Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Crack energy

Due to the plane-specific namre of crack nucleation under multiaxial tests. Mars and Fatemi proposed the cracking energy density as an equivalence parameter that represents the portion of strain energy density available to be released as crack growth on a specific material plane. The form of the cracking energy density Wc is... [Pg.675]

Based on comparison of three traditional equivalence parameters with cracking energy density, the maximum principal strain corresponded the closest to the cracking energy density. Thus, Mars and Fatemi judged that the maximum principal strain is the most robust and meaningful of the traditional parameters considered in their work. [Pg.675]

ABB Lummus Global/Solvay SA Ethylene dichloride (EDC) Ethylene and chlorine High-yield direct chlorination no purification prior to cracking energy efficient NA NA... [Pg.143]

The parameters include the critical cracking energy G and the mode-I tensile toughness of the coating. For the dual layer and triple layer systems presented here, the parameters deduced from three experiments for each type of sample are presented in Tables 6 and 7. The strain values are measured to an accuracy of 0.02% following a prior calibration. The applied stress is known to be within 0.1%, from a force sensor and the distance between two cracks is the average of twenty or so values determined to an accuracy of one micron in the central part of the specimen. [Pg.71]

In, the central zone, the regular distribution of transverse cracks shows that the induced strain is rather homogeneous. Consequently, many analytical models can be applied in order to determine the intrinsic parameters of the coatings. The critical cracking energy and the mode I fracture toughness of the deposited silicon carbide film were assessed by means of the model presented previously. It should be remembered that it was first established and developed for composite materials based on research by Kelly and subsequently by Hu ", that when the stress normal to the coating reaches a critical value... [Pg.72]

S. H. Ng, H. Seoud, M. Stanciulescu, and Y. Sugimoto, Conversion of Polyethylene to Transportation Fuels through Pyrolysis and Catalytic Cracking, Energy and Fuels, 9, 735-742 (1995). [Pg.68]

S. H. Ng, Conversion of polyethylene blended with VGO to transportation fuels by catalytic cracking. Energy Fuels, 9, 216 (1995). [Pg.110]

Schbek G., Thermodynamics and Thermal Activation of Dislocations in Dislocations in Solids, edited by E. R. N. Nabarro, North-Holland Pub. Co., Amsterdam The Netherlands, 1980. Schoeck G., Dislocation Emission from Crack Tips as a Variational Problem of the Crack Energy, J. Mech. Phys. Solids 44, 413 (1996). [Pg.767]

The relationship between the cracking energy or the critical stress intensity factor and porosity is more complex, and this relationship was establish quahtatively by Beaudoin [94] (Fig. 5.41). These both parameters depertd also on the sample drying procedure, which is understandable in the light of water irtflnence on paste strength, related to the humidity of envirorrment where it was stored. [Pg.328]

In the first case, the crack meets a particle which, provided it is strong enough, stops the crack s progress and forces the tip to broaden. Crack broadening will dissipate the crack energy and, thns, will relieve the stress concentration at this critical point, and will be manifested in some form of plastic deformation round the crack tip. [Pg.553]

In the second case, it is just possible that crack energy dissipation can occur by deformation of the second-phase particles at the tip actually deforming, while staying anchored on both sides of the crack, but its probability is low. Much more likely is that energy will be expended in deforming the particles to such an extent that they collapse in on themselves or they are pulled out of the matrix, leaving a void on one side of the crack and the deformed particle on the other. [Pg.553]


See other pages where Crack energy is mentioned: [Pg.287]    [Pg.673]    [Pg.675]    [Pg.675]    [Pg.680]    [Pg.681]    [Pg.682]    [Pg.46]    [Pg.46]    [Pg.48]    [Pg.49]    [Pg.73]    [Pg.73]    [Pg.109]    [Pg.417]    [Pg.294]    [Pg.53]    [Pg.73]    [Pg.73]    [Pg.78]    [Pg.333]    [Pg.462]    [Pg.104]    [Pg.334]    [Pg.165]    [Pg.118]    [Pg.363]    [Pg.364]    [Pg.185]    [Pg.185]   
See also in sourсe #XX -- [ Pg.130 , Pg.134 , Pg.135 , Pg.136 , Pg.137 , Pg.138 , Pg.139 , Pg.140 , Pg.141 , Pg.142 , Pg.143 , Pg.144 , Pg.145 , Pg.146 , Pg.147 , Pg.148 , Pg.149 , Pg.161 , Pg.229 , Pg.230 , Pg.232 , Pg.248 , Pg.255 , Pg.310 , Pg.345 , Pg.480 ]




SEARCH



Crack fracture, energy associated

Crack initiation energy

Crack potential energy

Crack propagation, energy required

Cracking energy consumption

Cracking energy density

Cracks dissipating energy

Elastic energy crack driving force

Energy balances cracking

Energy cracking

Estimation of Crack-Driving Force G from Energy Loss Rate (Irwin and Kies

Interface cracking energy

The energy balance of crack propagation

© 2024 chempedia.info