p. 656

1982 ◽  
Vol 22 (04) ◽  
pp. 493-502 ◽  
Author(s):  
Shapour Vossoughi ◽  
G. Paul Willhite ◽  
William P. Kritikos ◽  
Ibrahim M. Guvenir ◽  
Youssef El Shoubary

Abstract A fully automated in-situ combustion apparatus supported by a minicomputer was designed, constructed, and tested.Results obtained from four adiabatic dry combustion runs to investigate the effect on clay on crude oil combustion are reported. Sand mixtures of varying clay (kaolinite) content were saturated with crude oil and water. The fourth run was performed with amorphous silica powder in the sand mixture for comparison with clay results.We concluded that the large surface area of the clays was a major contributor to the fuel deposition process. However, different oxygen utilization efficiencies obtained from both types of sand mixtures indicated that mechanisms controlling the combustion reaction also depended on the composition of the porous matrix.A thermogravimetric analyzer (TGA) and a differential scanning calorimeter (DSC) were used to obtain kinetic data on the effects of kaolinite type clay on crude oil combustion. The addition of kaolinite clay or silica powder changed the shape of the crude oil TGA/DSC thermograms significantly, but sand had no effect. The major effect on DSC thermograms was a shifting of the large amount of heat produced from a higher to lower temperature range. Reduction of activation energy caused by the addition of kaolinite clay to the crude oil indicates both catalytic and surface area effects on combustion/cracking reactions. Introduction In-situ combustion is a thermal recovery process in which a portion of the crude oil is coked and burned in situ to recover the remaining oil. Design of the process involves experimental evaluation of process variables in laboratory experiments. Variables sought experimentally for the design of the process are usually fuel availability, air requirement, oxygen utilization efficiency, combustion peak temperature, combustion front velocity, effect of porous matrix, and kinetic parameters. Four methods have been used to obtain design data for in-situ combustion projects. These include (1) adiabatic in-situ combustion tube runs, (2) isothermal reactors, (3) flood pot tests, and (4) thermal analysis techniques.This paper describes an investigation of the effect of clay on in-situ combustion involving results from adiabatic combustion tube runs and thermal analysis methods. Part 1 describes the minicomputer-based insitu combustion system developed as part of the research program. Part 2 demonstrates application of the system to study the effect of clays on the in-situ combustion process. Combustion tube runs described in Part 2 are supplemented with thermal analysis methods to evaluate the effect of clay on in-situ combustion of a Kansas crude oil. Part 1-Development of an Automated In-Situ Combustion Tube Adiabatic tube runs have been the most commonly used approach for studying in-situ combustion. Since heat loss is small to nil in thick reservoirs, in-situ combustion is assumed to occur under adiabatic conditions. Adiabatic conditions in tube runs can be achieved either by insulating the tube or by reducing the temperature gradient between the sandpack and the environment surrounding the tube, or both. To attain adiabatic conditions in a partially or noninsulated tube, the temperature of the surroundings must be raised to that of the sandpack as the combustion front moves along the tube. Heater bands with proportional heat loads controlled by individual controllers are used. This requires a large number of controllers to control the temperature of the outside SPEJ P. 493^


2021 ◽  
Vol 14 (02) ◽  
pp. 2151011
Author(s):  
Jingwen Jia ◽  
Longfu Wei ◽  
Ziting Guo ◽  
Fang Li ◽  
Changlin Yu ◽  
...  

Metal–organic frameworks (MOFs) are the electrocatalytic materials with large specific surface area, high porosity, controllable structure and monodisperse active center, which is a promising candidate for the application of electrochemical energy conversion. However, the electrocatalytic performance of pure MOFs is seriously limited its poor conductivity and stability. In this work, high-performance electrocatalyst was fabricated through combining NiFe/MOF on nickel foam (NF) via in-situ growth strategy. Through rational control of the time and ratio in reaction precursors, we realized the effective manipulation of the growth behavior, and further investigated the electrocatalytic performance in water splitting. The catalyst presented excellent electrocatalytic performance for water splitting, with low overpotential of 260 mV in alkaline condition at a current density of 50 mA[Formula: see text], which is benefited from the large specific surface area and active sites. This study demonstrates that the rational design of NiFe MOF/NF plays a significant role in high-performance electrocatalyst.


2019 ◽  
Vol 55 (100) ◽  
pp. 15117-15120 ◽  
Author(s):  
Hong Wang ◽  
Wei Li ◽  
Zhiwei Zhu ◽  
Yijuan Wang ◽  
Pan Li ◽  
...  

An N-doped bio-carbon catalyst with a hierarchical interconnected macro/meso-porous structure and high specific surface area exhibited significantly enhanced electrocatalytic activity.


2014 ◽  
Author(s):  
E. A. Cavanzo ◽  
S. F. Muñoz ◽  
A.. Ordoñez ◽  
H.. Bottia

Abstract In Situ Combustion is an enhanced oil recovery method which consists on injecting air to the reservoir, generating a series of oxidation reactions at different temperature ranges by chemical interaction between oil and oxygen, the high temperature oxidation reactions are highly exothermic; the oxygen reacts with a coke like material formed by thermal cracking, they are responsible of generating the heat necessary to sustain and propagate the combustion front, sweeping the heavy oil and upgrading it due to the high temperatures. Wet in situ combustion is variant of the process, in which water is injected simultaneously or alternated with air, taking advantage of its high heat capacity, so the steam can transport heat more efficiently forward the combustion front due to the latent heat of vaporization. A representative model of the in situ combustion process is constituted by a static model, a dynamic model and a kinetic model. The kinetic model represents the oxidative behavior and the compositional changes of the crude oil; it is integrated by the most representative reactions of the process and the corresponding kinetic parameters of each reaction. Frequently, the kinetic model for a dry combustion process has Low Temperature Oxidation reactions (LTO), thermal cracking reactions and the combustion reaction. For the case of wet combustion, additional aquathermolysis reactions take place. This article presents a full review of the kinetic models of the wet in situ combustion process taking into account aquathermolysis reactions. These are hydrogen addition reactions due to the chemical interaction between crude oil and steam. The mechanism begins with desulphurization reactions and subsequent decarboxylation reactions, which are responsible of carbon monoxide production, which reacts with steam producing carbon dioxide and hydrogen; this is the water and gas shift reaction. Finally, during hydrocracking and hydrodesulphurization reactions, hydrogen sulfide is generated and the crude oil is upgraded. An additional upgrading mechanism during the wet in situ combustion process can be explained by the aquathermolysis theory, also hydrogen sulphide and hydrogen production can be estimated by a suitable kinetic model that takes into account the most representative reactions involved during the combustion process.


RSC Advances ◽  
2018 ◽  
Vol 8 (17) ◽  
pp. 9320-9326
Author(s):  
Q. Y. Yang ◽  
H. L. Zhou ◽  
M. T. Xie ◽  
P. P. Ma ◽  
Z. S. Zhu ◽  
...  

The combustion process of GOA, and the specific surface area and pore size distribution of P-RGO are shown in the images.


Author(s):  
Congming Tang ◽  
Juan Huang ◽  
Dong Zhang ◽  
Qingqing Jiang ◽  
Guilin Zhou

Abstract The mesoporous Ni/KIT-6 catalysts with different composition were prepared by altering reduction temperatures. In addition, their physicochemical properties were characterized by X-ray diffraction, in-situ X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller techniques. The results shown that the specific surface area, composition and metallic Ni crystallinity of the Ni/KIT-6 catalyst were significantly affected by reduction temperatures. The catalytic performances of the prepared Ni/KIT-6 catalysts were evaluated via the CO2 reforming of CH4 into syngas and followed the order: RT0 < RT250 < RT300 < RT350 < RT400 < RT450 ≈ RT500. The specific surface area, pore volume, pore diameter, and Ni0 content of the most representative RT450 catalyst among of them were 646.7 m2 g−1, 0.92 cm3 g−1, 6.5 nm, and 30.9%, respectively. The CH4 and CO2 conversions of RT450 catalyst reached to 69.0 and 39.4% under a reaction temperature of 600 °C, respectively. The CO selectivity was greater than 49% and the RT450 catalyst had good stability.


2019 ◽  
Vol 11 (11) ◽  
pp. 1477-1488
Author(s):  
Yonghang Xu ◽  
Fangya Zhou ◽  
Tao Zhang ◽  
Limiao Lin ◽  
Jingshu Wu ◽  
...  

Supported nano-silver composites, famous for large specific surface area, good dispersibility and high catalytic activity, have been widely used in chemistry and chemical engineering, biomedicine and new materials. In this paper, we report recent research progress on supported nano-silver composites as reviewed from preparation techniques (chemical reduction, physical reduction and in-situ formation), types of supporters (organic and inorganic) and anti-microbial/catalytic activity. Firstly, the principles and merits/demerits of three preparation techniques for silver nanoparticles are elaborated. Afterwards, preparation, structures and properties of supported nano-silver composites are summarized through different types of supporters, as well as their applications in catalytic reaction, pollutant control and antimicrobial. Furthermore, it has been demonstrated that silver nanoparticles produced by in-situ formation are more stable and well-distributed, readily meeting the demands for practical applications. Finally, superior supporters for nano-silver composites should be of high specific surface area and good stability, non-expensive, environmentally friendly and low-toxicity.


NANO ◽  
2018 ◽  
Vol 13 (12) ◽  
pp. 1850137 ◽  
Author(s):  
Qingna Xu ◽  
Tongchao Ji ◽  
Qingfeng Tian ◽  
Yuhang Su ◽  
Liyong Niu ◽  
...  

A series of silica surface-capped with hexamethyldisilazane (denoted as H-SiO2) were prepared by liquid-phase in-situ surface-modification method. The as-obtained H-SiO2 was incorporated into acrylic amino (AA) baking paint to obtain AA/H-SiO2 composite extinction paints and/or coatings. N2 adsorption–desorption tests were conducted to determine the specific surface area as well as pore size and pore volume of H-SiO2. Moreover, the effects of H-SiO2 matting agents on the physical properties of AA paint as well as the gloss and transmittance of AA-based composite extinction coatings were investigated. Results show that H-SiO2 matting agents possess a large specific surface area and pore volume than previously reported silica obtained by liquid-phase method. Besides, they have better dispersibility in AA baking paint than the unmodified silica. Particularly, H-SiO2 with a silica particle size of 6.7[Formula: see text][Formula: see text]m and the dosage of 4% (mass fraction) provides an extinction rate of 95.2% and a transmittance of 79.3% for the AA-based composite extinction coating, showing advantages over OK520, a conventional silica matting agent. Along with the increase in the silica particle size, H-SiO2 matting agents cause a certain degree of increase in the viscosity of AA paint as well as a noticeable decrease in the gloss of the AA-based composite extinction coating, but they have insignificant effects on the hardness and adhesion to substrate of the AA-based composite coatings. This means that H-SiO2 matting agents could be well applicable to preparing low-viscosity and low-gloss AA-based matte coatings.


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