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Interesting facts about plastics and rubber

We come across plastics and rubber everywhere in our daily lives. Discover fascinating stories, surprising facts and interesting background information – from historical developments and well-known products to key figures and innovations in the industry.

Results (423)

  • Directly printing 3D tissues within the body

    Image of a 3D lattice structure of a tissue implanted directly onto a soft living tissue. Image: Ohio State University In the TV series Westworld, human body parts are built on robotic frames using 3D printers. While still far from this scenario, 3D printers are being increasingly used in medicine. For example, 3D printing can be used to produce parts of the body such as orthopedic joints and prosthetics, as well as portions of bone, skin and blood vessels. However, the majority of these tissues are created in an apparatus outside of the body and surgically implanted. Such a procedure may involve making large surgical incisions, posing the added risk of infection and increased recovery time for the patient. And since there is a time lapse between when the tissue is created and when it is implanted in the patient, further complications may occur. To prevent these complications, a team of scientists have developed a technology to print tissues directly in the body. There are two basic components needed to produce an engineered tissue: (1) a fluid-like "bio-ink" that consists of a framework material mixed with living cells, and (2) growth factors to help the cells grow and develop into regenerated tissue. When developing tissues for direct implantation into the body, there are other things to consider: the construction of tissue would have to be conducted at body temperature (37°C), the tissue needs to be attached effectively to soft, live organ tissue and any procedural steps should not be harmful to the patient. One such harmful step in current methods is the application of harmful UV light necessary to solidify the constructed tissue. A collaboration among Ali Khademhosseini, Ph.D., Director and CEO of the Terasaki Institute, David J Hoelzle, Ph.D., from the Ohio State University Department of Mechanical and Aerospace Engineering and Amir Sheikhi, Ph.D. from the Pennsylvania State University Department of Chemical Engineering, has produced a specially-formulated bio-ink designed for printing directly in the body. "This bio-ink formulation is 3D printable at physiological temperature, and can be crosslinked safely using visible light inside the body." said first author Ali Asghari Adib, Ph.D. In order to build the tissue, they used robotic 3D printing, which uses robotic machinery affixed with a nozzle. Bio-ink may be dispensed through the nozzle, much like an icing tube squeezes out writing gel, only in a highly-precise, programmable manner. The team also worked on methods to attach pieces of the tissue formed with this bio-ink onto soft surfaces. In experiments attempting to attach the tissue onto pieces of raw chicken strips and agarose, the team employed a unique interlock technique using the robotic 3D printer and their specially-formulated bio-ink. The nozzle tip was modified to be able to penetrate the soft surfaces and fill the punctured space with bio-ink as it withdrew; this created an anchor for the tissue construct. As the nozzle tip reached the surface, it dispensed an additional blob of bio-ink to "lock in" the anchor. "The interlocking mechanism enables stronger attachments of the scaffolds to the soft tissue substrate inside the patient body," said Asghari Adib. Such improvements in tissue engineering are instrumental in providing lower-risk, minimally-invasive laparoscopic options for procedures such as the repair of tissue or organ defects, engineering/implanting patches to enhance ovarian function, or creating bio-functional hernia repair meshes. Such options would be safer for the patient, save time and be more cost-effective. Further modifications in tissue engineering design and the adjustment of other conditions may increase the potential for customization, thus leading the way to limitless possibilities for enhancing patient health. "Developing personalized tissues that can address various injuries and ailments is very important for the future of medicine. The work presented here addresses an important challenge in making these tissues, as it enables us to deliver the right cells and materials directly to the defect in the operating room," said Khademhosseini, "This work synergizes with our Personalized Implant Technology Platform at the Terasaki Institute which aims to develop approaches that address the variability in tissue defects in patients." Reference Adib et al., Direct-write 3D printing and characterization of a GelMA-based biomaterial for intracorporeal tissue engineering, IOPScience (2020), http://dx.doi.org/10.1088/1758-5090/ab97a1

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  • NIST study uncovers a potential driver of premature solar panel failures

    Cracks often form on solar panel backsheets in straight lines, along the gaps between solar cells. Image: NIST Unlike diamonds, solar panels are not forever. Ultraviolet rays, gusts of wind and heavy rain wear away at them over their lifetime. Manufacturers typically guarantee that panels will endure the elements for at least 25 years before experiencing significant drop-offs in power generation, but recent reports highlight a trend of panels failing decades before expected. For some models, there has been a spike in the number of cracked backsheets - layers of plastic that electrically insulate and physically shield the backsides of solar panels. The premature cracking has largely been attributed to the widespread use of certain plastics, such as polyamide, but the reason for their rapid degradation has been unclear. By closely examining cracked polyamide-based backsheets, researchers at the National Institute of Standards and Technology (NIST) and colleagues have uncovered how interactions between these plastics, environmental factors and solar panel architecture may be speeding up the degradation process. These findings could aid researchers in the development of improved durability tests and longer-lived solar panels. Cracks in backsheets often show up first near certain features - such as the grid-shaped space in between the blue or black electricity-producing solar cells - and can eventually propagate through the entire thickness of a sheet. These defects make way for oxygen and moisture to infiltrate and damage the interior where the cells lie and also allow electrical current to escape, increasing risks of electrocution. If left outside for long enough, any plastic-based backsheet will start to fall apart, but not all backsheets are created equal. Some plastics deteriorate much more rapidly than others. "In the 2010 to 2012 timeframe, many modules were deployed containing polyamide-based backsheets, which presented dramatic cracking failure in as little as four years despite meeting standard requirements," said Xiaohong Gu, NIST materials engineer and co-author of the study. Image: Although moisture and water wear away at the entire outer surface of backsheets, they crack more quickly in the area between solar cells where sunlight shines through. NIST researchers propose that degradation is worse there because acetic acid, which forms when sunlight hits the the rubbery upper layers, can pass between the solar cells towards the backsheets, causing them to decay from the inside out. (Source: N. Hanacek/NIST) To get to the root of polyamide's degradation problem, Gu and her team acquired backsheet samples from solar panels deployed in regions around the globe, including sites in the U.S., China, Thailand and Italy. Most of the panels, which were in use from three to six years, showed clear signs of premature cracking. With the weathered backsheets in hand, the researchers conducted a gamut of chemical and mechanical tests to examine the patterns and severity of degradation throughout the depth of the sheets. The results, described in the journal Progress in Photovoltaics: Research and Applications, showed that the areas of the sheets that had undergone the worst cracking were those that had become the most rigid. And curiously, the most brittle areas were on the inner side of the sheets, Gu said. How could the quality of the walled-off interior diminish more quickly than the exposed outer layer? Gu and her team speculated that the sunlight-induced degradation of the top side of the encapsulant - a film that surrounds the solar cells - produced damaging chemicals that descended toward the backsheets, speeding up their decay. If true, the proposed mechanism would explain why cracks form in between solar cells, as chemicals could find passage to the back through these regions. The researchers identified acetic acid as a prime suspect, as it is known to be harmful to polyamide and is produced during the degradation of a polymer commonly used as an encapsulant, called ethylene vinyl acetate (EVA). To test their hypothesis, the researchers stowed several polyamide strips away in vials of acetic acid and then, after five months, analyzed how they decayed compared with strips placed in either air or water. Under the microscope, cracks mirroring those from the weathered backsheets appeared on the surface of the plastic strips exposed to acetic acid, which appeared much worse than on those that had been in air or water. Chemical analysis showed that degradation products of polyamide were higher in the acetic-acid-exposed strips, providing further evidence that the acid accelerates the deterioration of the backsheet material. The study highlights the interplay between solar panel components (the EVA encapsulant and polyamide backsheet in this case) as a potentially critical factor to consider when designing solar panels that are built to last. These new insights into premature failures could also become valuable to NIST researchers and others who seek to replicate the degradation process in the lab as a way to test and predict the longevity of solar panel components. Reference Lyu et al., Drivers for the cracking of multilayer polyamide‐based backsheets in field photovoltaic modules: In‐depth degradation mapping analysis, Progress in Photovoltaics: Research and Applications (2020), https://doi.org/10.1002/pip.3260

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  • 'Deceptively simple' process could boost plastics recycling

    Eva Harth, director of the Welch-UH Center for Excellence in Polymer Chemistry at the University of Houston, said the new method addresses a long-standing need for industrial plastics producers, without requiring a new catalyst or expensive additives. Image: University of Houston Plastics are a victim of their own success, so inexpensive, easy to use and versatile that the world is awash in plastic waste. Now researchers from the University of Houston have reported a new method of producing polyolefins - made from hydrocarbons and the most common building block of plastics - structured to address one of the biggest stumbling blocks to plastics recycling. The process also would allow plastics to be produced from food oils and other natural substances. Eva Harth, director of the Welch-UH Center for Excellence in Polymer Chemistry, said the process addresses a long-standing need for industrial plastics producers, without requiring a new catalyst or expensive additives. "It's a very simple process," she said. Harth is a corresponding author for a paper describing the discovery, published in the German journal Angewandte Chemie. Co-authors include co-corresponding author Glen R. Jones, a post-doctoral researcher with the Welch-UH Center, and first author Hatice E. Basburg Alhan, a graduate student at UH. Polyolefins, and derivative products such as polyethylene and polypropylene, are used for everything from grocery bags to industrial pipes. The qualities of the plastics - rigidity vs. flexibility, for example - are determined in part by a chemical process known as branching: Jones said highly branched polyolefins are used in products that require softness or flexibility, such as grocery bags, while low branching is used to produce rigid plastics. Traditionally, different catalysts have been required to spark differing levels of branching, Harth said, meaning that only one type of plastic could be produced at a time. "You have to be specific about what material you are after, what type of branching you need," she said. Polymerization of internal alkenes proceeds via chain‐walking to give polymers with much higher branching than 1‐alkene analogues. Source: Angewandte Chemie The new method allows branching to be modulated using a palladium catalyst with varying amounts of added aluminum chloride, which functioned as a Lewis acid; the aluminum chloride - an abundant and inexpensive substance - can be added at different points in the process, allowing the resulting polyolefin to contain differing branching properties. The new process could address two growing issues faced by plastics producers - how to dispose of plastic waste in an environmentally friendly way, and how to reduce the use of oil and natural gas by instead using food oils and other natural substances. Current polymers used in everyday materials - grocery bags, milk jugs, toys and medical equipment, for example - won't readily mix when they are melted down for chemical recycling. "These new polymers could sit at the boundary," Jones said, allowing plastics with disparate properties to be more easily recycled. The process will work with a variety of molecules to produce a polymer, Harth said, suggesting that the concept provides a new platform to produce plastics. And that platform, she said, could lend itself to producing a variety of functional plastics from natural oils and other molecular sources. "This has exciting sustainability possibilities for the industry." Reference Hatice E. Basbug Alhan, Dr. Glen R. Jones and Prof. Eva Harth, Branching Regulation in Olefin Polymerization via Lewis Acid Triggered Isomerization of Monomers, Angewandte Chemie 132 (2019), https://doi.org/10.1002/ange.201914742

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  • Nanomaterial gives robots chameleon skin

    Graphic depicting gold nanorod film's color response to twisting. Image: UCR/Yadong Yin A new film made of gold nanoparticles changes color in response to any type of movement. Its unprecedented qualities could allow robots to mimic chameleons and octopi - among other futuristic applications. Unlike other materials that try to emulate nature's color changers, this one can respond to any type of movement, like bending or twisting. Robots coated in it could enter spaces that might be dangerous or impossible for humans, and offer information just based on the way they look. For example, a camouflaged robot could enter tough-to-access underwater crevices. If the robot changes color, biologists could learn about the pressures facing animals that live in these environments. Although some other color-changing materials can also respond to motion, this one can be printed and programmed to display different, complex patterns that are difficult to replicate. The UC Riverside scientists who created this nanomaterial documented their process in a Nature Communications paper published this past week. Nanomaterials are simply materials that have been reduced to an extremely small scale -- tens of nanometers in width and length, or, about the size of a virus. When materials like silver or gold become smaller, their colors will change depending on their size, shape, and the direction they face. "In our case, we reduced gold to nano-sized rods. We knew that if we could make the rods point in a particular direction, we could control their color," said chemistry professor Yadong Yin. "Facing one way, they might appear red. Move them 45 degrees, and they change to green." The problem facing the research team was how to take millions of gold nanorods floating in a liquid solution and get them all to point in the same direction to display a uniform color. Their solution was to fuse smaller magnetic nanorods onto the larger gold ones. The two different-sized rods were encapsulated in a polymer shield, so that they would remain side by side. That way, the orientation of both rods could be controlled by magnets. "Just like if you hold a magnet over a pile of needles, they all point in the same direction. That's how we control the color," Yin said. Once the nanorods are dried into a thin film, their orientation is fixed in place and they no longer respond to magnets. "But, if the film is flexible, you can bend and rotate it, and will still see different colors as the orientation changes," Yin said. Other materials, like butterfly wings, are shiny and colorful at certain angles, and can also change color when viewed at other angles. However, those materials rely on precisely ordered microstructures, which are difficult and expensive to make for large areas. But this new film can be made to coat the surface of any sized object just as easily as applying spray paint on a house. Though futuristic robots are an ultimate application of this film, it can be used in many other ways. UC Riverside chemist Zhiwei Li, the first author on this paper, explained that the film can be incorporated into checks or cash as an authentication feature. Under normal lighting, the film is gray, but when you put on sunglasses and look at it through polarized lenses, elaborate patterns can be seen. In addition, the color contrast of the film may change dramatically if you twist the film. The applications, in fact, are only limited by the imagination. "Artists could use this technology to create fascinating paintings that are wildly different depending on the angle from which they are viewed," Li said. "It would be wonderful to see how the science in our work could be combined with the beauty of art." Reference Li et al., Coupling magnetic and plasmonic anisotropy in hybrid nanorods for mechanochromic responses, Nature Communications (2020), http://dx.doi.org/10.1038/s41467-020-16678-8

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  • Tiny pump builds polyrotaxanes with precision

    Northwestern University researchers have developed the most precise way to build polyrotaxanes, a mechanically locked polymer for slide-ring gels, battery electrode materials and drug-delivery platforms. A necklace-like molecule made with rings threaded onto a polymer string, polyrotaxanes are notoriously difficult to construct. A new method from the laboratory of Nobel Prize-winning chemist Sir Fraser Stoddart uses two artificial molecular pumps to install rings onto each end of a polymer string. The tiny pumps allow researchers to control precisely how many rings pass onto the polymer. "These polyrotaxanes have never before been made with such precision," Stoddart said. "Without the ability to define accurately the polymer's structure, you cannot fine-tune the material's overall properties." The paper will be published on Friday, June 12 in the journal Science. Stoddart is the Board of Trustees Professor in Northwestern's Weinberg College of Arts and Sciences. Yunyan Qiu, a postdoctoral fellow in Stoddart's lab, is the paper's first author. Researchers have studied polyrotaxanes for years, fascinated by their stretchy mechanical properties and potential of materials containing them to self-heal. But, until now, it was impossible to build these promising polymers with a precise number of rings. "Traditionally, researchers mix the rings and polymers together, and they form inclusion complexes by noncovalent interactions," Qiu said. "But you couldn't know how many rings were threaded until you analyzed it later using nuclear magnetic resonance microscopy. People could roughly control the percentage of rings to some extent, but it was still an estimate." To overcome this challenge, the Northwestern researchers used an artificial molecular pump, which was developed in Stoddart's laboratory in 2015. The first of its kind, the pump draws power from redox reactions, driving molecules from a low-energy state to a high-energy state. To build polyrotaxanes, the pump employs repetitive redox reactions either chemically or electrochemically, in which a molecule gains or loses electrons. Initially, the pump - situated at both ends of the polymer string -- and the rings are both positively charged and, thus, repel each other. Upon injecting electrons, units in both pumps and rings change from dicationic to radical cationic states. Suddenly, the rings are attracted to the pump heads and thread onto both ends of the polymer string. Subsequent oxidation removes the electrons, restoring the positive charges. The rings try to escape but cannot due to the positively charged units at both end of the polymer string. Mild heating allows the ring to pass over a speed bump onto the polymer chain. The pump repeats this process to recruit rings in pairs onto the polymer string. "We can recruit up to 10 rings onto the thread," Qiu said. "But we believe we're only limited by the length of the chosen polymer chain. If we double the length of the polymer, we can double the number of rings." The team also believes that, with this method, they could use many different types of polymers to create untraditional polyrotaxanes with unusual properties. "I'm very excited about this research," Stoddart said. "I put it up there with some of the best papers I've been associated with during the past 50 years."

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  • Discovery of graphene switch

    Researchers at Japan Advanced Institute of Science and Technology (JAIST) have successfully measured the current-voltage curve of graphene nanoribbons (GNRs) that were suspended between two electrodes. Measurements were performed using transmission electron microscopy (TEM) observation. Results revealed that, in contrast to the findings of previous reports, the electrical conductance of GNRs with a zigzag edge structure (zigzag GNRs) abruptly increased above the critical bias voltage. This finding is worth noting because the abrupt change in these GNRs can be applied to switching devices, which are the smallest devices in the world. The electrical structure of GNRs have been systematically investigated through theoretical calculations. Studies have reported that both zigzag and armchair GNRs exhibit semiconducting behavior below several nm in width, although the origin of the energy gap is different. On the other hand, the electrical transport properties have rarely been calculated owing to the non-equiribrium calculations required. In 2009, Nikolic et al. predicted that sharp increments in electrical conductance would occur for extremely thin and short zigzag GNRs as the magnetic-insulator-nonmagnetic-metal phase transition occurs above a certain bias voltage [Phys. Rev.B 79, 205430 (2009)]. The obtained experimental results correspond closely to the results of this non-equilibrium calculation. Image: Researchers at Japan Advanced Institute of Science and Technology (JAIST) successfully developed the special in-situ transmission electron microscope technique to measure the current-voltage curve of graphene nanoribbon (GNR) with observing the edge structure and found that the electrical conductance of narrow GNRs with a zigzag edge structure abruptly increased above the critical bias voltage, indicating that which they are expected to be applied to switching devices, which are the smallest in the world. (Source: JAIST) A research team led by Ms. Chumeng LIU, Professor Yoshifumi OSHIMA and Associate Professor Xiaobin ZHANG (now of Shibaura Institute of Technology) has developed a special in situ TEM holder and a GNR device for TEM observation. This combination is aimed at clarifying the relationship between the edge structure of GNRs and electrical transport properties. Ms. Liu, the doctoral student of JAIST, said, "The fabrication process of our GNR device is much more difficult than the conventional one because we need to make very narrow GNR which should be stably suspended between both electrodes." She reviewed the literature focused on the fabrication process of GNR devices and verified their process en route to establishing her original fabrication method. Assoc. Prof. ZHANG said, "We were really happy to see that the I-V curve obviously changed when changing the edge structure to zigzag. I suppose we have encountered new possibilities for graphene nanoribbons." The team has successfully performed the in situ TEM observation of extremely narrow GNRs, and they plan to continue identifying electrical transport properties that are sensitive to the edge structure of these GNRs. Reference Liu et al., Origin of nonlinear current-voltage curves for suspended zigzag edge graphene nanoribbon, Carbon 165 (2020) 476-483, https://doi.org/10.1016/j.carbon.2020.05.010

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  • Twisted microfiber's network responses to water vapor

    Optical microscopy image of a single fiber of self-assembled polysaccharide in snaking, twisted, and straight structures. Image: JAIST Researchers at Japan Advanced Institute of Science and Technology (JAIST): graduate student Kulisara Budpud, Assoc. Prof. Kosuke Okeyoshi, Dr. Maiko Okajima and, Prof. Tatsuo Kaneko reveal a unique polysaccharide fiber in a twisted structure forming under drying process which showed spring-like behavior. The spring-like behavior of twisted structures is practically used as a reinforced structure in a vapor-sensitive film with millisecond-scale response time. This work is published in Small Full Paper titled "Vapor-Sensitive Materials from Polysaccharide Fibers with Self-Assembling Twisted Microstructures". Polysaccharides play a variety of roles in nature, including molecular recognition and water retention. Still, there is a lack of study in vitro microscale structures of polysaccharides because of the difficulties in regulating self-assembled structures. If the self-assembled structures of these natural polysaccharides can be reconstructed in vitro, it will lead not only to an increased understanding of the morphological changes involved in polysaccharide self-assembly in water but also to the development of a new class of bio-inspired materials, which exhibit regulated structures on a nanometer scale. In this research, it is demonstrated that a cyanobacterial polysaccharide named sacran, can hierarchically self-assemble as twisted fibers from nanoscale to microscale with diameters of ?1 μm and lengths >800 μm. this is remarkably larger than polysaccharides previously reported. Unlike other rigid fibrillar polysaccharides such as cellulose, the sacran fiber is capable of flexibly transforming into two-dimensional snaking and three-dimensional twisted structures at an evaporative air-water interface (Fig.1). This twisted sacran fiber behaves like a mechanical spring under a humid environment. To optimize the condition of the twisted structure is formed by controlling drying speeds. Actually, the drying speed and the capillary force are the dominant factors in creating these formations. To show the potential use of this spring-like polysaccharide fibers, a crosslinked polysaccharide film is prepared as a vapor-sensitive material and the effects of the microfiber's spring behaviors in an environment with humidity gradient are demonstrated (Fig.2). The film reversibly and quickly switched between flat and bent states within 300-800 ms. This repulsive motion displayed by the film is caused by the snaking and twisted structures of the fibers responding to the change of moisture. The sacran film shows a fast response to the water drop retreating, changing from the bent state to the flat state. Because the extended sacran fibers have extension stress like a spring, the network could quickly release water by shrinking. As a result, the bent film becomes flat immediately. Thus, the snaking and twisted fiber network enable millisecond bending and stretching responses to changes in local humidity. From the simple method, JAIST researchers could create unique micro-spring from natural polysaccharide which is practically used as a vapor-sensitive material. Besides, by introducing functional molecules into the microfiber, it would be possible to prepare a variety of soft actuators responding to other changes in the external environment, such as light, pH, and temperature. The method for preparing vapor sensors developed by this study not only improves understanding of how the motion of self-assembled structures responds to stimuli. But also contributes toward the design of environmentally adaptive materials with a high potential for sustainable use. Reference Budpud et al., Vapor‐Sensitive Materials from Polysaccharide Fibers with Self‐Assembling Twisted Microstructures, SMall (2020), http://dx.doi.org/10.1002/smll.202001993

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  • Plastic in the deep sea: Virtually unaltered after a quarter of a century

    Curd box next to manganese nodules at a water depth of more than 4000 metres in the so-called DISCOL area. This object was verifiably lying on the seafloor for 20 years. During a detailed analysis, researchers from GEOMAR found no traces of fragmentation or degradation. Photo: ROV Team/GEOMAR Even in the most remote regions of the oceans plastic debris can be found. Usually it is impossible to determine how long they have been lying on the seabed. Up to now, this has also hampered attempts to estimate how long plastic degradation might take. Scientists have now examined plastic items that have verifiably been at the abyssal seabed for more than 20 years. They could not find any traces of fragmentation or even degradation. Plastic products are durable. On one hand this is a great advantage, but on the other hand, if the plastic enters the environment, this advantage turns into a problem. According to current knowledge, natural degradation, as with organic matter, does not take place. It can only be estimated, how long plastic debris actually remains in the environment. Corresponding long-term experiments are lacking. This applies particularly to the deep sea that is only poorly explored itself. Plastic objects that are found by chance with the help of deep-sea robots or other underwater vehicles are difficult to date. However, during an expedition with the German research vessel SONNE in 2015, researchers from the GEOMAR Helmholtz Centre for Ocean Research Kiel, the Max Planck Institute for Marine Microbiology in Bremen and the Kiel University were able to recover several pieces of waste from the seabed of the Eastern Pacific Ocean in a depth of more than 4000 metre. Conducting a little detective work allowed to constrain the age of deposition quite accurately. For the first time, this offered the opportunity to conduct a long-term study on plastic degradation in the deep sea. The study was published today in the international journal Scientific Reports. In reality, in 2015 the team was out in the Pacific about 440 nautical miles (815 km) off the coast of Peru to investigate another long-term experiment in the so-called DISCOL area. There, German scientists had ploughed a piece of seafloor in 1989 in order to understand the environmental impacts arising from potential future mining of manganese nodules. They visited this site again in 1992, 1996 and in 2015 to study the recovery of the deep-sea ecosystem. In 2015, the remotely operated deep-sea robot ROV KIEL 6000 observed almost incidentally some waste and recovered it from the seafloor. Among it was a plastic bag containing a Coke can, which was part of a special edition produced for the Davis Cup 1988. "The aluminum can itself would have corroded in the deep sea, if it was not wrapped tightly inside a plastic garbage bag that preserved it. This also indicates that the garbage bag must be of the same age", says Dr. Matthias Haeckel from GEOMAR, project manager on board back then and now co-author of the study. A second recovered item was a curd box from a German manufacturer. The printed address shows a five-digit postal code. These were not introduced in Germany until 1990. However, the manufacturer was bought by a rival company in 1999, and the brand name disappeared. "Since the DISCOL area is far away from important shipping routes, the plastic bag and the curd box could be attributed to the DISCOL expeditions in 1989 and 1992 or 1996," says Dr Haeckel. After all, this offered the extremely rare opportunity to examine in detail datable plastic objects from the deep sea. "It turned out that neither the bag nor the curd box showed signs of fragmentation or even degradation", says biochemist Dr. Stefan Krause from GEOMAR, lead author of the study. He led the onshore analyses in the home laboratories. A scientifically most interesting finding was that the microbial community on the plastic surfaces differed from the one identified in the surrounding seafloor sediments. "All of the species can be found in the deep-sea sediment, but apparently, larger accumulations of plastics could locally cause a shift in the ratio of the predominant species," says Dr. Krause. Overall, the study provides the first scientifically sound indication of the fate of plastic debris in the deep sea. "This study builds also an important basis for our new project HOTMIC, where we aim to trace the plastic waste entering the ocean from the continents to the large oceanic eddies and further to their final sink, the abyssal seafloor", says Dr Haeckel. At the same time, the findings provide a good argument for him to pay even closer attention to compliance with regulations regarding waste on board. "Fortunately, the mentality has changed considerably since the 1990s. Today, both, the crews of the ships and the research teams on board take great care to ensure that no waste is disposed overboard," says Dr Haeckel. Reference Krause et al., Persistence of plastic debris and its colonization by bacterial communities after two decades on the abyssal seafloor, Scientific Reports 10 (2020), http://dx.doi.org/10.1038/s41598-020-66361-7

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  • Let’s rethink plastic!

    In 2015, packaging materials contributed 141 million tons to the global plastic waste generation. FlexFunction2Sustain will promote technologies and innovations to replace state-of-the-art packaging by sustainable solutions. Image: Jan Hosan On April 1st, the EU-funded initiative FlexFunction2Sustain was launched. The project, financed by the European Union’s Horizon 2020 research and innovation programme, will support Plastics and Paper Processing Industry in overcoming environmental challenges while entering the digital age. This Open Innovation Test Bed for nano-functionalized plastic and paper surfaces and membranes will support innovative SMEs and industries by drastically reducing the time-to-market for novel concepts, ideas and products. Plastic and paper based materials are used in a wide range of daily life products. Applications represent well established multi-billion Euro markets (e. g. food and pharma packaging, furniture surfaces, membrane-based filter systems, medical products etc.). New business opportunities will arise from replacing glass and metal by nano-functionalized plastic or paper surfaces in many products. That allows the reduction in weight and cost and gains in mechanical flexibility together with additional properties. Such properties include e. g. the blocking of water and oxygen permeation, surface conductivity, antimicrobial and anti-viral properties or chemical and corrosion resistance. State-of-the-art solutions often rely on composite or multi-layer materials. Such composites, however, have a major drawback with respect to their environmental footprint: they are neither fully recyclable nor compostable/degradable. Further, most plastic products are synthesized from mineral oil instead of renewable resources. Many innovations come from the urgent need to reduce plastic waste in the world addressing novel polymer formulations (bio-based, bio-degradable) and novel product designs. However, high access barriers to pre-commercial material development, testing and certification facilities and pilot-production capabilities in Europe prevent StartUps, SMEs and Industries from commercially exploiting novel ideas in nanotechnology and advanced materials. Investors, although willing to support innovative solutions, lack the technical knowledge and the institutional capabilities for evaluating new ideas, products and business models of StartUps. FlexFunction2Sustain – who is behind it and how does it work? The EU-funded initiative FlexFunction2Sustain aims at overcoming these limitations (often referred to as “Valley of Death” between research and industry) by creating an Open Innovation Test Bed (OITB) for nano-functionalisation technologies that enable sustainable and smart plastics and paper based products. The OITB will provide users an easy access to holistic innovation boosting services through a single entry point. The OITB will support its customers in material and product design, in process and product development, in product verification and certification, with pilot and small series production services and with accessing new markets and business opportunities. Integrating all these services to a complete, all-round offer will substantially reduce the time and cost to progress through the innovation chain from an idea to a successful product. FlexFunction2Sustain uniquely interconnects renowned Universities, Applied Research Organisations, and Companies offering pilot production services with Business Development, Networking and Intellectual Property Experts to support customers in any stage of the innovation chain. The consortium was assembled to improve competitiveness of Europe in the field of nano-functionalized materials, and to increase market share of European industries in the value chain of sustainable and smart plastic and paper related products. FlexFunction2Sustain member facilities cover all major nano-functionalisation techniques available for plastic and paper surfaces. This includes a large portfolio of techniques for atmospheric pressure and vacuum thin film coating; micro- and nano-structuring of surfaces; printed electronics processing; and lamination and product integration. Pilot-scale facilities for testing novel polymer formulations and for verifying recyclability and bio-degradability of innovative products complete the offer. Finally, application verification and pre-certification test facilities for food and non-food packaging and anti-microbial and antiviral applications will accelerate market Penetration of novel products in sensitive use scenarios. FlexFunction2Sustain will align the technical facilities according to the needs of six industrial use cases, including i.e.: recyclable and marine degradable food and cosmetic packaging, selective water filter membranes, innovative and smart plastic surfaces in automotive and bio-degradable security and fraud protection labels. Project coordinator Dr. John Fahlteich, Fraunhofer Institute for Organic Electronics, Electron Beam and Plasma Technology FEP, explains the unique potential of the ecosystem: “The strength of the FlexFunction2Sustain OITB is the unique cooperation between the research, technology and business development partners to set-up a combined offer of complementary services for boosting innovation. Customers will be able to gain access to a pan European innovation network through a single entry point without the need to speak multiple languages or to understand the law in multiple countries. This model allows the most appropriate technology selection and shaping among whole technological portfolio available in the EU. Users can expect optimum cost, time-to-market, reliability and performance.” Holistic services from a Single Entry Point in the whole European Market The services of the OITB will be made available to the industry though a novel “single entry point” company that will be created before Summer 2021. The company will act as general contractor for the customer managing all services and actions of the OITB for highest service quality and efficiency. Through this company, the customer will gain access to services from partners in more than 10 different EU countries in either its native language or English. The single entry point will eliminate the need to negotiate multiple service contracts in different countries and to organize material transfers and information exchange between different suppliers. Strategic partnerships with regional agents will ensure access in the whole European Market. To accelerate the uptake of the OITB services, FlexFunction2Sustain will launch two competitive calls for up to 20 pre-commercial SME-targeted pilot cases. The first call will open in January 2022 and will invite SMEs to submit innovation project proposals to FlexFunction2Sustain. The best rated projects will receive discounted services from the OITB. The FlexFunction2Sustain ecosystem will support innovative SMEs and industries by providing an expert support from an early development stage to the optimised transformation of prototypes into valuable and innovative products. The members of the consortium are convinced that only the complex response of this nature will provide the necessary service portfolio to create sustainable new products and business cases in the European Union.

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  • Liquid metals break down organic fuels into ultra-thin graphitic sheets

    For the first time, FLEET researchers at UNSW, Sydney show the synthesis of ultra-thin graphitic materials at room temperature using organic fuels (which can be as simple as basic alcohols such as ethanol). Image: UNSW, Sydney For the first time, FLEET researchers at UNSW, Sydney show the synthesis of ultra-thin graphitic materials at room temperature using organic fuels (which can be as simple as basic alcohols such as ethanol). Graphitic materials, such as graphene, are ultra-thin sheets of carbon compounds that are sought after materials with great promises for battery storage, solar cells, touch panels and even more recently fillers for polymers. These researchers were able to synthesize ultra-thin carbon-based materials on the surface of liquid metals at room temperature electrochemically. Before this report, others had shown electro-formation of such carbon-based materials only by transferring sheets onto the electrodes or electrode exfoliation of naturally-occurring carbon crystals from mines. "Using gallium liquid metal, we could catalytically break down the fuels and form carbon-carbon bonds (the base of graphitic sheets) from organic fuels at room temperature. The ultra-smooth surface of liquid metals could then template atomically-thin carbon based sheets. Removal of these sheets was easy as they do not stick to the liquid metal surface," suggested Prof Kalantar-Zadeh, the lead of this project and the Director of the Centre for Advanced Solid and Liquid based Electronics and Optics (CASLEO) at UNSW. "It is simple. Why has room temperature electro-synthesis of two-dimensional graphitic materials not been achieved before? We cannot offer a definitive answer. Perhaps disregarding ultra-catalysts such as liquid metals and too much emphasis on solid electrodes which are inherently not smooth." added Dr Mohannad Mayyas the first author of the paper. Reference Mayyas et al., Liquid‐Metal‐Templated Synthesis of 2D Graphitic Materials at Room Temperature, Advanced Materials (2020), http://dx.doi.org/10.1002/adma.202001997

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  • Self-healing bone cement

    Prof. Dr Frank A. Mueller, Chair of Colloids, Surfaces and Interfaces of Friedrich Schiller University Jena (Germany). Image: Anne Guenther Material scientists at the University of Jena have developed a bone replacement based on calcium phosphate cement and reinforced with carbon fibers. The fibers increase damage tolerance and ensure that cracks in the material repair themselves. Our body is able to treat many injuries and wounds all by itself. Self-healing powers repair skin abrasions and enable bones to grow back together. However, doctors often have to lend a helping hand to repair bones after a fracture or due to a defect. Increasingly, bone replacement materials are being used, which partially or completely restore the form and function of the bone at the site of the damage. To ensure that such implants do not have to be replaced or repaired through extensive surgery in the event of damage, they should themselves possess self-healing capabilities. Material scientists at Friedrich Schiller University Jena have now developed a bone replacement material that minimises the extent of damage to it and at the same time repairs itself. They report on their research in the prominent research magazine "Scientific Reports". Minimally invasive use of calcium phosphate cement The experts from Jena, who collaborated with colleagues from the University of Würzburg as part of the German Research Foundation's priority research programme "Self-healing Materials", concentrated on what is called calcium phosphate cement - a bone substitute that is already widely used in medicine. On the one hand, the material stimulates bone formation and increases the ingrowth of blood vessels. On the other hand, it can be introduced into the body as a paste in a minimally invasive procedure. There, its malleability allows it to bind closely to the bone structure. "Due to its high degree of brittleness, however, cracks form in the material when it is subjected to excessive load. These cracks can quickly widen, destabilise the implant and ultimately destroy it - similar to concrete on buildings," explains Prof. Frank A. Müller from the University of Jena. "For this reason, calcium phosphate cement has so far mainly been used on bones that do not play a load-bearing role in the skeleton, for example in the mouth and jaw area." Bridging and refilling cracks The material scientists in Jena have now developed a calcium phosphate cement in which any cracks do not develop into catastrophic damage. Instead, the material itself seals them. The reason for this is carbon fibres that have been added to the material. "Firstly, these fibres significantly increase the damage tolerance of the cement, because they bridge cracks as they form and thus prevent them from opening further," Müller explains. "Secondly, we have chemically activated the surface of the fibres. This means that as soon as the exposed fibres encounter body fluid, which collects in the openings created by the cracks, a mineralisation process is initiated. The resulting apatite - a fundamental building block of bone tissue - then closes the crack again." The Jena scientists have simulated this process in their experiments by deliberately damaging the calcium phosphate cement and healing it in simulated body fluid. This intrinsic self-healing ability - and the greater load-bearing capacity associated with fibre reinforcement - could considerably expand the areas in which bone implants made of calcium phosphate cement can be used, which could possibly also include load-bearing areas of the skeleton in the future. Anne V. Boehm, Susanne Meininger, Uwe Gbureck, Frank A. Mueller (2020): Self-healing capacity of fiber-reinforced calcium phosphate cements, Scientific Reports, DOI: https://doi.org/10.1038/s41598-020-66207-2

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  • Surprisingly strong and deformable silicon

    Researchers at ETH have shown that tiny objects can be made from silicon that are much more deformable and stronger than previously thought. In this way, sensors in smartphones could be made smaller and more robust. Since the invention of the MOSFET transistor sixty year ago, the chemical element silicon on which it is based has become an integral part of modern life. It ushered in the computer age, and by now the MOSFET has become the most produced device in history. Silicon is readily available, cheap, and has ideal electrical properties, but also one important drawback: it is very brittle and, therefore, breaks easily. This can become a problem when trying to make micro-?electro-mechanical systems (MEMS) from silicon, such as the acceleration sensors in modern smartphones. At ETH in Zurich, a team led by Jeff Wheeler, Senior Scientist at the Laboratory for Nanometallurgy, together with colleagues at the Laboratory for Mechanics of Materials and Nanostructures at Empa, has shown that, under certain conditions, silicon can be much stronger and more deformable than was previously thought. Their results have recently been published in the scientific journal Nature Communications. Ten-year effort The production process for strong, deformable silicon pillars (links). The pillars are first etched through a resist, then oxidized and finally cleaned. On the right, the end result can be seen (electron microscope image). Illustration: ETH Zurich "This is the result of a ten-year effort", says Wheeler, who worked as a researcher at Empa prior to his career at ETH. To understand how tiny silicon structures can deform, within the framework of an SNF project, he took a closer look at a widely used production method: the focused ion beam. Such a beam of charged particles can mill desired shapes into a silicon wafer very effectively, but in doing so leaves behind distinct traces in the form of surface damage and defects, which cause the material to break more easily. Lithography with final cleaning Wheeler and his collaborators had the idea to try a particular type of lithography as an alternative to the ion beam method. "First, we produce the desired structures - tiny pillars in our case - by etching away un-?masked material from the areas of the silicon surface using a gas plasma", explains Ming Chen, a former PhD student in Wheeler's group. In a further step, the surface of the pillars, some of which are narrower than a hundred nanometres, are first oxidized and then cleaned by completely removing the oxide layer with a strong acid. Chen then studied the strength and plastic deformability of silicon pillars of different widths with an electron microscope and compared the two production methods. To that end, he pressed a tiny diamond punch into the pillars and studied their deformation behaviour in the electron microscope. Striking results The results were striking: the pillars that had been milled with an ion beam collapsed at a width of less than half a micrometre. By contrast, the pillars produced by lithography only suffered brittle fractures at widths above four micrometres, while thinner pillars were able to withstand the strain much better. "These lithographic silicon pillars can deform at sizes ten times greater than what we've seen in ion beam-?machined silicon with the same crystal orientation, with double the strength!", Wheeler summarizes the results of his experiments. The strength of the lithographically produced pillars even reached values that one would only expect only in theory, for ideal crystals. What makes the difference here, says Wheeler, is the absolute purity of the surfaces of the pillars, which is achieved by the final cleaning step. This results in a much smaller number of surface defects from which a fracture could originate. With the assistance of Alla Sologubenko, a researcher with the microscopy centre ScopeM at ETH, this additional deformability also allowed the team to observe a striking change in deformation mechanisms at smaller sizes. This revealed new details on how silicon can deform. Applications in smartphones The results obtained by ETH researchers could have an immediate impact on the fabrication of silicon MEMS, Wheeler says: "In this way, the gyroscopes used in smartphones, which detect rotations of the device, could be made even smaller and more robust." That shouldn't be too difficult to realize, given that industry is already using the combination of etching and cleaning Wheeler and his colleagues investigated. The method could also be applied to other materials having crystal structures similar to that of silicon, the researchers believe. Moreover, more elastic silicon could also be used to further improve the electrical properties of the material for certain applications. By applying a large strain of the semiconductor the mobility of its electrons can be increased, which can lead, for instance, to shorter switching times. So far, one had to produce nanowires to achieve that, but now this could be done directly using structures integrated into a semiconductor chip. Further Information Video: Silicon lithography pillar Reference Chen, M., Pethö, L., Sologubenko, A.S. et al. Achieving micron-scale plasticity and theoretical strength in Silicon. Nat Commun 11, 2681 (2020), http://dx.doi.org/10.1038/s41467-020-16384-5

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