An environmentally friendlier approach to hydrometallurgy

Scientists from Belgium have developed an environmentally friendly route to separate cobalt from nickel, magnesium and calcium in chloride medium.

Koen Binnemans and colleagues from KU Leuven and Umicore, Belgium used undiluted phosphonium-based ionic liquids as the extractants with tri(hexyl)tetradecylphosphonium chloride (Cyphos IL 101) as the best ionic liquid tested in terms of commercial availability, separation characteristics and ease of handling.  The main advantage of their method is the fact that no organic diluents are required and thus volatile organic solvents can be avoided. The process enabled separation factors greater than 50 000 to be observed for cobalt/nickel separation.  In addition, the ionic liquid can easily be recovered and reused as extractant so there is potential for a continuous extraction process to be developed.

This article is free to access until the 6th June 2012!  Click on the link below to find out more…

An environmentally friendlier approach to hydrometallurgy: highly selective separation of cobalt from nickel by solvent extraction with undiluted phosphonium ionic liquids, Sil Wellens, Ben Thijs and Koen Binnemans, Green Chem., 2012, DOI: 10.1039/C2GC35246J

You may also be interested in this article too – free to access for 2 weeks:

Processing of metals and metal oxides using ionic liquids, Andrew P. Abbott, Gero Frisch, Jennifer Hartley and Karl S. Ryder, Green Chem., 2011, 13, 471-481

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Green Solvents 2012 – Submission deadline extended to the 15th May!

The deadline for submission of abstracts for the ‘Green Solvents – Advanced Concepts for Solution Phase Chemistry and Processes‘ has been extended to the 15th May 2012.  This conference will be taking place between the 7th-10th October in picturesque Boppard, Germany.

This event is part of the biennial conference series “Green Solvents” and this year’s scientific focus lies on energy-efficient processes, selectivity control for waste prevention, alternative and efficient use of raw materials, activation and capture of CO2 and integrated reaction and separation processes.

Submit your abstract now!

For more information about the many renowned invited speakers, the topics and abstract submission, please visit: www.dechema.de/gsfs2012.

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Green Chemistry issue 5 – now online!

The latest issue of Green Chemistryissue 5 – is now published online.

The front cover of this issue features work by James Dumesic and co-workers from the University of Wisconsin-Madison, USA.  In this paper, the authors report the selective hydrogenation of biomass-derived 5-hydroxymethylfurfural using heterogeneous catalysts.  A variety of supported catalysts in monophasic and biphasic reactions systems were studied to determine the effects of the metal, support, solution phase acidity and solvent on the selectivity of the reaction.  The authors found that Ru supported on materials with high isoelectric points (e.g. ceria and γ-alumina) gave the highest yields.

The selective hydrogenation of biomass-derived 5-hydroxymethylfurfural using heterogeneous catalysts, Ricardo Alamillo, Mark Tucker, Mei Chia, Yomaira Pagán-Torres and James Dumesic, Green Chem., 2012, 14, 1413-1419

The inside front cover of this issue highlights work by Klavs Jensen and Xiaoying Liu from Massachusetts Institute of Technology, USA, who report the direct oxidative amidation of aromatic aldehydes in a continuous flow microreactor system using aqueous hydrogen peroxide.  This method allows amides to be synthesized from secondary amines and aromatic aldehydes in a single operation under mild conditions within 15-40 mins.  The procedure does not require catalysts or promoting reagents.

Direct oxidative amidation of aromatic aldehydes using aqueous hydrogen peroxide in continuous flow microreactor systems, Xiaoying Liu and Klavs F. Jensen, Green Chem., 2012, 14, 1471-1474

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2012 Berkeley Centre for Green Chemistry Conference

The BCGC 2nd Annual Conference in Green Chemistry: Collaborative Approaches and New Solutions is being held at the University of California Berkeley on the 3rd May 2012.

The Spring 2012 BCGC Green Chemistry meeting will build awareness of Green Chemistry’s growing role in education, research and outreach on and off campus.

The morning speakers will each speak to one of the Center’s core research or outreach themes: (1) Advancing legislation to incentivize greener solutions (2) Creating new catalysts for green chemical transformations, (3) Promoting greener materials selection with quantitative tools and metrics, and (4) Developing an ethics for decision making in green chemistry. 

During the afternoon session we will host two panel discussions highlighting two of our most integrated interdisciplinary initiatives at the BCGC: (1) How should we advance an interdisciplinary approach to education in green chemistry at UC Berkeley and other Universities? (2) What is the role of biobased chemicals and products in a greener market place?

Confirmed speakers at the event include: Debbie Raphael, California Department of Toxic Substances Control; John Hartwig, UC Berkeley Department of Chemistry; Lauren Heine, Cleaner Production Action; John Warner, Warner Babcock Institute for Green Chemistry; Bill Tolman, University of Minnesota Department of Chemistry; Roger McFadden, Staples, Steve Hahn, Dow Chemical and Joan Blades, Founder of MoveOn.org and MomsRising.org.

Click here to find out more…

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Top ten most accessed articles in March

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

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

Synthesis and analytical applications of photoluminescent carbon nanodots
Pin-Che Hsu, Zih-Yu Shih, Chia-Hsin Lee and Huan-Tsung Chang
Green Chem., 2012, 14, 917-920 ,  DOI: 10.1039/C2GC16451E

A highly efficient Cu-catalyst system for N-arylation of azoles in water
Deping Wang, Fuxing Zhang, Daizhi Kuang, Jiangxi Yu and Junhua Li
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC35077G

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, Advance Article, DOI: 10.1039/C2GC35203F

The selective hydrogenation of biomass-derived 5-hydroxymethylfurfural using heterogeneous catalysts
Ricardo Alamillo, Mark Tucker, Mei Chia, Yomaira Pagán-Torres and James Dumesic
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC35039D

Highly efficient and selective sunlight-induced photocatalytic oxidation of cyclohexane on an eco-catalyst under a CO2 atmosphere
Yusuke Ide, Hideya Hattori, Shuhei Ogo, Masahiro Sadakane and Tsuneji Sano
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16594E

The synthesis of N-heterocycles via copper/TEMPO catalysed aerobic oxidation of amino alcohols
James C. A. Flanagan, Laura M. Dornan, Mark G. McLaughlin, Niall G. McCreanor, Matthew J. Cook and Mark J. Muldoon
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC35062A

Solvent-free bromination reactions with sodium bromide and oxone promoted by mechanical milling
Guan-Wu Wang and Jie Gao
Green Chem., 2012, 14, 1125-1131, DOI: 10.1039/C2GC16606B

Exploring the ruthenium catalysed synthesis of γ-valerolactone in alcohols and utilisation of mild solvent-free reaction conditions
Mohammad G. Al-Shaal, William R. H. Wright and Regina Palkovits
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16631C

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

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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4th International IUPAC Conference on Green Chemistry

The 4th International IUPAC Conference on Green Chemistry (4th ICGC) will be held in Foz do Iguaçu, Brazil between the 25-29th August 2012. 

The 4th ICGC will focus on broad topics including benign synthesis/processes, green chemistry for energy production, chemicals from renewable resources, green engineering, education in green chemistry and engineering and policy.  The conference will be held in Foz do Iguaçu, one of the most beautiful tourist destinations in Latin America.

Confirmed Plenary lectaures are: Paul Anastas (Yale University, USA), James Clark (University of York, UK), Jairton Dupont (University of Rio Grande do Sul, Brazil), Buxing Han (Chinese Academy of Sciences, China), Adelio Machado (Porto University, Portugal), Anita Marsaioli (University of Campinas, Brazil), Robin Rogers (University of Alabama, USA), Karl Barry Sharpless (Scripps Research Institute, USA), Roger Sheldon (Delft University, The Netherlands) and Rajendar S. Varma (EPA, USA).

Submission of abstracts and early bird registration must be completed by the 15th May.  For more information, please visit the website.

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Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water

A supported organaocatalyst has been developed for direct asymmetric Aldol reaction in water with higher enantioselectivity than the original homogeneous catalyst.

Asymmetric organocatalyst is considered to be a very powerful tool for stereoselective synthesis on enantiomerically enriched compounds.  However, organocatalytic reactions, whilst avoiding many of the problems associated with metal catalysts, often require high catalyst loadings and tedious purification of the products. 

In this work, Roser Pleixats and colleagues from the Autonomous University of Barcelona, the University of Alicante (Spain) and the Institute Charles Gerhardt Montpellier (France), have developed a recyclable silica-supported prolinamide organocatalyst.  The catalyst was applied to the direct asymmetric Aldol reaction, and allowed reactions to be conducted exclusively in water without the need of a co-catalyst.  This also resulted in easier isolation of the product and good recycling (at least three times) of the catalyst without the need for regeneration. 

This article is free to access until the 24th May 2012!  Click on the link below to find out more…

Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water, Amàlia Monge-Marcet, Xavier Cattoën, Diego A. Alonso, Carmen Nájera, Michel Wong Chi Man and Roser Pleixats, Green Chem., 2012, DOI: 10.1039/C2GC35227C

You may also be interested in the following article as well – free to access for 2 weeks!

Advances in catalytic metal-free reductions: from bio-inspired concepts to applications in the organocatalytic synthesis of pharmaceuticals and natural products, Magnus Rueping, Jeremy Dufour and Fenja R. Schoepke, Green Chem., 2011, 13, 1084-1105

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Meet our Authors: Pedro Lozano

Pedro Lozano in a Professor of Biochemistry and Molecular Biology at the University of Murcia, Spain.  His current research interests are related to enzyme technology with particular focus on the use of enzymes in ionic liquids and supercritical fluids.  Pedro took time out from his work to speak to Green Chemistry

Who or what initially inspired you to become a chemist?

My interest in experimental sciences began during my training at High School, which awoke my passion to know and understand all the phenomena of Nature. The choice to be a chemist was really accidental, because belonging to a family with few economic resources I had to study at the public University nearest my home, the University of Murcia. In 1979, Chemistry was the only experimental sciences degree offered this university. However, during the last two years of training in Chemistry, I chose the specialty of Biochemistry, allowing me to discover not only that the essence of life is chemistry, but also the enormous potential of applying biological systems to develop chemical processes of industrial interest in the context of Biotechnology. In fact, my PhD dealt with a cross-flow membrane reactor with immobilized pectinases to continuously produce clarified fruit juices.

What has been the motivation behind your recent research?

During the 90’s, my research was focused on the application of proteases to peptide synthesis in non-conventional media, mainly organic solvents and supercritical fluids. I came across supercritical fluids during my postdoctoral training at the Centre de Bioengenierie Gilbert Durand at Toulouse. I realized that there was a whole world to discover using biocatalytic systems in combination with these new solvents. Then by chance, in 1999 I met Dr. Michel Vaultier who was visiting the University of Murcia, and it was he who introduced me to ionic liquids. Also, the paper of Prof Joan F. Brennecke, (Nature, 1999, 399, 28-29) was a source of inspiration. Since that time, the combination of the catalytic excellence of enzymes with the unique characteristics of both supercritical fluids and ionic liquids has been a constant in my research activities. The idea of being able to perform clean and continuous catalytic processes under non-aqueous conditions using the inherent advantages of enzymes for processes of industrial interest is the final aim. At this moment, both dynamic kinetic resolutions and the enzymatic synthesis of biodiesel are the two processes under study, because of their possible application to important strategic sectors of the pharmaceutical and biofuels industries, respectively. However, the small size of our laboratory, the lack of human and material resources and an excessive teaching load are clear limitations to any research development.

What do you see as the main challenges facing research in this area?

Today, the big challenge, not only in this field, is to be able to do research in Spain in the deep economic crisis.

Outside this context, to provide a sufficiently high level of activity and stability to the enzymes to carry out synthetic processes in an overall reaction and separation approach is an important challenge. In the case of chemoenzymatic processes, it is important to have an active and selective chemical catalyst for the racemisation step, as it must also preserve (or at least, not destroy) the catalytic properties of enzymes for the kinetic resolution step. For instance, we have developed appropriate chemoenzymatic systems for the dynamic kinetic resolution of a sec-arylalcohol, but there are other sec-compounds like sec-amines, sec-thiols, etc. (in aryl and alkyl compounds), but there are many candidate reactions waiting to be studied. In the case of the enzymatic synthesis of biodiesel, our original contribution concerned the use of ILs with a large alkyl-side chain in their cations. This provides efficient monophasic reaction systems for enzyme catalysis, and opened the door to their industrial application. The full transformation of vegetable oil into biofuel molecules, without the undesirable production of glycerol is a very interesting challenge for any multicatalytic system.

Where do you see the field of Green Chemistry being in 5 or 10 years time?

The main overall challenge for the 21st century is to ensure truly sustainable development, as it is defined by the Brundtland Report, “development that meets the needs of the present without compromising the ability of future generations to meet their own need”, where the implementation of the twelve Principles of Green Chemistry, masterfully defined by Prof. Paul T. Anastas, is a good roadmap to follow. In the next 10 years, the interest of the society in green chemistry will be at its highest level, because of the profound changes that it should be occur in the chemical industry sector. Green Chemistry research should make efforts to combine selective catalysts with clean reaction media, by using sustainable approaches for product recovery and to enable the recycling/reuse of these reaction media. To transfer the exquisite efficiency shown by enzymes in nature to chemical processes may constitute the most powerful toolbox for developing a clean and sustainable chemical industry in the near future.

And finally…

If you could not be a scientist, but could be anything else, what would you be?

Really, research is vocational, and provides scientists with the enormous pleasure of having a job they enjoy. In my case, I am very lucky with my job. Furthermore, I like to work and I enjoy working…. As an undergraduate, I had many jobs during the summers to earn money to finance my studies. So, if I had not been a scientist, I do not know what other job had I would have chosen, but I am sure that it would be a job of service to society, which I would enjoy.

Take a look a couple of Pedro’s recent articles in Green Chemistryfree to access until the 22nd May 2012:

Stabilizing immobilized cellulase by ionic liquids for saccharification of cellulose solutions in 1-butyl-3-methylimidazolium chloride, Pedro Lozano, Berenice Bernal, Juana M. Bernal, Mathieu Pucheault and Michel Vaultier, Green Chem., 2011, 13, 1406-1410

An efficient activity ionic liquid-enzyme system for biodiesel production, Teresa De Diego, Arturo Manjón, Pedro Lozano, Michel Vaultier and José L. Iborra, Green Chem., 2011, 13, 444-451

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Green Solvents 2012 – Submission deadline extended to the 30th April 2012!

The latest event in the biennial ‘Green Solvents for Synthesis‘ conference series is being held on the 7th-10th October 2012 in Boppard, Germany – Advanced Concepts for Solution Phase Chemistry and Processes.

The submission deadline for abstracts for oral and poster presentations has now been extended to the 30th April 2012!  To submit your abstract or for more details, please click here.

This year’s scientific focus lies on energy-efficient processes, selectivity control for waste prevention, alternative and efficient use of raw materials, activation and capture of CO2 and integrated reaction and separation processes.

The scientific programme features the traditional Sunday evening lecture, keynote lectures by renowned experts in the field and submitted oral presentations.  An additional highlight is the poster session which will give you the opportunity for gripping discussions on cutting-edge research results.

More information can be found at the conference website: http://events.dechema.de/events/en/gsfs2012.html.  Registration for the event will open by the end of June.

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Perspective: Process intensification strategies and membrane engineering

In this perspective, Enrico Drioli and colleagues evaluate how membrane systems can help achieve ‘green process engineering’.

The principles of a process intensification strategy can lead to the development and redesign of new processes which are more compact and efficient than their traditional counterparts.  These new processes can allow for better exploitation of raw materials, lower energy consumption and a reduced plant volume.  Membrane technologies can be seen as contributing to these principles and over the last few years, the scope for membrane operations has become widely recognised.

In this perspective article, the authors provide an overview of membrane applications and their perspectives in the fields of hydrogen production and distillation will be analysied through case studies.  The aim of this review is to show how redesigning traditional operations as membrane systems might contribute to the realization of the goals of process intensification. 

This article is free to access until the 16th May 2012! Click on the link below to find out more…

Process intensification strategies and membrane engineering, Enrico Drioli, Adele Brunetti, Gianluca Di Profio and Giuseppe Barbieri, Green Chem., 2012, DOI: 10.1039/C2GC16668B

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