Fused silica contamination layer removal using magnetic field-assisted finishing

Fused silica optics used in lasing systems requires a high laser-induced damage resistance. Processes typically used to polish fused silica lenses induce subsurface and surface damage that collect ceria abrasive, creating a layer of contamination. The contamination can be a precursor to laser damage during use. A preliminary study showed the feasibility of magnetic field-assisted finishing (MAF) for polishing fused silica and suggested possible beneficial effects of the MAF-polished surface on the laser-induced damage threshold (LIDT). This paper proposes a method to examine the fundamental polishing characteristics of MAF for fused silica. Using the proposed method, this paper explores the material removal characteristics of the MAF process and improves the understanding of the MAF polishing mechanism. The 45% improvement of LIDT shows the efficacy of MAF for removing the contamination layer of fused silica surfaces with minimal changes in the surface roughness.     

Genes and Gene Networks Involved in Sodium Fluoride-Elicited Cell Death Accompanying Endoplasmic Reticulum Stress in Oral Epithelial Cells

Here, to understand the molecular mechanisms underlying cell death induced by sodium fluoride (NaF), we analyzed gene expression patterns in rat oral epithelial ROE2 cells exposed to NaF using global-scale microarrays and bioinformatics tools. A relatively high concentration of NaF (2 mM) induced cell death concomitant with decreases in mitochondrial membrane potential, chromatin condensation and caspase-3 activation. Using 980 probe sets, we identified 432 up-regulated and 548 down-regulated genes, that were differentially expressed by >2.5-fold in the cells treated with 2 mM of NaF and categorized them into 4 groups by K-means clustering. Ingenuity^® pathway analysis revealed several gene networks from gene clusters. The gene networks Up-I and Up-II included many up-regulated genes that were mainly associated with the biological function of induction or prevention of cell death, respectively, such as Atf3, Ddit3 and Fos (for Up-I) and Atf4 and Hspa5 (for Up-II). Interestingly, knockdown of Ddit3 and Hspa5 significantly increased and decreased the number of viable cells, respectively. Moreover, several endoplasmic reticulum (ER) stress-related genes including, Ddit3, Atf4 and Hapa5, were observed in these gene networks. These findings will provide further insight into the molecular mechanisms of NaF-induced cell death accompanying ER stress in oral epithelial cells.     

Epoxy nanocomposites with reduced coefficient of thermal expansion

Control of the coefficient of thermal expansion (CTE) of polymeric materials is critical in many applications, particularly the electronics industry where CTE mismatches have caused failures. In theory, adding exfoliated nanoplatelets with high aspect ratios would offer an effective solution for reducing CTE, but reported results have not been compelling due to poor dispersion. In this study, α-zirconium phosphate (ZrP) nanoplatelets, along with organic surfactants, were added to epoxy thermosets. The CTE reduction and glass-transition temperature (T_g) were measured while the molecular weight of the surfactant was varied. High-molecular-weight surfactants are effective for ZrP exfoliation and dispersion, but they can also lead to a reduction in T_g and hinder the drop in CTE. A combination of two low-molecular-weight tetrabutylammonium hydroxide and 2-methoxyethylamine surfactants for exfoliation of ZrP were found to give a CTE reduction of 40% with just 3.5 vol % of ZrP added. This CTE reduction correlates well with theory. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47703.     

Thioamide-Bridged Nucleic Acid (thioAmNA) Containing Thymine or 2-Thiothymine: Duplex-Forming Ability,Base Discrimination,and Enzymatic Stability

Oligonucleotides containing bridged nucleic acids (BNAs) show high duplex-forming ability towards target single-stranded RNA, so many BNAs have been developed for antisense applications. Amide-bridged nucleic acids (AmNAs), which are BNA analogues bearing an amide bond at the bridge, exhibit high duplex-forming ability, enzymatic stability, and antisense activity; thus, the AmNA motif represents a promising BNA scaffold. The high enzymatic stability of the AmNA motif is presumably attributable to the bulky amide structure, because it inhibits the access of nucleases to the phosphodiester linkage. Here, to improve enzymatic stability further, we designed thioAmNAs: thioamide-bridged nucleotides that have a bulkier bridge structure than AmNA. The synthesis of thioAmNAs bearing either thymine (thioAmNA-T) or 2-thiothymine (thioAmNA-S²T) bases was successful, and the obtained monomers were introduced into designed oligonucleotides without noticeable by-product generation. The thioAmNA-T- and thioAmNA-S²T-modified oligonucleotides showed strong binding affinity toward complementary single-stranded RNA, with the thioAmNA-S²T-modified oligonucleotide displaying excellent base-discrimination capability. Moreover, both thioAmNA-T and thioAmNA-S²T endowed oligonucleotides with higher resistance to enzymatic degradation than AmNA-T. These results indicate that thioAmNAs are potentially useful chemical modifications for oligonucleotide-based therapeutics.     

Enhancement of drawdown force in polypropylene containing nucleating agent

The effect of the nucleation efficiency of three commercial nucleating agents, such as 1,3:2,4-bis(3,4-dimethylbenzylidene)sorbitol (DMDBS), sodium 2,2′-methylene-bis-(4,6-di-tert-butylphenyl)phosphate (SMBP), and magnesium silicate (talc), on the melt-stretching performance of isotactic polypropylene (PP) is studied. It is found that the addition of 0.5 wt % of a nucleating agent enhances the crystallization temperature and that effect is pronounced for DMDBS and SMBP. Furthermore, DMDBS is more efficient than the other tested nucleating agents in enhancing the drawdown force, defined as a force required for stretching a molten strand. Nanofibers of DMDBS, which show significant alignment in the flow direction, are responsible for the rapid crystallization of PP in the flow field leading to an increase of drawdown force. The stretched strand shows a highly oriented structure in which the α-form crystals orient to the flow direction. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47295.     

Preparation of Highly Crystallized Strontium Titanate Powders at Room Temperature

Highly crystallized fine powder of strontium titanate (SrTiO₃) was obtained at room temperature simply by leaving a vial containing the powder mixture of Sr(OH)₂·8H₂O and hydrous titania gel (TiO₂·nH₂O) for 10 d. Solvent and additive(s) used in the conventional low‐temperature process were not used. The crystallinity judged from the FWHM of X‐ray diffraction peak was comparable to that obtained by a solid‐state reaction. To cause the reaction at room temperature, the titania gel had to contain a considerable amount of H₂O (n > 0.97). The reaction is considered to be neutralization of titanic acid [H₄TiO₄ or Ti(OH)₄] and strontium hydroxide (base). Using similar process, highly crystallized BaTiO₃ powder was also obtained at 60°C. In comparison with the formation temperature of BaTiO₃, tolerance factor in the perovskite structure was important for the room‐temperature synthesis of SrTiO₃. SrTiO₃ was hardly obtained at room temperature by the addition of saturated strontium hydroxide solution to the hydrous TiO₂ gel (n = 1.29). Therefore, the reaction seems to proceed in the hydrous titania gel. This process is characterized by three important points; “no solvent”, “no additional reagents”, and above all, “no heating”.     

Optical and electrochemical properties of oligo(1,5‐dialkoxynaphthalene‐2,6‐diyl)s with self‐assembled ordered structures in solid state

Oligo(1,5‐dialkoxynaphthalene‐2,6‐diyl)s were synthesized by Ni(cod)₂ (cod = 1,5‐cyclooctadiene)‐promoted condensation reactions of 1,5‐dialkoxy‐2,6‐dibromonaphthalenes. The UV–Vis, photoluminescence (PL), and powder X‐ray diffraction (XRD) measurements suggested that the oligomers have a self‐assembling ordered structure in the solid state. The oligomers underwent electrochemical oxidation (p‐doping), which occurred at lower potentials for films than for acetonitrile solutions containing [Et₄N]BF₄. This effect is caused by the longer π‐conjugation lengths of the oligomers in films, which was attributed to molecular self‐assembly leading to ordered structures in the solid state. The electrochemical reaction of the oligomers was accompanied by electrochromism. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41840.     

Direct ortho‐Hydroxylation of 2‐Phenylpyridines using Palladium(II) Chloride and Hydrogen Peroxide

Direct functionalization of the ubiquitous C H bond is receiving much attention because complex structures can be formed from simple precursors. This paper reports a useful method for the direct hydroxylation of 2‐phenylpyridines using palladium(II) chloride and aqueous hydrogen peroxide. In this method, hydrogen peroxide, which has high atom efficiency, is employed as the oxidant and phenol derivatives are generated via C H activation.

     

The consequences of engineering an extra disulfide bond in the Penicillium camembertii mono-and diglyceride specific lipase

The extracellular lipase from Penicillium camembertii has uniquesubstrate specificity restricted to mono- and diglycerides.The enzyme is a member of a homologous family of lipases fromfilamentous fungi. Four of these proteins, from the fungi Rhizomucormiehei, Humicola lanuginosa, Rhizopus delemar and P.camembertii,have had their structures elucidated by X-ray crystallography.In spite of pronounced sequence similarities the enzymes exhibitsignificant differences. For example, the thermo-stability ofthe P.camembertii lipase is considerably lower than that ofthe H.lanuginosa enzyme. Since only the P.camembertii enzymelacks the characteristic long disulfide bridge, correspondingto Cys22–Cys268 in the H.lanuginosa lipase, we have engineeredthis disulfide into the former enzyme in the hope of obtaininga significantly more stable fold. The properties of the doublemutant (Y22C and G269C) were assessed by a variety of biophysicaltechniques. The extra disulfide link was found to increase themelting temperature of the protein from 51 to 63°C. However,no difference is observed under reducing conditions, indicatingan intrinsic instability of the new disulfide. The optimal temperaturefor catalytic activity decreased by 10°C and the optimumpH was shifted by 0.7 units to more acidic.     

Cardioprotective Effects of a Nonsteroidal Mineralocorticoid Receptor Blocker,Esaxerenone, in Dahl Salt-Sensitive Hypertensive Rats

We investigated the effects of esaxerenone, a novel, nonsteroidal, and selective mineralocorticoid receptor blocker, on cardiac function in Dahl salt-sensitive (DSS) rats. We provided 6-week-old DSS rats a high-salt diet (HSD, 8% NaCl). Following six weeks of HSD feeding (establishment of cardiac hypertrophy), we divided the animals into the following two groups: HSD or HSD + esaxerenone (0.001%, w/w). In survival study, all HSD-fed animals died by 24 weeks of age, whereas the esaxerenone-treated HSD-fed animals showed significantly improved survival. We used the same protocol with a separate set of animals to evaluate the cardiac function by echocardiography after four weeks of treatment. The results showed that HSD-fed animals developed cardiac dysfunction as evidenced by reduced stroke volume, ejection fraction, and cardiac output. Importantly, esaxerenone treatment decreased the worsening of cardiac dysfunction concomitant with a significantly reduced level of systolic blood pressure. In addition, treatment with esaxerenone in HSD-fed DSS rats caused a reduced level of cardiac remodeling as well as fibrosis. Furthermore, inflammation and oxidative stress were significantly reduced. These data indicate that esaxerenone has the potential to mitigate cardiac dysfunction in salt-induced myocardial injury in rats.