Particle Morphology Research Articles

Peculiar Behavior of Methyl Methacrylate Emulsion Polymerization-Induced Self-Assembly Mediated by RAFT Using Poly(Methacrylic Acid) Macromolecular Chain Transfer Agent.

Reversible addition-fragmentation chain transfer (RAFT) emulsion polymerization of methyl methacrylate (MMA) is successfully performed in water in the presence of a poly(methacrylic acid) (PMAA) macromolecular chain transfer agent (macroCTA) leading to the formation of self-stabilized PMAA-b-PMMA amphiphilic block copolymer particles. At pH3.7, the reactions are well-controlled with narrow molar mass distributions. Increasing the initial pH, particularly above 5.6, results in a partial loss of reactivity of the PMAA macroCTA. The effect of the degree of polymerization (DPn) of the PMMA block, the solids content, the nature of the hydrophobic segment, and the pH on the morphology of the obtained diblock copolymer particles is then investigated. Worm-like micelles are formed for a DPn of PMMA of 20 (PMMA20), while "onion-like" particles and spherical vesicles are obtained for PMMA30 and PMMA50, respectively. In contrast, spherical particles are obtained for the DPns higher than 150. This unusual evolution of particle morphologies upon increasing the DPn of the PMMA block seems to be related to hydrogen bonds between hydrophilic MAA and hydrophobic MMA units.

Physicochemical characterisation and impact of Gryllus bimaculatus addition on gluten‐free flour blends

SummaryGryllus bimaculatus (field cricket) powder is a prospect in enriching gluten‐free food products' protein and mineral contents. However, the technological impacts of replacing common gluten‐free cereal flours with G. bimaculatus powder are still incipient. This study aimed to characterise nutritional composition, particle morphology, and particle size distribution of G. bimaculatus powder and the gluten‐free flours (maize, rice, finger millet and proso millet). Additionally, it investigated the effects of substituting these gluten‐free flours with 5%, 10%, 15% and 20% G. bimaculatus powder on proximate composition, hydration and colour properties. G. bimaculatus powder showed significantly (P ≤ 0.05) high protein (44.8 g/100 g) content and essential minerals such as zinc (208.5 mg/kg) and iron (132.2 mg/kg). Micrographs of G. bimaculatus powder revealed compact and heterogenous particles while the flours' particles varied in sizes, and the starch granules had different shapes, sizes and arrangements. Flour particles exhibited bi‐and trimodal size distributions ranging from 1.5 μm to 1100 μm with minor peaks preceding major peaks. Finger millet flour had a greater span of 4.12, while proso millet flour had a lower span of 1.97. Particle size correlated negatively with water absorption capacity (WAC) (r = −0.938) and oil absorption capacity (OAC) (r = −0.955), respectively. G. bimaculatus powder addition significantly increased (P ≤ 0.05) fat, protein and fibre contents, decreased (P ≤ 0.05) nitrogen‐free extracts, but had no effect on ash content. Hydration properties differed significantly (P ≤ 0.05) except for WAC in proso millet blends. Samples exhibited significantly higher (P ≤ 0.05) WAC than OAC in exception of G. bimaculatus powder and showed no emulsifying activities. Addition of G. bimaculatus powder significantly (P ≤ 0.05) increased colour differences, reduced redness (a*), yellowness (b*) and lightness. The use of G. bimaculatus powder demonstrates the potential to enhance the nutritional properties and modify the colour and hydration of gluten‐free flours in the development of novel gluten‐free foods.

Quantitative characterization of microstructure and research on spatial variation characteristics of loess of different strata in Luochuan, Shaanxi, China.

The complete sequence of loess strata in Luochuan has become a typical section in loess strata, and is the main focus of research for many scholars studying loess. We were based on the theory of aeolian loess and established a set of quantitative index parameters for loess microstructure through our previous research, such as equivalent diameter, sphericity, morphology ratio, orientation angle Phi, orientation angle Theta, pore Eq-Radius, throat Eq-Radius and throat channelLength. Through the quantitative characterization of various index parameters of the Luochuan loess, we found that the probability density of each index parameter meets a specific distribution well, and in terms of spatial dimension, it shows that as the depth of the strata increases, the average particle size and the mode of pore Eq-Radius, throat Eq-Radius and throat channelLength generally increase, while the mode of particle morphology ratio generally decreases. In addition, loess particles in deeper strata are less prone to vertical sedimentation and tend to deposit gently or horizontally. Most particles in different strata are distributed in a northwest or southwest direction. During the formation period of strata, the main cause for spatial differences is the material carrying force. We conducted a statistical analysis on the correlation between the macroscopic physical properties of loess and its microstructure index parameters. Specifically, we found a positive correlation between loess density and the average particle size and the mode of particle equivalent diameter, Additionally, we found a negative correlation between loess liquid limit and plastic limit, and the mode of particle morphology ratio. Furthermore, there was a negative correlation between permeability coefficient and the mode of pore Eq-Radius, throat Eq-Radius, and throat channelLength.

Morphological effect on Core@shell AuAg nanoparticles for detecting p‐aminothiophenol dimerization by surface‐enhanced Raman spectroscopy

AbstractA series of non‐spherical metallic Au and bimetallic core@shell AuAg nanoparticles (NPs) have been synthesized for SERS improvements. The bimetallic core@shell AuAg NPs were obtained through a controlled overgrowth of an Ag shell onto the surface of two types of non‐spherical Au NPs, used as seeds, Au nanooctaheda (Au NOc) and Au nanotriangles (Au NTs). This Ag overgrowth was able to produce bimetallic core@shell structures such as nanocubes and nanopyramids, respectively. Transmission electron microscopy (TEM) was used to determine the particle size and particle morphology for metallic and bimetallic NPs, and energy‐dispersive X‐ray (EDX) elemental mapping analysis confirmed the core@shell structure of the bimetallic NPs. The plasmonic absorption bands exhibited for each nanosystem were observed by UV–vis spectroscopy. The concentration of Au and Ag in the bimetallic systems was determined by inductively coupled plasma mass spectrometry (ICP‐MS). After synthesis and characterization, p‐aminothiophenol (PATP) was used as a model analyte to investigate the surface‐enhanced Raman spectroscopy (SERS) capabilities of the synthesized metallic and bimetallic nanosystems. In PATP, a dimerization reaction to 4,4′‐dimercaptoazobenzene (DMAB) is produced when it is adsorbed onto the surface of certain noble metals. This SERS analysis was performed at 10−4 M of PATP and by using two different laser wavelengths (532 and 785 nm) in all cases. In this context, we were able to detect the dimerization reaction of PATP to DMAB only for the bimetallic structures and under the 532 nm laser line. Moreover, we have found that the dimerization capacity also depends on the nanoparticle morphology.

PVP/aprepitant microcapsules produced by supercritical antisolvent process

The supercritical antisolvent (SAS) process was a green alternative to improve the low bioavailability of insoluble drugs. However, it is difficult for SAS process to industrialize with limited production capacity. A coaxial annular nozzle was used to prepare the microcapsules of aprepitant (APR) and polyvinylpyrrolidone (PVP) by SAS with N, N-Dimethylformamide (DMF) as solvent. Meanwhile, the effects of polymer/drug ratio, operating pressure, operating temperature and overall concentration on particles morphology, mean particle diameter and size distribution were analyzed. Microcapsules with mean diameters ranging from 2.04 μm and 9.84 μm were successfully produced. The morphology, particle size, thermal behavior, crystallinity, drug content, drug dissolution and residual amount of DMF of samples were analyzed. The results revealed that the APR drug dissolution of the microcapsules by SAS process was faster than the unprocessed APR. Furthermore, the drug powder collected every hour is in the kilogram level, verifying the possibility to scale up the production of pharmaceuticals employing the SAS process from an industrial point of view.

Comparison of Newtonian and glycerol-water solution-based SiO2 nanofluid droplets impacting on heated spherical surfaces

The dynamic interactions of liquid droplets with heated spherical particles, relevant across various scientific and engineering disciplines, display intriguing collision behaviors whose principles are yet to be fully deciphered. This investigation utilizes high-speed photography to explore the wetting and non-wetting responses of different Newtonian and glycerol-water solution-based SiO2 nanofluid droplets upon contact with heated particles. Findings indicate that nanofluid droplets disrupt the thermal field and modify the surface morphology of particles more extensively under wetting than non-wetting conditions. Wetting conditions lead to significant alterations in the liquid film thickness and notable velocity field disruptions for droplets of deionized water and glycerol solution. Conversely, in the non-wetting phase, droplets nearing full rebound cause less disturbance to the velocity field, a behavior consistent across all fluid types and particle temperatures. The shape changes nanofluid droplets undergo when rebounding and separating from the particle surface are similar to those seen in glycerol solution and water droplets. Droplets in the breakup-rebound phase experience shorter contact times than those merely rebounding. A phase diagram is presented, detailing wetting (receding-deposition and boiling-breakup) and non-wetting (rebound and breakup-rebound) actions. An increase in the Weber number necessitates a higher particle temperature for the transition from rebound to breakup-rebound, which corroborates with theoretical insights. Furthermore, droplets achieve their maximum spreading area during the boiling-breakup mode.

Heat Treatment of Calcite to Enhance Its Removal of Color Dye Alizarin Red S

The use of color dyes in modern society presents a great challenge to the environment. Thus, extensive studies have been conducted in the last 30 years on the removal of color dyes from aqueous solutions such industrial wastewater. In this study, the removal of alizarin red S (ARS), an anionic dye, from solution by raw calcite (Cal) and heat-treated calcite (HCal) was conducted and compared under different physico-chemical conditions. Based on the isotherm study, the ARS removal capacities increased from 167 to 251 mmol/kg after the Cal was heated to 1000 °C for 3 h. The X-ray diffraction analyses showed no difference in the calcite phase between Cal and HCal after ARS sorption. Fourier-transform infrared results also showed no change in the calcite phase after ARS sorption, except a slightly increase in wavenumber from 713 to 727 cm−1 for the OCO bending of HCal at high ARS sorption levels. SEM observations showed about the same particle size and morphology before and after ARS sorption. The TGA data showed the formation of CaO after Cal was heated, and CaO converted back into calcite after being in contact with water or ARS solution for 24 h and then being air-dried. Thus, the high ARS removal could be due to CaO produced after Cal being heated. The findings from this research proved that there is great potential in the use of calcite, a low-cost and readily available Earth material, after heat treatment for the removal of contaminants from water.

An Image-based method for evaluating changes in particle size and morphology distributions of aggregate materials after vibratory compaction test

Particle breakage and abrasion of aggregate materials can be induced by field compaction during construction, which adversely affects their mechanical properties. However, current compaction quality control testing does not evaluate changes in particle size distribution and particle morphology of aggregate materials due to the lack of fast and inexpensive testing methods. In this study, a modified watershed-based segmentation image analysis method and computational geometry algorithms were used to quickly quantify changes in particle size and morphology distributions of a large amount of contacting aggregate particles. The accuracy and required minimum sample size of the image analysis method were statistically evaluated. Compared to the conventional ASTM C136 aggregate sieve analysis test, the image analysis method conducted on a 40% sample size of the conventional method yielded less than 6% difference between the results, which can meet the ASTM C136 test repeatability criteria. In addition, demonstration tests were conducted to incorporate the image analysis method into a laboratory vibratory compaction test for evaluating the overall particle size and morphology changes of an aggregate material after compaction. Results indicate that the initial gradation and water content of the aggregate material can influence the particle breakage and abrasion characteristics of aggregate materials under compaction.

Resource potential of dust entrainment of asphalt-concrete plants

In the modern construction industry, the problem of finding materials with increased stability that would provide minimal environmental impact with optimal economic efficiency is urgent. Considering global trends in the field of ecology and sustainable development, attention is focused on recycling and reuse of industrial waste. Of particular interest is the pulverized material formed during the operation of asphalt concrete plants. In this paper, the potential of integrating this type of waste as an alternative construction resource is studied. This article focuses on the urgent need to adapt the principles of sustainability in construction practice through the integration of materials with minimal environmental footprint. The key aspect of the study is the concept of recycling of pulverized waste from asphalt concrete production, which can help optimize the resource potential and reduce the environmental burden on the ecosystem. The study examines various dust compositions obtained from asphalt plants of different operating principles. The morphology of particles and the bitumen capacity parameter were investigated. It was found that by replacing up to 50% of mineral powder with carryover dust, there can be a significant environmental and economic impact for the road construction industry.

Recycling kaolin from paper waste and assessment of its application for paper coating

In the cellulose industry, the paper coating process plays an essential role in reducing manufacturing costs while increasing the quality of the products. Given that cellulose products are being used increasingly, the ability to recycle and reuse these materials might be highly beneficial in this industry. Thus, kaolin—one of the most commonly utilized ingredients in the cellulose industry that has a major impact on the final quality—was recycled from paper waste for this study. Then, to confirm the successful recycling process, the particle distribution, morphology, and chemical composition of recycled kaolin were analyzed by DLS, SEM/EDS, FTIR, XRF, and XRD. The related results verified the recycled kaolin's high purity and crystallinity. Subsequently, coatings with thicknesses of 30, 60, 90, and 120 μm were applied to paper using a suspension of recycled kaolin. Their mechanical properties (burst strength and tensile strength), permeability (air passage, the amount of which indicates the porosity of the paper structure), wettability (the contact angle can reveal the wetting ability of the paper), and water absorbance (the Cobb test) were then assessed. The pertinent findings demonstrated that applying a coating considerably improves paper quality. So, a coating with a thickness of 30 µm is superior to uncoated paper. In addition, among all the coating thicknesses, the treatment with the best mechanical strength, permeability, contact angle, and Cob value values had a coating thickness of 120 µm. The corresponding values for the tensile index, burst index, air passage amount, and contact angle are 70 kNm/kgr, 3.61kPa m2/gr, 680 ml/min, and 46֯ ±2. Consequently, the 120 µm-thickness treatment was determined to be the most effective one in this investigation.

Exploring secondary aerosol formation associated with elemental carbon in the lower free troposphere

The variability of element carbon (EC) mixed with secondary species significantly complicates the assessment of its environmental impact, reflecting the complexity and diversity of EC-containing particles' composition and morphology during their ascent and regional transport. While the catalytic role of EC in secondary aerosol formation is recognized, the effects of heterogeneous chemistry on secondary species formation within diverse EC particle types are not thoroughly understood, particularly in the troposphere. Alpine sites offer a prime environment to explore EC properties post-transport from the ground to the free troposphere. Consequently, we conducted a comprehensive study on the genesis of secondary aerosols in EC-containing particles at Mt. Hua (altitude: 2069 m) from 1 May to 10 July, using a single particle aerosol mass spectrometer (SPAMS). Our analysis identified six major EC particle types, with EC-K, EC-SN, and EC-NaK particles accounting for 27.6 %, 27.0 %, and 19.6 % of the EC particle population, respectively. The concentration-weighted trajectory (CWT) indicated that the lower free troposphere over Mt. Hua is significantly affected by anthropogenic emissions at ground-level, predominantly from northwestern and eastern China. Atmospheric interactions are crucial in generating high sulfate levels in EC-SN and EC-OC particles (> 70 %) and notable nitrate levels in EC-K, EC-BB, and EC-Fe particles (> 80 %). The observed high chloride content in EC-OC particles (56 ± 32 %) might enhance chlorine's reactivity with organic compounds via heterogeneous reactions within the troposphere. Distinct diurnal cycles for sulfate and nitrate are mainly driven by varying transport dynamics and formation processes, showing minimal dependency on EC particle types. Enhanced nocturnal oxalate conversion in EC-Fe particles is likely due to the aqueous oxidation of precursors, with Fe-catalyzed Fenton reactions enhancing OH radical production. This investigation provides critical insights into EC's role in secondary aerosol development during its transport in the lower free troposphere.

DEVELOPMENT AND OPTIMIZATION OF A DOLUTEGRAVIR NANOSUSPENSION USING BOX BEHNKEN DESIGN

Objective: This study aimed to develop and optimize a nanosuspension of Dolutegravir, an integrase inhibitor with low aqueous solubility, using the sonoprecipitation technique. The objective was to enhance the drug's solubility and oral bioavailability by preparing nanosuspension. Methods: A box-behnken design was employed to systematically investigate the impact of stabilizer concentration, sonication amplitude, and time on the particle size and polydispersibility of the nanosuspension formulations. Various stabilizers, including Soluplus®, Poloxamer 188, Poly Vinyl Pyrrolidone (PVP) K90, Hydroxy Propyl Methyl Cellulose (HPMC), and Tween 80, were evaluated. Fourier transform infrared spectroscopy confirmed drug-polymer interactions, while differential scanning calorimetry and X-ray diffraction revealed partial amorphization. Scanning electron microscopy confirmed nanoscale particle size and morphology. Results: The optimized formulation (NS6) with 1% Soluplus®, 65 W amplitude, and 10 min sonication exhibited nanoparticles of 75.3 nm with low polydispersity. NS6 demonstrated enhanced drug release compared to the pure drug, attributed to particle size reduction and amorphization. In vitro tests indicated acceptable stability over time and temperature. Conclusion: The application of Box-Behnken design resulted in an optimized nanosuspension formulation capable of improving the oral bioavailability of poorly soluble Dolutegravir. The formulation exhibited favorable characteristics, including reduced particle size, amorphization, and enhanced drug release, highlighting its potential as an effective delivery system for Dolutegravir in Human Immuno Deficiency Virus (HIV) treatment.

Low-index mesoscopic surface reconstructions of Au surfaces using Bayesian force fields

Metal surfaces have long been known to reconstruct, significantly influencing their structural and catalytic properties. Many key mechanistic aspects of these subtle transformations remain poorly understood due to limitations of previous simulation approaches. Using active learning of Bayesian machine-learned force fields trained from ab initio calculations, we enable large-scale molecular dynamics simulations to describe the thermodynamics and time evolution of the low-index mesoscopic surface reconstructions of Au (e.g., the Au(111)-‘Herringbone,’ Au(110)-(1 × 2)-‘Missing-Row,’ and Au(100)-‘Quasi-Hexagonal’ reconstructions). This capability yields direct atomistic understanding of the dynamic emergence of these surface states from their initial facets, providing previously inaccessible information such as nucleation kinetics and a complete mechanistic interpretation of reconstruction under the effects of strain and local deviations from the original stoichiometry. We successfully reproduce previous experimental observations of reconstructions on pristine surfaces and provide quantitative predictions of the emergence of spinodal decomposition and localized reconstruction in response to strain at non-ideal stoichiometries. A unified mechanistic explanation is presented of the kinetic and thermodynamic factors driving surface reconstruction. Furthermore, we study surface reconstructions on Au nanoparticles, where characteristic (111) and (100) reconstructions spontaneously appear on a variety of high-symmetry particle morphologies.

Iron as recyclable metal fuel: Unraveling oxidation behavior and cyclization effects through thermogravimetric analysis, wide-angle X-ray scattering and Mössbauer spectroscopy.

The carbon-free chemical storage and release of renewable energy is an important task to drastically reduce CO2 emissions. The high specific energy density of iron and its recyclability makes it a promising storage material. Energy release by oxidation with air can be realized by the combustion of micron-sized iron powders in retro-fitted coal fired power plants and in fixed-bed reactors under milder conditions. An experimental parameter study of iron powder oxidation with air was conducted based on thermogravimetric analysis in combination with wide-angle X-ray scattering and Mössbauer spectroscopy. In agreement with literature the oxidation was found to consist of a very fast initial oxidation of the outer particle layer followed by much slower oxidation due to diffusion of iron ions through the Fe2O3/Fe3O4 layer being the ratelimiting step. Scanning electron microscopy analysis of the iron particle before and after oxidation reveal a strong particle morphology transformation. This impact on the reaction was studied by cyclization experiments. Up to 10 oxidation-reduction cycles show that both, oxidation and reduction rates, increase strongly with cycling due to increased porosity.

Preparation method and applicability evaluation of 3D printing alumina ceramic artificial coarse aggregate

Abstract The particle size and morphology of crushed stones impact their macroscopic mechanical and physical properties, which has become a hot topic in the study of road and geotechnical engineering. However, some reported studies fail to control the particle morphology as the only independent variable. This paper presented a new method to print artificial aggregates based on 3D printing technology of particles. The applicability of the new method was verified with uniaxial compression and dynamic modulus tests of asphalt mixtures formed by the printing aggregates. Results showed that the printing aggregates earned similar physical properties to real coarse when sintered at 1400℃ with alumina ceramic powder and CuO: TiO2 a 1:2 additive in mass. Besides, the gross volume density, compressive strength, and shrinkage of the printing aggregates show a similar trend of increasing and then decreasing with the increase of additives. The optimal mass percentage of additives was obtained to be 5%. Mechanical tests indicated that the mechanical indexes of the asphalt mixtures formed with the two types of coarse aggregates were similar, while the results of the specimens formed with artificial coarse aggregates showed less dispersion. The stability of test results was significantly improved for different asphalt mixture specimens prepared with 3D printed coarse aggregate. This provides a basic method for further research on the multi-scale properties of particle material.

Temperature sensing by means of a near-infrared luminescent Ca8NaBi(PO4)6F2:Nd3+ fluorapatite phosphor

Microrods of calcium sodium bismuth fluorapatite doped with neodymium, denoted as Ca8NaBi1-xNdx(PO4)6F2 (with x ranging from 0 to 0.5), were synthetized using a modified Pechini sol–gel method. The crystalline structure of these phosphors was refined using the Rietveld method and exhibited hexagonal symmetry with space group P63/m—C26h, where the lattice parameters were a = 9.3855(5) Å and c = 6.8998(6) Å for x = 0.2. The particles morphology was analyzed through SEM, revealing an average length of approximately 1.5 µm. When excited at 808 nm, the Ca8NaBi(PO4)6F2:0.2Nd3+ microrods emitted strongly at 872, 957 and 1055 nm, falling within the near-infrared region. These emissions correspond to the 4F3/2 → 4I9/2 (P2), 4F5/2 → 4I11/2(P3), 4F3/2 → 4I11/2(P1) transitions of Nd3+ ions, respectively, and are situated within the first and second biological windows. The luminescence lifetime of the 4F3/2 state of Nd3+ was measured to be 294.4 µs for the sample with the lowest Nd3+ concentration of x = 0.05. In addition, the luminescence intensity ratios P2/P1 and P3/P1 were found to be temperature dependent, potentially making it suitable for luminescent ratiometric thermal sensing. These findings suggest that the synthesized Ca8NaBi(PO4)6F2:Nd3+ microrod thermometers exhibit favorable characteristics in terms of relative sensitivity, temperature uncertainty, and repeatability within the temperature range of 303–403 K.

Rheological Insights into the Degradation Behavior of PP/HDPE Blends

The (re-)processing and degradation behavior of polypropylene (PP) blends with high-density polyethylene (HDPE) is a crucial topic in mechanical recycling due to the prevalence of PP/HDPE mixtures. In particular, small amounts of cross-contamination (below 10.0 wt.%) between these polyolefins are quite common. While much empirical data is available, systematic studies on such blends are scarce and rarely account for the polymers’ chain structure. This study employs time-resolved rheology, atomic force microscopy (AFM), differential scanning calorimetry (DSC) and chemiluminescence techniques to study the degradation of different PP types containing 0.5 to 10.0 wt.% of HDPE. It is observed that the addition of small amounts of HDPE can result in a prominent change in the viscoelastic properties of PP during the thermo-oxidative degradation. The substantial evolution of elasticity in the blends is mainly related to the gelation of fine PE particles dispersed within the PP matrix. It is also shown that a smaller viscosity ratio between the blend components can lead to a more significant degradation through morphology alterations. Remarkably, time-resolved rheology studies revealed that even a small amount of HDPE (2.5 wt.%) can lead to a reduction in the thermo-oxidative stability of the PP/HDPE blend through excessive branching/crosslinking of the HDPE phase. This effect was particularly more pronounced when the PP contained an ethylene comonomer in its backbone. The finer morphology of PE particles in PP copolymer can exacerbate the thermo-oxidative stability of the blend. These insights are essential in designing new life cycles for recycled PP cross-contaminated with HDPE, typically found in the light fraction of municipal solid plastic waste.

Chemical, structural, and techno-functional characterization of yam (Dioscorea) flour from South West Ethiopia

Yam (Dioscorea spp.) is a versatile tuber crop that holds nutritional, cultural, and economic values. Yam is a major source of carbohydrates for tropical Countries and provides various nutrients and health benefits. This study aims to characterize the chemical, structural, and thermal properties of yam flour using various analytical techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), and thermal analysis. Additionally, the pasting and rheological properties of yam flour were evaluated, as they are crucial for product development and enhancing the value of this unconventional vegetable. D. cayenensis complex had the highest total starch (64.63 ± 1.61 %) and soluble sugar (4.95 ± 0.46 %) content, which was significantly higher than other yam species. The amylose content of yam flours showed significant (p < 0.05) differences among the yam species. D. cayenensis flour exhibited significantly the highest peak (2923.66 cP) and steak back viscosity (2097.66 cP) among the yam species associated with their greater amylose content. There were notable variations in pasting and gelatinization parameters among the species. The peak temperatures of D. bulbifera and D. cayenensis complex were significantly (p < 0.05) higher than D. cayenensis and D. rotundata flours. The rheological measurements of yam flours demonstrated solid-like behavior with varying intensities. Furthermore, the morphology of tuber yam flour particles was oval to ellipsoidal shaped, with some appearing ovoid, and the smaller granules appearing spherical. The X-ray diffraction showed that all yam flours exhibit a B-type pattern. This study provide a better understanding of this unconventional vegetable's potential applications in the food industry and contribute to its value addition.

Amino acids as stabilizers for lysozyme during the spray-drying process and storage

Amino acids (AAs) have been used as excipients in protein formulations both in solid and liquid state products due to their stabilizing effect. However, the mechanisms by which they can stabilize a protein have not been fully elucidated yet. The purpose of this study was to investigate the effect of AAs with distinct physicochemical properties on the stability of a model protein (lysozyme, LZM) during the spray-drying and subsequent storage. Molecular descriptor based multivariate data analysis was used to select distinct AAs from the group of 20 natural AAs. Then, LZM and the five selected AAs (1:1 wt ratio) were spray-dried (SD). The solid form, residual moisture content (RMC), hygroscopicity, morphology, secondary/tertiary structure and enzymatic activity of LZM were evaluated before and after storage under 40 °C/75 % RH for 30 days. Arginine (Arg), leucine (Leu), glycine (Gly), tryptophan (Trp), aspartic acid (Asp) were selected because of their distinct properties by using principal component analysis (PCA). The SD LZM powders containing Arg, Trp, or Asp were amorphous, while SD LZM powders containing Leu or Gly were crystalline. Recrystallization of Arg, Trp, Asp and polymorph transition of Gly were observed after the storage under accelerated conditions. The morphologies of the SD particles vary upon the different AAs formulated with LZM, implying different drying kinetics of the five model systems. A tertiary structural change of LZM was observed in the SD powders containing Arg, while a decrease in the enzymatic activity of LZM was observed in the powders containing Arg or Asp after the storage. This can be attributed to the extremely basic and acidic conditions that Arg and Asp can create, respectively. This study suggests that when AAs are used as stabilizers instead of traditional disaccharides, in addition to the classic vitrification theory and water replacement theory, the microenvironmental pH condition that the basic or acidic AAs may create in the starting solution or during the storage of solid matter is crucial for the stability of SD protein products.

Size-controlled synthesis of copper oxide nanoparticles with a supercritical hydrothermal synthesis method

Supercritical hydrothermal synthesis (SCHS) is a promising technique for the preparation of copper oxide nanoparticles with fast reaction rate, green efficiency and low cost. In this paper, nanoparticles of copper oxide ranging from 53.0 to 94.0 nm were synthesized by supercritical hydrothermal method. The effects of different precursor concentrations, alkali addition, reaction pressure, reaction temperature and reaction time on the particle size, morphology and particle uniformity of copper oxide nanoparticles were also investigated, and the mechanism of each parameter was analyzed. The growth kinetic equation of copper oxide nanoparticles under supercritical hydrothermal conditions was established by analyzing the influence laws of temperature and reaction time on the grain size of the products. Further, the growth activation energy and the growth mechanism controlled by the grain surface process was obtained. The formation mechanism of copper oxide nanoparticles in rod form was analyzed by TEM results.