The interaction of diphosphonates with calcitic surfaces : understanding the inhibition activity in marble dissolution

The rates of dissolution of calcitic Carrara marble have been reported to be significantly reduced in alkaline pH (pH 8.25) at 25 degrees C in the presence of (1-hydroxyethylidene)-1,1 diphosphonic acid (HEDP). The adsorption takes place at the calcite/water interface at the double layer through the...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 22(2006), 5 vom: 28. Feb., Seite 2074-81
1. Verfasser: Spanos, Nikos (VerfasserIn)
Weitere Verfasser: Kanellopoulou, Dimitra G, Koutsoukos, Petros G
Format: Aufsatz
Sprache:English
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
LEADER 01000caa a22002652 4500
001 NLM160825547
003 DE-627
005 20250207033357.0
007 tu
008 231223s2006 xx ||||| 00| ||eng c
028 5 2 |a pubmed25n0536.xml 
035 |a (DE-627)NLM160825547 
035 |a (NLM)16489791 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Spanos, Nikos  |e verfasserin  |4 aut 
245 1 4 |a The interaction of diphosphonates with calcitic surfaces  |b understanding the inhibition activity in marble dissolution 
264 1 |c 2006 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 16.05.2007 
500 |a Date Revised 21.02.2006 
500 |a published: Print 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a The rates of dissolution of calcitic Carrara marble have been reported to be significantly reduced in alkaline pH (pH 8.25) at 25 degrees C in the presence of (1-hydroxyethylidene)-1,1 diphosphonic acid (HEDP). The adsorption takes place at the calcite/water interface at the double layer through the interaction of charged surface species with the charged solution species of the adsorbate. The present work focused on obtaining a better understanding of the interaction of the calcite surface with HEDP. Calculations were performed according to the triple layer model, assuming the formation of surface complexes between the charged surface species of calcite and the species of HEDP dominant at pH 8.25. According to the model, the adsorbed species are located at the inner Helmholtz plane of the electrical double layer. Strong lateral interactions between the adsorbed species were suggested and were corroborated from the calculation of the respective energy, which was equal to 69 kJ mol(-1). The adsorption isotherm was consistent with the proposed model at low surface coverage values, while discrepancies between the values experimentally measured and the predicted were found at higher adsorbate concentrations. The deviations from the predicted values were attributed to the fact that HEDP adsorption on calcite resulted in the formation of multiple layers. The model explained adequately the changes in the zeta-potential values of calcite in the presence of HEDP in the solution which resulted in charge reversal upon adsorption 
650 4 |a Journal Article 
700 1 |a Kanellopoulou, Dimitra G  |e verfasserin  |4 aut 
700 1 |a Koutsoukos, Petros G  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1991  |g 22(2006), 5 vom: 28. Feb., Seite 2074-81  |w (DE-627)NLM098181009  |x 0743-7463  |7 nnns 
773 1 8 |g volume:22  |g year:2006  |g number:5  |g day:28  |g month:02  |g pages:2074-81 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |d 22  |j 2006  |e 5  |b 28  |c 02  |h 2074-81