Strengthening Mechanisms in Nanostructured Al/Sicp Composite Manufactured by Accumulative
Total Page:16
File Type:pdf, Size:1020Kb
1 Strengthening mechanisms in nanostructured Al/SiCp composite
2 manufactured by accumulative press bonding
3 4 Sajjad Amirkhanlou a,b,c,*, Mehdi Rahimian c,d, Mostafa Ketabchi a, Nader Parvin a, Parisa
5 Yaghinali a, Fernando Carreño b
6 7 a Department of Mining and Metallurgical Engineering, Amirkabir University of Technology, Tehran,
8 Iran
9 b Department of Physical Metallurgy, CENIM-CSIC, Av. Gregorio del Amo 8, 28040 Madrid, Spain
10 c Institute of Materials and Manufacturing, Brunel University London, London UB8 3PH, United
11 Kingdom
12 d IMDEA Materials Institute, C/Eric Kandel 2, 28906, Getafe, Madrid, Spain
13 14 * Corresponding author: Email: [email protected]; [email protected] 15
16
17 Abstract
18 The strengthening mechanisms in nanostructured Al/SiCp composite deformed to
19 high strain by a novel severe plastic deformation process, accumulative press
20 bonding (APB), was investigated. The composite exhibited yield strength of 148
21 MPa which was 5 and 1.5 times higher than that of raw aluminum (29 MPa) and
22 aluminum-APB (95 MPa) alloys, respectively. A remarkable increase was also
23 observed in the ultimate tensile strength of Al/SiCp-APB composite, 222 MPa,
24 which was 2.5 and 1.2 times greater than the obtained values for raw aluminum
25 (88 MPa) and aluminum-APB (180 MPa) alloys, respectively. Analytical models
26 well described the contribution of various strengthening mechanisms. The
27 contribution of grain boundary, strain hardening, thermal mismatch, Orowan,
28 elastic mismatch and load-bearing strengthening mechanisms to the overall
29 strength of the Al/SiCp micro-composite were 64.9, 49, 6.8, 2.4, 5.4 and 1.5 MPa,
30 respectively. Whereas Orowan strengthening mechanism was considered as the 2
31 most dominating strengthening mechanism in Al/SiCp nanocomposites, it was
32 negligible for strengthening of the micro-composite. Al/SiCp nanocomposite
33 showed good agreement with quadratic summation model; however, experimental
34 results exhibited a good accordance with arithmetic and compounding summation
35 models in the micro-composite. While average grain size of the composite reached
36 380 nm, it was less than 100 nm in the vicinity of SiC particles as a result of
37 particle stimulated nucleation mechanism.
38 39 Keywords: Accumulative press bonding (APB); Severe plastic deformation (SPD);
40 Strengthening mechanisms; Analytical models; Metal matrix composites;
41 Nanostructured materials
42
43 1. Introduction
44 Aluminum matrix composites (AMCs), reinforced with particulate reinforcement,
45 have attracted considerable attention in automotive and aerospace industries, due
46 to their low weight and high mechanical properties [1, 2]. Silicon carbide (SiCp) is
47 considered as a typical cost effective particulate reinforcement used widely in
48 AMCs because of its high strength and modulus [3, 4]. Traditional processing
49 routes for fabrication of Al/SiCp composite, including casting, powder metallurgy
50 and spray forming encounter various shortcomings. The main drawbacks of those
51 liquid state techniques [5, 6] can be referred as SiCp agglomeration, weak
52 adhesion and undesirable chemical reaction occurred between Al and SiCp [7, 8].
53 However, manufacturing techniques in solid state can overcome the above
54 problems [9-11]. Microstructure and mechanical properties of Al/SiCp composite,
55 manufactured by accumulative roll bonding (ARB) as a solid-state process, was 3
56 evaluated by Jamaati et al. [12-14]. Accumulative press bonding (APB), introduced
57 for the first time in our previous works, is another severe plastic deformation
58 process [15, 16] enabling us to fabricate particle reinforced AMCs. Uniform
59 distribution of reinforcement, nano/ultra-fine structure and high mechanical
60 properties are obtained using APB process [17-20]. Many researches were focused
61 on the fabrication and characterization Al/SiCp composites prepared by metal
62 forming processes [21, 22]. However, individual contributions of various
63 micromechanics strengthening factors in AMCs deformed to high strain were not
64 investigated in previous studies. In this study the novel APB process was utilized
65 for fabrication of Al/SiCp composite and the effect and proportion of various
66 strengthening mechanisms on the final yield strength was assessed. Moreover,
67 advanced microstructural characterization techniques were employed to verify
68 each strengthening mechanism.
69
70 2. Experimental procedure
71 As-received AA1050 aluminum sheets, chemical composition is given in Table 1,
72 and SiC particles with an average size of 10 m were used as raw materials.
73 Aluminum sheets with the dimensions of 100 mm 50 mm 1.5 mm were
74 annealed at 623 K (350 ºC) for 1 h. The accumulative press bonding (APB)
75 process for manufacturing of the Al/10 vol.% SiCp composite was schematically
76 reported in ref. [23, 24]. The aluminum sheets were degreased in acetone bath
77 followed by scratch brushing with 0.4 mm wire diameter and peripheral speed of
78 2800 rpm. The reinforcement particles were uniformly spread between surfaces by
79 a hand sprayer. A hydraulic press machine was utilized to form a mechanical bond
80 between two stacked sheets, in a channel die, where the thickness of sheets 4
81 reduced by 50%. The APB process was performed at ambient temperature. The
82 fabricated sheet was cut in two pieces and the whole mentioned process was
83 repeated 5 times in order to increase SiC particles to 10 vol.%. Thereafter, the
84 above process was repeated 7 times but without any reinforcement addition. The
85 same process was employed for the production of the monolithic aluminum in
86 which the aluminum sheets were processed by APB without adding any SiCp
87 powder through the process.
88 Tensile tests were performed according to ASTM E8 standard at a rate of 1.6 by
89 a Houndsfield H50KS machine. The gauge width, thickness and length of
90 specimens were 6, 1.5 and 25 mm, respectively. Various microstructural aspects
91 of specimens were investigated by transmission electron microscopy (TEM, JEOL
92 JEM 2000 FX II, JEOL Ltd. Tokyo, Japan) operating at 200 kV and field-emission
93 scanning transmission electron microscopy (FE-STEM, HITACHI S-4800, Hitachi
94 Ltd., Tokyo, Japan) operating at 10 kV complemented by energy-dispersive
95 spectroscopy (EDS, 10mm2 SDD Detector X-ACT, Oxford instrument, Oxford,
96 England). Also the grain boundary characterization was performed by electron
97 backscattered diffraction (EBSD, JEOL JSM 6500 F) adjusted at 20 kV with a
98 working distance of 15 mm, step size of 80 nm and tilt angle of 70º. Thin foils
99 required for EBSD, TEM and STEM investigations were mechanically ground and
100 punched into 3 mm discs with an average thickness of less than 100 μm. The discs
101 were subsequently thinned to perforation using a twin-jet electropolishing facility
102 (TenuPol-5, Struers) with a solution of 30% nitric acid and 70% methanol at 11 V
103 and 245 K (−28 ºC). The X-ray pattern of the manufactured Al/SiCp composite was
104 recorded with an X-ray diffractometer (XRD). The XRD experiment was conducted by a
105 Philips X’PERT MPD X-ray diffractometer with CuKα radiation in the range of using a 5
106 step size of and a counting time of 1 s per step. Consequently, XRD patterns were
107 analyzed via X’Pert HighScore software.
108
109 3. Results and discussion
110 The stress-strain curves of annealed aluminum (Al), monolithic aluminum (Al-APB)
111 and Al/SiCp-APB composite are shown in Figure 1. According to the Figure 1, the
112 yield strength of the aluminum, which is 29 MPa, was improved by 5 times, as it
113 increases to 148 MPa. A remarkable increase was also observed in the ultimate
114 tensile strength of Al/SiCp-APB composite, 222 MPa, which was 2.5 and 1.2 times
115 greater than the obtained values for raw aluminum (88 MPa) and aluminum-APB
116 (180 MPa) alloys, respectively. Although this study has not been done previously,
117 relevant composites fabricated via other production processes are summarized
118 in Table 2. The superior strength of the produced composite through APB process
119 is obtained mainly due to the uniform distribution of particles, formation of ultra-fine
120 structure and low level of porosity. The enhancement of composite’s strength can
121 be described by different mechanisms. In following sections, microstructural
122 evidences and theoretical models are employed to explain each strengthening
123 mechanism.
124
125 3.1- Grain boundary
126 Figure 2 shows STEM micrographs of Al/SiCp composite after various cycles of
127 APB process. It is observed that gradual grain refining occurred during process
128 and grains are slightly elongated in the longitudinal direction. Average grain size
129 reduced to 380 nm after 14 cycles of APB, Figure 2e. Grain refining is the most
130 desirable strengthening mechanism because it is only mechanism which leads to 6
131 simultaneous increment of strength and toughness [25, 26]. The formation
132 mechanism of nano grains by the APB process is considered as continuous
133 dynamic recovery (CDR). In CDR the size of small (sub) grains remains constant,
134 whereas grains misorientation increases. In fact, there isn’t any nucleation and
135 growth of deformed nuclei in CDR, because the dislocations glide directly from one
136 side of grain to the other side resulting in the increment of grains misorientation.
137 This is the most equilibrated way of obtaining the finest and sharpest histogram of
138 grain sizes, which leads to the highest misorientation for the given processing
139 conditions. The grain refinement mechanisms of pure aluminum under APB
140 process were discussed in our previous studies [19, 20]. However, two other
141 factors encourage CDR of Al/SiCp composite including severe shear deformation
142 and micro-size particles. In fact, finer grain size can be obtained in APB process
143 on account of the present of non-deformable reinforcements. Figure 3 displays the
144 interface of the SiC particle and aluminum matrix. The finer grain sizes are
145 recognized in the vicinity of SiC particles where the average grain size measured
146 less than 100 nm. When the composite is exposed by deformation during the
147 process, the existence of non-deformable particles induces strain to their vicinity.
148 As a result, the vicinity of particles is fertilized to form new boundaries due to the
149 introduction of a high dislocation density, referred as particle stimulated nucleation
150 (PSN) [27, 28]. The accumulation of dislocations in the vicinity of particles
151 facilitated the formation of fine grains by continuous dynamic recovery mechanism.
152 Consequently, the average grain size of the composite, 380 nm, is finer than that
153 of monolithic aluminum which is 450 nm [19]. Other factor, considered for grain
154 refinement of pure aluminum and the composite, is severe shear deformation.
155 TEM micrographs of surface and center of the monolithic aluminum after one APB 7
156 cycle are shown in Figure 4. Comparison of Figure 4a and b demonstrates the
157 higher density of dislocation tangle zones on the surface. This observation is
158 attributed to the severe shear strain exists between the sample and press anvil. In
159 each APB cycle, the surface containing higher dislocation density is moved toward
160 the center resulting in homogeneous distribution of dislocation through the bulk
161 material. Therefore, dislocations formed because of severe shear contribute to the
162 final grain refinement. Grain boundary strengthening () can be explained by well-
163 known Hall-Petch equation (Eq. 1) [29]. Higher fractions of grain boundaries
164 existing in finer grain structures increase the number of obstacles against
165 dislocation movement.
166 (1)
167 where is average grain size, is constant and typically equal to 40 MPa for
168 aluminum alloys [19, 30]. While the grain boundary strengthening was calculated
169 5.2 MPa for Al [20], it increased to 59.6 MPa and 64.9 , for Al-APB and Al/SiCp
170 composite, respectively.
171
172 3.2- Thermal mismatch (TM)
173 Discrepancy of thermal expansion coefficient (CTE) between matrix and
174 reinforcement acts as a dislocation generation source [31, 32]. Since, thermal
175 expansion coefficient of the matrix, , differs from the SiCp reinforcement, , strain is
176 induced to the matrix around the particles resulting in dislocation formation, as
177 shown in Figure 5a. Multi-directional thermal stresses at the particle/matrix
178 interface, which are induced by the difference of thermal expansion between
179 aluminum and SiC particles, result in mismatch strain around the particles. The
180 system makes an attempt to reduce internal energy, mismatch strain, via 8
181 introducing new dislocations [33, 34]. High dislocation density in the vicinity of
182 particles, observed in Figure 5a, can arrange and form new grain boundaries via
183 continuous dynamic recovery during APB process, as shown in Figure 5b.
184 Strengthening effect of thermal mismatch () can be expressed by the following
185 equations [35, 36]:
186 (2)
187 where is shear modulus (~25.4 GPa for aluminum) and is the average value of
188 dislocation strengthening efficiency (∼1 for pure metals [37]) and is the Burgers
189 vector (=0.286 nm [38]). Dislocation density, resulted from CTE mismatch, is
190 governed by particles volume fraction, , difference between processing and
191 ambient temperature, [39], and variation between CTE of particles and matrix, .
192 Dislocation density induced by thermal mismatch can be calculated by [40]:
193 (3)
194 The amount of is calculated around 6.8 MPa for Al/SiCp composite, while this
195 mechanism is not taken into account for Al and Al-APB alloys.
196
197 3.3- Elastic mismatch (EM)
198 The difference of elastic modulus between matrix and reinforcement introduce an
199 additional dislocation into the composite in order to reduce induced plastic strain.
200 The density of generated dislocation due to elastic modulus mismatch can be 9
201 estimated by Eq. (4). These dislocations induce additional strength to the
202 composite which is expressed by Eq. (5) [41]:
203 (4)
204 (5)
205 where is yield strain (0.2%) and is density of dislocations caused by elastic
206 mismatch [42]. Whereas, due to absence of reinforcement in Al and Al-APB, there
207 is no elastic mismatch strengthening effect, it is calculated around 5.4 for Al/SiCp
208 composite.
209
210 3.4- Strain hardening
211 Figure 6 displays EBSD/orientation imaging microscopy (OIM) and grain boundary
212 maps of Al/SiCp composite. The red/gray lines correspond to the low angle grain
213 boundaries (LAGBs) having misorientations 2-15º, and the high angle grain
214 boundaries (HAGBs) are shown as black lines which have misorientations above
215 15º. The fraction of high angle grain boundaries () and the mean misorientation
216 angle of the boundaries () for the Al/SiCp composite were 73% and 35º,
217 respectively. According to EBSD results, it is obvious that APB process had a
218 significant effect on the development of an ultra-fine grain structure surrounded
219 mainly by high-angle boundaries. Formation of the well-developed high angle
220 boundary during APB process is attributed to the rearrangement of the
221 dislocations via short-range diffusion [43-46]. As a result of mechanical
222 deformation, dislocations will be generated resulting in the increment of strength. It
223 is well known that dislocations tend to array and form low angle grain boundaries
224 during severe plastic deformation process. Therefore, low angle grain boundaries
225 can be considered as a dislocation resource. In other word, HAGBs contribute to 10
226 the grain boundary strengthening mechanism which is determined by Hall-Petch
227 relation, whereas dislocation strengthening mechanism is related to LAGBs, as
228 explained by Hansen et al. [47]. The strength imposed by LAGBs to the system is
229 expressed by:
230 (6)
231 where is the dislocation strengthening efficiency (the average value = 0.24) and
232 M is the Taylor factor (for aluminum is 3.06). Following equation shows the density
233 of dislocations introduced by LAGBs to the system [48, 49]:
234 (7)
235 where , and are the mean misorientation of LAGBs, volume fraction of HAGBs and
236 average LAGBs spacing that is measured from EBSD results. is 8, 47 and 49
237 MPa for initial aluminum, Al-APB and Al/SiCp composite processed by APB,
238 respectively.
239
240 3.5- Orowan strengthening
241 Orowan mechanism corresponds to the interaction of the particles and dislocations
242 in which nano particles pin dislocations resulting in bowing dislocation around
243 particles and create Orowan rings. Increment of yield strength, in polycrystalline
244 materials, induced by Orowan mechanisms can be calculated by [41, 50]:
245 (8)
246 where is the Poisson’s ratio (0.33). A small contribution of Orowan strengthening
247 mechanism, , in Al/SiCp micro-composite can be interpreted by large distance of
248 micro-size particles.
249
250 3.6- Load-bearing 11
251 FE-SEM micrographs of Al/SiCp composite after several APB cycles are shown in
252 then Figure 7. With increasing number of cycles, the laminar structure is converted
253 into the homogeneous structure. The formation mechanism of this structure is
254 explained comprehensively in our previous study [17, 18]. It should be briefly
255 pointed out that aluminum plastic flow, because of applied stress during APB, led
256 to refinement and dispersion of SiCp clusters. The high pressures associated with
257 APB resulted in the squeezing of the Al-matrices within the SiCp clusters producing
258 homogenous structure. Formation of strong bond between the particles and matrix
259 due to extensive pressure can be another advantage of current process. Since, in
260 the tensile test a fraction of stress is transferred to particles, having higher
261 modulus and strength compared with matrix, composite can withstand higher load
262 than monolithic aluminum. In order to achieve maximum potential of load-bearing
263 effect, homogeneous distributed particles having strong bond with matrix are
264 required. Figure 8 displays SEM micrographs of Al/SiCp composite produced by
265 APB together with its EDS and X-ray maps. Al4C3 phase, observed usually in the
266 cast Al/SiCp composites, exhibits detrimental effect on interfacial bonding and
267 mechanical properties on account of its brittle nature [51]. The X-ray maps (Figure
268 8b-f) and X-ray diffraction pattern (Figure 9) show that there is no evidence of
269 undesired phase such as Al4C3 in the microstructure considered as the advantage
270 of solid state fabrication of Al/SiCp composite by the current process.
271 Well distributed particles endure a proportion of applied force imposed directly by
272 tensile test. The contribution of load-bearing mechanism in increasing of yield
273 strength is expressed by Eq. 9, which is the modification of shear-lag model:
274 (9) 12
275 where and are referred to volume fraction of particles and matrix yield strength,
276 respectively. is 1.5 MPa for Al/SiCp composite.
277 The total yield strength is calculated by three well-known models referred as
278 arithmetic summation (Eq. 10), quadratic summation (Eq. 11) and compounding
279 methods (Eq. 12) [41, 52, 53]:
280 (10)
281 (11)
282 (12)
283 Contribution of the various strengthening mechanisms as well as yield strength,
284 obtained by various models and tensile tests, are displayed in Table 3. The
285 influence of each factor on yield strength of micro-composite is evaluated against
286 that of nanocomposite, which was investigated in our previous study [20].
287 Matrix flow through micro-particles is easier than nanoparticles so nanocomposite
288 is associated with smaller grain (280 nm) compare with composites reinforced with
289 micro-particles (380 nm). Therefore, improvement of yield strength due to grain
290 boundary mechanism is 75.6 MPa for nanocomposite, while this value is 64.9 for
291 Al/SiCp micro-composite. Although grain boundaries strengthening mechanism has
292 conquered the second place enhancing mechanical properties in the
293 nanocomposite, it is promoted to first place in the micro-size composite. By
294 decreasing volume fraction of reinforcement/matrix interfaces in the macro-
295 composite compare with the nanocomposite, dislocation density formed in the
296 matrix of micro-composite due to thermal and elastic mismatch is significantly
297 decreased. Whereas Orowan strengthening mechanism was considered as the
298 most important strengthening mechanism in nanocomposites, it is negligible for
299 strengthening of the micro-size composites. As a result of large size and distance 13
300 of reinforcement, grains and subgrains interact with dislocations instead of
301 interacting with SiC particles. Strain hardening and grain boundary strengthening
302 mechanisms are considered as the two most effective strengthening mechanisms
303 in Al/SiCp micro-composite. The load transfer effect in both composites is
304 negligible because of particulate shape and low volume fraction of reinforcement.
305 Since the number of active strengthening mechanisms in Al/SiCp nanocomposite is
306 considerably higher than the micro-composite, the final experimental yield strength
307 of the nanocomposite increased up to 210 MPa. Based on the result of
308 calculations performed by each model, it is understood that experimental result
309 exhibits a good accordance with arithmetic summation and compounding models
310 in micro-composite. However, nanocomposite shows good agreement with
311 quadratic summation model, as demonstrated in previous study [20]. Short
312 dislocation gliding distance in the nanocomposites imposed by well distributed
313 nanoparticles and concomitant very fine grains results in the overestimating of
314 calculated results compared with experimental one. In other words, the first
315 obstacle on the way of dislocation movement, which can be LAGBs, HAGBs or
316 nanoparticles, leads to the strengthening of nanocomposite. Therefore, it is
317 expected that considering the contribution of strain hardening (LAGBs), grain
318 boundaries (HAGBs) and Orowan (nanoparticles) mechanisms together in
319 strengthening of nanocomposite, exhibiting an overestimation of the resistance of
320 the alloy.
321
322 4. Conclusions
323 In the present investigation, the micromechanics strengthening in nanostructured
324 Al/SiCp composite deformed to high strain by a novel severe plastic deformation 14
325 process, accumulative press bonding (ARB), was investigated. The improvement
326 in yield strength of Al/SiCp composite was described by various strengthening
327 mechanisms. Advanced microstructural techniques were employed to present
328 evidences of each strengthening mechanism. The conclusions drawn from the
329 results can be summarized as follows:
330 1) Homogeneous distribution of SiC particles (with average particle size of 10
331 µm) was successfully achieved after 14 cycles of APB process.
332 2) The EDS maps and X-ray diffraction pattern showed that there was no
333 evidence of detrimental phases in the microstructure of Al/SiCp composite
334 considered as the advantage of solid state fabrication process.
335 3) Nanostructured Al/SiCp composite with the average grain size of 380 nm and
336 well-developed high-angle grain boundaries (73% high angle boundaries and
337 35° average misorientation angle) was obtained by performing 14 cycles of
338 APB process.
339 4) As a result of particle stimulated nucleation mechanism, grain size of the
340 composite was less than 100 nm in the vicinity of SiC particles.
341 5) The yield strength of the aluminum, being 29 MPa, was improved by 5 times,
342 as it increased to 148 MPa.
343 6) The contribution of grain boundary, strain hardening, thermal mismatch,
344 Orowan, elastic mismatch and load-bearing strengthening mechanisms were
345 64.9, 49, 6.8, 2.4, 5.4 and 1.5 MPa, respectively. Clearly, strain hardening and
346 grain boundary mechanisms demonstrate higher contribution to the overall
347 strength of the Al/SiCp composite.
348 7) Al/SiCp nanocomposite showed good agreement with quadratic summation
349 model, however, based on the result of calculations performed by each model,
350 it is understood that experimental result exhibits a good accordance with
351 arithmetic and compounding summation models in micro-composite. 15
352
353 Acknowledgment
354 The authors acknowledge financial support from CICYT (Spain) under program
355 MAT2012-38962-C03-01, and the Ministry of Science, Research and Technology
356 of Iran.
357
358 16
359 References
360 [1] R. Jamaati, M. Naseri, M.R. Toroghinejad: Mater. Des., 2014, vol. 59, pp. 540-549.
361 [2] R. Jamaati, M.R. Toroghinejad, J. Dutkiewicz, J.A. Szpunar: Mater. Des., 2012, vol.
362 35, pp. 37-42.
363 [3] I. Ibrahim, F. Mohamed, E. Lavernia: J. Mater. Sci., 1991, vol. 26, pp. 1137-1156.
364 [4] E. Lacoste, C. Arvieu, J.M. Quenisset: J. Mater. Sci., 2015, vol. 50, pp. 5583-5592.
365 [5] H. Yue, H. Zhang, X. Gao, J. Chang, S. Zhang, J. Zhang, E. Guo, L. Wang, Z. Yu:
366 Mater. Charact., 2015, vol. 99, pp. 47-51.
367 [6] Š. Nagy, M. Nosko, Ľ. Orovčík, K. Iždinský, S. Kúdela, P. Krížik: Mater. Des., 2015,
368 vol. 66, pp. 1-6.
369 [7] S. Amirkhanlou, B. Niroumand: J. Mater. Process. Technol., 2012, vol. 212, pp. 841-
370 847.
371 [8] S. Amirkhanlou, B. Niroumand: J. Mater. Eng. Perform., 2013, vol. 22, pp. 85-93.
372 [9] Y. Ikoma, T. Toyota, Y. Ejiri, K. Saito, Q. Guo, Z. Horita: J. Mater. Sci., 2015, vol. 51,
373 pp. 138-143.
374 [10] M. Kawasaki, T.G. Langdon: J. Mater. Sci., 2015, vol. 51, pp. 19-32.
375 [11] S. Sabbaghianrad, T.G. Langdon: J. Mater. Sci., 2015, vol. 50, pp. 4357-4365.
376 [12] R. Jamaati, S. Amirkhanlou, M.R. Toroghinejad, B. Niroumand: Mater. Sci. Eng. A,
377 2011, vol. 528, pp. 2143-2148.
378 [13] S. Amirkhanlou, R. Jamaati, B. Niroumand, M.R. Toroghinejad: Mater. Sci. Eng. A,
379 2011, vol. 528, pp. 4462-4467.
380 [14] R. Jamaati, S. Amirkhanlou, M.R. Toroghinejad, B. Niroumand: J. Mater. Eng.
381 Perform., 2012, vol. 21, pp. 1249-1253.
382 [15] M.I. Latypov, M.G. Lee, Y.E. Beygelzimer, D. Prilepo, Y. Gusar, H.S. Kim: Metall.
383 Mater. Trans. A, 2016, vol. 47, pp. 1248-1260. 17
384 [16] Y. Zhang, S. Sabbaghianrad, H. Yang, T.D. Topping, T.G. Langdon, E.J. Lavernia,
385 J.M. Schoenung, S.R. Nutt: Metall. Mater. Trans. A, 2015, vol. 46, pp. 5877-5886.
386 [17] S. Amirkhanlou, M. Ketabchi, N. Parvin, S. Khorsand, R. Bahrami: Mater. Des.,
387 2013, vol. 51, pp. 367-374.
388 [18] S. Amirkhanlou, M. Ketabchi, N. Parvin, G. Drummen: Metall. Mater. Trans. B,
389 2014, vol. 45, pp. 1992-1999.
390 [19] S. Amirkhanlou, M. Askarian, M. Ketabchi, N. Azimi, N. Parvin, F. Carreño: Mater.
391 Charact., 2015, vol. 109, pp. 57-65.
392 [20] S. Amirkhanlou, M. Ketabchi, N. Parvin, A. Orozco-Caballero, F. Carreño: Scripta
393 Mater., 2015, vol. 100, pp. 40-43.
394 [21] M. Rezayat, A. Akbarzadeh, A. Owhadi: Metall. Mater. Trans. A, 2012, vol. 43, pp.
395 2085-2093.
396 [22] A. Ahmadi, M.R. Toroghinejad, A. Najafizadeh: Mater. Des., 2014, vol. 53, pp. 13-
397 19.
398 [23] S. Amirkhanlou, M. Ketabchi, N. Parvin, M. Askarian, F. Carreño: Mater. Sci. Eng.
399 A, 2015, vol. 627, pp. 374-380.
400 [24] S. Amirkhanlou, M. Ketabchi, N. Parvin, S. Khorsand, R. Bahrami: Mater. Des.,
401 2013, vol. 51, pp. 367-374.
402 [25] A. Mishra, B. Kad, F. Gregori, M. Meyers: Acta Mater., 2007, vol. 55, pp. 13-28.
403 [26] R. Jamaati, M.R. Toroghinejad, S. Amirkhanlou, H. Edris: Metall. Mater. Trans. A,
404 2015, vol. 46, pp. 4013-4019.
405 [27] J. Robson, D. Henry, B. Davis: Acta Mater., 2009, vol. 57, pp. 2739-2747.
406 [28] Y. Shen, R. Guan, Z. Zhao, R. Misra: Acta Mater., 2015, vol. 100, pp. 247-255.
407 [29] R. Jamaati, M.R. Toroghinejad, S. Amirkhanlou, H. Edris: Mater. Sci. Eng. A, 2015,
408 vol. 639, pp. 656-662. 18
409 [30] M. Alizadeh: J. Alloys Compd., 2011, vol. 509, pp. 2243-2247.
410 [31] J.G. Park, D.H. Keum, Y.H. Lee: Carbon, 2015, vol. 95, pp. 690-698.
411 [32] S. Dong, J. Zhou, D. Hui, Y. Wang, S. Zhang: Composites Part A: Applied Science
412 and Manufacturing, 2015, vol. 68, pp. 356-364.
413 [33] D. Cheng, J. Niu, Z. Gao, P. Wang: Mod. Phys. Lett. B, 2015, vol. 29, pp. 1540002.
414 [34] Z. Ni, H. Zhao, F. Ye: Vacuum, 2015, vol. 120, pp. 101-106.
415 [35] W. Kim, I. Park, S. Han: Scripta Mater., 2012, vol. 66, pp. 590-593.
416 [36] F. Chen, Z. Chen, F. Mao, T. Wang, Z. Cao: Mater. Sci. Eng. A, 2015, vol. 625, pp.
417 357-368.
418 [37] W. Miller, F. Humphreys: Scripta metallurgica et materialia, 1991, vol. 25, pp. 33-38.
419 [38] K. Edalati, D. Akama, A. Nishio, S. Lee, Y. Yonenaga, J.M. Cubero-Sesin, Z. Horita:
420 Acta Mater., 2014, vol. 69, pp. 68-77.
421 [39] S. Lee, Y. Saito, T. Sakai, H. Utsunomiya: Mater. Sci. Eng. A, 2002, vol. 325, pp.
422 228-235.
423 [40] R. Arsenault, N. Shi: Mater. Sci. Eng., 1986, vol. 81, pp. 175-187.
424 [41] L. Jiang, H. Yang, J.K. Yee, X. Mo, T. Topping, E.J. Lavernia, J.M. Schoenung: Acta
425 Mater., 2016, vol. 103, pp. 128-140.
426 [42] L. Dai, Z. Ling, Y. Bai: Compos. Sci. Technol., 2001, vol. 61, pp. 1057-1063.
427 [43] Y. Saito, N. Tsuji, H. Utsunomiya, T. Sakai, R.G. Hong: Scripta Mater., 1998, vol. 39,
428 pp. 1221-1227.
429 [44] S.H. Lee, Y. Saito, N. Tsuji, H. Utsunomiya, T. Sakai: Scripta Mater., 2002, vol. 46,
430 pp. 281-285.
431 [45] N. Tsuji, Y. Ito, Y. Saito, Y. Minamino: Scripta Mater., 2002, vol. 47, pp. 893-899.
432 [46] T. Yu, N. Hansen, X. Huang: Acta Mater., 2013, vol. 61, pp. 6577-6586.
433 [47] N. Hansen: Scripta Mater., 2004, vol. 51, pp. 801-806. 19
434 [48] J.R. Bowen, P. Prangnell, D.J. Jensen, N. Hansen: Mater. Sci. Eng. A, 2004, vol. 387,
435 pp. 235-239.
436 [49] N. Kamikawa, X. Huang, N. Tsuji, N. Hansen: Acta Mater., 2009, vol. 57, pp. 4198-
437 4208.
438 [50] Z. Zhang, D. Chen: Mater. Sci. Eng. A, 2008, vol. 483, pp. 148-152.
439 [51] J.-C. Lee, J.-Y. Byun, S.-B. Park, H.-I. Lee: Acta Mater., 1998, vol. 46, pp. 1771-
440 1780.
441 [52] Z. Zhang, D. Chen: Scripta Mater., 2006, vol. 54, pp. 1321-1326.
442 [53] C.-S. Kim, I. Sohn, M. Nezafati, J. Ferguson, B.F. Schultz, Z. Bajestani-Gohari, P.K.
443 Rohatgi, K. Cho: J. Mater. Sci., 2013, vol. 48, pp. 4191-4204.
444 [54] S.A. Sajjadi, H. Ezatpour, M.T. Parizi: Mater. Des., 2012, vol. 34, pp. 106-111.
445 [55] S. Amirkhanlou, B. Niroumand: Mater. Des., 2011, vol. 32, pp. 1895-1902.
446 [56] C. Tekmen, I. Ozdemir, U. Cocen, K. Onel: Mater. Sci. Eng. A, 2003, vol. 360, pp.
447 365-371.
448 [57] F. Khodabakhshi, H.G. Yazdabadi, A. Kokabi, A. Simchi: Mater. Sci. Eng. A, 2013,
449 vol. 585, pp. 222-232.
450 [58] C. Sun, M. Song, Z. Wang, Y. He: J. Mater. Eng. Perform., 2011, vol. 20, pp. 1606-
451 1612.
452 [59] B. Ogel, R. Gurbuz: Mater. Sci. Eng. A, 2001, vol. 301, pp. 213-220.
453
454
455
456
457
458 20
459 Table captions:
460 Table 1. Chemical composition of AA1050 sheets.
461 Table 2. Summary of AMCs strength from literatures.
462 Table 3. Contribution of strengthening mechanisms and yield strength obtained by
463 theoretical models and experiment in Al/SiCp composites.
464
465 Figure captions:
466 Figure 1. Engineering stress-strain curves of annealed aluminum (Al), monolithic
467 aluminum (Al-APB) and Al/10 vol.% SiCp composite produced by APB process.
468 Figure 2. STEM micrographs of Al/SiCp composite after different APB cycles; (a) 2,
469 (b) 5, (c) 7 and (d) 10 and (e) 14 cycles.
470 Figure 3. STEM micrograph of aluminum/SiCp interface.
471 Figure 4. TEM micrographs of aluminum after one cycle of APB process; (a)
472 surface (b) center of specimen.
473 Figure 5. TEM micrographs of Al/SiCp interface after 14 cycle of APB process.
474 Figure 6. Al/SiCp composite after 14 APB cycle: (a) EBSD/OIM and (b) grain
475 boundary maps.
476 Figure 7. FE-SEM micrographs of Al/SiCp composite after (a) 1, (b) 3, (c) 5 and (d)
477 10 and (e) 14 APB cycles.
478 Figure 8. (a) SEM micrograph of Al/SiCp composite along with its (b) aluminum, (c)
479 silicon and (d) carbon X-ray maps. EDS analysis of points (e) 1 and (f) 2.
480 Figure 9. X-ray diffraction (XRD) pattern of Al/SiCp composite.
481 21
482
483 Tables:
484 Table 1. Chemical composition of AA1050 sheets.
Element Al Si Fe Mn Cu Mg Zn Ti wt.% Bal. 0.2 0.22 0.02 0.01 0.01 0.01 0.01 485
486 22
487
488 Table 2. Summary of AMCs strength from literatures. AMCs Methods Reinforceme YS (MPa) UTS (MPa) Reference nt particle size
Al/5 wt.% Al2O3 Casting 20 µm ~112 ~157 [54]
Al/5 vol.% SiCp Casting 8 µm ~80 ~115 [55]
Al/3 wt.% Al2O3 Casting 50 nm ~107 ~162 [54]
Al/20 vol.% Al2O3 Casting+extrusion 12 µm ~175 ~220 [56]
Al/2 vol.% SiCp Friction stir welding 15 nm ~130 ~108 [57]
Al/20 vol.% SiCp Powder metallurgy 17 µm ~87 ~107 [58]
Al-5Cu/13vol.% SiCp Powder metallurgy 10 µm ~134 ~175 [59]
Al/10vol.% SiCp Accumulative press 10 µm 180 222 Present work bonding 489
490 23
491 Table 3. Contribution of strengthening mechanisms and yield strength obtained by
492 theoretical models and experiment in Al/SiCp composites.
Strengthening mechanisms and yield Al/SiCp micro-composite Al/SiCp nano-composite strength
Grain boundary () 64.9 75.6 Thermal mismatch () 6.8 39.6 Elastic mismatch () 5.4 34.4 Strain hardening () 49 42 Orowan looping () 2.4 172 Load-bearing () 1.5 0.3 Experimental yield strength () 148 210 Calculated arithmetic yield strength () 159 393 Calculated quadratic yield strength () 111 228 144 Calculated compounding yield strength () 289
493
494