Preparation of Spherical, Submicrometer Oxide Particles by Hydrolysis of Emulsified Alkoxide Droplets

A new method for forming spherical, submicrometer ceramic oxide particles by the hydrolysis of emulsified alkoxide droplets is reported. Emulsions are formed of alkoxide droplets dispersed in an inert, polar solvent. The alkoxide droplets are hydrolyzed to form oxide particles by adding water to the emulsion. It was shown that individual droplets acted as "microreactors" and controlled the powder size, shape, and composition. Both single-oxide and mixed-oxide powders were formed by this technique.     

Electrospun microporous gelatin–polycaprolactone blend tubular scaffold as a potential vascular biomaterial

The work reported involved the fabrication of an electrospun tubular conduit of a gelatin and polycaprolactone (PCL) blend as an adventitia‐equivalent construct. Gelatin was included as the matrix for increased biocompatibility with the addition of PCL for durability. This is contrary to most of the literature available for biomaterials based on blends of gelatin and PCL where PCL is the major matrix. The work includes the assiduous selection of key electrospinning parameters to obtain smooth bead‐free fibres with a narrow distribution of pore size and fibre diameter. Few reports elucidate the optimization of all electrospinning parameters to fabricate tubular conduits with a focus on obtaining homogeneous pores and fibres. This stepwise investigation would be unique for the fabrication of gelatin–PCL electrospun tubular constructs. The fabricated microfibrous gelatin–PCL constructs had pores of size ca 50–100 μm reportedly conducive for cell infiltration. The measured value of surface roughness of 57.99 ± 17.4 nm is reported to be favourable for protein adhesion and cell adhesion. The elastic modulus was observed to be similar to that of the tunica adventitia of the native artery. Preliminary in vitro and in vivo biocompatibility tests suggest safe applicability as a biomaterial. Minimal cytotoxicity was observed using MTT assay. Subcutaneous implantation of the scaffold demonstrated acute inflammation which decreased by day 15. The findings of this study could enable the fabrication of smooth bead‐free microfibrous gelatin–PCL tubular construct as viable biomaterial which can be included in a bilayer or a trilayer scaffold for vascular tissue engineering. © 2019 Society of Chemical Industry     

不同脱毒方法对玉米秸秆水解液酒精发酵的影响

利用湿热预处理(195℃,15 min)后的玉米秸秆水解液,考察了3种不同脱毒方法(中和法、饱和生石灰法和Na2SO3法)对水解液中的抑制剂的去除效果,研究了树干毕赤酵母(Pichia stipitis 58376)对脱毒后的水解液酒精发酵情况.结果表明:玉米秸秆水解液经过3种方法脱毒处理后,醛类抑制荆(糠醛和5-羟甲...     

A Highly Active and Selective Manganese Oxide Promoted Cobalt-on-Silica Fischer�CTropsch Catalyst

A highly active and selective manganese oxide-promoted silica-supported cobalt catalyst for the Fischer?CTropsch reaction is reported. Co/MnO/SiO₂ catalysts were prepared via impregnation of a cobalt nitrate and manganese nitrate precursor, followed by drying and calcination in an NO/He flow. The catalysts were studied with STEM?CEELS, infrared spectroscopy measurements of adsorbed CO and Steady-State Isotopic Transient Kinetic Analysis experiments. Based on those experiments, a relation between C₅₊-selectivity and surface-coverages of CH _x -intermediates on cobalt was found.     

Effect of Melt‐Memory on the Crystal Polymorphism in Molded Isotactic Polypropylene

The influence of γ‐quinacridone as a β‐crystal nucleating agent in injection molded isotactic polypropylene (iPP) is discussed. Samples are injection molded and characterized via polarized‐light optical microscopy and X‐ray diffraction. Mold‐filling simulation is used to understand the shear and cooling processes during sample preparation. The cooling rate associated with the quench near the mold wall is estimated to be greater than 600 K s^?1 using simulation, confirming previous studies that β‐crystal growth is not supported at that cooling rate. The non‐nucleated samples form β‐crystals at a distance of 100–300 µm from the skin and in the core of the sample, which is not expected based on quiescent cooling data. Since the mold‐filling simulation does not predict shear in the core, the formation of the β‐crystals formed in this region is attributed to shear‐induced crystallization effects in the injection unit of the molding machine that are not modeled in flow simulation, as they are typically excluded from any molding simulation analysis. This “melt‐memory” effect has shown to be significant, and it is suggested that the prediction of final properties of injection moldings requires understanding and knowledge of the entire shear history of the material including that of the injection unit.     

Effects of Radiographic Contrast Media on the Micromorphology of the Junctional Complex of Erythrocytes Visualized by Immunocytology

Effects of radiographic contrast media (RCM) application were demonstrated in vitro and in vivo where the injection of RCM into the A. axillaris of patients with coronary artery disease was followed by a significant and RCM-dependent decrease of erythrocyte velocity in downstream skin capillaries. Another study in pigs revealed that the deceleration of erythrocytes coincided with a significant reduction of the oxygen partial pressure in the myocardium—supplied by the left coronary artery—after the administration of RCM into this artery. Further reports showed RCM dependent alterations of erythrocytes like echinocyte formation and exocytosis, sequestration of actin or band 3 and the buckling of endothelial cells coinciding with a formation of interendothelial fenestrations leading to areas devoid of endothelial cells. Key to morphological alterations of erythrocytes is the membrane cytoskeleton, which is linked to the band 3 in the erythrocyte membrane via the junctional complex. Fundamental observations regarding the cell biological and biochemical aspects of the structure and function of the cell membrane and the membrane cytoskeleton of erythrocytes have been reported. This review focuses on recent results gained, e.g., by advanced confocal laser scanning microscopy of different double-stained structural elements of the erythrocyte membrane cytoskeleton.