Preparation and in Vitro Antitumor Study of Two-Dimensional Muscovite Nanosheets.

Inorganic nanosheets are endowed with many two-dimensional (2D) morphological features including ultra-high specific surface area, ultra-thin thickness, easy functionalization, and so on. They push forward an immense influence on effective cancer diagnosis and therapy, overcoming the inherent limitations of traditional treatment methods. However, long-term toxicity and poor biocompatibility are the critical issues for most inorganic nanosheets, which hinder their further oncological applications and clinical translations. Muscovite, also named white mica (WM), an aluminosilicate, is a major component of traditional Chinese medicine, which can be exfoliated into 2D nanosheets and expected to be a potential drug carrier. In this study, WM powder was exfoliated to prepare WM nanosheets (WMNs) through a polyamine intercalation method. In addition, doxorubicin hydrochloride (Dox) was loaded to WMNs via physical adsorption and electrostatic interaction to prepare Dox-loaded WMNs (Dox@WMNs). Then, we studied that Dox@WMNs released Dox in phosphate buffer saline. We also studied the cellular uptake and cytotoxicity of Dox@WMNs in vitro. The results illustrated that Dox@WMNs cumulatively released Dox much faster and more at acidic pH (6.0 and 4.6) compared with that at physiological pH. In addition, WMNs showed selective cytotoxicity. Within a certain concentration range, WMNs were cytotoxic to Hela cells but non-cytotoxic to RAW 264.7 cells. Compared with cytotoxicity at pH 7.4, the cytotoxicity of Dox@WMNs was significantly enhanced at pH 6.4 and 4.6. WMNs mainly promoted the immunostimulatory polarization of RAW 264.7 cells into M1 macrophages.

Colossal Volume Contraction in Strong Polar Perovskites of Pb(Ti,V)O3.

The unique physical property of negative thermal expansion (NTE) is not only interesting for scientific research but also important for practical applications. Chemical modification generally tends to weaken NTE. It remains a challenge to obtain enhanced NTE from currently available materials. Herein, we successfully achieve enhanced NTE in Pb(Ti1-xVx)O3 by improving its ferroelectricity. With the chemical substitution of vanadium, lattice tetragonality (c/a) is highly promoted, which is attributed to strong spontaneous polarization, evidenced by the enhanced covalent interaction in the V/Ti-O and Pb-O2 bonds from first-principles calculations. As a consequence, Pb(Ti0.9V0.1)O3 exhibits a nonlinear and much stronger NTE over a wide temperature range with a volumetric coefficient of thermal expansion αV = -3.76 × 10-5/°C (25-550 °C). Interestingly, an intrinsic giant volume contraction (∼3.7%) was obtained at the composition of Pb(Ti0.7V0.3)O3 during the ferroelectric-to-paraelectric phase transition, which represents the highest value ever reported. Such volume contraction is well correlated to the effect of spontaneous volume ferroelectrostriction. The present study extends the scope of the NTE family and provides an effective approach to explore new materials with large NTE, such as through adjusting the NTE-related ferroelectric property in the family of ferroelectrics.

Improved Mechanical Properties of Alumina Ceramics Using Plasma-Assisted Milling Technique.

In order to improve the mechanical properties of alumina ceramics, dielectric barrier discharge plasma-assisted milling (DBDPM) was employed to activate alumina powder. The effect of the plasma-assisted milling technique on the grinding behavior of alumina powder, as well as the microstructure and properties of fabricated alumina ceramic, was investigated in detail. Attributed to the great thermal stress induced via plasma heating, DBDPM showed significantly higher grinding efficiency than the common vibratory milling technique. Moreover, the lattice distortion of alumina grains occurred with the application of plasma, leading to an improved sintering activity of the produced alumina powders. Therefore, compared with the common vibratory milling technique, the fabricated alumina ceramics exhibited smaller grain sizes and improved mechanical properties when using alumina powder produced via the DBDPM method as the starting material.

Applications and perspectives of quaternized cellulose, chitin and chitosan: A review.

Recently, increasing attention has been paid to natural polysaccharides for their low cost, biocompatibility and biodegradability. Quaternization is a modification method to improve the solubility and antibacterial ability of natural polysaccharides. Water-soluble derivatives of cellulose, chitin and chitosan offer the prospect of diverse applications in a wide range of fields, such as antibacterial products, drug delivery, wound healing, sewage treatment and ion exchange membranes. By combining the inherent properties of cellulose, chitin and chitosan with the inherent properties of the quaternary ammonium groups, new products with multiple functions and properties can be obtained. In this review, we summarized the research progress in the applications of quaternized cellulose, chitin and chitosan in recent five years. Moreover, ubiquitous challenges and personal perspectives on the further development of this promising field are also discussed.

Investigation on Application Prospect of Refractories for Hydrogen Metallurgy: The Enlightenment from the Reaction between Commercial Brown Corundum and Hydrogen.

Hydrogenous environments put forward new requirements to refractories for the hydrogen metallurgy field. The temperature and impurities in refractories played an important role in stability. A commercial brown corundum with many impurities was adopted as a raw material, thermodynamic calculations and reduction experiments of the brown corundum by high-purity hydrogen (99.99%) were accepted to investigate the stability of the oxides. The weight loss and mass fraction were tested to estimate the stability of the oxides in the brown corundum. XRD and SEM were used to analyze the mineral compositions and microstructures. The results showed that: the thermodynamic stability of the oxides in the brown corundum under high-purity hydrogen was in the order of Al2O3 > CaO > MgO > SiO2 > TiO2 > Fe2O3 at temperatures lower than 1400 °C. Obvious weight loss appeared after heating at 1400 °C for 8 h. The content of CaO did not decline after reduction even at 1800 °C, owing to the formation of hibonite (CaAl12O19), high-purity Al2O3 and CaAl12O19 -based refractories had the prospect for lining materials in the hydrogen metallurgy field, owing to their excellent chemical stability under hydrogenous environments.

Tumor-triggered targeting ammonium bicarbonate liposomes for tumor multimodal therapy.

Tumor-triggered targeting ammonium bicarbonate (TTABC) liposomes were proposed to improve the uptake of ammonium bicarbonate (ABC) liposomes in tumor cells and retain their long circulation in vivo in our previous study. However, it must be solved how to precisely release the loaded drugs of the TTABC liposomes into tumor cells. In addition, synergistic multimodal therapy could result in better tumor treatment outcomes than monomodal chemotherapy. In the research, we prepared indocyanine green (ICG) and doxorubicin (DOX) encapsulated TTABC liposomes (ICG&DOX@TTABC) to achieve near-infrared (NIR) light-controlled chemo/photothermal/photodynamic multimodal therapy guided by fluorescence and photothermal imaging. In vitro and vivo studies show that ICG&DOX@TTABC can specifically accumulate in tumor tissues, effectively transform NIR light into local thermo-therapy, and have excellent anti-tumor ability without obvious side effects. ICG&DOX@TTABC could be promising for fluorescence and photothermal imaging-guided chemo/photothermal/photodynamic tumor treatment.

Hydrothermal synthesis of CdS nanorods anchored on α-Fe2O3 nanotube arrays with enhanced visible-light-driven photocatalytic properties.

As an n-type semiconductor with an excellent physicochemical properties, iron oxide (Fe2O3) has been extensively used in the fields of environmental pollution control and solar energy conversion. However, the high recombination rate of the photoinduced electron-hole pairs and poor charge mobility for Fe2O3 nanomaterial generally result in low photocatalytic efficiency. Herein, an uniform CdS nanorods grown directly on one-dimensional α-Fe2O3 nanotube arrays (NTAs) are successfully synthesized by a facile hydrothermal method and the constructed heterojunction can be a kind of efficient and recyclable photocatalysts. Successful deposition of CdS nanorods onto the α-Fe2O3 NTAs is verified by field emission scanning electron microscopy(FESEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy (EDS). UV-Vis diffuse reflectance spectroscopy indicates that α-Fe2O3/CdS NTAs possess the intense visible light absorption and also display a red-shift of the band-edge compared with the pure α-Fe2O3 NTAs. The as-obtained α-Fe2O3/CdS NTAs display excellent photocatalytic activity for decomposition of methylene blue (MB), methyl orange (MO), and phenol under visible light illumination. Among all the tested photocatalysts, the film synthesized for 3h with good stability exhibits the best photocatalytic properties and produces the highest photocurrent of 1.43 mA/cm2 at 0.8 V vs. Ag/AgCl electrode, owing to its well formed heterojunction structure, effective electron-hole pair separation and direct electron transfer pathway along the CdS nanorods and α-Fe2O3 NTAs. Besides, the photogenerated holes (h+) and superoxide radicals (O2-) play dominant roles in the photocatalytic process. On the basis of the photocatalytic results and energy band diagram, the photocatalytic process mechanism is proposed. Considering the easy preparation and excellent performance, α-Fe2O3/CdS NTAs could be a promising and competitive visible-light-driven photocatalyst in the field of environment remediation.

In situ growth of self-supported and defect-engineered carbon nanotube networks on 316L stainless steel as binder-free supercapacitors.

Self-supported and defect-engineered carbon nanotube networks directly grown on 316L stainless steel are used for binder-free supercapacitors. In situ growth of the carbon nanotube networks on 316L stainless steel is obtained through the chemical vaporization deposition and thermal treatment to generate various defects. The relationship between the microstructures of carbon nanotube networks and electrochemical characteristics is investigated. The as-prepared carbon nanotube networks are characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and Raman analysis. Cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy tests are also carried out to evaluate their capacitive properties, suggesting that the electrochemical characteristics are significantly affected by annealing time. The carbon nanotube networks annealed at 500 0C for 2 h display high capacitance of 11 mF cm-2 and excellent cycling lifetime with capacitance retention ration 97% at the scan rate of 0.5 mA cm-2 for 5000 periods, which is attributed to the defect engineering increasing the defects of carbon nanotube networks, enhancing hydrophilic property and facilitating the transportation of electrolyte ions.