Effects of isomalt on the quality of wheat flour dough and spicy wheat gluten sticks

The effects of different isomalt concentrations on the quality of wheat flour dough and spicy wheat gluten sticks (SWGS) were evaluated at the physical, structural and molecular levels. The results showed that the radial expansion rate (RER) and oil absorption rate (OAR) of SWGS increased first and then decreased with increased isomalt supplementation, which reached the maximum at 3 wt%. The pasting properties of wheat starch also changed, and the peak viscosity, breakdown and setback were decreased with the addition of isomalt. Dynamic rheological properties results showed that the storage modulus (G') and loss modulus (G'') increased with the addition of isomalt, which may be attributed to the reinforcement of gluten network structure by hydrogen bonding of isomalt. Scanning electron microscopy (SEM) images illustrated that the SWGS surface becomes smooth and the broken gluten structure was reduced after the addition of different isomalt levels compared with the control group. Overall, the wheat flour dough quality analysis showed that the addition of isomalt could generate a close binding with wheat starch and protein and further strengthen the internal structure of gluten through isomalt hydrogen bonds.     

In-vitro digestibility,textural and quality characteristics of ditalini pasta fortified with green banana flour and its type -IV modified starch

Resistant starch in unripe banana offers a possibility to alter the glycemic properties in convenience foods, such as pasta. In this study, pasta formulations were tried by replacing 30% semolina with varying proportions of green banana flour (GBF) and banana-modified starch (MS). The effect of substitution on physicochemical and functional properties, including in-vitro starch digestibility, antioxidant property and consumer acceptability, was evaluated. Among the composite flours, MS recorded higher swelling power and water holding capacity. The replacement of semolina with GBF resulted in higher resistant starch, 4–5 times enhanced indigestible fraction, phenols, flavonoids and antioxidant activity in pasta. Pronounced increment was also observed in potassium, calcium and magnesium content in blended pasta. Optimal cooking time was reduced with the addition of GBF, whereas it was enhanced with MS. GBF and MS in the blends, decreased the hydrolysis rate (up to 24%) and glycemic index (up to 17%) of pasta. However, the addition of MS beyond 10% negatively influenced springiness and chewiness. Microstructural studies explained the positive structural changes with the addition of GBF and MS. Sensory attributes disclosed that the addition of 25% GBF and 5% MS is a desirable proportion for pasta with a functional characteristics.     

电流模式和焊接方向对316L不锈钢增材制造成形的影响研究

目的 研究电流模式和焊接方向对316L不锈钢增材制造成形、内部微观组织和硬度的影响。方法 保持其他焊接工艺参数不变，采用Pulse、SpeedPulse、SpeedPulseXT这3种电流模式及同向和往复2种焊接方向进行单道多层堆积，采用光学显微镜观察增材制造件的微观组织并用洛氏硬度计测量其硬度值。结果 采用不同电流模式和不同焊接方向会影响增材制造件的冷却速率和凝固方式，进而影响增材制造件的表面成形和力学性能。同方向焊接时，随着电流模式的改变，焊接热输入增大，液态金属的流动性和铺展行为逐渐增强，增材制造件的高度尺寸减小，宽度尺寸增大，熔合线处δ铁素体受冷却速率的影响由块状变为蠕虫状，Pulse模式存在元素偏析;往复方向焊接时，外形尺寸没有明显的变化，熔合线处δ铁素体以胞状和蠕虫状为主。硬度测试结果表明，SpeedPulse模式硬度变化最小，SpeedPulseXT模式次之，Pulse模式硬度变化最大。结论 采用MIG焊进行316L不锈钢增材制造时，不同电流模式会对增材件的成形、内部金相组织和硬度产生影响。采用同方向焊接比往复方向焊接对增材件形貌的影响更大。     

Processing and characterization of an Li7La3Zr0.5Nb0.5Ta0.5Hf0.5O12 high-entropy Li–garnet electrolyte

In this paper, we demonstrated the processing of Li₇La₃Zr_0.5Nb_0.5Ta_0.5Hf_0.5O₁₂ (LLZNTH) high-entropy Li–garnet with promising properties for lithium batteries. We first synthesized the LLZNTH Li–garnet powders which have a single cubic garnet phase (space group: $\text{◂⋅▸}Ia\overline{3}d$; No. 230) without any secondary phases as well as uniform elements distributions. The prepared powders were further densified to a relative density of ∼94% with well-crystallized grains and good contact with the neighboring grains. Minimal grain growth can be observed in the sintering time range from 8 to 20 h, which is likely due to the sluggish effects of high-entropy compounds. The sample also maintains the cubic garnet phase along with uniform elements distribution after sintering. Electrochemical characterizations indicate that the densified sample has an adequate ionic conductivity of 4.67 × 10⁻⁴ S cm⁻¹ at room temperature, a low activation energy of 0.25 eV, and a low electronic conductivity in the order of 10⁻⁸ S cm⁻¹. The significance of designing high-entropy electrolyte is further discussed.     

Effects of Ni2+ concentration on the composition,structure, magnetic properties,and DC-bias superposition characteristics of NiCuZn ferrites

Ni_xCu_0.2Zn_yFe_1.98O₄ (x = 0.16, 0.26, 0.35, 0.43, 0.50; y = 0.8?x) ferrites were prepared via solid-state reaction. The influence of Ni²⁺ concentration on ferrites composition, microstructure, magnetic properties and DC-bias superposition characteristics was studied by XRD, SEM, XPS, and VSM. Then, the effect of magnetic properties on the DC-bias superposition characteristics was analyzed. The results showed that the ferrites sintered at 900 °C for 3 h were all in pure spinel phase with an average grain size of 7.5 μm and a relative density of about 5.15 g cm^?3. With the increase in Ni²⁺ concentration, the saturation magnetization (M_s) and coercivity (H_c) of ferrites increased, but the magnetocrystalline anisotropy constant (K₁) first increased and then decreased. And the M_s, H_c, and K₁ of the specimen with x = 0.43 were 63.62 emu·g^?1, 27.36 Oe, and 1813.17 Oe·emu·g^?1, respectively. In particular, the specimen of x = 0.50 achieved the best DC superposition characteristics, where the H_70% was about 220 A m^?1. The incremental permeability of the specimens decreased rapidly at a bias magnetic field <400 A m^?1. The variation mainly originated from the domain wall displacement, and the rate of decrease was influenced by both M_s and K₁. At a bias magnetic field ≥400 A m^?1, the incremental permeability of the specimens decreased slowly, mainly because the number of domain walls decreased until disappearing, and the specimens tended to become a single domain structure. And the rate of decrease of incremental permeability was mainly affected by K₁.     

Effect of Y2O3 on the structural,optical and radiation shielding properties of transparent Na-rich borate glass with diluted and fixed Fe2O3

We study the impact of yttrium oxide (Y₂O₃) on the optical properties of iron-doped borate glasses. A series of borate glasses, with a diluted and constant amount of Fe₂O₃, doped with various amounts of Y₂O₃ (labeled as BNaFeY-glasses) was prepared and studied. The impact of Y₂O₃ doping on the optical transitions of BNaFeY-glasses was studied by analyzing the optical absorption spectra. The presence of Fe cations, with their Fe³⁺ state, leads to the appearance of absorption in the ultraviolet region. Furthermore, the optical transmittance spectra proved the transparency of all BNaFeY-glasses. Moreover, the transmittance of the sample with the highest Y₂O₃ content is about 93 % within the visible range. Because of the diluted Fe content within BNaFeY-glasses, the five absorption bands of Fe are not observed. So, these bands are detected by magnifying the spectra within the visible region. These bands are labeled ?₁, ?₂, ?₃, ?₄ and ?₅ at wavelengths 454.5, 518.4, 652.5, 707 and 808 nm respectively. These bands were used to calculate the crystal field splitting (10Dq) for all BNaFeY-glasses. The outstanding 10Dq increment with further Y₂O₃ doping was explained in terms of more interactions between Fe cations and their surroundings. On the other side, the shielding parameters were considered to examine the competence of these transparent glasses against nuclear radiation. We found that the sample doped with the highest amount of Y₂O₃ has the highest linear attenuation coefficient and the lowest half-value layer (HVL). From the HVL results, we need a thickness of 3.646 cm from the sample with 5 mol% of Y₂O₃ to get protection from 50% of the photons with energy of 0.662 MeV, and this thickness is increased to 5.137 cm when the energy is 1.333 MeV.     

Phase transition induced morphotropic phase boundary behavior and the electric properties in strontium modulated Bi4.5Na0.5Ti4O15 lead-free ceramics

Lead-free (Bi_0.5Na_0.5)_1-xSr_xBi₄Ti₄O₁₅ ceramics (x = 0–0.9) are fabricated by solid state reaction process. XRD analysis shows the symmetry divergence from tetragonal to orthorhombic phase accompanied by morphotropic phase boundary with increasing strontium content. Raman spectra confirm the incorporation of strontium into (Bi_2.5Na_0.5Ti₄O₁₃)^2- layers. SEM graphs exhibit the typical plate-like morphology with regular variation of grain size and crystallization as strontium increases. Multistage ferroelectric transition is observed with x = 0.2–0.4. Piezoelectric performance measurements present the well thermal stability at x = 0.4. The dielectric properties display a shifting of Curie temperature towards low temperature with increasing strontium ions. It can be due to the crystal lattice distortion by larger radius of strontium and the increasing tolerance factor. ac conductivity and impedance measurements suggest that electron hopping mainly contributes to the low temperature region. Ionization conductivity by oxygen vacancy migration including first-ionization and double-ionization plays the dominating role in the middle and high temperature region. The controllable properties indicate the potential applications for electric devices of (Bi_0.5Na_0.5)_1-xSr_xBi₄Ti₄O₁₅ ceramic.     

Ionic liquid assisted polyetheretherketone-multiwalled carbon nanotubes nanocomposites: An environmentally friendly approach

Reinforcement of PEEK by nanoparticles such as multiwalled carbon nanotubes (MWCNTs), is a promising technique to prepare PEEK nanocomposites with improved properties for promising biomedical applications. However, proper dispersion of MWCNTs in the polymer matrices is a primary processing challenge. The present study reports a novel and environmentally beneficial approach for homogeneous dispersion of MWCNT in PEEK by using ionic liquid (IL) 1-ethyl-3-methylimidazolium hydrogen sulfate ([EMIM][HSO₄]). Neat PEEK, PEEK-MWCNTs (using conventional organic solvent dimethylformamide), and PEEK-MWCNTs-IL (using [EMIM][HSO₄]) nanocomposites were fabricated via melt-compounding and compression molding techniques. The fabricated composites were characterized for morphological, thermal, and mechanical properties and compared to those of neat PEEK and PEEK-MWCNTs. Ionic liquid provoked proficient dispersion of the MWCNTs in PEEK, as confirmed by FESEM and optical micrographs. The thermal stability of PEEK-MWCNTs-IL composite was significantly superior to that of the neat PEEK and PEEK-MWCNTs. Analysis of tensile strength and nanoindentation depicted that the modulus of elasticity of PEEK-MWNCTs-IL was significantly increased by 76% as compared to that of neat PEEK. We believe that the present work could provide a new and green platform for the manufacturing of PEEK nanocomposites with enhanced dispersion of nanofillers for biomedical applications.     

Effect of functionalized silicon carbide nano-particles as additive in cross-linked PVA based composites for vibration damping application

In this research study, a comprehensive effort has been made to functionalize silicon carbide particles using the acidic oxidation with nitric acid to obtain homogeneous stabilized distribution of activated SiC particles within a polymer matrix, and develop functionalized silicon carbide (f-SiC) particle reinforced polyvinyl alcohol (PVA) based cross-linked composite. After fabrication of functionalized silicon carbide (f-SiC) particle reinforced polyvinyl alcohol based cross-linked composite with varying f-SiC weight percentages of PVA (0%, 1%, 2%, 3%, and 4%) were placed to various investigations. Processed samples are initially examined based by the physical tests (water absorption tests), followed by mechanical test (tensile test) and then micro-structural tests (scanning electron microscopy). Lastly, thermal tests were also concluded which involved the dynamic mechanical, differential thermal and thermo gravimetric analysis. The cross-linked polyvinyl alcohol-based composite with 2 weight % of f-SiC content is observed to be the superlative of all the compositions under this research study that was confirmed by the mechanical and micro-structural tests. This composite material shows high storage modulus with visco-elastic behavior, therefore, the material can be utilized to diminish the transmission of noise, as a shock absorber and vibration isolator.     

镍基高温合金GH202高温氧化后的微观组织演变

研究了镍基高温合金GH202在800~1100 ℃高温氧化后晶粒、碳化物和强化相的演变过程。采用透射电子显微镜、扫描电子显微镜和电子背散射衍射对其微观结构进行了表征。结果表明：镍基高温合金的硬度随氧化温度的升高而降低，1100 ℃氧化100 h后，硬度降低了43.5%。800和900 ℃氧化后晶粒生长速度较慢，而经900 ℃氧化后晶界碳化物析出显著增加。在1000和1100 ℃氧化后，晶粒尺寸明显增大。氧化过程中晶界迁移是由晶界两侧自由能差决定，温度越高，晶界向曲率中心迁移越快，大量细小晶粒被吞并形成了大晶粒。大块状碳化物（MC）分解成大量的碳原子，与Cr原子结合形成少量的富Cr颗粒状M₂₃C₆。在900 ℃氧化150 h后，M₂₃C₆演化为富Ti的M₆C。随着氧化温度的升高，碳化物在γ相中回熔。在800、900和1000 ℃氧化后，γ′相逐渐长大，在1100 ℃氧化100 h后，完全溶解于γ相。