LCA study expresses caution over assuming bio-based is green

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.

A new study comparing life cycle assessments has shown that changing from a fossil derived feedstock to biomass is not necessarily beneficial to the environment. A reliance on food crops and inefficient conversion into chemical products will cause impact the environmental and result in an expensive product, also limiting its commercial opportunities.

Taking the example of hexamethylenediamine, the precursor to nylon-66, scientists based at Solvay in China have shown that the benefit of adopting a renewable feedstock (starch, in this instance) is counteracted by eutrophication concerns and greenhouse gas emissions. The issue largely stems from the cultivation of the biomass and the energy required to process the starch into chemical intermediates. The renewable route requires several high energy transformations to remove the original functionality of the biomass and obtain the conventional nylon monomer.

One lesson to be taken from this study is to give greater consideration to novel bio-based polymers that can be produced advantageously from bio-based feedstocks. Ideally, these would include wastes and agricultural by-products, thus making use of the reactive chemical groups inherent to the biomass rather than removing them.

Hexamethylenediamine (HMDA) from Fossil vs. Bio-based Routes: An Economic and Life Cycle Assessment Comparative Study

A. B. Dros et al., Green Chem., 2015, advanced article. DOI: 10.1039/C5GC01549A

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Recent HOT articles in Green Chemistry

The following HOT articles have been highlighted by the reviewers of the articles as being particularly interesting or significant pieces of research. These are all free to access until 30/09/2015. The order they appear in the list has no meaning or ranking.


Tandem Lewis/Brønsted homogeneous acid catalysis: conversion of glucose to 5-hydoxymethylfurfural in an aqueous chromium(III) chloride and hydrochloric acid solution
T. Dallas Swift, Hannah Nguyen, Andrzej Anderko, Vladimiros Nikolakis and Dionisios G. Vlachos
Journal Article
DOI: 10.1039/C5GC01257K, Paper

C5GC01257K GA


Expanding the scope of biogenic substrates for the selective production of formic acid from water-insoluble and wet waste biomass
Jakob Albert and Peter Wasserscheid
Journal Article
DOI: 10.1039/C5GC01474C, Paper

C5GC01474C GA


Hybrid bipolar membrane electrodialysis/ultrafiltration technology assisted by a pulsed electric field for casein production
Sergey Mikhaylin, Victor Nikonenko, Gérald Pourcelly and Laurent Bazinet
Journal Article
DOI: 10.1039/C5GC00970G, Paper

C5GC00970G GA


Solvent free depolymerization of Kraft lignin to alkyl-phenolics using supported NiMo and CoMo catalysts
Chowdari Ramesh Kumar, Narani Anand, Arjan Kloekhorst, Catia Cannilla, Giuseppe Bonura, Francesco Frusteri, Katalin Barta and Hero Jan Heeres
Journal Article
DOI: 10.1039/C5GC01641J, Paper
From themed collection Lignin chemistry and valorisation

C5GC01641J GA


An interchangeable homogeneous ⇔ heterogeneous catalyst system for furfural upgrading
Lu Wang and Eugene Y.-X. Chen
Journal Article
DOI: 10.1039/C5GC01648G, Communication

C5GC01648G GA


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Re-routing aromatic degradation to give pyridine dicarboxylic acids

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.

Biocatalytic conversion of lignin to aromatic dicarboxylic acids in Rhodococcus jostii RHA1 by re-routing aromatic degradation pathwaysBritish scientists, lead by Professor Tim Bugg at the University of Warwick, have reported a new method of converting lignin into useful monomers for the chemical industry. Processing difficulties mean that lignin remains an underutilised resource for the production of renewable chemicals. Only with the development of efficient depolymerisation methods will the potential of these waste products be realised. In this latest advance, the metabolic pathways in the bacterium Rhodococcus jostii RHA1 for the degradation of  lignin have been re-routed to generate aromatic dicarboxylic acids. Insertion of recombinant genes into R. jostii RHA1, followed by ammonia cyclisation generates pyridine-2,4-dicarboxylic acid or pyridine-2,5-dicarboxylic acid in yields of up to 125 mg L−1 from a wheat straw lignocellulose feed. The products have been identified as the building blocks of new bio-based polymers, and could help contribute to biomass resource efficiency and growth in the bio-polymer market.

This article is free to access untill 31st August 2015:

Biocatalytic conversion of lignin to aromatic dicarboxylic acids in Rhodococcus jostii RHA1 by re-routing aromatic degradation pathways, Z. Mycroft, M. Gomis, P. Mines, P. Law and T. D. H. Bugg, Green Chem., 2015, Advance Article. DOI: 10.1039/C5GC01347J

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From chip fat to biofuel

Abigail Hallowes writes about a hot Green Chemistry article for Chemistry World

Chips in deep fat fryer

© Shutterstock

Researchers from Singapore and China have developed a cheap and green catalytic system for turning fatty acids into fuel that doesn’t require hydrogen or a solvent.

Hydrocarbon biofuels made from waste fats and oils, such as leftover cooking oil could help reduce our dependence on fossil fuels. Traditionally, these biofuels are synthesised by transesterifying lipids under harsh alkaline conditions; in addition to generating waste solvent, this technique does not remove enough oxygen, so the products are incompatible with diesel engines. The process also doesn’t work with fatty acids as they become soapy and deactivate the catalyst. Read the full article in Chemistry World»


Read the original journal article in Green Chemistry – it’s free to access until 17th August:
Effective deoxygenation of fatty acids over Ni(OAc)2 in the absence of H2 and solvent
Wenjing Li, Yongjun Gao, Siyu Yao, Ding Ma and Ning Yan 
DOI: 10.1039/C5GC01147G, Paper

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Bread leavening proves useful for energy storage

Debbie Houghton writes about a hot Green Chemistry article for Chemistry World

Freshly baked bread

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 Just like bread, hierarchically porous carbons (HPCs), are judged on their texture; so researchers in China have called on their baking know-how to cook up a sustainable method for producing these supercapacitor components

 HPCs could prove useful in energy storage because of their high surface area and short ion transport pathway. But existing synthetic methods for producing HPCs, including nanocasting and soft-templating, are unfeasible for industrial application as they require complex, expensive processes. Read the full article in Chemistry World» 


Read the original journal article in Green Chemistry – it’s free to access until 3rd August:
Inspired by bread leavening: one-pot synthesis of hierarchically porous carbon for supercapacitors
Jiang Deng, Tianyi Xiong, Fan Xu, Mingming Li, Chuanlong Han, Yutong Gong, Haiyan Wang and Yong Wang 
DOI: 10.1039/C5GC00523J, Pape

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Green Chemistry Strategies for Drug Discovery

It is rapidly becoming clear that by incorporating green chemistry techniques earlier in drug development, pharmaceutical companies can greatly speed the production of a drug candidate.

Integrating green chemistry protocol into the drug discovery discipline is a relatively new phenomenon, as the scale at which chemists operate in drug discovery is smaller than in process and manufacturing chemistry.

Written by experts pioneering green chemistry efforts within their own institutions, Green Chemistry Strategies for Drug Discovery provides a practical guide illustrating to both academic and industrial labs how to implement greener process approaches for the greatest return on their investment, and without slowing down their science.

The Editors have taken a comprehensive approach to this emerging field, covering the entire drug discovery process from molecule conception, through synthesis, formulation and toxicology, with specific examples and case studies where green chemistry strategies have been implemented. They also address cutting-edge topics like biologics discovery, continuous processing and intellectual property.

Green Chemistry Strategies for Drug Discovery is the newest publication in the RSC Drug Discovery series. Further details on the content and scope of this book can be found on its Books Publishing page. If you like what you read, Green Chemistry Strategies for Drug Discovery is available now as a hardback from our Royal Society of Chemistry Bookshop. It is also in our 2015 eBook collection.

Front cover of "Green Chemistry for Drug Discovery"

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Chip fat to biofuel made easy

It is possible to synthesise hydrocarbon biofuel from waste fats and oils, such as cooking oils. Traditionally this process occurs with a catalyst under harsh alkaline conditions and in the presence of hydrogen. As a result, waste solvent is produced and not enough oxygen is removed for compatibility with diesel engines. In addition, with the presence of fatty acids the process does not work and the catalyst is deactivated.

In recent experiments, Ding Ma (Peking University) and Ning Yan (National University of Singapore), tested a series of nickel-based salts as pre-catalysits for deoxygenating fatty acids and triglycerides and forming shorter chain hydrocarbons, without the need for a solvent or hydrogen. The nickel nanoparticles that are formed act as a catalytic species and are stabilised by the presence of fatty acids. Although these preliminary results look promising, a lot more research into the applications and commercial viability of the findings are required.

Do you want to find out more?

Read the full Chemistry World article by Abigail Hallowes

Or, take a look at the original article which is free to access until 17th August 2015:

Effective deoxygenation of fatty acids over Ni(OAc)2 in the absence of H2and solvent” by W. Li et al., DOI:10.1039/c5gc01147g

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Christian Stevens wins Emerging Technologies Competition 2015

Green Chemistry Advisory Board member Christian Stevens has won first prize in the Energy & sustainability stream of the Royal Society of Chemistry’s Emerging Technologies Competition 2015. In this third year of the competition, applications were also accepted from outside the UK which enabled Christian and Wouter Ducheyne, of Ghent University and Caloritum in Belgium, achieve this success.

Their winning technology is a ‘Chemical pump for recovery of industrial waste heat’ and was developed jointly by the University of Ghent and Caloritum. It is an industrial chemical heat pump that can recover waste heat between 75-150°C and increase this to a useful heat level of over 200°C. This is a bio-inspired technology, being based on the phosphate transfer in the ATP-ADP cycle that occurs in the human body. Addressing a problem that cost the EU over €52bn per year, the patented technology can be implemented in production processes ranging from the petrochemical industry to food production and power generation.

The Emerging Technologies Competition is the Royal Society of Chemistry’s flagship annual innovation event and saw thirty teams pitch their emerging technologies to experienced judging panels. There are three streams to the competition: Healthcare, Energy & sustainability, and Materials and the top three teams in each stream received a prize at the ceremony on Monday 29th June 2015. First prize winners receive a cash prize of £20,000, a profile in Chemistry World magazine, and a personalised package of tailored business support from one or more of the competition partner companies – all of which are major multinationals (such as Croda, Procter & Gamble, Pfizer, GSK etc.) with considerable experience in bringing new products to market.

We would like to congratulate Christian Stevens and Wouter Ducheyne for achieving this accolade.

Pictured: Christian Stevens (left) and Wouter Ducheyne (right), pitching at the annual innovation event.

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New Green Chemistry Board Member: Martina Peters

We are pleased to welcome Dr Martina Peters as a new Green Chemistry Editorial Board Member.

Martina Peters studied Chemistry at RWTH Aachen University in Germany and at the University of Colorado at Boulder, USA. She finished her PhD with Prof. Walter Leitner at RWTH Aachen University in 2008 and continued as PostDoc at the CAT Catalytic Center at RWTH Aachen. In 2010 she joined Bayer Technology Services as project manager, focusing on chemical utilization of CO2 as C1-building block for polymers. In 2012 she became head of “Chemical Catalysis” at Bayer Technology Services, a team providing chemical expertise for different areas of application within Bayer. Since mid-2014 Martina is a senior strategists at Bayer AG in the area of Technology and Manufacturing Strategy. In her free time she enjoys doing sports, especially mountain biking.

Take a look at some of her contributions to Royal Society of Chemistry Journals (free to access until 30th August 2015):

Life cycle assessment of CO2 capture and utilization: a tutorial review, Niklas von der Assen, Philip Voll, Martina Peters and André Bardow , Chem. Soc. Rev., 2014,43, 7982-7994, DOI: 10.1039/C3CS60373C

Screening of new solvents for artemisinin extraction process using ab initio methodology, Alexei A. Lapkin, Martina Peters, Lasse Greiner, Smain Chemat, Kai Leonhard, Marcel A. Liauw and Walter Leitner, Green Chem., 2010,12, 241-251, DOI: 10.1039/B922001A

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Plant waste solar panels

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.

 A low cost, low energy route to solar grade silicon from rice hull ash (RHA), a sustainable source High purity silicon is essential for manufacturing solar panels. Unfortunately this prerequisite conversion of silica to elemental silicon requires a lot of energy, and the associated greenhouse gas emissions are significant. It has now been demonstrated that the ashes from burning biomass (rice hulls in this case) can provide a rich source of silica than can be reduced to give solar grade silicon.

For the preparation of the silica from rice hull ash only dilute acid and hot water are required. The energy requirement to then produce 99.9999% pure silicon is an order of magnitude less than the conventional process and is actually lower than the energy created by burning the rice hulls in the first place. As the carbon dioxide generated by burning biomass is originally fixed from the atmosphere by plants, the carbon footprint for the production of this sustainable silicon is very low.

Read the advanced article in Green Chemistry online now:

A low cost, low energy route to solar grade silicon from rice hull ash (RHA), a sustainable source

Julien C. Marchal, David J. Krug III, Patrick McDonnell, Kai Sun and Richard M. Laine

Green Chem., 2015, Advance Article. DOI: 10.1039/C5GC00622H

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