Studies on selective adsorbents for oxo-anions. Nitrate ion-exchange properties of layered double hydroxides with different metal atoms

被引:83
作者
Tezuka, S
Chitrakar, R
Sonoda, A
Ooi, K
Tomida, T
机构
[1] AIST Shikoku, Natl Inst Adv Sci & Technol, Inst Marine Resources & Environm, Takamatsu, Kagawa 7610395, Japan
[2] Univ Tokushima, Tokushima 7700814, Japan
关键词
D O I
10.1039/b314938m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Layered double. hydroxides (LDHs) with different kinds of metal ions (Mg-Al, Co-Fe, Ni-Fe, and Mg-Fe) in the brucite layers were prepared and their anion exchange properties were studied by measurements of distribution coefficient (K-d) and ion exchange capacity. The basal spacing of LDHs varied depending on the kind of metal ions in the brucite layer. A relatively high K-d value for NO3- ions was observed on Ni-Fe type LDHs, and a markedly high K-d value for the hydrothermally-treated Ni-Fe type LDHs (Ni-Fe (HT)), prepared at 120 degreesC. These high K-d values correlated with the basal spacing of 0.81 nm observed for this sample, where the interlayer distance (0.33 nm) is suitable for the stable fixing of NO3- ions (ionic size = 0.33 nm). A chemical analysis study showed a Cl-/NO3- ion-exchange mechanism for NO3- adsorption on Ni-Fe (HT). The NO3- uptake by Ni-Fe (HT) was nearly constant (NO3/Fe = 0.7) over a pH range between 5 and 10, which also supports the adsorption mechanism of Cl-/NO3- ion exchange. The Ni-Fe (HT) could remove NO3- ions from seawater effectively (NO3- uptake = 168 mumol g(-1)) even though seawater contains an extremely large amount of coexisting anions. This novel adsorbent thus has a NO3- ion-sieve property and will prove beneficial for the selective removal of NO3- ions from industrial effluents and seawater to clean the environment.
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页码:104 / 109
页数:6
相关论文
共 37 条
[1]  
ABE M, 1995, ION EX SOLV, V12, P381
[2]   Synthesis and thermal decomposition of Mn-Al layered double hydroxides [J].
Aisawa, S ;
Hirahara, H ;
Uchiyama, H ;
Takahashi, S ;
Narita, E .
JOURNAL OF SOLID STATE CHEMISTRY, 2002, 167 (01) :152-159
[3]   Direct intercalation of amino acids into layered double hydroxides by coprecipitation [J].
Aisawa, S ;
Takahashi, S ;
Ogasawara, W ;
Umetsu, Y ;
Narita, E .
JOURNAL OF SOLID STATE CHEMISTRY, 2001, 162 (01) :52-62
[4]   CRYSTALLINE ZR(R-PO3)2 AND ZR(R-OPO3)2 COMPOUNDS (R=ORGANIC RADICAL) - NEW CLASS OF MATERIALS HAVING LAYERED STRUCTURE OF ZIRCONIUM-PHOSPHATE TYPE [J].
ALBERTI, G ;
COSTANTINO, U ;
ALLULLI, S ;
TOMASSINI, N .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1978, 40 (06) :1113-1117
[5]   Ion exchange of different phosphate ions into the zinc-aluminium-chloride layered double hydroxide [J].
Badreddine, M ;
Legrouri, A ;
Barroug, A ;
De Roy, A ;
Besse, JP .
MATERIALS LETTERS, 1999, 38 (06) :391-395
[6]   ION EXCHANGE IN FELSPATHOIDS AS A SOLID-STATE REACTION [J].
BARRER, RM ;
FALCONER, JD .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1956, 236 (1205) :227-&
[7]   Hydrotalcites as sorbent for 2,4,6-trinitrophenol:: influence of the layer composition and interlayer anion [J].
Barriga, C ;
Gaitán, M ;
Pavlovic, I ;
Ulibarri, MA ;
Hermosin, MC ;
Cornejo, J .
JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (04) :1027-1034
[8]   THE CRYSTAL-CHEMISTRY AND PARAGENESIS OF HONESSITE AND HYDROHONESSITE - THE SULFATE ANALOGS OF REEVESITE [J].
BISH, DL ;
LIVINGSTONE, A .
MINERALOGICAL MAGAZINE, 1981, 44 (335) :339-343
[9]   HYDROTALCITE-TYPE ANIONIC CLAYS: PREPARATION, PROPERTIES AND APPLICATIONS [J].
Cavani, F. ;
Trifiro, F. ;
Vaccari, A. .
CATALYSIS TODAY, 1991, 11 (02) :173-301
[10]  
Clearfield A., 1982, INORGANIC ION EXCHAN