w. lemlikchi, p. sharrock, m. fiallo, a. nzihou and m.-o. mecherri (*)

2nd International Symposium on Innovation and Technology in the Phosphate Industry - [SYMPHOS 2013]

Hydroxyapatite and Alizarin sulfonate ARS modeling interactions for textile dyes removal from wastewaters

W. Lemlikchi, P. Sharrock, M. Fiallo, A. Nzihou and M.-O. Mecherri (*)

Hydroxyapatite (HA) Ca5(PO4)3(OH) is a calcium phosphate usually written as Ca10(PO4)6(OH)2

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Hydroxyapatite (HA) is more than an adsorbent and was previously used for eliminating heavy metals in water pollution by adsorption and ion exchange.

HA was also used for eliminating textile dyes from waste waters.

HA has multiple exchange capacities inside its structure, including formation of vacancies to accommodate ions with other valencies, in particular carbonate ions and alkali and other metal ions.

Our previous works showed that HA can be regenerated after calcination, and reused several times.

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Alirarin red sulfonate (ARS) sodium 3-alizarin-sulfonate (also called Alizarine Carmine, Alizarine Red S, Alizarine S) is a typical dihydroxyanthraquinone that has been used as a traditional natural dye originally derived from the roots of plants of the madder genus, also used a histochemical stain for calcium in bone tissues .

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http://en.wikipedia.org/wiki/Dihydroxyanthraquinone

http://en.wikipedia.org/wiki/Madder


Textile mordant dyes such as alizarin generally contain a functional ligand capable of reacting strongly with

Al(III), Cr(III), Co(II), Cu(II), Ni(II), or Fe(II), Fe(III) salts

to give different colored complexes with the textile.

The adsorption of alizarin red has long been used to assess the performance of the apatite before use in a water treatment facility.

This led us to investigate the way calcium ions interact simultaneously with ARS and phosphate.

Alizarin could therefore be used as a

model compound for more complex dyes.

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Anthraquinone and Alizarin forms and structures• Alizarin contains hydroquinone and catechol moiety

(with two adjacent OH phenol groups);

So, according to pH conditions, the catechol moiety could loose whether one proton or two protons

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Assuming pK values (pK (2-OH) = 5.49 and pK(1-OH) = 10.85) of the diacid alizarin sulfonate given by Wu and Forsling, we have drawn the theoretical distribution diagram of alizarin sulfonate (ARS) and that of phosphate system.

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Translated from: Jana Sanyova, Contribution à l'étude de la structure et des propriétés des laques de garance, Thèse ULB, Bruxelles 2001.

Formation of Metal-ARS complexes via two modes:¤ five-membered complex cycle: so-called « catecholate » or « diphenolate »;¤ six-membered complex cycle: so-called « chelate » or « ketophenolate ».

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Many authors like Moriguchi claimed two types of bonding of ARS could be observed on HA, one involving:• diphenolate or catecholate salt formation with 2 phenolic hydroxyl groups, • ketophenolate akin to chelate formation with a phenolic hydroxyl group

and adjacent quinone oxygen

Binding schemes according to Moriguchi et al., also reported by Ibsen and Birkedal

The complexation mechanisms reported in the literature never involve participation of the sulfonate group (‑SO3

-) of the alizarin-sulfonate ARS.

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Structures of Ca-ARS 1:1 and 1:2 complexes

The doubly deprotonated ARS forms a 1 to 1 calcium complex.

The monodeprotonated ARS forms a 1 to 2 complex.

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The ARS dye changes its color with the variation of the pH from violet (for basic pH) to pink, red, orange and therefore to yellow (for the most acidic pH values).

A very similar theoretical spectrum has been given by Turcanu and Bechtold for numerous pH values.

Our experimental UV spectrum given for different pH values after addition of NaOH to 0.1mM ARS solutions.

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T. Moriguchi et al. / Journal of Colloid and Interface Science 260 (2003) 19–25.

Our experimental IR spectrum of HA with increasing concentrations of ARS [HA + (5-10-20)% of ARS].

At right: IR spectra of (a) HAP (microscopic method) and (b) ARS (KBr method)

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pH shifts for some concentrations of alizarin during its titration with NaOH.

pH shift: corresponds to a difference of added volume of NaOH for a given constant pH value as a function of stoichiometry.

pH jump: corresponds to a difference of pH for a given added volume of NaOH: HBO2 appears to be stronger in presence of polyols.

The maximum pH shift occurs at 2 ARS for 1 Ca

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The maximum pH shift occurs for2 ARS for 1 Ca

Titration of 1.25 mm calcium ions in the presence of increasing ARS concentrations

The 1 to 2 calcium-alizarin complexforms as follows:Ca2+ + 2 ARS------ Ca(ARS)2 + 2 H+

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Titration of Ca/P solution with increasing amounts of alizarin

The pH shift is lower than in the case of Ca + Ars with no phosphate, but occurs for 2 ARS for 1 PO4

Thus, Alizarin reacts with surface bound apatite calcium ions

We had : Ca/PO4= 1.5 = 3:2 => 2 Ca/2PO4=3 ; the maximum shift occurs for ARS/PO4 = 2 or 2 ARS/PO4 = 4

The complex formulae will be: (ARS)4Ca3(PO4)2.14HAP-ARS-MECHERRI


For the mixtures calcium-alizarin, calcium-phosphate and calcium-phosphate-alizarin, there are both a pH jump and a pH shift of the equivalent points to the titration of alizarin and of the phosphorous species originating from apatite HA.

pH jumps and pH shifts

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Butmuch remains to be done to elucidate the mechanisms of formation of many other metal-dye complex and especially for metal-phosphates-dye complexes encountered in industrial textile mixtures and waste residues.Many thanks

for your attention !

Conclusion:We tried to show the interactions of calcium phosphate with alizarin dye model.

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Pacific berber warrior double deprotonated


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Pacific berber warrior double deprotonated

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Release of the potential acidity of (weak) boric acid via exaltation with polyols

pH jump during synergic titration of boric acid HBO2 0.1 M by NaOH 1M in presence of mannitol by the Sorensen method.


Illustrative example of a synergic titration of copper ions with alizarin in presence of borates.

Alizarin-borate complex structure as suggested by Panahi et al.

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w. lemlikchi, p. sharrock, m. fiallo, a. nzihou and m.-o. mecherri (*)

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