Melt Crystallization Research Articles

Impact of statistical poly(propylene co-ethylene) on the thermo-mechanical properties of high-density polyethylene

A series of high-density polyethylene and a statistical copolymer of poly(propylene-co-ethylene) blends in a wide range, namely (0, 10, 20, 30, 40, 50, 60,70, 80, 90, 100) abbreviated as HDPE/VM were systematically investigated by using a rheometer, differential scanning calorimetry (DSC) measurements, polarized optical microscopy (POM) and tensile tests. Rheometer results show that adding VM decreases dynamic viscosity, storage, and loss modulus. Han plot shows that HDPE and VM are compatible and miscible in the range from 20 to 60 VM % in the molten state. DSC results show little nucleation effect of VM on HDPE (HDPE’s melt crystallization temperature shifts 2 °C higher). Moreover, a linear composition dependence of ∆cp ∆Hc, ∆Hm shows that PE and VM are most probably compatible in the molten state in composition range from 20 to 60%. However, upon crystallization, the VM and PE domains occur distinctively. The results of the tensile tests demonstrated a decrease in elastic modulus, yield stress, and ultimate tensile strength as VM content increased. At low VM content (less than 20%), high elongation at break was detected for the blends, and very fine spherulites of HDPE were found across the sample by POM.

Insights on Arc Magmatic Systems Drawn from Natural Melt Inclusions and Crystallization Experiments at PH2O =800 MPa under Oxidizing Conditions

Abstract Whole rock compositions at Buldir Volcano, western Aleutian arc, record a strong, continuous trend of iron depletion with decreasing MgO, classically interpreted as a calc-alkaline liquid line of descent. In contrast, olivine-hosted melt inclusions have higher total iron (FeO*) than whole rocks and show little change in FeO* with decreasing MgO. To investigate this discrepancy and determine the conditions required for strong iron depletion, we conducted oxygen fugacity (ƒO2) buffered, water-saturated crystallization experiments at 800 MPa and ƒO2 = QFM+1.6 ± 0.4 (1$\sigma$) (where QFM refers to the quartz-fayalite-magnetite buffer) on a high-Al, basaltic starting material modeled after a Buldir lava. Experimental conditions were informed by olivine-hosted melt inclusions that record minimum entrapment pressures as high as 570 MPa, >6 wt.% H2O, and ƒO2 of QFM+1.4 (±0.2), making Buldir one of the most oxidized and wettest arc volcanoes documented globally. The experiments produce melts with Si-enrichment and Fe-depletion signatures characteristic of evolved, calc-alkaline magmas at the lowest MgO, although FeO* remains roughly constant over most of the experimental temperature range. Experiments saturate CrAl-spinel and olivine at 1160oC, followed by clinopyroxene and Al-spinel at 1085oC, hornblende at 1060oC, and, finally, plagioclase and magnetite between 1040oC and 960oC. Hornblende crystallization, not magnetite, generates the largest increase in SiO2 and largest decrease in FeO* in coexisting melts. Compositions of melt inclusions are consistent with experimental melts and reflect crystallization of a basaltic parent magma at high PH2O. In contrast, the whole rock compositional trends are influenced by magma mixing and phenocryst redistribution and accumulation. The crystallization experiments and natural liquids (melt inclusions and groundmass glass) from Buldir suggest that for an oxidized, hydrous primary basalt starting composition, significant Fe-depletion from the melt will not occur until intermediate to late stages of magma crystallization (< ~4.5 wt.% MgO). We conclude that the Buldir whole rock trend cannot be reproduced by crystallization at arc-relevant oxygen fugacities and is not a true liquid line of descent, warranting caution when interpreting volcanic trends globally.

Effect of Soret diffusion on the growth of spherical crystals in supercooled alloy melts under oscillatory flow.

The growth of spherical crystals in binary alloy melts with thermal diffusion effects under oscillatory flow is investigated analytically. Using the multiple scale method, we derive approximate analytical solutions for both the crystal interface growth rate and the solute concentration. Our results demonstrate that the Soret effect significantly influences both the solute concentration near the crystal interface and the crystal growth rate. Specifically, with a positive Soret coefficient, the growth rate of spherical crystals in a binary dilute alloy melt decreases as the coefficient increases, while the solute concentration near the interface increases. In contrast, with a negative Soret coefficient, the growth rate of the spherical crystals increases as the coefficient decreases, and the solute concentration near the interface decreases. Additionally, the presence of oscillatory flow markedly promotes the grain refinement induced by the Soret effect.

Preparation and melt-spun applications of PA6-based Poly(Amide-Ether) copolymers phase change fibers with passive temperature management

Phase change fiber, as an intelligent fiber material used in passive thermal management, can balance the temperature of the microenvironment near human skin. However, the traditional blending method makes phase change material prone to leakage during the processing and applications. Herein, this work introduces the phase change material PTMEG into the polyamide 6 (PA6) chain through melt polymerization to prepare a series of PA6-based poly(amide-ether) copolymers. Copolymers exhibit an obvious microphase separation structure, with the PA6 segments and the PTMEG segments can form independent crystalline and amorphous regions. PTMEG in copolymers through polymerization method exhibits better thermal stability compared with the blended way, which effectively solves the leakage problem of phase change materials. The copolymers can be directly melt-spun (1500 m/min) to prepare PA6-based phase change fibers. The fiber can maintain excellent mechanical properties (breaking strength of 2.12 cN/dtex). Meanwhile, the crystallization enthalpy and melting enthalpy of the PTMEG in the fiber are 10.59 J/g and 12.44 J/g, respectively. The thermal management time of the fiber in the hot environment is 349 s, and the maximum temperature difference is lower 5.6 ℃ from the PA6 fiber. In addition, the exothermic duration in a cold environment is 536 s, and the maximum temperature difference is higher 1.1 °C from the PA6 fiber. Meanwhile, the thermal enthalpy of the fiber remained stable (fluctuation within 2 %) after 20th thermal cycles, and the loss rate is less than 2 % after washing at 25 ℃, 50 ℃ and 90 ℃. The fiber exhibits good thermal stability, water washability and cyclic stability. Preparation of high enthalpy polymers directly by copolymerization will provide new ideas for phase change fibers for apparel.

Enhancing the Stereocomplex Crystallization of PLLA/PDLA Symmetric Blend by Controlling the Degree of Molecular Chain Entanglement

In order to enhance the content of stereocomplex crystals (SC) in poly L-lactic acid (PLLA)/poly D-lactic acid (PDLA) symmetric blend, thereby improving the defects of low crystallinity and poor heat resistance of polylactic acid (PLA)-based materials, the samples with different entanglement degrees were prepared by freezing extration method. The critical overlap concentration of the blend system was quantitatively obtained using an Ubbelohde viscometer. Based on this concentration, samples with a series of concentration gradient were prepared to control the different degrees of molecular chain entanglement inside. The results indicated that the chain disentanglement could greatly increase the content of SC in the blend, whether in the precipitation crystallization or the melt crystallization process. Especially after the isothermal crystallization for 30min at 130oC, the L/D-0.1 sample with the highest degree of disentanglement almost only formed SC, accounting for 95.2% of the total crystallinity. Samples with lower entanglement degree had more crystal nuclei and faster growth rate of formed spherulites. For completely entangled sample L/D-50, the crystal nucleus of homo-crystalls (HC) could be considered as SC. Besides, the Vicat softening temperature (VST) of L/D-0.1 sample increased from 79.9oC of L/D-50 sample to 103.8oC with an obvious increase of 24.9oC. All these results provide new ideas for improving the performance of PLA-based materials and show promising development prospects of green and sustainable polymers.

Preparation and scintillation properties of Eu3+-doped high crystallinity tellurite glass ceramics

In this study, a high-crystallinity glass-ceramic scintillator doped with Eu³⁺ containing Bi₂Te₄O₁₁ nanocrystals was prepared using a traditional melt crystallization method. The optimal heat treatment conditions, phase structure, and luminescent properties of the glass-ceramics were systematically investigated using various characterization techniques, including DSC, XRD, SEM, and spectrophotometry. To achieve glass-ceramic samples with high transmittance and excellent luminescent performance, the optimal heat treatment process was determined to be 500 °C for 10 minutes. The final sample was found to have a density of 5.9 g/cm³ and a crystallinity of 70%. Strong orange-red light emission was exhibited by the glass-ceramic under both 465 nm light and X-ray excitation. The maximum integral X-ray excited luminescence (XEL) intensity was found to reach 20.2% of that of the commercial Bi4Ge3O12 (BGO) scintillation crystal. It is indicated by the research that Eu³⁺-doped high-crystallinity tellurate glass-ceramics are promising candidate materials for scintillators in the field of X-ray detection.

Evaluation of critical process parameter on the production of sustainable bead foams based on polylactic acid

A commercial grade of polylactic acid (PLA) was foamed without using modifiers to obtain expanded polylactic acid bead foams (EPLA). Typically, the foaming process is influenced by both melt properties and crystallization behavior. While factors like water temperature, die structure, and die temperature are known to have effects on bead foam processing, these aspects have not been thoroughly explored in the context of PLA bead foam production. To address this gap, a comprehensive investigation was undertaken, varying water temperature, die structure, and die temperature to discern their impact on PLA processing behavior. Results revealed that water temperature significantly influenced foaming behavior, particularly at elevated temperatures near the glass transition of PLA. Additionally, the study demonstrated that die size wielded a notable influence on all foam properties, dictating process limits. With the selection of an appropriate die size, the die temperature could be manipulated within the range of 190°C to 160°C, revealing a substantial impact on the overall process. Remarkably, the lowest densities achieved were 63 kg/m3 with an average cell size of 36 µm and a cell density of 1.1*107 cells per cm3.

Advancing the development of supersonic natural gas liquefaction through understanding heavy hydrocarbon crystallization mechanism

During supersonic natural gas liquefaction, the solidification of heavy hydrocarbon molecules can be used to improve the efficiency of the liquefaction. This study investigates the supersonic crystallization of n-hexane using an experimental system designed by ourself for precise measurement of liquid heavy hydrocarbon vaporization. The results demonstrate that n-hexane gas condenses rapidly 1.5 cm downstream of the nozzle throat, releasing significant latent heat. The subsequent crystallization of these droplets transitions the substance fully from liquid to solid, and the latent heat released during crystallization is much lower than that during condensation. Under different conditions, we found that higher partial pressures intensify n-hexane crystallization, accelerating liquid phase growth despite slower solid phase mass increase. Furthermore, larger nozzle expansion ratios shorten the time and space distribution of the liquid phase mass fraction. Molecular dynamics simulations reveal n-hexane’s melting and surface crystallization temperatures to be approximately 160 ± 1 K and 158 ± 1 K, respectively, with a supercooling degree of 2 K, explaining the observed crystallization behavior in supercooled droplets.

GENESIS OF EXTREMELY MAGNESIAN DAUGHTER OLIVINE OF SECONDARY MELT INCLUSIONS FROM OLIVINE MACROCRYSTS IN KIMBERLITE FROM THE UDACHNAYA-EAST PIPE (SIBERIAN CRATON)

The paper presents the results of studies of daughter olivine within secondary melt inclusions marking healed cracks in olivine macrocrysts from unserpentinized kimberlite from the Udachnaya-East pipe. Macrocrysts compose four olivine generations: core olivine (Ol1); olivine marking healed cracks (Ol2); daughter olivine of melt inclusions (Ol3); thin outer rims of olivine (Olr) around macrocryst cores. The relationship between different olivine generations and variations in its chemical composition indicate that macrocrystal cores (Ol1) are grains or grain fragments of disintegrated mantle rocks; melt inclusions and Ol2 were formed due to infiltration of kimberlite melts into the grain cracks. Crystallization of a hybrid melt of inclusions and formation of an extremely magnesian daughter olivine (Ol3) occurred later, at lower PT conditions. Among the daughter minerals in the melt inclusions, in addition to Ol3 there were identified alkaline carbonates, sulfates, chlorides, oxides, and sulfides. It has been shown that the daughter olivine of melt inclusions (Ol3) has high Mg# (97–98) content, high MnO (0.18–0.41 wt. %) and CaO (0.12–0.25 wt. %) concentrations, and low NiO (0.02–0.04 wt. %) contents. The ratios between the daughter minerals of the melt inclusions indicate that the hybrid melt from which extremely magnesian olivine was formed was alkaline carbonate or silicate-carbonate liquid with a low water content. Our study directly showed for the first time that almost pure forsterite is able to be crystallized from evolved kimberlite melts of carbonate or silicate-carbonate composition, which confirms the previously proposed model for the formation of extremely magnesian outer rims of olivine crystals from worldwide kimberlites during crystallization of evolved kimberlite melts of carbonate composition.

Crystal melting influenced by particle cooperativity of the liquid

Crystal melting influenced by particle cooperativity of the liquid

Two Organic-Inorganic Hybrid Manganese Bromides with Highly Efficient Emission toward White LEDs.

Organic-inorganic metal halides have attracted great attention due to their tunable structural and spectroscopic properties. Here, two organic-inorganic hybrid manganese bromides, (TEMA)2MnBr4 (TEMA = triethylmethylammonium) and (TEBA)2MnBr4 (TEBA = benzyltriethylammonium), are synthesized using the evaporation crystallization method. Following a heat-induced phase transition at 363 K, the structure and optical properties of (TEMA)2MnBr4 change but return to their initial state upon cooling to room temperature, as confirmed by X-ray diffraction, photoluminescence (PL), and Raman spectra. Meanwhile, (TEBA)2MnBr4, with a larger Mn-Mn distance, exhibits a higher photoluminescence quantum yield of 98.1% and greater thermal quenching temperature. However, due to the poorer thermal stability of the organic cation, the crystal melts at 400 K, leading to fluorescence quenching. White LEDs based on (TEMA)2MnBr4 and (TEBA)2MnBr4 are successfully fabricated with color rendering indices of 97.4 and 97.2, respectively. The investigation provides deep insights into the structural and optical properties of (TEMA)2MnBr4 and (TEBA)2MnBr4, advancing research for LED display design by tuning organic cations.

Exact analytical solution of the equations for a quasiequilibrium two-phase domain: permeability and interdendritic spacing

This study is concerned with the theoretical description of a quasi-stationary process of directional crystallization of binary melts and solutions in the presence of a quasi-equilibrium two-phase region. The quasi-equilibrium process is ensured by the fact that the system supercooling is almost completely compensated by heat released during the phase transformation. Quasi-stationarity of the process determining constancy of the crystallization rate is ensured by given temperature gradients in the solid and liquid phases. The system of heat and mass transfer equations and boundary conditions to them under these assumptions is dependent on a single spatial variable in the reference frame moving with the crystallization rate relative to a laboratory coordinate system. Exact analytical solutions to the formulated problem in parametric form are obtained. The parameter of the solution is the solid phase fraction in a two-phase region. The distributions of temperature and impurity concentration in the solid, liquid and two-phase regions of the crystallizing system, the rate of solidification, and the spatial coordinate in the two-phase region depending on the solid phase fraction in it are found. An algebraic equation for the solid phase fraction at the interface between the solid material and the two-phase region is derived. Exact analytical solutions show that the impurity concentration in the two-phase layer increases as the solid phase fraction increases. Moreover, the solid phase fraction at the interface solid phase — two phase region and its thickness increase as the temperature gradient in the solid phase and the solidification rate increase. The developed theory allows us to determine analytically the permeability of the two-phase region and a characteristic interdendritic spacing in it. Analytical solutions show that the relative permeability in the two-phase region increases from a certain value at the interface with the solid phase to unity at the interface with the liquid phase. The selection theory of stable dendritic growth allows us to determine analytically a characteristic interdendritic distance in the two-phase layer that decreases as the temperature gradient in the solid phase increases. An increase of impurity in the molten phase gives a decrease in the interdendritic spacing within a two-phase region.

Investigation of high-temperature oxide-metal melts during induction melting in a cold crucible

The object of the study is high-temperature oxide-metal melts obtained in furnaces of induction melting in a cold crucible (IMCC). The results of pilot tests in IMCC furnaces at melt temperatures of more than 2200 оC in air, conducted to study the distribution of components between the oxide and metal phases of a two-phase melt with limited miscibility of components, are presented. The results of physicochemical studies of materials obtained by quenching crystallization of a high-temperature melt are presented, confirming the reduction of silicon and the oxidation of iron with the redistribution of these components between the oxide and metal phases. This experimental result contradicts the well-known Ellingham diagrams and thermodynamic calculations, but a similar effect is observed experimentally in the U–O–Fe system. Thus, the IMCC method allows for the inversion of redox processes in a number of oxide-metal systems, which can be used to obtain new materials and create technologies for high-temperature extraction of target components.

Internal radiation effect on semiconductor β-Ga2O3 crystals grown by the VB Method and anisotropic thermal stress

Gallium oxide crystals are semitransparent semiconductors with good optical and electrical properties, which allow their use for several technological applications. During the growth process of β-Ga2O3 crystals, internal radiation plays a crucial role that affects the growth process and then the crystal quality. In this work, the effect of the melt and the crystal transparency on the vertical Bridgman growth of β-Ga2O3 oxide is thoroughly studied. Using a global 2D/3D finite element model, temperature, melt flow, melt-crystal interface, and three-dimensional anisotropic thermal stress are computed at different growth stages. At each stage, four cases are considered, namely, opaque melt and crystal, semi-transparent melt and opaque crystal, semitransparent crystal and opaque melt, and finally semitransparent melt and crystal. The role of internal radiation in each case at different growth stages is then highlighted separately and then coupled together. It was found that the melt-crystal interface is shifted from a convex shape at the early stage to a nearly plane and then to a concave shape at the last stage. The melt flow is then changed from two rolls pattern at the beginning to a single-roll structure at the last stage. Thermal stress of the as-grown ingot is decreased during the growth due to the decrease of temperature non-linearities. Internal radiation inside the crystal acts to increase the melt-crystal interface convexity at the early and middle stages of the growth process and leads to a decrease in its concavity at the final stage. However, the melt transparency leads to the opposite effects, i.e., it decreases the interface convexity at the early stage and increases the interface concavity at the final stage. As a result, for semitransparent crystal and melt, the interface is between the two previous cases. The calculated thermal stresses are found to be more affected by the transparency of the crystal than the melt as the absorption coefficient of β-Ga2O3 crystal is smaller than that of the melt. At all stages, the thermal stresses are found to be larger for the opaque case due to the increase of temperature non-linearities in the crystal. Large values are found at the bottom and the lower part of the periphery. Furthermore, internal radiation inside the melt plays a major role during the early growth stage due to the large liquid volume. It reduces the melt flow intensity close to the free surface where the shear stress is combined with the buoyant force and leads to the flattening of the interface decreasing then the radial temperature gradients, which leads to small attenuation of the thermal stress. At the final stage, the transparency of the melt plays the opposite role due to the increase of the interface concavity which leads to an increase in both of the temperature gradients and the thermal stress inside the crystal. Due to the crystal anisotropy, and especially to the large thermal expansion coefficient in the [010] direction, the 3D thermal stress values are found to be larger in this direction, especially in the bottom part of the ingot. Comparisons with available experimental and numerical works are provided in this paper.

Investigations on the growth, spectral, optical, electrical, thermal and nonlinear optical properties of L-valine itaconic acid single crystal

A nonlinear optical single crystal of L-Valine Itaconic Acid (LVIA) was grown at room temperature from an aqueous solution by using the slow evaporation method. The grown crystal was undergone X-ray diffraction investigation, which confirm that the crystal belongs to orthorhombic system with the non-centro symmetric Pbca space group. This single crystal contains several functional groups, according to FTIR spectroscopic analysis there were identified. By analyzing the crystal's UV–visible spectrum, based on its optical transparency this crystal may use for optoelectronic device manufacturing. The emission happens at 553 nm wavelength, according to the photoluminescence spectrum. Thermo gravimetric and differential thermal analytical studies helps us to measure title crystal melting point and thermal stability. At various temperatures, the dielectric property of the crystal was found out. The Kurtz-powder method has been used to study the phenomenon of Second Harmonic Generation (SHG) in the crystal.

Influence of low voltage programmed thawing on the quality of frozen pork and its myofibrillar protein

This study explored the effects of low voltage programmed thawing (LVPT) on thawing period, water status, current density as well as physicochemical properties of porcine longissimus dorsi muscle, considering air thawing (AT), water immersion thawing (WT) and cold storage thawing (CST) for the comparison, additionally making fresh meat (FM) as the control. The thawing process used current limiting to gradually reduce the maximum output current to 500, 200 and 100 mA, respectively, by applying a safe voltage of 35 V in a home defrosting apparatus. Using two pairs of foil plate, the thawing (LVPT-2) with dual current loop accelerated the melting of ice crystals than the process with one pair of polar plate (LVPT-1) with one current loop. From −18 °C to −1 °C, the thawing period of LVPT-2 was reduced by 14.54 %, 11.72 %, and 15.95 % compared with that of LVPT-1 for samples within the thickness of 2, 3 and 4 cm, respectively. During the process, the intensity and density of the current loaded on the frozen meat gradually increased. LVPT-1 retained water and reduced its migration inside the meat, and protein solubility was better maintained. As the thickness increased, the effect of LVPT-2 on the moisture distribution and protein solubility of the sample decreased. LVPT-1 treatment resulted in less fat oxidation as well as stable secondary and tertiary structures of myofibrillar proteins compared to other treatments. At low voltage, the ability of LVPT −2 to maintain meat quality was reduced due to the increase in current density. In addition, LVPT-1 reduced muscle damage because of rapid melting of ice crystals. In contrast, LVPT-2 was conductive the formation of hot spots due to dual current loop passed through the pork in final phase of thawing, which would adversely influence the quality of thawed meat. Finally, LVPT could improve the rate of thawing, water binding capacity and meat quality, especially, there was no overheating effect on the meat because of current limiting.

Preparation of a trans-free fat blend to substitute partially hydrogenated oil

Partially hydrogenated oil (PHO) possesses a mild flavor and exceptional processing characteristics, making it historically the primary choice for creamer. The discovery of health problems of trans fatty acids has accelerated the development of alternative fats. This study aimed to develop an optimal PHO alternative fat by physical blending. Based on the correlation between physicochemical properties and sensory attributes, soybean oil, fully hydrogenated palm kernel oil, and fully hydrogenated soybean oil (45/45/10, w/w/w) were selected to make the alternative fat. The fat blend exhibited a solid fat content (SFC) curve identical to PHO, along with similar melting crystallization behavior, crystal nucleation pattern and growth mode, viscosity (705 mPa∙s), and taste profile. Pearson correlation analysis was used to further clarify the correlation between properties and tastes. The result showed that the SFCs and fatty acids compositions have strong correlations with tastes. It provides a reference scheme for preparing fats with ideal tastes.

Enhancing energy storage performance of dielectric capacitors: Tailoring CaO-SrO-Na2O-Nb2O5-SiO2 glass-ceramics through controlled crystallization for pulse power applications

As potential dielectric materials for capacitors, glass-ceramics exhibit significant promise in the realm of pulse power supply. Extensive research has been undertaken to explore the commendable voltage resistance and favorable dielectric properties of glass-ceramics. They exhibit a rapid charge and discharge rate. However, the limited energy storage density of glass-ceramics constrains their practical application. In this study, we focused on the preparation of CaO-SrO-Na2O-Nb2O5-SiO2(CSNNS) glass-ceramics through conventional melting and high-temperature crystallization processes. Our investigation delved into the impact of crystallization temperature on the phase composition, dielectric properties, and energy storage characteristics of the CSNNS glass-ceramics. The results indicate a direct correlation between the dielectric constant and dielectric loss, both exhibiting an upward trend with increasing crystallization temperature. Simultaneously, the microstructure of the glass-ceramics manifests signs of deterioration, characterized by larger grain size and heightened porosity, leading to a reduction in breakdown strength. At a crystallization temperature of 1100 °C, the CSNNS glass-ceramics demonstrated a remarkable combination of a high dielectric constant (∼280) and superior breakdown strength (481 kV/cm). The achieved maximum theoretical energy storage density reached 2.87 J/cm3. At an electric field of 100 kV/cm, the effective energy storage density is 0.23 J/cm3, and the energy storage efficiency is 72 %. These findings demonstrate the broad application potential of the CSNNS glass-ceramics in the domain of pulse power, highlighting their relevance for future developments in this field.

Crystallization and melting of Poly(4-hydroxybutyrate) characterized by fast scanning calorimetry

Poly (4-hydroxybutyrate) (P4HB) is a marine biodegradable polyester with promising applications. Unfortunately, the crystallization and melting behavior of P4HB has not been systematically studied, due to the rapid crystallization near room temperature. In particular, the characterization of crystallization and melting of P4HB by fast scanning calorimetry (FSC) has not been reported previously. In this article, the common differential scanning calorimeter (DSC), polarized optical microscopy (POM), atomic force microscopy (AFM) and FSC were performed to investigate the crystallization and melting behavior of P4HB. The results indicated that melt crystallization facilitated the formation of fragmented crystals rather than complete spherulites. Furthermore, the P4HB exhibited a broad crystallization temperature range from −19 °C to 49 °C, and the crystallization and melting of P4HB was notably affected by the temperature, in addition to the heating or cooling rates. The higher crystallization temperature and lower cooling rates facilitated the formation of well-developed crystals. Remarkably, the P4HB is found to be unable to crystallize at heating or cooling rates exceeding 6 K/s. Moreover, double melting peaks could be discerned at moderate isothermal crystallization temperature exhibiting faster crystallization rate. The findings will provide theoretical guidance on how to optimize the processing parameters in modulating the crystallization of P4HB.

Comprehensive Investigation into the Impact of Degradation of Recycled Polyethylene and Recycled Polypropylene on the Thermo-Mechanical Characteristics and Thermal Stability of Blends.

The impact of degradation on plastics is a critical factor influencing their properties and behavior, particularly evident in polyethylene (PE) and polypropylene (PP) and their blends. However, the effect of photoaging and thermal degradation, specifically within recycled polyethylene (rPE) and recycled polypropylene (rPP), on the thermo-mechanical and thermostability aspects of these blends remains unexplored. To address this gap, a range of materials, including virgin polyethylene (vPE), recycled polyethylene (rPE), virgin polypropylene (vPP), recycled polypropylene (rPP), and their blends with different ratios, were comprehensively investigated. Through a systematic assessment encompassing variables such as melting flow index (MFI), functional groups, mechanical traits, crystallization behavior, microscopic morphology, and thermostability, it was found that thermo-oxidative degradation generated hydroxyl and carboxyl functional groups in rPE and rPP. Optimal mechanical properties were achieved with a 6:4 mass ratio of rPE to rPP, as validated by FTIR spectroscopy and microscopic morphology. By establishing the chemical model, the changes in the system with an rPE-rPP ratio of 6:4 and 8:2 were monitored by the molecular simulation method. When the rPE-rPP ratio was 6:4, the system's energy was lower, and the number of hydrogen bonds was higher, which also confirmed the above experimental results. Differential scanning calorimetry revealed an increased crystallization temperature in rPE, a reduced crystallization peak area in rPP, and a diminished crystallization capacity in rPE/rPP blends, with rPP exerting a pronounced influence. This study plays a pivotal role in enhancing recycling efficiency and reducing production costs for waste plastics, especially rPE and rPP-the primary components of plastic waste. By uncovering insights into the degradation effects and material behaviors, our research offers practical pathways for more sustainable waste management. This approach facilitates the optimal utilization of the respective performance characteristics of rPE and rPP, enabling the development of highly cost-effective rPE/rPP blend materials and promoting the efficient reuse of waste materials.