Effect of ion implantation on the strength of sapphire at 300–600°C

Ion implantation with ¹¹B⁺ or ²⁸Si⁺ at 1000°C doubled the ring-on-ring flexure strength of c-plane sapphire disks tested at 300°C but had little effect on strength at 500 or 600°C. Disks were implanted on the tensile surface with 2 × 10¹⁷ B/cm² (half at 40 keV and half at 160 keV) or 1 × 10¹⁷ Si/cm² (80 keV). Sapphire implanted with 1 × 10¹⁸ B/cm² had only half as much flexure strength at 300° or 500°C as sapphire implanted with 2 × 10¹⁷ B/cm². Implantation with B, Si, N, Fe or Cr had no effect on the c-axis compressive strength of sapphire at 600°C. Boron ion implantation (2 × 10¹⁷ B/cm², half at 40 keV and half at 160 keV) induced a compressive surface force per unit length of 1.9 × 10² N/m at 20° and 1.4 × 10² N/m at 600°C. The infrared emittance at 550–800° of B-implanted sapphire at a wavelength of 5 m increased by 10–15% over that of unimplanted sapphire. Infrared transmittance of sapphire implanted with B, Si or N at either 1000°C or 25°C is within 1–3% of that of unimplanted material at 3.3 m. Implantation with Fe or Cr at 25°C decreases the transmittance by 4–8% at 3.3 m, but implantation at 1000°C decreased transmittance by only 2–4% compared to unimplanted material.     

Effect of matrix strength on the mechanical properties of Al–Zn–Mg/SiCP composites

The mechanical properties of Al–Zn–Mg alloy reinforced with SiC_P composites prepared by solidification route were studied by altering the matrix strength with different heat treatments. With respect to the control alloy, the composites have shown similar ageing behaviour in terms of microhardness data at 135°C. It was shown that although composites exhibited enhanced modulus values, the strengthening was found to be dependent on the damage that is occurring during straining. Thus the initial matrix strength plays an important role in determining the strengthening. Consequently, compression data had shown a different trend compared to tension.     

Effect of aging temper on the thermal stability of Al–Cu–Mg–Ag heat-resistant alloy

The thermal stability of Al–Cu–Mg–Ag alloy was tested by thermal exposure and creep performance. The results show that the under-aged Al–Cu–Mg–Ag alloy possessed better thermal stability compared to the peak-aged one, due to the secondary precipitations of the strengthening phases. The number of the precipitations in the under-aged sample increased and then decreased with increasing the thermal exposure or creep time while that of the peak-aged sample decreased gradually. The tensile strength of the under-aged sample increased and then decreased with increasing the thermal exposure time with a peak value of 524 MPa after exposed for 20 h, which was 19 MPa higher than that of the peak-aged alloy. The steady creep rate of the under-aged sample was much lower and the creep-life was much longer to that of the peak-aged one, indicating that the under-aged sample possessed excellent creep resistance property at elevated temperatures.     

Effect of bismuth–tin alloy particle diameter on bonding strength of copper nanoparticles/bismuth–tin solder hybrid joints

The effect of the diameter of Bi–Sn alloy particles on the bonding strength of hybrid joints formed between SiC chips and direct-bonded copper (DBC) plates using a Cu nanoparticles/Bi–Sn solder was studied. The bonding strength was the highest at 40 MPa for a Bi–Sn alloy particle diameter of 10 µm. Further, the bonding strength was dependent on the area of the bonding layer adhering to the SiC-side fracture surface, as determined by the die-shear test. Ni, which was deposited on the SiC chips and DBC plates before the bonding process, remained near the interfacial area of the bonding layer in the joints formed using the 5 µm particles. In contrast, Ni diffused all over the bonding area, with the exception of the interfacial area where Cu–Sn compounds were formed, in the joints produced using the larger alloy particles. The distribution of Sn in the bonding layer became more uniform and the segregation of Bi at the interface became more pronounced as the particle size was reduced. Further, with an increase in the particle size, the Ag layers deposited on the surfaces of the SiC chips and DBC plates diffused into the bonding layer after the first firing step at 473 K, which was performed before the secondary firing step at 623 K. These results imply that the diameter of the Bi–Sn solder particles in hybrid joints affects the interfacial structure, as it governs the wetting behavior of the Bi–Sn solder and hence has a determining effect on the bonding strength.     

Effect of solution pH on the surface morphology of sol–gel derived silica gel

We have examined the effect of solution acidity on the textural characteristics of silica gels prepared by sol–gel synthesis using tetraethyl orthosilicate (TEOS) as a silica precursor and cetyltrimethylammonium bromide (CTAB) as a template. Using IR spectroscopy, we have studied micellar TEOS solutions and the synthesized silica gel samples. The results demonstrate that, in an alkaline medium in a water–ethanol solution, SiO₂ experiences short-range ordering on the surface of micelles formed by CTAB molecules, whereas in an acid medium the process is not influenced by the presence of CTAB. Nitrogen porosimetry and electron microscopy data indicate that the silica gel obtained at pH 2 is microporous, with an average pore size of 2 nm. In an alkaline medium at pH 10, we obtained mesoporous SiO₂ (18 nm) with a narrow pore size distribution and a specific surface area of 110 m²/g.     

Effect of interfacial shear strength on reliability of strength and fracture process of SiC–Al composite

Abstract

A unidirectional SiC fibre reinforced pure aluminium composite was fabricated by the hot press method. Tensile testing of the SiC–Al was carried out to determine composite and interfacial shear strengths. A Monte Carlo procedure based on the elastic–plastic finite element method, involving the interfacial layer around the fibres, was constructed to simulate the tensile testing and to calculate the strength and Weibull parameters for the SiC–Al composite. The effect of the interfacial shear strength on the composite strength and its reliability is discussed. The results show that the composite strength and the Weibull shape parameter increase with increasing interfacial shear strength. The contribution of the interfacial shear strength to the composite strength and reliability is efficient when the interfacial shear strength is lower than the matrix shear strength. It is concluded that both composite strength and reliability are closely related to the fibre fracture process.     

Effect of γ-irradiation on the physical and mechanical properties of chitosan powder

In this study, locally produced chitosan powder was irradiated with pre-determined doses of γ-ray (Co-60) of 10 kGy, 25 kGy, 50 kGy and 100 kGy respectively. The properties of both chitosan powder and the chitosan film were examined and compared with unradiated chitosan. Physical characteristic of the irradiated powder and film was studied using stereo microscope. It was observed that the γ-ray induces a noticeable colour tone intensity change to the chitosan. Further investigation using Fourier Transformed Infrared Spectroscopy (FT-IR) analysis has confirmed that the chain scission reaction was occurred as a result of γ-ray exposure through the depolymerization mechanisms. Interestingly, the degree of deacetylation (DD) of chitosan measured using FT-IR showed a negligible effect due to the exposure of γ-ray radiation. Further investigation on the viscosity average molecular weight (M_v) showed a reduction of M_v from 577 kD of pure chitosan to 458 kD, 242 kD, 159 kD and 106 kD for 10 kGy, 25 kGy, 50 kGy and 100 kGy of γ-radiated chitosan respectively. In addition, the tensile strength and elongation at break showed a similar decreasing trend with increasing dosage of γ-ray.     

Effect of Y on the bio-corrosion behavior of extruded Mg–Zn–Mn alloy in Hank's solution

The bio-corrosion properties of Mg–Zn–Mn alloys with and without Y in Hank's solution at 37 °C were investigated by using electrochemical test and electrochemical impedance spectra (EIS). The results of open circuit potential (OCP) and polarization tests indicated that Y could reduce the cathodic current density. A passivative stage appeared in the Tafel curve of the Y containing magnesium alloy, indicating that a passivative film was formed on the surface of the Y containing magnesium alloy. EIS results showed that the Y containing alloy had higher charge transfer resistance and film resistance, but lower double layer capacity than the alloy without the Y element. The surface reaction product identification by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) showed that the surface corrosion products were hydroxide and phosphate (Mg₃Ca₃(PO₄)₄) for Mg–Zn–Mn alloy and phosphate (MgNaPO₄) for the Y containing Mg–Zn–Mn alloys. The XPS results also showed that a Y₂O₃ protective film was formed on the surface of the Y containing magnesium alloy which contributed mainly to the low cathodic current density and the high resistance.     

Optimization of the lyophilization process for long-term stability of solid–lipid nanoparticles

Objectives: To optimize a lyophilization protocol for solid–lipid nanoparticles (SLNs) loaded with dexamethasone palmitate (Dex-P) and to compare the long-term stability of lyophilized SLNs and aqueous SLN suspensions at two storage conditions.

Materials and Methods: The effect of various parameters of the lyophilization process on SLN redispersibility was evaluated. A three month stability study was conducted to compare changes in the particle size and drug loading of lyophilized SLNs with SLNs stored as aqueous suspensions at either 4°C or 25°C/60% relative humidity (RH).

Results and Discussion: Of nine possible lyoprotectants tested, sucrose was shown to be the most efficient at achieving SLN redispersibility. Higher freezing temperatures, slower freezing rates, and longer secondary drying times were also shown to be beneficial. Loading of the SLNs with Dex-P led to slightly larger particle size and polydispersity index increases, but both parameters remained within an acceptable range. Drug loading and particle shape were maintained following lyophilization, and no large aggregates were detected. During the stability study, significant growth and drug loss were observed for aqueous SLN suspensions stored at 25°C/60% RH. In comparison, lyophilized SLNs stored at 4°C exhibited a consistent particle size and showed <20% drug loss. Other storage conditions led to intermediate results.

Conclusions: A lyophilization protocol was developed that allowed SLNs to be reconstituted with minimal changes in their physicochemical properties. During a three month period, lyophilized SLNs stored at 4°C exhibited the greatest stability, showing no change in the particle size and a minimal reduction in drug retention.     

Effect of electrospark deposited surface layers on bond strength of titanium–porcelain

Abstract

Casting of titanium can be successfully used in prosthodontic applications, but it demands special machines and protection gas to avoid oxidation of the metal. The aims of this study are to investigate the bond compatibility between porcelain and titanium using three-point bending, oxide adherence and thermal expansion tests, and to compare the results with those of a conventional titanium–porcelain system. Titanium alloy surfaces were modified with Nb, YG8 and silicon electrode by electrospark surface modification process. The effect of electrospark surface depositing (ESD) layers on bond strength of titanium to porcelain was evaluated comparatively. Some reasons about bond strength of titanium to porcelain were discussed. Results indicate that ESD modified layer prepared in atmosphere using Si electrode can obtain the strongest bonding to porcelain. The ESD modified layer show metallurgical bond to Ti substrate. In addition, the facts that rough surface can help to improve physic bond, similar nature can also help to chemical link and compact ESD layer represent good high temperature oxidation resistance are the reasons that enhance good bond strength of titanium to porcelain.     

Effect of SiC nanoparticles on the wear behaviour of squeeze-cast AZ91–2.0Ca–0.3Sb alloy

The dry sliding wear behaviour of the AZ91–2.0Ca–0.3Sb alloy and the AZ91–2.0Ca–0.3Sb–xSiC_np nanocomposites have been investigated. The wear rate is lower for all the nanocomposites compared to the alloy. All the nanocomposites demonstrate the lower specific wear rates than the alloy. Among the nanocomposites, the one containing 2.0SiC_np exhibits the best tribological performance. The values of the coefficient of friction are lower for the nanocomposites than the alloy. The abrasion, adhesion, oxidation, and delamination are the dominant wear mechanisms. The 3D topography depicts that the addition of SiC_np to the AZ91–2Ca–0.3Sb alloy results in the reduced surface roughness during the wear tests, confirming the superior wear behaviour of the nanocomposites compared to the alloy.     

Effect of inadequate heat treatment on creep strength of 12Cr–Mo–V steel

Abstract

Solution treatment of 12Cr–Mo–V steels below the specified temperature range leads to the development of spheroidized microstructures with dramatically reduced creep resistance. This is known to have resulted in the premature service failures of superheater tubing. Compositional and mechanical property checks currently specified in the relevant standards may not be sufficient to reveal deficiencies. Steels with Cr–Ni equivalents at the uppermost extreme of the range possible within the compositional limits of the tube steel standards show enhanced susceptibility to both δ– and α–ferrite formation. The significance of this is discussed in relation to creep strength, with particular reference to the differences between the effects of α- and δ-ferrite.

MST/147     

Comments on ‘Effect of obstacle strength and spacing on the slope of Haasen plot’

In a recent paper, Mishra et al. [Effect of obstacle strength and spacing on the slope of Haasen plot. Mater Sci Technol. 2019;1–6. doi:10.1080/02670836.2019.1567043], discrepancy between theoretical and experimental results in the slope of the Haasen plot between pure metals and alloys were reported. The discrepancy arises from a common belief that when Haasen plot for pure metals is extended to metals with multiple strengthening mechanisms, the inverse of activation volume components can be linearly superposed. It is conjectured that the slope of the Haasen plot should remain the same for both the pure metals and alloys, as it is governed only by dislocation–dislocation interaction. The purpose of this note is to clarify that the conjecture of invariant Haasen slope is only a special case.     

Effect of pyrophosphate ions on the conversion of calcium–lithium–borate glass to hydroxyapatite in aqueous phosphate solution

The conversion of glass to a hydroxyapatite (HA) material in an aqueous phosphate solution is used as an indication of the bioactive potential of the glass, as well as a low temperature route for preparing biologically useful materials. In this work, the effect of varying concentrations of pyrophosphate ions in the phosphate solution on the conversion of a calcium–lithium–borate glass to HA was investigated. Particles of the glass (150–355 μm) were immersed for up to 28 days in 0.25 M K₂HPO₄ solution containing 0–0.1 M K₄P₂O₇. The kinetics of degradation of the glass particles and their conversion to HA were monitored by measuring the weight loss of the particles and the ionic concentration of the solution. The structure and composition of the conversion products were analyzed using X-ray diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy. For K₄P₂O₇ concentrations of up to 0.01 M, the glass particles converted to HA, but the time for complete conversion increased from 2 days (no K₄P₂O₇) to 10 days (0.01 M K₄P₂O₇). When the K₄P₂O₇ concentration was increased to 0.1 M, the product consisted of an amorphous calcium phosphate material, which eventually crystallized to a pyrophosphate product (predominantly K₂CaP₂O₇ and Ca₂P₂O₇). The consequences of the results for the formation of HA materials and devices by the glass conversion route are discussed.     

Effect of B content on thermal stability of nanocomposite Ti–B–N thin films

Abstract

Ti–B–N thin films with different B contents were deposited on Si (100) at room temperature, followed by vacuum annealed at 400, 600, 800 and 1000°C for 1 h respectively. Effect of boron content on thermal stability was investigated using X-ray diffraction, scanning electron microscopy, high resolution transmission electron microscopy and nanoindentation measurements. The results indicated that incorporation of B into TiN produced a nanocomposite structure, which had a positive effect on microstructure stability. A high B content resulted in an elevated recrystallisation temperature. The hardness stability was not consistent with that of microstructure, and depended on phase configuration and composition. The films with a high as deposited hardness showed high hardness stability. Excessive or lack of amorphous phase decreased hardness stability. The residual stress value was decreased with increasing annealing temperature owing to recovery of amorphous matrix, and crystallisation of amorphous phase made its direction transform from compression to tension.     

Effect of cobalt nanoparticles on mechanical properties of Sn–58Bi solder joint

Brittle phases are responsible for crack formation and propagation in tin–bismuth (Sn–58Bi) solder material. The purpose of this work is to investigate the effects of various cobalt (Co) nanoparticle (NP) concentrations on the tensile properties of the Sn–58Bi solder matrix. Different aging times were studied to find out the effect of Co NP on ultimate tensile strength. Tin–bismuth solder joints of different Co NP concentrations of 0%, 0.5%, 1%, and 2% were prepared. The reflow process was done at 180 °C for 1 min. Scanning Electron Microscopy and Energy-Dispersive X-ray spectroscopy were used to analyze the solder joints. The tensile test was carried out for the Sn–58Bi and Sn–58Bi–xCo (x?=?0.5, 1, and 2) solder joints. The tensile test was run before and after aging time. The tensile results reveal that the addition of Co NP increased the tensile strength significantly at different concentrations of Co NP. The Tensile test revealed that ductility was improved as the temperature was increased. As the aging time increased, the ultimate tensile strength of all samples decreased.

     

Effect of coordinated water of hexahydrate on nickel platings from choline–urea ionic liquid

Impacts of coordinated water of nickel chloride hexahydrate (NiCl₂·6H₂O) on the properties of choline–urea (ChCl–2Urea) ionic liquid (IL), including viscosity and electrical conductivity, and electrodeposition behavior of Ni coatings were investigated. Results reveal that the coordinated water exhibited a profound influence on reducing viscosity, improved electrical conductivity and promoted the formation of a nanocrystalline Ni coating, while the Ni nucleation mechanism was not altered by the presence of coordinated water, proceeding via that from the progressive three-dimensional nucleation to instantaneous nucleation with hemispherical diffusion-controlled growth when the deposition potential shifts to the negative direction. When water content was maintained no more than?~?8 wt%, a compact nanocrystalline Ni coating, with a current efficiency of almost 100%, was prepared from ChCl–2Urea–NiCl₂·6H₂O with an aid of 400 mg/L nicotinic acid (NA) at 318 K. These results indicate hydrated Ni salts can be used to replace anhydrous counterparts in preparation of Ni coating from choline–urea IL, which could reduce the impact on environment and product cost. Such a strategy may be extended to other hydrated metal salts in IL electrolyte electrodeposition for high-quality coating preparation.     

Effect of hyaluronic acid incorporation method on the stability and biological properties of polyurethane–hyaluronic acid biomaterials

The high failure rate of small diameter vascular grafts continues to drive the development of new materials and modification strategies that address this clinical problem, with biomolecule incorporation typically achieved via surface-based modification of various biomaterials. In this work, we examined whether the method of biomolecule incorporation (i.e., bulk versus surface modification) into a polyurethane (PU) polymer impacted biomaterial performance in the context of vascular applications. Specifically, hyaluronic acid (HA) was incorporated into a poly(ether urethane) via bulk copolymerization or covalent surface tethering, and the resulting PU–HA materials characterized with respect to both physical and biological properties. Modification of PU with HA by either surface or bulk methods yielded materials that, when tested under static conditions, possessed no significant differences in their ability to resist protein adsorption, platelet adhesion, and bacterial adhesion, while supporting endothelial cell culture. However, only bulk-modified PU–HA materials were able to fully retain these characteristics following material exposure to flow, demonstrating a superior ability to retain the incorporated HA and minimize enzymatic degradation, protein adsorption, platelet adhesion, and bacterial adhesion. Thus, despite bulk methods rarely being implemented in the context of biomolecule attachment, these results demonstrate improved performance of PU–HA upon bulk, rather than surface, incorporation of HA. Although explored only in the context of PU–HA, the findings revealed by these experiments have broader implications for the design and evaluation of vascular graft modification strategies.     

Effects of chitosan molecular weight on the physical and dissolution characteristics of amorphous curcumin–chitosan nanoparticle complex

Objective: To investigate the effects of varying molecular weight (MW) of chitosan (CHI) used in the complexation with curcumin (CUR) on the physical and dissolution characteristics of the amorphous CUR–CHI nanoparticle complex produced.

Significance: Amorphous CUR–CHI nanoparticle complex (or CUR nanoplex in short) recently emerged as a promising bioavailability enhancement strategy of CUR attributed to its fast dissolution, supersaturation generation capability, and simple preparation. Existing CUR nanoplex prepared using low MW CHI, however, exhibited poor colloidal stability during storage. Herein we hypothesized that the colloidal stability could be improved by using CHI of higher MW. The effects of this approach on the nanoplex’s other characteristics were simultaneously investigated.

Methods: The CUR nanoplex was prepared by electrostatically driven self-assembled complexation between CUR and oppositely charged CHI of three different MWs (i.e. low, medium, and high). Besides colloidal stability, the effects of MW variation were investigated for the nanoplex’s (1) other physical characteristics (i.e. size, zeta potential, CUR payload, amorphous state stability), (2) preparation efficiency (i.e. CUR utilization rate, yield), and (3) dissolutions under sink condition and supersaturation generation.

Results: CUR nanoplex prepared using CHI of high MW exhibited improved colloidal stability, larger size, superior morphology, and prolonged supersaturation generation. On the other hand, the effects of MW variation on the payload, amorphous state stability, preparation efficiency, and dissolution under sink condition were found to be insignificant.

Conclusions: Varying MW of CHI used was an effective means to improve certain aspects of the CUR nanoplex characteristics with minimal adverse effects on the others.