Hierarchically Structured Materials by Anodic Coagulation Casting of Fibrinogenic Alumina Suspensions

Anodic coagulation casting of fibrinogenic ceramic suspensions is a novel processing technology, which is based on the electrically induced transformation of the water soluble fibrinogen into the insoluble fibrin. Contrary to the direct coagulation casting (DCC) technology, green formation does not depend on a pH‐shift and as the fibrin coagulate forms on an anode, it can be combined with the electrophoretic deposition (EPD) technology. In this study, the conversion of fibrinogen into fibrin is activated via electron transfer processes at an electrode material and is combined with the green formation of alumina by embedding the ceramic particles in the protein matrix. The focus of this work was to establish a technology to shape thin hierarchically structured ceramic films and thick porous materials with a distinct pore structure. Film thickness and porosity were controlled by the applied voltage and the processing‐time. The range of the established green bodies included two‐dimensional and simple three‐dimensional shapes including multilayered deposition and fiber coatings. Overall the process of anodic coagulation casting can be reported to be successful for all established ceramic shapes except multilayers, where delamination was observed. The deposited alumina ceramics were characterized using light microscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), and synchrotron micro computed tomography (μCT), while the coagulation mechanism was studied using high‐performance liquid chromatography (HPLC).     

Detection of Pinosylvins in Solid Wood of Scots Pine Using Fourier Transform Raman and Infrared Spectroscopy

Abstract

Diffuse reflectance Fourier transform infrared (DRIFT) and near infrared (NIR) FT-Raman spectroscopy were used to detect pinosylvins in the wood of Pinus sylvestris L. trees. NIR FT-Raman spectroscopy offered the possibility of revealing pinosylvins simply by visual inspection of Raman spectra whereas DRIFT spectra needed a more complicated evaluation. Pinosylvin and resin acids from Scots pine were examined as to the possibility of their being the cause of observed spectral differences between sapwood and heartwood. Since pinosylvins are important compounds for the decay resistance of Scots pine wood, the detection of pinosylvins with Raman spectroscopy might be used to assess durability of wood products.     

The Kinetics of the Thermal Decomposition of Thermoplastic Polyurethane Elastomers under Thermoplastic Processing Conditions

A theoretical approach to the kinetics of the thermal decomposition of molten thermoplastic polyurethane elastomers, under conditions of thermoplastic processing, is described. On the basis of these considerations, the thermal decomposition in different instruments (melt index analyser and measuring extruder) can be described quantitatively and the various results can be compared. As a result, identical conditions of decomposition of the melt can be defined accurately, thus opening up the possibility of combining experimental values from different instruments. The fundamental kinetic equation obtained for the kinetics of the thermal decomposition of thermoplastic polyurethanes describes the decomposition reaction and the reverse reaction (formation reaction) – which is dependent on the system of measurement and processing – as a function of the molar mass (end‐group concentration) of the original product, determined from the velocity constants for the decomposition reaction and back reaction. The consideration of the limiting value for t → ∞ is in agreement with the equilibrium constant. Consequently, the development of physical characteristic functions of thermoplastic polyurethane elastomers – independent of the system of measurement – is possible.

Experimental values and calculated curves for the thermal decomposition of PUR‐Et in a melt index analyser.     

Polymer Ionomers for Rapid Prototyping and Rapid Manufacturing by Means of 3D Printing

Summary: The powder blend of poly(acrylic acid) (PAA) with zinc oxide or zinc oxide/magnesium oxide was applied successfully to produce zinc polycarboxylate during the 3D dispensing of an aqueous ink by means of 3D printers (Z402? from ZCorporation and Deskmodeler? from bmt Company). The layer‐by‐layer inkjet printing afforded zinc ionomer 3D objects with excellent water resistance, no inherent color formation and high mechanical and dimensional stabilities. In contrast to the 3D printing of conventional powders such as starch/cellulose/dextrose blends, poly(vinyl alcohol) (PVA) or plaster, no postprinting treatments were required. Excellent dimensional accuracy of the models, as evidenced by very small deviation of the dimensions from those of the corresponding CAD data, was achieved. The mechanical properties improved with increasing PAA content, ink amount (saturation value), decreasing particle size of the sintered zinc oxide ceramic. At high PAA content >7 wt.‐%, post‐treatment with aqueous zinc acetate solution improved the mechanical properties. The setting time of the zinc cements shows no significant effect on the mechanical properties, but on the water resistance of the models. The porosity of the 3D objects, measured by means of X‐ray microtomography (μ‐CT), had profound impact on the variations of the mechanical properties of the 3D objects prepared by 3D printing processes.

Comparison of three‐point‐bending tests of commercially available powders with selected zinc cements (ZC1, ZC2, ZC4, ZC19). Commercially available powders printed with recommended values of manufacturer. Zinc cements printed with saturation value 1.14 (Z402?).     

Tracking Protein S‐Fatty Acylation with Proteomics

Recently, Hang and co‐workers developed “acyl‐PEG exchange” (APE), which allows the investigation of protein S‐fatty acylation with mass‐tag labelling and gel electrophoresis, methods that are accessible to any biochemistry laboratory.     

Structure and Substrate Recognition of the Bottromycin Maturation Enzyme BotP

The bottromycins are a family of highly modified peptide natural products, which display potent antimicrobial activity against Gram‐positive bacteria, including methicillin‐resistant Staphylococcus aureus. Bottromycins have recently been shown to be ribosomally synthesized and post‐translationally modified peptides (RiPPs). Unique amongst RiPPs, the precursor peptide BotA contains a C‐terminal “follower” sequence, rather than the canonical N‐terminal “leader” sequence. We report herein the structural and biochemical characterization of BotP, a leucyl‐aminopeptidase‐like enzyme from the bottromycin pathway. We demonstrate that BotP is responsible for the removal of the N‐terminal methionine from the precursor peptide. Determining the crystal structures of both apo BotP and BotP in complex with Mn²⁺ allowed us to model a BotP/substrate complex and to rationalize substrate recognition. Our data represent the first step towards targeted compound modification to unlock the full antibiotic potential of bottro‐ mycin.     

How many object colors can we distinguish?

The question of how many different colors humans can perceive has been of interest to philosophers, psychologists and color scientists for centuries. In recent years the question of the number of distinguishable object color stimuli has been addressed by color scientists by defining a distinguishable color as a given stimulus surrounded by the contour of stimuli just noticeably different from the central stimulus. For a particular set of conditions the number of distinguishable object color stimuli assessed in this manner has recently been found to be slightly larger than 2 million. In this article an argument is made that the related rules are arbitrary and unnecessarily limiting. Based on logical arguments and experimental just noticeable difference data it is shown that, for the conditions involved, a more realistic if conservative number of distinguishable object color stimuli is ～40 million. © 2015 Wiley Periodicals, Inc. Col Res Appl, 41, 439–444, 2016     

Desktop manufacturing of complex objects,prototypes and biomedical scaffolds by means of computer‐assisted design combined with computer‐guided 3D plotting of polymers and reactive oligomers

Computer‐assisted design and image processing were combined with computer‐guided one‐ and two‐component air‐driven 3D dispensing of hotmelts, solutions, pastes, dispersions of polymers as well as monomers and reactive oligomers to produce solid objects with complex shapes and tailor‐made internal structures. During the 3D plotting process either individual microdots or microstrands were positioned in order to construct complex objects, fibers, tubes and scaffolds similar to non‐wovens. The resolution was in the range of 200 μm and depended upon inner nozzle diameter, air pressure, plotting speed, rheology, and plotting medium. Plotting in liquid media with densities similar to that of the dispensing liquid eliminated the need for construction of temporary support structures. The design capabilities of this computer‐guided 3D plotting process was demonstrated using conventional moisture‐curable silicone resin.