17th Annual Green Chemistry & Engineering Conference – Sustainable Chemistry & Engineering in the 21st Century

The ACS Green Chemistry Institute®’s Green Chemistry & Engineering Conference (GC&E) will be held on the 18–20 June 2013 in North Bethesda, Maryland, just outside of Washington DC. This event is an opportunity for scientists, businesses, students and educators, and advocates to broaden their understanding of green chemistry and engineering while building valuable connections with leaders in this growing field.

GC&E features three days of programming including world-renowned speakers, three poster sessions and more than 30 technical sessions on subjects such as designing safer chemicals and products, green chemistry education, and new business through green chemistry innovations.

Conference Highlights

• Daily Keynotes Speakers:  There will be a daily keynote presentation from Dr. Milton Hearn, Associate-Director, Green Chemical Futures-Industry; Dr. Michael J. Pcolinski, Vice President of Innovation & Technology, BASF Corporation; and Dr. Jim Hutchison, Professor of Chemistry, University of Oregon.

GC&E Student Workshop: This pre-conference workshop will be Monday, 17 June 2013 and is free to students registered for the conference. Lead by ACS Green Chemistry Institute® Director, Dr. David Constable, and other experts, this workshop will be a fast pasted, interactive series of sessions covering each of the 12 Principles of Green Chemistry.

ACS Careers Workshop: On Wednesday, 19 June 2013, expert consultants from ACS Careers will conduct a 4-hour workshop to help attendees accelerate professional development. Learn more about planning and résumé preparation, maintaining an effective job search, reviewing employment trends, and enhancing professional skills.

Online Session: A special session “Global Supplies for Chemical Feedstocks in the 21st Century” will be held on Tuesday, 18 June 2013 at 7:00 p.m. EDT (–4 GMT) and streamed live online for free to viewers around the world.

The Green Expo: The expo features vendors from business, government, and academia. Explore some of the 21st Century’s latest technology, resources, and marketplace opportunities.

For more information and to register, please visit the website www.gcande.org.

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Top 10 most accessed articles in February

For Green Chemistry, the top 10 most accessed articles in February were as follows:

Deconstruction of lignocellulosic biomass with ionic liquids
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton  
Green Chem., 2013, 15, 550-583
DOI: 10.1039/C2GC36364J, Critical Review

Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
Hailong Yang, Hong Yan, Peng Sun, Yan Zhu, Linhua Lu, Defu Liu, Guangwei Rong and Jincheng Mao  
Green Chem., 2013, 15, 976-981
DOI: 10.1039/C3GC37131J, Paper

Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications
Matthieu O. Sonnati, Sonia Amigoni, Elisabeth P. Taffin de Givenchy, Thierry Darmanin, Olivier Choulet and Frédéric Guittard  
Green Chem., 2013, 15, 283-306
DOI: 10.1039/C2GC36525A, Critical Review

Food waste biomass: a resource for high-value chemicals
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark  
Green Chem., 2013, 15, 307-314
DOI: 10.1039/C2GC36978H, Perspective

Ohmic heating as a new efficient process for organic synthesis in water
Joana Pinto, Vera L. M. Silva, Ana M. G. Silva, Artur M. S. Silva, José C. S. Costa, Luís M. N. B. F. Santos, Roger Enes, José A. S. Cavaleiro, António A. M. O. S. Vicente and José A. C. Teixeira  
Green Chem., 2013, 15, 970-975
DOI: 10.1039/C3GC36881E, Paper

Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic  
Green Chem., 2013, 15, 584-595
DOI: 10.1039/C3GC37065H, Critical Review

Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions
Maya Shankar Singh, Anugula Nagaraju, Girijesh Kumar Verma, Gaurav Shukla, Rajiv Kumar Verma, Abhijeet Srivastava and Keshav Raghuvanshi  
Green Chem., 2013, 15, 954-962
DOI: 10.1039/C3GC37047J, Paper

Catalytic etherification of glycerol with short chain alkyl alcohols in the presence of Lewis acids
Fei Liu, Karine De Oliveira Vigier, Marc Pera-Titus, Yannick Pouilloux, Jean-Marc Clacens, Floryan Decampo and François Jérôme  
Green Chem., 2013, 15, 901-909
DOI: 10.1039/C3GC36944G, Paper

Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
Sara E. Davis, Matthew S. Ide and Robert J. Davis  
Green Chem., 2013, 15, 17-45
DOI: 10.1039/C2GC36441G, Critical Review

Multicomponent reactions in unconventional solvents: state of the art
Yanlong Gu  
Green Chem., 2012, 14, 2091-2128
DOI: 10.1039/C2GC35635J, Critical Review
Take a look at the articles, and then let us know your thoughts and comments below.

Fancy submitting your own work to Green Chemistry? You can submit online today, or email us with your ideas and suggestions.

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Green Chemistry issue 5 now available online!

Issue 5 of Green Chemistry is now available to read online.

The front cover (left) this month features work by Etienne Grau and Stefan Mecking from Konstanz, Germany. In their work, caryophyllene and humulene, renewable sesquiterpenes from clove oil, were subject to metathesis polymerization to yield non-crosslinked linear polymers with unique microstructures and low glass transition temperatures.

Read the research: Polyterpenes by ring opening metathesis polymerization of caryophyllene and humulene, E. Grau and S. Mecking, Green Chem., 2013, 15, 1112–1115, DOI: c3gc40300a

The inside front cover (right) this month features work by Thomas-Xavier Métro, Frédéric Lamaty and co-workers from Montpellier, France. Their paper describes an original liquid-assisted ball-milling methodology for peptide bond synthesis – avoiding toxic solvents and reactants – and its application to the synthesis of Leu-enkephalin.

Read the research: Environmentally benign peptide synthesis using liquid-assisted ball-milling: application to the synthesis of Leu-enkephalin, J. Bonnamour, T.-X. Métro, J. Martinez and F. Lamaty, Green Chem., 2013, 15, 1116–1120, DOI: c3gc40302e

Both of these articles are free to access for 6 weeks!

Keep up-to-date with the latest content in Green Chemistry by registering for our free table of contents alerts.

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Creating biodegradable electronics using shellac

Scientists in Austria, Romania and Turkey have used the natural resin shellac to devise biocompatible organic field-effect transistors (OFETs), which could help make electronic gadgets biodegradable and allow easier use of OFETs in the body.

Multi-coloured row of nail polish bottles, illustrating a current application of shellac

© Shutterstock

Together with their better known cousins – organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs) – OFETs are already revolutionising the electronics industry, bringing us flexible displays and light-weight solar-powered chargers. Switching the synthetic substrate material and dielectric layer to the naturally occurring shellac has a number of advantages such as low cost, low toxicity and low environmental impact.

Currently used in the fashion and beauty industry as a hard-wearing nail varnish, shellac has also been used to make gramophone records and as a furniture finish. The material is composed of a mixture of aliphatic and alicyclic hydroxy acids that are easily cross-linked by heating, resulting in a smooth, glassy substrate for the OFET devices to be built upon. It is also easy to process.

 

Read the full article in Chemistry World

Read the original journal article in Green Chemistry:
Natural resin shellac as a substrate and a dielectric layer for organic field-effect transistors
Mihai Irimia-Vladu, Eric Daniel Głowacki, Günther Schwabegger, Lucia Leonat, Hava Zekiye Akpinar, Helmut Sitter, Siegfried Bauer and Niyazi Serdar Sariciftci
Green Chem., 2013, Advance Article 
DOI: 10.1039/C3GC40388B, Communication

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Sieving silica sieves from biomass ash

Burning biomass for heat and power could produce as much as 2000 TWh by 2020, which would produce 4–15.6 million tonnes of waste ash, per year, in Europe alone. To address the problem of what to do with all this waste, scientists in the UK have developed a method to convert this ash into mesoporous silica.

Although some of the waste ash produced from the combustion of biomass is currently used in construction, most of it ends up in landfill. Therefore, extracting alkali silicates, which can be used in cement, detergents, catalysts and catalyst supports, is one way of reusing the potentially huge quantities of ash due to be produced in the future.

The team, led by Duncan Maquarrie at the University of York, developed an efficient route for extracting the silicates by forming alkali silicate solutions. The silicate solutions were converted into the porous silica, MCM-41, a useful catalyst and molecular sieve.

Read what Duncan Macquarrie has to say about the research in Chemistry World.

Read the original research published in Green Chemistry:

Alkali silicates and structured mesoporous silicas from biomass power station wastes: the emergence of bio-MCMs, J. R. Dodson,  E. C. Cooper,  A. J. Hunt,  A. Matharu,  J. Cole,  A. Minihan,  J. H. Clark and D. J. Macquarrie, Green Chem., 2013, DOI: 10.1039/C3GC40324F

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Top 10 most accessed articles in January

For Green Chemistry, the top 10 most accessed articles in January were as follows:

Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
Sara E. Davis, Matthew S. Ide and Robert J. Davis
Green Chem., 2013, 15, 17-45
DOI: 10.1039/C2GC36441G, Critical Review

Food waste biomass: a resource for high-value chemicals
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark
Green Chem., 2013, 15, 307-314
DOI: 10.1039/C2GC36978H, Perspective

A simple metal-free catalytic sulfoxidation under visible light and air
Xiangyong Gu, Xiang Li, Yahong Chai, Qi Yang, Pixu Li and Yingming Yao
Green Chem., 2013, 15, 357-361
DOI: 10.1039/C2GC36683E, Communication

Deconstruction of lignocellulosic biomass with ionic liquids
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton
Green Chem., 2013, 15, 550-583
DOI: 10.1039/C2GC36364J, Critical Review

Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N,N-dimethylformamide
Donna S. MacMillan, Jane Murray, Helen F. Sneddon, Craig Jamieson and Allan J. B. Watson
Green Chem., 2013, 15, 596-600
DOI: 10.1039/C2GC36900A, Communication

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

Designing endocrine disruption out of the next generation of chemicals
T. T. Schug, R. Abagyan, B. Blumberg, T. J. Collins, D. Crews, P. L. DeFur, S. M. Dickerson, T. M. Edwards, A. C. Gore, L. J. Guillette, T. Hayes, J. J. Heindel, A. Moores, H. B. Patisaul, T. L. Tal, K. A. Thayer, L. N. Vandenberg, J. C. Warner, C. S. Watson, F. S. vom Saal, R. T. Zoeller, K. P. O’Brien and J. P. Myers
Green Chem., 2013, 15, 181-198
DOI: 10.1039/C2GC35055F, Paper

Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic
Green Chem., 2013, 15, 584-595
DOI: 10.1039/C3GC37065H, Critical Review

Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond
Rocío García-Álvarez, Pascale Crochet and Victorio Cadierno
Green Chem., 2013, 15, 46-66
DOI: 10.1039/C2GC36534K, Tutorial Review

Cyclometalated iridium complexes for transfer hydrogenation of carbonyl groups in water
Yawen Wei, Dong Xue, Qian Lei, Chao Wang and Jianliang Xiao
Green Chem., 2013, 15, 629-634
DOI: 10.1039/C2GC36619C, Communication

Take a look at the articles, then let us know your thoughts and comments below.

Interested in submitting your own work to Green Chemistry? You can submit online today, or email us with your ideas and suggestions.

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Recycling rare earth elements using ionic liquids

Recycling old magnets, so that rare-earth metals can be re-used, could help to solve an urgent raw material supply problem in the electronics industry. Researchers from the University of Leuven, Belgium, have used ionic liquids to separate neodymium and samarium from transition metals like iron, manganese and cobalt – all elements that are used in the construction of permanent rare-earth magnets, which are found in electronic devices ranging from hard drives to air conditioners and wind turbines.

‘The process involves the liquid-liquid extraction of rare-earth metals from the other elements present in neodymium-iron-boron and samarium-cobalt magnets,’ explains Koen Binnemans who leads the group developing the process. ‘These other elements – including iron, cobalt, manganese, copper and zinc – are extracted into the ionic-liquid phase, while the rare-earth metals are left behind in the aqueous phase,’ he says, adding that the ionic liquid itself – trihexyl(tetradecyl)phosphonium chloride – can also be re-used, after the transition metals have been stripped out.

In traditional liquid-liquid extractions of metal ions, an aqueous phase containing the metal salt is mixed with an organic phase containing an extraction agent. Simple though they are, these processes use organic phases comprising flammable and volatile solvents, like toluene, kerosene or diethyl ether. Ionic liquids are far more environmentally friendly, having very low vapour pressure and non-flammability.

Read the full article in Chemistry World

Read the original journal article in Green Chemistry:

Removal of transition metals from rare earths by solvent extraction with an undiluted phosphonium ionic liquid: separations relevant to rare-earth magnet recycling
Tom Vander Hoogerstraete,  Sil Wellens,  Katrien Verachtert and Koen Binnemans
Green Chem., 2013,15, 919-927

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Green Chemistry Issue 4 now online

Green Chemistry issue 4 is now online and you can read it here.

Issue 4 front coverThe cover features work by François Jérôme and co-workers from France.  Their Paper, ‘Pretreatment of microcrystalline cellulose by ultrasounds: effect of particle size in the heterogeneously-catalyzed hydrolysis of cellulose to glucose’ demonstrates that activity of a sulfonated carbon in the heterogeneously-catalyzed hydrolysis of cellulose was greatly improved by assistance of ultrasound. The paper demonstrates that the sonication method was as effective as conventional pre-treatments such as ball-milling or ionic liquids.

Pretreatment of microcrystalline cellulose by ultrasounds: effect of particle size in the heterogeneously-catalyzed hydrolysis of cellulose to glucose
Qinghua Zhang, Maud Benoit, Karine De Oliveira Vigier, Joël Barrault, Gwenaëlle Jégou, Michel Philippe and François Jérôme, Green Chem., 2013, 15, 963-969

Issue 4 inside cover

The inside front cover highlights a review article entitled ‘Green chemistry and the ocean-based biorefinery’ by Fran Kerton and co-workers at the Memorial University of Newfoundland in Canada.  This review highlights that competition for land use could be minimized if marine sourced feedstocks were used for chemicals and materials production rather than crops grown on fertile land. It focuses on achievements and potential opportunities surrounding the use of algae and waste from shellfish and finfish processing.

Green chemistry and the ocean-based biorefinery
Francesca M. Kerton, Yi Liu, Khaled W. Omari and Kelly Hawboldt, Green Chem., 2013, 15, 860-871

These articles are free to access for 6 weeks!

Keep up-to-date with the latest content in Green Chemistry by registering for our free table of contents alerts.

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‘Super solvents’ shortlisted for most important British innovation of the 21st Century

Work by scientists from Queen’s University Belfast on ionic liquid chemistry is in the running to be named the most important British innovation of the 21st Century. 

The work of staff in the Queen’s University Ionic Liquid Laboratories (QUILL) Research Centre is up against 11 other innovations from across the United Kingdom battling it out in a public vote to find the one that will have the greatest impact in the coming century. The vote is part of the Science Museum’s Initiative on Great British past and future Innovations. 

Ionic liquids are salts which can remain liquid at room temperature and do not form vapours, and so can be used as non-polluting alternatives to conventional solvents.  At QUILL, a team of nearly 100 scientists are exploring the potential of these green solvents and Fortune 100 energy giant Petronas is already using the technology in its plants.  The mercury removal unit, using 15 tons of supported ionic liquid, was developed by a team led by Professor Ken Seddon, Co-Director of QUILL at Queen’s, and Dr John Holbrey also from QUILL, who were listed last year as the number one and two chemists in the UK based on citations of their work.Professor Ken Seddon said: “Being shortlisted for the most important British innovation of the 21st century is recognition of the high calibre of research being undertaken at QUILL and throughout the University.  We would encourage people to take a moment to vote for our research as its application will eventually have a bearing on most of our lives.”

Other notable British innovations in the hunt for the prize are Quantum Dots, Graphene, Raspberry Pi and the discovery of the Higgs-Boson – you can vote for your favourite here.  Update Monday 25th March – Ionic Liquid Chemistry was voted the recent innovation that is most likely to shape the coming century.

Why not take a look at a collection of high quality research in this area from across RSC Journals – Increadible ionic liquids: an article collection.

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Top 10 most accessed articles in 2012

Do you want to know what your colleagues were reading during 2012? The following articles in Green Chemistry were the most accessed over the course of the year:

Multicomponent reactions in unconventional solvents: state of the art
Yanlong Gu
Green Chem., 2012,14, 2091-2128
DOI: 10.1039/C2GC35635J, Critical Review

Characterization and comparison of hydrophilic and hydrophobic room temperature ionic liquids incorporating the imidazolium cation
Jonathan G. Huddleston, Ann E. Visser, W. Matthew Reichert, Heather D. Willauer, Grant A. Broker and Robin D. Rogers
Green Chem., 2001,3, 156-164
DOI: 10.1039/B103275P, Paper

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

Transition metal based catalysts in the aerobic oxidation of alcohols
Camilla Parmeggiani and Francesca Cardona
Green Chem., 2012,14, 547-564
DOI: 10.1039/C2GC16344F, Tutorial Review

Evolution of asymmetric organocatalysis: multi- and retrocatalysis
Raffael C. Wende and Peter R. Schreiner
Green Chem., 2012,14, 1821-1849
DOI: 10.1039/C2GC35160A, Critical Review

Green synthesis of metal nanoparticles using plants
Siavash Iravani
Green Chem., 2011,13, 2638-2650
DOI: 10.1039/C1GC15386B, Critical Review

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

Continuous flow reactors: a perspective
Charlotte Wiles and Paul Watts
Green Chem., 2012,14, 38-54
DOI: 10.1039/C1GC16022B, Tutorial Review

Catalytic conversion of biomass using solvents derived from lignin
Pooya Azadi, Ronald Carrasquillo-Flores, Yomaira J. Pagán-Torres, Elif I. Gürbüz, Ramin Farnood and James A. Dumesic
Green Chem., 2012,14, 1573-1576
DOI: 10.1039/C2GC35203F, Communication

5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications
Andreia A. Rosatella, Svilen P. Simeonov, Raquel F. M. Frade and Carlos A. M. Afonso
Green Chem., 2011,13, 754-793
DOI: 10.1039/C0GC00401D, Critical Review

Take a look at the articles and then post your thoughts and comments below.

Interested in submitting your own work to Green Chemistry? Submit online today, or email us with your suggestions.

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