The incorporation of a naphthyl curing agent (NCA) can enhance the thermal stability of pressure-sensitive adhesives (PSAs). In this study, a PSA matrix was synthesized using a solution polymerization process and consisted of butyl acrylate, acrylic acid, and an ethyl acrylate within an acrylic copolymer. Benzoyl peroxide was used as an initiator during the synthesis. To facilitate the UV curing of the solvent-borne PSAs, glycidyl methacrylate was added to introduce unsaturated carbon double bonds. The resulting UV-curable acrylic PSA tapes exhibited longer holding times at high temperatures (150 °C) compared to uncross-linked PSA tapes, without leaving any residues on the substrate surface. The thermal stability of the PSA was further enhanced by adding more NCA and increasing the UV dosage. This may be attributed to the formation of cross-linking networks within the polymer matrix at higher doses. The researchers successfully balanced the adhesion performance and thermal stability by modifying the amount of NCA and UV radiation, despite the peel strength declining and the holding duration shortening. This research also investigated the effects of cross-linking density on gel content, molecular weight, glass transition temperature, and other properties of the PSAs.

Vinyl-capped cationic waterborne polyurethane (CWPU) was prepared using isophorone diisocyanate (IPDI), polycarbonate diol (PCDL), N-methyldiethanolamine (MDEA), and trimethylolpropane (TMP) as raw materials and hydroxyethyl methacrylate (HEMA) as a capping agent. Then, a crosslinked FPUA composite emulsion with polyurethane (PU) as the shell and fluorinated acrylate (PA) as the core was prepared by core-shell emulsion polymerization with CWPU as the seed emulsion, together with dodecafluoroheptyl methacrylate (DFMA), diacetone acrylamide (DAAM), and methyl methacrylate (MMA). The effects of the core-shell ratio of PA/PU on the surface properties, mechanical properties, and heat resistance of FPUA emulsions and films were investigated. The results showed that when w(PA) = 30~50%, the stability of FPUA emulsion was the highest, and the particles showed a core-shell structure with bright and dark intersections under TEM. When w(PA) = 30%, the tensile strength reached 23.35 ± 0.08 MPa. When w(PA) = 50%, the fluorine content on the surface of the coating film was 14.75% and the contact angle was as high as 98.5°, which showed good hydrophobicity; the surface flatness of the film was observed under AFM. It is found that the tensile strength of the film increases and then decreases with the increase in the core-shell ratio and the heat resistance of the FPUA film is gradually increased. The FPUA film has excellent properties such as good impact resistance, high flexibility, high adhesion, and corrosion resistance.

Slow-release fertilizer was developed by encapsulating NPK compound pellets with graphene oxide (GO) sheets employing a waterless synthesis technique. As-prepared GO sheets were characterized by XRD, Raman, XPS, FTIR, SEM, and EDS. The XRD patterns of the GO sheets indicate that the peak for the GO is observed at 2θ = 9.3°, and the peak (002) for graphite vanished. Moreover, a higher intensity ratio of the Raman ID/IG of the GO sheets than that of pristine graphite confirms the oxidation of the graphite. The FTIR and XPS analyses provided information on electronic structure, chemical structure, and oxygen-bonding neighbors. The SEM images indicated the GO sheet, whereby its morphology resembles a thin curtain or corrugated shape. The EDS spectrum of coated GO-F pellets revealed the distribution of C, O, N, P, and K elements in the synthesized materials. Afterwards, GO shell formation on fertilizer pellets greatly improved the slow-release characteristics of fertilizer, thus providing plants with their requisite nutrients and reducing environmental pollution.

Water-based chloroprene latex is a solvent-free, environmentally friendly adhesive. Currently, its market demand is growing rapidly. However, there are problems such as a lack of heat resistance and poor mechanical properties, which limit its application. The introduction of vinyl-POSS (OVS) into the resin structure can effectively improve the thermal stability of chloroprene adhesives. In this paper, modified waterborne chloroprene latex was prepared by copolymerization of methyl methacrylate and OVS with chloroprene latex. The results showed that vinyl-POSS was successfully grafted onto the main chain of the waterborne chloroprene latex, and the modified waterborne chloroprene latex had good storage stability. With the increase in vinyl-POSS, the tensile strength of the chloroprene latex firstly increased and then decreased, the tensile property (peel strength of 20.2 kgf) was maintained well at a high temperature (100 °C), and the thermal stability of the chloroprene latex was improved. When the addition amount was 4%, the comprehensive mechanical properties were their best. This study provides a new idea for the construction of a new and efficient waterborne chloroprene latex system and provides more fields for the practical application of waterborne chloroprene latex. This newly developed vinyl-POSS modified chloroprene latex has great application potential for use in home furniture, bags, and seat cushions.

The development of high-performance insulation materials that facilitate the reduction in building energy consumption is of paramount significance. In this study, magnesium–aluminum-layered hydroxide (LDH) was prepared by the classical hydrothermal reaction. By implementing methyl trimethoxy siloxane (MTS), two different MTS-functionalized LDHs were prepared via a one-step in situ hydrothermal synthesis method and a two-step method. Furthermore, using techniques, such as X-ray diffraction, infrared spectroscopy, particle size analysis, and scanning electron microscopy, we evaluated and analyzed the composition, structure, and morphology of the various LDH samples. These LDHs were then employed as inorganic fillers in waterborne coatings, and their thermal-insulation capabilities were tested and compared. It was found that MTS-modified LDH via a one-step in situ hydrothermal synthesis method (M-LDH-2) exhibited the best thermal insulating properties by displaying a thermal-insulation-temperature difference (ΔT) of 25 °C compared with the blank panel. In contrast, the panels coated with unmodified LDH and the MTS-modified LDH via the two-step method exhibited thermal-insulation-temperature difference values of 13.5 °C and 9.5 °C, respectively. Our investigation involved a comprehensive characterization of LDH materials and coating films, unveiling the underlying mechanism of thermal insulation and establishing the correlation between LDH structure and the corresponding insulation performance of the coating. Our findings reveal that the particle size and distribution of LDHs are critical factors in dictating their thermal-insulation capabilities in the coatings. Specifically, we observed that the MTS-modified LDH, prepared via a one-step in situ hydrothermal approach, possessed a larger particle size and wider particle size distribution, resulting in superior thermal-insulation effectiveness. In contrast, the MTS-modified LDH via the two-step method exhibited a smaller particle size and narrow particle size distribution, causing a moderate thermal-insulation effect. This study has significant implications for opening up the potential for LDH-based thermal-insulation coatings. We believe the findings can promote the development of new products and help upgrade industries, while contributing to local economic growth.

Graphene oxide (GO) was prepared by a waterless synthesis route to generate GO sheets, which were then applied to coat calcined oyster shell with fertilizer (OSF) pellets, resulting in the creation of an OSF-GO particle. The GO sheets (ID/IG = 0.86) were characterized by Raman spectroscopy, which showed that the GO-coated OSF pellet features a compact coating approximately 13.68 μm thick. SEM and AFM analyses revealed that the GO sheets displayed a monolayer configuration with a crinkled topography (about 0.91 nm). The EDS analysis confirmed that the core was primarily composed of Ca, K, P, O, N, and C elements. The hydroponic experiment results showed that a GO concentration of 80 mg/L significantly enhanced plant height, stem thickness, and root length in loose-leaf lettuce, while higher concentrations induced oxidative stress. In pot experiments, the OSF-GO composite effectively raised the soil pH from 5.38 to 6.41 and improved nutrient availability. OSF-GO composite functions effectively as both a soil conditioner and slow-release fertilizer (SRF), simultaneously remediating degraded soils and optimizing nutrient delivery.