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Valorization of Aloe barbadensis Miller. (Aloe vera) Processing Waste

Journal of Renewable Materials 2023年第3期11卷 1031-1061页

作者： Jeltzlin Semerel Nigel John Wim Dehaen Pedro Fardim SISSTEM Program Faculty of Arts and ScienceUniversity of ArubaOranjestadAruba Department of Chemistry KU LeuvenLeuvenBelgium Department of Chemical Engineering KU LeuvenLeuvenBelgium

Aloe vera plant is known worldwide for its medicinal properties and application in gel-based products such as shampoo,soap,and ***,the demand for these gel-based products has led to a surplus production of Aloe vera processing *** Aloe vera gel processing facility could generate up to 4000 kg of Aloe vera waste per *** the Aloe vera waste is being disposed to the landfill or used as fertilizer.A sustainable management system for the Aloe vera processing waste should be considered,due to the negative societal and environmental impacts of the currents waste disposal ***,this review focuses on various approaches that can be used to valorize Aloe vera waste into value-added products,such as animal and aquaculture feeds,biosorbents,biofuel and natural *** have reported Aloe vera waste for environmental applications biosorbents used for wastewater treatment of various *** studies have also reported on the valorization of Aloe vera waste for production of biofuels such as bioethanol,mixed alcohol fuels,biogas and *** vera waste could also be valorized through isolation and synthesis of natural polymers for application in wound dressing,tissue engineering and drug delivery *** vera waste valorization was also reviewed through extraction of value-added bioactive compounds such as aloe-emodin,aloin and *** value-added bioactive compounds have various applications in the cosmetics(non-steroidal anti-inflammatory,tyrosinase inhibitors)and pharmaceutical(anticancer agent and COVID 19 inhibitors)industry.

关键词： Aloe vera waste processing biomass conversion anthraquinone aloe-emodin aloin aloeresin

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Structural Properties of Ions and Polyelectrolytes in Aqueous Solutions under External Electric Fields:The Sign Effect

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Chinese Journal of Polymer science 2024年第9期42卷 1341-1352,I0007页

作者： Cheng-Jiang Lin Jun-Jun Wang Yuan Jiang Shu-Li Chen Hong-Fei Li Wen-Han Zhao Qing-Rong Huang Chang-Ru Rong Xiao-Zheng Duan State Key Laboratory of Polymer Physics and Chemistry Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun130022China School of Applied Chemistry and Engineering University of Science and Technology of ChinaHefei230026China National Key Laboratory of Advanced Vehicle Integration and Control China FAW Group Co.Ltd.Changchun130013China State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular ScienceFudan UniversityShanghai200438China Department of Food Science Rutgers University65 Dudley RoadNew BrunswickNew Jersey08901USA

We utilize molecular dynamics simulations to investigate the microstructures of ions and polyelectrolytes in aqueous solutions under external electric *** focusing on the multi-body interactions between ionic components and H_(2)O molecules,as well as their responses to the external electric fields,we clarify several nontrivial molecular features of the ionic and polyelectrolyte solutions,such as the solvations of cations and anions,clustering of the ions,and dispersions/aggregations of polyelectrolyte chains,as well as the corresponding responses of H_(2)O molecules in these *** simulations illustrate the variations in structures of ionic solutions caused by reversing the charge sign of the ions,and elucidate the disparity in structures between anionic and cationic polyelectrolyte solutions in the presence of the external electric *** work clarifies the mechanism for the alternations in complex multi-body interactions in aqueous solutions caused by the application electric field,which can contribute to the fundamental understanding of the physical and chemical natures of ion-containing and charged polymeric systems.

关键词： Polyelectrolyte Ions Aqueous solutions External electric fields Asymmetric dipole

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Smartly tuning supramolecular chirality in polymer gels via photoexcitation-induced cooperative self-assembly

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science China chemistry 2025年第3期68卷 1126-1135页

作者： Bingbing Yue Yulong Shi Fan Yang Danfeng Ye Jian Jin Pilan Zhang Shen Song Yifei Xu Hui Lin Shihui Zhu Liangliang Zhu School of Materials and Chemistry University of Shanghai for Science and TechnologyShanghai 200093China State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular ScienceFudan UniversityShanghai 200438China College of Material Science and Chemical Engineering Ningbo University of TechnologyNingbo 315211China Shanghai Depeac Biotechnology Co. Ltd.Shanghai 201900China Burn and Plastic Surgery Department Children’s Medical Center Affiliated to Shanghai Jiao Tong University School of MedicineShanghai 200120China

Although supramolecular chirality tuning is prosperous in systems with small molecular building blocks,these systems lack structural strength and have limited practical ***,polymer systems do not exhibit these drawbacks but suffer from topological chain entanglement,which often leads to large dynamic obstacles and therefore limits the tunability of supramolecular ***,we report that by manipulating stoichiometry and employing light to alter the H-bond crosslinking between a photoexcitation-induced aggregatable molecule and high molecular weight poly(L-lactic acids),supramolecular chirality tuning of the polymer gel systems can be achieved in different ways through a cooperative ***,the Cotton effects of the examined systems can be negatively tuned by varying their stoichiometry,while positive tuning can be realized by *** deexcitation,negative Cotton effect tuning occurs again spontaneously in some *** supramolecular chirality tuning is accompanied by rheological property tuning,demonstrating that our strategy can overcome polymer chain entanglement *** proposed strategy inspires further works on the precise control of polymer chirality and,hence,development of asymmetric materials with changeable optical activity and modulus.

关键词： supramolecular chirality polymer gels phototuning self-assembly rheological property

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A review on reactive oxygen species-induced mechanism pathways of pharmaceutical waste degradation:Acetaminophen as a drug waste model

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Journal of Environmental sciences 2025年第1期147卷 688-713页

作者： Saba Humayun Maan Hayyan Yatimah Alias Department of Chemistry Faculty of ScienceUniversity of MalayaKuala Lumpur 50603Malaysia University of Malaya Centre for Ionic Liquids University of MalayaKuala Lumpur 50603Malaysia Chemical Engineering Program Faculty of Engineering and TechnologyMuscat UniversityMuscat P.C.130Oman

Innately designed to induce physiological changes,pharmaceuticals are foreknowingly hazardous to the *** oxidation processes(AOPs)are recognized as a set of contemporary and highly efficient methods being used as a contrivance for the removal of pharmaceutical *** reactive oxygen species(ROS)are formed in these processes to interact and contribute directly toward the oxidation of target contaminant(s),a profound insight regarding the mechanisms of ROS leading to the degradation of pharmaceuticals is fundamentally *** conceptualization of some specific reaction mechanisms allows the design of an effective and safe degradation process that can empirically reduce the environmental impact of *** review mainly deliberates themechanistic reaction pathways for ROS-mediated degradation of pharmaceuticals often leading to complete mineralization,with a focus on acetaminophen as a drug waste model.

关键词： Wastewater treatment Ionic liquid Hydroxyl radical Superoxide Pharmaceutical contaminant Advanced oxidation process Deep eutectic solvent Hydrogen peroxide

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The Potential Game-Changer:A Concept-to-Proof Study on D:A Heterojunction-Free Organic Photovoltaics

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Chinese Journal of chemistry 2024年第3期42卷 252-258页

作者： Lijian Zuo Sae Byeok Jo Xueliang Shi Francis Lin Alex Jen State Key Laboratory of Silicon and Advanced Semiconductor Materials MOE Key Laboratory of Macromolecular Synthesis and FunctionalizationDepartment of Polymer Science and EngineeringZhejiang UniversityHangzhouZhejiang310058 China Department of Materials Science and Engineering University of WashingtonSeattleWAUSA School of Chemical Engineering Sungkyunkwan University (SKKU)Suwon16419 Republic of Korea School of Chemistry and Molecular Engineering East China Normal UniversityShanghai200062 China Department of Materials Science and Engineering City University of Hong KongKowloonHong KongChina Department of Chemistry City University of Hong KongKowloonHong KongChina Hong Kong Institute for Clean Energy Hong KongChina

Since 1986,the donor-acceptor (D:A) heterojunction has been regarded a necessity for high-efficiency organic photovoltaics (OPVs),due to its unique advantage in compensating the intrinsic limitations of organic semiconductors,such as high exciton binding energy and poor ambipolar charge mobility. While this adversely causes tremendous non-radiative charge recombination and instability issues,which currently become the most critical limits for commercialization of OPVs. Here,we present a concept-to-proof study on the potential of D:A heterojunction free OPV by taking advantage of recent progress of non-fullerene acceptors. First,we demonstrate that the “free carriers” can be spontaneously generated upon illumination in an NFA,i.e.,the 6TIC-4F single layer. Second,the 6TIC-4F layer also exhibits good ambipolar charge transporting property. These exceptional characteristics distinguish it from the traditional organic semiconductors,and relieve it from the reliance of D:A heterojunction to independently work as active layer. As a result,the subsequent OPV by simply sandwiching the 6TIC-4F layer between the cathode and anode yields a considerably high power conversion efficiency ~1%. Moreover,we find the D:A heterojunction free device exhibits two order of magnitude higher electroluminescence quantum efficiency and significantly reduced VOC loss by 0.16 eV compared to those of the D:A BHJ structure,validating its promise for higher efficiency in the future. Therefore,our work demonstrates the possibility of using D:A heterojunction-free device structure for high performance,that can potentially become the next game changer of OPV.

关键词： Organic solar cells Spontaneous charge generation Ambipolar charge transport Charge recombination Perovskite-like organic semiconductor Schottky-junction structure Single component

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High-performance polyimine vitrimers from an aromatic bio-based scaffold

RSC Applied Polymers

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RSC Applied Polymers 2023年第1期1卷 10-18页

作者： Stewart, Kevin A. Lessard, Jacob J. Cantor, Alexander J. Rynk, John F. Bailey, Laura S. Sumerlin, Brent S. George & Josephine Butler Polymer Research Laboratory Center for Macromolecular Science & Engineering Department of Chemistry University of Florida Gainesville 32611 FL United States

Bio-based vitrimers represent a promising class of thermosetting polymer materials, pairing the recyclability of dynamic covalent networks with the renewability of non-fossil fuel feedstocks. Vanillin, a low-cost lignin derivative, enables facile construction of polyimine networks marked by rapid exchange and sensitivity to acid-catalyzed hydrolysis. Furthermore, the aromatic structure makes it a promising candidate for the design of highly aromatic networks capable of high-performance thermal and dimensional stability. Such properties are paramount in polymeric thermal protection systems. Here, we report on the fabrication of polyimine networks with particularly high aromatic content from a novel trifunctional vanillin monomer prepared from the nucleophilic aromatic substitution of perfluoropyridine (PFP) on a multi-gram scale (>20 g) in high yield (86%). The trifunctional aromatic scaffold was then crosslinked with various diamines to demonstrate tunable viscoelastic behavior and thermal properties, with glass transition temperatures (T_g) ranging from 9 to 147 °C, degradation temperatures (5% mass loss) up to approximately 370 °C, and excellent char yields up to 68% at 650 °C under nitrogen. Moreover, the vitrimers displayed mechanical reprocessability over five destruction/healing cycles and rapid chemical recyclability following acidic hydrolysis at mild temperatures. Our findings indicate that vitrimers possessing tunable properties and high-performance thermomechanical behavior can be easily constructed from vanillin and electrophilic aromatic scaffolds for applications in heat-shielding materials and ablative coatings. © 2023 RSC.

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Tuning Polymer Molecular Weight Distribution in Cationic RAFT Polymerization by Mixing Chain Transfer Agents

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Chinese Journal of chemistry 2023年第14期41卷 1684-1690页

作者： Miao Chen Jiajia Li Dong Xing Xiangqiang Pan Jian Zhu State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials Jiangsu Key Laboratory of Advanced Functional Polymer Design and ApplicationSuzhou Key Laboratory of Macromolecular Design and Precision SynthesisDepartment of Polymer Science and EngineeringCollege of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhouJiangsu215123 China

Polymer dispersity (Đ) or molecular weight distribution (MWD) is a basic but vital parameter for the properties of polymeric materials. Developing new methodologies for controlling polymer MWD is emerging as a research hotspot. However, the methods to tune polymer MWD in cationic polymerization are still not well explored. Herein, we present a simple method to control the dispersity of poly(isobutyl vinyl ether) (PIBVE) by mixing two different chain transfer agents in batch visible light induced cationic RAFT polymerization. A broad dispersity range (Đ ≈ 1.16—1.80) was successfully achieved while maintaining monomodal MWD. Moreover, chain extension of PIBVE through both cationic polymerization and radical polymerization has been studied, which also provides a method to tune polymer MWD in mechanism transformation polymerization.

关键词： RAFT Photopolymerization Copolymers lonic polymerization Molecular weight distribution Dispersity

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Enhancing microplastic capture efficiencies with adhesive coatings on stainless-steel filters

RSC Applied Polymers

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RSC Applied Polymers 2024年第3期2卷 456-460页

作者： Ramkumar, Malavika Ji, Woojung Thurber, Henry E. Clough, Madeline E. Chirdon, Sarena McNeil, Anne J. Department of Chemistry University of Michigan 930 North University Avenue Ann Arbor 48109-1055 MI United States Macromolecular Science and Engineering Program University of Michigan 2300 Hayward Street Ann Arbor 48109-2800 MI United States

Microplastics have been found in our food, water, and air, raising concerns about their potential health impacts. While environmental remediation may be intractable, we should prioritize minimizing our exposure. In this context, an adhesive-coated stainless-steel filter was developed herein to remove microplastics from water. © 2024 RSC.

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Porphyrin-Grafted Poly(ethylene terephthalate) as a Reusable and Highly Selective Colorimetric Probe for Mercuric Ion Contaminants in Aqueous Samples

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ACS Applied Materials and Interfaces 2024年第30期16卷 39195-39205页

作者： Atayde, Eduardo C. Takenaka, Yasumasa Abe, Hideki Wu, Ming-Rou Wu, Kevin C.-W. Molecular Science and Technology Program Taiwan International Graduate Program Academia Sinica Department of Chemistry National Tsing Hua University Department of Chemical Engineering National Taiwan University Bioplastic Research Team RIKEN Center for Sustainable Resource Science Department of Chemical Engineering and Materials Science Yuan Ze University Department of Chemical Engineering Chung Yuan Christian University

Heavy metals are the most hazardous water pollutants, with severe health and environmental consequences. Among these, mercuric (Hg2+) ions are known to cause detrimental health issues in both humans and aquatic life. ... 详细信息

Heavy metals are the most hazardous water pollutants, with severe health and environmental consequences. Among these, mercuric (Hg²⁺) ions are known to cause detrimental health issues in both humans and aquatic life. Due to this, several analytical techniques have been devised to detect and quantify the amount of this ion. However, most of these require advanced instrumentation, prolonged analysis time, and sample preparation. In this study, a low-cost and highly reusable colorimetric probe was developed by grafting porphyrin to poly(ethylene terephthalate) sheets using an oxazoline polymer as covalent adhesive. Upon exposure to trace amounts of Hg²⁺ in solution, the fabricated material visually transitioned from faint brownish pink to green by the complexation mechanism. Additionally, the transparency of this probe allowed the quantitative spectrophotometric determination of the Hg²⁺ concentration in aqueous samples. It was also shown that the material is highly stable, which can be reused for more than 50 times without significant decline in its performance, hence, making it suitable for the onsite monitoring of mercuric ion contamination in different bodies of water. © 2024 The Authors. Published by American Chemical Society.

关键词： colorimetric probe mercuric ion oxazoline PET porphyrin

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Janus Polymerization:A One-Shot Approach towards Amphiphilic Multiblock Poly(ester-acetal)s Directly from 1,3-Dioxolane withε-Caprolactone

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Chinese Journal of chemistry 2022年第6期40卷 705-712页

作者： Huan Qiu Ting Shen Zhening Yang Feng Wu Xiaohong Li Yingfeng Tu Jun Ling MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and EngineeringZhejiang UniversityHangzhouZhejiang 310027China College of Chemistry Chemical Engineering and Materials ScienceSoochow UniversitySuzhouJiangsu 215123China

Janus polymerization consists of anionic and cationic ring opening polymerizations(AROP and CROP)at the two ends of a single propagating polymer chain,followed by a self-triggered chain extension generating multiblock copolymers(MBCPs)in one *** the contribution,Janus polymerization by Tm(OTf)_(3) or Er(OTf)_(3) catalyst with an epoxy initiator is applied to synthesize MBCPs of semi-crystalline poly(ε-caprolactone)(PCL)blocks from coordinated AROP and poly(1,3-dioxolane-co-ε-caprolactone)(P(DO-co-CL))blocks from CROP of DO with ***,amorphous random copolymers[P(DO-r-CL)]are synthesized as control by employing other rare earth triflates[RE(OTf)_(3),RE=Y,Nd,Gd and Lu]as catalysts or in the absence of an initiator via *** account of the distinguishable chemical structures and thermal properties between Janus MBCPs and cationic random copolymers,Janus features are confirmed including the CROP and AROP at a single propagating *** resultant amphiphilic copolymers self-assemble to nanoparticles in aqueous solution with designable diameters with the corresponding ratios of hydrophilic and hydrophobic *** exhibit good shape memory properties with appropriate deformation temperature close to human body's,providing a prospect on the applications in biomedical devices.

关键词： Janus polymerization Ring-opening polymerization Multiblock copolymers Homogeneous catalysis(?)Lanthanides

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