Growth characteristics of β-SiC by chemical vapour deposition

A twin-plane re-entrant corner effect (TPRE) in growth of chemical vapour deposited (CVD) -SiC is described by the film and particles of gas-phase homogeneous nucleation. The structural morphology has been characterized by scanning electron microscopy and transmission electron microscopy. Morphological characteristics of the deposited crystals, such as triangularity, hexagons or facets have been explained in terms of the re-entrant corner effect at twin junctions, which were proposed as preferential growth sites for perfect crystals. For real deposits, screw dislocations and/or the re-entrant corner effect are not expected to be compatible. The majority of chemical vapour deposited SiC crystals have a high defect density comprised of {111} twins and dislocations associated with the process variables. Infrared transmission spectra and electron spectroscopy of chemical analysis indicated that the major chemical bonds of CVD -SiC were Si-C and C-H bonds. The positions of the 1s or 2p corelevel peaks for deposits are described.     

Piezoelectric and acoustic properties of potassium titanyl phosphate (KTP) and its isomorphs

The bulk elastic and piezoelectric properties of potassium titanyl phosphate (KTP) and some of its family members such as RbTiOPO(4 ) (RTP) and RbTiOAsO(4) (RTA) have been determined. The piezoelectric, elastic, and dielectric matrix (P-E-D) of KTP has been completely characterized. Values for the temperature dependence of the expansion coefficients and elastic constants have been obtained, and the effects of variations in dielectric constant on coupling coefficient determined. The major diagonal elements of the piezoelectric and elastic matrices of RTP and RTA were measured as were the thermal expansion coefficient of all the KTP isomorphs, KTP in the temperature range 25-80 degrees C, is shown to have a combination of large coupling coefficients (up to k(t)=38% for hydrothermally grown KTP) and medium temperature dependence coefficients of elastic constant (as low as 40 p.p.m./ degrees C for tau(c33) for hydrothermally grown KTP) that makes it attractive for many piezoelectric applications.     

软件单元测试应用研究及案例分析

单元测试是软件测试过程的第一站,高质量的单元测试是软件质量保证的必要条件,本文就单元测试的概念、测试类型及规程作了简单的阐述,同时就单元测试进行了案例分析。     

Temperature dependence of high strain-rate impact fracture behaviour in highly filled polymeric composite and plasticized thermoplastic propellants

The effect of temperature and strain-rate on the fracture behaviour during high strain-rate ( 10³ sec^–1) impact of two highly filled polymeric composite propellants (containing segmented polyurethanes based on hydroxy-term inated polybutadiene (HTPB) or glycidyl azide polymer (GAP) filled with ammonium perchlorate (AP) particles) and a plasticized thermoplastic (cast double base (CDB) nitrocellulose-nitroglycerine) propellant have been examined over a wide temperature range encompassing the ittle-ductile transition. In the elastic region of the loaddisplacement curve, the yield stress and fracture toughness is highest for GAP/AP and lowest for HTPB/AP. In the elastic and post-yield ductile regions CDB is more fracture-resistant than GAP/AP and HTPB/AP over the temperature range –20 to 50° C, but below –40° C, where both CDB and GAP/AP are brittle, GAP/AP is more fracture-resistant than CDB (as observed in the elastic region). Although all the propellants are known to develop small cracks in the elastic and post-yield ductile regions of the load-displacement curve, the overall fracture behaviour is largely governed by viscoelastic properties (because the cracks close up in compression). The good mechanical properties of CDB, above the brittle-ductile transition temperature, can be attributed to the presence of a large-transition loss peak. In the composites, the fracture behaviour is also influenced to a lesser extent by the degree of filler-binder interactions. Dynamic mechanical analysis indicates that GAP/AP has a slightly higher degree of filler-binder interactions than HTPB/AP. A temperature-strain rate reduction has been obtained for the yield stress and the composite curve can be expressed by the equation _y =K ₁ +K ₂ log (ea _T ) whereK ₁ andK ₂ are constants anda _T is a shift factor.K ₂ is a material constant which reflects the temperature and strain-rate sensitivity.     

Preparation of Protein-Stabilized β-Carotene Nanodispersions by Emulsification–Evaporation Method

This work was initiated to prepare protein-stabilized β-carotene nanodispersions using emulsification–evaporation. A pre-mix of the aqueous phase composed of a protein and hexane containing β-carotene was subjected to high-pressure homogenization using a microfluidizer. Hexane in the resulting emulsion was evaporated under reduced pressures, causing crystallization and precipitation of β-carotene inside the droplets and formation of β-carotene nanoparticles. Sodium caseinate (SC) was the most effective emulsifier among selected proteins in preparing the nanodispersion, with a monomodal β-carotene particle-size distribution and a 17-nm mean particle size. The results were confirmed by transmission-electron microscopy analysis. SC-stabilized nanodispersion also had considerably high ζ-potential (−27 mV at pH 7), suggesting that the nanodispersion was stable against particle aggregation. Increasing the SC concentration decreased the mean particle size and improved the polydispersity of the nanodispersions. Nanodispersions prepared with higher β-carotene concentrations and higher organic-phase ratios resulted in larger β-carotene particles. Although increased microfluidization pressure did not decrease particle size, it did improve the polydispersity of the nanodispersions. Repeating the microfluidization process at 140 MPa caused the nanodispersions to become polydisperse, indicating the loss of emulsifying capacity of SC due to protein denaturation.     

Effects of enzymes and gamma irradiation on the tensile strength and morphology of poly(p-dioxanone) fibers

The objective of this study was to examine how and to what extent a new degradable polymeric fiber, poly(p-dioxanone), used as a surgical suture material, degrades in the presence of enzymes and after γ-irradiation. The degradation of the fiber was studied mechanically using an Instron and morphologically by SEM. Both esterase and trypsin enzymes and their corresponding buffer controls were used. The fibers were γ-irradiated at the dosages ranging from 0 to 20 Mrad, immersed in the solution for up to 70 days, and then removed for tensile strength and morphological examinations. It was found that γ-irradiation alone lowered the tensile strength of PDS fibers and made them more susceptible to hydrolysis. Esterase and trypsin did not accelerate the hydrolytic degradtion of this fiber to any significant level. Both γ-irradiation and enzymes influenced the gross morphological characteristic of PDS fibers when they were subjected to hydrolysis. The most important morphological observations were the formation of surface cracks and chips on the fibers and the subsequent peeling of the chips. Enzyme-treated PDS fibers exhibited similar morphological findings but the size of the chips was smaller. The morphological observations of PDS fibers were consistent with the tensile strength data.     

Hydrolytic degradation of polyglycolic acid: Tensile strength and crystallinity study

The hydrolytic degradation of polyglycolic acid (PGA) was studied by examining the changes of tensile strength and the level of crystallinity of the suture material. It was found that the breaking stress decreased from 6.369 × 10^?1 at 0 day to 3.97 × 10^?3 Newton/Tex at 49 days. The sigmodial shape of the stress–strain curves gradually disappeared with increase in the duration of in vitra degradation. The endpoint titration method used to assess the degree of degradation beyond the period of measurable tensile strength showed that the percent of PGA degraded were 42, 56, and 70% at 49, 60, and 90 days, respectively. The level of crystallinity of PGA at various durations of degradation exhibited an initial increase in the degree of crystallinity from 40% at 0 day to an upper limit of 52% at 21 days, then gradual decrease to 23% at 90 days. This observation is essentially parallel to hydrolysis of cellulose and polyethylene terephthalate. The concept of microfibrillar structure of fibers provides the basis for the proposed degradation mechanism of PGA in vitro. It is believed that degradation proceeds through two main stages which are different in rate of degradation.     

A rheological model for iron oxide suspensions

We have examined the rheological properties of a Co-adsorbed γ-Fe₂O₃ magnetic suspension with polyurethane (PU) as a binder and methyl ethyl ketone (MEK) or cyclohexanone (CH) as a solvent. A Haake RV20 viscometer was used to measure the suspension viscosity and the vane method was adopted to determine the fluid yield stress. A rheological model which can be viewed as a combination of the Casson model and the Bingham model is proposed to describe the suspension viscosity. The effects of temperature, particle content, and binder concentration are included in the model.     

Packed bed electrodes. I. The electrochemical extraction of copper ions from dilute aqueous solutions

A study has been made of the cathodic deposition of copper ions from flowing dilute aqueous solutions onto a packed bed of graphite. The electrodeposition reaction is mass transfer controlled and expressions are presented for the cathodic current as a function of time, solution flow rate and bed characteristics. These have been verified from potentiostatic experiments. The cathode current efficiency is shown to approach 100% and packed bed electrodes are shown to be an effective means of extracting or removing metal ions from dilute solutions.