Surface modification of CaCO3 nanoparticles by alkylbenzene sulfonic acid surfactant

被引:54
作者
Song, EunMin [1 ]
Kim, Do Won [1 ]
Kim, Byeorig Jo [2 ]
Lim, JongChoo [1 ]
机构
[1] Dongguk Univ Seoul, Dept Chem & Biochem Engn, Seoul 100715, South Korea
[2] AK ChemTech, Cent Res Lab, Taejon, South Korea
基金
新加坡国家研究基金会;
关键词
CaCO3; surface; Wetting property; Anionic surfactant; Hydrophobicity; Adsorption; QUARTZ-CRYSTAL MICROBALANCE; CALCIUM-CARBONATE; IN-SITU; QCM-D; PHASE INVERSION; ADSORPTION; ACTIVATION; PARTICLES; MULTILAYERS; COMPOSITES;
D O I
10.1016/j.colsurfa.2014.07.020
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Surface modification of CaCO3 nanoparticles by two kinds of anionic surfactants, such as linear alkylbenzene sulfonic acid (LABSA) and branched alkylbenzene sulfonic acid (BABSA), was investigated by a quartz crystal microbalance with dissipation monitoring (QCM-D) measurement and contact angle analysis. Basically, both surfactant systems showed the same trend in the measurements of QCM-D and contact angle. Contact angle measurement has shown that CaCO3 surface becomes more hydrophobic as surfactant concentration increases. However, the use of excess surfactant has led to the reverse change in surface property of CaCO3 particles from hydrophobic to hydrophilic. QCM-D measurement using a quartz crystal coated with CaCO3 revealed that monolayer adsorption of surfactant molecules at the particle water interface occurs in a low surfactant concentration region and the thickness of forming molecular layers was found to be in the order of the length of a single surfactant molecule. On the other hand, both mass of adsorbed surfactant molecules and the thickness of molecular layers indicated bilayer adsorption of surfactant molecules in a high surfactant concentration region, which evidently resulted in an increase in hydrophilicity of CaCO3 surface. Visual floating test has shown a good agreement with measurements of contact angle and QCM-D. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 43 条
[1]   Cellulose nanofibrils-adsorption with poly(amideamine) epichlorohydrin studied by QCM-D and application as a paper strength additive [J].
Ahola, Susanna ;
Osterberg, Monika ;
Laine, Janne .
CELLULOSE, 2008, 15 (02) :303-314
[2]   Quartz crystal microbalance-with dissipation monitoring (QCM-D) for real time measurements of blood coagulation density and immune complement activation on artificial surfaces [J].
Andersson, M ;
Andersson, J ;
Sellborn, A ;
Berglin, M ;
Nilsson, B ;
Elwing, H .
BIOSENSORS & BIOELECTRONICS, 2005, 21 (01) :79-86
[3]   Interactions of PAMAM Dendrimers with SDS at the Solid-Liquid Interface [J].
Arteta, Marianna Yanez ;
Eltes, Felix ;
Campbell, Richard A. ;
Nylander, Tommy .
LANGMUIR, 2013, 29 (19) :5817-5831
[4]   Particles as surfactants - similarities and differences [J].
Binks, BP .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2002, 7 (1-2) :21-41
[5]   Double phase inversion of emulsions stabilized by a mixture of CaCO3 nanoparticles and sodium dodecyl sulphate [J].
Cui, Z. -G. ;
Shi, K. -Z. ;
Cui, Y. -Z. ;
Binks, B. P. .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 329 (1-2) :67-74
[6]   Multiple Phase Inversion of Emulsions Stabilized by in Situ Surface Activation of CaCO3 Nanoparticles via Adsorption of Fatty Acids [J].
Cui, Z. -G. ;
Cui, C. -F. ;
Zhu, Y. ;
Binks, B. P. .
LANGMUIR, 2012, 28 (01) :314-320
[7]   Aqueous Foams Stabilized by in Situ Surface Activation of CaCO3 Nanoparticles via Adsorption of Anionic Surfactant [J].
Cui, Z-G. ;
Cui, Y-Z. ;
Cui, C-F. ;
Chen, Z. ;
Binks, B. P. .
LANGMUIR, 2010, 26 (15) :12567-12574
[8]   Interaction of silane coupling agents with CaCO3 [J].
Demjen, Z ;
Pukanszky, B ;
Foldes, E ;
Nagy, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 190 (02) :427-436
[9]   Evaluation of interfacial interaction in polypropylene surface treated CaCO3 composites [J].
Demjen, Z ;
Pukanszky, B ;
Nagy, J .
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING, 1998, 29 (03) :323-329
[10]   Possible coupling reactions of functional silanes and polypropylene [J].
Demjén, Z ;
Pukánszky, B ;
Nagy, J .
POLYMER, 1999, 40 (07) :1763-1773