With cellulose triacetate

Many ceUulosic derivatives form anisotropic, ie, Hquid crystalline, solutions, and cellulose acetate and triacetate are no exception. Various cellulose acetate anisotropic solutions have been made using a variety of solvents (56,57). The nature of the polymer—solvent interaction determines the concentration at which hquid crystalline behavior is initiated. The better the interaction, the lower the concentration needed to form the anisotropic, birefringent polymer solution. Strong organic acids, eg, trifluoroacetic acid are most effective and can produce an anisotropic phase with concentrations as low as 28% (58). Trifluoroacetic acid has been studied with cellulose triacetate alone or in combination with other solvents (59—64) concentrations of 30—42% (wt vol) triacetate were common. 

This paper examines two types of hydroxypropyl lignin based macromers, and these are illustrated schematically in Figure 1. Macromers with propylene oxide (PO) are formed by reducing the number of available hydroxyl groups on HPL followed by chain extension with PO and macromers with cellulose triacetate (CTA) are synthesized by attaching a monofunctional CTA chain to a limited number of terminal OH groups on HPL via a suitable grafting reaction. 

Cellulose acetate (CA), of poor chemical stability, tends to hydrolyze over time, is subject to biological attack, and can operate at only a limited pH range of 3.0 to 6.5 at 0 to 30°C. It is widely available at low cost and is tolerant of continuous low-level chlorine exposure, such as is found in city water). Often blended with cellulose triacetate (CTA), which provides reasonable hydrolysis and compaction characteristics. 

Known bicyclo[4.3.1]enone 15758 was converted into vinylsilane 158 with bis(trimethylsilyl)methyl lithium.55 Diene 158 underwent selective ozonolysis at the cis-olefin under conditions to produce differentially oxidized termini 90 alde-hydo-ester 159 was homologated with a phosphine oxide anion91 to enol 160. Subsequent hydrolysis of 161 provided substrate 162, which after tandem ozonolysis-acidification gave racemic 6,9-desmethyl analogue 155. Unfortunately, initial efforts failed to resolve 155 into its two optical isomers with cellulose triacetate.92 However, the antimalarial activity of racemate 155 is intriguing, as discussed in a later section. 

Cellulose esters (e.g., cellulose triacetate, cellulose diacetate, cellulose propionate, and cellulose butyrate) are prepared by initially treating cellulose with glacial acetic acid (or propionic acid and butyric acid) followed by the corresponding acid anhydride with a trace of strong acid as a catalyst in chlorinated hydrocarbon. Complete esterification reactions result in the formation of a triester, which undergoes water hydrolysis to form a diester. Cellulose acetate alone or in combination with cellulose triacetate or cellulose butyrate is used as a semipermeable membrane for osmotic pumping tablets, primarily in controlled release systems. The permeability of the membrane can be further modulated by adding water-soluble excipients to the cellulose esters. 

The color of cellulose acetate dyed with some disperse dyes is subject to gas fading. Treatment of the dyed material with diethanolamine or melamine can overcome the problem (3). Similarly, with cellulose triacetate, gas fading of dyes can occur. It has been stated that protection can be obtained by the application of an inhibitor (3). 

Figure 6. Liquid-chromatographic enantioseparation of hexobarbital on the column (2.5 x 85 cm) packed with cellulose triacetate [136].

To illustrate, chloroparalEns are compatible with cellulose triacetate up to 50% but do not render any plastieiziug actioa On heating these plasticized films become fragile. On immersion in water, the ehloroparafBns are washed away completely. Chloroparaffins are extracted from the other derivatives of eellnlose in a similar way. The increase in the chloroparaffin content in PVC has httle effect on Tg. Low temperature performance is degraded as the chloroparafBn fraction increases in a mixture with phthalate plasticizers. 

Vazquez-Torres and Cruz-Ramos studied blends of PCL with cellulose triacetate (CTA), cast from methylene chloride and dried for 48 h at 80 °C. No glass-transitions were observed and therefore no conclusions on polymer-polymer miscibility were drawn [121]. Double PCL melting peaks were seen and, in this case, the lower T j was the smaller, cf. CAB blends. Values of T j and AH of PCL were not increased by CTA. There was some evidence for CTA crystalHmty on heating to high temperatures in the differential scanning calorimeter [121]. 

Cellulose triacetate is obtained by the esterification of cellulose (qv) with acetic anhydride (see Cellulose esters). Commercial triacetate is not quite the precise chemical entity depicted as (1) because acetylation does not quite reach the maximum 3.0 acetyl groups per glucose unit. Secondary cellulose acetate is obtained by hydrolysis of the triacetate to an average degree of substitution (DS) of 2.4 acetyl groups per glucose unit. There is no satisfactory commercial means to acetylate direcdy to the 2.4 acetyl level and obtain a secondary acetate that has the desired solubiUty needed for fiber preparation. 

Polymer Plasticizer. Nylon, cellulose, and cellulose esters can be plasticized using sulfolane to improve flexibiUty and to increase elongation of the polymer (130,131). More importantly, sulfolane is a preferred plasticizer for the synthesis of cellulose hoUow fibers, which are used as permeabiUty membranes in reverse osmosis (qv) cells (131—133) (see Hollow-FIBERMEMBRANEs). In the preparation of the hoUow fibers, a molten mixture of sulfolane and cellulose triacetate is extmded through a die to form the hoUow fiber. The sulfolane is subsequently extracted from the fiber with water to give a permeable, plasticizer-free, hoUow fiber. 

Perchloric acid is a weU-known acetylation catalyst, especially in the fibrous method of preparing cellulose triacetate. Unlike sulfuric acid, perchloric acid does not combine with cellulose (78), ie, it does not form esters, and therefore virtually complete acetylation (DS 3.0, 44.8% acetyl) occurs. However, the extremely corrosive nature of perchloric acid and explosive nature of its salts have precluded its use industrially as an acetylation catalyst. 

The cellulose esters with the largest commercial consumption are cellulose acetate, including cellulose triacetate, cellulose acetate butyrate, and cellulose acetate propionate. Cellulose acetate is used in textile fibers, plastics, film, sheeting, and lacquers. The cellulose acetate used for photographic film base is almost exclusively triacetate some triacetate is also used for textile fibers because of its crystalline and heat-setting characteristics. The critical properties of cellulose acetate as related to appHcation are given in Table 10. 

It is difficult for dye solutions in water to penetrate synthetic fibers such as polyester, cellulose triacetate, polyamides, and polyacryUcs which are somewhat hydrophobic. The rate of water imbibition differs with each fiber as shown in Table 1 as compared to viscose (see Fibers, regenerated CELLULOSics), which imbibes water at the rate of 100% (1). The low imbibition rate is attributed to the high T obtained when the polymeric fibers are drawn. During this drawing operation the polymer chains become highly oriented and tightly packed, forming a stmcture practically free of voids. 

Cellulose Triacetate. Cellulose acetate having 92% or more of the hydroxyl groups acetylated is referred to as triacetate. This fiber is characteristically more resistant to alkaU than the usual acetate and may be scoured, generally, in openwidth, with aqueous solutions of a synthetic surfactant and soda ash. 

Rejection Rejection is defined in Background and Definitions. The highest-rejection membranes are those designed for single-pass production of potable water from the sea. The generally accepted criterion is 99.4 percent rejection of NaCl. Some membranes, notably cellulose triacetate fibers are rated even higher. A whole range of membranes is available as rejection requirements ease, and membranes with excellent chlorine resistance and hydrolytic stability can be made with salt rejection over 90 percent. 

This includes wire enamels on a base of polyvinyl formal, polyurethane or epoxy resins as well as moulding powder plastics on phenol-formaldehyde and similar binders, with cellulose fillers, laminated plastics on paper and cotton cloth base, triacetate cellulose films, films and fibres of polyethylene terephthalate. 

Cellulose triacetate [9012-09-3] M 72,000-74,000. Extracted with cold EtOH, dried in air, washed with hot distd water, again dried in air, then dried at 50° for 30min. [Madorsky, Hart and Straus J Res Nat Bur Stand 60 343 1958.]... 

R/0 unit Reverse Osmosis Unit for water purification in small aquariums and miniature yard-ponds, utilizes a membrane under pressure to filter dissolved solids and pollutants from the water. Two different filter membranes can be used the CTA (cellulose triacetate) membrane is less expensive, but only works with chlorinated water and removes 50-70% of nitrates, and the TFC membrane, which is more expensive, removes 95% of nitrates, but is ruined by chlorine. R/0 wastes water and a system that cleans 100 gallons a day will cost ft-om 400 to 600 with membrane replacement adding to the cost. A unit that handles 140 gallons a day will cost above 700,00. 

The purpose of this study is only intended to illustrate and evaluate the decision tree approach for CSP prediction using as attributes the 166 molecular keys publicly available in ISIS. This assay was carried out a CHIRBASE file of 3000 molecular structures corresponding to a list of samples resolved with an a value superior to 1.8. For each solute, we have picked in CHIRBASE the traded CSP providing the highest enantioselectivity. This procedure leads to a total selection of 18 CSPs commercially available under the following names Chiralpak AD [28], Chiral-AGP [40], Chiralpak AS [28], Resolvosil BSA-7 [41], Chiral-CBH [40], CTA-I (microcrystalline cellulose triacetate) [42], Chirobiotic T [43], Crownpak CR(-i-) [28], Cyclobond I [43], DNB-Leucine covalent [29], DNB-Phenylglycine covalent [29], Chiralcel OB [28], Chiralcel OD [28], Chiralcel OJ [28], Chiralpak OT(-i-) [28], Ultron-ES-OVM [44], Whelk-0 1 [29], (/ ,/ )-(3-Gem 1 [29]. 

The second system studied was the separation of the chiral epoxide enantiomers (la,2,7,7a-tetrahydro-3-methoxynaphth-(2,3b)-oxirane Sandoz Pharma) used as an intermediate in the enantioselective synthesis of optically active drugs. The SMB has been used to carry out this chiral separation [27, 34, 35]. The separation can be performed using microcrystalline cellulose triacetate as stationary phase with an average particle diameter greater than 45 )tm. The eluent used was pure methanol. A... 

---