# Difference between revisions of "Literature on Carbon Nanotube Research"

 Title: CNT Literature About: Moderator: [Markus Landgraf] Created: March 13th, 2009 Modified: March 20th, 2009 Tags: This is a collaborative article Discipline(s): Wiki, Engineering, Chemistry

I have hijacked this page to write down my views on the literature on Carbon Nanotube (CNT) growths and processing, a procedure that should give us the cable/ribbon we desire for the space elevator. I will try to put as much information as possible here. If anyone has something to add, please do not hesitate!

## Direct mechanical measurement of the tensile strength and elastic modulus of multiwalled carbon nanotubes

B. G. Demczyk et al., Materials and Engineering, A334, 173-178, 2002
The paper by Demczyk et al. (2002) is the basic reference for the experimental determination of the tensile strengths of individual Multi-wall nanotube (MWNT) fibers. The experiments are performed with a microfabricated piezo-electric device. On this device CNTs in the length range of tens of microns are mounted. The tensile measurements are obseverd by transmission electron microscopy (TEM) and videotaped. Measurements of the tensile strength (tension vs. strain) were performed as well as Young modulus and bending stiffness. Breaking tension is reached for the SWNT at 150GP and between 3.5% and 5% of strain. During the measurements 'telescoping' extension of the MWNTs is observed, indicating that single-wall nanotubes (SWNT) could be even stronger. However, 150GPa remains the value for the tensile strength that was experimentally observed for carbon nanotubes.

## Direct Spinning of Carbon Nanotube Fibers from Chemical Vapour Deposition Synthesis

Y.-L. Li, I. A. Kinloch, and A. H. Windle, Science, 304,276-278, 2004
The work described in the paper by Y.-L. Li et al. is a follow-on of the famous paper by Zhu et al. (2002), which was cited extensively in Brad's book. This article goes a little more into the details of the process. If you use a mixture of ethene (as the source of carbon), ferrocene, and theophene (both as catalysts, I suppose) into a furnace (1050 to 1200 deg C) using hydrogen as carrier gas, you apparently get an 'aerogel' or 'elastic smoke' forming in the furnace cavity, which comprises the CNTs. Here's an interesting excerpt:

Under these synthesis conditions, the nanotubes in the hot zone formed an aerogel, which appeared rather like “elastic smoke,” because there was sufficient association between the nanotubes to give some degree of mechanical integrity. The aerogel, viewed with a mirror placed at the bottom of the furnace, appeared very soon after the introduction of the precursors (Fig. 2). Itwas then stretched by the gas flow into the form of a sock, elongating downwards along the furnace axis. The sock did not attach to the furnace walls in the hot zone, which accordingly remained clean throughout the process.... The aerogel could be continuously drawn from the hot zone by winding it onto a rotating rod. In this way, the material was concentrated near the furnace axis and kept clear of the cooler furnace walls,...

The elasticity of the aerogel is interpreted to come from the forces between the individual CNTs. The authors describe the procedure to extract the aerogel and start spinning a yarn from it as it is continuously drawn out of the furnace. In terms of mechanical properties of the produced yarns, the authors found a wide range from 0.05 to 0.5 GPa/g/ccm. That's still not enough for the SE, but the process appears to be interesting as it allows to draw the yarn directly from the reaction chamber without mechanical contact and secondary processing, which could affect purity and alignment. Also, a discussion of the roles of the catalysts as well as hydrogen and oxygen is given, which can be compared to the discussion in G. Zhang et al. (2005, see below).

## Multifunctional Carbon Nanotube Yarns by Downsizing an Ancient Technology

M. Zhang, K. R. Atkinson, and R. H. Baughman, Science, 306, 1358-1361, 2004
In the research article by M. Zhang et al. (2004) the procedure of spinning long yarns from forests of MWNTs is described in detail. The maximum breaking strength achieved is only 0.46 GPa based on the 30micron-long CNTs. The initial CNT forest is grown by chemical vapour deposition (CNT) on a catalytic substrate, as usual. A very intersting formula for the tensile strength of a yarn relative to the tensile strength of the fibers (in our case the MWNTs) is given:

$\frac{\sigma_{\rm yarn}}{\sigma_{\rm fiber}} = \cos^2 \alpha \left(1 - \frac{k}{\sin \alpha} \right)$

where alpha is the helix angle of the spun yarn, i.e. fiber direction relative to yarn axis. The constant k=sqrt(dQ/mu)/3L is given by the fiber diameter d=1nm, the fiber migration length Q (distance along the yartn over which a fiber shifts from the yarn surface to the deep interior and back again), the mu=0.13 is the friction coefficient of CNTs (the friction coefficent is the ratio of maximum along-fiber force divided by lateral force pressing the fibers together), L=30micron is the fiber length. A critical review of this formula is given here.

In the paper interesting transmission electron microscope (TEM) pictures are shown, which give insight into how the yarn is assembled from the CNT forest. The authors describe other characteristics of the yarn, like how knots can be introduced and how the yarn performs when knitted, apparently in preparation for application in the textile industry.

## Ultra-high-yield growth of vertical single-walled carbon nanotubes: Hidden roles of hydrogen and oxygen

Important aspects of the production of CNTs that are suitable for the SE is the efficiency of the growth and the purity (i.e. lack of embedded amorphous carbon and imperfections in the Carbon bounds in the CNT walls). In their article G. Zhang et al. go into detail about the roles of oxygen and hydrogen during the chemical vapour deposition (CVD) growth of CNT forests from hydrocarbon sources on catalytic substrates. In earlier publications the role of oxygen was believed to be to remove amorphous carbon by oxidation into CO. The authors show, however, that, at least for this CNT growth technique, oxygen is important, because it removes hydrogen from the reaction. Hydrogen has apparently a very detrimental effect on the growth of CNTs, it even destroys existing CNTs as shown in the paper. Since hydrogen radicals are released during the dissociation of the hydrocarbon source compount, it is important to have a removal mechanism. Oxygen provides this mechanism, because its chemical affinity towards hydrogen is bigger than towards carbon.

In summary, if you want to efficiently grow pure CNT forests on a catalyst substrate from a hydrocarbon CVD reaction, you need a few percent oxygen in the source gas mixture. An additional interesting information in the paper is that you can design the places on the substrate, on which CNTs grow by placing the the catalyst only in certain areas of the substrate using lithography. In this way you can grow grids and ribbons. Figures are shown in the paper.

In the paper no information is given on the reason why the CNT growth stops at some point. The growth rate is given with 1 micron per minute. Of course for us it would be interesting to eliminate the mechanism that stops the growth so we could grow infinitely long CNTs.