C5510
Activated charcoal
acid-washed with phosphoric and sulfuric acids
Sinónimos:
Charcoal activated
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About This Item
Fórmula empírica (notación de Hill):
C
Número de CAS:
Peso molecular:
12.01
Número CE:
Número MDL:
Código UNSPSC:
23201100
ID de la sustancia en PubChem:
NACRES:
SB.52
Productos recomendados
presión de vapor
<0.1 mmHg ( 20 °C)
Nivel de calidad
Formulario
powder
temp. de autoignición
842 °F
características de los productos alternativos más sostenibles
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
resistividad
1375 μΩ-cm, 20°C (graphite)
impurezas
≤1.0% acid solubles
≤10% moisture content
mp
3550 °C (lit.)
categoría alternativa más sostenible
cadena SMILES
[C]
InChI
1S/C
Clave InChI
OKTJSMMVPCPJKN-UHFFFAOYSA-N
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Descripción general
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Click here for more details.
Aplicación
Activated charcoal was used to adsorb lignin and hemicelluloses in spent liquor from neutral sulfite semichemical (NSSC) pulping process.
Código de clase de almacenamiento
13 - Non Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
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Mehdi Dashtban et al.
Journal of environmental management, 136, 62-67 (2014-02-26)
Hemicelluloses and lignin present in the spent liquor (SL) of neutral sulfite semichemical (NSSC) pulping process can potentially be converted into value-added products such as furfural, hydroxymethylfurfural, levulinic acid, phenols and adhesives. However, the direct conversion of hemicelluloses and lignin
Yin Wang et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(1), 533-538 (2013-12-25)
Stomatal pores surrounded by a pair of guard cells in the plant epidermis control gas exchange between plants and the atmosphere in response to light, CO2, and the plant hormone abscisic acid. Light-induced stomatal opening is mediated by at least
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Nature chemistry, 6(1), 47-51 (2013-12-19)
The development of a general catalytic method for the direct and stereoselective construction of contiguous all-carbon quaternary stereocentres remains a formidable challenge in chemical synthesis. Here, we report a highly enantio- and diastereoselective [3+2] annulation reaction of 5-vinyloxazolidinones and activated
Nathalie Butt et al.
Ecological applications : a publication of the Ecological Society of America, 23(4), 936-943 (2013-07-20)
A typical way to quantify aboveground carbon in forests is to measure tree diameters and use species-specific allometric equations to estimate biomass and carbon stocks. Using "citizen scientists" to collect data that are usually time-consuming and labor-intensive can play a
Isabelle Aillaud et al.
Dalton transactions (Cambridge, England : 2003), (44)(44), 5105-5118 (2007-11-07)
The catalysed enantioselective formation of carbon-nitrogen bonds by the hydroamination reaction is reviewed. All examples deal with substrates containing non-activated carbon-carbon multiple bonds which are transformed either via intramolecular or intermolecular reactions. Structurally different complexes already provided nitrogen containing compounds/heterocycles
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