Carbon dots (CDs) with plenty of favorable properties have been extensively investigated in diverse areas including bioimaging, biomedicine, sensor, energy storage, anti-counterfeiting, photocatalysis, and optoelectronic devices. Herein, a simple, rapid, and green sonochemical-assisted method for fabricating nitrogen-doped CDs has been developed. In this approach, the nitrogen-doped CDs can be obtained through irradiation by intensive ultrasonic waves from ultrasonic probes in 30 min. The achieved CDs exhibit excellent water dispersibility, which can be ascribed to their high functionalization. Importantly, the CDs also demonstrate remarkable fluorescent properties, high photostability, and low cytotoxicity, which can be utilized for multicolor cellular imaging and anti-counterfeiting applications. As far as we know, the sonochemical-assisted method for rapidly synthesizing nitrogendoped CDs from gelatin has never been reported before. Significantly, the sonochemical-assisted approach to rapidly fabricate CDs is versatile for the facile construction of fluorescent CDs, and the obtained CDs can be potentially used in various areas including bioimaging and anti-counterfeiting.

Biodegradable mulch films are supposed to be a prospective substitute for poly­(ethylene)-based mulch films in the field of sustainable agriculture. Among them, weeding mulch films play significant roles. However, the large-scale production of weeding mulch films through the traditional high-temperature film blowing process would often cause serious pollution due to the diffusion of herbicides in the surroundings. Herein, a green and facile coating approach is developed to produce biodegradable weeding mulch films. In our strategy, a herbicide was added into a poly­(vinyl alcohol) aqueous solution with dopamine in it. After the subsequent low-temperature coating procedure on a biodegradable poly­(butylene adipate-co-terephthalate)/poly­(lactic acid) film, effective weeding mulch films were obtained. The morphology, structure, and mechanical property test results revealed the robustness and stability of the coating, and the pot experiments clearly demonstrated the effective weed suppression ability of the obtained weeding films. Evidently, this strategy to produce biodegradable weeding mulch films is green and facile, exhibiting great prospects in the large-scale production of weeding mulch films and other functional biodegradable mulch films.

The work presented herein focuses on developing the Al 2 O 3 based organic/ inorganic multifunctional composite films via an internal addition method in the presence of dripping agent, antifogging agent, light stabilizer and insulation barrier agent. The resulting composite films were systematically characterized using scanning electron microscope, FTIR, differential scanning calorimetry, UV, and tensile testing machine. The morphology changed obviously after introducing the inorganic fillers. In addition, the results indicated that the contact angle of the activated Al 2 O 3-10 film had the best stability and the film with ultrafine Al 2 O 3 possessed the best anti-dripping performance. The time of the first water drop of the film containing 10 g activated Al 2 O 3 (the activated Al 2 O 3-10) was 7 min and 18 s, and the time of each ten-drops was less than 120 s. The simulated anti-aging period of the films with antiaging agent was up to 423 days, which is superior to many other reported organic/inorganic composite films and can be applied to those extreme climate areas (such as Xinjiang, China).

Cellulose nanocrystal (CNC) was prepared through the hydrolysis of concentrated sulfuric acid using commercial bagasse pulp as a raw material. The performance of the developed CNC was tested through the atomic force microscope, particle size measurement, and zeta potential analysis. The melt blending method was adopted to prepare thermoplastic polyvinyl alcohol (TPVA) and CNC‐TPVA using the glycerol (GI)‐dicondensed triethylene glycol (TEG) complex. The TPVA and CNC‐TPVA were blended with poly(butylene adipate‐coterephthalate) and polylactic acid composite material (COM) through melt extrusion granulation and blown film, and then explored the effect of CNC on the UV aging properties of materials. The complex plasticizer could effectively break the PVA hydrogen bond and reduce its melting point. It had been observed that CNC had good interface compatibility with PVA, and CNC did not affect the crystallinity of PVA, but it could weaken the hydrogen bond between GI, TEG, and PVA, thereby reduce the plasticizing effect of PVA. Compared TPVA‐COM with CNC‐TPVA‐COM, detailed information of crystallization, the thermal stability of materials and mechanical properties was presented in the UV aging process, it was found that the cross‐section of CNC‐TPVA‐COM was rough, and its unevenness formed a striped structure, and its hydrogen bond strength, diffraction peak strength and anti‐aging performance were all improved.

The durable application of poly(butylene adipate- co -terephthalate) (PBAT) under atmospheric conditions is restricted by its poor ultraviolet (UV) stability. To improve the anti-aging capacity to UV radiation of the PBAT film, we describe a straightforward and highly producible synthesis of UV-resistant dendrimeric porous silica nanospheres (SiO 2 –HBT) by adding benzotriazole as a pore-expanding agent, more importantly demonstrating its detailed mechanism. Well-dispersed silica nanospheres are shown to offer the release property for benzotriazole triggered by UV and heat irradiation while durable UV protection due to the supplementary of benzotriazole in the PBAT matrix. With benzotriazole compensation, the halving period of elongation at break performance was extended from about 15 to 48 h. Combined with gel content and gel permeation chromatography analyses, it was inferred that the process of crosslinking resulting from Norrish I can be effectively minimized by the action of SiO 2 –HBT. The design of modified release strategy realizes the durable UV absorption ability of the hydroxyphenyl benzotriazole class of photostabilizers in particular but more generally highlights an important adding method that should be considered when utilizing a photostabilizer.