Micron-sized silica mesh for enhancing the performance of quantum dot sensitized solar cells

Three dimensional silica mesh structures are prepared through a new and simple method for enhancing the quantum dot sensitized solar cells performance and stability.Silica patterns are made on the top of the TiO₂ photoanodes and a marked improvement in light scattering properties of meshed structures is confirmed by diffuse reflectance spectroscopy measurements. This improvement enhances the current density and consequently the cells ‘efficiency. Parameters of electron transport in cells are explored by electrochemical impedance spectroscopy (EIS). According to the EIS results, silica mesh declines the recombination rate in cells in a clear way. Here more than 50% efficiency improvement is obtained in meshed structures in comparison to cells with normal TiO₂ photoanode structures. The insulated silica mesh, reduces the electrolyte's deleterious effect on the semiconductor layers and the cells’ stability is improved.     

Multilayer Si@SiOx@void@C anode materials synthesized via simultaneously carbonization and redox for Li-ion batteries

In the development of high-performance lithium-ion batteries (LIBs), the composition and structure of electrode materials are of critical importance. Silicon has a theoretical specific capacity 10 times that of graphite, nonetheless, its application as an anode material confronts challenge as it undergoes huge volume change and pulverization amidst the alloying and dealloying processes. Herein, a novel method to prepare a multilayer Si-based anode was proposed. Three layers, SiO₂, nickel and triethylene glycol (TEG), were coated successively on Si nanoparticles, which served respectively as the sources of SiO_x, sacrificial templates and carbon. Nickel can not only serve as a hollow template, but also play a catalytic role, which makes carbonization and redox reactions occur synchronously under a mild condition. Amid the carbonization process of TEG at 450 °C, several-nm-thick SiO₂ layer can react with the as-derived carbon to form a silicon suboxides (SiO_x (0 < x < 2)) intermedium layer. After removing the nickel template, a micro-nano scaled Si@SiO_x@void@C with conformal multilayer-structure can be obtained. The BET specific surface area and pore volume of powders were increased dramatically because of the derivation of abundant voids, which can not only buffer the swelling effect of silicon, but also provide richer ionic conductivity. The as-assembled half-cell with Si@SiOx@void@C as the anode material possesses high capacity (～1000 mAh g^?1 at 3 A g^?1), long cycle life (300 cycles with 77% capacity retention) and good rate performance (558 mAh g^?1 at 5 A g^?1).     

Compound surfactant-based emulsion method for the preparation of high-porosity alumina microspheres

Porous alumina microspheres have attracted significant attention owing to their high mechanical strength and excellent chemical and thermal stability. The emulsion method is considered as a simple and controllable method for the preparation of inorganic microspheres. However, preparing alumina microspheres with the emulsion method is challenging because the emulsification of the precursor is inhibited by the rapid hydrolysis of aluminum alkoxide. Herein, we report a new emulsion method for the preparation of high-porosity alumina microspheres using a combination of ionic and non-ionic surfactants; in this method, the compound surfactants act as a template agent to guide aluminum alkoxide to form a lamellar structure through self-assembly. The decomposition of the templating agent and transformation of the alumina crystal at a high temperature result in structural collapse and formation of lamellar pores. Compound surfactants increased the spheroidization rate of the emulsion from 47% to 63% after hydrolysis, whereas the particle size was decreased by almost half. Additionally, the morphology and porosity of the alumina microspheres were changed. With increasing anionic surfactant content, the porosity increased initially and then decreased. The porosity of the alumina microspheres reached a maximum value of 76% at the 1:1 mass ratio of the non-ionic to anionic surfactants. Heat treatment was found to change the size of lamellar pores, with the pore diameter reaching maximum value at 1300 °C. The compound surfactants also increased the compressive stress and specific surface area of the porous alumina microspheres.     

Effect of Nanoparticles on Viscosity and Interfacial Tension of Aqueous Surfactant Solutions at High Salinity and High Temperature

Surfactant flooding has widely been used as one of the chemically enhanced oil recovery (EOR) techniques. Surfactants majorly influence the interfacial tension, γ, between oil and brine phase and control capillary number and relative permeability behavior and, thus, influence ultimate recovery. Additives, such as nanoparticles, are known to affect surfactant properties and are regarded as promising EOR agents. However, their detailed interactions with surfactants are not well understood. Thus, in this work, we examined the influence of silica nanoparticles on the ability of surfactants to lower γ and to increase viscosity at various temperatures and salinities. Results show that the presence of nanoparticles decreased γ between n-decane and various surfactant formulations by up to 20%. It was found that γ of nanoparticles–surfactant solutions passed through a minimum at 35 °C when salt was added. Furthermore, the viscosity of cationic surfactant solutions increased at specific salt (1.5 wt.%) and nanoparticle (0.05 wt.%) concentrations. Results illustrate that selected nanoparticles–surfactant formulations appear very promising for EOR as they can lower brine/n-decane interfacial tension and act as viscosity modifiers of the injected fluids.     

Hollow hierarchical Ni/MgO-SiO2 catalyst with high activity,thermal stability and coking resistance for catalytic dry reforming of methane

The methane dry reforming (DRM) simultaneously converts the two greenhouse gases and produces syngas (CO + H₂), which is being significant for both environmental and industrial consideration. Employing well-defined crystal oxides as precursors can produce Ni-based DRM catalysts with good sintering and coking resistance by enhancing the metal-support interactions. Adding basic promoters also is considered as an effective way to improve the coking resistance of DRM catalysts, although challenge remains in the control over the structure, morphology and interaction of the promoter in the catalyst. To well combine the two methods together for better catalytic performance, in this work a Ni/MgO-SiO₂ catalyst was synthesized through a facile one-pot hydrothermal process, during which Ni-phyllosilicate formed as the precursor of Ni particles and MgO promoter was generated in form of Mg-phyllosilicate. This Ni/MgO-SiO₂ had a hierarchical hollow sphere structure with large surface area (477.4 m²/g). Both the Ni particles (avg. 6.0 nm) and MgO promoter uniformly distributed. This hollow hierarchical catalyst performed high activity, thermal stability and coking resistance for catalytic dry reforming of methane.     

Study of physicochemical properties of flutamide-loaded Ocimum basilicum microspheres with ex vivo mucoadhesion and in vitro drug release

Drug which shows extensive first pass effect is difficult task that, needs to be solved by formulators in the pharmaceutical science. The low oral bioavailability (49%) of flutamide may be due to poor wettability, low aqueous solubility and extensive first pass effect. The aim of present investigation was to prepare flutamide loaded microspheres and incorporate it into suppositories for rectal delivery to avoid first pass effect and enhance residence time. Flutamide loaded mucoadhesive microspheres of Ocimum Basilicum mucilage (OBM) were prepared using spray drying and characterized by percent production yield, encapsulation efficiency, particle size, zeta potential, polydispersity index, DSC, SEM, XRPD, in vitro drug release and stability studies. Moreover, ex vivo mucoadhesion was investigated using falling liquid film technique to determine the adhesion of microspheres to sheep rectal mucosa. The microspheres had nearly spherical shape and size about 2.53?μm. The encapsulation efficiency and mucoadhesion of optimized formulation MBF10 were found to be 69.6?±?2.3% and 89.01?±?2.18%, respectively. Percent CDR of optimized flutamide loaded mucoadhesive microspheres was found to be 88.7?±?1.3 at 7?h. In conclusion, OBM microparticles based suppository could be used to deliver drug through rectal delivery.     

Preparation of microencapsulated carbon microspheres coated by magnesium hydroxide/polyethylene terephthalate flame–retardant functional fibers and its flame retardant properties

In order to improve the compatibility between the flame retardants of carbon microspheres coated by magnesium hydroxide (MH@CMSs) and the PET matrix and improve the spinnability of the masterbatch, MH@CMSs have been microencapsulated by PET to obtain microencapsulated carbon microspheres coated by magnesium hydroxide flame retardants – MMH@CMSs.Morphologies and structures of MMH@CMSs have been studied by scanning electron microscope (SEM), transmission electron microscopy (TEM), and FTIR, which showed that an organic shell layer of PET as capsule wall was coated on the surface of MH@CMSs. A series of MMH@CMSs/PET fibers with different MMH@CMSs contents were successfully prepared through the melt-spinning method. The morphology and structure of MMH@CMSs/PET fibers were characterized by SEM and FTIR. The flame retardancy of MMH@CMSs/PET fibers was determined via limiting oxygen index (LOI) test and cone calorimeter. Results showed that the MMH@CMSs/PET fibers possessed optimum flame retardancy when the MMH@CMSs content is 0.6 wt.%, at which the LOI reached a maximum of 25.8, and the pk-HRR, total heat release, and total smoke release were reduced by 27.4, 20, and 13.6%, compared with pure PET fibers, respectively. Moreover, the flame-retardant mechanism was studied by thermogravimetric analysis, thermogravimetric analysis-infrared spectrometry, and the SEM of the residue char, which disclosed that MMH@CMSs enhanced the thermal stability of PET fibers, and promoted PET fibers to form a dense and continuous protective char layer that effectively blocked heat transfer and combustible gas release.     

炭黑和白炭黑对全钢载重子午线轮胎胎面胶生热和动态力学性能的影响

在全钢载重子午线轮胎胎面胶中加入不同用量炭黑N234,并将白炭黑与炭黑并用,考察炭黑用量和添加白炭黑对胶料性能的影响。结果表明:随着炭黑N234用量增大,不添加白炭黑的胶料Fmax和门尼粘度增大,门尼焦烧时间呈缩短趋势;密度、硬度和定伸应力提高,拉伸强度和回弹值降低,撕裂强度先提高后降低,耐磨性能提高,生热增大,炭黑用量不宜过大;在填料用量相当的条件下,添加白炭黑的胶料门尼粘度较小,门尼焦烧时间较短,撕裂强度和耐磨性能显著提高,生热明显降低;随着炭黑用量增大,不添加白炭黑的胶料弹性模量和损耗因子总体提高;总体来看,添加45份炭黑N234和10份白炭黑的胎面胶滞后损失和生热较低。     

Morphology control of ordered supermicroporous silicas

A feasible method has been developed for the morphology control of ordered supermicroporous silicas by adopting a kind of rosin-based surfactant as the templating agent. By adjusting the molar ratio of sodium silicate (SS) and ethyl acetate (EA), the morphologies of the materials can be changed from hollow sphere to hollow tube, and solid rod, while the degree of ordering of the samples showed a trend of firstly increasing and then decreasing. When the molar ratio of SS/EA was 0.38, an ordered supermicroporous silica with a hollow tubular morphology was obtained. The material had a surface area of 645.5 m²/g, a pore volume of 0.3 cm³/g, and a pore size distribution centered at 1.8 nm. When the molar ratio of SS/EA was increased to 0.46, the resulting sample exhibited a solid-rod morphology with a highly ordered hexagonal supermicroporous structure. This material had a large surface area of 1478.1 m²/g, a high pore volume of 0.7 cm³/g, and a uniform pore size distribution centered at 2.0 nm.     

Elastic modulus prediction based on thermal conductivity for silica aerogels and fiber reinforced composites

The speed of sound is a critical parameter in the test of mechanical and thermal properties. In this work, we proposed a testing method to obtain the elastic modulus of silica aerogel from the sound speed formulas. The solid thermal conductivity of the silica aerogel is experimentally measured for predicting the sound speeds, and then the elastic modulus is calculated based on the elasticity sound speed model. The experimental data of the solid thermal conductivity of silica aerogels with different densities are employed and the obtained elastic modulus is fitted as a power-law exponential function of the density. Two existing sound speed models and three groups of available experimental data are also employed to validate the present fitting relation, and good agreement is obtained for the silica aerogel in the density range of 150–350 kg/m³. The fitting formula can also be extended to estimate the elastic modulus of the glass fiber-reinforced silica aerogel composite. The results show that the elastic modulus of the aerogel composite is sensitive to the glass fiber volume fraction, while the thermal conductivity is weakly dependent on the glass fiber volume fraction at room temperature in the studied range of fiber volume fraction.