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Organic compound properties

Activated carbon is commonly acknowledged to be very efficient as a VOC adsorbent. However, in the last decade, interests arose to develop new materials, such as alumni-silicate molecular sieve, towards operating conditions for which activated carbon was inappropriate due to its inflammability and adsorption capacity dependence on effluent relative humidity. Apart from hydrophobicity, the advantages of High Silica Zeolites (HSZ) are notably a thermal and chemical stability, a high steric selectivity and a complete regeneration at low temperatures [11]. Yet, for adsorption and separation processes development, organic compounds properties impact on adsorption and crystalline framework influence on selectivity are to be clarified and efficiently modeled. [Pg.259]

Properties of surface Properties of organic compound Properties of medium... [Pg.164]

Alen R. Collection of organic compounds - properties and uses. Helsinki (Finland) Consalen Consulting 2009.1370 p [in Finnish]. [Pg.123]

Vassiliev PM (2000) Strategies of computer prediction of organic compound properties. In Proceedings of International scientific and technical conference Modem information technology. Section Information technologies in scientific experiments , PenzTI, Penza, P7... [Pg.428]

If you want to get your hands on NMR or IR data right away for common organic compounds, Properties of Organic Compounds and the Handbook of Data on Organic Compounds are very useful. [Pg.23]

Typical organic acids contain the --C(0)0H group, but many other acid groupings, e.g. the sulphonic -S(0)20H give acidic properties to organic compounds. Phenols have acidic properties and are classified with enols as pseudo-acids. [Pg.12]

Lydersen, A.L. (1955), Estimation of critical properties of organic compounds by the method of group contributions . Uniu. Wisconsin Coll., Eng. Exp. Stn. report No. 4, Madison, Wl. [Pg.457]

The abbreviation QSAR stands for quantitative structure-activity relationships. QSPR means quantitative structure-property relationships. As the properties of an organic compound usually cannot be predicted directly from its molecular structure, an indirect approach Is used to overcome this problem. In the first step numerical descriptors encoding information about the molecular structure are calculated for a set of compounds. Secondly, statistical methods and artificial neural network models are used to predict the property or activity of interest, based on these descriptors or a suitable subset. A typical QSAR/QSPR study comprises the following steps structure entry or start from an existing structure database), descriptor calculation, descriptor selection, model building, model validation. [Pg.432]

On pp. 410—415 Tables are given showing some of the properties of the simpler members of certain classes of organic compounds. These tables should be useful to the elementary student working with a limited range of compounds. It must be emphasised that these tables serve primarily to summarise some of the detailed descriptions given in the foregoing sections, and should be used w-hen the student is familiar with these sections. [Pg.409]

Location of the compound within a class (or homologous series) of compounds. Reference to the literature or to tables of the physical properties of the class (or classes) of organic compounds to which the substance has been assigned, will generally locate a number of compounds which boil or melt within 6° of the value observed for the unknown. If other physical properties e.g., refractive index and density for a hquid) are available, these will assist in deciding whether the unknown is identical with one of the known compounds. In general, however, it is more convenient in practice to prepare one, but preferably two, crystalhne derivatives of the substance. [Pg.1027]

Separations based upon differences in the physical properties of the components. When procedures (1) or (2) are unsatisfactory for the separation of a mixture of organic compounds, purely physical methods may be employed. Thus a mixture of volatile liquids may be fractionally distilled (compare Sections 11,15 and 11,17) the degree of separation may be determined by the range of boiling points and/or the refractive indices and densities of the different fractions that are collected. A mixture of non-volatile sohds may frequently be separated by making use of the differences in solubilities in inert solvents the separation is usually controlled by m.p. determinations. Sometimes one of the components of the mixture is volatile and can be separated by sublimation (see Section 11,45). [Pg.1092]

Organic chemistry demands much from chlorine, both as an oxidizing agent and in substitution, since it often brings many desired properties in an organic compound when substituted for hydrogen, as in one form of synthetic rubber. [Pg.42]

Appendix 1 lists selected physical properties for repre sentative alkanes as well as members of other families of organic compounds... [Pg.80]

Combustion in air is of course a chemical property of ethers that IS shared by many other organic compounds Write a balanced chemical equa tion for the complete combustion (in air) of diethyl ether... [Pg.673]

References D. D. Wagman, et ah, The NBS Tables of Chemical Thermodynamic Properties, in J. Phys. Chem. Ref. Data, 11 2,1982 M. W. Chase, et ah, JANAF Thermochemical Tables, 3rd ed., American Chemical Society and the American Institute of Physics, 1986 (supplements to JANAF appear in J. Phys. Chem. Ref. Data) Thermodynamic Research Center, TRC Thermodynamic Tables, Texas A M University, College Station, Texas I. Barin and O. Knacke, Thermochemical Properties of Inorganic Substances, Springer-Verlag, Berlin, 1973 J. B. Pedley, R. D. Naylor, and S. P. Kirby, Thermochemical Data of Organic Compounds, 2nd ed.. Chapman and Hall, London, 1986 V. Majer and V. Svoboda, Enthalpies of Vaporization of Organic Compounds, International Union of Pure and Applied Chemistry, Chemical Data Series No. 32, Blackwell, Oxford, 1985. [Pg.533]


See other pages where Organic compound properties is mentioned: [Pg.58]    [Pg.988]    [Pg.101]    [Pg.428]    [Pg.58]    [Pg.988]    [Pg.101]    [Pg.428]    [Pg.18]    [Pg.166]    [Pg.179]    [Pg.226]    [Pg.231]    [Pg.1904]    [Pg.1904]    [Pg.2807]    [Pg.407]    [Pg.495]    [Pg.513]    [Pg.539]    [Pg.596]    [Pg.1]    [Pg.590]    [Pg.32]    [Pg.149]    [Pg.150]    [Pg.1026]    [Pg.1028]    [Pg.1057]    [Pg.1193]    [Pg.99]    [Pg.109]    [Pg.115]    [Pg.1]    [Pg.7]    [Pg.57]    [Pg.1283]    [Pg.1286]   
See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.363 ]




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