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EMBARGOED FOR RELEASE: Monday, April 5, 2021, 5 a.m. Eastern Time
Note to journalists: Please report that this research will be presented at a meeting of the American Chemical Society.
Newswise — WASHINGTON, April 5, 2021 — Polyurethanes, a type of plastic, are nearly everywhere — in shoes, clothes, refrigerators and construction materials. But these highly versatile materials can have a major downside. Derived from crude oil, toxic to synthesize, and slow to break down, conventional polyurethanes are not environmentally friendly. Today, researchers discuss devising what they say should be a safer, biodegradable alternative derived from fish waste — heads, bones, skin and guts — that would otherwise likely be discarded.
The researchers will present their results today at the spring meeting of the American Chemical Society (ACS). ACS Spring 2021 is being held online April 5-30. Live sessions will be hosted April 5-16, and on-demand and networking content will continue through April 30. The meeting features nearly 9,000 presentations on a wide range of science topics.
If developed successfully, a fish-oil based polyurethane could help meet the immense need for more sustainable plastics, says Francesca Kerton, Ph.D., the project’s principal investigator. “It is important that we start designing plastics with an end-of-life plan, whether it’s chemical degradation that turns the material into carbon dioxide and water, or recycling and repurposing.”
To make the new material, Kerton’s team started out with oil extracted from the remains of Atlantic salmon, after the fish were prepared for sale to consumers. “I find it interesting how we can make something useful, something that could even change the way plastics are made, from the garbage that people just throw out,” says Mikhailey Wheeler, a graduate student who is presenting the work at the meeting. Both Kerton and Wheeler are at Memorial University of Newfoundland (Canada).
The conventional method for producing polyurethanes presents a number of environmental and safety problems. It requires crude oil, a non-renewable resource, and phosgene, a colorless and highly toxic gas. The synthesis generates isocyanates, potent respiratory irritants, and the final product does not readily break down in the environment. The limited biodegradation that does occur can release carcinogenic compounds. Meanwhile, demand for greener alternatives is growing. Previously, others have developed new polyurethanes using plant-derived oils to replace petroleum. However, these too come with a drawback: The crops, often soybeans, that produce the oil require land that could otherwise be used to grow food.
Leftover fish struck Kerton as a promising alternative. Salmon farming is a major industry for coastal Newfoundland, where her university is located. After the fish are processed, leftover parts are often discarded, but sometimes oil is extracted from them. Kerton and her colleagues developed a process for converting this fish oil into a polyurethane-like polymer. First, they add oxygen to the unsaturated oil in a controlled way to form epoxides, molecules similar to those in epoxy resin. After reacting these epoxides with carbon dioxide, they link the resulting molecules together with nitrogen-containing amines to form the new material.
But does the plastic smell fishy? “When we start the process with the fish oil, there is a faint kind of fish smell, but as we go through the steps, that smell disappears,” Kerton says.
Kerton and her team described this method in a paper last August, and since then, Wheeler has been tweaking it. She has recently had some success swapping out the amine for amino acids, which simplifies the chemistry involved. And while the amine they used previously had to be derived from cashew nut shells, the amino acids already exist in nature. Wheeler’s preliminary results suggest that histidine and asparagine could fill in for the amine by linking together the polymer’s components.
In other experiments, they have begun examining how readily the new material would likely break down once its useful life is over. Wheeler soaked pieces of it in water, and to speed up the degradation for some pieces, she added lipase, an enzyme capable of breaking down fats like those in the fish oil. Under a microscope, she later saw microbial growth on all of the samples, even those that had been in plain water, an encouraging sign that the new material might biodegrade readily, Wheeler says.
Kerton and Wheeler plan to continue testing the effects of using an amino acid in the synthesis and studying how amenable the material is to the microbial growth that could hasten its breakdown. They also intend to study its physical properties to see how it might potentially be used in real world applications, such as in packaging or fibers for clothing.
A press conference on this topic will be held Thursday, April 8 at 11 a.m. Eastern time online at www.acs.org/acsspring2021conferences.
The researchers acknowledge support and funding from the Natural Sciences and Engineering Research Council of Canada and Memorial University of Newfoundland.
The American Chemical Society (ACS) is a nonprofit organization chartered by the U.S. Congress. ACS’ mission is to advance the broader chemistry enterprise and its practitioners for the benefit of Earth and all its people. The Society is a global leader in promoting excellence in science education and providing access to chemistry-related information and research through its multiple research solutions, peer-reviewed journals, scientific conferences, eBooks and weekly news periodical Chemical & Engineering News. ACS journals are among the most cited, most trusted and most read within the scientific literature; however, ACS itself does not conduct chemical research. As a specialist in scientific information solutions (including SciFinder® and STN®), its CAS division powers global research, discovery and innovation. ACS’ main offices are in Washington, D.C., and Columbus, Ohio.
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Note to journalists: Please report that this research was presented at a meeting of the American Chemical Society.
Title
Waste fish oil for the production of greener polyurethane materials
Abstract
Polyurethanes are oil-based synthetic polymers frequently used in the manufacture of various materials such as synthetic fibres or hard plastics. Traditionally, polyurethanes are synthesized by reacting polyols with isocyanates, both derived from crude oil, to form the urethane linkage. Along with depleting our natural resources, this process can be toxic to both humans and the environment. Phosgene, a toxic gas, is used to make the required isocyanates and can cause negative health effects. Isocyanates themselves are also considered toxic, and therefore the production of polyurethanes requires high levels of safety measures. Even with low levels of biodegradability, small amounts of polymer degradation can lead to the formation of carcinogenic aromatic amines released into the environment. These safety, toxicity, and biodegradability issues have led to the need for safer and greener alternatives to polymer synthesis.
In this presentation, we will discuss greener methods to produce polyurethane materials. Previous synthetic routes have avoided the use of isocyanates by incorporating plant-based oils into the process. However, using these oils for polymer synthesis can compete with food production. Our research incorporates fish oil derived from aquaculture waste, a biomass-derived material that does not compete for land space. It was found that capelin-herring fish oil or fish oil extracted from salmon offal can be epoxidized and reacted with CO2 to form carbonated fish oil, which can then form a non-isocyanate polyurethane material (NIPU) from a reaction with a diamine. Biodegradability studies were performed on the resulting films under enzymatic conditions to determine the level of degradation the polymer would undergo, and Scanning Electron Micrographs suggest high levels of degradation. Further improvement of the synthetic process was then attempted by screening the reactivity of biocompatible amino acids in the crosslinking process. L-histidine, L-glutamine, and L-asparagine were chosen and tested for a reaction with the carbonated fish oil via Differential Scanning Calorimetry. Results show an exothermic reaction between the carbonated fish oil and the L-histidine, showing the potential of a crosslinking reaction to form a NIPU.
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