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In this study, epoxidized natural rubber (ENR) was mixed using a two-roller mixer. Water hyacinth fiber (WHF) acted as a reinforcing agent in the preparation of the rubber composite at 10 phr (ENRC/WHF). Chlorhexidine gluconate (CHG) was added at different concentrations (1, 5, 10, and 20 phr) as an antimicrobial and coupling agent. The tensile strength increased with a CHG content of 1 phr (4.59 MPa). The ENRC/WHF/CHG20 blend offered high hardness (38) and good morphology owing to the reduction in cavities and fiber pull-out from the rubber matrix. The swelling of the sample blends in oil and toluene decreased as the CHG content increased. Reactions of -NH/epoxy groups and -NH/-OH groups occurred during the preparation of the ENRC/WHF/CHG blend. The FTIR spectroscopy peak at 1730 cm confirmed the reaction between the -NH groups of CHG and epoxy groups of ENR. The ENRC/WHF/CHG blend at 10 phr and 20 phr exhibited zones of inhibition against three bacterial species (, , and ). CHG simultaneously acted as a crosslinking agent between ENR and WHF and as an antimicrobial additive for the blends. CHG also improved the tensile strength, hardness, swelling, and antimicrobial properties of ENR composites.
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http://dx.doi.org/10.3390/polym16213089 | DOI Listing |
Org Biomol Chem
September 2025
Phosphorus Laboratory, Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
Herein, we report a simple, microwave-assisted and open-air strategy for gram-scale C3-alkylation of indoles, along with an economically viable strategy for epoxide opening followed by α-alkylation, using the [RuCl(bpy){-PhPCHCONCHPPh-}-κ-(,,,,)] complex (hereafter referred to as [PNP-Ru]). This transformation proceeds an alcohol dehydrogenation (oxidation) mechanism, with water being the sole byproduct in both reactions, underscoring the environmentally benign and sustainable nature of the methodology. The protocol efficiently delivers both mono- and bis(indolyl) derivatives in good to excellent yields.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou, 450000, China.
With growing public attention to environmental issues and sustainable development, biodegradable bio-based plastics have attracted widespread interest. This study reveals the chemical-physical synergistic regulation mechanism of biodegradable PLA/PBAT blends through the synergistic modification of epoxidized natural rubber (ENR) and epoxy chain extender (ADR). Interfacial interaction analysis shows that PBAT tends to encapsulate ENR to form aggregates.
View Article and Find Full Text PDFAdv Mater
September 2025
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Developing amphibious adhesives that combine high adhesion strength with on-demand erasability in both dry and wet environments remains a significant challenge. In this study, biomass-derived, amphibious, and erasable adhesives are fabricated by grafting 3-aminobenzoic acid and 3-aminobenzeneboronic acid onto epoxidized soybean oil (ESO), yielding ESO-Am adhesives. These adhesives are dynamically cross-linked with boroxines, hydrogen bonds, and hydrogen-bonded hydrophobic nanodomains.
View Article and Find Full Text PDFZhongguo Zhong Yao Za Zhi
July 2025
Key Lab of Natural Product Chemistry and Application at Universities of Education Department of Xinjiang Uygur Autonomous Region, School of Chemistry and Chemical Engineering, Yili Normal University Yining 835000, China Jiangxi Provincial Key Laboratory of Natural and Biomimetic Drugs Research, Scho
Three taraxerane nortriterpenoids were isolated from mastic by using various modern chromatographic separation techniques. They were identified as(5R,8R,9R,10S,11S,12R,13S,17R,18R)-28-norlupa-11,12-epoxy-14-taraxerene-3,16-dione(1),(5R,8R,9R,10S,11S,12R,13S,17S,18S)-17-hydroxy-28-norlupa-11,12-epoxy-14-taraxerene-3-one(2), and(5R,8R,9R,10R,11S,12R,13R,14S,17S,18S)-14,17-epoxy-28-norlupa-11,12-oxidotaraxerone(3) through the high-resolution electrospray ionization mass spectrometry(HR-ESI-MS), infrared(IR), ultraviolet(UV), nuclear magnetic resonance(NMR), and single-crystal X-ray diffraction techniques as well as comparison with literature data. Compounds 1-3 were C-28 nortriterpenoids and isolated from mastic for the first time, and compounds 1-2 were new ones.
View Article and Find Full Text PDFRSC Adv
August 2025
Department of Marine Biotechnology and Resources, National Sun Yat-sen University Kaohsiung 804201 Taiwan
Two new 14,18-cycloapoeuphane triterpenoids, cumingianols G (1) and H (2), along with 12 known compounds, cumingianol C (3), cumingianol A (4), cumingianol D (5), 3,3-ethylenedioxy-5α-cycloart-24-en-23-one (6), 24,25(,)-24,25-epoxy-20()-hydroxydammar-3-one (7), (3β,7α)-stigmast-5-ene-3,7-diol (8), 7α-hydroxystigmasterol (9), 7β-hydroxysitosterol (10), 7β-hydroxystigmasterol (11), ethylcholest-5-en-3-hydroxy-7-one (12), coniferaldehyde (13) and 4-hydroxy-3,5-dimethoxy-benzaldehyde (14), have been isolated from collected in Taiwan. The structures of these metabolites were determined through mass spectrometry and 1D and 2D NMR analyses, combined with comparisons to reference data. The cytotoxic effects of these isolates were evaluated against human oral squamous cell carcinoma (SCC2095), human breast adenocarcinoma (MCF-7), and human gastric adenocarcinoma (SCM-1).
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