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Transparent polymers and plastics are used to create molded parts and films for many applications. The colors of these products are of great importance for the suppliers, manufacturers, and end-users. However, for simplicity of the processing, the plastics are produced in the form of small pellets or granules. The predictive measurement of the color of such materials is a challenging process and needs consideration of a complex set of factors. A combination of color measurement systems in transmittance and reflectance modes need to be used for such materials, along with the techniques for minimizing the artifacts based on surface texture and particle sizes. This article provides an extensive overview and discussion of the various factors that can affect the perceptive colors and the methods used for the characterization of the colors and minimizing the measuring artifacts.

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Sustainable practices that reduce food loss are essential for enhancing global food security. We report a 'wrap and plant' seed treatment platform to protect crops from soil-borne pathogens. Developed from the abundantly available wastes of banana harvest and recycled old, corrugated cardboard boxes via chemical-free pulping, these paper-like biodegradable seed wraps exhibit tunable integrity and bioavailability of loaded moieties. These wraps were used for nematode control on yam (Dioscorea cayenensis-rotundata) seed pieces in Benin, a major producer of this staple crop in the sub-Saharan African 'yam belt'. Our seed wraps loaded with ultra-low-volume abamectin (1/100 ≤ commercial formulation) consistently controlled yam nematode (Scutellonema bradys) populations while considerably increasing the yield at various locations over 2015-2018. Substantial reduction in post-harvest tuber weight loss and cracking was observed after 3 and 5 months of storage, contributing to increased value, nutrition and stakeholders' preference for the wrap and plant treatment.

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This review explores biobased polymers for industrial applications, their end fate, and most importantly, origin and key aspects enabling soil biodegradation. The physicochemical properties of biobased synthetic and natural polymers and the primary factors governing degradation are explored. Current and future biobased systems and factors allowing for equivalent comparisons of degradation and possible sources for engineering improved biodegradation are reviewed. Factors impacting ultraviolet (UV) stability of biopolymers have been described including methods to enhance photoresistance and impact on biodegradation. It discusses end-fate of biopolymers in soil and impact of residues on soil health. A limited number of studies examine side effects (e.g., microbial toxicity) from soil biodegradation of composites and biopolymers. Currently available standards for biodegradation and composting have been described with limitations and scope for improvements. Finally, design considerations and implications for sustainable polymers used, under consideration, and to be considered within the context of a rational biodegradable strategy are elaborated.

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Replacing synthetic polymers with renewable alternatives is a critical challenge for the packaging industry. This research investigated the use of leaf-based proteins as a sustainable co-binder in the coating formulations for paper-based packaging and other applications. Protein isolates from tobacco leaf and alfalfa concentrates were characterized using the Pierce protein assay, Kjeldahl nitrogen, and gel electrophoresis. The proteins were tested as co-binders in a typical latex-based paper coating formulation. The rheology and water retention properties of the wet coating and the surface, optical, structural, and strength properties of coated papers were measured. The coating performance was affected by the purity, solubility, and molecular weight of the tobacco protein and exhibited a shear-thinning behavior with lower water retention than soy protein. Analysis by scanning electron microscopy and time of flight secondary ion mass spectroscopy on the dried coating layer containing tobacco protein showed enhanced porosity (advantageous for package glueability) relative to the control latex coating. The tobacco protein offers adequate coverage and coating pigment distribution, indicating that this protein can be a suitable option in coatings for packaging applications.

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Hydrogels are three-dimensional porous polymeric networks prepared by physical or chemical cross-linking of hydrophilic molecules, which can be made into smart materials through judicious chemical modifications to recognize external stimuli; more specifically, this can be accomplished by the integration with stimuli-responsive polymers or sensing molecules that has drawn considerable attention in their possible roles as sensors and diagnostic tools. They can be tailored in different structures and integrated into systems, depending on their chemical and physical structure, sensitivity to the external stimuli and biocompatibility. A panoramic overview of the sensing advances in the field of hydrogels over the past several decades focusing on a variety protocols of hydrogel preparations is provided, with a major focus on natural polymers. The modifications of hydrogel composites by incorporating inorganic nanoparticles and organic polymeric compounds for sensor applications and their mechanisms are also discussed.

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A hybrid poly(N-isopropylacrylamide) (PNIPAm)/cellulose nanofibrils (CNFs) hydrogel composite was fabricated by inverted stereolithography 3D printing to provide a new platform for regulating lower critical solution temperature (LCST) properties and thus tuning optical and bioadhesive properties. The phenomena of interest in the as-printed PNIPAm/CNF hydrogels may be attributed to the fiber-reinforced composite system between crosslinked PNIPAm and CNFs. The optical tunability was found to be correlated to the micro/nano structures of the PNIPAm/CNF hydrogel films. It was found that PNIPAm/CNF hydrogels exhibit switchable bioadhesivity to bacteria in response to CNF distribution in the hydrogels. After 2.0 wt% CNF was incorporated, it was found that a remarkable 8°C reduction of the LCST was achieved relative to PNIPAm hydrogel crosslinked by TEGDMA without CNF. The prepared PNIPAm/CNF hydrogels possessed highly reversible optical, bioadhesion, and thermal performance, making them suitable to be used as durable temperature-sensitive sensors and functional biomedical devices.

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Rational spatiotemporal irradiation of cellulose-based hydrogels (carboxymethylcellulose (CMC), citric acid, and riboflavin) using a laser diode stereolithography 3D printer obtained architectures referred to as photodegradation addressable hydrogels (PAHs). Under irradiation, these PAHs engage in an unprecedented spatially resolved zonal swelling illustrating marked but controllable changes in swelling and thickness while concomitantly obtaining improved oxygen transmission rate values by 5 times. XPS, carboxyl content, and swelling data comparisons of hydrogel formulations show that photodegradation and ablation of the material occur, where hydroxyl sites of CMC are converted to aldehydes and ketones. XRD data show that the total number of crystalline aggregates in the material are lowered after photoablation. The spatially tuned (photoablated) hydrogel films can thus be shaped into a lens form. The energy required for the lens tuning process can be lowered up to 30 times by incorporation of riboflavin in the films. The method demonstrated here enables the processing of a material that is difficult to be machined or cast by popular contact lens making methods.

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A hybrid materials system to modulate lower critical solution temperature (LCST) and moisture content for thermo-responsivity and optical tunability was strategically developed by incorporating cellulose nanocrystals (CNCs) into a poly(N-isopropylacrylamide) (PNIPAm) hydrogel matrix. The PNIPAm/CNC hydrogel films exhibit tunable optical properties and wavelength bandpass selectivity as characterized by PROBE Spectroscopy and Dynamic Light Scattering (DLS). Importantly, the micro/nano structures of the PNIPAm/CNC hydrogel films were completely different when dried below and above the LCST. Below the LCST, PNIPAm/CNC hydrogel films exhibit transparency or semi-transparency due to the uniform bonding of hydrophilic PNIPAm and CNC through hydrogen bonds. Above the LCST, the hydrogel films engage in both hydrophobic PNIPAm and hydrophilic CNC interactions due to changes in PNIPAm conformation which lead to light scattering effects and hence opacity. Furthermore, the incorporation of CNC induces a ∼ 15 °C reduction of the LCST relative to pure PNIPAm hydrogel films.

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Flexible-hybrid printed electronics (FHPE) is a rapidly growing discipline that may be described as the precise imprinting of electrically functional traces and components onto a substrate such as paper to create functional electronic devices. The mass production of low-cost devices and components such as environmental sensors, bio-sensors, actuators, lab on chip (LOCs), radio frequency identification (RFID) smart tags, light emitting diodes (LEDs), smart fabrics and labels, wallpaper, solar cells, fuel cells, and batteries are major driving factors for the industry. Using renewable and bio-friendly materials would be advantageous for both manufacturers and consumers with the increased use of (FHPE) electronics in our daily lives. This review article describes recent developments in cellulose and nanocellulose-based materials for FHPE, and the necessary developments required to propagate their use in commercial applications. The aim of these developments is to enable the creation of FHPE devices and components made almost entirely of cellulose materials.