Scheme 1. Design Concept for Realizing a Photocatalyst for the Direct Synthesis of Imines from Alkenes and Amines Using Iminium Activation Communication pubs.acs.org/IC
To enhance hydrate formation kinetics, we presented a novel spiral‐agitated reactor, where hydrates were synthetized in pure water systems, and fast hydrate kinetics was observed under extremely mild conditions. Hydrates can nucleate within 4 min under 3.5 MPa and 275.15 K at a rotating speed of 60 rpm, and large water‐to‐hydrate conversion (>85%) was obtained at a moderate condition of 4.85 MPa, 275.15 K, and 30 rpm with an average methane uptake of 139.78 V/V, demonstrating that pure water systems are feasible for hydrate‐based solidified natural gas (SNG) technology. Numerical simulations of flow fields inner the reactor were carried out, and four mechanisms behind the excellent promotion were proposed, dual‐agitation, two‐way convection, interfacial impact and micro bubbles, which significantly improve mass transfer, giving rise to fast hydrate nucleation and growth kinetics. These findings suggest extraordinary performance of spiral agitation, and this may pave way on the industrial application of hydrate‐based SNG technology.
Due to the hybrid effect of physical adsorption and hydration, methane storage capacity in pre-adsorbed water-activated carbon (PW-AC) under hydrate favorable conditions is impressive, and fast nucleation and growth kinetics are also anticipated. Those fantastic natures suggest the PW-AC-based hydrates to be a promising alternative for methane storage and transportation. However, hydrate formation refers to multiscale processes, the nucleation kinetics at molecule scale give rise to macrohydrate formation, and the presence of activated carbon (AC) causes this to be more complicated. Although adequate nucleation sites induced by abundant specific surface area and pore texture were reported to correspond to fast formation kinetics at macroperspective, the micronature behind that is still ambiguous. Here, we evaluated how methane would be adsorbed on PW-AC under hydrate favorable conditions to improve the understanding of hydrate fast nucleation and growth kinetics. Microbulges on AC surface were confirmed to provide numerous nucleation sites, suggesting the contribution of abundant specific surface area of AC to fast hydrate nucleation and growth kinetics. In addition, two-way convection of water and methane molecules in micropores induced by methane physical adsorption further increases gas–liquid contact at molecular scale, which may constitute the nature of confinement effect of nanopore space.
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