scholarly journals Bubble-Size Evolution during Polyurethane Foam Expansion.

2016 ◽  
Author(s):  
Lisa Ann Mondy ◽  
Christine Cardinal Roberts ◽  
Grant Soehnel ◽  
Casper Brady ◽  
Bion Shelden ◽  
...  
2020 ◽  
Author(s):  
Rekha Rao ◽  
Lisa Mondy ◽  
Weston Ortiz ◽  
Christine Roberts ◽  
Melissa Soehnel

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Karina D. Martínez ◽  
Cecilio Carrera Sanchez

The objective of this work was to determine the effects of high intensity ultrasound application on the foaming properties of soy protein-polysaccharides mixed solutions. To this end, foaming parameters during foam formation were analyzed. The samples were sonicated for 20 min using ultrasonic processor Vibra Cell Sonics, and model VCX 750 at a frequency of 20 kHz and an amplitude of 20%. The foams were produced by a Foamscan instrument. The evolution of the bubble size change in the foam was also determined by a second CCD camera. For all foamed systems, at two pHs 3 and 7, Foam expansion and Relative Foam Conductivity showed a great increase after ultrasonic treatment. Other parameters studied did not show difference. On the other hand, Final Time of Foaming and the Total Gas Volume incorporation for foams formation were correlated with the Relative Foam Conductivity decrease and the Foam Expansion increase when HIUS were applied in every system. Comparative bubble size and shape during the foam formation according to the treatments and pH used confirmed the parameters results.


2018 ◽  
Vol 137 ◽  
pp. 461-466 ◽  
Author(s):  
Hongzheng Zhu ◽  
Alejandro López Valdivieso ◽  
Jinbo Zhu ◽  
Shaoxian Song ◽  
Fanfei Min ◽  
...  

Procedia CIRP ◽  
2017 ◽  
Vol 66 ◽  
pp. 62-67 ◽  
Author(s):  
Jürgen Tröltzsch ◽  
Kay Schäfer ◽  
Dariusz Niedziela ◽  
Ikenna Ireka ◽  
Konrad Steiner ◽  
...  

2018 ◽  
Vol 175 ◽  
pp. 20-35 ◽  
Author(s):  
Rekha Rao ◽  
Lisa Mondy ◽  
David Noble ◽  
Victor Brunini ◽  
Kevin Long ◽  
...  

AIChE Journal ◽  
2022 ◽  
Author(s):  
Christine Roberts ◽  
Lisa Mondy ◽  
Grant Soehnel ◽  
Casper Brady ◽  
Bion Shelden ◽  
...  

2015 ◽  
Vol 19 (sup8) ◽  
pp. S8-149-S8-156 ◽  
Author(s):  
H. Abdessalam ◽  
B. Abbès ◽  
Y. Li ◽  
Y. Q. Guo ◽  
E. Kwassi ◽  
...  

Author(s):  
Harry A. Atwater ◽  
C.M. Yang ◽  
K.V. Shcheglov

Studies of the initial stages of nucleation of silicon and germanium have yielded insights that point the way to achievement of engineering control over crystal size evolution at the nanometer scale. In addition to their importance in understanding fundamental issues in nucleation, these studies are relevant to efforts to (i) control the size distributions of silicon and germanium “quantum dots𠇍, which will in turn enable control of the optical properties of these materials, (ii) and control the kinetics of crystallization of amorphous silicon and germanium films on amorphous insulating substrates so as to, e.g., produce crystalline grains of essentially arbitrary size.Ge quantum dot nanocrystals with average sizes between 2 nm and 9 nm were formed by room temperature ion implantation into SiO2, followed by precipitation during thermal anneals at temperatures between 30°C and 1200°C[1]. Surprisingly, it was found that Ge nanocrystal nucleation occurs at room temperature as shown in Fig. 1, and that subsequent microstructural evolution occurred via coarsening of the initial distribution.


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