2021
DOI: 10.1007/s00289-021-03683-0
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High-strength and long-term durable hydrophobic polystyrene microsphere: a promising ultra-lightweight proppant for fracturing technology

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Cited by 8 publications
(9 citation statements)
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“…Peaks at 700–760 cm −1 , corresponding to the C–H bending vibration, belong to the mono-substituted benzene ring, and the peak at 1500 cm −1 belongs to the C=C stretching of the benzene ring in St. For the poly(St- co -MMA)/30 wt.% FA composite, except for the vibration signals of MMA and St, more signal peaks can be observed. The peaks at 3538 cm −1 , 1035 cm −1 , and 400–600 cm −1 were attributed to the -OH bending of the silicate layers, Si–O stretching, and Si–O–Si bending vibration, respectively [ 24 , 27 ]. These indicated the presence of FA in the final poly(St- co -MMA)/30 wt.% FA composite.…”
Section: Resultsmentioning
confidence: 99%
“…Peaks at 700–760 cm −1 , corresponding to the C–H bending vibration, belong to the mono-substituted benzene ring, and the peak at 1500 cm −1 belongs to the C=C stretching of the benzene ring in St. For the poly(St- co -MMA)/30 wt.% FA composite, except for the vibration signals of MMA and St, more signal peaks can be observed. The peaks at 3538 cm −1 , 1035 cm −1 , and 400–600 cm −1 were attributed to the -OH bending of the silicate layers, Si–O stretching, and Si–O–Si bending vibration, respectively [ 24 , 27 ]. These indicated the presence of FA in the final poly(St- co -MMA)/30 wt.% FA composite.…”
Section: Resultsmentioning
confidence: 99%
“…25 The peak at 1080 cm À1 belongs to the Si-O vibrations of the "Si-O-CH 3 " group in KH570. 12 Due to the mass weight of fluororesin coated on the surface only accounts to 1% of the microspheres, the IR spectra of the LO-MSDBs and CO-MSDBs do not show any peaks belonging to groups of fluororesin. XPS was then used to prove the presence of the fluororesin on their surface.…”
Section: The Design and Structure Of The Msdbsmentioning
confidence: 95%
“…The O-MSDBs were synthesized by a suspension polymerization method that was accompanied by a sol-gel process, which has been reported in our previous work. 12 As shown in Figure 1, an aqueous phase composed of water (100 ml), PVA-1788 (1.0 g) and MC-400 (0.05 g) was prepared at 50 C in a three-neck flask equipped with a reflux condenser. Before the addition of the oil phase, the pH of the aqueous phase was tuned to about 10 (monitor by a pH meter) using NH 3 ÁH 2 O.…”
Section: The Preparation Of O-msdbsmentioning
confidence: 99%
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