boron and acrylic-acid

boron has been researched along with acrylic-acid* in 2 studies

Other Studies

2 other study(ies) available for boron and acrylic-acid

ArticleYear
Efficient sequestration of boron from liquid phase by amidoxime-functionalized poly(acrylonitrile-co-acrylic acid): experimental and modelling analyses.
    Water science and technology : a journal of the International Association on Water Pollution Research, 2022, Volume: 85, Issue:10

    This study aims to produce amidoxime-modified poly(acrylonitrile-co-acrylic acid) using an optimized method and to investigate the performance of amidoxime-modified poly(acrylonitrile-co-acrylic acid) on the adsorption of boron ions in batch operations. Batch adsorption was conducted at the physiochemical parameters of pH, adsorbent dosage, and initial boron concentration. The isotherms and kinetics of adsorption data were studied at various initial boron concentrations. The renewed synthesis process gave a production yield of 77%, and the conversion of nitrile group to amidoxime was 78%. The adsorption reached its optimum point at pH = 8, adsorbent dosage = 4 g·L

    Topics: Acrylates; Acrylonitrile; Boron; Oximes; Water Pollutants, Chemical; Water Purification

2022
Boron subphthalocyanine polymers by facile coupling to poly(acrylic acid-ran-styrene) copolymers synthesized by nitroxide-mediated polymerization and the associated problems with autoinitiation.
    Macromolecular rapid communications, 2013, Apr-12, Volume: 34, Issue:7

    Boron subphthalocyanines (BsubPcs) are macrocyclic aromatic small molecules containing a chelated boron atom. BsubPcs have interesting optoelectronic and physical properties, justifying their use in various organic electronic devices such as organic solar cells and organic light-emitting diodes. However, our group has only recently reported the first incorporation of a BsubPc moiety into a polymer using a two-step post-polymerization procedure. This communication outlines the use of acrylic acid as a method for obtaining carboxylic acid functional copolymers for the facile coupling to BsubPc post polymerization. In addition, the observations and the proposed mechanism of a side product unique to the copolymerization of acrylic acid and styrene due to autoinitiation are presented.

    Topics: Acrylates; Boron; Molecular Structure; Polymerization; Polymers; Styrene

2013