scholarly journals INFLUENCE OF THE TIME STORAGE OF ICE POWDER ON KINETICS OF FORMATION AND GROWTH OF FREON-12 GAS HYDRATE

2018 ◽  
pp. 77-83
Author(s):  
M. Sh. Madygulov ◽  
A. G. Zavodovsky ◽  
V. P. Shchipanov

The article explores the influence a storage time on the samples of pure ice powder and mod-ified ice powder with polyvinylpyrrolidone on process formation and growth of the gas hydrate by used P-V-T measurements. It has been established that increased storage time of the pure ice powder leads to a decrease the rate of growth of gas hydrate. Fresh modified ice powder has induction time of hydrate formation which increased in a polyvinylpyrrolidone concentration. At long-term storage of modified ice powder with a polyvinylpyrrolidone concentration less 0,3 % the induction time don’t registrate and growth rate of gas hydrate likes zero. In the samples of modified ice powder with a polyvinylpyrrolidone concentration more 0,75 % after 10 days a storage were retained growth rate of gas hydrate likes fresh modified ice powder. There is no induction effect.

2012 ◽  
Vol 616-618 ◽  
pp. 902-906 ◽  
Author(s):  
Chun Long Wang ◽  
Xue Min Zhang ◽  
Jin Ping Li ◽  
Lin Jun Wang ◽  
Liang Jiao

Predicting the driving force accurately is the key process to hydrate nucleating and growing of hydration reaction. The nucleating and growing process of hydrate is relevant to temperature, pressure and component of reactant, and the property of reaction tank and intermiscibility of reactant have notable effect on the formation process of hydrate with its nucleating position, the induction time, growth rate and hydration rate. However, the present driving force model of hydrate cannot predict nucleating area, induction time, growth rate and the reaction limit, and also can't explain the influence of some factors such as cooling rate, temperature disturbance and inlet way on the hydration reaction, it is uncertain of the process to gas hydrate nucleation. We introduced some driving force models, analyzed their merits and demerits, and looked into the distance of research direction to driving force in the future.


2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Qiang Zhang ◽  
Qiang Wu ◽  
Hui Zhang

In order to explore the method of accelerating hydration separation process to recover methane from mine gas, propane hydrate phase equilibrium was used to measure the equilibrium points of three kinds of mine gas in NaCl solution. Driving force was set as 1 MPa on this basis and high-pressure experimental apparatus of mine gas hydrate was used to carry out the nucleation kinetics experiments of mine gas hydrate for three gas samples in different concentrations of sodium chloride (NaCl) and sodium dodecyl sulfate (SDS) compound systems, which was to study the effect of propane and NaCl-SDS solution on nucleation process of mine gas hydrate. The results showed that induction time of multicomponent mine gas hydrate formation was shortened with the decrease of methane concentration and increase of propane concentration. The induction time of mine gas hydrate formation was shortened with the reduction of NaCl concentration and the increase of SDS concentration. It was found that methane and propane in multicomponent mine gas nucleated collaboratively, which simplified its nucleation process compared with the single component. NaCl has two kinds of functions.


2021 ◽  
Author(s):  
Khalik Mohamad Sabil ◽  
Omar Nashed ◽  
Bhajan Lal ◽  
Khor Siak Foo

Abstract Nanofluids are known of having the capability to increase heat and mass transfer and their suitability to be used as kinetic gas hydrate promoters have been recently investigated. They have favorable properties such as high thermal conductivity, large surface area, recyclable, ecofriendly, and relatively cheap that are favorable for kinetic gas hydrate promoters. However, the nanomaterials face challenges related to their stability in the base fluid. Therefore, it is crucial to investigate the impact of surfactant free nanofluid on hydrate formation and dissociation kinetics. In this work, COOH-MWCNT suspended in water is used to study the effect of surfactant free nanofluid on CO2 hydrates formation kinetic and stability. Kinetic study on CO2 hydrates formation as well as self-preservation are conducted in a stirred tank reactor. The kinetic experiments are carried out at 2.7 MPa and 274.15 K. The induction time, initial gas consumption rate, half-completion time t50, semi completion time t95 are measured to evaluate the effect of COOH-MWCNT. Furthermore, the dissociation rate was calculated to assess the impact of COOH-MWCNT on self-preservation at 271.15 K and atmospheric pressure. The results are compared with that of sodium dodecyl sulphate (SDS). The study of CO2 hydrates formation kinetic shows that the induction time is not affected by COOH-MWCNT. The impact of nanofluid is more pronounced during the hydrate growth. The initial formation rate is the highest at 0.01 wt% of COOH-MWCNT whereas 0.01 and 0.03 wt% shows the same and shortest t50. However, t95 found to be decreased with increasing the concentration. The effect of COOH-MWCNT is attributed to the strong functional group. Self-preservation results shows CO2 hydrates are less stable in the presence of COOH-MWCNT. The result of this work may provide significant finding that can be used to developed kinetic gas hydrate promoter based on nanofluid that work better than SDS to eliminate gas hydrate formation in oil and gas pipeline.


2021 ◽  
Author(s):  
Aleksander Voloshin ◽  
Nikolay Nifantiev ◽  
Mikhail Egorov ◽  
Robert Alimbekov ◽  
Vladimir Dokichev

Abstract The effect of biodegradable polysaccharides – sodium (NaCMC) and ethanolammonium salts of carboxymethylcellulose, dextran and arabinogalactan on the process of gas hydrate formation was studied in order to search for new "green" inhibitors of low-concentration gas hydrate formation. The ability of polysaccharides to inhibit gas hydrate formation was studied in a quasi-equilibrium thermodynamic experiment. A mixture of hydrocarbon gases with a composition typical of the composition of petroleum gas and containing 78% methane was used as a gas-hydrate-forming model medium. It was found that in concentrations of 0.005, 0.0065 and 0.008%, dextran, NaCMC and arabinogalactan as thermodynamic inhibitors exceed methanol by 170-270 times in inhibitory properties. Dextran is superior to NaCMC and arabinogalactan in terms of inhibition efficiency, reduction of gas hydrate formation rate and induction time. Since with an increase in the concentration of polysaccharides, the pressure drop of gas hydrate formation increases and the rate of formation of gas hydrates decreases according to the mechanism of action, the studied polysaccharides can be attributed to both thermodynamic and kinetic inhibitors. It is established that the molecular weight of water-soluble polysaccharides has a significant effect on their inhibitory properties. A polysaccharide with a molecular weight of 250,000 demonstrated the highest inhibitory activity among the studied samples of NaCMC, which is 400 times more effective than methanol. NaCMC with a mass of 700 thousand did not have any effect on the formation of hydrates. Among the ethanolammonium salts, the monoethanolammonium salt CMC showed the greatest effectiveness in inhibiting the formation of tetrahydrofuran hydrates. An increase in its concentration from 0.02 to 0.1% leads to an increase in the induction time required for the nucleation and subsequent growth of crystals by 10 times. When switching from mono - to di - and triethanolammonium salts of carboxymethylcellulose, the inhibition efficiency decreases. It is shown that sodium and ethanolammonium salts of carboxymethylcellulose, arabinogalactan and dextran are promising for creating new "green" highly effective inhibitors of gas hydrate formation on their basis. The results of laboratory and field tests of the preparative form of the "green" gas hydrate formation inhibitor at the fields of Western Siberia are presented. It was found that at dosages of 500 g/m3 or less, there is no formation of hydrate plugs in the annulus of wells.


SPE Journal ◽  
2017 ◽  
Vol 23 (03) ◽  
pp. 937-951 ◽  
Author(s):  
Ahmad A. Majid ◽  
Wonhee Lee ◽  
Vishal Srivastava ◽  
Litao Chen ◽  
Pramod Warrier ◽  
...  

Summary As the oil-and-gas industries strive for better gas-hydrate-management methods, there is the need for improved understanding of hydrate formation and plugging tendencies in multiphase flow. In this work, an industrial-scale high-pressure flow loop was used to investigate gas-hydrate formation and hydrate-slurry properties at different flow conditions: fully dispersed and partially dispersed systems. It has been shown that hydrate formation in a partially dispersed system can be more problematic compared with that in a fully dispersed system. For hydrate formation in a partially dispersed system, it was observed that there was a significant increase in pressure drop with increasing hydrate-volume fraction. This is in contrast to a fully dispersed system in which there is gradual increase in the pressure drop of the system. Further, for a partially dispersed system, studies have suggested that there may be hydrate-film growth at the pipe wall. This film growth reduces the pipeline diameter, creating a hydrate bed that then leads to flowline plugging. Because there are different hydrate-formation and -plugging mechanisms for fully and partially dispersed systems, it is necessary to investigate and compare systematically the mechanism for both systems. In this work, all experiments were specifically designed to mimic the flow systems that can be found in actual oil-and-gas flowlines (full and partial dispersion) and to understand the transportability of hydrate particles in both systems. Two variables were investigated in this work: amount of water [water cut (WC)] and pump speed (fluid-mixture velocity). Three different WCs were investigated: 30, 50, and 90 vol%. Similarly, three different pump speeds were investigated: 0.9, 1.9, and 3.0 m/s. The results from these measurements were analyzed in terms of relative pressure drop (ΔPrel) and hydrate-volume fraction (ϕhyd). It was observed that, for all WCs investigated in this work, the ΔPrel decreases with increasing pump speed, at a similar hydrate-volume fraction. Analysis conducted with the partially-visual-microscope (PVM) data collected showed that, at constant WC, the hydrate-particle size at the end of the tests decreases as the mixture velocity increases. This indicates that the hydrate-agglomeration phenomenon is more severe at low mixture velocity. Calculations of the average hydrate-growth rate for all tests conducted show that the growth rate is much lower at a mixture velocity of 3.0 m/s. This is attributed to the heat generated by the pump. At a high mixing speed of 3.0 m/s, the pump generated a significant amount of heat that then increased the temperature of the fluid. Consequently, the hydrate-growth rate decreases. It should be stated that this warming effect should not occur in the field. Flow-loop plugging occurred for tests with 50-vol% WC and pump speeds lower than 1.9 m/s, and for tests with 90-vol% WC at a pump speed of 0.9 m/s. In addition, in all 90-vol%-WC tests, emulsion breaking, where the two phases (oil and water) separated, was observed after hydrate formation. From the results and observations obtained from this investigation, proposed mechanisms are given for hydrate plugging at the different flow conditions. These new findings are important to provide qualitative and quantitative understanding of the key phenomena leading to hydrate plugging in oil/gas flowlines.


Author(s):  
Dongxu Zhang ◽  
Qiyu Huang ◽  
Wei Wang ◽  
Rongbin Li ◽  
Huiyuan Li ◽  
...  

Asphaltene was fractionated into four subfractions with different polarities, and used to conduct the hydrate formation and dissociation experiments. It was observed that the more polar fraction could result in a higher tendency of self-aggregation and fewer asphaltenes adsorbing at the water-oil interface mainly due to the larger C/H ratio, higher aromaticity, and shorter length of the alkyl side chain. The nucleation rate decreased with the presence of asphaltenes, and the induction time increased with a reduction in asphaltene polarity in water-in-oil emulsions. The results showed that the formed amount of hydrates were reduced by the addition of asphaltenes. For the asphaltene containing emulsions, less hydrate was formed with the presence of a more polar asphaltene fraction. The presence of asphaltenes was also found to affect the growth rate of hydrate, which varies with the polarity. Meanwhile, all four asphaltene fractions were found to promote the dissociation of hydrate.


2021 ◽  
Vol 2076 (1) ◽  
pp. 012086
Author(s):  
Shuai Wu ◽  
Mingzhong Li ◽  
Chongrui Zhang ◽  
Chengwei Liu ◽  
Shuai Zhao ◽  
...  

Abstract In order to explore the kinetic mechanism of hydrate formation in a system containing micron-sized SiO2 particles, this paper uses a high-pressure reactor device with stirring function to record changes in pressure, temperature and torque during the growth of hydrates through a data acquisition system, based on the conservation of mass in the system The principle and gas equation of state calculate the kinetic parameters of hydrate formation such as gas consumption in the reactor, hydrate formation rate and induction time, and analyze the influence of particle size and particle concentration on the kinetic characteristics of hydrate formation based on the experimental results. The experimental results show that the particle content has no obvious effect on the average growth rate of hydrate in the range of 1%-7%, but increasing the particle content can effectively reduce the hydration induction time; when the particle size is in the range of 2.5-85 μm, the larger the particle size, the shorter the hydrate induction time and the greater the hydrate growth rate.


2015 ◽  
Vol 93 (9) ◽  
pp. 992-997
Author(s):  
Xuemei Lang ◽  
Pingping Lv ◽  
Shurui Xu ◽  
Baoyao Li ◽  
Shuanshi Fan ◽  
...  

Within the oil and gas industry, low-dosage hydrate inhibitors (LDHIs) are a proven technology to control hydrates. Besides hydrate inhibitors, wax inhibitors (WIs) are frequently injected to prevent wax buildup in the crude oil pipeline. However, little attention has been focused on the effect of wax inhibitors on the performance of LDHIs. In this study, performance tests of 3 LDHIs in the presence of wax inhibitors were carried out for a 67% CH4/33% CO2 gas hydrate formation. Using the isothermal cooling method at pressures of 9 MPa and temperatures of 4 °C (subcooling is 9 °C), the results showed that the induction time of CH4-CO2 gas hydrate formation with LDHI/WI was shorter than the system with only LDHI. During the growth period, when the concentration of the WIs was 1 mass%, the growth time of the system with LDHI/WI was prolonged. Taking the induction time and the growth time into consideration, it was found that WIs had a more negative impact on the kinetic hydrate inhibitor performance at low dosage. The effect of WIs at high concentration could be negligible.


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