Sulfato de cálcio

Sulfato de cálcio monohidratado
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Outros nomes Gesso, Drierite
Identificadores
Número CAS 7778-18-9
Número RTECS WS6920000
Propriedades
Fórmula molecular CaSO4
CaSO4.1/2H2O (hemihidrato)
Massa molar 136.142 g/mol
(anidro)
145.15 g/mol
(hemihidrato)
Aparência sólido branco
Densidade 2.96 g/cm3, sólido
Ponto de fusão

1460 °C (anidro)

Solubilidade em água 0.24 g/100 mL (20 °C) ou 0,017M
Estrutura
Estrutura cristalina ortorômbico
Compostos relacionados
Outros aniões/ânions sulfeto de cálcio
sulfito de cálcio
Outros catiões/cátions sulfato de magnésio
sulfato de estrôncio
Compostos relacionados Gesso
Página de dados suplementares
Estrutura e propriedades n, εr, etc.
Dados termodinâmicos Phase behaviour
Solid, liquid, gas
Dados espectrais UV, IV, RMN, EM
Exceto onde denotado, os dados referem-se a
materiais sob condições normais de temperatura e pressão

Referências e avisos gerais sobre esta caixa.
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O sulfato de cálcio é um composto químico representado por CaSO4, em que um cátion de cálcio se soma a um ânion sulfato por atração iônica. É considerado um sal inorgânico. Normalmente é encontrado no estado sólido, sua coloração é branca, e é pouco solúvel na água.

Na natureza, pode se apresentar na forma de cristais de anidrita ou gipsita. A anidrita possui coloração que pode variar de incolor a cinza escuro, com brilho intenso, mas não é fluorescente; é muito utilizada na produção de fertilizantes agrícolas, fabricação de cimento e giz, e também é útil para absorver água.

É matéria-prima para fabricação de giz escolar.[1]

Gesso

O gesso usado na construção civil e em ortopedia para imobilização em caso de luxação e fratura óssea é o sulfato de cálcio di-hidratado (CaSO4.2H2O). Tem coloração que pode ser branca ou amarela, com brilho semelhante de pérolas.

Obtenção

O sulfato de cálcio pode ser obtido como subproduto de múltiplos procedimentos:

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Referências

  1. Joab Trajano Silva (15 de julho de 2011). «As múltiplas faces do carbonato de cálcio». Ciência Hoje das Crianças. UOL.com.br. Consultado em 1 de maio de 2013. Arquivado do original em 4 de março de 2016 
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