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Chain controller

Fig. 1.2 shows a gas turbine power plant operating on a closed circuit. The dotted chain control surface (F) surrounds a cyclic gas turbine power plant (or cyclic heat engine) through which air or gas circulates, and the combustion chamber is located within the second open control surface (Z). Heat (2b is transferred from Z to Y, and heat (2a is rejected from Y. The two control volumes form a complete power plant. [Pg.1]

Chain tensioners and skids for chain-controlled camshafts Heat, hot oil, swelling, and wear resistance... [Pg.573]

The secondary structure of a protein is the shape adopted by the polypeptide chain—in particular, how it coils or forms sheets. The order of the amino acids in the chain controls the secondary structure, because their intermolecular forces hold the chains together. The most common secondary structure in animal proteins is the a helix, a helical conformation of a polypeptide chain held in place by hydrogen bonds between residues (Fig. 19.19). One alternative secondary structure is the P sheet, which is characteristic of the protein that we know as silk. In silk, protein... [Pg.890]

Doganci A, Neurath MF, Finotto S The IL-6R alpha chain controls lung CD4-FCD25-F Treg development and function during allergic airway inflammation in vivo. J Clin Invest 2005 115 313-325. [Pg.91]

Bopp T, Kallen KJ, Herz U, Schmitt S, Luft C, Hecht 0, Hohlfeld JM, Ito H, Nishimoto N, Yoshizaki K, Kishimoto T, Rose-John S, Renz H, Neurath MF, Galle PR, Finotto S The IL-6R a chain controls lung CD4-FCD25-F Treg development and function during allergic airway inflammation in vivo. J Clin Invest 2005 115 313-325. [Pg.198]

Of course the tertiary amine terminated polymer thus produced Is capable of being quaternlzed by alkyl halides and this has been confirmed experimentally. Moreover, It can be reacted with further living polyTHF to yield a polymer possessing a quaternary ammonium salt moiety at a point along the chain controlled by the relative molecular weights of the two living THF polymers reacted In the system, and again experiments have shown this to occur. [Pg.351]

From these experimental results it was assumed that conformational transitions within single polymer chains — controlled via intramolecular hydrogen bonds — are causing the viscosity decrease. Chain scission could be excluded. [Pg.134]

As pointed out above (Section III) the side chain controls the rate of the catalytic reaction. It was subsequently observed that it also controls the conformative response, i.e., the effect of the substrate on the conformation of the enzyme (75). Significantly, the nature of the conformative response could be correlated with the effect on the catalytic activity. Thus, the conformative response to benzylpenicillin and other penicillins with side chains promoting the rate of catalysis is characterized by increased stability of the enzyme molecule. Conversely, penicillins which carry side chains interfering with the catalytic activity labilize the enzyme and facilitate inactivation by heat, urea, proteolysis, iodination, or photooxidation. Such penicillins act as competitive inhibi-... [Pg.45]

Diffusion of the macroradicals controls can be assumed to be the termination reaction. However, that is not the case the termination rate constant is absolutely independent of the degree of polymerization, as shown in Table I. Therefore, the assumption must be that the diffusion of the segment at the end of the radical chain controls the termination process (as long as the Trommsdorff effect is not rate-determining). [Pg.16]

A joint experimental and computational DFT/MM study [56, 57] on the copolymerization of ethene and 2-butene provided further proof of the validity of the growing chain control of stereoselectivity mentioned above. The idea is that, if the same steric interactions postulated for propene hold for 2-butene, insertion of Z-butene should be favored with C2-symmetric metallocenes like Zr(Me2Si(l-indenyl)2CH3+, while E-butene should be favored with Cs-symmetric metallocenes like Zr(Me2Si(cyclopentadienyl-9-fluorenyl) CH3+. DFT/MM calculations confirmed this qualitative view, predicting the barrier for Z-butene to be 1.6 kcal/mol lower in the case of C2-symmetric complexes, and the barrier for E-butene to be 1.8 kcal/mol lower in the case of Cs-symmetric complexes. These results were corroborated by experiments, which showed molar compositions of 14% and 25% when the appropriate 2-butene isomer was copolymerized with ethene, while the molar percent was in the range of 1% when the wrong isomer was used. [Pg.126]

This technique is the simplest as it generally requires only one step since the polymerizable function is incorporated via the initiator fragment. To obtain well-defined macromonomers with one polymerizable end group per chain, controlled length and narrow MWD, the following criteria should be fulfilled ... [Pg.48]

Martinek TA, Fiilop F. Side-chain control of P-peptide secondary structures. Design principles. Fur. J. Biochem. 2003 270 3657-3666. [Pg.1459]

How is the rate of the electron-transport chain controlled Under most physiological conditions, electron transport is tightly coupled to phosphory-lation. Electrons do not usually flow through the electron-transport chain to O unless... [Pg.772]

The first of these, proposed by Martyna, Tuckerman, and Klein (MTK), was based on the notion that the variable py, itself, has a canonical (Gaussian) distribution exp(- 3p /Q). However, there is nothing in the equations of motion to control its fluctuations. MTK proposed that the Nose-Hoover thermostat should, itself, be connected to a thermostat, and that this thermostat should also be connected to a thermostat. The result is that a chain of thermostats is introduced whereby each element of the chain controls the fluctuations of the element just preceding it. The equations of motion for such a thermostat chain are ... [Pg.315]

Sakatsume M, Finbloom DS. Modulation of the expression of the IFN-y receptor P-chain controls responsiveness to IFN-y in human peripheral blood T cells. J Immuno 1996 156 4160-6. [Pg.739]

How is the rate of the electron-transport chain controlled Linder most physiological conditions, electron transport is tightly coupled to phosphorylation. Electrons do not usually Jlow through the electron-transport chain let CT unless ADP is simullaneously phosphorylated to ATP. When ADP concentration rises, as would be the case in active muscle, the rate of oxidative phosphorylation increases to meet the ATP needs ot the muscle. T he regulation of the rate of oxidative phosphorylation by the ADP level is called res piratory control or acceptor control. Experiments on isolated mitochondria demonstrate the importance of ADP level (Figure 18,40). The rate of oxygen consumption by mitochondria increases markedly when ADP is added and then returns to its initial value when the added ADP has been converted... [Pg.532]

The food safety policy of the Republic of Bulgaria is based on the functioning in the legal regnlation. The basic law inclndes Low for the foods. National health Law, Veterinarian and medical activity Law, Plant safety law Feed safety law. These laws state the legal food requirements, the producer, manufacturer s and merchant s obligations and the sequences of the complete food chain control actions (Valkov 2003). [Pg.390]

The average secondary particle size of the polycrystalline abrasives in ceria slurry is thought to be determined predominantly by PAA adsorption on the abrasives particle in the ceria slurry suspension. Generally, the amount of anionic PAA adsorbed on the abrasive particle surfaces, the configuration of the adsorbed PAA molecules, and the electric surface charge adsorbed from the particles by the PAA polymer chains control the agglomeration state and the stability of the dispersion. [Pg.66]


See other pages where Chain controller is mentioned: [Pg.672]    [Pg.112]    [Pg.661]    [Pg.16]    [Pg.102]    [Pg.379]    [Pg.247]    [Pg.125]    [Pg.395]    [Pg.42]    [Pg.128]    [Pg.106]    [Pg.13]    [Pg.77]    [Pg.81]    [Pg.211]    [Pg.184]    [Pg.281]    [Pg.145]    [Pg.130]    [Pg.160]    [Pg.249]    [Pg.137]    [Pg.10]    [Pg.39]    [Pg.167]    [Pg.165]    [Pg.425]    [Pg.45]    [Pg.234]   
See also in sourсe #XX -- [ Pg.72 ]




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A Model for the Control of Metabolic Reaction Chains

Atom transfer radical polymerization controlled chain lengths

Chain composition control

Chain length control

Chain reaction, nuclear first controlled

Chain scission diffusion controlled

Chain shape, controlling

Chain topology, control

Chain-end control

Chain-end control isotactic polymers

Chain-end control mechanism

Chain-end control syndiotactic polymers

Chain-end controlled polymerizations

Chain-growth polymerization controlled radical

Chain-growth polymerization sequence-controlled polymers

Chemically controlled systems pendant chain

Diffusion-controlled chain termination

Double stereoselection chain-end and site control

Electron transport chain respiratory control

Fatty acid control of chain length

HACCP-based systems for integrated control of pathogen transfer into organic food supply chains

Inventory control supply chain management

Molecular weight distribution controlled long chain branching

Negative polymerase chain reaction controls

Nuclear Control of Respiratory Chain Expression

Optimization of Mixed Control Supply Chain Logistics Planning Under Uncertain Environment

Polymer chain end control

Polymer living/controlled chain polymerization

Polymerase chain reaction control

Polymerase chain reaction performance, controls

Polymerase chain reaction temperature control

Positive polymerase chain reaction controls

Radical polymerization controlled chain length models

Radical polymerization controlled chain lengths

Rate-controlling step, chain reaction sequence

Reversible addition fragmentation chain equilibrium control

Supply chain planning and control

Temperature dependence controlled chain lengths

Terminated chains, controlled

Terminated chains, controlled radical polymerization

Things That Are Beyond Our Control in the Supply Chain

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