No abstract

No abstract

Refined bleached deodorised palm oil (RBDPO) was blended with 4–25 wt‐% hydrogenated palm oil (HPO). The physical, chemical and rheological properties of these samples were studied during 4 wk of storage at 15 °C. During storage, it was observed that there was an increase in solid fat content, compression force, hardness index (HI), melting temperatures, and storage modulus (G') with increasing concentration of HPO in the blends and with storage time. X‐ray diffraction results showed that the crystal networks of the blends were stabilised in the β' polymorphic form. However, in pure RBDPO, a very weak β form was observed. An increase in storage modulus (G'), compression force and HI indicated that the crystal networks of the blends became more highly structured with increasing storage time and concentration of HPO, which implies that post‐hardening had occurred without transformation of the polymorphic form from β’ to β.

No abstract

In an effort to improve the physical and/or melting characteristics of solid fats, the enzymatic transesterification of palm stearin-palm kernel olein (40:60) in a solvent-free system was investigated. The enzymes used were Celite-bound lipases that include 1,3-specific lipases such as Aspergillus niger, Alcaligenes sp. and nonspecific lipases such as Pseudomonas sp. and Candida rugosa. Commercial immobilized lipase from Rhizomucor miehei (Lipozyme 1M60) was also used. The efficacies of these enzymes for improving the melting behaviour of the oil mixtures were followed by slip melting point (SMP), solid fat content (SFC) and differential scanning calorimetry (DSC) analyses. Results indicated that enzymatic transesterification was able to produce fat mixtures with substantially lower melting points by repositioning the fatty acids of triglycerides in the higher melting range to form lower-or middle-melting components. Pseudomonas lipase-catalyzed mixtures produced the highest degree (152.2%) and rate (50.0 h-1) of transesterification followed by R. miehei lipase at 151.7% and 27.1 h-1, respectively. The highest % FFA liberated was also from the reaction mixture catalysed by Pseudomonas (2.90%) and R. miehei (2.54%) lipases. The Pseudomonas-catalyzed mixture also produced the biggest drop in SMP (12.0°C) and the SFC results showed complete melting at 35°C. Our findings also suggest that the positional specificity of lipases may not play a significant role in producing a more fluid product.