09.04.2015 Views

Hydrosulfite Types - BASF

Hydrosulfite Types - BASF

Hydrosulfite Types - BASF

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Technical Information<br />

<strong>Hydrosulfite</strong> <strong>Types</strong><br />

TI/T 7015 e<br />

October 1997 (RB)<br />

Supersedes TI/T 1489 dated January 1993<br />

® = Registered trademark of<br />

<strong>BASF</strong> Aktiengesellschaft<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> N<br />

<strong>Hydrosulfite</strong> F Conc. <strong>BASF</strong><br />

<strong>Hydrosulfite</strong> FE Conc. <strong>BASF</strong><br />

Reducing agents for the textile industry<br />

Textile and Leather Dyes and Chemicals


Nature<br />

Physical form<br />

Storage stability<br />

Anhydrous sodium dithionite (Na 2<br />

S 2<br />

O 4<br />

), technical grade, stabilized<br />

Powder<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> and <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> N have a shelf life<br />

of up to 24 months.<br />

<strong>Hydrosulfite</strong> F Conc. <strong>BASF</strong> and <strong>Hydrosulfite</strong> FE Conc. <strong>BASF</strong> have a shelf<br />

life of up to 12 months.<br />

Storage<br />

All <strong>Hydrosulfite</strong> types must be stored in closed containers, and the<br />

containers must be protected from moisture.<br />

If the products are not stored under suitable conditions or if moist scoops<br />

are used to take product out of the containers, or if moisture enters a containers,<br />

the product decomposes. The moist product becomes lumpy and<br />

it develops heat and gases (with the odour of sulphur dioxide), resulting<br />

finally in spontaneous combustion, particularly in the presence of atmospheric<br />

oxygen (cf. “Action in the case of spontaneous combustion” on<br />

page 7).<br />

Handling of partially<br />

decomposed product<br />

Impurities<br />

<strong>Hydrosulfite</strong> that has become lumpy must immediately be removed from<br />

the drum by passing it through a coarse sieve, after which the lumps must<br />

be dissolved in water. Only the residual, powdery product is fit for use.<br />

<strong>BASF</strong>’s <strong>Hydrosulfite</strong> types are practically free of heavy metals (below the<br />

level of detectability).<br />

2


Properties<br />

Physical and chemical data<br />

Appearance<br />

Solubility<br />

White powder<br />

Readily soluble in dilute alkalis: approx. 250 g/l at 20 °C. The solution is<br />

water-white without any turbidity.<br />

,,,<br />

500<br />

,,,<br />

400<br />

,,,<br />

300<br />

,,,<br />

dissolved<br />

undissolved<br />

,,,<br />

200<br />

,,,<br />

100<br />

,,,<br />

,,,<br />

0<br />

0 100 200 300 400<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> (g/l)<br />

Caustic soda 38 °Bé (ml/l)<br />

Fig. 1<br />

Solubility of <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> in the presence of alkali<br />

Stability of the solutions<br />

<strong>Hydrosulfite</strong> solutions have a strong reducing action and bind atmospheric<br />

oxygen. 1 m 3 of air binds roughly 1.7 kg of hydrosulfite. <strong>Hydrosulfite</strong> reacts<br />

with atmospheric oxygen many times more rapidly than its own relatively<br />

slow decomposition. In working with dissolved hydrosulfite, contact with<br />

air must therefore be avoided as far as possible. In acid media, hydrosulfite<br />

decomposes to form mainly sulphur dioxide, sulphur and other<br />

sulphur-containing compounds. Alkalis have a stabilizing action on<br />

solutions of hydrosulfite, particularly when the solution is exposed to air.<br />

3


<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> (g/l)<br />

30<br />

20<br />

exclusion of air<br />

presence of air<br />

without alkali<br />

10<br />

50 ml/l NaOH 38 °Bé<br />

30 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

25 °C<br />

0<br />

0 2 4 6 8 10<br />

h<br />

Fig. 2<br />

Stability of hydrosulfite solutions under various conditions<br />

pH value<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> and<br />

(50 g/l in water) <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> N 7– 9<br />

<strong>Hydrosulfite</strong> F Conc. <strong>BASF</strong> and<br />

<strong>Hydrosulfite</strong> FE Conc. <strong>BASF</strong> 6 – 7<br />

For pH measurements, oxygen must be completely excluded. The<br />

measurement must be carried out under nitrogen and with air-free water.<br />

Bulk density<br />

The <strong>Hydrosulfite</strong> types vary in their bulk density. This must be taken into<br />

consideration in volumetric metering.<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> 1300 –1400 g/dm 3<br />

<strong>Hydrosulfite</strong> Conc. <strong>BASF</strong> N 1150 –1250 g/dm 3<br />

<strong>Hydrosulfite</strong> F Conc. <strong>BASF</strong> and<br />

<strong>Hydrosulfite</strong> FE Conc. <strong>BASF</strong> 750 – 900 g/dm 3<br />

Action<br />

Preparation of<br />

hydrosulfite solutions<br />

In the textile industry, hydrosulfite is used mainly as a reducing agent for<br />

vat dyes and for the reductive clearing of dyeings on polyester. It is also<br />

suitable for stripping dyeings and for cleaning dye becks, dyeing<br />

machines, etc.<br />

<strong>Hydrosulfite</strong> solutions are best prepared immediately before use. The alkali<br />

should be added to the bath first, after which the hydrosulfite powder is<br />

strewed into the bath with stirring.<br />

The process can be carried out very economically by using a dissolving<br />

station and obtaining the product in containers.<br />

This method has the following advantages:<br />

– no dusting<br />

– less risk of fire<br />

– lower product wastage<br />

4


In this method, a solution is prepared containing approx. 130 g/l of hydrosulfite<br />

together with the requisite amount of alkali (260 ml/l of NaOH<br />

38 °Bé). The solution is then piped to the department where it is required.<br />

This concentrated reducing agent solution only has to be diluted and is<br />

then ready for use.<br />

Applications<br />

As a reducing agent for vat dyes<br />

The main field of application for hydrosulfite is the reduction of vat dyes in<br />

order to convert them into a water-soluble form with affinity for the fibre.<br />

The vat dyes are either reduced direct in the dyebath or, as in pigmentation<br />

dyeing processes, pigment padding processes, and two-phase printing,<br />

they are first applied to the textile material in an insoluble form and<br />

then subsequently developed with hydrosulfite and caustic soda.<br />

The reducing action of hydrosulfite depends on the temperature and the<br />

pH. Under the conditions of an IN vat, the redox potential is approx.<br />

–1000 mV. This potential is sufficient to convert all commercially available<br />

vat dyes into the water-soluble sodium leuco compound, because all of<br />

these dyes are reduced in the potential range of approx. – 650 to – 950 mV.<br />

The dye must remain completely vatted throughout the whole dyeing process.<br />

However, since the hydrosulfite is continuously decomposed by the<br />

action of air, with consumption of alkali, the vat must always contain an<br />

excess of hydrosulfite and caustic soda.<br />

The presence of this excess must be ensured throughout the entire<br />

dyeing process. The simplest method is to check the alkalinity with<br />

phenolphthalein paper, and the reducing action with Vat Yellow paper.<br />

The amounts of hydrosulfite necessary for the various dyeing processes<br />

are indicated in our pattern card for Indanthren ® dyes, MK/T 266.<br />

For the reductive clearing of dyeings<br />

Dyeings and prints produced with disperse dyes on polyester fibres,<br />

triacetate fibres, and various fibre blends are cleared with alkaline<br />

hydrosulfite solutions in order to obtain the best possible standard of<br />

fastness.<br />

4– 8 ml/l caustic soda 38 °Bé<br />

2– 3 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

0.5 g/l Uniperol ® EL<br />

20 min at 70 – 80 °C<br />

Vat dyes Liquor ratio 10 :1 to 30 :1<br />

For stripping or partial stripping of dyeings and prints<br />

<strong>Hydrosulfite</strong> is suitable for the reductive stripping of dyeings and prints<br />

produced with vat, direct, and reactive dyes on cellulosic fibres.<br />

In package systems<br />

and winches<br />

Set the bath at 75 – 80 °C with<br />

0.5 g/l Dekol ® S<br />

2– 3 g/l Setamol ® WS<br />

10– 15.5 ml/l caustic soda 38 °Bé<br />

5 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

1 g/l glucose<br />

(for vat dyes that are sensitive to over-reduction)<br />

2– 3 ml/l Albigen ® A<br />

and treat the textile material for 3 min at 75 – 80 °C (with indirect steam).<br />

Ensure that a fully vatted state is maintained.<br />

5


Rinse with<br />

1 ml/l caustic soda 38 °Bé<br />

1 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

1 g/l Setamol WS<br />

for 5 min at room temperature, and then rinse with cold water with<br />

overflow. If necessary, then oxidize at 55 °C with<br />

1– 2 ml/l hydrogen peroxide 35%.<br />

On the jig<br />

Liquor ratio 5 :1 for pale shades and up to 10 :1 for dark shades<br />

Set the bath at 75 – 80 °C with<br />

1 g/l Dekol S<br />

3– 5 g/l Setamol WS<br />

20 ml/l caustic soda 38 °Bé<br />

10 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

1 g/l glucose<br />

(for dyes that are sensitive to over-reduction)<br />

2– 3 g/l Albigen A<br />

and treat the dyeing over 4 ends, but never longer than for 40 min at<br />

75 – 80 °C (with indirect steam). Ensure that a fully vatted state is<br />

maintained.<br />

As the dye-Albigen A addition compounds have low solubility (with formation<br />

of tarry deposits under certain conditions), short liquor ratios and long<br />

treating times must be avoided. If necessary, the stripping process should<br />

be repeated. The goods are then rinsed with cold water with overflow, and<br />

than oxidized with 1– 2 ml/l of hydrogen peroxide 35% at 55 °C.<br />

Direct dyes 1.5 g/l soda ash<br />

2 g/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

2 g/l Albigen A<br />

30 – 60 min at 50 °C<br />

followed by intensive rinsing.<br />

Reactive dyes 15 ml/l caustic soda 38 °Bé<br />

5 ml/l <strong>Hydrosulfite</strong> Conc. <strong>BASF</strong><br />

2 ml/l Albigen A<br />

30 – 60 min at 60 – 80 °C<br />

followed by intensive rinsing.<br />

For cleaning dyeing machines and equipment<br />

Alkaline solutions of hydrosulfite are used to remove dye residues from<br />

dyeing machines, mixing vessels, rollers, etc. The cleaning action of the<br />

solutions can be promoted by adding Albigen A or Uniperol AC.<br />

Safety<br />

When using this product, the information and advice given in our Safety<br />

Data Sheet should be observed. Due attention should also be given to<br />

the precautions necessary for handling chemicals.<br />

Contact of the products with oxidizing agents (hydrogen peroxide, sodium<br />

chlorite, and sodium hypochlorite) must be avoided under all conditions.<br />

<strong>Hydrosulfite</strong> must always be kept at a safe distance away from these<br />

agents.<br />

Action in the case of spontaneous combustion<br />

See our Technical Information Bulletin TI/T 311 e of July 1997:<br />

Measures to be taken in the case of fire or accidents in transportation.<br />

6


Note<br />

The information submitted in this publication is based on our current<br />

knowledge and experience. In view of the many factors that may affect<br />

processing and application, these data do not relieve processors of the<br />

responsibility of carrying out their own tests and experiments; neither do<br />

they imply any legally binding assurance of certain properties or of suitability<br />

for a specific purpose. It is the responsibility of those to whom we<br />

supply our products to ensure that any proprietary rights and existing laws<br />

and legislation are observed.<br />

7


Printed in Germany<br />

Regional Marketing<br />

Asia<br />

Regional Marketing<br />

North America, Canada<br />

and Mexico<br />

Regional Marketing<br />

South America<br />

Regional Marketing<br />

Europe, Africa and West Asia<br />

<strong>BASF</strong> Textile and Leather<br />

Dyes and Chemicals Pte. Ltd.<br />

7 Temasek Boulevard<br />

#35-01 Suntec Tower One<br />

Singapore 038987<br />

Tel.: (65) 432 34 00<br />

Fax.: (65) 432 34 34<br />

<strong>BASF</strong> Corporation<br />

Textile /Leather Colors and<br />

Chemicals<br />

4330 Chesapeake Drive<br />

Charlotte, NC 28216, USA<br />

Tel.: (1) 704 398 43 80<br />

Fax.: (1) 704 398 42 50<br />

<strong>BASF</strong> S.A.<br />

Química Têxtil<br />

Estrada Samuel Aizemberg 1707<br />

09851-550 São Bernardo do Campo/<br />

São Paulo - Brazil<br />

Tel.: (55) 11 751 22 33<br />

Fax.: (55) 11 751 69 89<br />

<strong>BASF</strong> Aktiengesellschaft<br />

Textil- und Lederchemie<br />

67056 Ludwigshafen/Germany<br />

Tel.: (49) 621 60 41366<br />

Tel.: (49) 621 60-0<br />

Fax.: (49) 621 60 78452<br />

Telex: 46499-0 bas d<br />

Textile and Leather Dyes and Chemicals

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!