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FOOD SCIENCE AND BIOTECHNOLOGY · 2023 · IF 2.9

Enhancing effect on postharvest quality of potatoes through combined treatment of edible coating with UV-C irradiation

Lee Jung-Soo,Ahn Jiwon,Han Jaejoon

Various edible polymers [sodium alginate, carboxyl methylcellulose, sodium oleate, liquid paraffin, pectin, pullulan, polyvinyl acetate, and shellac (SHE)] as potato-coating materials and their effect on extending the shelf life of potatoes when combined with an edible coating and UV-C irradiation treatments were evaluated. As a result of the characterization of the edible polymers, SHE was selected as the optimal coating material because it had the best moisture and light barrier properties. SHE coating successfully prevented the greening, respiration, and sprouting of potatoes caused by exposure to light and oxygen. Additionally, it reduced weight loss by inhibiting transpiration on the potato surface. While the SHE coating did not exhibit antimicrobial effects, a significant effect was observed when combined with UV-C irradiation. This study suggests the potential of combined treatment of SHE coating and UV-C irradiation in extending the postharvest quality of potatoes.

CAS / MDL: 9002-89-5
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POLYMER DEGRADATION AND STABILITY · 2023 · IF 5.9

High toughness, UV & blue light shielding and antibacterial bio-based PEF/TiO2 nanowires composites for packaging application

Yuhao Zhao,Yuxuan Li,Yuze Dai,Ying Zhang,Min Jiang,Guangyuan Zhou

As a candidate of fossil-based poly(ethylene terephthalate) (PET), bio-based poly(ethylene 2,5-furandicarboxylate) (PEF) that could be converted from renewable resources has attracted attention from academia and industry. Here, we prepare a series of new type of PEF/TiO 2 NWs composites from 2,5-furandicarboxylic acid (FDCA), ethylene glycol (EG), titanium dioxide nanowire (TiO 2 NWs, diameter∼100 nm, length∼20 µm) and dipentaerythritol (Di-PE) via in-situ polymerization. The TiO 2 nanowires (0.5∼10 wt‰ based on PEF) and Di-PE (3 mol‰ based on FDCA) were added as fillers and extenders. TiO 2 nanowires were distributed in the PEF uniformly, shown by SEM. Compared with pure PEF, the T g and thermal stability of all nanocomposites got improved. And the impact strength of nanocomposites could reach 60 kJ/m 2 in contrast to brittle pure PEF. The UV-A and blue-light shielding of nanocomposites increased from 53 % to 98 % and 28 % to 86 %, respectively, and the nanocomposites still maintained good gas barrier properties. Moreover, the antibacterial activity of nanocomposites against E. coli had increased to 98 %, better than that of the PEF/Ag NWs composites. By uniaxial pre-stretching, the tensile modulus and the elongation at break were improved obviously, from 1840 MPa to 5466 MPa and 4 % to 54 % respectively with pre-stretching ratio increasing. Compared to the PET/TiO 2 NWs composites, the PEF/TiO 2 NWs composites shows batter thermal property and mechanical property. The PEF/TiO 2 NWs composites exhibit potential foreground in the packaging application.

CAS / MDL: 126-58-9
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2023 · IF 8.2

Modification of nanocellulose via atom transfer radical polymerization and its reinforcing effect in waterborne UV-curable resin

Qi Wang,Zhaozhe Yang,Xinhao Feng,Xinyou Liu

Cellulose nanocrystals (CNCs) are green reinforcing materials, and their potential has been evaluated in the preparation of waterborne UV-curable resin composites with high-performance. Herein, we present a novel and scalable approach for preparing surface-modified CNCs with acrylic-based polymers to strengthen the compatibility and interaction between CNCs and UV-curable resins. Using tert-butyl acrylate as the monomer, the nanocellulose grafted copolymer CNC-g-PtBA was successfully synthesized via atom transfer radical polymerization (ATRP) in the presence of a macromolecular initiator. Then, the CNC-g-PtBA is blended into the acrylic resin as a nanofiller to prepare the UV-curable nanocomposite. The results indicated that the contact angle of the CNCs increased from 38.7° to approximately 74.8°, and their thermal stability was significantly improved after graft modification. This contributed to the effective alleviation of the agglomeration phenomenon of nanocomposites due to the high hydrophilicity of pure CNCs. Notably, not only was the UV curing efficiency of the nanocomposites greatly increased but the mechanical properties were also further enhanced. Specifically, with the addition of 0.5 wt% CNC-g-PtBA, the curing time of the nanocomposite was shortened from >30 mins down to approximately 6 mins, and the bending strength was increased from 10 MPa for the original resin and 5 MPa for the addition of pure CNCs to 14.3 MPa, and the bending modulus was also greatly increased (up to approximately 730 MPa). Compared to pure CNCs, they are compatible with the resin, exhibiting high mechanical strength and flexibility, and have virtually no effect on the light transmission of the nanocomposites. Additionally, dielectric analysis (DEA) was used to monitor the dielectric constant and conductivity of the UV-curable nanocomposites in real time to further characterize their curing kinetics. The permittivity of these nanocomposites increased by 125 % compared to pristine resin, which shows potential for applications in high dielectric composites or for improving electrical conductivity . This work provides a feasible method for preparing UV-curable nanocomposites with high curing efficiency and permittivity, realizing a wider application of this high-performance nanocomposite.

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PROCESS SAFETY AND ENVIRONMENTAL PROTECTION · 2023 · IF 7.8

Degradation of bisphenol A by Fe-doped BiOBr enhanced UV/persulfate system: Significant role of superoxide radicals

Zezheng Lin,Yang Guo,Xiaoxuan Qu,Yuying Xiang,Shuwen Shen,Xin Zhu

Widely diffused pollution of endocrine disrupting chemicals (EDCs) has indeed threatened the safety of ecological environment and human health. A hydrangea-like Fe doped BiOBr (Fe-BiOBr) microsphere was synthesized and used to enhance the performance of UV/persulfate (PS) system using bisphenol A (BPA) as the targeted contaminant. The photochemical characterization of Fe-BiOBr showed that Fe doping markedly improved the separation efficiency of photoelectron and hole, and enhanced the utility rate of luminous energy of BiOBr. Degradation test demonstrated that with the assistance of Fe-BiOBr, the efficiency of UV/PS system was increased by 1.8 times, while 85.7% of BPA can be degraded within 10 min. Through scavenging experiments, sulfate radical (SO 4 •− ), superoxide radical (O 2 •− ), and hole were demonstrated as the dominate reactive species (RSs) in UV/Fe-BiOBr/PS system. Then, the role and mutual transformation of RSs was further clarified by radicals steady-state concentrations estimation and X-ray photoelectron spectroscopy (XPS) analysis. Based on the results, the produced O 2 •− can be subdivided into confined O 2 •− and free O 2 •− from the UV induced oxygen vacancy and photoelectron, respectively. Of which, SO 4 •− and confined O 2 •− were symbiotic via the redox cycle of Fe species. Significantly, only 2.6% of TOC can be simultaneously removed within 10 min treatment time, suggesting the incomplete degradation of BPA. For this, 16 organics was detected using LC-MS and the degradation route of BPA was also determined based on the intermediates analysis. Finally, the application possibility of the system was evaluated from the perspective of ecotoxicity by ECOSAR and T.E.S.T. softwares. This study investigates the dual effect of transition metal doped semiconductor on coupling system, and provides new insights into the role of O 2 •− .

CAS / MDL: 80-05-7
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Surfaces and Interfaces · 2023 · IF 6.2

Atomic layer deposition of TiO2 nanolayer coated Vectran fabrics with enhanced UV-blocking performance and structural colors

Jiahao He,Zhijiang Liu,Wenlu Zhang,Chong He,Wenbin Li

Vectran fabrics are widely employed as the key material for the manufacturing of stratospheric airship. Nonetheless, Vectran faber would decompose due to the UV aging during the prolonged flying process. Herein, atomic layer deposition (ALD) technology was introduced to coat TiO 2 nanolayers on the surface of Vectran fabrics. Titanium isopropoxide liquid was employed as the Ti source precursor throughout the deposition process. Compared with sol-gel vacuum infiltration technic, ALD modified Vectran yarns possessed higher surface uniformity, better UV blocking performance and lower density. Notably, thickness of the TiO 2 nanocoating prepared through the ALD method was adjustable, which can optimize the UV resistance of Vectran yarn without significantly affect its density. Additionally, the nanolayer interface can induce structural coloration on the Vectran strand via diffraction phenomena. These outstanding merits endow ALD technic a promising choice to modify the surface of Vectran fiber used as the skin of stratospheric airships.

CAS / MDL: 1843-05-6 546-68-9
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JOURNAL OF MOLECULAR STRUCTURE · 2022 · IF 3.841

HPLC, fluorescence spectroscopy, UV spectroscopy and DFT calculations on the mechanism of scavenging •OH radicals by Hypericin

Wan-ping Chen,Run-quan Wang,Yue-rong Zhang,Kai Song,Yuan Tian,Jia-xian Li,Guo-ying Wang,Gao-feng Shi

In this article, the scavenging ability of hypericin on hydroxyl radicals was evaluated by UV spectra, HPLC and fluorescence spectra. The reaction mechanism of the scavenging of free radicals by hypericin was also investigated. The Gaussian calculations obtained for the spatial structure and electrostatic potential of hypericin revealed that the active site for the reaction of hypericin with hydroxyl radicals is on the phenolic hydroxyl group of hypericin. The dissociation energy, spin density and frontline orbitals of the dehydrogenated hypericin radicals yielded that hypericin 7-OH and 7′ -OH are most likely to react with hydroxyl radicals. the transition state structure, enthalpy change and Gibbs free energy change and energy change of the reaction between hypericin and hydroxyl radicals,and the results of the above calculations indicate that hypericin 7-OH and 7′ -OH have the highest activity, can be directly involved in the scavenging process of radicals, followed by 5-OH and 5′ -OH, and finally 4-OH (4′ - OH).In-depth study of the antioxidant mechanism of hypericin molecules can help to design and synthesize new antioxidants in a more rational way.

CAS / MDL: 5144-89-8
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ACS Sustainable Chemistry & Engineering · 2023 · IF 8.4

Sustainable Multiblock Copolymer Elastomers Derived from Lignin with Tunable Performance toward Strong Adhesives and UV-Shielding Materials

Pengfei Tang,Zhiqiang Wang,Chao Wen,Chuantao Yin,Yuxian Xing,Haoming Tai,Feng Jiang

With the increasing concern about global environmental issues, reducing the carbon footprint to achieve carbon neutrality has been particularly important. Sustainable multiblock copolymer elastomers (MBCPEs) have received tremendous interest due to their unprecedented performance and huge potential applications. However, complex multistep polymerization and postpolymerization processes are needed to design MBCPEs. In this work, a series of MBCPEs, in which vanillin acrylate (VA) derived from lignin was selected as the renewable rigid segments for the glassy block, while methyl acrylate (MA) was chosen as the soft segments for the rubbery block, were prepared by two successive reversible addition–fragmentation chain transfer (RAFT) polymerization processes with polytrithiocarbonate (PTTC). These thermally stable MBCPEs exhibit distinct microphase-separated morphology, where the hard poly(vanillin acrylate) (PVA) blocks self-assemble into discrete glassy domains serving as the physical cross-linking points in the soft poly(methyl acrylate) (PMA) matrix. The macroscopic mechanical performance, such as tensile strength, stretchability, toughness, and elastic recovery, can be adjusted well by changing the molecular weights and PVA contents. Moreover, these sustainable MBCPEs can be applied as strong adhesives and excellent UV-shielding materials, broadening their potential applications. This novel strategy is convenient and robust by combining RAFT polymerization and renewable resources toward high-performance MBCPEs, which can open a new avenue for the development of sustainable biobased elastomers.

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POLYMER · 2023 · IF 4.6

Self-healing icephobic coating with UV shielding and removability based on biobased epoxy and reversible disulfide bonds

Xiangzhao Wang,Xiaobin Huang,Zemin Ji,Wenbin Hu,Haoqiang Sheng,Xiaofei Li

Icephobic coatings have attracted wide attention due to low energy consumption, low cost, and high efficiency. However, the icephobic coating is vulnerable to external damage due to long-term exposure, which can result in icephobic properties loss and limit its industrial application. Herein, the novel amphiphilic epoxy self-healing icephobic coating was designed by a compound with multiple hydrophilic groups, polydimethylsiloxane (PDMS) with hydrophobic groups and 4, 4′-diaminodiphenyldisulfide (APD) with reversible bonds. Moreover, considering the resource crisis, the biobased epoxy (GTE) was selected as the compound containing hydrophilic groups. In this study, the GTE will form hydrogen bonds with water molecules to achieve an anti-icing effect, while PDMS mainly play a deicing effect due to low surface energy. Due to the reasonable design, the icephobic coating showed good comprehensive icephobic properties: a 12.5-fold increase in icing delay time (802 s) and a 6.6-fold decrease in ice adhesion strength (32.6 kPa) compared with bare aluminum . Furthermore, the crystallization temperature of water was reduced by about 11 °C. More importantly, the APD with reversible disulfide bonds provides the icephobic coating with self-healing performance, removability, and excellent UV shielding performance. The coating provides a new idea for the preparation of sustainable and durable coatings with comprehensive icephobic performance.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Comparative effectiveness of sequential and synergistic (VUV/)UV and chlorine disinfection on DBPs and humic acid reduction

Jiayu Du,Decai Liu,Zhiyong Zhang,Huiying Ai,Ming-Lai Fu,Wenjie Sun,Baoling Yuan

The widespread use of chlorine during disinfection has led to the problems of disinfection by-products (DBPs). Recently, the combination of ultraviolet (UV, 254 nm) and vacuum ultraviolet (VUV, 185 nm) with chlorine has been considered a promising strategy to mitigate the formation of DBPs. This study systematically evaluated the efficacy of six different disinfection methods in abating humic acid (HA), a common precursor of DBPs (UV-Chlorine, VUV/UV-Chlorine, Chlorine-UV, Chlorine-VUV/UV, UV/Chlorine, and VUV/UV/Chlorine). Under 40 mJ/cm 2 UV fluence and 3 mg/L chlorine dose, the synergistic processes yielded DBP levels below 20 μg/L, whereas sequential disinfection resulted in DBP levels exceeding 100 μg/L. Additionally, there was no significant difference in the formation of DBPs between the two methods of chlorination followed by irradiation. However, for irradiation followed by chlorination, the addition of VUV led to an increase of 50 μg/L in trihalomethanes (THMs). As the irradiation time increased, the inclusion of VUV demonstrated enhanced control of DBP levels in the sequential disinfection process. Moreover, compared to UV/Chlorine, at 13 mg/L chlorine dose in VUV/UV/Chlorine process, the inclusion of VUV expedited the appearance of peak DBPs by two minutes and reduced the peak value by 25.6 %, but the DBP yield was 12.9 times higher than that at a chlorine dose of 3 mg/L. This study, comparing six combination disinfection methods, will provide deeper insights into precursor abatement and DBP control during drinking water disinfection.

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POLYMER · 2023 · IF 4.6

Synthesis of UV rapid curing silicone coatings via photoinitiated thiol-ene click polymerization for pressure-sensitive adhesive

Wei Zhang,Ruolin Wang,Zhen Yang,Yongping Bai,Linghui Meng,Yu Wang

UV-curable silicone pressure-sensitive adhesive (SPSA) is composed of silicone rubber and silicone resin. Generally, the C C double bond in acryloyloxy group provides a photocurable group for SPSA. However, oxygen inhibition of acryloyloxy group block the degree of cure and C C double bond conversion of SPSA during the photopolymerization . Therefore, efficient photocurable groups for UV curing SPSA is particularly important to be developed. Thiol-ene click polymerizations have been widely used in photocrosslinked polymers due to the rapid efficiency of reactions. In this study, sulfhydryl functionalized silicone resin (SFSR) and methacrylate functionalized amino silicone rubber (MFASR) were synthesized to prepare a SPSA via photoinitiated thiol-ene click polymerization. The double bond in MSASR and sulfhydryl in SFSR were characterized by FT-IR spectroscopy and 1 H NMR spectroscopy . The double bond conversion of SPSA was calculated after polymerization. The cohesion of SPSA was improved by SFSR, while the crosslinking degree was improved by thiol-ene. The loop tack of SPSA with 50 wt% SFSR was 9.01 N, and the 180° peel strength was 11.37 N/25 mm. The SPSA maintained good bonding adhesion to steel at various temperature.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2023 · IF 8.2

Protein-based coating strategy for preparing durable sunlight-driven rechargeable antibacterial, super hydrophilic, and UV-resistant textiles

Ning Zhang,Yujie Xu,Rongjin Shi,Man Zhou,Yuanyuan Yu,Ping Wang,Qiang Wang

With the improvement of the hygiene awareness and pathogen prevention awareness of patients and medical staff, textiles with efficient and long-lasting pathogen inactivation effects are urgently needed. Photodynamic therapy (PDT) has rapidly developed into a new type of antibacterial technology due to its high antibacterial activity and has received widespread attention. However, the commonly used photosensitizers are mostly inorganic nanomaterials, which have poor adhesion to textiles and are not environmentally or human friendly. Here, we report a strategy of preparation of a sunlight-driven rechargeable antibacterial textiles based on natural antibacterial agents, which can work in light and dark conditions. The prepared BD-PTL@wool has long-lasting antibacterial properties, can rapidly produce ROS, and can store sterilization activity under light irradiation, ensuring all-day bacterial killing (>99.95 % under light irradiation and >99.80 % under dark conditions after light irradiation). BD-PTL@wool has excellent reusability, and the antibacterial rate can still above 95 % after repeated use for 5 times. In addition, BD-PTL@wool has excellent hydrophilic, UV resistance, biocompatibility and can withstand 50 washing cycles. The successful application of this strategy in textile preparation broadens the research idea for exploring the application of green photosensitive antibacterial materials in textile field.

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MATERIALS RESEARCH BULLETIN · 2023 · IF 5.4

Enhanced performance of self-powered ZnO-based PEC type UV photodetectors by loading GQDs to construct heterojunctions

Meixian Li,Jun Liu,Tao Zhang,Nina Liang,Lijuan Yan,Fengzhen Lv,Wenjie Kong,Fuchi Liu,Lizhen Long

The construction of semiconductor heterojunctions is an effective approach to enhance the performance of optoelectronic devices. In this study, graphene-quantum-dots (GQDs) were grown on ZnO nanorods arrays in - situ to form intimate heterojunctions. The fabricated photoelectrochemical (PEC) photodetector based on ZnO/GQDs heterojunctions displayed good self-powering characteristics, with an on/off current ratio of approximately 21 at zero bias, which was almost seven-fold higher than that of the bare ZnO device. The responsivity and detectivity of the ZnO/GQDs-based photodetector were also enhanced compared with those of bare ZnO devices. A unique type-II band alignment was established at the ZnO/GQDs heterojunction interface, which facilitated the carrier transfer. Moreover, the ZnO/GQDs heterojunction reduced the passivation of the surface states, resulting in large energy-band bending and an internal electric field at the semiconductor/electrolyte interface, which provided a powerful driving force for the separation and transport of photogenerated carriers. These combined effects enhance the performance of the photodetector, indicating that this approach can be used to fabricate high-performance PEC optoelectronic devices.

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