Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fiber staple

Traditional textile fabrics are made by weaving or knitting. Nonwoven fabrics are similar to woven and knitted fabrics in that both are planar, inherently flexible, porous stmctures composed of polymer-based materials. The main difference between the two is the manner in which the fabric is made. [Pg.145]

A nonwoven fabric can be assembled by mechanically, chemically, or thermally interlocking layers or networks of fibers, filaments, or yams. Fabrics made from textile fibers in this manner have been classified as dry-laid nonwovens. [Pg.145]

Other companies with early involvement in developing nonwovens as textile replacements include Avondale Mills, Kimberly-Clark, The Kendall Company, and the West Point Manufacturing Company. Freudenburg of Germany, a worldwide producer of nonwoven interlinings (another woven fabric replacement), began efforts in the 1930s to find a substitute for leather (qv) (7). [Pg.145]

Kirk-Othmer Encyclopedia of Chemical Technology (4th Edition) [Pg.145]

As engineered stmctures, nonwovens can be designed to have appearances, textures, and other aesthetic properties comparable to traditional wovens and knits, and performance and functional properties superior to traditional wovens and knits. Nonwovens are, indeed, a distinct class of fiber-based materials with the characteristics of fabric and many of its useful properties. [Pg.146]


Fig. 2. Typical stress—strain properties of staple fibers at 65% rh and 21°C. Rate of elongation is 50%/min. To convert N/tex to gf/den, multiply by 11.3. Fig. 2. Typical stress—strain properties of staple fibers at 65% rh and 21°C. Rate of elongation is 50%/min. To convert N/tex to gf/den, multiply by 11.3.
An example of a commercial semibatch polymerization process is the early Union Carbide process for Dynel, one of the first flame-retardant modacryhc fibers (23,24). Dynel, a staple fiber that was wet spun from acetone, was introduced in 1951. The polymer is made up of 40% acrylonitrile and 60% vinyl chloride. The reactivity ratios for this monomer pair are 3.7 and 0.074 for acrylonitrile and vinyl chloride in solution at 60°C. Thus acrylonitrile is much more reactive than vinyl chloride in this copolymerization. In addition, vinyl chloride is a strong chain-transfer agent. To make the Dynel composition of 60% vinyl chloride, the monomer composition must be maintained at 82% vinyl chloride. Since acrylonitrile is consumed much more rapidly than vinyl chloride, if no control is exercised over the monomer composition, the acrylonitrile content of the monomer decreases to approximately 1% after only 25% conversion. The low acrylonitrile content of the monomer required for this process introduces yet another problem. That is, with an acrylonitrile weight fraction of only 0.18 in the unreacted monomer mixture, the low concentration of acrylonitrile becomes a rate-limiting reaction step. Therefore, the overall rate of chain growth is low and under normal conditions, with chain transfer and radical recombination, the molecular weight of the polymer is very low. [Pg.279]

Electrically Conducting Fibers. FlectricaHy conducting fibers are useful in blends with fibers of other types to achieve antistatic properties in apparel fabrics and carpets. The process developed by Nippon Sanmo Dyeing Co., for example, is reportedly used by Asahi in Casbmilon 2.2 dtex (2 den) staple fibers. Courtaulds claims a flame-resistant electrically conductive fiber produced by reaction with guanadine and treatment with copper sulfide (97). [Pg.285]

Staple. PET staple is widely used in 100% polyester or cotton-blend fabrics for apparel. Typical cotton-blend polyester staple fibers have a linear... [Pg.333]


See other pages where Fiber staple is mentioned: [Pg.68]    [Pg.121]    [Pg.168]    [Pg.257]    [Pg.295]    [Pg.337]    [Pg.347]    [Pg.389]    [Pg.394]    [Pg.416]    [Pg.433]    [Pg.489]    [Pg.537]    [Pg.553]    [Pg.601]    [Pg.663]    [Pg.687]    [Pg.721]    [Pg.788]    [Pg.811]    [Pg.868]    [Pg.870]    [Pg.921]    [Pg.922]    [Pg.922]    [Pg.926]    [Pg.926]    [Pg.932]    [Pg.937]    [Pg.980]    [Pg.982]    [Pg.1036]    [Pg.1067]    [Pg.1067]    [Pg.1068]    [Pg.264]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.274]    [Pg.283]    [Pg.283]    [Pg.310]    [Pg.318]    [Pg.331]    [Pg.334]   
See also in sourсe #XX -- [ Pg.355 ]

See also in sourсe #XX -- [ Pg.318 ]

See also in sourсe #XX -- [ Pg.355 ]

See also in sourсe #XX -- [ Pg.429 , Pg.430 ]

See also in sourсe #XX -- [ Pg.94 ]

See also in sourсe #XX -- [ Pg.304 , Pg.305 ]

See also in sourсe #XX -- [ Pg.94 ]

See also in sourсe #XX -- [ Pg.735 ]




SEARCH



Staple

© 2024 chempedia.info