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Category: Research
Type: News
Source: PNNL
Date: Tuesday, March 8th, 2016

New composite material that traps oxygen selectively could be useful for energy applications such as fuel cells

March 08, 2016 Share

  • Squeezing iron-containing ferrocene (not to scale) in the pores of the metal-organic framework known as MIL-101 lets ferrocene's iron snag oxygen from passing air.

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RICHLAND, Wash. - Inexpensive materials called MOFs pull gases out of air or other mixed gas streams, but fail to do so with oxygen. Now, a team has overcome this limitation by creating a composite of a MOF and a helper molecule in which the 2 work in concert to separate oxygen from other gases simply and cheaply.

The results, reported in today's Advanced Materials, might help with a wide variety of applications, including making pure oxygen for fuel cells, using that oxygen in a fuel cell, removing oxygen in food packaging, making oxygen sensors, or for other industrial processes. The technique might also be used with gases other than oxygen as well by switching out the helper molecule.

Currently, industry uses a common process called cryogenic distillation to separate oxygen from other gases. It is costly and uses a lot of energy to chill gases. Also, it can't be used for specialty applications like sensors or getting the last bit of oxygen out of food packaging.

A great oxygen separator would be easy to prepare and use, be inexpensive and be reusable. MOFs, or metal-organic frameworks, are materials containing lots of pores that can suck up gases like sponges suck up water. They have potential in nuclear fuel separation and in lightweight dehumidifiers.

But of the thousands of MOFs out there, less than a handful absorb molecular oxygen. And those MOFs chemically react with oxygen, forming oxides - think rust - that render the material unusable.

"When we 1st worked with MOFs for oxygen separation, we could only use the MOFs a few times. We thought maybe there's a better way to do it," said materials scientist Praveen Thallapally of the D.O.E.'s Pacific Northwest National Lab.

The new tack for Thallapally and colleagues at PNNL involved using a 2nd molecule to mediate the oxygen separation - a helper molecule would be attracted to but chemically uninterested in the MOF. Instead, the helper would react with oxygen to separate it from other gases.

They chose a MOF called MIL-101 that is known for its high surface area - making it a powerful sponge - and lack of reactivity. One teaspoon of MIL-101 has the same surface area as a football field. The high surface area comes from a MOF's pores, where reactive MOF's work their magic.

MOFs that react with oxygen need to be handled carefully in the laboratory, but MIL-101 is stable at ambient temperatures and in the open atmosphere of a lab. For their helper molecule, they tried ferrocene, an inexpensive iron-containing molecule.

The scientists made a composite of MIL-101 and ferrocene by mixing them and heating them up. Initial tests showed that MIL-101 took up in excess of its weight in ferrocene and at the same time lost surface area. This indicated that ferrocene was taking up space within the MOF's pores, where they need to be to snag the oxygen.

Then the team sent gases through the black composite material. The material bound up a large percentage of oxygen, but almost none of the added nitrogen, argon or carbon dioxide. The material behaved this way whether the gases went through individually or as a mix, showing that the composite could in fact separate oxygen from the others.

Additional analysis showed that heating caused ferrocene to decompose in the pores to nanometer-sized clusters, which made iron accessible to react with oxygen. This reaction formed a stable mineral known as maghemite, all within the MOF pores. Maghemite could be removed from the MOF to use the MOF again.

Together, the results on the composite showed that a MOF might be able to do unexpected things - like purify oxygen - with a little help. Future research will explore other combinations of MOF and helper molecules.

In addition to PNNL, participating researchers hailed from and used analytical instruments at 2 Office of Science User Facilities, the Environmental Molecular Sciences Lab at PNNL and the Advanced Photon Source at Argonne National Laboratory, as well as the University of Amsterdam. This work was supported by the D.O.E. Office of Science.


Reference: Wen Zhang, Debasis Banerjee, Jian Liu, Herbert T. Schaef, Jarrod V. Crum, Carlos A. Fernandez, Ravi K. Kukkadapu, Zimin Nie, Satish K. Nune, Radha K. Motkuri , Karena W. Chapman, M. H. Engelhard, James C. Hayes, Kurt L. Silvers, Rajamani Krishna, B. Peter McGrail, Jun Liu and Praveen K. Thallapally. Redox-Active Metal-Organic Composites for Highly Selective Oxygen Separation Applications, Advanced Materials, March 8, 2016, DOI:10.1002/adma201600259.

Tags: Energy, Fundamental Science, EMSL, Renewable Energy, Fuel Cells, Energy Production, Chemistry, Molecular Biology and Biochemistry, Mass Spectrometry and Separations, Materials

EMSL, the Environmental Molecular Sciences Lab, is a national scientific user facility sponsored by the D.O.E.'s Office of Science. Located at Pacific Northwest National Lab in Richland, Wash., EMSL offers an open, collaborative environment for scientific discovery to researchers around the world. Its integrated computational and experimental resources enable researchers to realize important scientific insights and create new technologies. Follow EMSL on Facebook, LinkedIn and Twitter.

Interdisciplinary teams at Pacific Northwest National Lab address many of America's most pressing issues in energy, the environment and national security through advances in basic and applied science. Founded in 1965, PNNL employs 4,400 staff and has an yearly budget of nearly $1 billion. It is managed by Battelle for the D.O.E.'s Office of Science. As the single biggest supporter of basic research in the physical sciences in the United States, the Office of Science is working to address some of the most pressing challenges of our time. For more information on PNNL, visit the PNNL News Center, or follow PNNL on Facebook, Google+, LinkedIn and Twitter.

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