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  2. Hafnium compounds - Wikipedia

    en.wikipedia.org/wiki/Hafnium_compounds

    The white hafnium(IV) oxide (HfO 2), also known as hafnium dioxide or hafnia, with a melting point of 2,812 °C and a boiling point of roughly 5,100 °C, is very similar to zirconia, but slightly more basic. [13] It is an electrical insulator with a band gap of 5.3~5.7 eV. [15] Hafnium(IV) oxide typically adopts the same structure as zirconia ...

  3. List of named alloys - Wikipedia

    en.wikipedia.org/wiki/List_of_named_alloys

    1.16 Platinum. 1.17 Plutonium. 1.18 Potassium. 1.19 Rare earths. 1.20 ... Some of the main alloying elements are optionally listed after the alloy names. Alloys by ...

  4. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  5. Actinide - Wikipedia

    en.wikipedia.org/wiki/Actinide

    The actinide series derives its name from the first element in the series, actinium. The informal chemical symbol An is used in general discussions of actinide chemistry to refer to any actinide. [1] [2] [3] The 1985 IUPAC Red Book recommends that actinoid be used rather than actinide, since the suffix -ide normally indicates a negative ion.

  6. Nitrogen - Wikipedia

    en.wikipedia.org/wiki/Nitrogen

    The earliest military, industrial, and agricultural applications of nitrogen compounds used saltpetre (sodium nitrate or potassium nitrate), most notably in gunpowder, and later as fertiliser. In 1910, Lord Rayleigh discovered that an electrical discharge in nitrogen gas produced "active nitrogen", a monatomic allotrope of nitrogen. [ 20 ]

  7. Oxidoreductase - Wikipedia

    en.wikipedia.org/wiki/Oxidoreductase

    Proper names of oxidoreductases are formed as "donor:acceptor oxidoreductase"; however, other names are much more common. [ citation needed ] The common name is " donor dehydrogenase " when possible, such as glyceraldehyde-3-phosphate dehydrogenase for the second reaction above.