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Naphthalene sulfonate oxidizing

The electrochemical oxidation at BDD as final treatment in a combined two-step biological/electrochemical process was investigated by Panizza et al. (2006) for the removal of naphthalene sulfonates contained in infiltration water of an industrial site. Mono and disulfonate naphthalenes were easily removed in the biological step, whereas bio-refractory compounds with complex molecules were oxidised by electrolysis at BDD anodes. With this combination the energy demand was significantly lowered with respect to mat required in a single electrochemical step. [Pg.222]

Also, HPLC methods with electrochemical or fluorescent detection are used (H19, M3). In proteins, dityrosine can be estimated by immunochemical methods employing dityrosine-specific antibodies (K5). Measurements of o,o -dityrosine and o-tyrosine levels in rat urine express dityrosine contents in skeletal muscle proteins, and have been proposed as the noninvasive oxidative stress test in vivo. One should be aware, however, that A-formylkynurenine, also formed in protein oxidation, has similar fluorescence properties as dityrosine (excitation 325 nm, emission at 400-450 nm) (G29). Also, oxidation of mellitin when excited at 325 nm produces an increase in fluorescence at 400—450 nm, despite the fact that mellitin does not contain tyrosine. Oxidation of noncontaining Trp residues ribonuclease A and bovine pancreatic trypsin inhibitor with "OH produces loss of tyrosine residues with no increase in fluorescence at 410 nm (S51). There are also methods measuring the increased hydrophobicity of oxidized proteins. Assays are carried out measuring protein binding of a fluorescent probe, 8-anilino-l-naphthalene-sulfonic acid (ANS). Increase in probe binding reflects increased surface hydrophobicity (C7). [Pg.229]

Evidence has been accumulated that shows that transaldolase is a half the sites enzyme, in which binding of substrate to one site almost completely inactivates the other active site. As mentioned above, only 1 mole of substrate is bound to the active site, even though the enzyme is a dimer. In the presence of excess F-6-P a burst of one equivalent of G-3-P is produced followed by a slower conversion of F-6-P to G-3-P plus DHA. It appears therefore, that the blocking of one active site by adduct formation with dihydroxyacetone results in a modified second active site which is able to slowly cleave F-6-P [76], This second site behavior is identical to that found in transaldolase in which one active site has been modified by reducing the dihydroxyacetone adduct with borohydride. Photo-oxidation of one of the two histidine residues in isoenzyme III results in the loss of activity of the enzyme, as is consistent with half-sites reaction [77]. The dye l-anilino-8-naphthalene sulfonate on the other hand is bound with 2 moles of dye per mole of enzyme, indicating two binding sites for F-6-P [78]. [Pg.288]

Add solutions may be used for the preparation of certain naphthalene-sulfonic acids incapable of formation by other means. Both aliphatic and aromatic sulfides or hydrosulfides are oxidized to corresponding sulfonic adds. o-Iodobenzoic acid is oxidized to o-iodosobenzoic acid. [Pg.490]

C. Basavaraja, W. J. Kim, D. G. Kim, D. S. Huh, Microwave Absorption Studies of Polyaniline Nanocomposites Encapsulating Gold Nanoparticles on the Surface of Reduced Graphene Oxide in the Presence of 2-Naphthalene Sulfonic Acid. Colloid Polym Sci 2012,290, 829-838. [Pg.511]

The fabrication of CP nanocomposites with metal oxides has become an important aspect for their potential applications in sensors and energy devices. The synergy between CPs and metal oxides provides the resultant nanocomposites with added functionalities compared to their individual parent materials. Wan and co-workers demonstrated that PANI/TiO, PANI/FejO and PANI/y-Fe Oj nanocomposites can be readily fabricated by a self assembling process [90-92]. The mechanism of the self-assembly can be related to the formation of micelles by (1-naphthalene sulfonic acid... [Pg.696]

Octoxynol-50 PEG-80 sorbitan laurate Sodium diisopropyl naphthalene sulfonate Sodium, nonoxynol-4 sulfate foam builder, paints/coatings Sodium C14-16 olefin sulfonate foam builder, paper lsodeceth-6 Trideceth-10 foam builder, personal care Ammonium lauryl sulfate Ammonium lauryl sulfosuccinate Ammonium myreth sulfate Behenamine oxide Behenyl betaine Bishydroxyethyl dihydroxyethyl stearaminium chloride Cocamidopropyl hydroxysultaine Cocamidopropyl PG-dimonium chloride phosphate N,N-Dimethyl-N-stearamidopropyl-N-(3-sulfopropyl)-ammonium betaine Disodium cocoamphodiacetate Disodium lauryl sulfosuccinate Disodium oleamido MEA-sulfosuccinate Disodium PEG-4 cocamido MIPA sulfosuccinate Disodium undecylenamido MEA-sulfosuccinate Distearyidimonium chloride Isostearamidopropyl morpholine lactate Lactamide MEA Lapyrium chloride Lauramidopropyl PEG-dimonium chloride phosphate Lauroampho PEG-glycinate phosphate... [Pg.5307]

Ammonium decyl sulfate Ammonium lauryl sulfate Cocamidopropylamine oxide Cocodimethylammonium-3-sulfopropylbetaine Cocoyl sarcosine C10-12 pareth-5 C12-14 pareth-9 C12-16 pareth-1 C12-16 pareth-2 C12-16 pareth-3 C12-16 pareth-5 C12-16 pareth-6 C12-16 pareth-7 C12-16 pareth-8 C12-16 pareth-11 DEA-lauryl sulfate Disodium deceth-6 sulfosuccinate Disodium myristamido MEA-sulfosuccinate lsodeceth-6 Lauramidopropyl PEG-dimonium chloride phosphate Lauroampho PEG-glycinate phosphate Magnesium lauryl sulfate Myristoyl sarcosine Sodium cocoamphoacetate Sodium cocoyl sarcosinate Sodium Cl2-15 pareth sulfate Sodium diisopropyl naphthalene sulfonate Sodium myristyl sulfate Sodium trideceth sulfate Stearoyl sarcosine TEA-lauryl sulfate Trideceth-10 foam builder, thickeners N,N-Dimethyl-N-lauric acid-amidopropyl-N-(3-sulfopropyl)-ammonium betaine N,N-Dimethyl-N-myristyl-N-(3-sulfopropyl)-ammonium betaine N,N-Dimethyl-N-palmityl-N-(3-sulfopropyl)-ammonium betaine N,N-Dimethyl-N-stearyl-N-(3-sulfopropyl)-ammonium betaine N,N-Dimethyl-N-tallow-N-(3-sulfopropyl)-ammonium betaine N,N-Distearyl-N-methyl-N-(3-sulfopropyl)-ammonium betaine foam builder, toothpaste Magnesium lauryl sulfate TEA-lauryl sulfate foam builder, topical cleansers Trideceth-7 carboxylic acid foam builder, upholstery shampoo DEA-lauryl sulfate Magnesium lauryl sulfate Sodium caproamphoacetate Sodium cocoamphoacetate TEA-lauryl sulfate... [Pg.5310]

Acenaphthene n-Amyl alcohol Arachidic acid Arachidyl alcohol Benzidine dihydrochloride 2-Butyl octanoic acid Butyloctanol Calcium sulfate Cetylarachidol Cocamine Cocopropylenediamine Cyclodextrin p-Cyclodextrin 1,10-Decanediol 2-Decyl tetradecanoic acid Dihydroxyethyl cocamine oxide Dodecylhexadecanol 2-Hexyl decanoic acid Hydroxypropyl-o-cyclodextrin Hydroxypropyl-P-cyclodextrin Hydroxypropyl-y-cyclodextrin 12-Hydroxystearyl alcohol Isobutyl oleate Kelp Lead phthalate, basic Methoxyethanol 2-Methoxy-5-nitroaniline Methoxy tripropylene glycol acrylate Methylene chloride 2-Octyl dodecanoic acid Oleamine PEG-25 castor oil PEG-30 castor oil PEG-36 castor oil PEG-40 castor oil PEG-200 castor oil PEG-5 hydrogenated castor oil PEG-25 hydrogenated castor oil Polyamide Polysorbate 85 Pyridine Quartz Sodium isopropyl naphthalene sulfonate Soybean (Glycine soja) meal Sucrose Sulfur Tallow amine N-Tallow-1,3-diaminopropane dioleate p-Toluene sulfonic acid Tri methyl amine Tungstic acid Undecylenic acid Vinyl compounds and polymers plastics additive... [Pg.5551]

Panizza M, Zolezzi M, Nicolella C (2006) Biological and electrochemical oxidation of naphthalene sulfonates in a contaminated site leachate. J Chem Technol Biotechnol 81 225-232... [Pg.1428]

The so-called template free method was discovered accidentally by the group of Wan. " In this method, typically, a solution of aniline is mixed with a dopant such as (3-naphthalene sulfonic acid, camphorsulfonic acid (or no dopant at all) before the oxidant ammonium persulfate is added to the solution. The mixture is kept stirring at room temperature and the precipitated tubes are washed with water. While this method does not offer the same amount of control over the morphology and the inner and outer diameter of the tubes compared to the hard template methods, its key feature is simplicity and ease of preparation. ... [Pg.228]

Ethoxylated diamines Ethoxylated amine oxides Alkyl naphthalene sulfonates... [Pg.223]


See other pages where Naphthalene sulfonate oxidizing is mentioned: [Pg.507]    [Pg.81]    [Pg.593]    [Pg.507]    [Pg.81]    [Pg.593]    [Pg.487]    [Pg.16]    [Pg.537]    [Pg.189]    [Pg.48]    [Pg.1573]    [Pg.23]    [Pg.8]    [Pg.45]    [Pg.48]    [Pg.2071]    [Pg.368]    [Pg.550]    [Pg.14]    [Pg.508]    [Pg.699]    [Pg.395]    [Pg.338]    [Pg.486]    [Pg.1501]    [Pg.88]    [Pg.314]    [Pg.318]    [Pg.425]    [Pg.575]    [Pg.377]    [Pg.184]    [Pg.375]    [Pg.218]    [Pg.2824]    [Pg.2861]    [Pg.368]    [Pg.496]   


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1-oxide sulfonation

Naphthalene oxidation

Naphthalene sulfonates

Naphthalenes sulfonation

Oxidation sulfones

Sulfonated naphthalene

Sulfonation, oxidative

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