Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Oxidation processes initiation

Fermentation. The term fermentation arose from the misconception that black tea production is a microbial process (73). The conversion of green leaf to black tea was recognized as an oxidative process initiated by tea—enzyme catalysis circa 1901 (74). The process, which starts at the onset of maceration, is allowed to continue under ambient conditions. Leaf temperature is maintained at less than 25—30°C as lower (15—25°C) temperatures improve flavor (75). Temperature control and air diffusion are faciUtated by distributing macerated leaf in layers 5—8 cm deep on the factory floor, but more often on racked trays in a fermentation room maintained at a high rh and at the lowest feasible temperature. Depending on the nature of the leaf, the maceration techniques, the ambient temperature, and the style of tea desired, the fermentation time can vary from 45 min to 3 h. More highly controlled systems depend on the timed conveyance of macerated leaf on mesh belts for forced-air circulation. If the system is enclosed, humidity and temperature control are improved (76). [Pg.372]

Antioxidants may intervene at any of the three major steps of the oxidative process initiation (oxygen consumption), propagation (conjugated dienes and peroxides formation), or termination (lipid peroxidation products). [Pg.271]

Many plants produce coumarins coumarin itself is found in sweet clover and contributes to the smell of new-mown hay. However, if sweet clover is allowed to ferment, oxidative processes initiated by the microorganisms lead to the formation of 4-hydroxycoumarin rather than coumarin. 4-Hydroxycoumarin then reacts with formaldehyde, also produced via the microbial degradative reactions, and provides dicoumarol. [Pg.419]

The oxidation process initiated in this way leads ultimately to the breakdown of the amide. The same mechanism was later shown to hold for polyamides also, and this is why polyamides with structure... [Pg.381]

Substituted pyran-2-ones can be conveniently obtained from saturated alcohols by a free radioed carbonylation / oxidation process initiated by lead tetraacetate (94JA5473). The cyclisation of 1,3,5-triketones by PPha in CCI4 has been used to synthesise the two pyran-2-one halves of the marine metabolite onchitriol (94TL9581). [Pg.275]

The oxidative process initiated during sterilization can continue during shelf storage and implantation. The rate and the extent of the process will depend on the storage temperature in the shelf and on the human body temperature, together with the amount of available oxygen in vivo. [Pg.256]

In the case of the developed oxidation process, initiation occurs owing to the decomposition of hydroperoxides with the formation of radicals by monomolecular or bimolecular reactions [4] ... [Pg.22]

Two Other chemical processes that rely on hydrothermal processing chemistry are wet oxidation and supercritical water oxidation (SCWO). The former process was developed in the late 1940s and early 1950s (3). The primary, initial appHcation was spent pulp (qv) mill Hquor. Shordy after its inception, the process was utilized for the treatment of industrial and municipal sludge. Wet oxidation is a term that is used to describe all hydrothermal oxidation processes carried out at temperatures below the critical temperature of water (374°C), whereas SCWO reactions take place above this temperature. [Pg.499]

Wet Oxidation Reactor Design. Several types of reactor designs have been employed for wet oxidation processes. Zimpro, the largest manufacturer of wet oxidation systems, typically uses a tower reactor system. The reactor is a bubble tower where air is introduced at the bottom to achieve plug flow with controlled back-mixing. Residence time is typically under one hour. A horizontal, stirred tank reactor system, known as the Wetox process, was initially developed by Barber-Cohnan, and is also offered by Zimpro. [Pg.502]

Manganate(VI) formed in the initial oxidation process must first be dissolved in a dilute solution of potassium hydroxide. The concentrations depend on the type of electrolytic cell employed. For example, the continuous Cams cell uses 120 150 g/L KOH and 50 60 g/L K MnO the batch-operated Bitterfeld cell starts out with KOH concentrations of 150 160 g/L KOH and 200 220 g/L K MnO. These concentration parameters minimize the disproportionation of the K MnO and control the solubiUty of the KMnO formed in the course of electrolysis. [Pg.520]

Isobutjiene [115-11-7] or tert-huty alcohol can be converted to methacrylic acid in a two-stage, gas-phase oxidation process via methacrolein as an intermediate. The alcohol and isobutjiene may be used interchangeably in the processes since tert-huty alcohol [75-65-0] readily dehydrates to yield isobutjiene under the reaction conditions in the initial oxidation. Variations of this process have been commercialized by Mitsubishi Rayon and by a joint venture of Sumitomo and Nippon Shokubai. Nippon Kayaku, Mitsui Toatsu, and others have also been active in isobutjiene oxidation research. [Pg.253]

The partial-oxidation process differs only in the initial stages before the water gas shift converter. Because it is a noncatalyzed process, desulfurization can be carried out further downstream. The proportions of a mixture of heavy oil or coal, etc, O2, and steam, at very high temperature, are so adjusted that the exit gases contain a substantial proportion of H2 and carbon monoxide. [Pg.83]

Initial production of the dimethyl terephthalate started with the oxidation of -xylene to terephthaUc acid using nitric acid both companies reportedly used similar technology (43—45). Versions of the nitric acid oxidation process, which has been abandoned commercially, involved the use of air in the initial oxidation step to reduce the consumption of nitric acid (44,46,47). The terephthaUc acid was then esterified with methanol to produce dimethyl terephthalate, which could be purified by distillation to the necessary degree (48). [Pg.487]

Polymerization of olefins such as styrene is promoted by acid or base or sodium catalysts, and polyethylene is made with homogeneous peroxides. Condensation polymerization is catalyzed by acid-type catalysts such as metal oxides and sulfonic acids. Addition polymerization is used mainly for olefins, diolefins, and some carbonyl compounds. For these processes, initiators are coordination compounds such as Ziegler-type catalysts, of which halides of transition metals Ti, V, Mo, and W are important examples. [Pg.2095]

In the absence of added radical generators the relatively unstable hydroperoxides, which are themselves generated by the oxidation process, are the major source of chain initiating radicals. [Pg.139]

While carburisation itself is not a normal corrosion process, in that there is no metal wastage, absorption and diffusion of carbon can lead to significant changes in the mechanical properties of the affected material and in particular to marked embrittlement. Furthermore, initial carburisation can produce an acceleration of the normal oxidation process, a phenomenon that is notable in nickel-chromium alloys. [Pg.1074]

Nevertheless, the system, composed of chain fragments of oxyfluoroniobate complexes, is thermodynamically less stable. Dipole properties of fragments of a certain length are re-orientated so as to be linked into typical infinite chains. There is no doubt that the fragment re-orientation and linking process initiates the partial reduction of niobium to Nb4+ and the oxidation of fluoride to elementary fluorine. The process scheme can be presented as follows ... [Pg.213]

Equations (37) and (38), along with Eqs. (29) and (30), define the electrochemical oxidation process of a conducting polymer film controlled by conformational relaxation and diffusion processes in the polymeric structure. It must be remarked that if the initial potential is more anodic than Es, then the term depending on the cathodic overpotential vanishes and the oxidation process becomes only diffusion controlled. So the most usual oxidation processes studied in conducting polymers, which are controlled by diffusion of counter-ions in the polymer, can be considered as a particular case of a more general model of oxidation under conformational relaxation control. The addition of relaxation and diffusion components provides a complete description of the shapes of chronocoulograms and chronoamperograms in any experimental condition ... [Pg.391]

Thus P is a structural parameter ranging between 0 and 1 that acts at the initial moments of the oxidation process of every segment the higher the degree of closure (v), the lower the probability (P) of any spontaneous conformational changes and the greater the anodic overpotential required to create a relaxation nucleus. Under these conditions both magnitudes are related by... [Pg.410]

So a linear dependence between the potential of the voltammetric peak and the increasing cathodic initial potential for the voltammograms (Fig. 57) points to an oxidation process occurring under conformational relaxation control of the electrode structure. [Pg.413]

Lipid hydroperoxides are either formed in an autocatalytic process initiated by hydroxyl radicals or they are formed photochemically. Lipid hydroperoxides, known as the primary lipid oxidation products, are tasteless and odourless, but may be cleaved into the so-called secondary lipid oxidation products by heat or by metal ion catalysis. This transformation of hydroperoxides to secondary lipid oxidation products can thus be seen during chill storage of pork (Nielsen et al, 1997). The secondary lipid oxidation products, like hexanal from linoleic acid, are volatile and provide precooked meats, dried milk products and used frying oil with characteristic off-flavours (Shahidi and Pegg, 1994). They may further react with proteins forming fluorescent protein derivatives derived from initially formed Schiff bases (Tappel, 1956). [Pg.316]

Scheme 4 The initial steps in the metaholism of morphine and codeine hy Pseudomonas putida MIO involved in the oxidation process... Scheme 4 The initial steps in the metaholism of morphine and codeine hy Pseudomonas putida MIO involved in the oxidation process...

See other pages where Oxidation processes initiation is mentioned: [Pg.561]    [Pg.938]    [Pg.88]    [Pg.25]    [Pg.351]    [Pg.425]    [Pg.298]    [Pg.33]    [Pg.317]    [Pg.561]    [Pg.938]    [Pg.88]    [Pg.25]    [Pg.351]    [Pg.425]    [Pg.298]    [Pg.33]    [Pg.317]    [Pg.3]    [Pg.499]    [Pg.459]    [Pg.479]    [Pg.256]    [Pg.339]    [Pg.796]    [Pg.1039]    [Pg.392]    [Pg.407]    [Pg.65]    [Pg.216]    [Pg.269]    [Pg.389]    [Pg.317]    [Pg.742]    [Pg.32]    [Pg.40]   
See also in sourсe #XX -- [ Pg.405 ]




SEARCH



Initial processing

Initiated Processes

Initiated oxidation

Initiation process

© 2024 chempedia.info