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Bisulfite effect

Embs, R.J., and P. Markakis. 1969. Bisulfite effect on the chemistry and activity of horseradish peroxidase. J. FoodSci. 34 500-501. [Pg.321]

Heavy metals often can be removed effectively by chemical precipitation in the form of carbonates, hydroxides, or sulfides. Sodium carbonate, sodium bisulfite, sodium hydroxide, and calcium oxide are all used as precipitation agents. The solids precipitate as a floe containing a large amount of water in the structure. The precipitated solids need to be separated by thickening or filtration and recycled if possible. If recycling is not possible, then the solids are usually disposed of to a landfill. [Pg.311]

Sulfur Dioxide and Sulfites. Sulfur dioxide [7446-09-5], SO2, sodium bisulfite [15181-46-1], NaHSO, and sodium metabisulfite [23134-05-6] ate effective against molds, bacteria, and certain strains of yeast. The wine industry represents the largest user of sulfites, because the compounds do not affect the yeast needed for fermentation. Other appHcations include dehydrated fmits and vegetables, fmit juices, symps and concentrates, and fresh shrimp (79). Sulfites ate destmctive to thiamin, and cannot be used in foods, such as certain baked goods, that ate important sources of this vitamin. [Pg.443]

A.lkyl Sulfosuccinate Half Asters. These detergents are prepared by reaction of maleic anhydride and a primary fatty alcohol, followed by sulfonation with sodium bisulfite. A typical member of this group is disodium lauryl sulfosucciaate [26838-05-1]. Although not known as effective foamers, these surfactants can boost foams and act as stabilizers when used ia combination with other anionic surfactants. In combination with alkyl sulfates, they are said to reduce the irritation effects of the latter (6). [Pg.450]

YeUowing of wool can occur during dyeing, depending on pH, temperature and time, and chlorinated wools ate especially sensitive. Bleaching agents that can be added to the dyebath have been developed based on sodium bisulfite and hydroxylamine sulfate (108). Addition of hydrogen peroxide to the dyebath after exhaustion can also be effective. [Pg.349]

Alternatively, the metathesis can be effected by sulfites or bisulfites that convert cystine iato one cysteiae residue and one thiosulfate (Bunte salt) residue. Hair waving based on sulfites is slower than that based on mercaptans and is more likely to cause changes ia hair color. [Pg.303]

Common impurities found in aldehydes are the corresponding alcohols, aldols and water from selfcondensation, and the corresponding acids formed by autoxidation. Acids can be removed by shaking with aqueous 10% sodium bicarbonate solution. The organic liquid is then washed with water. It is dried with anhydrous sodium sulfate or magnesium sulfate and then fractionally distilled. Water soluble aldehydes must be dissolved in a suitable solvent such as diethyl ether before being washed in this way. Further purification can be effected via the bisulfite derivative (see pp. 57 and 59) or the Schiff base formed with aniline or benzidine. Solid aldehydes can be dissolved in diethyl ether and purified as above. Alternatively, they can be steam distilled, then sublimed and crystallised from toluene or petroleum ether. [Pg.63]

Decontaminants. Area decontamination is not required as CS has a short duration, of effectiveness. Personnel exposed to CS may shower as necessary however, when CS dust or particles are on the skin, showering should be delayed for 6 hours to prevent stinging and reddening of the skin. Individuals affected by CS should move to fresh air, face the wind, and remain well spaced and should not rub their eyes. To remove accidental gross contamination, personnel should remove clothing and immediately flush body with copious amts of water to remove most of the agent apply 5% Na bisulfite soln to remove remainder (except in or around eyes) and then rinse body... [Pg.408]

The effect of various types of inhibitors with respect to structure and solubility on the formation of N-Nitrosodiethanolamine was studied in a prototype oil in water anionic emulsion, Nitrosation resulted from the action of nitrite on diethanolamine at pH 5.2-5.A, Among the water soluble inhibitors incorporated into the aqueous phase, sodium bisulfite and ascorbic acid were effective. Potassium sorbate was much less so. The oil soluble inhibitors were incorporated into the oil phase of the emulsion. [Pg.149]

Sulfoalkylated naphthol compounds are effective as dispersants in aqueous cement slurries. The compounds can also be applied in an admixture with water-soluble inorganic compounds of chromium to provide additives of increased overall effectiveness. Particularly suitable are sodium chromate or ammonium dichromate. a-Naphthol is reacted in an alkaline aqueous medium with formaldehyde to create condensation products. The aldehyde can be reacted with bisulfite to produce sulfoalkylated products [1404,1410]. [Pg.310]

Stablizers. Stabilizers are ingredients added to a formula to decrease the rate of decomposition of the active ingredients. Antioxidants are the principal stabilizers added to some ophthalmic solutions, primarily those containing epinephrine and other oxidizable drugs. Sodium bisulfite or metabisulfite are used in concentration up to 0.3% in epinephrine hydrochloride and bitartrate solutions. Epinephrine borate solutions have a pH range of 5.5 7.5 and offer a more difficult challenge to formulators who seek to prevent oxidation. Several patented antioxidant systems have been developed specifically for this compound. These consist of ascorbic acid and acetylcysteine, and sodium bisulfite and 8-hydroxyquinoline. Isoascorbic acid is also an effective antioxidant for this drug. Sodium thiosulfate is used with sodium sulfacetamide solutions. [Pg.458]

A flowsheet for the Wellman-Lord process is shown in Figure 25.26. Again the gas stream with S02 enters a scrubber into which is sprayed a sodium sulfite solution. This then goes to an evaporator/crystallizer to crystallize out the resulting sodium bisulfite, which converts the sodium bisulfite back to sodium sulfate, releasing the S02. The crystals are dissolved in water and recycled to the scrubber. The effect of the Wellman-Lord process is to produce a concentrated S02 stream from a dilute S02 stream. The resulting concentrated S02 still needs to be treated. [Pg.568]

Braga, T.G. "Effects of Commonly Used Oilfield Chemicals on the Rate of Oxygen Scavenging by Sulfite/Bisulfite," SPE Production Engineering, May 1987, 137-142. [Pg.104]

In terms of economical synthetic approaches to indoles, the synthesis of this heterocycle from anilines and trialkylammonium chlorides was effected in an aqueous medium (H20-dioxane) at 180°C in the presence of a catalytic amount of ruthenium(III) chloride hydrate and triphenylphosphine together with tin(II)chloride <00TL1811>. Muchowski devised a novel synthetic route to indole-4-carboxaldehydes and 4-acetylindoles 86 via hydrolytic cleavage of W-alkyl-5-aminoisoquinolinium salts 85 to homophthaldehyde derivatives upon heating in a two phase alkyl acetate-water system containing an excess of a 2 1 sodium bisulfite-sodium sulfite mixture <00JHC1293>. [Pg.118]

The enhancement effect of magnesia on S02 removal is caused by increased concentrations of basic sulfite species, SO3 and MgS0 , that react with the strong acid S02(aq) to form bisulfite ion, HSO3. [Pg.266]

In a perfectly-buffered solution the SO2 vapor pressure will be directly proportional to the total concentration of SO2 and bisulfite, giving a linear equilibrium relationship. In simple alkali sulfite solution without added buffer, the equilibrium relationship is highly nonlinear, because H-1" accumulates as SO2 is absorbed. Under these conditions is it not possible to carry out reversible SO2 absorption/stripping in a simple system, resulting in greater steam requirements than expected with a linear equilibrium relationship. Weak acid buffers such as sodium citrate have been proposed to "straighten" the equilibrium relationship and thereby reduce ultimate steam requirements (Jl, 2, 7). Citrate buffer is attractive because it is effective over a wide range, from pH 2.5 to pH 5.5 in concentrated solutions. [Pg.269]

Series 8 in combination with earlier series was intended to provide data on the effects of total anion concentration. The results are internally consistant with the correlation, having a standard deviation of about 15% around the mean error. However the measured values of PSO2 were about 40% lower than the general correlation. An SO2 analyzer, rather than iodine titration, was used to determine SO2 gas concentration from the saturator. The analyzer was calibrated with dry SO2/N2 span gas. In later experiments it was shown that humid gas gives a lower analyzer response. With constant fraction neutralization increased anionic concentration increases PSO2 because pH decreases faster than effective bisulfite activity. [Pg.284]

The dependence on fraction neutralization and total anion concentration should reflect the extent to which the bisulfite activity is not proportional to total dissolved SO2. As expected, the dependence on f is quite small, since dissolved SO2 is present primarily as bisulfite at pH 3.5 to 5.0. The effect of anion concentration is in the direction expected since bisulfite activity would be reduced by ion pairing in more concentrated solutions. [Pg.284]

All reactions were stirred at speeds in excess of 500 rpm to eliminate any effects due to stirring rate (17). Initially, polymerizations were conducted at 60 C in cyclohexanone solution. When 18-crown-6 was used as the catalyst, little difference was observed in the presence or absence of sodium bisulfite. [Pg.121]

Phenylcalcium iodide metallates dibenzothiophene in the 3-position however, it has no effect on the corresponding sulfone. Mercuration of dibenzothiophene has been accomplished by adding mercuric acetate to a melt of dibenzothiophene, but the position of mercuration was not established. Mercuric nitrate or bisulfite give no identifiable products. An unsuccessful attempt to metallate dibenzothiophene with cross-linked poly(p-lithiost5Tene) in ether has been recorded. ... [Pg.284]

Epidural/Intrathecal administration Limit epidural or intrathecal administration of preservative-free morphine and sufentanil to the lumbar area. Intrathecal use has been associated with a higher incidence of respiratory depression than epidural use. Asthma and other respiratory conditions The use of bisulfites is contraindicated in asthmatic patients. Bisulfites and morphine may potentiate each other, preventing use by causing severe adverse reactions. Use with extreme caution in patients having an acute asthmatic attack, bronchial asthma, chronic obstructive pulmonary disease or cor pulmonale, a substantially decreased respiratory reserve, and preexisting respiratory depression, hypoxia, or hypercapnia. Even usual therapeutic doses of narcotics may decrease respiratory drive while simultaneously increasing airway resistance to the point of apnea. Reserve use for those whose conditions require endotracheal intubation and respiratory support or control of ventilation. In these patients, consider alternative nonopioid analgesics, and employ only under careful medical supervision at the lowest effective dose. [Pg.883]

More definite evidence for the transient existence of the un-cyclized l-(jS-aminoethyl)-3,4-benzoquinones has been obtained recently by Kodja and Bouchilloux,77 78 who noted that a transient yellow color (Amax ca. 385 mp) was occasionally observed during the enzymic oxidations of catecholamines (particularly in unbuffered systems at low temperatures). This phenomenon was probably due to the formation of the transient o-quinones. (The absorption maximum of o-benzoquinone, the effective chromophore of the open-chain quinones, is known to occur at ca. 390 mp.79) An absorption maximum at 390 mp is characteristic of the formation of the dopa-quinone chromophore during oxidation of small C -terminal tyrosine peptides in the presence of tyrosinase.37 48 Similar spectroscopic features were observed when the oxidations were carried out with lead dioxide in sulfuric acid solutions (pH> 1). If the initial oxidation was carried out for a short period of time, it was possible to regenerate the original catecholamines by reduction (e.g. with sodium bisulfite, potassium iodide, and zinc powder) and to show that the 385 mp peak disappeared.77,78 Kodja and Bouchilloux were also able to identify 2,4-dinitrophenylhydrazones of several of the intermediate non-cyclized quinones by paper chromatography and spectroscopy (Amax n weakly acid solution ca. 350 mp with a shoulder at ca. 410 mp).77,78... [Pg.220]

The 7-iodoaminochromes also form addition products with sodium bisulfite, although formation of these adducts usually appears to be accompanied by some deiodination, with the consequent formation of the corresponding deiodinated complexes.155 The 7-iodonor-adrenochrome-sodium bisulfite addition product has been reported to be more stable in this respect (i.e. it shows less tendency to deiodinate) than the corresponding 7-iodoadrenochrome adduct.119 Although it has not proved possible to demonstrate effectively the presence of both the 7-iodoaminochrome complex and the corres-... [Pg.264]

Nitrous acid, formed from organic precursors such as nitrosamines and from nitrite and nitrate salts, is a potent accelerator of the deamination of bases. Bisulfite has similar effects. Both agents are used as preservatives in processed foods to prevent the growth of toxic bacteria. They do not appear to increase cancer risks... [Pg.294]

Bisulfite ions, HS03", condense with anthocyanins. This reversible reaction decreases the color by forming a colorless compound (12) (16). This effect is less evident in strongly acid media because the bisulfite ions are not as numerous since they are being converted to the undissociated acid. This property explains the decolorization of red wines following sulfite treatment but, since it is reversible, the color gradually reappears as the free S02 (bisulfite ions) disappears. The major role of tannins in the color of old wines explains their insensitivity to color change with SOo. [Pg.61]


See other pages where Bisulfite effect is mentioned: [Pg.278]    [Pg.278]    [Pg.460]    [Pg.359]    [Pg.457]    [Pg.383]    [Pg.150]    [Pg.439]    [Pg.348]    [Pg.352]    [Pg.149]    [Pg.240]    [Pg.941]    [Pg.315]    [Pg.55]    [Pg.548]    [Pg.974]    [Pg.895]    [Pg.97]    [Pg.108]    [Pg.48]    [Pg.191]    [Pg.150]    [Pg.149]    [Pg.203]   
See also in sourсe #XX -- [ Pg.159 , Pg.162 , Pg.163 ]




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