Mullite-bonded SiC-whisker-reinforced SiC matrix composites: Preparation,characterization, and toughening mechanisms

A novel mullite-bonded SiC-whisker-reinforced SiC matrix composite (SiCw/SiC, SiC whisker-to-SiC powder mass ratio of 1:9) was designed and successfully prepared. Before preparing the composite, the inexpensive lab-made SiCw was first modified by an oxidation/leaching process and then coated with Al₂O₃. The kinetics results indicate that the oxidation process can be described by improved shrinking-cylinder models. The aspect ratio of SiCw improved after modification. Subsequently, raw materials with a SiC–SiO₂–Al₂O₃ triple-layered structure were obtained after the Al₂O₃-coating process and used as feedstocks during the subsequent hot-pressing sintering. Finally, the characterization of the composites indicates that the mullite-bonded sample performs better (relative density of 93.8?±?1.4%, flexural strength of 533.3?±?18.2?MPa, fracture toughness of 13.6?±?2.1?MPa?m^1/2, and Vickers hardness of 20.6?±?2.5?GPa) than the reference sample without the mullite interface. The improved toughness could essentially be attributed to the moderately strong interface bonding and effective load transfer effects of the mullite interface.     

ICP—OES法测定钛合金中A1元素含量的不确定度评定

将钛合金样品用10mL1：1硫酸溶解后,用ICP—OES法对其中A1元素含量进行测定,测得样品中W（A1）=6．91％。对测定过程中的不确定度来源进行了分析,依据不确定度评定的步骤,计算得到了各分量标准不确定度及合成标准不确定度,W（A1）测定结果的扩展不确定度为U=0．17％,K=2。     

直读光谱与电感耦合等离子体发射光谱测定不锈钢中硅、锰、磷、铬、镍的方法比较

通过对比试验,从样品前处理、测定结果等方面对直读光谱法（OES）与电感耦合等离子体发射光谱法（ICP-OES）进行分析。结果表明,两种方法无显著差异,OES的前处理更简单,检测速度更快,但对样品大小、形状要求较高,无法对直径过小的钢铁样品进行检测,而ICP-OES更符合对不同形状钢铁的检测需求。     

氢气流量对大面积金刚石膜沉积的影响

为了实现大面积金刚石膜的高速均匀沉积,在新型多模微波等离子体装置中,利用微波等离子体(Microwave plasma chemical vapor deposition,MPCVD)技术,对大面积金刚石膜沉积过程中气体流场、电子密度和温度、基团分布及金刚石膜质量进行研究。流场模拟结果表明,多模MPCVD装置在高气体流量下依旧保持良好的流场稳定性。等离子体光谱结果表明,随着氢气流量的上升活性基团的强度上升。氢气流量在400 cm~3/min以内时,活性基团可在基底表面对称均匀分布。电子密度和电子温度随着氢气流量的上升先上升后下降,在500 cm3/min达到最大,分别为2.3×1019/m~3和1.65 eV。在氢气流量为300 cm~3/min时可在直径为100 mm的钼基底上实现大面积金刚石膜的均匀沉积,金刚石膜中心和边缘处拉曼光谱FWHM值为4.39 cm~(-1)和4.51 cm~(-1),生长速率为5.8μm/h。     

Comparison of oral,intravenous, and subcutaneous fluid therapy for resuscitation of calves with diarrhea

Neonatal diarrhea remains the primary cause of mortality in dairy calves around the world, and optimal treatment protocols are needed. The main goals of therapy are to restore hydration and electrolyte concentrations, correct strong ion (metabolic) acidemia, and provide nutritional support. Administration of oral electrolyte solutions (OES) has long been the primary method used to treat neonatal diarrhea in humans and calves because OES are capable of addressing each of the primary goals of therapy. In calves with moderate dehydration, we hypothesized that oral electrolytes would be as good as or better than small volumes of intravenous (IV) or subcutaneous (SC) fluids. Therefore, the main goal of this study was to compare the ability of a commercially available oral electrolyte solution (OES) administered alone or in combination with hypertonic saline with small volumes of IV or SC fluid therapy to resuscitate calves with diarrhea. Thirty-three Holstein calves from 5 to 14 d of age were utilized in this clinical trial. Diarrhea and dehydration were induced by adding sucrose to the milk replacer. In addition, hydrochlorothiazide and spironolactone were given orally and furosemide intramuscularly. Depression status, clinical hydration scores, fecal consistency, and body weight were recorded at regular intervals. Treatment began when calves had severe diarrhea and had a decrease in plasma volume of at least 10%. Calves were randomly assigned to 1 of 4 treatment groups of 8 to 9 calves per group: (1) OES; (2) OES with hypertonic saline (4 mL/kg, IV); (3) IV fluids (lactated Ringer's, 2 L); or (4) SC fluids (lactated Ringer's, 2 L). Treatments were given at 0 and 12 h. Changes in plasma volume, blood pH, electrolyte levels, and physical examination scores were determined before therapy and again at 1, 2, 4, 8, and 12 h after each treatment. All 4 treatments were ultimately successful in improving hydration as well as increasing blood pH; however, animals in both groups that received OES had much faster resuscitation than those in either the IV or SC fluid group. In conclusion, oral electrolyte products remain the gold standard for resuscitating diarrheic calves with moderate dehydration and acidemia and will likely perform better than small volumes of IV lactated Ringer's solution. Subcutaneous fluids by themselves are a poor treatment option and should be only be used as supportive therapy following the initial correction of hypovolemia and metabolic acidosis.     

Estimation of plasma parameters in the process of micro-scale powder plastic and characteristics of its products

The temperature and density of plasma jets were estimated with a Boltzmann plot and Stark broadening of Ar I (696.54 nm) lines by optical emission spectroscopy (OES) in the process of plasma plastic, and the morphology and microstructure of tungsten (W) powders were investigated by scanning electron microscope (SEM) and x-ray Diffraction (XRD), respectively. The results show that the assumption of local thermodynamic equilibrium (LTE) was invalid at the end of the plasma jets, and earlier than this after the injection of tungsten powder. The temperature and electron density of the plasma jets were up to about T=6797 K with Q_c=50 slpm and n_e=1.05×10¹⁶ cm⁻³ with Q_s=115 slpm at Z=60 mm, respectively, and both dropped rapidly with the injected tungsten powders of 20 μm. After the plasma plastic process, the spherical tungsten powders were prepared and there were some satellite particles on the surface of the spherical products. The tungsten powders were both composed of a single equilibrium α-W phase with a body centered cubic (bbc) crystal structure before and after plasma treatment.     

Evolution of plasma parameters in an Ar-N2/He inductive plasma source with magnetic pole enhancement

Magnetic pole enhanced inductively coupled plasmas(MaPE-ICPs) are a promising source for plasma-based etching and have a wide range of material processing appUcations.In the present study Langmuir probe and optical emission spectroscopy were used to monitor the evolution of plasma parameters in a MaPE-ICP Ar-N_2/He mixture plasma.Electron density(n_e) and temperature(T_e),excitation temperature(T_(exc)),plasma potential(V_p),skin depth(δ) and the evolution of the electron energy probability function(EEPF) are reported as a function of radiofrequency(RF) power,pressure and argon concentration in the mixture.It is observed that n_e increases while T_e decreases with increase in RF power and argon concentration in the mixture.The emission intensity of the argon line at 750.4 nm is also used to monitor the variation of the 'high-energy tail' of the EEPF with RF power and gas pressure.The EEPF has a'bi-Maxwellian' distribution at low RF powers and higher pressure in a pure N_2 discharge.However,it evolves into a 'Maxwellian' distribution at RF powers greater than 70 W for pure N_2,and at 50 W for higher argon concentrations in the mixture.The effect of argon concentration on the temperatures of two electron groups in the 'bi-Maxwellian' EEPF is examined.The temperature of the low-energy electron group T_L shows a decreasing trend with argon addition until the 'thermalization' of the two temperatures occurs,while the temperature of high-energy electrons T_H decreases continuously.     

The effect of current mode and discharge type on the corrosion resistance of plasma electrolytic oxidation (PEO) coated magnesium alloy AJ62

Magnesium alloys are increasingly being used as lightweight materials in the automotive, defense, electronics, biomaterial and aerospace industries. However, their inherently poor corrosion and wear resistance have, so far, limited their application. Plasma electrolytic oxidation (PEO) in an environmentally friendly aluminates electrolyte has been used to produce oxide coatings with thicknesses of ~ 80 μm on an AJ62 magnesium alloy. Optical emission spectroscopy (OES) in the visible and near ultraviolet (NUV) band (285 nm–800 nm) was employed to characterize the PEO plasma. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to characterize the coated materials, and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) in a 3.5% NaCl solution were used to determine the corrosion behavior. It was found that the plasma discharge behavior significantly influenced the microstructure and the morphology of the oxide coatings and, hence the corrosion resistance. The corrosion resistance of the coated alloy was increased by changing the current mode from unipolar to bipolar, where the strong plasma discharges had been reduced or eliminated.     

Determination of corrosion rate of orthodontic wires based on nickel‐titanium alloy in artificial saliva

The goal of this study was to determine corrosion behavior of three orthodontic wires based on nickel‐titanium alloy (NiTi) in artificial saliva at temperature of 37 °C as function of immersion time. Following orthodontic wires were used: uncoated (NiTi), rhodium coated (Rh NiTi) and nitrified (N NiTi) orthodontic wires. Corrosion of investigated orthodontic wires were monitored by measuring of Ni²⁺ and Ti⁴⁺ ions released in artificial saliva by inductively coupled plasma‐optical emission spectroscopy (ICP‐OES) after 3, 7, 14, 21 and 28 days of immersion. Obtained results indicate that corrosion reaction of the NiTi wires in artificial saliva follows the parabolic rate law. According to the obtained values of parabolic corrosion rate constants, corrosion susceptibility of orthodontic wires decreases in the following order: Rh NiTi wire (K_p = 2.48 μg²/cm⁴ h) > NiTi wire (K_p = 1.6 × 10^–3 μg²/cm⁴ h) > N NiTi wire (K_p = 6.0 × 10^–4 μg²/cm⁴ h). These results indicate that in comparison with uncoated NiTi wire, rhodium coating significantly increases corrosion susceptibility, while nitrification effectively suppresses the release of Ni²⁺ and Ti⁴⁺ ions.     

Optimization of a slurry dispersion method for minerals and trace elements analysis in infant formulae by ICP OES and FAAS

Infant formula developed by manufacturers requires a rigorous control of composition, particularly those elements added routinely in an attempt to mimic the mineral composition of human milk. A total of 97 different types of powdered infant formulae (preterm, adapted starter, adapted follow-up, toddler, specialised and soy-based formulae) commercially available in Spain were studied. It is noteworthy great differences in mineral (Ca, P, Mg) and trace element (Zn, Fe, Cu, Mn) contents found between analysed and listed in label information. The development of a fast, simple and direct slurry method for the determination of these essential micronutrients in infant formula by inductively coupled plasma optical emission spectrometry (ICP OES) and flame atomic absorption spectrometry (FAAS) was performed in order to help in quality control tasks. Infant formula samples were solubilised using different amounts of several different solvents. An addition of 250 μL of a solution 10% tetramethylammonium hydroxide and 25% ammonium hydroxide were required for the accurate quantification of Ca and P, Mg, Zn, Fe, Cu and Mn, respectively. The standard reference material 1549 non-fat milk powder was solubilised to compare the validity of assayed methodology following slurry nebulisation and traditional microwave-assisted acid digestion method. Good agreement of the analytical results by both ICP OES and FAAS, with the certified values was obtained. Method performance parameters (accuracy, precision and methodological detection limits) were determined for studied elements to check the quality and usefulness of the optimised slurry method. The analytical procedure was applied successfully to the analysis of a representative group of infant formulae. Levels of analysed elements were graphically represented, showing an acceptable comparability between slurry and acid-mineralisation method set by linear correlation coefficients and slopes close to the unit. The described simple and slurry method is appropriate, as an attractive alternative, for routine control analysis of added essential elements in infant formulae regardless of predominant protein type used in manufacture.