一种谱分解降维的模糊有监督局部保持投影策略

提出一种谱分解降维的模糊有监督局部保持投影策略。首先针对监督局部保持投影SLPP存在过学习和不能较好地保持图像空间的差异信息等问题,通过最小化局部离散度和最大化差异离散度准则提取投影方向,找到一种线性鉴别分析的等价形式。其次,通过采用模糊k近邻(FKNN)方法得到相应的样本分布隶属度信息,同时考虑到离群样本对整个分类结果的不利影响,提出一种模糊化方法,根据样本的隶属度对样本分布矩阵重定义所做的贡献,将每个样本的隶属度融入到SLPP特征抽取的过程中,从而得到完整有效的模糊样本特征向量集,有效解决了小样本问题的特征抽取问题。第三,提出一种谱分解的矩阵分析方法,在SLPP投影准则下,对散布矩阵实现降维。在ORL和NUST603人脸库上的实验结果验证了该方法的有效性。     

两轴稳定平台大俯仰角状态控制技术研究

在对两轴稳定平台一般构型分析的基础上,指出了其在俯仰方向大角度时稳定控制存在的不足,提出了采用三正交陀螺稳定控制方式解决大俯仰角控制问题的方法,最后利用MATLAB进行了数学仿真,结果表明该方法有效提高了系统的稳定精度。     

20MnVBH钢的奥氏体晶粒度及淬透性研究

研究了用电弧炉，平炉和非真空感应炉冶炼的２０ＭｎＶＢＨ钢的奥氏体晶粒度及淬透性。结果表明，有效钛是决定钢奥氏体晶粒度的主要参数；有效硼是决定该钢淬透性的主要参数。     

用局部法评定焊接接头的疲劳性能

采用16Mn钢非承载十字焊接接头疲劳试验结果对使用Dang Van准则的疲劳评定局部方法进行了研究。结果表明，有限元分析中应力集中区单元尺寸对局部参量计算有明显影响，为获得比较合理的预测结果需对焊趾应力集中区所划分的单元尺寸限定，当接头焊趾半径在0．15-0．8mm变化时应选择最小单元尺寸0．32-0．62mm计算局部参量；在此基础上Dang Van准则可以对焊态接头做出合理的评定，但Dang Van建议的卢值偏安全。此外，通过计算发现焊趾半径只影响局部很小区域(约0．5mm内)的应力集中分布，在某一深度(约0．5mm)后存在稳定的应力集中，因而建议采用距应力集中区最大应力处某一深度的应力参数计算Dang Van局部参量可能更为合理，这将减小局部参数对焊趾半径及单元尺寸的依赖性。     

高温水冷后循环加卸载条件下花岗岩的渗透性

针对水下隧道火灾喷水灭火降温过程中围岩的渗透性问题,对高温水冷后循环加卸载条件下花岗岩的渗透性开展了试验研究.以高温(25、400和900 ℃)水冷后的花岗岩试样为研究对象,通过轴向压应力循环加卸载过程中气体渗透性试验,研究花岗岩渗透率变化规律.结果表明:轴向压应力循环加卸载试验过程中,花岗岩试样的卸载模量随着高温水冷处理温度升高而减小,随着轴向压应力增大,卸载模量总体呈上升趋势,气体渗透率随温度升高而增大;花岗岩BET比表面积与BJH孔体积在900 ℃高温水冷后明显减小.     

Destabilising persistent coal froth using silicone oil

Persistent froth is becoming more and more common in coal and mineral flotation plants and presents safety and operational challenges. No effective method has been developed to destabilise persistent froth. As a new initiative, this study examined the structural difference between persistent foam and coal froth, based on which a solution was developed to maximumly destabilise coal froth. Destabilisation test, oscillatory rheology measurement and scanning electron microscopy (SEM) analysis indicated that the coal froth was more stable than the foam due to the formation of thin capillaries and tightly arranged coal particles on bubble surfaces. Although 107 µm silicone oil droplet could completely destabilise the foam at 2 mmol/L concentration, it only destabilised less than 50% coal froth even at 6 mmol/L concentration. To maximumly destabilise the coal froth formed by −38 and −20 µm particles, 24 and 18 µm silicone oil droplets were required to pass through the thin capillaries and enter the bubble films, respectively. However, smaller silicone oil droplets could not bridge the bubble films to destabilise coal froth and therefore a critical droplet size occurred depending on the size of particles stabilising the froth.     

Experimental research into the effect of gas pressure,particle size and nozzle area on initial gas-release energy during gas desorption

Coal and gas outburst is a violent disaster driven by released energy from gas desorption. The initial expansion energy of released gas(IEERG) is a new method to predict coal and gas outburst. In this paper,an instrument for IEERG measurement was developed. Compared with previous setups, the new one which is equipped with three convergent nozzles and quick-release mechanism gets improved in data acquisition and gas sealing and releasing performance. To comprehensively know the effect of gas pressure, particle size, and nozzle area on IEERG, a series of experiments were carried out with this new setup.The variable control test results indicated that the gas pressure-IEERG curves remain the linear trend and the particle size-IEERG curves maintain the negative exponential trend for nozzle areas at 1.13, 2.26, and3.39 mm2, respectively. The increase in nozzle area leads to deceases in value of IEERG and absolute value of slope of fitting curves in each test. In addition, the orthogonal experiment showed that the influence of gas pressure, nozzle area, and particle size on IEERG decreases in turn. Only gas pressure had a marked impact on IEERG. This work offers great importance in improving the accuracy of prediction of coal and gas outburst.     

Continuous size fractionation of magnetic nanoparticles by using simulated moving bed chromatography

The size fractionation of magnetic nanoparticles is a technical problem, which until today can only be solved with great effort. Nevertheless, there is an important demand for nanoparticles with sharp size distributions, for example for medical technology or sensor technology. Using magnetic chromatography, we show a promising method for fractionation of magnetic nanoparticles with respect to their size and/or magnetic properties. This was achieved by passing magnetic nanoparticles through a packed bed of fine steel spheres with which they interact magnetically because single domain ferro-/ferrimagnetic nanoparticles show a spontaneous magnetization. Since the strength of this interaction is related to particle size, the principle is suitable for size fractionation. This concept was transferred into a continuous process in this work using a so-called simulated moving bed chromatography. Applying a suspension of magnetic nanoparticles within a size range from 20 to 120 nm, the process showed a separation sharpness of up to 0.52 with recovery rates of 100%. The continuous feed stream of magnetic nanoparticles could be fractionated with a space-time-yield of up to 5 mg/(L∙min). Due to the easy scalability of continuous chromatography, the process is a promising approach for the efficient fractionation of industrially relevant amounts of magnetic nanoparticles.     

基于BPA潮流的电力系统中长期频率电压稳定仿真方法

随着电力系统的复杂化,电力系统中长期动态过程频率电压稳定对系统安全性的影响愈加明显。针对该问题,提出了基于潮流计算的中长期准稳态时域仿真方法。该方法在传统时域仿真方法的基础上综合利用准稳态思想和潮流计算模块,再进一步针对效率问题提出自适应变步长仿真策略和多时步预测辅助方法。所提方法的算法主体部分和潮流计算部分分别在Mathematica科学计算软件和BPA潮流计算功能模块中实现,通过自定义数据接口进行数据对接。通过在Nordic32标准算例系统和某大区电网实际算例系统中对该方法进行验证,表明该方法显著降低实现成本,并提高了仿真计算的效率。     

b型流感嗜血杆菌精制多糖分子大小分布及重均分子质量检测方法的改良

目的改良HPLC(AKTA层析)系统,采用HPLC-MALLS系统检测b型流感嗜血杆菌(Haemophilus influenzae type b,Hib)精制多糖的分子大小分布及重均分子质量(MW),并进行方法的验证。方法采用HPLC(AKTA层析)系统连接示差分析仪检测9批Hib精制多糖供试品的分配系数(KD)及K_D值为0.5的回收率(R_X)。采用HPLC连接18角度静态光散射分析系统MALLS(HPLC-MALLS)检测供试品的M_W、K_D及R_X,并对两种系统的测试结果进行相关性分析;验证HPLC-MALLS方法的重复性、准确性及定量限。结果 9批供试品经AKTA层析系统检测,K_D为0.29~0.37,RX为78%~90%;经HPLC-MALLS系统检测,KD为0.31~0.38,RX为84%~93%,MW为(1.418~2.281)×10⁵g/moL,两种系统检测同批供试品的KD值回归方程为Y=0.903 X+0.051,r为0.978,表明检测结果具有显著相关性,两种方法等效。9批供试品经HPLC-MALLS/RI系统重复检测6次,M_W、K_D及R_X的RSD均小于3.8%,多糖回收率及其RSD分别为80%~87%和0.05%~3.46%;定量限为1 mg/mL。结论 HPLC-MALLS系统能与HPLC系统基本对接,在准确检测Hib精制多糖M_W的同时还可检测K_D及R_X,且方法的准确性及重复性良好,可作为检测Hib精制多糖分子大小的改良方法。