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Sulfur dioxide binding

Weeks, C. (1969). Production of sulfur dioxide-binding compounds and of sulfur dioxide by two Saccharomyces yeasts. Am. J. Enol. Vitic., 20, 32-39. [Pg.56]

Table 8.7. Sulfur-dioxide binding sugar derivatives (based on Burroughs and Sparks, 1964 and 1973)... Table 8.7. Sulfur-dioxide binding sugar derivatives (based on Burroughs and Sparks, 1964 and 1973)...
The improvement in must quality is not only limited to an increase in potential alcohol content. These musts have the same characteristics as their late-harvested counterparts they are more difficult to ferment the risk of volatile acidity production is greater and the sulfur dioxide binding rate is higher. However, these ciyoextraction selected wines are clearly preferred over the control wines (Chauvet et al, 1986) due to their increased concentration, finesse and distinctiveness. [Pg.454]

Two-component methods represent the most widely applied principles in sulfone syntheses, including C—S bond formation between carbon and RSOz species of nucleophilic, radical or electrophilic character as well as oxidations of thioethers or sulfoxides, and cheletropic reactions of sulfur dioxide. Three-component methods use sulfur dioxide as a binding link in order to connect two carbons by a radical or polar route, or use sulfur trioxide as an electrophilic condensation agent to combine two hydrocarbon moieties by a sulfonyl bridge with elimination of water. [Pg.166]

Sulfurdiimines RN=S=NR and thionitrites RN=S=0 (R = alkyl, aryl) have been relatively little investigated as ligands in metal complexes. This lack of attention has been little deserved as both types of ligands have interesting ambident coordination properties, since they may bind via N, S, O, the 7t-N=S or jr-S=0 bond for example. They may be compared with allenes and naturally also with the isostructural and the isoelectronic sulfur dioxide 0=S—O.13 We will first discuss some relevant data concerning RNSNR and RNSO and subsequently the properties of the metal complexes. [Pg.190]

Fig. 7.7. Sulfonation of coniferaldehyde end groups and substituted structures containing a-carbonyl groups (see Gellerstedt, 1976). At lower temperatures aldehyde end groups can bind sulfur dioxide because of the formation of a-hydroxysulfonic acid. Fig. 7.7. Sulfonation of coniferaldehyde end groups and substituted structures containing a-carbonyl groups (see Gellerstedt, 1976). At lower temperatures aldehyde end groups can bind sulfur dioxide because of the formation of a-hydroxysulfonic acid.
Bindings covered with vegetable-tanned leather are washed with pure toilet soap, saddle soap, or mild, high quality surgical toilet soap and a 7-10% solution of potassium lactate. 0.25% of p-nitrophenol can be added as a fungicide, but this is not necessary if the temperature and relative humidity are constantly satisfactory (see p. 5). The lactate, when applied to new vegetable-tanned leather, is thought to protect the leather from the deleterious action of sulfuric acid which usually forms in leather when sulfur dioxide is absorbed. It is. probable that it has little efficacy once chemical deterioration has started, and for some years doubt has been cast on its effectiveness, even on new leather, despite favorable results in laboratory tests. However, it is used, and its use is advocated just in case it is beneficial. [Pg.21]

Most inhaled sulfur dioxide is absorbed into the bloodstream, widely distributed throughout the body, and rapidly metabolized to sulfate by the sulfite oxidase enzyme system. Sulfate is then primarily excreted by way of the urinary tract (HSDB 2000). However, results from studies that used 35S indicate that some residual sulfur dioxide can persist in the respiratory system for a week or more after exposure possibly as a result of the sulfur binding with protein (Yokoyama et al. 1971 as cited in Costa and Amdur 1996). [Pg.272]

The bis(tricyclohexylphosphine) complexes are 14-electron species and are highly reactive. They are easily oxidized by air,48 and even decompose when stored in an inert atmosphere. However, they will readily coordinate an additional small ligand. Many of these small ligands bind through carbon and are, therefore, outside the scope of this review. Both dinitrogen48,49 and sulfur dioxide form adducts (equations 9 and 10).so... [Pg.907]

X-ray crystallography has shown that the S02 ligand binds through both sulfur and oxygen.1310,1316 The sulfur dioxide complex (132) is easily oxidized by dioxygen in benzene solution to form the sulfato complex [Rh(N0)(S04)(PPh3)2].1310,1316 The product distribution when 1802 is the reactant implies that an intermediate sulfur bound sulfato complex is formed.1316... [Pg.1068]

Although the study of sulfur dioxide-transition metal coordination chemistry is an area of relatively recent intensive pursuit, structural information now spans a large number of stereochemically distinct coordination situations. The types of M-SO2 binding which have been identified, excluding insertion compounds and compounds containing SO2 bridging metal centers, are shown in Fig. 1. Several examples of complexes containing each type... [Pg.48]

An X-ray structure determination Cmcm i i= 0.061 of pale yellow crystals of compound B obtained from the sulfur dioxide reaction, shows a neutral complex of symmetry mm2 to be present in the solid. The anionic part of the molecule consists of two anellated l,2-dihydro-5-oxo-l,2,4-triphosphol-3-olate rings which share the central P-P group (P-P 215.3 P-C 189.1 P-C 178.4 C-O 123.9pm C-P-P 98.4° C-P-C 91.2° C P C 98.7°). The lithium cations are coordinated square pyramidally (Li-0 193.5 to 209.1 pm), each binding a 1,2-dimethoxyethane and a tetrahydrofiiran ligand in addition [30]. [Pg.171]

Model examples will be the study of the competitive clustering of ammonia and water on the ammonium ion and the determination of the characteristics of binding of water, carbon dioxide and sulfur dioxide on the nitrite ion, in relation to gas phase experimental measurements. [Pg.25]

As soon as the fermentation is stopped sulfur dioxide is added to bring the free SO2 concentration to 25 ppm for the subsequent clarification steps. This prevents oxidation, assists in biological stabilization, and binds aldehydes in the new wine. The binding of aldehydes (mostly acetaldehyde) improves the taste of the wine. [Pg.524]

Under this convention, member countries agreed to a non-binding commitment to aim to reduce transboundary air pollution. Focusing on the worst identified offender of air pollution, CLRTAP calls for an extensive international program for monitoring and evaluating air movement patterns of sulfur dioxide. This convention established a base for air pollution policy that mandated international cooperation in research, development, and publishing of emission levels, a trend the European Community has incorporated into its own subsequent policies. [Pg.326]


See other pages where Sulfur dioxide binding is mentioned: [Pg.126]    [Pg.126]    [Pg.233]    [Pg.168]    [Pg.278]    [Pg.216]    [Pg.269]    [Pg.297]    [Pg.316]    [Pg.351]    [Pg.635]    [Pg.470]    [Pg.97]    [Pg.50]    [Pg.93]    [Pg.21]    [Pg.33]    [Pg.52]    [Pg.53]    [Pg.78]    [Pg.79]    [Pg.758]    [Pg.134]    [Pg.269]    [Pg.474]    [Pg.17]    [Pg.232]    [Pg.18]    [Pg.436]    [Pg.829]   


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