Massimo Bagnani

Last Name

Bagnani

First Name

Massimo

ORCID

0000-0002-1326-1600

Show all metadata

Search Results

Publications1 - 5 of 5

From Soy Waste to Bioplastics: Industrial Proof of Concept
Bagnani, Massimo; Peydayesh, Mohammad; Knapp, Thomas; et al. (2024)
Biomacromolecules
The global plastic waste problem is pushing for the development of sustainable alternatives, encouraged by stringent regulations combined with increased environmental consciousness. In response, this study presents an industrial-scale proof of concept to produce self-standing, transparent, and flexible bioplastic films, offering a possible solution to plastic pollution and resource valorization. We achieve this by combining amyloid fibrils self-assembled from food waste with methylcellulose and glycerol. Specifically, soy whey and okara, two pivotal protein-rich byproducts of tofu manufacturing, emerge as sustainable and versatile precursors for amyloid fibril formation and bioplastic development. An exhaustive industrial-scale feasibility study involving the transformation of 500 L of soy whey into similar to 1 km (27 kg) of bioplastic films underscores the potential of this technology. To extend the practicality of our approach, we further processed a running kilometer of film at the industrial scale into transparent windows for paper-based packaging. The mechanical properties and the water interactions of the novel film are tested and compared with those of commercially used plastic films. By pioneering the large-scale production of biodegradable bioplastics sourced from food byproducts, this work not only simultaneously addresses the dual challenges of plastic pollution and food waste but also practically demonstrates the feasibility of biopolymeric building block valorization for the development of sustainable materials in real-world scenarios.
Single-Step Control of Liquid–Liquid Crystalline Phase Separation by Depletion Gradients
Lin, Dongdong; Bagnani, Massimo; Almohammadi, Hamed; et al. (2024)
Advanced Materials
Fine-tuning nucleation and growth of colloidal liquid crystalline (LC) droplets, also known as tactoids, is highly desirable in both fundamental science and technological applications. However, the tactoid structure results from the trade-off between thermodynamics and nonequilibrium kinetics effects, and controlling liquid–liquid crystalline phase separation (LLCPS) in these systems is still a work in progress. Here, a single-step strategy is introduced to obtain a rich palette of morphologies for tactoids formed via nucleation and growth within an initially isotropic phase exposed to a gradient of depletants. The simultaneous appearance is shown of rich LC structures along the depleting potential gradient, where the position of each LC structure is correlated with the magnitude of the depleting potential. Changing the size (nanoparticles) or the nature (polymers) of the depleting agent provides additional, precise control over the resulting LC structures through a size-selective mechanism, where the depletant may be found both within and outside the LC droplets. The use of depletion gradients from depletants of varying sizes and nature offers a powerful toolbox for manipulation, templating, imaging, and understanding heterogeneous colloidal LC structures.
Hybrid Amyloid-Chitin Nanofibrils for Magnetic and Catalytic Aerogels
Peydayesh, Mohammad; Boschi, Enrico; Bagnani, Massimo; et al. (2024)
ACS Nano
In the quest for a sustainable and circular economy, it is essential to explore environmentally friendly alternatives to traditional petroleum-based materials. A promising pathway toward this goal lies in the leveraging of biopolymers derived from food waste, such as proteins and polysaccharides, to develop advanced sustainable materials. Here, we design versatile hybrid materials by hybridizing amyloid nanofibrils derived by self-assembly of whey, a dairy byproduct, with chitin nanofibrils exfoliated from the two distinct allomorphs of α-chitin and β-chitin, extracted from seafood waste. Various hydrogels and aerogels were developed via the hybridization and reassembly of these biopolymeric nanobuilding blocks, and they were further magnetized upon biomineralization with iron nanoparticles. The pH-phase diagram highlights the significant role of electrostatic interactions in gel formation, between positively charged amyloid fibrils and negatively charged chitin nanofibrils. Hybrid magnetic aerogels exhibit a ferromagnetic response characterized by a low coercivity (<50 Oe) and a high specific magnetization (>40 emu/g) at all temperatures, making them particularly suitable for superparamagnetic applications. Additionally, these aerogels exhibit a distinct magnetic transition, featuring a higher blocking temperature (200 K) compared to previously reported similar nanoparticles (160 K), indicating enhanced magnetic stability at elevated temperatures. Finally, we demonstrate the practical application of these hybrid magnetic materials as catalysts for carbon monoxide oxidation, showcasing their potential in environmental pollution control and highlighting their versatility as catalyst supports.
Structural Colors from Amyloid-Based Liquid Crystals
Jin, Tonghui; Yuan, Ye; Bagnani, Massimo; et al. (2024)
Advanced Materials
The helical periodicity and layered structure in cholesteric liquid crystals (CLCs) may be tuned to generate structural color according to the Bragg's law of diffraction. A wide range of natural-based materials such as condensed DNA, collagen, chitin, cellulose, and chiral biopolymers exhibit cholesteric phases with left-handed helixes and ensued structural colors. Here, the possibility of using amyloid CLCs is reported to prepare films with iridescent color reflection and opposite handedness. Right-handed CLCs assembled by left-handed amyloid fibrils are dried into layered structures with variable pitch controlled by the addition of glucose. Circularly polarized light with the same handedness of amyloid CLCs helix is reflected in the Bragg regime. Varying the drying speed leads to the switching between films with a rainbow-like color gradient and large area uniform color. It is confirmed that the origin of the colors derives from the layered structures of the amyloid CLCs, given the negligeable birefringence of the films, calculated from optical rotatory dispersion. These findings provide a facile approach to constructing biosourced cholesteric materials and introduce an original class of proteinaceous materials for the generation of structural colors from right-handed circularly polarized light.
Cholesteric Tactoids with Tunable Helical Pitch Assembled by Lysozyme Amyloid Fibrils
Wu, Chao; Bagnani, Massimo; Jin, Tonghui; et al. (2024)
Small
Amyloid fibrils are biological rod-like particles showing liquid–liquid crystalline phase separation into cholesteric phases through a complex behavior of nucleation, growth, and order-order transitions. Yet, controlling the self-assembly of amyloids into liquid crystals, and particularly the resulting helical periodicity, remains challenging. Here, a novel cholesteric system is introduced and characterized based on hen egg white lysozyme (HEWL) amyloid fibrils and the results rationalized via a combination of experiments and theoretical scaling arguments. Specifically, the transition behaviors are elucidated from homogenous nematic, bipolar nematic to cholesteric tactoids following the classic Onsager model and the free energy functional model from Frank–Oseen elasticity theory. Additionally, the critical effects of pH and ionic strength on these order–order-transitions, as well as on the shape and helical pitch of the cholesteric tactoids are demonstrated. It is found that a small increase in pH from 2.0 to 2.8 results in a 34% decrease in pitch, while, on the contrary, increasing ionic strength from 0 to 10 mm leads to a 39% increase in pitch. The present study provides an approach to obtain controllable chiral nematic structures from HEWL amyloid fibrils, and may contribute further to the application of protein-based liquid crystals in pitch-sensitive biosensors or biomimetic architectures.

Publications1 - 5 of 5

Massimo Bagnani

Last Name

First Name

ORCID

Organisational unit

Filters

Search Results