15 research outputs found

    Standard Nitrogen Adsorption Data for Manganese Oxide and like (C = 40–60) Surfaces

    No full text
    Calcination to 1170 K of materials obtained by mild and intensive reduction of KMnO 4 and HMnO 4 solutions was found to produce manganese oxides assuming the crystalline bulk structure of α-Mn 2 O 3 Nitrogen adsorption isotherms at 77 K revealed that they also assume non-porous surfaces of low specific area (4 ± 1 m 2 /g) with C BET equal to 40–60; t- and α s -curves derived therefrom were found to coincide with those determined reportedly on non-porous surfaces of 11 < C BET < ∞, irrespective of the surface chemical similarity. The experimental and reported standard adsorption data were used to analyze a type-IV nitrogen adsorption isotherm determined at 77 K on a porous manganese oxide (δ-MnO 2 ) which was obtained by sol–gel processing of a KMnO 4 solution, and found to similarly reveal a mesoporous surface of S BET = 73 m 2 /g and C BET = 125. The close agreement between the surface area values (S t and S α ) derived for the test material (δ-MnO 2 ) from the t- and α s -plots thus obtained and its C BET value (73 m 2 /g) was the basis on which reference materials with 11 < C BET < ∞ were found to be appropriate. Since most of the appropriate reference materials were dissimilar chemically to the test material, the results of the present investigation may imply that the surface chemical similarity demanded by the α s -method is better manifested in terms of the surface activity (heat of adsorption monitored by the C BET value) than the chemical composition

    Surface Modification with Alginate-Derived Polymers for Stable, Protein-Repellent, Long-Circulating Gold Nanoparticles

    No full text
    Poly(ethylene) glycol is commonly used to stabilize gold nanoparticles (GNPs). In this study, we evaluated the ability of cysteine-functionalized alginate-derived polymers to both provide colloidal stability to GNPs and avoid recognition and sequestration by the body's defense system. These polymers contain multiple reactive chemical groups (hydroxyl and carboxyl groups) that could allow for ready functionalization with, for example, cell-targeting ligands and therapeutic drugs. We report here that alginate-coupled GNPs demonstrate enhanced stability in comparison with bare citrate-coated GNPs and a similar lack of interaction with proteins in vitro and long in vivo circulation as PEG-coated GNPs

    Surface Modification with Alginate-Derived Polymers for Stable, Protein-Repellent, Long-Circulating Gold Nanoparticles

    No full text
    Poly(ethylene) glycol is commonly used to stabilize gold nanoparticles (GNPs). In this study, we evaluated the ability of cysteine-functionalized alginate-derived polymers to both provide colloidal stability to GNPs and avoid recognition and sequestration by the body’s defense system. These polymers contain multiple reactive chemical groups (hydroxyl and carboxyl groups) that could allow for ready functionalization with, for example, cell-targeting ligands and therapeutic drugs. We report here that alginate-coupled GNPs demonstrate enhanced stability in comparison with bare citrate-coated GNPs and a similar lack of interaction with proteins <i>in vitro</i> and long <i>in vivo</i> circulation as PEG-coated GNPs
    corecore