畜禽骨蛋白质材料化利用的研究现状与发展趋势分析

作为畜禽屠宰的副产物,动物骨因其丰富的蛋白质和广阔的深加工利用的发展前景而成为当今环境、农业和能源等领域的研究热点.受自身骨骼结构和综合利用技术的制约,骨骼的深加工利用率不足2％,造成了严重的资源浪费与环境污染.蛋白水解作为蛋白质资源深加工领域最有效的技术手段,可实现大宗蛋白质资源的高效回收利用;而蛋白水解物优异的溶解性、可降解性、生物相容性和独特的生物功能活性使其具有开发高值材料的潜力.随着石化资源的短缺和人们健康环保意识的增强,人们对环保型可再生型新材料的需求逐渐迫切,而畜禽骨蛋白质材料的开发利用紧密结合国家新型战略产业——生物制造业,将促进农副产品加工业的持续健康发展.针对畜禽骨蛋白质材料化开发利用的发展历程及当前的研究热点,本文阐述了絮凝剂、粘结剂、可降解塑料、表面活性剂、医用材料等近年来研究较广的畜禽骨蛋白质材料化利用途径,并总结了各种利用途径的应用效果和局限性;同时,总结分析了现今利用蛋白水解物开发新型材料的相关理论及研究成果,为开发畜禽骨蛋白质材料提供了理论支持;最后,基于目前生物基材料的发展趋势及畜禽骨深加工技术的难点问题,客观展望了畜禽骨蛋白质材料的制备及应用发展方向.     

基于三相幅度测量的相控阵天线快速校准方法

提出了一种基于三相幅度测量的相控阵天线快速校准方法。该方法将天线阵列进行分组,利用每种分组在三种配相下的阵面合成场幅度测量值,可解算出各个天线单元的初始幅相值。该方法仅需幅度测量,避免了相位测量误差影响单元幅相值的计算精度,而且所需幅度测量次数仅为(2N+1)次,可显著提高校准时效性。另外,利用分组思想,同时改变多个单元相位,使总辐射场的幅度变化显著,提升校准准确性。仿真结果表明:校准后相位均方根误差为2.2°,幅度均方根误差为0.2 dB。     

Effect of an abrupt change in pulling rate on microstructures of directionally solidified Al2O3-Er3Al5O12 eutectic and off-eutectic composite ceramics

Directionally solidified microstructures of Al₂O₃-Er₃Al₅O₁₂ eutectic and off-eutectic in situ composite ceramics were explored under abrupt-change pulling rate conditions. Corresponding temperature distributions and interface locations were studied. In eutectic composition, fluctuation of eutectic spacing occurred when the pulling rate increased abruptly. A gradually increase or abrupt increase in eutectic spacing was observed when the pulling rate decreased abruptly. In hypoeutectic and hypereutectic compositions, formation of the primary phases were suppressed when the pulling rate increased abruptly from 10?µm/s to 100?µm/s, while primary phases precipitated when the pulling rate decreased abruptly from 100?µm/s to 10?µm/s. The interface altitude decreased after the pulling rate increased abruptly, but increased after the pulling rate decreased abruptly. The liquid composition restriction (around the eutectic composition) at the eutectic interface plays an important role in the suppression of the primary dendrite and coupled eutectic oxides can be obtained in off-eutectic compositions even under higher solidification rate conditions.     

Catalytic Hydrocracking of a Bitumen‐Derived Asphaltene over NiMo/γ‐Al2O3 at Various Temperatures

Hydrocracking of a bitumen‐derived asphaltene over NiMo/γ‐Al₂O₃ was investigated in a microbatch reactor at varying temperatures. The molar kinetics of asphaltene cracking reaction was examined by fitting the experimental data. Below a defined temperature, the molar reaction showed the first‐order kinetic feature while at higher temperatures secondary reactions such as coke formation became significant, causing deviation of the reaction behavior from the proposed first‐order kinetic model. Selectivity analysis proved that dominant products varied from gases to liquids to gases with increasing temperature, shifting the dominant reaction from C–S bonds cleavage to C–C bonds cleavage.     

3-三氟甲基-5,6,7,8-四氢-1,2,4-三唑[4,3-α]吡嗪盐酸盐的合成

乙二胺与氯乙酸乙酯经取代、环合反应制得2-哌嗪酮,2-哌嗪酮与Boc酸酐进行氨基保护反应后,再与五硫化二磷进行硫代反应制得4-(N-叔丁氧羰基)-2-哌嗪硫酮,其与三氟乙酰肼经取代、环合、脱叔丁氧羰基成盐,得标题化合物,总收率为45.7%(以氯乙酸乙酯计)。为磷酸西他列汀中间体的工业化生产提供了一条较理想的工艺路线。