Persulfates production

A two-step mediated oxidation method can be proposed that separates the persulfate production step from its activation and organic pollutants oxidation. In this way, the optimum conditions of temperature and concentration can be adopted in order to reach the maximum efficiency of mediated oxidation. 

An improvement in mediated oxidation can be expected by increasing the efficiency of persulfate production and the oxidation rate of organic pollutants. These objectives can be reached with a new two-step mediated oxidation method that separates... 

The second generation includes latices made with functional monomers like methacrylic acid, 2-hydroxyethyl acrylate [818-61 -17, acrylamide/75 -(9ti-/7, 2-dimethylaminoethylmethacrylate [2867-47-2] and sodiumT -vinyl-benzenesulfonate [98-70-4] that create in polymeric emulsifier. The initiator decomposition products, like the sulfate groups arising from persulfate decomposition, can also act as chemically bound surfactants. These surfactants are difficult to remove from the latex particle. 

The original SBR process is carried out at. 50° C and is referred to as hot polymerization. It accounts for only about 5% of aU the mbber produced today. The dominant cold polymerization technology today employs more active initiators to effect polymerization at about 5°C. It accounts for about 85% of the products manufactured. Typical emulsion polymerization processes incorporate about 75% butadiene. The initiators are based on persulfate in conjunction with mercaptans (197), or organic hydroperoxide in conjunction with ferrous ion (198). The rest of SBR is produced by anionic solution polymerization. The density of unvulcanized SBR is 0.933 (199). The T ranges from —59" C to —64 C (199). 

Oxidation. Citric acid is easily oxidized by a variety of oxidizing agents such as peroxides, hypochlorite, persulfate, permanganate, periodate, hypobromite, chromate, manganese dioxide, and nitric acid. The products of oxidation are usually acetonedicarboxyhc acid (5), oxaUc acid (6), carbon dioxide, and water, depending on the conditions used (5). 

Fluorine and persulfates were also produced electrochemicaHy. All product values ate based on prices quoted in Ref. 2. 

Diaminoazobenzene was reported by Nietzki to have been prepared by diazotizing -nitroaniline and coupling the product with aniline. The resulting 4-nitrodiazoaminobenzene is rearranged and the nitro group reduced. The submitters tried several times to carry out this procedure but were unsuccessful. 4,4 -Diaminoazobenzene has been prepared by the oxidation of -nitroaniline with potassium persulfate followed by the reduction of the nitro groups. ... 

A -Pyrroline has been prepared in low yield by oxidation of proline with sodium hypochlorite (71), persulfate (102), and periodate (103). A -Pyrroline and A -piperideine are products of enzymic oxidation via deamination of putrescine and cadaverine or ornithine and lysine, respectively (104,105). This process plays an important part in metabolism and in the biosynthesis of various heterocyclic compounds, especially of alkaloids. 

The reaction of peracids with ketones proceeds relatively slowly but allows for the conversion of ketones to esters in good yield. In particular, the conversion of cyclic ketones to lactones is synthetically useful because only a single product is to be expected. The reaction has been carried out with both percarboxylic acids and Caro s acid (formed by the combination of potassium persulfate with sulfuric acid). Examples of both procedures are given. 

The oxidizing agent is prepared in a 500-ml flask equipped with a magnetic stirrer and cooled in an ice bath as follows In the flask are placed 60 ml of concentrated sulfuric acid and 20 ml of water, and the solution is cooled to 10°. Potassium persulfate (42 g, 0.15 mole) is added slowly to the stirred solution while maintaining the temperature below 10°. The solution is diluted with an additional 65 ml of water maintaining the temperature below 15°. The solution is now cooled to about 7° and 0.08 mole of the ketone is added over 40 minutes. After the addition has been completed, the solution is allowed to come to room temperature and stirring is continued for 20 hours. The solution is diluted carefully with 150 ml of water and extracted twice with 75-ml portions of ether. The ether is washed with sodium bicarbonate solution, followed by water, and the ethereal solution is dried. Removal of the solvent, followed by fractional distillation, affords the product ester. 

Figure 28.21 The reactions of R u (11) pby 3 + are catalyzed by light at 452 nm that begins by forming an excited state intermediate. In the presence of persulfate, a sulfate radical is formed concomitant with the oxidative product Ru(III)bpy33+. This form of the chelate is able to catalyze the formation of a radical on a tyrosine phenolic ring that can react along with the sulfate radical either with a nucleophile, such as a cysteine thiol, or with another tyrosine side chain to form a covalent linkage. The result of this reaction cascade is to cause protein crosslinks to form when a sample containing these components is irradiated with light.

The quest for a solvent-free deprotection procedure has led to the use of relatively benign reagent, ammonium persulfate on silica, for regeneration of carbonyl compounds (Scheme 6.10) [48]. Neat oximes are simply mixed with solid supported reagent and the contents are irradiated in a MW oven to regenerate free aldehydes or ketones in a process that is applicable to both, aldoximes and ketoximes. The critical role of surface needs to be emphasized since the same reagent supported on clay surface delivers predominantly the Beckmann rearrangement products, the amides [49]. 

Polymerizations were carried out in a jacketed, 1-gal, stirred, pressure tank reactor. Typical reactions were run by adding water, alcohol, or chain transfer agent, phosphate buffer, and persulfate to the reactor. The reactor was pressurized with CTFE monomer. Sulfite solution was fed at a rate to maintain reaction. Copper and iron ions were used at times as catalysts by adding cupric sulfate or ferrous sulfate.3 The product was filtered, washed with 90 10 water methanol followed with deionized water. The product was dried at 110°C. 

Potassium peroxomonosulfate, 14 67 Potassium peroxydisulfate, 14 292 Potassium peroxymonosulfate, 26 189 Potassium persulfate, 7 856 Potassium phosphates, 18 834-835 20 637 manufacture of, 18 854 Potassium polymetaphosphate, 18 848 Potassium products, 20 5991 Potassium pyrophosphates, 18 843 Potassium residues, 20 603 Potassium salts, 20 609... 

In grafting reactions initiated by redox processes, there is an interaction of the intermediate products with the substrate polymer chains. There may also be a chain transfer reaction involved. It is sometimes difficult to make a clear distinction between a direct redox reaction and a chain transfer process. Three redox systems have been studied extensively in grafting onto cellulose persulfate ions 1, hydroperoxide/ferrous ions 2> 3 and cerium (IV) ions. ... 

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