Adsorption Behaviour of Pyrazolo [3, 4-b] Pyridine on Corrosion of Stainless Steel in HCl Solutions
The properties of stainless steel makes the alloy suitable for many application; but this tends to change at very aggressive conditions thereby making its properties to fail. The corrosion inhibition efficiency of 2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl) acetic acid butylester (PP) on stainless steel in HCl solution was studied by weight loss method. The adsorption mechanism was investigated using adsorption isotherms. The experimental data fit Flory-Huggins and Thermodynamic/El-Awady models. The values for free energy of adsorption, ΔGoads, of PP at different surface coverage, θ, were also calculated by applying the mathematical model of Bockris-Swinkels adsorption isotherm. The variation of free energy of adsorption ΔGoads.with surface coverage, θ, was rationalised in term of interaction between adsorbed PP molecules. A possible adsorption model of PP molecules on to the steel surface was suggested.
et al., 2007; Baddoo, 2008; Cardoso
et al., 2008). Stainless steels are also known to exhibit resistance
to corrosion under conditions of erosion and cavitation such as occurred on
the blade of water turbines and on ship propellers (Nethercot
and Gardner, 2002). However, the esteemed corrosion resistance properties
give way in aggressive media (Garcia-Alonso et al.,
2007). Thus, as it is the practice with less corrosion resistance metals,
in order to retard the corrosion rate, the use of inhibitor had also been employed
for some stainless steels (Noor and Al-Moubaraki, 2008).
The assessment and corrosion prevention study of metals in pipeline also has
become imminent as a means of protecting public, financial, investment and environment
from such failures (Noor et al., 2011).
A number of heterocyclic organic compounds have been investigated for corrosion
protection of stainless steel in aggressive media and it is generally agreed
that the inhibitors passivate the metals by forming protective films on their
surfaces (Assaf et al., 2007; El-Maksoud,
2008; Oluwadare and Agbaje, 2007). The readily polarisable
high electron density centres of the inhibitor molecule are frequently considered
as their interaction centre with the metal surface. Therefore, the development
of efficient inhibitors demands an understanding, evaluation and optimization
of the adsorption interactions between the inhibitor molecules and the metal
surface. These adsorption interaction are often evaluated with adsorption isotherms
such Langmuir, Temkin, Frumkin, Flory-Huggins and El Awady/thermodynamic model
(Ebenso, 2003; Tang et al.,
2006; Abiola and Otaigbe, 2008).
According to Abiola and Otaigbe (2008), a review of
the literature revealed scanty application of Bockris-Swinkels isotherm in investigating
adsorption mechanism of hererocyclic compounds on metal surfaces despite the
valuable information that can be deduced from its thermodynamic parameters Pyrazolo[3,4-b]pyridine,
PP, had been indicated to inhibit the corrosion of stainless steel in HCl solution
but its adsorption mechanism is yet to be examined (El-Mhammedi
and Chtaini, 2007). In continuation of our efforts at exploring Bockris-Swinkels
isotherm to study the adsorption of organic corrosion inhibitors on metal surfaces,
this study reports adsorption thermodynamics parameters of PP on stainless steel.
MATERIALS AND METHODS
Synthesis of the pyrazolo[3,4-b]pyridine derivatives: PP (Scheme1) was
synthesized under microwave irradiation according to the procedure of Xiang
et al. (2006). The synthesis can be described by the reaction shown
in scheme 1.
||Synthesis of 2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo
[3, 4-b] pyridin-4-yl) acetic acid butylester
A dry flask (25 mL) was charged with 3-amino-1-phenylpyrazol-5-one (1 mmoL)
butyl (5-chlorohex-3-one-4-enoate)nn 2 (1 mmoL), glycol (2 mL) and catalyst
ZnCl2 (0.05 mmoL). The flask was then connected with refluxing equipment.
After microwave irradiation for 8-12 min, the reaction mixture was cooled and
washed with ethanol. The crude products obtained were purified by recrystallization
from 95% ethanol to afford 3.
The experiments were performed with commercial stainless steel 316 having the chemical composition given in Table 1 and the corrosion rate was monitored by weight loss method.
Weight loss measurements: The Stainless steel was mechanically pressed-cut
into coupons of dimension 3x3 cm and used as procured without further polishing
but were degreased in absolute ethanol, dried in acetone, weighed and stored
in a moisture-free desiccator prior to use. All reagents are BDH grade and used
as sourced without further purification. Double distilled water was used for
all solution preparations. The heterocyclic compound (2-(4-Methyl-3-oxo-2-phenyl-2,
3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl) acetic acid butylester) was added
to acidic media without pre-treatment. The effect of addition of the inhibitor
pyridazine compounds tested at different concentrations on the corrosion of
steel in 0.1 M HCl solution was studied by weight-loss at 298 K after 6 h of
immersion period at concentrations of 4.57x10-5, 9.13x10-5,
3.65x10-4, 4.57x10-4 and 6.85x10-3 M at 25°C.
0.1 M HCl solutions were employed as blank.
|| Chemical composition of commercial 316 stainless steel
Inhibition efficiency (I.E%) is calculated as follows:
where, W and Wo are the corrosion rates of steel with and without the inhibitor, respectively.
The surface coverage values θ at electrode are calculated from the corrosion rate of stainless steel in the electrolytes: surface coverage values θ was calculated by:
RESULTS AND DISCUSSION
The dependence of corrosion rate on concentration of PP in the supporting electrolyte
(0.1 M HCl) at 25°C is shown in Fig. 1. The corrosion
rate of the stainless steel in the electrolytes decreases with increasing concentration
of PP in the electrolytes; suggesting that PP is a corrosion inhibitor for stainless
steel in these electrolytes. And this result is in agreement with previous reports
on pyridine derivatives as corrosion inhibitors (Abd El-Maksoud
and Fouda, 2005).
The variation of the inhibition efficiency with the logarithm of bulk concentration is presented in Fig. 2. The S-shaped curve of the graph portrays the formation of a protective barrier film of inhibitor molecules on the steel surface. The electron rich centres of the heteroatoms of the inhibitor molecules are potential centres of Lewis acid-base interaction with the metal surface. Although, the N- and O-atoms in PP have lone pair of electron, Lewis acid-base of PP with metal surface is more likely through the N-atoms.
It had been suggested that metal corrosion inhibition of pyridine derivatives
is often through coverage or blocking the metal surface from excessive contact
with the corrosion media. Upon adsorption on the metal surface it imposes higher
energy barrier to the dissolution of the metal in the corrosion media.
||Variation of corrosion rate (mg cm-2 h) with concentration
of (2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl)
acetic acid butylester) on the stainless steel in 0.1 M HCl at 25°C
||Relationship between Inhibition Efficiency and concentration
of 2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl)
acetic acid butylester) (PP)
It is explained that the protective action is a function of the π-electron
density on the nitrogen atom and the size of the organic molecule (Kuprin
et al., 1999). The corrosion inhibitive properties of pyrazole derivatives
and some pyridine-pyrazole compounds had also been reported (Abdallah,
2003; Tebbji et al., 2005; Elayyachy
et al., 2005; Chetouani et al., 2005)
no study of the adsorption behaviour of the fusion of Pyrazolo [3, 4-b] Pyridine
groups has been conducted. Table 2 depicts the linearization
parameters and the free energies of adsorption of PP on stain steel surface
in 0.1 M HCl.
Precise elucidation of the mechanism of adsorption of the inhibitor on metal surface is crucial for the design and evaluation of corrosion inhibitors. This makes adsorption isotherms imperative for elucidating the mechanism of surface (organo-electrochemical) reactions. Evaluation with an adsorption isotherm involves: fitting the data with the isotherm, optimisation of the adjustable parameters of the isotherm and appraisal of the physical reasonableness of the optimizing parameters in terms of the physical/chemical principle (s) on which the isotherm. The result presented in Table 2 revealed that the data are reasonably fitted by Flory-Huggins and El-Awady model. The data did not agree with a active centre 1:1 type adsorption mechanism. However, it is consistent with localized adsorption models that take into consideration for adsorbate-adsorbate interactions and adsorbent-adsorbate interaction via displacement of solvent molecules. Also, the data displayed less agreement for models with consideration for mobility of the adsorbed molecules (Volmer and Hill-De Boer isotherms).
Quasilattice models considered the surface of the electrode in aqueous solution to be covered with water dipoles and for adsorption of organic molecules to occur, these water dipoles must be replaced by organic molecules in a reaction as follows:
The thermodynamics of the substitution process depends on the numbers of water
molecules (n) removed by the organic molecules. The values of the apparent free
energy change (ΔGoads) for the adsorption process
can be evaluated from θ values with Bockris-Swinkels equation (Bockris
and Khan, 1993).
Based on substitutional adsorption process for the space filling models of
adsorption of organic molecules on electrode surface, for 5≤n≤1 for adsorption
of PP on the stainless steel surface, the values of ΔGoads
for the adsorption process were calculated at each θ values by using Bocris-Swinkels
equation is presented in Fig. 3.
||ΔGoads J moL-1 for
2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl)
acetic acid butylester (PP) on stainless steel as a function of surface
coverage θ in 0.1 M HCl as the suporting electrolyte
||Parameters of linearization of adsorption models for 2-(4-Methyl-3-oxo-2-phenyl-2,
3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl) acetic acid butylester (PP)
adsorption in acidic solutions
The graph showed that the free energies of adsorption decreases with increasing
surface coverage for when n value = 1, on the other hand, for n>1 ΔGoads
value increases with increasing surface coverage. This suggests positive or
cooperative adsorption at higher concentration and surface coverage.
It is important to put in to consideration that, the butyl ester group fragment of the in the inhibitor molecule is susceptible hydrolysis to give butanol and the remaining acid fragment. In addition the three N-atom centres are also prone to protonation in the acidic media. The resulting cation in solution is shown in scheme 2.
||The hydrolysis and protonation reaction of 2-(4-Methyl-3-oxo-2-phenyl-2,
3-dihydro-1H-pyrazolo [3, 4-b] pyridin-4-yl) acetic acid butylester) in
These cations can adsorb on the stainless steel metal surface even at high
chloride ion concentration. It had been shown that anions (from the electrolyte)
on the electrode surface provide a better electrostatic condition which promotes
a direct adsorption of cations on the surface via formation of ion pair.
||Adsorption models for 2-(4-Methyl-3-oxo-2-phenyl-2, 3-dihydro-1H-pyrazolo
[3, 4-b] pyridin-4-yl) acetic acid butylester) (PP) on the stainless steel
surface in HCl media; * the steel surface
On this basis, adsorption models for PP on the stainless steel surface in the
acidic media are proposed.
At low concentrations of PP or surface coverage [θ = 0.7] PP, cations
(R3+) from solution cluster around Cl¯ and neighbourhood by
strong coulombic attraction on the metal surface where, Cl¯ are previously
adsorbed (Fig. 4; Model I). The strong coulombic attraction
restricts the mobility of the cations which may be responsible for the relatively
low conformity of the data with isotherms that give provisions for mobility
of adsorbed molecules. The cations which are essentially acid fragment of the
hydrolysis product can interact with one another through condensation reaction.
The secondary amine group of one cation fragment can undergo amide formation
with the acid group of another. This reaction is accompanied with the release
of a molecule of water. This accounts in part for the considerable fitting of
the data with models that take into consideration for adsorbate-adsorbate interaction
and the observed increasing value of ΔGoads with
increasing surface coverage for n value>1. A model similar to model I had
been proposed for adsorption of Vitamin B1 derivatives in HCl solution (Abiola
and Oforka, 2004). For a situation of weak adsorption of chloride ions,
R3+ at high concentration withdraw the anions on the surface into
the solution, coadsorption of the cations and Cl¯ ions is possible as in
model II with increasing the concentration of PP. The degrees of desorption
of Cl¯ ions from the surface depends on the degree of adsorption of R3+
which is a function of the concentration of PP. At much higher concentrations
of PP, the Cl¯ ions on the surface provide a better electrostatic condition
which promotes a direction adsorption of the cations on the surface through
its pie electron system as depicted in model III (Abiola,
Although on the basis of energetics of the adsorption process: two types of
adsorption process had been established; physisorption (electrostatic interaction
between the electron density of the molecules and surface atoms of the metal)
in which the ΔGoads is up to -20 kJ mol-1
and chemisorption (in which there exist a chemical bond between the molecule
or ion and the metal surface) where the ΔGoads is
more negative than -40 kJ mol-1 (Abiola, 2005;
Abiola, 2006). The values of Δgoads
obtained (from Bocris-Swinkels equation for n = 1, 2, .., 5) range 45.54
to53.83 kJ mol-1 K-1 support chemisorption mechanism
with strong extra coulombic bonding of the inhibitor to the stain steel surface.
From the present study, following conclusion can be made:
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||The corrosion rate of the stainless steel in the supporting
electrolytes decrease with the increase in adsorbability of PP (values of
surface coverage, θ
||The negative values of ΔGoads suggest the spontaneous
adsorption of PP on the mild steel
||The magnitude of ΔGoads indicates physisorption
mechanism and PP molecules in cationic form adsorb on the stainless steel
surface via formation of ion pair with chloride ion acting as bridge between
||The adsorption data is consistent with Flory-Huggins and Thermodynamic/El-Awady