Isoprene and Rubber. Part 29. High Molecular Hydrorubbers

1932 ◽  
Vol 5 (2) ◽  
pp. 136-140
Author(s):  
H. Staudinger ◽  
W. Feisst
Keyword(s):  
Molecular Weight ◽  
Catalytic Reduction ◽  
Molecular Form ◽  
Average Molecular Weight ◽  
Molecular Size ◽  
Decomposition Products ◽  
Molecular Weights ◽  
Rubber Part ◽  
Derivatives Of ◽  
Suitable Process

Abstract The molecular concept in organic chemistry is based upon the fact that the molecules, whose existence is proved by vapor density determinations, enter into chemical reactions as the smallest particles. If now it is assumed that organic molecular colloids like rubber are dissolved in dilute solution in molecular form then it must be proved that in the chemical transposition of macromolecules as well no change in the size of the macromolecules occurs. In the case of hemicolloids, therefore for molecular colloids with an average molecular weight of 1000 to 10,000, this has been proved by the reduction of polyindenes, especially of polysterenes, to hydroproducts with the same average molecular weight, and also by the fact that cyclorubbers do not change their molecular weight upon autoöxidation. The molecular weights of hemi-colloidal hydrocarbons are therefore invariable. This is much more difficult to prove in the case of rubber, although there are many more ways in which unsaturated rubber can be transposed than the stable polysterenes, polyindenes, and poly cyclorubbers. In most of the reactions with rubber, as in its action with nitrosobenzene, oxidizing agents, hydrogen halides, and halogens, an extensive decomposition takes place as a result of the instability of the molecule, which is referred to in another work. Therefore derivatives of rubber are not formed, but derivatives of hemi-colloidal decomposition products. The catalytic reduction of rubber in the cold appears to be the most suitable process of making it react without changing its molecular size in order to prove that in a chemical transposition its molecular weight remains the same.

Isoprene and Rubber. XIX. The Molecular Size of Rubber and Balata

1930 ◽  
Vol 3 (3) ◽  
pp. 519-521 ◽  
Author(s):  
H. Staudinger ◽  
H. F. Bondy
Keyword(s):  
Molecular Weight ◽  
Organic Solvent ◽  
Average Molecular Weight ◽  
Molecular Size ◽  
Dilute Solution ◽  
Decomposition Products ◽  
Viscosity Measurements ◽  
Gutta Percha ◽  
Preceding Work

Abstract It was shown in the preceding work that a very dilute solution of balata in an organic solvent contains macromolecules in solution and not micelles. The same is true of rubber. On the basis of these findings it is possible to calculate the molecular weight of rubber and balata from viscosity measurements by means of the formula developed in a previous work: M=η8p/c. Km. The supposition is made that the molecules of rubber and balata have the form of threads and double threads, respectively. Also it is necessary to determine the constant KKm, and this may be calculated in the case of low molecular products, where the average molecular weight can be determined as well as the viscosity of the solutions. Such semi-colloidal decomposition products were obtained by heating rubber or gutta-percha in either tetralin or xylene. As shown by the following table the four samples thus obtained gave the constant: 0.3×10−3,5

Isoprene and Rubber. Part 20. The Colloidal Nature of Rubber, Gutta-Percha, and Balata

1930 ◽  
Vol 3 (4) ◽  
pp. 586-595
Author(s):  
H. Staudinger
Keyword(s):  
Molecular Weight ◽  
Characteristic Viscosity ◽  
Specific Viscosity ◽  
Decomposition Products ◽  
Molecular Weights ◽  
Gutta Percha ◽  
Viscosity Increase ◽  
Preceding Work ◽  
Rubber Part

Abstract I. The Molecular Weight of Rubber, Gutta-Percha, and Balata In the preceding work the molecular weight of rubber and balata was calculated on the basis of relations between specific viscosity ηsp and molecular weight which are shown by semi-colloidal decomposition products, on the assumption that this relation is also true for eucolloids. The value ηr−1 was taken as the specific viscosity, i. e., the characteristic viscosity increase of a substance of definite concentration and known solvent. The expression “specific viscosity” has already been used by J. Duclaux. In viscosity investigations of nitrocellulose solutions he represents this by a constant K which is calculated from the relations of the change of viscosity at various concentrations derived by Arrhenius: Based on these constants, nitrocelluloses show different average molecular weights for the increase in viscosity, that is, this constant K is greater with high molecular products than with low. In the following, this constant represents not the specific viscosity, but the viscosity-concentration constant Kc; the earlier constant Km which, on the basis of the formula: expressed the relation between the specific viscosity and the molecular weight, is called the viscosity-molecular weight constant.

Isoprene and Rubber. Part 32.The Constitution of Rubber

1931 ◽  
Vol 4 (3) ◽  
pp. 368-380
Author(s):  
H. Staudinger
Keyword(s):  
Molecular Weight ◽  
Colloidal Particles ◽  
Molecular Size ◽  
Group Method ◽  
Decomposition Products ◽  
True Solution ◽  
Rubber Part ◽  
Molecular Substances ◽  
Molecular Compounds ◽  
End Group

Abstract 1. The establishment of the molecular size of high molecular compounds which are composed of fiber molecules by the end-group method of determination is only possible if homologous polymeric series of similar type are concerned. 2. The end-group method assures reliable values with molecules up to a molecular weight of 1000 at the highest. With higher molecular products, like cellulose and rubber, the method is inexact. 3. The molecular weight of rubber and balata may be determined by viscosity determinations in the following two ways: (a) M=ηsp/cKm (b) M=Kc.Kcm. The constants Km and Kcm are determined with low molecular decomposition products. 4. Rubber and balata are composed of fiber molecules, which in one dimension have the magnitude of colloidal particles and in both the others, the dimensions of low molecular substances. 5. In highly viscous rubber solutions, there is the characteristic state of solution. As a result, the sphere of action of the dissolved molecule is greater than the volume at the disposal of the solution. This solution is midway between a true solution and a gel, and is therefore designated as a gel solution. It occurs only with high molecular substances, and is characteristic of them. 6. The readiness with which rubber solutions vary is explained by the fact that the rubber molecules are very sensitive to chemical influences and to changes in temperature as a result of the position of the double bonds. This sensitivity varies with the length of the molecules.

Effect of extractant and molecular size on the optical and chemical properties of soil humic acids

Soil Research ◽  
1969 ◽  
Vol 7 (3) ◽  
pp. 229 ◽  
Author(s):  
JHA Butler ◽  
JN Ladd
Keyword(s):  
Molecular Weight ◽  
Amino Acid ◽  
Humic Acids ◽  
Gel Filtration ◽  
Chemical Properties ◽  
Molecular Size ◽  
Carboxyl Content ◽  
Peptide Bonds ◽  
Molecular Weights ◽  
Amino Acid Contents

Humic acids extracted from soil with sodium pyrophosphate have greater proportions of lower molecular weight material, less acid-hydrolysable amino acid nitrogen contents, but greater carboxyl contents and extinction values (260 and 450 nm) than humic acids extracted subsequently from the same sample with alkali. Humic acids extracted with alkali from fresh soil samples have intermediate values. Extinction values at 260 nm are directly correlated with carboxyl contents for a given soil. Different crop histories have no significant effect on the measured properties of the extracted humic acids. An alkali-extracted humic acid has been fractionated by gel filtration into seven fractions of different nominal molecular weight ranges. As the molecular weights of the fractions increase, both aliphatic C-H (based on infrared absorption at 2900 cm-1) and acid-hydrolysable amino acid contents increase, whereas extinction values at 260 nm and carboxyl contents decrease. The infrared spectra of the high molecular weight fractions have peaks at 1650 and 1510 cm-1 which correlate with acid-hydrolysable amino acid contents and which correspond to amide I and II bands of peptide bonds. Alkaline hydrolysis to split peptide bonds eliminates both these peaks. The spectra also have peaks at 1720 and 1210 cm-1 which correlate with the carboxyl content.

scholarly journals The molecular form of acetylcholinesterase as determined by irradiation inactivation (Short Communication)

1974 ◽  
Vol 137 (1) ◽  
pp. 123-125 ◽  
Author(s):  
S. R. Levinson ◽  
J. C. Ellory
Keyword(s):  
Molecular Weight ◽  
Short Communication ◽  
Molecular Form ◽  
Electric Organ ◽  
Molecular Size ◽  
Erythrocyte Ghosts ◽  
Multiple Forms ◽  
Electrophorus Electricus ◽  
Membrane Bound

The molecular size of acetylcholinesterase (EC 3.1.1.7) from the electric organ of Electrophorus electricus and erythrocyte ‘ghosts’ was estimated in both membrane-bound and purified preparations by irradiation inactivation. Results suggest that the form of the enzyme in the membrane is a monomer of molecular weight approx. 75000 and that multiple forms of the enzyme observed in solubilized preparations are aggregates of this monomer.

Probing the molecular weights of sweetgum and pine kraft lignin fractions

TAPPI Journal ◽  
2021 ◽  
Vol 20 (6) ◽  
pp. 381-391
Author(s):  
JULIANA M. JARDIM ◽  
PETER W. HART ◽  
LUCIAN LUCIA ◽  
HASAN JAMEEL
Keyword(s):  
Molecular Weight ◽  
Black Liquor ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Systematic Investigation ◽  
Kraft Pulping ◽  
Molecular Weights ◽  
Lignin Recovery ◽  
Lignin Reactivity ◽  
Kinetics Of

The present investigation undertook a systematic investigation of the molecular weight (MW) of kraft lignins throughout the pulping process to establish a correlation between MW and lignin recovery at different extents of the kraft pulping process. The evaluation of MW is crucial for lignin characterization and utilization, since it is known to influence the kinetics of lignin reactivity and its resultant physicochemical properties. Sweetgum and pine lignins precipitated from black liquor at different pHs (9.5 and 2.5) and different extents of kraft pulping (30–150 min) were the subject of this effort. Gel permeation chromatography (GPC) was used to deter- mine the number average molecular weight (Mn), mass average molecular weight (Mw), and polydispersity of the lignin samples. It was shown that the MW of lignins from both feedstocks follow gel degradation theory; that is, at the onset of the kraft pulping process low molecular weightlignins were obtained, and as pulping progressed, the molecular weight peaked and subsequently decreased. An important finding was that acetobromination was shown to be a more effective derivatization technique for carbohydrates containing lignins than acetylation, the technique typically used for derivatization of lignin.

scholarly journals Characterization of proteins from the cytoskeleton of Giardia lamblia

1983 ◽  
Vol 59 (1) ◽  
pp. 81-103 ◽  
Author(s):  
R. Crossley ◽  
D.V. Holberton
Keyword(s):  
Molecular Weight ◽  
Sodium Dodecyl Sulphate ◽  
Giardia Lamblia ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Gel Filtration ◽  
Molecular Size ◽  
Molecular Weights

Proteins from the axonemes and disc cytoskeleton of Giardia lamblia have been examined by sodium dodecyl sulphate/polyacrylamide gel electrophoresis. In addition to tubulin and the 30 X 10(3) molecular weight disc protein, at least 18 minor components copurify with the two major proteins in Triton-insoluble structures. The most prominent minor bands have the apparent molecular weights of 110 X 10(3), 95 X 10(3) and 81 X 10(3). Protein of 30 X 10(3) molecular weight accounts for about 20% of organelle protein on gels. In continuous 25 mM-Tris-glycine buffer it migrates mostly as a close-spaced doublet of polypeptides, which are here given the name giardins. Giardia tubulin and giardin have been purified by gel filtration chromatography in the presence of sodium dodecyl sulphate. Well-separated fractions were obtained that could be further characterized. Both proteins are heterogeneous when examined by isoelectric focusing. Five tubulin chains were detected by PAGE Blue 83 dye-binding after focusing in a broad-range ampholyte gel. Giardin is slightly less acidic than tubulin. On gels it splits into four major and four minor chains with isoelectric points in the pI range from 5.8 to 6.2. The amino acid composition of the giardin fraction has been determined, and compared to Giardia tubulin and a rat brain tubulin standard. Giardins are rich in helix-forming residues, particularly leucine. They have a low content of proline and glycine; therefore they may have extensive alpha-helical regions and be rod-shaped. As integral proteins of disc microribbons, giardins in vivo associate closely with tubulin. The properties of giardins indicate that in a number of respects - molecular size, charge, stoichiometry - their structural interaction with tubulin assemblies will be different from other tubulin-accessory protein copolymers studied in vitro.

scholarly journals Average molecular weight of surfactants in aerosols

2007 ◽  
Vol 7 (5) ◽  
pp. 13805-13838 ◽  
Author(s):  
M. T. Latif ◽  
P. Brimblecombe
Keyword(s):  
Molecular Weight ◽  
Surface Tension ◽  
Atmospheric Aerosols ◽  
Average Molecular Weight ◽  
Molecular Size ◽  
Weight Fraction ◽  
Ozone Exposure ◽  
Before And After ◽  
Fine Mode ◽  
Active Substances

Abstract. Surfactants in atmospheric aerosols determined as methylene blue active substances (MBAS) and ethyl violet active substances (EVAS). The MBAS and EVAS concentrations can be correlated with surface tension as determined by pendant drop analysis. The effect of surface tension was more clearly indicated in fine mode aerosol extracts. The concentration of MBAS and EVAS was determined before and after ultrafiltration analysis using AMICON centrifuge tubes that define a 5000 Da (5 K Da) nominal molecular weight fraction. Overall, MBAS and to a greater extent EVAS predominates in fraction with molecular weight below 5 K Da. In case of aerosols collected in Malaysia the higher molecular fractions tended to be a more predominant. The MBAS and EVAS are correlated with yellow to brown colours in aerosol extracts. Further experiments showed possible sources of surfactants (e.g. petrol soot, diesel soot) in atmospheric aerosols to yield material having molecular size below 5 K Da except for humic acid. The concentration of surfactants from these sources increased after ozone exposure and for humic acids it also general included smaller molecular weight surfactants.

SIZE, STABILITY, AND HETEROGENEITY OF APURINIC ACID

1956 ◽  
Vol 34 (6) ◽  
pp. 1107-1117 ◽  
Author(s):  
G. C. Wood ◽  
David B. Smith
Keyword(s):  
Molecular Weight ◽  
Nucleic Acid ◽  
Acid Treatment ◽  
Average Molecular Weight ◽  
Weight Average Molecular Weight ◽  
Molecular Weights ◽  
Size Stability ◽  
Mild Acid

Apurinic acid prepared by mild acid treatment of sodium desoxyribonucleate and of fractions of sodium desoxyribonucleate was sufficiently stable to permit estimations of molecular weight and polydispersity. Apurinic acid from unfractionated desoxyribonucleate had a weight-average molecular weight of 25,000 and was very polydisperse. Preparations from fractionated desoxyribonucleate representing about half the original nucleic acid were much less polydisperse and had molecular weights of about 10,000.

Relative Efficacy of Separation of "Free" and "Bound" [3',5'-3H]Pteroylglutamate by Charcoal Coated with Various Materials

1975 ◽  
Vol 21 (13) ◽  
pp. 1927-1931 ◽  
Author(s):  
Alfred Zettner ◽  
Peggy E Duly
Keyword(s):  
Molecular Weight ◽  
Average Molecular Weight ◽  
Relative Efficacy ◽  
Molecular Weights

Abstract We studied the effectiveness with which various charcoal preparations separate free [3H]pteroylglutamate from that complexed with milk folate binder. We tested, in various concentrations, uncoated charcoals and charcoals coated with dextrans of various molecular weights, or with albumin, hemoglobin, or polyvinylpyrrolidone with an average molecular weight of 40 000. Although there was some distinction between the "bound" and "free" fractions with all charcoals, those treated with dextrans of average molecular weights of 43 500 or 70 000, or with polyvinylpyrrolidone gave the best separation over a greater range of charcoal concentration. Uncoated charcoal and charcoals coated with albumin, hemoglobin, or dextran T10 (average molecular weight, 10 500) were least effective.

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