Thermal properties of plasma-sprayed thermal barrier coating with bimodal structure

Nanostructured zirconia coatings have been prepared by atmospherical plasma spraying (APS) on NiCrAlY-coated superalloy substrates. The isothermal oxidation test results indicate that the oxidation kinetics of nanostructured TBC follows a parabolic law and the oxidation resistance of the nanostructured TBC is comparable to that of the conventional TBC. The nanostructured thermal barrier coatings exhibit excellent thermal cyclic resistance and low thermal diffusivity. The failure of the nanostructured TBC occurs within the top coat and close to the YSZ/thermal growth oxide interface. The thermal diffusivity of the coating is 90% of that of conventional thermal barrier coatings, and it increases after heat treatment at 1050 °C for 34 h. The increase in the thermal diffusivity of the coating is ascribed to grain growth, the crack healing as well as sintering neck formation.     

Monomer sequence of partially hydrolyzed poly(4-tert-butoxystyrene) and morphology of diblock copolymers composing this polymer sequence as one block

The molecular characteristics of poly(4-tert-butoxystyrene) (O) upon hydrolysis reaction were investigated. It is known that O can be converted into poly(4-hydroxystyrene) (H) through hydrolysis reaction using strong acid. In this study, a set of poly(4-tert-butoxystyrene-co-4-hydroxystyrene)s (O/H copolymers) having various conversion rates, f_Hs, were prepared. Hydrolysis reaction is found to occur uniformly by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) where the average f_H obtained was consistent with that from ¹H NMR though a certain distribution in the number of hydrolyzed units was conceived. Monomer sequence of O/H copolymers was determined by ¹³C NMR and the changes in triad concentration were obtained by spectra subtraction method. As a result, ¹³C NMR reveals that O and H are statistically distributed. To evaluate the effect of hydrolysis on microphase-separated structure, we observed the morphology of partially hydrolyzed poly(4-tert-butylstyrene-block-4-tert-butoxystyrene) (BO) by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS). Samples with f_H from 0.21 to 0.67 form both lamellar (major component) and cylindrical (minor component) structures reflecting both the statistical manner of hydrolysis reaction and the possible localized distribution of H sequence.     

Propylsulfonic acid-functionalized partially crystalline silicalite-1 materials: synthesis and characterization

Propylsulfonic acid-functionalized partially crystalline silicalite-1 materials were synthesized via one step co-condensation technique by varying the molar ratio of organosilane source, 3-mercaptopropyltrimethoxysilane (3MP) to tetraethylorthosilicate (TEOS) in the range of 0.05–0.30, and subsequent oxidation of thiol group to propylsulfonic acid using hydrogen peroxide (H₂O₂). These materials were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM) and nitrogen adsorption–desorption method. The structure of these materials was determined by Fourier transform infrared spectroscopy (FT-IR) and ²⁹Si and ¹³C solid state NMR. XRD results show that % crystallinity of the materials decreased with the increase in 3MP concentration in the synthesis mixture. Selected area electron diffraction (SAED) showed the presence of crystalline and amorphous phases in the samples. An amorphous phase was formed when 3MP concentration was 30 mol% of the total silica source. After elimination of the structure directing agent (SDA) by calcination at 420 °C, thermogravimetric analysis (TGA) shows that the structure was thermally stable up to 550 °C. Ammonia temperature-programmed desorption (NH₃-TPD) shows that the acid capacity of these materials was in the range of 1.19–1.83 mmol H⁺/g, which shows that these materials could be used as potential heterogeneous acid catalyst.     

Spectroscopic studies and evaluation of thermorheological properties of softwood and hardwood lignin

Fourier transform infrared spectroscopy ( FTIR) was used to determine characteristic absorption peaks of softwood kraft lignin and soda hardwood lignin. Remarkable spectral differences were noticed between the different lignins due to their various chemical structures. Proton nuclear magnetic resonance spectrometry (¹H NMR) was employed to analyze the structure of lignin. Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry ( MALDI‐TOF) provided important data regarding the molecular weight distribution of lignin. Thermal stability of softwood lignin was found to be remarkably higher than that of hardwood lignin. Softening temperature and glass transition temperature of lignin were measured by differential scanning calorimetry (DSC) which was useful in selecting an optimal temperature profile during extrusion process. Rheological studies provided valuable information about the viscosity of lignins. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Curing behavior and properties of benzoxazine‐co‐self‐promoted phthalonitrile polymers

A new high‐performance copolymer was successfully obtained via concerted catalysis polymerization of mono‐functional benzoxazine (P‐a) and self‐promoted 4‐aminophenoxy phthalonitrile (4‐APN) monomers. The FTIR and DSC curves of the P‐a/4‐APN in different blend ratios suggested that the monomer blends can be completely cured without the addition of curing additive. The P‐a/4‐APN copolymers were cured at relatively lower curing temperatures and time. The TGA curves revealed that the P‐a/4‐APN copolymers have good thermal stability in terms of T₅, T₁₀, and char yield. A gradual increase in the glass transition temperature (T_g) values and decline were seen in the storage modulus as the loading of 4‐APN was increased from 10 to 30 wt % in the copolymer. The SEM analyses showed that copolymer's fracture surface is dendritic, showing the stress has been dispersed to a certain extent. The study revealed that the poly(P‐a/4‐APN) copolymer have much better thermal stabilities than the poly(P‐a), and the prepared copolymer can be used as a high‐performance thermosetting resin. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46578.     

Thermal Evaluation of Diesel/Hydrogen Peroxide Fuel Blend

Thermal properties of fossil fuel are the key fundamental characteristics, which can distinguish any compound as a potential fuel. The performance of diesel fuel blend along with stability and solubility parameter designs are evaluated. The results from the experimental study indicate that the increase in hydrogen peroxide (H₂O₂) amount enhances the cetane number of diesel fuel blend significantly. However, the calorific value decreases as compared to pure diesel fuel. All values performed well according to the ASTM D‐975 diesel testing method. The thermodynamics of the prepared fuel blends also revealed that substantial solubility and diesel/H₂O₂ blend stability are provided even at lower temperatures. Such blends can be used as a feasible replacement of pure diesel fuel.     

Magnetic Nanoparticle Arrays Self-Assembled on Perpendicular Magnetic Recording Media

We study magnetic-field directed self-assembly of magnetic nanoparticles onto templates recorded on perpendicular magnetic recording media, and quantify feature width and height as a function of assembly time. Feature widths are determined from Scanning Electron Microscope (SEM) images, while heights are obtained with Atomic Force Microscopy (AFM). For short assembly times, widths were ~150 nm, while heights were ~14 nm, a single nanoparticle on average with a 10:1 aspect ratio. For long assembly times, widths approach 550 nm, while the average height grows to 3 nanoparticles, ~35 nm; a 16:1 aspect ratio. We perform magnetometry on these self-assembled structures and observe the slope of the magnetic moment vs. field curve increases with time. This increase suggests magnetic nanoparticle interactions evolve from nanoparticle–nanoparticle interactions to cluster–cluster interactions as opposed to feature–feature interactions. We suggest the aspect ratio increase occurs because the magnetic field gradients are strongest near the transitions between recorded regions in perpendicular media. If these gradients can be optimized for assembly, strong potential exists for using perpendicular recording templates to assemble complex heterogeneous materials.     

Pseudohalogenation of methyl 9-hydroxy-cis-12-and 12-hydroxy-cis-9-octadecenoate

Pseudohalogenation of methyl 9-hydroxy-cis-12-octadecenoate (I) and methyl 12-hydroxy-cis-9-octadecenoate (II) has been carried out with N,N-dibromobenzenesulfonamide (NNDBS). Compounds I and II, on reaction with NNDBS, formed four and three products, respectively. The interesting feature of these reactions was the formation of 1,4-epoxy compounds. The structures of individual compounds were established with the help of elemental and spectral analysis.     

Effects of functionalization conditions of sulfonic acid grafted SBA-15 on catalytic activity in the esterification of glycerol to monoglyceride: a factorial design approach

A series of propyl sulfonic acid-modified SBA-15 catalysts (SBA-15SO₃H) was prepared under various conditions using post-functionalization approach. A factorial design coupled with response surface analysis were employed to evaluate the effects of the preparation conditions on the catalyst activity. Optimization of the conditions to find the most active SBA-15SO₃H catalyst with the highest activity in glycerol esterification with lauric acid at 160?°C for 6?h was also made. Amount of 3-(mercaptopropyl)trimethoxysilane (MPTMS) and reflux time were chosen as parameters of the preparation conditions. The presence of propyl sulfonic acid groups in SBA-15SO₃H catalysts was confirmed by FT-TIR method. The catalysts were also characterized by means of surface analysis, XRD, TEM and TGA. The results obtained from the statistical models suggested that the amount of MPTMS was more important parameter to influence the activity compared to the reflux time. The optimum preparation condition was achieved at a reflux time of 20?h and an MPTMS amount of 1?mL/gram SBA-15 to obtain the SBA-15SO₃H(1) with the highest monoglyceride selectivity (70.2%) and corresponding lauric acid conversion (95%) in the esterification process.     

Substrate Temperature Dependent Surface Morphology and Photoluminescence of Germanium Quantum Dots Grown by Radio Frequency Magnetron Sputtering

The visible luminescence from Ge nanoparticles and nanocrystallites has generated interest due to the feasibility of tuning band gap by controlling the sizes. Germanium (Ge) quantum dots (QDs) with average diameter ~16 to 8 nm are synthesized by radio frequency magnetron sputtering under different growth conditions. These QDs with narrow size distribution and high density, characterized using atomic force microscopy (AFM) and field emission scanning electron microscopy (FESEM) are obtained under the optimal growth conditions of 400 °C substrate temperature, 100 W radio frequency powers and 10 Sccm Argon flow. The possibility of surface passivation and configuration of these dots are confirmed by elemental energy dispersive X-ray (EDX) analysis. The room temperature strong visible photoluminescence (PL) from such QDs suggests their potential application in optoelectronics. The sample grown at 400 °C in particular, shows three PL peaks at around ~2.95 eV, 3.34 eV and 4.36 eV attributed to the interaction between Ge, GeO_x manifesting the possibility of the formation of core-shell structures. A red shift of ~0.11 eV in the PL peak is observed with decreasing substrate temperature. We assert that our easy and economic method is suitable for the large-scale production of Ge QDs useful in optoelectronic devices.