Evaluation of the effects of sodium laurate on calcium carbonate precipitation: Characterization and optimization studies

被引:21
作者
Polat, Sevgi [1 ]
机构
[1] Marmara Univ, Fac Engn, Dept Chem Engn, TR-34722 Istanbul, Turkey
关键词
Calcium carbonate; Crystallization; Experimental design; Sodium laurate; Vaterite; CRYSTALLIZATION; ULTRASONICATION; TRANSFORMATION; POLYMORPHS; ARAGONITE; DESIGN;
D O I
10.1016/j.jcrysgro.2018.12.017
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The effects of using sodium laurate as an additive on the calcium carbonate precipitation process and on the product characteristics were investigated experimentally through X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), particle size, and Brunauer, Emmett, and Teller (BET) analysis. The characterization results showed that the addition of sodium laurate to the crystallization media contributed to the formation of the vaterite form of calcium carbonate. The average particle size changed from 32 mu m to 14 mu m with increasing sodium laurate concentration. The SEM results suggested that the presence of sodium laurate had a strong influence on the calcium carbonate morphology and the crystals transformed from cubic to ellipsoidal shape. This study also emphasized the application of a statistical tool, response surface methodology (RSM) based on Box-Behnken design (BBD), to determine the optimal conditions for the production of calcium carbonate crystals with high specific surface area. The precipitation process was performed using different combinations of additive concentration, pH, and temperature, which are the main parameters affecting this process. The effects of these parameters on the responses, i.e., average particle size, surface area, and the relative fraction of vaterite, were investigated. Second-order polynomial equations were developed for the particle size, specific surface area and vaterite composition to correlate the parameters. The maximum specific surface area (12.430 mg/g) was obtained under the optimal conditions of 50 ppm additive concentration, pH 8.5, and 40 degrees C.
引用
收藏
页码:8 / 18
页数:11
相关论文
共 32 条
[21]   CRYSTAL-STRUCTURE OF CACO3(II), A HIGH-PRESSURE METASTABLE PHASE OF CALCIUM-CARBONATE [J].
MERRILL, L ;
BASSETT, WA .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1975, 31 (FEB15) :343-+
[22]   Formation of thin calcium carbonate films on chitosan biopolymer substrates [J].
Payne, Simon R. ;
Heppenstall-Butler, Mary ;
Butler, Michael F. .
CRYSTAL GROWTH & DESIGN, 2007, 7 (07) :1262-1276
[23]   Composition of Calcium Carbonate Polymorphs Precipitated Using Ultrasound [J].
Price, Gareth J. ;
Mahon, Mary F. ;
Shannon, James ;
Cooper, Crispin .
CRYSTAL GROWTH & DESIGN, 2011, 11 (01) :39-44
[25]   Enhanced Polymer Induced Precipitation of Polymorphous in Calcium Carbonate: Calcite Aragonite Vaterite Phases [J].
Siva, T. ;
Muralidharan, S. ;
Sathiyanarayanan, S. ;
Manikandan, E. ;
Jayachandran, M. .
JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS, 2017, 27 (03) :770-778
[26]   The effect of different amino acids on spontaneous precipitation of calcium carbonate polymorphs [J].
Stajner, Lara ;
Kontrec, Jasminka ;
Dzakula, Branka Njegic ;
Maltar-Strmecki, Nadica ;
Plodinec, Milivoj ;
Lyons, Daniel M. ;
Kralj, Damir .
JOURNAL OF CRYSTAL GROWTH, 2018, 486 :71-81
[27]   Polymorphism of CaCO3 precipitated in a constant-composition environment [J].
Tai, CY ;
Chen, FB .
AICHE JOURNAL, 1998, 44 (08) :1790-1798
[28]   Quantitative analysis of synthetic calcium carbonate polymorphs using FT-IR spectroscopy [J].
Vagenas, NV ;
Gatsouli, A ;
Kontoyannis, CG .
TALANTA, 2003, 59 (04) :831-836
[29]   INFRARED STUDIES OF ARAGONITE, CALCITE, AND VATERITE TYPE STRUCTURES IN BORATES, CARBONATES, AND NITRATES [J].
WEIR, CE ;
LIPPINCOTT, ER .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1961, A 65 (03) :173-+
[30]   Exploring the Influence of Reaction Parameters on the Preparation of Calcium Carbonate by Spontaneous Precipitation [J].
Wu, Zhi Gang ;
Wang, Jian ;
Guo, Yang ;
Jia, Yan Rong .
CRYSTAL RESEARCH AND TECHNOLOGY, 2018, 53 (04)