改进的遗传算法在同步器优化中的应用

汽车同步器是自动变速器的重要组成部分.对同步器的模拟优化能为同步器的设计生产提供重要的参考.为了获得一个较好的优化效果,提出了一种改进的遗传算法.通过对遗传算法选择过程的标准进行了改进,结合适应度函数与染色体之间差异,形成一种新的适应度函数.该函数同时考虑了选择压力和物种多样性.通过对函数中两个常量的调整,可以使算法在不同情况下可以有不同的偏重.引入两种典型测试函数的分别从高纬度变量和低纬度变量进行试验,分析改进算法中两个影响因子的作用.并与几类遗传算法进行比较,结果表明该改进的遗传算法能更快更稳定的找到较优的解.最后将改进选择策略结合自适应遗传算法对同步器进行优化,证明了该选择策略具有良好的鲁棒性和实效性.     

Engineering Bioactive M2 Macrophage-Polarized Anti-Inflammatory,Antioxidant, and Antibacterial Scaffolds for Rapid Angiogenesis and Diabetic Wound Repair

Diabetic wound healing still faces great challenges due to the excessive inflammation, easy infection, and impaired angiogenesis in wound beds. The immunoregulation of macrophages polarization toward M2 phenotype that facilitates the transition from inflammation to proliferation phase has been proved to be an effective way to improve diabetic wound healing. Herein, an M2 phenotype-enabled anti-inflammatory, antioxidant, and antibacterial conductive hydrogel scaffolds (GDFE) for producing rapid angiogenesis and diabetic wound repair are reported. The GDFE scaffolds are fabricated facilely through the dynamic crosslinking between polypeptide and polydopamine and graphene oxide. The GDFE scaffolds possess thermosensitivity, self-healing behavior, injectability, broad-spectrum antibacterial activity, antioxidant and anti-inflammatory ability, and electronic conductivity. GDFE effectively activates the polarization of macrophages toward M2 phenotype and significantly promotes the proliferation of dermal fibroblasts, the migration, and in vitro angiogenesis of endothelial cells through paracrine mechanisms. The in vivo results from a full-thickness diabetic wound model demonstrate that GDFE can rapidly promote the diabetic wound repair and skin regeneration, through fast anti-inflammation and angiogenesis and M2 macrophage polarization. This study provides highly efficient strategy for treating diabetic wound repair through designing the M2 polarization-enabled anti-inflammatory, antioxidant, and antibacterial bioactive materials.     

挤出型3D打印混凝土力学性能研究进展

介绍了3D打印混凝土的特点与前景,综述了挤出型工艺的3D打印混凝土的压、拉、折、剪基本力学性能以及增强措施。研究表明:打印层在喷嘴的挤压作用下密实度有所提高,但同时层间易形成薄弱界面,造成性能的各向异性,通过调整胶凝材料、掺入纤维、优化工艺、水浴养护、布筋等措施能有效改善。此外,提出了还需进一步研究的问题。     

盾构接收对地铁车站接收端的影响研究

以西安地铁14号线某区间盾构接收施工为依托,通过数值模拟手段,对比分析了接收端结构板在不同施作时机条件下,盾构出洞对接收端影响并提供最优盾构接收方案.研究表明,接收端仅结构中板完成条件下盾构接收对接收端结构的影响,要明显小于接收端仅底板完成条件下接收的影响.在实际施工中,中板完成后盾构接收还应重点控制接收端端头加固质量、保证接收端混凝土结构达到强度要求,同时盾构接收过程中加强监测点的布设及监测频次.研究结果对类似工程具有一定的指导意义及参考价值.     

Characteristics of reaction and product microstructure during light calcination of magnesite in transport bed

A gas-heating laboratory transport bed was adopted to simulate the industrial transportbed reactor for flash calcination of magnesite, and a method based on TG analysis of a reacted sample was further developed to calculate the decomposition rate or conversion of its containing MgCO₃. The study investigated how the conversion and product reactivity as well as microstructure vary with reaction conditions including temperature, particle size and times of re-calcination for powder magnesite. Magnesite powder (<150 μm) calcination is a quick reaction that reaches 98% decomposition of its containing MgCO₃ in 1—2 s,corroborating the feasibility of magnesite flash-calcination in transport bed reactors. The coloration time given by the citric acid chromogenic method was 17—55 s and 294 s for the obtained products from transport and fixed beds, respectively. This proves the obviously higher activity and thus improved microstructure of the product from transport bed. During the calcination process, the MgO grain size of the product gradually increases, and the surface structure changes from loose and porous to dense and smooth. This structural change can be completed within a few seconds.     

湿法回收钒高氨氮废水处理工程实例

湿法提钒回收处理过程中的废水具有高硬度、高含盐、高氨氮等特征,采用预处理+负压亚沸碱析脱氨及微负压氨回收工艺,可使出水水质稳定氨氮达到15 mg/L以下,同时超级吸氨器以及两级氨水吸收罐可制得浓度为18％～25％的氨水作为产品,降低项目整体运行费用.     

基于蛋白质组学技术研究秦川牛肉宰后贮藏过程中肌红蛋白含量及其衍生物转化

本实验采用4D-非标记蛋白质组学技术研究秦川牛肉贮藏过程中（0～8 d）肌红蛋白含量及其衍生物的转化情况，阐释冷却秦川牛肉中肌红蛋白含量及其衍生物转化的分子机制。结果表明：贮藏过程中，肌红蛋白表达量在宰后0～4 d上升、4～8 d下降，利用非标记蛋白质组学技术鉴定出与肌红蛋白及其衍生物相关的差异蛋白14 种，具体包括代谢酶、氧化还原酶、过氧化物酶、伴侣蛋白4 类，这4 类蛋白的表达共同调控贮藏过程中肌红蛋白含量的变化及其3 种衍生物之间的转化，具体表现为贮藏过程中肌红蛋白表达量整体呈下降趋势，氧合肌红蛋白相对含量持续下降，脱氧肌红蛋白、高铁肌红蛋白相对含量逐渐增加，导致肉色发生褐变。本研究结果有利于理解秦川牛肉贮藏过程肉类变色的复杂生化变化机制。     

Aqueous dispersion of 1D van der Waals Mo6S3I6 crystal using biocompatible tri-block copolymer

To achieve the stable dispersion of 1D van der Waals crystal Mo₆S₃I₆ in aqueous media, the tri-block copolymer (Poloxamer) is used as dispersant. The head group of Poloxamer, hydrophobic polypropylene oxide parts can be adsorbed to Mo₆S₃I₆ surface by hydrophobic interaction and the tail group with hydrophilic polyethylene oxide exposed to the outside of the Mo₆S₃I₆ is soluble in water and can form sufficient steric hindrance, resulting in stable aqueous dispersion in nm scale. The excellent biocompatibility of aqueous dispersed nm scale 1D Mo₆S₃I₆ was demonstrated by effective proliferation of C2C12 cells.     

Peptide-Mimicking Poly(2-oxazoline)s Displaying Potent Antimicrobial Properties

Poly(2-oxazoline)s have excellent biocompatibility and have been used as FDA-approved indirect food additives. The inert property of the hydrophilic poly(2-oxazoline)s suggests them as promising substitutes for poly(ethylene glycol) (PEG) in various applications such as anti-biofouling agents. It was recently reported that poly(2-oxazoline)s themselves have antimicrobial properties as synthetic mimics of host defense peptides. These studies revealed the bioactive properties of poly(2-oxazoline)s as a new class of functional peptide mimics, by mimicking host defense peptides to display potent and selective antimicrobial activities against methicillin-resistant Staphylococcus aureus both in vitro and in vivo, without concerns about antimicrobial resistance. The high structural diversity, facile synthesis, and potent and tunable antimicrobial properties underscore the great potential of poly(2-oxazoline)s as a class of novel antimicrobial agents in dealing with drug-resistant microbial infections and antimicrobial resistance.