使用者:Woclass/鈣礬石
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鈣礬石 | |
---|---|
![]() 鈣礬石, 3.3×2.6×2.5 cm. 產自南非北開普省卡拉哈里錳田 | |
基本資料 | |
類別 | 硫酸鹽 |
化學式 | Ca 6Al 2(SO 4) 3(OH) 12·26H 2O |
施特龍茨分類 | 7.DG.15 |
晶體分類 | Ditrigonal pyramidal (3m) 赫爾曼–莫甘記號: (3m) |
晶體空間群 | P31c |
晶胞 | a = 11.23, c = 21.44 [Å]; Z = 2 |
性質 | |
顏色 | 無色、淡黃色或乳白色 |
晶體慣態 | 針狀生長、棱紋狀晶體; 纖維狀至棉絮狀 |
晶系 | 六方晶系 |
解理 | {1010} 完全 |
莫氏硬度 | 2-2.5 |
光澤 | 玻璃光澤 |
條痕 | 白色 |
透明性 | 透明至不透明 |
比重 | 1.77 |
光學性質 | 單軸 (-) |
折射率 | nω = 1.491, nε = 1.470 |
雙折射 | δ = 0.021 |
發光性 | 無熒光性 |
溶解度 | 部分溶於水 |
可轉變為 | 在空氣中部分脫水,變得不透明 |
參考文獻 | [1][2][3] |
鈣礬石 是一種含水的鈣鋁硫酸鹽礦物,其化學式為Ca
6Al
2(SO
4)
3(OH)
12·26H
2O。它呈無色到黃色,晶係為三方晶系。其柱狀晶體通常情況下無色,部分脫水後顯白色。[2][3]鈣礬石類礦物包括硅灰石膏和鈣鉻礬。[4]
Discovery and occurrence
![](http://images.weserv.nl/?url=//upload.wikimedia.org/wikipedia/commons/thumb/7/73/Ettringite.jpg/170px-Ettringite.jpg)
Ettringite was first described in 1874 by J.Lehmann,[5] for an occurrence near the Ettringer Bellerberg volcano, Ettringen, Rheinland-Pfalz, Germany.[2][3] It occurs within metamorphically altered limestone adjacent to igneous intrusive rocks or within xenoliths. It also occurs as weathering crusts on larnite in the Hatrurim Formation of Israel.[2] It occurs associated with portlandite, afwillite and hydrocalumite at Scawt Hill, Ireland and with afwillite, hydrocalumite, mayenite and gypsum in the Hatrurim Formation.[2] It has also been reported from the Zeilberg quarry, Maroldsweisach, Bavaria; at Boisséjour, near Clermont-Ferrand, Puy-de-Dôme, Auvergne, France; the N』Chwaning mine, Kuruman district, Cape Province, South Africa; in the US, occurrences were found in spurrite-merwinite-gehlenite skarn at the 910 level of the Commercial quarry, Crestmore, Riverside County, California[6] and in the Lucky Cuss mine, Tombstone, Cochise County, Arizona.[2][3]
Occurrence in cement
![](http://images.weserv.nl/?url=//upload.wikimedia.org/wikipedia/commons/thumb/9/98/CaOH2SEM.jpg/170px-CaOH2SEM.jpg)
In concrete chemistry ettringite is a hexacalcium aluminate trisulfate hydrate, of general formula:
- (CaO)6(Al2O3)(SO3)3·32H2O
or
- (CaO)3(Al2O3)(CaSO4)3·32H2O.
Ettringite is formed in hydrated Portland cement system as a result of the reaction of calcium aluminate with calcium sulfate, both present in Portland cement.[7] Ettringite, the more prominent representative of AFt phases or (Al2O3-Fe2O3-tri), can also be synthesized in the laboratory by reacting stoichiometric amounts of calcium, aluminium and sulfate in water.
- C3A + 3 CaSO4 → ettringite
In the cement system, the presence of ettringite depends on the ratio of calcium sulfate to tri-calcium aluminate (C3A); when this ratio is low, ettringite forms during early hydration and then converts to the calcium aluminate monosulfate (AFm phase or (Al2O3-Fe2O3-mono)). When the ratio is intermediate, only a portion of the ettringite converts to AFm and both can coexist, while ettringite is unlikely to convert to AFm at high ratios.
The following characters designate standard notations:[8]
- C = CaO
- S = SiO2
- A = Al2O3
- F = Fe2O3
- S̅ = SO3
- H = H2O
- K = K2O
- N = Na2O
- m = mono
- t = tri
AFt and AFm phases
- AFt: abbreviation for "alumina, ferric oxide, tri-sulfate" or (Al2O3 – Fe2O3 – tri). It represents a group of calcium sulfoaluminate hydrates. AFt has the general formula [Ca3(Al,Fe)(OH)6·12 H2O]2·X3·nH2O where X represents a doubly charged anion or, sometimes, two singly charged anions. Ettringite is the most common and important member of the AFt group (X in this case denoting sulfate).
- AFm: abbreviation for "alumina, ferric oxide, mono-sulfate" or (Al2O3 – Fe2O3 – mono). It represents another group of calcium aluminate hydrates with general formula [Ca2(Al,Fe)(OH)6)]·X·nH2O where X represents a singly charged anion or 'half' a doubly charged anion. X may be one of many anions. The most important anions involved in Portland cement hydration are hydroxyl, sulfate and carbonate.
結構
The mineral ettringite has a structure that runs parallel to the c axis -the needle axis-; in the middle of these two lie the sulfate ions and H2O molecules, the space group is P31c. Ettringite crystal system is trigonal, crystals are elongated and in a needle like shape, occurrence of disorder or twining is common, which affects the intercolumn material.[9] The first X-ray study was done by Bannister, Hey & Bernal (1936), which found that the crystal unit cell is of a hexagonal form with a=11.26 and c=21.48 with space group P63/mmcand Z=2. From observations on dehydration and chemical formulas there were suggestions of the structure being composed of Ca2+ and Al(OH)63−, were between them lie SO42− ions and H2O molecules. Further X-ray studies ensued; namely Wellin (1956) which determined the crystal structure of thaumasite, and Besjak & Jelenic (1966) which gave affirmation of the structure nature of ettringite.[9]
An ettringite sample extracted from Scawt Hill was analysed by C. E. Tilley, the crystal was 1.1 x 0.8 0.5 mm, with specific gravity of 1.772±0.002, the density was determined by immersing the sample in a solution of carbon tetrachloride mixed with bromoform. The crystal showed five prism faces of the form m {1010} and a small face a{1120}, with no pyramidal or basal faces, upon x-ray diffraction a Lauer gram along the c-axis revealed a hexagonal axis with vertical planes of symmetry, this study showed that the structure has a hexagonal and not a rhombohedral lattice.[10] further studies conducted on synthetic ettringite by use of x-ray and powder diffraction confirmed earlier assumptions and analyses.[11]
Upon analyzing the structure of both ettringite and thaumasite, it was deduced that both minerals have hexagonal structures, but different space groups. Ettringite crystals have a P31c with a=11.224 Å, c= 21,108 Å, while thaumasite crystals fall into space group P63 with a= 11.04 Å, c= 10.39 Å. While these two minerals form a solid solution, the difference in space groups lead to discontinuities in unit cell parameters. Differences between structures of ettringite and thaumasite arise from the columns of cations and anions: Ettringite cation columns are composed of Ca3[Al(OH)6·12H2O]3+, which run parallel to the c axis, and the other columns of sulfate anions and water molecules in channels parallel to these columns. In contrast, thaumasite consists of a cylindrical column of Ca3[Si(OH)6·12H2O]3+ in the c axis, with sulfate and carbonate anions in channels between these columns which contain water molecules as well.[12]
Further research
Ongoing research on ettringite and cement phase minerals is in general to find ways to immobilize wastes and heavy metals from soils and the environment; this can be done by use of the proper cement phase forming mineral by use of lattice to extract according elements. For example, it is reported that copper immobilization at high pH can be achieved through formation of CSH/CAH and ettringite.[13] It is suggested that the crystal morphology of ettringite Ca6Al2(SO4)3(OH)12·26H2O can incorporate a variety of divalent ions: Cu2+, Pb2+, Cd2+ and Zn2+, which can substitute for the Ca2+ by incorporating these ions into the lattice.[13]
參見
參考文獻
![](http://images.weserv.nl/?url=//upload.wikimedia.org/wikipedia/commons/thumb/4/4a/Commons-logo.svg/30px-Commons-logo.svg.png)
- ^ Ettringite data, Webmineral
- ^ 2.0 2.1 2.2 2.3 2.4 2.5 Ettringite in Handbook of Mineralogy
- ^ 3.0 3.1 3.2 3.3 Ettringite. Mindat.org
- ^ Ettringite-group.
- ^ Lehmann, J. (1874): Über den Ettringit, ein neues Mineral in Kalkeinschlüssen der Lava von Ettringen (Laacher Gebiet). N. Jb. Mineral. Geol. Paläont., 273-275
- ^ Carpenter, A.B. (1963): Oriented overgrowths of thaumasite on ettringite. Am. Mineral. 48
- ^ Merlini, Marco; Artioli, Gilberto; Cerulli, Tiziano; Cella, Fiorenza; Bravo, Anna. Tricalcium aluminate hydration in additivated systems. A crystallographic study by SR-XRPD. Cement and Concrete Research (Elsevier). 2008, 38 (4): 477–486. doi:10.1016/j.cemconres.2007.11.011.
- ^ Bazant, Z.P.; Wittmann F.H. Creep and shrinkage in concrete structures. John Wiley and Sons. 1982. ISBN 0-471-10409-4.
- ^ 9.0 9.1 Moore A E , Taylor H F W (1970), Crystal structure of ettringit, Acta Crystallographica Section B , 26 p.386-393
- ^ Bannister, M.A. (1935): Ettringite from Scawt Hill, Co. Antrim. Mineralogical Magazine, 24, 324-329
- ^ Goetz-Neunhoeffer, F. and Neubauer, J. (2006): Refined ettringite (Ca6Al2(SO4)3(OH)12·26H2O) structure for quantitative X-ray diffraction analysis. Powder Diffr. 21, 4-11.
- ^ Rachel L. Norman a,b, Sandra E. Dann a, Simon C. Hogg c, Caroline A. Kirk. (2013): Synthesis and structural characterisation of new ettringite and thaumasite type phases: Ca6[Ga(OH)6.12H2O]2(SO4)3.2H2O and Ca6[M(OH)6.12H2O]2(SO4)2(CO3)2, M = Mn, Sn, Solid State Sciences 25.
- ^ 13.0 13.1 Moon DH, Park JW, Cheong KH, Hyun S, Koutsospyros A, Park JH, Ok YS. (2013): Stabilization of lead and copper contaminated firing range soil using calcined oyster shells and fly ash, Environ Geochem Health 35