Revealing internal flow behaviour in arc welding and additive manufacturing of metals.

Internal flow behaviour during melt-pool-based metal manufacturing remains unclear and hinders progression to process optimisation. In this contribution, we present direct time-resolved imaging of melt pool flow dynamics from a high-energy synchrotron radiation experiment. We track internal flow streams during arc welding of steel and measure instantaneous flow velocities ranging from 0.

Synthesis of Cu₂O nanospheres decorated with TiO₂ nanoislands, their enhanced photoactivity and stability under visible light illumination, and their post-illumination catalytic memory.

A novel Cu2O/TiO2 composite photocatalyst structure of Cu2O nanospheres decorated with TiO2 nanoislands were synthesized by a facile hydrolyzation reaction followed by a solvent-thermal process. In this Cu2O/TiO2 composite photocatalyst, Cu2O served as the main visible light absorber, while TiO2 nanoislands formed heterojunctions of good contact with Cu2O, beneficial to the photoexcited electron transfer between them. Their band structure match and inner electrostatic field from the p-n heterojunction both favored the transfer of photoexcited electrons from Cu2O to TiO2, which effectively separated the electron-hole pairs.

Exceptional arsenic (III,V) removal performance of highly porous, nanostructured ZrO2 spheres for fixed bed reactors and the full-scale system modeling.

Highly porous, nanostructured zirconium oxide spheres were fabricated from ZrO2 nanoparticles with the assistance of agar powder to form spheres with size at millimeter level followed with a heat treatment at 450 °C to remove agar network, which provided a simple, low-cost, and safe process for the synthesis of ZrO2 spheres. These ZrO2 spheres had a dual-pore structure, in which interconnected macropores were beneficial for liquid transport and the mesopores could largely increase their surface area (about 98 m(2)/g) for effective contact with arsenic species in water. These ZrO2 spheres demonstrated an even better arsenic removal performance on both As(III) and As(V) than ZrO2 nanoparticles, and could be readily applied to commonly used fixed-bed adsorption reactors in the industry.

Strong adsorption of phosphate by amorphous zirconium oxide nanoparticles.

Phosphate removal is important in the control of eutrophication of water bodies. Adsorption is one of the promising approaches for the removal of phosphate, which could serve as a supplement for the biological phosphate removal process commonly used in the wastewater treatment industry to meet the discharge requirement when the biological performance is deteriorated from changes of operation conditions. Amorphous zirconium oxide nanoparticles were synthesized by a simple and low-cost hydrothermal process, and their phosphate removal performance was explored in aqueous environment under various conditions.

Superparamagnetic magnesium ferrite nanoadsorbent for effective arsenic (III, V) removal and easy magnetic separation.

By doping a proper amount of Mg(2+) (~10%) into α-Fe2O3 during a solvent thermal process, ultrafine magnesium ferrite (Mg0.27Fe2.50O4) nanocrystallites were successfully synthesized with the assistance of in situ self-formed NaCl "cage" to confine their crystal growth.

The synthesis of nitrogen/sulfur co-doped TiO2 nanocrystals with a high specific surface area and a high percentage of {001} facets and their enhanced visible-light photocatalytic performance.

Nitrogen/sulfur co-doped anatase TiO2 nanocrystals with a high specific surface area and a high percentage of {001} facets were synthesized by a solvent-thermal process followed by the calcination with thiourea at an optimum heat treatment temperature. Under current experimental conditions, the optimum heat treatment temperature was found at 300°C, which successfully introduced nitrogen and sulfur dopants into the anatase lattice to replace a small portion of oxygen atoms while preserving the geometry of these anatase TiO2 nanocrystals to maintain a high percentage of {001} facets. These nitrogen/sulfur co-doped anatase TiO2 nanocrystals demonstrated a largely enhanced light absorption in the whole visible-light range and exhibited much higher photocatalytic performance than both P25 TiO2 nanoparticles and anatase TiO2 nanocrystals with a high percentage of {001} facets under visible-light illumination.

NH4+ directed assembly of zinc oxide micro-tubes from nanoflakes.

A simple precipitation process followed with the heat treatment was developed to synthesize ZnO micro-tubes by self-assembly of nanoflakes composed of nanoparticles. The resulting ZnO micro-tubes demonstrated excellent photocatalytic performance in degrading methylene blue (MB) under UV illumination. It was found that NH4+ ion played a critical role in directing the assembly of the nanoflakes to form the micro-tube structure.

Arsenic (III,V) removal from aqueous solution by ultrafine α-Fe2O3 nanoparticles synthesized from solvent thermal method.

Ultrafine iron oxide (α-Fe(2)O(3)) nanoparticles were synthesized by a solvent thermal process and used to remove arsenic ions from both lab-prepared and natural water samples. The α-Fe(2)O(3) nanoparticles assumed a near-sphere shape with an average size of about 5 nm. They aggregated into a highly porous structure with a high specific surface area of ∼ 162 m(2)/g, while their surface was covered by high-affinity hydroxyl groups.

As(III) removal by hydrous titanium dioxide prepared from one-step hydrolysis of aqueous TiCl(4) solution.

Hydrous titanium dioxide (TiO(2)·xH(2)O) nanoparticles were synthesized by a low-cost one-step hydrolysis process with aqueous TiCl(4) solution. These TiO(2)·xH(2)O nanoparticles ranged from 3 to 8 nm and formed aggregates with a highly porous structure, resulting in a large surface area and easy removal capability from aqueous environment after the treatment. Their effectiveness on the removal of As(III) (arsenite) from water was investigated in both laboratory and natural water samples.