VINYL SULFONIC ACID 30% (Vinilslfonik asit)

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VINYL SULFONIC ACID 30% (Vinilslfonik asit)

VINYL SULFONIC ACID 30% (Vinilsülfonik asit)

CAS Number: 3039-83-6

synonyms:

 

Ethylenesulfonic acid ;sodium salt, 278416_ALDRICH, 278424_ALDRICH, 1184-84-5 (Parent), MolPort-003-929-071;EINECS 214-676-1;UNII-GJ6489R1WE;monomer;polymerization;ethylenesulfonic acid;ethenesulfonic acid;polyelectrolytes;1,4-NAPHTHOQUINONE-2-SULFONIC ACID, K DEUTEROPORPHYRIN IX 2,4-DISULFONIC ACID DIMETHYL ESTER DISODIUM SALT, ETHYLENESULFONIC ACID SODIUM SALT,Ethylenesulfonic acid sodium salt, Vinylsulfonic acid sodium salt,Ethylenesulfonic acid sodium salt, Sodium vinylsulfonate solution, Vinylsulfonic acid sodium salt, DEUTEROPORPHYRIN IX, 2,4-DISULFONIC ACID, DIHYDROCHLORIDE 1,2-NAPHTHOXY-DIAZOLE-4-SULFONIC ACID, Fuchsin Acid, BROMOSULFALEIN, Egualen AKOS, BBS-00000808 1,2-NAPHTHOQUINONE-4-SULFONIC ACID SODIUM SALT 4,4-DIFLUORO-1,3,5,7,8-PENTAMETHYL-4-BORA-3A,4A-DIAZA-S-INDACENE-2,6-DISULFONIC ACID, DISODIUM SALT POTASSIUM 1,2-NAPHTHOQUINONE-4-SULFONIC ACID 2-DIAZO-1-NAPHTHOL-4-SULFONIC ACID HYDRATE ACID FUCHSIN CALCIUM SALT 8-((4,5-DIMETHOXY-2-NITROBENZYL)OXY)PYRENE-1,3,6-TRISULFONIC ACID, TRISODIUM SALT, PHENYL VINYLSULFONATE, Sodium gualenate, Sulfobromophthalein sodium;18162-48-6,872-50-4,Methylene Chloride,naphthalene,THF,Titanium Dioxide; Einecs 214-676-1;VINYLSULPHONICACID;Vinylsulfonic acid;Ethenesulfonic acid;1-Ethenesulfonic acid;ethylenesulfonic acid;ethylenesulphonic acid;3039-83-6 (Hydrochloride salt);1,4-NAPHTHOQUINONE-2-SULFONIC ACID, K DEUTEROPORPHYRIN IX 2,4-DISULFONIC ACID; DIMETHYL ESTER DISODIUM SALT; ETHYLENESULFONIC ACID SODIUM SALT,Ethylenesulfonic acid sodium salt, Vinylsulfonic acid sodium salt,Ethylenesulfonic acid sodium salt, Sodium vinylsulfonate solution, Vinylsulfonic acid sodium salt; DEUTEROPORPHYRIN IX 2,4-DISULFONIC ACID DIHYDROCHLORIDE 1,2-NAPHTHOXY-DIAZOLE-4-SULFONIC ACID Fuchsin Acid BROMOSULFALEIN Egualen AKOS BBS-00000808 1,2-NAPHTHOQUINONE-4-SULFONIC ACID SODIUM SALT; 4,4-DIFLUORO-1,3,5,7,8-PENTAMETHYL-4-BORA-3A,4A-DIAZA-S-INDACENE-2,6-DISULFONIC ACID, DISODIUM SALT POTASSIUM; 1,2-NAPHTHOQUINONE-4-SULFONIC ACID; 2-DIAZO-1-NAPHTHOL-4-SULFONIC ACID; HYDRATE ACID; FUCHSIN CALCIUM SALT; 8-((4,5-DIMETHOXY-2-NITROBENZYL)OXY)PYRENE-1,3,6-TRISULFONIC ACID, TRISODIUM SALT PHENYL VINYLSULFONATE; Sodium gualenate; Sulfobromophthalein sodium; 1184-84-5 ethylenesulfonic acid; Vinylsulfonic acid; ethylenesulphonic acid; VINYLSULPHONICACID; CH2CHSO3H 1-Ethenesulfonic acid; Ethenesulfonic acid; 3039-83-6 (Hydrochloride salt;) Einecs 214-676-1;Ethenesulfonic acid,phenyl ester;Ethylenesulfonicacid, phenyl ester; Phenyl ethenesulfonate; Phenyl ethylenesulfonate; Phenylvinylsulfonate

Ethenesulfonic acid homopolymer;Ethenesulfonicacid,sodiumsalt,homopolymer;POLY(VINYLSULFONIC ACID, SODIUM SALT);VINYL SULFONATE, SODIUM SALT POLYMER;POLY(VINYLSULFONIC ACID, SODIUM S…;Ethenesulfonic acid ethyl ester;Ethenesulfonic acid ethyl ester;Ethyl ethenesulfonate;Ethyl ethylenesulfonate;Ethenesulfonic acid methyl ester;Ethenesulfonic acid methyl ester;Methyl ethenesulfonate;Methyl ethylenesulfonate;Ethenesulfonic acid, dimethylphenylsilyl ester;Ethenesulfonic acid,4-chlorophenyl ester;Ethenesulfonicacid, p-chlorophenyl ester (6CI,7CI,8CI);Ethenesulfonic acid, 4-methylphenyl ester;Ethenesulfonic acid, 4-methoxyphenyl ester;Ethenesulfonic acid, 1-methylethyl ester;Ethenesulfonic acid, 1,2,3-benzenetriyl ester;Ethenesulfonic acid, 2-phenyl-, (E)-;Ethenesulfonic acid, 2-(trimethylsilyl)-, (E)-;Ethylenesulfonicacid;VSA-H;VSA-S;Vinylsulfonic acid;SVS;Nsc 8957;Vinyl sulfonate;Einecs 221-242-5;SODIUM;VINYLSULFONATE;SODIUM VINYLSULPHONATE;Sodium ethenesulfonate;SODIUM ETHYLENESULFONATE;Natriumethylensulfonat15;sodium ethylenesulphonate; Vinyl Sul; Ethenesulfonic acid, sodium salt (1:1);vinilsülfonik asit sodyum tuzu çözeltisi, sodyum ethylenesulphonate, Vinylsulfonatesodiumsaltsolid; Vinylsulphonic asit, sodyum tuzu; etensülfonik asit, sodyum tuzu; vinil sülfonat; VS, SVS, vinil sülfonat, sodyum tuzu; Ethenesulfonicacid, sodiumsalt; etilensülfonik asit sodyum tuzu, sodyum vinilsülfonattan, sodyum VINYLSULPHONATE , SODYUM ETHYLENESULFONATE; vinilsülfonik AST SODYUM TUZ;etil sülfonat, sar sodyum vinil, etil sülfonat, sodyum vinil sar, etan sülfonat;Vinylsulfonic acid sodium salt solution, Ethylenesulfonic acid sodium salt solution, Sodium vinylsulfonate solution;

SVS;Nsc 8957;Vinyl sulfonate;Einecs 221-242-5;SODIUM VINYLSULFONATE;SODIUM VINYLSULPHONATE;Sodium ethenesulfonate;SODIUM ETHYLENESULFONATE;Natriumethylensulfonat15;sodium ethylenesulphonate; Vinyl Sul; Ethenesulfonic acid, sodium salt (1:1);C2H3O3S.Na; Vinylsulfonic acid sodium salt solution, Ethylenesulfonic acid sodium salt solution, Sodium vinylsulfonate solution;SVS;Nsc 8957;Vinyl sulfonate;Einecs 221-242-5;SodiuM ethylenesulph;SODIUM VINYLSULFONATE;SODIUM VINYLSULPHONATE;Sodium ethenesulfonate;SODIUM ETHYLENESULFONATE;Natriumethylensulfonat15;Sodium benzoate; 8-((4,5-DIMETHOXY-2-NITROBENZYL)OXY)PYRENE-1,3,6-TRISULFONIC ACID, TRISODIUM SALT 1,2-NAPHTHOQUINONE-4-SULFONIC ACID SODIUM SALT BROMOSULFALEIN 4,4-DIFLUORO-1,3,5,7,8-PENTAMETHYL-4-BORA-3A,4A-DIAZA-S-INDACENE-2,6-DISULFONIC ACID, DISODIUM SALT; Sodium gualenate; BETA-STYRENESULFONIC ACID; SODIUM SALT; Sulfobromophthalein sodium; DEUTEROPORPHYRIN IX; 2,4-DISULFONIC ACID, DIMETHYL ESTER; DISODIUM SALT; Sodium ethylenesulphonate; 1-DODECANESULFONIC ACID; SODIUM SALT; Sodium formate; Sodium hydroxide; Molasses Sodium gluconate; Sodium acetate; Sodium lignosulfonate; Diclofenac sodium;Ethenesulfonicacid,sodiumsalt; ETHYLENESULFONIC ACID; SODIUM SALT; 3039-83-6; Building Blocks SODIUM VINYLSULFONATE; SODIUM VINYLSULPHONATE; SODIUM ETHYLENESULFONATE;sodium ethylenesulphonate; VINYL SULFONATE, SODIUM SALT VINYLSULFONIC ACID; SODIUM SALT; Organic Building Blocks Sulfur Compounds; Sulfonic/Sulfinic Acid; Salts Vinyl sulfonate; Vinylsulfonatesodiumsalt;solid Vinylsulfonic acid; sodium salt solution; Vinylsulphonic acid sodium salt; VINYLSULFONIC ACID, SODIUM SALT, TECH., 25 WT. % SOLUTION IN WATER VINYLSULFONIC ACID SODIUM SALT SOLUTION, ~30% IN WATER C2H3O3SNa C2H3NaO3S sodium vinylsulfonate solution VINYLSULFONICACIDSODIUMSALT,25%AQUEOUSSOLUTION,TECHNICAL 3039-83-9 ETHENESULPHONICACID,SODIUMSALT Natriumethylensulfonat15 Vinyl sulphonate, sodium salt VINYL SULFONIC ACID SODIUM SALT, 25% WATER SVS; C2H3SO3Na; Sodium vinylsulfonate, tech. ca 25% aq. soln. Sodium Vinylsulfonate (25% in Water, ca. 2.3mol/L) (stabilized with MEHQ) Ethylenesulfonic acid sodium salt, Sodium vinylsulfonate solution, Vinylsulfonic acid sodium salt Vinylsulfonic acid solution sodium salt Ethylenesulfonic acid sodium salt, Vinylsulfonic acid sodium salt; CH2CHSO3Na; 1-Ethenesulfonic acid sodium salt; Ethene-1-sulfonic acid sodium salt; Vinylsulfonic acid sodium Sodium ethenesulfonate Einecs 221-242-5 Ethenesulfonic acid, sodium salt (1:1) Nsc 8957 Sodium Vinylsulfonate (25% in Water, ca. 2.3mol/L) Sodium vinylsulfonate solution,Ethylenesulfonic acid sodium salt, Vinylsulfonic acid sodium salt Sodium vinylsulphonate, tech. ca 25% aq. soln. Vinylsulfonic acid sodium salt solution,Ethylenesulfonic acid sodium salt, Sodium vinylsulfonate solution, Vinylsulfonic acid sodium salt SodiuM vinylsulfonate (SVS) SodiuM Vinylsulfonate, 25wt.% in H2O (25% in Water, ca. 2.3Mol/L) SodiuM Vinylsulfonate ; SodiuM ethylenesulph ;SodiuM ethylenesulfonate(SVS); SodiuM ethenesulfonate(25% in H2O) SVS,Sodium ethylenesulphonate; Vinylsulfonic acid sodium salt solution 25 wt. % in H2O, technical grade;ETHYLENESULFONIC ACID SODIUM SALT

SODIUM ETHYLENESULFONATE;sodium ethylenesulphonate;SODIUM VINYLSULFONATE;SODIUM VINYLSULPHONATE;VINYL SULFONATE, SODIUM SALT;VINYLSULFONIC ACID SODIUM SALT;Ethenesulfonicacid,sodiumsalt;Vinyl sulfonate;Vinylsulfonatesodiumsaltsolid;Vinylsulfonic acid sodium salt solution;Vinylsulphonic acid sodium salt;VINYLSULFONIC ACID, SODIUM SALT, TECH., 25 WT. % SOLUTION IN WATER;VINYLSULFONIC ACID SODIUM SALT SOLUTION, ~30% IN WATERsodium vinylsulfonate ; VINYL SULFONIC ACID 30% ;ethylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; Sodium ethylenesulphonate; Sodium ethylenesulfonate; Sodium Vinyl sulfonate; UNII F7K3L38Z7B; Lyapolate sodium [USAN]; Ethenesulfonic acid, sodium salt (1:1); Sodium apolate (INN); Sodium apolate [INN]; Lyapolate sodium; Lyapolate sodium (USAN); W-106946; Sodium ethenesulfonate(25% in H2O); CAS-3039-83-6; Ethenesulfonic acid, sodium salt, homopolymer;NCGC00185758-01; Peson; Sodium apolate;ethylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; Sodium ethylenesulphonate; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; vinil sülfonik asit; vinil sülfonik asit; acide vinylsulfonique; L’acide vinylsulfonique; vinilsülfonik asit; VNLSÜLFONK AST; VNL SÜLFONK AST; VINILSÜLFONIK AST; VINILSÜLFONIK ASIT; VINILSULFONIK ASIT; thylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; Sodium ethylenesulphonate; Sodium ethylenesulfonate; Sodium Vinyl sulfonate; UNII F7K3L38Z7B; Lyapolate sodium [USAN]; Ethenesulfonic acid, sodium salt (1:1); Sodium apolate (INN); Sodium apolate [INN]; Lyapolate sodium; Lyapolate sodium (USAN); W-106946; Sodium ethenesulfonate(25% in H2O); CAS-3039-83-6; Ethenesulfonic acid, sodium salt, homopolymer;NCGC00185758-01; Peson; Sodium apolate;ethylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; ethylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; Sodium ethylenesulphonate; Sodium ethylenesulfonate; Sodium Vinyl sulfonate; UNII F7K3L38Z7B; Lyapolate sodium [USAN]; Ethenesulfonic acid, sodium salt (1:1); Sodium apolate (INN); Sodium apolate [INN]; Lyapolate sodium; Lyapolate sodium (USAN); W-106946; Sodium ethenesulfonate(25% in H2O); CAS-3039-83-6; Ethenesulfonic acid, sodium salt, homopolymer;NCGC00185758-01; Peson; Sodium apolate;ethylenesulfonic acid polymer;lyapolate; lyapolate ammonium salt; lyapolate sodium; lyapolate sodium salt; poly(sodium vinyl sulfonate); poly(vinyl sulfonic acid); poly(vinylsulfonic acid); polyethylene sulfonate; polyvinyl sulfonic potassium; polyvinylsulfonic acid; PVS acid; sodium apolate; Sodium ethenesulfonate; Sodium vinylsulfonate, 3039-83-6; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; Sodium ethylenesulphonate; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; vinil sülfonik asit; vinil sülfonik asit; acide vinylsulfonique; L’acide vinylsulfonique; vinilsülfonik asit; VNLSÜLFONK AST; VNL SÜLFONK AST; VINILSÜLFONIK AST; VINILSÜLFONIK ASIT; VINILSULFONIK ASIT; Sodium ethylenesulphonate; Vinylsulfonic acid sodium salt; Ethenesulfonic acid, sodium salt; vinil sülfonik asit; vinil sülfonik asit; acide vinylsulfonique; L’acide vinylsulfonique 30; vinilsülfonik asit 30; VNLSÜLFONK AST 30 ; VNL SÜLFONK AST30; VINILSÜLFONIK AST 30; VINILSÜLFONIK ASIT 30 ; VINILSULFONIK ASIT 30; vinil sülfonik asit 30; vinil sülfonik asit; acide vinylsulfonique; L’acide vinylsulfonique; vinilsülfonik asit; VNLSÜLFONK AST; VNL SÜLFONK AST; VINILSÜLFONIK AST; VINILSÜLFONIK ASIT30; VINILSULFONIK ASIT 30%; Sodium ethylenesulphonate 30 %; Vinylsulfonic acid sodium salt 30 %; Ethenesulfonic acid, sodium salt 30%; vinil sülfonik asit; vinil sülfonik asit 30; acide vinylsulfonique 30 ; L’acide vinylsulfonique 30 ; vinilsülfonik asit 30 ; VNLSÜLFONK AST30; VNL SÜLFONK AST %30; VINILSÜLFONIK AST %30; VINILSÜLFONIK ASIT 30%; VINILSULFONIK ASIT 30 %; Vinylsulfonic acid; VinylSulfonic acid; VNL SÜLFONK AST; VNLSÜLFONK AST;VNL SÜLFONK ASTE; Vinilsülfonik asite; Vinyl sulfonic acid; Vinylsulfonic acide; Vinylcsulfonic acide; Vinylsulfonic acid 30 ; VNLSÜLFONK AST 30 ;VNLSÜLFONK AST 30%; Vinilsülfonik asit 30 ; Vinilsülfonik asit 30%; Vinilsülfonik asit30; Vinil sülfonik asit 30 ; Vinil sülfonik asit 30%; Vinil sülfonik asit30; Vinylsulfonic acid 30 ; Vinylsulfonic acid 30%; Vinylsulfonic acid -30%; Vinylsulfonic acid %30

 

 

 

Vinylsulfonic acid (VSA)

 

Laboratory Chemical Safety Summary (LCSS) Datasheet

Vinylsulfonic acid Molecular Formula: C2H3O3S

 

 

IUPAC name

ethenesulfonic acid

Identifiers of Vinylsulfonic acid

CAS Number of Vinylsulfonic acid

1184-84-5

3039-83-6 (sodium salt)

3D model (JSmol)

Interactive image

ChemSpider of Vinylsulfonic acid 

56254

ECHA InfoCard 100.013.342

PubChem CID of Vinylsulfonic acid

62474

 

 

Properties of Vinylsulfonic acid

Chemical formula of Vinylsulfonic acid

C2H4O3S

Molar mass of Vinylsulfonic acid 108.11 g·mol-1

Appearance of Vinylsulfonic acid colouless liquid

 

Vinylsulfonic acid is the organosulfur compound with the formula CH2=CHSO3H. Vinylsulfonic acid is the simplest unsaturated sulfonic acid.[2][3] The C=C double bond is a site of high reactivity. polymerize gives polyvinylsulfonic acid, especially when used as a comonomer with functionalized vinyl[4] and (meth)acrylic acid compounds.[5] Vinylsulfonic acid is a colorless, water-soluble liquid,[2] although commercial samples can appear yellow or even red.

 

Preparation of Vinylsulfonic acid

Vinylsulfonic acid is produced industrially by the alkaline hydrolysis of carbyl sulfate with subsequent acidification of the resulting vinyl sulfonate salt:[6]

 

 

The reaction is highly exothermic (reaction enthalpy: 1,675 kJ/kg) and requires exact maintenance of temperature and pH during the hydrolysis. When calcium hydroxide is used as the hydrolysis medium, a solution of calcium vinyl sulfonate is obtained. Acidification of this hydrolysis mixture with sulfuric acid gives vinylsulfonic acid, together with the poorly soluble calcium sulfate.

 

Vinylsulfonic acid also can be prepared by dehydration of isethionic acid with phosphorus pentoxide:[7]

Vinylsulfonic acid can also be prepared by sulfochlorination of chloroethane, dehydrohalogenation to vinylsulfonyl chloride and subsequent hydrolysis of the acid chloride.

 

use

The activated C=C double bond of vinylsulfonic acid reacts readily with nucleophiles in an addition reaction. 2-Aminoethanesulfonic acid is formed with ammonia and 2-methylaminoethanesulfonic acid with methylamine.[8]

 

Vinylsulfonic acid is the monomer in the preparation of highly acidic or anionic homopolymers and copolymers. These polymers are used in the electronic industry as photoresists, as ion-conductive polymer electrolyte membranes (PEM) for fuel cells. For example, transparent membranes with high ion exchange capacity and proton conductivity can be produced from polyvinylsulfonic acid.[9]

 

Research of Vinylsulfonic acid

Vinylsulfonic acid may also be grafted to polymeric supports (e.g. polystyrene) to give highly acidic ion exchangers, which used as catalysts for esterification and Friedel-Crafts acylations.[10] Where the sulfonic acid functionality is not essential, the much more usable alkaline aqueous solution of sodium vinylsulfonate is used, which is obtained directly in the alkaline hydrolysis of the carbyl sulfate and is commercially supplied as an aqueous solution.

 

 

Applications of Vinylsulfonic acid

Vinylsulfonic acid is a useful reagent (monomer) for the formation of poly(anionic) polymers and copolymers. Vinylsulfonic acid is employed as a basic brightener and leveling agent in nickel baths. Vinylsulfonic acid is also used as intermediate for organic synthesis, surfactant, pharmaceutical industry.

Vinylsulfonic acid CAS#: 9002-97-5

Molecular Weight of Vinylsulfonic acid: 4,000-6,000

Soluble In: 25% soln. in water (25g polymer). May contain a small percentage of insoluble material.

TSCA 

Hazards of Vinylsulfonic acid: Harmless-use normal precautions

Handling of Vinylsulfonic acid: Exercise normal care

Storage of Vinylsulfonic acid: Room Temperature 

Notes

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is sensitive to light. Incompatible with oxidizing agents.

The subject invention provides:

a method for producing vinyl sulfonic acid, comprising conducting demetallation of vinyl sulfonate salt, wherein the demetallation rate is not less than 95% according to the following formula:

Demetallation rate(%)={(acid value after demetallation)/(acid value before demetallation)}×100;

a method for producing vinyl sulfonic acid, comprising conducting demetallation of vinyl sulfonate salt, wherein demetallation is carried out using a strongly acidic ion exchange resin; and

said method further comprising the step of purifying a product of the demetallation using a thin film evaporator.

vinylsulfonic acid) (PVS) possesses a high acid content (ion‐exchange capacity in the chemical formula = 9.2 meq · g-1). Its monomer, vinylsulfonic acid (VSA), had a high acid dissociation ability (Hammett acid function = 0.74 in water), and a high ionic conductivity (0.04-0.11 S · cm-1). The radical polymerization of Vinylsulfonic acid with various initiators was kinetically investigated. The ESR spectrum of the Vinylsulfonic acid polymerization mixture showed a strong signal ascribed to the propagation carbon radical of Vinylsulfonic acid. The molecular weight of PVS increased with the increasing monomer concentration and decreasing radical initiator concentration to yield the PVS with a molecular weight of 4.0 × 104. Proton‐conductivity of PVS under hydrated and nonhumidified conditions was on the order of 10-1 and 10-3-10-6 S · cm-1, respectively.

 

 

CAS25053-27-4

Synonyms POLY(VINYLSULFONIC ACID, SODIUM SALT);VINYL SULFONATE, SODIUM SALT POLYMER;sodiumpoly(vinylsulfonate);Poly(vinyl sulfonate , sodium salt) (solid);Poly(vinylsulfonic acid, sodium salt) solution;sodium apolate;Sodium poly(vinylsulfonate), 25% in water;Lyap

IUPAC Namesodium ethenesulfonate

Molecular FormulaC2H3NaO3S

Molecular Weight130.0982

Exact Mass129.97000

Density1.267 g/mL at 25 °C

Appearanceyellow liquid

InChI KeyBWYYYTVSBPRQCN-UHFFFAOYSA-M

H-Bond Donor0

H-Bond Acceptor3

Safty Description26-36

Hazard StatementsXi: Irritant;

StabilityStable. Incompatible with strong oxidizing agents.

 

 

Vinylsulfonic acid is the organosulfur compound with the formula CH2=CHSO3H. It is the simplest unsaturated sulfonic acid.[2][3] The C=C double bond is a site of high reactivity. polymerize gives polyvinylsulfonic acid, especially when used as a comonomer with functionalized vinyl[4] and (meth)acrylic acid compounds.[5] It is a colorless, water-soluble liquid,[2] although commercial samples can appear yellow or even red.

Preparation of Vinylsulfonic acid

Vinylsulfonic acid is produced industrially by the alkaline hydrolysis of carbyl sulfate with subsequent acidification of the resulting Vinylsulfonic acid

Use of Vinylsulfonic acid

The activated C=C double bond of vinylsulfonic acid reacts readily with nucleophiles in an addition reaction. 2-Aminoethanesulfonic acid is formed with ammonia and 2-methylaminoethanesulfonic acid with methylamine.[8]

 

Vinylsulfonic acid is the monomer in the preparation of highly acidic or anionic homopolymers and copolymers. These polymers are used in the electronic industry as photoresists, as ion-conductive polymer electrolyte membranes (PEM) for fuel cells. For example, transparent membranes with high ion exchange capacity and proton conductivity can be produced from polyvinylsulfonic acid.[9]

 

Research

Vinylsulfonic acid may also be grafted to polymeric supports (e.g. polystyrene) to give highly acidic ion exchangers, which used as catalysts for esterification and Friedel-Crafts acylations.[10] Where the sulfonic acid functionality is not essential, the much more usable alkaline aqueous solution of sodium vinylsulfonate is used, which is obtained directly in the alkaline hydrolysis of the carbyl sulfate and is commercially supplied as an aqueous solution..

 

CHEMICAL PROPERTIES of Vinylsulfonic acid

 

Chemical Name: Sodium vinyl sulfonate, Vinylsulfonic acid

Chemical Formula of Vinylsulfonic acid: C2H3NaO3S

Molecular Weight of Vinylsulfonic acid 130.1

Form of Vinylsulfonic acid: liquid

Odour of Vinylsulfonic acid: product specific

Odour threshold: No data available.

Colour of Vinylsulfonic acid: colourless to yellow

Density of Vinylsulfonic acid: 1.18 – 1.22 g/cm3 ( 23 °C) (DIN 51757)

pH value of Vinylsulfonic acid: approx. 8 – 10 ( 23 °C) (DIN 53785)

Melting temperature of Vinylsulfonic acid: -14 °C

solidification temperature of Vinylsulfonic acid: -20 °C

boiling temperature of Vinylsulfonic acid: approx. 100 °C contains water

Flash point of Vinylsulfonic acid : > 100 °C (DIN EN 22719; ISO 2719) Aqueouspreparation

Flammability of Vinylsulfonic acid: not flammable

Autoignition of Vinylsulfonic acid: > 200 °C (DIN 51794)

Vapour pressure of Vinylsulfonic acid: 23.4 mbar ( 20 °C)

Water Solubility of Vinylsulfonic acid: Soluble in water.

Sensitive of Vinylsulfonic acid: Light Sensitive

Stability of Vinylsulfonic acid:: Stable. Incompatible with strong oxidizing agents.

 

 

DESCRIPTION of Vinylsulfonic acid

 

 

Low Color Stabilizer Vinylsulfonic acid Contains Sulphonate Group that Polymerize, Also Modify Olefinic Bond And Boost End Solubility Of The End Product. Water-Based Adhesive, Water-Based Paint Resin And Nickel Shine Producer.Vinylsulfonic acid is a polymerizable organic compound which has many industrial uses, particularly as an antistatic agent and as an agent improving the tinctorial affinity of synthetic fibres, such as polyacrylonitrile and polypropylene, to cationic dyes, as a dispersing agent in polymer emulsions, as a wetting agent for lowering the mixing water content of cement, as a starting material for the production of cation exchange resins and synthetic rubber.Vinylsulfonic acid and its derivatives can be prepared from ß-chloroethanesulfonyl chloride or carbyl sulfate (ß-hydroxysulfonyloxyethanesulfonic anhydride). The chemistry of vinylsulfonic acid has assumed industrial importance since the discovery of a simple synthesis of ß-chloroethanesulfonyl chloride from chloroethane or ethane, sulfur dioxide, and chlorine by the Reed process. Carbyl sulfate is as important a starting material as ß-chloroethanesulfonyl chloride, and surpasses the latter in some respects, e.g. on account of the low price of its components ethylene and sulfur trioxide. Vinylsulfonates undergo addition reactions with alcohols, phenols, thiols, sulfinic acids, carboxylic acids, amides, imides, and hydrazides, as well as with amines, ureas, diazonium salts, and nitroparaffins. Furthermore, they undergo halogenation, nitration, olefination, and the Diels-Adler reaction. – Methods for the preparation of the free vinylsulfonic acid are described. Alkyl vinylsulfonates are excellent alkylating agents. The derivatives of vinylsulfonic acid are used e.g. as plasticizers, emulsifiers, and fungicides.More easily handled than the acid is the salt, sodium vinylsulfonate, which is commercially supplied as an aqueous solution.

 

APPLICATION of Vinylsulfonic acid

Vinylsulfonic acid is a useful reagent (monomer) for the formation of poly(anionic) polymers and copolymers.Sodium ethylenesulphonate(3039-83-6) is widely used in the synthesis of auxiliary materials for environment friendly water treatment emulsifier, pure acrylic emulsion, styrene-acrylic, acetic styrene-acrylic emulsion and other emulsions. Vinylsulfonic acid used in synthetic fibre and polymeric invert monomer for its many good characteristics, such as stability, resistibility and reducing shrinkage cavity. Sodium ethylenesulphonate(3039-83-6) also used as sulfo-group ethyl auxiliaries, electrofacing gloss agent, surfactant, pharmaceutical intermediates and other fields. Vinylsulfonic acid’s application areas are Wetting Agents, Coatings, Dyes, Fibers, Polymers, Resins.

Vinylsulfonic acid also can be prepared by dehydration of isethionic acid with phosphorus pentoxide:[7]

Vinylsulfonic acid can also be prepared by sulfochlorination of chloroethane, dehydrohalogenation to vinylsulfonyl chloride and subsequent hydrolysis of the acid chloride.

 

use

The activated C=C double bond of vinylsulfonic acid reacts readily with nucleophiles in an addition reaction. 2-Aminoethanesulfonic acid is formed with ammonia and 2-methylaminoethanesulfonic acid with methylamine.[8]

 

Vinylsulfonic acid is the monomer in the preparation of highly acidic or anionic homopolymers and copolymers. These polymers are used in the electronic industry as photoresists, as ion-conductive polymer electrolyte membranes (PEM) for fuel cells. For example, transparent membranes with high ion exchange capacity and proton conductivity can be produced from polyvinylsulfonic acid.[9]

 

Research of Vinylsulfonic acid

Vinylsulfonic acid may also be grafted to polymeric supports (e.g. polystyrene) to give highly acidic ion exchangers, which used as catalysts for esterification and Friedel-Crafts acylations.[10] Where the sulfonic acid functionality is not essential, the much more usable alkaline aqueous solution of sodium vinylsulfonate is used, which is obtained directly in the alkaline hydrolysis of the carbyl sulfate and is commercially supplied as an aqueous solution.

 

 

Applications of Vinylsulfonic acid

Vinylsulfonic acid is a useful reagent (monomer) for the formation of poly(anionic) polymers and copolymers. Vinylsulfonic acid is employed as a basic brightener and leveling agent in nickel baths. Vinylsulfonic acid is also used as intermediate for organic synthesis, surfactant, pharmaceutical industry.

Vinylsulfonic acid CAS#: 9002-97-5

Molecular Weight of Vinylsulfonic acid: 4,000-6,000

Soluble In: 25% soln. in water (25g polymer). May contain a small percentage of insoluble material.

TSCA 

Hazards of Vinylsulfonic acid: Harmless-use normal precautions

Handling of Vinylsulfonic acid: Exercise normal care

Storage of Vinylsulfonic acid: Room Temperature 

Notes

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is sensitive to light. Incompatible with oxidizing agents.

The subject invention provides:

a method for producing vinyl sulfonic acid, comprising conducting demetallation of vinyl sulfonate salt, wherein the demetallation rate is not less than 95% according to the following formula:

Demetallation rate(%)={(acid value after demetallation)/(acid value before demetallation)}×100;

a method for producing vinyl sulfonic acid, comprising conducting demetallation of vinyl sulfonate salt, wherein demetallation is carried out using a strongly acidic ion exchange resin; and

said method further comprising the step of purifying a product of the demetallation using a thin film evaporator.

vinylsulfonic acid) (PVS) possesses a high acid content (ion‐exchange capacity in the chemical formula = 9.2 meq · g-1). Its monomer, vinylsulfonic acid (VSA), had a high acid dissociation ability (Hammett acid function = 0.74 in water), and a high ionic conductivity (0.04-0.11 S · cm-1). The radical polymerization of Vinylsulfonic acid with various initiators was kinetically investigated. The ESR spectrum of the Vinylsulfonic acid polymerization mixture showed a strong signal ascribed to the propagation carbon radical of Vinylsulfonic acid.

 

 

 

Vinilsülfonik asit

 

 

Vinilsülfonik asit moleküler formül C2H4O3S

Vinilsülfonik asit moleküler arlk 108.11

Vinilsülfonik asit CAS Numaras 1184-84-5

 

Vinilsülfonik asit

 

Vinilsülfonik asit Moleküler Formül: C2H3O3S

 

 

IUPAC ad

etensülfonik asit

Tanmlayclar

Vinilsülfonik asit CAS numaras

1184-84-5

3039-83-6 (sodyum tuzu)

3D model (JSmol)

Etkileimli görüntü

ChemSpider

56254

ECHA Bilgi Kart 100.013.342

Vinilsülfonik asit PubChem CID

62474

 

 

Vinilsülfonik asit Özellikleri

Vinilsülfonik asit Kimyasal formül

C2H4O3S

 

 

Vinilsülfonik asidin Molar kütle 108.11 g · mol – 1

Görünüm renksiz sv

 

Vinilsülfonik asit, CH2 = CHS03H formülüne sahip organosülfür bileiidir. En basit doymam sülfonik asittir. [2] [3] C = C çift ba, yüksek reaktivite bölgesidir. polimerize, özellikle ilevselletirilmi vinil [4] ve (met) akrilik asit bileiklerine sahip bir komonomer olarak kullanldnda polivinilsülfonik asit verir. Vinilsülfonik asit renksiz, suda çözünür bir svdr, ancak ticari örnekler sar veya hatta krmz görünebilir.

 

Hazrlk

Vinilsülfonik asit, elde edilen vinil sülfonat tuzunun daha sonra asitletirilmesi ile karbil sülfatn alkalin hidrolizi ile endüstriyel olarak üretilir: [6]

 

 

Vinilsülfonik asit in Reaksiyonu oldukça ekzotermiktir (reaksiyon entalpisi: 1.675 kJ / kg) ve hidroliz srasnda tam scaklk ve pH korunmasn gerektirir. Hidroliz ortam olarak kalsiyum hidroksit kullanldnda, bir kalsiyum vinil sülfonat çözeltisi elde edilir. Bu hidroliz karmnn sülfürik asit ile asitletirilmesi, az çözünür kalsiyum sülfat ile birlikte vinilsülfonik asit verir.

Vinilsülfonik asit, izetiyonik asidin fosfor pentoksit ile dehidrasyonu ile de hazrlanabilir: [7]

Vinilsülfonik asit ayrca kloroetann sülflorizasyonu, vinilsülfonil klorüre dehidrohalojenasyon ve daha sonra asit klorürün hidrolizi ile de hazrlanabilir.

 

Vinilsülfonik asit kullanm

Aktifletirilmi C = C çift vinilsülfonik asit ba, bir ilave reaksiyonunda nükleofiller ile kolayca reaksiyona girer. 2-Aminoetansülfonik asit, amonyak ve 2-metilaminoetansülfonik asit, metilamin ile oluturulur. [8]

 

Vinilsülfonik asit, oldukça asidik veya anyonik homopolimerlerin ve kopolimerlerin hazrlanmasnda monomerdir. Bu polimerler elektronik endüstrisinde, fotoresistler olarak, yakt hücreleri için iyon iletken polimer elektrolit membranlar (PEM) olarak kullanlr. Örnein, yüksek iyon deiim kapasitesi ve proton iletkenlii olan effaf membranlar polivinilsülfonik asitten üretilebilir. [9]

 

Aratrma

Vinilsülfonik asit ayrca esterletirme ve Friedel-Crafts asilasyonlar için katalizör olarak kullanlan yüksek asidik iyon deitiricileri vermek üzere polimerik desteklere (örnein polistiren) alanabilir. [10] Sülfonik asit ilevselliinin gerekli olmad durumlarda, dorudan karbil sülfatn alkalin hidrolizinde elde edilen ve ticari olarak sulu bir çözelti olarak temin edilen çok daha kullanl olan sodyum Vinilsülfonik asit alkali sulu çözeltisi kullanlr.

 

 

Uygulamalar

Vinilsülfonik asit, poli (anyonik) polimerlerin ve kopolimerlerin oluumu için yararl bir reaktiftir (monomer). Vinilsülfonik asit, nikel banyolarnda bazik bir parlatc ve tesviye maddesi olarak kullanlr. Vinilsülfonik asit ayrca organik sentez, yüzey aktif madde, ilaç endüstrisi için ara madde olarak kullanlr.

Vinilsülfonik asit CAS #: 9002-97-5

Vinilsülfonik asidin Moleküler Arl: 4.000-6.000

Çözünür In:% 25 soln. suda (25g polimer). Az miktarda çözünmeyen malzeme içerebilir.

TSCA

Tehlikeler: Zararsz kullanm için normal önlemler

Kullanm: Normal bakm yapn

Depolama: Oda Scakl

notlar

Serin yerde saklayn. Kab skca kapal olarak kuru ve iyi havalandrlm yerlerde saklaynz. Ia duyarldr. Oksitleyici maddelerle badamaz.

Söz konusu bulu unlar salar:

vinilsülfonik asit üretmek için bir yöntem olup, vinil sülfonat tuzunun demetallasyonunun yaplmasn içerir, burada demetallasyon oran aadaki formüle göre% 95’ten az deildir:

Demetallasyon oran (%) = {(demetallasyondan sonra asit deeri) / (demetallasyondan önce asit deeri)} × 100;

Vinilsülfonik asit üretmek için bir yöntem olup, vinil sülfonat tuzunun demetallasyonunun gerçekletirilmesini içerir, burada demetallasyon güçlü bir asidik iyon deiim reçinesi kullanlarak gerçekletirilir; ve

ad geçen yöntem ayrca bir ince film buharlatrc kullanlarak demetallasyonun bir ürününün saflatrlmas aamasn içerir.

vinilsülfonik asit) (PVS) yüksek asit içeriine sahiptir (kimyasal formülde iyon deiim kapasitesi = 9.2 meq · g – 1). Monomeri, vinilsülfonik asit (VSA), yüksek bir asit ayrma kabiliyetine (Hammett asit fonksiyonu = suda 0.74) ve yüksek bir iyonik iletkenlie (0.04-0.11 S · cm-1) sahipti. Vinilsülfonik asit’nn çeitli balatclarla radikal polimerizasyonu kinetik olarak aratrld. Vinilsülfonik asit polimerizasyon karmnn ESR spektrumu, Vinilsülfonik asit’nn yaylma karbon radikaline atfedilen güçlü bir sinyal gösterdi. PVS’nin moleküler arl, artan monomer konsantrasyonu ve azalan radikal balatc konsantrasyonu ile artt ve 4.0 × 104 molekül arlna sahip PVS’yi verdi. Hidratlanm ve nemlendirilmemi koullar altnda vinilsülfonik Asit’in proton tivity iletkenlii 10-1 ve 10- mertebesinde idi. Srasyla 3-10-6 S · cm – 1.

 

 

Vinilsülfonik asit

Düük renk stabilizatörü 

Vinilsülfonik asit polimerleebilen, ayrca modifiye edilebilen bir olefinik ba ve son ürünün sudaki çözünürlüünü arttran sülfonat grubu içerir.

Su bazl yaptrc, su bazl boya reçinesi ve nikel parlatc üretiminde Vinilsülfonik asit kullanlr.

VinilSülfonik Asit, Sodyum Tuzu: Etilen vinilsülfonik Asit Sodyum tuzu homopolimeri

Vinilsülfonik Asit Sondaj svlarnda viskozitenin ayarlanmas, ya geri kazanm veriminin arttrlmas için özellikle yüksek basnç, scaklk ve tuzluun olduu sondaj kuyularnda kullanr.

 

 

Vinilsülfonik asit olan organosülfür bileimi , formül CH 2 = CHSO 3 H Bu basit olan doymam sülfonik asit . [2] [3] C = C çift ba, yüksek reaktivite bölgesidir. polimerize , özellikle ilevselletirilmi vinil [4] ve (met) akrilik asit bileiklerine sahip bir komonomer olarak kullanldnda polivinilsülfonik asit verir . [5] Bu, renksiz, suda çözünür bir svdr [2] ticari örnekleri, sar ya da krmz görünebilir olmasna ramen.

Vinilsülfonik asit, oldukça asidik veya anyonik homopolimerlerin ve kopolimerlerin hazrlanmasnda monomerdir. Bu polimerler elektronik endüstrisinde fotoresistler olarak, yakt hücreleri için iyon iletken polimer elektrolit membranlar (PEM) olarak kullanlr . Örnein, yüksek iyon deiim kapasitesi ve proton iletkenlii olan effaf membranlar polivinilsülfonik asitten üretilebilir. [9]

 

 

Aratrma 

Vinilsülfonik asit ayrca esterletirme ve Friedel-Crafts asilasyonlar için katalizör olarak kullanlan yüksek asidik iyon deitiricileri vermek üzere polimerik desteklere (örnein polistiren ) alanabilir . [10] Vinilsülfonik asit ilevsellii gerekli olmad durumlarda, sodyum çok daha fazla kullanlabilir alkalik sulu çözelti, Vinilsülfonik asit Karbilsülfat alkalin hidrolizi dorudan elde edilen ve ticari olarak bir sulu çözelti olarak tedarik edildii, kullanlr ..

 

Vinilsülfonik asit uygulama: Yardmcs parlatc için nikel kaplama

noktas:kaplama ekleyin ve dalm yetenei, süneklik kaplama beyaz etkisi olabilir.

 

kimyasal ad hidroksil vinil sulfonate, sodyum tuzu

moleküler formülü C2H5O3SNa

CAS No. 1562-00-1

deneyi 45% (min)

görünüm sarms renksiz sv

PH deeri 2-4

lgili younluk @ 20 °C 1.31-1.34

suda çözünürlük oldukça su içinde çözünür

uygulama temel parlatc sünek kalite andUniformly kaplama yetenei gelitirmek için kullanlan.

 

Vinilsülfonik asitin KMYASAL ÖZELLKLER

 

Vinilsülfonik asit Kimyasal Ad: Sodyum vinil sülfonat

Vinilsülfonik asit Kimyasal Formül: C2H3Na03S

Vinilsülfonik asit Moleküler Arlk 130.1

Vinilsülfonik asit Form: sv

Vinilsülfonik asit Koku: Ürüne özgü

Vinilsülfonik asit Koku eik deeri: Veri mevcut deil.

Vinilsülfonik asitRenk: renksizden sarya

Vinilsülfonik asit Younluk: 1.18 – 1.22 g / cm3 (23 ° C) (DN 51757)

Vinilsülfonik asit PH deeri: yakl. 8-10 (23 ° C) (DIN 53785)

Vinilsülfonik asit Erime scakl: -14 ° C

Vinilsülfonik asit Katlama scakl: -20 ° C

Vinilsülfonik asit Kaynama scakl: yakl. 100 ° C su içerir

Vinilsülfonik asit Parlama noktas:> 100 ° C (DIN EN 22719; ISO 2719) Sulu hazrlama

Vinilsülfonik asit Yanclk: yanc deildir

Vinilsülfonik asit Kendiliinden alevlenebilirlik:> 200 ° C (DIN 51794)

Vinilsülfonik asit Buhar basnc: 23.4 mbar (20 ° C)

Vinilsülfonik asit Suda Çözünürlük: Suda özünebilir.

Hassas: Ik Hassasiyeti

Vinilsülfonik asit Kararllk :: Kararl. Güçlü oksitleyici ajanlarla uyumaz.

 

 

Vinilsülfonik asit GENEL TANIMI

Düük Renk Sabitleyici Sodyum Vinilsülfonik asit Polimerize Sülfonat Grubu çerir, Ayrca Olefinik Bond Deitirir ve Son Ürünün Uç Çözünürlüünü Artrr. Su Bazl Yaptrc, Su Bazl Boya Reçine ve Nikel Parlatma Üreticisi Vinilsülfonik asit, polistiren nitril gibi sentetik elyaflarn tinektial afinitesini artran, özellikle antistatik bir ajan ve bir ajan olarak birçok endüstriyel kullanma sahip polimerize olabilen bir organik bileiktir Katyon deitirici reçineler ve sentetik kauçuk üretimi için bir balangç ​​maddesi olarak polimer emülsiyonlarnda bir datma maddesi olarak katyonik boyalara, çimentonun kartrma su içeriini düürmek için slatc bir ajan olarak katyonik boyalara dönütürülebilir. Vinilsülfonik asit ve bunun türevleri ß-kloroetansülfonil klorit veya karbil sülfattan (β-hidroksisülfoniloksietansülfonik anhidrit) hazrland. Vinilsülfonik asit kimyas, kloroetan veya etandan, kükürt dioksitten ve klordan Reed süreci ile basit bir sentezin bulunmasndan bu yana endüstriyel öneme sahiptir. Karbil sülfat, ß-kloroetansülfonil klorür kadar önemli bir balangç ​​materyali olup, baz açlardan, örn. Bileenleri etilen ve kükürt trioksitin düük fiyat nedeniyle. Vinilsülfonatlar, alkoller, fenoller, tioller, sülfinik asitler, karboksilik asitler, amidler, imidler ve hidrazidler ile ayrca aminler, üreler, diazonyum tuzlar ve nitroparafinler ile ilâve reaksiyona girerler. Dahas, halojenasyon, nitrasyon, olefinasyon ve Diels-Adler reaksiyonundan geçer. – Serbest vinilsülfonik asit hazrlama yöntemleri anlatlmtr. Vinilsülfonik asit mükemmel alkile edici ajanlardr. Vinilsülfonik asitin türevleri örn. Emülgatörler ve fungisitler olarak kullanlr. Asitten daha kolay ele alnr, ticari olarak sulu bir solüsyon olarak tedarik edilen tuz, sodyum Vinilsülfonik asit

 

Vinilsülfonik asit UYGULAMA ALANLARI

 

Vinilsülfonik asit, poli (anyonik) polimerler ve kopolimerler oluturmak için yararl bir reaktiftir (monomer). Sodyum etilen sülfonat (3039-83-6), çevre dostu su artm emülsiyon yapc, saf akrilik emülsiyon için yardmc maddelerin sentezinde yaygn olarak kullanlmaktadr , Stiren akrilik, asetik stiren-akrilik emülsiyon ve dier emülsiyonlar. Sentetik elyaf ve polimerik ters monomerlerde stabilite, direnç ve büzülme boluunun azaltlmas gibi pek çok iyi özellii kullanlmtr. Ayrca sülfo grubu etil yardmclar, elektrofacing parlak ajan, yüzey aktif madde, ilaç ara maddeleri ve dier alanlar olarak kullanlan sodyum etilen sülfonat (3039-83-6). Sodyum fosfat sülfonatn uygulama alanlar Islatclar, Kaplamalar, Boyalar, Lifler, Polimerler, Reçinelerdir.

Vinilsülfonik asit in Reaksiyonu oldukça ekzotermiktir (reaksiyon entalpisi: 1.675 kJ / kg) ve hidroliz srasnda tam scaklk ve pH korunmasn gerektirir. Hidroliz ortam olarak kalsiyum hidroksit kullanldnda, bir kalsiyum vinil sülfonat çözeltisi elde edilir. Bu hidroliz karmnn sülfürik asit ile asitletirilmesi, az çözünür kalsiyum sülfat ile birlikte vinilsülfonik asit verir.

 

Vinilsülfonik asit, izetiyonik asidin fosfor pentoksit ile dehidrasyonu ile de hazrlanabilir: [7]

Vinilsülfonik asit ayrca kloroetann sülflorizasyonu, vinilsülfonil klorüre dehidrohalojenasyon ve daha sonra asit klorürün hidrolizi ile de hazrlanabilir.

 

Vinilsülfonik asit kullanm

Aktifletirilmi C = C çift vinilsülfonik asit ba, bir ilave reaksiyonunda nükleofiller ile kolayca reaksiyona girer. 2-Aminoetansülfonik asit, amonyak ve 2-metilaminoetansülfonik asit, metilamin ile oluturulur. [8]

 

Vinilsülfonik asit, oldukça asidik veya anyonik homopolimerlerin ve kopolimerlerin hazrlanmasnda monomerdir. Bu polimerler elektronik endüstrisinde, fotoresistler olarak, yakt hücreleri için iyon iletken polimer elektrolit membranlar (PEM) olarak kullanlr. Örnein, yüksek iyon deiim kapasitesi ve proton iletkenlii olan effaf membranlar polivinilsülfonik asitten üretilebilir. [9]

 

Aratrma

Vinilsülfonik asit ayrca esterletirme ve Friedel-Crafts asilasyonlar için katalizör olarak kullanlan yüksek asidik iyon deitiricileri vermek üzere polimerik desteklere (örnein polistiren) alanabilir. [10] Sülfonik asit ilevselliinin gerekli olmad durumlarda, dorudan karbil sülfatn alkalin hidrolizinde elde edilen ve ticari olarak sulu bir çözelti olarak temin edilen çok daha kullanl olan sodyum Vinilsülfonik asit alkali sulu çözeltisi kullanlr.

 

 

 

Acide vinylsulfonique

 

Fiche technique Résumé de sécurité chimique en laboratoire (LCSS)

Formule moléculaire: C2H3O3S

 

 

Nom IUPAC

acide éthènesulfonique

Identifiants

Numero CAS

1184-84-5

3039-83-6 (sel de sodium)

Modèle 3D (JSmol)

Image interactive

ChemSpider

56254

ECHA InfoCard 100.013.342

PubChem CID

62474

 

 

Propriétés du Acide vinylsulfonique

Formule chimique du Acide vinylsulfonique

C2H4O3S

Masse molaire du Acide vinylsulfonique 108,11 g · mol – 1

Aspect liquide sans couleur

 

L’acide vinylsulfonique est le composé organosulfuré de formule CH2 = CHSO3H. C’est l’acide sulfonique insaturé le plus simple. [2] [3] La double liaison C = C est un site de forte réactivité. polymériser donne de l’acide polyvinylsulfonique, en particulier lorsqu’il est utilisé comme comonomère avec des composés d’acide vinylique [4] et (méth) acrylique fonctionnalisés. [5] L’acide vinylsulfonique est un liquide incolore et soluble dans l’eau [2], bien que les échantillons commerciaux puissent apparaître jaunes ou même rouges.

 

Préparation de l’Acide vinylsulfonique

L’acide vinylsulfonique est produit industriellement par l’hydrolyse alcaline du sulfate de carbyle avec une acidification subséquente du sel de sulfonate de vinyle résultant: [6]

 

 

La réaction est hautement exothermique (enthalpie de réaction: 1 675 kJ / kg) et nécessite un maintien précis de la température et du pH pendant l’hydrolyse. Lorsque l’hydroxyde de calcium est utilisé comme milieu d’hydrolyse, une solution de vinylsulfonate de calcium est obtenue. L’acidification de ce mélange d’hydrolyse avec de l’acide sulfurique donne de l’acide vinylsulfonique, ainsi que du sulfate de calcium peu soluble.

 

L’acide vinylsulfonique peut également être préparé par déshydratation de l’acide iséthionique avec du pentoxyde de phosphore: [7]

L’acide vinylsulfonique peut également être préparé par sulfochloration du chloroéthane, déshydrohalogénation en chlorure de vinylsulfonyle et hydrolyse ultérieure du chlorure d’acide.

 

utilisation de L’Acide vinylsulfonique

La double liaison C = C activée de l’acide vinylsulfonique réagit facilement avec les nucléophiles dans une réaction d’addition. L’acide 2-aminoéthanesulfonique est formé avec de l’ammoniac et l’acide 2-méthylaminoéthanesulfonique avec de la méthylamine. [8]

 

L’acide vinylsulfonique est le monomère dans la préparation d’homopolymères et copolymères hautement acides ou anioniques. Ces polymères sont utilisés dans l’industrie électronique comme résines photosensibles, comme membranes électrolytiques polymères conductrices d’ions (PEM) pour les piles à combustible. Par exemple, des membranes transparentes avec une capacité d’échange ionique élevée et une conductivité protonique peuvent être produites à partir d’acide polyvinylsulfonique. [9]

 

Recherche

L’acide vinylsulfonique peut également être greffé sur des supports polymères (par exemple le polystyrène) pour donner des échangeurs d’ions hautement acides, qui sont utilisés comme catalyseurs pour l’estérification et les acylations de Friedel-Crafts. [10] Lorsque la fonctionnalité Acide vinylsulfonique n’est pas essentielle, la solution aqueuse alcaline beaucoup plus utilisable de vinylsulfonate de sodium est utilisée, qui est obtenue directement dans l’hydrolyse alcaline du sulfate de carbyle et est commercialisée sous forme de solution aqueuse.

 

 

Applications

L’acide vinylsulfonique est un réactif utile (monomère) pour la formation de polymères et copolymères poly (anioniques). L’acide vinylsulfonique est utilisé comme azurant de base et agent de nivellement dans les bains de nickel. L’acide vinylsulfonique est également utilisé comme intermédiaire pour la synthèse organique, le surfactant, l’industrie pharmaceutique.

Acide vinylsulfonique N ° CAS: 9002-97-5

Poids moléculaire de l’acide vinylsulfonique: 4 000-6 000

Soluble In: 25% de solution. dans l’eau (25g de polymère). Peut contenir un petit pourcentage de matière insoluble.

TSCA

Dangers: précautions normales d’utilisation inoffensive

Manipulation: exercer des soins normaux

Stockage: température ambiante

Remarques

Conserver dans un endroit frais. Conserver le récipient bien fermé dans un endroit sec et bien ventilé. Il est sensible à la lumière. Incompatible avec les agents oxydants.

La présente invention prévoit:

un procédé de production d’acide vinyl sulfonique, comprenant la conduite de la démétallation du sel de sulfonate de vinyle, dans lequel le taux de démétallation n’est pas inférieur à 95% selon la formule suivante:

Taux de démétallation (%) = {(indice d’acide après démétallation) / (indice d’acide avant démétallation)} × 100;

un procédé de production d’acide vinyl sulfonique, comprenant la conduite de la démétallation du sel de sulfonate de vinyle, dans lequel la démétallation est effectuée en utilisant une résine échangeuse d’ions fortement acide; et

ledit procédé comprenant en outre l’étape de purification d’un produit de la démétallation en utilisant un évaporateur à film mince.

acide vinylsulfonique) (PVS) possède une teneur élevée en acide (capacité d’échange ionique dans la formule chimique = 9,2 meq · g – 1). Son monomère, l’acide vinylsulfonique , avait une capacité de dissociation acide élevée (fonction acide Hammett = 0,74 dans l’eau) et une conductivité ionique élevée (0,04-0,11 S · cm – 1). La polymérisation radicalaire de acide vinylsulfoniqueavec divers initiateurs a été étudiée cinétiquement. Le spectre ESR du mélange de polymérisation de L’Acide vinylsulfonique a montré un signal fort attribué au radical carbone de propagation de VSA. Le poids moléculaire du PVS augmentait avec l’augmentation de la concentration en monomère et la diminution de la concentration de l’initiateur radicalaire pour donner l’acide vinylsulfonique avec un poids moléculaire de 4,0 × 104. La conductivité protonique de L’Acide vinylsulfonique dans des conditions hydratées et non humidifiées était de l’ordre de 10-1 et 10- 3-10-6 S · cm – 1, respectivement.

 

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