Characterizing the Adsorption of Poly(vinyl alcohol) on Colloidal Silica with Aggregation-Induced Emission Fluorophore

被引:9
作者
Zhu, Zhichao [1 ,4 ]
Dong, Xiaobiao [2 ]
Zhang, Guanxin [2 ]
Xiang, Junfeng [3 ]
Qiu, Dong [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Key Lab Organ Solids, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Anal & Test Ctr, Inst Chem, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
ANGLE NEUTRON-SCATTERING; DYNAMIC LIGHT-SCATTERING; SURFACE POLYMER LAYER; AROMATIC AMINO-GROUPS; SHEAR; PARTICLE; SUSPENSIONS; FLOW; MICROSTRUCTURE; DISPERSIONS;
D O I
10.1021/acs.langmuir.6b00288
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The adsorption of polymer on colloidal particle has significant influence on colloid structure and dynamics. Here we introduce a new method to monitor the adsorption in situ, based on the different emission behavior of aggregation induced emission (AIE) luminogen in different micro environments. Poly(vinyl alcohol) (PVA) and colloidal silica (CS) were used as a model system. It was found that AIE molecules exhibited extremely low fluorescence intensity in water and PVA solution, while their emission efficiency was enhanced when adsorbed on CS, and became significantly boosted when PVA was adsorbed on CS at the same time. The fluorescence intensity increases with the amount of added PVA and reaches a saturation point, which is earlier than that obtained by the well-established solvent relaxation NMR method, due to their different sensitivities for adsorption segments in specific conformation. This new method is advantageous in quick response, where the measurement can be finished within 2 min, while others usually take hours. Therefore, it is expected that this new method may be used to monitor the dynamical adsorption process of polymer on colloidal particles.
引用
收藏
页码:2145 / 2150
页数:6
相关论文
共 30 条
[1]   Reversible shear thickening in monodisperse and bidisperse colloidal dispersions [J].
Bender, J ;
Wagner, NJ .
JOURNAL OF RHEOLOGY, 1996, 40 (05) :899-916
[2]   RELAXATION EFFECTS IN NUCLEAR MAGNETIC RESONANCE ABSORPTION [J].
BLOEMBERGEN, N ;
PURCELL, EM ;
POUND, RV .
PHYSICAL REVIEW, 1948, 73 (07) :679-712
[3]   Formation of a highly ordered colloidal microstructure upon flow cessation from high shear rates [J].
Butera, RJ ;
Wolfe, MS ;
Bender, J ;
Wagner, NJ .
PHYSICAL REVIEW LETTERS, 1996, 77 (10) :2117-2120
[4]   Required polymer lengths per precipitated protein molecule in protein-polymer interaction [J].
Capito, Florian ;
Kolmar, Harald ;
Stanislawski, Bernd ;
Skudas, Romas .
JOURNAL OF POLYMER RESEARCH, 2014, 21 (02)
[5]   EFFECTS OF DIFFUSION ON FREE PRECESSION IN NUCLEAR MAGNETIC RESONANCE EXPERIMENTS [J].
CARR, HY ;
PURCELL, EM .
PHYSICAL REVIEW, 1954, 94 (03) :630-638
[6]   Surfactant-Mediated Desorption of Polymer from the Nanoparticle Interface [J].
Cattoz, Beatrice ;
Cosgrove, Terence ;
Crossman, Martin ;
Prescott, Stuart W. .
LANGMUIR, 2012, 28 (05) :2485-2492
[7]   Competition between Polymers for Adsorption on Silica: A Solvent Relaxation NMR and Small-Angle Neutron Scattering Study [J].
Cooper, Catherine L. ;
Cosgrove, Terence ;
van Duijneveldt, Jeroen S. ;
Murray, Martin ;
Prescott, Stuart W. .
LANGMUIR, 2013, 29 (41) :12670-12678
[8]   POLYMER ADSORPTION - THE EFFECT OF THE RELATIVE SIZES OF POLYMER AND PARTICLE [J].
COSGROVE, T ;
GRIFFITHS, PC ;
LLOYD, PM .
LANGMUIR, 1995, 11 (05) :1457-1463
[9]   NUCLEAR-MAGNETIC-RESONANCE STUDIES OF ADSORBED POLYMER LAYERS [J].
COSGROVE, T ;
GRIFFITHS, PC .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 1992, 42 :175-204
[10]   Effects of surfactants and electrolytes on adsorbed layers and particle stability [J].
Flood, Charlie ;
Cosgrove, Terence ;
Espidel, Youssef ;
Howell, Ian ;
Revell, Patricia .
LANGMUIR, 2008, 24 (14) :7323-7328