HLA环境下基于聚合属性的数据采集方法

该文分析了HLA体系结构对数据采集的影响 ,提出了聚合属性 (AggregateAttribute)的概念以及基于聚合属性的数据采集方法 ,并且分析了该方法的优缺点。最后 ,介绍了基于该研究自行开发的聚合属性生成工具 3AT(AggregateAttributeAuto generationTool)的使用方法和效果。

聚合保障理念解析

为适应信息化条件下联合作战后勤保障特点及需求,提出聚合保障理念。从聚合保障的概念和核心特征阐释聚合保障的内涵,从静态结构和动态机制界定聚合保障的外延,依据聚合属性和需求对聚合保障进行分类,并以此构建聚合保障模式,可为指导作战后勤聚合保障实践提供理论基础。

Transition metal catalysis in lithium‐ion batteries studied by operando magnetometry

Owing to the potential ability of metal nanoparticles to enhance the performance of energy storage devices,their catalytic performance has been studied by many researchers.However,a limited number of suitable characterization techniques does not allow fully elucidating their catalytic mechanism.Herein,high‐accuracy operando magnetometry is employed to investigate the catalytic properties of a cobalt oxide electrode for lithium‐ion batteries fabricated by magnetron sputtering.Using this technique,the magnetic responses generated by the Co‐catalyzed reversible formation and decomposition of a polymer/gel‐like film are successfully detected.A series of CoO/Co films are prepared by magnetron sputtering in different environments at various sputtering times to study the influence of Co content and film thickness on their catalytic properties.It is clearly demonstrated that increasing the Co content enhances the magnetic signal associated with the catalysis process.Furthermore,decreasing the electrode thickness increases the area affected by the catalytic reactions,which in turn enhances the corresponding magnetic responses.The obtained results experimentally confirm the catalytic activity of Co metal nanoparticles and provide a scientific guidance for designing advanced energy storage devices.This work also shows that operando magnetometry is a versatile technique for studying the catalytic effects of transition metals.

Ionic polymer metal composites actuators with enhanced driving performance by incorporating graphene quantum dots

In order to further improve the driving performance of ionic polymer metal composites(IPMCs),Nafion/graphene quantum dots(GQDs)hybrid membranes incorporating GQDs with various contents of 0,0.1 wt.%,0.5 wt.%,1.0 wt.%,2.0 wt.%and 4.0 wt.%were fabricated by solution casting,and then IPMCs were manufactured by electroless plating.The water contents and elastic moduli of the hybrid membranes were tested.The morphology characteristics of the hybrid membranes and the IPMCs were observed,and the current,AC impedance,blocking force and displacement of the IPMCs were measured.The results show that the elastic modulus of the hybrid membranes decreases,the water content increases,and the actuation performance of the IPMCs improves significantly after the addition of GQDs.IPMC with 1.0 wt.%GQDs exhibits the best driving property.Compared with the IPMC without GQDs,the working current,ion conductivity,blocking force,and tip displacement increase by 94.67%,311.11%,53.66%,and 66.07%,respectively.These results lay a solid foundation for the preparation of IPMCs with high performance,and further broaden their applications in biomedical devices and bionic robots.

STUDY ON SYNTHESIS AND RELAXIVITY OF PARAMAGNETIC POLYESTER METAL COMPLEXES FOR MRI

Fifteen new polyester ligands were prepared by copolymerndion Of EDTA(ethylenediaminetetraacetic acid ) dianhydride or DTPA (dikthylenetriaminepenlaacetic acid) dianhydrtde and dihydric alcohol or dihydric phenol. Theirparanzagnetic metal complexes were also synthesized. All polyester ligands andmetal complexes were characterized by IHNMR, IR spectra and elemental analyses. Preliminary study showed that the polyester .metal complexes had higher relaxation effectiveness as compared to corresponding small molecular metal complexes.

Biosorption of Toxic Zn（ll） Ion from Water Using Ion Imprinted Interpenetrating Polymer Networks

Toxic Zn（II） ion imprinted interpenetrating polymer networks were synthesized for the selective sorption of Zn（ll） from aqueous solutions using a biopolymer alginic acid. The polymeric biosorbant was prepared using Zn（II） ion as template, acrylamide as functional monomer, cross linker NNMBA （N,N＇ Methylene-bis-acrylamide） and potassium persulphate as an initiator. The non-imprinted polymer networks were also prepared without use of the Zn（II） ion. The synthesized interpenetrating networks were characterized by various spectral techniques. Metal ion binding studies were carried out and the factors affecting binding were also optimized. Competitive sorption studies were investigated to determine the selectivity of Zn（II） ion imprinted interpenetrating polymer network. Zinc ion imprinted polymer networks showed good selectivity for the target ion.

Porous coordination polymers based on three planar rigid ligands

During the last two decades,porous coordination polymers(PCPs),usually called as metal-organic frameworks(MOFs),have been developed rapidly due to their versatile structural diversities and potential physical and chemical functions.This article provides a short review of recent advances in the design and constructions of porous coordination polymers based on three planar rigid ligands,including imidazole-4,5-dicarboxlate(H3IDC),1H-tetrazole(HTz),as well as 1H-tetrazole-5-carboxylate(H2Tzc).Their preparations,crystal structures,and desirable properties have been reviewed.

Facile synthesis of poly(aroxycarbonyltriazole)s with aggregation-induced emission characteristics by metal-free click polymerization

Regioseletive 1,3-dipolar polycycloadditions of 4,4'-isopropylidenediphenyl dipropiolate (1) and tetraphenylethene (TPE)-containing diazides (2) are carried out in polar solvents such as DMF/toluene at a moderate temperature of 100℃ for 6 h,producing poly(aroxycarbonyltriazole)s (PACTs) P3 with high molecular weights (Mw up to 23900) and regioregularities (F1,4 up to ～90%) in high yields (up to ～99%).These metal-free click polymerizations can propagate smoothly in an open atmosphere without protection from oxygen and moisture.The obtained polymers are soluble in common organic solvents and thermally stable at temperatures up to 375℃.Thanks to their contained TPE moieties,the PACTs show aggregation-induced emission and can serve as fluorescent chemosensors for superamplified detection of explosives.

Probing the effects of external species on poly(acrylate acid) chain dynamics by using cationic AIE-active fluorophore

We report here our results on the investigation of the chain dynamics of poly(acrylic acid) in aqueous solution. The concentration of poly(acrylic acid) was approximately 3.8×10^(-4) mol/L, two orders of magnitude higher than that reported in the literature. The p H value of the solution was 3.9, and the hydrogen bonds between the intrinsic and ionized carboxylic acid groups formed dynamic networks, which captured aggregation-induced emission-active molecules(a tetra-quaternary ammonium modified tetraphenylethene derivative) inside the polymer coils and induced fluorescence emission. The hydrogen bonds can be classified as intra- or intermolecular; both can be probed based on the emission change of the tetra-quaternary ammonium modified tetraphenylethene probes. The effects of different external stimuli on the polymer chain dynamics were investigated using different metal cations(including Na^+, Li^+, Zn^(2+), Ni^(2+), Ca^(2+), and Co^(2+)), different cation concentrations(1×10^(-6) to 4×10^(-4) mol/L), different poly(acrylic acid) molecular weights(5, 240, and 450 k Da), and different copolymers. The experimental results indicate that the long poly(acrylic acid) chains(high molecular weight) tend to form dense globular coils and exclude the probe molecules outside, which are robust and unsusceptible to water-soluble metal cations. However, the shorter poly(acrylic acid) chains tend to form intermolecular hydrogen bonds, which are helpful in capturing more probe molecules inside the networks, thus inducing stronger emission. Because of the dual functions of forming hydrogen bonds with carboxylic groups and acting as an acceptor of protons from the carboxylic acid group to form cationic species, copolymerization with acrylate amide [poly(acrylic acid)-co-poly(acrylamide)] can greatly affect the chain dynamics of poly(acrylic acid) segments, which is reflected by the drastically decreased emission intensity from the fluorescent probes.