Influence of Fluorine Content in Apatite–Mullite Glass-Ceramics

The nucleation and crystallization of a series of glasses based on 4.5SiO₂·3Al₂O₃·1.5P₂O₅·(5 − z )CaO · z CaF₂ with a Ca:P ratio corresponding to apatite were studied. In these glasses, the objective was to investigate the influence of fluorine content and z was varied from 3 to 0. All the glasses studied crystallized to fluorapatite (FAP) and mullite with the exception of the glass containing no fluorine, which crystallized to β-tricalcium phosphate (Ca₃(PO₄)₂) and anorthite (CaAl₂Si₂O₈). Glasses that contained sufficient fluorine to form FAP bulk nucleated to give FAP without a nucleation hold. Thermal gravimetric analysis demonstrated a significant weight loss corresponding to the crystallization of mullite, which increased with the fluorine content of the glass and also with decreased particle size. The loss was attributed to volatile SiF₄. The glass transition temperature decreased with increased fluorine content of the glass.     

Novel process for biodiesel by reactive absorption

Process integration and intensification is increasingly applied also in the biodiesel production, as shown by recent research papers. This study takes previous work on reactive separation processes for biodiesel production to a new level by proposing an innovative technology based on reactive absorption using solid acid catalysts. This is a major step forward since reactive absorption offers significant benefits over reactive distillation, such as: reduced capital investment and operating costs due to the absence of the reboiler and condenser, higher conversion and selectivity as no products are recycled in the form of reflux or boil-up vapors, as well as no occurrence of thermal degradation of the products due to a lower temperature profile in the column. Rigorous simulations embedding experimental results were performed in AspenTech AspenONE engineering suite to design this novel reactive absorption process and evaluate the technical and economical feasibility. The main results are given for a plant producing 10 ktpy biodiesel from waste vegetable oil with high free fatty acids content, using solid acids as green catalysts. This innovative process eliminates all conventional catalyst-related operations, and efficiently uses the raw materials and the reactor volume in an integrated setup that allows significant savings in CapEx and OpEx of the plant.     

Molten Salt Synthesis of Bi4(V0.85Co0.15)2O11−δ (BICOVOX) Ceramic Powders

Cobalt (15 at.%)-doped bismuth vanadate, Bi₄(V_0.85Co_0.15)₂O_11−δ (BICOVOX) is known to have high oxygen ion conduction. However, the conductivity is highly anisotropic due to its layered structure. In this paper, we report the synthesis of BICOVOX powders with platelet habit by molten salt synthesis using a NaCl–KCl eutectic mixture as the reaction medium. The effects of treatment temperature and time on the morphology and phase content of the BICOVOX powders were investigated. By this method, it is possible to synthesize powders with platelets of major face dimension ∼50 μm and aspect ratio (major face dimension to thickness) as high as 15.     

LanV, a bifunctional enzyme: aromatase and ketoreductase during landomycin A biosynthesis

LanV is involved in the biosynthesis of landomycin A. The exact function of this enzyme was elucidated with combinatorial biosynthesis by using Streptomyces fradiae mutants that produce urdamycin A. After expression of lanV in S. fradiae DeltaurdM, which is a mutant that accumulates rabelomycin, urdamycinon B and urdamycin B were found to be produced by the strain. This result indicates that LanV is involved in the 6-ketoreduction of the angucycline core, which preceeds a 5,6-dehydration reaction. 9-C-D-Olivosyltetrangulol was also produced by this strain; this demonstrates that LanV catalyses the aromatization of ring A of the angucycline structure. Coexpression of lanV and lanGT2 in S. fradiae AO, a mutant that lacks all four urdamycin glycosyltransferases, resulted in the production of tetrangulol and the glycoside landomycin H, both of which have an aromatic ring A. As glycosylated angucyclines were not observed after expression of lanGT2 in the absence of lanV, we conclude that LanGT2 needs an aromatized ring A for substrate recognition.     

Ligand-directed immobilization of proteins through an esterase 2 fusion tag studied by atomic force microscopy

Atomically flat mica surfaces were chemically modified with an alkyl trifluoromethyl ketone, a covalent inhibitor of esterase 2 from Alicyclobacillus acidocaldarius, which served as a tag for ligand-directed immobilization of esterase-linked proteins. Purified NADH oxidase from Thermus thermophilus and human exportin-t from cell lysates were anchored on the modified surfaces. The immobilization effectiveness of the proteins was studied by atomic force microscopy (AFM). It was shown that ligand-esterase interaction allowed specific attachment of exportin-t and resulted in high-resolution images and coverage patterns that were comparable with immobilized purified protein. Moreover, the biological functionality of immobilized human exportin-t in forming a quaternary complex with tRNA and the GTPase Ran-GTP, and the dimension changes before and after complex formation were also determined by AFM.     

Multiscale, Multiphysics Numerical Modeling of Fusion Welding with Experimental Characterization and Validation

Various physical interfacial phenomena occur during the process of welding and influence the final properties of welded structures. As the features of such interfaces depend on physics that resolve at different spatial scales, a multiscale and multiphysics numerical modeling approach is necessary. In a collaborative research project Modeling of Interface Evolution in Advanced Welding, a novel strategy of model linking is employed in a multiscale, multiphysics computational framework for fusion welding. We only directly link numerical models that are on neighboring spatial scales instead of trying to link all submodels directly together through all available spatial scales. This strategy ensures that the numerical models assist one another via smooth data transfer, avoiding the huge difficulty raised by forcing models to attempt communication over many spatial scales. Experimental activities contribute to the modeling work by providing valuable input parameters and validation data. Representative examples of the results of modeling, linking and characterization are presented.     

Magnetically Controlled Carbonate Nanocomposite with Ciprofloxacin for Biofilm Eradication

Biofilms are the reason for a vast majority of chronic inflammation cases and most acute inflammation. The treatment of biofilms still is a complicated task due to the low efficiency of drug delivery and high resistivity of the involved bacteria to harmful factors. Here we describe a magnetically controlled nanocomposite with a stimuli-responsive release profile based on calcium carbonate and magnetite with an encapsulated antibiotic (ciprofloxacin) that can be used to solve this problem. The material magnetic properties allowed targeted delivery, accumulation, and penetration of the composite in the biofilm, as well as the rapid triggered release of the entrapped antibiotic. Under the influence of an RF magnetic field with a frequency of 210 kHz, the composite underwent a phase transition from vaterite into calcite and promoted the release of ciprofloxacin. The effectiveness of the composite was tested against formed biofilms of E. coli and S. aureus and showed a 71% reduction in E. coli biofilm biomass and an 85% reduction in S. aureus biofilms. The efficiency of the composite with entrapped ciprofloxacin was higher than for the free antibiotic in the same concentration, up to 72%. The developed composite is a promising material for the treatment of biofilm-associated inflammations.     

Effect of Mn doping on hydrolysis of low-temperature synthesized metastable alpha-tricalcium phosphate

In the present work, effect of Mn doping on hydrolysis rate of low-temperature synthesized metastable α-tricalcium phosphate (α-TCP) was investigated. α-TCP powders containing different amount of Mn²⁺ ions (0, 0.5 and 1 mol%) were synthesized by wet co-precipitation process, followed by annealing and crystallization of as-precipitated amorphous calcium phosphate at 700 °C. It was demonstrated that the presence of Mn²⁺ ions significantly retards hydrolysis rate of α-TCP. While pristine α-TCP fully hydrolyzed with a conversion to calcium-deficient hydroxyapatite in 10 h, complete hydrolysis of α-TCP doped with 0.5 and 1 mol% of Mn occurred only after 20 and 35 h, respectively. Initial and final products were characterized by X-ray diffraction (XRD) analysis, infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). Chemical composition of starting and fully hydrolyzed α-TCP powders was determined by inductively coupled plasma optical emission spectrometry (ICP-OES).