1999
DOI: 10.1016/s1381-5148(99)00034-6
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Characterisation and sorption performance of a Hypersol–Macronet polymer and an activated carbon

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Cited by 37 publications
(23 citation statements)
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“…In most cases, the data available were chemical interpretations. If this work is compared with sorption data on PAH removal by hypercrosslinked polymeric resins, the range of the apparent surface diffusivities are very close to the result reported for this specific sorbent [27,36]. The apparent surface diffusivity coefficients were compared (Table 8) with measured values of functionalized aromatic hydrocarbons such as phenol, p-bromophenol, p-nitrophenol, p-toluenesulphonate and dodecylbenzenesulphonate [37][38][39][40][41][42].…”
Section: Pore and Surface Diffusion Coefficientssupporting
confidence: 52%
“…In most cases, the data available were chemical interpretations. If this work is compared with sorption data on PAH removal by hypercrosslinked polymeric resins, the range of the apparent surface diffusivities are very close to the result reported for this specific sorbent [27,36]. The apparent surface diffusivity coefficients were compared (Table 8) with measured values of functionalized aromatic hydrocarbons such as phenol, p-bromophenol, p-nitrophenol, p-toluenesulphonate and dodecylbenzenesulphonate [37][38][39][40][41][42].…”
Section: Pore and Surface Diffusion Coefficientssupporting
confidence: 52%
“…Toluene (10 mmol) was added to anhydrous 1,2-dichloroethane (10 mL) under a flow of nitrogen, followed by formaldehyde dimethyl acetal (15,16,17,19,20,23,25,27,30,40, or 50 mmol for 1.5, 1.6, 1.7, 1.9, 2, 2.3, 2.5, 2.7, 3, 4, or 5 equivalents of FDA, respectively). An equimolar amount of iron(III) chloride (15,16,17,19,20,23,25,27,30,40, or 50 mmol) was added and the reaction mixture heated at 80°C for 18 hours. After cooling the solid product was removed by filtration and washed with methanol several times.…”
Section: Methodsmentioning
confidence: 99%
“…34 Similarly, modification of HCPs with imidazolium ionic liquids helped to increase polarity for enhanced adsorption of catechin from herbal plants. 35 The propensity of HCPs to swell has led their use in a number of applications including the trapping of organic vapors, 36 ion exchange, 37,38 removal of toxic trace metals, 39,40 solid phase extraction, 41 and recovery of organic compounds from water. 42,43 Knitting of the triptycene monomer can produce HCPs which show high adsorption for solvents including DMSO, toluene, and ethyl acetate, with a 30 times increase in the mass of the polymer observed for adsorption of chloroform.…”
Section: Introductionmentioning
confidence: 99%
“…Sorption of metal ions strongly depends on the chemistry of the carbon surface. The shapes of the pH titration curves indicate the presence of polyfunctional weakly-acidic groups on the activated surface (Tai et al, 1999). A significant difference is observed between the curves of the adsorbents and K500.…”
Section: Resultsmentioning
confidence: 93%