scholarly journals Studies on Sheet Explosive Formulation Based on Octahydro-1,3,5,7-Tetranitro-1,3,5,7-Tetrazocine and Hydroxyl Terminated Polybutadiene

2017 ◽  
Vol 67 (6) ◽  
pp. 617 ◽  
Author(s):  
Suresh Kumar Jangid ◽  
Mrityunjay Kumar Singh ◽  
Vasant Jadavji Solanki ◽  
Rabindra Kumar Sinha ◽  
Krothapalli Prabhakara Subrahmania Murthy
Keyword(s):  
Mechanical Properties ◽  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Kinetic Method ◽  
Decomposition Kinetics ◽  
Thermal And Mechanical Properties ◽  
Binder System ◽  
Scanning Calorimetry ◽  
Velocity Of Detonation ◽  
Kinetics Of

<p class="p1">The effect of replacing hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) in HTPB-binder on the performance, sensitivity, thermal, and mechanical properties of the sheet explosive formulation has been studied. The maximum loading of HMX was achieved up to 78 per cent in HTPB-binder system. The velocity of detonation (VOD) of HMX-based sheet explosive was observed about 7300 m/s which is marginally higher than existing RDX-based sheet explosive formulation (RDX/HTPB-binder, 80/20). The VOD trends were verified by theoretical calculation by BKW code using FORTRAN executable program. The thermal decomposition kinetics of sheet explosive formulations was investigated by differential scanning calorimetry. The activation energy for sheet explosive formulation HMX/HTPB-binder (78/22) was calculated using Kissinger kinetic method and found to be 170.08 kJ/mol, infer that sheet explosive formulation is thermally stable.</p>

Study on Curing Kinetics of MEP-15/593/660 System

2014 ◽  
Vol 988 ◽  
pp. 31-35
Author(s):  
Jia Le Song ◽  
Chan Chan Li ◽  
Zhi Mi Zhou ◽  
Chao Qiang Ye ◽  
Wei Guang Li
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Kinetic Parameters ◽  
Curing Kinetics ◽  
Conversion Ratio ◽  
Scanning Calorimetry ◽  
Degree Of Cure ◽  
Curing Kinetic ◽  
The Relationship ◽  
Kinetics Of

Curing kinetics of MEP-15/593 system and MEP-15/593/660 system is studied by means of differential scanning calorimetry (DSC). Curing kinetic parameters are evaluated and the relationship between diluent 660 and the curing properties is investigated. The results show that the diluent 660 can not only reduce viscosity and activation energy, but also improve the degree of cure and conversion ratio.

Thermal and Mechanical Properties of Cyclized Polybutadiene Dielectrics

1986 ◽  
Vol 76 ◽  
Author(s):  
C. W. Wilkins ◽  
H. E. Bair ◽  
M. G. Chan ◽  
R. S. Hutton
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Physical And Mechanical Properties ◽  
Mechanical Analysis ◽  
Infrared Analysis ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
The Difference ◽  
Thermal Mechanical Analysis ◽  
Lower Glass Transition Temperature

ABSTRACTWe have studied some of the physical and mechanical properties of cyclized polybutadiene (CBR) dielectrics by dynamic mechanical analysis, thermal mechanical analysis, thermogravimetry, infrared analysis, and differential scanning calorimetry. Of interest is the difference in properties between thin (<30 μm) films which have been cured under vacuum and those which have been cured in air. Our results indicate that curing under vacuum prevents oxidation and reduces crosslinking. Vacuum cured films have 20% smaller moduli and 200 lower glass transition temperature than do films produced in air.

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.

Effect of Meta- and Para-Substitution of the Aromatic Diamines on the Properties of Poly(Amidoimidourethane)

2016 ◽  
Vol 721 ◽  
pp. 23-27 ◽  
Author(s):  
Ilya Kobykhno ◽  
Oleg Tolochko ◽  
Ekaterina Vasilyeva ◽  
Andrei Didenko ◽  
Danila Kuznetcov ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Thermal Analysis ◽  
Differential Scanning Calorimetry ◽  
Thermogravimetric Analysis ◽  
Polymer Structure ◽  
Multiblock Copolymers ◽  
Thermal And Mechanical Properties ◽  
Amino Groups ◽  
Scanning Calorimetry ◽  
Aromatic Diamines

The paper experimentally studies the effect of meta and para- substitution of the amino groups in the diamine used in the synthesis of multiblock copolymers. The way for synthesis of new multiblock copolymers with the possibility of replacing the diamine in the polymer structure was shown. Thermal and mechanical properties of synthesized copolymers had been characterized by means of differential scanning calorimetry, thermogravimetric analysis, dynamic mechanical thermal analysis and by nanoindentation and tensile test.

Study on the β1→α+β2 Transformation Kinetics of Ti-6Al-4V Alloy by DSC

2014 ◽  
Vol 508 ◽  
pp. 110-113
Author(s):  
Rong Hua Zhang ◽  
Biao Wu ◽  
Xiao Ping Zheng
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Phase Transformation ◽  
Cooling Rate ◽  
Volume Fraction ◽  
Avrami Exponent ◽  
Transformation Kinetics ◽  
Cooling Process ◽  
Scanning Calorimetry ◽  
Kinetics Of

The temperature and duration of β1→α+β2 transformation of Ti-6Al-4V alloy in cooling process were measured by differential scanning calorimetry, and transformation activation energy and Avrami exponent of β1→α+β2 were also calculated. The results show that the cooling rate is in the range of 在5～20°C/min, the transformation temperature and the transformation duration β1→α+β2 transformation of Ti-6Al-4V alloy decreased with the increasing cooling rate, its transformation activation energy decreased with the increasing phase transformation volume fraction, and Avrami exponent was between 1 and 2 at 660°C.

Non—Isothermal Differential Scanning Calorimetry Studies on Nanocrystallization Kinetics of Fe81Si3.5B13.5C2 Amorphous Alloy

2011 ◽  
Vol 688 ◽  
pp. 180-185
Author(s):  
Yu Zhang ◽  
Wei Lu ◽  
Biao Yan ◽  
Yu Xin Wang ◽  
Ying Yang
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Amorphous Alloy ◽  
Three Dimensional ◽  
Crystallization Mechanism ◽  
Scanning Calorimetry ◽  
Average Value ◽  
Initial Stage ◽  
Friedman Method ◽  
Kinetics Of

The nanocrystallization kinetics of the Fe81Si3.5B13.5C2amorphous alloy was investigated by differential scanning calorimetry (DSC). The apparent activation energy Ea, as well as the nucleation and growth kinetic parameters has been calculated by Kissinger and Ozawa methods. The changeable activation energy Eawith crystalline fraction α was obtained by the expended Friedman method without assuming the kinetic model function, and the average value of Eawas 364±20 kJ/mol. It was shown that the crystallization mechanism of initial stage (0<α<0.7) of the transformation was bulk crystallization with two and three dimensional nucleation graining growth which was controlled by diffusion. For the middle stage (0.7<α<0.9), the crystallization mechanism is surface crystallization with one dimensional nucleation graining growth at a near-zero nucleation rate. In the final stage(α>0.9)，the local Avrami exponents rose anomalously from 1.4 to about 2.0.

scholarly journals Curing Reaction Kinetics of the EHTPB-Based PBX Binder System and Its Mechanical Properties

Coatings ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1266
Author(s):  
Xing Zhang ◽  
Yucun Liu ◽  
Tao Chai ◽  
Zhongliang Ma ◽  
Kanghui Jia
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Reaction Kinetics ◽  
Testing Machine ◽  
Curing Process ◽  
Binder System ◽  
Isophorone Diisocyanate ◽  
Scanning Calorimetry ◽  
Curing Reaction ◽  
Kinetics Of

In this research, differential scanning calorimetry (DSC) was employed to compare the curing reaction kinetics of the epoxidized hydroxyl terminated polybutadiene-isophorone diisocyanate (EHTPB-IPDI) and hydroxyl terminated polybutadiene-isophorone diisocyanate (HTPB-IPDI) binder systems. Glass transition temperature (Tg) and mechanical properties of the EHTPB-IPDI and HTPB-IPDI binder systems were determined using the DSC method and a universal testing machine, respectively. For the EHTPB-IPDI binder system, the change of viscosity during the curing process in the presence of dibutyltin silicate (DBTDL) and tin 2-ethylhexanoate (TECH) catalysts was studied, and the activation energy was estimated. The results show that the activation energies (Ea) of the curing reaction of the EHTPB-IPDI and HTPB-IPDI binder systems are 53.8 and 59.1 kJ·mol−1, respectively. While their average initial curing temperatures of the two systems are 178.2 and 189.5 °C, respectively. The EHTPB-IPDI binder system exhibits a higher reactivity. Compared with the HTPB-IPDI binder system, the Tg of the EHTPB-IPDI binder system is increased by 5 °C. Its tensile strength and tear strength are increased by 12% and 17%, respectively, while its elongation at break is reduced by 10%. Epoxy groups and isocyanates react to form oxazolidinones, thereby improving the mechanical properties and thermal stability of polyurethane materials. These differences indicate that the EHTPB-IPDI binder system has better thermal stability and mechanical properties. During the EHTPB-IPDI binder system’s curing process, the DBTDL catalyst may ensure a higher viscosity growth rate, indicating a better catalytic effect, consistent with the prediction results obtained using the non-isothermal kinetic analysis method.

Pad Degradation During CMP Process: Effect of Soak in Slurry and Water on Thermal and Mechanical Properties of the CMP Pads

2003 ◽  
Vol 767 ◽  
Author(s):  
A. Tregub ◽  
G. Ng ◽  
M. Moinpour
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Thermal Gravimetric Analysis ◽  
Mechanical Analysis ◽  
Gravimetric Analysis ◽  
Thermal And Mechanical Properties ◽  
Thermal Gravimetric ◽  
Scanning Calorimetry ◽  
Modulated Differential Scanning Calorimetry ◽  
Thermal Mechanical Analysis

AbstractSoak of polyurethane-based CMP pads in tungsten slurry and de-ionized water and its effect on retention of thermal and mechanical properties of the pads was studied using Dynamic Mechanical Analysis (DMA), Thermal Mechanical Analysis (TMA), Thermal Gravimetric Analysis (TGA), and Modulated Differential Scanning Calorimetry (MDSC). Simultaneous cross-linking and plastisizing due to soak were established using DMA and MDSC analysis. The stable operating temperature range and its dependence on soak time were determined using TMA analysis. Substantial difference in diffusion behavior of the “soft” and “hard” pads was discovered: diffusion into the hard pads followed Fickian law [1], while diffusion into the multi-layer soft pads was dominated by the fast filling of the highly porous pad surface with liquid.During a traditional CMP process, which involves application of polishing pads and slurry, the pad properties can be substantially and irreversibly changed as the result of slurry/rinse water absorption.The retention of the pad properties after exposure was monitored using such thermal and mechanical techniques, as Thermal Mechanical Analysis (TMA), Dynamical Mechanical Analysis (DMA), Modulated Differential Scanning Calorimetry (MDSC), Thermal Gravimetric Analysis (TGA).

Crystallization kinetics of amorphous Ga–Sb–Te chalcogenide films: Part I. Nonisothermal studies by differential scanning calorimetry

2004 ◽  
Vol 19 (10) ◽  
pp. 2929-2937 ◽  
Author(s):  
Chain-Ming Lee ◽  
Yeong-Iuan Lin ◽  
Tsung-Shune Chin
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Crystallization Kinetics ◽  
Crystallization Temperature ◽  
Ternary Phase Diagram ◽  
Film Deposition ◽  
Rate Dependency ◽  
Scanning Calorimetry ◽  
Kinetics Parameters ◽  
Kinetics Of

Nonisothermal crystallization kinetics of amorphous chalcogenide Ga–Sb–Te films with compositions along the pseudo-binary tie-lines connecting Sb7Te3−GaSb and Sb2Te3–GaSb of the ternary phase diagram were investigated by means of differential scanning calorimetry. Powder samples were prepared firstly by film deposition using a co-sputtering method; the films were then stripped from the substrate. The activation energy (Ea) and rate factor (Ko) were evaluated from the heating rate dependency of the crystallization temperature using the Kissinger method. The kinetic exponent (n) was deduced from the exothermic peak integrals using the Ozawa method. The crystallization temperature (Tx = 181 to 327 °C) and activation energy (Ea= 2.8 to 6.5 eV) increased monotonically with increasing GaSb content and reached a maximum value in compositions located at the vicinity of GaSb. The kinetic exponent is temperature dependent and shows higher values in the SbTe-rich compositions. Promising media compositions worthy of further studies were identified through the determined kinetics parameters.

scholarly journals KINETIC STUDY OF SYNTHESIS REACTION OF LIGNOSULFONATE USING ISOTHERMAL DIFFERENTIAL SCANNING CALORIMETRY METHOD

2017 ◽  
Vol 55 (4) ◽  
pp. 443 ◽  
Author(s):  
Giang Truong Nguyen ◽  
Kien Trung Tran ◽  
Thiem Van Pham ◽  
Hoa Thi Nguyen
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Kinetic Study ◽  
Preexponential Factor ◽  
Synthesis Reaction ◽  
Scanning Calorimetry ◽  
Differential Scanning Calorimetry Method ◽  
Kinetics Of

The kinetics of lignin methylsulfonation were studied in solution by using differential scanning calorimetry (DSC) techniques under an isothermal program, at 55, 65, 75 and 85°C, respectively. It was found that activation energy, Eα =  41.26 kJ/mol, and preexponential factor A was 1.85×103 s-1.

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