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A promoting

Studies of electrical interactions in proteins, polypeptides, and amino acids started over 60 years ago [1]. To a large extent, electrostatic properties of proteins are determined by the ability of certain amino acids to exchange protons with their environment and the dependence of these processes on pH. The proton occupies a special position as a promoter and iiuxliator in... [Pg.176]

The metallocene catalyst is used m combination with a promoter usually methyl alumoxane (MAO)... [Pg.612]

FIGURE 28 10 During transcription a molecule of mRNA is assembled from a DNA template Transcription begins at a promoter sequence and proceeds in the 5 3 direction of the mRNA until a termination sequence of the DNA is reached Only a region of about 10 base pairs is unwound at any time... [Pg.1174]

In the first step cumene is oxidized to cumene hydroperoxide with atmospheric air or air enriched with oxygen ia one or a series of oxidizers. The temperature is generally between 80 and 130°C and pressure and promoters, such as sodium hydroxide, may be used (17). A typical process iavolves the use of three or four oxidation reactors ia series. Feed to the first reactor is fresh cumene and cumene recycled from the concentrator and other reactors. Each reactor is partitioned. At the bottom there may be a layer of fresh 2—3% sodium hydroxide if a promoter (stabilizer) is used. Cumene enters the side of the reactor, overflows the partition to the other side, and then goes on to the next reactor. The air (oxygen) is bubbled ia at the bottom and leaves at the top of each reactor. [Pg.95]

Vapor-phase oxidation over a promoted vanadium pentoxide catalyst gives a 90% yield of maleic anhydride [108-31-6] (139). Liquid-phase oxidation with a supported palladium catalyst gives 55% of succinic acid [110-15-6] (140). [Pg.108]

The metals are impregnated together or separately from soluble species, eg, Na2PdCl4 and HAuCl or acetates (159), and are fixed by drying or precipitation prior to reduction. In some instances sodium or potassium acetate is added as a promoter (160). The reaction of acetic acid, ethylene, and oxygen over these catalysts at ca 180°C and 618—791 kPa (75—100 psig) results in the formation of vinyl acetate with 92—94% selectivity the only other... [Pg.385]

A one-step LPO of cyclohexane directly to adipic acid (qv) has received a lot of attention (233—238) but has not been implemented on a large scale. The various versions of this process use a high concentration cobalt catalyst in acetic acid solvent and a promoter (acetaldehyde, methyl ethyl ketone, water). [Pg.344]

Naphtha desulfurization is conducted in the vapor phase as described for natural gas. Raw naphtha is preheated and vaporized in a separate furnace. If the sulfur content of the naphtha is very high, after Co—Mo hydrotreating, the naphtha is condensed, H2S is stripped out, and the residual H2S is adsorbed on ZnO. The primary reformer operates at conditions similar to those used with natural gas feed. The nickel catalyst, however, requires a promoter such as potassium in order to avoid carbon deposition at the practical levels of steam-to-carbon ratios of 3.5—5.0. Deposition of carbon from hydrocarbons cracking on the particles of the catalyst reduces the activity of the catalyst for the reforming and results in local uneven heating of the reformer tubes because the firing heat is not removed by the reforming reaction. [Pg.420]

Trade secrets become unprotectable when they are found in the pubHc domain, are independentiy developed, or are disclosed out of confidence. Events of the latter type may occur in any number of controUed or uncontroUed situations. For example, a promotional event such as a trade show or a required disclosure to a governmental agency may result in disclosure of the trade secret. Further, pubHcations in journals or maga2ines which may be necessary to promote products may lead to a disclosure of trade secrets. Idle correspondence, conversations, or communications with sales associates, suppHers, or distributors may also result in disclosure of trade secret information. [Pg.40]

Often the requisite THF oxonium ion is generated m situ by using a combination of reagents based on the Meerwein syntheses of trialkyl oxonium salts (150). These combinations include epichlorohydrin or a reactive haUde with a Lewis acid, a reactive hahde with a metal salt, or sometimes just a Lewis acid alone. The epoxide portion is often referred to as a promoter. [Pg.362]

Sodium bisulfate, NaHSO, is a convenient mild acid and is safe for uses as a household toilet-bowl cleaner, automobile-radiator cleaner, and for swimming pool pH adjustment. It is used for metal pickling, as a dye-reducing agent, for soil disinfecting, and as a promoter in hardening certain types of cement. [Pg.207]

Catalysts. In industrial practice the composition of catalysts are usuaUy very complex. Tellurium is used in catalysts as a promoter or stmctural component (84). The catalysts are used to promote such diverse reactions as oxidation, ammoxidation, hydrogenation, dehydrogenation, halogenation, dehalogenation, and phenol condensation (85—87). Tellurium is added as a passivation promoter to nickel, iron, and vanadium catalysts. A cerium teUurium molybdate catalyst has successfliUy been used in a commercial operation for the ammoxidation of propylene to acrylonitrile (88). [Pg.392]

Oxidation. Benzene can be oxidized to a number of different products. Strong oxidizing agents such as permanganate or dichromate oxidize benzene to carbon dioxide and water under rigorous conditions. Benzene can be selectively oxidized in the vapor phase to maleic anhydride. The reaction occurs in the presence of air with a promoted vanadium pentoxide catalyst (11). Prior to 1986, this process provided most of the world s maleic anhydride [108-31 -6] C4H2O2. Currendy maleic anhydride is manufactured from the air oxidation of / -butane also employing a vanadium pentoxide catalyst. [Pg.39]

Three commercial processes that use these various hot carbonate flow arrangements are the promoted Benfield process, the Catacarb process, and the Giammarco-Vetrocoke process (26—29). Each uses an additive described as a promoter, activator, or catalyst, which increases the rates of absorption and desorption, improves removal efficiency, and reduces the energy requirement. The processes also use corrosion inhibitors, which aHow use of carbon—steel equipment. The Benfield and Catacarb processes do not specify additives. Vetrocoke uses boric acid, glycine, or arsenic trioxide, which is the most effective. [Pg.21]

The amount of promoter used can also be a variable in influencing the degree of CO combustion. A promoted catalyst system can be classified as fully or partially promoted. A partially promoted system is one in which an increase in promoter content results in a decrease in the dilute-dense AT... [Pg.213]

In addition to platinum and related metals, the principal active component ia the multiflmctioaal systems is cerium oxide. Each catalytic coaverter coataias 50—100 g of finely divided ceria dispersed within the washcoat. Elucidatioa of the detailed behavior of cerium is difficult and compHcated by the presence of other additives, eg, lanthanum oxide, that perform related functions. Ceria acts as a stabilizer for the high surface area alumina, as a promoter of the water gas shift reaction, as an oxygen storage component, and as an enhancer of the NO reduction capability of rhodium. [Pg.370]

Application. Polyesters are cured by free radicals, most commonly produced by the use of peroxides. A wide range of peroxide initiators (qv) are available for use in curing polyesters. Most peroxide initiators are thermally decomposed into free radicals, and the common initiators used at room temperature requke the use of a promoter such as dimethylaniline or cobalt octoate. [Pg.18]

Organic peroxides need to be stored separately from the polyester resins and promoters. If a peroxide is contaminated with a promoter, violent decomposition can result. Promoters should always be thoroughly mixed into the resin prior to the addition of the peroxide to prevent violent peroxide decomposition. Peroxides can become unstable if stored for too long or at too high a temperature. Peroxide manufacturers advice for storage and disposal must be stricdy followed. [Pg.19]

Under polymerisation conditions, the active center of the transition-metal haHde is reduced to a lower valence state, ultimately to which is unable to polymerise monomers other than ethylene. The ratio /V +, in particular, under reactor conditions is the determining factor for catalyst activity to produce EPM and EPDM species. This ratio /V + can be upgraded by adding to the reaction mixture a promoter, which causes oxidation of to Examples of promoters in the eadier Hterature were carbon tetrachloride, hexachlorocyclopentadiene, trichloroacetic ester, and hensotrichloride (8). Later, butyl perchlorocrotonate and other proprietary compounds were introduced (9,10). [Pg.503]

The initiation stage may be activated by free-radical or ionic systems. In the following example a free-radical system will be discussed. In this case a material which can be made to decompose into free radicals on warming, or in the presence of a promoter or by irradiation with ultraviolet light, is added to the monomer and radicals are formed. Two examples of such materials are benzoyl peroxide and azodi-isobutyronitrile, which decompose as indicated in Figure 2.13. [Pg.25]

This process has many similarities to the Phillips process and is based on the use of a supported transition metal oxide in combination with a promoter. Reaction temperatures are of the order of 230-270°C and pressures are 40-80 atm. Molybdenum oxide is a catalyst that figures in the literature and promoters include sodium and calcium as either metals or as hydrides. The reaction is carried out in a hydrocarbon solvent. [Pg.211]

The reluctance of acrylic monomers to polymerise in the presence of air has been made a virtue with the anaerobic acrylic adhesives. These are usually dimethacrylates such as tetramethylene glycol dimethacrylate. The monomers are supplied with a curing system comprising a peroxide and an amine as part of a one-part pack. When the adhesive is placed between mild steel surfaces air is excluded, which prevents air inhibition, and the iron present acts as a polymerisation promoter. The effectiveness as a promoter varies from one metal to another and it may be necessary to use a primer such as cobalt naphthenate. The anaerobic adhesives have been widely used for sealing nuts and bolts and for a variety of engineering purposes. Small tube containers are also available for domestic use. [Pg.420]

Between 10 and 15 parts of hexa are used in typical moulding compositions. The mechanism by which it cross-links novolak resins is not fully understood but it appears capable of supplying the requisite methylene bridges required for cross-linking. It also functions as a promoter for the hardening reaction. [Pg.646]

For many materials scientists the database for which they automatically reach when a problem arises like the one with which 1 opened this chapter is the Handbook of Chemistry and Physics, now in its 81st edition, with over 2500 pages of densely packed information. This Handbook was first published in 1914 (a few years were missed because of wars), at the instigation of Arthur Friedman, a mechanical engineer and entrepreneur one of his eompanies was the Chemical Rubber Company, CRC, in Cleveland, Ohio, which supplied laboratory items in rubber. The CRC published the Handbook from the start, and still does... hence the Handbook s nickname. The Rubber Bible. In the early years, Friedman used the Handbook as a promotional device for the sale of such items as rubber stoppers. [Pg.493]

Metal oxides. Zinc oxide is the most effective metal oxide. The zinc oxide should have a low lead content. Zinc oxide has three main functions (a) promote cure (b) improves ageing, heat and weathering resistance (c) acid acceptor. In general, 2-5 phr zinc oxide is added in latex formulations. [Pg.668]


See other pages where A promoting is mentioned: [Pg.584]    [Pg.946]    [Pg.2144]    [Pg.202]    [Pg.242]    [Pg.135]    [Pg.359]    [Pg.477]    [Pg.458]    [Pg.132]    [Pg.200]    [Pg.481]    [Pg.5]    [Pg.36]    [Pg.419]    [Pg.163]    [Pg.198]    [Pg.212]    [Pg.213]    [Pg.396]    [Pg.1657]    [Pg.127]    [Pg.129]    [Pg.410]    [Pg.227]    [Pg.291]   
See also in sourсe #XX -- [ Pg.201 ]




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A-actin promoter

Acrylonitrile, a-chloroDiels-Alder reactions Lewis acid promoted

Carbon as promoter

Cu-Promoted Catalytic Decarboxylative Biaryl Synthesis, a Biomimetic Type Aerobic Decarboxylation

Diels-Alder reactions clays as promoters

Diels-Alder reactions silica gel as promoter

Electrochemical Promotion Using a Bipolar Monolithic Reactor

Electrochemical Promotion of C2H4 Oxidation on Pt Using a Bipolar Design

Factors promoting a negative culture

HB Polymers as Adhesion Promoters

Haemoglobin as a promoter of oxidative processes

Hormones as Inhibitors or Promoters

Kogls auxin-a and -b. the plant-growth promoters

Metal oxides as promoters

Microwave-Promoted Carbonylations Using the Solvent as a Source of Carbon Monoxide

PROMOTING A POSITIVE HEALTH AND SAFETY CULTURE

Potassium as promoter

Termination of the Metal-promoted or catalysed Reactions and a Catalytic Cycle

Water as promoter

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