1991
DOI: 10.5006/1.3585307
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Acid Corrosion Inhibition of Nickel by 2-(Triphenosphoranylidene) Succinic Anhydride

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Cited by 319 publications
(108 citation statements)
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“…It has been reported that values of ðÀDG 0 ðadsÞ Þ up to À20 kJ/mol are consistent with the physisorption; those around À40 kJ/mol or higher are consistent with chemisorption [38] and [62]. The high values of ðÀDG 0 ðadsÞ Þ and relative increase with temperature in the range of 25-55°C suggest a chemisorption.…”
Section: Adsorption Isothermsupporting
confidence: 62%
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“…It has been reported that values of ðÀDG 0 ðadsÞ Þ up to À20 kJ/mol are consistent with the physisorption; those around À40 kJ/mol or higher are consistent with chemisorption [38] and [62]. The high values of ðÀDG 0 ðadsÞ Þ and relative increase with temperature in the range of 25-55°C suggest a chemisorption.…”
Section: Adsorption Isothermsupporting
confidence: 62%
“…The most frequently used isotherms to describe the adsorption process are: Langmuir, Frumkin, Hill de Boer, Parsons, Temkin, Flory-Huggins, Dhar-Flory-Huggins, and Bockris-Swinkels [38].…”
Section: Introductionmentioning
confidence: 99%
“…The negative values of ∆G o ads ensure the spontaneity of the adsorption process and stability of the adsorbed layer on the electrode surface. Generally, values of ∆G o ads lower than -40 kJ mol -1 are consistent with the electrostatic interaction between the charged molecules and the charged metal (physisorption); those around -50 kJ mol -1 or higher involve charge shairing or charge transfer from organic molecules to the metal surface to form a coordinate type of bond (chemisorption) [32,34]. In the present work, the calculated values of ∆G o ads are lower than -40 kJ mol -1 , indicating, therefore, that the adsorption mechanism of SA on LCS surface in 1.0 M HCl solutions (pH 4) was typical of physisorption (see Table 3).…”
Section: Adsorption Isotherms and Thermodynamic Functions Of The Adsomentioning
confidence: 83%
“…It seems that the thermodynamic functions of the adsorption process obtained from the two methods are parallel and in a good agreement. The calculated values of ∆G o ads are low and negative, suggesting that the nature of this inhibitor adsorption is mainly physisorption and spontaneous [22][23][24][25]. It is usually accepted that the value of ∆G o ads around -20 kJ mol -1 or lower indicates the electrostatic interaction between charged metal surface and charged organic inhibitor in the bulk of the solution [26], while those around -40 kJ mol -1 or higher involve charge sharing transfer between the metal surface and the organic inhibitor [27].…”
Section: Adsorption Isotherms and Thermodynamic Functions Of Adsorptimentioning
confidence: 99%