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A simplified radiation-induced emulsion graft polymerization (SREG) method is proposed. This method involves a convenient and easy degassing process of a monomer solution using a commercially available sealed glass jar. A loaded weight on the lid of the jar was used to control the jar's internal pressure as the degassing of the monomer solution took place using a vacuum pump. The degassing method was highly reproducible, resulting from no bumping of the monomer solution. The initial grafting velocity was proportional to the absorbed doses of pre-irradiation between 5 and 20 kGy. This result indicates that dissolved oxygen was sufficiently eliminated from the monomer solution at such a level where the remaining oxygen had little effect on the grafting reaction at a dose of 5 kGy. The method was then applied to the fabrication of a heavy metal adsorbent that possessed a sufficient adsorption capacity of Co(II) ions. The SREG method is applicable to the fabrication of a wide variety of functional graft polymers because high-dose-rate gamma-ray radiation and expensive experimental equipment are not necessary.
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http://dx.doi.org/10.3390/polym11081373 | DOI Listing |
J Am Chem Soc
September 2025
State Key Laboratory of Advanced Materials for Intelligent Sensing and Key Laboratory of Organic Integrated Circuits, Ministry of Education & Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Institute of Molecular Plus, Department of Chemistry, Tianjin University, Tianjin 300072, China.
Incorporating boron atoms into organic macrocycles imparts unique chemical, electronic, and optical properties. The concept of making use of dative boron-nitrogen (B ← N) bonds for the construction of macrocycles has been proposed, but very few examples have been prepared with functional structures, much less pillar-like and other prismatic macrocycles, and their various functionalities have not been fully exploited. Here, we introduce a "functional molecular wall" synthetic protocol based on the self-assembly characteristics of B ← N dative bonds to construct highly symmetrical macrocycles, forming a quasi-pentagonal-shaped macrocycle (named [5]pyBN-) with a pillar-like structure.
View Article and Find Full Text PDFLangmuir
September 2025
Advanced Polymer Laboratory, Department of Polymer Science and Technology, Government College of Engineering and Leather Technology (Post Graduate), Maulana Abul Kalam Azad University of Technology, Salt Lake City, Kolkata 700106, West Bengal, India.
This research provides a constructive approach for developing high-performance polymer nanohybrids toward enhancing optoelectronic properties, fluorogenic viscosity sensing, and metal-free electrocatalytic oxidation of glycerol to value-added organic(s). Herein, reduced graphene oxide (RGO) and mildly oxidized RGO (MRGO) are strategically combined with fluorescent electroactive polymers (FEPs) to develop a promising sustainable metal-free electrocatalytic system suitable for amplifying opto-electrochemical properties, multiplatform sensing capacity, and electrocatalytic efficiency. The optimized polymeric counterpart (FEP2) promotes dual-state emission in the supramolecular network of RGO-/MRGO-incorporated fluorescent electroactive hybrid polymers (RFEHPs/MFEHPs) through physicochemically confined atypical electron-rich -C(═O)NH-/-C(═O)O-/-SOH fluorophores of (hydroxyethyl)methacrylate and 2-acrylamido-2-methylpropane-1-sulfonic acid monomers.
View Article and Find Full Text PDFJ Mater Chem B
September 2025
School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia 4072, Australia.
Surface modification of poly(ε-caprolactone) (PCL) to facilitate interactions with high pI proteins is a strategy used to enhance 3D PCL scaffolds for tissue engineering applications. The approach of the current study was to firstly optimise the surface modification on 2D films and then apply to 3D scaffolds. Melt-pressed PCL films were grafted with 2-aminoethyl methacrylate gamma radiation induced grafting to introduce amine functional groups to the substrate surfaces.
View Article and Find Full Text PDFChem Sci
August 2025
Department of Chemistry, Graduate School of Science, Osaka University Toyonaka Osaka 560-0043 Japan.
Liquid is the most flexible state of condensed matter and shows promise as a functional soft material. However, these same characteristics make it challenging to achieve efficient room-temperature phosphorescence (RTP) from metal-free organic molecular liquids. Herein, we report efficient RTP from liquefied thienyl diketones bearing one or two dimethyloctylsilyl (DMOS) substituents.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Department of Chemistry, University of Houston, Houston, Texas 77204-5003, USA.
In conflict with standard notions of thermodynamics, mesoscopically sized inclusions ("clusters") of a solute-rich liquid have been observed in equilibrated solutions of proteins and other molecules. According to a complexation scenario proposed earlier, a steady-state ensemble of finite-sized droplets of a metastable solute-rich liquid can emerge in a solution, if the solute molecules can form transient complexes with each other and/or solute. Here, we solve for the thermodynamics of an explicit model of a self-associating fluid in which particles can form transient dimers.
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