Crystalline Regions Research Articles

Determination and molecular simulation of ternary solid–liquid phase equilibrium of succinic acid + maleic acid + water from 283.15 K to 333.15 K

This study used the isothermal saturation gravimetric method to examine the solid–liquid phase equilibrium relationships composed of succinic acid + maleic acid + water spanning from 283.15 K to 333.15 K. The experimental data were utilized for the purpose of plotting the equilibrium phase diagrams of ternary systems in the studied temperature range. There were three crystalline regions in each isothermal ternary phase diagram, two saturation boundary curves, and a co-saturation point. To broaden the use of data from binary and ternary phase equilibrium measurements, Wilson and NRTL models were utilized for correlation and expectation, while relative average deviation (RAD) and root mean square deviation (RMSD) were utilized to evaluate the computational exactness. The results show that the theoretically calculated values were found to be in near agreement with the experimental values, and both models were able to obtain more precise theoretical data under different experimental conditions. In addition, molecular simulation was employed to elucidate the interaction between succinic acid, maleic acid, and water. This study provides accurate and reliable data for the separation of succinic acid and maleic acid mixture in water. These findings can be utilized to make sense of the dissolvability conduct of succinic acid and maleic acid in aqueous solution.

Eco-friendly fiberboards with low formaldehyde content and enhanced mechanical properties produced with activated soybean protein isolate modified urea-formaldehyde resin

Urea-formaldehyde (UF) resin is one of the most widely used resin adhesive for wood-based panels. The main concern of UF resin bonded wood-based panels is formaldehyde emission and poor water resistance. In this study, activated soybean protein isolate (SPI) was used to modify UF resin for the production of eco-friendly fiberboard panels. The effects of different activated SPI on the properties of UF resins and the resin bonded medium-density fiberboard (MDF) panels were investigated. The free formaldehyde content of the urea-activated SPI modified UF resin was only 0.13 %. Approximately 27.8 % lower than that of the unmodified UF resin. The resin bonded MDF panel with a density of 760 kg/m3 shows a modulus of rupture (MOR) and modulus of elasticity (MOE) of 45.73 MPa and 4005 MPa, which is increased by 25 % and 15 % compared to the unmodified UF resin group. The internal bonding strength (IB) reaches 0.71 MPa, which is about 15 % higher than that of the unmodified UF resin group. The tested 24-hour thickness swelling (24 h TS) of the modified UF resin group is only 8.1 %. The tested formaldehyde content of the sodium dodecyl sulfate (SDS)-activated SPI modified UF resin bonded MDF panel is only 4.8 mg/100 g, which is 20 % lower than that of the control UF resin group. The activated SPI modified UF resin shows great improvement in bonding strength and lower formaldehyde content for MDF panels as compared to the pure UF resin. The chemical groups, crystalline properties, and thermal stability of the pure and the modified UF resins were characterized via Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric (TG) analysis. It is confirmed that the activated SPI modified UF resin has similar chemical structure, higher ratio of crystalline regions, and slightly lower thermal stability with compared to the pure UF resin. This study proposes a practical and applicable solution for the utilization of eco-friendly UF resin in wood-based panel production.

Nanoscale visualization of fast carrier dynamics in organic thin-film transistors by time-resolved electrostatic force microscopy

Fast carrier dynamics in organic thin-film transistors (OTFTs) was investigated by time-resolved electrostatic force microscopy (tr-EFM). We found that the carrier diffusion in the OTFTs proceeded in two stages: fast diffusion and slow diffusion. By applying the instantaneous frequency method to EFM, the temporal evolution of the spatial distribution of fast carriers in the channel region of the OTFTs, which took place on the timescale of several hundreds of nanoseconds, was evaluated. The inhomogeneous distribution of the local decay time constant showed that the carrier diffusion of the OTFTs was limited by the grain boundaries between each crystalline region. The quantitative capability of the method was verified by comparing the values of the carrier mobility estimated by the tr-EFM measurement and a numerical simulation. The mobility estimated from the experiment and the simulation showed good agreement, showing the possibility of the tr-EFM to evaluate the time evolution of dynamic phenomena in semiconductor devices.

Exploring the functional abilities of PVA–combeite composites as potential candidates for bone substitutes

Abstract The field of biomaterials continually seeks novel materials to meet the requirements of bone tissue engineering. This manuscript explores polyvinyl alcohol (PVA)–combeite composites. The composites were characterized using X-ray diffraction and scanning electron microscopy. Notably, the X-ray diffraction patterns unveil a combination of amorphous and crystalline regions attributed to PVA and combeite, respectively. More importantly, PVA–combeite composites exhibit reduced swelling and degradation rates compared to pure PVA. The percentage swelling and degradation values (%) for the prepared materials fall within the range of 190–340 and 55–75, respectively. The spherical apatite structures formed post the immersion in Hanks’ Balanced Salt Solution indicate that these materials could be used in the field of bone tissue engineering.

Tailoring the physicochemical properties of starch: impact of integrated ultrasonic and ethanol pretreatment on the oil uptake of infrared fried ginkgo seeds.

The structural changes of starch would have a more crucial impact on oil absorption and quality changes in starch-rich fruits and vegetables during frying process with enhanced heat transfer (such as infrared frying). In the present study, the influence of integrated ultrasonic and ethanol (US + ethanol) pretreatment on oil uptake in infrared fried (IF) ginkgo seeds was evaluated regarding modifications in the physicochemical properties of starch. The pretreatment was performed with ultrasonic (40 kHz, 300 W) and ethanol osmotic (95%, v/v) treatment individually or integrated for 40 min. The mass transfer in the pretreatment was facilitated by combined ultrasound and ethanol. The swelling power, solubility, and gelatinization degree of starch was significantly increased. Low-frequency-NMR curves and images revealed that the bound water fraction in ginkgo seeds was increased and the water distribution was homogenized. The results of Fourier transform-infrared spectrum and differential scanning calorimeter revealed that the crystalline regions of starch were reduced and the thermal enthalpy was decreased after US + ethanol pretreatment. The total, surface and structural oil content in IF ginkgo seeds with US + ethanol pretreatment was reduced by 29.10%, 34.52% and 29.73%, respectively. The US + ethanol pretreatment led to a thinner crust layer with increased porosity and smaller-sized pores in the IF ginkgo seeds as observed by stereo microscopy and scanning electron microscopy. The changes in structural and physicochemical properties of starch by combined ultrasound and ethanol affect the crust ratio and pore characteristics in fried high-starch fruits and vegetables, thereby reducing oil absorption. © 2024 Society of Chemical Industry.

Glueless formaldehyde-free biocomposites with high strength based on the three-dimensional structure of wood fibres

The efficient utilization of small-diameter shrub resources holds significant potential in averting forest resource waste and mitigating carbon emissions. Herein, glueless biocomposites were prepared using waste small-diameter Buxus megistophylla via alkali pre-treatment and thermal molding. Instead of simple hot-pressing, the biocomposites were prepared using thermal molding, which allows the release of edge stresses in a high-pressure environment. After alkali pretreatment, the flexural and tensile strength of the biocomposites increased by 66.08% and 74.12%. Alkali pre-treatment forms reactive alkali-cellulose, facilitating fiber bonding. Structural disruption leads to fiber swelling, increasing surface area and hydrogen bonding, especially on cellulose. This process disrupts and reconstitutes crystalline regions, enhancing crystallinity. Lignin liberated from the lignin-hemicellulose polymer transitions to a molten state, serving as an adhesive to fortify fiber bonds, creating a 3D lattice structure and hydrophobic surface (Water contact angle 85°). Furthermore, these biocomposites, being adhesive-free and non-emitters of harmful gases like formaldehyde, hold promise as sustainable materials for architectural decoration and furniture applications.

Trap-induced hydro-charging polylactic acid nonwovens with high charge storage capability for stable and efficient air filtration

Under the background of carbon neutrality, eco-friendly biodegradable polylactic acid (PLA) melt-blown nonwovens have been developed in air filtration. Nevertheless, the filtration performance of existing PLA melt-blown nonwovens is in an embarrassing situation and fails to meet the requirement of high efficiency air filters. Here, with controllable doping of N, N′-ethylene bis-stearamide (EBS), and barium titanate (BaTiO3) into PLA, through the melt-blown process, the charge-storage capacity of PLA nonwovens enhanced significantly. By utilizing the hydro-charging technology thereafter, we have prepared hydro-charged PLA/EBS/BaTiO3 nonwovens (HCP-EB) with excellent filtration performances. The doped EBS and BaTiO3 could improve the crystallization and charge storage capacity of PLA during the melt-blown process, thus constructing a large number of interfacial traps between crystalline and amorphous regions, leading to more electric charges captured during the hydro-charging process. The HCP-EB exhibited a high filtration efficiency (99.69 %) for PM0.3, a low pressure drop (27.44 Pa), and superior charge storage stability. Furthermore, the HCP-EB, remained at 99.18 % filtration efficiency after 48 h of treatment at 90 % relative humidity. After 3 months of storage, it still possessed an excellent filtration efficiency (99.02 %). Our work will contribute to the practical application of PLA melt-blown nonwovens in air filters and masks, and inspire the research of next-generation biodegradable electret air filtration materials.

The Crystallization Morphology and Conformational Changes of Polypropylene Random Copolymer Induced by a Novel β-Nucleating Agent.

The crystal morphology and conformational changes during crystallization of a polypropylene random copolymer (PPR) are the basis for understanding its crystallization process. In this work, novel rare-earth β-nucleating agent WBN-28 was directly added into PPR to induce β-crystallization. The results of differential scanning calorimetry (DSC) showed that it has an excellent β-crystal-induced effect. The β-crystal content could surpass 85%, calculated from wide-angle X-ray diffraction (WAXD) data. The morphology of the β-crystal and α-crystal was intuitively observed via a polarizing optical microscope (POM). The β-crystallites were interconnected to naturally develop plate-like crystalline regions possessing a certain size, and the α-crystallites with sufficient thicknesses possessed a cross-hatched phenomenon. The bundle-like supramolecular structure of the β-crystal induced by WBN-28 was further observed via a scanning electron microscope (SEM). The conformational changes in the crystallization process of PPR were resolved via high-resolution infrared spectroscopy to understand its β-crystallization in depth. The conformational changes during the crystallization of PPR were found to be different from those of the isotactic polypropylene homopolymer (PPH); they had their own characteristics. This will provide guidance for understanding the β-crystallization of PPR in depth.

Absorption of water molecules on the surface of stereocomplex-crystal spherulites of polylactides: An in-situ FT-IR spectroscopy investigation

The correlation between water molecules and polylactide was clarified. The crystallinity in stereocomplex (SC) crystal spherulites was investigated using microbeam wide-angle X-ray diffraction. The crystallinity was higher in the central region, and edge-on lamellae grew in a twisted manner. The hydrogen bonding in SC-crystal spherulites was evaluated via microbeam FT-IR spectroscopy in a humidity-controlled cell. The water-derived bands corresponding to OH vibration and HOH bending increased with increasing humidity. Microbeam FT-IR spectroscopy was used to evaluate the water absorption behavior of crystalline films depending on their position. Coarse-grained molecular dynamics simulations indicated that the number of adsorbed water molecules increased with decreasing crystallinity. In SC-crystal spherulites, water molecules are absorbed in both amorphous and crystalline regions but with greater difficulty in the crystalline regions. These insights into water molecule absorption on SC-crystal spherulite can facilitate the development of polylactide materials with controlled biodegradability for advanced medical and optical applications.

Impact of crystalline domains on long-term stability and mechanical performance of anisotropic silk fibroin sponges.

Sponge-like materials made from regenerated silk fibroin biopolymers are a tunable and advantageous platform for in vitro engineered tissue culture and in vivo tissue regeneration. Anisotropic, three-dimensional (3D) silk fibroin sponge-like scaffolds can mimic the architecture of contractile muscle. Herein, we use silk fibroin solution isolated from the cocoons of Bombyx mori silkworms to form aligned sponges via directional ice templating in a custom mold with a slurry of dry ice and ethanol. Hydrated tensile mechanical properties of these aligned sponges were evaluated as a function of silk polymer concentration (3% or 5%), freezing time (50% or 100% ethanol), and post-lyophilization method for inducing crystallinity (autoclaving, water annealing). Hydrated static tensile tests were used to determine Young's modulus and ultimate tensile strength across sponge formulations at two strain rates to evaluate rate dependence in the calculated parameters. Results aligned with previous reports in the literature for isotropic silk fibroin sponge-like scaffolds, where the method by which beta-sheets were formed and level of beta-sheet content (crystallinity) had the greatest impact on static parameters, while polymer concentration and freezing rate did not significantly impact static mechanical properties. We estimated the crystalline organization using molecular dynamics simulations to show that larger crystalline regions may be responsible for strength at low strain amplitudes and brittleness at high strain amplitudes in the autoclaved sponges. Within the parameters evaluated, extensional Young's modulus is tunable in the range of 600-2800 kPa. Dynamic tensile testing revealed the linear viscoelastic region to be between 0% and 10% strain amplitude and 0.2-2 Hz frequencies. Long-term stability was evaluated by hysteresis and fatigue tests. Fatigue tests showed minimal change in the storage and loss modulus of 5% silk fibroin sponges for more than 6000 min of continuous mechanical stimulation in the linear regime at 10% strain amplitude and 1 Hz frequency. Furthermore, we confirmed that these mechanical properties hold when decellularized extracellular matrix is added to the sponges and when the mechanical property assessments were performed in cell culture media. We also used nano-computed tomography (nano-CT) and simulations to explore pore interconnectivity and tortuosity. Overall, these results highlight the potential of anisotropic, sponge-like silk fibroin scaffolds for long-term (>6 weeks) contractile muscle culture with an in vitro bioreactor system that provides routine mechanical stimulation.

Enhancing polyamide 6: Acid hydrolysis for functionalization and amino group quantification

In this study, our primary aim was to increase the presence of amine groups in polyamide 6 fibers. To achieve this, we employed a functionalization process that mainly depended on increasing the number of reactive sites via acid-catalyzed hydrolysis. The effects of several acids were rigorously examined, including hydrochloric acid (HCl), sulfuric acid (H2SO4), and formic acid (HCOOH). Following this comprehensive acid-based treatment, the method that demonstrated the most significant increase in amine groups was selected for further evaluation in dyeing experiments and full characterization. The quantification of amino groups was performed using potentiometry, evaluating the equilibrium state of acid removal from the fibers. To corroborate these results, the acid dye Levaset Blue 2R was employed, which measured the amount of dye bound to the fibers during the dyeing process. Characterization of the polyamide 6 fiber structural changes was conducted using multiple techniques, including tensile tests, Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC). Among the acid treatments, the 11% HCl treatment exhibited the most significant increase in amine groups, amounting to an approximately 110% increase as measured by potentiometry and an approximately 150% increase using the dyeing method. During the dyeing process, the 11% HCl-treated fibers absorbed 91% of the dye from the dye bath, indicating enhanced color intensity and K/S value, thus affirming the efficacy of the amine group increasing. Tensile testing revealed a decrease in the strength of the functionalized fiber. In the FTIR spectra, there was a notable increase in the intensity of bands associated with the fiber's crystalline regions and hydrogen bonds. DSC tests validated the FTIR results, demonstrating a 9% increase in crystallinity. Furthermore, SEM micrographs depicted surface alterations induced by the hydrolysis process. These results collectively highlight the effectiveness of hydrolysis in introducing functional groups, enhancing color intensity during dyeing with acid dyes, and reducing dye content in the bath. Additionally, the potentiometric method for quantifying amine group demonstrated practicality and accuracy, serving as a valuable contribution to the field.

Molecular mechanism analysis of apoptosis induced by silk fibroin peptides

Silk fibroin derived from silkworm cocoons exhibits excellent mechanical properties, good biocompatibility, and low immunogenicity. Previous studies showed that silk fibroin had an inhibitory effect on cells, suppressing proliferation and inducing apoptosis. However, the source of the toxicity and the mechanism of apoptosis induction are still unclear. In this study, we hypothesized that the toxicity of silk fibroin might originate from the crystalline region of the heavy chain of silk fibroin. We then verified the hypothesis and the specific induction mechanism. A target peptide segment was obtained from α-chymotrypsin. The potentially toxic mixture of silk fibroin peptides (SFPs) was separated by ion exchange, and the toxicity was tested by an MTT assay. The results showed that SFPs obtained after 4 h of enzymatic hydrolysis had significant cytotoxicity, and SFPs with isoelectric points of 4.0–6.8 (SFPα II) had a significant inhibitory effect on cell growth. LC-MS/MS analysis showed that SFPα II contained a large number of glycine-rich and alanine-rich repetitive sequence polypeptides from the heavy-chain crystallization region. A series of experiments showed that SFPα II mediated cell death through the apoptotic pathway by decreasing the expression of Bcl-2 protein and increasing the expression of Bax protein. SFPα II mainly affected the p53 pathway and the AMPK signaling pathway in HepG2 cells. SFPα II may indirectly increase the expression of Cers2 by inhibiting the phosphorylation of EGFR, which activated apoptotic signaling in the cellular mitochondrial pathway and inhibited the Akt/NF-κB pathway by increasing the expression of PPP2R2A.

Molecular Simulations of Hydrogen Sorption in Semicrystalline High-Density Polyethylene: The Impact of the Surface Fraction of Tie-Chains.

The modeling of the barrier properties of semicrystalline polymers has gained interest following the possible application of such materials as protective liners for the safe supply of pressurized hydrogen. The mass transport in such systems is intimately related to the complex intercalation between the crystal and amorphous phases, which was approached in this work through an all-atom representation of high-density polyethylene structures with a tailored fraction of amorphous-crystalline connections (tie-chains). Simulations of the polymer pressure-volume-temperature data and hydrogen sorption were performed by means of molecular dynamics and the Widom test particle insertion method. The discretization of the simulation domains of the semicrystalline structures allowed us to obtain profiles of density, degree of order, and gas solubility. The results indicated that the gas sorption in the crystalline regions is negligible and that the confinement of the amorphous phase between crystals induces a significant increase in density and a drop in the sorption capacity, even in the absence of tie-chains. Adding ties between the crystal and the amorphous phase results in further densification, an increase of the lamella tilt angle, and a decrease in the degree of crystallinity and hydrogen sorption coefficient, in agreement with several literature references.

Photooxidation‐induced conformational changes and degradation behaviors of poly(butylene succinate) and poly(butylene succinate‐co‐adipate)

AbstractTwo biodegradable polyesters, poly(butylene succinate) (PBS) and poly(butylene succinate‐co‐adipate) (PBSA), were artificially aged in a UV irradiation test chamber, and their photodegradation behaviors investigated. The attenuated total reflection (ATR) infrared (IR) spectra of the initial and UV‐aged samples revealed conformational changes in the tetramethylene sequences of the photoaged PBS and PBSA. The one‐dimensional wide‐angle X‐ray scattering (WAXS) profiles showed that the (110) d‐spacing of the α‐form crystal progressively decreased during UV aging, suggesting that the crystalline polymer chains became arranged more closely along the fiber axis. Accordingly, we conclude that PBS and PBSA transform from their TGTGT to nearly TTTTT conformations upon photoaging. The observed WAXS, small‐angle X‐ray scattering, and IR spectral data suggest that photodegradation preferentially occurs in the amorphous phase of each polymer. The less crystallizable butylene adipate co‐unit enhances the degradability of PBSA, with prolonged photooxidation leading to partial degradation of the crystalline region of the copolymer. This finding is consistent with and may be linked to the higher biodegradability of PBSA compared to PBS.

Influence of TEMPO-oxidation on pulp fiber chemistry, morphology and mechanical paper sheet properties

In this contribution, we report on the TEMPO-mediated oxidation of pulp fibers used in the general context of papermaking and for the future design of tailor-made paper in advanced applications. We focus in our studies on properties of TEMPO-oxidized pulp fibers to explain the characteristics of the paper made thereof. 13C solid-state NMR analysis reveals that in particular amorphous regions of the fibers are being chemically oxidized, while at the same time the crystalline regions of the fibers are not significantly affected. Investigation of the fiber morphology before and after oxidation shows that the fiber length is not changed, yet the fibers do exhibit an increase in width if in contact with water, which is attributed to an increase in fiber swelling. In addition, fibrillation decreases due to the oxidative removal of loosely bound fines and fibrils, rendering the surface of the resulting oxidized fibers much smoother in comparison to the original fibers. Finally, we observe that both, dry and wet tensile strengths are also higher for paper made of oxidized fibers, most likely due to cross linkable aldehyde groups formed during oxidation (i.e. hemiacetal bond formation in the sheet during thermal drying). Our results of the oxidation of paper fibers thus offer a systematic study helpful for the design of tailor-made paper useful in several applications where a fiber-modification with fiber-immobilized functional motifs is crucial, such as for example in paper-based microfluidic sensors (µPADs) or lab-on a chip-devices.

Using bacterial cellulose to bridge covalent and physical crosslinks in hydrogels for fabricating multimodal sensors

Network optimization is vital for the polysaccharide based hydrogels with multiple crosslinks. In this study, we developed a ‘two-step’ strategy to activate synergistic effect of chemical and physical crosslinks using a poly (vinyl alcohol) (PVA)/bacterial cellulose (BC) hydrogel as a template. The BC nanofibers, on the one hand, acted as nucleating agents, participating in the crystallization of PVA, and on the other hand, were also involved in the formation of boronic ester bond, anchored with the PVA chains via chemical bonding. Therefore, the existence of BC nanofibers, as ‘bridge’, linked the crystalline regions and amorphous parts of PVA together, associating the two characteristic crosslinks, which was conducive to load transfer. The mechanical properties of resultant hydrogels, including the tensile elongation and strength, as well as fracture toughness, were significantly improved. Moreover, the dually cross-linked hydrogels possessed ionic conductivity, which was sensitive to the tensile deformation and environmental temperature. This study clarifies a unique role of BC nanofibers in hydrogels, and proposes an effective approach to construct multiple networks in the nanocellulose reinforced PVA hydrogels.

Influence of Carbon Black on Conductivity and Structure of Polyethylene Oxide Based Polymer Electrolyte Film

AbstractThe potential applications of carbon black are expected to grow as science and technology improve offering up new possibilities for innovation throughout disciplines included in the field of energy storage. The present work shows the influence of carbon black to improve the ionic conductivity of the polymer electrolyte. The synthesis of polyethylene oxide: ammonium iodide based polymer electrolyte incorporated with carbon black varying from 0.01 to 0.06 wt% with respect to PEO: NH4I system by solution casting method. Different characterizations like polarized optical microscopy (POM), impedance spectroscopy, and ionic transference number (tion) are studied in detail. The maximum ionic conductivity is achieved at 0.05 wt% carbon black shows 1.20 × 10−5 S cm−1 at ambient temperature. In accordance with POM data, the amorphous region has increased whereas the crystalline region has shrunk which further indicated the increase in ionic conductivity. The value of (tion) is calculated to be 0.97 which shows the system is ionic in nature. PEO based polymer electrolyte doped carbon black can be used for the fabrication of energy storage devices.

Comparative analysis of granular starch hydrolysis and multi-structural changes by diverse α-amylases sources: Insights from waxy rice starch

Three cultivars of waxy rice starch with different multi-scale structures were subjected to α-amylase hydrolysis to determine amylopectin fine structure, production of oligosaccharides, morphology, and crystallinity of the partially hydrolyzed starch granules. α-amylases hydrolyzed the amylopectin B2 chain during the initial stage of hydrolysis, suggesting that it is primarily located in the outer shell of the granules. For waxy rice starch with loose structure, α-amylases attacked the crystalline and amorphous regions simultaneously in the initial stage, while for starch granules with compact structure, the outer shell blocklet (crystalline structure) can be a hurdle for α-amylases to proceed to hydrolysis of the internal granule structure. The ability of α-amylases from porcine pancreatic α-amylases to attack the outer shell crystalline structure was lower than that of α-amylases from Bacillus amyloliquefaciens and Aspergillus oryzae. These results show that α-amylase source and rice cultivar combinations can be used to generate diverse structures in degraded waxy rice starch.

Polyetheramine‐Type Semi‐Biobased Long‐Chain Polyamide 1210 Elastomer: Synthesis, Structure, and Unique Thermal Behavior

AbstractBiobased thermoplastic polyamide elastomers (TPAEs) have received increasing attention in both academia and industry. Here, a series of semi‐biobased long‐chain TPAEs are successfully synthesized via one‐step melt polymerization, employing polyamide 1210 (PA1210) and polyetheramines (PEAs) as hard and soft segments, respectively. The prepared TPAEs demonstrate excellent mechanical properties, energy dissipation capabilities, low density, good damping, high resilience, and low melting temperature. More interestingly, the properties of the TPAEs can be customized by adjusting the content and molecular weight of PEA. By varying the molecular weights of the PEAs, two different thermal behaviors can be observed in the prepared TPAEs. Specifically, PEA with low molecular weight has good compatibility with PA1210, leading to an increase in the conformation of the crystalline region and a significant decrease in melting temperature. Meanwhile, high molecular weight PEA causes strong phase separation with PA1210, leading to limited crystalline regions and inadequate physical cross‐linking, further resulting in suboptimal mechanical properties. This work provides new insights into the design and preparation of PEA‐type biobased long‐chain TPAEs.

TEM Image Analysis and Simulation Physics for Two-Step Recrystallization of Discretely Amorphized C3H5-Molecular-Ion-Implanted Silicon Substrate Surface

In this study, we investigate the initial rapid recrystallization of a discretely amorphized C3H5-molecular-ion-implanted silicon (Si) substrate surface in the subsequent thermal annealing treatment through the analysis of plan-view transmission electron microscopy (TEM) images and technology computer-aided design (TCAD) process simulation. In the approach of the analysis of the plan-view TEM image of the Si substrate surface, we found that initial rapid recrystallization occurs in the intermediate regions between the residual crystalline and discrete amorphous regions formed in the C3H5-molecular-ion-implanted Si substrate surface. In addition, the TCAD process simulation results indicate that the intermediate regions correspond to the amorphous pockets formed around the discrete amorphous regions in the C3H5-molecular-ion-implanted Si substrate surface and are recrystallized preferentially during the short thermal annealing time. These plan-view TEM image analysis and TCAD process simulation results reveal a two-step recrystallization of the discretely amorphized C3H5-molecular-ion-implaned Si substrate surface. After the initial rapid recrystallization of amorphous pockets in the 1st step, the recrystallization of discrete amorphous regions starts in the 2nd step. The incubation period between the 1st and 2nd steps is the time required to recrystallize the amorphous pockets around the discrete amorphous regions completely and redefine the amorphous/crystalline interface.