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Polymer/Boron Nitride Nanotube
   (BNNTs) Nanocomposites

                 METE 560



             Ümit TAYFUN

    Middle East Technical University
        Polymer Science & Technology
Boron nitride nanotubes
Boron nitride nanotubes, firstly synthesized in
1995, are structural analogues of carbon
nanotubes with boron and nitrogen atoms
instead of carbon atoms.


BNNTs can be imagined as a rolled up
hexagonal BN layer or as a carbon nanotube
(CNTs) in which alternating B and N atoms
entirely substitute for C atoms

Similar to CNTs, BNNTs have chiralities, an
important geometrical parameter, but for them,
the chiralities do not play an important role in
determining electrical properties

Atomic models of BNNT;

 (a)arm-chair
 (b)zig-zag
 (c)chiral
Properties of BNNTs
BNNTs are chemically inert, oxidation resistant, and
structurally stable.

BNNTs are electrically isolating materials with uniform
electronic properties independent of their size and
chirality.

Therefore, they are evaluated as suitable fillers for the
fabrication of mechanically and thermally enhanced
polymer composites, while preserving the electrical         TEM images of single to multi-wall BNNTs with six walls
isolation of the polymer matrix

Excellent mechanical and thermal properties
Unusually efficient electrical insulators
Structurally stable and inert to most chemicals
Uniform band gap (5.5 eV)
High sensitivity for sensor materials
High resistance to oxidation

TGA showed that the oxidation of BNNTs starts
approximately at 800 °C, which is much higher
than the oxidation temperature of CNTs, which is
about 400 °C. High oxidation resistance of BNNTs
allows their applications in high temperature
environments.
BNNT vs CNT
Besides their structure, mechanical and thermal properties of BNNTs are very similar to CNTs.

Both BNNTs and CNTs have superb mechanical properties: the Young’s modulus of them has
been predicted to reach a TPa level.

However, BNNTs have better resistance to thermal oxidation than CNTs.

The electronic properties of BNNTs are also different from CNTs. BNNTs have a constant and
wide band-gap of 5.5 eV. Therefore, they are electrically isolating independent of their size or
chirality‟s. The electronic properties of BNNTs make them suitable nanofillers for the
production of isolating polymeric materials.

The obvious and most appealing difference between BNNTs and CNTs is their visible
appearance:
BNNTs are pure white (sometimes slightly yellowish due to N vacancies) while CNTs are totally
black




Comparison of properties of carbon nanotubes and boron nitride nanotubes   Images of (a) CNTs and (b) BNNTs
Synthesis Methods of BNNTs




There are several methods used for synthesizing boron nitride nanotubes.
Mainly used methods are:

arc-discharge,
laser ablation,
ball milling,
chemical vapor deposition
Polymer/BNNT composites
The studies on the polymeric composites of BNNTs have been flourished
only over the last years.

The exciting properties of BNNTs, such as high elastic modulus and high
thermal conductivity make them advantageous for novel nanofillers in
composite materials to obtain mechanical reinforcement, high thermal
conductivity and a low coefficient of thermal expansion in a matrix.

Polymer/BNNT composites that have been studied to date were prepared as
thin films via solution–mixing, evaporation and melt-mixing techniques
Mechanical Properties
     C. Zhi et al. fabricated PS/BNNT composites using a solution method

     The mechanical properties of a polymer were improved
     It was found that the results were solvent-
     dependent, that is, when chloroform
      was used to disperse BNNTs, the elastic
     modulus of the composite film was decreased.
     However, improvements can be obtained by
      using DMF as a solvent. This is attributed to
     different BNNT dispersions in different organic
      solvents
     Benefiting from the pure white appearance of BNNTs,
     the composite films retained good transparency

   (a) a blank PS film (b) BNNT/PS film           (c) BNNT/PmPV/PS film




C. Zhi, Y. Bando, C. Tang, S. Honda and H. Kuwahara, J. Mater. Res., 2006, 21, 2794.
Mechanical Properties

    Zhou et al. used isophorone diisocyanate (IPDI) activated BNNTs to
    synthesize BNNT/polyvinyl alcohol (PVA) and hydroxypropyl methylcellulose
    (HPMC) composites
                                                              Addition of a small fraction of activated
                       3 wt%IPDI–BNNTs                        IPDI–BNNTs leads to a considerable
                       1 wt%IPDI–BNNTs    3 wt%IPDI–BNNTs     increase in both Young’s modulus and
                           Pure PVA
                                          1 wt%IPDI–BNNTs
                       1 wt% BNNTs                            tensile strength.
                       3 wt% BNNTs         Pure HPMC
                                          1 wt% BNNTs
                                           3 wt% BNNTs
                                                              When the amount of ap-BNNTs was
                                                              added, both tensile strength and Young’s
               BNNT/PVA                           BNNT/HPMC
                                                              modulus were decreased

                                                              Activated IPDI–BNNTs exhibit good
                                                              dispersibility and chemical activity.

                                                              Adding IPDI–BNNTs into the solution of
                                                              PVA or HPMC, the strong interfacial
                                                              interactions between BNNTs and polymers
                                                              were achieved

                                                              In contrast, due to the well-crystallized
          BNNT/PVA                                BNNT/HPMC
                                                              surface, pristine BNNTs exhibit limited
                                                              dispersibility and poor interfacial
S-J Zhou et al, Nanotechnology 23 (2012) 055708               interactions with PVA and HPMC.
Mechanical Properties

 PMMA/BNNTs composites were fabricated using a solution method by C. Y. Zhi et
 al.


 The elastic modulus of PMMA was improved up to 19% while using only a 1wt.%
 BNNTs loading fraction. These results show that the external force can be
 transferred to BNNTs in some degree

 Tensile strength decreased

 The elongation also decreased, indicates that the interaction between
 BNNTs and polymer chains exists.




C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
Mechanical Properties




Four kinds of polymeric composites with BNNTs were fabricated by Chunyi
Zhi et al.

Vickers hardness of polymethyl methacrylate (PMMA), polystyrene (PS),
polyvinyl butyral (PVB), and polyethylene vinyl alcohol (PEVA) was only
slightly affected when they were loaded with the BN nanotubes.

This indicates that there is no obvious negative effect on the mechanical
properties of the composites.

With the exception of PVB, the Vickers hardness did not notably
decrease after adding BNNTs
Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
Mechanical Properties
NASA have developed new materials with greater anti-penetration characteristics.
By using BNNT polymer composites, researchers have successfully fabricated the
new materials to demonstrate enhanced material toughness and hardness.

Nonwoven mats of BNNTs are used as toughening layers to maximize energy
absorption and/or high hardness layers to rebound or deform penetrators.

They can also be used as reinforcing inclusions, combining with other polymer
matrices to create reinforcing composite layers to maximize anti-penetrator
protection




   Microindentation test of BNNT composite




NASA Langley, Jefferson Lab, www.nianet.org
Thermal Properties

    After adding BNNTs, the coefficient of thermal
    expansion (CTE) of PMMA dramatically decreases,
     This indicates that BNNTs significantly restrict the
    mobility of polymer chains

    Tg of a PMMA/BNNT composite becomes 85.2 °C
    In case of organic-inorganic nanocomposites, the mobility
    of polymer chains is significantly affected by the
    confinement and strength of polymer-surface interactions.
    This applies to the interactions between BNNTs and
    PMMA chains.




C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
Thermal Properties
Low CTE is a thermal parameter in polymeric composites used in packaging materials.

Chunyi Zhi et al. fabricated polymethyl methacrylate
(PMMA), polystyrene (PS), polyvinyl butyral (PVB), and
polyethylene vinyl alcohol (PEVA) composites filled with
BNNTs by solution mixing.

All composites exhibit much lower CTE compared
with the corresponding neat polymers. This implies the
appearance of constraints to the polymer chain
movements due to their interactions with BNNTs.
Due to the different affinity of BNNTs for various
polymers, the BNNT absorb different fractions of
polymer.
The weight fractions of BNNTs in the composites
range from 18 to 37 wt%. It was found that the weight
fraction of BNNTs in a composite can be controlled by
the concentration of the polymer solution.


   Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
Thermal Conductivity




Chunyi Zhi et al. also performed Thermal conductivity measurements;

Neat polymers possess low thermal conductivity.
After embedding BNNTs, this property was improved.
Thermal conductivity of PMMA sample drastically increases up to a
21-fold gain after adding BNNT.
 The thermal conductivity improvements of the composites are
roughly related to the BNNTs fractions in them.
In the case of a PVB composite loaded with BNNTs, a 7-fold increase
was documented.

 It is also assumed that an interfacial (BNNT–polymer) thermal transfer
varies from one polymer to another, inducing the observed discrepancy
in thermal conductivity values for almost the same BNNT loading
fractions in different matrices.
 Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
Thermal Conductivity

                                                           Composite films with 5wt.% and 10wt.%
                                                           BNNTs fractions of PMMA nanocomposites
                                                            were chosen by Zhi et al. for the thermal
                                                           conductivity measurements.

                                                           Thermal conductivity of PMMA loaded with
                                                           a 10wt.% BNNT fraction was improved 3
                                                           times
                                                           compared to blank PMMA

                                                           It should be emphasized that this gain is
                                                           likely to display the lower estimate for the
                                                           observed improvement since the BNNT
                                                           texture within the film is generally misaligned
                                                           with the direction used for the heat flow
                                                           measurements




C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
Thermal Conductivity
                                                          Huang et al. demonstrated that POSS modified
                                                          BNNTs are very effective nanofillers for making
                                                          dielectric epoxy composites with high thermal
                                                          conductivity.

                                                          The room temperature thermal conductivity of
                                                          the pure epoxy is about 0.2. The highest
                                                          measured room-temperature thermal
                                                          conductivity is 2.77 at 30.0 wt% BNNT fraction,
                                                          which is 13.6 times higher than that of the pure
                                                          epoxy resin.

                                                          Improvement of thermal conductivity in
                                                          the present epoxy/BNNT nanocomposites
                                                          is nonlinear: at a high fraction of BNNTs, a
                                                          more effective improvement was observed.

                                                          This implies that efficient thermal transfer
                                                          pathways start to form at a high fraction of
                                                          BNNTs due to tube-to-tube connections
Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
Dielectric Properties

  The dielectric loss tangent is closely
  associated with the electrical conductivity in
  the epoxy composites, which is determined
  by a charge carrier density at the certain
  temperature.

  Therefore, the decreased dielectric loss
  tangent of epoxy/BNNT nanocomposites
  should be attributed to a reduction of the
  electrical conductivity, which is confirmed by
  the conductivity spectra of the composites

  One of the possible reasons for lower
  dielectric constant obtained in the
  epoxy/BNNT composites is the relatively low
  intrinsic dielectric constant of hexagonal
  BNNTs

   Besides this factor, the other contribution
  may come from the restriction of bulk
  polarization in epoxy resin due to the
  immobility of polymer chains hindered
  by BNNTs.
Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
Dielectric Properties

Chunyi Zhi et al. examined the breakdown electric fields of neat polymers
with that of their BNNTs composites.

Only in the case of PS does the breakdown electric field decrease, while in
the other three cases, it marginally increases.

 In any case, all the materials remain insulating and possess a high
breakdown electric field, which is fully suitable for dielectric packages.




Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
Dielectric Properties

The appealing point of BNNT usage in polymeric composites is that the original
dielectric nature of a polymer is kept in the resultant composite. This fact is crucial in
many cases, such as packing materials for electrical circuits and power modules.

                                                             The electrical breakover voltages of a
                                                             blank PMMA and its composites
                                                             are compared.

                                                             This reveals that both blank PMMA
                                                             and its BNNTs composites have a
                                                             similar breakover electric field

                                                             Therefore, the presently developed
                                                             BNNTs/polymer composites are surely
                                                             suitable materials for heat-releasing
                                                             parts due to unique combination of
                                                             decent thermal conductivity and perfect
                                                             electrical insulation.
  C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
Radiation Shielding Properties
NASA have developed a neutron shielding material using boron-containing
polymer nanocomposites, which include boron nanoparticles (BNPs) (0D),
boron nitride nanotubes (BNNTs) (1D), and boron nitride nano-platelets (2D).

The large neutron absorption cross section, along with the light weight and
large surface area of BNNT, enable effective shielding with much less volume
and weight.




NASA Langley, Jefferson Lab, www.nianet.org
Morphology


  10 wt% BNNT-POSS               10 wt% BNNT-POSS

                                                          Huang et al. performed the SEM
                                                          observations of the fractured surface of the
                                                          BNNT-POSS based epoxy composites

                                                          It is seen that BNNTs are uniformly
                                                          dispersed in the epoxy matrix.

                                                          In addition, interface-debonding between
   20 wt% BNNT-POSS              30 wt% BNNT-POSS         BNNTs and the epoxy resin is not
                                                          observed, suggesting the strong interfacial
                                                          adhesion.

                                                          Such uniform dispersion of BNNTs and
                                                          strong interface are beneficial to the
                                                          thermal conductivity enhancement




Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
Morphology

D. Lahiri et al reinforced biodegradable
                           b
polylactide–polycaprolactone copolymer
(PLC) with 0, 2 and 5 wt.% BNNTs

Figures show the BNNTs bridges
within PLC matrix.

Dangling BNNTs with the other end fully
embedded in the polymer matrix are also
observed.

BNNTs behave as rigid reinforcements and
provide benefits of short fiber strengthening.




D. Lahiri et al., Acta Biomaterialia, 2010
Conclusion
Mechanical properties of CNTs and BNNTs are similar. They are both ideal for
mechanical applications.

High oxidation resistance of BNNTs allows their applications in high temperature
environments.

The electronic properties of BNNTs are different from CNTs. BNNTs have a constant
and wide band-gap of 5.5 eV. The electronic properties of BNNTs make them suitable
nanofillers for the production of isolating polymeric materials

The exciting properties of BNNTs, such as high elastic modulus and high thermal
conductivity make them advantageous for novel nanofillers in polymer composites to
obtain mechanical reinforcement, high thermal conductivity and a low coefficient of
thermal expansion in a matrix.

Chemical modification of inert BNNTs results dispersibility improvement in polymeric
matrices.

Future research efforts are needed to demonstrate the performance of functionalized
BNNTs in mechanical, electronic, chemical, and biological applications.
References
Sheng-Jun Zhou et al., 2012 Nanotechnology, 23, 055708

C. Zhi, Y. Bando, C. Tang, S. Honda and H. Kuwahara, J. Mater. Res., 2006, 21,
2794.

C. Y. Zhi, Y. Bando, C. Tang, H. Kuwahara, and D. Golberg, Journal of
Nanomaterials, 2008, 642036

Chunyi Zhi, Yoshio Bando, Takeshi Terao, Chengchun Tang, Hiroaki Kuwahara, and
Dimitri Golberg, Adv. Funct. Mater. 2009, 19, 1857–1862

Xingyi Huang , Chunyi Zhi , Pingkai Jiang , Dmitri Golberg , Yoshio Bando,
Toshikatsu Tanaka, Adv. Funct. Mater. 2012, 201201824

NASA Langley, Jefferson Lab, www.nianet.org

D. Lahiri et al., Acta Biomaterialia, 2010

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Polymer/Boron Nitride Nanotube (BNNTs) Nanocomposites

  • 1. Polymer/Boron Nitride Nanotube (BNNTs) Nanocomposites METE 560 Ümit TAYFUN Middle East Technical University Polymer Science & Technology
  • 2. Boron nitride nanotubes Boron nitride nanotubes, firstly synthesized in 1995, are structural analogues of carbon nanotubes with boron and nitrogen atoms instead of carbon atoms. BNNTs can be imagined as a rolled up hexagonal BN layer or as a carbon nanotube (CNTs) in which alternating B and N atoms entirely substitute for C atoms Similar to CNTs, BNNTs have chiralities, an important geometrical parameter, but for them, the chiralities do not play an important role in determining electrical properties Atomic models of BNNT;  (a)arm-chair  (b)zig-zag  (c)chiral
  • 3. Properties of BNNTs BNNTs are chemically inert, oxidation resistant, and structurally stable. BNNTs are electrically isolating materials with uniform electronic properties independent of their size and chirality. Therefore, they are evaluated as suitable fillers for the fabrication of mechanically and thermally enhanced polymer composites, while preserving the electrical TEM images of single to multi-wall BNNTs with six walls isolation of the polymer matrix Excellent mechanical and thermal properties Unusually efficient electrical insulators Structurally stable and inert to most chemicals Uniform band gap (5.5 eV) High sensitivity for sensor materials High resistance to oxidation TGA showed that the oxidation of BNNTs starts approximately at 800 °C, which is much higher than the oxidation temperature of CNTs, which is about 400 °C. High oxidation resistance of BNNTs allows their applications in high temperature environments.
  • 4. BNNT vs CNT Besides their structure, mechanical and thermal properties of BNNTs are very similar to CNTs. Both BNNTs and CNTs have superb mechanical properties: the Young’s modulus of them has been predicted to reach a TPa level. However, BNNTs have better resistance to thermal oxidation than CNTs. The electronic properties of BNNTs are also different from CNTs. BNNTs have a constant and wide band-gap of 5.5 eV. Therefore, they are electrically isolating independent of their size or chirality‟s. The electronic properties of BNNTs make them suitable nanofillers for the production of isolating polymeric materials. The obvious and most appealing difference between BNNTs and CNTs is their visible appearance: BNNTs are pure white (sometimes slightly yellowish due to N vacancies) while CNTs are totally black Comparison of properties of carbon nanotubes and boron nitride nanotubes Images of (a) CNTs and (b) BNNTs
  • 5. Synthesis Methods of BNNTs There are several methods used for synthesizing boron nitride nanotubes. Mainly used methods are: arc-discharge, laser ablation, ball milling, chemical vapor deposition
  • 6. Polymer/BNNT composites The studies on the polymeric composites of BNNTs have been flourished only over the last years. The exciting properties of BNNTs, such as high elastic modulus and high thermal conductivity make them advantageous for novel nanofillers in composite materials to obtain mechanical reinforcement, high thermal conductivity and a low coefficient of thermal expansion in a matrix. Polymer/BNNT composites that have been studied to date were prepared as thin films via solution–mixing, evaporation and melt-mixing techniques
  • 7. Mechanical Properties C. Zhi et al. fabricated PS/BNNT composites using a solution method The mechanical properties of a polymer were improved It was found that the results were solvent- dependent, that is, when chloroform was used to disperse BNNTs, the elastic modulus of the composite film was decreased. However, improvements can be obtained by using DMF as a solvent. This is attributed to different BNNT dispersions in different organic solvents Benefiting from the pure white appearance of BNNTs, the composite films retained good transparency (a) a blank PS film (b) BNNT/PS film (c) BNNT/PmPV/PS film C. Zhi, Y. Bando, C. Tang, S. Honda and H. Kuwahara, J. Mater. Res., 2006, 21, 2794.
  • 8. Mechanical Properties Zhou et al. used isophorone diisocyanate (IPDI) activated BNNTs to synthesize BNNT/polyvinyl alcohol (PVA) and hydroxypropyl methylcellulose (HPMC) composites Addition of a small fraction of activated 3 wt%IPDI–BNNTs IPDI–BNNTs leads to a considerable 1 wt%IPDI–BNNTs 3 wt%IPDI–BNNTs increase in both Young’s modulus and Pure PVA 1 wt%IPDI–BNNTs 1 wt% BNNTs tensile strength. 3 wt% BNNTs Pure HPMC 1 wt% BNNTs 3 wt% BNNTs When the amount of ap-BNNTs was added, both tensile strength and Young’s BNNT/PVA BNNT/HPMC modulus were decreased Activated IPDI–BNNTs exhibit good dispersibility and chemical activity. Adding IPDI–BNNTs into the solution of PVA or HPMC, the strong interfacial interactions between BNNTs and polymers were achieved In contrast, due to the well-crystallized BNNT/PVA BNNT/HPMC surface, pristine BNNTs exhibit limited dispersibility and poor interfacial S-J Zhou et al, Nanotechnology 23 (2012) 055708 interactions with PVA and HPMC.
  • 9. Mechanical Properties PMMA/BNNTs composites were fabricated using a solution method by C. Y. Zhi et al. The elastic modulus of PMMA was improved up to 19% while using only a 1wt.% BNNTs loading fraction. These results show that the external force can be transferred to BNNTs in some degree Tensile strength decreased The elongation also decreased, indicates that the interaction between BNNTs and polymer chains exists. C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
  • 10. Mechanical Properties Four kinds of polymeric composites with BNNTs were fabricated by Chunyi Zhi et al. Vickers hardness of polymethyl methacrylate (PMMA), polystyrene (PS), polyvinyl butyral (PVB), and polyethylene vinyl alcohol (PEVA) was only slightly affected when they were loaded with the BN nanotubes. This indicates that there is no obvious negative effect on the mechanical properties of the composites. With the exception of PVB, the Vickers hardness did not notably decrease after adding BNNTs Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
  • 11. Mechanical Properties NASA have developed new materials with greater anti-penetration characteristics. By using BNNT polymer composites, researchers have successfully fabricated the new materials to demonstrate enhanced material toughness and hardness. Nonwoven mats of BNNTs are used as toughening layers to maximize energy absorption and/or high hardness layers to rebound or deform penetrators. They can also be used as reinforcing inclusions, combining with other polymer matrices to create reinforcing composite layers to maximize anti-penetrator protection Microindentation test of BNNT composite NASA Langley, Jefferson Lab, www.nianet.org
  • 12. Thermal Properties After adding BNNTs, the coefficient of thermal expansion (CTE) of PMMA dramatically decreases,  This indicates that BNNTs significantly restrict the mobility of polymer chains Tg of a PMMA/BNNT composite becomes 85.2 °C In case of organic-inorganic nanocomposites, the mobility of polymer chains is significantly affected by the confinement and strength of polymer-surface interactions. This applies to the interactions between BNNTs and PMMA chains. C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
  • 13. Thermal Properties Low CTE is a thermal parameter in polymeric composites used in packaging materials. Chunyi Zhi et al. fabricated polymethyl methacrylate (PMMA), polystyrene (PS), polyvinyl butyral (PVB), and polyethylene vinyl alcohol (PEVA) composites filled with BNNTs by solution mixing. All composites exhibit much lower CTE compared with the corresponding neat polymers. This implies the appearance of constraints to the polymer chain movements due to their interactions with BNNTs. Due to the different affinity of BNNTs for various polymers, the BNNT absorb different fractions of polymer. The weight fractions of BNNTs in the composites range from 18 to 37 wt%. It was found that the weight fraction of BNNTs in a composite can be controlled by the concentration of the polymer solution. Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
  • 14. Thermal Conductivity Chunyi Zhi et al. also performed Thermal conductivity measurements; Neat polymers possess low thermal conductivity. After embedding BNNTs, this property was improved. Thermal conductivity of PMMA sample drastically increases up to a 21-fold gain after adding BNNT.  The thermal conductivity improvements of the composites are roughly related to the BNNTs fractions in them. In the case of a PVB composite loaded with BNNTs, a 7-fold increase was documented. It is also assumed that an interfacial (BNNT–polymer) thermal transfer varies from one polymer to another, inducing the observed discrepancy in thermal conductivity values for almost the same BNNT loading fractions in different matrices. Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
  • 15. Thermal Conductivity Composite films with 5wt.% and 10wt.% BNNTs fractions of PMMA nanocomposites were chosen by Zhi et al. for the thermal conductivity measurements. Thermal conductivity of PMMA loaded with a 10wt.% BNNT fraction was improved 3 times compared to blank PMMA It should be emphasized that this gain is likely to display the lower estimate for the observed improvement since the BNNT texture within the film is generally misaligned with the direction used for the heat flow measurements C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
  • 16. Thermal Conductivity Huang et al. demonstrated that POSS modified BNNTs are very effective nanofillers for making dielectric epoxy composites with high thermal conductivity. The room temperature thermal conductivity of the pure epoxy is about 0.2. The highest measured room-temperature thermal conductivity is 2.77 at 30.0 wt% BNNT fraction, which is 13.6 times higher than that of the pure epoxy resin. Improvement of thermal conductivity in the present epoxy/BNNT nanocomposites is nonlinear: at a high fraction of BNNTs, a more effective improvement was observed. This implies that efficient thermal transfer pathways start to form at a high fraction of BNNTs due to tube-to-tube connections Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
  • 17. Dielectric Properties The dielectric loss tangent is closely associated with the electrical conductivity in the epoxy composites, which is determined by a charge carrier density at the certain temperature. Therefore, the decreased dielectric loss tangent of epoxy/BNNT nanocomposites should be attributed to a reduction of the electrical conductivity, which is confirmed by the conductivity spectra of the composites One of the possible reasons for lower dielectric constant obtained in the epoxy/BNNT composites is the relatively low intrinsic dielectric constant of hexagonal BNNTs  Besides this factor, the other contribution may come from the restriction of bulk polarization in epoxy resin due to the immobility of polymer chains hindered by BNNTs. Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
  • 18. Dielectric Properties Chunyi Zhi et al. examined the breakdown electric fields of neat polymers with that of their BNNTs composites. Only in the case of PS does the breakdown electric field decrease, while in the other three cases, it marginally increases.  In any case, all the materials remain insulating and possess a high breakdown electric field, which is fully suitable for dielectric packages. Chunyi Zhi et al., Adv. Funct. Mater. 2009, 19, 1857–1862
  • 19. Dielectric Properties The appealing point of BNNT usage in polymeric composites is that the original dielectric nature of a polymer is kept in the resultant composite. This fact is crucial in many cases, such as packing materials for electrical circuits and power modules. The electrical breakover voltages of a blank PMMA and its composites are compared. This reveals that both blank PMMA and its BNNTs composites have a similar breakover electric field Therefore, the presently developed BNNTs/polymer composites are surely suitable materials for heat-releasing parts due to unique combination of decent thermal conductivity and perfect electrical insulation. C. Y. Zhi et al., Journal of Nanomaterials, 2008, 642036
  • 20. Radiation Shielding Properties NASA have developed a neutron shielding material using boron-containing polymer nanocomposites, which include boron nanoparticles (BNPs) (0D), boron nitride nanotubes (BNNTs) (1D), and boron nitride nano-platelets (2D). The large neutron absorption cross section, along with the light weight and large surface area of BNNT, enable effective shielding with much less volume and weight. NASA Langley, Jefferson Lab, www.nianet.org
  • 21. Morphology 10 wt% BNNT-POSS 10 wt% BNNT-POSS Huang et al. performed the SEM observations of the fractured surface of the BNNT-POSS based epoxy composites It is seen that BNNTs are uniformly dispersed in the epoxy matrix. In addition, interface-debonding between 20 wt% BNNT-POSS 30 wt% BNNT-POSS BNNTs and the epoxy resin is not observed, suggesting the strong interfacial adhesion. Such uniform dispersion of BNNTs and strong interface are beneficial to the thermal conductivity enhancement Xingyi Huang et al., Adv. Funct. Mater. 2012, 201201824
  • 22. Morphology D. Lahiri et al reinforced biodegradable b polylactide–polycaprolactone copolymer (PLC) with 0, 2 and 5 wt.% BNNTs Figures show the BNNTs bridges within PLC matrix. Dangling BNNTs with the other end fully embedded in the polymer matrix are also observed. BNNTs behave as rigid reinforcements and provide benefits of short fiber strengthening. D. Lahiri et al., Acta Biomaterialia, 2010
  • 23. Conclusion Mechanical properties of CNTs and BNNTs are similar. They are both ideal for mechanical applications. High oxidation resistance of BNNTs allows their applications in high temperature environments. The electronic properties of BNNTs are different from CNTs. BNNTs have a constant and wide band-gap of 5.5 eV. The electronic properties of BNNTs make them suitable nanofillers for the production of isolating polymeric materials The exciting properties of BNNTs, such as high elastic modulus and high thermal conductivity make them advantageous for novel nanofillers in polymer composites to obtain mechanical reinforcement, high thermal conductivity and a low coefficient of thermal expansion in a matrix. Chemical modification of inert BNNTs results dispersibility improvement in polymeric matrices. Future research efforts are needed to demonstrate the performance of functionalized BNNTs in mechanical, electronic, chemical, and biological applications.
  • 24. References Sheng-Jun Zhou et al., 2012 Nanotechnology, 23, 055708 C. Zhi, Y. Bando, C. Tang, S. Honda and H. Kuwahara, J. Mater. Res., 2006, 21, 2794. C. Y. Zhi, Y. Bando, C. Tang, H. Kuwahara, and D. Golberg, Journal of Nanomaterials, 2008, 642036 Chunyi Zhi, Yoshio Bando, Takeshi Terao, Chengchun Tang, Hiroaki Kuwahara, and Dimitri Golberg, Adv. Funct. Mater. 2009, 19, 1857–1862 Xingyi Huang , Chunyi Zhi , Pingkai Jiang , Dmitri Golberg , Yoshio Bando, Toshikatsu Tanaka, Adv. Funct. Mater. 2012, 201201824 NASA Langley, Jefferson Lab, www.nianet.org D. Lahiri et al., Acta Biomaterialia, 2010