Methanedisulfonic acid dipotassium salt Property

Density 

1.622[at 20℃]

Water Solubility 

34.438g/L at 20℃

LogP

-1.83 at 20℃

Safety

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26

WGK Germany 

3

F 

10-21

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Methanedisulfonic acid dipotassium salt Chemical Properties,Usage,Production

Uses

Methanedisulfonic acid dipotassium salt is widely used in electroplating process. As the main component of chromium plating additives, it can significantly improve the corrosion of the plating solution on the anode plate, resulting in a brighter surface, higher hardness of the coating, more microcracks and higher corrosion resistance.

Flammability and Explosibility

Not classified

Synthesis

Methanedisulfonic acid dipotassium salt is synthesised using 1,1-dibromomethane as a raw material by chemical reaction. The specific synthesis steps are as follows:
Raw Materials: CH₂Br₂: 140 g/0.8 mol K₂SO₃ (45% in water) 600 g/1.7 mol [(C₄H₉)4N]Br: 6 g KI: 0.8 g; A mixture of 600 g K₂SO₃-solution (45% in water), 6 g of [(C₄H₉)₄N]Br and 0.8 g KI in 400 ml of water, was heated to 70° C. Within a period of 16 hours, 140 g of CH₂Br₂ were transferred under the surface of the reaction mixture. During the addition of CH₂Br₂, the pressure in the reactor was determined with 1007-1008 mbar. Afterwards the reaction mixture was heated up to 90° C. After a total reaction time of 24 h, K₂[CH₂(SO₃)₂] started to precipitate. After 72 hours at 90° C., complete conversion of CH₂Br₂ to [CH₂(SO₃)₂]^2- has been achieved. The reaction mixture was cooled down to 20° C. The precipitated K₂[CH₂(SO₃)₂] was isolated by suction filtration and washed three times with 100 ml of water. The product was dried 6 hours at 80° C. under atmospheric pressure. Yield: 175 g (86.7%) Composition: Assay: 99.7% (Titration) Br^-: 111 ppm (Ion-chromatography) SO₃^2-:<50 ppm (Ion-chromatography) SO₄^2-: 54 ppm (Ion-chromatography); Purification by Recrystallization 175 g of K₂[CH₂(SO₃)₂] were suspended in 600 ml of water. The suspension was heated to about 100° C. At a pressure of about 40 mbar, 362 ml of water were evaporated out of the mixture. The remaining suspension was cooled down to 20° C. The precipitated K₂[CH₂(SO₃)₂] was isolated by suction filtration and dried 6 h at 80° C. under atmospheric pressure. Yield: 165.4 g (94.5%) Overall yield: 81.9% Composition: Assay: 99.8% (Titration) Br-: <10 ppm (potentiometric titration) SO₃^2-: <50 ppm (Ion-chromatography) SO₄^2-: <50 ppm (Ion-chromatography).