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Journal articles on the topic "Decomposition of CoCl2 hydrates"

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S., B. Kanungo. "Kinetics of thermal dehydration and decomposition of hydrated chlorides of some 3d transition metals (Mn-Co series). Part-III. Dehydration and decomposition of CoCl2 hydrates." Journal of Indian Chemical Society Vol. 81, Oct 2004 (2004): 842–49. https://doi.org/10.5281/zenodo.5832472.

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Regional Research Laboratory, Bhubaneswar-751 013, India <em>Manuscript received 4 July 2003, revised 19 March 2004, accepted 13 April 2004</em> An attempt has been made to study the thermal dehydration behavior of CoCI<sub>2</sub> with different states of hydration in static air as well as in !&quot;lowing nitrogen atmosphere by TG/DTA method. It is observed that the salt containing more than two moles of water of hydration dehydrates in three steps and only the dihydrate salt dehydrates in two steps losing one mole of H<sub>2</sub>O in each step. Because of the variable nature of the loss of H<sub>2</sub>O moles in the first step of dehydration, kinetics of this have not been studied. However, the kinetics of the dehydration of the last two moles of H<sub>2</sub>O in air as well as in flowing N<sub>2</sub> atmosphere have been studied by using the isoconversion method. While nucleation and/or growth is found to he the best fit model for dehydration in static air, in N<sub>2</sub> atmosphere progress of reactant/product interphase appears to be the most appropriate model. The anhydrous salt is stable up to about 400&deg; above which CoCI<sub>2</sub> decomposes with the formation of spinel oxide (Co<sub>3</sub>O<sub>4</sub>) The kinetics of decomposition also tends to follow the progress of phase boundary model.
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Mishra, S. K., and S. B. Kanungo. "Thermal dehydration and decomposition of cobalt chloride hydrate (CoCl2·xH2O)." Journal of Thermal Analysis 38, no. 11 (1992): 2437–54. http://dx.doi.org/10.1007/bf01974622.

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Sun, Jian Ye, Yu Guang Ye, Chang Ling Liu, and Jian Zhang. "Experimental Study on Gas Hydrates Dissociation in Sands by Depressurization." Advanced Materials Research 690-693 (May 2013): 3557–60. http://dx.doi.org/10.4028/www.scientific.net/amr.690-693.3557.

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Depressurization method is a more potential way for gas production from gas hydrates. The behavior of gas hydrates dissociation by depressurization method is observed by the use of an experimental apparatus. The hydrates saturation is tracked by TDR during hydrates decomposition. The decomposition process consist three stages: fast dissociation, stable dissociation and the end. Significantly one of major factors that determine gas production rate by depressurization: degree of depressurization is discussed. t1/2 is used to characterize the hydrates decomposition rate. The greater of degree of depressurization is the faster of the hydrates decomposition rate gets.
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Lykova, A. Yu, A. N. Kabirov, R. T. Gordanov, and A. A. Hovhannisyan. "Simulation of the Decomposition Process of Methane Hydrate by Injection of Hot Water." Oil and Gas Technologies 149, no. 6 (2023): 33–37. http://dx.doi.org/10.32935/1815-2600-2023-149-6-33-37.

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To extract natural gas from hydrates by injection of hot water, the decomposition of natural gas hydrates in a porous medium under the influence of a heat flow was experimentally and numerically simulated. It is assumed that the radial diffusion model describes the decomposition of natural gas hydrates in a porous medium due to the injection of hot water, and the decomposition of hydrates is a first-order reaction. By combining the decomposition reaction rate equation with the heat transfer rate equation and the heat balance equation, the relationship between the accumulatedamount of methane (n -n ) and the decomposition time t was obtained. By comparing the results of the experiment0 Hand numerical simulation, it was found that under the experimental conditions, the hydrate decomposition ratecoefficient is consistent with the results of the obtained analytical dependences.
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Wang, Bin, Zi-Ang Nan, Qing Li та ін. "Trapping an Ester Hydrate Intermediate in a π-Stacked Macrocycle with Multiple Hydrogen Bonds". Molecules 28, № 15 (2023): 5705. http://dx.doi.org/10.3390/molecules28155705.

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Ester hydrates, as the intermediates of the esterification between acid and alcohol, are very short-lived and challenging to be trapped. Therefore, the crystal structures of ester hydrates have rarely been characterized. Herein, we present that the mono-deprotonated ester hydrates [CH3OSO2(OH)2]−, serving as the template for the self-assembly of a π-stacked boat-shaped macrocycle (CH3OSO2(OH)2)0.67(CH3OSO3)1.33@{[ClLCoII]6}·Cl4·13CH3OH·9H2O (1) (L = tris(2-benzimidazolylmethyl) amine), can be trapped in the host by multiple NH···O hydrogen bonds. In the solution of CoCl2, L, and H2SO4 in MeOH, HSO4− reacts with MeOH, producing [CH3OSO3]− via the ester hydrate intermediate of [CH3OSO3(OH)2]−. Both the product and the intermediate serve as the template directing the self-assembly of the π-stacked macrocycle, in which the short-lived ester hydrate is firmly trapped and stabilized, as revealed by single-crystal analysis.
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Li, Yaobin, Xin Xin, Tianfu Xu, et al. "Production Behavior of Hydrate-Bearing Sediments with Mixed Fracture- and Pore-Filling Hydrates." Journal of Marine Science and Engineering 11, no. 7 (2023): 1321. http://dx.doi.org/10.3390/jmse11071321.

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Most hydrate-bearing sediments worldwide exhibit mixed pore- and fracture-filling hydrates. Due to the high exploitation value, pore-filling hydrate production is the focus of current hydrate production research, and there is a lack of systematic research on the decomposition of fracture-filling hydrates and their effects on the evolution of temperature and pressure in hydrate-bearing sediments. If only the decomposition characteristics of pore-filling hydrates are studied while the fracture-filling hydrates decomposition and its effects on the hydrate-bearing sediments production process are ignored, the obtained research results would be inconsistent with the actual situation. Therefore, in this study, the effects of fracture-filling hydrates with different dipping angles on the hydrate production process were studied, and the necessity of considering the phenomenon of mixed pore- and fracture-filling hydrates in hydrate-bearing sediments was illustrated. On this basis, the simulation of a typical site (GMGS2-16) with mixed pore- and fracture-filling hydrates was constructed, and the production process was researched and optimized. The results indicated that: (a) fracture-filling hydrates formed in shallow fine-grained sediments and gradually approached the area of pore-filling hydrates, before a stable mixed zone was formed; (b) the occurrence of fracture-filling hydrates was conducive to the hydrate-bearing sediment depressurization production, and the promoting effect of the fracture-filling hydrate with smaller dipping angles was stronger; and (c) depressurization combined with heat injection could effectively compensate for the local low temperature and secondary hydrate caused by the mass decomposition of fracture-filled hydrates.
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Geletii, Yurii V., Alan J. Bailey, Jennifer J. Cowan, Ira A. Weinstock, and Craig L. Hill. "Highly efficient and stable catalyst for peroxynitrite decomposition." Canadian Journal of Chemistry 79, no. 5-6 (2001): 792–94. http://dx.doi.org/10.1139/v01-035.

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The new cobalt substituted-polyoxometalate K7[CoAlW11O39]·15H2O and the simple CoCl2·6H2O salt are efficient catalysts for peroxynitrite decomposition. These compounds also catalyze the oxidation of ascorbic acid and the nitration of phenol by peroxynitrite.Key words: peroxynitrite, polyoxometalates, antioxidant.
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Sumathirathne, Lasanthi, and William B. Euler. "Catalysis of the Thermal Decomposition of Transition Metal Nitrate Hydrates by Poly(vinylidene difluoride)." Polymers 13, no. 18 (2021): 3112. http://dx.doi.org/10.3390/polym13183112.

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Poly(vinylidene difluoride) (PVDF) doped with transition metal nitrate hydrates are cast into thin films giving a high β-phase content. Analysis of the thermal behavior of the doped PVDF shows that the decomposition of the metal (II) nitrate hydrates to metal (II) oxides is catalyzed by the PVDF, as evidenced by reduction in the decomposition temperature by as much as 170 °C compared to the pure metal salts. In contrast, there is little to no apparent catalysis for the decomposition of the metal (III) nitrate hydrates. The FTIR spectra of the gas phase decomposition products show H2O and NO2 are the major components for both PVDF-doped material and the pure metal nitrate hydrates. A mechanism for the role of PVDF is proposed that uses the internal electric field of the ferroelectric phase to orient the nitrate ions and polarize the N-O bonds.
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Bishnoi, P. Raj, and V. Natarajan. "Formation and decomposition of gas hydrates." Fluid Phase Equilibria 117, no. 1-2 (1996): 168–77. http://dx.doi.org/10.1016/0378-3812(95)02950-8.

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Sato, Taichi. "Thermal decomposition of uranium peroxide hydrates." Journal of Applied Chemistry and Biotechnology 26, no. 1 (2007): 207–13. http://dx.doi.org/10.1002/jctb.5020260133.

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Dissertations / Theses on the topic "Decomposition of CoCl2 hydrates"

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Haligva, Cef. "Natural gas recovery from hydrates in a silica sand matrix." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/2791.

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This thesis studies methane hydrate crystal formation and decomposition at 1.0, 4.0 and 7.0°C in a new apparatus. Hydrate was formed in the interstitial space of a variable volume bed of silica sand particles with an average diameter equal to 329μm (150 to 630μm range). The initial pressure inside the reactor was 8.0MPa for all the formation experiments. Three bed sizes were employed in order to observe the effects of the silica sand bed size on the rate of methane consumption (formation) and release (decomposition). The temperature at various locations inside the silica sand bed was measured with thermocouples during formation and decomposition experiments. For the decomposition experiments, two different methods were employed to dissociate the hydrate: thermal stimulation and depressurization. It was found that more than 74.0% of water conversion to hydrates was achieved in all hydrate formation experiments at 4.0°C and 1.0°C starting with a pressure of 8.0MPa. The dissociation of hydrate was found to occur in two stages when thermal stimulation was employed whereas three stages were found during depressurization. In both cases, the first stage was strongly affected by the changing bed size whereas it was not found to depend on the bed size afterwards.
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Narasimhan, Sridhar. "Dynamic behavior characterization of fine powders consisting of a homogeneous emulsion & Synthesis and decomposition of methane gas hydrate : a reaction engineering study /." Morgantown, W. Va. : [West Virginia University Libraries], 2000. http://etd.wvu.edu/templates/showETD.cfm?recnum=1644.

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Nam, Sung Chan, Praveen Linga, Cef Haligva, John A. Ripmeester, and Peter Englezos. "KINETICS OF HYDRATE FORMATION AND DECOMPOSITION OF METHANE IN SILICA SAND." 2008. http://hdl.handle.net/2429/1027.

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Kinetics of hydrate formation and decomposition of methane hydrate formed in silica sand particles were studied in detail at three temperatures of 7.0, 4.0 and 1.0°C, respectively. A new apparatus was setup to study the decomposition behavior of the methane hydrate formed in the bed of silica sand particles. Six thermocouples are placed in different locations to study the temperature profiles during hydrate formation and decomposition experiments. Gas uptake measurement curves for the formation experiments and the gas release measurement curves for the decomposition experiment were determined from the experimental data. Percent conversion of water to hydrates was significantly higher for the experiments conducted at 4.0 and 1.0°C compared to 7.0°C. Recovery of methane occurred in two stages during the decomposition experiments carried out with a thermal stimulation approach at constant pressure. Methane recovery in the range of 95 to 98% was achieved.
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Falenty, Andrzej. "Formation and decomposition processes of CO2 hydrates at conditions relevant to Mars." Doctoral thesis, 2008. http://hdl.handle.net/11858/00-1735-0000-0006-B27B-4.

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Yoon, Yong Seok, Myung Ho Song, Jung Ho Kang, and Peter Englezos. "HEAT AND MASS TRANSFER DURING NONEQUILIBRIUM DECOMPOSITION OF HYDRATE PELLET." 2008. http://hdl.handle.net/2429/1029.

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Mathematical model, which depicts on macroscopic scale the physical phenomena occurring during the decomposition of gas hydrate, was set up and applied to the spherical methane hydrate pellet decomposing into ice. Initially, porous hydrate pellet is at uniform temperature and pressure within hydrate stable region. The pressure starts to decrease at t=0 with a fixed rate down to the final pressure and is kept constant afterwards. The bounding surface of pellet is heated by convection. Governing equations are based on the conservation principles, the phase equilibrium relation, equation of gas state and phase change kinetics. The single-domain approach and volume average formulation are employed to take into account transient change of local pressure, volumetric liberation of latent enthalpy, and convective heat and mass transfer accompanied by the decomposed gas flow through hydrate/ice solid matrix. The algorithm called “enthalpy method” is extended to deal with non-equilibrium phase change and utilized to determine local phase volume fractions. Predicted results suggest that the present numerical implementation is capable of predicting essential features of heat and mass transfer during non-equilibrium decomposition of hydrate pellet.
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Rovetto, Laura J., Steven F. Dec, Carolyn A. Koh, and E. Dendy Sloan. "NMR studies on CH4 + CO2 binary gas hydrates dissociation behavior." 2008. http://hdl.handle.net/2429/1143.

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The dissociation behavior of the CH4+CO2 binary gas hydrate has been investigated using Nuclear Magnetic Resonance (NMR) spectroscopy. This technique allows us to distinguish the hydrate structure present, as well as to quantify phase concentrations. Single-pulse excitation was used in combination with magic-angle spinning (MAS). Time-resolved in situ decomposition experiments were carried out at different compositions in sealed, pressurized samples. The decomposition profiles of the CH4+CO2 binary gas hydrate system obtained at various compositions suggest that the decomposition rate is a strong function of the fractional cage occupancy and temperature. An unexpected CH4 hydrate reformation was observed during our decomposition experiments when the temperature reached the ice melting point. A decrease on the CO2 content in the hydrate phase was found during the decomposition experiment, as the pressure and temperature of the system increases.
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Lu, Hailong, and John A. Ripmeester. "A LABORATORY PROTOCOL FOR THE ANALYSIS OF NATURAL GAS HYDRATES." 2008. http://hdl.handle.net/2429/1090.

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For a number of years the NRC group has been working on a laboratory protocol for the analysis of gas hydrate that has been recovered from various natural sites. The expectation was that a comprehensive set of techniques would become available for the general use of hydrate researchers around the world. With the current set of available techniques a good picture of natural gas hydrates can be obtained, although the emerging complexity of the hydrate-mineral system still demands additional work. Here we present a suite of techniques that will take a researcher from preservation techniques to hydrate occurrence, gas/water/sediment ratios, gas and isotope analysis, P-T behaviour, structure, composition, degree of water conversion to hydrate, hydrate homogeneity and decomposition behaviour. As more detailed studies become possible a variety of more subtle features are revealed, for instance the role of minor gas components in hydrate stability, decomposition behaviour and heterogeneity in structure and composition.
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Falenty, Andrzej [Verfasser]. "Formation and decomposition processes of CO2 hydrates at conditions relevant to Mars / vorgelegt von Andrzej Falenty." 2008. http://d-nb.info/993257631/34.

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Feneyrou, Guillaume. "Elucidation of the formation and decomposition of clathrate hydrates of natural gases through gas solubility measurements." Thesis, 1996. http://hdl.handle.net/1911/17045.

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Through isobaric temperature ramping experiments, the solubility of pure methane, ethane, propane, carbon dioxide gases and a methane-propane gas mixture in pure liquid water has been measured. The experiments are conducted at low temperatures and pressures corresponding to the clathrate hydrate formation and decomposition region. The inhibitory effect of a 10 weight percent methanol aqueous solution and a 0.5 weight percent polyvinylpyrrolidone aqueous solution on the hydrate formation and decomposition conditions has been estimated. A study of the pH-induced change in the hydrate stability has also been performed. The isobaric solubility data obtained show a significant divergence from Henry's law prior to and during hydrate formation. A molecular mechanism of hydrate nucleation is hypothesized, based on an analysis of the gas supersaturation observed and the current knowledge on the structure of liquid water.
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Zhang, Keni, George J. Moridis, Yu-Shu Wu, and Karsten Pruess. "A DOMAIN DECOMPOSITION APPROACH FOR LARGE-SCALE SIMULATIONS OF FLOW PROCESSES IN HYDRATE-BEARING GEOLOGIC MEDIA." 2008. http://hdl.handle.net/2429/1166.

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Simulation of the system behavior of hydrate-bearing geologic media involves solving fully coupled mass- and heat-balance equations. In this study, we develop a domain decomposition approach for large-scale gas hydrate simulations with coarse-granularity parallel computation. This approach partitions a simulation domain into small subdomains. The full model domain, consisting of discrete subdomains, is still simulated simultaneously by using multiple processes/processors. Each processor is dedicated to following tasks of the partitioned subdomain: updating thermophysical properties, assembling mass- and energy-balance equations, solving linear equation systems, and performing various other local computations. The linearized equation systems are solved in parallel with a parallel linear solver, using an efficient interprocess communication scheme. This new domain decomposition approach has been implemented into the TOUGH+HYDRATE code and has demonstrated excellent speedup and good scalability. In this paper, we will demonstrate applications for the new approach in simulating field-scale models for gas production from gas-hydrate deposits.
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Book chapters on the topic "Decomposition of CoCl2 hydrates"

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Yang, Jinhai, and Bahman Tohidi. "23. Geophysical Properties and Dynamic Response of Methane-Hydrate-Bearing Sediments to Hydrate Formation and Decomposition." In Geophysical Characterization of Gas Hydrates. Society of Exploration Geophysicists, 2010. http://dx.doi.org/10.1190/1.9781560802197.ch23.

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Conference papers on the topic "Decomposition of CoCl2 hydrates"

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Yang, J., and Y. Wang. "Experimental Study on Formation and Decomposition Characteristics of Tetrahydrofuran and Methane Hydrate Based on Microfluidic Chip Technology." In Innovative Geotechnologies for Energy Transition. Society for Underwater Technology, 2023. http://dx.doi.org/10.3723/zjsz8344.

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Gas hydrates are considered a promising energy source for the 21st century, and understanding their formation and decomposition processes is crucial. This study utilized micro-fluidic technology to observe the secondary formation and decomposition of hydrates at the pore scale, comparing methane-tetrahydrofuran(THF)-water and methane-water systems. The study found that hydrates tended to form and decompose at the gas-liquid interface, and the second formation rate of hydrates was higher than the first. During depressurization, hydrates located at the solid-liquid interface decomposed first, followed by decomposition towards the interior of the hydrate. The study sheds light on the formation and decomposition characteristics of gas hydrates at the pore scale, providing some insights for the safe and efficient exploitation of gas hydrate.
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Dou, Bin, Guosheng Jiang, Xiang Wu, Mingju Qing, and Hui Gao. "Numerical Solution for Gas Recovery from Hydrates Decomposition by Depressurization." In International Oil and Gas Conference and Exhibition in China. Society of Petroleum Engineers, 2010. http://dx.doi.org/10.2118/131016-ms.

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Uddin, Mafiz, Dennis Allan Coombe, David Hin-Sum Law, and William Daniel Gunter. "Numerical Studies of Gas-Hydrates Formation and Decomposition in a Geological Reservoir." In SPE Gas Technology Symposium. Society of Petroleum Engineers, 2006. http://dx.doi.org/10.2118/100460-ms.

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Fopah Lele, Armand, Fréderic Kuznik, Holger Urs Rammelberg, Thomas Schmidt, and Wolfgang K. L. Ruck. "Modeling Approach of Thermal Decomposition of Salt-Hydrates for Heat Storage Systems." In ASME 2013 Heat Transfer Summer Conference collocated with the ASME 2013 7th International Conference on Energy Sustainability and the ASME 2013 11th International Conference on Fuel Cell Science, Engineering and Technology. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/ht2013-17022.

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Heat storage systems using reversible chemical solid-fluid reactions to store and release thermal energy operates in charging and discharging phases. During last three decades, discussions on thermal decomposition of several salt-hydrates were done (experimentally and numerically) [1,2]. A mathematical model of heat and mass transfer in fixed bed reactor for heat storage is proposed based on a set of partial differential equations (PDEs). Beside the physical phenomena, the chemical reaction is considered via the balances or conservations of mass, extent conversion and energy in the reactor. These PDEs are numerically solved by means of the finite element method using Comsol Multiphysics 4.3a. The objective of this paper is to describe an adaptive modeling approach and establish a correct set of PDEs describing the physical system and appropriate parameters for simulating the thermal decomposition process. In this paper, kinetic behavior as stated by the ICTAC committee [3] to understand transport phenomena and reactions mechanism in gas and solid phases is taking into account using the generalized Prout-Tompkins equation with modifications based on thermal analysis experiments. The model is then applied to two thermochemical materials CaCl2 and MgCl2 with experimental activation energies and a comparison is made with TGA-DSC measurement results.
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Chepyzhenko, Alexey I., and Anna A. Chepyzhenko. "Hydrooptical signs of gas-hydrates decomposition and phase transformation in the Black Sea." In XXV International Symposium, Atmospheric and Ocean Optics, Atmospheric Physics, edited by Gennadii G. Matvienko and Oleg A. Romanovskii. SPIE, 2019. http://dx.doi.org/10.1117/12.2540383.

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Liu, Liguo, Jiafei Zhao, Chuanxiao Cheng, et al. "Experimental Study of Gas Production From Methane Hydrate by Depressurization and Combination Method Under Different Hydrate Saturations." In ASME 2012 31st International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/omae2012-84078.

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In this work, different saturated methane hydrates were formed by controlling the methane gas filling pressure on the three-dimensional experimental systems. The hydrates were dissociated using by depressurization and combination method, respectively. The results indicated that, as the saturation enhancing, the gas production was enlarged, however, the gas production rate became extremely volatile, and the decomposition cycle increased. Furthermore, compared with single depressurization, the combination method has the high gas production rate and efficiency, and the short decomposition cycle. So the combination method is worthy for further study of the gas hydrate exploitation.
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Zhang, Jianbo, Shujie Liu, Yilong Xu, et al. "Experimental Investigation on Hydrate Formation and Decomposition Behaviors in Micro-Pore Channels." In ADIPEC. SPE, 2023. http://dx.doi.org/10.2118/216581-ms.

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Abstract Hydrate formation and decomposition are important factors affecting fluid flow in porous media. To reveal the characteristics of hydrate formation and decomposition in the pores of porous media, pore-scale experiments under different types of flow in micromodel were conducted using a visual microflow experimental apparatus. The experimental results suggested that heterogeneous hydrates were formed in the pore channels, which was mainly affected by the gas-water distribution and temperature &amp; pressure. Compared with the gas-dominated and water-dominated flow, the hydrate formation rate was the maximum under gas-water two-phase flow, and the risk of hydrate blocking the flow channel was the maximum. Moreover, the hydrates were gradually decomposed from the pressure-reduced outlet to the inlet. The methane produced by hydrate decomposition in the pore channel would gather and form a continuous gas flow channel under pressure difference, and the methane dissolved in the water phase would also gradually precipitate out as the pressure decreases to form bubbles, which would form large methane bubbles with adjacent bubbles, thus driving the surrounding water phase flow. This paper lays a foundation for future research on hydrate formation, decomposition and flow in porous media.
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Huang, Haochen, Yiqun Zhang, Xiaoya Wu, Chengyu Hui, Yawen Tan, and Gensheng Li. "Study on the Decomposition of Natural Gas Hydrate Induced by Cavitation Damage." In 57th U.S. Rock Mechanics/Geomechanics Symposium. ARMA, 2023. http://dx.doi.org/10.56952/arma-2023-0366.

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ABSTRACT Natural gas hydrate (NGH) is a clean and abundant emerging energy source that develops in pores of soil deposits in permafrost regions and deep seabed, which are difficult to exploit. Cavitation bubbles contain powerful energy that can effectively break hydrate and may bring higher exploitation efficiency. However, the decomposition of hydrate induced by cavitation damage is still unclear, and the damage characteristics of hydrate need further research. In this paper, a study is conducted based on experiments of laser induced cavitation damage to methane hydrate to evaluate the influence of cavitation on the decomposition of hydrate under different cavitation parameters. The results show that: 1) Cavitation exerts a strong promotion effect on the decomposition of hydrate, and microjet induced by bubble collapse is a key factor accelerating hydrate dissociation; 2) During hydrate decomposition, the generated methane bubbles have an influence on the cavitation damage effect. 3) Larger cavitation energies can lead to stronger hydrate damage, while closer standoff distances do not always lead to more sustained cavitation damage. This paper conducts a preliminary study on the influence of cavitation bubbles on the decomposition of hydrate, which provides a theoretical guidance for further research on the mechanism of cavitation effects on hydrate. INTRODUCTION Natural gas hydrate is an important unconventional energy source, which is considered to be one of the most promising alternative energy sources in the 21st century. The proven reserves of natural gas hydrates are up to 80 billion tons of oil equivalent and are predominantly distributed under seabed (Fitzgerald, G. C. et al., 2012; Li et al., 2020; Sloan, 2003; Song et al., 2021). Currently, there are many problems in the process of gas hydrate exploitation by conventional methods, such as low efficiency of gas production, poor sustainability and risk of reservoir destabilization and collapse. Thus, commercial extraction of gas hydrate cannot be achieved for the moment based on the existing technology and equipment (Luo et al., 2021; Terzariol et al., 2017; Zhang et al., 2022). The cavitation phenomenon is a destructive effect with enormous energy and was first discovered in the shipbuilding industry (Lauterborn, W. &amp; Bolle, H. J., 1975). The high temperature and pressure generated during the collapse of a bubble can cause significant damage to the surrounding wall (Li et al., 2007; Zhou et al., 2018), which has a strong damaging effect on hydrated soft sediments (Zhang et al., 2022). In recognition of the powerful destructive effect of cavitation, Li et al. proposed a new idea of integrated method of drilling radial horizontal wells by cavitation jets with screen tubing completion to extract hydrates based on the characteristics of unconformable gas hydrate resources in the South China Sea (Li et al., 2020). In particular, the hydro-jet erosion effect plays an important role in improving the efficiency of jet breaking underwater and increasing the production of hydrate. Peng et al. optimized a contraction-expansion cavitation nozzle and verified the cavitation erosion ability of cavitation jets based on laboratory experiments (Peng, K., 2018). Zhang et al. conducted a macroscopic study for the cavitation jet's erosion performance on natural gas hydrates and verified that the cavitation jet has a stronger destructive effect than classic water jets (Zhang et al., 2020). Existing studies and results argue for the effectiveness of cavitation jets for efficient gas hydrate fragmentation, while most of the work is conducted based on macroscopic jet experiments, and the results are difficult to characterize the specific effects of cavitation on hydrate. Few experimental studies have been conducted to investigate the effect of the bubble collapse process on the hydrate breakage.
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Yin, Q. S., J. X. Tang, X. Zhang, et al. "Numerical Simulation of Conductor Stability in Deepwater Hydrate-Bearing Formation." In Offshore Technology Conference. OTC, 2025. https://doi.org/10.4043/35712-ms.

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Abstract Deepwater natural gas hydrates have attracted widespread attention as a clean energy resource, but their decomposition process will significantly change the physical and mechanical properties of the formation, posing a threat to the stability of the casing during drilling. Deepwater natural gas hydrates have attracted widespread attention as a clean energy resource, but their decomposition process will significantly change the physical and mechanical properties of the formation, posing a threat to the stability of the casing during drilling. Based on the multi-physics coupling theory, this study comprehensively analyzes the impact of hydrate decomposition on formation stability and the bearing capacity of the conductor. A coupled model integrating gas-water two-phase flow, thermal fields, and mechanical fields is constructed using finite element software to simulate the stability changes of the conductor passing through hydrate-bearing formations. The results indicate that during the early stages of hydrate decomposition, pore pressure in the near-well region rises rapidly, and the stress on the bottom and surrounding formation of the conductor increases significantly, resulting in intensified formation settlement and substantial conductor displacement. As the decomposition proceeds, the pore pressure and stress distribution tend to be stable, and the conductor displacement changes gradually slow down; the decomposition rate, pore pressure, and temperature changes show obvious time correlation, with violent fluctuations in the initial stage and gradually stabilizing over time. This study elucidates the dynamic mechanism of hydrate decomposition's impact on conductor stability and provides theoretical support for optimizing deepwater drilling design and natural gas hydrate development.
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Kim, Tatyana, Valery Dyrdyn, and Vyacheslav Smirnov. "The Study of Natural Gas Hydrates Decomposition Conditions in Order to Determine Their Possible Influence on Gasodynamic Processes." In 9th China-Russia Symposium “Coal in the 21st Century: Mining, Intelligent Equipment and Environment Protection". Atlantis Press, 2018. http://dx.doi.org/10.2991/coal-18.2018.57.

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Reports on the topic "Decomposition of CoCl2 hydrates"

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Bishnoi, P. R., R. B. Saeger, N. E. Kalogerakis, and J. Jeje. The kinetcs of formation & decomposition of hydrates from mixtures of natural gas components. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/293492.

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