scholarly journals Erratum to : The Solution Viscosity and Molecular Weight of the Coconut Fatty Acid Modified Alkyd Resins Which Use Benzoic Acid for the Chain Stopper

1983 ◽  
Vol 40 (12) ◽  
pp. xviic-xviic
Keyword(s):  
Molecular Weight ◽  
Fatty Acid ◽  
Benzoic Acid ◽  
Solution Viscosity ◽  
Alkyd Resins ◽  
Coconut Fatty Acid

Structure and Solution Properties of High Molecular Weight Butadiene-Styrene Copolymers

1957 ◽  
Vol 30 (1) ◽  
pp. 315-325
Author(s):  
R. B. MacFarlane ◽  
L. A. McLeod
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Complex Structure ◽  
Mixed Solvents ◽  
Solution Time ◽  
Solution Viscosity ◽  
Solution Properties ◽  
Molecular Weight Range ◽  
Viscosity Measurements ◽  
Commercial Practice

Abstract Production of high molecular weight copolymers of butadiene and styrene for use in oil-extended rubbers has aroused interest in the solution properties of copolymers above the molecular weight range commonly encountered in commercial practice. It has been observed that solubility of such polymers in toluene is a time-dependent phenomenon and the apparent solubility can increase continuously, in the absence of agitation, for as long as 800 hours. Although a standard Harris cage solubility test may show the presence of 50% gel, other properties do not confirm the presence of any appreciable quantities of insoluble material. Mild agitation rapidly promotes almost complete solubility. Dilute solution viscosity measurements are very misleading unless the influence of solution time is recognized and apparent intrinsic viscosities rise progressively with time of contact of the sample with solvent. This time-dependence of solution has been found to occur at conversions higher than 50% and is also a function of the amount of modifier used in the polymerization recipe. It has not been possible to shorten the solution time for viscosity measurements by mild heating or gentle agitation. Mixed solvents cause a change in the amount of increase of the apparent intrinsic viscosity but do not shorten the time to equilibrium. Measurement of the slope constant in the Huggins viscosity equation indicate that these solubility and viscosity effects coincide with the appearance of a marked degree of branching in the polymer molecules. The effect is, therefore, interpreted as being caused by the relatively slow disentanglement of molecules of complex structure.

Effect of viscoelasticity on the soft-wall transition and turbulence in a microchannel

2017 ◽  
Vol 812 ◽  
pp. 1076-1118 ◽  
Author(s):  
S. S. Srinivas ◽  
V. Kumaran
Keyword(s):  
Molecular Weight ◽  
Reynolds Number ◽  
Reynolds Stress ◽  
Mass Fraction ◽  
Rectangular Cross Section ◽  
Pure Water ◽  
Polymer Concentration ◽  
Wall Turbulence ◽  
Solution Viscosity ◽  
Soft Wall

The modification of soft-wall turbulence in a microchannel due to small amounts of polymer dissolved in water is experimentally studied. The microchannels are of rectangular cross-section with height ${\sim}$160 $\unicode[STIX]{x03BC}\text{m}$, width ${\sim}$1.5 mm and length ${\sim}$3 cm, with three walls made of hard polydimethylsiloxane (PDMS) gel, and one wall made of soft PDMS gel with an elasticity modulus of ${\sim}$18 kPa. Solutions of polyacrylamide of molecular weight $5\times 10^{6}$ and mass fraction up to 50 ppm, and of molecular weight $4\times 10^{4}$ and mass fraction up to 1500 ppm, are used in the experiments. In all cases, the solutions are in the dilute limit below the critical overlap concentration, and the solution viscosity does not exceed that of water by more than 10 %. Two distinct types of flow modifications are observed below and above a threshold mass fraction for the polymer, $w_{t}$, which is ${\sim}$1 ppm and 500 ppm for the solutions of polyacrylamide with molecular weights $5\times 10^{6}$ and $4\times 10^{4}$, respectively. At or below $w_{t}$, there is no change in the transition Reynolds number, but there is significant turbulence attenuation, by up to a factor of 2 in the root-mean-square velocities and a factor of 4 in the Reynolds stress. When the polymer concentration increases beyond $w_{t}$, there is a decrease in the transition Reynolds number and in the intensity of the turbulent fluctuations. The lowest transition Reynolds number is ${\sim}$35 for the solution of polyacrylamide with molecular weight $5\times 10^{6}$ and mass fraction 50 ppm (in contrast to 260–290 for pure water). The fluctuating velocities in the streamwise and cross-stream directions are lower by a factor of 5, and the Reynolds stress is lower by a factor of 10, in comparison to pure water.

Properties of Acetate Kinase Isozymes and a Branched-Chain Fatty Acid Kinase from a Spirochete

1982 ◽  
Vol 152 (1) ◽  
pp. 246-254
Author(s):  
Caroline S. Harwood ◽  
Ercole Canale-Parola
Keyword(s):  
Amino Acids ◽  
Fatty Acids ◽  
Molecular Weight ◽  
Fatty Acid ◽  
Branched Chain Amino Acids ◽  
Chain Fatty Acid ◽  
Acetate Kinase ◽  
Nucleoside Triphosphate ◽  
Branched Chain ◽  
Chain Fatty Acids

Spirochete MA-2, which is anaerobic, ferments glucose, forming acetate as a major product. The spirochete also ferments (but does not utilize as growth substrates) small amounts of l -leucine, l -isoleucine, and l -valine, forming the branched-chain fatty acids isovalerate, 2-methylbutyrate, and isobutyrate, respectively, as end products. Energy generated through the fermentation of these amino acids is utilized to prolong cell survival under conditions of growth substrate starvation. A branched-chain fatty acid kinase and two acetate kinase isozymes were resolved from spirochete MA-2 cell extracts. Kinase activity was followed by measuring the formation of acyl phosphate from fatty acid and ATP. The branched-chain fatty acid kinase was active with isobutyrate, 2-methylbutyrate, isovalerate, butyrate, valerate, or propionate as a substrate but not with acetate as a substrate. The acetate kinase isozymes were active with acetate and propionate as substrates but not with longer-chain fatty acids as substrates. The acetate kinase isozymes and the branched-chain fatty acid kinase differed in nucleoside triphosphate and cation specificities. Each acetate kinase isozyme had an apparent molecular weight of approximately 125,000, whereas the branched-chain fatty acid kinase had a molecular weight of approximately 76,000. These results show that spirochete MA-2 synthesizes a branched-chain fatty acid kinase specific for leucine, isoleucine, and valine fermentation. It is likely that a phosphate branched-chain amino acids is also synthesized by spirochete MA-2. Thus, in spirochete MA-2, physiological mechanisms have evolved which serve specifically to generate maintenance energy from branched-chain amino acids.

Fatty acid binding protein is a major determinant of hepatic pharmacokinetics of palmitate and its metabolites

2003 ◽  
Vol 284 (3) ◽  
pp. G423-G433 ◽  
Author(s):  
Daniel Y. Hung ◽  
Frank J. Burczynski ◽  
Ping Chang ◽  
Andrew Lewis ◽  
Paul P. Masci ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Fatty Acid ◽  
Fatty Acid Binding Protein ◽  
Binding Protein ◽  
Low Molecular Weight ◽  
Metabolic Clearance ◽  
Pharmacokinetic Models ◽  
Fatty Acid Binding ◽  
Acid Binding Protein ◽  
Rat Livers

Disposition kinetics of [3H]palmitate and its low-molecular-weight metabolites in perfused rat livers were studied using the multiple-indicator dilution technique, a selective assay for [3H]palmitate and its low-molecular-weight metabolites, and several physiologically based pharmacokinetic models. The level of liver fatty acid binding protein (L-FABP), other intrahepatic binding proteins (microsomal protein, albumin, and glutathione S-transferase) and the outflow profiles of [3H]palmitate and metabolites were measured in four experimental groups of rats: 1) males; 2) clofibrate-treated males; 3) females; and 4) pregnant females. A slow-diffusion/bound model was found to better describe the hepatic disposition of unchanged [3H]palmitate than other pharmacokinetic models. The L-FABP levels followed the order: pregnant female > clofibrate-treated male > female > male. Levels of other intrahepatic proteins did not differ significantly. The hepatic extraction ratio and mean transit time for unchanged palmitate, as well as the production of low-molecular-weight metabolites of palmitate and their retention in the liver, increased with increasing L-FABP levels. Palmitate metabolic clearance, permeability-surface area product, retention of palmitate by the liver, and cytoplasmic diffusion constant for unchanged [3H]palmitate also increased with increasing L-FABP levels. It is concluded that the variability in hepatic pharmacokinetics of unchanged [3H]palmitate and its low-molecular-weight metabolites in perfused rat livers is related to levels of L-FABP and not those of other intrahepatic proteins.

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