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Organic compounds techniques

Grant, D.J.W and Higuchi, T. Group contributions in prediction.Satubility Behavior of Organic Compounds, Techniques of Chemistry, Vol. 21, John Wiley Sons, New York, NY, 1990, Chapter 7. [Pg.192]

Many semiempirical methods have been created for modeling organic compounds. These methods correctly predict many aspects of electronic structure, such as aromaticity. Furthermore, these orbital-based methods give additional information about the compounds, such as population analysis. There are also good techniques for including solvation elfects in some semiempirical calculations. Semiempirical methods are discussed further in Chapter 4. [Pg.284]

The wastewater produced in this process consists mostly of water used in cleanup and propellant conveyance and sorting operations. Techniques such as the use of activated carbon and biological treatment are being investigated for the removal of solvents and dissolved organic compounds (143). [Pg.44]

In addition to the Hquid—Hquid reaction processes, there are many cases in both analytical and industrial chemistry where the main objective of separation is achieved by extraction using a chemical extractant. The technique of dissociation extraction is very valuable for separating mixtures of weakly acidic or basic organic compounds such as 2,4-dichlorophenol [120-83-2] and 2,5-dichlorophenol [583-78-8] which are difficult to separate by... [Pg.62]

The deterrnination of hydrogen content of an organic compound consists of complete combustion of a known quantity of the material to produce water and carbon dioxide, and deterrnination of the amount of water. The amount of hydrogen present in the initial material is calculated from the amount of water produced. This technique can be performed on macro (0.1—0.2 g), micro (2—10 mg), or submicro (0.02—0.2 mg) scale. Micro deterrninations are the most common. There are many variations of the method of combustion and deterrnination of water (221,222). The oldest and probably most reUable technique for water deterrnination is a gravimetric one where the water is absorbed onto a desiccant, such as magnesium perchlorate. In the macro technique, which is the most accurate, hydrogen content of a compound can be routinely deterrnined to within 0.02%. Instmmental methods, such as gas chromatography (qv) (223) and mass spectrometry (qv) (224), can also be used to determine water of combustion. [Pg.430]

The two most useful supplementary techniques for the light microscope are EDS and FTIR microscopy. Energy dispersed x-ray systems (EDS) and Eourier-transform infrared absorption (ETIR) are used by chemical microscopists for elemental analyses (EDS) of inorganic compounds and for organic function group analyses (ETIR) of organic compounds. Insofar as they are able to characterize a tiny sample microscopically by PLM, EDS and ETIR ensure rapid and dependable identification when appHed by a trained chemical microscopist. [Pg.334]

Other. Numerous other supercritical fluid processes and techniques have been and are continuing to be developed. The novel spray appHcation UNICARB uses supercritical CO2 to replace volatile diluents in coating formulations, thereby reducing the volatile organic compound emissions by up to 80% (128). Rapid expansion of CO2 iu the spray can also improve the quaUty of coatings, thus performance benefits are obtained in a process developed for environmental advantages. [Pg.229]

Zone refining can be appHed to the purification of almost every type of substance that can be melted and solidified, eg, elements, organic compounds, and inorganic compounds. Because the soHd—Hquid phase equiHbria are not favorable for all impurities, zone refining often is combined with other techniques to achieve ultrahigh purity. [Pg.446]

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]

Nowadays all over the world considerable attention is focused on development of chemical sensors for the detection of various organic compounds in solutions and gas phase. One of the possible sensor types for organic compounds in solutions detection is optochemotronic sensor - device of liquid-phase optoelectronics that utilize effect of electrogenerated chemiluminescence. In order to enhance selectivity and broaden the range of detected substances the modification of working electrode of optochemotronic cell with organic films is used. Composition and deposition technique of modifying films considerably influence on electrochemical and physical processes in the sensor. [Pg.335]

Additions have been made to Chapters 1 and 2 in order to include more recent developments in techniques (e.g. Schlenk-type, cf p. 10), and chromatographic methods and materials. Chapter 3 still remains the core of the book, and lists in alphabetical order relevant information on ca 4000 organic compounds. Chapter 4 gives a smaller listing of ca 750 inorganic and metal-organic substances, and makes a total increase of ca 13% of individual entries in these two chapters. Some additions have also been made to Chapter 5. [Pg.624]

Hundreds of chemical species are present in urban atmospheres. The gaseous air pollutants most commonly monitored are CO, O3, NO2, SO2, and nonmethane volatile organic compounds (NMVOCs), Measurement of specific hydrocarbon compounds is becoming routine in the United States for two reasons (1) their potential role as air toxics and (2) the need for detailed hydrocarbon data for control of urban ozone concentrations. Hydrochloric acid (HCl), ammonia (NH3), and hydrogen fluoride (HF) are occasionally measured. Calibration standards and procedures are available for all of these analytic techniques, ensuring the quality of the analytical results... [Pg.196]

Historically, measurements have classified ambient hydrocarbons in two classes methane (CH4) and all other nonmethane volatile organic compounds (NMVOCs). Analyzing hydrocarbons in the atmosphere involves a three-step process collection, separation, and quantification. Collection involves obtaining an aliquot of air, e.g., with an evacuated canister. The principal separation process is gas chromatography (GC), and the principal quantification technique is wdth a calibrated flame ionization detector (FID). Mass spectroscopy (MS) is used along with GC to identify individual hydrocarbon compounds. [Pg.202]

Within 6 months after enactment of the Qean Air Act Amendments of 1990, and at least every 3 years thereafter, the Administrator shall review and, if necessary, revise, the methods ( emission factors ) used for purposes of this Act to estimate the quantity of emissions of carbon monoxide, volatile organic compounds, and oxides of nitrogen from sources of such air pollutants (including area sources and mobile sources). In addition, the Administrator shall permit any person to demonstrate improved emissions estimating techniques, and following approval of such techniques, the Administrator shall authorise the use of such techniques. Any such technique may be approved only after appropriate public participation. Until the Administrator has completed the revision required by this section, nothing in this section shall be construed to affect the validity of emission factors established by the Administrator before the date of the enactment of the Clean Air Act Amendments of 1990. [Pg.405]


See other pages where Organic compounds techniques is mentioned: [Pg.17]    [Pg.211]    [Pg.17]    [Pg.1708]    [Pg.22]    [Pg.1702]    [Pg.17]    [Pg.211]    [Pg.17]    [Pg.1708]    [Pg.22]    [Pg.1702]    [Pg.150]    [Pg.1028]    [Pg.1028]    [Pg.103]    [Pg.115]    [Pg.20]    [Pg.214]    [Pg.639]    [Pg.442]    [Pg.274]    [Pg.321]    [Pg.414]    [Pg.443]    [Pg.401]    [Pg.144]    [Pg.162]    [Pg.226]    [Pg.226]    [Pg.194]    [Pg.530]    [Pg.458]    [Pg.14]    [Pg.9]    [Pg.452]    [Pg.452]    [Pg.16]    [Pg.29]    [Pg.192]    [Pg.391]    [Pg.396]   
See also in sourсe #XX -- [ Pg.47 ]




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Compounding techniques

Extraction techniques, for semivolatile organic compounds

Organization techniques

Separation techniques soluble organic compounds

Separation techniques volatile organic compound

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