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Cellulose triacetate, triacetate, CTA or TAC is a chemical compound produced from cellulose and a source of acetate esters, typically acetic anhydride. Triacetate is commonly used for the creation of fibres and film base .
Cellulose diacetate and cellulose triacetate are mistakenly referred to as the same fiber; although they are similar, their chemical identities differ. Triacetate is known as a generic description or primary acetate containing no hydroxyl group.
Cellulose diacetate film was first created by the German chemists Arthur Eichengrün and Theodore Becker, who patented it under the name Cellit, from a process they devised in 1901 for the direct acetylation of cellulose at a low temperature to prevent its degradation, which permitted the degree of acetylation to be controlled, thereby avoiding total conversion to its triacetate.
Cellulose acetate and cellulose triacetate are film- and fiber-forming materials that find a variety of uses. Nitrocellulose was initially used as an explosive and was an early film forming material. When plasticized with camphor , nitrocellulose gives celluloid .
The chemical structure of cellulose with substitutions that characterize coex materials. Coex is a biopolymer with flame-retardant properties derived from the functionalization of cellulosic fibers such as cotton, linen, jute, cannabis, coconut, ramie, bamboo, raffia palm, stipa, abacà, sisal, nettle and kapok.
Disperse dyes were originally developed for the dyeing of cellulose acetate, and are water-insoluble. The dyes are finely ground in the presence of a dispersing agent and sold as a paste, or spray-dried and sold as a powder. Their main use is to dye polyester, but they can also be used to dye nylon, cellulose triacetate, and acrylic
Cellulose diacetate, sometimes called diacetate, is a synthetic polymer made by treating cellulose with acetic acid. It consists of two acetyl functional groups on each unit of D-anhydroglucopyranose of the cellulose molecule. It was first developed in the United States. It is fragile since it is based on cellulose.
Structure formula of cellulose diacetate with one of the acetate groups on the cellulose backbone shown by the red circle. Cellulose acetate is non-toxic, odorless, tasteless, and weakly flammable plastic. It is resistant to weak acids and is largely stable to mineral and fatty oils as well as petroleum.