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A trace level of N

Carbon nanotube (CNT) fibers were strengthened by wet stretching with 1-Methyl-2-pyrrolidinone (NMP) or chlorosulfonic acid (CSA) as the wetting liquid, and the change of hierarchical structure of CNT fibers was observed at a nanometer level. Two kinds of voids were present in a CNT fiber: inter-bundle void and intra-bundle void. Wet stretching was a very effective method to aggregate CNT bundles and to remove the voids in a CNT fiber. CNT bundle thickness and the number of CNTs in a bundle increased and the bundle-to-bundle distance decreased as a result of the aggregation of the bundles. After infiltration of liquids, CNTs with elliptical and non-circular cross-sections appeared and the distance between CNTs in a bundle i.e., intra-bundle voids, decreased. It was confirmed that the stretch alone did not affect the intra-bundle void. CSA infiltrated CNT bundles better than NMP did, so CSA yielded better densification than NMP. Load at failure, specific strength (SS) and tensile strength of CNT fibers increased with wet-stretching. SS of the CNT fiber increased from 0.95 to 2.19 N/tex (CSA13%). Understanding structure and morphology of CNT fibers in nanoscale will be helpful to build better strengthening strategies.

We present pure CH4 and CH4/C3H8 mixed hydrate phase equilibria formed from a mixture of NaCl (10 wt %) and monoethylene glycol (MEG, 10 and 30 wt %) solutions. As expected for thermodynamic inhibitors, the mixture of salt and glycol causes the hydrate phase equilibrium boundary to shift to lower temperatures and higher pressures, and on increasing the MEG concentration, the hydrate stable region shifted more. The measured experimental data are also compared with a thermodynamic model recently developed, named the Hu–Lee–Sum correlation, showing that the data match well with the predictions. The experimental data were used to calculate the enthalpy of hydrate dissociation. The enthalpies of CH4 hydrates in the mixture of 10 wt % NaCl brine and 10 or 30 wt % MEG were found to be ∼58.7 and 54.63 kJ/mol, respectively, corresponding to structure I hydrates, whereas for the CH4/C3H8 (91.98:8.02 mol %) mixed gas system, the enthalpies of dissociation were found to be ∼101.10 kJ/mol (10 wt % NaCl + 10 wt % MEG) ...

Gas hydrates are considered a nuisance in the flow assurance of oil and gas production since they can block the flowlines, consequently leading to significant losses in production. Hydrate avoidance has been the traditional approach, but recently, hydrate management is gaining acceptance because the practice of hydrate avoidance has become more and more challenging. For better management of hydrate formation, we investigated the risk of hydrate formation based on the subcooling range in which hydrates form by associating low, medium, and high probability of formation for a gas+oil+water system. The results are based on batch experiments which were performed in an autoclave cell using a mixture gas (CH4: C3H8=91.9 : 8.1 mol%), total liquid volume (200 ml), mineral oil, watercut (30%), and mixing speed (300 rpm). From the measurements of survival curves showing the minimum subcooling required before hydrate can form and hydrate conversion rates for the initial 20 minutes, we developed a risk map for hydrate formation.

Both CO 2 and SF 6 are potent greenhouse gases responsible for global warming and associated environmental issues. Hydrate-based separation and capture of these gases from gas mixtures produced by industry have been proposed, and improving the commercial viability of these processes is crucial. Here, we report the phase equilibria and characterization of binary hydrates containing CO 2 and SF 6 . The introduction of SF 6 considerably lowered the formation pressure of CO 2 hydrates by readily occupying the structure II hydrate cages and hence altering the crystal structure. Hydrate phases with different crystalline structures were found to coexist as a result of competition in occupying different hydrate cages. The structural instability caused by the coexistence of structure I and II hydrates was observed, and this feature would be important to understand the mixed gas hydrate systems. The ability of SF 6 to significantly reduce the formation pressure of hydrates suggests that it has a potential to serve as a hydrate promoter. This feature of SF 6 combined with its non-toxic and non-flammable properties would be efficient for practical applications such as CO 2 sequestration using hydrates.

Gas hydrates are crystalline ice-like solid materials enclosing gas molecules inside. The possibility of the presence of gas hydrates with amino acids in the universe is of interest when revealing the potential existence of life as they are evidence of a source of water and organic precursors, respectively. However, little is known about how they can naturally coexist, and their crystallization behavior would become far more complex as both crystallize with formation of hydrogen bonds. Here, we report abnormal incorporation of amino acids into the gas hydrate crystal lattice that is contrary to the generally accepted crystallization mode, and this resulted in lattice distortion and expansion. The present findings imply the potential for their natural coexistence by sharing the crystal lattice, and will be helpful for understanding the role of additives in the gas hydrate crystallization.

Natural gas hydrates are solid hydrogen-bonded water crystals containing small molecular gases. The amount of natural gas stored as hydrates in permafrost and ocean sediments is twice that of all other fossil fuels combined. However, hydrate blockages also hinder oil/gas pipeline transportation, and, despite their huge potential as energy sources, our insufficient understanding of hydrates has limited their extraction. Here, we report how the presence of amino acids in water induces changes in its structure and thus interrupts the formation of methane and natural gas hydrates. The perturbation of the structure of water by amino acids and the resulting selective inhibition of hydrate cage formation were observed directly. A strong correlation was found between the inhibition efficiencies of amino acids and their physicochemical properties, which demonstrates the importance of their direct interactions with water and the resulting dissolution environment. The inhibition of methane and natural gas hydrate formation by amino acids has the potential to be highly beneficial in practical applications such as hydrate exploitation, oil/gas transportation, and flow assurance. Further, the interactions between amino acids and water are essential to the equilibria and dynamics of many physical, chemical, biological, and environmental processes.

As the foundation of energy industry moves towards gas, flow assurance technology preventing pipelines from hydrate blockages becomes increasingly significant. However, the principle of hydrate inhibition is still poorly understood. Here, we examined natural hydrophobic amino acids as novel kinetic hydrate inhibitors (KHIs) and investigated hydrate inhibition phenomena by using them as a model system. Amino acids with lower hydrophobicity were found to be better KHIs to delay nucleation and retard growth, working by disrupting the water hydrogen bond network, while those with higher hydrophobicity strengthened the local water structure. It was found that perturbation of the water structure around KHIs plays a critical role in hydrate inhibition. This suggestion of a new class of KHIs will aid development of KHIs with enhanced biodegradability and the present findings will accelerate the improved control of hydrate formation for natural gas exploitation and the utilization of hydrates as next-generation gas capture media.