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  2. Orthosilicic acid - Wikipedia

    en.wikipedia.org/wiki/Orthosilicic_acid

    Orthosilicic acid (/ ˌ ɔːr θ ə s ɪ ˈ l ɪ s ɪ k /) is an inorganic compound with the formula Si(O H) 4. Although rarely observed, it is the key compound of silica and silicates and the precursor to other silicic acids [H 2 x SiO x +2 ] n .

  3. Stöber process - Wikipedia

    en.wikipedia.org/wiki/Stöber_process

    The Stöber process is a chemical process used to prepare silica (SiO 2) particles [1] of controllable and uniform size [2] for applications in materials science.It was pioneering [3] when it was reported by Werner Stöber and his team in 1968, [1] and remains today the most widely used wet chemistry synthetic approach to silica nanoparticles. [3]

  4. Empirical formula - Wikipedia

    en.wikipedia.org/wiki/Empirical_formula

    Glucose (C 6 H 12 O 6), ribose (C 5 H 10 O 5), Acetic acid (C 2 H 4 O 2), and formaldehyde (CH 2 O) all have different molecular formulas but the same empirical formula: CH 2 O.This is the actual molecular formula for formaldehyde, but acetic acid has double the number of atoms, ribose has five times the number of atoms, and glucose has six times the number of atoms.

  5. Potassium silicate - Wikipedia

    en.wikipedia.org/wiki/Potassium_silicate

    Potassium silicate can be synthesized in the laboratory by treating silica with potassium hydroxide, according to this idealized equation: nSiO 2 + 2 KOH → K 2 O·nSiO 2 + H 2 O. These solutions are highly alkaline. Addition of acids causes the reformation of silica. K 2 SiO 3 adopts a chain or cyclic structures with interlinked SiO 2− 3 ...

  6. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    Organic synthesis is a special type of chemical synthesis dealing with the synthesis of organic compounds. For the total synthesis of a complex product, multiple procedures in sequence may be required to synthesize the product of interest, needing a lot of time. A purely synthetic chemical synthesis begins with basic lab compounds.

  7. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    2 ((CH 3) 3 SiCl + H 2 O → [(CH 3) 3 Si] 2 O + 2 HCl. The analogous reaction of dimethyldichlorosilane gives siloxane polymers or rings: n (CH 3) 2 SiCl 2 + n H 2 O → [(CH 3) 2 SiO] n + 2n HCl. Many compounds containing Si-Cl bonds can be converted to hydrides using lithium aluminium hydride, This kind of conversion was demonstrated for the ...

  8. Organosilicon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosilicon_chemistry

    Although proportionately a minor outlet, organosilicon compounds are widely used in organic synthesis. Notably trimethylsilyl chloride Me 3 SiCl is the main silylating agent. One classic method called the Flood reaction for the synthesis of this compound class is by heating hexaalkyldisiloxanes R 3 SiOSiR 3 with concentrated sulfuric acid and a ...

  9. ZSM-5 - Wikipedia

    en.wikipedia.org/wiki/ZSM-5

    Pentasil-zeolites are defined by their structure type, and more specifically by their X-ray diffraction patterns. ZSM -5 is the trade name of a pentasil-zeolite. As early as 1967, Argauer and Landolt worked out parameters for the synthesis of pentasilzeolites, particularly those relating to the following molar ratios: OH − /SiO 2 = 0.07–10, SiO 2 /Al 2 O 3 = 5–100, H 2 O/SiO 2 = 1–240. [1]