Caprolactam

caprolactam

[¦ka·prō¦lak·təm] (organic chemistry) (CH₂)₅NH·CO White flakes, melting point 68-69°C, made from cyclohexanone; used to make synthetic fiber, particularly nylon-6.

Caprolactam

a lactam of €-aminocaproic acid; a white crystalline substance. Melting point, 68°-69°C; boiling point, 262.5°C; index of refraction n²⁰_D, 1.4768.

Caprolactam is highly soluble in water and organic solvents, such as alcohol, ether, and benzene, and is hydrolyzed in aqueous acid and alkaline solutions to €-aminocaproic acid, H₂NN-(CH₂)₅CCOOH. An important property of caprolactam is its ability to polymerize, forming the vaulable polymer polycaproa-mide.

All of the commercial methods of preparing caprolactam include preparation of an intermediate—cyclohexanon oxime— and its conversion (Beckmann rearrangement) into caprolactam under the action of fuming sulfuric acid or concentrated H₂ SO ₄ at 60°-120°C. One of the main methods of preparing caprolactam from cyclohexane (I) involves the catalytic oxidation of cyclohexane (by atmospheric oxygen) into cyclohexanone (II). Upon interaction with hydroxylamine, the latter is converted into cyclohexanon oxime (III):

The most efficient and economical method is direct photochemical nitrosation of (I) into cyclohexanon oxime chlorhydrate. The procedure is simple: upon continuous saturation with gaseous HC1, a solution of nitrosylchloride, NOC1, in (I) is irradiated using a 10-kilowatt mercury lamp. The oxime (III) can also be obtained from other available raw material, such as benzoic acid, C₆H⁵COOH; it is hydrogenated to cyclohexanocarboxylic acid, C⁶H¹¹COOH, which is subsequently treated with nitrosylsulfu-ric acid. The original commercial method of preparation of caprolactam from phenol is still widely used.

In all methods, the caprolactam produced is isolated rectification (redistillation) or extraction (for example, by benzene), with subsequent rectification.

Caprolactam is used primarily in the preparation of polyamide plastics, films, and fibers. In 1970 the world production of caprolactam reached 1.6 million tons.

REFERENCE

Sovremennye metody sinteza monomerov dlia geterotsepnykh voloknoo-brazuiushchikh polimerov. Sb. statei. Edited by I. L. Knuniants. Mos-cow, 1961.

单词	caprolactam
释义	caprolactam caprolactam (ˌkæprəʊˈlæktæm) n (Elements & Compounds) a white crystalline cyclic imine used in the manufacture of nylon. Formula: C5H10NHCO[C20: from capro(ic acid) + lactam] cap•ro•lac•tam (ˌkæp roʊˈlæk tæm) n. a white, water-soluble compound, C₆H₁₁NO, used to produce a type of nylon. [1940–45; capro(ic acid) + lact(one) + am(ide)] Translations Caprolactam caprolactam [¦ka·prō¦lak·təm] (organic chemistry) (CH₂)₅NH·CO White flakes, melting point 68-69°C, made from cyclohexanone; used to make synthetic fiber, particularly nylon-6. Caprolactam a lactam of €-aminocaproic acid; a white crystalline substance. Melting point, 68°-69°C; boiling point, 262.5°C; index of refraction n²⁰_D, 1.4768. Caprolactam is highly soluble in water and organic solvents, such as alcohol, ether, and benzene, and is hydrolyzed in aqueous acid and alkaline solutions to €-aminocaproic acid, H₂NN-(CH₂)₅CCOOH. An important property of caprolactam is its ability to polymerize, forming the vaulable polymer polycaproa-mide. All of the commercial methods of preparing caprolactam include preparation of an intermediate—cyclohexanon oxime— and its conversion (Beckmann rearrangement) into caprolactam under the action of fuming sulfuric acid or concentrated H₂ SO ₄ at 60°-120°C. One of the main methods of preparing caprolactam from cyclohexane (I) involves the catalytic oxidation of cyclohexane (by atmospheric oxygen) into cyclohexanone (II). Upon interaction with hydroxylamine, the latter is converted into cyclohexanon oxime (III): The most efficient and economical method is direct photochemical nitrosation of (I) into cyclohexanon oxime chlorhydrate. The procedure is simple: upon continuous saturation with gaseous HC1, a solution of nitrosylchloride, NOC1, in (I) is irradiated using a 10-kilowatt mercury lamp. The oxime (III) can also be obtained from other available raw material, such as benzoic acid, C₆H⁵COOH; it is hydrogenated to cyclohexanocarboxylic acid, C⁶H¹¹COOH, which is subsequently treated with nitrosylsulfu-ric acid. The original commercial method of preparation of caprolactam from phenol is still widely used. In all methods, the caprolactam produced is isolated rectification (redistillation) or extraction (for example, by benzene), with subsequent rectification. Caprolactam is used primarily in the preparation of polyamide plastics, films, and fibers. In 1970 the world production of caprolactam reached 1.6 million tons. REFERENCE Sovremennye metody sinteza monomerov dlia geterotsepnykh voloknoo-brazuiushchikh polimerov. Sb. statei. Edited by I. L. Knuniants. Mos-cow, 1961.
随便看	trotted her out trotted him out trotted me out trotted out trotted someone out trotted them out trotted us out trotted you out trotter trotters trotter syndrome trotter, w trotter, w. trotter, william monroe trot them out trotting trotting her out trotting him out trotting horse trotting me out trotting out trotting race trotting races trotting someone out trotting them out

caprolactam

caprolactam

cap•ro•lac•tam

Caprolactam

caprolactam

Caprolactam

REFERENCE