A Composition Rule to Predict the Linear Viscoelastic Properties of Polybutadienes with Varying Microstructure

2006 ◽  
Vol 79 (5) ◽  
pp. 859-869 ◽  
Author(s):  
O. Robles-Vásquez ◽  
A. González-Álvarez ◽  
J. E. Puig ◽  
O. Manero

Abstract A composition rule is proposed here to predict the glass transition temperature (Tg), the zero shear-rate dynamic viscosity (η0′), the plateau modulus (G0) and the terminal relaxation time (λ) of narrow molecular weight distribution (MWD) polybutadienes with various vinyl contents in solution and in the melt from the knowledge of the vinyl fraction, polymer fraction in solution and average molecular weight. The predictions of the composition rule are compared with data of a variety of narrow MWD polybutadienes with varying microstructure.

1973 ◽  
Vol 9 (11) ◽  
pp. 1231-1249 ◽  
Author(s):  
G.V. Vinogradov ◽  
A.Ya. Malkin ◽  
N.K. Blinova ◽  
S.I. Sergeyenkov ◽  
M.P. Zabugina ◽  
...  

1998 ◽  
Vol 10 (3) ◽  
pp. 273-283 ◽  
Author(s):  
J W Connell ◽  
J G Smith ◽  
P M Hergenrother

As part of a programme to develop high-performance/high-temperature structural resins for aeronautical applications, imide oligomers containing pendent and terminal phenylethynyl groups were prepared, characterized and the cured resins evaluated as composite matrices. The oligomers were prepared at a calculated number-average molecular weight of 5000 g mol−1 and contained 15–20 mol% pendent phenylethynyl groups. In previous work, an oligomer containing pendent and terminal phenylethynyl groups exhibited a high glass transition temperature (∼313 °C), and laminates therefrom exhibited high compressive properties, but processability, fracture toughness, microcrack resistance and damage tolerance were less than desired. In an attempt to improve these deficiencies, modifications in the oligomeric backbone involving the incorporation of 1,3-bis(3-aminophenoxy)benzene were investigated as a means of improving processability and toughness without detracting from the high glass transition temperature and high compressive properties. The amide acid oligomeric solutions were prepared in N-methyl-2-pyrrolidinone and were subsequently processed into imide powder, thin films, adhesive tape and carbon fibre prepreg. Neat resin plaques were fabricated from imide powder by compression moulding. The maximum processing pressure was 1.4 MPa and the cure temperature ranged from 350 to 371 °C for 1 h for the mouldings, adhesives, films and composites. The properties of the 1,3-bis(3-aminophenoxy)benzene modified cured imide oligomers containing pendent and terminal phenylethynyl groups are compared with those of previously prepared oligomers containing pendent and terminal phenylethynyl groups of similar composition and molecular weight.


1996 ◽  
Vol 455 ◽  
Author(s):  
A. Sahnoune ◽  
L. Piché

ABSTRACTWe present measurements of the glass transition and the ultrasonic relaxation modulus in a series of monodisperse polystyrenes. The temperature dependence of the modulus was analyzed using Havriliak-Negami relaxation model (HN) and Vogel-Tammann-Fulcher equation (VTF) for the relaxation time. The results allowed us to determine the fragility index, m, which decreases with increasing molecular weight, Mn. Furthermore, the relaxation time was found to saturate at high molecular weights and varies as Mnp, in the low molecular weight region. The exponent is p≈2 at high temperatures and p ≈ 7 at low temperatures close to Tg.


1990 ◽  
Vol 63 (5) ◽  
pp. 734-746 ◽  
Author(s):  
Jacques Roovers ◽  
Paul M. Toporowski

Abstract In the course of work on linear and ring polybutadienes with 62% 1,2 units, a number of discrepancies were noted with data on polybutadienes of various microstructure available in the literature. For example, GNο=870 kPa for our 62% 1,2-polybutadiene. This is larger than GNο=730 kPa for a 56% 1,2-polybutadiene and GNο=550 kPa for a 78% 1,2-polybutadiene sample. The cis : trans ratio of our 62% 1,2-polybutadiene, prepared with potassium counterion, is 1 : 4, On the other hand, the cis : trans ratio of 62% 1,2-polybutadiene prepared with a modified Li catalyst is estimated to be 1 : 2. It is conceivable that the different cis : trans ratio leads to different properties at constant 1,2 content. Nevertheless, the low levels of both the cis and the trans units are not expected to cause more than minor differences in the properties of the polybutadienes. Correct values for GNο of model polymers are important for the study of the influence of the chemical structure on the melt characteristics of a polymer. For this reason, it was thought useful to reinvestigate 1,2-polybutadiene itself in some detail. The synthesis of narrow molecular-weight distribution 1,2-polybutadiene by anionic polymerization techniques has been described recently. The dilute-solution properties of 1,2-polybutadiene has been investigated. The melt rheology of two 1,2-polybutadiene samples have been studied, but no systematic study of the molecular-weight dependence of the melt properties was made. 1,2-Polybutadiene has been used as a component in block copolymers with 1,4-polybutadiene. These studies have permitted an investigation of the phase behavior of two rubbery blocks at room temperature. Poly(l,4-butadiene-graft-l,2-butadiene)s with well-defined composition and architecture have also been prepared. Hydrosilylated 1,2-polybutadiene has found use as the coupling agent for multiarm star polymer, and this method can easily be extended to the preparation of poly( l,2-butadiene-graft-l,4-butadiene). Hydrogenated 1,2-polybutadienes are prepared as model polymers for poly(l-butene). The synthesis and characterization of a series of 1,2-polybutadienes are described here. Special attention is given to low-molecular-weight polymers. The linear viscoelastic properties of the melts are also described. In the discussion, the relation between the characteristic ratio, C∞, and the plateau modulus, GNο, of a number of model polymer systems is explored.


2011 ◽  
Vol 217-218 ◽  
pp. 1066-1069 ◽  
Author(s):  
Hong Chi Zhao ◽  
Qi Li ◽  
Li Bin Bai ◽  
Fan Huang

Polyvinylamine (PVAm) was synthesized by Hofmann degradation of polyacrylamide (PAM). The thermal properties of the Polyvinylamine hydrochloride (PVAm•HCl) were studied by differential scanning calorimeter (DSC). The degradation rate (a) decreased with increasing weight-average molecular weight (Mw) of PAM and decreasing amount of NaOH, and a were the better values when the concentration of PAM was 5% and the amount of NaClO was 10 mL. DSC curves showed that the glass transition temperature (Tg) of PVAm•HCl increased with increasing Mw of PAM, concentration of NaClO and decreasing concentration of NaOH. Tg of PVAm•HCl appeared the minimum value when the concentration of PAM was 5.0%.


1998 ◽  
Vol 10 (1) ◽  
pp. 51-59
Author(s):  
Amane Mochizuki ◽  
Masahiro Yoshioka ◽  
Michie Sakamoto ◽  
Takahiro Fukuoka ◽  
Mitsuru Ueda

A one-pot synthesis of aromatic polycarbodiimide from aromatic diamine has been developed. This method involves the preparation of carbamate by the reaction of 4, 4′-hexafluoroisopropylidenebis( p-phenyleneoxy)dianiline (6FPA) with phenylchloroformate, followed by the transformation of the carbamate with trimethylsilylchloride-triethylamine to diisocyanate, and then the polycondensation of the resulting diisocyanate in the presence of 3-methyl-1-phenyl-2-phosopholene-1-oxide. The polycarbodiimide (6FPCD) from 6FPA was obtained in quantitative yield having a number average molecular weight up to 5000. The thermal treatment of 6FPCD gave a crosslinkined polymer having a high glass transition temperature up to 200 °C.


2005 ◽  
Vol 480-481 ◽  
pp. 281-286 ◽  
Author(s):  
J. Llorens ◽  
E. Rudé ◽  
R.M. Marcos

We apply a model that connects rheological properties of linear polymer blends with their molecular weight distributions (MWDs). The model is based on the assumption that the relaxation time, ti, of a chain depends on an average molecular weight, M, which determines the effect of the environment where the molecule reptates, and its own molecular weight according to ti = (kE / 0 N G )·M 3.4 - b·Mi b where kE is the constant of proportionality between zero shear viscosity, ho, and weight average molecular weight, Mw, in unimodal polydisperse systems and 0 N G is the plateau modulus. We deduce that the MWD is related to the relaxation spectrum as H(t) = ( 0 N G /b)·M·W(M). Therefore, the MWD is obtained from the relaxation spectrum, which is deduced from the dynamic moduli, G’(w) and G’’(w), constrained by the plateau modulus, the zero shear viscosity and the steady state compliance, 0 e J . The maximum entropy method has been used to solve the integral equation that provides the relaxation spectra from experimental dynamic moduli. The model has been tested in polydimethylsiloxane blends with weight average molecular weight ranging from 94 to 630 kDa and polydispersity from 1.5 to 3.3. Good agreement is found between experimental and calculated MWDs.


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