scholarly journals Ultrasound-assisted intensified crystallization of L-glutamic acid: Crystal nucleation and polymorph transformation

2020 ◽  
Vol 68 ◽  
pp. 105227 ◽  
Author(s):  
Chen Fang ◽  
Weiwei Tang ◽  
Songgu Wu ◽  
Jingkang Wang ◽  
Zhenguo Gao ◽  
...  
2012 ◽  
Vol 463-464 ◽  
pp. 36-40 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu

Large-sized hydroxyapatite (HA) crystals with different morphologies, such as whisker-like, tubular and plate-form shape were prepared at different hydrothermal temperatures. Reaction solutions with small concentration of Ca2+, PO43- and OH- ions were used for HA synthesis. Phase identifications and morphological characterizations indicated that HA crystal grew along c axis under the modulation of glutamic acid adsorbent. The formation mechanism was explained according to the interfacial structures between glutamic acid and HA, as well as thermodynamic and kinetic considerations of crystal nucleation and growth. Understanding the evolution of crystal morphology in a specified reaction solution might favor to control the shape of crystals by the hydrothermal method.


1974 ◽  
Vol 3 (6) ◽  
pp. 551-554
Author(s):  
Minoru Ohki ◽  
Akio Takenaka ◽  
Hirotaka Shimanouchi ◽  
Yoshio Sasada

2015 ◽  
Vol 179 ◽  
pp. 451-461 ◽  
Author(s):  
Shuqin Jiang ◽  
Haihua Pan ◽  
Yan Chen ◽  
Xurong Xu ◽  
Ruikang Tang

Generally, a solution nucleation model is used to study biomineralization kinetics. However, we found that the amorphous calcium phosphate (ACP)-mediated hydroxyapatite (HAP) nucleation in simulated body fluids (SBF) had a different profile from the linear relationship between ln J and ln−2 S (J, nucleation rate; S, supersaturation). This behaviour was alternatively explained by a developed heterogeneous nucleation theory, which indicated that HAP was nucleated at the ACP–solution interface via a polymorph transformation. Based upon this new model, we demonstrated experimentally that the embedded polymer molecules inside ACP were inert on HAP nucleation kinetics; rather, the polymers adsorbed on ACP surface could inhibit HAP nucleation from ACP. It further confirmed the heterogeneous nucleation pathway of HAP on the precursor phase. The present study provides an in-depth understanding of HAP formation for ACP-mediated crystallization.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Rubén Sierra-Ávila ◽  
Marissa Pérez-Alvarez ◽  
Janett Valdez-Garza ◽  
Carlos Alberto Avila-Orta ◽  
Enrique Javier Jiménez-Regalado ◽  
...  

A nylon 6 nanocomposite with copper nanoparticles processed by ultrasound-assisted extrusion was prepared at concentrations between 0.01 and 0.50 wt.%, and its thermal and mechanical properties were determined. The presence of the crystalline phase α (α1 and α2) in the polymer matrix was confirmed by X-ray diffraction, and the presence of the α2 phase showed a greater increase than the α1 phase as a function of the copper nanoparticle concentration. This process was attributed to secondary crystallization. Furthermore, it was determined that the chemical composition of the nanoparticles is a blend of metallic copper and cupric oxide. The formation of copper nanowires was observed by scanning electron microscopy, and the concentration of 0.10% exhibited the best dispersion in comparison with the other concentrations. The melting temperature of the nanocomposites underwent a slight decrease in comparison with the nylon 6, while thermal stability, crystallization temperature, and crystallinity were increased in relation to the pure polymer. This behavior is attributed to an efficient dispersion of the nanoparticles and to their functionality as crystal nucleation sites. For the 0.10% concentration nanocomposite, higher mechanical properties were obtained; tensile strength increased by 8.9%, and the tensile modulus increased by 25.4%; as a consequence, elongation at break was 62% less than that of the polymer matrix.


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