Crystallization Rate Research Articles

Super-tough poly(lactic acid)/silicone rubber thermoplastic vulcanizates: The organic and inorganic synergistic interfacial compatibilization

Polymer modification using silicone rubber represents a promising avenue for enhancing physico-mechanical properties. However, achieving optimal performance through direct blending is hindered by the poor interface compatibility between silicone rubber and the matrix. In this study, we prepared super-tough thermoplastic vulcanizates (TPVs) of polylactic acid/silicone rubber through dynamic vulcanization with PLA, methyl vinyl silicone rubber (MVQ), glycidyl methacrylate grafted MVQ (MVQ-g-GMA), and fumed silica nanoparticles (SiO2). The impact of the SiO2 addition in MVQ on the morphology, mechanical properties, crystallization, and thermal properties of the TPVs was investigated. The results showed that MVQ-g-GMA and SiO2 exhibited a synergistic compatibilization effect significantly improving the interfacial adhesion between PLA and MVQ. Therefore, the impact and tensile strength of the TPVs increased from 8.0 kJ/m2 and 22.2 MPa to 62.6 kJ/m2 and 36.7 MPa, respectively. Moreover, the TPVs also presented good low-temperature toughness with a maximum impact strength of 40.4 kJ/m2 at −20 °C. Additionally, improvements in thermal stability and crystallization rate were also observed. Overall, combining organic and inorganic synergistic compatibilization is a feasible and effective method to fabricate outstanding low-temperature toughness to PLA.

Effects of crystal growth rate and pressure on shape controllability in the dewetting micro-pulling-down method

The dewetting micro-pulling-down (μ-PD) method is a type of μ-PD method that utilizes low-wettability insulating materials with melts. This method enables the direct fabrication of difficult-to-process alloy wires from molten material. Using this method, in certain systems, a deviation between the theoretically predicted wire diameter based on the static contact angle and the experimentally obtained wire diameter has been observed. In this study, it was hypothesized that this deviation could be explained by the velocity-dependence of the advancing contact angle, based on previous theoretical considerations. This hypothesis was experimentally verified by observing changes in the wire diameter during the pulling process of iridium and ruthenium. Furthermore, crystal growth was carried out under different pressure conditions, demonstrating that the behavior and surface state during crystal growth can be explained by variations in the angle conditions at the meniscus endpoint.

Synthesis and Characterization of Phase Change Microcapsules Containing Nano-Graphite

This study uses the sol-gel method to modify the phase change microcapsules. The phase change material (PCM) is encapsulated by a polymer shell to reduce the leakage in the solid-liquid transition. Furthermore, the nano-graphite particle (NGP) is introduced into the shell to increase its thermal conductivity. The particle size and enthalpy value of the obtained microcapsules are approximately 3 μm and 150.3 J/g, respectively. The results show that the encapsulation efficiency of PCM in the prepared microcapsules is increased and the crystallization rate of PCM becomes faster when the NGP is added. The obtained microcapsules and wood flour are incorporated into high-density polyethylene (HDPE) to form a wood-plastic composite (WPC). The results indicate that the tensile and impact strengths of the WPC are 24.1 MPa and 48.7 J/m, respectively. Moreover, it is observed that the addition of these phase-change microcapsules can improve the heat dissipation of HDPE and accelerate the speed of thermal diffusion.

Crystallinity, Rheology, and Mechanical Properties of Low-/High-Molecular-Weight PLA Blended Systems.

As semi-crystalline polyester (lactic acid) (PLA) is combined with other reinforcing materials, challenges such as phase separation, environmental pollution, and manufacturing difficulties could hinder the benefits of PLA, including complete biodegradability and strong mechanical properties. In the present investigation, melt blending is utilized to establish a mixture of low- and high-molecular-weight polylactic acids (LPLA and HPLA). The crystallinity, rheology, and mechanical properties of the combination were analyzed using rotational rheometry, differential scanning calorimetry, X-ray diffraction, polarized optical microscopy, scanning electron microscopy, and universal testing equipment. The results demonstrate compatibility between LPLA and HPLA. Moreover, an increase in LPLA concentration leads to a decrease in the crystallization rate, spherulite size, fractional crystallinity, and XRD peak intensity during isothermal crystallization. LPLA acts as a diluent during isothermal crystallization, whereas HPLA functions as a nucleating agent in the non-isothermal crystallization process, promoting the growth of LPLA crystals and leading to co-crystallization. The blended system with a 5% LPLA mass fraction exhibits the highest tensile strength and enhances rheological characteristics. By effectively leveraging the relationship between various molecular weights of PLA's mechanical, rheological, and crystallization behavior, this scrutiny improves the physical and mechanical characteristics of the material, opening up new opportunities.

Analysis of the Non-isothermal Crystallization Kinetics of the Polyamide 6/M-lignin Composites

In this study, investigations of the non-isothermal crystallization kinetics of polyamide 6 (PA6) and PA6/m-lignin composites were conducted by differential scanning calorimetry (DSC). The crystallization kinetics of the PA6, including crystallization temperature and rate, were characterized by monitoring the heat flow during cooling. The study found that the crystallization temperature shifted to lower temperatures and the crystallization kinetics slowed down with increasing lignin. Besides, the Avrami equation modified by Jeziorny and Mo’s method were used to study the non-isothermal crystallization kinetics of the neat PA6 and PA6 composites. The curve fit resulting from the modified Avrami equation was not convincing. However, Mo’s method did successfully characterize the overall non-isothermal crystallization kinetics for neat PA6 and the PA6 composites. In addition, the activation energies of the non-isothermal crystallization were calculated by the Kissinger method. It was found that the PA6 composite crystallization rate increased when adding less than 10% lignin. However, the more the content of m-lignin, the slower the crystallization rate. The same conclusion was reached based on the fitting results of the non-isothermal crystallization activation energies.

Effect of Surface Properties of Nanoparticles on the Crystallization Behavior of Polypropylene/Polypropylene‐g‐Silica Nanocomposites

AbstractIn order to investigate the effect of surface properties of nanoparticles (NPs) on the crystallization behavior of nanocomposite, three kinds of silica (SiO2) NPs are dispersed in isotactic polypropylene (iPP) matrix by solution blending method. Specifically, the poor compatibility between inorganic bare SiO2 NPs and organic PP matrix triggers the formation of aggregates and induces the fractionated crystallization with two crystallization peaks at higher particle loading (Φ), i.e., main crystallization peak (MCP) and low temperature crystallization peak (LCP, always located at 124.0 °C). Once short PP chains (0.9 × 104 g mol−1) are grafted onto the surface of SiO2 NPs, the nanocomposites with all Φ only exhibit a single MCP which is attributed to the strong interfacial interaction. With the increase of grafting chain length (9 × 104 g mol−1), the more stretched conformation of grafting chains can provide numerous heterogeneous nucleation sites and significantly accelerate the crystallization rate of PP chains near the surface of SiO2 NPs, which lead to the formation of an extra high temperature crystallization peak (HCP, almost kept constant at 133.0 °C). The occurrence of various crystallization peaks implies that the surface properties of nanoparticles play a vital role in the nucleation ability of nanoparticles.

Tunable wide-angle high-efficiency polarization selectivity based on a one-dimensional photonic crystal containing elliptical metamaterials

Recently, researchers achieved wide-angle high-efficiency polarization selectivity based on polarization-sensitive photonic bandgaps in one-dimensional photonic crystals containing elliptical metamaterials. However, wide-angle high-efficiency polarization selectivity can only operate at fixed wavelengths (around band edges), which intensively limits the practical applications. To overcome this limitation, we construct a one-dimensional photonic crystal containing phase-change-material-based elliptical metamaterials. The position of the polarization-sensitive photonic bandgap can be flexibly controlled by the crystallization rate of the phase change material. Empowered by the wavelength-tunable polarization-sensitive photonic bandgap, we achieve wavelength-tunable wide-angle high-efficiency polarization selectivity. As the crystallization rate increases from 0 % to 100 %, the operating wavelength of polarization selectivity can be flexibly tuned from 1440 to 1796 nm. Meanwhile, the operating angular width remains larger than 50° and the optimal polarization extinction ratio remains on the order of 104. Our work provides a viable route to designing tunable high-performance polarizers.

Induced crystallization for the simultaneous removal of hardness-iron–manganese in groundwater: An experimental study

Hardness, iron, and manganese are common groundwater pollutants, that frequently surpass the established discharge standard concentrations. They can be effectively removed, however, through induced crystallization. This study has investigated the effectiveness of the simultaneous removal of hardness-iron-manganese and the crystallization kinetics of calcium carbonate during co-crystallization using an automatic potentiometric titrator. The impacts pH, dissolved oxygen (DO), and ion concentration on the removal efficiency of iron and manganese and their influence on calcium carbonate induced crystallization were assessed. The results suggest that pH exerts the most significant influence during the removal of hardness, iron, and manganese, followed by DO, and then the concentration of iron and manganese ions. The rate of calcium carbonate crystallization increased with pH, stabilizing at a maximum of 10−10 m/s. Iron and manganese can be reduced from an initial level of 4 mg/L to <0.3 mg/L and 0.1 mg/L, respectively. The removal rate of iron, however, was notably higher than that of manganese. The DO concentration correlates positively with the removal of iron and manganese but has minimal impact on the calcium carbonate crystallization process. During the removal of iron and manganese, competitive interactions occur with the substrate, as increases in the concentration of one ion will inhibit the removal rate of the other. Characterization of post-reaction particles and mechanistic analysis reveals that calcium is removed through the crystallization of CaCO3, while most iron is removed through precipitation as Fe2O3 and FeOOH. Manganese is removed via two mechanisms, crystallization of manganese oxide (MnO2/Mn2O3) and precipitation. Overall, this research studies the removal efficiency of coexisting ions, the crystallization rate of calcium carbonate, and the mechanism of simultaneous removal, and provides valuable data to aid in the development of new removal techniques for coexisting ions.

Diopside-like based ceramics prepared via one-step sintering of extracted titanium slag and coal fly ash

Diopside-Like based ceramics as the main crystalline phase (expressed as ‘Diopside’) were prepared via one-step sintering using extracted titanium slag (ETS) and coal fly ash (CFA) as raw materials. The effects of CFA content and sintering temperature on the crystal phase composition, microstructure, properties and crystallization kinetics were studied by X-ray fluorescence, X-ray diffraction, scanning electron microscopy, and inductively coupled plasma emission spectrometry. According to the findings, the addition of CFA supplemented the deficiency of Si and Al in ETS and balanced the Ca/Al/Si molar ratio in the system. Moreover, at the CFA doping of 20 %, melilite was gradually transformed into ‘diopside’ at 800–1100 °C that further remained stable at 1160–1200 °C. ‘Despite’ the fact that the crystallization activation energy increased and the Avrami index was at its lowest level (1.75), the crystallization temperature was reduced, whereas the crystallization rate increased, causing the ceramic body and surface to crystallize and thereby improving the properties of ceramics. Sintering at 1180 °C for 1 h resulted in ceramics with ‘diopside’ as the primary crystal phase composition. The water absorption, linear shrinkage, bulk density, bending strength, and acid resistance were respectively 1.3 %, 13 %, 2.89 g cm−3, 141.8 MPa, and 97.36 %. Finally, ‘diopside’ possessed the higher acid resistance than melilite and anorthite.

Titanium Dioxide Promotes the Growth and Aggregation of Calcium Phosphate and Monosodium Urate Mixed Crystals.

The increased utilization of titanium dioxide (TiO2) nanoparticles (TNPs) in various industrial and consumer products has raised concerns regarding its harmful effect due to its accumulation within the different systems of the human body. Here, we focused on the influence of TNPs on the growth and aggregation of two crucial crystalline substances, calcium phosphate (CaP) and monosodium urate (MSU), particularly its implications in gout disease. In this study, we adopted microscopic techniques and generated kinetic models to examine the interactions between TNPs, CaP and MSU, and crystallization, under controlled laboratory conditions. Our findings reveal that TNPs not only facilitate the growth of these crystals but also promote their co-aggregations. Crystal dissolution kinetics also exhibit that an increase in TNPs concentration corresponds to a reduction in the dissolution rate of CaP and MSU crystals in presence of the dissoluting agent hydroxycitrate (Hcit). These observations suggest that TNPs can stabilize CaP+MSU mixed crystals, which underscores the significance of TNPs' exposure in the pathogenesis of gout disease.

Conductive Metal-Organic Framework Nanosheets Constructed Hierarchical Water Transport Biological Channel for High-Performance Interfacial Seawater Evaporation.

Solar interfacial water evaporation shows great potential to address the global freshwater scarcity. Water evaporation being inherently energy intensive, Joule-heating assisted solar evaporation for addressing insufficient vapor under natural conditions is an ideal strategy. However, the simultaneous optimization of low evaporation enthalpy, high photothermal conversion, and excellent Joule-heating steam generation within a single material remain a rare achievement. Herein, inspired by the biological channel structures, a large-area film with hierarchical macro/microporous structures is elaborately designed by stacking the nanosheet of a conductive metal-organic framework (MOF), Ni3(HITP)2, on a paper substrate. By combining the above three features in one material, the water evaporation enthalpy reduces from 2455Jg-1 to 1676 J g-1, and the photothermal conversion efficiency increases from 13.75% to 96.25%. Benefiting from the synergistic photothermal and Joule-heating effects, the evaporation rate achieves 2.60kg m-2 h-1 under one sun plus input electrical power of 4W, surpassing the thermodynamic limit and marking the highest reported value in MOF-based evaporators. Moreover, Ni3(HITP)2-paper exhibits excellent long-term stability in simulated seawater, where no salt crystallization and evaporation rate degradation are observed. This design strategy for nanosheet films with hierarchical macro/microporous channels provides inspiration for electronics, biological devices, and energy applications.

Effect of Dilution on the Crystallization Kinetics of Neodymium-Based Rare Earth Polybutadiene Rubber.

The crystallization behavior of neodymium-based rare earth polybutadiene rubber (Nd-BR) is studied in the presence of small-molecule treated distillate aromatic extract (TDAE) and high-molecular-weight polybutadiene-isoprene copolymer rubber (BIR). Pronounced inhibitory effects on the crystallization of Nd-BR are exhibited by both materials, as evidenced by reductions in the crystallization temperature (Tc), melting point (Tm), and corresponding enthalpy change. It is found that, at equal concentrations, a greater influence on the crystallization rate is exerted by TDAE oils, whereas nucleation inhibition is more potently affected by BIR. Incomplete crystallization during cooling is exhibited by Nd-BR when the TDAE oil concentration reaches 40 parts per hundreds of rubber (PHR) (31 wt.%), or BIR achieves a 60 wt.% concentration; subsequently, a noticeable cold crystallization phenomenon is observed upon heating. Insights into the isothermal crystallization kinetics are offered by the data, which reveal that the Avrami index n value for Nd-BR predominantly ranges between 2.5 and 3.0. A decrease in the n value is induced by a small amount of TDAE oil, while a noticeable decline in the n value is observed only when the BIR concentration is 60 wt.%. A correlation between the crystallization activation energy, the concentration of TDAE oil and BIR, and the crystallization temperature is established; a negative activation energy is recorded, and a decrease in the crystallization rate is noted when both concentrations are low and the crystallization temperature exceeds -50 °C. In contrast, positive activation energy and an increase in the crystallization rate are observed when the BIR concentration reaches 60%, and the crystallization temperature resides between -50 °C and -70 °C.

Thermal behavior of gadolinium-silica gels prepared via sol–gel route combined to γ-irradiation process

Gadolinium-silica (Gd-silica) gels were prepared via sol–gel route combined to γ-irradiation (0–30 kGy), starting from Tetra-Ethyl-Orthosilicate (Si(OCH2CH3)4, TEOS) and gadolinium nitrate Gd(NO3).6H2O used as raw materials. The phase transformation and morphology of the gels derived from both precursors were characterized by XRD and TEM analysis. Differential scanning calorimetry (DSC) under non-isothermal conditions was used to determine the crystallization activation energy (E c) at different γ-doses (0, 8, 15, 25 and 30 kGy), using the methods suggested by Kissinger, Moynihan and Ozawa. XRD analysis of the samples calcined up to 1100°C for 2 h reveals the formation of gadolinium silicate (Gd4.67 (SiO4)3O) apatite crystalline phase with the presence of small traces of gadolinium pyrosilicate (Gd2Si2O7), the average particle sizes about 50 nm. TEM observations show spherical Gd-silicate nanoparticles homogeneously dispersed in silica matrix, the mean diameter size is about 40 nm. From DSC analysis, it was observed that the onset crystallization temperature (T x) and peak crystallization temperature (T c) both increase with increasing γ-dose. According to Kissinger, Moynihan and Ozawa models, the crystallization activation energies for Gd-silicate phase formation were found to be 465.2, 474.5 and 465.7 kJ mol−1, respectively for unirradiated samples and 429.1, 447 and 438 kJ mol−1 when the γ-irradiation reaches 30 kGy respectively. Results revealed that the values of E c decreased when the γ-dose increases and attains the minimum value at the dose of 15 kGy and then increase at higher doses. The crystallization rate factor (K) was also seen to decrease with increasing of γ-dose. Gamma irradiation increases the crystallization peak temperature (T c). The crystallization activation energy (E c) estimated from the three models is in good agreement and much well with those reported for silicate systems. Gamma irradiation decreases the E c and crystallization rate factor (K). These preliminary results can provide useful technical information for a better understanding and control of the crystallization process of this type of nanomaterial.

Uniform infrared light field induced rapid crystallization and enhanced stability of perovskite solar cells

Infrared (IR) light has exhibited remarkable efficacy in facilitating the annealing crystallization process of perovskite film. However, the precise mechanisms underpinning the promotional effects of IR remain a subject of ongoing investigation. Herein, we address this critical knowledge gap by presenting a comprehensive investigation into the mechanisms governing IR-induced crystallization and its impact on the performance of perovskite solar cells. Our computational simulations reveal that IR light create a swift, stable, and homogenous annealing environment during the crystallization. The incident light field on the perovskite film surface orchestrates the controlled departure of excess iodide ions from the surface, consequently inducing the formation of iodine vacancies. This transformative process leads to a transition of the surface from a strong p-doped state to a more delicate n-doped state. Furthermore, the application of IR treatment demonstrates a pronounced propensity for facilitating the integration of methylammonium iodide (MAI) into the less compacted PbI2 lattice, thereby expediting the crystallization rate. Remarkably, devices processed within this uniform and stable light field exhibit augmented performance and heightened stability.In summary, our study furnishes invaluable insights into the intricate interplay underlying IR-assisted crystallization in perovskite solar cells. The elucidation of these mechanisms holds significant promise for advancing future industrial-scale fabrication techniques for enhanced perovskite solar cell production.

Micromechanical modeling of the effects of crystal content on the visco-hyperelastic-viscoplastic behavior and fracture of semi-crystalline polymers

In this work, we present a novel physically based visco-hyperelastic-viscoplastic micromechanical constitutive model, which establishes a link between the evolution of the macromolecular network properties to the mechanical and fracture behavior of variable-crystallinity semi-crystalline polymers. Unlike previous micromechanical constitutive models that were only time independent, we propose a time-dependent scheme. It employs the computational effective eight-chain model for micro-macro transition while assuming a composite structure for the polymer. Thus, an innovative approach that couples the deformation and damage of individual polymer chains is developed. The proposed constitutive framework assumes that the stress developed through the deformation of semi-crystalline polymers is the sum of a macromolecular network and an intermolecular part. The macromolecular part accounts for the conformational change associated with Kuhn segments reorientation and the bond potential associated with the deformation of the bonds between Kuhn segments. Meanwhile, the intermolecular part accounts for the deformation of the crystalline and the amorphous phases. The constitutive equations are integrated using a mixed explicit/implicit integration algorithm. To validate and calibrate our model, we utilize uniaxial tensile experimental data obtained from three different polyethylene materials with varying crystallinity levels and different strain rates. We propose a robust calibration procedure, ensuring the identification of a single set of parameters that remain independent of crystal content and strain rate. Finally, we assess the model's predictive capabilities in predicting the mechanical behavior and fracture at different strain rates for variable-crystallinity polyethylene is evaluated. This comprehensive approach enhances our understanding and predictive capacity in modeling the intricate mechanical response up to fracture of semi-crystalline polymers under diverse conditions.

Valorization of acid mine drainage into potable water and valuable minerals through membrane distillation crystallization

Owing to the rise in population growth and demands for the current living standards, mineral and water resources are depleting at the alarming rate. Also, the mineral–water-energy nexus raises a concern of high-quality water and mineral production at low costs. Membrane distillation crystallization (MDC) has emerged as a promising technology capable of simultaneous water and mineral recovery from wastewater or industrially discharged brines. Herein, the MDC was evaluated for recovery of water and precious minerals from acid mine drainage discharged from the mine tailings. High quality fresh water with 99.9 % salt rejection and permeate flux of 2.32 kg·m−2·h−1 was recovered at 52 °C feed inlet temperature. Also, feed temperatures were varied to determine their impact on mineral crystal morphology, size distribution and growth rate. Predominantly recovered minerals were gypsum, manganese fluoride, potassium iron oxide, nickel oxide hydroxide, sodium sulphate and dihydrogen sulphate. Orthorhombic crystal structure of mineral salts was attained at low feed inlet temperature (34 °C). Higher feed inlet temperatures (i.e. 41° C and 52° C) promoted co-crystallization giving rise to orthorhombic polymorph structures. Narrow crystal size distribution was reported at low water recovery factor (initial growth) for all temperatures. However, the particle size distribution broadened as the recovery factor increased. The crystal sizes ranged from 3.91 ± 0.97 µm to 14.04 ± 3.31. Remarkably, crystal growth rate increased with an increase in feed inlet temperature. These findings open a research direction towards economic recovery of mineral and water to supplement the existing shortages. With a myriad of crystals obtained from the MDC process, an additional operational unit is required to selectively recover high economic minerals.

Two-step nucleation and crystal growth in a metastable solution

This study is concerned with a theory of two-step nucleation and growth of crystals in a metastable liquid. This mechanism is that crystalline nuclei formation occurs in dense liquid clusters suspended in the solution. These clusters contain higher solution concentration and viscosity, leading to a lower surface free energy barrier and faster phase transition route. The theory is based on growth laws of crystals during the two-step bulk phase transformation. At the initial stage, the crystals evolve in a diffusion-limited environment with almost unchanged supersaturation. At the second stage, they become larger, move beyond these clusters, and evolve in accordance with a hyperbolic tangent law. A generalized particle growth law joining the first and second stages is obtained by stitching the diffusion limited and hyperbolic tangent laws. On this basis, an integrodifferential model of the evolution of a polydisperse ensemble of crystals was formulated and solved. The crystal-size distribution function increases and the solution supersaturation remains practically unchanged until the particle size corresponds to a transition in the particle growth rate from a diffusion-limited branch to a hyperbolic tangent branch. This is followed by an increase in the crystal growth rate, a decrease in the distribution function and solution supersaturation. Then the distribution function increases up to the maximum size of crystals grown in the solution. A sufficiently long time interval of almost constant supersaturation and the N-shaped behavior of the distribution function are the consequences of a two-step nucleation and growth mechanisms.

In operando study of gypsum crystal growth through in-cell environmental SEM

Thanks to their setting ability, hydraulic binder materials (e.g., cements, plasters) are used for a wide variety of applications (e.g., construction, medical). The setting reaction occurs through a dissolution–precipitation mechanism during which initial particles dissolve releasing ionic species from which new crystals precipitate. The development of such a microstructure governs the final properties of the material and are thus of uttermost interest.In this paper, the in operando study of the precipitation of gypsum crystals from the dissolution of bassanite particles using a specific cell for scanning electron microscope (SEM) observation is presented. Image analysis based on segmentation enabled to give quantitative results on the growth of crystals at global and local scales. Single crystal facets are indexed based on crystallography and literature results, which enables the quantification of crystal growth rates for the indexed crystallographic planes. Different growth regimes are identified; they are attributed to the transition from unfavored to the most favored crystal facets known for gypsum. The {111} and {110} planes were the fastest growing planes, whereas the {120} and {010} planes were the most stable and grew slowly.

Domain Growth in Polycrystalline Graphene.

Graphene is a two-dimensional carbon allotrope which exhibits exceptional properties, making it highly suitable for a wide range of applications. Practical graphene fabrication often yields a polycrystalline structure with many inherent defects, which significantly influence its performance. In this study, we utilize a Monte Carlo approach based on the optimized Wooten, Winer and Weaire (WWW) algorithm to simulate the crystalline domain coarsening process of polycrystalline graphene. Our sample configurations show excellent agreement with experimental data. We conduct statistical analyses of the bond and angle distribution, temporal evolution of the defect distribution, and spatial correlation of the lattice orientation that follows a stretched exponential distribution. Furthermore, we thoroughly investigate the diffusion behavior of defects and find that the changes in domain size follow a power-law distribution. We briefly discuss the possible connections of these results to (and differences from) domain growth processes in other statistical models, such as the Ising dynamics. We also examine the impact of buckling of polycrystalline graphene on the crystallization rate under substrate effects. Our findings may offer valuable guidance and insights for both theoretical investigations and experimental advancements.

A deep insight into the dynamic crystallization of coal slags and the correlation with melt microstructure

In liquid discharging furnace, crystallization can occur in slags during the cooling process. The presence of crystal changes the structure, flow, heat transfer, especially the viscosity with a sharp increase. A deep understanding of the crystal kinetics is significant to optimize the flow of liquid slag. Crystal kinetics varies significantly with different slags due to the complexity and variability of the multi components in slags. In this paper, a high-temperature microscopy with high-resolution is used to clearly observe the in situ precipitation of different crystals and the kinetic parameters of different crystals are analyzed. Microscopic structure analysis of both the melt and the precipitated crystal shows that the proportion of basic oxygen structure and the diffusion coefficient of the basic cation in the melt have a direct correlation with the growth of crystal. A structural parameter St of the melt is developed, which has a positive correlation with the crystal growth rate. This is a new discovery in bridging the gap between the melt and precipitated crystals and it provides a way to control the crystal growth during slag cooling.