U.S. patent application number 13/459755 was filed with the patent office on 2012-09-20 for mass production of carbon nanostructures.
Invention is credited to Viktor I. Petrik.
Application Number | 20120237435 13/459755 |
Document ID | / |
Family ID | 36574632 |
Filed Date | 2012-09-20 |
United States Patent
Application |
20120237435 |
Kind Code |
A1 |
Petrik; Viktor I. |
September 20, 2012 |
Mass Production of Carbon Nanostructures
Abstract
Carbon nanostructures are mass produced from graphite. In
particularly preferred aspects, graphene is thermo-chemically
derived from graphite and used in numerous compositions. In further
preferred aspects, the graphene is re-shaped to form other
nanostructures, including nanofractals, optionally branched
open-ended SWNT, nanoloops, and nanoonions.
Inventors: |
Petrik; Viktor I.; (Moscow,
RU) |
Family ID: |
36574632 |
Appl. No.: |
13/459755 |
Filed: |
April 30, 2012 |
Related U.S. Patent Documents
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Application
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Filing Date |
Patent Number |
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12939144 |
Nov 3, 2010 |
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13459755 |
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11007614 |
Dec 7, 2004 |
7842271 |
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12939144 |
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Current U.S.
Class: |
423/447.1 ;
977/743; 977/750; 977/842 |
Current CPC
Class: |
Y10S 423/10 20130101;
Y10T 428/2991 20150115; B82Y 40/00 20130101; C01B 2202/02 20130101;
Y10S 977/734 20130101; C01B 32/162 20170801; B82Y 30/00 20130101;
Y10S 977/742 20130101 |
Class at
Publication: |
423/447.1 ;
977/842; 977/750; 977/743 |
International
Class: |
D01F 9/12 20060101
D01F009/12 |
Claims
1.-22. (canceled)
23. A method of producing an open-ended single-wall carbon nanotube
the method comprising providing a graphene, and providing energy to
the graphene to thereby form the open-ended single-wall carbon
nanotube.
24. The method of claim 23, wherein providing energy to the
graphene comprises heating the graphene to a temperature of between
200.degree. C. and 600.degree. C.
25. The method of claim 23, further comprising placing the graphene
under reduced pressure of between about 100 mbar and about 1 mbar
prior to providing energy to the graphene.
26. The method of claim 23, wherein providing energy comprises
providing radiant heat, providing induction heating or providing
microwave heating.
27. The method of claim 23, wherein the nanotube is open ended on
both ends.
Description
FIELD OF THE INVENTION
[0001] The field of the invention is carbon nanostructures, carbon
nanostructure-containing materials, and their manufacture.
BACKGROUND OF THE INVENTION
[0002] Carbon nanostructures include single-wall carbon nanotubes
(SWNT), multi-wall carbon nanotubes (MWNT), fullerenes,
nanodiamonds, and nanoonions, and such nanostructures can be
manufactured in various manners.
[0003] For example, in one relatively common manner, nanotubes can
be produced by electric arc discharge. Nanotubes formed by such a
process are typically MWNT. To produce SWNT, various catalytic
metals (e.g., cobalt) can be added to the graphite electrodes. Arc
discharge typically provides relatively low yield. Moreover, the so
formed nanotubes will have in most cases relatively large
inhomogeneity in length and chirality. Fullerenes can be obtained
in similar manner from soot prepared in an arc generator using a
carbonaceous electrode (typically without catalyst). When the
electrodes are immersed in water, nanoonions can be formed that
float to the surface of the water. So formed fullerenes and
nanoonions can then be processed (typically in a shockwave
compression) to form nanodiamonds.
[0004] Alternatively, especially where increased yield or localized
synthesis of nanostructures is desired, chemical vapor deposition
(CVD) can be employed in which a feed gas (e.g., methane or
ethylene) is decomposed in the presence of a metal catalyst to grow
nanotubes. For example, numerous nanotubes can be grown at the same
time on a silicon dioxide template (that can be patterned) in
predetermined positions. Such process may further be modified by
the choice of the particular catalyst to influence the type of
nanotube that is to be produced. While CVD synthesis is directional
and relatively simple, industrial significant yields are typically
not achieved. CVD was reported to also yield nanodiamonds under
certain conditions, however, other nanostructures are rarely formed
using CVD.
[0005] In yet another manner, laser ablation may be employed in
which a laser pulse evaporates a solid target of graphite that
contains a small amount of metal catalyst (.about.1 atomic % Ni and
.about.1% Co). The ablated material is transferred into a
background gas (e.g., Ar) which is gently flowing through a quartz
tube inside a high temperature (e.g., 1000.degree. C.) oven. Laser
ablation generally allows for tighter control of reaction
conditions, and with that tends to provide a more defined
population of nanotubes. Furthermore, nanotubes (and also
fullerenes under certain conditions) can be produced in relatively
good quantities. However, such a process is relatively energy
consuming, requires expensive equipment, and highly trained
personnel.
[0006] Other less common methods of forming nanostructures include
plasma based synthesis of nanotubes. Such methods advantageously
allow for mass production of nanotubes, but generally require
megawatt quantities of energy. Similarly, nanostructures have been
produced by impulse heating of fluorinated graphite dust in a 27.12
MHz inductively coupled plasma. Again, which such method may yield
a relatively high yield of SWNT, the energy demand in most cases is
cost-prohibitive. "Two-dimensional" carbon nanostructures, and
particularly graphene, were until recently thought to be difficult,
if not even impossible to manufacture. However, advances in plasma
assisted CVD have yielded doped carbon flakes as described in WO
2004/095494, and more recently, graphene layers were reported that
were extracted as an individual plane from a graphite crystal
(Novoselov et al., Electric Field Effect in Atomically Thin Carbon
Films, Science 2004 306: 666-669).
[0007] Therefore, while various materials and methods for
manufacture of carbon nanostructures are known in the art, all or
almost all of them suffer from one or more disadvantages,
especially where large quantities of carbon nanostructures are
desired. Thus, there is still a need to provide improved
compositions and methods for manufacture of carbon
nanostructures.
SUMMARY OF THE INVENTION
[0008] The present invention is directed to compositions and
methods of carbon nanostructures, and especially those comprising,
or formed from graphene or graphene-containing compositions. In
generally contemplated aspects, graphene is thermo-chemically
derived from a carbonaceous starting material, and the so obtained
graphene can then be used directly or can be reformed into other
carbon nanostructures.
[0009] In one aspect of the inventive subject matter, a composition
is contemplated comprising at least 0.1 wt %, more preferably at
least 10 wt %, and most preferably at least 50 wt % carbon
fractals. The carbon fractals in such compositions may be metal
coated, and particularly preferred metals include noble metals.
[0010] In another aspect of the inventive subject matter, a device
is contemplated that comprises at least 0.1 wt %, more preferably
at least 10 wt %, and most preferably at least 50 wt % graphene as
an added component. Similar to the carbon fractals, it is
contemplated that at least some of the graphene is coated with a
metal, and especially a noble metal. Among other devices, suitable
devices include electrical devices (e.g., electric conductors,
electron emitters, electrodes, etc.) and non-electrical devices
(e.g., structural elements, a heat conductors, etc.).
[0011] Therefore, in still other aspects of the inventive subject
matter, a bulk composition of at least 1000 gram is contemplated
that includes at least 10 gram of graphene and/or carbon fractals.
Most preferably, the graphene and/or carbon fractals are present in
an amount effective to increase (e.g., at least two fold, more
typically at least five fold, most typically at least ten fold)
thermal conductivity, electrical conductivity, adsorption, and/or a
mechanical stability of the bulk composition.
[0012] In a further aspect of the inventive subject matter, a
method of preparing a composition comprising a nanostructured
carbon includes a step in which a carbonaceous starting material is
contacted with an activated acid catalyst to form an activated
intermediate. In yet another step, energy is provided to the
activated intermediate to thereby form a carbon nanostructure
(e.g., a graphene, a carbon nanotube, and/or a carbon fractal).
Most preferably, the carbonaceous starting material is graphite,
coal, tar, and/or coke, and the activated acid catalyst comprises
plasma-activated hydrochloric acid. While numerous manners of
providing energy are deemed suitable, it is typically preferred
that the energy is thermal energy of a temperature between about
200.degree. C. and 1200.degree. C.
[0013] Additionally, the carbon nanostructure in contemplated
methods may be contacted with an additional activated acid catalyst
to form an activated carbon nanostructure, to which in a still
further step energy is provided to thereby form a secondary carbon
nanostructure (e.g., a single-wall carbon nanotube, a branched
carbon nanotube, and a carbon fractal).
[0014] In yet another aspect of the inventive subject matter,
method of producing an open-ended single-wall carbon nanotube
includes a step of providing graphene, and another step of
providing energy to the graphene to thereby form the open-ended
single-wall carbon nanotube. Most preferably, the energy is thermal
energy at a temperature of 200.degree. C. and 600.degree. C., and
the heating step is performed in inert gas (e.g., nitrogen, argon,
helium, etc.).
[0015] Various objects, features, aspects and advantages of the
present invention will become more apparent from the figures and
the following detailed description of preferred embodiments of the
invention.
BRIEF DESCRIPTION OF THE DRAWING
[0016] FIG. 1A is an exemplary electronmicrograph depicting
graphene produced using methods according to the inventive subject
matter.
[0017] FIG. 1B is a detail view of the graphene of FIG. 1B at a
higher magnification.
[0018] Prior Art FIG. 2A is an exemplary electronmicrograph
depicting expanded graphite in a characteristic worm-like form.
[0019] Prior Art FIG. 2B is a detail view showing honeycomb-like
features in the worm-like material of FIG. 2A.
[0020] FIG. 3 is an exemplary electronmicrograph depicting an
open-ended carbon nanotube formed from graphene according to the
inventive subject matter.
[0021] FIG. 4 is a detail view of the open end of the nanotube of
FIG. 3 at a higher magnification.
[0022] FIG. 5 is an exemplary electronmicrograph depicting a
branched carbon nanotube formed from graphene according to the
inventive subject matter.
[0023] FIG. 6 is an exemplary electronmicrograph depicting a metal
coated carbon fractal formed from graphene according to the
inventive subject matter.
[0024] FIG. 7 is an exemplary electronmicrograph depicting a
ring-shaped carbon nanotube.
DETAILED DESCRIPTION
[0025] The inventors have surprisingly discovered that graphene can
be produced in a simple and cost-effective manner, and that the so
formed graphene can be formed into other nanostructures, including
open-ended single-wall carbon nanotubes, branched carbon nanotubes,
and carbon fractals.
[0026] As used herein, the term "graphene" refers to a molecule in
which a plurality of carbon atoms (e.g., in the form of
five-membered rings, six-membered rings, and/or seven-membered
rings) are covalently bound to each other to form a (typically
sheet-like) polycyclic aromatic molecule. Consequently, and at
least from one perspective, a graphene may be viewed as a single
layer of carbon atoms that are covalently bound to each other (most
typically sp.sup.2 bonded). It should be noted that such sheets may
have various configurations, and that the particular configuration
will depend (among other things) on the amount and position of
five-membered and/or seven-membered rings in the sheet. For
example, an otherwise planar graphene sheet consisting of
six-membered rings will warp into a cone shape if a five-membered
ring is present the plane, or will warp into a saddle shape if a
seven-membered ring is present in the sheet. Furthermore, and
especially where the sheet-like graphene is relatively large, it
should be recognized that the graphene may have the
electron-microscopic appearance of a wrinkled sheet. It should be
further noted that under the scope of this definition, the term
"graphene" also includes molecules in which several (e.g., two,
three, four, five to ten, one to twenty, one to fifty, or one to
hundred) single layers of carbon atoms (supra) are stacked on top
of each other to a maximum thickness of less than 100 nanometers.
Consequently, the term "graphene" as used herein refers to a single
layer of aromatic polycyclic carbon as well as to a plurality of
such layers having a thickness of less than 100 nanometers.
Typically, the dangling bonds on the edge of the graphene are
saturated with a hydrogen atom. The term "about" where used in
conjunction with a numeral refers to a numeric range of +/-10% of
the numeral, inclusive. For example, the term "about 100" refers to
a numerical value of between 90 and 110, inclusive.
[0027] As further used herein, the term "carbon nanotube" refers to
a cylindrical single- or multi-walled structure in which the
wall(s) is (are) predominantly composed of carbon, wherein the
diameter may be uniform or decreasing over the length of the
nanotube. In some instances, the carbon nanotube can be curved, and
is therefore also termed "carbon nanohorn".
[0028] The term "carbon fractal" as used herein refers to a
macromolecule in which at least two graphene portions are coupled
to each other such that the first and second portions form an angle
of 90 degrees (4-/-20 degrees). Most typically, the coupling is
covalent, and the first and second portions have a length
L.sub.first, L.sub.second, respectively, and a width W.sub.first,
W.sub.second, respectively, wherein the ratio of L.sub.first to
W.sub.first, and L.sub.second to W.sub.second is at least 2:1, more
typically at least 5:1, and most typically at least 10:1.
Therefore, a typical carbon fractal will appear in an electron
micrograph as a cross-like structure having a longitudinal portion
from which at least one other longitudinal portion extends. It
should be noted that the graphene in at least one of the portions
may have a configuration that is other than flat, and most
typically the graphene will have a curved (and sometimes even
cylindrical) configuration. The term "isolated" as used in
conjunction with the term "carbon fractal" herein means that the
presence of the carbon fractal in a composition is ascertained
(e.g., by electron microscopy, or by following a synthetic protocol
known or proven to produce at least some carbon fractals) and that
that composition is then enriched in the carbon fractal. For
example, carbon fractals obtained by at least partial removal of a
solvent or undesired non-carbon fractal component from a
composition containing a carbon fractal are considered isolated
carbon fractals.
[0029] As still further used herein, the term "activated acid
catalyst" refers to an acidic solution of a compound, wherein the
solution (typically, but not necessarily aqueous) is subjected to
an electromagnetic field, electromagnetic radiation, and/or laser
irradiation. Most preferably, the activated acid catalyst comprises
an acidic solution that is plasma-activated and/or comprises a
compound having the general formula MXO.sub.n, wherein M is
selected from the group consisting of H, NH.sub.4, Na, and K,
wherein X is selected from the group consisting of Cl, Br, and I,
and wherein n is an integer between 0 and 4, inclusive. It should
be noted that the term "activated acid catalyst" also includes one
or more oxidizers (typically, but not necessarily in aqueous
solution) that were previously subjected to electromagnetic
radiation, an electromagnetic field, and/or laser irradiation.
Alternatively, and in less preferred aspects, activation using the
electromagnetic radiation, electromagnetic field, and/or laser
irradiation may replaced by admixing the acid or oxidizer with a
penetration enhancer (e.g., compounds and/or mixtures commonly
found in lubricating formulations, etc.).
[0030] In one preferred aspect of the inventive subject matter, the
inventors discovered graphene can be produced from commercially
available graphite (e.g., Natural crystalline flake graphite from
Superior Graphite Co., 10 S. Riverside Plaza, Chicago, Ill. 60606)
using commercially available activated acid catalyst (e.g.,
Activated Acid Catalyst #3[Plasma-activated hydrochloric acid] from
SupraCarbonic, LLC., 348 N. Eckhoff Street, Orange, Calif. 92868,
USA). For example, the crystalline flake graphite is granulated to
a size between about 0.1 and several millimeter and mixed with the
activated acid catalyst in approximately same weight proportions
(e.g., 10 gram graphite with 10 ml activated acid catalyst). The so
prepared activated graphite is then subjected to heating at a
temperature of about 120.degree. C. for up to two minutes
(typically less than 40 seconds) to expansion (up to 500-fold in
volume). Exemplary electronmicrographs of the so produced material
are depicted in FIG. 1A and FIG. 1B at different magnification.
[0031] It should be especially noted that so prepared compositions
are significantly distinct in structural and molecular aspects from
currently known expanded graphite/intercalated graphite. Among
other differences, graphene produced according to the inventive
subject matter is a substantially monoatomic (and in some cases
oligoatomic) flat or wrinkled layer of polycyclic aromatic carbon,
while expanded graphite typically has a worm-like configuration
with wall strengths in the micrometer range as depicted in Prior
Art FIG. 2A. Also, the interconnected thick walls of expanded
graphite in the worms form a honeycomb structure as depicted in
Prior Art FIG. 2B, whereas the monoatomic (and in some cases
oligoatomic) flat or wrinkled graphene layers in contemplated
compositions are independent layers.
[0032] While not wishing to be bound by any hypothesis or theory,
the inventors contemplate that the graphene produced according to
the inventive subject matter is a result of complete penetration of
the acid catalyst between each of the graphene layers in the
graphite and violent and exothermic reaction of the catalyst with
the graphite. Moreover, due to the exothermic nature and other
factors, it should be recognized that the acid catalyst may be
substantially completely (i.e., greater 99%) removed from the
graphene. However, and especially where alternative acid catalysts
are employed, it should also be recognized that the catalyst (or
portions thereof) may be partially (between 1-10%, 10-25%, 25-50%,
5075%, or 75-90%) or even entirely (90-99%) retained within the
graphene.
[0033] In alternative aspects, numerous carbonaceous starting
materials other than crystalline flake graphite may be employed,
and it should be recognized that many carbon-containing materials
are suitable for use herein. However, especially preferred
carbonaceous materials include those predominantly (>80 atom %)
comprising carbon. Therefore, suitable carbonaceous starting
materials include coal, tar, natural and synthetic graphite,
pyrolysis products, coke, carbonized organic matter, and/or
carbonized synthetic fibers. Suitable carbonaceous materials also
include various synthetic compounds, and especially synthetic
(preferably polycyclic) aromatic compounds.
[0034] Contemplated starting materials, and especially graphite may
also be doped or derivatized with one or more heteroatoms (e.g.,
optionally substituted nitrogen, oxygen, sulfur, boron, etc.)
and/or substituents. The term "substituted" as used herein also
refers to a replacement of a chemical group or substituent (e.g.,
hydrogen) with a functional group, and particularly contemplated
functional groups include nucleophilic (e.g., --NH.sub.2, --OH,
--SH, --NC, etc.) and electrophilic groups (e.g., C(O)OR, C(X)OH,
etc.), polar groups (e.g., --OH), non-polar groups (e.g., aryl,
alkyl, alkenyl, alkynyl, etc.), ionic groups (e.g.,
--NH.sub.3.sup.+), halogens (e.g., --F, --Cl), and all chemically
reasonable combinations thereof. Thus, the term "substituent"
includes nucleophilic (e.g., --NH.sub.2, --OH, --SH, --NC, etc.)
and electrophilic groups (e.g., C(O)OR, C(X)OH, etc.), polar groups
(e.g., --OH), non-polar groups (e.g., aryl, alkyl, alkenyl,
alkynyl, etc.), ionic groups (e.g., --NH.sub.3.sup.+), halogens
(e.g., --F, --Cl), and all chemically reasonable combinations
thereof. Such substituted or doped starting materials may then
result in chemically modified nanostructures.
[0035] Depending on the particular starting material, it should be
appreciated that the structure of the graphene obtained by
contemplated methods may vary considerably. For example, where a
high-quality flake graphite is employed, relatively large graphene
sheets will be produced. On the other hand, where a low grade
graphite is employed as a starting material, fractured or otherwise
imperfect graphene is obtained. Thus, and at least to some degree,
the graphene structure will influence the structure of
nanostructured derived from the graphene. For example, where a
relatively large proportion of fractured graphene is present,
formation of nanofractals is favored.
[0036] Similarly, where moderately fractured graphene is produced
from an intermediate-grade graphite, formation of branched
nanotubes is favored.
[0037] With respect to the acid catalyst it is contemplated that
the particular chemical nature of the catalyst and/or activation of
the catalyst may vary considerably. However, it is generally
contemplated that the catalyst has a composition such that the
catalyst will soak throughout the entire starting material.
Preferred acid catalysts include acidic solutions that are
plasma-activated and/or comprises a compound having the general
formula MXO.sub.n, wherein M is selected from the group consisting
of H, NH.sub.4, Na, and K, wherein X is selected from the group
consisting of Cl, Br, and I, and wherein n is an integer between 0
and 4, inclusive. Further preferred acid catalysts include
oxidizing agents, activated or formulated such that the oxidizing
agent will entirely penetrate the starting material.
[0038] It should also be recognized that the ratio of carbonaceous
material to acid catalyst may vary, and suitable ratios are
typically between 100:1 and 1:100, more preferably between 10:1 and
1:10, and most preferably between 4:1 and 1:4 on a weight-by-weight
basis. The exact ratio will depend on the nature of the starting
material and/or the degree of fractionation of the graphite. For
example, where the starting material is relatively solid and has a
relatively low degree of porosity, larger quantities of acid
catalyst relative to the starting material may be required. On the
other hand, where the starting material is powdered flake graphite,
less than equal amounts of acid catalyst may be required be
determined. Moreover, and at least to some degree, the ratio of
acid catalyst to carbonaceous material will not only determine the
degree of breakage between graphene layers, but also the degree of
breakage of carbon-carbon bonds within one layer. Therefore, it
should be recognized that preferred acid catalysts also break one
or more carbon-carbon bonds within one layer.
[0039] Heating or provision of energy other than thermal energy to
expand the activated intermediate (e.g., flake graphite comprising
the activated acid catalyst) may be performed in numerous manners,
and it should be recognized that any energy is suitable for use in
conjunction with the teachings presented herein. Therefore,
generally contemplated energies include chemical (e.g., via
exothermic reaction), thermal (e.g., via heater, IR radiation),
electrical (e.g., resistive or inductive heating), electromagnetic
(e.g., via microwave irradiation), and/or mechanical (e.g., via
compression), etc. Most typically the energy is provided in an
amount sufficient to initiate some expansion, which itself is an
exothermic process. Once the critical amount of energy is
delivered, heat generated from the exothermic expansion reaction
will carry the remaining energy requirement for expansion of the
entire load of activated intermediate. For example, where thermal
energy is used as energy, heating of the activated intermediate to
a temperature of about 100-200.degree. C. for several seconds is
generally sufficient. However, higher temperatures (e.g., between
200-400.degree. C., or between 400-800.degree. C., and even higher)
are also contemplated. Similarly, the time required and/or desired
for providing the energy may vary considerably. For example, where
the energy is provided as a mechanical impact energy, several
milliseconds may be sufficient. On the other hand, where the energy
is provided as radiant heat, heating may be performed for between 5
seconds to several minutes. While heating of the graphite is
typically done in a static manner, it should be recognized that
heating may also be performed in a container in which the heated
material is suspended (e.g., in a counter current of inert gas, or
fluidized bed). Moreover, it should be recognized that the further
processing of graphene into nanostructures other than the graphene
obtained by the expansion reaction may be performed in the same
step as the expansion. Therefore, heating may be performed using
different temperature profiles and durations. Consequently, it
should be recognized that the starting material after expansion may
include one or more of graphene, an open-ended nanotube, a branched
nanotube, a ring-shaped nanotube, and a carbon fractal.
[0040] The so obtained graphene or graphene-containing composition
may optionally be treated using one or more solvents to remove
impurities/undesirable material, and/or to dilute the so obtained
material (for further especially preferred chemical modifications,
and especially metal deposition, see below). Where desirable, the
material may also be chemically or physically treated. For example,
the graphene or graphene-containing composition may be chemically
modified to add a substituent or doping element. Contemplated
physical treatments include compaction and or heating, sonication,
size separation, etc.
[0041] In especially preferred aspects of the inventive subject
matter, the graphene or graphene-containing composition is further
processed to provide a re-shaped nanostructured material. Most
preferably, reshaping of the graphene is performed by providing
energy to the graphene, typically heating using radiant heat,
induction heating, or microwave heating. Preferably, the
temperature for the re-shaping is between about 200.degree. C. and
1200.degree. C., more preferably between 300.degree. C. and
1000.degree. C., and most preferably between 400.degree. C. and
800.degree. C. Where desired, the graphene or graphene-containing
composition is evacuated before the energy for reshaping is
provided. It should be recognized that the particular shape of the
re-shaped nanostructured material will to a relatively large degree
depend on both the starting material and process conditions:
[0042] For example, where high-quality flake graphite is provided
as starting material, relatively large and structurally homogeneous
graphene layers are obtained, which will favor formation of
open-ended single wall nanotubes. Lower-quality graphite will
typically result in a more inhomogeneous population of graphene,
which will typically favor formation of branched nanotubes and/or
ring-shaped nanotubes. In most cases, technical graphite will yield
fractured graphene, which in turn will favor formation of carbon
fractals. Similarly, excess of acid catalyst will generally favor
breaking of carbon-carbon bonds within a graphene layer, and
therefore tend to favor branched nanotubes and/or carbon fractals.
Heating of the graphene for relatively short periods will typically
favor relatively short nanotubes and/or formation of carbon
fractals, while heating over a relatively long period will
generally favor long carbon nanotubes.
[0043] It should still further be appreciated that the
nanostructures according to the inventive subject matter (e.g.,
graphene, carbon fractal, de-novo open-ended SWNT, branched
nanotube, ring-shaped nanotube) may be further derivatized by
chemical compounds (e.g., fluorination, oxidation, amidation, etc.)
to introduce pendant (within the graphene plane) or terminal (at
the end of a graphene) functional groups or dopants.
[0044] Most preferably, however, it is contemplated that the
nanostructures according to the inventive subject matter are coated
with one or more metals, and especially noble metals. The term
"noble metal" as used herein refers to metals of groups VIIb, VIII,
and Ib of the second and third transition series. Particularly
contemplated noble metals therefore include rhenium, ruthenium,
rhodium, palladium, silver, osmium, iridium, platinum, and gold.
Furthermore, it generally preferred that the coating of the metal
to the nanostructure is relatively thin. For example, suitable
coatings will typically have a thickness of less than 100 atoms,
more typically less than 50 atoms, even more typically less than 10
atoms, and most typically less than 5 atoms. Therefore,
contemplated coating processes will preferably include those in
which the metal is deposited from a gas phase (e.g., physical vapor
deposition, chemical vapor deposition, plasma deposition,
sputtering, etc.). It should still further be noted that the metal
coating of graphene from vapor phase will typically coat the
graphene on both faces of the graphene layer. Therefore, reformed
structures, and especially nanotubes from metal coated graphene may
have a metal coat on the inside of the nanotube. However,
alternative coating processes are also considered such as galvanic
plating and electroless plating. Thus, the term "plating" or
"coating" as used in conjunction with metal deposition on
contemplated nanostructures excludes processes in which a
nanostructure is placed or grown on a metal and/or in which a metal
is placed onto the nanostructure to cover the nanostructure.
[0045] Therefore, the inventors contemplate numerous compositions
comprising contemplated nanostructures, and especially those
comprising at least 0.1 wt % to at least 1 wt %, more typically at
least 5 wt % graphene, even more typically at least 10-20 wt %,
20-40 wt %, 40-80 wt %, and most typically at least 80-90 wt %, or
90-99.9 wt % graphene, carbon fractals, and/or other carbon
nanostructures presented herein. Still further, it should be
appreciated that at least some of the graphene, carbon fractals,
and/or other carbon nanostructures may be coated with a metal (most
preferably a noble metal). It should further be recognized that in
such compositions the balance of the material may be any material,
and exemplary balance materials include carbonaceous starting
materials, silicon-based materials, metal-containing materials,
and/or materials other than graphene, carbon fractals, and/or other
carbon nanostructures presented herein.
[0046] Contemplated compositions may be advantageously used in
numerous manners, and according to their desirable properties. For
example, where the nanostructures are uncoated, they may provide
substantial stability of thermal conductivity to materials into
which they are integrated. Integration may be merely by admixing,
but also by covalent bonding with other materials. For example,
contemplated nanostructures may be partly oxidized (e.g. at high
temperatures), and the so introduced oxygen may be further reacted
to for a acid, alcohol, or keto group that is then used for
covalent binding (via crosslinker or otherwise). In another
example, and especially where the nanostructure is metal coated,
such nanostructures may be employed in an electric conductor, an
electron emitter, and/or an electrode.
[0047] Based on the simple manner of production, it should be noted
that the nanostructures according to the inventive subject matter
have now become available in bulk quantities (e.g., several hundred
tons per year) at relatively low cost of manufacture. Therefore,
the inventors contemplate bulk composition of at least 1000 gram
comprising at least 10 gram of at least one of a graphene, an
open-ended carbon nanotube, and a carbon fractal. Typically, the
graphene, the open-ended carbon nanotube, and/or the carbon fractal
are present in an amount effective to increase thermal
conductivity, electrical conductivity, adsorption, and/or a
mechanical stability of the bulk composition (e.g., at least ten
fold, and more typically at least hundred fold). Further aspects,
compositions, methods, and uses are disclosed in our commonly owned
copending U.S. applications with the title "Compositions and
Methods for Gas and liquid Purification" (filed Dec. 7, 2004) and
"Binding And In Situ Destruction Of Chemical Agents And Other
Contaminants" (filed Dec. 7, 2004), both of which are incorporated
by reference herein.
EXAMPLES
[0048] The following examples are provided only to illustrate
selected aspects of the inventive subject matter and are not
limiting to the inventive concept presented herein.
Production of Graphene
[0049] 100 g of flake graphite (e.g., commercially available from
Superior Graphite Company, 10 South Riverside Plaza, Chicago, Ill.
60606, or Crystal Graphite Corp., Vancouver, B.C., Canada) was
admixed with 100 ml activated acid catalyst (e.g., Activated Acid
Catalyst #3, commercially available from SupraCarbonic, 348 N.
Eckhoff Street--Orange, Calif. 92868, USA) and briefly heated to
expansion at about 100.degree. C. to about 20.degree. C. The so
obtained material was used without further purification for
electron microscopy and exemplary electron micrographs at different
magnifications are shown in FIG. 1A and FIG. 1B. Depending on the
purity and quality of the graphite, the so obtained material
typically comprises between 30 wt % and 99 wt % graphene.
Production of Open-Ended SWNT from Graphene
[0050] 1 g of graphene produced as described above was placed into
a refractory container, hermetically sealed and evacuated to a
pressure between about 100 mbar to about 1 mbar. After evacuation,
the graphene was heated to a temperature of between 500.degree. C.
and 700.degree. C. Depending on the starting material and purity,
heating is performed between several seconds and several minutes.
After cool-down, the reaction product was mixed with acetone and/or
toluene, sonicated where appropriate, and the floating material was
captured and dried under vacuum. The so obtained material was used
without further purification for electron microscopy and exemplary
electron micrographs are shown in FIG. 3 and FIG. 4. Depending on
the reaction conditions and starting materials (e.g., where
intermediate-grade graphite was used as starting material), varying
amounts of branched nanotubes were obtained, and exemplary branched
nanotubes are depicted in FIG. 5.
Production of Carbon Fractals and Carbon Rings from Graphene
[0051] Similar to the procedure for open-ended SWNT from graphene,
1 g of low grade graphite (e.g., technical, synthetic, or
amorphous) was used to produce low grade, fractured graphene by
mixing the graphite with 1 ml of activated acid catalyst (e.g.
Activated Acid Catalyst #3) and subsequent thermal expansion. The
so obtained low grade graphene was placed into a refractory
container, hermetically sealed, and evacuated to a pressure between
about 100 mbar to about 1 mbar. After evacuation, the graphene was
heated to a temperature of between 500.degree. C. and 700.degree.
C. for about 60 seconds. After cool-down, the reaction product was
mixed with acetone and/or toluene, sonicated where appropriate, and
the floating material was captured and dried under vacuum to
isolate or enrich the carbon fractals. The so obtained material was
used without further purification for electron microscopy and an
electron micrograph is shown in FIG. 6. Depending on the reaction
conditions (e.g., where less activated acid catalyst was used and
heating time was above one minute), varying amounts of ring-shaped
nanotubes were also obtained, and exemplary ring-shaped nanotubes
are depicted in FIG. 7.
[0052] Thus, specific embodiments and applications of compositions
and methods for binding and in situ destruction of chemical agents
have been disclosed. It should be apparent, however, to those
skilled in the art that many more modifications besides those
already described are possible without departing from the inventive
concepts herein. The inventive subject matter, therefore, is not to
be restricted except in the spirit of the appended claims.
Moreover, in interpreting both the specification and the claims,
all terms should be interpreted in the broadest possible manner
consistent with the context. In particular, the terms "comprises"
and "comprising" should be interpreted as referring to elements,
components, or steps in a non-exclusive manner, indicating that the
referenced elements, components, or steps may be present, or
utilized, or combined with other elements, components, or steps
that are not expressly referenced. Furthermore, where a definition
or use of a term in a reference, which is incorporated by reference
herein is inconsistent or contrary to the definition of that term
provided herein, the definition of that term provided herein
applies and the definition of that term in the reference does not
apply.
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