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Addition direction

It also is possible to make a standard addition directly to the sample after measuring Ssamp (Figure 5.6). In this case, the final volume after the standard addition is Vo + Vs and equations 5.5-5.7 become... [Pg.112]

In addition, directive effects have been reported to operate for A4 26 A -steroids. On the other hand, both the 3a- and... [Pg.5]

The reaction of hexa-2,4-diyn-l-al (64) with mercaptoacetaldehyde leads to 2-formyl-5-(prop-l-ynyl)thiophene (65). The addition direction is governed by the aldehyde group via intramolecular aldol condensation in the intermediate (77HOU947). [Pg.175]

The absence of overlapping of bands of various matrix-isolated compounds and the possibility of freezing highly reactive intermediates make this method very convenient for the direct study of reaction mechanisms. Additionally, direct IR spectroscopy of intermediates allows estimation of important structural parameters, e.g. valence force fields, which show the character of bonds in these species. [Pg.6]

Food additives are authorized at the EU level for all 15 member states, as well as for Norway and Iceland. The use of food additives is controlled by legislation that is harmonized across the EU. Domestic legislation in each member state is based on the various additive directives incorporated into specific national legislation. The community legislation on food additives consists of the following directives ... [Pg.575]

Council Directive 89/107/EEC, as amended by Directive 94/34/EC ° — This framework directive provides umbrella legislation under which the individual additives directives are developed. It includes a definition of a food additive, exclusions from the scope of the definition, and a list of food additive categories, one of which is colors. Additionally, general criteria for use of food additives are described. ... [Pg.575]

The bridging by bromine prevents rotation about the remaining bond and back-side nucleophilic opening of the bromonium ion by bromide ion leads to the observed anti addition. Direct evidence for the existence of bromonium ions has been obtained from NMR measurements.31 A bromonium ion salt (with Br3 as the counterion) has been isolated from the reaction of bromine with the very hindered alkene adamantylide-neadamantane.32... [Pg.299]

When the flame is lit, adjust the gas flow and oxygen flow so that the flame is blue with an inner light-blue cone. A yellow flame is too cool and needs more oxygen. Your teacher may have additional directions on the operation of the Bunsen burner. [Pg.6]

The results thus show that ammonia DCI-MS/MS using a triple quadrupole mass spectrometer is a convenient method for the detection of additives in PE samples. The softness and selectivity provided by ammonia DCI in combination with the specificity provided by CID, demonstrate great potential for identification of additives directly from PE extracts. The utility of DCI in the quantitative analysis of additives has still to be explored. DCI-MS/MS (B/E) with high collision... [Pg.366]

In the deformulation of PE/additive systems by mass spectrometry, much less fragmentation was observed with DCI-MS/MS using ammonia as a reagent gas, than with FAB-MS [69]. FAB did not detect all the additives in the extracts. The softness and the lack of matrix effect make ammonia DCI a better ionisation technique than FAB for the analysis of additives directly from the extracts. Applications of hyphenated FAB-MS techniques are described elsewhere low-flow LC-MS (Section 7.3.3.2) and CE-MS (Section 7.3.6.1) for polar nonvolatile organics, and TLC-MS (Section 7.3.5.4). [Pg.371]

Selection of a suitable ionisation method is important in the success of mixture analysis by MS/MS, as clearly shown by Chen and Her [23]. Ideally, only molecular ions should be produced for each of the compounds in the mixture. For this reason, the softest ionisation technique is often the best choice in the analysis of mixtures with MS/MS. In addition to softness , selectivity is an important factor in the selection of the ionisation technique. In polymer/additive analysis it is better to choose an ionisation technique which responds preferentially to the analytes over the matrix, because the polymer extract often consists of additives as well as a low-MW polymer matrix (oligomers). Few other reports deal with direct tandem MS analysis of extracts of polymer samples [229,231,232], DCI-MS/MS (B/E linked scan with CID) was used for direct analysis of polymer extracts and solids [69]. In comparison with FAB-MS, much less fragmentation was observed with DCI using NH3 as a reagent gas. The softness and lack of matrix effect make ammonia DCI a better ionisation technique than FAB for the analysis of additives directly from the extracts. Most likely due to higher collision energy, product ion mass spectra acquired with a double-focusing mass spectrometer provided more structural information than the spectra obtained with a triple quadrupole mass spectrometer. [Pg.403]

For this purpose, the WEEE Directive has been complemented with an additional directive that limits the use of certain pollutants in these products. The EC Directive 2002/95/EC on the Restriction of the use of certain Hazardous Substances in electrical and electronic equipment (RoHS Directive) ([7], recast 2011 [9]) restricts the use of the six harmful substances/substance families lead, mercury, hexavalent chromium, polybrominated biphenyls (PBB), and polybrominated diphenyl ethers (PBDE) to 0.1% and cadmium to 0.01% w/w per homogenous material in equipment and components, but with several exemptions for a wide range of applications (Annex III and IV). [Pg.140]

Freund s incomplete adjuvant (FIA) is a similar product. It differs from FCA in that it lacks the mycobacterial component and, consequently, displays somewhat lesser adjuvanticity. The mode of action of FIA is largely attributed to depot formation. The mycobacterial components in FCA have additional direct immunostimulatory activities. Although it is one of the most potent adjuvant substances known, FCA is too toxic for human use. [Pg.414]

Miscellaneous Food Additives Directive 95/2/EC (e.g. preservatives, antioxidants, emulsifiers, stabilisers, thickeners, flavour enhancers, acidity regulators, etc.)... [Pg.5]

Additives, other than Sweeteners and Colours (Directive 95/2/EC) -Miscellaneous Additives Directive... [Pg.249]

Mathematical models for Ca + signaling were subsequently developed in two additional directions. First, waves of intra- or intercellular Ca + can be modeled by incorporating the diffusion of cytosolic Ca + or the passage of Ca + or InsPs from cell to cell through gap junctions [62-65]. While most models for... [Pg.262]


See other pages where Addition direction is mentioned: [Pg.313]    [Pg.427]    [Pg.187]    [Pg.672]    [Pg.796]    [Pg.102]    [Pg.38]    [Pg.127]    [Pg.514]    [Pg.42]    [Pg.186]    [Pg.19]    [Pg.366]    [Pg.406]    [Pg.493]    [Pg.542]    [Pg.149]    [Pg.98]    [Pg.230]    [Pg.295]    [Pg.75]    [Pg.94]    [Pg.242]    [Pg.205]    [Pg.104]    [Pg.127]    [Pg.298]    [Pg.22]    [Pg.27]    [Pg.251]    [Pg.5]    [Pg.136]    [Pg.131]    [Pg.69]    [Pg.102]   
See also in sourсe #XX -- [ Pg.16 , Pg.17 , Pg.685 , Pg.707 ]




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1,4-addition directed

Addition charge-directed

Addition reactions direct

Addition reactions, gas-phase radical directive effects

Addition template-directed

Additional research directions

Alkenes heteroatom-directed addition

Alkoxide-directed 1,6-addition

Amines direct addition

Chelation directed addition

Chinensin via ortho directed addition

Direct Conjugate Additions via Enamine Activation

Direct Determination of Additives in Polymers and Rubbers

Direct Oxidative Addition of Magnesium to Organic Halides

Direct Oxidative Addition of Reactive Zinc to Functionalized Alkyl, Aryl, and Vinyl Halides

Direct addition

Direct addition

Direct additives

Direct additives

Direct additives to food

Direct and indirect food additives

Direct catalysis alkyne/alkene additions

Direct conjugate addition via C-H activation nonan-2-one

Direct ligand addition, transition metal

Direct potentiometry standard addition method

Direct potentiometry standard additions

Directed Conjugate Addition Reactions

Directed aldol addition

Directive effects in gas-phase radical addition reactions

Functionalized Grignard reagents direct oxidative addition

Hydrogen cyanide conjugate vs. direct addition

In Situ Direct Generation of Enolates and Their Asymmetric Aldol Addition Reactions

Incorporation of Liquid Additives and Dispersions by Direct Addition

Intramolecular addition reactions amines, direct irradiation

Organic halides direct oxidative addition

Oxazoline directed nucleophilic additions

Phosphoranes, acylcharge-directed conjugate addition

Preservatives Food Additives Directive

Proline-catalyzed direct aldol additions

Secondary direct additives

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