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Amine Functional Groups (amine + functional_groups)

Distribution by Scientific Domains
Polymers and Materials Science75%

Selected Abstracts

Chemical Bonding Assembly of Multifunctional Oxide Nanocomposites

ADVANCED FUNCTIONAL MATERIALS, Issue 2 2010
Gary Evans
Abstract The synthesis, functionalization and assembly of metal oxide nanoparticles BaTiO3 and CoFe2O4 is presented. The ferroelectric (BaTiO3) and ferromagnetic (CoFe2O4) oxide nanoparticle surfaces are directly functionalized via the anchoring of phosphonic acid and aminosilane molecules that engender the nanoparticles with terminal carboxylic acid and amine functional groups, respectively. These promote the electrostatic self-assembly of the particles in non-polar solvents and permit the synthesis of more chemically robust assemblies linked by the covalent amide bond via the addition of the chemical coupling agent N - N, -dicyclohexylcarbodiimide. This functionalization and assembly procedure is applied to two systems: the first comprised of 50,nm BaTiO3 and 10,nm CoFe2O4 particles and the second of 200,nm BaTiO3 and 12.5,nm CoFe2O4 particles. The latter composites possess magnetoelectric properties when processed into dense ceramics and, as a direct result of the assembly performed in solution, have a high degree of homogeneity between the ferroelectric and ferromagnetic phases. The developed functionalization and assembly procedure is considered to be adaptable to the preparation of other hybrid oxide nanomaterials with different property combinations. [source]

Synthesis of morphologically different, metal absorbing aniline-formaldehyde polymers including micron-sized sphere using simple alcohols as morphology modifier

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008
Rik Rani Koner
Abstract Aniline-formaldehyde condensate (AFC) is an amine functional group containing polymer. The sticky resinous nature of the polymer limits its usefulness. Synthesis of AFC in presence of methanol, isopropanol, t -butanol, n -octanol or glycerine formed solid cakes instead of resinous material. The scanning electron microscopic (SEM) picture of the polymer synthesized in presence of t -butanol shows the formation of micron sized spheroids while the presence of methanol, isopropanol, n -octanol and glycerine leads to amorphous polymer. The polymers were characterized with IR, MALDI-TOF mass and Energy Dispersive X-ray (EDAX) analysis. To probe the accessibility of the amine functional groups by external reagents and as an application, metal removal property of the polymers were tested using aqueous Cr(VI) solution. All the polymers remove Cr(VI) efficiently at pH 3 with extent of metal removal depends on their morphology. Polymer synthesized in presence of isopropanol removes , 66% Cr(VI) removal from an initial concentration of 9 mg/L. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

Torque-rheometry investigation of model transreactions involving condensation polymers.

POLYMER ENGINEERING & SCIENCE, Issue 2 2006

The chemical transformations taking place when poly(ethylene terephthalate) (PET) or poly(ethylene naphthalate) (PEN) are blended in the melt with different low molar mass substances containing hydroxyl, carboxyl, or amine functional groups have been investigated as models of the transreactions, undergone by the polyesters in reactive blending operations. The polyester molecular weight changes caused by the alcoholysis, acidolysis, aminolysis, and esterolysis reactions have been monitored by torque-rheometry, using a Brabender Plasticorder static mixer. The degradation of the polyesters by hydrolysis was also studied, under similar conditions, by the addition of a water-releasing substance (wet polyamide-6), and was shown to occur quite rapidly, although most of the added water was lost by flash vaporization caused by the high temperature of the polyester melt. It has been shown that the rate constants of the reactions leading to breakage of the inner ester bonds of the polyester macromolecules decrease in the following order: aminolysis (with aliphatic amines, either primary and secondary) > alcoholysis (with aliphatic alcohols) , hydrolysis > acidolysis (with aromatic acids) , acidolysis (with aliphatic acids) , aminolysis (with aromatic amines) > alcoholysis (with phenols) , esterolysis. POLYM. ENG. SCI. 46:139,152, 2006. © 2005 Society of Plastics Engineers [source]

Acid,Base Bifunctional Catalytic Surfaces for Nucleophilic Addition Reactions

CHEMISTRY - AN ASIAN JOURNAL, Issue 8-9 2008
Ken Motokura Dr.
Abstract This article illustrates the modification of oxide surfaces with organic amine functional groups to create acid,base bifunctional catalysts, summarizing our previous reports and also presenting new data. Immobilization of organic amines as bases on inorganic solid,acid surfaces afforded highly active acid,base bifunctional catalysts, which enabled various organic transformations including CC coupling reactions, though these reactions did not proceed with either the homogeneous amine precursors or the acidic supports alone. Spectroscopic characterization, such as by solid-state MAS NMR and FTIR, revealed not only the interactions between acidic and basic sites but also bifunctional catalytic reaction mechanisms. [source]