Crystallization Peak Research Articles

Effective attainment of a substantial proportion of the PbTiO3 crystalline phase through a non-isothermal crystallization process

The crystallization kinetics studies were performed on a lead–titanium borate glass with a composition 50PbO–25TiO2–25B2O3 (mol %) to well understand the crystallization process by a non-isothermal method in an attempt to obtain a substantial proportion of the lead titanate (PbTiO3) crystalline phase. Based on the DTA result, the glassy material was heat-treated to induce crystallization and then produced a glass-ceramic. The broad hump observed in the XRD patterns of a glassy sample affirmed its amorphous nature. However, XRD studies conducted on a glass-ceramic revealed the evolution of the crystalline phase of PbTiO3 and a minor phase of TiO2. The phase relationship of PbTiO3 resulting from the reaction between PbO and TiO2 during a non-isothermal crystallization process has been examined. The activation energy for the crystallization of PbTiO3 is evaluated to be 135 kJ/mol (at PbO/TiO2 ratio = 2/1 mol %). When the Pb/Ti ratio exceeds 1, the process progresses nearly to completion by the first crystallization peak, and the PbTiO3 phase formation is easier. The fraction of PbTiO3 phase in the present glass is 98.3 % at PbO/TiO2 ratio = 2/1 mol %. In addition, FTIR spectra provided the presence of Ti4+ ions in the glass-ceramic. According to the values of crystal growth and Avrami index, surface crystallization and one-dimensional growth mechanisms are suitable mechanisms for contributing to the crystallization of this glassy sample. The obtained findings provided details on the crystallization behaviour of this glassy sample and excellent insight into obtaining the PbTiO3 crystalline phase in a large proportion, which is of great importance in future technological applications.

Study of the effect of SMAW welding speed on the microstructure and crystal stability of X70 steel using X-ray diffraction

This study investigates the impact of manual electric arc welding (SMAW) speed on the microstructure of X70 steel. Welding was performed at two distinct speeds: S1 = 20 mm/min and S2 = 35 mm/min, at the COSIDER BISKRA workshop in Algeria. X-ray diffraction (XRD) analysis was conducted on the welded zones to examine crystal orientation, size, dislocation density, and structural stability across different welding areas, including the base metal (MB), heat-affected zones (HAZ1 and HAZ2), and weld zones (WZ1 and WZ2). The XRD results revealed that key crystal peaks, such as {110} and {200}, retained their positions at both welding speeds, though variations in {110} peak intensity were noted. The lower welding speed (S1) resulted in a higher heat input, which enhanced crystal stability, increased crystal size, and reduced dislocation density. On the other hand, the higher speed (S2) produced lower heat input, leading to smaller crystal sizes, increased residual stresses, and a greater number of defects due to rapid cooling. These findings underscore the critical influence of welding speed on heat input, cooling rates, and their consequent effects on microstructure. The study highlights the importance of optimizing welding parameters to balance microstructural integrity, mechanical performance, and production efficiency.

Preparation of g-C3N4 from mixed ammonium salts containing NH4SCN and characterization of its cobalt-modified photocatalytic degradation of formaldehyde

This paper aims to achieve high-quality utilization of desulfurization waste liquid mixed salt. CN-MIX was prepared through pyrolysis of a mixture containing ammonium thiocyanate, ammonium thiosulfate, and ammonium sulfate. Additionally, CN-MIX/Co-a was produced via an impregnation-pyrolysis method with cobalt modification. The performance of the photocatalysts was evaluated using the formaldehyde degradation rate as an index, and their stability was tested. The results indicate that the specific surface area and pore volume of CN-MIX/Co-a increase by 1.53-fold and 1.44-fold, respectively, compared to CN prepared from single salt. The cobalt loading inhibits the thermal polymerization of CN-MIX, leading to a reduction in the intensity of the (002) crystal diffraction peaks. Additionally, CN-MIX/Co-a exhibits an increase in the CN peak at 2000–2200 cm−1, generating more photocatalytic active sites. The absorption sideband in the visible range red-shifts from 429 nm to 458 nm, broadening the photoresponse range. The emission peak in the photoluminescence (PL) diagram decreases, reducing the photogenerated electron-hole recombination rate. The photocatalyst demonstrates enhanced photocatalytic degradation of formaldehyde gas, with the degradation rate of CN-MIX/Co-a increasing from 13.28 % to 99.2 %. Furthermore, after eight cycles of use, the degradation efficiency of CN-MIX/Co-a for formaldehyde remains above 90 %, indicating high stability.

Effect of rare earth ions on the optical and electronic properties of defect chalcopyrite: Experimental and theoretical investigation

The present research is a systematic experimental and computational study focused on structural, electronic, and optical properties of ZnGa2S4 doped with neodymium rare earth ions for the first time. High-intensity, narrow-band luminescence peaks are observed in the visible and infrared regions by doping the matrix with Nd ions. These peaks in the background of the broadband spectrum are due to intercenter 4f-4f transitions of Nd3+ ions. The fact that the Raman peaks of the alloy crystal are more intense than that of the pure crystal confirms that the neodymium does not move freely in the lattice and occupies the place of defects. This confirms the results from our X-ray structural analysis. The crystal lattice parameters of the studied materials were determined as follows: a = 5.496 Å, c = 10.99 Å, c/a = 2. To explain the electronic, optical and magnetic properties, using ATK-DFT method, electronic energy band structure, density of states and optical spectrum for pure and doped with ZnGa2S4:Nd compound are computed and discussed. DFT result shows that impurity Nd leads to a decreased bandgap of ZnGa2S4 due to the hybridization of Nd-4d with S-3p orbital in the forbidden gap. The peaks in the optical spectrum are shifted toward the lower energy range for doped supercell.

Structural features of polylactide and natural rubber films produced by solution casting

Composite film samples of polylactide-natural rubber with a rubber content of 5, 10 and 15 wt. % were obtained by the solution method. The study of morphology showed the presence of rubber inclusions in the form of drops in the polylactide matrix. Thermophysical characteristics were determined by differential scanning calorimetry. It was determined that when rubber was added, the peak of cold crystallization of polylactide disappears on melting thermograms, the melting temperature decreases by 1–4°C compared to 100% polylactide. The structure of the obtained compositions was studied by nuclear magnetic resonance, electron paramagnetic resonance, and X-ray diffraction. The diffraction patterns of the samples contain reflections characteristic of the crystalline α-form of polylactide.

Influence of functional group structures in nucleating agents on the crystallization behavior of poly(ethylene terephthalate)

AbstractNucleating agents are crucial for modifying semi‐crystalline polymers, but the impact of different end‐group structures on crystallization behavior remains unclear. This study synthesized succinic dihydrazide nucleating agents with various end groups (methyl, ethyl, and tert‐butyl) for PET composite materials. The tert‐butyl‐terminated nucleating agent showed the best performance, increasing the crystallization peak temperature to 203.8°C, crystallinity to 27.3%, and reducing half‐crystallization time to 2.8 min at 220°C. It also enhanced the impact strength to 47.2 kJ·m−2 and flexural modulus to 2623 MPa, while improving Vicat softening temperature and heat distortion temperature by 41 and 8°C, respectively. The results from FTIR and Raman Spectroscopy indicate that the interactions between the end groups of the nucleating agent and the CH bonds in the PET structure, the π–π interactions between the nucleating agent and the PET molecular structure, as well as the modulation of the PET chain conformation by the nucleating agent, are the primary factors contributing to the enhanced crystallinity of PET. This study provides a new approach for designing efficient nucleating agents for high‐performance materials.

Effect of Sm2O3 on thermal, optical, mechanical, gamma and neutron shielding properties of zinc-boro-vanadate glasses

Abstract The effect of Sm2O3 on thermal, optical, mechanical, gamma and neutron shielding properties of newly prepared zinc borovanadate glasses has been investigated. Density is found increased and molar volume decreased with Sm2O3 content. The glass transition temperature ( T g ) , crystallization temperature ( T c ) and the peak crystallization temperature ( T P ) increased with increase of rare earth oxide content. These findings demonstrated an excellent glass-forming ability and thermal stability of the glasses. The optical properties have been explored through UV–vis spectroscopy. The indirect optical band gap energy ( E opt ) decreased from 2.978 to 2.679 eV, Urbach energy ( ∆ E ) increased from 0.273 to 0.299 eV and refractive index increased from 2.403 to 2.489 with increase in Sm2O3. Elastic moduli, Poisson’s ratio, Hardness and fractal bond connectivity were computed theoretically as per Makishima Mackenzie model. It is found that these glasses have appreciable mechanical strength and rigidity. Phy-X/PSD software has been used to determine different radiation shielding characteristics for the energy range 0.015–15 MeV. The mass and linear attenuation coefficients are found higher, and half value layer, tenth value layer and mean free paths are found lower than many radiation shielding glasses quoted in the literature values. The obtained Z eq values varied from 15.828–29.118 for energy range from 0.015 to 15 MeV, which are greater than those reported for several commercial glasses, concretes and rocks. Due to the Compton scattering process, exposure build up and energy absorption factor are found to be highest in the medium energy region. The fast neutron removal cross-sections of the glasses are observed to be significantly high. For the first time, thermally stable and mechanically strong zinc borovanadate glasses mixed with Sm2O3 have been thoroughly investigated for various properties and concluded that these glasses are suitable for optoelectronics and γ-shielding applications.

Effect of the synergistic interaction of zinc adipate, hydrotalcite and ethylene propylene rubber on the performances of polypropylene

Polypropylene (PP) is widely used in a range of areas due to its excellent physical and chemical properties, but its low-temperature brittleness and low-impact resistance largely limits its application. Hence, this study investigated the changes in mechanical and thermal properties of isotactic polypropylene (iPP) modified by the addition of the β-nucleating agent zinc adipate (ZnAA), the inorganic rigid particle hydrotalcite (HT), and the rubber elastomer bipropylene rubber (EPR). The structure and properties of modified PP were investigated by Fourier transform infrared (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), electronic universal material testing machine, and simple-beam impact testing machine. At last, the non-isothermal crystallization kinetics of iPP was investigated by the Caze method. It was found that with the addition of EPR reached 30 wt%, the notched impact strength of iPP was 34.74 kJ/m2, which was 542.43 % higher than that of pure iPP, and more than twice as high as that of ZnAA and HT modification, and the relative crystallinity ( K β) value of the β-crystalline form reached 79.66 % when 10 wt% EPR was added to the iPP. The addition of ZnAA, HT and EPR could significantly increase the crystallisation peak temperature ( T c), shorten the half-crystallisation time ( t 1/2) and increase the crystallisation activation energy ( ΔE) of iPP.

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.

The Impact of Water on Polylactide – Polybutylene Adipinate Terephthalate Blends

Mixing in the melt followed by pressing, blends of polylactide — polybutylene adipate terephthalate of various compositions were obtained. The content of polybutylene adipate terephthalate in blends was 10, 20 and 30 wt. %. The effect of water on film samples at a temperature of 22 ± 2°C for 270 days was studied. After exposure to water, a change in morphology was detected: turbidity of the samples and the appearance of defects. The thermophysical characteristics before and after hydrolytic degradation were determined by differential scanning calorimetry. A decrease in the cold crystallization temperature in pure polylactide and with a low content of polybutylene adipate terephthalate, and the disappearance of the cold crystallization peak at a content of 20 and 30 wt. % of polybutylene adipate terephthalate were shown. The degree of crystallinity of polylactide after exposure to water tended to increase. Changes in the chemical structure of mixed samples were monitored by IR spectroscopy.

Effect of boron oxide on the structure and properties of Li2O‐Al2O3‐SiO2 transparent glass‐ceramics

AbstractTransparent lithium aluminum silicon glass‐ceramics are prepared via heat treatment and the effect of boron oxide (B2O3) content on the structure and properties of Li2O‐Al2O3‐SiO2 glass‐ceramics is investigated. The X‐ray photoelectron spectroscopy results reveal that the parent glass containing B2O3 exhibits a higher concentration of bridging oxygen (BO). With an increase in B2O3 content, the relative amount of BO changes from 76.64% to 79.86% and then to 79.52%. Simultaneously, the second crystallization peak temperature TP2 of the samples increases from 715°C to 720°C and then to 724°C by differential scanning calorimeter analysis. The X‐ray diffractometer and scanning electron microscope results indicate that the addition of B2O3 facilitates grain growth, while an increase in B2O3 substitution for Al2O3 hinders the precipitation of LiAlSi4O10 but promotes quartz formation. The glass containing 2 wt% B2O3 with the heat treatment of 560°C/ 4 h+ 680°C/2 h shows a Vickers Hardness value of approximately 7.75 GPa, and a transmittance at 550 nm reaching ∼85%.

Warpage evaluation and mechanical characterisation of modified polyamide-6 specimens produced by Arburg plastic freeformer

AbstractIn injection moulding and additive manufacturing processes, it is common for the final product to exhibit warpage induced by a non-uniform cooling rate after material deposition. Residual stresses can be generated in the built parts, with a volume shrinkage that leads to dimensional inaccuracy and reduced usability. This phenomenon is even amplified in the presence of semi-crystalline polymers, which still need to be more widespread among additive manufacturing processes despite their capacity to show better mechanical properties when compared to amorphous ones. This study evaluates the degree of deformation and subsequently characterises the mechanical properties of a novel modified Polyamide 6 formulation (i.e., RADILON® S X21351 NT) printed through the Arburg Plastic Freeforming process. This new proprietary formulation modified the crystallisation behaviour during cooling. The whole exothermic crystallisation peak was shifted to lower temperatures, allowing the processing envelope of the modified formulation to widen. More specifically, after preliminary polymer characterisation analyses and after evaluating the warpage, a mechanical characterisation was performed using tensile tests on specimens (dry-as-moulded and conditioned) printed with different filling strategies on the build platform (XY-0°; XY- ± 45°; XY-90°; ZX-0°). Measured mechanical properties were ultimately compared to those achieved by applying the injection moulding technique on the same non-modified material. The specimens produced through the Arburg Plastic Freeforming process showed brittle behaviour that was more marked than those obtained by injection moulding. Moreover, the infill direction and water content significantly influenced the mechanical properties of specimens.

Influence of Ni Doping on Oxygen Vacancy-Induced Changes in Structural and Chemical Properties of CeO2 Nanorods

In recent years, cerium dioxide (CeO2) has attracted considerable attention owing to its remarkable performance in various applications, including photocatalysis, fuel cells, and catalysis. This study explores the effect of nickel (Ni) doping on the structural, thermal, and chemical properties of CeO2 nanorods, particularly focusing on oxygen vacancy-related phenomena. Utilizing X-ray powder diffraction (XRD), alterations in crystal structure and peak shifts were observed, indicating successful Ni doping and the formation of Ni2O3 at higher doping levels, likely due to non-equilibrium reactions. Thermal gravimetric analysis (TGA) revealed changes in oxygen release mechanisms, with increasing Ni doping resulting in the release of lattice oxygen at lower temperatures. Raman spectroscopy corroborated these findings by identifying characteristic peaks associated with oxygen vacancies, facilitating the assessment of Ni doping levels. Ni-doped CeO2 can catalyze the ultrasonic degradation of methylene blue, which has good application prospects for catalytic ultrasonic degradation of organic pollutants. Overall, this study underscores the substantial impact of Ni doping on CeO2 nanorods, shedding light on tailored catalytic applications through the modulation of oxygen vacancies while preserving the nanorod morphology.

Preparation and optical properties of ZnO/ZnS heterostructured nanomaterials

Firstly, Nano-ZnO materials are obtained by hydrothermal method, and Zinc acetate (Zn(CH3COO)2·2H2O) is selected as the Zn source, and potassium hydroxide (KOH) is used as the analytical reagent. Secondly, ZnO/ZnS composites are prepared by hydrothermal method using monomer nano-ZnO as a template, thioacetamide (CH3CSNH2) as a sulfur source, hexadecyl trimethyl Ammonium bromide (CTAB) as a surface modifier, and adjusting the molar mass ratio of Zn/S. The structure, morphology, and optical properties of the composite are characterized respectively by XRD, SEM, and PL, and the growth mechanism and fluorescence characteristics of the composite are explored. The results indicate that the crystal structure of the ZnO/ZnS complex is initially a hexagonal wurtzite structure. With the gradual increase of S element concentration, only the crystal plane diffraction peak of sphalerite structure ZnS is shown in the XRD spectrum. Besides, the morphology of the composite also grows from microsphere like to flocculent layered nano-crystals. There are strong characteristic absorption and green light absorption capabilities at 523 nm, and there is a relatively weak ultraviolet emission peak appeared at 380 nm in the PL spectrum. The optical properties and visible light absorption capabilities of the nano-ZnO/ZnS composite are superior to those of the monomer ZnO. Finally, the growth mechanism and luminescence mechanism of ZnO/ZnS are explored at the micro-level.

Novel nanostructured transparent Na2O–Al2O3–SiO2 carnegieite-based glass ceramics with high crystallinity

Developing next-generation cover glasses with high crystallinity and transmittance, such as transparent nanocrystalline Na2O–Al2O3–SiO2 (NAS) glass, has proved highly challenging. Herein, we propose a novel nanostructured transparent NAS glass–ceramic with high crystallinity (65 %) and transmittance (91 %) owing to the involved separation of crystallization peaks and the diffusion barrier properties of ZrO2. Compared with untreated glass, this glass-ceramic shows a considerable increase in hardness (from 5.18 to 7.15 GPa, i.e. >38 %). With the increased crystallinity, no substantial reduction in transmission is detected and the crystal type and size can be effectively controlled by the limitation of ZrO2. Hence, the findings project a novel method for creating high crystallinity and transmittance, providing new directions for transparent NAS glass–ceramic.

Kinetics study and fragility of (Cu50Zr43Al7)98Y2 bulk metallic glass

Crystallization transformation kinetics and fragility of (Cu50Zr43Al7)98Y2 bulk metallic glass (BMG) were investigated at non-isothermal and isothermal conditions by differential scanning calorimetry. Activation energies for the BMG were calculated for the glass transition, onset crystallization, and crystallization peak using various methods of non-isothermal analysis. Results suggested that atomic rearrangement during glass transition is more complex than crystallization, and growth poses greater challenges than nucleation. Isothermal analysis conducted in the supercooled liquid region provides evidence of crystallization being controlled by diffusion, with a calculated mean Avrami exponent of 2.2. Additionally, the findings of fragility studies and kinetic studies demonstrated a strong correlation with the glass-forming ability (GFA), thereby validating the high GFA of the BMG analyzed in this study. Thus, this research results provide a detailed understanding of the complex crystallization kinetics, thermal behavior, and GFA of (Cu50Zr43Al7)98Y2 BMG, emphasizing its potential in materials science applications.

Effect of optical and electronic structure on the photocatalytic activity of Al doped ZnO ALD thin films on glass fibers

Photocatalytic water treatment can be promising for eliminating toxic pollutants via a more sustainable approach using renewable sources. However, the technique still requires materials design to optimize/maximize the performance of the photocatalytic materials. Immobilizing the thin film photocatalytic materials onto high surface area textile substrates via atomic layer deposition (ALD) can offer a practical design approach. Al-doped ZnO (AZO) ALD films are deposited onto glass fabric substrates, and their photocatalytic performances were investigated in relation to the FESEM, XRD, XPS, UV–Vis, and PL characterizations. The amount of Al and the post-deposition annealing changed the materials structure, thus the photocatalytic activity of the films. Maximum performance was achieved with the 20 % Al-doped ZnO films after a post-deposition thermal annealing step at 450 °C. The sample also showed the highest UV–Vis absorption and PL emission among the samples. However, this sample didn’t show any crystal peaks in the XRD analysis. Furthermore, the charge carrier concentrations and the mobility of the films were investigated via Hall-Effect, which showed that the 20 % AZO sample has very different features with a p-type nature compared to the other AZO films.

Physical, chemical and radiation shielding properties of metakaolin-based geopolymers containing borosilicate waste glass

Upcycling waste borosilicate glass (BS) is a viable and sustainable way of preserving the natural resources required for the production of new materials and ensuring environmental sanitation and safety. This study was aimed at investigating how the addition of BS influences the physical, chemical, and mechanical properties and shielding performance against neutrons and charged particles on metakaolin-based geopolymer G. Four batches of G infused with 10%, 20%, and 30% wt BS samples and coded as G, G-10BS, G-20BS, and G-30BS, respectively, were fabricated based on the solid-state reaction method. The samples were characterized accordingly using experimental and theoretical procedures. X-ray diffraction analysis of the materials showed that the addition of BS suppressed crystal peaks in the geopolymers. The Vickers hardness values were calculated as 554, 503, 517, and 528 HV under a 0.1 kg load. The values of fast neutron macroscopic cross-section increased from 0.0601 cm−1 to 0.0706 cm−1 as BS content increased from 0 to 30 wt%. The coherent, incoherent, absorption, and total interaction probabilities of thermal neutrons increased in the geopolymer samples. For electrons, the stopping powers were in the range of 1.575–13.17 cm2/g, 1.571–13.15 cm2/g, 1.571–13.16 cm2/g, and 1.571–13.18 cm2/g for G, G-10BS, G-20BS, and G-30BS, respectively. The projected ranges of carbon ions in G, G-10BS, G-20BS, and G-30BS are within the limits 0.069–17.87 μm, 0.064–16.99 μm, 0.064–16.99 μm, and 0.057–15.24 μm. The trend of the projected ranges of electrons, protons, α-particles, and C ions with kinetic energies within 15 keV and 15 MeV was mostly in the sequence G > G-10BS > G-20BS > G-30BS. This order was consistent with the density and BS content of the geopolymer samples. The addition of BS to the metakaolin-based geopolymer improved the fast neutron moderating capacity and thermal neutron cross-sections and reduced the range of charged particle radiation in the geopolymers. The neutron shielding ability of G-30BS was found to be better than that of some existing shielding materials. The BS-infused concrete can be useful for the production of concrete used for radiation control.

Quantifying Asymmetric Zinc Deposition: A Guide Factor for Designing Durable Zinc Anodes.

Zinc metal is recognized as the most promising anode for aqueous energy storage but suffers from severe dendrite growth and poor reversibility. However, the coulombic efficiency lacks specificity for zinc dendrite growth, particularly in Zn||Zn symmetric cells. Herein, a novel indicator (fD) based on the characteristic crystallization peaks is proposed to evaluate the growth and distribution of zinc dendrites. As a proof of concept, triethylenetetramine (TETA) is adopted as an electrolyte additive to manipulate the zinc flux for uniform deposition, with a corroborating low fD value. A highly durable zinc symmetric cell is achieved, lasting over 2500h at 10mAcm-2 and 400h at a large discharge of depth (10mAcm-2, 10mAhcm-2). Supported by the low fD value, the Zn||TETA-ZnSO4||MnO2 batteries overcome the sudden short circuit and fast capacity fading. The study provides a feasible method to evaluate zinc dendrites and sheds light on the design of highly reversible zinc anodes.

Self‐nucleation in poly(butylene adipate‐co‐terephthalate) of initially different crystal forms

AbstractPoly(butylene adipate‐co‐terephthalate) (PBAT) is an important biodegradable copolymer, but its crystallization rate is slow. Herein, the effect of self‐nucleation on the crystallization behavior of PBAT with initially different crystalline modifications (melt‐crystallized specimens and as‐received pellets) was investigated. The melt‐crystallized and as‐received PBAT specimens are confirmed as the α‐ and β‐form, respectively. It is found that the self‐nucleation domains of β‐form PBAT are almost the same as those of α‐form one. After self‐nucleation, the maximum shift of the crystallization peak toward higher temperature is around 60 °C upon the followed cooling process, suggesting that self‐nucleation remarkably promotes PBAT crystallization. The self‐nucleation temperature span of self‐nucleation domain is about 10 °C, which provides substantial benefits to industrial processing. Moreover, for both the initial α‐ and β‐form PBAT, the final crystal is α‐form after self‐nucleation treatment. This work demonstrates that self‐nucleation is highly effective in enhancing PBAT crystallization.