scholarly journals Studies on the prevention of calcium carbonate scale deposition by the addition of polyelectrolytes. II. Effect of molecular weight and chemical composition of polyelectrolyte on the inhibition of scale deposition.

1988 ◽  
pp. 266-271
Author(s):  
Masaru OKAMOTO ◽  
Shiro HAYASHI
Heliyon ◽  
2020 ◽  
Vol 6 (3) ◽  
pp. e03506
Author(s):  
K. Palanisamy ◽  
K. Sanjiv Raj ◽  
S. Bhuvaneswari ◽  
M. Rajasekaran ◽  
V.K. Subramanian

1968 ◽  
Vol 7 (1) ◽  
pp. 59-65 ◽  
Author(s):  
David Hasson ◽  
Mordecai Avriel ◽  
William Resnick ◽  
Tzvi Rozenman ◽  
Shlomo Windreich

Author(s):  
Xiuhua Si ◽  
Jinxiang Xi ◽  
Xihai Tao

Scale deposition on heat transfer surfaces from water containing dissolved salts reduces the efficiency and performance of heat transfer equipments considerably. Scale deposition could be reduced through physical or chemical methods. In some cases, chemical methods are unacceptable, due to cost, contamination issues, etc. In these cases, physical methods are the only acceptable choices. Surface energy of the heat exchanger has been thought to be one important factor affecting the growth of fouling. Applying low energy surfaces to reduce scaling deposition is one of the effective physical methods. The formation and the characteristics of the calcium carbonate scaling on low energy surfaces have been studied in this paper. Copper and stainless steel surfaces were modified by micro-scale (μm thickness) PTFE (Poly-Tetrofluorethylene) films and nano-scale (nm thickness) thiolate SAMs (Self-Assembly Monolayers). The resulting surface energy of PTFE films and SAMs layers based on copper and stainless steel were significantly reduced compared with the original metal surfaces. To study the formation of the calcium carbonate scale, a recirculation cooling water system was used. The formation of the calcium carbonate scale on PTFE surfaces, SAMs surfaces, polished copper surfaces, and polished stainless steel surfaces were investigated respectively. The rate of calcium carbonate scale formation was decreased and the induction period was prolonged with the decrease of the heat transfer surface energy. The characteristics of the calcium carbonate scale formed on heat transfer surfaces with different surface energies was analyzed with fractal theory after taking photos with SEM (Scanning Electron Microscope). The fractal dimension values of the calcium carbonate scale on different heat transfer surfaces with different surface energies were calculated. The results showed that the fractal dimension values of calcium carbonate scale formed on lower energy PTFE and Cu-SAMs surfaces were greater than those that formed on higher energy Cu and stainless steel surfaces. Results of this study clearly indicated that the formation of calcium carbonate scaling on lower energy heat transfer surfaces is reduced.


2016 ◽  
Vol 75 (2) ◽  
pp. 255-262 ◽  
Author(s):  
Zhanhui Shen ◽  
Jialu Shi ◽  
Shuzhan Zhang ◽  
Jing Fan ◽  
JianSheng Li

The mixture of 1-hydroxyethane-1,1-diphosphonic acid (HEDP), and polyacrylic acid (PAA) and synthesized hydrolyzed polymaleic anhydride (HPMA) was optimized by using simplex lattice of Design-Expert software through calcium carbonate precipitation method. The optimum mass ratio of HEDP, PAA and synthesized HPMA was obtained at 10/10/80, which showed excellent performance on controlling calcium carbonate deposition. The antiscale efficiency of the optimum mixture was 84% and 95%, respectively, in the calcium carbonate precipitation test and the calcium carbonate scale deposit test. The optimum mixture could disturb the crystal growth of calcium carbonate and then affect the morphology and crystal structure of the calcium carbonate precipitates.


Desalination ◽  
1968 ◽  
Vol 5 (1) ◽  
pp. 107-119 ◽  
Author(s):  
D. Hasson ◽  
M. Avriel ◽  
W. Resnick ◽  
T. Rozenman ◽  
S. Windreich

2018 ◽  
Author(s):  
Khadouja Harouaka ◽  
Yi Tsung Lu ◽  
Gedeng Ruan ◽  
H. Dushanee Sriyarathne ◽  
Wei Li ◽  
...  

Author(s):  
Xiuhua Si ◽  
Sungmin Youn ◽  
Jinxiang Xi

Scale deposition (or fouling) on metal surfaces from salt-containing water considerably reduces the efficiency and performance of heat transfer equipments. In industrial practices, scale deposition could be reduced through physical or chemical methods. However, in some cases chemical methods are unpractical due to cost and contamination issues, rendering the physical methods the only feasible options. The objective of this study was to evaluate the effectiveness of two physical treatments in reducing scale depositions. One is to decrease the surface energy of the heat exchanger wall through surface modification; the other one is to change the crystallography of the small solid particles formed in the solution by applying a magnetic field. For the first method, the scale deposition on PTFE surfaces, SAMs (self-assembly monolayers) surfaces, polished copper surfaces, and polished stainless steel surfaces are investigated respectively. Copper and stainless steel surfaces were modified by micro-scale (μm thickness) PTFE (Poly-Tetrofluorethylene) films and nano-scale (nm thickness) thiolate SAMs. The surface energy of PTFE films and SAMs layers based on copper and stainless steel were significantly reduced compared with the untreated metal surfaces. To study the magnetic treatment effect on the formation of the calcium carbonate scale, a magnetic field up to 0.6 T was implemented in a simulated recirculation cooling water system. A large number of experiments were performed to study the effects of fluid velocity, heat flux, and the bulk concentration of the solution on the fouling rate and induction period of calcium carbonate on various modified surfaces. The experiments showed that the formation rate of the calcium carbonate scale was decreased on modified surfaces and the induction period was prolonged with the decrease of the surface energy. The study also showed that the nucleation and nucleate growth of calcium carbonate particles were enhanced through magnetic water treatment. In addition, using a higher flow rate and/or filtration of suspended calcium carbonate particles achieves a longer induction period.


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