灰度／深度图像序列的三维空间内插──一种新的计算机图像生成技术

本文提出的灰度／深度图像序列的三维内插方法,摆脱了原实摄路径限制,可在空间内任意巡行,采用空间稀疏化采样,从而达到大量节省存储量和高度灵活地可控再现空间场景的目的,为解决三维内插中庞大的计算量,我们研究了快速而实用的散点算法和深度适应的Ｗａｒｐ算法。通过介绍三维内插的几种简单情形,导出了一些简单、实用的算法。计算机仿真结果显示了这一新方法是完全可行的。     

Himawari-8气溶胶变分同化对PM2.5污染模拟的改进

利用地球静止轨道卫星Himawari-8 气溶胶光学厚度 (AOD) 产品能够估算空间覆盖范围广、时间分辨率高的 近地表 PM2.5 浓度。基于三维变分同化系统将AOD估算得到的 PM2.5 资料同化进入WRF-Chem大气化学模式中, 通过 控制实验与同化实验的对比与分析, 探讨了AOD估算得到的PM2.5资料同化对 PM2.5 污染模拟的改进作用。实验结果 表明： (1) AOD估算得到的 PM2.5 资料同化能够改进 PM2.5 污染模拟效果;(2) PM2.5 污染模拟改进效果存在时空差异。 此外, 与其他研究中使用AOD观测算子直接同化AOD的方法相比, 该方法的操作更加简单。     

Latch Applicator for Efficient Delivery of Dissolving Microneedles Based on Rapid Release of Elastic Strain Energy by Thumb Force (Adv. Funct. Mater. 11/2023)

Dissolving microneedle (DMN) is an attractive alternative to parenteral and enteral drug administration owing to its painless self-administration and safety due to non-generation of medical waste. For reproducible and efficient DMN administration, various DMN application methods, such as weights, springs, and electromagnetic devices, have been studied. However, these applicators have complex structures that are complicated to use and high production costs. In this study, a latch applicator that consists of only simple plastic parts and operates via thumb force without any external complex device is developed. Protrusion-shaped latches and impact distances are designed to accumulate thumb force energy through elastic deformation and to control impact velocity. The optimized latch applicator with a pressing force of 25 N and an impact velocity of 5.9 m s⁻¹ fully inserts the drug-loaded tip of the two-layered DMN into the skin. In an ovalbumin immunization test, DMN with the latch applicator shows a significantly higher IgG antibody production rate than that of intramuscular injection. The latch applicator, which provides effective DMN insertion and a competitive price compared with conventional syringes, has great potential to improve delivery of drugs, including vaccines.     

基于峰宽修正的玻璃药瓶内氧气残留浓度的检测研究

玻璃药瓶中的氧气残留对瓶中药品的无菌特性造成了严重的威胁。采用波长调制光谱（Wavelength Modulated Spectrum, WMS）技术解调得到的二次谐波信号峰高值作为氧浓度反演的基础。然而,在用二次谐波信号测量气体浓度时,由于调制深度的变化会导致二次谐波峰值的变化,这通常会给系统带来误差,进而降低浓度的反演精度。而调制深度受调制电流波动、温度和压强变化等因素的影响不能直接计算获得进而修正。针对这一问题,本文成功地将调制深度与二次谐波峰高的关系转换为二次谐波峰宽和峰高的关系。然后,利用峰宽校正后的谐波峰高对气体浓度进行反演。初步实验表明,利用峰宽校正后的谐波峰高对瓶内气体浓度进行预测的准确性提高了2.1%,且系统的整体鲁棒性也得以提升。本文提出的校正方法不需要系统参数信息与气体成分信息,可以直接从谐波信号本身出发对调制深度进行校正,十分适合于工业现场的在线氧气浓度预测。     

基于改进的SSD监理目标检测研究

针对装饰装修工程中由人工验收带来的诸多问题,文中提出了一种改进的SSD算法并将其应用于监理工作来代替人工验收,推动智能监理的实现。由于SSD算法存在对同一目标复检以及小目标检测效果欠佳等问题,故文中利用DPN网络替换基础特征提取网络VGG16。DPN结合了Resnet和Densenet的优点,具有更好的特征提取能力。通过加权FPN融合特征图,突出不同层特征图的贡献,丰富用于预测的特征图语义。利用深度可分离卷积降低模型的参数量,提高算法的推理速度。实验对比发现,改进后模型的平均精度提升了3.47%,对小数目检测平均精度的提升可达15%,证明新模型在监理目标检测任务中效果良好。     

XPS in‐depth composition study on commercial monocrystalline silicon solar cells

From large‐scale production, two monocrystalline silicon solar cells of different quality, i.e. I_SC = 3.0 A (good cell) and I_SC = 1.6 A (bad cell), have been studied by XPS combined with 4 keV Ar⁺ depth profiling. Depth profiling was carried out through the anti‐reflection coating (TiO₂), the passivation layer (SiO₂) and up into the phosphorus‐doped silicon bulk. At the solar cell surface the elemental composition is similar for both cells, although the bad one presents slightly more carbon, phosphorus and lead but less silver than the good one. During profiling, carbon and silver could be followed by XPS. It was found that the carbon content is distinguishably higher in the bad cell than in the good one. Furthermore, it was found that silver atoms have not diffused in the same way in both cells. Only the good cell presents silver atoms up into the silicon bulk. Copyright © 2003 John Wiley & Sons, Ltd.     

Error surface calculations on the parameters defining oxygen depth profile models fitted to ARXPS data obtained from polystyrene exposed to an oxygen/helium plasma

Error surfaces are calculated for the fitting of concentration–depth profiles to angle‐resolved x‐ray photoelectron spectroscopy (ARXPS) data. The shapes of the error surfaces indicate that model parameters related to composition (especially at the very surface of the sample) are well constrained by the data, whereas parameters related to depth have a less significant impact on the fit. It is then shown that certain parameters in the different depth profile models employed are highly correlated and that the different models convey essentially the same information in different ways. Finally, a compromise profile definition is proposed for the fitting of constrained but flexible depth profiles to ARXPS data. Copyright © 2003 John Wiley & Sons, Ltd.     

Degradation of poly(acrylates) under SF5+ primary ion bombardment studied using time‐of‐flight secondary ion mass spectrometry. 1. Effect of main chain and pendant methyl groups

Polyatomic primary ions have been applied recently to the depth profiling of organic materials by secondary ion mass spectrometry (SIMS). Polyatomic primary ions offer low penetration depth and high damage removal rates in some polymers, but the relationship between polymer chemistry and degradation under polyatomic primary ion bombardment has not been studied systematically. In this study, positive and negative ion time‐of‐flight SIMS (ToF‐SIMS) was used to measure the damage of ～100 nm thick spin‐cast poly(methyl methacrylate) (PMMA), poly(methyl acrylate) (PMA) and poly(methacrylic acid) (PMAA), films under extended (～2 × 10¹⁴ ions cm^?2) 5 keV SF₅⁺ bombardment. These polymers were compared to determine the effect of the main chain and pendant methyl groups on their degradation under SF₅⁺ bombardment. The sputter rate of PMMA was approximately twice that of PMA or PMAA and the rate of damage accumulation was higher for PMA and PMAA than PMMA, suggesting that the main chain and pendant methyl groups played an important role in the degradation of these polymers under SF₅⁺ bombardment. These results are consistent with the literature on the thermal and radiation‐induced degradation of these polymers, which show that removal of the main chain or pendant methyl groups reduces the rate of depolymerization and increases the rate of intra‐ or intermolecular cross‐linking. Copyright © 2004 John Wiley & Sons, Ltd.     

Eco-dyeing and functional finishing of wool fabric based on Portulaca oleracea L. as colorant and Musa basjoo as natural mordant

Biomass energy is the most acknowledged renewable resource due to its universality, richness, and renewability. This study utilized a Portulaca oleracea L. plant as a natural colorant for wool fabric dyeing with a high color yield at optimum extraction and dyeing conditions. To evaluate the dyeing mechanism and feasibility of the extracted dyes, we analyzed and characterized the molecular structure and nano-level particle size. The dyeing kinetics and the morphology of dyed fabrics were integratedly explored; the adsorption process of wool fabric on natural colorant molecules was increasingly in line with the pseudo-second-order kinetic adsorption model. Further, the dyeing effects of wool fabrics were compared to that of Musa basjoo mordant and synthetic dyes to confirm the superior color depth (K/S value 23.53), biological function as anti-ultraviolet (UPF value 253.47), and anti-bacterial activity (antibacterial rate of Staphylococcus aureus/Escherichia coli was 71.3%/37%). Our findings provide a feasible scheme for providing deep color and biological activity to wool fabrics. This has broad application prospects in the field of eco-friendly textile materials.