基于机器视觉的加工刀具磨损监测方法

为了对加工过程中刀具的磨损状态进行监测,针对麻花钻的磨损形式,提出基于机器视觉的加工刀具磨损监测方法. 根据磨损刀具图像的灰度分布特点,提出基于积分图加速和Turky bi-weight核函数的非局部均值去噪方法;采用单、双阈值大津法获取磨损区域的灰度区间,实现对图像的自适应对比度增强;提出基于形态学重构方法的磨损区域局部极值点提取方法,有效完成对磨损区域的检测和边界提取. 该刀具磨损检测方法成功应用于麻花钻头磨损状态的监测过程,实验结果表明,相较于目前已有的机器视觉监测方法,所提出的方法具有更高的检测精度和效率,准确地提取磨损轮廓,从而有效实现对刀具磨损状态的监测和自动化监控加工过程,达到降低人工成本和产品不合格率的目的.     

换热器结构发展综述及展望

主要介绍换热器200余年的发展历程,对不同结构换热器的产生及典型应用进行综述。重点阐述管壳式换热器、板式换热器、微结构换热器和印刷电路板换热器四种不同结构的换热器,及其为了实现强化传热所开展的相关几何参数优化和结构改进的发展工作。分析现有换热器结构设计中存在的问题与限制,总结换热器结构更新的具体建议和发展趋势。     

纳米颗粒强化胺法吸收CO2研究进展

碳捕集、利用与封存（CCUS）技术是缓解全球气候变化的重要措施之一。纳米颗粒因具有良好表面效应和体积效应,能够强化CO2捕集传质性能而备受青睐,其可增大胺法吸收CO2过程中的传质系数并减少溶剂再生所需的能量,有望进一步提高CO2捕集效率、降低能耗。本文从纳米颗粒强化胺法吸收CO2过程出发,讨论了纳米颗粒强化吸收的3种机理（抑制气泡聚并机理、传输机理、边界层混合机理）,总结了近年来国内外最新研究进展,论述了纳米颗粒强化CO2吸收过程中的主要影响因素,指出纳米颗粒对CO2吸收过程的强化是多重因素共同作用的结果,并对该技术的未来研究方向作了展望。     

下喷式环流反应器环隙气含率影响因素

下喷式环流反应器是一种用于强化气-液两相反应过程的新型装置，虽然已在工业上有了较广泛的应用，但对其理论研究远未成熟，其工业装置的设计仍依赖于实验和经验。本文借助实验室自制实验装置，对下喷式环流反应器环隙气含率的影响规律进行了研究。首先，对喷射器的吸气量进行了测量，获得了不同条件下喷射器最大吸气量的性能曲线；在此基础上，分别研究了气相流量、液相流量以及喷射器安装位置对环隙气含率的影响规律。结果表明：气相流量和液相流量对气含率具有重要的影响，随着气相流量和液相流量的增大，气含率快速提高，而喷嘴位置对气含率的影响相对较小；考虑到增加气相流量和液相流量所需要的能耗和设备代价，通过增加液相流量来达到提高气含率的目的是优选方案。     

Miscibility and Probe Tack of Acrylic Pressure Sensitive Adhesives—Acrylic Copolymer/Tackifier Resin Systems

Miscibility between acrylic copolymers and tackifier resins are investigated in terms of phase diagrams, and the probe tack of the blends are measured as a function of both temperature and rate of separation in order to obtain the master curves. It is found that the probe tack of the pressure sensitive adhesives are closely related to the miscibility between the components. The master curves of the miscible blends shift along the X(rate)-axis according to the change of T_g of the bulk materials with a gradual variation of the peak heights. However, those of the immiscible blends will not shift along the X(rate)-axis, but the magnitude will decrease with increase of a dispersed phase.     

异形管内水力、传热性能的数值模拟

通过数值计算考察了横纹管、缩放管两种异形管内的流动与传热性能。计算时采用标准k-ε湍流模型：采用控制容积法对控制方程进行离散化；采用SIMPLE算法进行压力修正：代数方程采用超松弛法迭代求解。很出了在充分发展流时的传热努塞尔数、速度、瘴撩系数及湍动能分布，并与光滑管内的流动传热进行了比较，分析了异形管在强化传热方面的机理。计算结果和实验值比较吻合。     

Study of miscibility,crystallization, mechanical properties,and thermal stability of blends of poly(3‐hydroxybutyrate) and poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate)

Natural amorphous polymer poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) (P3HB4HB) containing 41 mol % of 4HB was blended with poly(3‐hydroxybutyrate) (PHB) with an aim to improve the properties of PHB. The influence of P3HB4HB contents on thermal and mechanical properties of the blends was evaluated with differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, stress–strain measurement and thermo gravimetric analyzer. Miscibility of PHB/P3HB4HB blends was mainly decided by the contents of P3HB4HB. When P3HB4HB exceeded 50 wt %, the two polymer phases separated and showed immiscibility. The addition of P3HB4HB did not alter the crystallinity of PHB, yet it diluted the PHB crystalline phase as revealed by DSC studies. DSC and FTIR results showed that the overall crystallinity of the blends decreased remarkably with increasing of P3HB4HB contents. Decreased glass transition temperature and crystallinity imparted desired flexibility for the blends. The ductility of the blends increased progressively with increasing of P3HB4HB content. Thus, the PHB mechanical properties can be modulated by changing the blend composition. P3HB4HB did not significantly improve the thermal stability of PHB, yet it is possible to melt process PHB without much molecular weights loss via blending it with suitable amounts of P3HB4HB. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Activation of a Au/TiO2 Catalyst by Loading a Large Amount of Fe–Oxide: Oxidation of CO Enhanced by H2 and H2O

Catalytic activity of a 1 wt% Au/TiO₂ catalyst is markedly improved by loading a large amount of FeO_x, on which the oxidation of CO in excess H₂ is selectively promoted at temperature lower than 60 °C. Oxidation of CO with O₂ on the FeO_x/Au/TiO₂ catalyst is markedly enhanced by H₂, and H₂O moisture also enhances the oxidation of CO but its effect is not so large as the promotion by H₂. We deduced that activation of Au/TiO₂ catalyst by loading FeO_x is not caused by the size effect of Au particles but a new reaction path via hydroxyl carbonyl intermediate is responsible for the superior activity of the FeO_x/Au/TiO₂ catalyst.     

Isothermal crystallization and spherulite structure of partially miscible polypropylene–linear low-density polyethylene blends

Polypropylene (PP) was blended with a linear low-density polyethylene (LLDPE, containing 5% hexene comonomer) over a composition range of 10–90% of PP. The crystallization and morphology of the PP–LLDPE blends were studied by differential scanning calorimetry (DSC), polarized optical microscopy with a hot stage (HSOM), and scanning electron microscopy (SEM). In particular, the isothermal crystallization of PP in molten LLDPE was investigated. It was observed that the crystallization and melting behavior of PP and LLDPE changed in the blends, indicating that there was some degree of miscibility between the PP and the LLDPE. A depression of the equilibrium melting temperature (T) of PP in the blends with no more than 15% of PP confirmed that PP was miscible with LLDPE at and below 15% of PP. In addition, a drastic decrease in T from the 25% PP blend to the 20% blend led us to conclude that the miscible behavior between PP and LLDPE became favorable at a PP concentration of 20%. The optical microscopic images showed that, in the blends with 10 and 15% of PP, the PP crystallized as open-armed diffuse spherulites, similar to those in the miscible blends. In contrast, the PP crystallized in a phase-separated matrix or droplets with more than 25% of PP, when obvious phase separation occurred. The SEM image revealed that the PP lamella was able to penetrate the PP and LLDPE phase boundary and grow in the LLDPE phase. The above results displayed that the PP dissolved in the LLDPE, and, particularly, when the PP concentration was below 20%, the dissolution was substantial. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 628–639, 2001     

基于模糊梯度卷积核的在线棒材断面中心识别

针对传动带上严重堆叠、形状尺寸不规则的棒材,提出基于模糊梯度卷积核的在线棒材断面中心识别方法.以标准圆边缘为中心环,结合棒材断面边缘点偏离中心环的程度定义一个模糊梯度卷积核;通过模糊梯度卷积核与实时棒材断面梯度图像的卷积操作,实现棒材断面中心的增强;依次执行候选点选取、局部峰值抑制、距离检测步骤确定中心位置.实验结果表明,该方法能有效抑制棒材中心增强过程中易产生的峰值扩散现象,减少误识别和漏识别;平均计算时间为8.3 ms,满足系统实时性要求.