Dry Fractionation Approach in Concentrating Tocopherols and Tocotrienols from Palm Fatty Acid Distillate: A Green Pretreatment Process for Vitamin E Extraction

Palm fatty acid distillate (PFAD) is a rich source of vitamin E. As compared to other vegetable oil, PFAD has higher tocotrienol (70–80%) over tocopherol content, which makes it a valuable source for vitamin E extraction. Current vitamin E extraction methods are not sustainable due to the intensive usage of chemical and high operational cost. Hence, the present study investigated for the first time using dry fractionation process as a green and economical pretreatment method for separating solid fraction (stearin) and liquid fraction (olein) in order to concentrate vitamin E from PFAD in olein fraction. We examined the dry fractionation conditions: crystallization ending temperature (36–44 °C), cooling rate (0.3 and 1.5°C min⁻¹), stirring speed (20–125 rpm), and holding time (0–60 min) on the composition of unsaturated and saturated fatty acids as well as vitamin E content in liquid fraction (olein) and solid fraction (stearin) using gas chromatography and high performance liquid chromatography, respectively. In most of these conditions, vitamin E was ultimately higher in olein fraction as compared to stearin fraction, which is correlated with the high degree of unsaturation. Under a cooling rate of 0.3°C min⁻¹, 90 rpm stirring speed, and ending crystallization of 38 °C, the highest vitamin E rich olein fraction was attained with 1479 ± 10.51 ppm in 50 g olein fraction as compared to 1366 ± 7.94 ppm in 500 g of unfractionated PFAD.     

棉籽油的深度分提工艺

新疆棉籽油含有700 mg/kg的蜡质和26%～28%的固体脂，由于新疆气温多在零度以下，棉籽油在运输、储存和销售过程中易产生固化、沉淀、发朦，影响棉籽油的外观、食用和销售。为了保持包装棉籽油透明，提高棉籽油的质量和附加值，对棉籽油进行深度分提以脱蜡脱脂。介绍了棉籽油深度分提工艺，即在15 ℃脱除蜡质，在7 ℃分提出棕榈酸甘三酯，继续降温至-10 ℃分提出棕榈酸甘二酯、棕榈酸甘一酯及其他硬脂，最终得到在低温下保持透明的棉籽液油。     

Quantitative UPLC‐MS/MS analysis of chlorogenic acid derivatives in antioxidant fractionates from dandelion (Taraxacum officinale) root

While qualitative studies have identified chlorogenic acids in antioxidant extracts, particularly ethyl acetate‐derived extracts, of Taraxacum officinale, quantitative analysis of these phenolic compounds remains largely unreported for this species. In this study, bioactivity‐guided fractionation of an antioxidant crude ethyl acetate extract (DPPH = 295.481 ± 0.955 mg TE g^?1 extract) from T. officinale root resulted in a number of reverse‐phase fractions that demonstrated high antioxidant activity (DPPH = 1058.733–1312.136 mg TE g^?1 extract), stronger than that of the synthetic antioxidant Trolox^®. UPLC‐MS/MS screening of these fractions for the presence of selected mono‐ and di‐caffeoylquinic acids revealed large quantities of 1,5‐dicaffeoylquinic acid present in several fractions (853.052–907.324 μg mg^?1), respectively. Due to the antioxidant potency and high levels of 1,5‐dicaffeoylquinic acid observed in these fractions, it was concluded that specifically this chlorogenic acid derivative is a major contributor to the antioxidant efficacy of dandelion root.     

Solvent fractionation of hard palm stearin to increase the concentration of tripalmitoylglycerol and dipalmitoyl-stearoyl-glycerol as substrates for synthesis of human milk fat substitute

This research aimed to produce triacylglycerols fraction rich in palmitic acid (PA) at the sn-2 position from hard palm stearin (HPS) through acetone fractionation. Fractionations were done at HPS-to-acetone ratios of 1:3, 1:5 and 1:7 (w/v) and at temperatures of 25, 30 and 35 °C for 3 h. Triacylglycerols with PA at the sn-2 position, such as tripalmitoylglycerol (PPP) and dipalmitoyl-stearoyl-glycerol (PPS), were concentrated in the solid fraction, obtained after separation by filtration. The optimal fractionation conditions were at a HPS-to-acetone ratio of 1:5 (w/v) and 30 °C. The total PPP and PPS content was more than 91%, with a corresponding yield of more than 59%. Triacylglycerols obtained were composed of more than 91% PA in which 88% were at the sn-2 position. Conclusively, the solvent fractionation is a suited alternative method for the preparation of triacylglycerols used for the enzymatic synthesis of 1,3-dioleoyl-2-palmitoylglycerol which is the main triacylglycerol for human milk fat substitute.     

Dry Fractionation of Cupuassu (Theobroma grandiflorum) Fat: Physical–Chemical Properties and Polymorphic Behavior

Physical chemical properties of cupuassu fat were modified by dry fractionation. Stearin and olein fractions were obtained at 29, 26, and 24 °C. Polymorphic behavior of unfractionated cupuassu fat (UCF) and its fractions were studied in situ by small-angle (SAXS) and wide-angle (WAXS) X-ray scattering using synchrotron light. Polymorphic transitions were followed in real time tempering samples with a thermal cycle. For UCF, the main polymorphic form crystallized under selected conditions was the β’₂. α and β’₁-forms appeared in trace amounts. β₂-form was obtained after storage at 25 °C for 3 months. Stearins obtained at 26 (S-26) and 24 °C (S-24) showed a similar polymorphic behavior. However, S-26 with improved physical properties might be more suitable for chocolate production or as a trans-fat alternative than UCF. Stearin fraction obtained at 29 °C (S-29) had a complex polymorphic behavior. The α-form was the first polymorphic form detected followed by β’₂-form. There was a polymorphic transition from α to β’₁-form but no transition between β’-forms. They were independent to each other showing fractionation in two different solid solutions. Increased contents of the triacylglycerols (TAG) SOA and SOB together with lower contents of SOO compared to UCF led to co-crystallization because there was no complete compatibility among all TAG present in S-29. β₁-form crystallized after storage forming crystals with a double-layer arrangement and a characteristic morphology. This form could be useful for accelerating crystallization process in melted liquid systems.     

Effect of malting and roasting of chickpea on functional and nutritional qualities of its protein fractions

Chickpea is gaining importance as a sustainable plant-based protein source due to its high protein content and protein bioavailability. Malting and roasting, the traditional processing techniques, can be used to improve the protein quality of chickpea. The effect of two processing techniques on the water-soluble albumin fraction, salt-soluble globulin fraction, alcohol-soluble prolamin fraction, and alkali-soluble glutelin fraction was studied. Globulin content decreased from 45.85% to 37.08%, whereas the albumin fraction was found to increase from 4.16% to 7.08%, after 6 days of germination. It was observed that malting and roasting resulted in significant changes in the protein quality parameters and decrease in anti-nutritional factors. Tannin content reduced by 53.18% and 40.44%, and the trypsin inhibitor activity reduced by 14.91% and 34.59% after malting and roasting, respectively. The protein efficiency ratio, biological value, and nutritional index improved due to malting and roasting. The biological value of raw chickpea protein was found to be 74.97%, and it increased to 81.89% and 79.27% on malting and roasting, respectively, and protein digestibility values were also increased. Microstructural and diffraction patterns of chickpea flours were examined. Amino acid scores for infants and adults were calculated, and sulphur-containing amino acids were found to be the limiting amino acids in chickpea.     

Comprehensive branching analysis of polyethylene by combined fractionation and thermal analysis

Linear low density polyethylene (LLDPE) and low density polyethylene (LDPE) differ significantly in their branching types and branching distributions. For a comprehensive analysis, preparative temperature rising elution fractionation and/or preparative molar mass fractionation are used to fractionate typical LLDPE and LDPE bulk resins into narrowly distributed fractions. The chain structures of the bulk resins and their fractions are further analysed using SEC, crystallization analysis fractionation, DSC and high‐temperature HPLC to provide detailed information on short chain branching in LLDPE and long chain branching in LDPE. For LDPE it is shown that the multiple fractionation approach is a powerful source of sample libraries that may have similar molar masses and different branching structures or alternatively similar branching but different molar masses. The analysis of these library samples by thermal analysis provides a much deeper insight into the molecular heterogeneity of the samples compared to bulk sample analysis. © 2018 Society of Chemical Industry     

Analytical fractionation of dissolved organic matter in water using on-line carbon detection

A routine method is described for the analytical fractionation of dissolved organic matter (DOM) in natural freshwater and in used waters. The fractionation is based on the different adsorption behaviours of various constituents of the DOM on octadecyl-silica as a function of pH. The DOM is separated into a hydrophilic, an acid and a hydrophobic fraction. The detection is carried out by an on-line carbon detector. The method requires only small water samples (20 ml) with low dissolved organic carbon (DOC) concentrations (1–5 mg Cl⁻¹). The samples can be analysed rapidly with no preconcentration. Fractionation of model compounds and mixtures demonstrates the performance of the method. The application of the method is illustrated by an investigation of the changes of the DOC composition occurring in a longitudinal transect of a river and during the infiltration of river water to groundwater.