Automated 3D Scenes Reconstruction Using Multiple Stereo Pairs from Portable Four-Camera Photographic Measurement System

An effective automatic 3D reconstruction method using a portable four-camera photographic measurement system (PFCPMS) is proposed. By taking advantage of the complementary stereo information from four cameras, a fast and highly accurate feature point matching algorithm is developed for 3D reconstruction. Specifically, we first utilize a projection method to obtain a large number of dense feature points. And then a reduction and clustering treatment is applied to simplify the Delaunay triangulation process and reconstruct a 3D model for each scene. In addition, a 3D model stitching approach is proposed to further improve the performance of the limited field-of-view for image-based method. The experimental results tested on the 172 cave in Mogao Grottoes indicate that the proposed method is effective to reconstruct a 3D scene with a low-cost four-camera photographic measurement system

Construction of NIR Light Controlled Micelles with Photothermal Conversion Property: Poly(poly(ethylene glycol)methyl ether methacrylate) (PPEGMA) as Hydrophilic Block and Ketocyanine Dye as NIR Photothermal Conversion Agent

Polymeric nanomaterials made from amphiphilic block copolymers are increasingly used in the treatment of tumor tissues. In this work, we firstly synthesized the amphiphilic block copolymer PBnMA-b-P(BAPMA-co-PEGMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization using benzyl methacrylate (BnMA), poly (ethylene glycol) methyl ether methacrylate (PEGMA), and 3-((tert-butoxycarbonyl)amino)propyl methacrylate (BAPMA) as the monomers. Subsequently, PBnMA-b-P(APMA-co-PEGMA)@NIR 800 with photothermal conversion property was obtained by deprotection of the tert-butoxycarbonyl (BOC) groups of PBAPMA chains with trifluoroacetic acid (TFA) and post-modification with carboxyl functionalized ketocyanine dye (NIR 800), and it could self-assemble into micelles in CH3OH/water mixed solvent. The NIR photothermal conversion property of the post-modified micelles were investigated. Under irradiation with NIR light (λmax = 810 nm, 0.028 W/cm2) for 1 h, the temperature of the modified micelles aqueous solution increased to 53 °C from 20 °C, which showed the excellent NIR photothermal conversion property

Achieving Secondary Dispersion of Modified Nanoparticles by Hot-Stretching to Enhance Dielectric and Mechanical Properties of Polyarylene Ether Nitrile Composites

Enhanced dielectric and mechanical properties of polyarylene ether nitrile (PEN) are obtained through secondary dispersion of polyaniline functionalized barium titanate (PANI-f-BT) by hot-stretching. PANI-f-BT nanoparticles with different PANI content are successfully prepared via in-situ aniline polymerization technology. The transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopic instrument (XPS) and Thermogravimetric analysis (TGA) results confirm that the PANI layers uniformly enclose on the surface of BaTiO3 nanoparticles. These nanoparticles are used as functional fillers to compound with PEN (PEN/PANI-f-BT) for studying its effect on the mechanical and dielectric performance of the obtained composites. In addition, the nanocomposites are uniaxial hot-stretched by 50% and 100% at 280 °C to obtain the oriented nanocomposite films. The results exhibit that the PANI-f-BT nanoparticles present good compatibility and dispersion in the PEN matrix, and the hot-stretching endows the second dispersion of PANI-f-BT in PEN resulting in enhanced mechanical properties, crystallinity and permittivity-temperature stability of the nanocomposites. The excellent performances of the nanocomposites indicate that a new approach for preparing high-temperature-resistant dielectric films is provided

Polyethylenimine Assisted Bio-Inspired Surface Functionalization of Hexagonal Boron Nitride for Enhancing the Crystallization and the Properties of Poly(Arylene Ether Nitrile)

Semi-crystalline poly(arylene ether nitrile) (PEN) has exhibited remarkable potential in various fields. However, the inherent drawbacks of PEN such as slow crystalline rate and low crystallinity limit its further development. To alleviate this problem, the choice of nanofiller as nucleation agent and the interfacial compatibility between nanofiller and PEN matrix are two momentous factors that need to be considered. Accordingly, in this work, functionalized hexagonal boron nitride (h-BN@(PDA+PEI)) was successfully synthesized via polyethylenimine (PEI) assisted bio-inspired surface functionalization, and then homogeneously dispersed in the PEN resin using solution casting method to obtain functional polymer nanocomposite films with strengthening the crystallization behavior, mechanical and dielectric properties. Various testing methods including differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X-ray diffraction (XRD), and polarizing microscope (POM) were applied to intricately analyze the effect of h-BN@(PDA+PEI) on the crystallization behavior of PEN composites. The testing results certificated that the h-BN@(PDA+PEI) can effectively improve the crystallinity (from 6.56% to 14.90%), and the spherulite size of PEN was reduced while the nucleation density of nanocomposites was raised. Furthermore, the non-isothermal crystallization kinetics demonstrated that 2 wt% h-BN@(PDA+PEI) could significantly reduce the cold crystallization temperature (Tp) and the crystallization activation energy (Ea) (from 359.7 KJ/mol to 292.8 KJ/mol), while it improved the crystallization rate (Kc) of PEN. In addition, the mechanical and dielectric properties of nanocomposite films were also reinforced to further broaden the application of semi-crystalline PEN. Therefore, the h-BN@(PDA+PEI) can function as an effectual nucleating agent and enhance the performance of PEN

A New Wood Adhesive Based on Recycling <i>Camellia oleifera</i> Cake-Protein: Preparation and Properties

In order to improve the initial viscosity and stability of Camellia oleifera cake-protein adhesive, Camellia oleifera cake-protein was blended with defatted soybean protein (DSP), soybean protein isolate (SPI), and casein, followed by adhesive preparation through degradation and crosslinking methods. The performance of Camellia oleifera cake-protein adhesive was investigated by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), scanning electron microscopic (SEM), and thermogravimetric (TG) and X-ray diffraction (XRD). The results showed that DSP, SPI, and casein likely promoted the effective degradation of Camellia oleifera cake-protein, and, thus, more active groups were formed in the system, accompanied by more reactivity sites. The prepared adhesive had a lower curing temperature, and higher initial viscosity and stability, but the storage time was shortened. Moreover, DSP, SPI, and casein, themselves, were degraded into peptide chains with lower molecular weights; thus, improving the overall flexibility of the adhesive, facilitating a better elastic contact and regular array between crosslinking products, and further strengthening the crosslinked structure and density of the products. After curing, a compact and coherent reticular structure was formed in the adhesive layer, with both bonding strength and water resistance being significantly improved. According to the results obtained, the next step will be to study the DSP-modified Camellia oleifera cake-protein adhesive in depth