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Short chains

Table 5.4 gives the specific energies of selected organic liquid compounds. Compared with the isooctane chosen as the base reference, the variations from one compound to another are relatively small, on the order of 1 to 5%, with the exception of some particular chemical structures such as those of the short chain nitroparaffins (nitromethane, nitroethane, nitropropane) that are found to be energetic . That is why nitromethane, for example, is recommended for very small motors such as model airplanes it was also used in the past for competitive auto racing, for example in the Formula 1 at Le Mans before being forbidden for safety reasons. [Pg.186]

The adliesion and fiision mechanisms between bilayers have also been studied with the SEA [M, 100]. Kuhl et al [17] found that solutions of short-chained polymers (PEG) could produce a short-range depletion attraction between lipid bilayers, which clearly depends on the polymer concentration (fignre Bl.20.1 It. This depletion attraction was found to mduce a membrane fusion widiin 10 minutes that was observed, in real-time, using PECO fringes. There has been considerable progress in the preparation of fluid membranes to mimic natural conditions in the SEA [ ], which promises even more exciting discoveries in biologically relevant areas. [Pg.1742]

Kuhl T Let al 1994 Modulation of interaction forces between bilayers exposing short-chained ethylene oxide headgroups Biophys. J. 66 1479-88... [Pg.1749]

R N. The exponent v = 0.588 has been calculated using renonnalization group teclmiques [9, 10], enumeration teclmiques for short chain lengths and Monte Carlo simulations [13]. [Pg.2365]

Figure C2.1.2. Polymers witli linear and nonlinear chain architectures. The nonlinear polymers can have branched chains. Short chains of oligomers can be grafted to tire main chain. The chains may fonn a. stor-like stmcture. The chains can be cross-linked and fonn a network. Figure C2.1.2. Polymers witli linear and nonlinear chain architectures. The nonlinear polymers can have branched chains. Short chains of oligomers can be grafted to tire main chain. The chains may fonn a. stor-like stmcture. The chains can be cross-linked and fonn a network.
Short chains of amino acid residues are known as di-, tri-, tetrapeptide, and so on, but as the number of residues increases the general names oligopeptide and polypeptide are used. When the number of chains grow to hundreds, the name protein is used. There is no definite point at which the name polypeptide is dropped for protein. Twenty common amino acids appear regularly in peptides and proteins of all species. Each has a distinctive side chain (R in Figure 45.3) varying in size, charge, and chemical reactivity. [Pg.331]

Environmental Considerations. Environmental problems in Ziegler chemistry alcohol processes are not severe. A small quantity of aluminum alkyl wastes is usually produced and represents the most significant disposal problem. It can be handled by controlled hydrolysis and separate disposal of the aqueous and organic streams. Organic by-products produced in chain growth and hydrolysis can be cleanly burned. Wastewater streams must be monitored for dissolved carbon, such as short-chain alcohols, and treated conventionally when necessary. [Pg.457]

Selectivity. Solvent selectivity is intimately linked to the purity of the recovered extract, and obtaining a purer extract can reduce the number and cost of subsequent separation and purification operations. In aqueous extractions pH gives only limited control over selectivity greater control can be exercised using organic solvents. Use of mixed solvents, for example short-chain alcohols admixed with water to give a wide range of compositions, can be beneficial in this respect (6). [Pg.88]

When PET is extracted with water no detectable quantities of ethylene glycol or terephthaUc acid can be found, even at elevated extraction temperatures (110). Extractable materials are generally short-chained polyesters and aldehydes (110). Aldehydes occur naturally iu foods such as fmits and are produced metabohcaHy iu the body. Animal feeding studies with extractable materials show no adverse health effects. [Pg.333]

PVF displays several transitions below the melting temperature. The measured transition temperatures vary with the technique used for measurement. T (L) (lower) occurs at —15 to —20 " C and is ascribed to relaxation free from restraint by crystallites. T (U) (upper) is in the 40 to 50°C range and is associated with amorphous regions under restraint by crystallites (63). Another transition at —80° C has been ascribed to short-chain amorphous relaxation and one at 150°C associated with premelting intracrystalline relaxation. [Pg.380]

Lactulose. 4-O-P -D-Galactopyranosyl-4-D-fmctofuranose [4618-18-2] (Chronolac) (12) may be made from lactose using the method described in Reference 9. It is a synthetic disaccharide that is not hydroly2ed by gastrointestinal enzymes in the small intestine, but is metabolized by colonic bacteria to short-chain organic acids. The increased osmotic pressure of these nonabsorbable organic acids results in an accumulation of fluid in the colon. Lactulose may not be tolerated by patients because of an extremely sweet taste. It frequently produces flatulence and intestinal cramps. [Pg.202]

Light and photosynthetic electron transport convert DPEs into free radicals of undetermined stmcture. The radicals produced in the presence of the bipyridinium and DPE herbicides decrease leaf chlorophyll and carotenoid content and initiate general destmction of chloroplasts with concomitant formation of short-chain hydrocarbons from polyunsaturated fatty acids (37,97). [Pg.44]

It is estimated that mote than 25 x 10 different potentially toxic OP esters can be made using Schrader s classic (27) formula for effective phosphorylating agents, (39), where R and are short-chain alkyl, alkoxy, alkylthio, or alkylamino groups, and X is a displaceable moiety with a high energy P-bond such as E or acyl anhydride, and the pentavalent phosphoms atom is bonded to oxygen or sulfur. [Pg.279]

The newly formed short-chain radical A then quickly reacts with a monomer molecule to create a primary radical. If subsequent initiation is not fast, AX is considered an inhibitor. Many have studied the influence of chain-transfer reactions on emulsion polymerisation because of the interesting complexities arising from enhanced radical desorption rates from the growing polymer particles (64,65). Chain-transfer reactions are not limited to chain-transfer agents. Chain-transfer to monomer is ia many cases the main chain termination event ia emulsion polymerisation. Chain transfer to polymer leads to branching which can greatiy impact final product properties (66). [Pg.26]

Fat. Milk fat is a mixture of triglycerides and diglycerides (see Fats and fatty oils). The triglycerides are short-chain, C. —C., medium-chain, 24 46 ... [Pg.351]

Structure. The physical properties of LDPE depend on the molecular weight, the molecular weight distribution, as well as the frequency and distribution of long- and short-chain branching (2). [Pg.371]

Both propylene and isobutylene ate comonomers that are incorporated along the chain, resulting in additional short-chain branching. One important factor in controlling polymer crystallinity is the choice of chain-transfer agent. Ethane and methane, for example, are inefficient agents whose presence in the monomer feed stream must be considered in reaction control. [Pg.374]

Crystallinity and Density. Crystallinity and density of HDPE resins are derivative parameters both depend primarily on the extent of short-chain branching in polymer chains and, to a lesser degree, on molecular weight. The density range for HDPE resins is between 0.960 and 0.941 g/cm. In spite of the fact that UHMWPE is a completely nonbranched ethylene homopolymer, due to its very high molecular weight, it crystallines poorly and has a density of 0.93 g/cm. ... [Pg.379]


See other pages where Short chains is mentioned: [Pg.193]    [Pg.309]    [Pg.320]    [Pg.371]    [Pg.2377]    [Pg.2378]    [Pg.2574]    [Pg.2646]    [Pg.447]    [Pg.465]    [Pg.1008]    [Pg.1010]    [Pg.348]    [Pg.613]    [Pg.884]    [Pg.120]    [Pg.127]    [Pg.418]    [Pg.418]    [Pg.498]    [Pg.31]    [Pg.94]    [Pg.451]    [Pg.367]    [Pg.371]    [Pg.374]    [Pg.382]    [Pg.389]    [Pg.395]    [Pg.403]    [Pg.427]    [Pg.448]    [Pg.114]   
See also in sourсe #XX -- [ Pg.37 ]

See also in sourсe #XX -- [ Pg.4 ]




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3- Hydroxybutyrate common short-chain-length

Alcohol dehydrogenases, short-chain

Aliphatic diols, short-chain

Aliphatic hydrocarbons short-chain aliphatics

Alkenes short-chain

Amino acids short chain

Amylose hybrids with short alkyl chains

Aromatic short-chain peptides

Aromatics from short-chain alkanes

Behavior of the Sugars with Short Carbon Chains

Branched short chain

Branching short chain

Carboxylic acid volatile short chain

Catalytic Reaction Mechanism of Drosophila ADH, a Short-Chain Dehydrogenase

Chain Polymetallocenes with Short Spacer Groups

Characterization of Short-Chain Branching (SCB) in LDPE

Degradation modelling short-chain diffusion

Dehydrogenase short-chain alcohol

Determination of short-chain sulphonates

Diffusion equation short chains

Effects of Short-Chain Branching

Elimination of short range divergences for a chain with two-body interactions

Elucidation of Short Chain Branching in Polyethylene

Fasting glucose short-chain

Fatty acids saturated short-chain

Fatty acids short-chain

Fatty adds short-chain

Fatty short-chain

Formation of Short Chain Oligomers

Friction coefficient short chains

Fructooligosaccharides short-chain

Glass transition temperature short chains

Higher olefin copolymers, short chain branching

How Common Is Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

How Do People Inherit Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Hydrocarbons short-chain

Hydrogenases. short-chain

Intra-Chain Transport at Short Time Scales

Inulin short-chain fatty acids

Long-short-chain mixture, adsorption

Macromolecules short chain-branched

Membranes short side chains

Mixture of short and long chains

Molecular branched short-chain

Network chain — continued short

Network short-chain

Networks, bimodal short-chain model

Networks, bimodal short-chain unimodal

Non-Self-Entangled Long Chains in a Short-Chain Matrix

PFSA Polymers with Short Side Chains

PHAscl (short chain length

Peptides short-chain

Perfluorosulfonic acid short side chain

Polar-Endcapped Short Hydrocarbon Chains on Silica

Poly short-chain branches

Polyethylene short-chain

Polyethylene short-chain branches

Polyhydroxyalkanoates short-/medium-chain-length

Polymer structure short-chain branches

Polymetallocenes main-chain with short spacer group

Relaxation short chain

SHORT-CHAINED

SHORT-CHAINED CHLORINATED

SHORT-CHAINED PARAFFINS

Self-Entangled Long Chains in a Short-Chain Matrix

Short Chain Alkanes on

Short Chain Chlorinated Paraffins (SCCP)

Short Chain Dynamics

Short Chain Fatty Acids (SFAS)

Short chain branches

Short chain branching content

Short chain branching level

Short chain chlorinated paraffins

Short chain chlorinated paraffins production

Short chain chlorinated paraffins toxicity

Short chain diffusion

Short chain fatty acids, absorption

Short chain fatty acids, dietary fiber

Short chain length

Short chain length monomers

Short chain primary alcohols

Short chain reactions

Short chain soaps

Short chains production

Short side chain PFSA

Short- and Long-Chain Acyl Triglyceride

Short- and Long-Chain Acyl Triglyceride Molecules

Short-Chain Analogues of Surfactants and Other Nonmicelle-Forming Amphiphiles

Short-Chain Dehydrogenases

Short-Chain Kurrols Salts

Short-Chain-Length PHA

Short-chain FOS

Short-chain Olefins

Short-chain TAGs

Short-chain TAGs Triacylglycerols

Short-chain acyl-CoA dehydrogenase

Short-chain acyl-CoA dehydrogenase SCAD)

Short-chain acyl-CoA dehydrogenase deficiency

Short-chain alcohols

Short-chain aliphatics

Short-chain amines

Short-chain branch distribution

Short-chain branch distribution SCBD)

Short-chain branch, definition

Short-chain branching (intramolecular

Short-chain branching distribution

Short-chain carboxylic acids

Short-chain ceramides

Short-chain dehydrogenase

Short-chain dehydrogenase/ reductases SDRs)

Short-chain dehydrogenase/reductase

Short-chain dispersants

Short-chain fatty acid derivation

Short-chain fatty acids -3-hydroxybutyric acid

Short-chain fatty acids colorectal cancer

Short-chain fatty acids dietary fiber fermentation

Short-chain fatty acids functional foods

Short-chain fatty acids metabolism

Short-chain fatty acids properties

Short-chain fatty acids resistant starch fermentation

Short-chain fatty adds metabolism

Short-chain lipid species

Short-chain molecules

Short-chain phospholipids

Short-chain polyamines

Short-chain saturated phospholipid

Short-chain sulfonates

Short-chain volatile FFAs

Short-chain volatile aldehydes

Short-chain, Primary Derivatives of Polysaccharides

Short-chain-length polyhydroxyalkanoates

Short-chained chlorinated paraffins

Short-side-chain ionomer

Short-side-chain polymers

Short-side-chain vinyl ether polymer

Studies on Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Unimodal networks, short chain

What Genes Are Related to Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

What Is Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

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