Differential scanning calorimetry applied to cross-linking of a filled epoxy resin: Accuracy of the Borchardt and Daniels equation for describing the curing process kinetics

1986 ◽  
Vol 31 (6) ◽  
pp. 1351-1358 ◽  
Author(s):  
L. Elegant ◽  
P. Tomi ◽  
G. Augier ◽  
J. P. Nicolas ◽  
G. Pecqueux
Keyword(s):  
Differential Scanning Calorimetry ◽  
Epoxy Resin ◽  
Cross Linking ◽  
Curing Process ◽  
Scanning Calorimetry ◽  
Process Kinetics

scholarly journals Kinetic Analysis of the Curing Process of Biobased Epoxy Resin from Epoxidized Linseed Oil by Dynamic Differential Scanning Calorimetry

Polymers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1279
Author(s):  
Diego Lascano ◽  
Alejandro Lerma-Canto ◽  
Vicent Fombuena ◽  
Rafael Balart ◽  
Nestor Montanes ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Epoxy Resin ◽  
Epoxy Resins ◽  
Linseed Oil ◽  
Single Step ◽  
Curing Process ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Step Process ◽  
Epoxidized Linseed Oil

The curing process of epoxy resin based on epoxidized linseed oil (ELO) is studied using dynamic differential scanning calorimetry (DSC) in order to determine the kinetic triplet (Ea, f(α) and A) at different heating rates. The apparent activation energy, Ea, has been calculated by several differential and integral isoconversional methods, namely Kissinger, Friedman, Flynn–Wall–Ozawa (FWO), Kissinger–Akahira–Sunose (KAS) and Starink. All methods provide similar values of Ea (between 66 and 69 kJ/mol), and this shows independence versus the heating rate used. The epoxy resins crosslinking is characterized by a multi-step process. However, for the sake of the simplicity and to facilitate the understanding of the influence of the oxirane location on the curing kinetic, this can be assimilated to a single-step process. The reaction model has a high proportion of autocatalytic process, fulfilling that αM is between 0 and αp and αM < αp∞. Using as reference the model proposed by Šesták–Berggren, by obtaining two parameters (n and m) it is possible to obtain, on the one hand, the kinetic parameters and, on the other hand, a graphical comparison of the degree of conversion, α, versus temperature (T) at different heating rates with the average n and m values of this model. The good accuracy of the proposed model with regard to the actual values obtained by DSC gives consistency to the obtained parameters, thus suggesting the crosslinking of the ELO-based epoxy has apparent activation energies similar to other petroleum-derived epoxy resins.

scholarly journals Improved Processing and Properties for Polyphenylene Oxide Modified by Diallyl Orthophthalate Prepolymer

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2016
Author(s):  
Honghua Wang ◽  
Qilin Mei ◽  
Yujie Ding ◽  
Zhixiong Huang ◽  
Minxian Shi
Keyword(s):  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Phase Separation ◽  
Dilution Effect ◽  
Gradual Decrease ◽  
Gel Point ◽  
Dynamic Mode ◽  
Curing Process ◽  
Scanning Calorimetry ◽  
Polyphenylene Oxide

Diallyl orthophthalate (DAOP) prepolymer was investigated as a reactive plasticizer to improve the processability of thermoplastics. The rheology of blends of DAOP prepolymer initiated by 2,3-dimethyl-2,3-diphenylbutane (DMDPB) and polyphenylene oxide (PPO) was monitored during the curing process, and their thermal properties and morphology in separated phases were also studied. Differential scanning calorimetry (DSC) results showed that the cure degree of the reactively plasticized DAOP prepolymer was reduced with increasing PPO due to the dilution effect. The increasing amount of the DAOP prepolymer led to a gradual decrease in the viscosity of the blends and the rheology behavior was consistent with the chemical gelation of DAOP prepolymer in blends. This indicated that the addition of the DAOP prepolymer effectively improved processability. The phase separation occurring during curing of the blend and the transition from the static to dynamic mode significantly influences the development of the morphology of the blend corresponding to limited evolution of the conversion around the gel point.

Corrosion Property Analysis of Coating Formulated Using Acrylic Polyol and Silicone Resin Hybrid Systems

2013 ◽  
Vol 746 ◽  
pp. 363-368
Author(s):  
S.K.M. Jamaria ◽  
K. Rameshb ◽  
B. Vengadaesvaranc ◽  
S. Rameshd ◽  
S.R. Raue ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Corrosion Property ◽  
Cross Linking ◽  
Silicone Resin ◽  
Scanning Calorimetry ◽  
Maximum Value ◽  
Infra Red ◽  
Protection Property

Coating systems consist of acrylic polyol resin and silicone intermediate resins were tested for their corrosion resistance properties. The corrosion protection property of the coating was evaluated by using Electrochemical Impedance Spectroscopy (EIS) which showed that system with 70 % of acrylic has the highest corrosion resistance. The maximum value of corrosion resistance obtained was found to be 1.40 x 109Ω on the 30thday for the 70 % of acrylic sample. The glass transition temperature (Tg) obtained using the Differential Scanning Calorimetry (DSC) were in the range of 23 °C to 65 °C. It showed that all samples are suitable for decorative paints, general industrial coatings and floor care coatings. The functional groups and also the cross-linking between the organic resins were analyzed using Fourier Transform Infra-Red Spectroscopy.

A comparative study on the effect of higher acrylate on cross-linkable PMMA used as environment friendly latexes

2020 ◽  
Vol 32 (2) ◽  
pp. 135-141
Author(s):  
Sweta Shukla
Keyword(s):  
Thermal Analysis ◽  
Differential Scanning Calorimetry ◽  
Butyl Methacrylate ◽  
Cross Linking ◽  
Scanning Calorimetry ◽  
Environment Friendly ◽  
Glycol Diacrylate ◽  
Poly Propylene ◽  
Kinetics Of ◽  
Scanning Electron

The kinetics of emulsion polymerization of monomers methyl methacrylate (MMA)/ n-butyl methacrylate (BMA) was studied to investigate the effect of cross-linkable monomer poly(propylene glycol diacrylate) (PPGDA). The results showed that by the incorporation of PPGDA rate constant of reaction decreased. Fourier transform infrared spectroscopy and scanning electron microscope were used to characterize the synthesized polymers. The thermal analysis of samples was done by differential scanning calorimetry, and the results were compared by the previous studies with MMA/ n-butyl acrylate (BA) and MMA/2-ethylhexyl acrylate (EHA). The glass transition temperature ( T g) values show that the latexes prepared using BA and EHA as comonomer was suitable for binder purpose, but in the present study the T g is not suitable in case of BMA as higher acrylate comonomer. That may be due to more cross-linking in MMA-BMA-PPGDA. The results conclude that the BA and EHA can be used as the binder, but the use of BMA is limited for the binder in coating applications.

scholarly journals Structural and Thermo-Mechanical Properties of Poly(ε-caprolactone) Modified by Various Peroxide Initiators

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1101 ◽  
Author(s):  
Przybysz ◽  
Hejna ◽  
Haponiuk ◽  
Formela
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Cross Linking ◽  
Mechanical And Thermal Properties ◽  
Dicumyl Peroxide ◽  
Organic Peroxides ◽  
Reactive Processing ◽  
Scanning Calorimetry ◽  
Melting Temperatures ◽  
Gel Fraction

The modification of poly(ε-caprolactone) (PCL) was successfully conducted during reactive processing in the presence of dicumyl peroxide (DCP) or di-(2-tert-butyl-peroxyisopropyl)-benzene (BIB). The peroxide initiators were applied in the various amounts of 0.5 or 1.0 pbw (part by weight) into the PCL matrix. The effects of the initiator type and its concentration on the structure and mechanical and thermal properties of PCL were investigated. To achieve a detailed and proper explication of this phenomenon, the decomposition and melting temperatures of DCP and BIB initiators were measured by differential scanning calorimetry. The conjecture of the branching or cross-linking of PCL structure via used peroxides was studied by gel fraction content measurement. Modification in the presence of BIB in PCL was found to effectively increase gel fraction. The result showed that the cross-linking of PCL started at a low content of BIB, while PCL modified by high DCP content was only partially cross-linked or branched. PCL branching and cross-linking were found to have a significant impact on the mechanical properties of PCL. However, the effect of used initiators on poly(ε-caprolactone) properties strongly depended on their structure and content. The obtained results indicated that, for the modification towards cross-linking/branching of PCL structure by using organic peroxides, the best mechanical properties were achieved for PCL modified by 0.5 pbw BIB or 1.0 pbw DCP, while the PCL modified by 1.0 pbw BIB possessed poor mechanical properties, as it was related to over cross-linking.

DEA and DSC study of cubic silsesquioxane epoxy resin nanocomposites

e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Newton Luiz Dias Filho ◽  
Hermes Adolfo de Aquino
Keyword(s):  
Mechanical Properties ◽  
Activation Energy ◽  
Fracture Toughness ◽  
Differential Scanning Calorimetry ◽  
Epoxy Resin ◽  
Loss Factor ◽  
Tensile Modulus ◽  
Dielectric Analysis ◽  
Epoxy Nanocomposites ◽  
Scanning Calorimetry

AbstractNon-isothermal dielectric analysis (DEA) and differential scanning calorimetry (DSC) techniques were used to study the epoxy nanocomposites prepared by reacting 1,3,5,7,9,11,13,15-octa[dimethylsiloxypropylglycidylether] pentaciclo [9.5.1.13,9.15,15 .17,13] octasilsesquioxane (ODPG) with methylenedianiline (MDA). Loss factor (ε”) and activation energy were calculated by DEA. The relationships between the loss factor, the activation energy, the structure of the network, and the mechanical properties were investigated. Activation energies determined by DEA and DSC, heat of polymerization, fracture toughness and tensile modulus show the same profile for mechanical properties with respect to ODPG content.

scholarly journals Investigation on cure kinetics of epoxy resin containing carbon nanotubes modified with hyper-branched polyester

RSC Advances ◽  
2018 ◽  
Vol 8 (52) ◽  
pp. 29830-29839 ◽  
Author(s):  
Li Lu ◽  
Liao Xia ◽  
Hao Zengheng ◽  
Sheng Xingyue ◽  
Zhang Yi ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Differential Scanning Calorimetry ◽  
Epoxy Resin ◽  
Cure Kinetics ◽  
Scanning Calorimetry ◽  
Kinetics Of

The cure kinetics of epoxy resin cured by D-EP, D-EP/CNT composites and D-EP/CNTs-H20 were investigated by non-isothermal differential scanning calorimetry (DSC).

Perfluoropolyether Modified Waterborne Shape Memory Polyurethaneurea Ionomers for Potential Medical Implant Application

2012 ◽  
Vol 499 ◽  
pp. 53-57
Author(s):  
Qun Xia Li ◽  
Zhong Yu Hou
Keyword(s):  
Molecular Structure ◽  
Differential Scanning Calorimetry ◽  
Transition Temperature ◽  
Shape Memory ◽  
Soft Segment ◽  
Cross Linking ◽  
Isophorone Diisocyanate ◽  
Scanning Calorimetry ◽  
Weight Percentage ◽  
Ft Ir

A series of cross-linked fluorinated waterborne shape memory polyurethaneurea (PUU) ionomers were synthesized from polycaprolactone diol, perfluoropolyether diol (PFPE), dimethylolproionic acid, isophorone diisocyanate, ethylenediamine (EDA) and diethylenetriamine (DETA). The effect of PFPE content in the soft segment and the degree of cross-linking on the molecular structure and the properties of for these PUU films was examined and studied. Differential scanning calorimetry showed that the transition temperature for these Tm type shape memory PUU could be facially tuned by PFPE weight percentage and EDA/DETA ratio in the range between 30°C to 50°C, in the vicinity of body temperature. The dependence of their properties on hydrogen-bonds evaluated by FT-IR was also discussed.

Sign in / Sign up

Export Citation Format

Share Document