Kontturi Katri S, Holappa Susanna, Kontturi Eero, Johansson Leena-Sisko, Hyvärinen Sari, Peltonen Soili, Laine Janne
Laboratory of Forest Products Chemistry, Helsinki University of Technology, P.O. Box 6300, FIN-02015 TKK, Finland.
J Colloid Interface Sci. 2009 Aug 1;336(1):21-9. doi: 10.1016/j.jcis.2009.03.026. Epub 2009 Mar 31.
Arrangements of cationic starches hydrophobized by acetylation (CS-acet) deposited from aqueous electrolyte solutions onto hydrophilized and hydrophobized silica surfaces were investigated by atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and contact angle measurements. The influence of electrolyte composition, acetylation degree of cationic starch (DS(ACET)), and deposition method was examined. On a hydrophobic substrate, CS-acet formed an open film with structure strongly dependent on DS(ACET) and electrolyte composition of the solution. On a hydrophilic substrate, acetylation increased the hydrophobicity of the film when the starch was deposited by adsorbing. When deposition was made by spin coating, i.e., the CS-acet was forced onto the substrate, the hydrophobic tuning by acetylation was lost. The films deposited by spin coating were thicker and considerably rougher than those deposited by adsorbing.
通过原子力显微镜(AFM)、X射线光电子能谱(XPS)和接触角测量,研究了由乙酰化疏水化的阳离子淀粉(CS-acet)从水性电解质溶液沉积到亲水和疏水二氧化硅表面的排列情况。研究了电解质组成、阳离子淀粉的乙酰化程度(DS(ACET))和沉积方法的影响。在疏水基底上,CS-acet形成了一种开放膜,其结构强烈依赖于DS(ACET)和溶液的电解质组成。在亲水基底上,当淀粉通过吸附沉积时,乙酰化增加了膜的疏水性。当通过旋涂进行沉积时,即CS-acet被强制沉积到基底上,乙酰化的疏水调节作用消失。通过旋涂沉积的膜比通过吸附沉积的膜更厚且粗糙度更大。