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Biological Reductions

The effectiveness of a combined reduction-biological treatment system for the decolorization of nonbiodegradable textile dyeing wastewater has been investigated. The bench-scale experimental comparison of this technique with other reported combined chemical-biological methods showed higher efficiency and lower cost for the new technique [35]. [Pg.139]

Biological reduction. Biological reduction of chlorate and bromate was still in development at the time of decision-making [2, 3]. It is known that this anaerobic process works well on a bench-scale. Studies on a full-scale basis are presently being conducted. [Pg.190]

In still other aldehyde and ketone reductions, biological systems use NADPH as a reducing agent. This molecule, which is a phosphate ester of NADH, functions in the same manner as NADH as a biological reducing agent. [Pg.673]

The transformation of toxic substances in soil can have a profound effect on their potential for transport and accumulation at different soil depths. The rate of transformation processes impact the effective penetration depth of contaminants in soil, which in turn determines the length scale needed to define the soil compartment dimensions in mass transfer models. Transformation processes in soil include chemical conversions such as photolysis, hydrolysis, and oxidation/reduction biological processes such as microbial transformations and physical processes such as radioactive decay. [Pg.166]

By partial hydrogenation with DIBAL, or reaction with RMgX, of O-protected cyanohydrins, metallated primary imines are formed initially. Upon protonation these can be subjected to transimination with primary amines to furnish, upon reduction, biologically interesting N-substituted amino alcohols [106,108,124,143], e.g., ephedrine, tembamide, aegeline, denopamine, and some analogs of salbutamol [144]. (1 R,2S) Aimno alcohols have been converted to (5)-amphetamines by catalytic hydrogenation of their oxazolidi-nones [108]. [Pg.314]

Some fairly typical results, obtained by LaMer and co-workers [275] are shown in Fig. IV-24. At the higher film pressures, the reduction in evaporation rate may be 60-90%—a very substantial effect. Similar results have been reported for the various fatty acids and their esters [276,277]. Films of biological materials may offer little resistance, as is the case for cholesterol [278] and dimyristoylphosphatidylcholine (except if present as a bilayer) [279]. [Pg.147]

An important aspect of biological transport is that nature makes extensive use of the reduction of dimensionality to speed up search and discovery (SD) (see also section C2.14.6.2). SD is enonnously enlranced upon moving from tliree to two or one dimensions, because the spatial extent to be explored is drastically reduced. Affinity follows kinetics in being enlranced upon moving from tliree dimensions to two dimensions 1791. [Pg.2829]

Adam G and Delbrtick M 1968 Reduction of dimensionality in biological diffusion processes Structural Chemistry and Molecular Biology ed A Rich and N Davidson (San Francisco Freeman)... [Pg.2850]

Biological reduction of pyruvic acid catalyzed by the enzyme... [Pg.300]

Many biological processes involve oxidation of alcohols to carbonyl compounds or the reverse process reduction of carbonyl compounds to alcohols Ethanol for example is metabolized m the liver to acetaldehyde Such processes are catalyzed by enzymes the enzyme that catalyzes the oxidation of ethanol is called alcohol dehydrogenase... [Pg.645]

We shall encounter other biological processes m which the NAD" conversion plays a prominent role m biological oxidation-reduction... [Pg.647]

In spite of the rationale on which the testing of dyestuffs as antibiotics rested subsequent research re vealed that the antibacterial properties of Prontosil had nothing at all to do with its being a dye In the body Prontosil undergoes a reductive cleavage of its azo linkage to form sulfanilamide which is the sub stance actually responsible for the observed biological activity This is why Prontosil is active in vivo but not in vitro... [Pg.951]

Dichromated Resists. The first compositions widely used as photoresists combine a photosensitive dichromate salt (usually ammonium dichromate) with a water-soluble polymer of biologic origin such as gelatin, egg albumin (proteins), or gum arabic (a starch). Later, synthetic polymers such as poly(vinyl alcohol) also were used (11,12). Irradiation with uv light (X in the range of 360—380 nm using, for example, a carbon arc lamp) leads to photoinitiated oxidation of the polymer and reduction of dichromate to Ct(III). The photoinduced chemistry renders exposed areas insoluble in aqueous developing solutions. The photochemical mechanism of dichromate sensitization of PVA (summarized in Fig. 3) has been studied in detail (13). [Pg.115]

Despite advances, it seems unlikely that the reductive approaches outlined above can, by themselves, teach the level of control, fiexibiUty, discrimination, and versatiUty of atomic and molecular manipulation that will be needed to manufacture the molecular and suptamoleculat nanodevices envisaged to be the products of nanotechnology. Studies of biological nanodevices (eg, proteins) suggest that under proper conditions, atoms and molecules can assemble into functional nanoscale units that can carry out all the functions of life. [Pg.204]

Ornithine-Derived Alkaloids. Ornithine (23) undergoes biological decarboxylation reductively to generate either putrescine [110-60-1] (36), or its biological equivalent, and subsequent oxidation and cyclization gives rise to the pyrroline [6724-81-2], (37), C H N. [Pg.535]


See other pages where Biological Reductions is mentioned: [Pg.734]    [Pg.275]    [Pg.734]    [Pg.202]    [Pg.734]    [Pg.734]    [Pg.237]    [Pg.340]    [Pg.37]    [Pg.547]    [Pg.547]    [Pg.548]    [Pg.353]    [Pg.734]    [Pg.275]    [Pg.734]    [Pg.202]    [Pg.734]    [Pg.734]    [Pg.237]    [Pg.340]    [Pg.37]    [Pg.547]    [Pg.547]    [Pg.548]    [Pg.353]    [Pg.713]    [Pg.1719]    [Pg.2825]    [Pg.2991]    [Pg.492]    [Pg.209]    [Pg.182]    [Pg.1147]    [Pg.24]    [Pg.36]    [Pg.207]    [Pg.537]    [Pg.16]    [Pg.46]    [Pg.108]    [Pg.411]   
See also in sourсe #XX -- [ Pg.90 , Pg.139 ]




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Aldehyde biological reduction

Alkene biological reduction

Biological Catalysis of Respiratory Oxygen Reduction

Biological N2 Reduction

Biological N2O Reduction

Biological activity reduction

Biological and other reduction reactions

Biological reaction, alcohol aldehyde reduction

Biological reaction, alcohol ketone reduction

Biological reaction, alcohol reduction

Biological reaction, alcohol reductive amination

Biological reaction, alcohol thioester reduction

Biological redox proteins, oxidation-reduction

Biological redox proteins, oxidation-reduction potentials

Biological reductants

Biological reductants

Biological reduction processes, sediment

Biological standard reduction potentials

Biological sulfate reduction

Biological sulfate reduction process

Biological systems oxidation reduction

Biological systems oxidation-reduction reactions

Coenzymes in Biologically Important Oxidation-Reduction Reactions

Direct Bioelectrocatalysis Oxygen Reduction for Biological Fuel Cells

Electron Affinities of Biological Molecules from Reduction Potentials

Enantioselective reactions biological reduction

Ketone biological reduction

Mechanism biological reduction with NADH

Mechanism biological reduction with NADPH

Nicotinamide adenine dinucleotide biological reductions with

Nicotinamide adenine dinucleotide reduced), biological reduction with

Nicotinamide adenine dinucleotide reduced), biological reductions

Oxidation-reduction potential, biological compounds

Oxygen reduction biological proteins

Phosphate biological reduction

Pyruvic acid biological reduction

Reduction biological processes

Reduction micro-biological

Reduction, biological enzymatic

Reductive amination biological example

Thioester biological partial reduction

Thioester biological reduction

Vanadium Compounds on Biological Systems Cellular Growth, Oxidation-Reduction Pathways, and Enzymes

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