@article {43990, title = {Molecular dynamics simulation and experimental study on the growth of methane hydrate in presence of methanol and sodium chloride}, journal = {Energy Procedia}, volume = {105}, year = {2017}, month = {MAY}, pages = {5026-5033}, type = {Article}, abstract = {The plugging of processing and transportation lines by gas hydrate formation is a challenging problem for safe exploitation of oil and gas. The existence of water soluble third component (like methanol and sodium chloride) in the aqueous phase influence the gas hydrate formation thermodynamically also possibly affects the kinetics of hydrate growth. Inorganic salt and organic molecule (alcohols) at high concentration in the aqueous phase have been used as thermodynamic inhibitors to effectively prevent the hydrate formation. This study utilizes molecular dynamics as well as an experimental method to investigate the mechanism of the hydrate formation and the effect of additives. The MD simulation showed that at moderate temperature and pressure, a low concentration (1 wt \%) of methanol and NaCl enhances methane hydrate growth kinetics. Significant numbers of methanol molecules were observed inside the gas hydrate cages whereas Na$^{+}$/Cl$^{-}$ ions leach out during hydrate formation.}, doi = {10.1016/j.egypro.2017.03.1008}, author = {Choudhary, Nilesh and Kushwaha, Omkar Singh and Bhattacharjee, Gaurav and Chakrabarty, Suman and Kumar, Rajnish} } @article {46444, title = {Methane recovery from marine gas hydrates: a bench scale study in presence of low dosage benign additives}, journal = {Applied Energy}, volume = {253}, year = {2019}, month = {NOV }, pages = {113566}, type = {Article; Proceedings Paper}, abstract = {

De-pressurization is one approach which has been found to be economically feasible for methane recovery from marine hydrates. Hydrate dissociation being an endothermic process suggests that de-pressurization alone would not be sufficient and some additional stimulation would be required for sustained production from one such reservoir. Thermal stimulation may overcome the challenge posed by the endothermic dissociation process; however, economically it may not be ideal. A possible way out is to use thermal stimulation, but at relatively low temperatures as compared to conventional practice. This would be economical and can be accomplished in the presence of small doses of additives mixed in with the water stream used for thermal stimulation. In the present study, a number of benign additives were identified which when used in low concentrations enhance the kinetics of methane hydrate dissociation compared to pure water. Additives were first shortlisted from a wide potential pool using quantum mechanical calculations. These additives were later tested for their efficacy in stirred tank reactor to quickly identify the best additives for the job and few selected additives were then studied in a larger bench scale setup (fixed bed configuration) where they were injected in the form of an additive-water stream to dissociate already formed hydrates. Factors such as toxicity of the additive, fluidity of additive-water stream, foam formation on mixing of additive with water, etc. were also taken into account. An energy and efficiency analysis revealed that reported additives enhance the energy ratio and thermal efficiency of the process as compared to pure water stimulation.

}, keywords = {Bench scale, kinetics, Marine hydrate, methane hydrate, Methane recovery, Natural gas hydrate, Process}, issn = {0306-2619}, doi = {10.1016/j.apenergy.2019.113566}, author = {Bhattacharjee, Gaurav and Choudhary, Nilesh and Barmecha, Vivek and Kushwaha, Omkar S. and Pande, Nawal K. and Chugh, Parivesh and Roy, Sudip and Kumar, Rajnish} } @article {46627, title = {Macro and molecular level insights on gas hydrate growth in the presence of hofmeister salts}, journal = {Industrial \& Engineering Chemistry Research}, volume = {59}, year = {2020}, month = {NOV }, pages = {20591-20600}, type = {Article}, abstract = {

The effect of few monovalent salts (NaCl, NH4Cl, and GdmCl) as additives, according to the Hofrneister series on the growth of methane gas hydrates, has been studied using experiments as well as molecular dynamics (MD) simulation. Further, the Hofmeister effects on hydrate crystallization have been correlated with the methanol as an additive, which is a known thermodynamic hydrate inhibitor for hydrate growth. One of the previous studies (discussed later in this article) available in the literature concludes that methane hydrate formation from ice might show enhanced kinetics in the presence of salts; this behavior is contrary to the general usage of such salts as hydrate inhibitors. This conclusion may not necessarily be true for experiments done with liquid water, and therefore, this work explores the behavior of these salts in a lab-scale setup. In addition, current work reports detailed MD simulation studies to gain insight into the mechanism of hydrate formation in the presence of Hofmeister series salts at two different concentrations of 1 and 10 wt \% in water and compare the results with hydrate formation in the methanol-water system. Our study suggests that the presence of these additives at low concentrations (1 wt \%) does enhance the hydrate growth kinetics. However, at higher concentrations (10 wt \%), inhibition by these additives persisted, and prolonged nucleation, as well as retarded growth, was observed.

}, issn = {0888-5885}, doi = {10.1021/acs.iecr.0c04389}, author = {Choudhary, Nilesh and Kushwaha, Omkar Singh and Bhattacharjee, Gaurav and Chakrabarty, Suman and Kumar, Rajnish} } @article {46618, title = {Morphology and dynamics of self-assembled structures in mixed surfactant systems (SDS plus CAPB) in the context of methane hydrate growth}, journal = {Journal of Molecular Liquids}, volume = {319}, year = {2020}, month = {DEC }, pages = {114296}, type = {Article}, abstract = {

Presence of small dosages of surfactants in the aqueous phase has been reported to enhance the rate of gas hydrate (clathrate) formation. In this work, using extensive atomistic molecular dynamics (MD) simulations, we have investigated how SDS (surfactant) aggregates in the presence/absence of CAPB (co-surfactant) at ambient conditions (temperature 298 K and pressure 1 bar) and at hydrate forming conditions (temperature 275 K and pressure 50 bar) resulting in altered growth kinetics of methane hydrate. We observe that SDS forms aggregates of different sizes and shapes depending on the thermodynamic condition starting from random distributions of the surfactants. In the presence of the CAPB co-surfactant, tightly packed mixed aggregates are formed. Using various structural order parameters, we demonstrate that shape of the aggregates deviates from spherical as well as cylindrical symmetry. During the aggregation process in presence of methane, the methane molecules get absorbed into the aggregates, enhance the aggregation kinetics and provide structural flexibility to the aggregates. This result is partly in agreement with previous experimental observations that SDS (with or without a co-surfactant) may form micelle-like structures under hydrate forming conditions and that methane gets absorbed by these aggregates leading to enhanced solubility of methane in the aqueous phase. Further, we have investigated the dynamics of shape fluctuations of the aggregates and observed that several distinct relaxation timescales exist in these heterogenous systems. (C) 2020 Elsevier B.V. All rights reserved.

}, issn = {0167-7322}, doi = {10.1016/j.molliq.2020.114296}, author = {Hande, Vrushali and Choudhary, Nilesh and Chakrabarty, Suman and Kumar, Rajnish} }