Flaxseed oil was emulsified in whey protein isolate (WPI) and spray-dried. Powder characteristics and oxidative stability of oil at relative humidities (RH) from RH approximately 0% to RH 91% at 37 degrees C were analyzed. Oil droplets retained their forms in drying and reconstitution, but the original droplet size of the emulsion was not restored when the powder was dispersed in water. The particles seemed to be covered by a protein-rich surface layer as analyzed by electron spectroscopy for chemical analysis (ESCA). Oxidation of flaxseed oil dispersed in the WPI matrix was retarded from that of bulk oil but followed the same pattern as bulk oil with respect to humidity. A high rate of oxidation was found for both low and high humidity conditions. The lowest rate of oxidation as followed by peroxide values was found at RH 75%, a condition that is likely to diverge significantly from the monolayer moisture value. A weak baseline transition observed for the WPI matrix in a differential scanning calorimetry (DSC) thermogram suggested a glassy state of the matrix at all storage conditions. This was not consistent with the observed caking of the powder at RH 91%. Scanning electron microscopy (SEM) images revealed a considerable structural change in the WPI matrix in these conditions, which was suggested to be linked with a higher rate of oxygen transport. Possible mechanisms for oxygen transport in the whey protein matrix under variable RHs are discussed.

Sodium caseinate was chemically modified in order to alter its isoelectric point (pI). Negatively charged carboxylic groups were introduced to lower the pI, and positively charged amino groups to achieve the opposite. Different chemical amino acid modification approaches were studied and the modified proteins were characterized using free amino group assays, SDS-PAGE, MALDI-TOF mass spectrometry, and zeta potential measurements. Oil-in-water emulsions were prepared using these modified caseinates. The pH stability behavior of the emulsions was monitored, and interestingly, the stability of the emulsion could be modulated through steering the pI of caseinate. Using different modified caseinates, it was possible to create emulsions that were stable in the acid, neutral, and alkaline regions of the pH spectrum. The stability behavior of the emulsions correlated well with the theoretical and experimentally determined pI values of the caseinates. Storage stability of emulsions was also studied at pH values around 7, and emulsions made of modified caseinates showed storage stability similar to that of unmodified caseinate emulsions.

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Many of the amphiphilic molecules, or surfactants, are produced from fossil-based raw materials. With the increasing awareness of the climate situation, focus has shifted toward more environmentally friendly solutions to replace fossil-based products. This has led to more interest towards the forest. The circular bioeconomy is focused on making use of residues and waste and on optimizing the value of biomass over time via cascading. Nowadays, bark is seen as a waste product by industries and mainly incinerated as solid fuel. The bark contains interesting compounds but some of these are only available in low amounts, less than 1 % in the bark, while other components are present in several percentages. However, some of these components are potential candidates for the manufacture of amphiphiles and there seems to be a strong match between bark availability and surfactant demand. The global amount of bark available is approximately 359 million m3 and more than 10 million m3 of industrial bark are generated annually in Sweden and Finland. The bark of Norway spruce, Scots pine and silver birch contains approximately 25–32 % of extractives and part of these extractives has a potential as a surfactant backbone. This matches the global surfactant demand of about 15.6 million tons. Therefore, industrial bark has a significant potential value as a raw material source for amphiphilic molecules and polymers. This review focuses on betulin, condensed tannin and suberin. These compounds have been studied on individually and methods to extract them out from the bark are well investigated, but to utilize them as amphiphilic compounds has not been explored. With this review, we want to emphasis the potential of using bark, what today is seen as a waste product, as a raw material for production of amphiphiles. Moreover, a techno-economic analysis has been performed on betulin, tannins and suberin.

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The influence of surface treatments including pigment coating, surface sizing and calendering on the mechanical strength of hotmelt adhesive joints in pilot made cartonboards was studied. The mechanical strength of the joints was investigated using the Y-peel test device at 23 • C and 50% relative humidity. Some of the samples were investigated with respect to the failure mode by scanning electron microscopy. The surfaces were characterized in terms of surface roughness, surface chemical composition, and adhesion behaviour. A strong adhesive bond displayed fibre tear. In addition to fibre tear, interfacial failure, i.e., failure between the cartonboard and the adhesive, was the main reason for fracture in the bonded assembly. The most important factor controlling the integrity of adhesive joints seemed to be the real contact area. The adhesive joints showed significantly higher strength when the hotmelt adhesive was first applied onto the rougher cartonboard of the assembly and then the smoother cartonboard was pressed on the adhesive than vice versa. The surface roughness of cartonboards mainly depended on whether the surface was pigment coated or not. Calendering displayed only a minor effect. No clear influence of surface chemical composition of the cartonboards on the adhesive joint strength was found due to the fact that changes in surface chemistry in this study also led to changes in surface roughness. The strongest adhesive joint was created between two medium-rough and surface-sized cartonboards.

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