Palm Olein Organogelation Using Mixtures of Soy Lecithin and Glyceryl Monostearate

The present work investigated the interaction between soy lecithin (SL), glyceryl monostearate (GMS), and water in structuring palm olein (PO) to create an organogel having similar mechanical properties to commercial spread. Extreme vertices mixture design was used to optimize the composition of PO-based organogel. The resulting model showed a good fit to the predicted data with R2 ≥ 0.89. The optimum composition was 8% SL, 22% GMS, 28% water, and 42% PO (w/w) to produce a mean firmness of 1.91 N, spreadability of 15.28 N s−1, and oil binding capacity (OBC) of 83.83%. The OBC of optimized organogel was 10% higher than commercial spread product, and no significant difference was observed in the mechanical properties (p > 0.05). The microstructure, as well as the rheological and thermal properties of the optimized organogel were characterized. Fourier transform infrared analysis indicated that hydrogen bonding and van der Waals interactions were the key driving forces for organogelation. The mixture of SL and GMS favored the formation of β′ + β form crystals with a predominance of the β′ form. These results have important implications for the development of PO-based organogel as a potential fat replacer in the production of low-fat spread.

A Quasi-Nondestructive Evaluation Method for Physical-Mechanical Properties of Fragile Archaeological Wood with TMA: A Case Study of an 800-Year-Old Shipwreck

Archaeological wood is a kind of ‘new material’ that has deteriorated due to long-term degradation. The existing wood science theory and evaluation methods are not fully applicable to archaeological wood. Moreover, current physical-mechanical evaluation methods are inadequate for fragile archaeological wood due to their insufficient accuracy and the large sample amount required, causing difficulties in many necessary physical-mechanical repeatability tests. In light of these limitations, the representative samples on Nanhai No. 1, a merchant shipwreck in the Song Dynasty, were selected as the research objects in this paper. The shipwreck is a typical waterlogged wooden artifact. A quasi-nondestructive physical-mechanical evaluation technique for archaeological wood was developed with the thermomechanical analyzer (TMA). This study used TMA to evaluate the bending strength of representative waterlogged archaeological samples of Nanhai No. 1 shipwreck and sound wood with the same species. Besides, the thermal linear expansion coefficients in the ambient temperature range were obtained. The sizes of the samples used in the tests were only 2 mm × 8 mm × 0.3 mm and 1 cm × 1 cm × 1 cm, respectively. Bending strength results of archaeological wood by the TMA method conformed to the tendency that the bending strength decreases with the increase of decay degree. In addition, the longitudinal linear expansion coefficients of archaeological wood reached 80%–115% of those in the transverse grain direction, which were about 10 times higher than those of the sound wood. The linear expansion coefficients of archaeological wood in three directions were similar. Based on the results of Fourier transform infrared analysis (FT-IR), the significant differences in the physical-mechanical properties of the archaeological wood and the sound wood were induced to be mainly ascribed to the decomposition and the loss of hemicellulose in the archaeological wood. The cell wall substrate could not stabilize the cellulose skeleton, which led to the instability of the tracheid structure of the archaeological wood. This study provided a proven quasi-nondestructive method for the preservation state evaluation of waterlogged archaeological wood (WAW) from the Nanhai I shipwreck and other similar waterlogged wooden relics.

Development and Evaluation of 2-Amino-7-Fluorophenazine 5,10-Dioxide Polymeric Micelles as Antitumoral Agents for 4T1 Breast Cancer

2-Amino-7-fluorophenazine 5,10-dioxide (FNZ) is a bioreducible prodrug, poorly soluble in water, with potential anticancer activity on hypoxic-tumors. This poor solubility limits its potential applications in clinic. Amphiphilic pristine polymeric micelles (PMs) based on triblock copolymers Pluronic® and Tetronic®, glycosylated derivatives and their mixtures with preformed-liposomes (LPS), were analyzed as strategies to improve the bioavailability of FNZ. FNZ encapsulations were performed and the obtaining nanostructures were characterized using UV-visible spectroscopy (UV-VIS), Transmission Electron Microscopy (TEM), Fourier transform infrared analysis and Dynamic Light Scattering (DLS). The most promising nanoformulations were analyzed for their potential toxicity and pharmacologically, at 20 mg/kg FNZ-doses, in a stage-IV murine metastatic-breast tumor model. The results revealed that the solubility of the encapsulated-FNZ increased up to seven times and the analysis (UV-VIS, DLS and TEM) confirmed the interaction between vehicles and FNZ. In all the cases appropriate encapsulation efficiencies (up to 70%), monodisperse nanometric particle sizes (PDI = 0.180–0.335), adequate Z-potentials (−1.59 to −26.4 mV), stabilities and spherical morphologies were obtained. The in vitro profile of FNZ controlled releases corresponded mainly to a kinetic Higuchi model. The in vitro/in vivo biological studies revealed non-toxicity and relevant tumor-weight diminution (up to 61%).

Sustainable insulating foams based on recycled polyurethanes from construction and demolition wastes

Background: Polyurethane (PU) foams contained in construction and demolition wastes (CDW) represent a great environmental impact, since they usually end in landfill or incineration processes. The goal of this work is to develop a way to formulate PU foams, maintaining (or ever improving) their performance, by the re-use of those industrial wastes. This procedure will allow minimize both the volume of disposal to be treated by other ways and the amount of pristine raw material needed to produce new PU foams. Methods: In this work, new rigid and soft polyurethane (PU) foams have been formulated with addition of recycled PU foams coming from demolition of buildings. Density, Fourier transform infrared analysis, compression properties and thermal conductivity were measured to characterize the resulting foams. Results: The work showed that addition of filler coming from recycled PU foams should be limited to low percentages, in order to allow good foam evolution from the reactants. Thermal conductivity values of modified rigid foams are worse than those of pristine foam, which is undesirable for thermal insulation purposes; however, in the case of soft foams, this parameter improved to some extent with low levels of recycled PU foam addition. Conclusions: The studied procedure could contribute to reduce the thermal conductivity of pristine soft PU foam, which would be of interest for applications where thermal insulation matters.

Engineered properties of polyurethane laden with beetroot and cerium oxide for cardiac patch application

The cardiac patch provides appropriate physicochemical properties and mechanical strength for the regeneration of damaged heart tissues. In this work, for the first-time, beetroot (BR) is blended with cerium oxide (CeO2) to produce nanofibrous polyurethane (PU) composite patch using electrospinning. The objective of this work is to fabricate the composite and examine its feasibility for cardiac patch applications. Morphological analysis revealed a dramatic reduction of fiber diameter of PU/BR (233 ± 175 nm) and PU/BR/CeO2 (331 ± 176 mm) compared to the pristine PU (994 ± 113 mm). Fourier transform infrared analysis (FTIR) analysis indicated functional peak intensities of the newly formed composite PU/BR and PU/BR/CeO2 were not similar to PU. The addition of beetroot rendered PU/BR hydrophilic (86° ± 2), whereas PU/BR/CeO2exhibited hydrophobic nature (99° ± 3). Atomic force microscopy (AFM) analysis depicted the reduced surface roughness of the PU/BR (312 ± 12 nm) and PU/BR/CeO2 (390 ± 125 nm) than the pristine PU (854 ± 32 nm). The incorporation of beetroot and CeO2 into PU enhanced the tensile strength compared with the pristine PU. The blood clotting time of PU/BR (APTT-204 ± 3 s and PT-103 ± 2 s) and PU/BR/CeO2 (APTT-205 ± 3 s and PT-105 ± 2s) were delayed significantly than the pristine PU(APTT-176 ± 2 s and PT-94 ± 2 s) as revealed in the coagulation study. Further, hemolysis assay showed the less toxic nature of the fabricated composites than the pristine PU. Hence, it can be inferred that the advanced physicochemical and blood compatible properties of electrospun PU/BR and PU/BR/CeO2 nanocomposite can be engineered successfully for cardiac patch applications.

Layered Double Hydroxide Nanomaterial as Highly Efficient Adsorbent and its Recycling after Removal of a Carcinogenic Tartrazine Dye from Wastewater

In this work, the tartrazine dye is removed from the wastewater by the layered double hydroxide (LDH) [Zn2-Al-Cl]. LDH materials have proven to be highly effective in removing pollutants, with a low cost of synthesis, non-toxic, and they do not regenerate the sludge. Several parameters were studied, the retention of dye by LDH nanomaterial is optimized for a pH between 6 and 8, the equilibrium retention is obtained after 24 hours, and retention kinetics follows the pseudo-second-order model. The isotherms are the H type, and they follow the Langmuir model, retention capacity reaches 100% for a mass ratio (adsorbate/adsorbent) between 0.1 and 0.5, and the maximum amount retained of the dye is 740.35 mg/g for an initial concentration of tartrazine was 1200 mg/L and 100 mg of mass of LDH. X-ray diffraction (XRD) showed that the synthesized matrix is crystallized in a lamellar structure. Two processes affect the removal of the dye, adsorption of the surface of LDH, and intercalation between the layers. Infrared analysis indicated the appearance of the band's dye in the spectrum of the matrix after retention. Moreover, scanning electron microscopy showed the lamellar character of the two phases obtained before and after retention. The thermodynamics study showed that the process is endothermic, and the adsorption mechanism is governed by physisorption. The LDH nanomaterial is a good adsorbent with low cost, high efficiency, and recyclable.

Investigation of TiO2 Nanoparticles Synthesized by Sol-Gel Method for Effectual Photodegradation, Oxidation and Reduction Reaction

Metal oxide titanium dioxide (TiO2) nanoparticles were synthesized by using a simple and economical sol-gel method. The prepared nanoparticles were used to evaluate methylene blue dye degradation and as catalysts in the oxidation of benzaldehyde. The crystallite size of the titanium dioxide nanoparticle was 18.3 nm, which was confirmed by X-ray diffraction analysis. The spherical morphology was confirmed by scanning electron microscopy (SEM), and the elemental composition of the nanoparticle was found by energy dispersive X-ray (EDAX) analysis. The anatase form of the nanoparticle was confirmed by the bandgap 3.2 eV, which was measured using UV–DRS analysis. The bond between metal and oxygen was confirmed by the peaks at 485 and 606 cm–1 analyzed by Fourier transform infrared analysis (FTIR). The efficiency of the catalyst in dye degradation was 60.08, 68.38, and 80.89% with respect to 50, 75, and 100 mg catalyst weight. The yield % of benzoic acid was 94%, and the reduction efficiency against 4-nitrophenol was 98.44%.

Facile thermal synthesis of g-C3N4/ZnO nanocomposite with antibacterial properties for photodegradation of Methylene blue

Semiconductors as photocatalysts are ideal materials for wastewater remediation. A nanocomposite of g-C3N4 and ZnO was produced using a two-step in-situ synthesis technique to achieve a better photocatalyst. The samples were assessed via UV-vis diffuse reflection spectroscopy, transmission electron microscopy, photoluminescence spectroscopy, Fourier transform infrared analysis, and X-ray diffraction. The photodegradation of methylene blue as an organic dye model was assessed to examine the photocatalytic properties of the synthesized samples. The antibacterial characteristics of synthesized samples were also investigated. The findings revealed that the photodegradation efficiency of the binary g-C3N4/ZnO systems was greater than that of pristine g-C3N4. Under irradiation, the photodegradation yield of g-C3N4/ZnO with a 15 wt.% of ZnO was up to 3.5 times better than that of pristine g-C3N4. The feature of enhanced separation of photoinduced holes and electrons resulting from heterojunction formation between g-C3N4 and ZnO surfaces might be attributed to this photocatalytic activity enhancement. The synthesized binary nanocomposites showed good antibacterial properties against Escherichia coli and Staphylococcus aureus bacteria.