Friday, October 31, 2008

Hot nanotube sheets produce music on demand

16:08 31 October 2008
  • NewScientist.com news service
  • Colin Barras
Carbon nanotube speaker

Sheets made of carbon nanotubes behave like a loudspeaker when zapped with a varying electric current, say Chinese researchers. The discovery could lead to new generation of cheap, flat speakers.

Since the early 1990s, nanotubes have been intensively studied by researchers across the globe. The tiny structures are widely touted as potential drug delivery devices but might also be useful in more exotic gadgets including artificial photosynthesis devices and space elevators. But no one has thought to test their acoustic properties until now.

Shoushan Fan and his research team at Tsinghua University in Beijing, China, working with colleagues at Beijing Normal University, created a thin sheet by roughly aligning many 10-nanometer-diameter carbon nanotubes. When they sent an audio frequency current through the sheet, they discovered it acted as a loudspeaker.

A standard loudspeaker consists of three basic elements – a speaker cone, a voice coil and a magnet. The cone and coil are attached and sit in a permanent magnetic field created by the magnet. When an audio frequency current passes through the voice coil, it creates a temporary magnetic field, and the coil and cone shift relative to the permanent magnetic field. Those shifts induce vibrations in the air molecules near the speaker cone, generating sound.

How it works

Fan's team wondered whether the nanotube speaker behaved in a similar way. They used a laser vibrometer to look for vibrations in their nanotube speaker as it produced sound, but the sheet remained resolutely static throughout. Instead, they think that the nanotube speaker functions as a thermoacoustic device.

When an alternating current passes through the nanotube sheet, the sheet alternates between room temperature and 80 °C. Those rapid temperature oscillations lead to pressure oscillations in the air next to the film. It is those thermally induced pressure oscillations that are responsible for the sound, rather than any physical movement of the nanotube sheet itself.

In fact, the researchers realised this phenomenon was first observed over a century ago independently by William Henry Preece and Karl Ferdinand Braun. Those nineteenth century researchers realised they could get sound from a thin metal foil by passing an alternating current through it, a discovery that led to the invention of a device called the "thermophone".

But the thermophone produced a very weak sound, whereas the nanotube sheets can be very loud (see video). That's because of the unusual properties of carbon nanotubes, says Fan. "A key parameter that determines the sound generation efficiency is the heat capacity per unit area," he says. Put simply, that's a measure of how much heat energy must be applied to a material to raise its temperature. The heat capacity per unit area of a carbon nanotube sheet is 260 times smaller than that of a platinum foil sheet. That means a nanotube sheet can generate sound waves 260 times more efficiently than a platinum sheet, and so produce a much louder sound.

'Singing jackets'

The nanotube loudspeakers have several key advantages over standard speaker systems, says Fan. "Conventional loudspeakers which [produce sound] due to the vibration of the cone will fail to emit sound if the cone is broken," he says. "The carbon nanotube loudspeaker does not vibrate, which means it will still emit sound if part of the film is broken."

The flexible nanotube sheets can be stretched or flexed into complicated shapes and they still produce sound, Fan says. When fully stretched, the sheets are transparent and so they could be attached to the front of an LCD screen to replace standard speakers.

Watch a video of a carbon nanotube speaker being stretched

But more exotic uses might see nanotube sheets stitched into clothing to create "singing and speaking jackets", Fan's team thinks.

Cees Dekker, a nanoscience expert at Delft University of Technology in the Netherlands, finds the new study very interesting. "It's just amazing how widespread the diversity of applications of these nanotubes are," he says.

Journal reference: Nano Letters (DOI: 10.1021/nl802750z)

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Thursday, October 30, 2008

Diamond structures as fuel capsules for nuclear fusion

United States Patent Application 20080256850
Kind Code A1
Kley; Victor B. October 23, 2008

Diamond structures as fuel capsules for nuclear fusion

Abstract

Fuel capsules usable in inertial confinement fusion (ICF) reactors have shells made from materials having a diamond (sp.sup.3) lattice structure, including diamond materials in synthetic crystalline, polycrystalline (ordered or disordered), nanocrystalline and amorphous forms. The interior of the shell is filled with a fusion fuel mixture, including any combination of deuterium and/or tritium and/or helium-3 and/or other fusible isotopes.


Inventors: Kley; Victor B.; (US)
Correspondence Name and Address:
    IMPERIUM PATENT WORKS
P.O. BOX 587
SUNOL
CA
94586
US
Assignee Name and Adress: General Nanotechnology LLC

Serial No.: 152032
Series Code: 12
Filed: May 10, 2008

U.S. Current Class: 44/502; 427/551
U.S. Class at Publication: 44/502; 427/551
Intern'l Class: G21C 3/07 20060101 G21C003/07; B05D 3/06 20060101 B05D003/06


Claims



1-113. (canceled)

114. An article of manufacture, comprising:a shell enclosing a hollow volume; wherein a nanocrystalline diamond film having a surface roughness less than about 400 nm comprises the wall of said shell.

122. The article of claim 120, wherein at least one fusion fuel selected from deuterium and tritium is disposed therein said hollow volume.

123. The article of claim 122, wherein said fusion fuel further comprises a frozen layer of deuterium-tritium (DT) fuel and a central DT gas core.

124. The article of claim 122, wherein said fusion fuel comprises a pressure greater than about 1 atm.

130. A method of fabricating a diamond shell, comprising:providing a substrate; symmetrically depositing a diamond film on said substrate; removing said substrate so as to produce a hollow core; refilling said hollow core with a nuclear fuel; and focusing an ion beam on one or more fill perforations in a C.sub.14H.sub.10 atmosphere so as to produce a target use for inertial confinement fusion.

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Tuesday, October 28, 2008

Graphene could accelerate genomics

Oct 28, 2008
DNA moving through a graphene nanogap

Artist's impression of a DNA molecule (helix) moving through a tiny slit in a graphene sheet (shown in blue). (Courtesy: Henk Postma)

The “wonder material” graphene could soon be used to analyse DNA at a record-breaking pace. That’s the claim of a physicist in the US who has proposed a new way of reading the sequence of chemical bases in a DNA strand by sending the molecule through a tiny slit in a graphene sheet.

While the technique has yet to be verified experimentally, if successful it could be eligible for the $10 million X Prize for Genomics, which has set the challenge of developing a new rapid and low-cost sequencing technology.

The genetic profile — or “genome” — of an organism is determined by recording the full sequence of acid base pairs that make up its DNA. In 2003, the Human Genome Project made history by determining the entire human genetic code — 3 billion DNA base pairs that took 13 years to analyse using a technique that has changed very little since the late 1970s.

This “shotgun” approach first isolates a DNA strand and forces it to copy itself millions of times over in a chemical reaction. These are then “blasted” into tiny fragments because current techniques for sequence reading can detectors can only analyse very short sections of DNA. Finally, a supercomputer matches up overlapping base patterns to piece together the full genome.

No processing required

Now, Henk Postma at California State University Northridge has proposed a way of sequencing an entire DNA strand without the need for blasting or computer processing (arXiv:0810.3035v1 ).

Rapid Sequencing of Individual DNA Molecules in Graphene Nanogaps
http://arxiv.org/PS_cache/arxiv/pdf/0810/0810.3035v1.pdf

The technique involves cutting a very narrow slit or “nanogap” along the length of a piece of graphene — an extremely strong sheet of carbon just one atom thick. A voltage is applied perpendicular to the graphene’s surface, which causes the DNA strand to pass slowly through the slit one base at a time.

A second voltage is applied across slit and electrons are able to “tunnel” across the nanogap via the base that happens to be passing through the slit. There are four different types of base in a DNA molecule, and each should support a different tunnelling current — allowing the base type to be identified.

While the idea of sequencing DNA by sending it through a tiny gap is not new, previous schemes had relied on using separate materials for the membrane and electrodes — and aligning the two materials has proved to be a considerable challenge. Postma’s design gets around this problem by having the graphene function as both membrane and electrode.

Postma believes that detector could be made from a graphene sheet sandwiched between glass plates that are held together by van der Waals forces.

Technology should be possible

According to Changgu Lee, a mechanical engineer at Colombia University, some of the technology to realize Postma’s design may be available already. “Creating the nanogaps in graphene was demonstrated this year using both STM [scanning tunnelling microscopy] and catalytic cutting with metal particles”, he said.

Postma told physicsworld.com that traditional sequencing techniques are limited to determining about 800 base pairs per recording. By contrast, he estimates his design could yield 100,000 bases per recording, and if run continuously it would read the whole human genome in two and a half hours. He also believes that his technique could lead to sequencing devices that are smaller and cheaper than existing systems.

If successful, Postma's system could be a contender for the X Prize for Genomics, which aims to award $10m to the inventor of a device that can sequence 100 human genomes within 10 days or less,to a specified accuracy and costing no more than $10,000 per genome.

Postma said he is continuing to develop his design, but added: “I published the paper to get feedback from the scientific community, in the open, because I believe that will lead to the best possible technology.”

And it seems DNA experts are ready for a new technology. Geoffrey Baldwin, a molecular biologist from Imperial College in the UK said “to truly develop health care we need the profile of 100s of genomes not just the few we have at the moment”. He added “there is now a great opportunity for a new technique to become the standard in base sequencing”.

About the author

James Dacey is a science journalist based in the UK

Source

Strikes me as a DNA computer in the making.

Killing Cancer Cells Using Cobalt Nanoparticles Coated with Graphitic Shells

A team of scientists at Arkansas Nanotechnology Center at UALR (the University of Arkansas at Little Rock) has developed what promises to be a non-invasive method of eradicating cancer cells while reducing the life-threatening side effects of chemotherapy and radiation.

The new technique, described in the current issue of the journal Nanotechnology, was developed by a team led by Dr. Alexandru Biris, assistant professor of applied science and chief scientist at the Nanotechnology Center. Working in collaboration with the University of Arkansas for Medical Sciences, the team successfully killed more than 98 percent of the cervical cancer cells used in the study.

The technique introduces nano-sized cobalt particles encased in graphitic carbon layers inside the cells and thermally activates them by using radio frequency radiation. By applying low radio frequency radiation – used in some electronic or electromagnetic devices – the magnetic portion in the nanoparticles heats up the cancerous cells, destroying them.

The procedure promises a non-invasive method of eradicating cancer cells while reducing the life-threatening side effects of chemotherapy and radiation.

The technique is described in their new research paper, Cobalt Nanoparticles Coated with Graphitic Shells as Localized Radio Frequency Absorbers for Cancer Therapy.

"We have demonstrated that using a combination of a low frequency, low power radio frequency radiation – which has a high penetration ability in human tissue – with graphitic-magnetic composite nanoparticles could prove an excellent means of raising the temperature at the cellular level above the threshold required for DNA fragmentation or protein denaturation,” Biris said. “The result is death of the cells. This technique is less invasive and possesses higher efficiency for targeting localized cells. It also has the potential to reduce the side effects associated with traditional cancer therapies.”

With approved research protocols, UAMS scientists are expanding on previous work involving use of nanostructural materials for killing tumors with lasers. Using this method, the nanomaterials are introduced through the bloodstream to be activated with radio frequency energy once they are in the tumors.

“We believe this method is extremely promising for killing cancer cells,” said Dr. Vladmir Zharov, professor and director of the Phillips Classic Laser Laboratories in the UAMS Winthrop P. Rockefeller Cancer Institute. “We are working now to move this technology toward clinical trials with the ultimate goal of achieving a safe, effective procedure that leaves a patient cancer free.”

Biris, a native of Romania who earned a Ph.D. in applied science at UALR in 2004, said the delivery of the encased nanoparticle to tumors will also be explored by binding them to cancer-specific antibodies.

By using antibodies or other nanoparticle bioconjugations – the coupling of two substances – the nanoparticles are expected to find the cancer cells even in advanced cases, including places that before now have been considered inoperable. The nanoparticles can also find undiagnosed micrometastasis, or the spread of cancer cells from the primary site with the secondary tumors too small to be detected clinically.

“This research has extended the understanding of the mechanisms that are responsible for effective nanoparticle targeting and eventually the death of cancer cells,” Zharov said.

The team’s work is helping to explain the mechanism that is responsible for the death of the cells by figuring out the localized thermal damages such as protein denaturation and DNA fragmentation associated with the process. The finding can be applied to bacteria, viruses, or other biological systems.

Members of the research team working with Biris are:

* Yang Xu, Meena Mahmood, Zhongrui Li, and Enkeleda Dervishi, Nawab Ail, and Viney Saini, all of all of the Nanotechnology Center and Department of Applied Science at UALR.
* Vladimir P. Zharov’ group: Ekaterina Galanzha and Evgeny Shashkov, the Philips Classic Laser Laboratories at UAMS.
* Steve Trigwell of ASRC Aerospace, NASA’s Electrostatic and Surface Physics Laboratory at Kennedy Space Center in Florida.
* Alexandru R. Biris and Dan Lupu of the National Institute for Research and Development of Isotopic and Molecular Technologies, Cluj Napoca, Romania.
* Dorin Boldor of Louisiana State University’s AgCenter, Biological and Agricultural Engineering Department in Baton Rouge, LA.

To read Biris’ paper, visit http://www.iop.org/EJ/journal/Nano.

Posted October 28th, 2008

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Cobalt nanoparticles coated with graphitic shells as localized radio frequency absorbers for cancer therapy

Yang Xu et al 2008 Nanotechnology 19 435102 (9pp) doi: 10.1088/0957-4484/19/43/435102 Help


PDF (1.18 MB) | Supplementary data | References


Yang Xu1, Meena Mahmood1, Zhongrui Li1, Enkeleda Dervishi1, Steve Trigwell2, Vladimir P Zharov3, Nawab Ali1, Viney Saini1, Alexandru R Biris4, Dan Lupu4, Dorin Boldor5 and Alexandru S Biris1
1 Nanotechnology Center and Applied Science Department, University of Arkansas at Little Rock, Little Rock, AR 72204, USA
2 NASA, Electrostatics and Surface Physics Laboratory, ASRC Aerospace, Kennedy Space Center, FL 32899, USA
3 Philips Classic Laser Laboratories, University of Arkansas for Medical Sciences, Little Rock, AR 72204, USA
4 National Institute for Research and Development of Isotopic and Molecular Technologies, Cluj Napoca, RO-3400, Romania
5 Louisiana State University, AgCenter, Baton Rouge, LA, USA
E-mail: yxxu@ualr.edu and asbiris@ualr.edu

Abstract. Graphitic carbon-coated ferromagnetic cobalt nanoparticles (C–Co-NPs) with diameters of around 7 nm and cubic crystalline structures were synthesized by catalytic chemical vapor deposition. X-ray diffraction and x-ray photoelectron spectroscopy analysis indicated that the cobalt nanoparticles inside the carbon shells were preserved in the metallic state. Fluorescence microscopy images and Raman spectroscopy revealed effective penetrations of the C–Co-NPs through the cellular plasma membrane of the cultured HeLa cells, both inside the cytoplasm and in the nucleus. Low radio frequency (RF) radiation of 350 kHz induced localized heat into the metallic nanoparticles, which triggered the killing of the cells, a process that was found to be dependent on the RF application time and nanoparticle concentration. When compared to carbon nanostructures such as single-wall carbon nanotubes, these coated magnetic cobalt nanoparticles demonstrated higher specificity for RF absorption and heating. DNA gel electrophoresis assays of the HeLa cells after the RF treatment showed a strong broadening of the DNA fragmentation spectrum, which further proved the intense localized thermally induced damages such as DNA and nucleus membrane disintegration, under RF exposure in the presence of C–Co-NPs. The data presented in this report indicate a great potential of this new process for in vivo tumor thermal ablation, bacteria killing, and various other biomedical applications.

Print publication: Issue 43 (22 October 2008)
Received 17 July 2008, in final form 25 August 2008
Published 22 September 2008

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Monday, October 20, 2008

Sun + Water = Fuel

November/December 2008

With catalysts created by an MIT chemist, sunlight can turn water into hydrogen. If the process can scale up, it could make solar power a dominant source of energy.

By Kevin Bullis


Leaf envy: MIT chemist Daniel Nocera has mimicked the step in photosynthesis in which green plants split water.
Credit: Christopher Harting

"I'm going to show you something I haven't showed anybody yet," said Daniel Nocera, a professor of chemistry at MIT, speaking this May to an auditorium filled with scientists and U.S. government energy officials. He asked the house manager to lower the lights. Then he started a video. "Can you see that?" he asked excitedly, pointing to the bubbles rising from a strip of material immersed in water. "Oxygen is pouring off of this electrode." Then he added, somewhat cryptically, "This is the future. We've got the leaf."

What Nocera was demonstrating was a reaction that generates oxygen from water much as green plants do during photosynthesis--an achievement that could have profound implications for the energy debate. Carried out with the help of a catalyst he developed, the reaction is the first and most difficult step in splitting water to make hydrogen gas. And efficiently generating hydrogen from water, Nocera believes, will help surmount one of the main obstacles preventing solar power from becoming a dominant source of electricity: there's no cost-effective way to store the energy collected by solar panels so that it can be used at night or during cloudy days.

Solar power has a unique potential to generate vast amounts of clean energy that doesn't contribute to global warming. But without a cheap means to store this energy, solar power can't replace fossil fuels on a large scale. In Nocera's scenario, sunlight would split water to produce versatile, easy-to-store hydrogen fuel that could later be burned in an internal-combustion generator or recombined with oxygen in a fuel cell. Even more ambitious, the reaction could be used to split seawater; in that case, running the hydrogen through a fuel cell would yield fresh water as well as electricity.

Storing energy from the sun by mimicking photosynthesis is something scientists have been trying to do since the early 1970s. In particular, they have tried to replicate the way green plants break down water. Chemists, of course, can already split water. But the process has required high temperatures, harsh alkaline solutions, or rare and expensive catalysts such as platinum. What Nocera has devised is an inexpensive catalyst that produces oxygen from water at room temperature and without caustic chemicals--the same benign conditions found in plants. Several other promising catalysts, including another that Nocera developed, could be used to complete the process and produce hydrogen gas.

Nocera sees two ways to take advantage of his breakthrough. In the first, a conventional solar panel would capture sunlight to produce electricity; in turn, that electricity would power a device called an electrolyzer, which would use his catalysts to split water. The second approach would employ a system that more closely mimics the structure of a leaf. The catalysts would be deployed side by side with special dye molecules designed to absorb sunlight; the energy captured by the dyes would drive the water-splitting reaction. Either way, solar energy would be converted into hydrogen fuel that could be easily stored and used at night--or whenever it's needed.

Nocera's audacious claims for the importance of his advance are the kind that academic chemists are usually loath to make in front of their peers. Indeed, a number of experts have questioned how well his system can be scaled up and how economical it will be. But Nocera shows no signs of backing down. "With this discovery, I totally change the dialogue," he told the audience in May. "All of the old arguments go out the window."

The Dark Side of Solar
Sunlight is the world's largest potential source of renewable energy, but that potential could easily go unrealized. Not only do solar panels not work at night, but daytime production waxes and wanes as clouds pass overhead. That's why today most solar panels--both those in solar farms built by utilities and those mounted on the roofs of houses and businesses--are connected to the electrical grid. During sunny days, when solar panels are operating at peak capacity, homeowners and companies can sell their excess power to utilities. But they generally have to rely on the grid at night, or when clouds shade the panels.

This system works only because solar power makes such a tiny contribution to overall electricity production: it meets a small fraction of 1 percent of total demand in the United States. As the contribution of solar power grows, its unreliability will become an increasingly serious problem.

If solar power grows enough to provide as little as 10 percent of total electricity, utilities will need to decide what to do when clouds move in during times of peak demand, says Ryan Wiser, a research scientist who studies electricity markets at Lawrence Berkeley National Laboratory in Berkeley, CA. Either utilities will need to operate extra natural-gas plants that can quickly ramp up to compensate for the lost power, or they'll need to invest in energy storage. The first option is currently cheaper, Wiser says: "Electrical storage is just too expensive."

But if we count on solar energy for more than about 20 percent of total electricity, he says, it will start to contribute to what's called base load power, the amount of power necessary to meet minimum demand. And base load power (which is now supplied mostly by coal-fired plants) must be provided at a relatively constant rate. Solar energy can't be harnessed for this purpose unless it can be stored on a large scale for use 24 hours a day, in good weather and bad.

In short, for solar to become a primary source of electricity, vast amounts of affordable storage will be needed. And today's options for storing electricity just aren't practical on a large enough scale, says Nathan Lewis, a professor of chemistry at Caltech. Take one of the least expensive methods: using electricity to pump water uphill and then running the water through a turbine to generate elec­tricity later on. One kilogram of water pumped up 100 meters stores about a kilojoule of energy. In comparison, a kilogram of gasoline stores about 45,000 kilojoules. Storing enough energy this way would require massive dams and huge reservoirs that would be emptied and filled every day. And try finding enough water for that in places such as Arizona and Nevada, where sunlight is particularly abundant.

Batteries, meanwhile, are expensive: they could add $10,000 to the cost of a typical home solar system. And although they're improving, they still store far less energy than fuels such as gasoline and hydrogen store in the form of chemical bonds. The best batteries store about 300 watt-hours of energy per kilogram, Lewis says, while gasoline stores 13,000 watt-hours per kilogram. "The numbers make it obvious that chemical fuels are the only energy-dense way to obtain massive energy storage," Lewis says. Of those fuels, not only is hydrogen potentially cleaner than gasoline, but by weight it stores much more energy--about three times as much, though it takes up more space because it's a gas.

The challenge lies in using energy from the sun to make such fuels cheaply and efficiently. This is where Nocera's efforts to mimic photosynthesis come in.

Photosynthesis in a beaker: In an experimental setup that duplicates the benign conditions found in photosynthetic plants, -Daniel ¬Nocera has demonstrated an easy and potentially cheap way to produce hydrogen gas. When a voltage is applied, cobalt and phosphate in solution (left) accumulate on an electrode to form a catalyst, which releases oxygen gas from the water as electrons flow out through the electrode. Hydrogen ions flow through a membrane; on the other side, hydrogen gas is produced by a nickel metal catalyst (Nocera has also used a platinum catalyst).
Credit: Bryan Christie

Imitating Plants
In real photosynthesis, green plants use chlorophyll to capture energy from sunlight and then use that energy to drive a series of complex chemical reactions that turn water and carbon dioxide into energy-rich carbohydrates such as starch and sugar. But what primarily interests many researchers is an early step in the process, in which a combination of proteins and inorganic catalysts helps break water efficiently into oxygen and hydrogen ions.

The field of artificial photosynthesis got off to a quick start. In the early 1970s, a graduate student at the University of Tokyo, Akira Fujishima, and his thesis advisor, Kenichi Honda, showed that electrodes made from titanium dioxide--a component of white paint--would slowly split water when exposed to light from a bright, 500-watt xenon lamp. The finding established that light could be used to split water outside of plants. In 1974, Thomas Meyer, a professor of chemistry at the University of North Caro­lina, Chapel Hill, showed that a ruthenium-based dye, when exposed to light, underwent chemical changes that gave it the potential to oxidize water, or pull electrons from it--the key first step in water splitting.

Ultimately, neither technique proved practical. The titanium dioxide couldn't absorb enough sunlight, and the light-induced chemical state in Meyer's dye was too transient to be useful. But the advances stimu­lated the imaginations of scientists. "You could look ahead and see where to go and, at least in principle, put the pieces together," Meyer says.

Over the next few decades, scientists studied the structures and materials in plants that absorb sunlight and store its energy. They found that plants carefully choreograph the movement of water molecules, electrons, and hydrogen ions--that is, protons. But much about the precise mechanisms involved remained unknown. Then, in 2004, researchers at Imperial College London identified the structure of a group of proteins and metals that is crucial for freeing oxygen from water in plants. They showed that the heart of this catalytic complex was a collection of proteins, oxygen atoms, and manganese and calcium ions that interact in specific ways.

"As soon as we saw this, we could start designing systems," says Nocera, who had been trying to fully understand the chemistry behind photosynthesis since 1984. Reading this "road map," he says, his group set out to manage protons and electrons somewhat the way plants do--but using only inorganic materials, which are more robust and stable than proteins.

Initially, Nocera didn't tackle the biggest challenge, pulling oxygen out from water. Rather, "to get our training wheels," he began with the reverse reaction: combining oxygen with protons and electrons to form water. He found that certain complex compounds based on cobalt were good catalysts for this reaction. So when it came time to try splitting water, he decided to use similar cobalt compounds.

Nocera knew that working with these compounds in water could be a problem, since cobalt can dissolve. Not surprisingly, he says, "within days we realized that cobalt was falling out of this elaborate compound that we made." With his initial attempts foiled, he decided to take a different approach. Instead of using a complex compound, he tested the catalytic activity of dissolved cobalt, with some phosphate added to the water to help the reaction. "We said, let's forget all the elaborate stuff and just use cobalt directly," he says.



Solar goes solo: Artificial photosynthesis could provide a practical way to store energy produced by solar power, freeing people’s homes from the electrical grid. In this scheme, electricity from solar panels powers an electrolyzer, which breaks water into hydrogen and oxygen. The hydrogen is stored; at night or on cloudy days, it is fed into a fuel cell to produce electricity for lights, appliances, and even electric cars. On sunny days, some of the solar power is used directly, bypassing the hydrogen production step.
Credit: Bryan Christie

The experiment worked better than Nocera and his colleagues had expected. When a current was applied to an electrode immersed in the solution, cobalt and phosphate accumulated on it in a thin film, and a dense layer of bubbles started forming in just a few minutes. Further tests confirmed that the bubbles were oxygen released by splitting the water. "Here's the luck," Nocera says. "There was no reason for us to expect that just plain cobalt with phosphate, versus cobalt being tied up in one of our complexes, would work this well. I couldn't have predicted it. The stuff that was falling out of the compounds turned out to be what we needed.

"Now we want to understand it," he continues. "I want to know why the hell cobalt in this thin film is so active. I may be able to improve it or use a different metal that's better." At the same time, he wants to start working with engineers to optimize the process and make an efficient water-splitting cell, one that incorporates catalysts for generating both oxygen and hydrogen. "We were really interested in the basic science. Can we make a catalyst that works efficiently under the conditions of photosynthesis?" he says. "The answer now is yes, we can do that. Now we've really got to get to the technology of designing a cell."

Catalyzing a Debate
Nocera's discovery has garnered a lot of attention, and not all of it has been flattering. Many chemists find his claims overstated; they don't dispute his findings, but they doubt that they will have the consequences he imagines. "The claim that this is the answer for artificial photosynthesis is crazy," says Thomas Meyer, who has been a mentor to Nocera. He says that while Nocera's catalysts "could prove technologically important," the advance is "a research finding," and there's "no guarantee that it can be scaled up or even made practical."

Many critics' objections revolve around the inability of ­Nocera's lab setup to split water nearly as rapidly as commercial electrolyzers do. The faster the system, the smaller a commercial unit that produced a given amount of hydrogen and oxygen would be. And smaller systems, in general, are cheaper.

The way to compare different catalysts is to look at their "current density"--that is, electrical current per square centimeter--when they're at their most efficient. The higher the current, the faster the catalyst can produce oxygen. Nocera reported results of 1 milliamp per square centimeter, although he says he's achieved 10 milliamps since then. Commercial electrolyzers typically run at about 1,000 milliamps per square centimeter. "At least what he's published so far would never work for a commercial electrolyzer, where the current density is 800 times to 2,000 times greater," says John Turner, a research fellow at the National Renewable Energy Laboratory in Golden, CO.

Other experts question the whole principle of converting sunlight into electricity, then into a chemical fuel, and then back into electricity again. They suggest that while batteries store far less energy than chemical fuels, they are nevertheless far more efficient, because using electricity to make fuels and then using the fuels to generate electricity wastes energy at every step. It would be better, they say, to focus on improving battery technology or other similar forms of electrical storage, rather than on developing water splitters and fuel cells. As Ryan Wiser puts it, "Electrolysis is [currently] inefficient, so why would you do it?"

The Artificial Leaf
Michael Grätzel, however, may have a clever way to turn Nocera's discovery to practical use. A professor of chemistry and chemical engineering at the École Polytechnique Fédérale in Lausanne, Switzerland, he was one of the first people Nocera told about his new catalyst. "He was so excited," Grätzel says. "He took me to a restaurant and bought a tremendously expensive bottle of wine."

In 1991, Grätzel invented a promising new type of solar cell. It uses a dye containing ruthenium, which acts much like the chlorophyll in a plant, absorbing light and releasing electrons. In ­Grätzel's solar cell, however, the electrons don't set off a water-splitting reaction. Instead, they're collected by a film of titanium dioxide and directed through an external circuit, generating electricity. Grätzel now thinks that he can integrate his solar cell and ­Nocera's catalyst into a single device that captures the energy from sunlight and uses it to split water.

If he's right, it would be a significant step toward making a device that, in many ways, truly resembles a leaf. The idea is that Grätzel's dye would take the place of the electrode on which the catalyst forms in Nocera's system. The dye itself, when exposed to light, can generate the voltage needed to assemble the catalyst. "The dye acts like a molecular wire that conducts charges away," Grätzel says. The catalyst then assembles where it's needed, right on the dye. Once the catalyst is formed, the sunlight absorbed by the dye drives the reactions that split water. Grätzel says that the device could be more efficient and cheaper than using a separate solar panel and electrolyzer.

Another possibility that Nocera is investigating is whether his catalyst can be used to split seawater. In initial tests, it performs well in the presence of salt, and he is now testing it to see how it handles other compounds found in the sea. If it works, Nocera's system could address more than just the energy crisis; it could help solve the world's growing shortage of fresh water as well.

Artificial leaves and fuel-producing desalination systems might sound like grandiose promises. But to many scientists, such possibilities seem maddeningly close; chemists seeking new energy technologies have been taunted for decades by the fact that plants easily use sunlight to turn abundant materials into energy-rich molecules. "We see it going on all around us, but it's something we can't really do," says Paul Alivisatos, a professor of chemistry and materials science at the University of California, Berkeley, who is leading an effort at Lawrence Berkeley National Laboratory to imitate photosynthesis by chemical means.

But soon, using nature's own blueprint, human beings could be using the sun "to make fuels from a glass of water," as Nocera puts it. That idea has an elegance that any chemist can appreciate--and possibilities that everyone should find hopeful.

Kevin Bullis is Technology Review's Energy Editor.

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Saturday, October 18, 2008

Hybrid Material Could Vastly Increase Energy Potential From the Sun

10.17.2008 9:03 AM

Harnessing Light's Full Spectrum: Scientists Claim Solar Power Breakthrough

By Dan Shapley


Chemists at Ohio State University say they have produced a next-generation material that not only absorbs the full spectrum of sunlight, but also make makes the electrons generated more easy to capture.

The hybrid material -- a combination of electrically conductive plastic and metals like molybdenum and titanium -- is the first of its kind to capture the full solar spectrum, according to Malcolm Chisholm, one of the authors of the paper describing the research, which appears in Proceedings of the National Academy of Sciences. Solar panels in use today capture only a small fraction of the energy contained in sunlight.

The material is years from being made into a commercial product, but is another example of how innovations in the field of solar energy could make vastly more of the sun's energy available for human use. Recent action by Congress to extend industry tax incentives should keep companies investing in new technology research and development. And according to the Department of Energy, "Under the ongoing global financial crisis, a lack of available credit is causing projects to be delayed or canceled, but the clean energy sector is continuing to attract substantial amounts of investment capital."

If coupled with new battery technology, solar energy technology has the potential to revolutionize the way we generate electricity. Millions of homes could be outfitted with their own power sources, and they could store enough electricity -- if efficient enough -- to eliminate the need for power plants in the residential sector.

That's been the promise of solar energy for a long time. Breakthroughs like this one announced by Ohio State brings the vision that much closer to reality.

Here's how the university described the breakthrough:

The material generates electricity just like other solar cell materials do: light energizes the atoms of the material, and some of the electrons in those atoms are knocked loose.

Ideally, the electrons flow out of the device as electrical current, but this is where most solar cells run into trouble. The electrons only stay loose for a tiny fraction of a second before they sink back into the atoms from which they came. The electrons must be captured during the short time they are free, and this task, called charge separation, is difficult.

In the new hybrid material, electrons remain free much longer than ever before.

To design the hybrid material, the chemists explored different molecular configurations on a computer at the Ohio Supercomputer Center. Then, with colleagues at National Taiwan University, they synthesized molecules of the new material in a liquid solution, measured the frequencies of light the molecules absorbed, and also measured the length of time that excited electrons remained free in the molecules.

They saw something very unusual. The molecules didn't just fluoresce as some solar cell materials do. They phosphoresced as well. Both luminous effects are caused by a material absorbing and emitting energy, but phosphorescence lasts much longer.

To their surprise, the chemists found that the new material was emitting electrons in two different energy states -- one called a singlet state, and the other a triplet state. Both energy states are useful for solar cell applications, and the triplet state lasts much longer than the singlet state.

Electrons in the singlet state stayed free for up to 12 picoseconds, or trillionths of a second -- not unusual compared to some solar cell materials. But electrons in the triplet state stayed free 7 million times longer -- up to 83 microseconds, or millionths of a second.

When they deposited the molecules in a thin film, similar to how they might be arranged in an actual solar cell, the triplet states lasted even longer: 200 microseconds.

Source

Thursday, October 16, 2008

The Materialist

He designs nanomaterials with outrageous abilities

By Gregory Mone Posted 10.16.2008 at 1:45 pm

Earlier this year, Francesco Stellacci announced that his group had developed a material that can suck 20 times its weight in oil out of a sample of water. The material could be used to clean up massive crude spills, and chemist Joerg Lahann of the University of Michigan called the work a blueprint for scientists who hope to design nanomaterials that protect the environment. Yet Stellacci doesn’t consider this his best work. He’s excited about tricking cells.

Stellacci’s first major step came in 2003, when he created a peculiar coating for metallic nanoparticles. He had been wondering what would happen if hydrophilic, or water-loving, molecules, and their opposites, hydrophobes, were stuck together on the surface of a nanosize sphere. So he ran an experiment and found that the molecules self-organized into alternating stripes, like lines of latitude on a globe. A belt of tiny, spherical hydrophilic molecules sat atop a band of hydrophobes, and so on from top to bottom.

These stripes are not only aesthetically attractive, they gave his particles new properties. Typically, when materials try to enter a cell, they either get swallowed up and spat out, or they damage it by poking a hole in its membrane. But Stellacci’s striped nanoparticles slipped right in. “The cell has a security system,” he says, “and somehow my particles trick it.”

He hasn’t figured out how this works, but he has shown that the particles could improve drug delivery by giving molecules safe passage into cells. This finding, along with the oil-absorbing material and a new genetic testing technique he developed, has his contemporaries buzzing. “From time to time you see those big leaps in science,” Lahann says. “Francesco is one of those people who has taken several big leaps.”

Source

CANCER CELL TARGETING USING NANOPARTICLES

(WO/2008/121949)

Pub. No.:
WO/2008/121949
International Application No.:
PCT/US2008/058873
Publication Date:09.10.2008 International Filing Date:31.03.2008
IPC: A61K 9/14 (2006.01), B82B 1/00 (2006.01)
Applicants:MASSACHUSETTS INSTITUTE OF TECHNOLOGY [US/US]; Room NE25-230, 5 Cambridge Center, Kendall Square, Cambridge, MA 02142 (US) (All Except US).
ZALE, Stephen, E. [US/US]; 101 Binney Street, Cambridge, MA 02142 (US) (US Only).
Inventor:ZALE, Stephen, E.; 101 Binney Street, Cambridge, MA 02142 (US).
Agent:HANLEY, Elizabeth, A.; Lahive & Cockfield, LLP, One Post Office Square, Boston, MA 02109-2127 (US).
Priority Data:
PCT/US2007/007927
30.03.2007
US
60/976,197
28.09.2007
US
Title: CANCER CELL TARGETING USING NANOPARTICLES
Abstract:
The present invention generally relates to polymers and macromolecules, in particular, to polymers useful in particles such as nanoparticles. One aspect of the invention is directed to a method of developing nanoparticles with desired properties. In one set of embodiments, the method includes producing libraries of nanoparticles having highly controlled properties, which can be formed by mixing together two or more macromolecules in different ratios. One or more of the macromolecules may be a polymeric conjugate of a moiety to a biocompatible polymer. In some cases, the nanoparticle may contain a drug. Other aspects of the invention are directed to methods using nanoparticle libraries.

Source

Wednesday, October 15, 2008

Synthesis and Characterization of Selenium−Carbon Nanocables

ASAP Nano Lett., ASAP Article, 10.1021/nl801635b
Web Release Date: October 9, 2008

Copyright © 2008 American Chemical Society

Synthesis and Characterization of Selenium−Carbon Nanocables

O. E. D. Rodrigues,* G. D. Saraiva, R. O. Nascimento, E. B. Barros, J. Mendes Filho, Y. A. Kim,§ H. Muramatsu,§ M. Endo,§ M. Terrones, M. S. Dresselhaus, and A. G. Souza Filho*

Área de Ciências Naturais e Tecnológicas, Centro Universitário Franciscano - UNIFRA, 97010-032 Santa Maria, RS, Brazil., Departamento de Física, Universidade Federal do Ceará, C.P. 6030 Fortaleza-CE, 60455-900, Brazil, Faculty of Engineering, Shinshu University, 4-17-1 Wakasato, Nagano-shi 380-8553, Japan, Advanced Materials Department, IPICyT, Camino a la Presa San Jose 2055, 78216 San Luis Potosi, SLP, Mexico, Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, and Faculdade de Educação, Ciências e Letras do Sertão Central, Universidade Estadual do Ceará, Quixadá-CE, 63.900-000, Brazil

Received June 8, 2008

Revised August 22, 2008

Download the full text: PDF | HTML

Abstract:
In this letter, we report the synthesis and characterization of a novel Se−C hybrid nanostructure. X-ray diffraction data indicates a high degree of crystallinity for the nanostructured Se shell. High resolution transmission electron microscopy images show that the Se−C nanostructures consist of coaxial nanocables made of single wall carbon nanotubes, as the core, surrounded by a trigonal Selenium shell. Resonance Raman spectroscopy was used to access the properties of both the carbon nanotubes and selenium. The behavior of the radial breathing mode and the G-band indicates that the Se shell primarily covers semiconducting nanotubes. X-ray photoelectron spectroscopy show that the nanocables have a thin coverage of seleniun oxide. We envisage that this system could be used in the fabrication of photonic devices as an interface between electronic and photonic materials.

Source

Tuesday, October 14, 2008

Pores open the door to death

New prospects for improved methods of treatment of virus infections and cancer

by Mary Carter
Published 10/6/2008 in Research


Granzymes going about their deadly work. A killer cell makes contact
with a tumour cell (left) and detaches itself after one hour. After a
further two hours, blisters appear (right, red arrow) on the surface of
the cell that had been attacked. The tumour cell shrinks, dies and
disintegrates.
Image: Max Planck Institute of Neurobiology / Jenne


Our body is almost constantly being threatened by pathogens and cancerous cells that appear out of the blue. But the body puts up a fight: specialized cells in the immune system smuggle small molecules (granzymes) into cancer cells and those body cells that have fallen prey to viruses.

The molecules then trigger off the diseased cells built-in suicide program. There are two possible ways in which the granzymes gain entry into the cells under attack. Despite more than twenty years of research, however, it remained unclear as to which of these pathways is used to smuggle the lethal amount of granzymes into a cell.

Scientists at the Max Planck Institute of Neurobiology have now shown that minute pores on the cell surface open the door to the granzymes for a short period of time. These results provide new prospects for improved methods of treatment of chronic virus infections and cancer.

During our day-to-day life, we are rarely aware of the battles taking place in our own bodies. The body is almost always in a state of war against countless pathogens. And so, with every litre of blood that is pumped through our bodies, up to five billion white blood cells are sent out on patrol. Some of these cells react to pathogens by producing antibodies specially designed to attack precisely those pathogens that have been discovered. At the same time, they develop memory cells which recognize these pathogens immediately, should they attack anew.

In addition to these tacticians, a second group of white blood cells takes up arms against the enemy without further hesitation. The group consists of T-cells and killer cells that specialize in singling out body cells that have already been infected by viruses and tumor cells - swift action is therefore essential. However, these attackers also require tactics: in order to destroy a target cell, the attackers need to smuggle their weapons, known as granzymes, into the afflicted cell. Once inside, the granyzmes can carry out their deadly work by manipulating the diseased cell in such a way that it activates its suicide program. But how do the granzymes gain entry into the cell to begin with?

This is a question that scientists have been discussing for over twenty years. Granzymes were believed to gain entry into a cell either via pores or by membrane transport. T-cells and killer cells release a molecule called perforin which creates small holes in the cell membrane. Perforin might thus provide the granzymes with the openings they require. However, granzymes also bind to the surface of the attacked cells and are then internalized by membrane inversions and formation of small vesicles. Since the membrane pores created by perforin holes are fairly small and are quickly closed again by the besieged cell, most scientists favoured the latter theory that the granzymes main mode of entry into a cell was membrane transport.

To determine what path the lethal dose of granzymes takes to enter a cell is no trivial matter. Such knowledge could be used to develop new therapeutic methods in the fight against viruses and cancer. Some twenty years on, scientists at the Max Planck Institute of Neurobiology now appear to have solved this question. Contrary to the generally accepted view, the membrane holes now seem to be the main point of entry for granzymes. The scientists proved this with artificially manipulated granzymes which no longer bound to membranes and which therefore could not enter the cell via membrane transport. "Interestingly enough, despite this restriction, the attacker cells were observed to be no less effective" declares Dieter Jenne. "We were also able to show that the pores are large enough to allow enough granzymes into the cell before the holes are resealed."

"The exciting thing about these results is not only that we have finally managed to answer a long-standing question", Florian Kurschus explains, "but that our granzyme variations, together with the knowledge that the membrane holes are the most important means of entry into the cell, can lead to improved therapeutic methods in the fight against viruses and cancer." High doses of artificially added granzymes can also damage healthy cells by entering them via membrane transport. The new granzyme variants do not accumulate in healthy cells, however, since they can only avail themselves of the pathway opened by T-cells or killer cells using perforin. In an infected cell that has been recognized by a T-cell or killer cell as an enemy, this door will be opened -wide enough for granzymes to enter and perform their deadly task.

Source

Ref:

http://www.neuro.mpg.de/english/news_events/news/pdf/0809_Jenne_E.pdf

Pores open the door to death

Scientists settle the question as to how our immune defences enter and attack its own cells when they fall prey to viruses and tumour cells

Our body is almost constantly being threatened by pathogens and cancerous cells that appear out of the blue. But the body puts up a fight: specialized cells in the immune system smuggle small molecules (granzymes) into cancer cells and those body cells that have fallen prey to viruses. The molecules then trigger off the diseased cells’ built-in suicide program. There are two possible ways in which the granzymes gain entry into the cells under attack. Despite more than twenty years of research, however, it remained unclear as to which of these pathways is used to smuggle the lethal amount of granzymes into a cell. Scientists at the Max Planck Institute of Neurobiology have now shown that minute pores on the cell surface open the door to the granzymes for a short period of time. These results provide new prospects for improved methods of treatment of chronic virus infections and cancer. (PNAS, 2. September 2008)

****

Not unlike the pores created by Inovio-VGX in their vaccine/cancer work that facilitate the introduction of DNA vaccines or a useful biopharmaceutical into electrically stimulated cells (electroporation) thereby forming the open pore passageways!

Saturday, October 11, 2008

Sensitive Nanowire Disease Detectors Made by Yale Scientists

Published: October 10, 2008

New Haven, Conn. — Yale scientists have created nanowire sensors coupled with simple microprocessor electronics that are both sensitive and specific enough to be used for point-of-care (POC) disease detection, according to a report in Nano Letters.

The sensors use activation of immune cells by highly specific antigens — signatures of bacteria, viruses or cancer cells — as the detector. When T cells are activated, they produce acid, and generate a tiny current in the nanowire electronics, signaling the presence of a specific antigen. The system can detect as few as 200 activated cells.

In earlier studies, these researchers demonstrated that the nanowires could detect generalized activation of this small number of T cells. The new report expands that work and shows the nanowires can identify activation from a single specific antigen even when there is substantial background “noise” from a general immune stimulation of other cells.

Describing the sensitivity of the system, senior author Tarek Fahmy, Yale assistant professor of biomedical engineering, said:. “Imagine I am the detector in a room where thousands of unrelated people are talking — and I whisper, ‘Who knows me?’ I am so sensitive that I can hear even a few people saying, ‘I do’ above the crowd noise. In the past, we could detect everyone talking — now we can hear the few above the many.”

According to the authors, this level of sensitivity and specificity is unprecedented in a system that uses no dyes or radioactivity. Beyond its sensitivity, they say, the beauty of this detection system is in its speed — producing results in seconds — and its compatibility with existing CMOS electronics.

“We simply took direction from Mother Nature and used the exquisitely sensitive and flexible detection of the immune system as the detector, and a basic physiological response of immune cells as the reporter,” said postdoctoral fellow and lead author, Eric Stern. “We coupled that with existing CMOS electronics to make it easily usable.”

The authors see a huge potential for the system in POC diagnostic centers in the US and in underdeveloped countries where healthcare facilities and clinics are lacking. He says it could be as simple as an iPod-like device with changeable cards to detect or diagnose disease. Importantly, Stern notes that the system produces no false positives — a necessity for POC testing.

The authors suggest that in a clinic, assays could immediately determine which strain of flu a patient has, whether or not there is an HIV infection, or what strain of tuberculosis or coli bacteria is present. Currently, there are no electronic POC diagnostic devices available for disease detection.

“Instruments this sensitive could also play a role in detection of residual disease after antiviral treatments or chemotherapy,” said Fahmy. “They will help with one of the greatest challenges we face in treatment of disease — knowing if we got rid of all of it.

The work resulted from collaboration between the laboratories of Fahmy and Mark Reed, the Harold Hodgkinson Professor of Engineering & Applied Science within the Yale Institute for Nanoscience and Quantum Electronics (YINQE). Reed and biomedical engineering graduate student Erin Steenblock [erin.steenblock@yale.edu] are also authors on the study that was funded by the Department of Defense, the National Institutes of Health, the Department of Homeland Security and the National Science Foundation.

Citation: Nano Letters 8(10): 3310-3314 (October 1, 2008)

PRESS CONTACT: Janet Rettig Emanuel [janet.emanuel@yale.edu] 203-432-2157

Source

Nano Lett., 8 (10), 3310–3314, 2008. 10.1021/nl801693k

Web Release Date: September 3, 2008
Copyright © 2008 American Chemical Society

Label-free Electronic Detection of the Antigen-Specific T-Cell Immune Response

Eric Stern,† Erin R. Steenblock,† Mark A. Reed,*‡§ and Tarek M. Fahmy*†∥

Departments of Biomedical Engineering, Electrical Engineering, Applied Physics, and Chemical Engineering, Yale University, 55 Prospect Street, New Haven, Connecticut 06511

Received June 13, 2008

Revised August 1, 2008


Abstract:

Detection of antigen-specific T-cells is critical for diagnostic assessment and design of therapeutic strategies for many disease states. Effective monitoring of these cells requires technologies that assess their numbers as well as functional response. Current detection of antigen-specific T-cells involves flow cytometry and functional assays and requires fluorescently labeled, soluble forms of peptide-loaded major histocompatability complexes (MHC). We demonstrate that nanoscale solid-state complementary metal-oxide-semiconductor (CMOS) technology can be employed to allow direct, label-free electronic detection of antigen-specific T-cell responses within seconds after stimulation. Our approach relies on detection of extracellular acidification arising from a small number of T-cells (as few as ~200), whose activation is induced by triggering the T-cell antigen receptor. We show that T-cell triggering by a nonspecific anti-CD3 stimulus can be detected within 10 s after exposure to the stimulus. In contrast, antigen-specific T-cell responses are slower with response times greater than 40 s after exposure to peptide/MHC agonists. The speed and sensitivity of this technique has the potential to elucidate new understandings of the kinetics of activation-induced T-cell responses. This combined with its ease of integration into conventional electronics potentially enable rapid clinical testing and high-throughput epitope and drug screening.

Download the full text: PDF | HTML

Friday, October 10, 2008

Sticky Nanotape

Thursday, October 09, 2008

Carbon-nanotube adhesive outperforms gecko feet and could aid climbing robots.

By Katherine Bourzac

Gecko tape: Arrays of carbon nanotubes with a vertically aligned section (lower left) and a branched, tangled upper layer (lower right) mimic the structures of gecko feet but are 10 times more adhesive.
Credit: Science/AAAS
Multimedia
video Watch the tape in action.

For years, materials scientists have been trying to catch up with geckos. Adhesives that, like gecko feet, are dry, powerful, reusable, and self-cleaning could help robots climb walls or hold together electrical components, even in the harsh conditions of outer space. But it's been difficult to design strong adhesives that can be lifted back up again. Now researchers have developed an adhesive made of carbon nanotubes whose structure closely mimics that of gecko feet. It's 10 times more adhesive than the lizards' feet and, like the natural adhesive, easy to lift back up. And it works on a variety of surfaces, including glass and sandpaper.

Developed by a group led by Liming Dai, a professor of materials engineering at the University of Dayton, and Zhong Wang, director of the Center for Nanostructure Characterization at Georgia Tech, the adhesive is not the first made from carbon nanotubes. However, it's much stronger than previous nanotube adhesives. Its branched structure more closely mimics the structures on gecko feet, which are covered with millions of microscale hairs that branch into many smaller hairs, each of which has a weak electrical interaction with a surface. These many weak interactions add up to strong adhesion over the area of the foot. Previously, researchers have shown that arrays of vertically aligned carbon nanotubes have similar interactions with a surface.

"People have tried to mimic the gecko structures, but it's not easy," says Dai. Using a silicon substrate, he and his group grew arrays of vertically aligned carbon nanotubes topped with an unaligned layer of nanotubes, like rows of trees with branching tops. The adhesive force of these nanotube arrays is about 100 newtons per square centimeter--enough for a four-by-four-millimeter square of the material to hold up a 1,480-gram textbook. And its adhesive properties were the same when tested on very different surfaces, including glass plates, polymer films, and rough sandpaper.

One advantage of this adhesive over others is that its strength is strongly direction dependent. When it's pulled in a direction parallel to its surface, it's very strong. That's because the branched nanotubes become aligned, says Dai. But when it's pulled up with little force, as one would peel a piece of Scotch tape, the nanotubes lose contact one by one.

The greater the adhesive strength, the better, says Ali Dhinojwala, a professor of polymer science at the University of Akron. However, says Dhinojwala, who works on carbon-nanotube adhesives as well, "we also need to solve other problems before they're commercially viable." Wall-climbing robots will require adhesives that work again and again without wearing out or getting clogged with dirt. "We want a robot to take more than 50 steps in a dirty environment," says Dhinojwala. No one has demonstrated strong gecko-inspired adhesives that can do this. And nanotube adhesives will need to be grown on different substrates than those used so far. Carbon nanotubes are easy to grow on silicon wafers; creating large areas of the adhesive wouldn't be a problem. But "we're not going to stick silicon wafers to robot feet," says Dhinojwala.

Dai says that carbon nanotubes' versatility may help overcome the dirt problem. These structures can readily be functionalized with proteins and other polymers. Dai is developing adhesive nanotube arrays coated with proteins that change their shape in response to temperature changes. A robot could have feet that heat up when they get clogged, shedding dirt so that it can keep walking.

Other applications of the adhesive may take better advantage of carbon nanotubes' properties than robotics would. Carbon nanotubes are highly conductive to electricity and have promising thermal properties, Dai notes. Nanotube adhesives created to replace solder for holding together electronics components could also act as heat sinks. Other gecko-inspired adhesives made of polymers can't hold up to high temperatures, says Metin Sitti, who heads the nanorobotics lab at Carnegie Mellon. Spacecraft using nanotube adhesives instead of polymers could go to hotter areas.

Source


Coating carbon nanotubes with colloidal nanocrystals by combining an electrospray technique with directed assembly using an electrostatic field

Shun Mao, Ganhua Lu and Junhong Chen1
Department of Mechanical Engineering, University of Wisconsin-Milwaukee, Milwaukee,
WI 53211, USA
E-mail: jhchen@uwm.edu

Received 4 July 2008, in final form 30 August 2008
Published 9 October 2008
Online at stacks.iop.org/Nano/19/455610

Abstract
A simple method that combines an electrospray technique with directed assembly using an electrostatic field was used for decorating carbon nanotubes (CNTs) with nanocrystals. Colloidal CdSe and Au nanocrystals were electrosprayed and assembled onto random CNTs and vertically aligned CNTs in a controlled manner. The high level of electrical charge on the electrosprayed aerosol nanocrystals was responsible for the assembly. The technique can be used to assemble various compositions of nanomaterials onto different substrates and provides a versatile route for producing novel hybrid nanostructures.


Figure 1. Schematic of the nanocrystal aerosolization by an electrospray process and the subsequent assembly of nanocrystals onto random CNTs or vertically aligned CNTs by ESFDA (Electrostaic Force Directed Assembly).

4. Conclusion
In summary, an electrospray process was combined with an ESFDA process to coat CNTs with nanocrystals produced in the solution. Colloidal CdSe and Au nanocrystals were successfully electrosprayed and assembled onto random CNTs and CNT array in a controlled manner. No agglomeration of the nanocrystals was found after the assembly. The surface charge of electrosprayed aerosol was responsible for the successful assembly. This simple technique could be extended to other colloidal nanocrystals that are readily available, with proper adjustments of the nanocrystal concentration and the solution conductivity. The resulting novel hybrid nanostructures are expected to provide tremendous opportunities for exploring nanoscience, nanotechnology, and biotechnology.

Source

Thursday, October 9, 2008

Nano-fusion reaction

United States Patent Application 20080247930
Kind Code A1
Hotto; Robert October 9, 2008

Nano-fusion reaction

Abstract

A nano-fusion reactor comprised of nano-particles such as carbon based nanotubes, endohedral fullerenes and other nano materials encapsulating fusible fuels such as the hydrogen isotopes, deuterium, and tritium. The nano-devices encapsulate the fusible materials and ignite fusion reactions which in some of the embodiments consume the nano-fusion reactor device requiring the replenishment of these devices so to continue the fusible reactions. The reactions can be controlled and scaled through modulated presentation of fusion targets to the ignition chamber. The fusion reactions are ignited in the embodiments through one or more of the applied forces in the fusion reactor: electromagnetic compressive, electrostatic, and thermo. These applied forces in conjunction with the extreme structural strength, the ablation forces and purity of the nano-fusion device produces maximum forces necessary for the production of a shock wave on the nano-encapsulated device to ignite one or a plurality of fusion reactions. The lower ignition energy is due to a smaller device with less fuel, more efficient coupling of applied energy by the nano-device, along with purer encapsulated fuels, and improved geometries has provided improvements over conventional ICF reactions.


Inventors: Hotto; Robert; (Carlsbad, CA)
Correspondence Name and Address:
    LAW OFFICE OF DONALD L. WENSKAY
16909 VIA DE SANTA FE, 200, P.O. BOX 7206
RANCHO SANTA FE
CA
92057
US
Serial No.: 725604
Series Code: 11
Filed: March 17, 2007




Claims



1. A nano-device encapsulating deuterium and tritium.

2. The nano-device of claim 1, further comprising endohedral fullerenes.

3. The nano-device of claim 1, further comprising clusters of endohedral fullerenes.

4. The nano-device of claim 1, further comprising single and multi-walled nanotubes.

5. The nano-device of claim 4, wherein the nanotubes further comprise nano-laser devices.

6. A device for directing energy to nano-devices encapsulating fusible fuels.

7. The device of claim 5, being joined with an ignition chamber, whereby the output of the ignition chamber, such as tritium, is fed into the breeder device.

BACKGROUND OF THE INVENTION

[0002]1. Field of the Invention

[0003]The present invention relates to controlled fusion reaction devices, processes and products. More particularly, the present invention is directed to a fusion fuel container for use in a fusion reactor system.

SUMMARY OF THE DISCLOSURE

[0018]Briefly stated, endohedral fullerenes, clusters of the same, carbon nanotubes and the like nano-devices house hydrogen isotopes as targets presented to, and manipulable about a reactor system which re-circulates and recaptures both useful products and ash. A nano-fusion reactor comprised of nano-particles such as carbon based nanotubes, endohedral fullerenes and other nano devices encapsulating fusible fuels such as the hydrogen isotopes, deuterium, and tritium. The nano devices encapsulate the fusible materials and ignite fusion reactions and consume the nano-fusion devices requiring the replenishment of these devices to the plant so to continue the fusible reactions. The reactions can be controlled and scaled through fusible target material presentation the ignition chamber. The nano-fusion reactions are ignited in the embodiments through one or more of the generated forces. These in situ generated forces in conjunction with the extreme structural strength and hardness of the nano-fusion targets produces maximum forces necessary for the production of a shock wave impinging directly on the nano-encapsulated materials necessary to ignite fusion reactions. Lower ignition energy and more efficient use of coupling is energy efficient to generate improvements over conventional ICF reactions.

[0019]According to a feature of the present invention, there is provided at least a nano-device encapsulating hydrogen isotopes. In particular, a nano-fusion target encapsulating deuterium and tritium is offered for consideration.

[0020]According to another feature of the present invention there is provided a device for directing energy to nano-devices encapsulating fusible fuels.

[0021]According to yet another feature of the present invention there is provided an inertial confinement fusion process which comprises, in combination, a plurality of nano-devices encapsulating deuterium-tritium fuel.

[0022]According to yet still another feature of the present invention there is provided a device for producing endohedral fullerenes encapsulating deuteriums and tritium.

[0023]According to yet still another and further feature of the present invention, there is provided a device for igniting nano-devices encapsulating deuteriums and tritium and employing byproducts of the reaction for breeding nano-devices encapsulating deuteriums and tritium to further continue the fuel ignition and breeding cycle.

[0038]FIG. 13 shows prior art including ICF with conventional laser irradiation;

[0039]FIG. 14 shows cluster arrangement of endohedral fullerenes and/or single or multi-walled nanotubes, according to the teachings of the present invention;

[0040]FIG. 15 schematically illustrates peaks of lasers and at least one of endohedral fullerenes and single-walled or multi-walled carbon nanotubes, according to the teachings of the present invention.

Click pic to enlarge


Source

See also:
http://www.chaienergy.org/index.htm
Nano-scale Fusion: An exciting alternative energy technology with tremendous potential. Patent applications have been submitted and early development in progress. (View PDF description here)
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Wednesday, October 8, 2008

Structure Of 'Beneficial' Virus That Can Infect Cancer Cells Solved


A research team has solved the 3-D structure of Seneca Valley Virus-001. (Credit: Image courtesy of Scripps Research Institute)

ScienceDaily (Oct. 8, 2008) — The 3-D structure of the virus, known as Seneca Valley Virus-001, reveals that it is unlike any other known member of the Picornaviridae viral family, and confirms its recent designation as a separate genus "Senecavirus." The new study reveals that the virus's outer protein shell looks like a craggy golf ball — one with uneven divets and raised spikes — and the RNA strand beneath it is arranged in a round mesh rather like a whiffleball.

"It is not at all like other known picornaviruses that we are familiar with, including poliovirus and rhinoviruses, which cause the common cold," says the study's senior author, Associate Professor Vijay S. Reddy, Ph.D., of The Scripps Research Institute. "This crystal structure will now help us understand how Senecavirus works, and how we can take advantage of it."

The Senecavirus is a "new" virus, discovered several years ago by Neotropix Inc., a biotech company in Malvern, Pennsylvania. It was at first thought to be a laboratory contaminant, but researchers found it was a pathogen, now believed to originate from cows or pigs. Further investigation found that the virus was harmless to normal human cells, but could infect certain solid tumors, such as small cell lung cancer, the most common form of lung cancer.

Scientists at Neotrophix say that, in laboratory and animal studies, the virus demonstrates cancer-killing specificity that is 10,000 times higher than that seen in traditional chemotherapeutics, with no overt toxicity. The company has developed the "oncolytic" virus as an anti-cancer agent and is already conducting early phase clinical trials in patients with lung cancer.

But the researchers still did not know how the virus worked, so they turned to Reddy. He and his Scripps Research team, especially Sangita Venkataraman, Ph.D., a postdoctoral researcher, determined the Senecavirus crystal structure.

Reddy describes the differences they found between other picornaviruses and the Senecavirus as like variations among car models of the same manufacturer. "The chassis is the same, but the body style is different," he says. "How the body of a virus is shaped determines how it infects cells."

The structure of the Senecavirus is also depicted at http://viperdb.scripps.edu/, the "Virus Particle Explorer" developed at Scripps Research by Reddy and his colleagues. The online database is a worldwide resource for information on the structure of viral particles; it contains details of 253 viruses to date.

Once the structure of Seneca Valley Virus-001 was solved, researchers went on to identify several areas on the viral protein coat that they think might hook onto receptors on cancer cells in the process of infecting them. The researchers are now conducting further investigations on this process. "It will be critically important to find out what region of its structure the virus is using to bind to tumor cells, and what those cancer cell receptors are," Reddy says. "Then we can, hopefully, improve Senecavirus enough to become a potent agent that can be used with many different cancers."

The research was supported by grants from the National Institutes of Health.


Journal reference:

  1. S. Venkataraman, V. Reddy, Seshidhar P. Reddy, Neeraja Idamakanti, Paul L. Hallenbeck and Jackie Loo. Structure of Seneca Valley Virus-001, an oncolytic picornavirus representing a new genus. Structure, Vol 16, 1555-1561, 08 October 2008 [link]
Adapted from materials provided by Scripps Research Institute.
APA

MLA
Scripps Research Institute (2008, October 8). Structure Of 'Beneficial' Virus That Can Infect Cancer Cells Solved. ScienceDaily. Retrieved October 8, 2008, from http://www.sciencedaily.com­ /releases/2008/10/081008151320.htm

Tuesday, October 7, 2008

Copper inkjettable inks - Applied Nanotech Holdings

Applied Nanotech Holdings, Inc. Expands Research Agreement and Enters Negotiations to Finalize an Exclusive License Agreement With Leading Industrial Chemical Products Company

Tuesday October 7, 11:46 am ET

AUSTIN, TX--(MARKET WIRE)--Oct 7, 2008 -- Applied Nanotech Holdings, Inc. (OTC BB:APNT.OB - News) today announced that the third phase of its research project with a leading industrial chemical products company in Japan, announced on September 29, 2008, has been expanded and the previously announced funding of $700,000 has been increased to $1.2 million over the next twelve months in order to accelerate the prototyping of copper inkjettable inks and product introduction. The parties also expect a fourth phase of the project, of at least the same magnitude, to begin in October 2009 to expand the applications.

In addition, the companies agreed to enter negotiations to finalize an exclusive worldwide license to Applied Nanotech's copper inks technology within the parameters set forth in the current research agreement between the companies. These parameters include an upfront payment of up to $2.0 million and a running royalty rate of 4% on sales of the copper ink product. The parties agreed to finalize and execute the license agreement no later than April 15, 2009. During the period until then, the parties will formulate a comprehensive worldwide license agreement drafted in both English and Japanese, based on the results of the R&D partnership.

"I believe that the almost immediate expansion of this program by $500,000 following on the heals of last week's announcement, along with the significant agreement for the overall terms for a license, show the seriousness of this application in the minds of our customer. Printable inks may redefine the manufacturing process for a wide variety of electronic devices and ANI is at the forefront of these developments, with this partner, as well as two additional Phase I studies that we have underway," said Tom Bijou, Chairman and CEO of Applied Nanotech Holdings, Inc.

ABOUT APPLIED NANOTECH HOLDINGS, INC.

Applied Nanotech Holdings, Inc. is a premier research and commercialization organization dedicated to developing applications for nanotechnology with an extremely strong position in the fields of electron emission applications from carbon film/nanotubes, sensors, functionalized nanomaterials, and nanoelectronics. It also possesses investments related to electronic digitized sign technology. ANI has over 250 patents or patents pending. Its business model is to license its technology to partners that will manufacture and distribute products using the technology. ANI's website is www.appliednanotech.net.

Contact:
     COMPANY CONTACT
Doug Baker
Applied Nanotech Holdings, Inc.
248.391.0612
Email Contact

MEDIA CONTACT
William J. Spina
781.378.2000
Email Contact


Source: Applied Nanotech Holdings, Inc.

Thursday, October 2, 2008

METHODS OF ENHANCING IMMUNE RESPONSE USING ELECTROPORATION-ASSISTED VACCINATION AND BOOSTING

(WO/2008/063555) METHODS OF ENHANCING IMMUNE RESPONSE USING ELECTROPORATION-ASSISTED VACCINATION AND BOOSTING

Latest bibliographic data on file with the International Bureau
Pub. No.:
WO/2008/063555
International Application No.:
PCT/US2007/024051
Publication Date:29.05.2008 International Filing Date:16.11.2007
IPC: A61K 39/00 (2006.01)
Applicants:GENETRONICS, INC. [US/US]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (All Except US).
MATHIESEN, Iacob [NO/NO]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (US Only).
TJELLE, Elisabeth, Torunn [NO/NO]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (US Only).
KJEKEN, Rune [NO/US]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (US Only).
RABUSSAY, Dietmar [AT/US]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (US Only).
LIN, Feng [CN/US]; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US) (US Only).
Inventors:MATHIESEN, Iacob; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US).
TJELLE, Elisabeth, Torunn; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US).
KJEKEN, Rune; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US).
RABUSSAY, Dietmar; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US).
LIN, Feng; 11494 Sorrento Valley Road, San Diego, CA 92121-1318 (US).
Agent:CHAMBERS, Daniel, M.; Biotechnology Law Group, 527 N. Hwy. 101, Suite E, Solana Beach, CA 92075-1173 (US).
Priority Data:
60/859,724
17.11.2006
US
Title: METHODS OF ENHANCING IMMUNE RESPONSE USING ELECTROPORATION-ASSISTED VACCINATION AND BOOSTING
Abstract:
Disclosed are methods of enhancing immune responses. Such methods involve the administration of vaccine compositions to different tissues to elicit an enhanced immune response. The enhanced response arises from the vaccination and boosting route of administration in two separate patient tissues, for example, by first administering a priming vaccination into skin and later administering a boost vaccination in muscle. In each case, priming and boosting, the administration of the vaccine composition is preferably carried out using contemporaneous electroporation-assisted delivery of the antigenic agent.


Source

Electroporation device and injection apparatus

United States Patent Application 20080234655
Kind Code A1
Mathiesen; Iacob ; et al. September 25, 2008

Electroporation device and injection apparatus

Abstract

An apparatus is provided for injecting a fluid into body tissue, the apparatus comprising: a hollow needle; and fluid delivery means, wherein the apparatus is adapted to actuate the fluid delivery means in use so as to automatically inject fluid into body tissue during insertion of the needle into the said body tissue.


Inventors: Mathiesen; Iacob; (Oslo, NO) ; Tjelle; Torunn; (Oslo, NO) ; Rekdahl; Knut Arvid Sorensen; (Tarnasen, NO) ; David-Andersen; Bjorn; (Oslo, NO)
Assignee Name and Adress: INOVIO AS
San Diego
CA


Claims

1. Apparatus for injecting a fluid into body tissue, the apparatus comprising: a hollow needle; and fluid delivery means, wherein the apparatus is adapted to actuate the fluid delivery means in use so as to concurrently inject fluid into body tissue during insertion of the needle into the said body tissue.

2. Apparatus as claimed in claim 1 adapted to automatically inject fluid into body tissue during insertion.

14. A method of injecting a fluid into body tissue, the method comprising: injecting the fluid into the body tissue through a hollow needle while the said needle is being inserted into the said body tissue.

[0007]From a first aspect, the present invention provides an apparatus for injecting a fluid into body tissue, the apparatus comprising: a hollow needle; and fluid delivery means, wherein the apparatus is adapted to actuate the fluid delivery means in use so as to concurrently (preferably automatically) inject fluid into body tissue during insertion of the needle into the said body tissue. This has the advantage that the ability to inject the fluid gradually while the needle is being inserted leads to a more even distribution of the fluid through the body tissue. It is also believed that the pain experienced during injection is reduced due to the distribution of the volume of fluid being injected over a larger area.

Source


See also - WO/2004/004825
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Wednesday, October 1, 2008

Modular electroporation device with disposable electrode and drug delivery components

Click pics to ENLARGE.


United States Patent Application 20080058706

Zhang; Lei ; et al.

March 6, 2008

Modular electroporation device with disposable electrode and drug delivery components

Abstract

The invention comprises a modular electroporation device for use in clinical settings. The device includes components which may be varied or adapted for application of electroporation-based delivery of therapeutic agents to cells of a subject in a variety of electroporation formats such as intratissue electroporation or transsurface electroporation. The device components include a hand-manipulable handle with activation switch and a disposable head comprising electrodes, injection port, electrode directional and depth guide, and a slideably engaged electrode safety shield.

Inventors: Zhang; Lei; (San Diego, CA) ; Gamelin; Andre S.; (Vista, CA) ; Rabussay; Dietmar; (Solana Beach, CA)

Assignee Name and Adress:
Genetronics, Inc.
San Diego
CA

Serial No.: 784892
Series Code: 11
Filed: April 10, 2007

Claims

1. An electroporation device comprising: a handle in electrical communication with an electric pulse generating source; and in electrical communication with said handle a head component comprising elements selected from the group consisting of a plurality of electrodes, an injection port, and an electrode safety shield.

BACKGROUND OF THE INVENTION

[0003] Electroporation has proven to be useful in the delivery of substances directly into biologic cells of tissues. The methodologies employed for electroporation of such materials into tissues have varied and the devices designed for such electroporation have been numerous. However, there remains a need in the art for a clinically-friendly and user-friendly device that can be employed to administer therapeutic agents to patients in need thereof. To date there is no single device designed to have modular components, some of which are intended to be disposable after a single use, that is inexpensive to produce yet highly effective in the clinic and that incorporates various components including a disposable component for carrying a fluid therapeutic or a disposable needle tipped head with safety shield and other functional features. Of particular need is a device that can be easily employed to administer therapeutic compounds to large numbers of patients in a short period of time and while maintaining accuracy in the administration of a therapeutic agent into patient tissues relative to positioning of electrodes in such tissues.

Source

Neat, nifty little device! Very practical at a clinic.
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