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General scheme

In principle, these stages are dealt with in a consecutive manner. However, as further information on the system is revealed only during the course of work of an LCA, adjustments may become necessary and in consequence the stages might rather be reworked in an iterative process. [Pg.189]

ISO 14040 states an apphcation of LCA, for example, product development and improvement, strategic planning, or public pohcy making. LCA can be used to not [Pg.189]

The clear statement of goal and the intended application and audience (e.g., the commissioner of a study) is the main prerequisite of transparency of an LCA. At the same time, it is the basis for defining the systems boundary of modeling as to space and time as well as to the production systems investigated. [Pg.190]

The first phase may also incorporate procedural decisions of how to perform the LCA, for example, the incorporation of a review panel. Specifically, ISO 14040 asks whether the results are intended to be used in comparative assertions intended to be disclosed to the publid -, if so, a critical review, that is, a validation of the study by independent experts, has to be scheduled. [Pg.190]

The PFR of phenyl acetate, which affords o-hydroxyacetophenone, p-hydroxyacetophenone, and phenol, is a convenient model to illustrate the basic mechanistic aspects of the process. Initial homolysis of the carbonyl-oxygen bond from the singlet excited state gives an acetyFphenoxyl radical pair within a solvent cage, where spin is delocalized through the oxygen atom and the o- and [Pg.889]

Arene Chemistry Reaction Mechanisms and Methods for Aromatic Compounds, First Edition. Edited by Jacques Mortier. [Pg.889]

A similar mechanism is accepted for the photo-Claisen rearrangement of aromatic ethers, where allyl, benzyl, or other activated alkyl groups migrate from the oxygen to the o- andp-carbons of the aromatic ring [17]. [Pg.890]

Glucose + 2 + H2O Gluconic acid dissociates into hydrogen ion and gluconate anion  [Pg.201]


The main purpose of AUGUR4.2 expert ISI is the application to zones where some flaws (indications) had been revealed by scheduled manual ultrasonic inspections. Information provided by AUGUR 4.2 is used for decision-making further surveillance of these zones or corrective measures. The procedure of AUGUR 4.2 examination is included into the approved general scheme of ISI [1]... [Pg.195]

A3.13.4.3 IVR WITHIN THE GENERAL SCHEME OF ENERGY REDISTRIBUTION IN REACTIVE SYSTEMS... [Pg.1058]

We employ the general scheme presented above as a starting point in our discussion of various approaches for handling the R-T effect in triatomic molecules. We And it reasonable to classify these approaches into three categories according to the level of sophistication at which various aspects of the problem are handled. We call them (1) minimal models (2) pragmatic models (3) benchmark treatments. The criterions for such a classification are given in Table I. [Pg.489]

A further example is given below illustrating the use of a dibasic anhydride (succinic anhydride) the succinoylation reaction is a valuable one since it leads to aroyl carboxylic acids and ultimately to polynuclear hydrocarbons. This general scheme of synthesis of substituted hydrocarbons through the use of succinic anhydride is sometimes called the Haworth reaction. Thus a-tetralone (see below) may be reduced by the Clemmensen method to tetralin (tetrahydronaphthalene) and the latter converted into naphthalene either catal3d.ically or by means of sulphur or selenium (compare Section, VI,33). [Pg.726]

TABLE XI,9,1. GENERAL SCHEME FOR SEPARATION OF A WATER-INSOLUBLE MIXTURE... [Pg.1097]

As indicated in the general scheme below, butatrienes are the first products from base-induced 1,4-elinination of hydrogen and a suitable leaving group. The butatriene in general very readily undergoes isomerization into enynes, if sufficiently "acidic" protons are available (see Chapter 11 in Ref. 3a). In aprotic media cumulenic ethers are fixed as their lithio derivatives if an excess of alkyllithium is applied... [Pg.115]

Several 4-amino-2,5-disubstituted thiazoles (257) have been obtained recently (702, 756, 776, 814, 820) by a ring cyclization reaction of halogeno compounds with cyanamide derivatives (263) according to the general Scheme 135. [Pg.302]

Proof. The general scheme of reasoning is the same as that in the previous subsection we will pay attention to those details related to the interior nonsmooth boundary Tc. [Pg.304]

Proof. The general scheme of reasoning coincides with that used in the proof of Theorem 5.3 and our attention now focuses on details related to the nonsmoothness of the boundary. [Pg.318]

Fig. 3. General scheme for producing benzene, PX, and OX from catalytic reforming. Fig. 3. General scheme for producing benzene, PX, and OX from catalytic reforming.
General schemes for the identification of natural and synthetic fibers have been estabhshed by the Textile Institute and by the American Association of Textile Chemists and Colorists (8). A comprehensive treatment of burning, solvent, staining, microscopy, and density techniques has been given (9) and a general discussion of procedures for identifyiag synthetic fibers has been presented (10). [Pg.277]

TFEO is by fai the most reactive epoxide of the series. However, ail the reported perfluoroepoxides undergo similar ring-opening reactions. The most important reactions of these epoxides ate those with the fluoride ion or perfluoroalkoxides. The reaction of PIBO and the fluoride ion is an example (27). It also illustrates the general scheme of oligomerization of perfluoroepoxides (eq 5). [Pg.303]

The mechanism of anionic polymerization of cyclosiloxanes has been the subject of several studies (96,97). The first kinetic analysis in this area was carried out in the early 1950s (98). In the general scheme of this process, the propagation/depropagation step involves the nucleophilic attack of the silanolate anion on the sUicon, which results in the cleavage of the siloxane bond and formation of the new silanolate active center (eq. 17). [Pg.46]

Dyeing Mechanism. Unmodified polyester fibers are very hydrophobic and absorb only minimal amounts of water and are therefore only dyeable with hydrophobic disperse dyes. The mechanism of dyeing is by simple partition, the so-called soHd solution mechanism. The dyeing process can be described by the general scheme... [Pg.364]

Most ground state syntheses of oxaziridines and diaziridines follow the general scheme outlined for (242). Syntheses from starting materials containing a hetero-hetero bond, reported in the older literature, have not been confirmed. [Pg.227]

FIG. 16-9 General scheme of adsorbent particles in a packed bed showing the locations of mass transfer and dispersive mechanisms. Numerals correspond to mimhered paragraphs in the text 1, pore diffusion 2, solid diffusion 3, reaction kinetics at phase boundary 4, external mass transfer 5, fluid mixing. [Pg.1510]

Figure 8.9(b) illustrates a general scheme to achieve speed control through such couplings. These couplings, up to 90 kW, are easily available. [Pg.202]

Figure 8.9(b) A general scheme illustrating speed control by feedback control system using an eddy current coupling... [Pg.203]

Various specific experiments support this general scheme. For example, in 80% aqueous acetone, the rate constant for lacemization ofp-chlorobenzhydiyl p-nitrobenzoate (/ ) and that for exchange of label in the carbonyl group can both be measured. At 100 C, kjk = 2.3. [Pg.270]

The reaction is generally carried out in an alcoholic solvent, resulting in formation of the acetal the general scheme is called the Mattox rearrangement, and the yields are usually high. If a nonalcoholic solvent and acid are used, the aldehyde is obtained directly, but in lower yield. However, the use of zinc acetate as catalyst instead of an acid permits isolation of the aldehyde in ca. 50 % yield. Tire use of refluxing acetic acid alone... [Pg.215]

What is the likelihood of missing an industry specific hazard when using a general scheme ... [Pg.53]

Incorporation of a third heteroatom into S-N compounds is now well established, e.g. for C, Si P, As O Sn and Pb, together with the S2N2 chelates of Fe, Co, Ni, Pd and Pt mentioned on p. 725. The field is very extensive but introduces no new concepts into the general scheme of covalent heterocyclic molecular chemistry. Illustrative examples are in Fig. 15.44 and fuller... [Pg.736]

The general scheme for this type of tautomeric reaction is 310a 310b. [Pg.264]

The Diels-Alder reaction catalyzed by this chiral titanium catalyst 31 has wide generality (Scheme 1.53, 1.54, Table 1.22, 1.23). Acryloyl- and fumaroyl-oxazolidinones react with isoprene giving cycloadducts in high optical purity. 2-Ethylthio-l,3-buta-diene can also be successfully employed as the diene [42]. [Pg.36]

This fact can serve as a model system for the study of PS-MA-Lewis acid systems. Results obtained allow one to present the general scheme for the side chain modification of PS in the presence of Lewis acid in the following way ... [Pg.266]

General scheme of kerogen evolution from diagenesis to metagenesis in the van Krevelen diagram. [Pg.916]

Rydon and co-workers (73) have shown that the reaction of simple alcohols with triphenylphosphite methiodide and triphenylphosphite dihalides gives alkyl halides according to the general scheme. [Pg.180]

Fig. 115. General scheme of the processing of tantalum and niobium including treatment of fluoride compounds. Fig. 115. General scheme of the processing of tantalum and niobium including treatment of fluoride compounds.
Fig. 118. General scheme of liquid-liquid extraction of a system containing two dissolved components. Fig. 118. General scheme of liquid-liquid extraction of a system containing two dissolved components.

See other pages where General scheme is mentioned: [Pg.1056]    [Pg.2998]    [Pg.73]    [Pg.550]    [Pg.1091]    [Pg.274]    [Pg.462]    [Pg.239]    [Pg.248]    [Pg.248]    [Pg.564]    [Pg.186]    [Pg.355]    [Pg.276]    [Pg.238]    [Pg.426]    [Pg.154]    [Pg.225]    [Pg.132]    [Pg.593]    [Pg.15]   
See also in sourсe #XX -- [ Pg.260 ]




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Hartree-Fock scheme, general

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