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This study aimed to improve the dispersion state of single-walled carbon nanotubes (SWCNTs) in a cyclo-olefin polymer (COP) matrix by introducing extensional flow during the compounding through a twin-screw extruder (TSE). A modified mixing element with multiple holes, called a fixed blister disc (XBD), was developed. To describe the mixing performance of XBD, the flow state was characterized via numerical simulation and acquisition of process data such as pressure drop ([DELTA]P) at XBD and specific mechanical energy (SME), while the operational conditions of TSE were varied. The dispersion state of SWCNTs was evaluated from the viewpoint of the melt viscoelastic property, surface resistivity of extruded samples and mechanical properties of injection molded samples. Furthermore, the dispersion morphology was observed via optical microscopy and scanning electron microscopy. As a result, the mixing performance of XBD was improved by increasing the ratio of throughputs Q to screw speed [N.sub.s] (Q/[N.sub.s]) since [DELTA]P, which is related to extensional stress, was increased. However, the trade-off relationship between [DELTA]P and SME was confirmed versus Q/[N.sub.s]. Although the dispersion state at the submicron level was markedly improved with higher SME inputs, higher [DELTA]P reduced the largest agglomerate size and improved dispersion uniformity. Consequently, the mechanical properties were improved significantly. KEYWORDS dispersive mixing, extensional flow, nanocomposite, single-walled carbon nanotube, twinscrew extrusion, 1 | INTRODUCTION The introduction of extensional flow during compounding in a corotating twin-screw extruder (TSE) to improve the dispersion of nanofillers into a polymer matrix has been studied at [...]

We report Cu, Fe, N‐doped carbon nanotubes, (Cu,Fe)−N−CNT, as electrocatalysts for the oxygen reduction reaction (ORR) in acidic media. (Cu,Fe)−N−CNT was prepared using a silica coating method in pyrolysis to minimize the formation of carbon‐coated metal oxide or carbide nanoparticles, which are known to be inactive for the H2O2 reduction. (Cu,Fe)−N−CNT shows a turnover frequency of 0.66 e− site−1 s−1 at +0.8 V vs. RHE and H2O2 yields of <1 % for the ORR with a utilization factor of active sites of 82 %. Kinetic analysis reveals that 4e− transfer rates for (Cu,Fe)−N−CNT are higher than those of a monometallic counterpart of Fe−N−CNT. In situ X‐ray absorption spectroscopy enables us to determine redox potentials: E°'(FeIII/FeII)=0.65 V vs. RHE and E°'(CuII/CuI)=0.45 V for (Cu,Fe)−N−CNT, and E°'(FeIII/FeII)=0.65 V for Fe−N−CNT. These results indicate that bimetallic doping into carbon nanotubes gives the effect on kinetic parameters but not on thermodynamic ones. In other words, there is no direct electronic interactions between the Cu and Fe active sites for (Cu,Fe)‐N‐CNT because such interactions should modulate their redox potentials. [ABSTRACT FROM AUTHOR]

Recently, biomolecular condensates formed through liquid–liquid phase separation have been widely reported to regulate key intracellular processes involved in cell biology and pathogenesis. BRD4 is a nuclear protein instrumental to the establishment of phase-separated super-enhancers (SEs) to direct the transcription of important genes. We previously observed that protein droplets of BRD4 became hydrophobic as their size increase, implying an ability of SEs to limit the ionization of water molecules by irradiation. Here, we aim to establish if SEs confer radiation resistance in cancer cells. We established an in vitro DNA damage assay that measures the effect of radicals provoked by the Fenton reaction on DNA integrity. This revealed that DNA damage was markedly reduced when BRD4 underwent phase separation with DNA. Accordingly, co-focal imaging analyses revealed that SE foci and DNA damage foci are mutually exclusive in irradiated cells. Lastly, we observed that the radioresistance of cancer cells was significantly reduced when irradiation was combined with ARV-771, a BRD4 de-stabilizer. Our data revealed the existence of innately radioresistant genomic regions driven by phase separation in cancer cells. The disruption of these phase-separated components enfolding genomic DNA may represent a novel strategy to augment the effects of radiotherapy. [ABSTRACT FROM AUTHOR]

We previously developed a simplified finite element (FE) "unit" model to reproduce the mechanical interaction between the smooth muscle layer and elastic lamina (EL) in the aortic media. Nevertheless, whether this simplified FE model can represent the structure of a real medial wall and whether its modeling technique can help in developing a highly sophisticated and structure-based aortic FE model should be determined. Therefore, this study aimed to computationally represent EL buckling in the aortic medial ring at an unloaded state based on the integrated unit models and reproduce transmural variations in EL waviness across the vascular wall. We confirmed that the inner and outer layers of the medial wall were relatively subjected to compressive and tensile residual stresses, respectively, at the unloaded state, implying that the ring model will open spontaneously when it is radially cut. In addition, the residual stresses computed under such a stress-free condition were comparable to the analytically estimated values, partially supporting the validity of our modeling approach. Although further study is still required, the information obtained in this study will greatly improve the understanding of basic aortic physiology and pathophysiology and provide a basis for performing more sophisticated computational modeling of the aortic wall. [ABSTRACT FROM AUTHOR]

Bacteria regulate virulence by using two‐component systems (TCSs) composed of a histidine kinase (HK) and a response regulator (RR). TCSs respond to environmental signals and change gene‐expression levels. The HK QseE and the RR QseF regulate the virulence of Enterobacteriaceae bacteria such as enterohemorrhagic Escherichia coli. The operon encoding QseE/QseF also contains a gene encoding an outer membrane lipoprotein, qseG. The protein product QseG interacts with QseE in the periplasmic space to control the activity of QseE and constitutes a unique QseE/F/G three‐component system. However, the structural bases of their functions are unknown. Here, crystal structures of the periplasmic regions of QseE and QseG were determined with the help of AlphaFold models. The periplasmic region of QseE has a helix‐bundle structure as found in some HKs. The QseG structure is composed of an N‐terminal globular domain and a long C‐terminal helix forming a coiled‐coil‐like structure that contributes to dimerization. Comparison of QseG structures obtained from several crystallization conditions shows that QseG has structural polymorphisms at the C‐terminus of the coiled‐coil structure, indicating that the C‐terminus is flexible. The C‐terminal flexibility is derived from conserved hydrophilic residues that reduce the hydrophobic interaction at the coiled‐coil interface. Electrostatic surface analysis suggests that the C‐terminal coiled‐coil region can interact with QseE. The observed structural fluctuation of the C‐terminus of QseG is probably important for interaction with QseE. [ABSTRACT FROM AUTHOR]

Furanopyrimidine (FPy) and 2,6-diamino-3-deazapurine (DC3Pu) nucleosides with the ability to interact in DDD and AAA H-bonding patterns, respectively, were prepared. The N-1 pKa value of the DC3Pu nucleoside was estimated to be 6.4, which is due to the lack of a nitrogen atom at the 3-position, suggesting that DC3Pu acts as a base interacting in a DDD H-bonding pattern under near physiological conditions. As DC3Pu and FPy are expected to form a thermally stable DDD:AAA type of base pair in an oligodeoxynucleotide (ODN) duplex, they were incorporated into ODNs, and the Tm value of the ODN duplex was determined. However, the ODN duplex containing a DC3Pu:FPy pair has a lower thermal stability than that containing a G:C pair does, although its thermal stability is equal to that of an ODN duplex with an A:T pair even under acidic conditions. [ABSTRACT FROM AUTHOR]

The introduction of nanofillers into conventional microsized fiber-reinforced plastic composites has great potential to improve the fracture toughness and crystalline properties of composites, especially for semicrystalline thermoplastic polymers. Although the selective reinforcement is possible by nanofiller addition, the influence of the addition position of nanofillers on the mechanical properties and crystalline properties still has not been revealed. In this work, the cellulose nanofibers (CNFs) as the secondary filler were added (i) into a polypropylene (PP) matrix by a melt-mixing process and (ii) onto a carbon fiber (CF) surface by a dip-coating process in a CF-reinforced PP composite. By focusing on the transcrystals surrounding CFs, which enable improvement of the interfacial strength, the crystalline properties and mechanical properties were investigated through polarized optical microscopy, differential scanning calorimetry, X-ray diffraction, and 3-point bending tests in this study. We revealed that (i) CNF addition into the PP matrix disturbed the transcrystallization surrounding CFs and that the mechanical properties slightly decreased. Conversely, (ii) CNF addition onto the CF surface promoted transcrystallization surrounding the CF, and the flexural yield strength and modulus significantly improved by a maximum of 30% and 63%, respectively. [ABSTRACT FROM AUTHOR]