Rational design and characterization of bioplastics from Hermetia illucens prepupae proteins

In this study proteins extracted from prepupae of Hermetia illucens, also known as black soldier fly,are investigated as promising base for a new type of bioplastics for agricultural purposes. Designof experiments techniques are employed to perform a rational study on the effects of differentcombination of glycerol as plasticizer, citric acid as cross-linking agent and distilled water as solventon the capability of proteins to form a free-standing film through casting technique, keeping asfixed the quantity of proteins. Glycerol shows interesting properties as plasticizer contributing tothe formation of homogenous and free-standing film. Moreover, mechanical and thermalcharacterizations are performed to estimate the effect of increasing amounts of proteins on thefinal properties and thickness of the specimens. Proteins derived from H. illucens can be success-fully employed as base for bioplastics to be employed for agricultural purposes

Diblock Copolymers as Emulsifying Agents in Polymer Blends: Influence of Molecular Weight, Architecture, and Chemical Composition

Interfacial agents used in the compatibilization of immiscible polymer blends often consist of block copolymers containing at least one segment compatible with each of the two phases of the blend. This work examines the influence of the molecular weight, architecture, and chemical composition of the interfacial agent on its ability to emulsify a polymer blend. The system chosen is a blend containing 80% polystyrene and 20% ethylene-propylene rubber, compatibilized by diblock copolymers of poly(styrene-hydrogenated butadiene). The emulsification curve, which relates the dispersed phase particle size to the concentration of interfacial agent added to the system, was used as a tool to characterize the efficacy of the different interfacial agents. The observed behavior is similar to that of classical emulsions: a rapid drop in phase size at low concentrations of interfacial modifier, followed by a levelling off to an equilibrium diameter value once a critical concentration has been reached. For systems compatibilized by symmetrical diblocks (i.e., containing approximately 50% styrene by weight), the volume average particle diameter decreased from 2.7 m for the unmodified system to about 0.4 m once interfacial saturation is reached. The critical concentration for emulsification decreased with increasing interfacial agent molecular weight, due to the higher interfacial area occupied by longer molecules; however, this parameter did not affect the equilibrium particle diameter. The asymmetrical diblock copolymer (30% styrene) was found to be less effective than the symmetrical ones over the entire range of concentrations studied (5 to 35% modifier, based on the volume of the minor phase). Asymmetrical diblock copolymers would tend to form micelles, whereas symmetrical copolymers are less constrained at the interface. No significant difference was observed between the emulsifying capability of tapered and pure diblocks of similar composition and molecular weight

Water effects in polyurethane block copolymers

Equilibrium and dynamic sorption isotherm measurements, differential scanning calorimetry (DSC) measurements, and, mainly, dielectric relaxation spectroscopy (DRS) measurements by means of the thermally stimulated depolarization currents (TSDC) method were used to investigate the hydration properties of linear segmented polyurethane copolymers. Three types of samples were investigated with various fractions of hard and soft block segments. They were based on polyethylene adipate (PEA), 4,4′-diphenylmethane diisocyanate (MDI) and 1,4-butanediol (BDO). At 20°C the water content h of the samples at various values of relative humidity rh increases in proportion to the weight fraction of soft block segments phase. At saturation (rh = 100%) the ratio of sorbed water molecules to polar carbonyl polyester groups is 0.13. At saturation at 20°C there is no fraction of freezable water. The glass transition temperature, Tg, measured by DSC and by TSDC, shifts to lower temperature with increasing h by about 8-10 K at saturation at 20°C. A dielectric relaxation mechanism related to interfacial polarization in the phase-separated morphology is also plasticized by water in a way similar to that observed for the main (α) relaxation, © 1996 John Wiley & Sons, Inc

Diblock Copolymers as Emulsifying Agents in Polymer Blends: Influence of Molecular Weight, Architecture, and Chemical Composition

peer reviewedaudience: researcherInterfacial agents used in the compatibilization of immiscible polymer blends often consist of block copolymers containing at least one segment compatible with each of the two phases of the blend. This work examines the influence of the molecular weight, architecture, and chemical composition of the interfacial agent on its ability to emulsify a polymer blend. The system chosen is a blend containing 80% polystyrene and 20% ethylene-propylene rubber, compatibilized by diblock copolymers of poly(styrene-hydrogenated butadiene). The emulsification curve, which relates the dispersed phase particle size to the concentration of interfacial agent added to the system, was used as a tool to characterize the efficacy of the different interfacial agents. The observed behavior is similar to that of classical emulsions: a rapid drop in phase size at low concentrations of interfacial modifier, followed by a levelling off to an equilibrium diameter value once a critical concentration has been reached. For systems compatibilized by symmetrical diblocks (i.e., containing approximately 50% styrene by weight), the volume average particle diameter decreased from 2.7 m for the unmodified system to about 0.4 m once interfacial saturation is reached. The critical concentration for emulsification decreased with increasing interfacial agent molecular weight, due to the higher interfacial area occupied by longer molecules; however, this parameter did not affect the equilibrium particle diameter. The asymmetrical diblock copolymer (30% styrene) was found to be less effective than the symmetrical ones over the entire range of concentrations studied (5 to 35% modifier, based on the volume of the minor phase). Asymmetrical diblock copolymers would tend to form micelles, whereas symmetrical copolymers are less constrained at the interface. No significant difference was observed between the emulsifying capability of tapered and pure diblocks of similar composition and molecular weight