Calculation of the contents of low molecular weight fractions when determining the molecular weight distribution of polydispersed polymers from the rate of sedimentation

1976 ◽  
Vol 18 (4) ◽  
pp. 1079-1082 ◽  
Author(s):  
M.P. Platonov ◽  
T.P. Petrova ◽  
S.Ya. Frenkel'
1970 ◽  
Vol 43 (6) ◽  
pp. 1439-1450 ◽  
Author(s):  
W. V. Smith ◽  
S. Thiruvengada

Abstract A preparative fractionation of about 23 g of a commercial cis-polybutadiene rubber is described. The method employed was a solvent elution chromatographic method with very little temperature gradient. The molecular weight distributions of the fractions obtained were determined by an analytical fractionation of 20 mg of polymer. The method was similar to the preparative fractionation and involved solvent elution chromatography. The fractions obtained were assayed for quantity, molecular weight, and molecular weight distribution by GPC. The low molecular weight fractions of the preparative fractionation had molecular weight distributions which could be closely approximated by two log normal distributions, the low molecular weight component having the narrower width. The ratio of weight to number average molecular weight was found to be about 1.1 for these samples. The higher molecular weight fractions could also be approximated by two log normal distributions; however, in these fractions the low molecular weight component had a very broad distribution but constituted only a small portion of the sample. The widths of the GPC curves of the fractions correlate satisfactorily with the molecular weight distributions found by the analytical refractionations. The GPC width is a sensitive criterion of the width of the molecular weight distribution even when only two columns are used. It is felt that the analytical fractionation procedure presented gives more detailed information on the molecular weight distribution than is easily obtainable from an ordinary GPC curve.


1998 ◽  
Vol 180 (16) ◽  
pp. 4184-4191 ◽  
Author(s):  
Gregory M. York ◽  
Graham C. Walker

ABSTRACT In Rhizobium meliloti (Sinorhizobium meliloti) cultures, the endo-1,3-1,4-β-glycanases ExoK and ExsH depolymerize nascent high-molecular-weight (HMW) succinoglycan to yield low-molecular-weight (LMW) succinoglycan. We report here that the succinyl and acetyl modifications of succinoglycan influence the susceptibility of succinoglycan to cleavage by these glycanases. It was previously shown that exoH mutants, which are blocked in the succinylation of succinoglycan, exhibit a defect in the production of LMW succinoglycan. We have determined that exoZ mutants, which are blocked in the acetylation of succinoglycan, exhibit an increase in production of LMW succinoglycan. For both wild-type andexoZ mutant strains, production of LMW succinoglycan is dependent on the exoK + andexsH + genes, implying that the ExoK and ExsH glycanases cleave HMW succinoglycan to yield LMW succinoglycan. By supplementing cultures of glycanase-deficient strains with exogenously added ExoK or ExsH, we have demonstrated directly that the absence of the acetyl group increases the susceptibility of succinoglycan to cleavage by ExoK and ExsH, that the absence of the succinyl group decreases the susceptibility of succinoglycan to cleavage, and that the succinyl effect outweighs the acetyl effect for succinoglycan lacking both modifications. Strikingly, nonsuccinylated succinoglycan actually can be cleaved by ExoK and ExsH to yield LMW succinoglycan, but only when the glycanases are added to cultures at greater than physiologically relevant concentrations. Thus, we conclude that the molecular weight distribution of succinoglycan in R. meliloti cultures is determined by both the levels of ExoK and ExsH glycanase expression and the susceptibility of succinoglycan to cleavage.


1978 ◽  
Vol 173 (1) ◽  
pp. 179-183 ◽  
Author(s):  
A W Davis ◽  
D R Phillips

Concentrated solutions of low-molecular-weight DNA (Mw=35000) with a known molecular-weight distribution can be prepared in several hours, and require no additional fractionation procedures. This is achieved by sonication of the DNA in 1.0 M-NaCl at high power at 0–2 degrees C. No denaturation of the DNA is detectable, even after 8h of continuous sonication. After 2h, the molecular-weight distribution of the total DNA sample is that of the most probably Schulz distribution, described by-Mn:-Mw:-Mz …=1:2:3 …etc. Such a molecular-weight distribution is expected for a random break-up of indefinitely long macromolecules and indicates that the sonication process is essentially by random double-strand scission. DNA was also sonicated in the presence of ligands capable of modifying the DNA tertiary structure. The results support the idea that inflexibility of the DNA is required for efficient sonic degradation.


2012 ◽  
Vol 518-523 ◽  
pp. 5550-5554
Author(s):  
Ming Hui ◽  
Chun Yuan Gao ◽  
Qing Tian ◽  
Xiao Bo Du ◽  
Xiang Long Yin

Molecule structures of poly(γ-glutamic acid) (γ-PGA) were modified by ultrasonic, UV and 60Co γ-rays irradiation treatments, which might be used to prepare the polymer with low molecular weight. When 10 g/l γ-PGA solution was sonicated 60 times (400W, working time 3 s and interval 4 s) or that of 20 g/l solution was irradiated from 2 kGy to 10 kGy, the long-chain molecules were broken into smaller fragments. But, as the same solution of 10 g/l was irradiated by UV rays for 10 min, the molecular aggregates were observed in the solution so that the molecular weight distribution of γ-PGA became narrower compared with the control through the analysis of SDS-PAGE. These results would have a reference of the modification of γ-PGA molecules and the production of low molecular weight γ-PGA.


The shear mechanical impedance of six polydimethylsiloxane liquids of viscosity grades ranging from 100 to 100000 cS has been measured over the frequency range 10 kc/s to 78 Mc/s, and at temperatures from –50 to +50 °C. It was found possible to reduce the experimental data for each liquid to give a single curve for each component of the mechanical impedance by using the method of reduced variables. From these curves the components of the shear modulus and the dynamic viscosity have been determined as a function of frequency, normalized to a temperature of 30 °C. The theory of Rouse, as developed by Ferry and others, describes adequately the viscoelastic relaxation of those siloxane liquids of comparatively low molecular weight in which entanglement coupling between molecules is absent. Quantitative predictions from the theory require a knowledge only of the variation of viscosity as a function of molecular weight and of the molecular weight distribution. In order to account for the viscoelastic behaviour of the higher molecular weight siloxanes the theory has been further developed to describe the properties of polydisperse polymers in which considerable entanglement coupling is present. Good agreement between the experimental and the theoretical results has been obtained. It has thus proved possible to predict the viscoelastic behaviour of polydimethylsiloxane liquids from a knowledge only of the molecular weight distribution and of the variation of viscosity with molecular weight.


2019 ◽  
Vol 78 ◽  
pp. 02004
Author(s):  
Tingting Li ◽  
Yan Yang ◽  
Linjun Chen ◽  
Wanling Yang

The physicochemical properties of Phellinus baumii polysaccharides extracted from the fruiting bodies by different grinding methods were studied in this paper. Compared with ordinary grinding methods, superfine grinding technology exerts significantly higher yields of crude polysaccharides, polysaccharide contents and β-Glucan contents of six samples. HPSEC-MALLS- RI analysis shows the molecular weight distribution of P.baummii crude polysaccharides, which indicates superfine grinding technique generates higher molecular weight fractions and larger polydispersities. The 6 kinds of crude polysaccharides have obvious effects on NO generation of RAW264.7 cells, which indicated that crude polysaccharides from P.baumii may have some immune-enhancing effects. Meanwhile, CW30 and FP30 show the best immune enhancing effects. However, CW50 and CW70 exert weaker immune-enhancing effects compared with FP50 and FP70.


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