Single-layer graphene is interesting as a flexible 2D material, with xy-dimensions variable up to a centimetre in length and a z-thickness of a single carbon atom. It conducts heat and electricity, has excellent mechanical strength, and is impermeable to gases except hydrogen gas. Its drawback: how to disperse it in a liquid. When you try to do this flexible sheets of graphene tend to stack as a result of attractive van der Waals interactions, making it virtually an impossible material to disperse as single sheets.

Labels are big business. A typical label has multiple layers: a topcoat for protection, the face stock, which contains the message in the form of text and/or images, a pressure-sensitive adhesive, and a release liner, which often has a release coating. The release liner and coating are only there to protect the label from sticking to things you do not wish it would stick to. You remove the liner when you wish to apply the label onto your substrate of choice, for example, a bottle containing a drink.

Imagine a label without a release liner and coating, imagine a label that could be activated at the moment you want it to stick to a substrate, a stick-on-demand linerless label.

BonLab has designed and developed a concept and prototype for a sustainable solution: a mesh reinforced pressure-sensitive adhesive for linerless label design.

When we synthesize polymer colloids by emulsion polymerization, molecular surfactants are often employed. These are required to keep the polymer latex particles dispersed in the water phase, so that they do not clump together, a phenomenon known as coagulation. Keeping polymer dispersions stable is especially important in end applications, such as waterborne coatings and adhesives.

A downside of the use of surfactant molecules is that they can desorb from the surface of the latex particles. This makes the particles colloidally unstable, and they coagulate. This can be disastrous in product formulations, such as water-based paints which have many components. Another downside of this mobility of the surfactant molecules is that they can migrate in the final coating, once applied on a substrate. This leads to deterioration of the properties of the coated film.

Polymer latex particles, typically 50-600 nm in diameter, are used in many applications, such as paper manufacturing, water-based adhesives, printing, and coatings. Commonly, a water-based formulation that contains these polymer colloids is used, often together with other components, such as pigments for opacity and color, fillers, and rheology modifiers. Each of the polymer latex particles consists of many individual polymer chains. These water-based dispersions are applied onto a substrate as a droplet or a film, after which these systems are dried. Visualizing this drying and film formation process in real time would greatly help in understanding how the properties of a dried film come about. In our paper, published in the American Chemical Society’s journal Langmuir, we used TeraHertz Time-Domain Spectroscopy (THz-TDS) to map the water content spatially in real-time during the drying process.

Single-layer graphene oxide sheets are interesting as a flexible 2D material, with xy-dimensions variable up to a centimetre in length and a z-thickness of a single carbon atom. The presence of oxygen atoms with functional groups, such as hydroxy, epoxy, carboxylic acid, ketone, or aldehyde, provides graphene oxide (GO) with polarity. This unique property allows GO to disperse as single sheets in polar solvents like water or DMSO at low concentrations, in the absence of electrolytes or other colloidal particles.

Water-based pressure sensitive adhesives (PSAs) are typically made by emulsion polymerization using a low glass transition temperature base monomer, such as n-butyl acrylate or 2-ethyl hexylacrylate, together with a range of functional comonomers. Typically these include a high glass transition temperature comonomer, such as styrene or methyl methacrylate and monomers that can promote wetting and undergo secondary interactions such as (meth)acrylic acid.

Single-layer graphene is interesting as a flexible 2D material, with xy-dimensions variable up to a centimetre in length and a z-thickness of a single carbon atom. It conducts heat and electricity, has excellent mechanical strength, and is impermeable to gases except hydrogen gas. Its drawback: how to disperse it in a liquid. When you try to do this flexible sheets of graphene tend to stack as a result of attractive van der Waals interactions, making it virtually an impossible material to disperse as single sheets.

Labels are big business. A typical label has multiple layers: a topcoat for protection, the face stock, which contains the message in the form of text and/or images, a pressure-sensitive adhesive, and a release liner, which often has a release coating. The release liner and coating are only there to protect the label from sticking to things you do not wish it would stick to. You remove the liner when you wish to apply the label onto your substrate of choice, for example, a bottle containing a drink.

Imagine a label without a release liner and coating, imagine a label that could be activated at the moment you want it to stick to a substrate, a stick-on-demand linerless label.

BonLab has designed and developed a concept and prototype for a sustainable solution: a mesh reinforced pressure-sensitive adhesive for linerless label design.

Researchers at The University of Warwick have made significant progress in the search for sustainable alternatives to conventional plastics. In response to growing environmental concerns, the move towards a circular economy and changing consumer preferences, the research team has identified that certain mixtures of small organic molecules form interesting glasses and viscous liquids. These so-called organic eutectics are promising candidates for replacing polymers in various products.

Water-based pressure sensitive adhesives (PSAs) are typically made by emulsion polymerization using a low glass transition temperature base monomer, such as n-butyl acrylate or 2-ethyl hexylacrylate, together with a range of functional comonomers. Typically these include a high glass transition temperature comonomer, such as styrene or methyl methacrylate and monomers that can promote wetting and undergo secondary interactions such as (meth)acrylic acid.

Labels are big business. A typical label has multiple layers: a topcoat for protection, the face stock, which contains the message in the form of text and/or images, a pressure-sensitive adhesive, and a release liner, which often has a release coating. The release liner and coating are only there to protect the label from sticking to things you do not wish it would stick to. You remove the liner when you wish to apply the label onto your substrate of choice, for example, a bottle containing a drink.

Imagine a label without a release liner and coating, imagine a label that could be activated at the moment you want it to stick to a substrate, a stick-on-demand linerless label.

BonLab has designed and developed a concept and prototype for a sustainable solution: a mesh reinforced pressure-sensitive adhesive for linerless label design.

Fibers are interesting. They are made by a spinning process in which a liquid based mixture, referred to as spinning dope, is extruded through an orifice hereby generating a jet, which subsequently is solidified through either coagulation/precipitation and/or gelation. Two extreme fibers found in Nature are spidersilk, a super strong and extensible liquid-crystalline fiber, and the soft hydrogel double-strings of toad eggs, as spawn by the common toad (Bufo bufo). The production of manmade fibers using dry and wet spinning techniques – both starting from a liquid mixture – goes back to the 19th century. An early example is the development of Rayon fibers initiated by the discovery of Schweizer in 1857, who found that cellulose could be dissolved in and re-precipitated from an aqueous solution of ammonia and copper (II) hydroxide (coined Schweizer’s reagent (dry or wet)). Examples of wet-spun high performance fibers include ultrahigh molecular weight poly(ethylene) fibers, and polyaramid fibers.

An emerging trend is to make soft, hydrogel-based, fibers wet spun into water. Applications for example are in the area of tissue engineering. Microfluidic technologies are often employed to manufacture these fibers.

We asked ourselves whether it would be possible to fabricate fibers through assembly of thousands of emulsion droplets? We call these HIPE (High Internal Phase Emulsion) fibers.

Hydrogels are soft objects that are mainly composed of water. The water is held together by a 3D cross-linked mesh. In our latest work we show that hydrogel beads made from the bio-sustainable polymer alginate can be loaded up with different types of molecules so that the beads can communicate via chemistry.

Chemical communication underpins a plethora of biological functions and behaviours. Plants, animals and insects rely on it for cooperative action, your body uses it to moderate its internal environment and your cells require it to survive.

A key goal of materials science is to mimic this biological behaviour, and synthetic objects that are able to communicate with one another by the sending and receiving of chemical messengers are of great interest at a range of length scales. The most widely explored platform for this kind of communication is between nanoparticles, and to a lesser extent, vesicles, but to date, very little work explores communication between large (millimetre-sized), soft objects, such as hydrogels.

In our work published in the Journal of Materials Chemistry B, we present combinations of large, soft hydrogel objects containing different signalling and receiving molecules, can exchange chemical signals. Beads encapsulating one of three species, namely the enzyme urease, the enzyme inhibitor silver (Ag+), or the Ag+ chelator dithiothreitol (DTT), are shown to interact when placed in contact with one another. By exploiting the interplay between the enzyme, its reversible inhibitor, and this inhibitor’s chelator, we demonstrate a series of ‘conversations’ between the beads.

A hydrogel is a solid object predominantly composed of water. The water is held together by a cross-linked 3D mesh, which is formed from components such as polymer molecules or colloidal particles. Hydrogels can be found in a wide range of application areas, for example food (think of agar, gelatine, tapioca, alginate containing products), and health (wound dressing, contact lenses, hygiene products, tissue engineering scaffolds, and drug delivery systems).

In Nature hydrogels can be found widely in soft organisms. Jellyfish spring to mind. These are intriguing creatures and form an inspiration for an area called soft robotics, a discipline seek to fabricate soft structures capable of adaptation, ultimately superseding mechanical hard-robots. Hydrogels are an ideal building block for the design of soft robots as their material characteristics can be tailored. It is however, challenging to introduce and program responsive autonomous behaviour and complex functions into man-made hydrogel objects.

Ross Jaggers and prof.dr.ir. Stefan Bon at BonLab have now developed technology that allows for temporal and spatial programming of hydrogel objects, which we made from the biopolymer sodium alginate. Key to its design was the combined use of enzyme and metal-chelation know-how.