Mixing of nickel and silicon by incoherent-light-pulse annealing

Mixed layers of Ni and Si were formed by pulsed incoherent-light annealing of Ni thin films evaporated on Si substrates. Incoherent light pulse of 36 μs produced in an arc-discharge plasma system was used as the energy source for annealings. A thin layer (300 Å) of amorphous silicon (a-Si) deposited on 800–1000 Å thick Ni films was found to increase light absorption significantly. The light energy needed to form uniform mixing was measured to be about 23 J/cm². Rutherford backscattering and Auger electron spectroscopy techniques were used for qualitative analysis of a-Si/Ni/Si samples. Optimum operating conditions of the light source was determined.     

How Microbes Affect Depression: Underlying Mechanisms via the Gut–Brain Axis and the Modulating Role of Probiotics

Accumulating evidence suggests that the gut microbiome influences the brain functions and psychological state of its host via the gut–brain axis, and gut dysbiosis has been linked to several mental illnesses, including major depressive disorder (MDD). Animal experiments have shown that a depletion of the gut microbiota leads to behavioral changes, and is associated with pathological changes, including abnormal stress response and impaired adult neurogenesis. Short-chain fatty acids such as butyrate are known to contribute to the up-regulation of brain-derived neurotrophic factor (BDNF), and gut dysbiosis causes decreased levels of BDNF, which could affect neuronal development and synaptic plasticity. Increased gut permeability causes an influx of gut microbial components such as lipopolysaccharides, and the resultant systemic inflammation may lead to neuroinflammation in the central nervous system. In light of the fact that gut microbial factors contribute to the initiation and exacerbation of depressive symptoms, this review summarizes the current understanding of the molecular mechanisms involved in MDD onset, and discusses the therapeutic potential of probiotics, including butyrate-producing bacteria, which can mediate the microbiota–gut–brain axis.     

Mixing effects of metal hydrides on equilibrium behavior and reaction kinetics

Mixing effects of hydriding alloys on equilibrium and kinetic properties are studied, and experimental results are presented for the binary mixtures of LaNi₅/TiMn_1.5, MmNi₅/TiMn_1.5, MmNi_4.8Al_0.2/TiMn_1.5, and LaNi₅/Ti_0.8Zr_0.2Cr_0.8Mn_1.2 under isothermal conditions of 30–60°C with 10° intervals. Major known advantages of mixing are to give desirable P-T-C properties, to enhance reaction rate, and to increase the available temperature and pressure ranges. The authors' objective is to provide a method of designing a particular pair of hydride mixtures with increased hydride composition ranges for transferring hydrogen fairly quickly, increasing availability, improving unit performance, and increasing operational flexibility for a given application.     

Hydrolyzed collagen‐grafted‐poly[(acrylic acid)‐co‐(methacrylic acid)] hydrogel for drug delivery

Hydrolyzed collagen‐grafted‐poly[(acrylic acid)‐co‐(methacrylic acid)] hydrogels were synthesized by solution polymerization and confirmed by infrared spectroscopy. From sequential univariate analysis, the optimal molar ratio of acrylic acid: methacrylic acid was 92:8 in the presence of N,N′‐methylenebisacrylamide, ammonium persulfate, and N,N,N′,N′‐tetramethylethylenediamine at 0.12, 0.015, and 0.2% mol of the monomers, respectively. The water absorbency of this hydrogel was both pH‐ and temperature‐dependent, but was higher in nonbuffered water than in boric acid/citric acid/phosphate buffer under the same conditions. The optimal hydrogel could swiftly swell and deswell in neutral and acid solutions, respectively. Its potential application in drug delivery was examined using insulin and methylene blue as model payload drugs. Loading in a 50% (v v^?1) ethanol solution gave a higher insulin loading level than in the buffer water. Insulin and methylene blue were both released at pH 6.8 but not at pH 1.2, but followed first order kinetics and the Higuchi equation, respectively. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45654.     

Multilayer‐coated NPK compound fertilizer hydrogel with controlled nutrient release and water absorbency

A novel trilayered controlled‐release nitrogen, phosphorous, and potassium (NPK) fertilizer hydrogel was prepared by dipping the NPK fertilizer granules sequentially in 7% w v^?1 poly(vinyl alcohol) (PVA) and 2% w v^?1 chitosan (CS) solutions and then cross‐linking the CS layer (cross‐CS) via glutaraldehyde vapor deposition. Different NPK fertilizer hydrogels were then synthesized by inverse suspension polymerization of the dried PVA/cross‐CS bilayer‐coated fertilizer granules in various molar ratios of acrylamide (AM) and acrylic acid (AA) monomers, and polymerization with varying molar ratios of ammonium persulfate, N,N,N′,N′‐tetramethylethylenediamine and N,N′‐methylenebisacrylamide (N‐MBA). The water dissolution time of the obtained PVA/cross‐CS/poly (AA‐co‐AM) trilayer‐coated NPK fertilizer hydrogel granules was prolonged, while the water absorbency increased with increasing AA contents, and decreased with increasing N‐MBA contents in the outer poly(AA‐co‐AM) coating. The optimal trilayer‐coated NPK fertilizer hydrogel obtained released 84 ± 18, 63 ± 12, and 36 ± 15% of the N, P, and K nutrients, respectively, after a 30‐day immersion in water. The release phenomena of the N, P, and K nutrients of the fertilizer hydrogel obeyed both the Korsmeyer‐Peppas and Ritger‐Peppas models with a pseudo‐Fickian diffusion mechanism. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41249.     

Synthesis of Succinic Gemini Surfactants and the Effect of Stereochemistry on Their Monolayer Behaviors

In this work, succinic gemini surfactants, dl‐ and meso‐2,3‐bis(alkyl)succinic acids (alkyl: C₆H₁₃–C₁₃H₂₇), were successfully synthesized by oxidative coupling of enolates of fatty acid tert‐butyl esters with copper(II) bromide followed by treatment with CF₃COOH. Focusing on the influence of stereochemistry (dl‐ and meso‐) of succinic geminis, their monolayer behaviors at the air–water interface were explored using surface pressure–area (Π–A) isotherms, the compression modulus of monolayers (ε_s), and Brewster angle microscope (BAM) analysis. meso‐2,3‐Bis(undecyl)succinic acid showed a unique isotherm where the surface pressure drastically decreased at A = ~0.56 nm² (Π = 21.9 mN m^?1) regardless of compression rates and subphase temperatures, while dl‐isomer showed the common isotherm of gas → liquid‐expanded → liquid‐condensed phase transitions. BAM analysis on meso‐2,3‐bis(undecyl)succinic acid films at the air–water interface showed that small islands of aggregates appear just after the maximum pressure (A = ~0.56 nm²), and on further compression needle‐shaped assemblies appear that can grow in size. It was reasonably concluded that hydrophobic interactions can operate more effectively in meso‐isomers than in dl‐isomers, and that meso‐molecules can “jump up” to cause a transition from monolayer to bilayer. This is the first finding of the “jumping‐up” phenomenon of gemini surfactants having meso‐stereochemistry.     

Formation of Tetravalent Fe Ions in LaFeO3 Perovskite Through Mechanochemical Modification by Ball Milling

Mechanochemical modification of previously synthesized LaFeO₃ perovskite‐type oxide by a high‐energy ball milling was investigated to introduce Fe⁴⁺ ions or transform some Fe³⁺ into Fe⁴⁺ in LaFeO₃. X‐ray absorption fine structure studies revealed that the formation of Fe⁴⁺ ions into LaFeO₃ perovskite has been achieved at first time by ball milling at room temperature without any additives or replacement of La³⁺ ions by some divalent cations. The structural model of Fe⁴⁺ containing LaFeO₃ could be described as with a modified perovskite having equal amounts of La and Fe vacancies, which is supported by a good correlation between the results of Fe K‐edge XANES spectra and O₂‐TPD. The synthesis of Fe⁴⁺‐containing LaFeO₃ perovskite by ball milling was able to produce the O₂ adsorption capacity of nonsubstituted perovskite‐type oxide.     

Optical resolution of racemic amino acid derivatives with chiral polyamides bearing glutamyl residue as a diacid component

Novel chiral polyamides with chiral environment in their main chains were obtained from aromatic diamine, 4,4′‐diaminodiphenylmethane (DADPM), and the D ‐isomer or the L ‐isomer of N‐α‐protected glutamic acid, such as N‐α‐benzyloxycarbonyl‐D ‐glutamic acid (Z‐D ‐Glu‐OH) or N‐α‐benzyloxycarbonyl‐L ‐glutamic acid (Z‐L ‐Glu‐OH), in the presence of triphenyl phosphite (TPP). Two types of newly prepared polyamide showed optical rotation, implying that there were asymmetric carbons in their main chains. Circular dichroism studies demonstrated that resulting chiral poly‐ amides took a helical structure. Optical resolution ability of those two types of polyamide was studied by adopting potential difference as a driving force for membrane transport. Membranes showed permselectivity toward racemic mixture of N‐α‐acetyltryptophan (Ac‐Trp). The permselectivity was dependent on the absolute configuration of diacid component. The permselectivity was expressed by diffusivity selectivity, which was determined by the presence of chiral helicity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Synthesis and characterization of styrenic‐based polymerized toner and its composite for electrophotographic printing

Suspension polymerization in an aqueous medium was applied to the syntheses of styrenic‐based polymerized toner particles. Poly(vinyl alcohol) and benzoyl peroxide were used as a dispersant and an initiator, respectively. The resulting polymerized toners were found to be smooth on their spherical surfaces, and the particle sizes were 4–10 μm with a coefficient of variation of 20–30%. In most cases, a correlation between small particle sizes with high weight‐average molecular weights was observed. The glass‐transition temperature (T_g) of the polymerized toner could be controlled by the molar ratio of the comonomer between styrene and n‐butyl acrylate (nBA). T_g decreased when the content of nBA in copolymer increased, due to its rubbery state along with the increasing carbon black feed level, because the surface functional groups of the carbon black pigment inhibited the rate of polymerization and decreased the molecular weight of the resulting polymerized toners. The T_g's of the resulting polymerized toners were 66–70°C. Triboelectricity [the charge‐to‐mass ratio (q/m)] of the resulting polymerized toners was 7–20 μCg^?1 in the presence of borobis(1,1‐diphenyl‐1‐oxo‐acetyl)potassium salt. An analysis of print quality showed high background fog, low maximum density, and a small amount of image raggedness. The print result correlated with the q/m values. This article elucidates the polymerization technique, charging properties, and image qualities. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 238–248, 2003     

Morphology and drug release behavior of <Emphasis Type="Italic">N</Emphasis>-isopropylacrylamide/acrylic acid copolymer as stimuli-responsive nanogels

Thermo- and pH-responsive N-isopropylacrylamide (NIPAM) nanogels can be obtained by copolymerization of acrylic acid (AA) comonomer through differential microemulsion polymerization. The effects of comonomer, cross-linker, surfactant contents, and water/oil ratio were preliminarily investigated by a 2⁴ full factorial design in order to eliminate the insignificant parameters from the polymerization analysis. The smallest poly(NIPAM-co-AA) nanogel particles were 40 ± 1 nm in diameter with 6 wt% of solid content and 98% conversion without coagulation. The comonomer amounts controlled the morphologies and LCST of the poly(NIPAM-co-AA) nanogels. The hairy microgels of poly(NIPAM-co-AA) with a 10:90 mol ratio of AA/ NIPAM had a lower critical solution temperature (LCST) of 6 °C. With an increase in the AA amount to a 17 mol ratio, the LCST increased to 27 °C, resulting in core-shell morphology. The morphology of resultant nanogels was characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, and differential scanning calorimetry. Nuclear magnetic resonance spectroscopy was used to calculate the mole ratio of NIPAM and AA in resultant nanogels after dialysis. Both nanogel mole ratio and morphology effectively retained the cationic anti-cancer drug of methylene blue for several hours, an important basic requirement for a drug delivery system. Compared to core-shell microgels, a higher methylene blue release was obtained from the hairy microgels in simulated intestinal fluid.