平纹机织玄武岩纤维/环氧树脂复合材料冲击拉伸行为

以常规机织工艺生产织物增强体,以真空辅助树脂转移模塑法(VARTM)制备成型复合材料,研究单层平纹玄武岩长丝增强环氧树脂复合材料在准静态和高应变率加载下的拉伸性能。准静态和高应变率拉伸试验分别在MTS-810.23试验仪和分离式霍普金森拉杆(SHTB)测试系统上完成。试验结果表明该材料的力学性能具有应变率依赖性:随着应变速率的增加,拉伸模量和拉伸强度单调增加,失效应变单调减小,弹性能先增加后减小。材料的失效破坏特征也呈现明显的应变率效应:准静态拉伸时,材料断口整齐,树脂的破碎少,几乎没有纤维的抽拔和经纬向纤维束间的滑移;高应变率拉伸时,材料断口参差错乱,树脂完全破碎,纤维束抽拔严重、相互崩裂和滑移,织物增强体结构的整体性破坏严重。     

Al-Ti-B-RE细化剂对Al-7．0Si-0．55Mg合金显微组织和力学性能的影响

研究添加Al-5Ti-lB-RE细化剂对Al-7．0Si-0．55Mg（A357）合金的显微组织和力学性能的影响。先利用真空熔炼技术制各Al-7．0Si-0．55Mg合金,然后在Al-7．0Si-0．55Mg合金中加入不同成分的Al-5Ti-1B-RE中间合金。通过X射线衍射仪（XRD）、金相显微镜（OM）和扫描电子显微镜（SEM）对显微组织和拉伸试样的断口形貌进行观察。在室温下对合金的力学性能进行测试。观察Al-5Ti-1B-RE细化剂的形态以及内部结构,可以发现以TiB,为异质形核核心的TiAl3／Ti2Al20RE的壳层结构相。在Al-7．0Si-0．55Mg合金中加入Al-5Ti-1B-3．0RE细化剂后,抗拉强度会有明显提升,直到0．2％添加量时,抗拉强度会达到峰值。     

EFFECT OF REDUCTION CONDITIONS ON THE ACTIVITY OF Ni/γAl2O3 CATALYST FOR METHANATION REACTION

The effect of reduction conditions, mainly reduction temperature and duration time on the activity of Ni/γAl₂O₃ catalyst were studied for a methanation reaction in a gradientless Berty reactor. The methanation reaction was investigated using a feed containing CO (6.7 mole%), H₂ (26 mole%) and the balance being nitrogen at a pressure of 30 psig and a fixed temperature of 350°C. The reduction temperature was varying from 250 to 500°C, in order to investigate its effect on the methanation reaction. The methanation activity of the catalyst increased to a maximum by increasing the reduction temperature up to a maximum at 300-350°C and showed a slight negative decline afterward. The second parameter investigated was reduction duration time which was varied from 2 to 16 hours. It was observed that the methanation reaction activity increased by increasing the reduction duration time up to 6 hours. After six hours, there was no increase in activity. Based on the finding of this investigation, a recommended set of reduction conditions is given: reduction temperature of 300°C and a duration time of six hours.     

CHARACTERIZATION AND INHIBITION OF POLYPHENOL OXIDASE FROM PEARS (PYRUS COMMUNIS L. CV. BOSC AND RED)

Red pears had higher PPO activity, total phenolics and chlorogenic acid concentration than Bosc pears. PPO activity and phenolics both decreased in fruits held at room temperature. pH and temperature optima for Bosc and Red pears PPOs were 5.0 and 5.5, and 20 and 23C, respectively. 4-Methylcatechol, catechol and dopamine were good substrates for PPO from both pear cultivars; however, no activity was observed with any of the mono-hydroxy substrates studied. Higher K_m and lower V_max values were observed for Bosc pear PPO. Heating at 75C for 30 min completely inactivated the enzyme from both cultivars. Heating at 55 and 65C for the same duration resulted in partial inactivation (45–60%) of this enzyme. Ascorbic acid, L-cysteine, sodium metabisulfite and thiourea effectively inhibited browning due to pear PPOs.     

EFFECT OF HOT WATER IMMERSION ON PEEL COLOR OF PEARS AND ON WHITE ROT CAUSED BY BOTRYOSPHAERIA BERENGERIANA

Abstract The effectiveness of hot water immersion (HWI) on peel color and the control of white rot caused by Botryosphaeria berengeriana on wound-inoculated European pears, cv. La-France, were investigated. After HWI at 40, 45, 48, 50, 52 and 54C for varying immersion periods, the pears were held at 20C, ≥ 90% RH (simulated retail conditions). The peel color (L*, a*, b*) was determined before and after HWI treatment. The dominant role of L* suggested that peel darkening was the major factor in color change of the HWI treated pears. The L* value of 54 was judged as the border line for acceptability and less than 51 resulted in browning. Similarly the critical points for a*, b*, chroma, hue and ΔE* were found to be −6, 34, 35, 100, and 8, respectively. Disease incidence recorded 7 days after treatment revealed that High Temperature Short Time (HTST) treatment of 54C for 3 min reduced incidence about 85% with good retention of color. Both temperature and immersion period are to be carefully selected to prolong shelf-life and retain the peel color quality of 'La-France'pears.     

SiCp及Al2O3w增强铸态混杂金属基复合材料的疲劳裂纹扩展机理（英文）

研究了一种SiCp及Al2O3w增强铸态混杂金属基复合材料(MMC)的疲劳裂纹扩展(FCG)机理,同时对比研究了Al2O3w增强铸态金属基复合材料和铸态铝合金的疲劳裂纹扩展机理。在研究近临界和裂纹稳定扩展区域的疲劳裂纹扩展(FCG)机理时,发现混杂MMC的临界应力强度因子?Kth值高于其他两种材料的?Kth值,说明应力强度因子?K值较低时混杂MMC可以更好地抵抗裂纹扩展。随着?K值的降低,两种MMC在近临界区域显示出相似的FCG机理,即主要由增强相–基体界面的剥离控制,随后由铝基体中空隙的形核与合并控制;在裂纹稳定或中等扩展区域,?K值较高时FCG除了受界面上周期性裂纹扩展引起的增强相–基体界面剥离的影响之外,还显著受到铝基体中疲劳条带的影响。此外,在高?K值下,因为局部失稳断裂机制,可见铝基体中空隙的形核与合并以及SiCp和Al2O3w中的穿晶断裂。对于铸态铝合金,在低?K值下,FCG主要受空隙的形核与合并所控制;在高?K值下,FCG主要受铝晶粒的疲劳条带控制,随后受Si团簇中空隙的形核与合并控制。     

BROWNING OF SAGO (METROXYLON SAGU) PITH SLURRY AS INFLUENCED BY HOLDING TIME, pH AND TEMPERATURE

The effect of holding time, pH and temperature of sago pith slurry on its browning was evaluated. Holding time of sago pith slurry, which browning took place, proved to be an important factor in determining the amount of soluble phenolic compounds that were oxidized. This subsequently led to the development of color. The amount of (+)-catechin and (-)-epicatechin that was oxidized increased with pH particularly above pH 4.5. This resulted in simultaneous development of color in the sago pith slurry. The oxidation of phenolic compounds in acidic conditions was suggested to be caused by latent polyphenol oxidase (LPPO) as it is activated by acidic pH. The amount (+)-catechin and (-)-epicatechin oxidized also increased with increase in temperature particularly above 30C.