Browse > Article

Synthesis and Characterization of Chelating Resins Containing Thiol Croups  

박인환 (한국화학연구원)
방영길 (한국화학연구원)
김경만 (한국화학연구원)
주혁종 (충남대학교 고분자공학과)
Publication Information
Polymer(Korea) / v.27, no.4, 2003 , pp. 330-339 More about this Journal
Abstract
Three kinds of macro-reticular bead-typed chelating resins having thiol groups were obtained from basic resins like poly(strene-co-divinylbenzene) (PSD) and poly(styrene-co-methyl methacrylate-co-divinylbenzene) (PSMD): the chelating resin (I) was prepared by chloromethylation of phenyl rings of PSD followed by thiolation using thiourea. The chelating resin (ll) was designed to provide enough space to chelate heavy metal ions; one chloromethyl group was obtained by chlorination of hydroxymethyl group provided by reduction of carboxylic ester group of PSMD and another chloromethyl group was obtained by direct chloromethylation of pendent phenyl group using chloromethyl methyl ether. Both of chloromethyl groups were thiolated by using thiourea. The chelating resin (III) was prepared by chlorosulfonation of phenyl rings of PSD followed by thiolation using sodium hydrosulfide. The adsorbtivity toward heavy metal ions was evaluated. The hydrophobic chelating resin (I) with thiol groups showed highly selective adsorption capacity f3r mercury ions. However, the chelating resin (II) with thiol groups showed mere effective adsorption capacity toward mercury ions than chelating resin (I) with thiol groups, and showed some adsorption capacity for other heavy metal ions like Cu$\^$2+/, Pb$\^$2+/, Cd$\^$2+/ and Cr$\^$3+/. On the other hand, the chelating resin (III) which have hydrophilic thiosulfonic acid groups was found to be effective adsorbents for some heavy metal ions such as Hg$\^$2+/, Cu$\^$2+/, Ni$\^$2+/, Co$\^$2+/, Cr$\^$3+/ and especially Cd$\^$2+/ and Pb$\^$2+/.
Keywords
chelating resin; thiol group; poly(styrene-co-divinylbenzene); Poly(styrene-co-methyl methacrylate-co-divinylbenzene); heavy metal ions;
Citations & Related Records

Times Cited By Web Of Science : 0  (Related Records In Web of Science)
Times Cited By SCOPUS : 0
연도 인용수 순위
  • Reference
1 /
[ H.Egawa;Y.Jogo;H.Maeda ] / Nippon Kagaku Kaishi
2 /
[ A.Spiro;C.A.Shelley;E.P.Horitz;R.Chiarizia;J.Michael;X.Xue ] / PCT Int. Appl.WO2000001458 A1
3 /
[ R.J.Phillips;J.S.Fritz ] / Anal. Chem.   DOI
4 /
[ B.S.Chokina;L.N.Prodius; E.E.Ergozhin ] / Izv. Akad. Nauk Kaz. USSR. Ser. Khim.;Chem.Abstr.
5 /
[ K.Mori;N.Asabe;Y.Nakamura ] / J. Polym. Sci. Polym. Lett. Ed.   DOI
6 /
[ M.Tomoi;O.Abe;N.Takasu;H.Kakiuchi ] / Makromol. Chem.   DOI
7 /
[ T.Nonaka;Y.Uemura,K.Enishi;S.Kurihara ] / J. Appl. Polym. Sci.   DOI   ScienceOn
8 /
[ S.Tamura;K.Takase; H.Hisayama ] / Japan. Kokai JP52121692
9 /
[ G.S.Bylina;T.A.Nikolaeva ] / Vysokomol. Soedin., Ser. A Ser. B
10 /
[ Y.V.Svetkin;M.V.Burmistr;A.N.Talanov;O.E.Degtyarev;V.E.Zak;N.S.Malovichko ] / Chem. Abstr.
11 /
[ F.Abassi;P.Hodge;E.Khoshdel ] / Chem. Abstr.
12 /
[ A.Spiro;C.A.Shelley;E.P.Horitz;R.Chiarizia;J.Michael;X.Xue ] / Chem. Abstr.
13 /
[ T.Fujisawa;I.Sachio;T.Sato ] / Chem. Lett.
14 /
[ Y.Kamitori;M.Hojo;R.Masuda;T.Inoue;T.Izumi ] / Tetrahedron Lett.   DOI   ScienceOn
15 /
[ L.V.Dunkerton;B.C.Barot ] / J. Hetrocycl. Chem.   DOI
16 /
[ D.W.Jeon;H.J.Lee ] / J. Korean Fiber Soc.
17 /
[ N.Kabay;M.Demircioglu;H.Ekinci;M.Yueksel;M.Mehmet;M.Akcay;M.Streat ] / Ind. Eng. Chem. Res.   DOI   ScienceOn
18 /
[ I.H.Park;J.M.Suh ] / Angew. Makromol. Chem.   DOI   ScienceOn
19 /
[ E.Santaniello;P.Ferraboschi ] / J. Org. Chem.   DOI
20 /
[ H.Maeda;H.Egawa ] / Anal. Chim. Acta   DOI
21 /
[ H.Maeda;H.Egawa ] / Nippon Kagaku Kaishi
22 /
[ D.J.Cram ] / J. Am. Chem. Soc.   DOI
23 /
[ M.Date;I.Tanaka ] / Chem. Abstr.
24 /
[ K.S.Kim;D.W.Jeon;K.H.Park ] / J. Kor. Pharm.
25 /
[ F.Abassi;P.Hodge;E.Khoshdel ] / Polym. Commun.
26 /
[ H.Egawa;T.Nonaka;M.Ikari ] / J. Appl. Polym. Sci.   DOI   ScienceOn
27 /
[ T.Matsuo; Y.Kizaki ] / Chem. Abstr.
28 /
[ N.Bicak;G.Koza;Y.Yusuf ] / J. Polym. Mater.
29 /
[ T.Matsuo;Y.Kizaki ] / Jpn. Kokai Tokkyo Koho JP 2000273179
30 /
[ H.U.Blank ] / Chem. Abstr.
31 /
[ Y.Gao;K.B.Sharpless ] / J. Org. Chem.   DOI
32 /
[ M.Sakamoto;S.Tomita;Y.Takashima;H.Koga ] / PCT Int. Appl.WO20001040176 A1
33 /
[ B.Saha;M.Iglesias;I.W.Cumming;M.Streat ] / Solvent Extr. Ion Exch.   DOI   ScienceOn
34 /
[ A.Deratani;B.Sebille ] / Anal. Chem.   DOI
35 /
[ B.Saha;M.Iglesias;I.W.Cumming;M.Streat ] / Chem. Abstr.
36 /
[ J.M.Frechet;M.D.De Smet;M.J.Farall ] / Polymer   DOI   ScienceOn
37 /
[ H.U.Blank ] / Ger. Offen. DE 2635281
38 /
[ M.Sakamoto;S.Tomita;Y.Takashima;H.Koga ] / Chem. Abstr.
39 /
[ K.Morimoto;T.Sato;S.Yamamoto;H.Takeuchi ] / J. Heterocycl. Chem.   DOI
40 /
[ L.Feistel;G.Popov;G.Schwachula ] / Plaste Kautsch.
41 /
[ B.A.Utkelov;E.E.Ergozhin;R.K.Ashkeeva ] / React. Polym.   DOI   ScienceOn
42 /
[ S.Tamura;K.Takase; H.Hisayama ] / Chem. Abstr.
43 /
[ E.M.Moyers;J.S.Fritz ] / Anal. Chem.   DOI
44 /
[ I.H.Park;J.C.Jung;S.C.Hwang;J.O.Joo ] / Angew. Makromol. Chem.   DOI
45 /
[ S.Savaskan;N.Besirli;B.Hazer ] / J. Appl. Polym. Sci.   DOI   ScienceOn
46 /
[ N.Daniel;A.K.Srivastava ] / J. Macromol. Sci.,Pure Appl. Chem.
47 /
[ M.Date;I.Tanaka ] / Jpn. Kokai Tokkyo Koho JP0182688
48 /
[ E.W.Collington;A.I.Meyers ] / J. Org. Chem.   DOI
49 /
[ H.C.Brown;Y.M.Choi;S.Narasimhan ] / J. Org. Chem.   DOI
50 /
[ I.H.Park;J.M.Rhee;Y.S.Jung ] / Angew. Makromol. Chem.   DOI   ScienceOn
51 /
[ Y.V.Svetkin;M.V.Burmistr;A.N.Talanov;O.E.Degtyarev;V.E.Zak;N.S.Malovichko ] / Khim. Tekhnol.(Kiev)
52 /
[ Y.Shimano;K.Sato;D.FuKui;Y.Onodera;Y.Kimura ] / Polym. J.   DOI   ScienceOn
53 /
[ M.Camps;M.Chatzopoulos;J.M.Camps;J.E.Montheard ] / J. Macromol Sci.,Rev. Macromol. Chem. Phys.