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  2. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  3. Monopropellant rocket - Wikipedia

    en.wikipedia.org/wiki/Monopropellant_rocket

    This system is based on a hydroxylammonium nitrate (HAN)/water/fuel monopropellant blend which is extremely dense, environmentally benign, and promises good performance and simplicity. [ 16 ] The EURENCO Bofors company produced LMP-103S as a 1-to-1 substitute for hydrazine by dissolving 65% ammonium dinitramide , NH 4 N(NO 2 ) 2 , in 35% water ...

  4. Weak base - Wikipedia

    en.wikipedia.org/wiki/Weak_base

    Bases are proton acceptors; a base will receive a hydrogen ion from water, H 2 O, and the remaining H + concentration in the solution determines pH. A weak base will have a higher H + concentration than a stronger base because it is less completely protonated than a stronger base and, therefore, more hydrogen ions remain in its solution.

  5. Portable water purification - Wikipedia

    en.wikipedia.org/wiki/Portable_water_purification

    Secondary factors are pathogen species, water temperature, pH, and organic contaminants. In field-water disinfection, use of concentrations of 1–16 mg/L for 10–60 min is generally effective. Of note, Cryptosporidium oocysts, likely Cyclospora species, Ascaris eggs are extremely resistant to halogens and field inactivation may not be ...

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. [1] [2] In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step.

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