Study on the preparation and characterization of high-dispersibility nanosilica

2016 ◽  
Vol 23 (4) ◽  
pp. 401-406 ◽  
Author(s):  
Yu Guo ◽  
Yan-qing Wang ◽  
Zhong-ming Wang ◽  
Cheng-jin Shen

AbstractThis article reports on experiments aimed at modifying nanosilica powder by adding a silane coupling agent, KH570, to achieve high dispersibility and strengthen the compatibility and interface bonding between it and the organic phases. Experiments were first done to prepare the common nanosilica powder, dried at 120°C for 4 h in a drying oven; second, an ethanol/water solution (volume ratio 11:1, total volume not more than two-thirds of the capacity of the flask) was blended in a three-necked flask with a reflux condenser and magnetic stirring; third, appropriate amount of dried nanosilica powder and appropriate mass fraction ratio of the silane coupling agent KH570 were added into the ethanol/water solution, and the pH of the mixture was adjusted to about 4–5 by adding acetic acid solution; fourth, the three-necked flask was placed in a water bath, and the modification reaction of the above mixing solution was sustained for an appropriate time in the appropriate temperature with magnetic stirring; fifth, the above mixing solution was separated by using a centrifuge (10,000 rpm) for 3 min, and the precipitate at the bottom of the flask was obtained after the supernatant was poured out; sixth, the precipitate was dried at 120°C for 48 h in a drying oven after it was washed with acetone several times, finally yielding the high-dispersibility nanosilica powder. The orthogonal test method was adopted to optimize three key test parameters: mass fraction ratio of the silane coupling agent KH570, modification reaction temperature, and modification reaction time. The dispersion effect of the high-dispersibility nanosilica powder was characterized by using infrared, X-ray diffraction, and scanning electron microscopic analyses from different views. The results revealed that the best dispersibility effect was achieved when the mass fraction ratio of the silane coupling agent KH570 was 3%, the modification reaction temperature was 80°C, and the modification reaction time was 2 h. Furthermore, the modification reaction resulted in chemical bonding, but not simple physical adsorption, owing to the presence of organic bond groups in the nanosilica modified by the silane coupling agent. The crystal structure of the nanosilica powder remained amorphous after the modification reaction.

2018 ◽  
Vol 36 (4) ◽  
pp. 638-643 ◽  
Author(s):  
Jin Hou ◽  
Qiwang Jiang

AbstractNanosized NaA zeolite was successfully synthesized by hydrothermal method using tetraethyl orthosilicate (TEOS) and aluminum isopropoxide (AIP) as the main raw materials. The surface modification of NaA zeolite was carried out by silane coupling agent 3-aminopropyltriethoxysilane (KH-550). The effects of silane coupling agent dosage, reaction temperature, reaction time, hydrolysis time and pH value on grafting rate of NaA zeolite were investigated in detail. The zeolites were characterized by XRD, SEM-EDS, FT-IR and TG-DTA. The results showed that the surface of NaA zeolite was modified successfully by KH-550. The optimal modification conditions obtained were as follows: the dosage of coupling agent in 95 % ethanol – 1.6 %, reaction temperature − 70 °C, reaction time – 2 h, hydrolysis time – 20 min, and pH value – 3.5. Under these conditions, the grafting rate of modified NaA zeolite was 3.95 %.


2014 ◽  
Vol 21 (4) ◽  
pp. 471-477 ◽  
Author(s):  
Yan-qing Wang ◽  
Yu Guo ◽  
Rong-xin Cui ◽  
Zhong-ming Wang ◽  
You-liang Wu

AbstractThis article mainly aims at experiments used for modifying unsaturated polyester resin (UPR), and trying to enhance the strengthening and toughening performance of nano-silica/UPR polymer composite in order to improve its integrated mechanical properties and to expand its field of application. Experiments were initially used to get high dispersibility nano-silica powder by adding silane coupling agent KH570 as a dispersant into commonly and commercially available nano-silica powder. Then, high dispersibility nano-silica powder was added as a filling with different mass fraction ratios into UPR and nano-silica/UPR polymer composite samples were fabricated. Infrared spectroscopy analysis, X-ray diffraction analysis, and scanning electron microscopy (SEM) analysis were conducted for high dispersibility nano-silica powder. Mechanical properties test and SEM observation of fracture morphology were investigated for nano-silica/UPR polymer composite samples. The results revealed that adding silane coupling agent KH570 with a mass fraction ratio 3% into nano-silica powder made nano-silica best dispersed after the modification reaction at a temperature of 80°C for 2 h. When the high dispersibility nano-silica powder was added into UPR with a mass fraction ratio 1.5%, the impact strength of nano-silica/UPR polymer composite improved greatly by 9.6%. However, when the high dispersibility nano-silica powder was added into UPR with a mass fraction ratio 2%, the tensile strength, bending strength and extension rate of nano-silica/UPR polymer composite improved greatly by 152%, 102%, and 167%, respectively.


2014 ◽  
Vol 490-491 ◽  
pp. 222-226
Author(s):  
Heng Wang ◽  
Chuan Bai Yu ◽  
Chun Wei

In this paper, the mesoporous silica SBA-15 surface was modified by using silane coupling agent KH-540. In order to investigate the best modification conditions, effects of KH-540 dosage, reaction time and temperature were studied. The modified mesoporous silica SBA-15 was characterized by TGA, FTIR, XRD and N2 adsorption-desorption etc. The best modification conditions were obtained as follows: KH-540 dosage is 0.5g, reaction temperature is 90°C and reaction time is 4 hours. The results showed that KH-540 is successfully grafted on the surface of SBA-15, the SBA-15-KH540 possess a well ordered hexagonal mesoporous structure. Compared with pure SBA-15, the surface area, the pore size and the pore volume of the SBA-15-KH540 are decreased slightly.


Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2254
Author(s):  
Adeleke A. Oyekanmi ◽  
N. I. Saharudin ◽  
Che Mohamad Hazwan ◽  
Abdul Khalil H. P. S. ◽  
Niyi G. Olaiya ◽  
...  

Hydrophilic behaviour of carrageenan macroalgae biopolymer, due to hydroxyl groups, has limited its applications, especially for packaging. In this study, macroalgae were reinforced with cellulose nanofibrils (CNFs) isolated from kenaf bast fibres. The macroalgae CNF film was after that treated with silane for hydrophobicity enhancement. The wettability and functional properties of unmodified macroalgae CNF films were compared with silane-modified macroalgae CNF films. Characterisation of the unmodified and modified biopolymers films was investigated. The atomic force microscope (AFM), SEM morphology, tensile properties, water contact angle, and thermal behaviour of the biofilms showed that the incorporation of Kenaf bast CNF remarkably increased the strength, moisture resistance, and thermal stability of the macroalgae biopolymer films. Moreover, the films’ modification using a silane coupling agent further enhanced the strength and thermal stability of the films apart from improved water-resistance of the biopolymer films compared to unmodified films. The morphology and AFM showed good interfacial interaction of the components of the biopolymer films. The modified biopolymer films exhibited significantly improved hydrophobic properties compared to the unmodified films due to the enhanced dispersion resulting from the silane treatment. The improved biopolymer films can potentially be utilised as packaging materials.


2005 ◽  
Vol 04 (01) ◽  
pp. 117-126
Author(s):  
N. L. MA ◽  
P. WU

Using density functional theory, we predicted the solution structure of the hydrolyzed 3–aminopropyltriethoxysilane (h–APS), which is a silane coupling agent commonly used in many industrial applications. We have located five stable minima on the potential energy surface of h–APS in which four of them are "neutral", and the remaining one is zwitterionic (dipolar) in nature. Our calculations suggested that the stability of the most stable form of h–APS in water (denoted as II_N) arose from strong intramolecular OH ⋯ N hydrogen bond. The least stable form is the zwitterionic form (I_ZW), which is estimated to be over 90 kJ mol -1 less stable than II_N. The factors governing the relative stabilities of different forms are discussed.


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