Preparation and Characterization of Acrylic Pressure-Sensitive Adhesives Crosslinked with UV Radiation-Influence of Monomer Composition on Adhesive Properties

In this study, syntheses of acrylate copolymers were performed based on the monomers butyl acrylate (BA), 2-ethylhexyl acrylate (2-EHA), and acrylic acid (AA) and the second-type unsaturated photoinitiator 4-acryloyloxybenzophenone (ABP). The structure of the obtained copolymers was confirmed via FT-IR spectroscopic analysis, and the viscosity and the content of non-volatile substances were determined. The adhesive films were then coated and cross-linked using ultraviolet radiation in the UV-C range at various doses (5–50 mJ/cm²). Due to the dependence of the self-adhesive properties of the adhesive layer on the basis weight, various basis weights of the layer in the range of 30–120 g/m² were tested. Finally, the self-adhesive properties were assessed: tack, peel adhesion, shear strength (cohesion) at 20 °C and 70 °C, as well as the SAFT test and shrinkage. The aim of the study was to determine the effect of the type of monomer used, the dose of ultraviolet radiation, and the basis weight on the self-adhesive and usable properties of the obtained self-adhesive tapes.     

A New Wood Adhesive Based on Recycling Camellia oleifera 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.     

Inspired by Skeletal Muscles: Study of the Physical and Electrochemical Properties of Derived Lignocellulose-Based Carbon Fibers

Skeletal muscles exhibit excellent properties due to their well-developed microstructures. Taking inspiration from nature that thick filaments and thin filaments are linked by “cross-bridges”, leading to good stability and ion transport performance of muscles. In this work, extracted poplar lignin and microcrystalline cellulose (MCC) were connected by biomimetic covalent bonds, akin to biological muscle tissue, in which isophorone diisocyanate was used as the chemical crosslinking agent. Then, poplar lignin–MCC was mixed with polyacrylonitrile to serve as the precursor for electrospinning. The results show that due to the effective covalent-bond connection, the precursor fibers possess excellent morphology, smooth surface, good thermal stability, and high flexibility and toughness (average elongation-at-break is 51.84%). Therefore, after thermal stabilization and carbonization, derived lignocellulose-based carbon fibers (CFs) with a reduced cost, complete fiber morphology with a uniform diameter (0.48 ± 0.22 μm), and high graphitization degree were obtained. Finally, the electrodes fabrication and electrochemical testing were carried out. The results of electrochemical impedance spectroscopy (EIS) indicate that the Rs and Rct values of CFs supercapacitors are 1.18 Ω and 0.14 Ω, respectively. Results of cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) suggest that these CFs demonstrate great application potential in electrochemical materials.     

一种新型巴布剂基质配方的优选

目的：在传统巴布剂基质材料基础上,优选一种基于透明质酸的新型巴布剂基质材料的配方。方法：以初黏力、剥离强度、赋形性和感官评价的综合评分为指标,以聚丙烯酸钠、明胶、透明质酸钠为黏合剂,甘油、丙二醇、聚乙二醇为保湿剂,高岭土、氧化锌为填充剂,氯化铝为交联剂,采用正交试验考察优选巴布剂基质配方。结果：最佳基质配方为聚丙烯酸钠-明胶-透明质酸钠-甘油-丙二醇-聚乙二醇-三氯化铝（4.5：2.5：2.0：13：13：13：0.2）。结论：优选的新型巴布剂初黏力、剥离强度、赋型性、光泽均良好,具有一定的推广应用价值。     

Synthesis of π‐Conjugated Organometallic Polymer Networks

The present paper reports the synthesis of π‐conjugated organometallic polymer networks based on poly[2,5‐dioctyloxy‐1,4‐diethynyl‐phenylene‐alt‐2,5,‐bis(2′‐ethylhexyloxy)‐1,4‐phenylene] (EHO‐OPPE), a soluble poly(p‐phenylene ethynylene) (PPE) derivative. The ethynylene moieties of the polymer coordinate to Pt⁰ centers, which act as conjugated cross‐links. These materials are readily accessible through ligand‐exchange reactions between the linear PPE and Pt(styrene)₃. The in‐situ NMR investigation of model reactions of Pt(styrene)₃ with diphenylacetylene (DPA) has shown that the ethynylene moieties comprised in the PPE readily coordinate to Pt⁰ centers under release of the relatively weakly‐bound styrene ligands. Spin‐coating has resulted in cross‐linked films of good optical quality. We also have been able to produce PPE‐Pt‐gels with high solvent content (> 95 wt.‐%). As expected, the coordination of Pt markedly influences the photophysical characteristics of the PPE. The photoluminescence is efficiently quenched, and the absorption maximum in the visible regime experiences a hypsochromic shift.

Ligand‐exchange reaction between EHO‐OPPE and [Pt(PhCH?CH₂)₃] leading to the target EHO‐OPPE‐Pt⁰ networks.     

Study on Different Modification Methods of Collagen for Tissue Engineering

Because of the excellent biocompatibility and its specific amino sequences, collagen is an ideal biomedical material for tissue engineering applications. But collagen is usually lack of mechanical strength to form a rigid 3-D matrix and lack of ability to resist collagenase. In order to be a tissue engineering scaffold, collagen must strengthen its structures by modifying with chemical crosslinkers. Chemical crosslinkers used for modif- ying collagen fibers include glutaraldehyde （GA）, epoxy compounds （PC） and carbodiim- ides （EDC）. The aim of this study is to choose the best chemical crosslinker from the three reagents. In terms of the resistance to collagenase degradation, chemical cross-link- ing with PC provided the best protection; in terms of the mechanical characterization, chemical cross-linking with GA provided the best;and in terms of the biocompatibility, chemical cross-linking with EDC provided the best. There is not a reagent which has all merits for collagen crosslinking, so we should select the crosslinking reagent as the demands of use ask.     

1,4‐Bisbenzil: Visible‐Light‐ and Heat‐Assisted Crosslinking of Polystyrene Films

Polystyrene (PS) film containing 1,4‐bisbenzil is efficiently crosslinked in two steps. In the first step, visible light (λ > 400 nm) causes molecular oxygen to insert between two carbonyl groups of one of the 1,2‐dicarbonyl groups. The peroxide is subsequently decomposed by absorption of another photon, forming acyloxy radicals, which add to the aromatic ring of the PS chain. The remaining 1,2‐dicarbonyl group is then photoperoxidized to form PS with pendant benzoyl peroxide moieties. In the second step, pendant benzoyl peroxide groups are decomposed thermally to form acyloxy macroradicals responsible for the crosslinking. Crosslinking proceeds simultaneously with degradation. Finally, the gel content in the film may exceed 80 wt%.

     

Parameter Study on the Preparation of UV Depth‐Cured Chemically Resistant Polysulfone‐Based Membranes

Polysulfone‐based membranes with excellent chemical resistance and a wet thickness up to 200 μm are obtained via UV curing of unmodified polymers after careful tuning of the photoinitiating system and the crosslinker structure. Combinations of photoinitiator and crosslinker are studied in depth, followed by a characterization of the formed macromolecular structure. The performance of the resulting membranes is then evaluated through long‐term immersion in solvents. Classical depth‐curing acyl phosphine oxide‐based photoinitiators in combination with a pentaacrylate crosslinker are found to be the optimal system.

     

Photo‐Crosslinked Side‐Chain Liquid‐Crystalline Elastomers for Microsystems

Photo‐crosslinkable side‐chain liquid‐crystalline polymers (LCPs) containing photoreactive benzophenone cores are synthesized in order to obtain their corresponding side‐chain liquid‐crystalline elastomers (LCEs). This strategic synthesis allows thin elastomeric films and their integration into microsystems for actuators and micromachines to be obtained. As an example of this principle, a gripper was developed. The position of its arms can be changed by applying voltages from 1.5 to 3.5 V at different rates. Small changes in the liquid‐crystalline elastomer film cause strains of up to 150% in the microdevice and the capacity to move up to 400 times its own mass due to the nematic‐to‐isotropic transformation.