Natural adhesive brings new life to old carpets

Sarah Kenwright writes about a hot Green Chemistry paper for Chemistry World

A biotechnological process to transform lignin into an adhesive opens the door on an eco-friendly strategy for recycling carpets, new research shows.

Traditional carpets consist of yarns stuck to a backing fabric by an adhesive – usually synthetic latex. As part of the production process, the latex is cured at high temperatures, but this creates a non-recyclable material as the latex is almost impossible to remove at the end of a carpet’s life. As a result, almost all carpets are disposed of by burning in an incinerator.

With a view to finding a more environmentally friendly solution to carpet disposal, Tzanko Tzanov and his team at the Polytechnic University of Catalonia in Barcelona, Spain, decided to replace the synthetic latex with an organic lignin-based adhesive to produce a renewable woollen floor covering.

Lignin is an aromatic polymer that reinforces cellulose fibres in plants and is readily available as a waste product of paper and biofuel production. 

It can be easily converted into an adhesive using laccase, an enzyme found in plants and fungi. ‘Lignin is transformed by an oxidative enzymatic process that activates the phenolic structures, which can then react chemically with the wool fibres and bind them to the backing,’ explains Tzanov. The process is carried out at much lower temperatures than in latex production – around 50°C rather than 150°C – making it much more environmentally friendly.

The carpets can degrade and be recycled as a soil fertiliser

The laccase enzymes that convert lignin into an adhesive are also involved in its biodegradation, meaning that the carpets can be recycled at the end of their usable life. Instead of being incinerated, the carpets are shredded and returned to nature, where they degrade and can be used as a soil fertiliser.

Diego Moldes Moreira, an expert in natural products and bioprocesses at the University of Vigo in Spain is impressed by the innovative and sustainable solution. ‘We could expect to find the proposed biotech carpets in stores in the short–medium term,’ he says. In fact, Tzanov’s team are already working with Dutch companies, James and Best Wool Carpets, on an industrial scale-up.


You can also read this article in Chemistry World»

Read the original journal article in Green Chemistry – it’s free to access until 27th March:
An enzymatic approach to develop a lignin-based adhesive for wool floor coverings
Elisabetta Aracri, Carlos Díaz Blanco and Tzanko Tzanov  
Green Chem., 2014, Accepted Manuscript, DOI: 10.1039/C4GC00063C, Paper

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Top 10 most accessed Green Chemistry articles in 2013

The 10 most downloaded Green Chemistry articles in 2013 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

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

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

Photocatalysis on supported gold and silver nanoparticles under ultraviolet and visible light irradiation
Sarina Sarina, Eric R. Waclawik and Huaiyong Zhu  
Green Chem., 2013,15, 1814-1833
DOI: 10.1039/C3GC40450A, Tutorial Review

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

Hydrolysis of cellulose to glucose by solid acid catalysts
Yao-Bing Huang and Yao Fu  
Green Chem., 2013,15, 1095-1111
DOI: 10.1039/C3GC40136G, Tutorial Review

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

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
From themed collection Green Chemistry and the Environment

Take a look at the articles, and if you have any comments, please leave them 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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Direct conversion of chitin into a N-containing furan derivative

Chitin is a main constituent of the exoskeletons of insects and crustaceans. Utilizing this biopolymer in the production of value-added chemicals, particularly nitrogen-containing aromatic compounds (e.g., furans), is a more sustainable route than their energy-intensive synthesis from ammonia. Chitin may be subjected to hydrolysis reactions to produce N-acetyl-D-glucosamine (NAG), its monomeric constituent. Kerton et al. previously reported a high-yielding synthesis of 3-acetamido-5-acetylfuran (3A5AF) by the direct dehydration of NAG. In this paper, Kerton and researchers from the National University of Singapore aimed to combine the two steps to generate NAG in situ from chitin and convert it to 3A5AF.Chitin can be transformed into a nitrogen-containing furan derivative (3A5AF)

In order to dissolve chitin, its extensive hydrogen-bonding network must be tempered. The use of polar, aprotic solvents in combination with metal salts can accomplish this challenging task, enabling the dehydration reaction to occur more easily. Chloride-containing salts or additives also facilitate the reaction, which is suspected to occur through their disruptive effect on the hydrogen bonds. Dual or tri-component additive systems of boric acid with alkali or alkaline earth metal chlorides resulted in the highest yields of 3A5AF. The optimized conditions used boric acid and sodium chloride in NMP (N-methyl-2-pyrrolidone) to give ca. 7.5% 3A5AF, while 50% chitin conversion was achieved, representing an array of other products. Pre-treatment of chitin to initiate the depolymerisation was suggested as a potential means to increase 3A5AF yields.

Read this article now, we’ve made it free to access until 3rd March:

Direct conversion of chitin into a N-containing furan derivative
Xi Chen, Shu Ling Chew, Francesca M. Kerton, and Ning Yan
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42436G

Jenna Flogeras obtained her B.Sc. and M.Sc. in Chemistry from the University of New Brunswick (Fredericton), Canada. She is currently working towards her Ph.D. at Memorial University of Newfoundland, under the supervision of Dr. Francesca Kerton. Her research is focused on the synthesis of biodegradable polymers using main-group metal complexes as catalysts.

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A new approach to bio-based PET

Jennifer Lee and George Kraus of Iowa State University have published a new method of producing dimethyl terephthalate, a precursor to polyethylene terephthalate (PET), from renewable sources. In this new work the reaction between methyl coumalate (the esterified dimer of malic acid) and methyl pyruvate (the ester of pyruvic acid) is optimised to provide dimethyl terephthalate in 95% yield.

This is the latest of several approaches currently being developed to supplant the current manufacturing process that produces PET from finite fossil resources. These include the valorisation of citrus waste and the reaction of ethylene with 2,5-dimethylfuran. As is true for the zeolite catalysed fast pyrolysis of certain bio-based resources, these other green methods produce an intermediate aromatic compound, p-xylene or sometimes p-cymene, which must later be oxidised to terephthalic acid. This oxidation reaction is present in the conventional petroleum derived synthesis of PET. The new uncatalysed, solvent-free method of Lee and Kraus circumvents the oxidation stage, and by doing so shortens the synthetic procedure and avoids the use of cobalt or manganese oxidation catalysts, which from an elemental sustainability perspective are vulnerable to depletion.

Free to access until 4th March:

One-pot formal synthesis of biorenewable terephthalic acid from methyl coumalate and methyl pyruvate, J. J. Lee and G. A. Kraus, Green Chemistry, DOI: 10.1039/C3GC42487A

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Green Chemistry issue 2 is now available online

Issue 2 of Green Chemistry is a themed issue on the conversion of biomass with heterogeneous catalysts, Guest Edited by Professors Paul Dauenhauer and George Huber. It’s available to read online now.

GC issue 2 coverThe front cover this month (pictured left) features a review by Jesse Hensley and co-workers from Golden, Colorado. In their article they focus on recent model compound studies of catalysts for hydrodeoxygenation of biomass pyrolysis products, with an emphasis on mechanisms, reaction networks, and structure–function relationships.

Read the full article:
Recent advances in heterogeneous catalysts for bio-oil upgrading via “ex situ catalytic fast pyrolysis”: catalyst development through the study of model compounds
Daniel A. Ruddy, Joshua A. Schaidle, Jack R. Ferrell III, Jun Wang, Luc Moens and Jesse E. Hensley  
Green Chem., 2014, 16, 454-490, DOI: 10.1039/C3GC41354C


GC issue 2 inside coverThe inside front cover this month (pictured right) features work by Andreas Heyden and co-workers from Columbia, South Carolina. In their work they report a theoretical study of the effects of various solvents on the mechanism of the hydrodeoxygenation of propanoic acid over Pd(111).

Read the full article:
Solvent effects on the hydrodeoxygenation of propanoic acid over Pd(111) model surfaces
Sina Behtash, Jianmin Lu, Muhammad Faheem and Andreas Heyden  
Green Chem., 2014, 16, 605-616, DOI: 10.1039/C3GC41368C

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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Magdalena Titirici speaks to Chemistry World about her research on biowaste conversion

Magdalena Titirici is interviewed in Chemsitry Word

Magdalena Titirici speaks to Green Chemistry Deputy Editor Anna Simpson in a recent Chemistry World interview.

Magdalena joined the School of Engineering and Materials Science at Queen Mary, University of London, UK, as a reader in materials science at the beginning of 2013. Before that, she spent over six years leading the sustainable materials for renewable energy group at the Max Planck Institute of Colloids and Interfaces in Potsdam, Germany. Research in the Titirici group involves trying to create porous carbon materials from renewable resources such as lignin, cellulose and chitin, as well municipal and agricultural wastes.

Click here to read the interview with her in Chemistry World, where she discusses her not only her research, but also her love of photography, street art and the electronic music scene!

Some of Magdalena’s most recent Green Chemistry papers are listed below. We’ve made these papers free to access for the next 2 weeks, so click on the links below to find out more about Magdalena’s research…

Original design of nitrogen-doped carbon aerogels from sustainable precursors: application as metal-free oxygen reduction catalysts, Nicolas Brun, Stephanie A. Wohlgemuth, Petre Osiceanu and Magdalena M. Titirici, Green Chem., 2013,15, 2514-2524, DOI: 10.1039/C3GC40904J

A one-pot hydrothermal synthesis of sulfur and nitrogen doped carbon aerogels with enhanced electrocatalytic activity in the oxygen reduction reaction, Stephanie-Angelika Wohlgemuth, Robin Jeremy White, Marc-Georg Willinger, Maria-Magdalena Titirici and Markus Antonietti, Green Chem., 2012,14, 1515-1523, DOI: 10.1039/C2GC35309A

A one-pot hydrothermal synthesis of tunable dual heteroatom-doped carbon microspheres, Stephanie-Angelika Wohlgemuth, Filipe Vilela, Maria-Magdalena Titirici and Markus Antonietti, Green Chem., 2012,14, 741-749, DOI: 10.1039/C2GC16415A

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HOT papers in Green Chemistry

Here are the latest HOT papers published in Green Chemistry as recommended by the referees:

Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis
Nicholas A. Isley, Sebastian Dobarco and Bruce H. Lipshutz  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42188K


Design and evaluation of switchable-hydrophilicity solvents
Jesse R. Vanderveen, Jeremy Durelle and Philip G. Jessop  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42164C

 


Cleaving C–H bonds with hyperthermal H2: facile chemistry to cross-link organic molecules under low chemical- and energy-loads
Tomas Trebicky, Patrick Crewdson, Maxim Paliy, Igor Bello, Heng-Yong Nie, Zhi Zheng, Xiaoli Fan, Jun Yang, Elizabeth R. Gillies, Changyu Tang, Hao Liu, K. W. Wong and W. M. Lau  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC41460D

 


Sustainable polyesters for powder coating applications from recycled PET, isosorbide and succinic acid
C. Gioia, M. Vannini, P. Marchese, A. Minesso, R. Cavalieri, M. Colonna and A. Celli  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42122H

 

All the papers listed above are free to access for the next 4 weeks!

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AMI to hold 3rd international conference on sustainable production of plastics and elastomers

For the future generations the world needs to move towards a renewable supply structure including materials and AMI is bringing together a group of concerned professionals and expert scientists at Green Polymer Chemistry 2014, which takes place from 18th to 20th March 2014 at the Maritim Hotel in Cologne, Germany.

Green Polymer Chemistry 2014 provides an ideal forum for today’s market, as the polymer industry looks at alternatives to petrochemical sources to ensure a viable long-term future. The conference will stimulate a debate on feedstock for polymers, green polymers, performance plastics and monomer sourcing.

Green Polymer Chemistry 2014 offers an excellent networking and sourcing opportunity for brand owners, environment and sustainability managers, business development and innovation professionals, chemical engineers, plastics manufacturers, agriculture specialists, biorefinery experts, biochemists, researchers, and suppliers to the industry to debate sustainable, economic solutions for polymer synthesis.

Attending, Exhibiting and Sponsoring
For details on attending, exhibiting or sponsoring this event, please contact Kat Langner.
E: kl@amiplastics.com T: +44 (0) 117 924 9442

Green Polymer Chemistry 2014
18–20th March 2014, Maritim Hotel, Cologne, Germany
Website:
http://amiplastics.com/events/Event.aspx?code=C564&sec=3717
Brochure: http://amiplastics.com/Events/Resources/Programme/Green%20Polymer%20Chemistry%202014%20Brochure.pdf

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HOT papers in Green Chemistry

Here are the latest HOT papers published in Green Chemistry, as recommended by the referees:

One-pot two-step mechanochemical synthesis: ligand and complex preparation without isolating intermediates
Michael Ferguson, Nicola Giri, Xu Huang, David Apperley and Stuart L. James  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42141D


Studies on the oxidative N-demethylation of atropine, thebaine and oxycodone using a FeIII-TAML catalyst
Duy D. Do Pham, Geoffrey F. Kelso, Yuanzhong Yang and Milton T. W. Hearn  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC41972J


Lignin extraction from biomass with protic ionic liquids
Ezinne C. Achinivu, Reagan M. Howard, Guoqing Li, Hanna Gracz and Wesley A. Henderson  
Green Chem., 2014, Advance Article, DOI: 10.1039/C3GC42306A


In an attempt to provide green solvent selection guide for olefin metathesis
Tomasz Krzysztof Olszewski, Krzysztof Skowerski, Andrzej Tracz and Jacek Bialecki  
Green Chem., 2013, Accepted Manuscript, DOI: 10.1039/C3GC41943F

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All the papers listed above are free to access for the next 4 weeks!

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Professor Buxing Han elected as Academician of the Chinese Academy of Sciences

Professor Buxing Han has been elected as an Academician of the Chinese Academy of Sciences

Professor Buxing Han (pictured) has been elected as an Academician of the Chinese Academy of Sciences

Professor Buxing Han has been awarded the prestigious honour of Academician of the Chinese Academy of Sciences. Academician is a lifelong honour and the highest academic title given to Chinese scientists and experts working in scientific and technological fields. Professor Han has received this award for his contribution to the chemical sciences; his research interests include the chemical thermodynamics of green solvent systems and applications of green solvents in chemical reactions and material synthesis. We would like to take this opportunity to congratulate him on this great achievement.

Professor Han has also taken on the role of  Associate Editor for Green Chemistry from 2014, handling submissions in the areas of green solvents, CO2 and biomass conversion. He joins Professor C.-J. Li and our experienced in-house Editorial team in handling submissions to the Journal. We welcome him to this new role.

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