Kinetic Pathways of Order-Disorder and Order-Order Transitions in Weakly Segregated Microstructured Systems

The kinetics of hexagonal to disordered and hexagonal to body-centered-cubic phase transitions in weakly segregated, microstructured systems (e.g., diblock copolymers) is studied using a time-dependent Ginzburg-Landau (TDGL) approach. Both computer simulation of the TDGL equation and analysis of a simplified two-mode model reveal nontrivial pathways during the transition

Transient instability upon temperature quench in weakly ordered block copolymers

We report a novel transient instability upon temperature quench in weakly ordered block copolymer microphases possessing a soft direction or directions, such as the lamellar and hexagonal cylinder (HEX) phases. We show that reequilibration of the order parameter is accompanied by transient long wavelength undulation of the layers or cylinders—with an initial wavelength that depends on the depth of the temperature quench—that eventually disappears as the structure reaches its equilibrium at the new temperature. Such undulation leads to a transient transverse broadening of the scattering peaks near the Bragg positions. We argue that this instability might be responsible for the experimentally observed unusual ordering dynamics of the HEX phase of a diblock copolymer after quenching from the disordered state

Numerical study on the impact of wall structure on the thermal performance of double-channel porous solar wall

With the improvement of people’s living standards, they have higher requirements for indoor thermal comfort in the cold season. Solar wall utilizing solar energy for heating can reduce carbon emissions and achieve carbon neutrality. In the aspect of solar wall research, the influence of wall structure on the thermal performance of double-channel porous solar wall is limitedly investigated. In fact, the optimization design of wall structure is important for the thermal performance of solar wall and its applications. Therefore, a simplified three dimensional room model is built to study the influence of the wall structure on the thermal performance of porous solar wall by numerical simulation. With this model, different channel spacing and thickness of porous walls were used to determine the optimal design for a double-channel porous solar wall in terms of enhancing the heat storage. Moreover, the influence of the surface emissivity on the characteristics of heating and temperature field of double-channel porous solar wall are studied based on the optimal structure. The CFD simulation results indicate that the optimal structure parameters should include spacing of 0.08 m for channel 1, the porous wall thickness should be 0.08 m, and the air channel 2 spacing should be 0.06 m. The temperature of air channel 1 and air channel 2, the indoor temperature, and the heat storage of porous wall decrease with the increase of the surface emissivity of the porous wall. In order to improve the heat storage performance of double-channel porous solar wall, the outer surface of the porous wall should use a lower emissivity material. The outer surface emissivity of porous wall has a significant impact on the heat storage of the porous wall and little effect on the thermal storage wall. The temperature of porous wall is always higher than that of outdoor environment temperature

Metal–Organic‐Framework‐Derived Carbons: Applications as Solid‐Base Catalyst and Support for Pd Nanoparticles in Tandem Catalysis

The facile pyrolysis of a bipyridyl metal‐organic framework, MOF‐253, produces N‐doped porous carbons (Cz‐MOF‐253), which exhibit excellent catalytic activity in the Knoevenagel condensation reaction and outperform other nitrogen‐containing MOF‐derived carbons. More importantly, by virtue of their high Lewis basicity and porous nature, Cz‐MOF‐253‐supported Pd nanoparticles (Pd/Cz‐MOF‐253‐800) show excellent performance in a one‐pot sequential Knoevenagel condensation‐hydrogenation reaction

Corrigendum: Inhibition of O-GlcNAc transferase sensitizes prostate cancer cells to docetaxel

The expression of O-GlcNAc transferase (OGT) and its catalytic product, O-GlcNAcylation (O-GlcNAc), are elevated in many types of cancers, including prostate cancer (PC). Inhibition of OGT serves as a potential strategy for PC treatment alone or combinational therapy. PC is the second common cancer type in male worldwide, for which chemotherapy is still the first-line treatment. However, the function of inhibition of OGT on chemotherapeutic response in PC cells is still unknown. In this study, we show that inhibition of OGT by genetic knockdown using shRNA or by chemical inhibition using OGT inhibitors sensitize PC cells to docetaxel, which is the most common chemotherapeutic agent in PC chemotherapy. Furthermore, we identified that microRNA-140 (miR-140) directly binds to OGT mRNA 3′ untranslated region and inhibits OGT expression. Moreover, docetaxel treatment stimulates miR-140 expression, whereas represses OGT expression in PC cells. Overexpression of miR-140 enhanced the drug sensitivity of PC cells to docetaxel, which could be reversed by overexpression of OGT. Overall, this study demonstrates miR-140/OGT axis as therapeutic target in PC treatment and provides a promising adjuvant therapeutic strategy for PC therapy

Role of CD34 in inflammatory bowel disease

Inflammatory bowel disease (IBD) is caused by a variety of pathogenic factors, including chronic recurrent inflammation of the ileum, rectum, and colon. Immune cells and adhesion molecules play an important role in the course of the disease, which is actually an autoimmune disease. During IBD, CD34 is involved in mediating the migration of a variety of immune cells (neutrophils, eosinophils, and mast cells) to the inflammatory site, and its interaction with various adhesion molecules is involved in the occurrence and development of IBD. Although the function of CD34 as a partial cell marker is well known, little is known on its role in IBD. Therefore, this article describes the structure and biological function of CD34, as well as on its potential mechanism in the development of IBD