Tag Archives: plastic

Turning Biofuel Waste Into Valuable Platform Chemicals

Scientists have recently demonstrated a faster and more efficient way of turning biofuel waste into highly valuable chemicals. These findings could have a significant impact on the economics of making fuels and other products from renewable sources.

Lignin is a component of an abundant dry plant matter called lignocellulosic biomass. This biomass source makes up the cell walls of plants and enables the upwards transport of water and provides protection against environmental stress and microbial attacks. Due to the rigidness of its structure, lignin is difficult to break down. Scientists have been trying to find methods for extracting its valuable compounds for decades, as these compounds could subsidize biofuel production, making the cost of biofuel a more competitive alternative to petroleum.

Lignin Structure. Source: Wikimedia Commons

Seema Singh and a group of researchers from Sandia National Laboratories recently studied the metabolic pathway of a soil bacteria that can naturally break down lignin. They used this metabolic pathway to come up with a method of extracting lignin’s valuable platform chemicals. The method involved genetically engineering a tobacco plant to produce large amounts of an intermediate compound called protocatechuate (PCA) as it grew. This compound was then extracted from the plant without the need to break down the lignin. Next, an engineered E. coli was added to convert the PCA into muconic acid with a yield 34% greater than previous conversion methods.

Muconic acid and pyrogallol, another product obtained using this method, are platform chemicals that are currently only derived from petroleum, and together, have a combined market value of $255.7 billion. Muconic acid can be turned into plastics, nylon, resins, and lubricants; and pyragallol has applications in cancer treatment drugs.

Nylon 6,6. Source: Wikimedia Commons

The next challenge in this field will be to maximize the yield and rate of production of these chemicals. In order for this method to be used on an industrial scale, large amounts of muconic acid and pyragallol must be produced in a short amount of time to compete with the current petroleum derived methods.

– Joseph Bergvinsom

New Bioinspired Polymer

Materials chemists have designed a polymer that is both stretchy and strong. This polymer could lead to a new family of biomaterials which are able to heal themselves upon sustaining damage, along with being able to disparate materials such as metals and wood.

Linear Polymers – Taken by Yurko – Own work, CC BY-SA 3.0, Wikimedia Creative Commons

The most common approach to polymer synthesis is to covalently link monomers – the building blocks of polymers – together into long chains. These polymers are typically stiff and not too strong. Another approach involves ionically linking charged polymer chains together to create loosely-linked, flexible materials. Due to the electrostatic interactions between these polymers, they will reattach or “heal” upon separation.

Saltwater mussels naturally create polymers using a combination of these two methods, which result in polymers with both covalent and ionic bonds. Scientists have been trying to synthetically replicate these polymers by adding negatively charged groups called catechols to a gel containing covalently linked polymers. Upon adding positively charged iron atoms to a solution of this, the catechols, located on the polymer strands form ionic bonds with them. This results in strong polymers which are able to heal themselves. The problem with this method is that the salt water in which the reaction takes place causes the gel to expand, thus limiting the stretching ability of the resulting polymer.

Saltwater Mussels – Taken by Mark A. Wilson (Department of Geology, The College of Wooster). Public Domain

Valentine and a team of researchers were able to adapt this strategy to work in a dry environment. They added catechol groups to a gel containing covalently linked polyethylene glycol (PEG) polymers. Capping reagents were added to the catechols during the reaction to prevent their reaction with oxygen in the air or water. Before spritzing in iron, these capping groups were removed with acid. The iron atoms diffused through the PEG to react with the catechols to form additional linkage. The resulting polymer was found to be 100 to 1000 times stiffer than the polyethylene glycol, yet very flexible.

Given that this new polymer forms materials that can withstand forces that would rupture normal PEG-based materials, it might lead to a new family of biomaterials which are able to heal themselves upon sustaining damage and could be used in artificial tendons or joints for prosthetics to help minimize wear and tear.