Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals

Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethyl...
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Autor*in:	Malović, Ljiljana [verfasserIn] Nastasović, Aleksandra [verfasserIn] Sandić, Zvjezdana [verfasserIn] Marković, Jelena [verfasserIn] Đorđević, Dragana [verfasserIn] Vuković, Zorica [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2007

Schlagwörter:	Sorption Capacity Epoxy Group Teta Diethylene Triamine EGDMA

Übergeordnetes Werk:	Enthalten in: Journal of materials science - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966, 42(2007), 10 vom: 22. März, Seite 3326-3337
Übergeordnetes Werk:	volume:42 ; year:2007 ; number:10 ; day:22 ; month:03 ; pages:3326-3337

Links:	Volltext

DOI / URN:	10.1007/s10853-006-0958-y

Katalog-ID:	SPR013817221

Internformat


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100	1		\|a Malović, Ljiljana \|e verfasserin \|4 aut
245	1	0	\|a Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
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520			\|a Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1.
650		4	\|a Sorption Capacity \|7 (dpeaa)DE-He213
650		4	\|a Epoxy Group \|7 (dpeaa)DE-He213
650		4	\|a Teta \|7 (dpeaa)DE-He213
650		4	\|a Diethylene Triamine \|7 (dpeaa)DE-He213
650		4	\|a EGDMA \|7 (dpeaa)DE-He213
700	1		\|a Nastasović, Aleksandra \|e verfasserin \|4 aut
700	1		\|a Sandić, Zvjezdana \|e verfasserin \|4 aut
700	1		\|a Marković, Jelena \|e verfasserin \|4 aut
700	1		\|a Đorđević, Dragana \|e verfasserin \|4 aut
700	1		\|a Vuković, Zorica \|e verfasserin \|4 aut
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773	1	8	\|g volume:42 \|g year:2007 \|g number:10 \|g day:22 \|g month:03 \|g pages:3326-3337
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912			\|a GBV_ILN_24
912			\|a GBV_ILN_31
912			\|a GBV_ILN_32
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_90
912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_120
912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_152
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2057
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2070
912			\|a GBV_ILN_2086
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2116
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2119
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2144
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2188
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2446
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
912			\|a GBV_ILN_4012
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4046
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4246
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4335
912			\|a GBV_ILN_4336
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
936	b	k	\|a 51.00 \|q ASE
951			\|a AR
952			\|d 42 \|j 2007 \|e 10 \|b 22 \|c 03 \|h 3326-3337

Indexfelder

author_variant	l m lm a n an z s zs j m jm d đ dđ z v zv
matchkey_str	article:15734803:2007----::ufcmdfctoomcoooslcdlehcyaeaecplmrfree
hierarchy_sort_str	2007
bklnumber	51.00
publishDate	2007
allfields	10.1007/s10853-006-0958-y doi (DE-627)SPR013817221 (SPR)s10853-006-0958-y-e DE-627 ger DE-627 rakwb eng 670 ASE 51.00 bkl Malović, Ljiljana verfasserin aut Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1. Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213 Nastasović, Aleksandra verfasserin aut Sandić, Zvjezdana verfasserin aut Marković, Jelena verfasserin aut Đorđević, Dragana verfasserin aut Vuković, Zorica verfasserin aut Enthalten in Journal of materials science Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966 42(2007), 10 vom: 22. März, Seite 3326-3337 (DE-627)315293969 (DE-600)2015305-3 1573-4803 nnns volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337 https://dx.doi.org/10.1007/s10853-006-0958-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 51.00 ASE AR 42 2007 10 22 03 3326-3337
spelling	10.1007/s10853-006-0958-y doi (DE-627)SPR013817221 (SPR)s10853-006-0958-y-e DE-627 ger DE-627 rakwb eng 670 ASE 51.00 bkl Malović, Ljiljana verfasserin aut Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1. Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213 Nastasović, Aleksandra verfasserin aut Sandić, Zvjezdana verfasserin aut Marković, Jelena verfasserin aut Đorđević, Dragana verfasserin aut Vuković, Zorica verfasserin aut Enthalten in Journal of materials science Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966 42(2007), 10 vom: 22. März, Seite 3326-3337 (DE-627)315293969 (DE-600)2015305-3 1573-4803 nnns volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337 https://dx.doi.org/10.1007/s10853-006-0958-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 51.00 ASE AR 42 2007 10 22 03 3326-3337
allfields_unstemmed	10.1007/s10853-006-0958-y doi (DE-627)SPR013817221 (SPR)s10853-006-0958-y-e DE-627 ger DE-627 rakwb eng 670 ASE 51.00 bkl Malović, Ljiljana verfasserin aut Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1. Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213 Nastasović, Aleksandra verfasserin aut Sandić, Zvjezdana verfasserin aut Marković, Jelena verfasserin aut Đorđević, Dragana verfasserin aut Vuković, Zorica verfasserin aut Enthalten in Journal of materials science Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966 42(2007), 10 vom: 22. März, Seite 3326-3337 (DE-627)315293969 (DE-600)2015305-3 1573-4803 nnns volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337 https://dx.doi.org/10.1007/s10853-006-0958-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 51.00 ASE AR 42 2007 10 22 03 3326-3337
allfieldsGer	10.1007/s10853-006-0958-y doi (DE-627)SPR013817221 (SPR)s10853-006-0958-y-e DE-627 ger DE-627 rakwb eng 670 ASE 51.00 bkl Malović, Ljiljana verfasserin aut Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1. Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213 Nastasović, Aleksandra verfasserin aut Sandić, Zvjezdana verfasserin aut Marković, Jelena verfasserin aut Đorđević, Dragana verfasserin aut Vuković, Zorica verfasserin aut Enthalten in Journal of materials science Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966 42(2007), 10 vom: 22. März, Seite 3326-3337 (DE-627)315293969 (DE-600)2015305-3 1573-4803 nnns volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337 https://dx.doi.org/10.1007/s10853-006-0958-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 51.00 ASE AR 42 2007 10 22 03 3326-3337
allfieldsSound	10.1007/s10853-006-0958-y doi (DE-627)SPR013817221 (SPR)s10853-006-0958-y-e DE-627 ger DE-627 rakwb eng 670 ASE 51.00 bkl Malović, Ljiljana verfasserin aut Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1. Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213 Nastasović, Aleksandra verfasserin aut Sandić, Zvjezdana verfasserin aut Marković, Jelena verfasserin aut Đorđević, Dragana verfasserin aut Vuković, Zorica verfasserin aut Enthalten in Journal of materials science Dordrecht [u.a.] : Springer Science + Business Media B.V, 1966 42(2007), 10 vom: 22. März, Seite 3326-3337 (DE-627)315293969 (DE-600)2015305-3 1573-4803 nnns volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337 https://dx.doi.org/10.1007/s10853-006-0958-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 51.00 ASE AR 42 2007 10 22 03 3326-3337
language	English
source	Enthalten in Journal of materials science 42(2007), 10 vom: 22. März, Seite 3326-3337 volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337
sourceStr	Enthalten in Journal of materials science 42(2007), 10 vom: 22. März, Seite 3326-3337 volume:42 year:2007 number:10 day:22 month:03 pages:3326-3337
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Sorption Capacity Epoxy Group Teta Diethylene Triamine EGDMA
dewey-raw	670
isfreeaccess_bool	false
container_title	Journal of materials science
authorswithroles_txt_mv	Malović, Ljiljana @@aut@@ Nastasović, Aleksandra @@aut@@ Sandić, Zvjezdana @@aut@@ Marković, Jelena @@aut@@ Đorđević, Dragana @@aut@@ Vuković, Zorica @@aut@@
publishDateDaySort_date	2007-03-22T00:00:00Z
hierarchy_top_id	315293969
dewey-sort	3670
id	SPR013817221
language_de	englisch
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Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. 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author	Malović, Ljiljana
spellingShingle	Malović, Ljiljana ddc 670 bkl 51.00 misc Sorption Capacity misc Epoxy Group misc Teta misc Diethylene Triamine misc EGDMA Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
authorStr	Malović, Ljiljana
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topic_title	670 ASE 51.00 bkl Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals Sorption Capacity (dpeaa)DE-He213 Epoxy Group (dpeaa)DE-He213 Teta (dpeaa)DE-He213 Diethylene Triamine (dpeaa)DE-He213 EGDMA (dpeaa)DE-He213
topic	ddc 670 bkl 51.00 misc Sorption Capacity misc Epoxy Group misc Teta misc Diethylene Triamine misc EGDMA
topic_unstemmed	ddc 670 bkl 51.00 misc Sorption Capacity misc Epoxy Group misc Teta misc Diethylene Triamine misc EGDMA
topic_browse	ddc 670 bkl 51.00 misc Sorption Capacity misc Epoxy Group misc Teta misc Diethylene Triamine misc EGDMA
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title	Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
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title_full	Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
author_sort	Malović, Ljiljana
journal	Journal of materials science
journalStr	Journal of materials science
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author_browse	Malović, Ljiljana Nastasović, Aleksandra Sandić, Zvjezdana Marković, Jelena Đorđević, Dragana Vuković, Zorica
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author-letter	Malović, Ljiljana
doi_str_mv	10.1007/s10853-006-0958-y
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author2-role	verfasserin
title_sort	surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
title_auth	Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
abstract	Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1.
abstractGer	Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1.
abstract_unstemmed	Abstract Two samples of macroporous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate), poly(GMA-co-EGDMA), were synthesized by suspension copolymerization and modified with amines. Initial poly(GMA-co-EGDMA), and the samples modified with ethylene diamine [poly(GMA-co-EGDMA)-en], diethylene triamine [poly(GMA-co-EGDMA)-deta] and triethylene tetramine [poly(GMA-co-EGDMA)-teta], were characterized by mercury porosimetry, FTIR spectroscopy and elemental analysis. The most pronounced increase of specific surface area (75%) was observed for poly(GMA-co-EGDMA)-teta sample with smaller particles (D < 150 μm). The Cu(II) sorption was rapid, depending on porosity of amino-functionalized samples and ligand type. For poly(GMA-co-EGDMA)-deta and poly(GMA-co-EGDMA)-teta sorption half time required to reach 50% of total sorption capacity, t1/2, were around 3 min. Sorption capacities for Cu(II), Co(II), Cd(II) and Ni(II) as well as for Cr(VI), Co(II), Cd(II) and Ni(II) ions were determined under competitive conditions as a function of pH, ligand type and porosity at room temperature. The results indicate selectivity of poly(GMA-co-EGDMA)-deta for Cu(II) over Cd(II) of 3:1 and for Cu(II) over Ni(II) and Co(II) of 6:1. The decrease in particle size of poly(GMA-co-EGDMA)-teta caused the increase of sorption capacities for all metal ions. At pH 1.8 the selectivity of poly(GMA-co-EGDMA)-teta with smaller particles for Cr(VI) over Ni(II), Co(II) and Cd(II) ions was 8.5:1.
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container_issue	10
title_short	Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals
url	https://dx.doi.org/10.1007/s10853-006-0958-y
remote_bool	true
author2	Nastasović, Aleksandra Sandić, Zvjezdana Marković, Jelena Đorđević, Dragana Vuković, Zorica
author2Str	Nastasović, Aleksandra Sandić, Zvjezdana Marković, Jelena Đorđević, Dragana Vuković, Zorica
ppnlink	315293969
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doi_str	10.1007/s10853-006-0958-y
up_date	2024-07-03T22:20:32.358Z
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Surface modification of macroporous glycidyl methacrylate based copolymers for selective sorption of heavy metals

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