2009
DOI: 10.1016/j.biortech.2009.03.014
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Selective recovery of precious metals by persimmon waste chemically modified with dimethylamine

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Cited by 88 publications
(53 citation statements)
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“…The shifting of the free ionization carboxy (C=O) peaks is attributed to the polymerization during the modification (Liang et al 2010a). Moreover, two new peaks at 1315.7 and 459.1 cm -1 are due to amino (N-H) stretching, which infers the polyphenol groups have combined with glycine (Xiong et al 2009). …”
Section: Ft-ir Analysismentioning
confidence: 98%
“…The shifting of the free ionization carboxy (C=O) peaks is attributed to the polymerization during the modification (Liang et al 2010a). Moreover, two new peaks at 1315.7 and 459.1 cm -1 are due to amino (N-H) stretching, which infers the polyphenol groups have combined with glycine (Xiong et al 2009). …”
Section: Ft-ir Analysismentioning
confidence: 98%
“…Although, as mentioned earlier, CPT and PP gels were found to exhibit extraordinary high selectivity for gold(III), we further attempted to enhance the affinity also for platinum(IV) and palladium [35][36][37][38][39][40]. It is easy to chemically modify persimmon tannin extract and persimmon waste including persimmon peel by immobilizing a variety of functional groups which exhibit special affinities for some metal ions onto their surface similar to other biomass wastes [41,42].…”
Section: Chemical Modification Of Persimmon Tannin Extract and Persimmentioning
confidence: 99%
“…It is easy to chemically modify persimmon tannin extract and persimmon waste including persimmon peel by immobilizing a variety of functional groups which exhibit special affinities for some metal ions onto their surface similar to other biomass wastes [41,42]. In our research works, persimmon waste was chemically modified by immobilizing functional group of dimethylamine (DMA) to prepare the adsorption gel functioning as a typical weak base type of anion exchange material and investigated its adsorption behavior for some precious and base metals from hydrochloric acid solutions [35,36]. Further, a variety of adsorption gels were prepared from persimmon tannin extract powder by the chemical modifications immobilizing other functional groups such as tertiary amine where the immobilized tertiary amine groups function as quaternary ammonium compounds (QA) [37], a typical strong base, as well as tetraethylenepentamine (TEPA) [38], glycidyltrimethyl ammonium (GTA), aminoguanidine (AG) [40], and bisthiourea (BTU) [41].…”
Section: Chemical Modification Of Persimmon Tannin Extract and Persimmentioning
confidence: 99%
“…The dimethylamine modified persimmon peel gel (abbreviated as DMA-PP) was prepared according to Scheme 2. 1.0 g PP was mixed together with 5 ml acetic acid, 10 ml phosphoric acid, 1.0 g para-formaldehyde, 10 ml 1,4-dioxane and 20 ml hydrochloric acid and the mixture stirred for 18 h at 358 K. The chlorinated product was washed with 0.1 mol/l sodium hydroxide and dried for 3 h at 323 K. Then, it was mixed with 10 ml dimethylamine solution, and heated at 363 K with continuous stirring for 3 h. The product was filtered and washed by 0.1 mol/l NaCl, and finally dried and sieved to 150 mesh size [9].…”
Section: Preparation Of the Dimethylamine Modified Persimmon Peel Gelmentioning
confidence: 99%