Structural Regeneration of Coatings in Friction

Materials Science - We propose a mechanism for increasing the durability of friction surfaces in the presence of in-service defects caused by the intrastructural regeneration. It is shown that, in...     

Catalytic activity of char produced from brown coal for steam-gasification of bitumen oil

There are several kinds of catalyst for tar reduction such as Ni-based catalysts, alkali catalysts, metal catalysts, and char. Char is a nonmetallic material which be generated by the devolatilization of organic materials. In this article, by using an experimental setup we tried to study the effect of char particles as a catalyst on the tar concentration and produced gas from steam gasification of bitumen oil and to introduce effective parameters in the process of syngas generation. With the increase of gasification temperature from 800 to 950°C, the hydrogen increased sharply from 28.4 vol% to 34.9 vol% and 18.5 vol% to 21.3 vol%, while CO decreased from 12.5 vol% to 14.9 vol% and 14.8 vol% to 18.1 vol% for gasification with and without char, respectively. As a result, it was found that the gas produced is not sensitive to the pressure changes.     

Vacuum desorption of gases from inorganic solvents with various boiling points

The vacuum desorption of gases from inorganic solvents with low and high boiling points is reported. A thin-film evaporator consisting of regular tubular packing elements is considered. A laminar downward cocurrent flow of liquid and vapor is analyzed. General theoretical propositions are illustrated by the example of the desorption of simple gases from lower alcohols (methanol, ethanol) and liquid naphthalene, as well as by the example of removing the products of ester decomposition from esters at high temperatures.     

Sonochemical Synthesis and Characterization of A Nano-Rod Lead(II) Supramolecular, Three Dimensional Coordination Compound: New Precursor to Produce Pure Phase Nano-Sized Lead(II) Oxide

Nanorods of a lead(II) supramolecular three-dimensional (3D) coordination compound, [Pb(tfpb)₂]_n (1) (Htfpb?=?4,4,4-trifluoro-1-phenyl-1,3-butanedione), was prepared by the sonochemical method. The new nano-structure was characterized by scanning electron microscopy, X-ray powder diffraction, elemental analyses and IR spectroscopy. A single-crystal structure of the compound showed that the coordination number of Pb(II) is eight with six O-donor atoms from the tfpb ligand and two F-donors from anionic ligands. The 3D supramolecular structure of 1 is realized by weak directional C–F···F–C and π–π stacking interactions. After calcination of nano-sized 1 at 500?°C, pure phase nano-sized lead(II) oxide is produced.     

Solvothermal Synthesis of a Nano-sized Aza-aromatic Base Adduct of a Cadmium(II) 4,4-Difluoro-1-phenyl-1,3-butandionate Coordination Compound

A new nano-structured cadmium(II) coordination compound, [Cd(phen)(dfpb)₂] (1) (phen?=?1,10-phenanthroline, dfpb?=?4,4-difluoro-1-phenyl-1,3-butandion), was synthesized by a solvothermal method and produced a coordination polymer in the nano-size range. The new nanostructure was characterized by scanning electron microscopy, X-ray powder diffraction elemental analysis and IR spectroscopy. Compound 1 was structurally characterised by single crystal X-ray diffraction. The single crystal structure shows a coordination number for the Cd ion of six with two N-donor atoms from the phen ligand and four O-donors from the two dfpb moieties. Self-assembly occurs by CH····F–C and π–π stacking interactions. The supramolecular features in these complexes are controlled by weak directional intermolecular interactions.     

Human Cellular Retinol Binding Protein II Forms a Domain-Swapped Trimer Representing a Novel Fold and a New Template for Protein Engineering

Domain-swapping is a mechanism for evolving new protein structure from extant scaffolds, and has been an efficient protein-engineering strategy for tailoring functional diversity. However, domain swapping can only be exploited if it can be controlled, especially in cases where various folds can coexist. Herein, we describe the structure of a domain-swapped trimer of the iLBP family member hCRBPII, and suggest a mechanism for domain-swapped trimerization. It is further shown that domain-swapped trimerization can be favored by strategic installation of a disulfide bond, thus demonstrating a strategy for fold control. We further show the domain-swapped trimer to be a useful protein design template by installing a high-affinity metal binding site through the introduction of a single mutation, taking advantage of its threefold symmetry. Together, these studies show how nature can promote oligomerization, stabilize a specific oligomer, and generate new function with minimal changes to the protein sequence.     

Analysis and Optimization of a Synthetic Milkweed Floral Attractant for Mosquitoes

A pentane extract of flowers of common milkweed, Asclepias syriaca (Asclepiadaceae), elicited significant orientation from both male and female Culex pipiens in a dual-port flight olfactometer. Analysis of the extract by gas chromatography-mass spectrometry revealed six major constituents in order of relative abundance: benzaldehyde, (E)-β-ocimene, phenylacetaldehyde, benzyl alcohol, nonanal, and (E)-2-nonenal. Although not all were collected from the headspace profile of live flowers, a synthetic blend of these six compounds, when presented to mosquitoes in the same levels and proportions that occur in the extract, elicited a response comparable to the extract. Subtractive behavioral bioassays demonstrated that a three-component blend consisting of benzaldehyde, phenylacetaldehyde, and (E)-2-nonenal was as attractive as the full blend. These findings suggest the potential use of synthetic floral-odor blends for monitoring or control of both male and female disease-vectoring mosquitoes.     

Unsteady-State Mass Transfer of Gases between Two Quiescent Phases

It is shown that many gases interact with water by reactions similar to that characteristic of sulfur dioxide. The unsteady-state transfer of such gases from one quiescent phase into another is studied in the cases where these gases are absorbed by a liquid or released from a liquid solution.     

Biodegradable polypropylene/thermoplastic starch nanocomposites incorporating halloysite nanotubes

In this work, polypropylene/thermoplastic starch (PP/TPS) with and without halloysite nanotubes (HNTs) was prepared via melt mixing in order to obtain environmentally friendly plastics. PP‐grafted maleic anhydride (PP‐g‐MA) was used to improve the compatibility among the highly incompatible polymers. The mechanical characterization showed a reduction in the tensile properties of the polymer when TPS increased; however, HNT successfully compensated for some of the observed losses. The results from the thermogravimetric analysis (TGA) indicated that HNT is an efficient reinforcement for the thermal stability improvement. TPS caused an increase in the storage modulus (G′) and the complex viscosity (η*) which marks a change in the viscoelastic properties of the system. The scanning electron microscope (SEM) images showed the effective plasticization of starch and better dispersion of TPS in the presence of HNT. Some samples were also buried in the soil to measure their sustainability after their lifetime lapse. The results indicated that TPS improves the biodegradability of the PP/TPS system. PP considerably lowered the moisture uptake of TPS; nevertheless, HNT caused a slight increase in the moisture absorption. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45740.