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Careful estimates suggest that the total losses to agricultural crops from insect attacks in the United States average about 10% of production and amount to more than 14 biUion annually (1). Worldwide agricultural losses from insect attacks have been estimated as about 14% of production (2). [Pg.267]

Mineral dust also has important effects on the amounts of nutrients supplied to the oceans, thereby affecting biological productivity and amounts of CO2 released into the atmosphere (Martin and Gordon, 1988 Watson, 1997). Iron is thought to be a limiting factor for phytoplankton productivity in remote marine areas (Falkowski et al., 1998 Fung et al., 2000 Gao et al., 2001). [Pg.2009]

The requirements to be given below for the different cooling systems all refer to the natural size characteristics for that cooling system. The listed D2O requirement is all the D2O that is needed for the operation at the production level given. As far as the U is concerned, one must remember that the U is consumed by the operation and that the pile operation is followed by a chemical one. However, the consumption of U does not depend on the cooling system. It is proportional to the 49 production and amounts to about 2000 kg of U for 1 kg 49 produced. Similarly, the chemical operation is also independent of the cooling system used (except for the 6th system). For these reasons, the U requirement includes only the amount of U which is tied up in the pile and subsidiary equipment. The data for other piles (cf. W pile) are also always given in the same form. [Pg.362]

Fig. 5.1. Production and amount of adhesives in Japan (Japan Adhesive... Fig. 5.1. Production and amount of adhesives in Japan (Japan Adhesive...
CjHiaNO, [Mc3NCH= CH2] OH. A liquid forming a crystalline trihydrate, It is present free and combined in brain and other animal and vegetable products and is formed as a product of putrefaction of lecithin. It can be prepared synthetically from choline and decomposes easily to trimethylamine. neutralization, heat of The amount of heat evolved when I g equivalent of an acid is neutralized by 1 g equivalent of a base. For strong acids and strong bases in dilute solution the only reaction which occurs is H -h OH ---> H2O and the heat of neutral-... [Pg.272]

It is clear that the freight value depends on the type and amount of film and how the production is spread over time. Figure 3 shows 2 simulations of silver concentration in fixer for different processing regimes. In one case, 10 m of film is processed over 3 hours. In another case, 10 m of film is processed over 16 hours. It is clear that the silver level in the fixer not only depends on the amount of film processed, but also on the distribution of the working load. The simulated daily freight values are 44 and 16 mgW respectively. ... [Pg.607]

It is designed to deal with large families of products and/or for horizontal risks, limiting thereby the amount of internal market directives needed to a manageable number ... [Pg.938]

Initially, the only means of obtaining elements higher than uranium was by a-particle bombardment of uranium in the cyclotron, and it was by this means that the first, exceedingly minute amounts of neptunium and plutonium were obtained. The separation of these elements from other products and from uranium was difficult methods were devised involving co-precipitation of the minute amounts of their salts on a larger amount of a precipitate with a similar crystal structure (the carrier ). The properties were studied, using quantities of the order of 10 g in volumes of... [Pg.443]

The theoretical yield in an organic reaction is the amount which would be obtained under ideal conditions if the reaction had proceeded to completion, i.e., if the starting materials were entirely converted into the desired product and there was no loss in isolation and purification. The yield (sometimes called the actual yield) is the amount of pure product which is actually isolated in the experiment. The percentage yield is... [Pg.201]

Apart from using an environmentally friendly solvent, it is also important to clean up the chemical reactions themselves by reducing the number and amount of side-products formed. For this purpose catalysts are a versatile tool. Catalysts have been used for thousands of years in processes such as fermentation and their importance has grown ever since. In synthetic oiganic chemistry, catalysts have found wide applications. In the majority of these catalytic processes, organic solvents are used, but also here the use of water is becoming increasingly popular . [Pg.2]

Palladation of aromatic compounds with Pd(OAc)2 gives the arylpalladium acetate 25 as an unstable intermediate (see Chapter 3, Section 5). A similar complex 26 is formed by the transmetallation of PdX2 with arylmetal compounds of main group metals such as Hg Those intermediates which have the Pd—C cr-bonds react with nucleophiles or undergo alkene insertion to give oxidized products and Pd(0) as shown below. Hence, these reactions proceed by consuming stoichiometric amounts of Pd(II) compounds, which are reduced to the Pd(0) state. Sometimes, but not always, the reduced Pd(0) is reoxidized in situ to the Pd(II) state. In such a case, the whole oxidation process becomes a catalytic cycle with regard to the Pd(II) compounds. This catalytic reaction is different mechanistically, however, from the Pd(0)-catalyzed reactions described in the next section. These stoichiometric and catalytic reactions are treated in Chapter 3. [Pg.14]

In contrast to oxidation in water, it has been found that 1-alkenes are directly oxidized with molecular oxygen in anhydrous, aprotic solvents, when a catalyst system of PdCl2(MeCN)2 and CuCl is used together with HMPA. In the absence of HMPA, no reaction takes place(100]. In the oxidation of 1-decene, the Oj uptake correlates with the amount of 2-decanone formed, and up to 0.5 mol of O2 is consumed for the production of 1 mol of the ketone. This result shows that both O atoms of molecular oxygen are incorporated into the product, and a bimetallic Pd(II) hydroperoxide coupled with a Cu salt is involved in oxidation of this type, and that the well known redox catalysis of PdXi and CuX is not always operalive[10 ]. The oxidation under anhydrous conditions is unique in terms of the regioselective formation of aldehyde 59 from X-allyl-A -methylbenzamide (58), whereas the use of aqueous DME results in the predominant formation of the methyl ketone 60. Similar results are obtained with allylic acetates and allylic carbonates[102]. The complete reversal of the regioselectivity in PdCli-catalyzed oxidation of alkenes is remarkable. [Pg.30]

In steroid systems, the homoannular diene in ring A and the heteroannular diene in AB rings are generated. The allylic 3a-carbonate 514 affords the homoannular conjugated diene 515 as a main product and a small amount of the heteroannular diene 516. On the other hand, the heteroannular conjugated diene 516 is obtained exclusively from 33-carbonates 517. The elimination reaction proceeds smoothly at room temperature. [Pg.359]

Table 3. Top Aquaculture Producing Nations in 1992 and Amount of Production in Each ... Table 3. Top Aquaculture Producing Nations in 1992 and Amount of Production in Each ...
Secondary Treatment and Uses. The vast majority of OSB panels are used "as is," without further processing or treatment. Primary uses are as wall and roof sheathing, floor decking, and other constmction panel uses in home and commercial constmction. OSB products are effectively filling in for the decline in plywood production. Small amounts of OSB are used in furniture, primarily as frame stock, and in other uses in which plywood might be used. [Pg.396]

By-product acetic acid is obtained chiefly from partial hydrolysis of cellulose acetate [9004-35-7]. Lesser amounts are obtained through the reaction of acetic anhydride and cellulose. Acetylation of saHcyHc acid [69-72-7] produces one mole of acetic acid per mole of product and the oxidation of allyl alcohol using peracetic acid to yield glycerol furnishes by-product acid, but the net yield is low. [Pg.69]

Little is known of the market for acetyl chloride. The production and sales are beUeved to be small, but may have potential for very large scale-up. The total U.S. market may amount to only 500 t annually. Acetyl chloride must be shipped in polyethylene-lined dmms having capacities of only 220 L it must be labeled as a corrosive substance. Acetyl chloride generated captively from purchased raw materials probably has a unit value of no more than 0.92—0.95/kg. Shipping costs and other factors set the price at about 3/kg for the commercial trade. [Pg.82]

The type of initiator utilized for a solution polymerization depends on several factors, including the solubiUty of the initiator, the rate of decomposition of the initiator, and the intended use of the polymeric product. The amount of initiator used may vary from a few hundredths to several percent of the monomer weight. As the amount of initiator is decreased, the molecular weight of the polymer is increased as a result of initiating fewer polymer chains per unit weight of monomer, and thus the initiator concentration is often used to control molecular weight. Organic peroxides, hydroperoxides, and azo compounds are the initiators of choice for the preparations of most acryUc solution polymers and copolymers. [Pg.167]

The temperature and humidity should be maintained at comfort conditions consistent with the operator s expected level of activity in order to minimise perspiration. Constant temperature and humidity may also be required in machine rooms to prevent the etching or corrosion of machine parts. If perspiration causes only minor damage to the product and results in few rejects, then inside design conditions at 27°C and 40% rh are satisfactory. Where even small amounts of perspiration cause extreme damage to precision-machined parts and result in a high amount of rejects, inside design conditions of 21°C and 40% rh are recommended. [Pg.357]

When coal is coked at a temperature of approximately 1000°C, about 70—75% of the product is coke. Nearly 20% of the product is a light gas, mostiy methane and hydrogen, that typically is used as fuel to heat the ovens. Coal tars amount to about 4% of the product and light oil or naphtha is about 1%. Ammonia is recovered in an amount equal to about 0.3% of the feed coal. The ammonia is usually converted to ammonium sulfate and sold as a fertilizer. Littie or no ammonia [7664-41-7] is produced inlow temperature carbonization (3). [Pg.161]

In 1980, the last year for which a breakdown has been pubUshed, the amount of benzene derived from coal in the United States was 168,000 t or 2.5% of domestic benzene production. Coal-derived toluene was 0.8% of production, and xylenes from coal were only 0.1% of total chemical production (9). The amounts and proportions of BTX components derived from coal in the United States are expected to be nearly the same today as in 1980. Based on information submitted to the International Trade Commission, approximately 25 companies participated in the coal-tar industry in the United States in 1990. [Pg.162]

Certain factors and product precursors are occasionally added to various fermentation media to iacrease product formation rates, the amount of product formed, or the type of product formed. Examples iaclude the addition of cobalt salts ia the vitamin fermentation, and phenylacetic acid and phenoxyacetic acid for the penicillin G (hen ylpenicillin) and penicillin V (phenoxymethylpenicillin) fermentations, respectively. Biotin is often added to the citric acid fermentation to enhance productivity and the addition of P-ionone vastly iacreases beta-carotene fermentation yields. Also, iaducers play an important role ia some enzyme production fermentations, and specific metaboHc inhibitors often block certain enzymatic steps that result in product accumulation. [Pg.180]

Since 1960, about 95% of the synthetic ammonia made in the United States has been made from natural gas worldwide the proportion is about 85%. Most of the balance is made from naphtha and other petroleum Hquids. Relatively small amounts of ammonia are made from hydrogen recovered from coke oven and refinery gases, from electrolysis of salt solutions, eg, caustic chlorine production, and by electrolysis of water. In addition there are about 20 ammonia plants worldwide that use coal as a hydrogen source. [Pg.243]


See other pages where Products and amounts is mentioned: [Pg.365]    [Pg.27]    [Pg.162]    [Pg.580]    [Pg.365]    [Pg.27]    [Pg.162]    [Pg.580]    [Pg.25]    [Pg.337]    [Pg.695]    [Pg.208]    [Pg.2]    [Pg.216]    [Pg.461]    [Pg.112]    [Pg.42]    [Pg.44]    [Pg.387]    [Pg.392]    [Pg.410]    [Pg.423]    [Pg.449]    [Pg.479]    [Pg.517]    [Pg.33]    [Pg.125]    [Pg.182]    [Pg.225]    [Pg.231]    [Pg.231]   
See also in sourсe #XX -- [ Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 ]




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