Effect of silica coating thickness on the thermal conductivity of polyurethane/SiO2 coated multiwalled carbon nanotube composites

Silica coated multiwalled carbon nanotubes (SiO₂@MWCNTs) with different coating thicknesses of ∼4 nm, 30–50 nm, and 70–90 nm were synthesized by a sol–gel method and compounded with polyurethane (PU). The effects of SiO₂@MWCNTs on the electrical properties and thermal conductivity of the resulting PU/SiO₂@MWCNT composites were investigated. The SiO₂ coating maintained the high electrical resistivity of pure PU. Meanwhile, incorporating 0.5, 0.75 and 1.0 wt% SiO₂@MWCNT (70–90 nm) into PU, produced thermal conductivity values of 0.287, 0.289 and 0.310 W/mK, respectively, representing increases of 62.1%, 63.3% and 75.1%. The thermal conductivity of PU/SiO₂@MWCNT composites was also increased by increasing the thickness of the SiO₂ coating.     

Strength development of alkali-activated fly ash produced with combined NaOH and Ca(OH)2 activators

Alkali-activated matrices can attain compressive strengths of the order of 30–120 MPa, primarily depending on the mix formulation. The objective of this study is to evaluate compressive strength development by testing, at different ages, fly-ash-based mortars alkali-activated with activating solutions containing varying proportions of a combination of NaOH and Ca(OH)₂. The NaO/SiO₂ ratio was constant for all samples (N/S = 0.3). Three different CaO/SiO₂ molar ratios of the total quantity of CaO to the total quantity of SiO₂ present in the mix were studied; specifically: 0.05 (C/N = 0.033) – M5; 0.15 (C/N = 0.370) – M15; and 0.25 (C/N = 0.700) – M25. The M25 mix attained compressive strength of 30 MPa at 7 days. However, after periods of 28 and 91 days, M25 compressive strength had decreased to 22 MPa and 16 MPa respectively. The M15 matrices exhibited similar compressive strength results. In contrast, the M5 mix exhibited increasing compressive strength over time. The SEM micrographs of M5 and M25 matrices showed the presence of two different aluminosilicate gels: the M5 sample developed a massive aluminosilicate gel over time, while the M25 sample began to exhibit a spongy gel at 28 days, resulting in a weaker material. Therefore, the reduction in compressive strength appears to be related to increasing amounts of CaO (higher C/S and C/N) for the alkali-activated matrices tested in this study.     

Enhanced photocatalytic property of nanoporous TiO2/SiO2 micro-particles prepared by aerosol assisted co-assembly of nanoparticles

Nanoporous TiO₂/SiO₂ composite micro-particles were prepared by an aerosol assisted co-assembly (AACA) and their characteristics were investigated for photocatalytic application. The average diameter of resulting co-assembled TiO₂/SiO₂ particles was ranged 4–10 μm, and increased as the precursor concentration increased. The TiO₂/SiO₂ particles were spherical in shape and pores ranged 1–100 nm in diameter. Photocatalytic activity of the as-prepared nanoporous TiO₂/SiO₂ particles was evaluated by measuring the photodegradation of methylene blue (MB) and NO_x. Furthermore, the photocatalytic activity of nanoporous TiO₂/SiO₂ particles was compared with those of commercial TiO₂ nanoparticles and nanoporous TiO₂ particles. The nanoporous TiO₂/SiO₂ particles exhibited the highest photodegradation of MB and NO_x among three samples, which was 80% after 3 h and 55% at 10 min, respectively.     

Synthesis and functionalization of SiO2 coated Fe3O4 nanoparticles with amine groups based on self-assembly

The purpose of this research was to synthesize amino modified Fe₃O₄/SiO₂ nanoshells for biomedical applications. Magnetic iron-oxide nanoparticles (NPs) were prepared via co-precipitation. The NPs were then modified with a thin layer of amorphous silica. The particle surface was then terminated with amine groups. The results showed that smaller particles can be synthesized by decreasing the NaOH concentration, which in our case this corresponded to 35 nm using 0.9 M of NaOH at 750 rpm with a specific surface area of 41 m² g^? 1 for uncoated Fe₃O₄ NPs and it increased to about 208 m² g^?1 for 3-aminopropyltriethoxysilane (APTS) coated Fe₃O₄/SiO₂ NPs. The total thickness and the structure of core-shell was measured and studied by transmission electron microscopy (TEM). For uncoated Fe₃O₄ NPs, the results showed an octahedral geometry with saturation magnetization range of (80–100) emu g^?1 and coercivity of (80–120) Oe for particles between (35–96) nm, respectively. The Fe₃O₄/SiO₂ NPs with 50 nm as particle size, demonstrated a magnetization value of 30 emu g^?1. The stable magnetic fluid contained well-dispersed Fe₃O₄/SiO₂/APTS nanoshells which indicated monodispersity and fast magnetic response.     

Effect of SiO2 nanoparticles on the phase transformation of TiO2 in micron-sized porous TiO2–SiO2 mixed particles

Spherical and nanoporous TiO₂ and TiO₂–SiO₂ mixed micro-particles with four different compositions (20/80, 50/50, 80/20, 90/10 in weight ratio of TiO₂/SiO₂) were prepared by spray drying method from colloidal mixtures of amorphous silica and anatase titania nanoparticles. The as-prepared particles were heat-treated at 900 °C for 0.5–5 h. The TiO₂ and TiO₂–SiO₂ particles were spherical in shape and the average particle diameter was about 1 μm. The anatase mass fraction and the specific surface area of TiO₂–SiO₂ (50 wt.% SiO₂) mixed particles were kept to 61.5% and 30.6%, respectively, of their initial values after 5 h heat-treatment whereas these values of TiO₂ particles were rapidly decreased to 13.0% and 1.2% of their initial values, respectively, within 30 min after heat-treatment. And the anatase mass fraction and specific surface area increased as SiO₂ content in the TiO₂–SiO₂ mixed particles increased.     

The photoluminescence and optical constant of ZnSe/SiO2 thin films prepared by sol–gel process

In this paper, ZnSe/SiO₂ thin films were prepared by sol–gel process. X-ray diffraction results indicate that the phase structure of ZnSe particles embedded in SiO₂ thin films is sphalerite (cubic ZnS). The dependence of ellipsometric angle ψ on wavelength λ of ZnSe/SiO₂ thin films was investigated by spectroscopic ellipsometers. The optical constant, thickness, porosity and the concentration of ZnSe/SiO₂ composite thin films were fitted according to Maxwell–Garnett effective medium theory. The thickness of ZnSe/SiO₂ thin films was also measured by surface profile. The photoluminescence properties of ZnSe/SiO₂ thin films were investigated by fluorescence spectrometer. The photoluminescence results reveal that the emission peak at 487 nm (2.5 eV) excited by 395 nm corresponds to the band-to-band emission of sphalerite ZnSe crystal (2.58 eV). Strong free exciton emission and other emission peaks corresponding to ZnSe lattice defects are also observed.     

Compressive strength and microstructural characteristics of class C fly ash geopolymer

Geopolymers prepared from a class C fly ash (CFA) and a mixed alkali activator of sodium hydroxide and sodium silicate solution were investigated. A high compressive strength was obtained when the modulus of the activator viz., molar ratio of SiO₂/Na₂O was 1.5, and the proper content of this activator as evaluated by the mass proportion of Na₂O to CFA was 10%. The compressive strength of these samples was 63.4 MPa when they were cured at 75 °C for 8 h followed by curing at 23 °C for 28 d. In FTIR spectroscopy, the main peaks at 1036 and 1400 cm^?1 have been attributed to asymmetric stretching of Al–O/Si–O bonds, while those at 747 cm^?1 are due to the Si–O–Si/Si–O–Al bending band. The main geopolymeric gel and calcium silicate hydrate (C–S–H) gel co-exist and bond some remaining unreacted CFA spheres as observed in XRD and SEM–EXDA. The presence of gismondine (zeolite) was also observed in the XRD pattern.     

Optical characterization of In2S3–SiO2 nanocomposite thin films synthesized by sol–gel technique

In₂S₃–SiO₂ nanocomposite films (with molar ratios of In₂S₃:SiO₂ = 15:85, 10:90 and 5:95) were prepared on quartz substrates by sol–gel method. Highly confined nanoparticles of In₂S₃ (radius ∼ 1.8–7 nm) were obtained in SiO₂ matrix, indicating SiO₂ to be a good capping agent for the nanoparticles. The films were annealed in air at different temperatures (473–623 K) and characterized by optical, microstructural and photoluminescence measurements. XRD studies showed that annealing in air upto 623 K leads to the formation of oxide free In₂S₃ nanoparticles. The broad Photoluminescence peak observed at ∼353 nm showed a marked blue shift associated with a decrease in intensity with increasing concentration of In₂S₃ in the matrix.     

CdS nanoparticles incorporated onion-like mesoporous silica films: Ageing-induced large stokes shifted intense PL emission

CdS nanoparticles (NPs) were generated in onion-like ordered mesoporous SiO₂ films through a modified sol–gel process using P123 as a structure directing agent. Initially Cd²⁺ doped (12 equivalent mol% with respect to the SiO₂) mesoporous SiO₂ films were prepared on glass substrate. These films after heat-treatment at 350 °C in air yielded transparent mesoporous SiO₂ films having hexagonally ordered onion-like pore channels embedded with uniformly dispersed CdO NPs. The generated CdO NPs were transformed into CdS NPs after exposing the films in H₂S gas at 200 °C for 2 h. The as-prepared CdS NPs incorporated mesoporous SiO₂ films (transparent and bright yellow in color) showed a band-edge emission at 485 nm and a weak surface defect related emission at 530 nm. During ageing of the films in ambient condition the band-edge emission gradually weakened with time and almost disappeared after about 15 days with concomitant increase of defect related strong surface state emission band near 615 nm. This transformation was related to the decay of initially formed well crystalline CdS to relatively smaller and weakly crystalline CdS NPs with surface defects due to gradual oxidation of surface sulfide. At this condition the embedded CdS NPs show large Stokes shifted (∼180 nm) intense broad emission which could be useful for luminescent solar concentrators. The detailed process was monitored by UV–Visible, FTIR and Raman spectroscopy, XPS, XRD and TEM studies. The evolution of photoluminescence (PL) and life times of CdS/SiO₂ films were monitored with respect to the ageing time.     

Crystallization and spectroscopic properties investigations of Er3+ doped transparent glass ceramics containing CaF2

Transparent oxyfluoride glass ceramics with composition of 45SiO₂–25Al₂O₃–5CaCO₃–10NaF–15CaF₂–0.5ErF₃ (in mol%) were developed through controlled crystallization of melt-quenched glass. Non-isothermal crystallization kinetics investigation showed that the average apparent activation energy E_a and Avrami exponent n are about 283 kJ/mol and 2.22, respectively, indicating the crystallization a three dimensional crystal growth process controlled by the diffusion with a decreasing nucleation rate. X-ray diffraction (XRD) analysis and transmission electron microscopy (TEM) observation revealed the precipitation of CaF₂ crystallites sized about 15 nm among the glass matrix after heat-treatment at 650 °C for 2 h. For as-made glass, no upconversion signals were detected when excited with a 30 mW diode laser at 980 nm, while strong upconversion emissions at 545, 660 and 800 nm were obtained for transparent glass ceramic under similar excitation condition.     

Evolution of alkaline activated ground blast furnace slag–ultrafine palm oil fuel ash based concrete

The two locally available pozzolanic solid wastes (PMs) – ultrafine palm oil fuel ash (UPOFA) and ground blast furnace slag (GBFS) – have been used as base materials to develop high alkaline activated strength concrete. The samples were prepared with combined aggregate modulus of 3.66 and at constant GBFS/PM that varied from 0 to 0.3. The combined alkaline activators (CAA) (Na₂SiO₃ and NaOH) to PMs ratios (CAA/PMs), temperature and curing durations also varied as 0.45–0.55, 25–90 °C, and 6–24 h, respectively. The findings revealed that the strength at 3-day and 28-day were 69.13 and 71.2 MPa, respectively and the respective optimum GBFS/PM, CAA/PM, temperature and curing duration are 0.2, 0.5, 60 °C and 24 h. GBFS was found to contribute to the soluble Ca, heterogeneity, and amorphousity of the product. This eventually facilitated the formation of suspected calcium-silicate-hydrate and the geopolymer products of Ca/Na-aluminosilicate-hydrate (C/NASH) that enhanced the compressive-strength results.     

Agglomerating vibro-fluidization behavior of nano-particles

An experiment study of agglomerating fluidization behavior of three kinds of nano-particles (SiO₂, TiO₂, ZnO) in vibro-fluidized bed (VFB) has been performed. At certain amplitude (3 mm) of vibrations applied, the minimum fluidization velocity decreases, whilst the equilibrium pressure drop increases with increase in the vibration frequency. The minimum fluidization velocity is nearly independent of the vibration amplitude at almost constant frequency of about 40 Hz, whilst the equilibrium pressure increases. Using the linear regression, the Richardson–Zaki exponents of three kinds of nano-particles have been calculated. R–Z analyses indicate that the particulate fluidization degree of cohesive particles can be greatly improved by vibration force.     

Preparation of organic and carbon xerogels using high-temperature–pressure sol–gel polymerization

To prepare organic gels at temperatures higher than normal boiling point of solvent, a method was developed using sol–gel polymerization in atmosphere saturated by vapor of solvent. To illustrate the advantages of proposed method, two series of gels were prepared using the conventional (T_curing = 70 °C) and the high temperature (T_curing = 140–170 °C) sol–gel polymerization. While no drying shrinkage was observed in our proposed method, 5–18% linear shrinkage occurred in conventional method depending on resin concentration in sol. Moreover, rising of curing temperature reduced the required time for preparation of organic gels from 5 days to lower than 5 h. The effects of processing parameters were investigated on physical and mechanical properties of organic xerogels. The results revealed that resin concentration significantly affects both density and compressive strength of final xerogels. While the curing temperature had no obvious effect on density, the raising of curing temperature significantly enhance the strength of organic xerogels. Carbon xerogels prepared by pyrolysis of novolac aerogels in inert atmosphere. The textures of the carbon xerogels were denser than corresponding organic xerogels, as evidenced by scanning electron microscopy (SEM) images. N₂ adsorption tests indicated that carbon aerogels were mainly meso or macroporous depending on resin concentration in initial sol.     

Tunable BT@SiO2 core@shell filler reinforced polymer composite with high breakdown strength and release energy density

Barium titanate@silicon dioxide (BT@SiO₂) core@shell fillers with an average diameter of 100 nm were prepared by a facile sol–gel synthesis. The thickness of SiO₂ shell can be easily tuned by varying different mass ratio of BT to tetraethyl orthosilicate (TEOS). Polyvinylidene fluoride (PVDF) based composite films reinforced by BT and BT@SiO₂ were fabricated via a solution casting method. The effects of SiO₂ shell on morphology structure, wettability, interfacial adhesion, dielectric, electrical and energy performances of composites were investigated. Compared with BT/PVDF, BT@SiO₂/PVDF composites show significantly increased breakdown strength due to enhanced interfacial adhesion and suppressed charge carrier conduction. Benefiting from enhanced breakdown strength and reduced remnant polarization induced by SiO₂ shell, BT@SiO₂/PVDF shows increased release energy density (energy density which can be fully discharged and applicable). Especially, BT@SiO₂/PVDF with SiO₂ thickness of 4 nm exhibits the highest release energy density of 1.08 J/cm³ under applied electric field of 145 kV/mm.     

Transformation of the geopolymer gels to crystalline bonds in cold-setting refractory concretes: Pore evolution,mechanical strength and microstructure

Two K₂O–MgO–Al₂O₃–SiO₂ based geopolymer gels with bulk chemical composition corresponding to cordierite (Co) and 1:1 mullite-cordierite (MuCo) were successfully transformed to crystalline bonds in high temperature service of cold-setting made refractory concretes. Kyanite aggregates changed the flexural strength of the gels from 11 to 28 MPa due to the development of good adhesive bonds. Under thermal cycles, up to 1250 °C, the cumulative pore volume remained at 0.09 mL/g, as from the absence of important densification/shrinkage. However, the behavior of the cumulative pore volume curves changed from that of a matrix with a wide range of distribution of pore sizes to that, of matrix, consisting of relatively coarse grains. The latter exhibits a rise at 10 μm as void spaces created around the contact points among the coarse kyanite grains and that at 0.054 μm as pores within the crystalline phases (cordierite, kalsilite, leucite, mullite, enstatite) formed. The microstructural observations confirmed the transformation of gel pores (size around 0.01 μm) to interparticle and intergranular pores due to the crystallization. The flexural strength of refractory concretes increased from 28 MPa to 40 MPa in agreement with the increase in the elastic modulus from 9 to 30 GPa. The crystallization was enhanced by the MgO content (being important in Co compared to MuCo) and the kyanite concentration as particles of kyanite effectively acted as phase separation and nucleation sites.     

Growth of SiO2 hierarchical nanostructure on SiC nanowires using thermal decomposition of ethanol and titanium tetrachloride and its FTIR and PL property

Novel SiO₂ hierarchical nanostructure has been grown on SiC nanowires using thermal decomposition of a mixture of ethanol and titanium tetrachloride. Novel nanostructure was realized in one synthesis route. Based on SEM and TEM observations, the hierarchical nanostructure consists of core-shell SiC–SiO₂ main stem nanowire and a lot of SiO₂ nanorod branches grown on the main stem. A mean diameter of SiC central cores was about 40 nm and their lengths reach about 100 μm. The lengths and diameters of SiO₂ nanorod-like branches were ranged in 400–800 nm and 30–120 nm, respectively. The growth of core-shell SiC–SiO₂ nanowires obeyed vapor–liquid–solid mechanism and the SiO₂ nanorod-like branches grew via vapor–solid mechanism. The infrared absorption and photoluminescence properties of the grown nanostructure were investigated.     

Studies on optical,chemical, and electrical properties of rapid SiO2 atomic layer deposition using tris(tert-butoxy)silanol and trimethyl-aluminum

Rapid SiO₂ atomic layer deposition (ALD) was used to deposit amorphous, transparent, and conformal SiO₂ films using tris(tert-butoxy)silanol (TBS) and trimethyl-aluminum (TMA) as silicon oxide source and catalytic agent, respectively. The growth rate of the SiO₂ films drastically increased to a maximum value (2.3 nm/cycle) at 200 °C and slightly decreased to 1.6 nm/cycle at 275 °C. The SiO₂ thin films have C–H species and hydrogen content (～8 at%) at 150 °C because the cross-linking rates of SiO₂ polymerization may reduce below 200 °C. There were no significant changes in the ratio of O/Si (～2.1) according to the growth temperatures. On the other hand, the film density slightly increased from 2.0 to 2.2 although the growth rate slightly decreased after 200 °C. The breakdown strength of SiO₂ also increases from 6.20 ± 0.82 to 7.42 ± 0.81 MV/cm. These values suggest that high cross-linking rate and film density may enhance the electrical property of rapid SiO₂ ALD films at higher growth temperature.     

Influence of 15 and 80 nano-SiO2 particles addition on mechanical and physical properties of ternary blended concrete incorporating rice husk ash

This study demonstrates the effects of SiO₂ nanoparticles as additives with two different sizes of 15 and 80?nm on compressive strength and porosity of rice husk ash (RHA) blended concrete. Up to 20% of ordinary Portland cement (OPC) was replaced by RHA with average particle size of 5 micron. Also, SiO₂ nanoparticles were added to the above mixture at four different weight percentages of 0.5, 1.0, 1.5 and 2.0 and cured in lime solution. The results indicated that compressive strength of Portland cement–nano SiO₂–rice husk ash (PC–NS–RHA) ternary blended concrete was considerably increased. Moreover, the total amount of porosity decreased to a minimum with respect to the control concrete. This improvement was observed at all the curing ages and replacement levels, but there was a gain in the optimal point with 20% of RHA plus 2% of 80?nm SiO₂ particles at 90 days of curing.     

Synthesis and characterization of rice grains like Nitrogen-doped TiO2 nanostructures by electrospinning–photocatalysis

Rice grain-shaped Nitrogen-doped titanium dioxide (N–TiO₂) nano/mesostructures were fabricated through a combination of sol–gel and electrospinning methods. As-spun nanofibers were continuous and upon thermal treatment at 500° C for 1 h in air, the continuous fibers break into rice grain-shaped TiO₂ nanostructures of average diameter 50–80 nm. The nanostructures were characterized by spectroscopy, microscopy and powder X-ray diffraction. The rice grains consist of spherical particles of average diameter of ~ 18 nm and with N doping, their average diameters decrease from ~ 18 to ~ 12 nm. The presence of N in the TiO₂ lattice was confirmed by X-ray photoelectron spectroscopy (XPS). The band-gap of TiO₂ reduced from 3.19 eV to 2.83 eV upon increasing doping level of N from 0% to 5% (w/w), respectively. The N–TiO₂ rice grains showed an enhanced UV light-assisted photocatalysis compared to pure TiO₂ in the photodegradation of Alizarin Red S dye, an industrially important anthraquinone dye.     

Enhanced thermal transfer and bending strength of SiC/Al composite with controlled interfacial reaction

The interface and its effect on the thermal conductivity and bending strength of SiC/Al composite were investigated. The results indicated that the compact interfacial layer could be obtained when holding the SiC particles for 4 h at 1200 °C. The decrease of the holding time reduced the thickness of the interfacial layer, yet harmful for the thermal transfer of the interface due to the formation of pores and Al₄C₃. The prolongation of the holding time introduced SiO₂ layer owning the very low instinct thermal conductivity, resulting in the increase of interfacial thermal resistance. However, the addition of SiO₂ layer seems less harmful for the interfacial thermal transfer with respect to the thin SiO₂ layer. The critical thickness of SiO₂ layer is confirmed to be 210 nm. Very similar to the variation of thermal conductivity, the bending strength follows a first increase until reaches a maximum value 435 MPa and then trends to decrease. The composite after T6 treatment exhibits a better bending strength compares to T2 treated composite.