Effect of acetic acid content on in situ preparation of epoxy/zirconia hybrid materials

Epoxy/zirconia hybrid materials were synthesized via in situ polymerization of acetic acid-modified zirconium alkoxide. The reactivity of acetic acid-modified zirconium alkoxide changed with the amount of acetic acid added. In the hybrid materials, the phase structure varied between the homogeneous phase and nanophase separation as the reactivity of zirconium alkoxide changed. At the molecular level, the storage modulus in the rubbery region significantly increased and the peak area of tan δ in the glass-transition temperature region decreased with increasing zirconia contents in the hybrid dispersed zirconia. Additionally, the optical properties of the hybrid materials in the homogeneous phase were better than those in the system with nanophase separation.     

Interfacial properties of HIP joints between beryllium and reduced activation ferritic/martensitic steel

ITER test blanket modules are the most important components to validate energy production and fuel breeding for future fusion demonstration reactors. Reduced activation ferritic/martensitic steel is recognized as one of the promising structural materials for the breeding blanket systems. Beryllium is a primary candidate plasma facing materials for ITER blanket. In this work, the interfacial properties of Be/reduced activation ferritic/martensitic steel (RAF/Ms) joints were investigated for the first wall of an ITER test blanket module (TBM). The joints were produced by the solid-state hot isostatic pressing (HIP) method. Chromium (Cr) was used as a diffusion barrier with a thickness of 1 μm or 10 μm, formed by plasma vapor deposition on the Be surface. The HIPping was conducted at 1023 K and 1233 K with 160 MPa of static pressure. The temperatures are standard normalizing and tempering temperatures of F82H. EPMA showed the Cr layer effectively worked as a diffusion barrier at 1023 K. However, for the F82H/Be interface which underwent HIP at 1233 K followed by tempering a Be rich layer was formed. Bend tests revealed that a thin Cr layer and low temperature HIP is preferable. The joint with a thick Cr layer suffer from brittleness of Cr itself.     

High-pressure torsion of TiFe intermetallics for activation of hydrogen storage at room temperature with heterogeneous nanostructure

TiFe is a potential candidate for the stationary hydrogen storage systems, but it requires initial activation to absorb hydrogen. This study shows that TiFe processed by high-pressure torsion (HPT) absorbs and desorbs 1.7 wt.% hydrogen at room temperature without activation. The absorption pressure decreases from 2 MPa in the first hydrogenation cycle to 0.7 MPa in the latter cycles. The HPT-processed TiFe exhibits heterogeneous microstructures composed of nanograins, coarse-grains, amorphous-like phases and disordered phases with a high hardness of ∼1050 Hv.     

Phase and morphology evolution study of ball milled Mg–Co hydrogen storage alloys

Ball milled Mg–Co alloys with body-centered cubic structure (BCC) may absorb hydrogen at 258 K with a hydrogen capacity around 3 mass%. The phase and morphology evolution process of Mg₅₀Co₅₀ alloys ball milled for 0.5 h–400 h was studied by X-ray diffraction and scanning electron microscope. The formation mechanism of the Mg₅₀Co₅₀ alloys was clarified. Mg₅₀Co₅₀ alloys ball milled for various durations were found to present different hydrogen storage properties which could result from the phase and morphology difference in these samples.     

Sphingomyelinase C from Streptomyces sp. A9107: Unusual primary structure for bacterial sphingomyelinase C

A sphingomyelinase C (SMase) was identified in the culture supernatant of Streptomyces sp. A9107 (S-SMase). Although S-SMase seems to be a typical bacterial SMase, the primary structure of S-SMase was unusual for known bacterial SMase. The gene was functionally overexpressed in the culture medium of recombinant Rhodococcus erythropolis.     

UV Light-Generated Superhydrophilicity of a Titanium Surface Enhances the Transfer,Diffusion and Adsorption of Osteogenic Factors from a Collagen Sponge

It is a significant challenge for a titanium implant, which is a bio-inert material, to recruit osteogenic factors, such as osteoblasts, proteins and blood effectively when these are contained in a biomaterial. The objective of this study was to examine the effect of ultraviolet (UV)-treatment of titanium on surface wettability and the recruitment of osteogenic factors when they are contained in an atelocollagen sponge. UV treatment of a dental implant made of commercially pure titanium was performed with UV-light for 12 min immediately prior to the experiments. Superhydrophilicity on dental implant surfaces was generated with UV-treatment. The collagen sponge containing blood, osteoblasts, or albumin was directly placed on the dental implant. Untreated implants absorbed only a little blood from the collagen sponge, while the UV-treated implants absorbed blood rapidly and allowed it to spread widely, almost over the entire implant surface. Blood coverage was 3.5 times greater for the UV-treated implants (p < 0.001). Only 6% of the osteoblasts transferred from the collagen sponge to the untreated implants, whereas 16% of the osteoblasts transferred to the UV-treated implants (p < 0.001). In addition, a weight ratio between transferred albumin on the implant and measured albumin adsorbed on the implant was 17.3% in untreated implants and 38.5% in UV-treated implants (p < 0.05). These results indicated that UV treatment converts a titanium surface into a superhydrophilic and bio-active material, which could recruite osteogenic factors even when they were contained in a collagen sponge. The transfer and subsequent diffusion and adsorption efficacy of UV-treated titanium surfaces could be useful for bone formation when titanium surfaces and osteogenic factors are intervened with a biomaterial.     

Activation of TiFe for hydrogen storage by plastic deformation using groove rolling and high-pressure torsion: Similarities and differences

Intermetallics of TiFe were processed using three different routes: annealing, plastic deformation using groove rolling and severe plastic deformation using high-pressure torsion (HPT). Hydrogen absorption was less than 0.2 wt.% in the coarse-grained annealed sample because of difficult activation. The groove-rolled sample, with subgrain structure and high density of dislocations and cracks, absorbed 0.3, 1.0, 1.4 and 1.7 wt.% of hydrogen in the first, second, third and fourth hydrogenation cycles, respectively. The HPT-processed sample, containing nanograins, absorbed 1.7–2 wt.% of hydrogen in any hydrogenation cycles. Both samples activated by groove rolling and HPT were not deactivated by long time exposure to the air. No surface segregation was detected after groove rolling, while the HPT-processed sample exhibited surface segregation. The current study confirmed the significance of plastic deformation and formation of grain boundaries and cracks on activation for hydrogen storage.