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Cellulose state

Carbonyl or carboxyl group profiles can also be evaluated numerically. This way, the amount of functionalities in preselected regions of the MWD are compared, provided that the samples have similar molecular weights. Certain characteristics of the cellulose state of oxidation or the distribution of... [Pg.29]

Chahal DS (1982) Enzymatic hydrolysis of cellulose, state-of-the-art. National Research Council of Canada, p 101... [Pg.92]

The overall objective of this and a companion paper (22) is to define the extent to which board formaldehyde emission is controlled by resin hydrolysis or other processes. In the companion paper I have critically reviewed the literature and presented original Forest Products Laboratory (FPL) data in three related aspects of the formaldehyde emission phenomenon the chemistry of and formaldehyde liberation from formaldehyde-urea and formaldehyde-phenol states the chemistry of and formaldehyde liberation from formaldehyde-cellulose and resin-cellulose states and our knowledge of the board emission mechanism derived from actual board and wood systems. Whereas my oral presentation at the American Chemical Society (ACS) Symposium made use of information from all three of those parts, this written paper, in the interest of saving space, is limited to literature and FPL data dealing with actual wood-containing systems. The Conclusions section of this paper, however, makes use of the results from all three parts of the companion paper. Experimental details of the... [Pg.88]

Many continuous extractions involving solid samples are carried out with a Soxhiet extractor (Figure 7.18). The extracting solvent is placed in the lower reservoir and heated to its boiling point. Solvent in the vapor phase moves upward through the tube on the left side of the apparatus to the condenser where it condenses back to the liquid state. The solvent then passes through the sample, which is held in a porous cellulose filter thimble, collecting in the upper reservoir. When the volume of solvent in the upper reservoir reaches the upper bend of the return tube, the solvent and any extracted components are siphoned back to the lower reservoir. Over time, the concentration of the extracted component in the lower reservoir increases. [Pg.214]

Most of the acetic acid is produced in the United States, Germany, Great Britain, Japan, France, Canada, and Mexico. Total annual production in these countries is close to four million tons. Uses include the manufacture of vinyl acetate [108-05-4] and acetic anhydride [108-24-7]. Vinyl acetate is used to make latex emulsion resins for paints, adhesives, paper coatings, and textile finishing agents. Acetic anhydride is used in making cellulose acetate fibers, cigarette filter tow, and ceUulosic plastics. [Pg.64]

Acetic anhydtide is a mature commodity chemical ia the United States and its growth rate in the 1970s and 1980s was negative until 1988 when foreign demand neatly doubled the exports of 1986. This increase in exports was almost certainly attributable to the decline in the value of the U.S. doUar. Over four-fifths of all anhydtide production is utilized in cellulose acetate [9004-35-7] manufacture (see Cellulose esters). Many anhydtide plants are integrated with cellulose acetate production and thus employ the acetic acid pyrolysis route. About 1.25 kg acetic acid is pyrolyzed to produce 1.0 kg anhydtide. [Pg.79]

Lead azide is not readily dead-pressed, ie, pressed to a point where it can no longer be initiated. However, this condition is somewhat dependent on the output of the mixture used to ignite the lead azide and the degree of confinement of the system. Because lead azide is a nonconductor, it may be mixed with flaked graphite to form a conductive mix for use in low energy electric detonators. A number of different types of lead azide have been prepared to improve its handling characteristics and performance and to decrease sensitivity. In addition to the dextrinated lead azide commonly used in the United States, service lead azide, which contains a minimum of 97% lead azide and no protective colloid, is used in the United Kingdom. Other varieties include colloidal lead azide (3—4 pm), poly(vinyl alcohol)-coated lead azide, and British RE) 1333 and RE) 1343 lead azide which is precipitated in the presence of carboxymethyl cellulose (88—92). [Pg.10]

The two procedures primarily used for continuous nitration are the semicontinuous method developed by Bofors-Nobel Chematur of Sweden and the continuous method of Hercules Powder Co. in the United States. The latter process, which uses a multiple cascade system for nitration and a continuous wringing operation, increases safety, reduces the personnel involved, provides a substantial reduction in pollutants, and increases the uniformity of the product. The cellulose is automatically and continuously fed into the first of a series of pots at a controlled rate. It falls into the slurry of acid and nitrocellulose and is submerged immediately by a turbine-type agitator. The acid is deflvered to the pots from tanks at a rate controlled by appropriate instmmentation based on the desired acid to cellulose ratio. The slurry flows successively by gravity from the first to the last of the nitration vessels through under- and overflow weirs to ensure adequate retention time during nitration. The overflow from the last pot is fully nitrated cellulose. [Pg.14]

There is more activity in dairy products than anywhere else in the food industry. Ice milk and fro2en yogurt, early leaders in the field, rose rapidly in sales then plummeted. Fat-free ice cream has been marketed, but final results are not yet available. Sales of these products have not cannibalized traditional ice cream (35). Standards for traditional ice cream call for a minimum of 10% butterfat. One fat-free ice cream product is prepared from nonfat milk (skim) and cellulose gum. Fat-free ice creams have encountered strong resistance in some segments of the retail trade. Retailers in Maine and New York, states with important dairy producing industries, refuse to sell such products (36). [Pg.118]

Eastman Goal Chemicals. In 1983 Eastman Chemical Co. became the first chemical producer in the United States to return to coal as a raw material for large-scale manufacture of industrial chemicals (35). In that year, Eastman started manufacturing acetic anhydride from coal. Acetic anhydride is a key intermediate for production of coatings, ceUulosic plastics, and cellulose acetate fibers. Acetic anhydride from other sources also is used in the manufacture of pharmaceuticals, starches and sweeteners, and flavors and fragrances. [Pg.166]

Most of the commercial tree plantations that produce wood for captive use as a raw material in manufacturing operations use a portion as fuel. Examples of short-rotation plantations are Hsted in Table 38 (127). Paper companies in the southeastern United States are reported to have short-rotation plantings also, eg, Weyerhaeuser, James River Corp., Buckeye Cellulose, and Lykes Brothers, but the intensity of maintenance is not known (127). [Pg.42]

Magnesium acetate also has uses as a dye fixative in textile printing, as a deodorant, disinfectant, an antiseptic in medicine, and as a reagent chemical (see Disinfectants AND ANTISEPTICS Textiles) (6). In the United States, Hoescht-Celanese and Tennessee Eastman are the principal producers of magnesium acetate. These companies make about 36,000 t/yr, which is largely used in-house for the production of cellulose acetate. [Pg.339]

Sulfates of sodium are iadustriaUy important materials commonly sold ia three forms (Table 1). In the period from 1970 to 1981, > 1 million metric tons were consumed aimuaHy ia the United States. Siace then, demand has declined. In 1988 consumption dropped to 890,000 t, and ia 1994 to 610,000 t (1,2). Sodium sulfate is used principally (40%) ia the soap (qv) and detergent iadustries. Pulp and paper manufacturers consume 25%, textiles 19%, glass 5%, and miscellaneous iadustries consume 11% (3). About half of all sodium sulfate produced is a synthetic by-product of rayon, dichromate, phenol (qv), or potash (see Chromium compounds Fibers, regenerated cellulosics Potassium compounds). Sodium sulfate made as a by-product is referred to as synthetic. Sodium sulfate made from mirabilite, thenardite, or naturally occurring brine is called natural sodium sulfate. In 1994, about 300,000 t of sodium sulfate were produced as a by-product another 300,000 t were produced from natural sodium sulfate deposits (4). [Pg.203]

Traditionally, these dyes are appHed from a dyebath containing sodium sulfide. However, development in dyeing techniques and manufacture has led to the use of sodium sulfhydrate, sodium polysulfide, sodium dithionite, thiourea dioxide, and glucose as reducing agents. In the reduced state, the dyes have affinity for cellulose (qv) and are subsequendy exhausted on the substrate with common salt or sodium sulfate and fixed by oxidation. [Pg.162]

Dextrose (D-glucose) is by far the most abundant sugar in nature. It occurs either in the monosaccharide form (free state) or in a polymeric form of anhydrodextrose units. As a monosaccharide, dextrose is present in substantial quantities in honey, fmits, and berries. As a polymer, dextrose occurs in starch, cellulose (qv), and glycogen. Sucrose is a disaccharide of dextrose and fmctose. [Pg.288]

The principal chemical iadustry based on wood is pulp and paper. In 1995, 114.5 x 10 metric tons of wood were converted iato - 60 x 10 metric tons of fiber products ranging from newsptint to pure cellulose ia the United States (1,76). Pure cellulose is the raw material for a number of products, eg, rayon, cellulose acetate film base, cellulose nitrate explosives, cellophane, celluloid, carboxymethylceUulose, and chemically modified ceUulosic material. [Pg.331]

Cellulose I. The majority of celluloses in the native state were previously thought to have the same crystal stmcture (Cellulose I), varying only in perfection of the crystaUites. Now, at least two different crystal stmctures are known for these materials, named la and ip. These two phases coexist in... [Pg.240]

Many cellulose derivatives form Hquid crystalline phases, both in solution (lyotropic mesophases) and in the melt (thermotropic mesophases). The first report (96) showed that aqueous solutions of 30% hydroxypropylceUulose [9004-64-2] (HPC) form lyotropic mesophases that display iridescent colors characteristic of the chiral nematic (cholesteric) state. The field has grown rapidly and has been reviewed from different perspectives (97—101). [Pg.243]

John A. Cuculo (Cellulose Solvents) North Carolina State University... [Pg.245]

From 1980 to 1988, aimual cellulose acetate flake production in the United States showed a slight decrease in production from 392,000 t to 323,000 t with an aimual decline of —0.4 to —0.1% (Table 6). World demand for cellulose acetate flake has also fallen. A modest recovery has occurred in recent years as a result of the increased demand for cigarette-filter tow world consumption of cigarette-filter tow has risen about 2.5% per year since 1980 (Tables 7 and 8). In contrast, world demand for textile fibers and cellulose ester plastics decline 4.6% and 4.2% per year, respectively (Fig. 9). [Pg.255]

Cellulose acetate ester plastics are produced largely in the United States, Western Europe, and Japan. World consumption is assumed to be approximately equivalent to production of cellulose ester plastics in these three regions. Courtesy of CEH Estimates. [Pg.256]

Demand for cellulose acetate flake in the United States is projected to decline slightly from 1988 to 1993. Cigarette-filter tow for export is the only market projected to grow. Cellulose acetate for textile fibers is expected to decline, as will flake demand for plastics, with the growth of photographic films somewhat offsetting declining markets in other plastics end uses. [Pg.256]

From 1946 to mid-1987, Farbenfabriken Bayer AG in Germany was the European producer of cellulose acetate, cellulose acetate butyrate (CAB), and cellulose acetate propionate (CAP) before closing its faciUties. Bayer s exit from the cellulose acetate mixed esters business leaves Eastman Chemical Co. in the United States as the sole producer of CAB/CAP resins. [Pg.256]

Other two-dimensional techniques, such as COSY (122), DEPT (123), HOHAHA, soHd state (124) etc. give varying degrees of success when apphed to the stmcture-property relationship of cellulose triesters. The recent appHcation of multiple-bond correlation (HMBC) spectroscopy for... [Pg.258]


See other pages where Cellulose state is mentioned: [Pg.1482]    [Pg.440]    [Pg.463]    [Pg.565]    [Pg.284]    [Pg.2522]    [Pg.1482]    [Pg.440]    [Pg.463]    [Pg.565]    [Pg.284]    [Pg.2522]    [Pg.429]    [Pg.2604]    [Pg.352]    [Pg.11]    [Pg.14]    [Pg.30]    [Pg.34]    [Pg.451]    [Pg.181]    [Pg.292]    [Pg.482]    [Pg.321]    [Pg.238]    [Pg.21]    [Pg.239]    [Pg.340]    [Pg.240]    [Pg.241]    [Pg.243]    [Pg.249]    [Pg.256]   
See also in sourсe #XX -- [ Pg.128 , Pg.129 ]




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