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Journal articles on the topic 'Melt crystallization'

Author: Grafiati

Published: 4 June 2021

Last updated: 24 January 2023

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1

Ulrich, Joachim, Jutta Bierwirth, and Sabine Henning. "Solid Layer Melt Crystallization." Separation and Purification Methods 25, no. 1 (January 1996): 1–45. http://dx.doi.org/10.1080/03602549608006625.

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2

Matsuoka, M. "Morphology control in melt crystallization." Journal of Physics D: Applied Physics 26, no. 8B (August 14, 1993): B149—B155. http://dx.doi.org/10.1088/0022-3727/26/8b/024.

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3

Shtukenberg, Alexander G., Melissa Tan, Leslie Vogt-Maranto, Eric J. Chan, Wenqian Xu, Jingxiang Yang, Mark E. Tuckerman, Chunhua T. Hu, and Bart Kahr. "Melt Crystallization for Paracetamol Polymorphism." Crystal Growth & Design 19, no. 7 (June 17, 2019): 4070–80. http://dx.doi.org/10.1021/acs.cgd.9b00473.

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4

Gupta, Rakesh K., and Kim F. Auyeung. "Crystallization in polymer melt spinning." Journal of Applied Polymer Science 34, no. 7 (November 20, 1987): 2469–84. http://dx.doi.org/10.1002/app.1987.070340711.

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5

Berezhiani, Malkhaz. "Simulation of melt crystallization kinetics." International Journal of Material Forming 4, no. 4 (January 6, 2011): 421–28. http://dx.doi.org/10.1007/s12289-010-1016-5.

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6

Beierling, T., J. Micovic, P. Lutze, and G. Sadowski. "Using complex layer melt crystallization models for the optimization of hybrid distillation/melt crystallization processes." Chemical Engineering and Processing: Process Intensification 85 (November 2014): 10–23. http://dx.doi.org/10.1016/j.cep.2014.07.011.

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7

Tseng, Chen-Rui, Shoei-Chin Wu, Jeng-Jue Wu, and Feng-Chih Chang. "Crystallization behavior of syndiotactic polystyrene nanocomposites for melt- and cold-crystallizations." Journal of Applied Polymer Science 86, no. 10 (September 25, 2002): 2492–501. http://dx.doi.org/10.1002/app.11020.

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8

Marukovich, E. I., and V. Yu Stetsenko. "Thermodynamic metal crystallization basics." Litiyo i Metallurgiya (FOUNDRY PRODUCTION AND METALLURGY), no. 2 (June 9, 2020): 8–11. http://dx.doi.org/10.21122/1683-6065-2020-2-8-11.

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On the basis of thermodynamic calculations it is shown that crystallization of metals is a thermodynamic process, which takes place mainly at constant temperature. The exception is crystallization at very high cooling rates of the metal melt when the released solidification heat is not enough to stabilize the crystallization temperature of the liquid metal. In crystallization, the specific interfacial surface energy of crystals is not a constant value, but is proportional to their dimensions (bend radius).Nanocrystals of crystallizing phases exist in the metal melt steadily. Metal crystallization aggregates nanocrystals and free metal melt atoms into microcrystals. Mechanism of dendritic crystallization of metals is proposed.

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9

MISHIMA, Naofumi, Rikuo OTA, Takashi WAKASUGI, and Jiro FUKUNAGA. "Crystallization Behavior of Li2O⋅2SiO2 Melt and a Melt Model." Journal of the Ceramic Society of Japan 101, no. 1179 (1993): 1206–9. http://dx.doi.org/10.2109/jcersj.101.1206.

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10

Panine, P., E. Di Cola, M. Sztucki, and T. Narayanan. "Early stages of polymer melt crystallization." Polymer 49, no. 3 (February 2008): 676–80. http://dx.doi.org/10.1016/j.polymer.2007.12.026.

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11

Ulrich, Joachim. "Is Melt Crystallization a Green Technology?" Crystal Growth & Design 4, no. 5 (September 2004): 879–80. http://dx.doi.org/10.1021/cg0300432.

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12

Chernov, A. A., and A. A. Pil’nik. "Melt cavitation at its volumetric crystallization." International Journal of Heat and Mass Transfer 55, no. 1-3 (January 2012): 294–301. http://dx.doi.org/10.1016/j.ijheatmasstransfer.2011.09.017.

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13

Zhang, Jingming, Changning Li, Jason Armstrong, and Shenqiang Ren. "Eutectic melt crystallization of L10-FePt." Chemical Communications 55, no. 5 (2019): 656–58. http://dx.doi.org/10.1039/c8cc08199a.

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14

Zhang, Shuai, Thomas W. Y. Lee, and Albert H. L. Chow. "Crystallization of Itraconazole Polymorphs from Melt." Crystal Growth & Design 16, no. 7 (May 26, 2016): 3791–801. http://dx.doi.org/10.1021/acs.cgd.6b00342.

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15

Buevich, Yu A., and V. V. Mansurov. "Oscillatory crystallization of a binary melt." Journal of Engineering Physics 49, no. 3 (September 1985): 1077–84. http://dx.doi.org/10.1007/bf00872754.

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16

Alfonso, Giovanni C., and Paolo Scardigli. "Melt memory effects in polymer crystallization." Macromolecular Symposia 118, no. 1 (June 1997): 323–28. http://dx.doi.org/10.1002/masy.19971180143.

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17

Ulrich, J., and M. Neumann. "Purification by solid layer melt crystallization." Journal of Thermal Analysis 48, no. 3 (March 1997): 527–33. http://dx.doi.org/10.1007/bf01979499.

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18

Gilbert, Samuel W. "Melt crystallization: Process analysis and optimization." AIChE Journal 37, no. 8 (August 1991): 1205–18. http://dx.doi.org/10.1002/aic.690370810.

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19

Wesson, R. D. "Melt crystallization kinetics of syndiotactic polystryrene." Polymer Engineering and Science 34, no. 14 (July 1994): 1157–60. http://dx.doi.org/10.1002/pen.760341409.

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20

Ziabicki, Andrzej, and Leszek Jarecki. "Crystallization-controlled limitations of melt spinning." Journal of Applied Polymer Science 105, no. 1 (2007): 215–23. http://dx.doi.org/10.1002/app.26121.

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21

Wu, Defeng, Liang Wu, Lanfeng Wu, Bin Xu, Yisheng Zhang, and Ming Zhang. "Comparison Between Isothermal Cold and Melt Crystallization of Polylactide/Clay Nanocomposites." Journal of Nanoscience and Nanotechnology 8, no. 4 (April 1, 2008): 1658–68. http://dx.doi.org/10.1166/jnn.2008.18229.

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The isothermal cold and melt crystallization behavior of intercalated polylactide (PLA)/clay nanocomposites (PLACNs) were studied using differential scanning calorimetry (DSC), polarized optical microscope (POM), X-ray diffractometer (XRD) and Fourier Transform Infra-Red Spectrometer (FT-IR). The results show that the degree of crystallinity of PLA matrix decreases monotonously with increasing clay loadings for both the cold and melt crystallization. The cold crystallized sample shows a double melting behavior and lower melting temperature compared to that of melt-crystallized sample, especially in the presence of clay. The crystallization kinetics was then analyzed by the Avrami and Lauritzen-Hoffman methods for further comparison between these two crystallization behaviors. The results reveal that PLA and its nanocomposites present higher activation energy in melt crystallization than that in cold crystallization due to the reptation of entire polymer chains. The addition of clay facilitates the overall kinetics of melt crystallization, which is attributed to both the nucleation effect of clay and enhanced diffusion of PLA chains. However, for cold crystallization, only very small amounts of clay can slightly increase the kinetics, while larger amounts impede the process. The presence of clay leads to a diffusion-controlled growth of nucleation of PLA matrix in the cold crystallization process and, the hindrance effect of clay hence becomes the dominant factor gradually with increasing clay loadings in the case of high-rate nucleation.

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22

Dong, Beibei, Xiaokang Yang, Youxin Ji, Fengmei Su, Chunguang Shao, and Chuntai Liu. "Polymorph selection during melt crystallization of the isotactic polybutene-1 homopolymer depending on the melt state and crystallization pressure." Soft Matter 16, no. 39 (2020): 9074–82. http://dx.doi.org/10.1039/d0sm01231a.

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This work investigated the crystalline forms obtained from melt crystallization in the isotactic polybutene-1 (iPB-1) homopolymer via manipulation of the temperature at which samples were melted (T_melt) and crystallization pressure (P_cry).

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23

Zhao, Li-Sha, Jun Qiao, Wei Chen, and Yan-hua Cai. "Thermal and mechanical properties of poly(L-lactic acid) nucleated with N,N’-bis(phenyl) 1,4-naphthalenedicarboxylic acid dihydrazide." Polimery 66, no. 4 (April 30, 2021): 234–44. http://dx.doi.org/10.14314/polimery.2021.4.3.

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The modified poly(L-lactic acid) (PLLA) with different contents (0.5−3 wt %) of N,N’-bis(phenyl) 1,4-naphthalenedicarboxylic acid dihydrazide (NAPH) were prepared to evaluate effects of NAPH on melt-crystallization behavior (DSC), thermal degradation (TGA) and mechanical properties of PLLA. The melt-crystallization results demonstrated that NAPH as a heterogeneous organic nucleating agent enhanced crystallization ability of PLLA in cooling, and PLLA/1%NAPH had the best crystallization ability because of the highest onset crystallization temperature and the sharpest melt-crystallization peak. However, melt-crystallization behavior also depended on the cooling rate and final melting temperature, overall, a relative slow cooling rate and low final melting temperature were beneficial for crystallization of PLLA. The cold-crystallization results indicated that NAPH had an inhibition for cold-crystallization process of PLLA, and the cold-crystallization peak shifted towards lower temperature and became wider with an increase of NAPH concentration. The different melting behaviors ofPLLA/NAPH after melt-crystallization and isothermal-crystallization efficiently reflected the accelerating role of NAPH for PLLA crystallization; the double melting peaks formed in heating were thought to result from melting-recrystallization, as well as that a higher crystallization temperature could cause melting peak to appear in higher temperature regions and possess larger melting enthalpy. A comparative analysis on thermal degradation in air illustrated that the addition of NAPH accelerated decomposition of PLLA, but a decrease of onset decomposition temperature was inhibited by the probable interaction of PLLA with NAPH. Moreover, the tensile test showed that NAPH decreased tensile modulus and elongation at break of PLLA, whereas PLLA with low concentration of NAPH had higher tensile strength than pure PLLA.

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24

Huang, Hao, Yan-Hua Zhang, Li-Sha Zhao, Guang-Ming Luo, and Yan-Hua Cai. "Insight into the Role of a Isophthalic Dihydrazide Derivative Containing Piperonylic Acid in Poly(L-lactide) Nucleation: Thermal Performances and Mechanical Properties." Materiale Plastice 57, no. 3 (September 30, 2020): 28–40. http://dx.doi.org/10.37358/mp.20.3.5377.

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This work was aimed at synthesizing the N, N -isophthalic bis(piperonylic acid) dihydrazide (PAID) to be as a new crystallization accelerator for poly(L-lactide) (PLLA), and a detailed investigations of the non-isothermal crystallization, melting behavior, thermal decomposition behavior and mechanical properties of PLLA nucleated by PAID were performed applying differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and electronic tensile tester. The melt-crystallization proved that the PAID could act as a heterogeneous nucleating agent to significantly promote the crystallization in cooling, even the crystallization was still able to be accelerated upon the fast cooling at 50 oC/min. The final melt temperature was another crucial factor for PLLA�s melt crystallization, and when the final melt temperature was 170 oC, the onset crystallization temperature and melt-crystallization enthalpy was almost up to 150 oC and 56.8 J/g upon cooling of 1 oC/min, respectively. Furthermore, the chemical nucleation was proposed to be the nucleation mechanism of PAID for PLLA via the preliminary theoretical calculation. For the cold-crystallization, the addition of PAID exhibited an inhibition for the crystallization of PLLA, but the total crystallization process depended on the heating rate and PAID concentration. The single melting peak after cooling of 1 oC/min indicated that the crystallization had been thoroughly completed in cooling. Additionally, the single melting peak with different locations after full crystallization resulted from the different crystallization temperatures. A comparison in the onset decomposition temperature implied that the presence of PAID only slightly decreased the thermal stability of PLLA. The mechanical testing showed that, in contrast with the elongation at break, the existence of PAID enhanced the tensile strength of PLLA.

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25

Purwantoro, Dwi Utami, Ilma Nugrahani, and Slamet Ibrahim Surantaatmadja. "Studies of preparation, characterization, and solubility of mefenamic acid-nicotinamide co-crystal synthesized by using melt crystallization method." Asian Journal of Pharmaceutical and Clinical Research 10, no. 5 (May 1, 2017): 135. http://dx.doi.org/10.22159/ajpcr.2017.v10i5.15863.

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Objective : The objective of this study is to develop the formation mefenamic acid (MFA) – nicotinamide (NCT) co-crystal by using melt crystallization method and investigate its solubility.Method : Co-crystal was prepared by using melt crystallization method of MFA-NCT (1:2) at (220±3) ° C. The initial co-crystal formation was performed by powder x-ray diffraction (PXRD). The thin layer chromatography (TLC) method was done to confirm the chemical stability of MFA and NCT due to synthesized process. The melt crystallization of MFA-NCT (1:2) was characterized by DSC/TG, Infrared spectrophotometry, and scanning electron microscopy. The solubility of the melt crystallization of MFA-NCT (1:2) was evaluated by incubated the samples in water at 25 °C and shaken for 24 h. The solubility of MFA was measured by UV-Vis spectrophotometer.Result : Characterizations of a co-crystal MFA-NCT (1:2) including PXRD, FTIR, DSC and SEM have indicated the formation of new solid crystal phase that differ from MFA, NCT and its physical mixture. The chromatogram of the TLC study exhibited two spot that corresponds to MFA and NCT. The solubility of the melt crystallization of MFA-NCT (1:2) was 57.97 % higher than MFA solubility.Conclusion : These results suggest that MFA-NCT co-crystal can be synthesized by using melt crystallization method without decomposition of its component and provides an opportunity for the development of MFA solid form.Keywords: co-crystal, mefenamic acid, nicotinamide, melt crystallization, solubility

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26

Jiang, Xiaobin, Wu Xiao, and Gaohong He. "Falling film melt crystallization (III): Model development, separation effect compared to static melt crystallization and process optimization." Chemical Engineering Science 117 (September 2014): 198–209. http://dx.doi.org/10.1016/j.ces.2014.06.027.

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27

Cai, Yan-Hua, Li-Sha Zhao, and Yan-Hua Zhang. "Composites Based Green Poly(L-Lactic Acid) and Dioctyl Phthalate: Preparation and Performance." Advances in Materials Science and Engineering 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/289725.

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The effects of dioctyl phthalate (DOP) on performances of poly(L-lactic acid) (PLLA) were investigated in detail using optical depolarizer, X-ray diffraction, melt index instrument, and electronic tensile tester. Crystallization performance showed that the half time of overall PLLA crystallizationt1/2decreased with increasing of crystallization temperature (80°C to 105°C), but thet1/2of PLLA/DOP composites firstly decreased and then increased, andt1/2of PLLA/DOP exhibited minimum value at 85°C. Compared to neat PLLA, 20%DOP made thet1/2decrease from 7258.3 s to 265.4 s. X-ray diffraction experiment further confirmed that DOP could accelerate the crystallization of PLLA. The fluidity of PLLA/DOP composites indicated that the melt mass flow rate firstly decreased and then greatly increased with increasing of DOP content. The mechanical performance showed that DOP could improve the general mechanical performance, and the elongation at break of PLLA/25%DOP was about 30 times longer than that of neat PLLA.

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28

Clavaguera-Mora, M. T., M. D. Baró, S. Suriñach, and N. Clavaguera. "Crystallization behavior of some melt spun Nd–Fe–B alloys." Journal of Materials Research 5, no. 6 (June 1990): 1201–6. http://dx.doi.org/10.1557/jmr.1990.1201.

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The kinetics of crystallization of four amorphous (or partially amorphous) melt spun Nd–Fe–B alloys induced by thermal treatment is studied by means of differential scanning calorimetry and scanning electron microscopy, In the range of temperatures explored experimentally, the crystallization process is thermally activated and generally proceeds in various stages. The Curie temperature and the crystallization behavior have been measured. The apparent activation energy of crystallization of most of the crystallization stages has been determined for each melt spun alloy. The explicit form of the kinetic equation that best describes the first stage of crystallization has been found. It follows in general the Johnson-Mehl-Avrami-Erofe'ev model, but clear deviations to that model occur for one alloy. Scanning electron microscopy demonstrates that preferentially hetereogeneous nucleation occurs at the ribbon surface which was in contact with the wheel. From crystallization kinetics results the lower part of the experimental time-temperature-transformation curves for all studied alloys are deduced and extrapolated to the high temperature limit of their range of validity, also deduced.

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29

Kirdyashkin, A., and A. Kirdyashkin. ". Influence of crystallization differentiation on the composition of the residual melt for plagioclase under different p-t conditions." Transbaikal State University Journal 26, no. 7 (2020): 53–61. http://dx.doi.org/10.21209/2227-9245-2020-26-7-53-61.

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Crystallization differentiation processes in the melt volume for albite-anorthite solid solution series have been studied. For the albite-anorthite system, the change in the melt composition due to crystallization differentiation is calculated for pressure values P = 6,3 kbar and 1 bar and temperature T = 1410 °C, 1350 and 1300 °C. A calculation technique is presented for composition of the melt remaining after settling of plagioclase particles. The residual melt compositions have been calculated for different initial melt compositions and different P-T parameters. The change in composition due to crystallization differentiation of the melt is the difference in the percentage composition for each oxide on the liquidus line and the initial melt composition. The dimensionless ratios (similarity criteria) for the initial melt composition and the change of the oxide content , , , have been obtained. The change of each oxide percentage is calculated in weight percents and in the dimensionless form (as values of above-mentioned similarity criteria). The initial melt is depleted in different components. The depletion is due to settling of plagioclase particles and melt volume reduction. The latter is the sum of the solid particles and the melt volumes in the intercrystalline spaces of the settled particles’ layer. It is shown that the processes of crystallization differentiation are the sum total of hydrodynamic (geodynamic) and petrological processes. These processes can be studied using the methods of similarity theory. The compositional change in the melt due to crystallization differentiation can be represented in the form of an analytical relationship between the petrological similarity criteria

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30

Baek, Ji-Yeon, Seung-Ho Shin, Sung-Hee Hyun, and Jung-Wook Cho. "Glass structure and crystallization via two distinct thermal histories: Melt crystallization and glass crystallization." Journal of the European Ceramic Society 41, no. 1 (January 2021): 831–37. http://dx.doi.org/10.1016/j.jeurceramsoc.2020.08.036.

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31

Jabarin, S. A. "Crystallization kinetics of polyethylene terephthalate. I. Isothermal crystallization from the melt." Journal of Applied Polymer Science 34, no. 1 (July 1987): 85–96. http://dx.doi.org/10.1002/app.1987.070340107.

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32

Zhang, Hong Ya, Feng Wang, and Hua Cheng. "Effects of Crystallization Degree on Rate during Isothermal Crystallization from PET Melt." Applied Mechanics and Materials 174-177 (May 2012): 1520–23. http://dx.doi.org/10.4028/www.scientific.net/amm.174-177.1520.

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In this study, one new function is defined as change of relative crystallization degree in unit time and named relative crystallization rate (1/min.). The curve of heat flow rate to time is transmitted to that of to . The produced curve was fitted using one high-order polynomial equation with a variable of and the coefficient vector （Ai ,in this paper，the values of i were from 0 to 9）was produced. It was found that, even during the accelerated stage of crystallization from PET melt，both aspects to promote and delay the relative crystallization rate existed， furthermore， both aspects of promotion and delay declined with the crystallization process and appeared “internal exhaustion”.

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33

Vapnik, Ye. "Melt inclusions in granitoids of the Timna Igneous Complex, Southern Israel." Mineralogical Magazine 62, no. 1 (February 1998): 29–40. http://dx.doi.org/10.1180/002646198547440.

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AbstractHigh temperature microthermometry and Scanning Electron Microprobe (SEM) analyses were used to study natural magmatic remnants in quartz crystals in granitoids from the Timna Igneous Complex, southern Israel, and to constrain physicochemical parameters during their crystallization. For the porphyritic granite, alkali granite and quartz monzodiorite, liquidus temperatures are 710–770, 770–830 and 770–840°C, respectively; solidus temperatures are 690–770, 710–790 and 770°C, respectively. Pressures during crystallization and water content in the magmas were determined using the phase diagram of the modal granite system. The determined P-T-conditions are typical for water-saturated granitoid magmas (>4–8 wt.%) generated and crystallized at a shallow crustal level.SEM data on melt inclusions support conclusions of previous investigations on two types of granitoid magmas exposed in the Timna Igneous Complex: the porphyritic and alkali granites. Different trends of crystallization are proposed for these granites. Crystallization of the porphyritic granite started with cotectic crystallization of plagioclase and terminated in residual K-feldspar-rich crystallization; crystallization of the alkali granite took place at higher temperatures, starting with K-rich alkali-feldspar crystallization and terminating in residual Na-rich eutectic crystallization.Parameters not available from other sources — temperature and pressure of the liquidus and solidus stages, water content, trends of crystallization — were obtained for the porphyritic and alkali granites.

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34

Xu, Qing Yan, Lin Wang, Yuan Liu, Zhi Hong Guo, Pei Jie Lin, Yan Ping Wang, and Yi Min Wang. "Study on Non-Isothermal Crystallization Kinetics of PBT with High Melt Flow Index." Advanced Materials Research 487 (March 2012): 58–63. http://dx.doi.org/10.4028/www.scientific.net/amr.487.58.

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The non-isothermal crystallization process of PBT with high melt flow index has been investigated by DSC, and the nonisothermal crystallization process of PBT with high melt flow index was studied by Ozawa equation and Jeziorny equation respectively. It was found that Ozawa equation, rather than Jeziorny equation, could appropriately be applied to study the non-isothermal crystallization process of PBT with high melt flow index. The Avrami index, obtained by Ozawa equation, varied between 1.06-1.80 with the change in temperature.

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35

Kirdyashkin, А., and A. Kirdyashkin. "Forces generating crystallization differentiation, and the evolution of the melt composition on the example of plagioclase." Transbaikal State University Journal 26, no. 7 (2020): 44–52. http://dx.doi.org/10.21209/2227-9245-2020-26-7-44-52.

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Crystallization differentiation processes in the melt volume are investigated for albite-anorthite continuous solid solution series. It has shown that crystallization differentiation occurs in the isothermal melt volume due to hydrodynamic instability of the melt/solid particles system. The time of particle settling in a 10 cm thick melt layer is estimated for different particle sizes. In terrestrial conditions, the existence of large melt volumes with long lifetime is possible in the case of a long-lived heat source of high thermal power. This source is a mantle thermochemical plume with a mushroom-shaped head. The particle settling time is estimated for the melt layer thickness, i. e. plume head thickness equal to 10 km. A calculation technique is presented for composition of the melt remaining after settling of plagioclase particles. The results of calculations of changes in the melt composition due to crystallization differentiation at a temperature T = 1410 °C and a pressure P = 6,3 kbar are presented. For a melt whose composition corresponds to N 47,5 (weight percentage of anorthite is 47,5 %), the oxide content in the settled plagioclase, the composition of the melt in its intercrystalline spaces, and the residual melt composition are calculated. At constant temperature, the crystallization differentiation of the melt whose composition corresponds to plagioclase leads to the compositional changes in the initial melt. Calculations of the melt composition have shown that the melt is depleted in anorthite component owing to settling of plagioclase particles. The composition of plagioclase therewith shifts to the liquidus line, reaching its limit on this line

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36

Chen, Aimei, Jiawen Zhu, Bin Wu, Kui Chen, and Lijun Ji. "Continuous Melt Suspension Crystallization of Phosphoric Acid." Journal of Crystallization Process and Technology 02, no. 03 (2012): 111–16. http://dx.doi.org/10.4236/jcpt.2012.23014.

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37

Nakae, Hideo, and Noriyuki Kiuchi. "Crystallization of Fibrous Mullite from Glass Melt." Journal of the Japan Institute of Metals 57, no. 2 (1993): 195–202. http://dx.doi.org/10.2320/jinstmet1952.57.2_195.

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38

Schlossmacher, P., N. Boucharat, H. Rösner, and A. V. Shelyakov. "Crystallization studies of amorphous melt-spun Ti50Ni25Cu25." Journal de Physique IV (Proceedings) 112 (October 2003): 731–34. http://dx.doi.org/10.1051/jp4:2003986.

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39

RADHAKRISHNAN*, K. B., and A. R. BALAKRISHNAN*. "KINETICS OF MELT CRYSTALLIZATION IN FALLING FILMS." Chemical Engineering Communications 171, no. 1 (February 1999): 29–53. http://dx.doi.org/10.1080/00986449908912748.

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40

Kim, Kwang-Joo, and Alfons Mersmann. "Direct Contact Heat Transfer in Melt Crystallization." JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 31, no. 4 (1998): 527–35. http://dx.doi.org/10.1252/jcej.31.527.

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41

Crowder, C. E., J. U. Otaigbe, M. A. Barger, R. L. Sammler, B. C. Monahan, and C. J. Quinn. "Melt crystallization of zinc alkali phosphate glasses." Journal of Non-Crystalline Solids 210, no. 2-3 (March 1997): 209–23. http://dx.doi.org/10.1016/s0022-3093(96)00588-1.

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42

Diepen, P. J., O. S. L. Bruinsma, and G. M. van Rosmalen. "Crystal Size Engineering in Melt Suspension Crystallization." Chemical Engineering Research and Design 75, no. 2 (February 1997): 171–75. http://dx.doi.org/10.1205/026387697523417.

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43

Kim, Kwang-Joo, and A. Mersmann. "Melt Crystallization with Direct Contact Cooling Techniques." Chemical Engineering Research and Design 75, no. 2 (February 1997): 176–82. http://dx.doi.org/10.1205/026387697523426.

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44

Chernov, A. A., and A. A. Pil'nik. "Melt crystallization at large deviations from equilibrium." Materials Today: Proceedings 16 (2019): 144–50. http://dx.doi.org/10.1016/j.matpr.2019.05.241.

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45

Melikhov, I. V., and A. Pamiatnikh. "Dendrite relay crystallization of the dispersed melt." Journal of Crystal Growth 102, no. 4 (June 1990): 885–90. http://dx.doi.org/10.1016/0022-0248(90)90856-g.

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Gao, J., T. Volkmann, S. Yang, S. Reutzel, D. M. Herlach, and X. P. Song. "Crystallization of Nd2Fe17Bx from stoichiometric melt composition." Journal of Alloys and Compounds 433, no. 1-2 (May 2007): 356–62. http://dx.doi.org/10.1016/j.jallcom.2006.06.090.

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Vitorino, Maria B. C., Pâmela B. Cipriano, Renate M. R. Wellen, Eduardo L. Canedo, and Laura H. Carvalho. "Nonisothermal melt crystallization of PHB/babassu compounds." Journal of Thermal Analysis and Calorimetry 126, no. 2 (May 18, 2016): 755–69. http://dx.doi.org/10.1007/s10973-016-5514-7.

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Hiltunen, E. J., M. Kesti, Arja Ulvinen, and L. Takàcs. "Crystallization of melt-spun Fe81P19 metallic glass." Journal of Materials Science Letters 7, no. 5 (May 1988): 441–43. http://dx.doi.org/10.1007/bf01730682.

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Gibson, M. A., and G. W. Delamore. "Surface crystallization in melt-spun metallic glasses." Journal of Materials Science 23, no. 4 (April 1988): 1164–70. http://dx.doi.org/10.1007/bf01154574.

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Ding, Qian, Michelina Soccio, Nadia Lotti, Dario Cavallo, and René Androsch. "Melt Crystallization of Poly(butylene 2,6-naphthalate)." Chinese Journal of Polymer Science 38, no. 4 (November 15, 2019): 311–22. http://dx.doi.org/10.1007/s10118-020-2354-5.

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