Search results for "Molar mass"
showing 10 items of 239 documents
Hyperbranched Polyglycerols: From the Controlled Synthesis of Biocompatible Polyether Polyols to Multipurpose Applications
2009
Dendritic macromolecules with random branch-on-branch topology, termed hyperbranched polymers in the late 1980s, have a decided advantage over symmetrical dendrimers by virtue of typically being accessible in a one-step synthesis. Saving this synthetic effort once had an unfortunate consequence, though: hyperbranching polymerization used to result in a broad distribution of molecular weights (that is, very high polydispersities, often M(w)/M(n)5). By contrast, a typical dendrimer synthesis yields a single molecule (in other words, M(w)/M(n) = 1.0), albeit by a labor-intensive, multistep process. But 10 years ago, Sunder and colleagues reported the controlled synthesis of well-defined hyperb…
New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst
2017
International audience; In this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization…
Relations between the cohesive energy, atomic volume, bulk modulus and sound velocity in metals
2011
By analysing the experimental data available in the literature, it has been found that the bulk modulus B of metals is proportional to the cohesive energy density Ec/V. For metals which start to melt having the close packed structure A1 or A3 the proportionality factor in the forementioned correlation is distinctly greater than that for metals melting from the A2 type structure. The existence of the correlation between the bulk modulus and the cohesive energy density leads to another, hitherto unrevealed correlation between the sound velocity, cohesive energy and the molar mass of metals: u2 ~ Ec/μ.
Solution behavior of 4-arm poly(tert-butyl acrylate) star polymers
2010
Abstract This paper reports the synthesis of 4-arm poly( tert -butyl acrylate) stars of different molar masses up to 10 6 g/mol by the “core-first” method using ATRP. All obtained stars have a monomodal and narrow molar-mass distribution ( The dilute-solution properties of these star polymers were investigated in good solvents (tetrahydrofuran and acetone). Gel permeation chromatography and dynamic and static light scattering were used to measure the hydrodynamic properties including intrinsic viscosity [ η ], radius of gyration R g , hydrodynamic radius R h , second virial coefficient A 2 and diffusion coefficient D 0 . These data were used to establish relationships between these paramet…
Über die bestimmung des zahlenmittels des molekulargewichts von polyoxymethylenen. 36. Mitt. Über polyoxymethylene
1968
Die Bestimmung des Zahlenmittels des Molekulargewichts (Mn) von Polyoxymethylenen durch Osmose, durch Kryoskopie, durch chemische und infrarotspektroskopische Endgruppenbestimmung und durch andere Methoden wird diskutiert. Osmotische Messungen in Phenol bei 90°C gelangen mit Cellophanmembranen besser als mit Glasmembranen. Kryoskopische Messungen nach RAST in Campher ergaben nur in Gegenwart eines Antioxydans zuverlassige Ergebnisse. Zur Endgruppenanalyse wurde vor allem die infrarotspektroskopische Bestimmung von Acetatgruppen weiterentwickelt; zur Auswertung wurde die Intensitat der Carbonylbande bei 5,70 μ in Beziehung gesetzt zu der CH2-Bande bei 6,8 μ und eine Eichung mit Hilfe des Chr…
General Kinetic Analysis and Comparison of Molecular Weight Distributions for Various Mechanisms of Activity Exchange in Living Polymerizations
1997
The molecular weight distributions in many living (e.g. anionic, group transfer, cationic, and radical) polymerizations strongly depend on the dynamics of various equilibria between chain ends of d...
Synthesis of linear and three-arm star tert-chlorine-telechelic polyisobutylenes by a two-step conventional laboratory process
1997
A two-step conventional laboratory process was developed for the synthesis of mono- and difunctional linear and three-arm star tert-chlorine-telechelic polyisobutylenes (PIB) with desired molecular weights (MW) and narrow molecular weight distribution (MWD) by living carbocationic polymerization (LCCP). This polymerization method applies easy to handle operations and chemicals. LCCP of isobutylene (IB), was carried out in CH2Cl2 as solvent and with BCl3 as coinitiator in the first step to obtain soluble low MW PIB prepolymer with narrow MWD. This was followed by addition of hexane, TiCl4 and additional monomer in the second step to prepare PIBs with desired MW and narrow MWD in practically …
The calculation of the number-average degree of polymerization starting from intrinsic viscosity and overall rate
1962
The relation between the intrinsic viscosity [η] and the number-average degree of polymerization Pn is a function of the molecular weight distribution of the polymer. In a polymer in which the termination of polymer radicals occurs partly by combination of two growing chains, this molecular weight distribution depends on number and extent of additional reactions such as chain transfer; i.e., it is variable. Therefore Pn of such polymers cannot be obtained from intrinsic viscosity measurements by means of an equation of the type [η] = KPna. A new method is proposed which allows the evaluation of Pn in these cases, without necessity of osmotic (or related) measurements or fractionation. The v…
The Largest Synthetic Structure with Molecular Precision: Towards a Molecular Object
2010
Pushing the limits: A 200A - 10 Da structurally defined, linear macromolecule (PG5) has a molar mass, cross-section dimension, and cylindrical shape that are comparable to some naturally occurring objects, such as amyloid fibrils or certain plant viruses. The macromolecule is resistant against flattening out on a surface; the picture shows PG5 embracing the tobacco mosaic virus (TMV).
Modes of Structure Formation in Doped Discotic Polymers and Low Molar Mass Model Systems
1991
By doping low molar mass or polymeric liquid crystals containing flat disc-like units with electron acceptors one achieves a stabilization of columnar phases, the induction of a columnar phases in otherwise discotic nematic or even in amorphous systems. Theoretical models based on the assumption of strong electron donator-acceptor (EDA) complex formation are able to account for the structure formation on a molecular level and the thermodynamic properties of the mixtures and the model of diffusion limited aggregation (DLA) for the structure formation on a supermolecular structure.