Composite materials are widely used in temperature fluctuating environments, which make these materials highly prone to cracking. The cracking phenomenon is a result of high thermal stresses that are generated by the mismatch in properties of the composite constituents, particularly the mismatch in the thermal expansion coefficient. The main objective of this study is to understand the micromechanics of such a phenomenon. The problem has been investigated using the finite element method (FEM). The analyses were performed utilizing 3-D prism and axisymmetric models. Hexagonal fiber packing of unidirectional composites was considered. The dimensions of the models were assumed such that the models could provide sufficient information on the behavior near the free surface as well as the interior of fiber composites. Properties of the constituents were considered to be temperature dependent. The elasto-plastic and visco-elastic characteristics of the materials were also included. The transient thermal analysis of the models showed that, for most practical applications, the temperature gradient in the composite constituents has minor effects on the stresses generated. Therefore, several stress analyses were performed assuming a uniformly changing temperature throughout the composite. The elastic analysis of thermal stresses and deformations showed high radial and hoop stress concentrations occurring at the fiber end on the free surface. This is contrary to the shear-lag theorem, which assumes that these stress components are negligible. An overlapping hypothesis, based on the deformation of the fiber and matrix, is proposed to explain such high radial and hoop stresses. Using regular FEM elements, it was concluded that the stresses are singular in nature. The stress singularity was numerically investigated and found to be of the type r -á with á being dependent on the material properties but having a value close to 1/3. The elasto-visco-plastic behavior of composites was also analyzed. Large plastic strains were localized at the fiber end even for a small temperature change. Creep effects that were significant at elevated temperatures brought about some stress relaxation during the manufacturing process. Thermally induced stress concentration in composites can be controlled, to some extent, by changing the geometry of the free surface. The analysis of such effects indicated that reduction of the contact angle between the fiber and the matrix on the fire surface reduced the high radial and hoop stress magnitudes. Also, the influence of covering the free surface of the composite with a thin layer of matrix-like material was studied. The magnitudes of the radial and hoop stress components were substantially reduced. The case when the cover and the composite are made in separate stages (two-stage covering), was also studied. Based on the analysis, effective and practical ways of applying the cover are recommended. To verify the effects of the covering process, experiments were conducted on large-scale laboratory-made composite samples. The samples with the free surface covered with a thin layer of matrix-like material showed no trace of cracking or fiber/matrix debonding even after 1000 thermal cycles. On the other hand, in the samples without cover, exposed to identical thermal cycling, numerous matrix cracks and extensive fiber/matrix debonding were observed.

Sulfide Stress Cracking (SSC) resistance of the newly developed API-X100 High Strength Low Alloy (HSLA) steel was investigated in the NACE TM0177 "A" solution. The NACE TM0177 "A" solution is a hydrogen sulfide (H2S) saturated solution containing 5.0 wt.% sodium chloride (NaC1) and 0.5 wt.% acetic acid (CH3COOH). The aim of this thesis was to study the effect of microstructure, non-metallic inclusions and alloying elements of the X100 on H2S corrosion and SSC susceptibility. The study was conducted by means of electrochemical polarization techniques and constant load (proof ring) testing. Microstructural analysis and electrochemical polarization results for X100were compared with those for X80, an older generation HSLA steel. Uniaxial constant load SSC testing was conducted using X100 samples and the results were compared with those reported for older generation HSLA steels. Addition of H2S to the NACE TM0177 "A" solution increased the corrosion rate of X100from 51.6 to 96.7 mpy. The effect of H2S on the corrosion rate was similar for X80. The corrosion rate for X80 increased from 45.2 to 80.2 mpy when H2S was added to the test solution. Addition of H2S enhanced the anodic kinetics by forming a catalyst (FeHSads) on the metal surface and as a result, shifted the anodic polarization curve to more current densities. Moreover, the cathodic half cell potential increased due to the decrease in pH, from 2.9 to 2.7, which shifted the cathodic polarization curve to more current densities. The increase in both the anodic and cathodic currents, after H2S addition, caused the rise in the corrosion current density. In H2S saturated NACE TM-0177 "A" solution, the X100 steel corrosion rate was higher than the X80 steel by 20%. Longer phase boundaries and larger nonmetallic inclusions in the X100 microstructure generated more areas with dissimilar corrosion potentials and therefore, a stronger driving force for corrosion. Higher density of second phase regions and larger nonmetallic inclusions acted as an increased cathode area on the X100 surface which increased the cathodic current density and consequently, increased the corrosion current density. Proof ring tests on the X100 gave a threshold stress value, C5th, of 46% YS, 343.1 MPa(49.7 ksi). The main failure was caused by SSC cracking. SSC nucleated at corrosion pits on the metal surface and microcracks in the metal body and propagated perpendicular to the applied stress. Hydrogen Induced Cracking (HIC) was observed in the X100. HIC cracks nucleated at banded martensite-ferrite interfaces and propagated along the rolling direction parallel to the applied tensile stress through the softer ferrite phase. When compared to older HSLA grades, the X100 tested in this study had a high SSC susceptibility and therefore, is not be recommended for H2S service applications. The high X100 SSC susceptibility was caused by the material high corrosion rates in H2Smedia which formed corrosion pits that acted as crack initiation sites on the metal surface and provided more hydrogen that migrated into the steel. In addition, the X100 inhomogeneous microstructure provided a high density of hydrogen traps in front of the main crack tip which promoted SSC microcrack formation inside the metal. Microcracks in the metal body connected with the main crack tip that originated from corrosion pits which assisted SSC propagation.

No description available.

Environmental stress cracking (ESC) is one of the main, and probably the most common, failure mechanisms involved in polymer fractures. This type of failure is critically important as it occurs suddenly, without any visible pre-fracture deformation. Such failure can be catastrophic and costly in cases where structural integrity is required. In polyethylene (PE), ESC occurs through a slow crack growth mechanism. Cracks initiate from stress-concentrated imperfections, propagate through the bulk of PE, and ultimately result in a brittle fracture. In order to predict the environmental stress cracking resistance (ESCR) of PE, it is necessary to fully understand the molecular structure of the resin. In this thesis, attempts were made to find relationships between molecular structure characteristics and material responses, mainly inter-lamellar entanglements and strain hardening behaviour of PE resins, through mechanical and rheological experiments. Inter-lamellar entanglements are believed to be the main factor controlling slow crack growth of PE. Extent of entanglements and entanglement efficiency were investigated by monitoring the strain hardening behaviour of PE resins in the solid state through a uniaxial tensile test, and in the melt state, through extensional rheometry. ESCR is usually assessed by unreliable and time consuming testing methods such as the notch constant load test (NCLT) on notched PE specimens in the presence of an aggressive fluid and elevated temperatures. In this thesis, a practical, yet reliable, tensile test was developed for the evaluation and prediction of ESCR. The developed test offers a more reliable and consistent ESCR picture without the drawbacks of the subjective notching process and presence of aggressive fluids. Through this test, a factor called ???corrected hardening stiffness (cHS)??? was developed, which can easily be used for a relative ranking of ESCR of different PE resins. Studies were next extended to the melt state via shear and extensional rheometry. Through studies in the shear mode, a molecular weight-normalized average characteristic relaxation time (??N) was found to be efficient in predicting the extent of chain entanglements in resins. This provided a potential melt indicator for a relative measure of ESCR, for linear low density polyethylene (LLDPE), with different short chain branching levels. Extensional studies were conducted to evaluate the strain hardening behaviour in the melt state. An inverse correlation was obtained between ESCR and the melt strain hardening coefficient (MSHC), found from Sentmanat Extensional Rheometry (SER). This indicated an inverse relationship between ESCR and chain extensibility in the melt. In addition, a new factor called ???melt hardening stiffness (mHS)??? was developed from the slope of a stress-strain line, obtained from SER. This factor, analogous to cHS, can be used for a practical and reliable ranking of ESCR of PEs. ESCR is usually associated with classical crystalline phase property indicators, such as crystallinity and lamella thickness. In this thesis, the effect of processing and post processing temperature on the extent of inter-lamellar entanglements were investigated, evaluated, and correlated to ESCR. Also, analysis of the lamella surface area (LSA) was pursued since LSA reflects changes in phase interconnectivity more precisely. The focus of this part of the study was on the effect of temperature on LSA to identify the optimum processing and post-processing conditions which yield a higher LSA. It was reasonable to presume that PE with larger lamella lateral surface areas will have more inter-lamellar entanglements, hence higher ESCR. Finally, a well-controlled ultraviolet (UV) photoinitiated reactive extrusion (REX) process was developed for selective formation of long chain branches in the PE structure. This was conducted to impose restrictions against stretching of the polymer chain, which consequently enhanced ESCR.

Sulfide Stress Cracking (SSC) resistance of the newly developed API-X100 High Strength Low Alloy (HSLA) steel was investigated in the NACE TM0177 "A" solution. The NACE TM0177 "A" solution is a hydrogen sulfide (H2S) saturated solution containing 5.0 wt.% sodium chloride (NaC1) and 0.5 wt.% acetic acid (CH3COOH). The aim of this thesis was to study the effect of microstructure, non-metallic inclusions and alloying elements of the X100 on H2S corrosion and SSC susceptibility. The study was conducted by means of electrochemical polarization techniques and constant load (proof ring) testing. Microstructural analysis and electrochemical polarization results for X100were compared with those for X80, an older generation HSLA steel. Uniaxial constant load SSC testing was conducted using X100 samples and the results were compared with those reported for older generation HSLA steels. Addition of H2S to the NACE TM0177 "A" solution increased the corrosion rate of X100from 51.6 to 96.7 mpy. The effect of H2S on the corrosion rate was similar for X80. The corrosion rate for X80 increased from 45.2 to 80.2 mpy when H2S was added to the test solution. Addition of H2S enhanced the anodic kinetics by forming a catalyst (FeHSads) on the metal surface and as a result, shifted the anodic polarization curve to more current densities. Moreover, the cathodic half cell potential increased due to the decrease in pH, from 2.9 to 2.7, which shifted the cathodic polarization curve to more current densities. The increase in both the anodic and cathodic currents, after H2S addition, caused the rise in the corrosion current density. In H2S saturated NACE TM-0177 "A" solution, the X100 steel corrosion rate was higher than the X80 steel by 20%. Longer phase boundaries and larger nonmetallic inclusions in the X100 microstructure generated more areas with dissimilar corrosion potentials and therefore, a stronger driving force for corrosion. Higher density of second phase regions and larger nonmetallic inclusions acted as an increased cathode area on the X100 surface which increased the cathodic current density and consequently, increased the corrosion current density. Proof ring tests on the X100 gave a threshold stress value, C5th, of 46% YS, 343.1 MPa(49.7 ksi). The main failure was caused by SSC cracking. SSC nucleated at corrosion pits on the metal surface and microcracks in the metal body and propagated perpendicular to the applied stress. Hydrogen Induced Cracking (HIC) was observed in the X100. HIC cracks nucleated at banded martensite-ferrite interfaces and propagated along the rolling direction parallel to the applied tensile stress through the softer ferrite phase. When compared to older HSLA grades, the X100 tested in this study had a high SSC susceptibility and therefore, is not be recommended for H2S service applications. The high X100 SSC susceptibility was caused by the material high corrosion rates in H2Smedia which formed corrosion pits that acted as crack initiation sites on the metal surface and provided more hydrogen that migrated into the steel. In addition, the X100 inhomogeneous microstructure provided a high density of hydrogen traps in front of the main crack tip which promoted SSC microcrack formation inside the metal. Microcracks in the metal body connected with the main crack tip that originated from corrosion pits which assisted SSC propagation. / Applied Science, Faculty of / Materials Engineering, Department of / Graduate

No description available.

No description available.

The influence of two lubricating and cleaning agents and diesel fuel on environmental stress cracking of polyamide reinforced by glass fibers and polycarbonate was studied in this master thesis. Testing of environmental stress cracking was performed by the method of critical bending deformation. Bergen elliptical strain jig was used for testing. The test liquids caused varying levels of environmental stress cracking of amorphous polycarbonate, but they did not cause environmental stress cracking of glass fiber reinforced polyamide. The test method used allows testing the resistance of both materials against environmental stress cracking of any liquid. The results can be used to design products that are expected to be exposed to corrosive liquids. Quantification of the influence of stress free corrosion on the static and impact properties of polycarbonate and glass fiber reinforced polyamide was performed by accelerated test. Specimens were exposed to test liquid and an elevated temperature of 70 °C. The mechanical properties of the tested materials were significantly affected by elevated temperature exposure. The yield strength of the polycarbonate has increased and the toughness has decreased due to physical aging. The tensile strength of glass fiber reinforced polyamide has increased due to a decrease of the moisture content of the material.

Environmental stress cracking (ESC) is a significant problem that has plagued the plastics industry since its discovery nearly 70 years ago. The accelerated brittle failure brought about when a stressed polymer comes in contact with an aggressive environment can happen suddenly with destructive results. Many classes of polymers are susceptible to this type of slow crack growth; however special emphasis has typically been placed on polyolefins due to their wide range of working environments, market dominance and their seemingly chemical resistance. Much research has been focused on formulating environmentally resistant materials, while the evaluation techniques for gauging environmental stress cracking resistance (ESCR) seem to have been left behind. This research focuses on developing a reliable testing technique for evaluating the ESCR of polyethylene resins. Passive acoustic monitoring was adapted to an industrially accepted ESCR test in an attempt to hear polymer damage before it was visually apparent. It was discovered that the low energy released during the early stages of damage and excessive background noise masked passive signals, making this method of evaluation impractical. Alternatively, active ultrasonic monitoring through velocity and attenuation measurements was investigated to see if probing techniques could be used to detect structural damage. Active ultrasonic monitoring of static and tensile stressed samples were able to differentiate plasticization after ageing, however no indication of ESCR properties could be inferred. A novel forced based monitoring system was developed in response to the acoustic testing techniques. Force monitoring was able to provide useful information regarding the failure cycle of ESC and the acquired profiles could describe a failure onset time. Several ageing environments were also tested with force monitoring and a traditional ESCR test to reveal the stress cracking ability of biodiesel, an important finding. / Thesis / Master of Applied Science (MASc) / Accelerated failure of stressed plastics can occur upon exposure to fluids through a phenomenon known as environmental stress cracking (ESC). The following research outlines the development of a novel testing technique to gauge a material’s environmental stress cracking resistance (ESCR). Adaption of passive acoustics to an existing stress cracking test was unable to provide any indication of ESCR, however the use of active ultrasonics was able to show sample plasticization. A novel forced based measuring technique was found to uniquely map the failure progression of a sample undergoing ESC, providing valuable information for understanding the phenomenon. Additional testing was also completed on various environmental fluids to reveal biodiesel’s ability to provoke ESC, an important observation.

The first paper, “Dye Penetrant Induced Microcracking in High-Performance Thermoplastic Polyimide Composites”, studied the possibility of spurious microcracking in three high-performance thermoplastic polyimide composite materials due to zinc iodine dye penetrant. The material systems were IM7/LaRC™-IAX, IM7/LaRC™-IAX2, and IM7/LaRC™-8515. Specimens from each material system were subjected to one of three immersion tests. The first immersion test involved soaking composite specimens previously prepared with different polishing techniques in dye penetrant. In the second test, specimens were immersed in the individual components of the dye penetrant. The final test involved exposure of specimens to one of six solvents followed by exposure to dye penetrant. Results showed that the composite materials have sufficiently high thermal residual stresses to drive microcracking in the presence of dye penetrant without external mechanical loading. There was no evidence that the different polishing techniques had an effect on dye penetrant-induced stress cracking. The dye penetrant components did not produce microcracks in the composites. Some combination of the components must be present to induce microcracking. Observations also revealed that polishing had an effect on the microcracking process of the composites that were initially exposed to solvents then dye penetrant. The second paper, “The Effect of Environmental Stress Cracking on High-Performance Polymeric Composites”, studied solvent stress cracking and solvent-induced strength degradation on four polyimide matrix materials developed at NASA-Langley Research Center. These materials are LaRC™-IAX, LaRC™-IAX2, LaRC™-8515, and LaRC™-PETI-5. Cross-ply specimens were used to characterize solvent stress cracking in composites. Matrix cracking due to solvent exposure was observed in all of the materials. The solvent exposure time of the materials ranged from 1 minute to 96 hours. The results show that residual thermal stresses due to processing in the cross-ply composite specimens are sufficient to drive solvent stress cracking in the matrix. Solvent application lowers the microcracking toughness, G_mc ,values such that the available strain energy, G_m, within the transverse ply groups is sufficient to initiate microcracking. In the absence of a solvent, the same G_m value would not induce microcracking. Transverse flexure tests were performed on unidirectional specimens to determine the effects of the solvents on the material strengths. The presence of certain solvents severely degraded the materials. The manner in which the solvents were applied to the materials determined the degree of material degradation. The results revealed a synergistic effect between stress and solvent. The tests showed that diglyme, MEK, and acetone produced the most severe damage to the materials. The most solvent resistant material was LaRC™-PETI-5. This is followed by LaRC™-8515, LaRC™-IAX2, and LaRC™-IAX respectively. LaRC™- PETI-5 is a thermoset whereas the remaining materials are thermoplastics. / Master of Science