0000000000222333

AUTHOR

Gunter Büchel

Investigation of characterizing methods for the microstructure of cement

Volumetric, gravimetric, calorimetric, flow methods, mercury porosimetry and laser granulometry were used to investigate the surface structure and the sorption behavior of industrial cements and hydrated cement paste. The suitability of the measuring methods is assessed.

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Synthesis of spherical porous silicas in the micron and submicron size range: challenges and opportunities for miniaturized high-resolution chromatographic and electrokinetic separations.

Classical silica technology has reached its limit with respect to an ultimate minimum particle size of about 2 microm in diameter. Here, a novel process is presented which allows one to synthesize porous silica beads and control their particle diameter in situ, within the range of 0.2-2.0 microm. As a result, no sizing is required and losses of silica are avoided. Furthermore, the process enables one to control in situ the pore structural parameters and the surface chemistry of the silica beads. Even though surface funtionalized silicas made according to this process can principally be applied in fast HPLC the column pressure drop will be high even for short columns. In addition, the column…

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Rational design, tailored synthesis and characterisation of ordered mesoporous silicas in the micron and submicron size range

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A Novel Pathway for Synthesis of Submicrometer-Size Solid Core/Mesoporous Shell Silica Spheres

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Tailored syntheses of nanostructured silicas: Control of particle morphology, particle size and pore size

Ordered mesoporous silicas with spherical morphology and average particle size in the range between 100 nm and 2 μm were synthesised according to two novel routes. Both synthesis routes used tetraethoxysilane, water, alcohol and aqueous ammonia for producing spherical silica beads. The porosity was created by adding two different kinds of pore structure directing agents to the starting solution: one was an n-alkyltrialkoxysilane which was covalently bonded to the silica framework, the other was an n-alkylamine which acted as a nonionic template. After calcination and post treatment the resulting particles showed a specific surface area up to 1000 m2 g-1, a specific pore volume of up to 0.8 …

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Relationship between intrinsic pore-wall corrugation and adsorption hysteresis of N-2, O-2, and Ar on regular mesopores

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