Multi-Objective Optimization of Braun-Type Exothermic Reactor for Ammonia Synthesis

The exothermic reactor for ammonia synthesis is a primary device determining the performance of the energy storage system. The Braun-type ammonia synthesis reactor is used as the exothermic reactor to improve the heat release rate. Due to the entirely different usage scenarios and design objectives, its parameters need to be redesigned and optimized. Based on finite-time thermodynamics, a one-dimensional model is established to analyze the effects of inlet gas molar flow rate, hydrogen–nitrogen ratio, reactor length and inlet temperature on the total entropy generation rate and the total exothermic rate of the reactor. It’s found that the total exothermic rate mainly depends on the inlet molar flow rate. Furthermore, considering the minimum total entropy generation rate and maximum total exothermic rate, the NSGA-II algorithm is applied to optimize seven reactor parameters including the inlet molar flow rate, lengths and temperatures of the three reactors. Lastly, the optimized reactor is obtained from the Pareto front using three fuzzy decision methods and deviation index. Compared with the reference reactor, the total exothermic rate of the optimized reactor is improved by 12.6% while the total entropy generation rate is reduced by 3.4%. The results in this paper can provide some guidance for the optimal design and application of exothermic reactors in practical engineering.     

One‐Pot Synthesis of 2,5‐Furandicarboxylic Acid from 2‐Furoic Acid by a Pd‐catalyzed Bromination–Hydroxycarbonylation Tandem Reaction in Acetate Buffer

The one‐pot synthesis of 2,5‐furandicarboxylic acid from 2‐furoic acid with a yield of 57 % was achieved for the first time using a Pd‐catalyzed bromination‐hydroxycarbonylation tandem reaction in HOAc‐NaOAc buffer. This synthetic protocol shows major improvements compared to previously reported methods, such as using biomass‐based 2‐furoic acid as low‐cost raw material, one‐pot synthesis without isolation of intermediate products, and no need for an acidification procedure. Experiments indicate that the involved Xantphos‐modified Pd‐catalyst and the buffer solution play significant promoting roles for each individual reaction whereas Br₂ (as the brominating reagent) had a negative effect on the second hydroxycarbonylation step, while CO was deleterious for the first bromination step. Hence, in this practical one‐pot synthesis, Br₂ should be consumed in the first bromination step as fully as possible, and CO is introduced after the first bromination step has been completed.     

机顶盒与ADSL宽带故障处理分析

在数字化油田发展的今天,光纤通信已经普及,但仍有部分单位没有实现光纤入户.这些单位还在使用机顶盒与非对称数字用户线路(Asymmetric Digital Subscriber Line,ADSL)宽带,由此带来的故障不可避免.通过分析长期在边远地区实际工作中遇到的故障,总结了机顶盒与ADSL宽带故障的各种原因和常见的...     

纸基PVA无芯片RFID湿度传感器

传统湿度传感器制造工艺复杂、需有线连接信号,对此,文中提出一种纸基无芯片射频识别(Radio Frequency Identification, RFID)湿度传感器。为提升传感器谐振特性,选择非对称开口环内部分布式加载金属碎片作为传感器结构,聚乙烯醇(PVA)作为湿敏材料,使用遗传算法和HFSS射频仿真软件来设计并优化传感器结构。以喷墨打印技术制作传感器样品,采用滴涂法在传感器表面分别制备了5%、10%、15%三种质量浓度比的PVA薄膜。湿敏特性仿真及测试结果一致表明：PVA与纸基底协同作用可显著提高传感器灵敏度。随PVA浓度增加灵敏度增加,15%PVA传感器灵敏度最高,高湿灵敏度达到12.22 MHz/%RH,但随PVA浓度增加恢复特性变差,5%PVA湿度传感器具有良好的恢复特性,恢复度达83.87%。通过长期多次实验验证了PVA纸基湿度传感器具有良好的温度稳定性与中长期稳定性。与同类研究成果对比,文中设计在感湿范围及灵敏度方面有优势且制造工艺更简单,为低成本湿度传感器的大规模使用提供了可能。     

聚芴类电致发光材料

聚芴与其衍生物是一类重要的电致发光聚合物,它们具有较高的光致发光效率,并且易于进行结构修饰,因此受到材料化学家们的高度关注。本文叙述的线索是聚合物结构与其电致发光性能之间的构效关系。通过化学修饰,可以调节材料的前线分子轨道、热和光谱稳定性,进而开发新的发光材料。文中首先简单介绍了聚芴类发光材料的聚合方法,然后把这些聚合物按结构不同分成两个部分介绍：一部分是主链仅含有共轭芴单元的聚合物,它们的化学修饰依赖于芴9位的活性碳原子;另一部分是通过共聚方法得到的主链含有芴和其它基团的聚合物。     

实验室质量体系运行的关键控制点分析

通过对十几年来实验室计量认证的经验总结,对县级实验室质量体系运行情况进行了分析。指出了质量体系运行的关键控制点、存在的问题、解决问题的方法。经分析认为,基层实验室的生存和发展必然趋势是提高自身的检测能力。     

硬脂酸镉和山嵛酸镉混合LB膜的微结构

X-ray diffraction (XRD) was used to investigate the microstructure and phase separation of mixed multilayers of cadmium stearate (SA) and behenate (BA) deposited onto hydrophilic glass by the Langmuir-Blodgett technique. No unitary fatty acid diffraction peaks in the XRD spectra of the mixed LB films, which reveals that domains in these samples are small and uniform. The interplanar spacing of the mixed LB films changes with the ratio of BA to SA in a step-shaped curve, which suggests that with the changing of the ratio between BA and SA, only three kinds of ordered structure form in the mixed system, and each microstructure, in particular, the short chains against long chains meshed microstructure can be maintained in a certain ratio range . In addition, for the meshed microstructure, the alkyl chains of both SA and BA stand straight or may have exactly the same small tilted angle from the substrate normal, as is indicated by the symmetric and asymmetric stretching vibration of methylene (CH2) peaks which are at 2847.80 and 2914.37 cm-1respectively in the Fourier transform infrared (FT-IR) transmission spectra. The mixed system always goes through a longitudinal regularity decreasing process when BA/SA is out of the intermediate ratio range (BA/SA: 1/5-1/1), which is illustrated by the relative XRD intensity changing with the ratio of BA/ SA in a \W" shape. These results for the mixed LB films of BA/SA provide meaningful data for choosing the mixture ratio when fabricating composite films with special structure.     

催化链转移聚合制备接枝型两亲共聚物及其溶液性质研究

采用大分子单体法制备接枝型两亲共聚物, 通过表面张力仪、偏光显微镜、旋转流变仪和小角X射线衍射研究了两亲共聚物在水溶液中的聚集行为及其相结构. 首先末端带有可聚合双键的聚甲基丙烯酸叔丁酯大分子单体(PtBMA Macromonomer)通过催化链转移聚合法制备, 所用到的催化链转移剂为二水合双(二氟化硼苯二酮肟)合钴(II) (COPhBF). 然后将所得到的大分子单体与丙烯酸正丁酯(BA)进行自由基共聚得到接枝共聚物PBA-g-PtBMA, PBA-g-PtBMA中PtBMA的侧链部分在酸性条件下定量水解成聚甲基丙烯酸(PMAA)并用NaOH中和得到主链疏水侧链亲水的接枝型两亲共聚物PBA-g-P(MAA^－Na^＋). 用Wilhelmy吊片法研究了不同浓度的两亲共聚物水溶液的表面张力, 发现其行为与小分子表面活性剂不同. 同时用动态光散射法测量了两亲共聚物水溶液中聚集体的粒度, 发现在研究的浓度范围内(0.02～10 g/L)聚集体都存在两个粒度分布峰(约30和300 nm). 浓溶液(w＝37.5%)的偏光显微照片呈现层状液晶的特征图案, 而流变研究表明此时体系具有明显的粘弹性, 说明体系形成了层状液晶. 并且用小角度X射线衍射测定了层状液晶的层间距, 约为12.6 nm.     

气相色谱与气相色谱-质谱联用法对七氟醚降解产物的测定

七氟醚是一种新型临床麻醉剂,由于具有稳定性好,刺激性小,诱导麻醉迅速,恢复快,代谢能力强等优点,成功研制出后很快被推广应用.但有学者指出,七氟醚的降解产物氟甲基五氟丙烯醚(Compound A)对小鼠的肝肾功能具有损害作用[1],在人体内的毒性作用目前还没有明确的结论.为了观察Compound A降解量对人体肝肾功能的影响,本文建立了一种快速测定Compound A的气相色谱和气相色谱一质谱联用法.     

Isolation and Purification of Unstable Iridoid Glucosides from Traditional Chinese Medicine by Preparative High Performance Liquid Chromatography Coupled with Solid-phase Extraction

An efficient preparative method was successfully developed for isolation and purification of unstable components from medicinal plant extracts, using a combined method of preparative high performance liquid chro-matography(HPLC) and solid-phase extraction(SPE). The aim of this study was to obtain an effective method with high preparative efficiency and importantly to avoid the transformation of unstable compounds. The preparative HPLC system was based on an LC/MS controlled four-channel autopurification sys...