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Starch simple

The monosaccharide D-( + )-glucose, an aldohexose, is formed by plants in photosynthesis and is converted to the polysaccharides cellulose and starch. Simple saccharides are called sugars. Polysaccharides are hydrolyzable to monosaccharides e.g., a mol of trisaccharide gives 3 mol of monosaccharides. [Pg.494]

However, grasses contain a much wider variety of components that do most tree species. In addition to cellulose, hemicellulose and lignin, grasses often contain 10% or more of protein, in addition to minerals, starch, simple sugars, vitamins and other components. The wider variety of components in grasses versus woody plants offers the potential for producing additional valuable products, but may also complicate the processing required. [Pg.22]

Gums and starches were used in early attempts to replace the viscosity and lubricity of oils in foods. These were not well received by consumers because they assumed fats merely suppHed mouthfeel and a bit of flavor. On closer examination, it became evident that fats in food and in the diet performed many roles, some simple, some extremely complex, some understood, and some not understood. [Pg.117]

Quaternary ammonium alkyl ethers are prepared similarly an alkaline starch is reacted with a quaternary ammonium salt containing a 3-chloto-2-hydtoxyptopyl or 2,3-epoxyptopyl radical. Alternatively, such derivatives can be prepared by simple quaternization of tertiary aminoalkyl ethers by reaction with methyl iodide. Sulfonium (107) and phosphonium (108) starch salts have also been prepared and investigated. Further work has explained the synthesis of diethyl aminoethyl starch (109) as well as the production of cationic starches from the reaction of alkaline starch with... [Pg.345]

In the early years of the chemical industry, use of biological agents centered on fermentation (qv) techniques for the production of food products, eg, vinegar (qv), cheeses (see Milk and milk products), beer (qv), and of simple organic compounds such as acetone (qv), ethanol (qv), and the butyl alcohols (qv). By the middle of the twentieth century, most simple organic chemicals were produced synthetically. Fermentation was used for food products and for more complex substances such as pharmaceuticals (qv) (see also Antibiotics). Moreover, supports were developed to immobilize enzymes for use in industrial processes such as the hydrolysis of starch (qv) (see Enzyme applications). [Pg.113]

A simple test for ether peroxides is to add lOmL of the ether to a stoppered cylinder containing ImL of freshly prepared 10% solution of potassium iodide containing a drop of starch indicator. No colour should develop during one minute if free from peroxides. Alternatively, a 1% solution of ferrous ammonium sulfate, O.IM in sulfuric acid and O.OIM in potassium thiocyanate should not increase appreciably in red colour when shaken with two volumes of the ether. [Pg.65]

There are two types of glucose chains in starch. One is a simple chain called amylose, and the other is a complex branched form called amylopectin. In the starch grains in a plant, amylopectin makes up the bulk of the material, from 50 to 80 percent by weight, made up of several million amylopectin molecules per starch grain. The rest is a much larger number of the smaller amylose chains, made up of 500 to 20,000 glucose units in each chain. Amylopectin molecules are made of several million glucose units. [Pg.144]

The synthetic approach is very simple and does not require any special set up. In a typical room temperature reaction, 1.0 mL aqueous solution of cadmium chloride was added to 20 mL aqueous solution of soluble starch in a 50 mL one-necked round-bottom flask with constant stirring at room temperature. The pH of the solution was adjusted from 6 to 11 using 0.1 M ammonia solution. This was followed by a slow addition of 1.0 mL colourless selenide ion stock solution. The mixture was further stirred for 2 h and aged for 18 h. The resultant solution was filtered and extracted with acetone to obtain a red precipitate of CdSe nanoaprticles. The precipitate was washed several times and dried at room temperature to give a material which readily dispersed in water. The same procedure was repeated for the synthesis of PVA and PVP - capped CdSe nanoparticles by replacing the starch solution with the PVA and PVP polymers while the synthesis of elongated nanoparticles was achieved by changing the Cd Se precursor ratio from 1 1 to 1 2. The synthesis of polymer capped ZnSe nanoparticles also follows the same procedure except that ZnCb solution was used instead of CdCb solution. [Pg.167]

We have reported a simple, green, bench top, economical and environmentally benign room temperature synthesis of MSe (M=Cd or Zn) nanoparticles using starch, PVA and PVP as passivating agents. The whole process is a redox reaction with selenium acting as the oxidant and MSe as the reduction product. An entire "green" chemistry was explored in this synthetic procedure and it is reproducible. The optical spectroscopy showed that all the particles are blue shifted from the bulk band gap clearly due to quantum confinement. Starch capped CdSe nanoparticles showed the presence of monodispersed spherical... [Pg.179]

Most of the biomass used for energy is burned, either directly to provide heat or in a power station to provide electricity. Although biomass is a complex mixture of starch, cellulose, etc., in simple terms the burning process can be viewed as being represented by Equation 6.1. The CO2 output can be considered as being essentially neutral since a similar amount of CO2 is consumed in growing the biomass. [Pg.170]

Cellulose and starch are macromolecules with empirical formulas that resemble hydrated carbon, CX (H2 0)y, where x and y are integers. The monomers from which these macromolecules are consfructed are sugars such as glucose and fructose. These monomers and macromolecules are the carbohydrates. Structurally, carbohydrates are very different from simple combinations of carbon and water. Even the smallest carbohydrates contain carbon chains with hydrogen atoms, OH groups, and occasional ether linkages. [Pg.919]

In the Phadebas TM amylase test (72) (Pharmacia Labs) the substrate was a water insoluble cross-TTnked blue starch in tablet form which also contains some inert ingredients, sodium and potassium phosphate buffer salts and sodium chloride. This polymer was hydrolyzed by amylase into water soluble blue starch fragments. After centrifugation the absorbance of the blue supernatant was proportional to the activity of amylase present in the test samples. The day to day variation on a quality control serum had a coefficient of variation of 2.7% based on 30 days of data in our laboratory. The method is simple, reproducible and uses microquantities of serum. [Pg.210]

The diastase activity was traditionally determined according to the Schade method in the earlier years (Schade et al., 1958). One unit of diastase activity (or more specifically, a-amylase), DN, is defined as that amoimt of enz)nne that converts 0.01 g of starch to the prescribed endpoint in 1 h at 37 °C under the experimental conditions. In this assay, a standard solution of starch, which reacts with iodine to produce a color solution, is used as a substrate for honey enzymes under the standard conditions (Rendleman, 2003). A recently developed procedure uses an insoluble, dyed starch substrate (Persano Oddo and Pulcini, 1999). As this substrate is hydrolyzed by ot-amylase, soluble dyed starch fragments are released into solution. After reaction termination and insoluble substrate removal by centrifugation, absorbance of the supernatant solution (at 620 nm) is measured. The absorbance is proportional to the diastase activity. This procedure has been widely adopted in the honey industry due to the convenience of a commercially available substrate and the simple assay format. [Pg.106]

Carbohydrates are classified based upon the products formed when they are hydrolyzed. Monosaccharides are simple sugars that cannot be broken down into simpler sugars upon hydrolysis. Examples of monosaccharides are glucose, ribose, deoxyribose, and fructose. Disaccharides contain two monosaccharide units and yield two monosaccharides upon hydrolysis. Examples of disaccharides are lactose, maltose, and sucrose. Polysaccharides are polymers of monosaccharide units and yield many individual monosaccharides upon hydrolysis. Examples of polysaccharides are starch, glycogen, and cellulose. [Pg.177]

Desizing by chemical decomposition is applicable to starch-based sizes. Since starch and its hydrophilic derivatives are soluble in water, it might be assumed that a simple alkaline rinse with surfactant would be sufficient to effect removal from the fibre. As is also the case with some other size polymers, however, once the starch solution has dried to a film on the fibre surface it is much more difficult to effect rehydration and dissolution. Thus controlled chemical degradation is required to disintegrate and solubilise the size film without damaging the cellulosic fibre. Enzymatic, oxidative and hydrolytic degradation methods can be used. [Pg.101]


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Simple starch hydrolyzates

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