薄板结构加筋布局优化设计方法研究

提出一种两步优化策略，以加筋板结构的固有频率最大化为目标函数，以结构所受外载荷作用的最大静变形为约束条件，开展薄板结构加筋构件的布局优化设计研究。为了降低加筋布局优化的难度，提高优化设计的效率，将加筋等效为一系列弹性铰（点）支撑，以便快速获得加筋横向移动的灵敏度信息。在基本不改变结构重量的情形下，通过合理布局加筋位置，能显著改善结构的刚度分布，提高结构的整体承载能力。随后，小幅调整加筋的截面尺寸，以满足对结构最大变形的设计要求。最后，用两个算例验证了所提优化方法的可行性和有效性。     

考虑侧面摩擦的侧限压缩模型的数值解法

海上箱筒型基础结构下沉到位后，舱内土体的受力变形可以看作是侧限压缩模型问题，上部荷载引起的侧壁摩擦力与土体应力之间的关系较为复杂。本文通过简化模型，列出了侧限压缩模型的平衡微分方程，分析了方程解析计算时存在的难点，结合摩擦应力边界条件的特点，构造函数迭代法对该方程进行数值求解，展示了计算的收敛过程，得到接触侧面上水平应力和土体表面位移的非线性分布规律，并将其结果与ABAQUS数值模拟结果进行了对比。结果表明，函数迭代法收敛速度较快，计算过程稳定，对其他存在变量耦合边界条件的微分方程数值求解有一定的参考价值。     

Dynamic and buckling analysis of polymer hybrid composite beam with variable thickness

This work deals with a study of the dynamic and buckling analysis of polymer hybrid composite(PHC) beam. The beam has variable thickness and is reinforced by carbon nanotubes(CNTs) and nanoclay(NC) simultaneously. The governing equations are derived based on the first shear deformation theory(FSDT). A three-phase HalpinTsai approach is used to predict the mechanical properties of the PHC. We focus our attention on the effect of the simultaneous addition of NC and CNT on the vibration and buckling analysis of the PHC beam with variable thickness. Also a comparison study is done on the sensation of three impressive parameters including CNT, NC weight fractions, and the shape factor of fillers on the mechanical properties of PHC beams,as well as fundamental frequencies of free vibrations and critical buckling load. The results show that the increase of shape factor value, NC, and CNT weight fractions leads to considerable reinforcement in mechanical properties as well as increase of the dimensionless fundamental frequency and buckling load. The variation of CNT weight fraction on elastic modulus is more sensitive rather than shear modulus but the effect of NC weight fraction on elastic and shear moduli is fairly the same. The shape factor values more than the medium level do not affect the mechanical properties.     

THE SHEAR LAG EFFECT OF BOX BEAMS WITH VARYING LATERAL LOADING LOCATIONS 1)

对箱梁各翼板(顶板、悬臂板、底板)分设不同剪力滞广义纵向位移,其横向分布均取二次抛物线形式,并引入载荷横向位置参数η,以分析载荷横向变位对剪力滞效应的影响.运用能量变分原理,建立剪力滞控制微分方程,求解了简支梁和悬臂梁在均布载荷作用下的控制微分方程的解.算例分析表明:载荷横向变位改变直接承受载荷的翼板的正负剪力滞特性,对非直接承载翼板只改变其应力幅度;箱梁横向框架效应对直接承载翼板纵向应力的贡献远远大于剪切变形.与块体有限元分析结果较吻合,表明该算法能较准确分析载荷横向变位作用下箱梁剪力滞的变化规律.     

花岗岩单轴压缩侧向变形及脆性破坏机制实验研究

为研究花岗岩侧向变形及脆性破坏机制,对花岗岩试件进行单轴压缩实验。利用动态应变采集系统、数字散斑相关方法(DSCM)和显微观测手段,记录并分析花岗岩试件在单轴压缩过程中的宏观侧向应变、局部侧向应变以及破裂面形貌,并与水泥砂浆试件的破坏过程对比,讨论了花岗岩脆性破坏机制。实验与分析结果表明:(1)花岗岩试件在加载初期发生侧向收缩变形,产生并发展于压密阶段,消失于线弹性阶段初期,这主要由于试件内部裂纹闭合造成的;此后,宏观侧向应变持续增长,当侧向应变与轴向应变之比接近0.5时试件破坏;(2)在峰值载荷前很长一段时间内,局部侧向应变在一定范围内波动,临近试件破坏时局部侧向应变最大值和最小值均出现较大幅度的波动,二者差值迅速增大,试件不均匀程度增大,最终导致试件破坏;(3)在峰值载荷前有无塑性屈服阶段是峰值载荷后脆性破坏程度的重要影响因素,而宏观裂纹的贯通程度是峰值载荷后应力降大小的决定因素。     

双稳态结构中的1/2次谐波共振及其对隔振特性的影响

以典型的双稳态系统——屈曲梁结构为例,基于等效模型,结合解析、数值和实验手段,研究了双稳态结构中的1/2次谐波共振特性、演化过程、参数调节规律及其对隔振特性的影响.研究发现,当非线性刚度系数或激励幅值增加到一定程度时,系统会在一定带宽下产生显著的1/2次谐波共振;随着激励幅值增加,阻尼系统的1/2次谐波遵循“产生-增强-衰退-消失”的过程,该过程对峰值频率和峰值传递率有重要影响;适当提高非线性强度能有效改善双稳态结构隔振特性.针对双稳态屈曲梁结构开展的实验验证了1/2次谐波特性和隔振特性变化规律.     

基于正弦控制因子的Lateral变异鲨鱼优化算法

针对传统鲨鱼优化算法在求解高维目标函数时,易早熟收敛,陷入局部最优的缺陷.提出一种基于正弦控制因子的Lateral变异鲨鱼优化算法.通过正弦曲线的特性和自适应惯性权重,改善了传统鲨鱼优化算法中由于随机选取控制因子数值大小可能导致算法在迭代后期全局搜索能力降低的问题,提高了算法在迭代后期的全局收敛能力,并对最佳鲨鱼位置引入Lateral变异策略,加强了算法跳出局部最优的可能性.改进后的算法对多个shifted单峰,多峰以及固定维测试函数进行求解,实验结果表明,对比多种不同优化算法而言,本文所提LSSO算法具有更高的收敛精度和搜索速度.     

An estimated quantitative lateral flow immunoassay for determination of artesunate using monoclonal antibody

There have been reports of fake artesunate (ART), which has led to deaths from untreated malaria in South East Asia. To rapidly screen for fake and adulterated ART products in the drug market, a lateral flow immunoassay (LFIA) based on a colloidal gold–monoclonal antibody probe for detection of ART within samples was developed. With this method, the calibration curve for ART was determined by the intensity ratio of the test and control bands at various ART concentrations. The linearity range was 12.5–200 μg/ml of ART. Samples were tested by the developed LFIA and can be calculated for ART contents. The levels of ART in the samples were also confirmed by enzyme-linked immunosorbent assay. The results of the two methods were in good conformance. The proposed LFIA was demonstrated to be a simple and rapid analytical method for detecting ART in the pharmaceutical formulation.     

Dual gold nanoparticle lateflow immunoassay for sensitive detection of Escherichia coli O157:H7

Two patterns of signal amplification lateral flow immunoassay (LFIA), which used anti-mouse secondary antibody-linked gold nanoparticle (AuNP) for dual AuNP-LFIA were developed. Escherichia coli O157:H7 was selected as the model analyte. In the signal amplification direct LFIA method, anti-mouse secondary antibody-linked AuNP (anti-mouse-Ab-AuNP) was mixed with sample solution in an ELISA well, after which it was added to LFIA, which already contained anti-E. coli O157:H7 monoclonal antibody-AuNP (anti-E. coli O157:H7-mAb-AuNP) dispersed in the conjugate pad. Polyclonal antibody was the test line, and anti-mouse secondary antibody was the control line in nitrocellulose (NC) membrane. In the signal amplification indirect LFIA method, anti-mouse-Ab-AuNP was mixed with sample solution and anti-E. coli O157:H7-mAb-AuNP complex in ELISA well, creating a dual AuNP complex. This complex was added to LFIA, which had a polyclonal antibody as the test line and secondary antibody as the control line in NC membrane. The detection sensitivity of both LFIAs improved 100-fold and reached 1.14 × 10³ CFU mL⁻¹. The 28 nm and 45 nm AuNPs were demonstrated to be the optimal dual AuNP pairs. Signal amplification LFIA was perfectly applied to the detection of milk samples with E. coli O157:H7 via naked eye observation.     

Rapid and sensitive lateral flow immunoassay method for determining alpha fetoprotein in serum using europium (III) chelate microparticles-based lateral flow test strips

Alpha-fetoprotein (AFP), a primary marker for many diseases including various cancers, is important in clinical tumor diagnosis and antenatal screening. Most immunoassays provide high sensitivity and accuracy for determining AFP, but they are expensive, often complex, time-consuming procedures. A simple and rapid point-of-care system that integrates Eu (III) chelate microparticles with lateral flow immunoassay (LFIA) has been developed to determine AFP in serum with an assay time of 15 min. The approach is based on a sandwich immunoassay performed on lateral flow test strips. A fluorescence strip reader was used to measure the fluorescence peak heights of the test line (H_T) and the control line (H_C); the H_T/H_C ratio was used for quantitation. The Eu (III) chelate microparticles-based LFIA assay exhibited a wide linear range (1.0–1000 IU mL⁻¹) for AFP with a low limit of detection (0.1 IU mL⁻¹) based on 5ul of serum. Satisfactory specificity and accuracy were demonstrated and the intra- and inter-assay coefficients of variation (CV) for AFP were both <10%. Furthermore, in the analysis of human serum samples, excellent correlation (n = 284, r = 0.9860, p < 0.0001) was obtained between the proposed method and a commercially available CLIA kit. Results indicated that the Eu (III) chelate microparticles-based LFIA system provided a rapid, sensitive and reliable method for determining AFP in serum, indicating that it would be suitable for development in point-of-care testing.