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vì các mục khác nhau nên chỉ mang tính tương đối, buổi học cuối cùng nộp cho thầy,
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tiếng anh sẽ bị trừ 50% số điểm vì phải kiểm tra xem các em viết đúng ý hay không).

Nanocomposite Science and Technology

(P. M. Ajayan, L. S. Schadler, P. V. Braun)

1) 1.2 Ceramic/Metal Nanocomposites, 1.2.1 Nanocomposites by Mechanical

Alloying (P.3 – 8)
2) 1.2.2 Nanocomposites from Sol – Gel Synthesis (P. 8 – 11)
3) 1.2.3 Nanocomposites by Thermal Spray Synthesis (P.11 – 14)
4) 1.3 Metal Matrix Nanocomposites (P.14 – 18).
5) 1.4 Bulk Ceramic Nanocomposites for Desired Mechanical Prop (P. 18 – 23)
6) 1.6 Nanocomposites for Hard Coatings (P. 24 – 31)
7) 1.7 Carbon Nanotube-Based Nanocomposites (P. 31 – 34). 1.8.2 Applications of
Nanocomposite Wires, 1.8.3 Applications of Nanocomposite Particles (P. 44 –
46).
8) 1.8.1 Encapsulated Composite Nanosystems (P. 36 – 44)
9) 1.9 Inorganic Nanocomposites for Optical Applications (P. 46 – 49).
10) 1.10 Inorganic Nanocomposites for Electrical Applications (P. 49 – 52).
11) 1.11 Nanoporous Structures and Membranes: Other Nanocomposites (P. 53 – 57).
12) 1.12.1 Particle-Dispersed Magnetic Nanocomposites - 1.12.2
Magnetic Multilayer Nanocomposites, 1.12.2.1 Microstructure and Thermal
Stability of Layered Magnetic Nanocomposites (P. 57 – 61).
13) 1.12.2.2 Media Materials (P. 61 – 64).
14) 1.13 Nanocomposite Structures having Miscellaneous Properties, 1.14Concluding
Remarks on Metal/Ceramic Nanocomposites (P. 64 – 69).
15) 2.1 Introduction (P. 77 – 80).
16) 2.2.1.1 Carbon Nanotubes (P. 80 – 85).
17) 2.2.1.2 Nanotube Processing, 2.2.1.3 Purity (P. 85 – 89).
18) 2.2.1.4 Other Nanotubes, 2.2.2 Plate-like Nanofillers (P. 89 – 93).
19) 2.2.3 Equi-axed Nanoparticle Fillers (P. 93 – 95).
20) 2.3 Inorganic Filler – Polymer Interfaces (P. 96 – 100).
21) 2.4 Processing of Polymer Nanocomposites - 2.4.1
Nanotube/Polymer Composites (P. 100 – 103).
22) 2.4.2 Layered Filler – Polymer Composite Processing đến 2.4.2.2 Polyimide
Matrices (P. 103 – 108).
23) 2.4.2.3 Polypropylene and Polyethylene Matrices đến hết 2.4.3.3 In-Situ
Polymerization (P. 108 – 112).
24) 2.4.3.4 In-Situ Particle Processing – Ceramic/Polymer Composites, 2.4.3.5 In-Situ
Particle Processing – Metal/Polymer Nanocomposites (P. 112 – 116).
25) 2.4.4 Modification of Interfaces đến hết 2.5.1 Mechanical Properties (P.117-122)
26) 2.5.1.1 Modulus and the Load-Carrying Capability of Nanofillers đến hết
Nanotubes (P. 122-126).
27) Equi-axed nanoparticles, 2.5.1.2 Failure Stress and Strain – Toughness (P. 126-
131)
28) 2.5.1.3 Glass Transition and Relaxation Behavior, 2.5.1.4 Abrasion and Wear
Resistance (P. 131-134).
29) 2.5.3 Dimensional Stability, 2.5.4 Thermal Stability and Flammability (P. 135-
138).
30) 2.5.5 Electrical and Optical Properties, 2.5.5.1 Resistivity, Permittivity, and
Breakdown Strength, 2.5.5.2 Optical Clarity, 2.5.5.3 Refractive Index Control
(P.138-141).
31) 2.5.5.4 Light-Emitting Devices, 2.5.5.5 Other Optical Activity, 2.6 Summary (P.
141-144).
32) 3.1 Introduction, 3.2 Natural Nanocomposite Materials (P.155-158).
33) 3.2.1 Biologically Synthesized Nanoparticles, 3.2.2 Biologically Synthesized
Nanostructures (P. 159-165).
34) 3.3 Biologically Derived Synthetic Nanocomposites, 3.3.1 Protein-Based
Nanostructure Formation, 3.3.2 DNA-Templated Nanostructure Formation, 3.3.3
Protein Assembly (P. 165-170).
35) 3.4 Biologically Inspired Nanocomposites (P. 171-178).
36) 3.4.2 Liquid-Crystal Templating of Thin Films, 3.4.3 Block-Copolymer
Templating, (P. 194-197).
37) 4.1 Introduction – The Need For Modeling, 4.2 Current Conceptual Frameworks,
4.3 Multiscale Modeling (P. 215 -220).
Polymer nanocomposites
(Yiu-Wing Mai and Zhong-Zhen Yu)
38) 1.1 Introduction 1.2 Nylon 6-clay hybrid (NCH), 1.3 Synthesis of nylon 6-clay
hybrid (NCH) 1.3.1 Clay organization andmonomer swelling, 1.3.2 Synthesizing
the nylon-clay nanocomposite (P. 3-6).
39) 1.6 Properties of NCH, 1.6.1 Mechanical properties, 1.6.2 Gas barrier
characteristics of NCH, 1.6.3 Flame retardancy, 1.6.4 Self-passivation, 1.7
Synthesizing NCH using different types of clay, (P.19-23).
40) 2.1 Introduction, 2.2 Epoxy-layered silicate nanocomposites, 2.2.1 Layered silicate
surface modification, 2.2.2 Rheology of epoxy layered silicate network precursors
(P.29-34).
41) 2.2.3 Formation and microstructure of epoxy nanocomposites, (P. 34-39)
42) 2.2.4 Other strategies of layered silicate nanocomposite synthesis, 2.2.5
Mechanical properties (P. 39-43).
43) 2.2.6 Barrier properties and solvent uptake, 2.2.7 Thermal and flame retardation
properties, (P. 43-47).
44) 2.3 Epoxy-nanocomposites based on other nanofillers, 2.4 Ternary epoxy
nanocomposite systems, 2.4.1 Ternary composites containing layered
nanoparticles and a rubbery phase (P. 47-51).
45) 2.4.2 Ternary systems with other nanoadditives, 2.4.3 Epoxy composites
containing fibres and a nanostructured filler, 2.5 Future trends (P. 51-53).
46) 3.1 Introduction, 3.2 Definition and categories of biodegradable polymers, 3.3
Properties and drawbacks of biodegradable Polymers, 3.4 Polymer/layered silicate
nanocomposite Technology, (P. 57-62).
47) PHB and its nanocomposites, Plant oils-based polymers and their nanocomposites
(P. 69-74).
48) Cellulose and its nanocomposites, Gelatin and its nanocomposites, Chitosan and
its nanocomposites (P. 74-76).
49) 3.7.2 Biodegradable polymers from petroleum sources, PBS and its
nanocomposites (P. 76-80).
50) Biodegradable aliphatic polyesters, PCL and its nanocomposites, (P. 80-84).
51) PVA and its nanocomposites, 3.8 Properties, 3.8.1 Mechanical properties, (P. 84-
90).
52) Tensile properties (P. 90-94).
53) Flexural properties, Heat distortion temperature, 3.8.3 Thermal stability, (P. 94-
98).
54) 3.9.1 PLA and its nanocomposites, 3.9.2 PHB and its nanocomposites, 3.9.3 PBS
and its nanocomposites, 3.9.4 Other polyesters and their nanocomposites, (P. 101-
106).
55) 3.11 Foamprocessing of biodegradable Nanocomposites, 3.12 Conclusions, (P.
115-118).