Improvement In Thermal Stability Research Articles

Improving Thermal Stability of High-Efficiency Methylammonium-Free Perovskite Solar Cells via Chloride Additive Engineering.

Tin dioxide (SnO2), in perovskite solar cells (PSCs), stands out as the material most suited to the electron transport layer (ETL), yielding advantages with regard to ease of preparation, high mobility, and favorable energy level alignment. Nonetheless, there is a chance that energy losses from defects in the SnO2 and interface will result in a reduction in the Voc. Consequently, optimizing the interfaces within solar cell devices is a key to augmenting both the efficiency and the stability of PSCs. Herein this present study, we introduced butylammonium chloride (BACl) into the SnO2 ETL. The resulting optimized SnO2 film mitigated interface defect density, thereby improving charge extraction. The robust bonding capability of negatively charged Cl- ions facilitated their binding with noncoordinated Sn4+ ions, effectively passivating defects associated with oxygen vacancies and enhancing charge transport within the SnO2 ETL. Concurrently, doped BA+ and Cl- diffused into the perovskite lattice, fostering perovskite grain growth and reducing the defects in perovskite. In comparison to the control device, the Voc saw a 70 mV increase, achieving a champion efficiency of 22.86%. Additionally, following 1000 h of ambient storage, the unencapsulated device based on SnO2 preburied with BACl retained around 90% of its initial photovoltaic conversion efficiency.

Enhanced polyacrylamide polymer hydrogels using nanomaterials for water shutoff: Morphology, thermal and rheological investigations at high temperatures and salinity

This study focuses on the synthesis, characterization, and performance evaluation of polyacrylamide (PAM)/polyethyleneimine (PEI) hydrogels enhanced with nanomaterials for potential application in conformance control in oil wells. The materials used include PAM with a molar mass of 25,000 Kg mol−1, PEI with an average weight molar mass of 25 Kg mol−1, and synthetic brine (ionic strength 0.6). Nanomaterials such as titanium dioxide (TiO2) nanoparticles, oxidized carbon nanotubes (CNT-ox), and graphene oxide (GO) were incorporated into the hydrogel matrix. A simple method was used for the incorporation of nanomaterials into the polymeric matrix, ensuring their good dispersion in the hydrogels formed. Characterization techniques including thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) were employed to analyze the structure, morphology, and thermal stability of the hydrogels. Rheological measurements and gel strength evaluations were conducted to assess the performance of the hydrogels. Results indicate that the incorporation of nanomaterials enhanced the thermal stability, gel strength (Sydansk code), and resistance to syneresis of the hydrogels. Specifically, the addition of TiO2 nanoparticles exhibited the highest improvement in viscosity and thermal stability, attributed to strong interactions between TiO2 and PAM molecules. A notable decrease in syneresis percentages was observed with the inclusion of nanomaterials compared to the PAM reference sample, reaching 70.1 % for the hydrogel modified with GO. These findings suggest that nanomaterial-enhanced hydrogels hold promise for applications in conformance control in oil wells, offering improved stability and performance over extended periods of use.

Improving Thermal Stability of Perovskite Solar Cells by Suppressing Ion Migration

Ion migration presents a formidable obstacle to the stability and performance of perovskite solar cells (PSCs), hindering their progress toward commercial feasibility. Herein, the degradation mechanism of PSCs caused by iodide ion migration, which leads to abnormal changes in photoluminescence transients at the buried interface of perovskite films, is investigated. In light of this problem, a novel strategy is proposed to mitigate ion migration by introducing poly(2‐vinylnaphthalene) into poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] as the hole transport layer with improved ion‐blocking capability. Consequently, this layer effectively reduces defect concentration, suppresses ion migration, and modulates energy level alignment, leading to an impressive efficiency exceeding 23% for doctor‐bladed FAPbI3 PSCs. Moreover, the corresponding unencapsulated devices demonstrate remarkable durability, maintaining over 80% of their initial value after undergoing rigorous stress tests in accordance with the International Electrotechnical Commission 61215 standard for temperature, humidity, and illumination. These tests include 1000 h of thermal cycling and a long‐term operational test lasting 600 h under maximum power point tracking.

Design and Analysis of Mode-Matched Decoupled Mass MEMS Gyroscope with Improved Thermal Stability

Abstract This paper presents an efficient design approach for microelectromechanical systems (MEMS) gyroscope considering the design constraint of MEMSCAP's Silicon-on-Insulator Multi-User MEMS Processes (SOIMUMPs). A design for a decoupled mass MEMS resonant gyroscope with tuning electrodes is presented to minimize cross-axis coupling and optimize the gyroscope's performance. The device features a size of 1.8 ×2.772 mm^2. A decoupled mass MEMS gyroscope has been designed using a novel mechanical beam configuration that optimizes the structural design to reduce unwanted interactions between drive and sense axes motions. Mode order has been achieved by obtaining the first two modes as drive and sense modes at 9946.3 Hz and 10202.7 Hz, respectively. Parallel plate electrostatic tuning electrodes have been added to adjust and match the drive and sense modes at the resonant frequencies of 9946 Hz. This mode matching is crucial for optimizing gyroscope performance, accuracy, and sensitivity. The effects of temperature variation on the performance of the designed decoupled mass MEMS gyroscope have been investigated, particularly in terms of its mode-matched operation achieved using tuning electrodes. Finite Element Method (FEM) simulations were conducted, demonstrating that thermal stability was achieved, and mode-matched operation was maintained within the temperature range of -40 ºC to 80 ºC. The gyroscope exhibits enhanced performance compared to existing MEMS gyroscopes under mode-matched conditions, featuring a lower temperature coefficient of frequency (TCF) at 0.0415 Hz/ºC in the drive mode and 0.0165 Hz/ºC in the sense mode. FEM analysis for the fabrication process tolerances has been done, where MEMS gyroscope’s resonant frequencies, output capacitance, output displacement, and sense mode quality factor have shown negligible changes to fabrication process tolerances. Transient analysis was conducted using CoventorWare MEMS+ 3D schematic, which was integrated with MATLAB Simulink to measure the MEMS gyroscope’s output response, which corresponded with the varying input angular velocity signal.

Preparation and characterization of long carbon chain based polyacrylate latexes and their pressure sensitive adhesive application

Aqueous emulsion homo- and co-polymerization of lauryl methacrylate (LMA), a strong hydrophobic monomer with long carbon chain, is quite challenging. In this study, a long carbon chain emulsifier N-390 was used as the primary emulsifier to facilitate the emulsion copolymerization of LMA with other acrylate monomers through the mutual hydrophobic interaction between N-390 and LMA, and ultimately polyacrylate latex pressure sensitive adhesives modified by LMA via pre-emulsified semi-continuous seeded emulsion polymerization process were synthesized. The effects of LMA on the resulting latex and PSA properties was comprehensively examined. Both FTIR and 1H NMR spectra indicated that LMA has been successfully introduced into copolymer chain with the aid of long carbon chain emulsifier N-390. The results also showed that the introduction of LMA will contribute to decrease in particle size and zeta potential, while increase viscosity and gel content of the acrylate PSA latex. Moreover, as the LMA content increased, the latex PSA films demonstrated gradual improvements in both water resistance and thermal stability. Finally, for the long carbon chains adhesive film, the shear strength was improved greatly while at the sacrifice of loop tack and peel strength, when compared to counterparts without LMA.

Improved Thermal Stability and Oxygen‐Barrier Performance of SiO2 Thin Films by Modifying Amorphous Network Structure

Due to low‐refractive‐index and grain‐boundary‐free features, amorphous SiO2 thin films possess inherent advantages in serving as antireflective and protective layers against atmosphere. However, under high‐temperature and/or oxidation harsh environment, the thermodynamic instability of SiO bonds and “depolymerization” process among tetrahedral units [SiO4] would result in their insufficient thermal stability and oxygen‐barrier failure. By taking amorphous network former, small element electronegativity, and high oxide dissociation energy into considerations, low‐level Zr dopant is introduced to induce short‐ and medium‐range structural modification in amorphous SiO2 thin films, aiming to shorten SiO bond length and enhance network connectivity, respectively. As expected, the fabricated SiZrO thin films exhibit superior thermal stability and oxygen‐barrier performance without sacrificing their low‐index attribute. The Zr doping significantly elevates the oxygen‐inward‐diffusion activation energy from 0.94 to 1.95 eV in SiO2 network. Further, utilizing as protective layer for W‐SiO2 cermet, the SiZrO can effectively prevent the oxidation of W nanoparticles caused by oxygen inward diffusion. Undoubtedly, the exploration of amorphous SiZrO thin films offers exciting prospects for the application of functional coatings and devices under extreme conditions.

Modified Amber Particles as a Stabilizer to Construct Oil-in-Water Pickering Emulsions for Improved Thermal Stability of Acorus tatarinowii Essential Oil.

Lingzhu Pulvis is a classic formulation for treating febrile convulsions in children. However, Acorus tatarinowii essential oil (AT-EO) in this prescription is prone to volatilization and oxidation, compromising the efficacy and quality control of this formulation. Herein, based on the concept of "combination of medicine and adjuvant", Pickering emulsion technology was applied to enhance the stability of AT-EO using modified amber as a stabilizer. Amber was a resinous medicinal powder in Lingzhu Pulvis and was modified into a suitable stabilizer for Pickering emulsion through surface modification. A thermal stability study indicated that Pickering emulsion, stabilized by modified amber, exhibited a higher retention rate of AT-EO and lower levels of peroxide value and malondialdehyde content compared to those of the pure AT-EO group after heat treatment at 40 °C for 1, 3, and 8 h. Additionally, component analysis in content and composition revealed that the volatile components of AT-EO in the Pickering emulsion were more stable during the thermal treatment process. This study convincingly illustrates the potential of a Pickering emulsion stabilized with modified medicinal powders to improve the thermal stability of the essential oil.

Improvement of thermal stability by co-introducing Dy and Co with dual-alloy method in NdFeB magnets

A dual-main-phase magnet with excellent thermal stability was prepared by co-mixing two types of magnetic powders, which was the conventional N55-grade powder without Dy elements, while the Co and Dy contents reached 50 wt.% and 6 wt.% respectively in another Co-rich powder. Studies showed that the magnetic properties along with the thermal stabilities of the magnets exhibited significant differences with the changes in the mixing ratio of the two powders. Especially, when mixing the two powders in equal proportions, a great remanence temperature coefficient of -0.0725 %/°C at 20-100 °C was obtained with a rather high Curie temperature of 581 °C, possessing its magnetic properties with Br=12.58 kGs, Hcj=15.9 kOe, and (BH)max=36.88 MGOe. Note that as the proportion of Co-rich powder increased to 2/3, although the Curie temperature of the prepared magnets further increased to 622 °C, both the remanence temperature coefficient and the magnetic properties deteriorated significantly. The phase composition and microstructure analyses revealed that when the proportion of added Co-rich component exceeded 1/2, the RE(Fe,Co)2B phase transformed into the RE(Fe,Co)4B phase, and a significant amount of RE(Fe,Co)1.8B0.2 phase precipitated at the grain boundaries, leading to a deterioration in magnetic performance. In addition, dynamic domain evolution analyses under variable temperature conditions demonstrated the positive effect of the appropriate introduction of Co/Dy on the anti-demagnetization in high temperatures. This work provides insights and an experimental foundation for the development of high-performance magnets with high thermal stability, used in high-temperature environments.

Charge-Traps, Thermal Stability and Water-Uptakes of CaSiO3/EP and SiO2/EP Nanocomposites from Molecular Simulations and First-Principles Calculations

Various analytical methods were employed to elucidate the effects of filling nano-calcium-silicate or nano-silica on the electronic property, water-uptake, and thermal stability of an amine-crosslinked epoxy (EP) polymer. Molecular-mixture models consisting of a nanofiller or several calcium ions and EP crosslinked macro-molecules were used to simulate local regions of nanofiller/matrix interface or ion-infiltrated matrix, calculating their density of electron-states by first-principles method to determine whether and how the nanofillers introduce charge traps into EP matrix. Calcium cations on nanofiller surface dissociate away from coordinating with silicon-oxygen tetrahedron and infiltrate into void spaces in EP matrix, leaving a larger free volume at filler/matrix interface than in matrix. Calcium cations dissolved in EP matrix are adsorbed in the low electrostatic potential region or coordinate with carbonyl groups in EP matrix and thus introduce a miniband of deep electron traps at energy levels >1 eV lower than conduction band minimum of the amine-crosslinked EP polymer. Even at room temperature, thermal vibrations can break coordinate bonds between calcium cations and silicon-oxygen framework on calcium-silicate nanofiller surface and make considerable calcium ions infiltrating void spaces within EP matrix, leading to comprehensive improvements of cohesive energy, thermal stability, and charge trapping ability in the calcium-silicate/EP nanocomposite.

Water Absorption, Thermal, and Mechanical Properties of Bamboo Fiber with Chopped Glass Fiber Filler-Reinforced Polyester Composites

This study explores the investigations of bamboo fiber-reinforced polyester composites with chopped glass fiber (CGF) filler, focusing on addressing the challenges of low mechanical properties, limited thermal stability, and high moisture absorption. The two types of composites were fabricated using the hand layup method, that is, long unidirectional 0° bamboo fiber (BF) and randomly oriented short bamboo fiber (BP) reinforced a polyester matrix with chopped glass fiber (CGF) filler. By incorporating CGF filler, significant improvements in mechanical properties were achieved across both types of bamboo fiber, surpassing the limitations of unfilled composites. Notably, the composite formulation consisting of 40% wt. of unidirectional 0° BF and 5% wt. of CGF filler exhibited superior ultimate tensile strength, flexural strength, impact strength, water absorption, and thermal stability. This composite demonstrated remarkable enhancements, with increases of up to 131.22 MPa, 128.76 MPa, 113.3 kJ/m2, 1.94% water absorption, and up to 255°C (representing a 10% improvement) in thermal stability compared to the unfilled composite. Statistical analysis revealed quadratic models for the mechanical properties of long unidirectional 0° bamboo fiber composites, while water absorption exhibited a linear two-factor interaction model. For randomly oriented short bamboo fiber, the models for tensile, flexural, and water absorption properties were linear, while the impact energy model showed a quadratic relationship. These statistical models provide valuable insights into predicting the properties of bamboo fiber-reinforced polyester composites. This research underscores the significance of bamboo fiber-reinforced polyester composites in wall partition systems. This study paves the way for improved performance in these areas. The findings highlight the potential of incorporating CGF filler, enabling enhanced mechanical strength, increased thermal stability, and improved resistance to moisture-related issues. The derived statistical models offer valuable guidance for predicting the properties of these composites, facilitating their application and adoption in the construction industry.

An insight into the co-doping effect of d-d transitions of transition metal ions and hypersensitivity of rare-earth ions in multicomponent glass-system

A multicomponent glass system with composition (70B2O3-22.5Bi2O3-5SeO2-2CuO-0.5Sm2O3) was synthesized via the conventional melt-quench technique. X-ray diffraction analysis confirmed the amorphous nature of this glass. The co-doping of transition and rare-earth metal ions results in the gradual decrease in glass transition temperature and improvement in thermal stability as observed from differential scanning calorimetry. The addition of CuO has increased non-bridging oxygens in multicomponent glass system. The increase in non-bridging oxygens results in a decrease in the optical band gap energy of the glass. Various results reveal that the hypersensitive nature of rare-earth ions has been suppressed by the d-d transition. A decrease in the energy band gap upon co-doping of transition and rare earth ions, suggests its applications in the fields of optoelectronics.

Improvement of Thermal Stability and Photoelectric Performance of Cs2PbI2Cl2/CsPbI2.5Br0.5 Perovskite Solar Cells by Triple-Layer Inorganic Hole Transport Materials.

Conventional hole transport layer (HTL) Spiro-OMeTAD requires the addition of hygroscopic dopants due to its low conductivity and hole mobility, resulting in a high preparation cost and poor device stability. Cuprous thiocyanate (CuSCN) is a cost-effective alternative with a suitable energy structure and high hole mobility. However, CuSCN-based perovskite solar cells (PSCs) are affected by environmental factors, and the solvents of an HTL can potentially corrode the perovskite layer. In this study, a Co3O4/CuSCN/Co3O4 sandwich structure was proposed as an HTL for inorganic Cs2PbI2Cl2/CsPbI2.5Br0.5 PSCs to address these issues. The Co3O4 layers can serve as buffer and encapsulation layers, protecting the perovskite layer from solvent-induced corrosion and enhancing hole mobility at the interface. Based on this sandwich structure, the photovoltaic performances of the Cs2PbI2Cl2/CsPbI2.5Br0.5 PSCs are significantly improved, with the power conversion efficiency (PCE) increasing from 9.87% (without Co3O4) to 11.06%. Furthermore, the thermal stability of the devices is also significantly enhanced, retaining 80% of its initial PCE after 40 h of continuous aging at 60 °C. These results indicate that the Co3O4/CuSCN/Co3O4 sandwich structure can effectively mitigate the corrosion of the perovskite layer by solvents of an HTL and significantly improves the photovoltaic performance and thermal stability of devices.

Flexible and thermoresponsive AEMR-pNIPAM/Cs0.33WO3 composite hydrogel film with NIR shielding potential for smart windows and smart curtains

Thermoresponsive flexible smart windows and smart curtains having high near-infrared (NIR) shielding and tuned visible light transmittance are essential for improving the energy efficiency of the buildings. The lower critical solution temperature (LCST) of the cross-linked poly(N-isopropylacrylamide) (pNIPAM) hydrogel film was precisely modified to a desired LCST value at 27.4 °C through the free radical copolymerization with 10 wt% of acrylated epoxidized methyl ricinoleate (AEMR). Cs0.33WO3 as NIR shielding nanoparticles (particle size < 200 nm) were synthesized via high energy ball milling method with AEMR as a surfactant for high NIR shielding efficiency and dispersion—the composite flexible hydrogel films with different wt% (0.3, 0.5,0.7, and 0.9 wt%) of Cs0.33WO3 nanoparticles were fabricated to analyze the NIR shielding efficiency and thermal insulation performance. The copolymeric hydrogel film with 0.7 wt% of Cs0.33WO3 nanoparticles (0.7-CWO) demonstrates a significant reduction in the NIR transmittance (15.0 % to 2.3 %) and variation in visible light transmittance from 73.6 % to 15.7 % while undergoing temperature-induced phase transition. The smart window fabricated with composite hydrogel film exhibits good integral luminous transmittance (Tlum, 380–780 nm, 68.7 %, below LCST) and justifiable solar modulation ability (ΔTsol, 300–2500 nm, 53.6 %). A model house was designed to monitor the indoor temperature difference, and a noticeable variation of 7 °C was observed in the house with and without 0.7-CWO film. Further, the developed composite material showed improvement in flexibility, water resistance, and thermal stability, confirming its usage for energy-saving smart windows or smart curtains.

Investigation of the Effects of Phenolic Extracts Obtained from Agro-Industrial Food Wastes on Gelatin Modification.

In this study, modified bovine gelatin was produced using the alkaline technique with four different oxidized agro-industrial food waste (pomegranate peel (PP), grape pomace and seed (GP), black tea (BT), and green tea (GT)) phenolic extracts (AFWEs) at three different concentrations (1, 3, and 5% based on dry gelatin). The effect of waste type and concentration on the textural, rheological, emulsifying, foaming, swelling, and color properties of gelatin, as well as its total phenolic content and antioxidant activity, was investigated. Significant improvement in gel strength, thermal stability, and gelation rate of gelatin was achieved by modification with oxidized agro-industrial waste extracts. Compared to the control sample, 46.24% higher bloom strength in the GT5 sample, 5.29 and 6.01 °C higher gelling and melting temperatures in the PP5 sample, respectively, and 85.70% lower tmodel value in the GT3 sample were observed. Additionally, the total phenolic content, antioxidant activity, foam, and emulsion properties of the modified gels increased significantly. This study revealed that gelatins with improved technological and functional properties can be produced by using oxidized phenolic extracts obtained from agricultural industrial food wastes as cross-linking agents in the modification of gelatin.

Comparative Analysis of Crosslinking Methods and Their Impact on the Physicochemical Properties of SA/PVA Hydrogels.

Hydrogels, versatile materials used in various applications such as medicine, possess properties crucial for their specific applications, significantly influenced by their preparation methods. This study synthesized 18 different types of hydrogels using sodium alginate (SA) and two molecular weights of polyvinyl alcohol (PVA). Crosslinking agents such as aqueous solutions of calcium (Ca2+) and copper (Cu2+) ions and solutions of these ions in boric acid were utilized. The hydrogels were subjected to compression strength tests and drying kinetics analysis. Additionally, six hydrogel variants containing larger PVA particles underwent Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) post-drying. Some samples were lyophilized, and their surface morphology was examined using scanning electron microscopy (SEM). The results indicate that the choice of crosslinking method significantly impacts the physicochemical properties of the hydrogels. Crosslinking in solutions with higher concentrations of crosslinking ions enhanced mechanical properties and thermal stability. Conversely, using copper ions instead of calcium resulted in slower drying kinetics and reduced thermal stability. Notably, employing boric acid as a crosslinking agent for hydrogels containing heavier PVA molecules led to considerable improvements in mechanical properties and thermal stability.

Improved Thermal Stability of Al-Si Alloy Coated Steel Sheet with Cr Thin Film Deposition

We investigated the effect of Cr thin film deposition on the thermal stability and corrosion resistance of hot-dip aluminized steel. A high-quality Cr thin film was deposited on the surface of the Al-9 wt. % Si-coated steel sheets by physical vapor deposition. When the Al-Si coated steel sheets were exposed to a high temperature of 500℃, Fe from the steel substrate diffused into the Al-Si coating layer resulting in discoloration. However, the highly heat-resistant Cr thin film deposited on the Al-Si coating prevented diffusion and surface exposure of Fe, improving the heat and corrosion resistances of the Al-Si alloy coated steel sheet.

The effect of gamma rays and stearic acid on calcium carbonate and its impact on the properties of epoxy-based composites

Abstract The purpose of this research is to produce composites of epoxy resin and calcium carbonate (EP/CaCO3) and investigate how treating the CaCO3 filler with stearic acid and gamma radiation affects the properties of the epoxy composites, enhancing their suitability for a range of applications. The CaCO3 powder was subjected to stearic acid treatment and later exposed to γ-radiation at various doses namely (10, 20 and 30 kGy), Different weight percentages of untreated and treated CaCO3 powder were added to epoxy resin (EP) to create EP/CaCO3 composites loaded with varying amounts of CaCO3 filler (5 %, 10 %, 20 %, 30 %, and 40 %). The influence of both stearic acid treatment and different doses of gamma radiation on CaCO3 was investigated. The composites were subjected to characterization of various properties including mechanical (splitting tensile strength, impact strength), thermal (TGA and dimensional thermal analysis) as well as morphological SEM examination. The analysis’ findings demonstrated that the stearic acid monolayer functions as a coupling agent in the EP matrix and can coat CaCO3 particles efficiently. The modification of CaCO3 by stearic acid and exposure to 30 kGy of gamma radiation shows a notable improvement in thermal stability and mechanical qualities for the epoxy composites loaded with various CaCO3 concentrations.

Solubilization and stabilization of lipoic acid trisulfide by creation of various β-cyclodextrin clathrates.

Lipoic acid trisulfide, a sulfane sulfur-containing trisulfide of α-lipoic acid, holds promise in pharmaceuticals, yet knowledge gaps persist regarding its synthesis, properties, and stability. Here, we synthesized the lipoic acid trisulfide with a purity exceeding 99% from α-lipoic acid on a gram scale and obtained novel β-cyclodextrin clathrates (84-95% yield). Differential scanning calorimetry confirmed the inclusion of lipoic acid trisulfide in β-cyclodextrins. The resulting β-cyclodextrin clathrates exhibited significant improvements in water solubility and thermal stability. This pioneering study demonstrated a novel approach to the practical preparation of trisulfide and its β-cyclodextrin clathrates as active ingredients, paving the way for clinical development.

Improved Thermal Stability of a Novel Acidophilic Phytase.

Phytase increases the availability of phosphate and trace elements by hydrolyzing the phospho-monoester bond in phytate present in animal feed. It is also an important enzyme from an environmental perspective because it not only promotes the growth of livestocks but also prevents phosphorus contamination released into the environment. Here we present a novel phytase derived from Turicimonas muris, TmPhy, which has distinctive structure and properties compared to other previously known phytases. TmPhy gene expressed in the Pichia system was confirmed to be 41 kDa in size and was used in purified form to evaluate optimal conditions for maximum activity. TmPhy has a dual optimum pH at pH3 and pH6.8 and exhibited the highest activity at 70℃. However, the heat tolerance of the wildtype was not satisfactory for feed application. Therefore, random mutation, disulfide bond introduction, and N-terminal mutation were performed to improve the thermostability of the TmPhy. Random mutation resulted in TmPhyM with about 45% improvement in stability at 60℃. Through further improvements, a total of three mutants were screened and their heat tolerance was evaluated. As a result, we obtained TmPhyMD1 with 46.5% residual activity, TmPhyMD2 with 74.1%, and TmPhyMD3 with 66.8% at 80℃ heat treatment without significant loss of or with increased activity.

Development of soy protein isolate-based orally disintegrating film: Improvement of disintegration speed, mechanical properties, and thermal stability by β-Cyclodextrin

The effect of β-Cyclodextrin (β-CD) at different concentrations (0–20% w/w) on the function and properties of soy protein isolate (SPI)-based orally disintegrating films (ODF) was studied. The results of moisture content and contact angle indicate that the inclusion of β-CD enhances the moisture content and surface hydrophilicity of ODF. The thickness ODF samples is between 0.031 and 0.041 mm. Due to the addition of β-CD, ODF disintegration rates increased by 47.86%–64.62%. Scanning electron microscope, and mechanical analysis show that ODF with a β-CD concentration of 10% w/w has the best performance, presenting the smoothest surface, maximum tensile strength (TS) and elongation at break (EB). FTIR spectrum results show that there are physical entanglements and hydrogen bonding interactions between SPI and β-CD, and appropriate concentrations of β-CD (5% w/w and 10% w/w) can transform random coils into β-sheets. Once the concentration exceeding 10% w/w, β-CD will crystallize and precipitate on the ODF surface, which weakens the mechanical properties of the ODF and the strength of the SPI network structure. Thermogravimetric test results show that β-CD improves ODF thermal stability. This research offers a significant theoretical foundation for the advancement of ODF that are protein-based and not hydrolyzed.