Steven Wang

Biological liquid crystals, a rich set of soft materials with rod‐like structures widely existing in nature, possess typical lyotropic liquid crystalline phase properties both in vitro (e.g., cellulose, peptides, and protein assemblies) and in vivo (e.g., cellular lipid membrane, packed DNA in bacteria, and aligned fibroblasts). Given the ability to undergo phase transition in response to various stimuli, numerous practices are exercised to spatially arrange biological liquid crystals. Here, a fundamental understanding of interactions between rod‐shaped biological building blocks and their orientational ordering across multiple length scales is addressed. Discussions are made with regard to the dependence of physical properties of nonmotile objects on the first‐order phase transition and the coexistence of multi‐phases in passive liquid crystalline systems. This work also focuses on how the applied physical stimuli drives the reorganization of constituent passive particles for a new steady‐state alignment. A number of recent progresses in the dynamics behaviors of active liquid crystals are presented, and particular attention is given to those self‐propelled animate elements, like the formation of motile topological defects, active turbulence, correlation of orientational ordering, and cellular functions. Finally, future implications and potential applications of the biological liquid crystalline materials are discussed.

Developing flexible sensors with a high strain sensing range could enable widespread downstream applications, by allowing intimate, mechanically conformable integration with soft biological tissues. By characterizing interconnected metal electrode arrays on super-flexible substrates, we have established a surface deformation control strategy of an array of strain transducers. The strain gated switches are capable of measuring various compressive strains (up to 60%) by bringing metal electrodes into self-contact via creasing elastic instability beyond a threshold substrate strain. The designed devices have been developed to explore the geometry design effect on the electrode-elastomer “stiff film on soft elastomer” surface deformation. The enabled transducer array yielded a stepwise strain-electrical resistance switching mechanism which opens up the potential of future interconnected sensor array type of super-compressible devices.

High‐temperature pyrolysis of natural gas is the basis of the standard method for the manufacture of acetylene. The study of methane pyrolysis was designed to find optimum process conditions that would produce high yields of acetylene with minimal carbon formation. High temperatures and short residence times enhanced the selectivity for acetylene, while hydrogen dilution was found to suppress the generation of carbonous products. Carbon formation on reactor surfaces over time may be mainly responsible for the misalignment of predicted and measured product gas compositions, as the mechanisms reported do not consider the surface chemistry. In essence, the pyrolysis system favors the highest possible temperature and shortest possible residence time, suggesting that the selection of reactor materials is the key for pyrolysis process optimization. The operating temperature is likely dictated by the physical properties of the reactor materials rather than the selection of optimal pyrolysis conditions.

This study of methane pyrolysis was designed to look at carbon deposition on the internal reactor and wafer surface during CH₄ pyrolysis. The rate of carbon deposition on the internal reactor surfaces could be reduced with: lower methane/oxygen ratios, shorter residence times, and lower temperatures. The type of carbon formed appeared to have a significant effect on the pyrolysis process. Pyrolytic carbon with a lower order structure produces a higher selectivity for carbon formation compared to carbon with a higher order structure. Form a process perspective, there are two obvious means of addressing this: deposited carbon could be regularly removed; and/or pyrolysis conditions are selected that produce carbon with a higher order structure. From the results, it is very clear that any development of a commercial process for natural gas pyrolysis in ceramic reactor systems would have to carefully address the selection of reactor material. © 2018 American Institute of Chemical Engineers AIChE J, 65: 1035–1046, 2019

While nanometer‐scale capillaries have long been theoretically and experimentally studied, their transport mechanisms have not yet been fully understood. Here, the flow control mechanism is theoretically clarified by molecular dynamics (MD) simulations of graphene‐based nanoscale capillaries. The imbibition rate complies with a modified Lucas–Washburn equation. It changes non‐monotonically with the slit width due to a compromise in competition of density and slip length. Secondly, the relative scale of imbibition and evaporation rate is length dependent. From short slits to long ones, the imbibition–evaporation process alters from evaporation controlled to imbibition controlled. Finally, hydrophilic modification is employed to enhance the rates. External modification can spread the water and accelerate the evaporation. Within the slit, the flow is accelerated by a positive hydrophilic gradient but detained by a negative one. These findings can be applied in a novel nanofluidic diode.