Soluble polyimide as liquid crystal perpendicular alignment layer

Journal of Materials Science - Three polyimides (PIs) were prepared from a diamine containing biphenyl ester group as a side chain and a corresponding dianhydride chosen from...     

Cu掺杂对有序Sr3YCo4-xCuxO10.5+δ多晶的结构与物理性能的影响

采用固相反应法制备了四方Sr3YCo4-xCuxO10.5+δ(x=0~1.0)多晶。用热重-差示扫描量热分析,X射线衍射研究了多晶的有序化相变及结构。在固溶范围内(x=0~0.4),观察到有序峰(103)和(215),说明四方Sr3YCo4-xCuxO10.5+δ多晶为超结构,这是由于合成时在1000℃以上发生了吸氧(δ)有序化相变；当x=0.6~1.0时,978℃时在晶界处形成了单斜杂相,破坏了Sr3YCo4-xCuxO10.5+δ多晶的有序。当x=0~0.4时,多晶呈半导体输运行为。随着Cu掺杂量的增加,Co4+提供的空穴载流子浓度增大,电阻率明显下降；由于Cu的固溶,自旋熵增加,载流子浓度和自旋熵的共同作用使x=0~0.2多晶的热电势不变,x=0.4的热电势降低。并且Cu掺杂导致的晶格畸变使Co3+离子由高自旋态转变为高/低自旋混合态,磁化强度和铁磁转变温度(Tc)降低,磁结构由G-型反铁磁转变为铁磁。在进行二次烧结后,300K时电阻率明显降低,热电势为一次烧结的2倍,可能是二次烧结使多晶的有序化程度增大,提高了铁磁有序排列。     

Simultaneous fractionation of multiple classes of polyphenols from honeybush tea using solid-phase extraction

The structural diversity of polyphenols and the inherent limitations of current extraction techniques pose a challenge to extract polyphenols using a simple and green method. Hence, in this study, a method was developed to simultaneously fractionate multiple classes of polyphenols by only varying ethanol-water solutions. Honeybush tea, which is rich in polyphenols, was selected as a model for this study. Solvent extraction followed by solid-phase extraction (SPE) was developed to obtain a polyphenol-rich fraction from six honeybush samples. Based on a gradient elution programme (10%, 30%, 50%, 70% and 90% (v/v) ethanol-water solution) of SPE, the Strata X cartridge showed a better recovery of most targeted polyphenols under 0.9 mL of the drying volume and 1 mL min⁻¹ of the dispensing speed. The elution programme for fractionating most polyphenols was as follows: single elution with 50% ethanol, followed by twice elution with 70% ethanol. The antioxidant capacity was used to analyse the differences among the polyphenol-rich fractions from six honeybush samples. Principal component analysis (PCA) revealed that unfermented C. genistoides (GG) has the greatest antioxidant capacity among the honeybush species studied. Additionally, mangiferin, isomangiferin and vicenin-2 were the main contributors to the antioxidant capacity in six honeybush fractions according to the correlation study.     

乙烯精馏塔提馏段温度控制系统

针对乙烯精馏塔提馏段温度原控制方案的不足,采用提馏段温度ＧC３气流量组成串级控制方式,提高温度稳定性,同时采用提馏段温度Ｇ丙烯凝液储槽液位的选择性控制系统,克服丙烯凝液储槽出口排出气态丙烯的问题,从而保证生产安全平稳进行.与原控制效果比较,现提馏段温度稳定性和控制精度大大改善,控制质量获得提高。     

双功能催化剂上四氢萘加氢裂化生成单环芳烃的反应网络研究

Conversion of LCO (light cycle oil) to BTX (benzene, toluene, and xylene) is an economically valuable method for refineries. However, this approach still faces difficulties as the main reactions are not clearly understood. Here we study the detailed hydrocracking pathway of typical reactants, 1-methylnaphthalene and tetralin, through molecular simulations and experiments to improve our understanding of the conversion process of LCO to BTX. Molecular simulations demonstrate that the rate-determining step is the isomerization pathway of six-membered ring to five-membered ring in tetralin as its activation energy (ΔEa) is the highest among all the reactions and the order of ΔEa of reactions is isomerization > ring-opening ≈ side-chain cleavage. The results of experiments show that with the increase in reaction depth, i.e., through a high temperature (350 – 370 °C) and low LHSV (4.5 – 6.0 h−1), isomerization, ring-opening, and side-chain  cleavage reactions occurred, thus improving the selectivity and yield of alkyl aromatics.     

行李箱外板浮动整形模设计

介绍了某轿车行李箱外板的翻边侧整形模设计过程,行李箱外板的侧法兰翻边上存在凹包,其翻边方向和凹包成形方向不同,常规需要2道工序分别完成翻边和凹包成形。该模具突破了传统的设计结构,在翻边机构中设置了凹包成形机构,将2个不同方向的成形复合到1道工序中,减少了模具数量,降低了冲压成本和工装成本。     

GC-MS法测定缬草残渣中的化学组分

分别使用95％乙醇和四氯化碳作为提取溶剂,在78℃左右,对已提取过挥发油的缬草残渣中化学成分进行提取,借用气相色谱-质谱联用方法(GC-MS)对提取浸膏中化学组分进行分析.结果显示:以乙醇作为提取溶剂条件下,共鉴定出38中化学组分,数据出峰相对总质量分数为81.7％;以四氯化碳为提取溶剂条件下,共鉴定出44种化学组分,数据出峰相对总质量分数为84.4％.     

CFETR水冷陶瓷增殖剂包层模块产氚率实验验证

水冷陶瓷增殖剂（WCCB）包层作为中国聚变工程试验堆（CFETR）候选包层之一，承担着氚增殖、核热提取、屏蔽等重要涉核功能，其中子学设计的可靠性直接影响CFETR氚自持目标的实现。为验证中子学设计工具，即MCNP和FNEDL3.0数据库，在WCCB包层中子学设计中的可靠性，基于研制出的WCCB包层模块，在DT中子环境下开展中子学实验，对以产氚率（TPR）为代表的中子学参数进行了模拟值（C）和实验值（E）对比分析。结果表明，模块中轴线位置处TPR的C/E为0.97?1.08，而模块边缘位置处TPR的C/E为0.65?0.82；模块钛酸锂层边缘区197Au（n，γ）198Au反应率的C/E为0.72?0.90，表明模块边缘区存在非期望的散射中子，导致该区TPR模拟值和实验值偏离较大。