2019
DOI: 10.1016/j.cattod.2019.06.082
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Pushing the limits of electrostatic adsorption: charge enhanced dry impregnation of SBA-15

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Cited by 13 publications
(16 citation statements)
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“…In a colloid preparation, the colloid stability is a principal parameter that influences by the change of solution pH. A very high at pH above 9, the reduction rate of particle is slow resulting an aggregation of nanoparticles 45 . A conclusion has been reported by Eskandari et al .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In a colloid preparation, the colloid stability is a principal parameter that influences by the change of solution pH. A very high at pH above 9, the reduction rate of particle is slow resulting an aggregation of nanoparticles 45 . A conclusion has been reported by Eskandari et al .…”
Section: Resultsmentioning
confidence: 99%
“…A conclusion has been reported by Eskandari et al . 45 that the formation of nanoparticle can be defends owing to the strong electrostatic repulsion under the pH 8. Hence, pH of the solution was kept at 8 in this study in order to synthesise NiO nanoparticles onto the γ -alumina supports to produce macroscopic spherical γ -NA5 catalyst.…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, the formation of charged species on the adsorbent surface intensely depends on the pH of the solution [ 116 ]. pH PZC represents the pH of the solution when no charge species exist on the adsorbent surface [ 117 , 118 , 119 ]. At pH > pH PZC , functional groups, such as –COOH, –OH, and –H 3 PO 4 are deprotonated due to an excessive concentration of OH − in the aqueous solution that creates anions (such as –COO − ,–O − , –PO 4 3– , etc.)…”
Section: Adsorption Mechanismmentioning
confidence: 99%
“…Hence, strong electrostatic interactions occur between the positively charged adsorbent surface and anions. Conversely, the aqueous solution is deprotonated at pH > pH PZC , creating a negatively charged surface that interacts with cations [ 117 , 118 , 119 ]. The protonation and deprotonation mainly occur at different functional groups, such as carboxylic [ 105 ] or amine [ 174 , 178 ], and the precipitation of ions in HGs.…”
Section: Factors Affecting the Adsorption Capacity Of Cbhsmentioning
confidence: 99%
“…Both the WI and DI methods suffer from poor metal precursor–support interaction during metal deposition, especially when using “inert” supporting materials (SiO 2 , carbon, etc. ), resulting in severe sintering and a wide size distribution of metal particles during the thermal treatment. Thus, several innovative methods have been developed to prepare noble metal nanoparticles (NPs) with a narrow size distribution and high dispersion on support. Among them, strong electrostatic adsorption (SEA) and charge-enhanced dry impregnation (CEDI) methods have been proven to be simple and cost-effective to prepare supported noble and base metal catalysts with high dispersion and tight size distribution of metal particles. The SEA and CEDI methods involve a simple variation in the WI and DI methods, respectively, using an initially strongly acidified or basified impregnating solution according to the support’s point of zero charge (PZC) to enhance the electrostatic interaction between the metal ion/cation precursor and protonated/deprotonated surface hydroxyls on support. This strong interaction stabilizes the metal precursors during drying and prevents the metal particles from severe aggregation during thermal treatment, as opposed to WI and DI. , …”
Section: Introductionmentioning
confidence: 99%