CUPRIETHYLENEDIAMINE AS A REAGENT FOR HEMICELLULOSE SEPARATION FROM WHEAT STRAW HOLOCELLULOSE

1951 ◽  
Vol 29 (11) ◽  
pp. 974-985
Author(s):  
V. D. Harwood
Keyword(s):  
Molecular Weight ◽  
Vapor Pressure ◽  
Petroleum Ether ◽  
Wheat Straw ◽  
Periodate Oxidation ◽  
Chloroform Solution ◽  
Chemical Compositions ◽  
Distillation Method ◽  
Molecular Weights ◽  
Isothermal Distillation

Wheat straw and wheat straw holocellulose were dispersed in aqueous cupriethylenediamine solutions and fractionated by graded precipitation with acid and alcohol. From the holocellulose a 25.4% recovery of a hemicellulose containing negligible quantities of hexoses was achieved. The corresponding product from wheat straw was contaminated with both lignin and cellulose but a comparison of the chemical compositions of the two hemicelluloses showed that the acid chlorite used for delignification had caused very little hydrolytic action. The acetate of the hemicellulose from holocellulose was fractionated from chloroform solution by the addition of petroleum ether into a series of fractions and subfractions. Analysis of representative fractions from this series led to the conclusion that the hexoses present were not chemically combined with pentosan. Molecular weights were determined by periodate oxidation, the Signer isothermal distillation method, and from the lowering of the vapor pressure of their chloroform solutions and showed that the hemicellulose molecules were relatively small (mol. wt. < 10,000). The decreasing ratio of xylose to arabinose in the fractions of lower molecular weight indicated increasing chain branching.

Behavior of Rubber Hydrocarbon in a Molecular Still

1939 ◽  
Vol 12 (4) ◽  
pp. 789-793 ◽  
Author(s):  
W. Harold Smith ◽  
Henry J. Wing
Keyword(s):  
Molecular Weight ◽  
Vapor Pressure ◽  
High Molecular Weight ◽  
Molecular Species ◽  
Decomposition Temperature ◽  
Sedimentation Equilibrium ◽  
Chain Molecules ◽  
Molecular Weights ◽  
Average Value ◽  
Long Chain

Abstract Some investigators believe that rubber consists of associated molecules, and others accept Staudinger's view that long-chain molecules are formed by polymerization. Pummerer, Andriessen and Gündel have obtained a molecular weight as low as 600. Meyer and Mark believe that it is approximately 5,000, although they calculated on the basis of osmotic pressures values as high as 350,000. They, as well as Pummerer, consider that rubber is an associated colloid and that high molecular weights are caused by aggregates, sometimes called micelles. Staudinger, however, considers that the long-chain rubber molecule itself has a molecular weight of 200,000 or even 350,000, and that products with lower values, which may be formed in rubber, result from degradation. if the molecules are small it might be possible to distil them if their vapor pressure could be sufficiently increased, but none would distil without decomposition if the molecules are very large. Because the vapor pressure of rubber below its decomposition temperature is low, it appeared of interest to attempt to distil the material in a molecular still. Paraffin wax and sugar, both substances of relatively high molecular weight, have been successfully distilled in this type of apparatus. Subsequent to the work described in this paper, the molecular weight of sol rubber prepared at this Bureau was determined by Kraemer and Lansing of E. I. du Pont de Nemours & Co., Inc. They used the Svedberg method of sedimentation equilibrium in an ultracentrifuge with ethereal solutions of sol rubber. The temperature of the solutions during determinations was approximately 10° C, and an average value of 460,000 was obtained. There was evidenced of a mixture of molecular species.

THE MOLECULAR WEIGHT OF POLYVINYL ACETATE

1958 ◽  
Vol 36 (3) ◽  
pp. 543-549 ◽  
Author(s):  
A. F. Sirianni ◽  
R. Tremblay ◽  
I. E. Puddington
Keyword(s):  
Molecular Weight ◽  
Vapor Pressure ◽  
Polyvinyl Acetate ◽  
Molecular Weight Range ◽  
Weight Range ◽  
Molecular Weights ◽  
Approximate Molecular Weight ◽  
Low Degrees ◽  
Made In

The molecular weights of a series of unfractionated polyvinyl acetates of low degrees of polymerization have been measured by determining the lowering of the vapor pressure of their solutions. An approximate molecular-weight range of 5000–40,000 was examined. While most of the determinations were made in benzene solutions at 55 °C., other solvents and temperatures were used. Anomalous results were obtained with one sample of fractionated material.

scholarly journals The interplay between bi-modal molecular weight distribution in polystyrene and humidity induces self-assembly of biomimetic micropillars/honeycomb morphology in the thin polymer film

2021 ◽  
Author(s):  
Maciej Łojkowski ◽  
Adrian Chlanda ◽  
Emilia Choińska ◽  
Wojciech Swieszkowski
Keyword(s):  
Molecular Weight ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Self Assembly ◽  
Phase Segregation ◽  
Polymer Chains ◽  
Thin Polymer Film ◽  
Chemical Compositions ◽  
Molecular Weights ◽  
The Right

<p>Segregation of polymer chains of different molecular weights is a well-known process. A traditional experimental approach of studying phase segregation in thin films composed of polymer blends with identical chemical compositions but different molecular weights was focused on functionalisation of chemical group or modification of end-group. In this study, however, a different approach was proposed. Polystyrene with bimodal molecular weight distribution, but no additional chemical modification was used. The films were prepared by spin-coating and the segregation between polystyrene phases was investigated by force spectroscopy. The solubility of bimodal polystyrene was explored. At the right molecular weight distribution and soluted in Methyl Ethyl Ketone, the phase segregation occurred. Introduction of moist airflow induced the separation of the lower molecular weight into micropillars and the heavier fraction self-organized into a honeycomb. As a result, an easy, fast, and effective method of obtaining micropillar/honeycomb morphologies was demonstrated. The mechanism of formation of such structures was explained. </p>

scholarly journals Volatile and Non-Volatile Organic Compounds Stimulate Oviposition by Aphidophagous Predators

Insects ◽  
2020 ◽  
Vol 11 (10) ◽  
pp. 683
Author(s):  
Eric W. Riddick
Keyword(s):  
Molecular Weight ◽  
Volatile Organic Compounds ◽  
Vapor Pressure ◽  
Organic Compounds ◽  
Egg Production ◽  
United States Department ◽  
Oviposition Stimulants ◽  
Molecular Weights ◽  
Production Ratio ◽  
Volatile Organic

Introduction: Evidence that volatile organic compounds (VOCs) and non-VOCs stimulate oviposition by aphidophagous predators is scattered throughout the literature. The objectives of this review are to (1) compile records indicating that VOCs and non-VOCs are responsible for oviposition stimulation, (2) calculate an egg production ratio (EPR) for stimulated predators, and (3) determine if EPR is correlated with vapor pressure and molecular weight of active compounds. Methods: The USDA (United States Department of Agriculture), National Agricultural Library, online digital catalog system was used to retrieve abstracts, then the full text of manuscripts on oviposition stimulants for predators. Oviposition-stimulating VOCs and non-VOCS were tabulated with molecular weights and vapor pressure estimates. EPRs were calculated for stimulated coccinellids, syrphids, and chrysopids. Results: Both VOCs and non-VOCs stimulated oviposition behavior by coccinellids and syrphids, but not chrysopids. EPR was greatest for syrphids. Two VOCs, (E)-β-farnesene and 3-methyl-2-butenal, stimulated very high EPR values by the syrphid Episyrphusbalteatus. Regardless of predator taxa, EPR was negatively and positively correlated with molecular weight and vapor pressure, respectively. Conclusions: Syrphids (rather than coccinellids or chrysopids) produce more eggs in response to VOCs. Organic compounds with low-to-moderate molecular weights and moderate-to-high vapor pressures might be most effective oviposition stimulants for aphidophagous predators.

scholarly journals Exploiting the Interplay Between Bi-Modal Molecular Weight Distribution in Polystyrene and Humidity to Induce Self-Assembly of Biomimetic Micropillars/honeycomb Morphology in Thin Polymer Film

2021 ◽  
Author(s):  
Maciej Łojkowski ◽  
Adrian Chlanda ◽  
Emilia Choińska ◽  
Wojciech Swieszkowski
Keyword(s):  
Molecular Weight ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Self Assembly ◽  
Phase Segregation ◽  
Thin Polymer Film ◽  
Time Interval ◽  
Chemical Compositions ◽  
Short Time Interval ◽  
Molecular Weights

<p>Segregation of polymer chains of different molecular weights is a well-known process. A traditional experimental approach of studying phase segregation of thin films composed of polymer blends with identical chemical compositions but different molecular weights, was focused on functionalization of chemical group or modification of end-group. In this study however, a different approach was proposed, in which polystyrene with a bimodal molecular weight distribution but no additional chemical modification was implemented in order to examine and analyze its phase segregation. It was found that by choosing right molecular weight distribution it is possible to obtain controlled phase separation at short time interval and at microscale. By doing this, we have presented an easy, fast, effective and fully controlled method of obtaining biomimetic micropillar/honeycomb morphologies. In addition, the evaporation rate during spin-coating and the viscosity of a solution with a bimodal molecular weight distribution was studied.</p>

MOLECULAR WEIGHTS FROM MICRO QUANTITIES OF MATERIALS

1949 ◽  
Vol 27b (3) ◽  
pp. 151-157 ◽  
Author(s):  
I. E. Puddington
Keyword(s):  
Molecular Weight ◽  
Vapor Pressure ◽  
Chemical Compounds ◽  
Unknown Compound ◽  
Molecular Weights ◽  
Pure Solvent ◽  
Unknown Substance ◽  
The Difference

A method is proposed for the determination of the molecular weight of chemical compounds in which the unknown substance may be used successfully m quantities of 1 mgm. or less. The method depends on the accurate measurement of the difference in vapor pressure between a solution of the unknown compound and the pure solvent, and this is accomplished with a modified mercury U-tube manometer. The results presented indicate that the difference between the experimental and theoretical molecular weights is of the order of 2%. Determinations require from two to three hours and the sample may be recovered.

scholarly journals Exploiting the Interplay Between Bi-Modal Molecular Weight Distribution in Polystyrene and Humidity to Induce Self-Assembly of Biomimetic Micropillars/honeycomb Morphology in Thin Polymer Film

2021 ◽  
Author(s):  
Maciej Łojkowski ◽  
Adrian Chlanda ◽  
Emilia Choińska ◽  
Wojciech Swieszkowski
Keyword(s):  
Molecular Weight ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Self Assembly ◽  
Spin Coating ◽  
Phase Segregation ◽  
Polymer Chains ◽  
Thin Polymer Film ◽  
Chemical Compositions ◽  
Molecular Weights

<p>Segregation of polymer chains of different molecular weights is a well-known process. For many years, it was assumed that this process occurs over long-time intervals. On the contrary, solvent evaporation during spin-coating is very fast. A traditional experimental approach of studying phase segregation of thin films composed of polymer blends with identical chemical compositions but different molecular weights, was focused on functionalization of chemical group or modification of end-group. In this study however, a different approach was proposed, in which polystyrene with a bimodal molecular weight distribution but no additional chemical modification was implemented in order to examine and analyze its phase segregation. By doing this, we have presented an easy, fast, effective and fully controlled method of obtaining biomimetic micropillar/honeycomb morphologies. In addition, the evaporation rate during spin-coating and the viscosity of a solution with a bimodal molecular weight distribution was described.</p>

scholarly journals Exploiting the Interplay Between Bi-Modal Molecular Weight Distribution in Polystyrene and Humidity to Induce Self-Assembly of Biomimetic Micropillars/honeycomb Morphology in Thin Polymer Film

2021 ◽  
Author(s):  
Maciej Łojkowski ◽  
Adrian Chlanda ◽  
Emilia Choińska ◽  
Wojciech Swieszkowski
Keyword(s):  
Molecular Weight ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Self Assembly ◽  
Phase Segregation ◽  
Thin Polymer Film ◽  
Time Interval ◽  
Chemical Compositions ◽  
Short Time Interval ◽  
Molecular Weights

<p>Segregation of polymer chains of different molecular weights is a well-known process. A traditional experimental approach of studying phase segregation of thin films composed of polymer blends with identical chemical compositions but different molecular weights, was focused on functionalization of chemical group or modification of end-group. In this study however, a different approach was proposed, in which polystyrene with a bimodal molecular weight distribution but no additional chemical modification was implemented in order to examine and analyze its phase segregation. It was found that by choosing right molecular weight distribution it is possible to obtain controlled phase separation at short time interval and at microscale. By doing this, we have presented an easy, fast, effective and fully controlled method of obtaining biomimetic micropillar/honeycomb morphologies. In addition, the evaporation rate during spin-coating and the viscosity of a solution with a bimodal molecular weight distribution was studied.</p>

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