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1.
ChemSusChem ; 2(2): 158-60, 2009.
Article in English | MEDLINE | ID: mdl-19148915

ABSTRACT

A thirst for water: Organic-inorganic hybrid silica nanosieve membranes with narrow pore size distributions were developed for the separation of binary (bio)alcohol/water mixtures, for example, to remove water from wet biofuels during production. These membranes dehydrate lower alcohols and show a stable performance in the presence of significant amounts of acetic acid.


Subject(s)
Alcohols/isolation & purification , Membranes, Artificial , Acetic Acid , Energy-Generating Resources , Porosity , Silicon Dioxide , Water
2.
Chem Commun (Camb) ; (9): 1103-5, 2008 Mar 07.
Article in English | MEDLINE | ID: mdl-18292904

ABSTRACT

Unprecedented hydrothermal stability in functional membranes has been obtained with hybrid organic-inorganic nanoporous materials, enabling long-term application in energy-efficient molecular separation, including dehydration up to at least 150 degrees C.

3.
Chem Commun (Camb) ; (7): 834-5, 2004 Apr 07.
Article in English | MEDLINE | ID: mdl-15045087

ABSTRACT

The incorporation of methyl groups in microporous silica membranes was proven to enhance the service time in the dehydration of a butanol-water mixture at 95 degrees C from a few weeks to more than 18 months with a water flux of about 4 kg m(-2) h(-1) and a selectivity between 500 and 20 000.

4.
Inorg Chem ; 37(23): 6071-6077, 1998 Nov 16.
Article in English | MEDLINE | ID: mdl-11670745

ABSTRACT

A polycrystalline sample of a new phase in the Sr-Fe-Mn-O system has been prepared by standard solid-state techniques. Characterization at room temperature by X-ray diffraction, high-resolution electron microscopy, Mössbauer spectroscopy and neutron diffraction has led to it being described as a 15-layered, rhombohedral (15R) perovskite [space group R&thremacr;m: a = 5.4489(1) Å, c = 33.8036(7) Å] with a previously unobserved structure. The pseudo close-packed SrO(3) layers have a (cchch)(3) stacking sequence such that the occupation of the interstitial 6-coordinate sites by Mn (or Fe) leads to the formation of Mn(2)O(9) units which are linked to each other either directly by a common vertex, or indirectly via a single, vertex-sharing MnO(6) octahedron. The stoichiometry of the compound was determined to be SrMn(0.915(5))Fe(0.085(5))O(2.979(3)). The face-sharing sites are occupied by 0.957(3)Mn/0.043(3)Fe while the exclusively corner-linked sites show a higher Fe occupation; 0.745(4)Mn/ 0.255(4)Fe. A neutron diffraction experiment carried out at 3 K indicated the presence of long-range magnetic order with the Mn(4+) cations aligned antiferromagnetically with an ordered moment of 2.26(3)&mgr;(B)/Mn(4+). Both the neutron and the susceptibility data are consistent with the Fe cations remaining magnetically disordered to 3 K. The latter data show T(N) = 220 K, and suggest that some spin frustration is present at low temperatures.

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