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After concentration of the liquor by evaporation, sodium dithionite is precipitated
By the addition of sodium chloride. The salt, which is dried before shipment, contains
Up to 300 p.p.m. zinc.
The dominant process is the reaction of sodium formate with sulfur dioxide
and caustic soda under pressure. The reaction is described by:
HCOONa + 2SO2 + NaOH → NaS2O4 + CO2 + H2O
Commercial grades of sodium dithionite powder typically have a content of
about 88% sodium dithionite, with the sodium salts of bisulfite, sulfite, sulfate
And carbonate as the byproducts. Solutions of dithionite in water must be prepared
On-site. In pulp bleaching, the use of returnable steel containers with up to
Kg of technical-grade product is common. Typically, a small amount of a chelant
(e.g., ethylene diamine tetra-acetic acid; EDTA) is added. This avoids scaling
(precipitation of calcium carbonate) caused by the hardness of the dilution water.
An analysis of the stability of dithionite solutions in the presence of iron and manganese
[33] contradicted the speculation about the metal ion (Fe, Mn) -induced
decomposition of dithionite [34]. The fine powder reacts exothermically with atmospheric
Oxygen; the heat of oxidation can lead to ignition. Sodium dithionite is
therefore classified as “spontaneously combustible goods”, and the corresponding
Transport and storage regulations must be applied.
Alternatively, some mills operate an on-site process using a solution of sodium
borohydride (~12% by weight) with caustic soda (~40%). This mixture is reacted
with sulfur dioxide to yield dithionite solutions:
NaBH4 + 8NaOH + 8SO2 → 4Na2S2O4 + NaBO2 + 6H2O
Some pulp mills are supplied with an alkaline solution (pH > 12) of sodium
dithionite. Transportation requires cooling to a temperature below 10 °C to maintain
the content at ca. 11–12% dithionite. Cooling of the storage tank is not required
When there is a rapid turnover of the product. Exclusion of air is required
To avoid product losses, as dithionite reacts rapidly with oxygen in the air to yield
Sulfite. In the absence of air, decomposition reactions take place, with one of the
Products being thiosulfate; this, in turn, may accelerate corrosion reactions.
Bleaching with dithionite typically is conducted at moderately acidic pH, between
PH 4.5 and 6.5. The temperature in tower or tube bleaching is maintained
at 60–80 °C, although a higher temperature produces a faster response to the
Chemical addition. The reduction of chromophores occurs very quickly; so the
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Oxidative processes. | | | Bleaching with Dithionite 1125 |