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Ecklonia maxima is an endemic South African seaweed with numerous commercially valuable compounds, including sodium alginate. This polysaccharide contains 1,4-linked β-d-mannuronic (M) and α-l-guluronic acid (G) residues, and has enormous health and food applications and benefits for biomedicine. In this study, acid extraction of sodium alginate from Ecklonia maxima was performed, and its chemical and physical properties were compared with commercial sodium alginate. A yield of 58.7 % (w/w of dry alga) sodium alginate was recovered from the seaweed. As expected, Fourier-transform infrared spectroscopy and nuclear magnetic resonance spectroscopic analyses of sodium alginate revealed the presence of M and G residues in the polysaccharide. Circular dichroism (CD) spectroscopy revealed an M/G ratio of 1.86 from the extracted sodium alginate. The viscosity average molecular weight of sodium alginate was 429 kDa using the Mark–Houwink–Sakurada equation. Three-dimensional conformational analysis by Congo red and CD spectroscopy suggested that sodium alginate exhibits a triple-helix conformation in solution. Furthermore, X-ray powder diffraction analysis confirmed that the alginate has an amorphous structure. Sodium alginate extracted from E. maxima found on the coasts of Southern Africa exhibits a high mannuronic content and high viscosity, potentially beneficial for drug delivery and biomedical applications. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Gelatin is a derived, protein-based biopolymer used in nourishments to enhance consistency, strength, and flexibility. The aim of this research is to optimize the organic acid extraction of gelatin from fish skin. In this work, effect of parameters such as acid (based on its type) concentration (0.05-0.15 M), extraction temperature (40-60 °C), and types of acid (formic, acetic and propionic acids) on extraction yield of gelatin was examined at constant extraction time of 7 d and skin to acid mass ratio of 1:20. Collagenous material was separated from fish skin, and a basic protein, collagen, was hydrolyzed to gelatin, a derived protein. Response surface methodology (RSM) based Box-Wilson design was used for optimization and the optimization results revealed that the maximum gelatin extraction of 11.91% was achieved at 0.1 M formic acid and 52 °C. Thus, it would be concluded that the fish skin could be the potential feedstock for gelatin extraction.

Gelatin is a derived, protein-based biopolymer used in nourishments to enhance consistency, strength, and flexibility. The aim of this research is to optimize the organic acid extraction of gelatin from fish skin. In this work, effect of parameters such as acid (based on its type) concentration (0.05-0.15 M), extraction temperature (40-60 °C), and types of acid (formic, acetic and propionic acids) on extraction yield of gelatin was examined at constant extraction time of 7 d and skin to acid mass ratio of 1:20. Collagenous material was separated from fish skin, and a basic protein, collagen, was hydrolyzed to gelatin, a derived protein. Response surface methodology (RSM) based Box- Wilson design was used for optimization and the optimization results revealed that the maximum gelatin extraction of 11.91% was achieved at 0.1 M formic acid and 52 °C. Thus, it would be concluded that the fish skin could be the potential feedstock for gelatin extraction. [ABSTRACT FROM AUTHOR]

Establishing an alternative resource of rare earth elements (REEs) in coal by-products has been a topic of high interest for the past decade. Despite this, research that characterizes REEs in such materials produced in Australia is lacking. This paper focuses on the concentration and occurrence of REEs in power station coal ashes that represent a suite of major economic coal basins in Australia. The concentration of REEs in coal ash samples was determined by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). Fly ash and bottom ash generated at power stations that utilize coals from the Collie Basin in Western Australia contained elevated REE concentrations. A REE-rich fly ash containing 0.21% total rare earth oxides (REO) was subject to further analysis by Scanning Electron Microscopy with Energy Dispersive X-rays (SEM-EDX) and TESCAN Integrated Mineral Analysis (TIMA). Fine (avg. <5 μm) monazite grains were observed in the fly ash which were typically bound to Al/Si-rich phases. A substantial increase in the aqua regia-extractable fraction of REEs occurred when fly ash samples were milled to an ultrafine particle size. The current investigation has demonstrated that Australian coal ash may represent a promising resource of REEs as the demand for these metals increases. [ABSTRACT FROM AUTHOR]

In this study, the Glycyrrhiza polysaccharides were prepared from Glycyrrhiza residues with different pH acid solutions (HCl, pH 1[P1], pH 3[P3], pH 5[P5]) as extraction solution. The monosaccharide composition and relative molecular weight of Glycyrrhiza polysaccharides were determined by Dionex system and high performance size exclusion chromatography. The structures of Glycyrrhiza polysaccharides were analyzed and compared by FT-IR spectroscopy, atomic force microscope (AFM), nuclear magnetic resonance (NMR), scanning electron microscope (SEM) and X-Ray diffraction (XRD). The results showed that three Glycyrrhiza polysaccharides were heteropolysaccharides, which were mainly composed of Fuc (fucose), Rha (rhamnose-rhamnose), Ara (arabose), Gal (galactose), Glc (glucose) and GalA (galacturonic acid) in different proportions. The weight average molecular weight (Mw) of P3 exhibited a multicomponent distribution. Mw(682 kDa) accounted for about 7.3% (w/w), and Mw(7110 kDa) was about 92.7% (w/w), accounting for the largest proportion. The FT-IR spectroscopy and NMR verified that the backbone of Glycyrrhiza polysaccharides could be composed of→4)-β-D-Glcp-(1→. Congo red experiment showed that P1 and P5 might have a triple helix conformation. The SEM showed a similar morphological structure both in P3 and P5, which was a network structure with a rough surface cumulated by a large number of spherical particles. While P1 was a lamellar structure with an uneven surface and multiple pores. The AFM revealed a mutually branched and intertwined structure of Glycyrrhiza polysaccharide, and a small amount of Glycyrrhiza polysaccharide displayed a microstructure of spherical aggregates. The XRD showed that P1 had crystal and amorphous structure, while P3 and P5 had no crystal structure. Therefore, the structure of Glycyrrhiza polysaccharide by acid extraction was significantly affected by different pH.

This is an essay in the field of mining engineering. Deep-sea rare earth rich deposit, as a potential rare earth resource, are an important supplement to land rare earth resources and may become one of the first deep-sea minerals to be exploited. In this paper, four deep-sea REE rich deposit (REE rich deposits in the western Pacific Ocean, the southeast Pacific Ocean, the middle and east Pacific Ocean, and the Middle Indian Ocean basin-Wharton Basin.) are analyzed. This paper summarizes the basic resource characteristics of deep-sea rare earth rich deposit (such as large total reserves, large distribution differences, and the main occurrence mineral is biological apatite), and reviews two methods (acid leaching-extraction separation technology and separation-flotation method) used in the separation and extraction of deep-sea REE. The result shows that the acid leaching-extraction separation technology has the disadvantages of low recovery of REE and excessive acid consumption. The separation of sediment samples before flotation operation can achieve efficient enrichment of REE in deposit under the condition of low acid consumption, which is an important development direction to separate and extract REE resources from deep-sea REE rich deposit. Based on this, it is suggested to strengthen the research and development related to efficient classification of deep-sea REE rich deposit resources and in-situ mining and leaching technology in the future.

Industry represents a fundamental component of modern society, with the generation of massive amounts of industrial waste being the inevitable result of development activities in recent years. Red mud is an industrial waste generated during alumina production using the Bayer process of refining bauxite ore. It is a highly alkaline waste due to the incomplete removal of NaOH. There are several opinions in both the literature and legislation on the hazards of red mud. According to European and national legislation, this mud is not on the list of hazardous wastes; however, if the list of criteria are taken into account, it can be considered as hazardous. The complex processing of red mud is cost-effective because it contains elements such as iron, manganese, sodium, calcium, magnesium, zinc, strontium, lead, copper, cadmium, bismuth, barium and rare earths, especially scandium. Therefore, the selection of an extraction method depends on the form in which the element is present in solution. Extraction is one of the prospective separation and concentration methods. In this study, we evaluated the kinetic modelling of the solid–liquid acid extraction process of predominantly scandium as well as other elements present in red mud. Therefore, three acids (HCl, HNO3 and H2SO4) at different concentrations (10, 20 and 30%) were targeted for the extraction of Sc(III) from solid red mud. Specific parameters of the kinetics of the extraction process were studied, namely the solid:liquid ratio, initial acid concentration, contact time and temperature. The extraction kinetics of Sc(III) with acids was evaluated using first- and second-order kinetic models, involving kinetic parameters, rate constants, saturation concentration and activation energy. The second-order kinetic model was able to describe the mechanism of Sc(III) extraction from red mud. In addition, this study provides an overview on the mechanism of mass transfer involved in the acid extraction process of Sc(III), thereby enabling the design, optimization and control of large-scale processes for red mud recovery. [ABSTRACT FROM AUTHOR]

[Display omitted] • A Fe2+ pyrite /PMS conditioning method was developed with extremely low acid usage. • Fe2+ pyrite /PMS conditioning improved WAS dewaterability and released 22.75% of BWC. • Some PN in TB-EPS was decomposed into inorganic-N by Fe2+ pyrite /PMS conditioning. • The eco-toxicity of Cr in WAS was weakened by Fe2+ pyrite /PMS conditioning. • 94% pyrite was recovered after use and the recycled feasibility was verified. Wastewater activated sludge (WAS) has poor dewaterability and contains heavy metals (HMs), limiting its land application. Therefore, in this study, a novel pyrite acid eluent-activated peroxymonosulfate (Fe2+ pyrite /PMS) conditioning approach that can completely recover the residual pyrite and greatly reduce acid use was developed to improve WAS dewaterability, and the HMs chemical speciation and risks of conditioned WAS were assessed. Our results showed that under the optimized operational parameters, the capillary suction time (CST) and water content (Wc) of WAS decreased by 46.03% and 7.75%, respectively. Furthermore, during Fe2+ pyrite /PMS conditioning processing, sulfate radical (SO 4 − ) destroyed the extracellular polymeric substances (EPS) matrix, causing bound water release and the decrease of proteins/polysaccharides in outer layered EPS, even the decomposition of some protein-N in tightly bound EPS (TB-EPS) into inorganic-N. In addition, although the total concentration of HMs in the conditioned WAS matrix increased, the Ni concentration decreased in the solid fraction. Further, the risk assessment code (RAC) levels did not increase, and the eco-toxicity of Cr became weakened after Fe2+ pyrite /PMS conditioning. However, after acid extraction, the pyrite residue had worsened recycle performance because the passivation layer contained S0/S n 2− on its surface, and no additional elements were detected in the pyrite residue, which had almost no effect on its further usage. [ABSTRACT FROM AUTHOR]

The aims of this study were to extract pectin from selected indigenous fruits, including breadfruit, papaya and santol as well as investigate the chemical and physical properties of extracted pectin to address the potential of these fruits as an alternative source of commercial pectin. Different parts of fruits were used to extract pectin under the acid condition method. Pectin yield ranged from 8.52±0.05 to 49.96±0.89% and breadfruit was the highest pectin source. The extracted pectin from breadfruit was categorized as high methoxyl pectin with the degree of esterification between 93.57±0.22 to 96.70±0.17%, which was almost 2-time higher than the commercial pectin (53.10±1.25%). The galacturonic acid contents found in the extracted pectin varied widely from 41.41±0.09 to 73.19±0.59%. The significantly highest galacturonic acid content was found in the pectin extracted from the peel of breadfruit, which strongly indicated that pectin extracted from the peel of breadfruit was good quality. The FT-IR spectra also confirmed that the pectin obtained in this study was overall similar to the commercial pectin. Therefore, the breadfruit peel was highly recommended as a potential alternative source of pectin.

Recently, the applications of hydrate phenomena in industrial processes have been increasing. A clathrate or hydrate is a solid, ice-like compound that forms when water/guest is mixed under certain conditions. Hydrogen water molecules bond with the guest molecules to form a crystal lattice. Different guests can form the Clathrate (e.g., gases or liquids). Dilute Sulfuric acid is usually generated at different industrial plants, and these dilute acids are considered waste because they cannot be reused again. Many treatment processes handle this environmental problem, like electrochemistry, precipitation, adsorption, membrane filtration, and ion exchange. Although such processes have significant operational advantages, their disadvantage is that many of the high costs of the treatment process and the generated products of treatment are considered toxic pollutants. This work utilized clathrate phenomena experiments to re-concentrate dilute sulfuric acid. The selected clathrate guest was Cyclopentane. Each experiment s consists of a mixture of Cyclopentane and dilute sulfuric acids. The volume ratios of dilute sulfuric acid to Cyclopentane were (6:1, 4: 1, 3:1, and 2:1) with different initial concentrations (12.5%, 10%, 7.5%, 5%, 2.5%) of acid. It was found that the clathrate method was effective in re-concentrate dilute sulfuric acids with a maximum efficiency of 94% at the ratio of acid /cyclopentane (6:1) at 12.5% concentration. It can be concluded that the increase in dilute sulfuric acid /cyclopentane volume ratio leads increasing in removal efficiency while reducing the yield percentage and enriched Factor.

The specifi cs of the nuclear tests carried out on the territory of the former Semipalatinsk test site (STS) led to the emergence of various sites that diff er in levels of radioactive contamination and radionuclide composition. This also led to a signifi cant diff erence in the solubility of radioactive particles. Traditionally, the “Experimental Field” testing ground was characterized by the presence of sparingly soluble, vitrifi ed particles, which was determined by the features inherent in ground tests of nuclear weapons, namely, the interaction of the high-temperature explosion region with soil particles. The presence of such sparingly soluble particles in the soil cover makes it impossible to use 6–8 М HCl and 7–8 М HNO3 solutions which are most often used radiochemical analysis to determine the content of 90Sr and 239+240Pu. This paper considers methods for the acid extraction of anthropogenic radionuclides from soils of the STS using autoclaving. The aim of the research is to develop a method for the acid extraction of anthropogenic radionuclides from enlarged soil samples using autoclave decomposition. A blank soil sample was used to determine the optimal autoclave decomposition parameters; to test the acid extraction method, a soil sample was taken from the territory of the “experimental fi eld” testing ground. The radionuclide 137Cs has been used as the most optimal indicator of acid extraction due to its strong fi xation on clay and mineral soil particles and ease of detection by the gamma radiation. Autoclave decomposition has been carried out by dissolving the studied samples in a mixture of mineral acids (HCl, HNO3, HF, H2SO4). The specifi c activity of radionuclide has been determined on a BE3830 gamma spectrometer with a high-purity germanium detector (Canberra, USA), the amount of undecomposed soil residue has been determined gravimetrically (PA214C analytical balance, Ohaus, USA). The data obtained indicate that the most complete extraction of 137Cs occurs when using concentrated HF solutions (individually or in a mixture with other mineral acids). The degree of extraction of 137Cs varied from 85 to 100%. The worst results have been shown by the use of a mixture of acids 3HCl:HNO3. In this case the degree of extraction of 137Cs did not exceed 20%. The effi ciency of decomposition of soil samples weighing 10 g with a concentrated solution of HF at a temperature of 120 to 160 ºC was ≥95%.

Copyright of Multipurpose Utilization of Mineral Resources / Kuangchan Zonghe Liyong is the property of Multipurpose Utilization of Mineral Resources Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The evaluation of different methods for kafirin extraction was made to obtain techno-functional concentrates from two sorghum cultivars. The concentrates were rheologically evaluated in a “dough-like” resin system to assess their potential as a gluten substitute. Under acidic extractions (ethanol 70%, pH 2.5), yields of 56.98% and 46.31% for white (WS) and red sorghum (RS) were obtained, with the highest purity for WS (74.54%). A characteristic electrophoretic pattern was obtained for kafirins, including fractions α1, α2, β and γ. The WS protein was used to prepare resins with lactic acid (LA) as a plasticizing agent, showing similar extensibility to zein (11.37 vs. 11.89 mm respectively) but below wheat gluten (42.61 mm). The microstructure of kafirin resins showed air encapsulation and alignment as fibers. This study allowed to explore new food-compatible extractions for kafirin and evaluate how they will perform rheologically at the kneading stage using a simple resin method.

Summary: The industrial processing of passion fruit produces a huge quantity of rinds. This work evaluates the physicochemical and technological characteristics of passion fruit mesocarp flour (MF) and its pectin (PM), aiming to replace the commercial citrus pectin (PC) used as thickener and gelling agent. The pectin PM presented the lower degree of esterification (68.0%), content of galacturonic acids (72.0%) and molar mass than the pectin PC. Gels made with MF, pectin PM and pectin PC were formed at all concentrations (1%, 2% and 3%) and showed non‐Newtonian pseudoplastic fluid behaviour. Gel made with 3% MF (0.75% pectin) presented the higher hardness and viscosity than 1% PC gel, but the lower gel strength. The MF flour and its pectin PM have very good technological potential, when compared to the commercial pectin PC, mainly as thickener agent. [ABSTRACT FROM AUTHOR]

Pectin has numerous applications in the food industry because of its gelling capability. Dragon fruit peel is an ideal source of pectin since it contains pectin of around ± 10.8% of the weight. In this research, the extraction of pectin from dragon fruit peels used ultrasonic waves. This study was an experimental research with three independent variables that was a type of acid (HCl and CH3COOH), acid concentration (0.1 N and 0.2 N), and extraction time (30, 60, and 90 minutes). The control sample was pectin extracted by conventional methods, dipped in 0.1 N acids at room temperature for 24 hours. The result showed that the ultrasound-assisted extraction was an effective method to extract pectin from peels of red dragon fruits, whereas the yield was even twice that compared with the control sample. The treatment of 90 minutes of sonication in 0.2 N HCl produced the highest yield (2.71%). The pectin has a yellowish to a white degree of color and a 2.22 g.s/cm viscosity. It has a 902.2 mg equivalent weight, 6.14% methoxyl content, 54.4% galacturonic acid content and 63.8% esterification degree. The value of esterification degree and methoxyl content indicated that pectin from this research is high ester-pectin and low-methoxyl pectin.

Biopolymer-like collagen has great industrial potential in terms of its excellent properties, such as strong biocompatibility, high degradability, and low antigenicity. Collagen derived from fish by-products is preferable as it is safer (free from transmittable diseases) and acceptable to most religious beliefs. This study aimed to characterize the unicornfish (Naso reticulatus Randall, 2001) bone collagens prepared with different type of acids, i.e., acetic acid, lactic acid, and citric acid. A higher yield (Y) (p < 0.05) was obtained in the citric-acid-soluble collagen (CASC) (Y = 1.36%), followed by the lactic-acid-soluble collagen (LASC) (Y = 1.08%) and acetic-acid-soluble collagen (AASC) (Y = 0.40%). All extracted collagens were classified as type I due to the presence of 2-alpha chains (α1 and α2). Their prominent absorption spectra were located at the wavelengths of 229.83 nm to 231.17 nm. This is similar to wavelengths reported for other fish collagens. The X-ray diffraction (XRD) and infrared (IR) data demonstrated that the triple-helical structure of type I collagens was still preserved after the acid-extraction process. In terms of thermal stability, all samples had similar maximum transition temperatures (Tmax = 33.34–33.51 °C). A higher relative solubility (RS) of the unicornfish bone collagens was observed at low salt concentration (0–10 g/L) (RS > 80%) and at acidic condition (pH 1.0 to pH 3.0) (RS > 75%). The extracted collagen samples had an irregular and dense flake structure with random coiled filaments. Overall, bones of unicornfish may be used as a substitute source of collagen. [ABSTRACT FROM AUTHOR]

This study was carried out to compare the extractability and characteristics of barracuda (Sphyraena sp.) skin collagen using various organic acids. Acetic-solubilized collagen (ASBS), lactic-solubilized collagen (LSBS) and citric-solubilized collagen (CSBS) yielded 6.77 g/100 g, 10.06 g/100 g and 8.35 g/100 g, respectively, and those yields were significantly different (p < 0.05). All acid-solubilized collagens were considered as type I because of their two alpha chains (α1 and α2) detected in acrylamide gel after electrophoresis. Ultraviolet–visible (UV–vis) analysis confirmed that ASBS, LSBS and CSBS had similar absorption peaks (230.5 nm) and the results were in accordance with other fish collagens. Under infrared (IR) and X-ray diffraction (XRD) analysis, the triple helical structure of type I collagens extracted from barracuda skin was maintained. From a thermostability study, all type I collagens showed a higher maximum transition temperature (Tmax = 40.16 to 41.29 °C) compared to other fish skin collagens. In addition, the functional properties of the extracted collagens revealed the ASBS had higher water and oil absorption capacities than the CSBS and LSBS samples. The highest level of the emulsion ability index (EAI) (>200 m2/g) was detected under acidic conditions (pH 4), while lower EAIs were recorded under the alkaline (pH 10) and neutral treatments (pH 7). All type I collagens had a higher relative solubility (>60%) at a low pH test but the solubility level sharply decreased at a neutral pH. In addition to this, a lower concentration of NaCl (0–20 g/L) showed the higher percentage of solubility (>60%) while adding over 30 g/L of NaCl decreased solubility (>40%). From a microstructural test, all type I samples had an irregular and dense flake structure with random coiled filaments. Overall, collagen extracted from the barracuda skin may be applied as an alternative collagen from an industry perspective. [ABSTRACT FROM AUTHOR]

Two neutral Glycyrrhiza polysaccharide (GP), named GP-LA and GP-HA, with molecular weights of 3.023 × 105 and 1.291 × 105, respectively, were extracted from Glycyrrhiza residues by hot acid extraction (HA) and low-temperature acid extraction (LA) and purified by column chromatography. Comprehensive analysis showed that the backbone of GP was composed of →4)-β-D-Glcp-(1→. For GP-LA, the side chain probably composed of β-L-Araf-(1→, →5)-β-L-Araf-(1→, →4)-β-D-Xylp-(1→, β-D-Glcp-(1→, →3,4)-α-D-Glcp-(1→, →4,6)-α- D-Glcp-(1→, and for GP-LA, the side chain probably composed of→6)-β-D-Galp-(1→, -α-D-Glcp-(1→, →3,4)-α-D-Glcp-(1→, →2,4)-α-D-Glcp-(1→, →4,6)- D-Glcp-(1→. The GP had a triple helix conformation and numerous irregular spherical particles with smooth surfaces. Atomic force microscopy (AFM) confirmed that GP-HA possessed single-branched structures and GP-LA possessed cross-linked network structures. X-ray diffraction (XRD) analysis revealed that GP-LA had both crystalline and amorphous structures, but GP-HA had no crystal structure. Furthermore, the results indicated that GP-LA and GP-HA exhibited certain inhibition activity on α-glucosidase. CD spectra and fluorescence intensity measurements confirmed that the secondary structure of α-glucosidase changed with the addition of GP. • Two neutral polysaccharides extracted from Glycyrrhiza uralensis residues. • Structure characteristics of Glycyrrhiza polysaccharides were analyzed comprehensively. • Glycyrrhiza polysaccharides had better inhibitory activity on α-glucosidase. [ABSTRACT FROM AUTHOR]

Industry represents a fundamental component of modern society, with the generation of massive amounts of industrial waste being the inevitable result of development activities in recent years. Red mud is an industrial waste generated during alumina production using the Bayer process of refining bauxite ore. It is a highly alkaline waste due to the incomplete removal of NaOH. There are several opinions in both the literature and legislation on the hazards of red mud. According to European and national legislation, this mud is not on the list of hazardous wastes; however, if the list of criteria are taken into account, it can be considered as hazardous. The complex processing of red mud is cost-effective because it contains elements such as iron, manganese, sodium, calcium, magnesium, zinc, strontium, lead, copper, cadmium, bismuth, barium and rare earths, especially scandium. Therefore, the selection of an extraction method depends on the form in which the element is present in solution. Extraction is one of the prospective separation and concentration methods. In this study, we evaluated the kinetic modelling of the solid–liquid acid extraction process of predominantly scandium as well as other elements present in red mud. Therefore, three acids (HCl, HNO3 and H2SO4) at different concentrations (10, 20 and 30%) were targeted for the extraction of Sc(III) from solid red mud. Specific parameters of the kinetics of the extraction process were studied, namely the solid:liquid ratio, initial acid concentration, contact time and temperature. The extraction kinetics of Sc(III) with acids was evaluated using first- and second-order kinetic models, involving kinetic parameters, rate constants, saturation concentration and activation energy. The second-order kinetic model was able to describe the mechanism of Sc(III) extraction from red mud. In addition, this study provides an overview on the mechanism of mass transfer involved in the acid extraction process of Sc(III), thereby enabling the design, optimization and control of large-scale processes for red mud recovery.

Persimmon (Diospyros kaki L.) is a fruit generally consumed fresh, generating quantities that are discarded due to senescence or the presence of lesions. The extraction of pectin from persimmon could be an alternative to obtain a product with added value and to reduce post-harvest losses. Thus, the present work aimed to evaluate the potential of Fuyu persimmon for pectin extraction through acid and enzymatic extraction methods. The extractions were performed separately for each part of the fruit, dividing it into pulp and residues (peel and seeds). The highest yield was obtained from the enzymatic extraction of peel and seeds, resulting in an amount of pectin 14 times higher than the pectin obtained from the freeze-dried pulp.

The novelty of this study is the use of brewed black tea waste (BBTW) for pectin extraction. For this purpose, the effects of extraction conditions including extraction temperature, particle size, extraction duration and solid–liquid ratio (w/v) (SLR), on the yields (PY) and physicochemical properties of the extracted pectins were investigated. In the study, pectin extractions were accomplished using solutions of citric acid (CA) as organic acid and hydrochloric acid (HCl) as inorganic acid. Extracted pectin yields from BBTW were varied between 3.18 and 10.75% depending on the extraction conditions. Galacturonic acid values were observed between 29.39 and 73.99% for the extracted pectins. Obtained pectins showed 30.87–62.50% of degree of esterification, 5.31–10.49% of methoxyl content and equivalent weight values varied between 429 and 1238 g/mol. These values for the commercial pectin (CP) were found to be respectively 69.31%, 11.57% and 1250 g/mol. These results showed that brewed black tea waste can be considered as an alternative resource for pectin production. Graphical representation of pectin extraction steps from brewed black tea waste and black tea leaves. [ABSTRACT FROM AUTHOR]

Water pollution, resulting from the degradation of plastics into microplastics, exposes humans and other living organisms to contaminated drinking water. Microplastics are capable of adsorbing toxic heavy metals which are carcinogenic and may affect the reproductive functions of living organisms. Hence, this study focuses on the characterization and quantification of microplastics in water to raise the awareness and propose a method of dealing with this emerging pollutant in various aqueous environments. The microplastics were separated from water using polyvinylidene difluoride (PVDF) and PVDF modified with carbon nano-onions (CNOs). The PVDF exhibited the highest concentration of microplastics in the wastewater influent (140 ± 1.85 MP/L) compared to the effluent (8.8 ± 2.10 MP/L), tap water (6.5 ± 5.77 MP/L), and lake water (10 ± 2.65 MP/L). The stereo microscope displayed red, blue, and black colored plastics. The morphological properties were determined using SEM. ATR-FTIR, equipped with Spectrum 10 Spectroscopy Software was used to establish the presence of high-density polyethylene (50%), poly(1,4-butylene terephthalate) (16.6%), nylon 12 (16.6%), and cellulose (16.6%) in the influent. The quantification of heavy metals extracted from the microplastics indicated that the concentrations of As (1.759 to 8.699 mg/L), Cu (83.176 mg/L) and Zn (0.610 mg/L) were above the acceptable limits. Our work is beneficial for the development of a microplastics monitoring protocol for various municipalities. Water treatment plants may also include the treatment of microplastics in the influent and monitor the effluent before the water is released back into the environment. [ABSTRACT FROM AUTHOR]

Extraction methods are determinant in technological properties of non-conventional starches. Different steeping procedures are capable of modifying the starch regarding its proximal composition and its morphological thermal and rheological profile, also changing the residues produced during the extractions. Thus, this study aimed to characterize the modified loquat seed starch (LSS) by neutral (NS—neutral starch) and acid (AS—acid starch) steeping and their by-products (AEB—acid extraction by-product) and (NEB—neutral extraction by-product). This study was based on data from thermal analysis, viscosity profile, antioxidant properties and determination of structural and morphological characteristics. Regardless of the extraction method applied, LSS presented a C-type crystalline structure. The AS resulted in a less yellowish starch, with low protein (1.18%), lipid (0.34%) and ash content (0.15%). Compared with the NS, the AS provided more thermal stability. Using differential scanning calorimetry (DSC) and Rapid Visco Analyzer (RVA), was verified a low gelatinization temperature (60.53–60.55 °C) and a higher tendency to gelatinization of the starches. Furthermore, higher antioxidant capacity was observed for NS (600.20 mg GAE/100 g). Moreover, all by-products presented higher content of fiber (65.82%) and protein (8.92%), verified by their proximal composition and Scanning Electron Microscopy. The thermogravimetric analysis showed a low thermal stability for by-products. These findings demonstrate that all samples obtained from loquat seed showed potential characteristics for industrial usage in new processes. Their by-products can also be associated with the decreasing of agro-industrial waste and can be used in food formulations or biodegradable films. [ABSTRACT FROM AUTHOR]

The evaluation of different methods for kafirin extraction was made to obtain techno-functional concentrates from two sorghum cultivars. The concentrates were rheologically evaluated in a "dough-like" resin system to assess their potential as a gluten substitute. Under acidic extractions (ethanol 70%, pH 2.5), yields of 56.98% and 46.31% for white (WS) and red sorghum (RS) were obtained, with the highest purity for WS (74.54%). A characteristic electrophoretic pattern was obtained for kafirins, including fractions α1, α2, β and γ. The WS protein was used to prepare resins with lactic acid (LA) as a plasticizing agent, showing similar extensibility to zein (11.37 vs. 11.89 mm respectively) but below wheat gluten (42.61 mm). The microstructure of kafirin resins showed air encapsulation and alignment as fibers. This study allowed to explore new food-compatible extractions for kafirin and evaluate how they will perform rheologically at the kneading stage using a simple resin method. [ABSTRACT FROM AUTHOR]

This study was carried out to compare the extractability and characteristics of barracuda (Sphyraena sp.) skin collagen using various organic acids. Acetic-solubilized collagen (ASBS), lactic-solubilized collagen (LSBS) and citric-solubilized collagen (CSBS) yielded 6.77 g/100 g, 10.06 g/100 g and 8.35 g/100 g, respectively, and those yields were significantly different (p < 0.05). All acid-solubilized collagens were considered as type I because of their two alpha chains (α1 and α2) detected in acrylamide gel after electrophoresis. Ultraviolet–visible (UV–vis) analysis confirmed that ASBS, LSBS and CSBS had similar absorption peaks (230.5 nm) and the results were in accordance with other fish collagens. Under infrared (IR) and X-ray diffraction (XRD) analysis, the triple helical structure of type I collagens extracted from barracuda skin was maintained. From a thermostability study, all type I collagens showed a higher maximum transition temperature (Tmax = 40.16 to 41.29 °C) compared to other fish skin collagens. In addition, the functional properties of the extracted collagens revealed the ASBS had higher water and oil absorption capacities than the CSBS and LSBS samples. The highest level of the emulsion ability index (EAI) (>200 m2/g) was detected under acidic conditions (pH 4), while lower EAIs were recorded under the alkaline (pH 10) and neutral treatments (pH 7). All type I collagens had a higher relative solubility (>60%) at a low pH test but the solubility level sharply decreased at a neutral pH. In addition to this, a lower concentration of NaCl (0–20 g/L) showed the higher percentage of solubility (>60%) while adding over 30 g/L of NaCl decreased solubility (>40%). From a microstructural test, all type I samples had an irregular and dense flake structure with random coiled filaments. Overall, collagen extracted from the barracuda skin may be applied as an alternative collagen from an industry perspective.

Biopolymer-like collagen has great industrial potential in terms of its excellent properties, such as strong biocompatibility, high degradability, and low antigenicity. Collagen derived from fish by-products is preferable as it is safer (free from transmittable diseases) and acceptable to most religious beliefs. This study aimed to characterize the unicornfish (Naso reticulatus Randall, 2001) bone collagens prepared with different type of acids, i.e., acetic acid, lactic acid, and citric acid. A higher yield (Y) (p < 0.05) was obtained in the citric-acid-soluble collagen (CASC) (Y = 1.36%), followed by the lactic-acid-soluble collagen (LASC) (Y = 1.08%) and acetic-acid-soluble collagen (AASC) (Y = 0.40%). All extracted collagens were classified as type I due to the presence of 2-alpha chains (α1 and α2). Their prominent absorption spectra were located at the wavelengths of 229.83 nm to 231.17 nm. This is similar to wavelengths reported for other fish collagens. The X-ray diffraction (XRD) and infrared (IR) data demonstrated that the triple-helical structure of type I collagens was still preserved after the acid-extraction process. In terms of thermal stability, all samples had similar maximum transition temperatures (Tmax = 33.34–33.51 °C). A higher relative solubility (RS) of the unicornfish bone collagens was observed at low salt concentration (0–10 g/L) (RS > 80%) and at acidic condition (pH 1.0 to pH 3.0) (RS > 75%). The extracted collagen samples had an irregular and dense flake structure with random coiled filaments. Overall, bones of unicornfish may be used as a substitute source of collagen.

In this study; pectin was extracted using traditional acid extraction method using fruit peel waste such as mandarin, pomegranate and pumpkin peels. The pectins obtained by using different fruit peels and changing the extraction conditions were characterized and compared with commercial pectin. Pectin extractions were carried out with varying parameters such as three different fruit peels as raw materials, two different acid types (citric acid and hydrochloric acid) for the extraction medium and two different extraction temperatures (80 °C and 90 °C). The effects of these parameters on the pectin yield and properties of pectin were investigated. Moisture and ash content, FTIR analysis, esterification degree, equivalent weight, methoxyl content and anhydrouronic acid content were determined for the characterisation of the extracted pectin samples. The pectin yields were found to be; 4.70-14.50% for mandarin peel, 4.40-9.25% for pomegranate peel and 2.10-4.80% for pumpkin peel. Among the fruit peels used in the study for pectin extraction, the highest pectin yield was obtained as 14.50% from the mandarin peel, which is a citrus fruit. The results of the analysis and characterization show that the samples are mainly composed of high methoxy pectins. Considering the yields of extracted pectins from different fruit peels, their properties and environmental effects, it was concluded that it is more appropriate to use citric acid as the extraction medium and to select the extraction temperature of 90 °C. [ABSTRACT FROM AUTHOR]

Water pollution, resulting from the degradation of plastics into microplastics, exposes humans and other living organisms to contaminated drinking water. Microplastics are capable of adsorbing toxic heavy metals which are carcinogenic and may affect the reproductive functions of living organisms. Hence, this study focuses on the characterization and quantification of microplastics in water to raise the awareness and propose a method of dealing with this emerging pollutant in various aqueous environments. The microplastics were separated from water using polyvinylidene difluoride (PVDF) and PVDF modified with carbon nano-onions (CNOs). The PVDF exhibited the highest concentration of microplastics in the wastewater influent (140 ± 1.85 MP/L) compared to the effluent (8.8 ± 2.10 MP/L), tap water (6.5 ± 5.77 MP/L), and lake water (10 ± 2.65 MP/L). The stereo microscope displayed red, blue, and black colored plastics. The morphological properties were determined using SEM. ATR-FTIR, equipped with Spectrum 10 Spectroscopy Software was used to establish the presence of high-density polyethylene (50%), poly(1,4-butylene terephthalate) (16.6%), nylon 12 (16.6%), and cellulose (16.6%) in the influent. The quantification of heavy metals extracted from the microplastics indicated that the concentrations of As (1.759 to 8.699 mg/L), Cu (83.176 mg/L) and Zn (0.610 mg/L) were above the acceptable limits. Our work is beneficial for the development of a microplastics monitoring protocol for various municipalities. Water treatment plants may also include the treatment of microplastics in the influent and monitor the effluent before the water is released back into the environment.

This study evaluates the efficiency of acid extraction and total digestion to determine the presence of metals in geopropolis produced by the stingless bee Melipona scutellaris. Geopropolis samples were collected at five meliponaries in the city and in the metropolitan region of Salvador, Bahia State, Brazil. The sample treatment methods comprised acid extraction and total digestion. The Inductively Coupled Plasma Optical Emission Spectrometry (ICP OES) technique was used to quantify Cd, Cu, Cr, Pb, and Zn. Geopropolis samples submitted to both digestion methods showed statistical differences. For both methods, Cr and Zn showed the highest concentrations, while those of Cd were the lowest. The Cr concentration for determination by total digestion was 37.53 mg/kg, while for acid extraction it was 32.90 mg/kg. For Zn, the concentration was 17.65 mg/kg and 8.85 mg/kg for total digestion and acid extraction, respectively. The total digestion method showed the highest concentrations of the metals evaluated; however, acid extraction (USEPA 3050b) is a more straightforward procedure for metal evaluation in geopropolis samples and presented values that support the use of geopropolis as a bioindicator. The acid extraction method USEPA 3050b, in combination with detection using ICP OES, showed efficiency in analyses carried out to determine metals in geopropolis. [ABSTRACT FROM AUTHOR]

BACKGROUND Sugarcane bagasse is a heterogeneous and organized material that needs a pretreatment to access the polysaccharides (cellulose and xylan). The particle size of a non‐milled bagasse can influence the xylan and xylose solubilization, as well as the enzymatic hydrolysis of the pretreated material. Using bagasse selected on 16‐, 30‐, 40‐ and 50‐mesh sieves: xylan solubilization was performed with hydrogen peroxide; xylose was solubilized with diluted sulfuric acid; and enzymatic hydrolysis was conducted for glucose yield evaluation. RESULTS: The xylose solubilized by acid pretreatment resulted in a maximum of 6.59 g L−1 with no influence of particle size. The solubilized xylan showed linear correlation with a variation of 36.18% (16‐mesh bagasse) to 71.43% (<50‐mesh bagasse). Pretreated material submitted to enzymatic hydrolysis revealed that particle size influenced the pretreatment, increasing the glucose yield. CONCLUSIONS: The results showed that non‐milled sugarcane bagasse particle size selection positively influenced the solubilization of xylan, improving the enzymatic hydrolysis of the pretreated material. © 2020 Society of Chemical Industry (SCI) [ABSTRACT FROM AUTHOR]

This study aimed to fully recover ammonia contained at a high concentration in anaerobic digestate of piggery wastewater (ADPW) by forming struvite. As magnesium and phosphorus sources, ferronickel slag (FNS) and K2HPO4 were used, respectively. By leaching 200 g L−1 of FNS with 3.0 M H2SO4, 10,309 mg L−1 of magnesium ions were extracted, and this acid-leachate of FNS (FNSL) also contained 5965 mg L−1 of total iron. In order to simultaneously remove both high concentrations of organic matters in ADPW and iron in FNSL which were known to hinder struvite formation, the mixture of ADPW and FNSL was added with H2O2 at the H2O2/Fe molar ratio of 0.75 and pH 4.0. After Fenton reaction, removal efficiencies of COD and total iron reached 77.36% and 99.89%, respectively. Then COD and an iron-reduced mixture of ADPW and FNSL were added with K2HPO4 satisfying Mg:N:P molar ratio of 1.2:1:1.15 at pH 9.5 to produce struvite for 1 h. From 1 L of ADPW (2.21 g NH3-N), 0.65 L of FNSL (4.65 g Mg2+), and 5.63 g of PO43–P, 46.7 g of precipitates were obtained. Overall removal efficiencies of magnesium, NH3-N, and phosphorus were 98.59%, 94.25%, and 99.97%, respectively. Obtained precipitates were analysed by using XRD, XRF, SEM-EDX and found to be struvite with impurities of potassium and metals. Additionally, the economic feasibility of FNS was assessed by estimating chemical costs of various magnesium sources. [ABSTRACT FROM AUTHOR]

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A large number of iron ore tailings (IOTs) are produced in steel industry, posing threat to the environment during its storage and disposal. To effectively reutilize Fe in IOTs, we propose a comprehensive utilization scheme: (1) most Fe in IOTs is extracted by concentrated hydrochloric acid to form FeCl3 flocculants; (2) after separation from the FeCl3 flocculants, a small amount of Fe is absorbed on the residue solids, which is further washed out to synthesize micron Fe3O4 as magnetic seeds. Results show that the as-synthetic FeCl3 flocculants meet the product standard for FeCl3 flocculants in China (GB/T 4482-2018) after a series of treatments including rotary evaporation, neutralization, and dilution and have comparable performance with commercial polyaluminum chloride (PAC) and polyaluminum ferric chloride (PAFC). Moreover, the addition of synthetic superparamagnetic Fe3O4 (as magnetic seeds) doubled the flocculation rate compared with as-synthetic FeCl3 flocculants alone. Finally, the reutilization of Fe in IOTs can create a direct economic value of ¥ 1.27/kg IOTs, and produce 745 g high-silicon residues for further reutilization, which indicates that our comprehensive utilization scheme is of great application potential. [ABSTRACT FROM AUTHOR]

Waste foundry sand (WFS) from the brass and bronze casting and molding process include various potentially toxic elements (PTEs), such as copper, zinc, tin, and lead. Hence, the utilization of WFS in construction and geotechnical applications evokes environmental concerns due to the rain-induced leaching of PTEs into the groundwater system. The present study investigated the extractive decontamination of WFS using mineral acids, e.g., HCl, H2SO4, or HNO3. Favorable extraction efficiency was achieved with HCl as compared to the other mineral acids, which was further enhanced at high temperatures and increased acid concentrations. The thermodynamic analysis indicated that ≥ 4 mol L−1 of HCl and ≤ 100 °C temperature ensured maximum extraction of PTEs due to the endothermic interactions between the HCl and PTEs. The HCl-treated WFS needed to be rinsed with water to restrict the after treatment elution of PTEs. The hazardous environmental impact of acid-treated WFS was evaluated following the standard leaching test and comparison with legislative recommendations for PTEs, which showed the water-assisted leaching rate of all the PTEs are within the regulatory limits. [ABSTRACT FROM AUTHOR]

Experiments concerning hydrochloric acid assisted extraction of polysaccharides from foxtail millet were carried out. Various combinations of extraction conditions of hydrochloric acid concentration, liquid-solid ratio, extraction time and extraction temperature were investigated using the Response Surface Methodology at three levels and four variables of Box-Behnken designs to obtain the maximum yield of polysaccharides. The experimental data were fitted to a quadratic equation using multiple regression analysis and analysed. The antioxidant activity of the obtained polysaccharides was also investigated in vitro. The optimal conditions were an acid concentration of 2.4 mol L-1, a liquid-solid ratio of 19.3:1 mL g-1, an extraction time of 1.2 h, and an extraction temperature 80.6°C. Under these conditions, the experimental yield was 52.13 mg g-1, which was in close agreement with the value of 52.37 mg g-1 predicted by the model. The mathematical model had a high correlation with experimental data (p<0.05). The polysaccharides of foxtail millet display a high radical scavenging capacity against superoxide and hydroxyl radicals. [ABSTRACT FROM AUTHOR]

The present work aimed to extract proteins from tambatinga fish residue with physicochemical characterization, a hybrid of the crossing between the female tambaqui (Colossoma macropomum) and the male pirapitinga (Piaractus brachypomus). Protein extraction was performed by the following methods: acid (hydrochloric acid, acetic acid) and basic (sodium hydroxide). The protein fraction was characterized in relation to moisture content, ash, protein and yield. The moisture determination was performed with powder samples, submitted to drying at 40 ° C, in a forced circulation oven, which presented values of 7.29; 11.42 and 3.14% respectively. Regarding the fixed mineral residue (ash), the samples differed from each other, with valuesbetween 81.52; 50.65 and 44.76%. The samples obtained by the different processes presented protein contents of 3.63; 9.36 and 39.55% respectively. And the yield of protein extraction was 8.96; 3.64 and 6.43% for hydrochloric acid, acetic acid and sodium hydroxide, respectively. The obtained results indicate that it is possible to perform protein extraction for fish waste utilization, mainly by the basic extraction method. [ABSTRACT FROM AUTHOR]

To evaluate the pretreatment processing for Cd isotope analysis of environmental samples, acid extractions and total digestions were examined with various environmental certified reference materials. Four certified reference material samples, including fly ash, polluted soil, domestic sludge, and industrial sludge, were digested by six different acid extraction and total digestion methods, and then Cd was separated to remove other matrix by anion-exchange column. The Cd recovery rates of the acid extraction methods were 2.6–89.1%, while those of the total digestion methods were 21.6–88.7%. In these results, the Cd recovery rates were dependent on the sample type. More than 80% of the Cd in the polluted soil and domestic sludge samples could be recovered regardless of the decomposition method, except one method. On the other hand, the Cd recovery rate from fly ash was low when total digestion was performed using a HF mixture, and the recovery rate by total digestion methods for industrial sludge was higher than that by acid extraction. In our results, Cd isotope ratios tended to be more positive by increasing the Cd recovery rates, suggesting that the light isotope of Cd was decomposed preferentially during the decomposition procedures. However, when more than 80% of the Cd in the samples was recovered, the Cd isotope ratios were determined to be similar. This indicated that at least 80% of the Cd should be recovered from environmental samples to accurately measure the Cd isotopic ratio of environmental samples. [ABSTRACT FROM AUTHOR]

Marine organisms such as fish and shellfish are composed of compounds with properties and characteristics that have been proven useful in a variety of sectors such as cosmetics, healthcare (wound healing), food industries, and tissue engineering. Collagen extraction from fish waste as a "blue resource" has attracted research attention over the past decade. Around 75 % of fish waste contains a high concentration of collagen. This has driven research in the conversion of these low-cost by-products into valuable products. Collagen extracted by acidic or/and enzymatic methods is gaining a lot of attention today due to its low cost and high yield. Fermentation and enzymatic hydrolysis stand out as one of the most environmentally sustainable and ecologically friendly methods for collagen extraction. Because of its great biocompatibility, excellent bioactivity, and low antigenicity, marine collagen is receiving more attention. Furthermore, collagen-derived peptides may exhibit interesting antioxidant activity, potent antihypertensive activity, and antimicrobial activity against different strains of bacteria. This review focuses on the advancements in extraction and detection methods of marine collagen, both from a technological and legislative standpoint, in addition to exploring its diverse range of application domains. [Display omitted] • 75 % of fish waste contains collagen, making it an abundant and valuable source. • Acidic and enzymatic methods offer low-cost, high-yield collagen extraction. • Marine collagen is versatile, finding uses in cosmetics, healthcare and tissue engineering. • Collagen peptides show promise in antioxidants and antimicrobial properties. [ABSTRACT FROM AUTHOR]

The extraction of polysaccharides from proso millet was investigated experimentally using hot water and acid aqueous solution. Response surface methodology, based on a three-level, three- or four-variable Box-Behnken design for hot water extraction or acid extraction, respectively, was employed to obtain the best possible combination of acid concentration, liquid-solid ratio, extraction time, and extraction temperature for maximum polysaccharides yield. The obtained experimental data were fitted to a second-order polynomial equation and analyzed by appropriate statistical methods. The corresponding optimum extraction conditions of each method were obtained. Under the optimum conditions, the experimental yield was well in close agreement with the predicted value by the model. The results showed that the polysaccharides yield of acid extraction was 42.13 mg g-1, significantly higher than 20.07 mg g-1 of the yield of hot water extraction, the obtained equation could be used to predict the extraction experimental results.

Phosphorus depletion represents a significant problem. Ash of incinerated biological sewage sludge (BSS) contains P, but the presence of heavy metals (e.g., Fe and Al) is the main issue. Based on chemical characterization by SEM-EDS, ED-XRF and ICP-OES techniques, the characteristics and P content of bottom ash (BA) and fly ash (FA) of incinerated BSS were very similar. On BA, P extraction carried out in counter- current with an S:L ratio of 1:10 and H2SO4 0.5 M led to better extraction yields than those of a similar test with H2SO4 1 M and an S:L ratio of 1:5 (93% vs. 86%). Comparing yields with H2SO4 0.5 M (S:L ratio of 1:10), the counter-current method gave better results than those of the crossflow method (93% vs. 83.9%), also improving the performance obtained with HCl in crossflow (93% vs. 89.3%). The results suggest that the purification of the acid extract from heavy metals with pH variation was impractical due to metal precipitation as phosphates. Extraction with H2SO4 and subsequent treatment with isoamyl alcohol represented the best option to extract and purify P, leading to 81% extraction yields of P with low amounts of metals.

The potential of microbial enzyme-aided extraction of pectin from fruit processing wastes was evaluated to assess its possible use as an environment friendly alternative to acid extraction methods. Peel wastes from yellow passion fruit (Passiflora edulis Slims var. flavicarpa), 'Saba' banana (Musa 'saba' [Musa acuminata x Musa balbisiana]), 'Carabao'mango (Mangifera indica L. cv. 'Carabao') and soursop 'guyabano'(Annona muricata) were extracted of pectin using different microbial enzymes namely cellulase, xylanase, pectinase and a-amylase. The efficiency of the enzymatic extraction as well as pectin quality were compared with acid extraction. Generally, high yields were obtained using cellulase and a-amylase. The yields from enzymatic extractions were however significantly lower compared with the acid extraction. Highest yields were obtained from 'Carabao' mango peels. The chemical properties of the pectins extracted from the fruit peels highly varied depending on the fruit and the extraction method. Pectin from yellow passion fruit peels was classified as low methoxyl (LM) based on the degree of esterification values while the rest of the pectins were classified as high methoxyl(HM). Analyses of the anhydrouronic acid (AUA) content showed that 'Carabao' mango peel pectins had high purity while the pectins from the other fruits had low purities. Equivalent weights of the fruit peel pectins from microbial extraction were significantly higher than that from acid extraction and from commercial citrus peel pectin. 'Carabao'mango, 'Saba' banana, yellow passion fruit and soursop 'guyabano' peels are potential sources of pectin for food applications. Acid extraction was found to be more efficient compared with microbial enzyme-aided extraction. [ABSTRACT FROM AUTHOR]

Pectin is a naturally occurring biopolymer which can be used for food and pharmaceutical applications. In this study the effect of temperature, time and pH on the yield, physicochemical characteristics of pectin extracted from Bombax ceiba fruits was investigated. The extraction of pectin was done using citric acid buffer followed by 96% alcohol precipitation. The optimum temperature, time and pH for the extraction of pectin were determined to be 85 °C, 90 min and 2.0, respectively. The yield of pectin under these optimum conditions was found to be 16.35%. The physicochemical properties determined under these optimum conditions were found to be; equivalent weight; 765.40 mg/mol, methoxyl content: 6.62%, anhydrouronic acid content; 65.25%, degree of esterification; 72.45%, moisture content; 1.30% and ash content; 0.60% for Bombax ceiba fruits extracted pectin, respectively. FTIR was also utilized for characterizing the pectins. Generally, the findings of the study showed that the pectin extracted from Bombax ceiba fruit can find industrial applications, especially in food processing and pharmaceutical industries. [ABSTRACT FROM AUTHOR]

Typical fission product formation experiments utilize metal or oxide target materials that must be dissolved prior to product separation. We report here a novel study using metal–organic frameworks for recovery of fission products into acidic media. We further show that the frameworks are largely preserved, such that this bulk target material could be retained for additional irradiations or characterizations. Through this approach, fission products can be separated from the actinide-based metal–organic framework using 0.01 M HNO3 without the need to dissolve the framework itself, reducing the amount of acidic waste. Extraction yields of four frameworks with varying pore sizes are compared. The results suggest that it may be possible to use porous frameworks as target materials for the extraction of select fission products. [ABSTRACT FROM AUTHOR]

We report here an initial isolation study based upon the use of small uranium oxide particles dispersed in a soluble salt matrix to evaluate the relative recovery of fission products into acidic media. We further show that the macrostructures of the uranium microparticles are largely preserved, such that the bulk target material could be retained for additional irradiations or characterizations. Through this approach, fission products can be separated from the actinide-based target using low molarities of acid without the need to dissolve the actinide itself, reducing the amount of acidic waste. Extraction yields using two molarities of HCl and HNO3 are compared. [ABSTRACT FROM AUTHOR]

Abstract Extraction of pectin from pomelo peel was performed using water, acid and alkaline solutions with a microwave power of 1100 W for 2 min, and yield and structural/chemical characteristics of the extracted pectins were investigated. Extraction of pectin with water gave the lowest yield (6.5%, dry weight basis). The water-extracted pectin contained the highest amount of neutral sugar (29.5%), while equivalent molecular weight (MWeq) and degree of methylation (DM) were 43 kDa and 29.7%, respectively. Extraction of pectin with HCl solutions at concentrations of 25, 50, 100 and 200 mM resulted in a significant increase of pectin yields (12.1–20.5%) and pectins with high amount of galacturonic acid (83.3–85.6%). The MWeq and DM of the acid-extracted pectins ranged from 171 to 368 kDa and 53.9–82.5%, respectively. Compared to the acid, extraction with NaOH solutions at the same concentrations provided higher yields (13.9–24.2%), smaller size (142–187 kDa) and lower DM (<1.7%) pectins, while amount of galacturonic acid was comparable. The highest yield of extraction was found at a concentration of 50 mM for both HCl and NaOH solutions. Extraction of pomelo peel with 50 mM NaOH solution by reduction of the microwave power to 550 W and extending the extraction time to 15 min resulted in an increase of pectin yield (29.2%) and pectin with smaller size (76 kDa). Graphical abstract Image 1 Highlights • Pectin was extracted from pomelo peel using 25–200 mM HCl and NaOH solutions. • Extraction with 50 mM NaOH solution gave the highest pectin yield. • Alkaline extraction gave smaller size pectins as compared to the acid extraction. • Alkaline extracted pectin had very low amount of methyl ester group. • Low microwave power with long time could increase yield and reduce size of pectin. [ABSTRACT FROM AUTHOR]