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Lights, camera, action

Martyn Poliakoff, CBE, FRS, is research professor of chemistry at the University of Nottingham in the UK. His main research interest is the application of supercritical fluids with a focus on green and sustainable chemistry. He is one of the narrators of 'The Periodic Table of Videos', which are popular on YouTube. He is chair of the Green Chemistry editorial board.

Martyn Poliakoff talks to Kathleen Too about the periodic table of videos and passion for green chemistry

Can you tell us a little known fact about yourself? 

I’m an Honorary Professor at Moscow State University, something I share with Fidel Castro and Bill Clinton. 

Which of your academic achievements are you most proud of? 

To me, academic work is rather like journalism – journalists get excited about the story they are working on, but when they move on to the next story, that one is more exciting than the one before. So I think that the only way you can operate as an academic is to be excited about whatever you are doing at a particular time. When I was younger, I did a lot of work on the reactive molecule iron tetracarbonyl, which is completely useless in the green chemistry context because it only exists at room temperature for a millionth of a second or less , but I am still quite proud of my experiments. As a professor, I am proud of the little contributions I can make to the design of an experiment by my research group. Experiments are almost always done by my students or postdocs. Sometimes, as a supervisor, the contributions to the design of the experiments are not as big as one would like. Occasionally, I have a really good idea , which makes the experiments work and that always give me pleasure. 

You’re keen to promote science on YouTube. Could you tell us more? 

I began working with YouTube purely by accident. My university was collaborating with Brady Haran, a very talented video journalist, who wanted to make a periodic table of videos. I didn’t think there was enough to say about some of the more obscure elements but as it turned out, there was plenty to say, at least enough to make short videos. We wanted to show that we enjoy chemistry and how much fun it can be. 

We’re in the process of making videos about different molecules and reactions. There are also other videos that are rather difficult to define, for example, we made a video of gold dissolving in Aqua Regia – a mixture of nitric acid and hydrochloric acid – it’s not exactly a reaction or a molecule but we thought that people may be interested in seeing the gold dissolving. 

Which video was the most fun to make? 

They were all fun, but my favourite is about the element hassium. This is element 108 and I knew nothing about it. In fact, in the precredit sequence – the bit before the main title of the video – I was filmed saying ‘I don’t know anything about hassium, let’s make something up’. 

What is your favourite element? 

I’m very fond of sodium. The chemical symbol for sodium is Na, which was my mother’s nickname when she was a child. Each time I hear the word Na or see it written down, I get a warm feeling. I’m also fond of xenon, because it’s been an important element in my research. 

What excites you about chemistry and what does the future hold for green chemistry? 

Objects we use in everyday life, such as most of the clothes we wear, are made from synthetic chemicals. The jacket I’m wearing is actually leather but the inside is made of polyester – a synthetic material. We couldn’t enjoy any of these without the products of the chemical industry. Chemistry often has a bad image. People generally think about it polluting and destroying the planet but green chemistry allows young people to feel that they are helping both the planet and humanity at the same time. So it’s doubly good! 

With oil running out and the expanding world population leading to a greater demand for chemicals, we have got to do something. One of the greatest challenges is to get green chemistry to work. The future either holds success in delivering what people need or complete failure leading to society collapsing. We have to succeed. I hope that in the end the principles of green chemistry will be applied to most chemistry. You could argue that if green chemistry really succeeds, it will disappear because all chemistry will become green. 

What do you enjoy most about being the chair of Green Chemistry? 

I enjoy interacting with other chemists, inspiring young people and spreading the green chemistry message. I also enjoy promoting the subject in Ethiopia and encouraging people in economically developing countries to take up green chemistry so that they don’t make the same mistakes regarding pollution that we did in the past. 

What advice do you have for young scientists? 

Green chemistry offers terrific opportunities and there are different areas within the subject. It doesn’t matter that some people are using ionic liquids, others using new catalysts, the important message is that green chemistry is not about one area being better than another. We need all those areas and many more to solve our current problems. One of the attractions of green chemistry is that there are huge opportunities for new ideas. 

Which historical scientific figure would you most like to have dinner with and why? 

I have been fortunate to have met many fascinating famous scientists. One of the exciting things is actually finding out what they are like as people and not just learning about what they have discovered. However, historical figures come from a very different age. Possibly, they would strike us as being pompous or very formal compared to nowadays, not because they were famous scientists but because they lived 100 or 200 years ago. From my point of view, there are two quite exciting events that happened in 1869. One was Mendeleev propounding the Periodic Table for the first time. The other was that Thomas Andrews, a physical chemist in Belfast, described the critical point of carbon dioxide for the first time. Supercritical fluids have played a very important part in my research. It’s quite amusing that the two events took place in the same year. I would quite like to have dinner with Thomas Andrews and Mendeleev, though of course, they might not have been able to speak to each other because I am not sure whether Mendeleev could speak English. He definitely spoke German because he published some of his papers in German. It probably would be a rather strange triangular conversation. 

How would your family and friends describe you? 

Always doing chemistry.

When you got your CBE, how was your meeting with the Royal Family? 

A CBE is a British Award, which stands for Commander of the Order of the British Empire. It is presented at Buckingham Palace by a member of the Royal Family. I met with Prince Charles and he was very interested in my work. We had a 45 second discussion about recycling plastics, which was quite unexpected. He really had done his homework! 

You already have a number of fans; you even have a Martyn Poliakoff appreciation society on Facebook. How do you feel about being famous and how do you deal with fame? 

I’m not sure that I’m particularly famous. My brother is a well known playwright in the UK and much better known than me. Ten years ago I was walking through Helsinki with a friend of mine, who is very well known in Finland. I was with him and my postdoc who asked, ‘Have you noticed that everybody is looking at Neil?’ I replied ‘No’, because I am used to people staring at my hair anyway. So I didn’t notice anything different. 

Articles of interests:

Continuous heterogeneous catalytic oxidation of primary and secondary alcohols in scCO2
Adrian O. Chapman, Geoffrey R. Akien, Nicholas J. Arrowsmith, Peter Licence and Martyn Poliakoff, Green Chem., 2010, 12, 310
DOI:10.1039/b913434d

Solubilisation of -chymotrypsin by hydrophobic ion pairing in fluorous systems and supercritical carbon dioxide and demonstration of efficient enzyme recycling
Karima Benaissi, Martyn Poliakoff and Neil R. Thomas, Green Chem., 2010, 12, 54
DOI:10.1039/b904761a

Videos of interests:

Link icon The Periodic Table of Videos – Sodium
The Periodic Table of Videos – Sodium

Link icon The Periodic Table of Videos – Xenon
The Periodic Table of Videos – Xenon

Link icon The Periodic Table of Videos – Hassium
The Periodic Table of Videos – Hassium

Link icon Dissolving gold in aqua regia
Dissolving gold in aqua regia

Link icon Chemistry Christmas Tree
Chemistry Christmas Tree

Link icon Which element for Christmas?
Which element for Christmas?

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Top ten most accessed articles in October

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Catalytic conversion of biomass to biofuels 
David Martin Alonso, Jesse Q. Bond and James A. Dumesic 
Green Chem., 2010, 12, 1493-1513, DOI: 10.1039/C004654J, Critical Review  

Vegetable oil-based polymeric materials: synthesis, properties, and applications 
Ying Xia and Richard C. Larock 
Green Chem., 2010, 12, 1893-1909, DOI: 10.1039/C0GC00264J, Critical Review  

Production of jet and diesel fuel range alkanes from waste hemicellulose-derived aqueous solutions 
Rong Xing, Ayyagari V. Subrahmanyam, Hakan Olcay, Wei Qi, G. Peter van Walsum, Hemant Pendse and George W. Huber 
Green Chem., 2010, 12, 1933-1946, DOI: 10.1039/C0GC00263A, Paper  

Sulfonated silica/carbon nanocomposites as novel catalysts for hydrolysis of cellulose to glucose 
Stijn Van de Vyver, Li Peng, Jan Geboers, Hans Schepers, Filip de Clippel, Cedric J. Gommes, Bart Goderis, Pierre A. Jacobs and Bert F. Sels 
Green Chem., 2010, 12, 1560-1563, DOI: 10.1039/C0GC00235F, Communication  

Heterogeneous catalytic synthesis using microreactor technology 
Christopher G. Frost and Lynsey Mutton 
Green Chem., 2010, 12, 1687-1703, DOI: 10.1039/C0GC00133C, Tutorial Review 

Biorenewable polyethylene terephthalate mimics derived from lignin and acetic acid 
Laurent Mialon, Alexander G. Pemba and Stephen A. Miller 
Green Chem., 2010, 12, 1704-1706, DOI: 10.1039/C0GC00150C, Communication 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B, Communication  

Mild water-promoted selective deacetalisatison of acyclic acetals 
D. Bradley G. Williams, Adam Cullen, Alex Fourie, Hendrik Henning, Michelle Lawton, Wayne Mommsen, Portia Nangu, Jonathan Parker and Alicia Renison 
Green Chem., 2010, 12, 1919-1921, DOI: 10.1039/C0GC00280A, Communication  

Sulfated tungstate: a new solid heterogeneous catalyst for amide synthesis 
Pramod S. Chaudhari, Suresh D. Salim, Ravindra V. Sawant and Krishnacharya G. Akamanchi 
Green Chem., 2010, 12, 1707-1710, DOI: 10.1039/C0GC00053A, Communication 

Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: multiple benefits of CO2-expanded liquids 
Xiaobin Zuo, Fenghui Niu, Kirk Snavely, Bala Subramaniam and Daryle H. Busch 
Green Chem., 2010, 12, 260-267, DOI: 10.1039/B920262E, Paper  

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.  

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Top ten most accessed articles in September

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Catalytic conversion of biomass to biofuels 
David Martin Alonso, Jesse Q. Bond and James A. Dumesic 
Green Chem., 2010, 12, 1493-1513, DOI: 10.1039/C004654J , Critical Review 

Sulfonated silica/carbon nanocomposites as novel catalysts for hydrolysis of cellulose to glucose 
Stijn Van de Vyver, Li Peng, Jan Geboers, Hans Schepers, Filip de Clippel, Cedric J. Gommes, Bart Goderis, Pierre A. Jacobs and Bert F. Sels 
Green Chem., 2010, 12, 1560-1563, DOI: 10.1039/C0GC00235F , Communication 

Synthesis of cyclic carbonates from epoxides and CO2 
Michael North, Riccardo Pasquale and Carl Young 
Green Chem., 2010, 12, 1514-1539, DOI: 10.1039/C0GC00065E , Critical Review 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B , Communication 

Switchable adhesives for carpet tiles: a major breakthrough in sustainable flooring 
Peter S. Shuttleworth, James H. Clark, Robert Mantle and Nigel Stansfield 
Green Chem., 2010, 12, 798-803, DOI: 10.1039/B922735K , Paper 

Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: multiple benefits of CO2-expanded liquids 
Xiaobin Zuo, Fenghui Niu, Kirk Snavely, Bala Subramaniam and Daryle H. Busch 
Green Chem., 2010, 12, 260-267, DOI: 10.1039/B920262E , Paper 

Pausing a stir: heterogeneous catalysis in “dry water” 
Benjamin O. Carter, Dave J. Adams and Andrew I. Cooper 
Green Chem., 2010, 12, 783-785, DOI: 10.1039/B922508K , Communication 

A solvent having switchable hydrophilicity 
Philip G. Jessop, Lam Phan, Andrew Carrier, Shona Robinson, Christoph J. Dürr and Jitendra R. Harjani 
Green Chem., 2010, 12, 809-814, DOI: 10.1039/B926885E , Paper 

Production of liquid hydrocarbon transportation fuels by oligomerization of biomass-derived C9 alkenes 
David Martin Alonso, Jesse Q. Bond, Juan Carlos Serrano-Ruiz and James A. Dumesic 
Green Chem., 2010, 12, 992-999, DOI: 10.1039/C001899F , Paper 

Catalytic disassembly of an organosolv lignin via hydrogen transfer from supercritical methanol 
Katalin Barta, Theodore D. Matson, Makayla L. Fettig, Susannah L. Scott, Alexei V. Iretskii and Peter C. Ford 
Green Chem., 2010, 12, 1640-1647, DOI: 10.1039/C0GC00181C , Paper 

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.

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Singing Green Chemistry tools in Germany

The Green Solvents for Synthesis conference started on Sunday the 10th October 2010 with a boat trip on Lake Königsee which I was told was absolutely spectacular with plenty of mountain landscape.  The lake was described as the purest of all “green solvents” being a gorgeous emerald green in colour.

The delegates were then gathered for a welcome reception in the evening and an opening lecture delivered by Phil Jessop (Queen’s University, Canada) where he described the progress made in green solvents and categorised them in three areas: Replacement green solvents, Really green solvents, and Revolutionary green solvents. His comments were that the replacement solvents may not be enough to cover the different needs. Some solvents have been assessed thoroughly and found to be really green, but most “green” solvents have not been assessed.

On the first day of the conference, Peter Dunn of Pfizer Ltd gave us a broad overview of organic reactions carried out in water. Other talks of interest were by Takao Ikariya (Tokyo institute of Technology) on the use carbon dioxide as green solvent and reactant for organic reactions and Tadafumi Adschiri (Tohoku University) who brought along samples of the super hybrid materials made in his lab via supercritical routes. This was followed by a lecture by Andreas Jess (University of Bayreuth, Germany) on the evaporation and thermal decomposition of ionic liquids by thermogravimetry at ambient pressure and UHV.  The afternoon ended with an inspiring lecture by Peter Wassercheid (University of Erlangen-Nuremberg) on ionic liquids and heterogeneous catalysis and his recent progress on supported ionic liquid phase (SILP) and supported catalyst with an ionic liquid layer (SCILL). A poster session then followed with winners to be announced shortly.

The highlights of the second day were talks by Dieter Vogt (TU Eindhoven) on homogeneous catalysis and amine formations, followed by Alberto Puga (QUILL, Belfast) on new 6-membered  piperidine and 7-membered azepane derived ionic liquids. It became clear that toxicity is an important factor in determining the “greenness” of new ionic liquids. Other talks of interest were algae lipids for biodiesel production delivered by Lindsay Soh (PhD student at Yale University) and fluorous solvents for catalyst recovery, activation and product protection given by John Gladysz (Texas A&M University).

The delegates were spoilt for choices for lunch at either traditional Bavarian style restaurants or small cafes with plenty of outdoor seating to soak up the sun and the magnificent mountain views. The afternoon session resumed with an awe-inspiring talk by Steve Howdle (University of Nottingham, UK) where he used supercritical fluids to synthesize green polymers which were used in bone grafting and drug delivery. We later learnt that Steve, who is a keen footballer, had been invited to take a penalty shoot at half-time during the England-Montenegro qualifying match at Wembley Stadium and he had declined the FA invitation to be with us at the Green Solvents conference. Biocatalysis was also on the agenda with a talk from Udo Kragl (University of Rostock, Germany).

The day ended with a traditional Bavarian buffet and music. The atmosphere was light-hearted and spirits high. Walter Leitner, Steve Howdle, Istvan Horvath, Peter Wassercheid and Helen Olivier-Bourbigou grouped on stage for an excellent rendition of the “green chemistry song”, lyrics below:

Always Use Green Chemistry Tools

Music: guitar by Walter Leitner

Lyrics: Walter Leitner and Steve Howdle

Some syntheses are bad

They can really make you mad

Other chemistry just smells and makes a mess!

If the molecule’s a hassle

Don’t crumble- give a whistle

Green Chemistry will change things for the best!

Chorus:

And Always use the Green Chemistry tools

— whistle —

They make science fun and scientists cool

— whistle —

If the process seems absurd

And “waste” is the final word

Green Chemistry will show a better way!

Just save energy and steps

Of course, catalysis can help

And your profits will shoot up to the sky!

Chorus:

And Always use the Green Chemistry tools

— whistle —

They make science fun and scientists cool

— whistle —

Using carbon dioxide

Makes the future look so bright!

And with biomass we make the stuff we need

All the solvents are replaced

There is no more toxic waste

The business model is extremely neat!

Chorus:

And Always use the Green Chemistry tools

— whistle —

They make science fun and scientists cool

— whistle —

Unfortunately, I was unable to attend the last day of the conference but I am sure that the lectures were as inspiring as the previous days. Green solvents 2012 is a must and well done DECHEMA for organising this excellent conference!

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Making fuels from biomass waste

Jet and diesel fuel can be produced in a simple economic process using waste products of wood processing and pulp mills, claim US scientists. 

World decline in fossil fuel resources, rising oil prices, and an increased awareness in environmental impact has made the search for alternative renewable fuel sources extremely important. Sustainable production of fuels has been attempted using non-food biomass (composed of cellulose, hemicellulose, and lignin) and vegetable oils. But these methods only make light alkanes that are not suitable for use as jet and diesel fuel due to their high volatility, so jet and diesel fuels are currently still reliant on petroleum-based crude oils. 

In the search for alkanes more suited for transport fuels, George Huber at the University of Massachusetts in Amherst and colleagues have shown that waste feedstocks from biomass power plants or composite wood manufacturing facilities can be turned into jet fuel in an integrated and economical process. 

four step process

4 step process produces heavy alkanes suitable for diesel

Huber treats a hemicellulose extract from hardwood trees, a common by-product from the wood manufacturing industry, in a four-step process that includes acid hydrolysis and xylose dehydrogenation, aldol condensation, low temperature hydrogenation, and high temperature hydrodeoxygenation. High yields of 76 per cent are obtained and the cost works out to between $2.06/gal and $4.39/gal, depending on initial xylose concentration, refinery size and overall yield. 

‘Our society will always have a critical need to produce renewable liquid transportations fuels that can run heavy machinery like jet or diesel engines. It is imperative that we develop inexpensive routes to produce these liquid fuels from our renewable resources,’ comments Huber. Though in its beginning stages, Huber hopes it can be developed to a commercial level. 

David Shonnard, director of the Sustainable Futures Institute at Michigan Technological University in the US comments, ‘this is a significant step forward in achieving sustainable transportation. The economic analysis is also particularly important and the sensitivity analyses highlight promising pathways for improvement.’ 

Rebecca Brodie

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Top ten most accessed articles in August

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Catalytic conversion of biomass to biofuels 
David Martin Alonso, Jesse Q. Bond and James A. Dumesic 
Green Chem., 2010, 12, 1493 – 1513, DOI: 10.1039/c004654j, Critical Review 

Pausing a stir: heterogeneous catalysis in “dry water” 
Benjamin O. Carter, Dave J. Adams and Andrew I. Cooper 
Green Chem., 2010, 12, 783 – 785, DOI: 10.1039/b922508k, Communication 

Energy densification of levulinic acid by thermal deoxygenation 
Thomas J. Schwartz, Adriaan R. P. van Heiningen and M. Clayton Wheeler 
Green Chem., 2010, 12, 1353 – 1356, DOI: 10.1039/c005067a, Communication 

Green alcohol couplings without transition metal catalysts: base-mediated beta-alkylation of alcohols in aerobic conditions 
Laura J. Allen and Robert H. Crabtree 
Green Chem., 2010, 12, 1362 – 1364, DOI: 10.1039/c0gc00079e, Communication 

Synthesis of cyclic carbonates from epoxides and CO2 
Michael North, Riccardo Pasquale and Carl Young 
Green Chem., 2010, 12, 1514 – 1539, DOI: 10.1039/c0gc00065e, Critical Review 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570 – 573, DOI: 10.1039/b920000b, Communication 

Production of liquid hydrocarbon transportation fuels by oligomerization of biomass-derived C9 alkenes 
David Martin Alonso, Jesse Q. Bond, Juan Carlos Serrano-Ruiz and James A. Dumesic 
Green Chem., 2010, 12, 992 – 999, DOI: 10.1039/c001899f 

Sulfonated silica/carbon nanocomposites as novel catalysts for hydrolysis of cellulose to glucose 
Stijn Van de Vyver, Li Peng, Jan Geboers, Hans Schepers, Filip de Clippel, Cedric J. Gommes, Bart Goderis, Pierre A. Jacobs and Bert F. Sels 
Green Chem., 2010, 12, 1560 – 1563, DOI: 10.1039/c0gc00235f, Communication 

Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: multiple benefits of CO2-expanded liquids 
Xiaobin Zuo, Fenghui Niu, Kirk Snavely, Bala Subramaniam and Daryle H. Busch 
Green Chem., 2010, 12, 260 – 267, DOI: 10.1039/b920262e 

Accounting for clean, fast and high yielding reactions under microwave conditions 
Christopher Roy Strauss and David W. Rooney 
Green Chem., 2010, 12, 1340 – 1344, DOI: 10.1039/c0gc00024h, Critical Review 

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.

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1st PACN Green Chemistry Congress

15-17 November 2010
UN Economic Commisssion for Africa
Addis Ababa, Ethiopia

Africa is vastly abundant in natural resources and the richness offers valuable opportunities to pursue novel routes to sustainable processes and products. However, the concept of Green Chemistry for Sustainability is still at its infancy in most African countries. 

Focusing on the search for such routes, and expanding on their benefits, is an exciting challenge that can render African countries extremely competitive at international levels. Sustainable chemistry will contribute to the spreading of knowledge in such a frontier area of chemistry.

About the conference

Sessions at the conference will include:

  • catalysis and biocatalysis 
  • renewable feedstocks/ energy 
  • green solvents 
  • metrics 
  • product design       

Confirmed Speakers

  • Paul Anastas, Yale University, USA 
  • Vanderlan Bolzani, Sao Paulo State University, Brazil  
  • Colin Brennan, Syngenta, UK 
  • Erick Carreira, ETH Zurich, Switzerland 
  • Terry Collins, Carnegie Mellon University, USA 
  • Bob Crawford, Unilever, UK  
  • Buxing Han, Chinese Academy of Sciences, Beijing, China  
  • Walter Leitner, ITMC-RWTH, Germany 
  • Goverdhan Mehta, Bangalore, India 
  • Romeela Mohee, University of Mauritius, Madagascar 
  • Egid Mubofu, Dar es Salaam, Tanzania 
  • David Phillips, Imperial College, UK  
  • John Pickett, Rothamsted Research, UK 
  • Jay Siegel, University of Zurich, Switzerland         

Scientific Committee

  • Nigist Asfaw, Addis Ababa University, Ethiopia 
  • Yonas Chebude, Addis Ababa University, Ethiopia 
  • John Clough, Syngenta, UK 
  • Neil Coville, University of Witwatersrand, South Africa  
  • Lisa Hall, University of Cambridge, UK 
  • Pete Licence, The University of Nottingham, UK 
  • Jacob Midiwo, University of Nairobi, Kenya 
  • Alejandra Palermo, RSC, UK 
  • Martyn Poliakoff, The University of Nottingham, UK 
  • Sarah Ruthven, Green Chemistry Editor, RSC, UK 
  • Tom Welton, Imperial College, UK        

Key Dates

  • Deadline for abstract submission: 1 October 2010 
  • Early bird registration until: 30 September 2010      

Read more about this conference: http://www.rsc.org/ConferencesAndEvents/RSCEvents/International/Africa/GreenChem/Index.asp

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Top ten most accessed articles in July

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Glycerol as a sustainable solvent for green chemistry 
Yanlong Gu and François Jérôme 
Green Chem., 2010, 12, 1127-1138, DOI: 10.1039/C001628D , Critical Review 

Development of safe and scalable continuous-flow methods for palladium-catalyzed aerobic oxidation reactions 
Xuan Ye, Martin D. Johnson, Tianning Diao, Matthew H. Yates and Shannon S. Stahl 
Green Chem., 2010, 12, 1180-1186, DOI: 10.1039/C0GC00106F , Paper 

Catalytic production of hydrogen from glucose and other carbohydrates under exceptionally mild reaction conditions 
N. Taccardi, D. Assenbaum, M. E. M. Berger, A. Bösmann, F. Enzenberger, R. Wölfel, S. Neuendorf, Volker Goeke, N. Schödel, H. -J. Maass, H. Kistenmacher and P. Wasserscheid 
Green Chem., 2010, 12, 1150-1156, DOI: 10.1039/C002910F , Communication 

A two-step approach for the catalytic conversion of glucose to 2,5-dimethylfuran in ionic liquids 
Mandan Chidambaram and Alexis T. Bell 
Green Chem., 2010, 12, 1253-1262, DOI: 10.1039/C004343E , Paper 

Highly recyclable, imidazolium derived ionic liquids of low antimicrobial and antifungal toxicity: A new strategy for acid catalysis 
Lauren Myles, Rohitkumar Gore, Marcel Špulák, Nicholas Gathergood and Stephen J. Connon 
Green Chem., 2010, 12, 1157-1162, DOI: 10.1039/C003301D , Communication 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B , Communication 

Production of liquid hydrocarbon transportation fuels by oligomerization of biomass-derived C9 alkenes 
David Martin Alonso, Jesse Q. Bond, Juan Carlos Serrano-Ruiz and James A. Dumesic 
Green Chem., 2010, 12, 992-999, DOI: 10.1039/C001899F , Paper 

Technology development for the production of biobased products from biorefinery carbohydrates-the US Department of Energy’s “Top 10” revisited 
Joseph J. Bozell and Gene R. Petersen 
Green Chem., 2010, 12, 539-554, DOI: 10.1039/B922014C , Critical Review 

Green chemistry by nano-catalysis 
Vivek Polshettiwar and Rajender S. Varma 
Green Chem., 2010, 12, 743-754, DOI: 10.1039/B921171C , Tutorial Review 

Direct synthesis of hydrogen peroxide on palladium catalyst supported on sulfonic acid-functionalized silica 
Gema Blanco-Brieva, M. Pilar de Frutos Escrig, Jose M. Campos-Martin and Jose L. G. Fierro 
Green Chem., 2010, 12, 1163-1166, DOI: 10.1039/C003700A , Communication 

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.

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