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Solid Acids (solid + acid)

Distribution by Scientific Domains
Chemistry70%
Polymers and Materials Science30%

Terms modified by Solid Acids

  • solid acid catalyst
    		•

    Selected Abstracts

    ChemInform Abstract: Solid Acid Induced Heterocyclization under Microwave Irradiation.

    CHEMINFORM, Issue 13 2001
    Highly Selective Synthesis of Condensed Thiazole.
    Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

    An Efficient Solid Acid Promoted Synthesis of Quinoxaline Derivatives at Room Temperature

    CHINESE JOURNAL OF CHEMISTRY, Issue 6 2007
    Shaabani Ahmad
    Abstract Quinoxaline derivatives have been synthesized in a very short time with excellent yields by the condensation of 1,2-diamines with aliphatic or aromatic 1,2-dicarbonyl compounds or benzilmonoxime in the presence of silica sulfuric acid as a very inexpensive solid acid catalyst at room temperature. The recovery and reuse of the catalyst are also satisfactory. [source]

    ChemInform Abstract: Microwave-Induced Solvent-Free Synthesis of ,-Keto Esters Using Montmorillonite KSF and K10 Clays as Efficient and Recyclable Heterogeneous Solid Acids.

    CHEMINFORM, Issue 27 2008
    Omid Marvi
    Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

    ChemInform Abstract: Solid Acids as Fuel Cell Electrolytes.

    CHEMINFORM, Issue 31 2001
    Sossina M. Haile
    Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

    The Combined Catalytic Action of Solid Acids with Nickel for the Transformation of Polypropylene into Carbon Nanotubes by Pyrolysis

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 11 2007
    Rongjun Song
    Abstract The effects of both organically modified montmorillonite (OMMT) and Ni2O3 on the carbonization of polypropylene (PP) during pyrolysis were investigated. The results from TEM and Raman spectroscopy showed that the carbonized products of PP were mainly multiwalled carbon nanotubes (MWNTs). Surprisingly, a combination of OMMT and Ni2O3 led to high-yield formation of MWNTs. X-ray powder diffraction (XRD) and GC,MS were used to investigate the mechanism of this combination for the high-yield formation of MWNTs from PP. Brønsted acid sites were created in degraded OMMT layers by thermal decomposition of the modifiers. The resultant carbenium ions play an important role in the carbonization of PP and the formation of MWNTs. The degradation of PP was induced by the presence of carbenium ions to form predominantly products with lower carbon numbers that could be easily catalyzed by the nickel catalyst for the growth of MWNTs. Furthermore, carbenium ions are active intermediates that promote the growth of MWNTs from the degradation products with higher carbon numbers through hydride-transfer reactions. The XRD measurements showed that Ni2O3 was reduced into metallic nickel (Ni) in situ to afford the active sites for the growth of MWNTs. [source]

    H2xMnxSn3-xS6 (x,=,0.11,0.25): A Novel Reusable Sorbent for Highly Specific Mercury Capture Under Extreme pH Conditions

    ADVANCED FUNCTIONAL MATERIALS, Issue 7 2009
    Manolis J. Manos
    Abstract The H2xMnxSn3-xS6 (x,=,0.11,0.25) is a new solid acid with a layered hydrogen metal sulfide (LHMS). It derives from K2xMnxSn3,xS6 (x,=,0.5,0.95) (KMS-1) upon treating it with highly acidic solutions. We demonstrate that LHMS-1 has enormous affinity for the very soft metal ions such as Hg2+ and Ag+ which occurs via a rapid ion exchange process. The tremendous affinity of LHMS-1 for Hg2+ is reflected in very high distribution coefficient KdHg values (>106,mL g,1). The large affinity and selectivity of LHMS-1 for Hg2+ persists in a very wide pH range (from less than zero to nine) and even in the presence of highly concentrated HCl and HNO3 acids. LHMS-1 is significantly more selective for Hg2+ and Ag+ than for the less soft cations Pb2+ and Cd2+. The Hg2+ ions are immobilized in octahedral sites between the sulfide layers of the materials via Hg,S bonds as suggested by pair distribution function (PDF) analysis. LHMS-1 could decrease trace concentrations of Hg2+ (e.g. <100,ppb) to well below the acceptable limits for the drinking water in less than two min. Hg-laden LHMS-1 shows a remarkable hydrothermal stability and resistance in 6,M HCl solutions. LHMS-1 could be regenerated by treating Hg-loaded samples with 12,M HCl and re-used without loss of its initial exchange capacity. [source]

    Reactive extrusion to synthesize intumescent flame retardant with a solid acid as catalyst and the flame retardancy of the products in polypropylene

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008
    Yuan Liu
    Abstract Reactive extrusion and solid acid catalysis technologies were adopted in the pentaerythritol,melamine phosphate (PER-MP) reaction to synthesize intumescent flame retardant, melamine salt of pentaerythritol phosphate (MPP), which was applied in flame retardant polypropylene (PP). This environment-friendly synthesis method provided a solution to the problems of conventional methods. On one hand, reactive extrusion in a twin screw extruder can effectively mix and transfer viscous materials that usually results in a tough stir in a conventional reactor, and achieve a continuous synthesis process. On the other hand, the solid acid, silicotungstic acid (STA) serving as a catalyst, can maintain a satisfactory conversion even with a low extrusion temperature and a short residence time, thus effectively suppressing foaming in the process of the reaction. Furthermore, without removal like other catalysts in general chemical reactions, STA was kept in produced MPP to constitute a synergism flame retardant system, therefore further improved the flame retardancy. LOI and UL94 test showed that the STA-catalyzed MPP (by reactive extrusion) possessed much better flame retardancy in PP when compared with the noncatalyzed MPP (by reactive extrusion), as well as present commercial MPP (by POCl3 method). In our investigation, the catalytic and synergistic effects of STA, as well as the related factors of the reactive extrusion affecting the conversion of the PER-MP reaction, flame retardancy and mechanical performance of the corresponding flame retardant PP, were systematically investigated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

    A Comparison Study of Rhodamine,B Photodegradation over Nitrogen-Doped Lamellar Niobic Acid and Titanic Acid under Visible-Light Irradiation

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 14 2009
    Xiukai Li Dr.
    Abstract Slip between the sheets! The intercalation properties of lamellar solid acids have a profound impact on nitrogen doping as well as on the resultant visible-light photocatalysis, and the effects depend strongly on the protonic acidities of the samples (see figure). A solid-state reaction method with urea as a nitrogen precursor was used to prepare nitrogen-doped lamellar niobic and titanic solid acids (i.e., HNb3O8 and H2Ti4O9) with different acidities for visible-light photocatalysis. The photocatalytic activities of the nitrogen-doped solid acids were evaluated for rhodamine,B (RhB) degradation and the results were compared with those obtained over the corresponding nitrogen-doped potassium salts. Techniques such as XRD, BET, SEM, X-ray photoelectron spectroscopy, and UV-visible diffuse reflectance spectroscopy were adopted to explore the nature of the materials as well as the characteristics of the doped nitrogen species. It was found that the intercalation of the urea precursor helped to stabilize the layered structures of both lamellar solid acids and enabled easier nitrogen doping. The effects of urea intercalation were more significant for the more acidic HNb3O8 sample than for the less acidic H2Ti4O9. Compared with the nitrogen-doped KNb3O8 and K2Ti4O9 samples, the nitrogen-doped HNb3O8 and H2Ti4O9 solid acids absorb more visible light and exhibit a superior activity for RhB photodegradation under visible-light irradiation. The nitrogen-doped HNb3O8 sample performed the best among all the samples. The results of the current study suggest that the protonic acidity of the lamellar solid-acid sample is a key factor that influences nitrogen doping and the resultant visible-light photocatalysis. [source]

    Which Controls the Depolymerization of Cellulose in Ionic Liquids: The Solid Acid Catalyst or Cellulose?

    CHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 2 2010
    Roberto Rinaldi Dr.
    Abstract Cellulose is a renewable and widely available feedstock. It is a biopolymer that is typically found in wood, straw, grass, municipal solid waste, and crop residues. Its use as raw material for biofuel production opens up the possibility of sustainable biorefinery schemes that do not compete with food supply. Tapping into this feedstock for the production of biofuels and chemicals requires,as the first-step,its depolymerization or its hydrolysis into intermediates that are more susceptible to chemical and/or biological transformations. We have shown earlier that solid acids selectively catalyze the depolymerization of cellulose solubilized in 1-butyl-3-methylimidazolium chloride (BMIMCl) at 100,°C. Here, we address the factors responsible for the control of this reaction. Both cellulose and solid acid catalysts have distinct and important roles in the process. Describing the depolymerization of cellulose by the equivalent number of scissions occurring in the cellulosic chains allows a direct correlation between the product yields and the extent of the polymer breakdown. The effect of the acid strength on the depolymerization of cellulose is discussed in detail. Practical aspects of the reaction, concerning the homogeneous nature of the catalysis in spite of the use of a solid acid catalyst, are thoroughly addressed. The effect of impurities present in the imidazolium-based ionic liquids on the reaction performance, the suitability of different ionic liquids as solvents, and the recyclability of Amberlyst 15DRY and BMIMCl are also presented. [source]