Preparation of three-dimensional ordered macroporous SiCN ceramic using sacrificing template method

Three-dimensional (3D) long range well ordered macroporous SiCN ceramics were prepared by infiltrating sacrificial colloidal silica templates with the low molecular weight preceramic polymer, polysilazane. This was followed by a thermal curing step, pyrolysis at 1250 °C in a N₂ atmosphere, and finally the removal of the templates by etching with dilute HF. The produced macroporous SiCN ceramics showed high BET surface areas (pore volume) in the range 455 m²/g (0.31 cm³/g)–250 m²/g (0.16 cm³/g) with the pore sizes of 98–578 nm, which could be tailored by controlling the sizes of the sacrificial silica spheres in the range 112–650 nm. The sphere-inversed macropores were interconnected by 50 ± 30 nm windows and 3–5 nm mesopores embedded in the porous SiCN ceramic frameworks, which resulted in a trimodal pore size distribution. The surface of the achieved porous SiCN ceramic was then modified by Pt–Ru nanoparticle depositing under mild chemical conditions.     

Lithium/V6O13 cells using silica nanoparticle-based composite electrolyte

The electrochemical behavior of Li/V₆O₁₃ cells is investigated at room temperature (22 °C) both in liquid electrolyte consisting of oligomeric poly(ethyleneglycol)dimethylether+lithium bis(trifluoromethylsulfonylimide) and composite electrolytes formed by blending the liquid electrolyte with silica nanoparticles (fumed silica). The addition of fumed silica yields a gel-like electrolyte that demonstrates the desirable property of suppressing lithium dendrite growth due to the rigidity and immobility of the electrolyte structure. The lithium/electrolyte interfacial resistance for composite gel electrolytes is less than that for the corresponding base-liquid electrolyte, and the charge-discharge cycle performance and electrochemical efficiency for the Li/V₆O₁₃ cell is significantly improved. The effect of fumed silica surface group on the electrochemical performance is discussed; the native hydrophilic silanol surface group appears better than fumed silica that is modified with a hydrophobic octyl surface moiety.     

Thermo-mechanical properties of LLDPE/SiO2 nanocomposites

Two series of linear low density polyethylene (LLDPE)/SiO₂ nanocomposites were prepared. They were based on two types of commercial LLDPE, one prepared by metallocene (mLLDPE) and the other by traditional Ziegler-Natta (zLLDPE) catalysts, and silica nanoparticles surface treated with dimethyldichlorosilane. The silica nanonparticles used have an average diameter of 16 nm, and their weight fraction varied from 2 up to 10%. The structure and thermal-mechanical features of the nanocomposites were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), dynamic mechanical spectroscopy (DMA) as well as tensile tests. The effect of nanoparticles on crystallinity, and hence to the morphology of the materials was studied. The secondary transitions were also affected by the filler presence, while the tensile properties were reinforced with varying the nanoparticle weight fraction. The addition of the nanofillers brought up an increase in the elastic modulus and the tensile strength of mLLDPE accompanied by an unusual dramatic increase in the elongation at break. The same trend, although to a lesser extent, was observed for the zLLDPE/SiO₂ composites. The increment of the elastic modulus of the composites with increasing filler content was simulated with three micromechanical models developed in previous works. The model which assumes an effective interface between the matrix and the nanoparticles provided the best fitting with the experimental data of mLLDPE/SiO₂.     

Rheology of cementitious paste with silica fume or limestone

The rheological behaviour of cementitious pastes where cement has increasingly been replaced by densified silica fume (SF), untreated SF or limestone has been studied. The effect of SF on the flow resistance, taken as the area under the flow curve, was found to depend on the dispersing ability of the plasticizer as illustrated by pastes with naphtalene sulphonate-formaldehyde condensate (SNF) and polyether grafted polyacrylate (PA).The gel strengths increased with increasing SF replacement of cement independently of plasticizer type. The cementitious gel strength was, however, depending on the type of SF since pastes with densified SF developed lower gel strengths than pastes with untreated SF. This phenomenon was attributed to agglomerates in the densified SF which remained unbroken by the mixing and measurement sequence.Both flow resistance and gel strength decreased with increasing limestone replacement. Thus, silica fume may have an advantage over limestone filler as stabilizing agent for self-compacting concrete preventing segregation upon standing and reduced form pressure due to a more rapid gel formation.     

Properties of lightweight expanded polystyrene concrete reinforced with steel fiber

Expanded polystyrene (EPS) concrete is a lightweight, low strength material with good energy-absorbing characteristics. However, due to the light weight of EPS beads and their hydrophobic surface, EPS concrete is prone to segregation during casting, which results in poor workability and lower strength. In this study, a premix method similar to the ‘sand-wrapping’ technique was utilized to make EPS concrete. Its mechanical properties were investigated as well. The research showed that EPS concrete with a density of 800-1800 kg/m³ and a compressive strength of 10-25 MPa can be made by partially replacing coarse and fine aggregate by EPS beads. Fine silica fume greatly improved the bond between the EPS beads and cement paste and increased the compressive strength of EPS concrete. In addition, adding steel fiber significantly improved the drying shrinkage.     

Effect of silica fume and fly ash on heat of hydration of Portland cement

Results of calorimeter tests on Portland cement-silica fume-fly ash mixtures are presented. Data indicate that silica fume accelerates cement hydration at high water/cementitious ratios and retards hydration at low water/cementitious ratios. On the other hand, fly ash retards cement hydration more significantly at high water/cementitious ratios. When silica fume and fly ash are added together with cement, the reactivity of the silica fume is hampered and the hydration of the cementitious system is significantly retarded.     

石英砂高温改性对酯硬化水玻璃砂性能的影响

通过对由平度人造石英砂、围场砂和梧龙砂高温改性后混制的水玻璃砂铸造工艺性能的研究，发现在环境温度和湿度相同的条件下，随焙烧温度升高，型砂的抗拉强度提高；相同的焙烧温度下，高温焙烧对不同原砂的改性作用不同；对三种原砂而言，其抗拉强度还受到环境湿度和温度的影响，在相同的环境温度下，湿度越大，水玻璃砂的抗拉强度越低。提出了石英砂高温改性对酯硬化水玻璃砂性能的影响规律。     

Coating nanodiamonds with biocompatible shells for applications in biology and medicine

Use of nanodiamonds (NDs) as nontoxic nanoparticles for biological imaging, sensing, and drug delivery is expanding rapidly. The interest in NDs is triggered by their unique combination of optical properties. ND can accommodate nitrogen-vacancy color centers which provide stable fluorescence without photobleaching or photoblinking and their electronic structure is very sensitive to magnetic and electric fields. The limited options to control ND properties during synthesis or by direct surface functionalization leave room to be improved upon by employing surface coatings engineered precisely for a particular application. The major disadvantages of unmodified NDs are their limited colloidal stability and tendency to non-specifically adsorb biomolecules. This review aims to summarize recent advances in coating NDs (namely with silica and polymer shells), which addresses these disadvantages and enables the use of NDs in biological applications such as targeting of specific cells, drug delivery, and biological imaging.     

Experimental tracking of silica dispersion into silicone polymer

This work deals with the experimental tracking of a dispersion of very fine silica particles in PDMS using a new, easily implemented methodology. The dispersion experiments are carried out in an 8-l capacity mixer equipped with a torquemeter. Using a Couette analogy, the torque-rotational speed data can be converted into process viscosity-effective shear rate data. Simultaneously, the Particle Size Distribution (PSD) evolution is followed through Laser Light Scattering measurements on diluted samples. The PSD evolution allowed us to interpret the dispersion process in terms of different mechanisms, such as breaking-up and erosion of aggregates, as well as, in some cases, re-agglomeration (or flocculation) of particles.     

Quaternary Ammonium Salts (QAS) Modified Polysiloxane Biocide Supported on Silica Materials

Three types of silica particles modified with vinyl groups were obtained: (i) xerogel formed by hydrolytic polycondensation of the mixture of tetramethoxysilane (TMOS) and 1,1,1,7−tetramethoxy-3,5,7-trimethyl-3,5,7-trivinyltetrasiloxane, (ii) mesoporous silica obtained from the same precursors in the presence of the cetyltrimethylammonium bromide (CTAB), and (iii) commercial Fluka silica gel 60A with a vinyltriethoxysilane-treated surface. Vinyl groups on these silica materials were transformed into silyl chloride by hydrosilylation with HMe₂SiCl. These groups were used to graft living polysiloxane that was synthesized by anionic ring-opening polymerization of 2,4,6-tri(3-chloropropyl)-2,4,6-trimethylcyclotrisiloxane and initiated by BuLi. Chloropropyl groups on the grafted polymer were used to quaternize N,N-dimethyl-n-octylamine. Silica particles with grafted polysiloxane having quaternary ammonium salt (QAS) groups pendant to polymer chains were obtained. Silica material with QAS groups directly attached to the surface were generated by the action of N,N-dimethyl-n-octylamine on particles obtained by the sol–gel process involving tetraethoxysilane (TEOS) with 3-chloropropyltriethoxysilane. The bacteriocidal properties of all these materials were tested in water suspension against five representative strains for Gram-positive and Gram-negative bacteria. Some of the silica–polysiloxane hybrid materials have good antibacterial properties against Gram-positive strains, but not as good as the non-tethered QAS-substituted polysiloxane in water solution. The QAS groups that are directly bonded to the silica material surface are inactive.