Phytochemical Composition of <Emphasis Type="Italic">Oryza sativa</Emphasis> (Rice) Bran Oil Bodies in Crude and Purified Isolates

We describe a procedure for isolating and purifying oil bodies (OBs) from Oryza sativa bran, and present evidence that strongly suggests a physical association between the OB organelles and several antioxidant phytochemicals (γ-oryzanol and several tocochromanols). This suggestion arises from work showing that despite comprehensive washing steps (9 M urea, water), the majority of the tocotrienols and tocopherols (77 and 73 %, respectively) and oryzanols (91 %) remain integral to the oil bodies, not being released unless the latter are sacrificed. This in turn provides a valuable comparison with similar analyses of tocochromanols in other plant species, as well as indicating that rice bran, normally a waste product from the rice industry, may provide a valuable source of antioxidants as well as protein and unsaturated fat.     

Iterative Nonproteinogenic Residue Incorporation Yields α/β‐Peptides with a Helix–Loop–Helix Tertiary Structure and High Affinity for VEGF

Inhibition of specific protein–protein interactions is attractive for a range of therapeutic applications, but the large and irregularly shaped contact surfaces involved in many such interactions make it challenging to design synthetic antagonists. Here, we describe the development of backbone‐modified peptides containing both α‐ and β‐amino acid residues (α/β‐peptides) that target the receptor‐binding surface of vascular endothelial growth factor (VEGF). Our approach is based on the Z‐domain, which adopts a three‐helix bundle tertiary structure. We show how a two‐helix “mini‐Z‐domain” can be modified to contain β and other nonproteinogenic residues while retaining the target‐binding epitope by using iterative unnatural residue incorporation. The resulting α/β‐peptides are less susceptible to proteolysis than is their parent α‐peptide, and some of these α/β‐peptides match the full‐length Z‐domain in terms of affinity for receptor‐recognition surfaces on the VEGF homodimer.     

The performance of wood and tile roofing assemblies exposed to continuous firebrand assault

The performance of tile roofing assemblies as well as untreated cedar shake roofing assemblies exposed to continuous firebrand showers were compared. Specifically, experiments were conducted for two types of concrete tile roofing assemblies (flat and profiled), one type of terracotta tile roofing assembly (flat) and an untreated (without any fire retardant) cedar shake roofing assembly. The design of the roofing assemblies was based on construction guidelines in the USA. The duration of the firebrand flux was fixed at 20 min, and the wind speed was varied from 6 m/s to 9 m/s. These wind speeds were chosen to be able to compare roofing assembly performance to similar assemblies exposed to a batch‐feed firebrand generator which had limited duration of firebrand exposure (6 min). The average firebrand mass flux that arrived at the surface of the roofing assemblies was 0.3 g/m²s Results indicated that for the untreated cedar shake assemblies, ignition occurred easily from the firebrand assault, and this type of roofing assembly generated their own firebrands after ignition. To attempt to quantify the degree of penetration, the number of firebrands that penetrated the tile roofing assemblies, and deposited onto the underlayment/counter‐batten system was counted as function of wind speed for each assembly. Firebrand penetration was observed, even for the flat tile assemblies. It is believed that these are the first‐ever experiments described in the peer‐reviewed literature to expose wood and tile roofing experiments to continuous wind‐driven firebrand showers. Copyright © 2016 John Wiley & Sons, Ltd.     

Modification of absorbent poly(glycerol‐glutaric acid) films by the addition of monoglycerides

Monoglycerides (MGs) have been incorporated into the matrix of poly(glycerol‐co‐glutaric acid) films to investigate their effect on the thermal, mechanical, and solvent absorption properties of the resultant films. Solvent absorption studies revealed that poly(glycerol‐co‐glutaric acid‐co‐MG) films were able to absorb and resorb solvents better than poly(glycerol‐co‐glutaric acid) films, albeit they had higher erosion levels. Thermogravimetric analysis showed that the incorporated MGs did not affect the thermal stability of the glycerol‐based films. The MG‐incorporated films were observed to be much softer than the poly(glycerol‐co‐glycerol) films which was further proven by a 39‐fold reduction in Young's Modulus and 17‐fold reduction in fracture energy when compared to the poly(glycerol‐co‐glycerol). Mechanical property studies also revealed that the incorporation of MGs increased the elongation % and reduced the tensile strength of poly(glycerol‐co‐glutaric acid) films. Correlation analysis revealed a strong linear relationship between Young's Modulus and fracture energy (R² = 0.9962), and between Young's Modulus and tensile strength (R² = 0.9972). Our study proved that MGs can be successfully incorporated in the polymer matrix of poly(glycerol‐co‐glutaric acid) films to produce softer films with increased elongation and increased solvent absorption capacity. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45381.     

Toughening of epoxy systems by brominated epoxy

Blends of brominated epoxy (BE) and conventional epoxy resins were studied following curing with aliphatic triethylenetetramine (TETA), etheric (polyether diamine‐ PEA4), and aromatic (3,3′‐diamino diphenyl sulfone [DDS]) hardeners. The addition of BE resulted in an increase in T_g in all tested blends. Blends with 50 wt% BE cured with TETA demonstrated an increase in flexural modulus and flexural strength, while preserving the elongation. Blends with 40 wt% BE cured with PEA4 and 50 wt% BE cured with DDS resulted in a significant enhanced tensile elongation. The shear strength of all cured systems decreased moderately with the addition of BE exhibiting a mixed mode failure. Analysis of the fracture morphology using electron microscopy supported the increase of toughness levels as a result of incorporating BE to conventional epoxy. A unique nodular and rough fracture morphology was obtained, which is related to a toughening mechanism caused by the addition of BE. It was concluded that blends of BE and conventional epoxy could be used as structural adhesives having high T_g, enhanced mechanical properties and increased toughness. POLYM. ENG. SCI., 59:206–215, 2019. © 2018 Society of Plastics Engineers     

Morphology of Palladium Thin Film Deposited on a Two-Dimensional Bilayer Aluminosilicate

Topics in Catalysis - The morphology of a thin palladium film deposited on bilayer Al0.35Si0.65O2/Ru(0001), previously proposed as a two-dimensional zeolite model, is investigated using a set of...     

放电等离子烧结对纳米TiN增强Ti-6Al-4V显微组织和磨损行为的影响（英文）

采用放电等离子烧结(SPS)成功制备Ti-6Al-4V/TiN复合材料。加入Ti-6Al-4V中的TiN含量变化范围为1%~5%(体积分数)。研究添加TiN对Ti-6Al-4V材料致密度、显微组织、硬度和磨损行为的影响。实验结果表明,随着TiN含量的增加,材料的烧结密度从99%降低至97%;而显微硬度值却从HV_(0.1) 389增加至HV_(0.1) 488。X射线衍射(XRD)分析表明,伴随着少量二次Ti_2N相的形成,复合材料中TiN相的衍射峰强度增加。SEM分析表明,SPS烧结Ti-6Al-4V纳米复合材料具有细化的α/β相组织及均匀分散的TiN颗粒。与无添加烧结Ti-6Al-4V相比,Ti-6Al-4V/TiN复合材料的磨损表面呈现非连续的凹槽,抗磨粒磨损性能得到提高。     

Broadly tunable deep blue laser based on a star-shaped oligofluorene truxene

We report amplified spontaneous emission (ASE) and optically pumped deep-blue-emitting distributed feedback (DFB) lasers based on a star-shaped oligofluorene truxene molecule. A low ASE threshold of 2.1 kW/cm² at 439 nm was achieved. The material exhibits a high net gain of 38 cm^?1 and also low optical loss coefficient of 3.5 cm^?1. Second-order DFB lasers show tuning of the emission wavelength from 422 to 473 nm, and a minimum threshold density of 515 W/cm². This is the broadest tuning range (51 nm) reported for organic deep-blue/blue lasing materials.     

Vicia faba–Lygus rugulipennis Interactions: Induced Plant Volatiles and Sex Pheromone Enhancement

The profiles of volatile chemicals emitted by Vicia faba plants damaged by Lygus rugulipennis feeding, and by feeding plus oviposition, were shown to be quantitatively different from those released by undamaged plants. Samples of volatile chemicals collected from healthy plants, plants damaged by males as a consequence of feeding, plants damaged by females as a consequence of feeding and oviposition, plants damaged by feeding with mated males still present, and plants damaged by feeding and oviposition with gravid females still present, showed significant differences in the emission of hexyl acetate, (Z)-β-ocimene, (E)-β-ocimene, (E)-β-caryophyllene, and methyl salicylate. In particular, treatments with mated females present on plants had a significant increase in emission levels of the above compounds, possibly due to eggs laid within plant tissues or active feeding, compared with undamaged plants and plants damaged by males feeding, with or without insects still present. Furthermore, the pheromonal blend released by mated L. rugulipennis females, mainly comprising hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-4-oxo-2-hexenal, was enhanced when females were active on broad bean plants, whereas such an increase was not observed in males. Both sexes gave electroantennogram responses to green leaf volatiles from undamaged plants and to methyl salicylate and (E)-β-caryophyllene emitted by Lygus-damaged plants, suggesting that these compounds may be involved in colonization of host plants by L. rugulipennis. In addition, mated males and females were responsive to hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-4-oxo-2-hexenal released by mated females on V. faba, indicating that these substances could have a dual function as a possible aggregation pheromone in female–female communication, and as a sex pheromone in female–male communication. An erratum to this article can be found at     

MoO2 Diffusion in Aluminosilicate Glass

A diffusion couple of an oxidized molybdenum disk and a glass cylinder was used to measure the solubiiity and effective binary diffusion coefficient of MoO₂ in a non-alkali aluminosilicate glass. At 1400°C, the solubility limit was 8.4 mol%; the value of the diffusion coefficient (4.1 × 10⁻¹⁶ m²/s) was significantly lower than that estimated from the Stokes-Einstein relation.