Microstructure and Properties of TiCp/Fe Hierarchical Composites Prepared by a New Pressure Infiltration Method.

TiCp/steel composites are conventionally produced via powder metallurgy. In this paper, a liquid pressure infiltration method was developed to prepare a kind of spherical hierarchical architectured composite, in which spherical TiCp-rich hard phase regions were uniformly dispersed in TiCp-free soft phase region. The microstructure and mechanical properties of the architectured composites were carefully studied and compared with the common composite, as well as the effect of TiCp fraction on the properties. The results show that architecturual design can effectively improve both the toughness and strength of the composites. With TiCp content increasing from 30% to 50%, both the bending strength and the impact toughness of the architectured composites first increase, then decrease, and reach the highest at 40% TiCp. The highest impact toughness reaches 21.2 J/cm2, being 6.2 times that of the common composite and the highest strength being 67% higher. The pressure infiltration method possesses adaptability to varying shapes and sizes of the products, allowing for large-scale preparation. Therefore, for the first time, the combination of pressure infiltration preparation and architectural design was applied to TiCp/steel composites.

Highly efficient charge transfer from small-sized cadmium sulfide nanosheets to large-scale nitrogen-doped carbon for visible-light dominated hydrogen evolution.

Slow charge transfer and carrier recombination are key issues in photocatalytic reactions. The current solution is to load small-sized cocatalysts onto large-sized photocatalysts. Here a new strategy is proposed. Small-sized photocatalysts of cadmium sulfide (CdS) nanosheets are grown onto large-sized cocatalysts of N-doped amorphous carbon (a-CN) to construct CdS @ a-CN photocatalysts. Photoluminescence spectra and transient photocurrent demonstrate that optimized CdS @ a-CN shows effective charge separation compared with CdS. The corresponding photocatalytic H2 yield of optimized CdS @ a-CN is âˆ¼244 µmol, which is 3.6 times higher than that of CdS. Besides, the hydrogen yield for CdS under visible-light irradiation is significantly improved from âˆ¼44 µmol to âˆ¼217 µmol for the optimized CdS @ a-CN. Our design strategy provides an effective way to construct photocatalytic systems with outstanding photocatalytic performance.

Redox and pH responsive polymeric vesicles constructed from a water-soluble pillar[5]arene and a paraquat-containing block copolymer for rate-tunable controlled release.

Herein, for rate-tunable controlled release, pH and redox dual responsive polymeric vesicles were constructed based on host-guest interaction between a water soluble pillar[5]arene (WP5) and a paraquat-containing block copolymer (BCP) in water. The yielding polymeric vesicles can be further applied in the controlled release of a hydrophilic model drug, doxorubicin hydrochloride (DOX). The drug release rate is regulated depending on the type of single stimulus or the combination of two stimuli. Meanwhile, DOX-loaded polymeric vesicles present anticancer activity in vitro comparable to free DOX under the studied conditions, which may be important for applications in the therapy of cancers as a controlled-release drug carrier.

Glucose- and H2O2-Responsive Polymeric Vesicles Integrated with Microneedle Patches for Glucose-Sensitive Transcutaneous Delivery of Insulin in Diabetic Rats.

Herein, a dual-responsive insulin delivery device by integrating glucose- and H2O2-responsive polymeric vesicles (PVs) with transcutaneous microneedles (MNs) has been designed. This novel microneedle delivery device achieves a goal of fast response, excellent biocompatibility, and painless administration. The PVs are self-assembled from a triblock copolymer including poly(ethylene glycol), poly(phenylboronic acid) (glucose-sensitive block), and poly(phenylboronic acid pinacol ester) (H2O2-sensitive block). After loading with insulin and glucose oxidase (GO x), the drug-loaded PVs display a basal insulin release as well as a promoted insulin release in response to hyperglycemic states. The insulin release rate responds quickly to elevated glucose and can be further promoted by the incorporated GO x, which will generate the H2O2 at high glucose levels and further break the chemical links of phenylboronic acid pinacol ester group. Finally, the transdermal delivery of insulin to the diabetic rats ((insulin + GO x)-loaded MNs) presents an effective hypoglycemic effect compared to that of subcutaneous injection or only insulin-loaded MNs, which indicates the as-prepared MNs insulin delivery system could be of great importance for the applications in the therapy of diabetes.

Influence of Al-oxide on pesticide sorption to woody biochars with different surface areas.

Biochars' properties will change after application in soil due to the interactions with soil constituents, which would then impact the performance of biochars as soil amendment. For a better understanding on these interactions, two woody biochars of different surface areas (SA) were physically treated with aluminum oxide (Al-oxide) to investigate its potential influence on biochars' sorption property. Both the micropore area and mesopore (17∼500 Å in diameter) area of the low-SA biochar were enhanced by at least 1.5 times after treatment with Al-oxide, whereas the same treatment did not change the surface characteristics of the high-SA biochar due partly to its well-developed porosity. The enhanced sorption of the pesticide isoproturon to the Al-oxide-treated low-SA biochar was observed and is positively related to the increased mesopore area. The desorption hysteresis of pesticide from the low-SA biochar was strengthened because of more pesticide molecules entrapped in the expanded pores by Al-oxide. However, no obvious change of pesticide sorption to the high-SA biochar after Al-oxide treatment was observed, corresponding to its unchanged porosity. The results suggest that the influence of Al-oxide on the biochars' sorption property is dependent on their porosity. This study will provide valuable information on the use of biochars for reducing the bioavailability of pesticides.

Role of Alumina and Montmorillonite in Changing the Sorption of Herbicides to Biochars.

The influence of biochars on the fate of herbicides in soil depends mostly on environmental factors among which the role of soil minerals is not clear. Two wood-derived biochars produced at 400 °C (BC400) and 600 °C (BC600) were treated with alumina and montmorillonite to investigate their interaction with biochars and the influence of herbicide sorption. Both minerals exhibited a pore-expanding effect that was likely relative to the removal of authigenic organic matter away from the biochars' surface. Alumina brought more remarkable pore expansion by doubling the surface area of the BC400 biochar and the mesopore area of the BC600 biochar. Consequently, more adsorption sites were accessible for herbicide molecules, which resulted in higher sorption of herbicides (acetochlor and metribuzin) to the mineral-treated biochars than to the untreated biochars. The results are useful for understanding the change of surface and sorption properties of biochars with soil applications.