Sleeping sickness fly trap in a nutshell – GC article in Chemistry World

Written by Charlie Quigg

An international team of chemists has developed a green method for creating odour attractants to trap the insects that spread African sleeping sickness.

Sleeping sickness or African trypanosomiasis is transmitted by tsetse flies and is a threat to millions of people, and their livestock, across sub-Saharan Africa. Trapping these flies can reduce the number of sleeping sickness cases. Unfortunately, the odour attractants that draw the flies in are often prohibitively expensive – barring buffalo urine, which has unfortunate hygienic and olfactory detractions – limiting their use…

Tsetse flies feed on the blood of vertebrate animals © Image Quest Marine/Alamy

Interested to know more?

Read the full article by Charlie Quigg here

Read the research article in GC:

Synthesis of tsetse fly attractants from a cashew nut shell extract by isomerising metathesis

S. Baader, P.E. Podsiadly, D.J. Cole Hamilton and L.J. Goossen

Green Chem., 2014, Advance Article
DOI: 10.1039/C4GC01269K

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7th Green Solvents Conference, Dresden, Germany

Kylie L. Luska

Institute for Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 1, 52074 Aachen, Germany.

The 7th Green Solvents Conference took place in the Saxonian capital city of Dresden, Germany from October 19-22, 2014. This biennial Dechema conference brings together chemists and engineers from both academia and industry to discuss their latest research discoveries and future perspectives on the fundamental aspects and application of advanced fluids. An important aspect of the Green Solvents Conference series is the selection of a unique locale, in which previous meetings have been held in the lower Rhein Valley (Bruchsal), Lake Constance (Friedrichshafen), the Bavarian Alps (Berchtesgaden) and the middle Rhein Valley (Boppard). The latest edition of the Green Solvents Conference took place in Dresden; a city renowned for its magnificent baroque architecture and role in the reunification of Germany through the “Peaceful Revolution”.

The four-day conference provided an opportunity to discuss the scientific progress and application of such alternative solvents as water, ionic liquids, supercritical fluids, green organic solvents and controllable multiphase media. The conference presentations highlighted the wide variety of chemical syntheses and processes utilizing advanced fluids including: biomass conversion, supported ionic liquid phases and continuous flow processes. A common discussion point during the conference involved various life cycle characteristics of alternative solvents such as large-scale production, toxicity and end-of-life disposal. It was emphasized that such factors need to be considered during the early stages of advanced fluid development to ensure novel chemical syntheses or processes will have a reduced environmental impact compared to conventional methods.

On Sunday evening, the conference began with the awarding of the “Willi Keim Prize” to Roberto Rinaldi from the Max-Planck-Institut für Kohlenforschung. The section of “Advanced Fluids” of Dechema established this award in 2012 to recognize an outstanding young scientist working in the field of advanced fluids and was named in honour of Prof. emeritus Wilhelm Keim (RWTH Aachen University). Dr. Keim’s research investigated the use of alternative solvents in numerous catalytic processes, in which his work was important in the development of the SHOP process (Shell Higher Olefin Process) by demonstrating and implementing the principle of biphasic catalysis for the first time on an industrial scale. Dr. Rinaldi was the recipient of the 2014 Willi Keim Award for his work on the use of alternative solvents in the conversion of biomass. His intriguing talk outlined different aqueous, ionic liquid and solvent-free (mechanochemical) methods for the processing of biomass feedstocks that have been developed within his lab.

Green Chemistry photo 1

Willi Keim Prize winner Dr. Roberto Rinaldi

The Sunday evening program also included a keynote lecture from one of the pioneers in the field of advanced fluids, Martyn Poliakoff from the University of Nottingham. His research examines the development of continuous catalytic processes using scCO2 as a mobile phase. His lecture illustrated how supercritical carbon dioxide (scCO2), an “old” solvent, can be utilized in the development of novel chemical processes. As examples, he showcased how his lab has created a self-optimizing continuous flow reactor for the conversion of levulinic acid to δ-valerolactone, a continuous method for the creation of methylmethacrylate and a continuous photocatalytic procedure toward the synthesis of artemisinin.

The Monday program began with Mark Shiflett from Dupont Central Research and Development who outlined his work toward the implementation of ionic liquids within the chemical industry. His work examines the phase behaviour of hydrofluorocarbons in imidazolium ionic liquids, in which he stressed the importance in obtaining high quality data in order to properly understand the fundamental properties of advanced fluids. He illustrated how ionic liquids have potential application within Dupont as media for the purification of tetrafluoroethylene and for the separation of hydrofluorocarbon isomers and diastereomers.

Andreas Kirschning from the Leibniz Universität Hannover presented his work on the construction of continuous flow reactors in organic synthesis. He illustrated how consecutive reactions can be carried out in continuous flow to achieved complex organic transformations. He emphasized how this approach mimics biosynthetic routes, which are not necessarily “step-economic” but are highly efficient syntheses due to the continuous processing of reaction intermediates. His lab also investigates the use of inductive heating in continuous flow processes, which involves the application of an electromagnetic field to a tubular reactor constructed of a conductive metal or filled with magnetic nanoparticles. Inductive heating allows for the creation of very high reaction temperatures and has been applied in his work for such reactions as the Claisen rearrangement and alcohol oxidation.

François Jerome from the Université de Poitiers presented his work toward the application of deep eutectic solvents in the conversion of biomass resources. Deep eutectic solvents based on such materials as choline chloride represent inexpensive, non-toxic and environmentally benign ionic liquids. His work has explored the use of deep eutectic solvents in the dissolution of crystalline cellulose and for the catalytic transformation of various biomass-derived substrates. His research has shown that deep eutectic solvents can be created by mixing choline chloride directly with biomass substrates and thus avoid the requirement of a second component to form an ionic liquid phase.

Tuesday morning began with a lecture from Fabrice Gallou from Novartis who presented his perspective on the use of alternative solvents in the pharmaceutical industry. He outlined how the driving force toward the implementation of more benign solvents is mainly dependent on its performance characteristics (e.g., reaction yield, product purity) but is also related to legislation changes and literature precedence. He emphasized that the application of alternative solvents in the pharmaceutical industry is not a matter of “if” but “when” this switch will occur. He illustrated several examples of how such solvents as N-methylpyrrolidone (NMP) and dichloromethane (DCM) are being replaced with safer solvents. Furthermore, he showed how Novartis has investigated the use of surfactants to enable various organic transformations to take place in aqueous solution.

Phillip Jessop from Queen’s University outlined his research into the development of switchable solvents. He emphasized that “green solvents” are those that impart the lowest environmental impact on an entire chemical process, in which solvent separation has one of most significant influences on the efficiency of a procedure. He highlighted his work on the creation and application of switchable hydrophilicity solvents and switchable water through the use of nitrogen-based additives and CO2. The switchability of these solvents, triggered by the application or removal of CO2,  allows for facile product separations in a wide variety of processes including the production of latex, extraction of soybean oil or desalination of seawater. He also showed how his group is preparing an in silico screening method to identify the most appropriate nitrogen-based additives for the formation of switchable solvents, which combines together various performance characteristics and toxicity considerations.

The last day of the conference included a keynote lecture from David Bergbreiter from Texas A&M University who presented how “older solvents” based on oligomer hydrocarbons can accomplish “new tricks”. His work investigates the use of polyisobutylene, polyethylene and poly(N-alkylacrylamide) oligomers as recyclable solvents for catalytic reactions. Functionalization of homogeneous catalysts with polymer units imparted catalyst solubility and retention in these polymeric solvents. The thermomorphic behaviour of these polymeric solvents and catalysts allow for facile product or catalyst separation by which temperature can be used as a trigger to switch between a mono- and biphasic solvent system or a soluble and insoluble catalyst.

Phillip Savage of Pennsylvania State University presented his work on the valorization of algal biomass using aqueous phase reforming. He illustrated the advantages of converting algal biomass in comparison to lignocellulose resources (e.g., faster growth rates, avoid land usage, lignin-free feedstock) and outlined various strategies in which aqueous phase reforming of algae can be used in the production of biofuels. He also presented work within his group toward the formation of novel heterogeneous catalysts that operate under aqueous phase reforming conditions.

Poster Award Winners Jose I. Garcia, Manuela Facchin and Emilia Streng (receiving the award for Zacharias Amara)

Poster Award Winners Jose I. Garcia, Manuela Facchin and Emilia Streng (receiving the award for Zacharias Amara)

 The high quality of the oral and poster program presented at the 7th Green Solvents Conference provided a stimulating environment for the conference participants to engage and discuss the future challenges and applications of advanced fluids. Congratulations to the winners of the poster awards: Jorge I. Garcia (University of San Jorge), Manuela Facchin (Università Cà Foscari Venezia) and Zacharias Amara (University of Nottingham). The conference also provided a lively social program, which provided additional opportunities for the attendees to network and exchange ideas. The conference dinner was held at Festungsmauern am Brühlschen Garten, a baroque barrel vault dining hall located below the old city walls of Dresden, which offered a beautiful setting for the participants to enjoy some local food, drinks and entertainment.

Dr. Walter Leitner welcoming guests to the conference dinner

Dr. Walter Leitner welcoming guests to the conference dinner

 Academic and industrial researchers interested in the fundamental study and application of advanced fluids are encouraged to take part in the 8th Green Solvents Conference on October 16-19, 2016. In accordance with conference tradition, participants can expect the conference to be held in another inspiring city located near large amounts of the greenest solvent, water!

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Driving towards success with biomass-derived petrol – GC article in Chemistry World

Written by Anisha Ratan

Chinese scientists have overcome previous limitations to generate high octane number petrol from biomass-derived γ-valerolactone (GVL), an organic compound that is already often blended in small amounts with petrol or diesel. Using an ionic liquid catalyst, the conversion churned out a 2,2,4-trimethylpentane-rich substance with an octane number of 95.4, the highest reported for biomass derived fuel.

GA

Process for converting GVL into high octane number petrol

Petrol, the liquid many of us use to run our cars, is typically obtained from fossil fuels. But, with energy demands rocketing, producing a renewable and sustainable alternative has become a challenge for many researchers…

Interested to know more?

Read the full article by Anisha Ratan in Chemistry World here…

Read the article in GC:

Conversion of biomass derived valerolactone into high octane number gasoline with an ionic liquid
Jiayu Xin, Dongxia Yan, Olubunmi Ayodele, Zhan Zhang, Xingmei Lu and Suojiang Zhang
Green Chem., 2015, Advance Article
DOI: 10.1039/C4GC01792G

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Green Polymer Chemistry 2015

AMI’s Green Polymer Chemistry 2015 is the 4th edition of the international conference on sustainable synthesis of plastics and elastomers including materials currently available in the marketplace. The event will take place from 18-19 March 2014 at the Maritim Hotel, Cologne, Germany.

The conference kicks off with market papers on the global renewable plastics industry, discusses renewable packaging, new from old materials, synthesis, renewable plastics, measuring sustainability and new routes to bio-based polymers. This will be a 2-day conference with a networking cocktail reception for all delegates and speaker to attend, on the evening of the first day. Please follow the link here for full programme: http://www.amiplastics.com/Events/Resources/Programme/Green%20Polymer%20Chemistry%202015%20Brochure.pdf

For more information please visit the webiste or contact the Conference Organiser: Kat Langner, email: kl@amiplastics.com Tel: +44 (0) 117 314 8111

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EPA Announces Winners of 2014 Presidential Green Chemistry Challenge Awards

Green Chemistry would like to congratulate the recent winners of the EPA Presidential Green Chemistry Challenge Awards. The Presidential Green Chemistry Challenge Awards promote the environmental and economic benefits of developing and using novel green chemistry. These prestigious annual awards recognize chemical technologies that incorporate the principles of green chemistry into chemical design, manufacture, and use. The 2014 submissions were formally judged by an independent panel of technical experts convened by the American Chemical Society Green Chemistry Institute.

The winners include:

  • Academic: Professor Shannon S. Stahl, University of Madison for his work on developing aerobic oxidation methods for Pharmaceutical Synthesis.
  • Small Business: Amyris, for engineering a yeast to make a renewable fuel replacement for petroleum diesel.
  • Designing Greener Chemicals: The Solberg Company, for developing a new safer firefighting foam which is free from persistent toxic chemicals.
  • Greener Reaction Conditions: QD Vision, Inc., for the production of new LED lighting material that can bring massive energy savings.
  • Greener Synthetic Pathways: Solazyme, Inc., for making soaps, laundry detergents, food products and fuels while reducing energy and water use, waste and impacts on forests.

For further information on the award winning research and how to enter for the 2015 awards take a look at the EPA website.

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Lignin boosts sunscreen performance

Article written by Cally Haynes

Scientists in Canada and China have shown that the effectiveness of commercial sunscreens can be enhanced by the addition of lignin and, as an unprecedented bonus; sunlight exposure may help them work even better!

To read the full article written about this work visit Chemistry World.

The original research article is free to access until 14 November 2014.

Download it here: Y Qian, X Qiu and S Zhu, Green Chem., 2014, DOI: 10.1039/c4gc01333f

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Dissolving lignin

James Sherwood is a guest web-writer for Green Chemistry. James is a research associate in the Green Chemistry Centre of Excellence at the University of York. His interests range from the certification and application of bio-based products, to the understanding of solvent effects in organic synthesis.

The separation of lignocellulosic biomass into its three component polymers; cellulose, hemicellulose, and lignin, is an important field of research relevant to biorefineries and the production of bio-based products. The chemical valorisation of polysaccaharides (to bio-ethanol for example) and the paper industries leave the lignin behind as waste.

Rich in aromatic functionality, it is unfortunate that because of the poor solubility of lignin up to 40% of lignocellulosic biomass feedstock is consigned to low value applications.Graphical abstract ammonia lignin

The use of ammonia as a solvent for lignin has now been revisited by a team of Dutch scientists in order to resolve this solubilisation bottleneck. Ammonia was shown to readily dissolve most varieties of lignin at room temperature and 7-11 bar, and can be removed simply by releasing the pressure.

The mild conditions make ammonia an attractive solvent for biorefineries looking to maximise lignocellulosic biomass utilisation. Furthermore the necessary apparatus is already incorporated into biorefineries for the ammonia fibre explosion (AFEX) process.

This article is open access and available to everyone to read for free:

Lignin solubilisation and gentle fractionation in liquid ammonia

Zea Strassberger, Pepijn Prinsen, Frits van der Klis, Daan S. van Es, Stefania Tanasea and Gadi Rothenberg

Green Chem., 2014, Advance Article. DOI: 10.1039/C4GC01143K

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Alane without aluminum byproduct

pXRD alane synthesis under hydrogenResearchers from Iowa State University have recently developed a route to non-solvated aluminum trihydride (alane), free of metallic aluminum. The reaction occurs at room temperature by the mechanical milling of lithium aluminum hydride and aluminum chloride and a nearly complete conversion can be achieved in 30–60 mins. The formation of aluminum can be entirely avoided above a certain critical pressure, which depends on the nature of the gas and the milling parameters. An intermediate was identified in the process, which reacts to produce alane and lithium chloride.

Due to the impractical conditions required for the direct hydrogenation of aluminum, alternative routes that allow for the large-scale preparation of alane are essential, for example the one described in this paper. The authors have also recently introduced a mechanochemical synthesis of alane using lithium hydride as a starting material, which directly leads to adduct-free alane.

Check out the original article online now:

Solvent-free mechanochemical synthesis of alane, AlH3: effect of pressure on the reaction pathway
S. Gupta, T. Kobayashi, I. Z. Hlova, J. F. Goldston, M. Pruski, and V. K. Pecharsky
Green Chem. 2014, 16, 4378.
DOI: 10.1039/C4GC00998C

Jenna Flogeras obtained her B.Sc. and M.Sc. in Chemistry from the University of New Brunswick (Fredericton), Canada. She is currently a Ph.D. student at Memorial University in Newfoundland, where she studies aluminum-based catalysts under the supervision of Dr. Francesca Kerton.

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Waste office paper comes to a sticky end

Article written by Debbie Houghton

Paper cannot be recycled into new paper indefinitely

A process for generating aluminium–aluminium bonding adhesives from waste office paper could give a purpose to paper than can no longer be recycled into more paper. 

Paper can typically only be recycled as a new paper product 3–4 times, after this the fibres become too short to be used in new paper or cardboard. Finding alternative ways of reusing this readily available resource is crucial.

To read the full article please visit Chemistry World.

Low-temperature microwave-assisted pyrolysis of waste office paper and the application of bio-oil as an Al adhesive
Zhanrong Zhang, Duncan J. Macquarrie, Mario De bruyn, Vitaliy L. Budarin, Andrew J. Hunt, Mark J. Gronnow, Jiajun Fan, Peter S. Shuttleworth, James H. Clark and Avtar S. Matharu  
Green Chem., 2014, Advance Article
DOI: 10.1039/C4GC00768A, Paper

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Walter Leitner and Jürgen Klankermayer – Winners of the European Sustainable Chemistry Award

We are delighted to announce that Walter Leitner, Green Chemistry Editorial Board Chair, has been awarded the 2014 European Sustainable Chemistry Award alongside Jürgen Klankermayer, also from the Institute of Technical and Macromolecular Chemistry at the RWTH Aachen University.

The European Sustainable Chemistry Award is intended to be a prestigious scheme to raise the profile of sustainable chemistry and be a spur to innovation and competitiveness. The ESCA was initially launched in 2010 by EuCheMS and its current prize amounts to €10,000. A full list of sponsors can be found on the website.

The Award covers innovations in the following scientific areas:

– the use of alternative synthetic pathways, that increase resource efficiency and selectivity e.g. with the help of catalysis or natural processes

– the use of alternative feedstocks which are safer and/or renewable e.g. based on biomass

– the use of alternative reactor design and reaction conditions, such as use of solvents which deliver health and environmental benefits, or increased yield and reduced waste and emissions

– the design and use of chemicals and chemical products that are, for example, less environmentally harmful than current alternatives, or inherently safer with regard to hazardous concerns

Visit the website for more information on the EuCheMS and the prizes awarded.

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