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  2. Disulfur dibromide - Wikipedia

    en.wikipedia.org/wiki/Disulfur_dibromide

    Disulfur dibromide is the inorganic compound with the formula S 2 Br 2.It is a yellow-brown liquid that fumes in air. It is prepared by direct combination of the elements and purified by vacuum distillation. [3]

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  4. Flammability diagram - Wikipedia

    en.wikipedia.org/wiki/Flammability_diagram

    Such diagrams are available in the speciality literature. [1] [2] [3] The same information can be depicted in a normal orthogonal diagram, showing only two substances, implicitly using the feature that the sum of all three components is 100 percent. The diagrams below only concerns one fuel; the diagrams can be generalized to mixtures of fuels.

  5. Sulfur dibromide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dibromide

    Sulfur dibromide is the chemical compound with the formula S Br 2.It is a toxic gas. Sulfur dibromide readily decomposes into S 2 Br 2 and elemental bromine. In analogy to sulfur dichloride, it hydrolyzes in water to give hydrogen bromide, sulfur dioxide and elemental sulfur.

  6. Sulfur bromide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_bromide

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  7. List of interactive geometry software - Wikipedia

    en.wikipedia.org/wiki/List_of_interactive...

    Live Geometry is a free CodePlex project that lets you create interactive ruler and compass constructions and experiment with them. It is written in Silverlight 4 and C# 4.0 (Visual Studio 2010). The core engine is a flexible and extensible framework that allows easy addition of new figure types and features.

  8. Styrene-butadiene - Wikipedia

    en.wikipedia.org/wiki/Styrene-butadiene

    E-SBR produced by emulsion polymerization is initiated by free radicals. Reaction vessels are typically charged with the two monomers, a free radical generator, and a chain transfer agent such as an alkyl mercaptan. Radical initiators include potassium persulfate and hydroperoxides in combination with ferrous salts.

  9. Thionyl bromide - Wikipedia

    en.wikipedia.org/wiki/Thionyl_bromide

    Unlike with thionyl chloride, stoichiometric bases are problematic activating agents, because free bromide anions decompose thionyl bromide to tribromide, sulfur dioxide, and sulfur. [1] It can be used for brominations of certain α,β-unsaturated carbonyl compounds. [5] It may occasionally be used as a solvent. [6] [7]