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Article

A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium

by
Qing Yang
1,
Bing Lin
1,*,
Junlei Tang
1,2,*,
Yingying Wang
3,
Hongpeng Zheng
1,
Hailong Zhang
1,4,
Zhen Nie
5 and
Yanna Zhang
5
1
School of Chemistry and Chemical Engineering & Institute for Carbon Neutrality, Southwest Petroleum University, Chengdu 610500, China
2
Tianfu Yongxing Laboratory, Chengdu 610217, China
3
Key Laboratory of Optoelectronic Chemical Materials and Devices (Ministry of Education), Jianghan University, Wuhan 430056, China
4
Research Institute of Tianfu New Energy, Chengdu 610217, China
5
Research Institute of Petroleum Exploration and Development, CNPC, Beijing 100083, China
*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(3), 1314; https://doi.org/10.3390/molecules28031314
Submission received: 26 December 2022 / Revised: 19 January 2023 / Accepted: 19 January 2023 / Published: 30 January 2023
(This article belongs to the Special Issue Synthesis, Characterization and Theoretical Study of Corrosion Inhibitors)
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Abstract

:
To provide carbon steel a long-term corrosion protection effect in NaCl solutions with different pH values, based on poly-acrylamide (PAM) and oleate imidazoline (OIM), a solid corrosion inhibitor with the properties of pH-controlled release was synthesized. SEM, FTIR and TGA results indicated that the OIM inhibitors were successfully loaded into PAM hydrogel with a high OIM encapsulation content (39.64 wt.%). The OIM release behavior from the hydrogel structure has two stages, quick release and sustained release. The pH of solutions could affect the initial release kinetics of OIM inhibitors and the diffusion path in the hydrogel structure. Weight loss measurement of L80 steel in different pH solutions with OIM@PAM proved the inhibitor responsive release mechanism and anticorrosion performance. The inhibition efficiency of OIM@PAM can maintain over 80% after long-term immersion in a harsh corrosive environment (pH 3), which is much higher than the inhibition efficiency of OIM@PAM in a moderate corrosive solution.

1. Introduction

Corrosion leads to material degradation in various environments, which is due to the inter-chemical and electrochemical actions between metal substrates and environments [1]. Organic inhibitors have been wildly used to solve the corrosion issue due to their high inhibition efficiency, wild application range, good solubility and relatively low toxicity [2,3,4]. The inhibition mechanism of organic inhibitors has been explained by the formation of an adsorption film. Organic inhibitors adsorbed on metal surfaces through the delocalized electrical charge on the heteroatoms such as N, S, and O [1,5]. Many scholars have focused on the effect of inhibitor functional group type, quantity, and molecular structure on inhibition efficiency [5,6,7]. However, there are several drawbacks to the direct use of inhibitors in an aqueous corrosion environment. To ensure the corrosion protection effect of organic inhibitors, the excessive use of inhibitors will lead to a waste of resources, and the inhomogeneous distribution of inhibitors in corrosive environments will limit the long-lasting effect and anticorrosion effect of inhibitors. In addition, adding inhibitors is a high-selectivity corrosion protection method, which means the inhibitors are usually suitable for a certain material and corrosion environment.
Recently, scholars became interested in encapsulating corrosion inhibitors into containers to extend the inhibitor protection time and enhance anticorrosion effectiveness as the drawbacks of direct using inhibitors. Many researchers try to encapsulate organic inhibitors into MOFs [8], hollow particles [9], core–shell nanofiber [10], gel materials [11], and so on. A critical application of encapsulated inhibitors is to provide self-healing properties to organic coating [8,9,10,11]. However, the low inhibitor concentration and complex construction of self-healing coating limited the industrial applications. Another important application of encapsulated corrosion inhibitors is solid inhibitors. The inhibitor release behavior from encapsulated container is adjusted according to the change of environment by modifying the inhibitor container. Wang et al. [12] reported calcium alginate gel capsules loaded with inhibitors. The synthesized capsules could release inhibitors during the sinking process, and effectively prevent the tube in oil well from corrosion. Dong and his coworkers [13,14,15] reported a series of solid intelligent inhibitors. The container could release inhibitors faster in an acidic environment in comparison with a neutral environment, and provide better anticorrosion performance.
Hydrogel material is a hydrophilic 3D natural or synthetic polymer network structural gel, which could swell in water. Hydrogel has been used in drug delivery systems due to the controllable release rate [16]. Researchers have tried to use hydrogel in corrosion protection systems. Wen et al. [17] reported an solid hybrid hydrogel coating for steel corrosion protection. The weight percentage of loaded inhibitor is about 10%, and the releasing property of inhibitors rises as the external environment pH value decrease. Dong et al. [13] tried to use hydrogel to synthesize solid inhibitors, which benefits long-term corrosion inhibition due to the sustained inhibitor supply. Hydrogel is an ideal container material to synthesize a solid inhibitor, and still needs further investigation on increasing the inhibitor content, controlling inhibitor release behavior, and enhancing the mechanical property to make the application of a solid inhibitor based on the hydrogel.
Owing to the advantages of excellent corrosion protection performance, low toxicity, stability and low economy cost, imidazoline and its derivatives are widely utilized in the industrial fields. The high inhibition efficiency of oleate imidazoline (OIM) derivatives is associated with good adsorption characteristics and the ability to form a hydrophobic film on metal surfaces [11,18]. Imidazoline and its derivatives have excellent inhibition effects in acid [19], neutral [20] and alkaline [21] mediums. In our previous work [11], OIM was introduced into gel coating to enhance the anticorrosion performance of coating in 3.5 wt.% NaCl. In this study, the anticorrosion performance is mainly dependent on the physical shielding effect of the coating, but the combination of gel material and corrosion inhibitor to enhance the anticorrosion performance is feasible and effective. Inspired by this work, gel material could be an ideal carrier for encapsulating material to protect carbon steel. The controllable release behavior of inhibitors could enhance the environment applicability and protection time. Therefore, the drawbacks of directly using inhibitors in an aqueous corrosion environment would be significantly improved.
This work successfully synthesized a pH-controlled release solid inhibitor based on PAM hydrogel and OIM. Scanning electron microscope (SEM), Fourier-transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), and mechanical tests were employed to investigate the structure and characteristics of OIM@PAM. The OIM release behavior of OIM@PAM in various pH value aqueous environments was studied by the UV–visible spectrophotometer, and the release mechanism is discussed in-depth. The outstanding anticorrosion performance of OIM@PAM in different pH corrosion mediums was carried out by weight loss measurement and SEM observation, and the solid inhibitor might be applicable for the corrosion protection of facilities and pipelines in oil production.

2. Results and Discussion

2.1. Characteristics of OIM@PAM

2.1.1. Surface Morphology of OIM@PAM

Figure 1 shows the surface and interior morphologies of synthesized PAM hydrogel and OIM@PAM. It can be seen that OIM loaded into PAM hydrogel causes different morphology. For the PAM hydrogel (Figure 1a,b), the surface and interior morphology are relatively smooth and flat without pore canals. This result is due to the surface tension of water and the PAM interface, which lead to the tight bonding between PAM molecules during the evaporating progress [22], while the surface and interior morphology of OIM@PAM includes numerous pore canals, which is the characteristic structure of hydrogel containers loaded with corrosion inhibitors after vacuum drying [17]. The pores area distribution in the surface and interface of OIM@PAM is counted through the software of “Image–J”, and the results are displayed in Figure S1. The pore canals existing in OIM@PAM can provide space for OIM accommodation and release.

2.1.2. FTIR Analysis

Figure 2 illustrates the FTIR spectra of OIM@PAM, and the pure OIM and PAM were also tested as control samples. The high-intensity broad absorption peak located in 3440 cm−1 is assigned to the antisymmetric stretching vibration of the –NH– group that existed in OIM, PAM and OIM@PAM [23,24]. The sharpened peak at 1640 cm−1 contributed to the −C=C−, −C=N− and −C=O− double bonds [12,24], which can be found in OIM, PAM and OIM@PAM. The stronger peak at 1640 cm−1 of OIM@PAM than PAM indicates the load of OIM corrosion inhibitor. There are several characteristic peaks only appearing in OIM and OIM@PAM FTIR spectra. The weak peaks at 2923 cm−1 and 2861 cm−1 correspond to the symmetric and antisymmetric stretching vibrations of the −CH2− group, respectively, which only consisted of OIM and OIM@PAM [25]. The interferential peak at 2359 cm−1 is associated with the antisymmetric stretching vibration of CO2 due to infrared spectrometer optical path imbalance [26], and the peak located in 1290 cm−1 is attributed to the stretching vibration of the tertiary amine group in OIM’s imidazole ring [12,23]. The above peaks indicate that OIM was successfully loaded in PAM hydrogel. In addition, there is no new peak in OIM@PAM in comparison with the FTIR spectra of OIM or PAM. The OIM is doped into the network structure of PAM without a chemical reaction, which result is consistent with the interior morphology of PAM hydrogel.

2.1.3. Thermostability and Inhibitor Loading Content of OIM@PAM

Figure 3 compares the thermal gravimetric analysis (TGA) results of OIM, PAM and OIM@PAM. The investigated OIM and PAM hydrogel showed two main degradation stages. The first stage is related to the evaporation of water molecules and other volatile impurities through dehydration [27]. For OIM, the weight loss of this stage (40–190 °C) is 8.56%, and for PAM hydrogel, the weight loss of the first stage (40–190 °C) is 6.48%. These results reveal that the water content in PAM is lower than that of OIM. More importantly, the OIM has better thermal stability in comparison with PAM. The second stage is related to decomposition [27,28]. OIM started to decompose at 190 °C and achieved the maximum decomposition rate at 375 °C. The mass change of OIM stopped at 500 °C, the weight loss was 86.03%, and 3.60% substance remained. The decomposition of PAM started at about 190 °C and reached the highest decomposition rate at about 400 °C. The weight loss of PAM was 66.30% mainly due to the intramolecular and intermolecular imidization reactions on the amide group of PAM. These imidization reactions occurred when the temperature reached 190 °C, and released NH3, H2O and CO2 [29].
For the TGA curve of OIM@PAM, the first weight loss stage was at 40–190 °C. The weight loss caused by water volatilization was about 6.93%. As the temperature increased to 250 °C, the TGA curve of OIM@PAM was parallel to that of PAM. This result is due to the high thermal stability of OIM at this temperature, and the weight loss of synthesized composition is mainly caused by PAM. As the temperature further increased, the OIM@PAM rapidly decomposed. OIM@PAM had the highest decomposition rate at about 375 °C, which was consistent with OIM. The capacity of OIM in OIM@PAM could be calculated by the decomposition ratio of TGA curves using the following equation (1) [30]:
DOIM × COIM + DPAM × CPAM = DOIM@PAM
where DX is the decomposition ratio of the compound, and CX is the content of OIM or PAM in OIM@PAM. Therefore, the content of anticorrosion inhibitor OIM loaded in the OIM@PAM is 39.64%, which is quite a high value in comparison with other researchers [13,31]. The TGA results reveal the excellent thermal stability of synthesized OIM@PAM, which could be used in the corrosion environment of temperature lower than 190 °C, and the high OIM load content could ensure the anticorrosion performance of this solid inhibitor, which will be discussed in the following section.

2.1.4. Mechanical Properties of OIM@PAM

Appropriate mechanical property is the premise to ensure the practical application of OIM@PAM in a corrosion environment, especially for the flowing harsh corrosion environment. The stress–strain curves of PAM hydrogel and synthesized OIM@PAM are shown in Figure 4. The average tensile strength (σb) values of PAM and OIM@PAM are 17.69 MPa and 13.21 MPa, respectively. Compared with PAM, the hybrid of OIM into PAM leads to the decrease of OIM@PAM strength and a remarkable increase of elongation at break. From the TGA, the OIM load content in OIM@PAM is 39.64%, and the PAM content is almost 60.36%. The hybrid of OIM into PAM leads to the monomer concentration of PAM decreasing and weakening the length of the PAM polymer chains. PAM with a shorter chain length leads to the decrease of the physical entanglement strength. Therefore, a lower tensile strength of OIM@PAM is obtained compared with PAM [32]. When the OIM@PAM sample was stretched, reversible non–covalent interactions between the PAM network and OIM, such as π–π stacking and hydrogen bond, etc., can break to effectively dissipate energy and prevent crack propagation, thus increasing its elongation at break [33].

2.2. Inhibitor Releasing Characteristics and Mechanism of OIM@PAM

2.2.1. Release Behavior of OIM@PAM in Different pH Environment

Figure 5 shows the release behavior of OIM@PAM in wide range pH solutions. From Figure 5a, the concentration of OIM in the test solutions declined as the immersion time increased. In the first 24 h, the inhibitor concentration decreased from over 350 mg/L to about 100 mg/L. As the releasing time further increased, the inhibitor OIM concentration maintained at several dozen mg/L. The two release stages might be caused by the different releasing mechanisms. OIM is a highly effective corrosion inhibitor in various corrosive environments. In our previous study [11], the inhibition efficiency of 10 mg/L OIM in a simulated 3.5 wt.% NaCl corrosion environment could reach up to 92%. The inhibitor release behavior of OIM@PAM in different pH solutions had no definite difference. The released OIM concentration in pH 3 solution was the highest, which could reach 60 mg/L after 168 h of immersion. As the immersion solution pH increased to 7, the released OIM concentration after 168 h decreased to about 20 mg/L. As the solution pH value further increased, the OIM concentration increased to 30 mg/L. Figure 5b shows the cumulative release ratio of inhibitors from OIM@PAM in different pH solutions. In the first 24 h, the cumulative release ratio of the inhibitor reached about 20% to 30% for each condition. As the release time increased, the apparent release ratio could be observed. After the 168 h release test, the cumulative release ratio of the tested sample in pH 3 solution reached the highest value at 81.09%. As the test solution pH value increased, the release ratio decreased to 47.40% in a neutral environment, and then slightly increased in an alkaline solution. The release behavior of OIM from OIM@PAM is directly affected by the pH value of solutions.

2.2.2. Release Mechanism of OIM@PAM

From Figure 5, two release stages of OIM@PAM could be observed [34]. When OIM@PAM was immersed in solutions, OIM could be released quickly through the short diffusion path in the first 2 h, which led to the high concentration of OIM in the first 2 h. The OIM concentration gradually decreased over 2 to 24 h in the releasing process, which was related to the enlargement of the transport path of OIM from the interior of OIM@PAM to the test solution. As the immersion time increased, the decrease of the OIM amount in OIM@PAM and the increase of the transport distance led to the released OIM concentration continuing to decline from 24 h to 168 h. The two release stages of the cumulative release curve were fitted by the Korsmeyer–Peppas equation [17,35,36] and the Parabolic equation [37,38], respectively.
Stage   I   ( 0   to   24   h ) :   Korsmeyer – Peppas :   M t M ∞ = k t n
Stage   II   ( 24   to   168   h ) :   Parabolic :   ( M t / M ∞ ) t = k t − 0.5 + a
where Mt and M∞ are the cumulative release ratio of OIM at time t and infinite time, respectively. k is the release behavior kinetic constant, which is associated with the OIM delivery system. For the Korsmeyer–Peppas model in the first stage, n is an important exponent, which could determine the release mechanism of OIM from OIM@PAM [17]. If n ≤ 0.45, the release mechanism follows Fick diffusion, and the inhibitor release is controlled by inhibitor concentration gradient [39,40]. If 0.45 < n < 0.89, the release mechanism is dominated by Anomalous transport or non-Fick transport [17,41]. If n ≥ 0.89, the release behavior is followed Case II transport [39,41], which means the release rate is only controlled by the matrix relaxation [39]. For the second stage, a is a constant. The parabolic model of the second stage indicates a sustainable release range [38]. All fitted results are presented in Figure 6, and the fitted parameters are presented in Table 1.
Figure 7 shows the schematic of the two OIM releasing stages. For the first stage, the OIM release behavior is in good agreement with the Korsmeyer–Peppas equation, and the fitted R2 is above 0.99. The n values for this stage in different pH solutions are in the range of 0.45~0.89, which indicates the inhibitor release mechanism is in accord with the anomalous transport [17,41]. The inhibitor release behavior is controlled by both diffusion and matrix relaxation [39]. The released OIM due to the diffusion mechanism follows Fick’s law presented in Equation (4):
∂ c ∂ t = D ∂ 2 c ∂ x 2
The matrix relaxation of PAM gel is due to the absorption of water into the gel 3D network, and the swelling of the PAM network is caused by water invasion, resulting in the release of inhibitors. The OIM could dissolve in water. Once the OIM in OIM@PAM contacts with corrosion mediums, the dissolution of OIM becomes the initial dynamic force of the inhibitor release. The process of water invasion into gel also follows Fick’s second law [42,43], which means the axial water transfer is according to the concentration-dependent diffusivities in Equation (5):
∂ C w ∂ t = ∂ ∂ z ( D w ∂ C W ∂ z )
where Cw is the water concentration in hydrogel, z is the water transfer distance, t presents the time and Dw is the diffusion coefficient of water in the PAM gel at time t. Since it is assumed that the diffusion coefficient depends on the solvent concentration (water in this study), the Fujita model of free volume is used to model solvent ingress kinetics [42,44] in Equation (6):
D w = D w , e q e x p ⁡ ( - β w 1 - C w C w , e q )
where, Dw,eq is the diffusion coefficient of water in the fully swollen PAM, βw is a structural parameter related to the PAM swelling rate, which will be further disused in 3.2.3, and Cw,eq is the water concentration in the fully swollen PAM. In addition, this model is only concerned with the initial absorption of water, and the water concentration change in PAM at t = 0 and x = 0 is zero. The absorbed water into PAM gel could replace the inhibitor. Therefore, the inhibitor content released into solutions is equal to the volume fraction of the inhibitor in the PAM gel in Equation (7):
C i n h = V i n h V h y d r o - G e l C w
The total released amount of OIM consists of Fick diffusion and hydrogel swelling, as shown in Equation (8):
Qt = Qf + Qs
where Qt is the total release amount of inhibitor, and Qf and Qs are the release amount of inhibitor followed Fick and non-Fick diffusion, respectively. For this stage, the release behavior of OIM@PAM shows little difference in various pH immersion solutions. On the one hand, the pH values of solutions have no influence on the release behavior of Fick diffusion. That is, the Qf of OIM@PAM release behavior has no difference in various immersion solutions. On the other hand, the different dissolution behavior of PAM in solutions with various pH values causes the difference of release behavior, and the dissolution behavior of PAM will be discussed later. In brief, in the first stage, the stable status of OIM@PAM leads to little difference in inhibitor release behavior at various pH values.
For the second stage, the inhibitor release behavior turns into the Parabolic model. As the releasing time increased, the water penetrated into the PAM hydrogel and led to the swelling of the hydrogel. The major effect of water penetrant on the gel entanglement network is the inducement of viscoelastic stress [45]. During this process, water enhances the mobility of gel chains by converting the glassy matrix into a swollen material, and there are two moving fronts for this process:
(1) a sharp interface between unpenetrated gel and swollen gel (U–S interface), which propagates inwards into the gel.
(2) a gel–water interface (G–W interface), which moves outwards and progressively increases the gel layer thickness.
Several researchers used the water volume fraction Φ(xt) in the gel layer to describe the penetration process and the moving behavior of the two fronts [45,46,47,48]:
∂ Φ ∂ t = - ∂ J ∂ x = - ∂ ∂ x - D ∂ Φ ∂ x + ϑ s w Φ = ∂ y ∂ x ( D ∂ Φ ∂ x 1 - Φ )
where D is the water diffusivity in the gel material and ϑsw is the swelling velocity of the gel. x is the distance between the U–S interface and G–W interface.
Assuming the gel material would not dissolve during the immersion process means the volume expansion is only caused by water absorption. Therefore, the absorbed water and gel are incompressible and the mixture has no volume change. That is to say:
ϑ s w x , t = D ∂ Φ ∂ x
For this stage, the OIM release has three steps. Firstly, at the fronts between unpenetrated gel and swollen gel (U–S interface), the swelling of dry gel needs an initiate threshold concentration of water [49]. Therefore, the initial release process of the inhibitor at the U–S interface is controlled by the initial swelling of the gel, and the release kinetics of the process were described in Equtions (6) and (7). Secondly, the diffusion of the inhibitor in the swollen gel is influenced by the viscoelasticity of the hydrogel structure [50]. Finally, at the gel–water (G–W) interface, the gel 3D net structure is filled with water. The inhibitor release behavior could be regarded as an equilibrium state, which is only followed by Fick’s law.

2.2.3. Swelling Behavior and Micromorphology of OIM@PAM

The macro morphology and volume change of OIM@PAM before and after the 168 h releasing test are presented in Figure S2 and Figure 8, respectively. Before the release test, the length of the cube shape OIM@PAM is 12.5 mm and the surface color is yellow, which is mainly due to the color of OIM. After the 168 h test, the shape of OIM@PAM is still a cube, which indicates the solid inhibitor could maintain the mechanical strength during the immersion time. The surface color of OIM@PAM faded, especially for that immersed in the pH 3 solution. In combination with the OIM releasing curves in Figure 5, the fade of OIM@PAM is caused by OIM releasing. The side length of the OIM@PAM cube after immersion grew longer significantly in comparison with the pristine cube. These results indicate that the swelling rate of OIM@PAM is related to the pH value of the corrosive solution. According to Figure 8, the volume change rate of OIM in the pH 3 solution is about 85 mm3/h, which is the highest one of all the test conditions, and the change rate decreases as the immersion solution pH increases to 7, and then increase as the pH further increase. PAM can react with H+ or OH− in solution [51,52,53]. In the acid medium, the AM group in PAM has hydrolysis and imidization reactions [51]. As the medium pH decreases, the imidization reaction would be the major reaction. In the alkaline solution, PAM would hydrolyze into acrylic acid and ammonium salt [51,52]. Therefore, the volume change of PAM during immersion is composed of three factors: (1) the swelling of hydro–gel during immersion, (2) the dissolution of PAM material in an aqueous environment and (3) the release behavior of inhibitors. It follows from the above that the volume change of gel material is larger than the diffusion flux of water in Equation (12). This situation could enhance the inhibitor release at the interface between unpenetrated gel and swollen gel, and the initial release step of the inhibitor from PAM is strongly affected by the solution pH value.
The internal micro images of the freezing-drying OIM@PAM after a 168 h release test in different pH were observed via SEM at 20 kV, and the results are presented in Figure 9. For all conditions, the internal morphology showed a palisading arrangement due to the evaporation of water during the freezing-drying process. The fence-like channel could be the passage of inhibitor release. The distribution of channels of a solid inhibitor in pH 3 and 11 is dense and orderly, and the distance between two channels is about 100 μm. For the inhibitor immersed in pH 5 and 9, the distance between two channels slightly increased. The distribution of channels in a PAM inhibitor immersed in pH 7 is much looser than the other conditions. This result is consistent with the OIM release results in Figure 5. As we discussed above, the diffusion behavior of the inhibitor in swollen gel is controlled by the viscoelasticity of the gel structure and Fick’s law. Once the swollen gel material forms the ordered channel, the inhibitor release rate will be enhanced, and the distribution of inhibitor pathways could also affect the release behavior.

2.3. Corrosion Protection Effect of OIM@PAM in Various pH NaCl Solutions

2.3.1. Weight Loss Measurements

Figure 10a shows the corrosion behavior of L80 steel in the different pH solutions of 3.5 wt.% NaCl without OIM@PAM, and the relevant data are listed in Table S1. The corrosion rates of L80 steel in test solutions without a solid inhibitor have high values, especially in the acid solutions. As the immersion time increases, the corrosion rate of L80 steel in the test solutions slightly decreases. After the 168 h corrosion test, the corrosion rate of L80 steel remains above 0.2 mm/y, which is classified as severe corrosion for steel in pH 3 and 5 and high corrosion for steel in neutral and alkaline solutions, according to the NACE–RP0775 standards. The unprotected steel in the test solution underwent serious deterioration resulting from electrochemical corrosion. The corrosion mechanism of steel is changed by the pH value of the corrosive medium. In an acid solution, a localized electrochemical reduction–oxidation reaction is the main corrosion mechanism [54]. For steel immersed in neutral and alkaline NaCl solutions, the corrosion rate increases with the pH values augmented [55]. The corrosiveness of 3.5 wt.% NaCl solution at different pH for L80 steel long-term soaking follows: pH 3 > pH 5 > pH 11 > pH 9 > pH 7. Therefore, the corrosion protection requirements of L80 steel in various pH value test solution are different, which requires the release of a solid inhibitor that could adapt to the environment and provide an appropriate corrosion protection effect.
Figure 10b shows the corrosion rate of L80 steel in test solutions with OIM@PAM, and the inhibition efficiency of OIM@PAM is calculated. The corrosion rate of L80 steel immersed in inhibited test solutions is dramatically decreased in contrast with solutions without solid inhibitors. The released OIM, as an imidazoline derivative, could absorb on the steel surface and form a hydrophobic film to suppress the corrosion reactions on steel surface [1,11]. N atom in the imidazole ring could provide electrons to the steel surface, enhancing the adsorption effect of OIM on the steel surface. The oleate carbon chain tail in OIM would help to increase the hydrophobicity of the absorption film [56]. The good inhibition performance of OIM is the foundation of the solid inhibitor. For the steel immersed in acid solution (pH 3 and 5), the corrosion rate decreased obviously in comparison with the other conditions. After 168 h of immersion, the corrosion rate of L80 steel in the pH 3 and 5 test solutions was 0.0432 mm/y and 0.0511 mm/y, respectively. For the steel immersed in neutral and alkaline solutions, the corrosion rate was also reduced to below 0.076 mm/y according to Chinese standards SY/T 5329. The different inhibition effect of OIM@PAM is associated with the corrosivity of the test solution and the release characteristics of OIM@PAM. The inhibition efficiency (IE%) calculated by the weight loss results are also presented in Figure 10b and Table S1. The highest IE% value for each condition was obtained at 24 h due to the quick release of inhibitors from OIM@PAM in the first release stage (Figure 5). As the immersion time increased, the IE% slightly decreased, especially for the pH 7 solution. This result was due to the release difference of OIM@PAM in various pH solutions. According to the above discussion, the solid inhibitor of OIM@PAM could provide an appropriate corrosion protection effect for steel in different corrosive mediums, especially for an acid environment.

2.3.2. Surface Observation of L80 Steel after Immersion Test

The Raman spectrum is used to study the adsorption of OIM on a L80 steel surface after the immersion test, and the results are shown in Figure 11. The pure OIM molecule has three characteristic peaks. The peaks located at 1662 cm−1, 1440 cm−1 and 1302 cm−1 are attributed to vibrations of the C=N double bond, C−N bond and −CH2− group, respectively [11]. For the L80 steel immersed in a solution without OIM@PAM, there are characteristic peaks represented by γ−FeOOH (at 250 cm−1 and 389 cm−1), α−Fe2O3 (at 298 cm−1) and Fe3O4 (at 675 cm−1) [57]. For the L80 steel immersed in the pH 7 solution with OIM@PAM, the characteristic peaks caused by corrosion products and OIM could both be found. This result indicates the OIM released from OIM@PAM could be absorbed on a steel surface and provide excellent long-term protection performance for steel.
The SEM micrographs of L80 steel after the 168 h immersion test in uninhibited and inhibited pH 3, 7 and 11 solutions are presented in Figure 12. According to Figure 12a, the surface of L80 steel corroded in the pH 3 test solution looks similar to the lunar surface. The rough surface contains several pits with diameters about 30 μm. The surface of steel immersed in pH neutral and alkaline are presented in Figure 12b,c. The corrosion morphology in these conditions shows similar characteristics, which means the corrosion mechanism of these conditions is same. After adding OIM@PAM, the corrosion evidence on the steel surfaces of all conditions shows a significant reduction. The surface roughness of steel decreases in comparison with the uninhibited solution. For the steel in the pH 3 inhibited solution, there are some white dots and polishing traces on the steel surface. The surfaces of steel immersed in pH 7 and 11 inhibited solution are similar, while the polishing traces on the surface of steel in pH 11 is more obvious than that of steel in pH 7. The SEM results further confirmed the excellent inhibition effect of OIM@PAM in NaCl solution with a wide pH range, especially for the more corrosive environment.

3. Materials and Methods

3.1. Synthesis of OIM@PAM Solid Corrosion Inhibitor

Acrylamide (AM), N,N-methylene-bis-acrylamide (BIS), ammonium persulfate (APS), tetramethylethylenediamine (TEMED) and oleate imidazoline (OIM) all purchased from Shanghai Macklin Biochemical Technology Co., Ltd. (Shanghai, China) for the preparation of the solid corrosion inhibitor.
Firstly, as Figure 13 shows, 1.88 g acrylamide (AM) was dissolved into 5 mL deionized water. Secondly, 1 g oleic imidazoline (OIM) was dispersed to the above solution with continuous stirring until the inhibitor dissolved completely, followed by adding 0.032 g N,N-methylene-bis-acrylamide (BIS) to the mixed solution, and all of the above steps were processed under the temperature range of 0–4 °C to prevent acrylamide from polymerizing prematurely. Thirdly, 0.015 g ammonium persulfate (APS) was introduced into the above solution to convert acrylamide monomers to free radicals. The free radicals would react with unactivated monomers to begin the polymerization chain reaction, while the addition of TEMED aims to accelerate the rate of formation of free radicals from APS and, consequently, catalyze the polymerization. After that, the as-prepared mixed solution was poured into a silica gel mold (20 mm × 20 mm × 20 mm) and polymerized at 45 °C for 12 h. Finally, after drying in a vacuum oven (D2T–6050, Jinghong Experimental Equipment Co., Ltd., Shanghai, China) at 45 °C for 24 h, the solid corrosion inhibitor was successfully synthesized and recorded as OIM@PAM. The average weight of obtained OIM@PAM is 2.5583 g, and the side length is 12.5 mm.

3.2. Characterization Methods

The micromorphology of OIM@PAM was observed by scanning electron microscope (ZEISS EV0 MA15, Carl Zeiss, Dublin, CA, USA) with the accelerating voltage of 20 kV. The structure of OIM@PAM was measured by a fourier-transform infrared analyzer (Nicolet 6700, Thermo Scientific, Waltham, MA, USA) with a wavelength range of 500 cm−1–4000 cm−1. Thermo-gravimetric analysis (DSC823, METTLER TOLEDO, Greifensee, Switzerland) was employed to estimate the loaded amount of OIM at a heating rate of 10 °C/min in a temperature range of 40–600 °C in the N2 atmosphere. The tensile test of OIM@PAM mainly referred to the ASTM standard D822 at room temperature in atmosphere, which was measured by an electronic universal testing machine (ETM502C, Wance Co. Ltd., Shenzhen, China) with the crosshead speed of 5 mm/min [58]. Each sample was measured three times to guarantee the accuracy of the results. A raman spectrometer (BWS465–785S, B&W TEK, Newark, DE, USA) was used to study the OIM adsorption behavior at the L80 steel/corrosive solution interface. The selected laser wavelength was 785 nm.

3.3. Release Behavior of OIM from OIM@PAM

A UV–Visible spectrophotometer was used to investigate the release behavior of OIM from OIM@PAM. The standard OIM solutions with concentrations of 50, 100, 125, 150, 175 and 200 mg/L were prepared. The UV–Vis curves of the standard OIM solution are shown in Figure 14a, and the relationship between absorbance and OIM concentrations was linearly fitted and is shown in Figure 14b.
To investigate the OIM release behavior from OIM@PAM, OIM@PAM was completely immersed in 100 mL solution with various pH (3, 5, 7, 9 and 11). After a certain time (2 h, 4 h, etc.), 5 mL immersion solution was taken out and used to test the OIM concentration by UV–Vis, and the OIM release amount can be calculated according to OIM standard curve (Figure 14). At the same time, the rest solution was replaced by the appropriate pH solution to simulate the flow state of the corrosive medium. According to the results of the releasing test and TGA test, the cumulative release ratio of OIM from OIM@PAM can be calculated.

3.4. Corrosion Protection Performance of OIM@PAM

The L80 carbon steel (wt. %: 0.36%C, 0.45%Si, 1%Mn, 0.03%P, 0.004%S, 0.25%Ni, 0.38%Mo, and balance Fe) purchased from China Jiangsu Xinyou Instrument Co., Ltd. (Changzhou, China) was used as the corrosion substrate. The surfaces of L80 coupons were polished with 160# to 2000# SiC grit paper [59] and rinsed with acetone, deionized water and ethanol. The 3.5 wt.% NaCl solutions with different pH values (3, 5, 7, 9 and 11) were selected as the corrosive medium. The above-mentioned reagents were purchased from Chengdu Kelong Chemical Reagent Factory (Chengdu, China).
The corrosion protection performance of OIM@PAM on L80 steel in a wide range pH value environments was tested by a weight loss experiment. The original qualities of the L80 samples were recorded using an analytical balance with a precision of ±0.1 mg. Then, the L80 samples were immersed in different pH values of 3.5 wt.% NaCl solution with and without OIM@PAM. The above experiments were carried out at 25 °C, and the different pH value corrosive solutions were replaced every 24 h to simulate the flow state of the mediums.
Corrosion products were removed using an acid-washing solution composed of 10% HCl + 0.5% ammonioformaldehyde (C6H12N4) [60]. After that, each L80 sample was weighted three times through electronic balance to ensure the reliability of the tested data. The corrosion rate (CR) and inhibition efficiency (IE) of L80 are calculated according to the following equations [61]:
C R = Δ w × 87600 S t ρ
I E % = 1 - C R C R 0 × 100
where Δw with the unit of gram (g) is the mass diffidence of L80 before and after the experiment. S with the unit of square centimeter (cm2) is the surface of L80. t with the unit of hour (h) is the experiment time of L80. ρ with the unit of gram per cubic centimeter (g·cm−3) is the density of L80. CR and CR0 with the unit of millimeter per year (mm·y−1) are the corrosion rate of L80 in the medium with and without OIM@PAM, respectively.

4. Conclusions

(1) OIM is successfully loaded into the PAM gel network, and the load amount is up to 39.64%. The synthesized OIM@PAM has good thermal stability, which could be used in an environment below 190 °C, and OIM@PAM also has good mechanical properties.
(2) The release behavior of OIM from OIM@PAM depends on the external solution pH values, and its release has two stages. The first stage is the OIM quick release from the PAM, which is followed by Fick’s law and hydro-gel swelling. The second stage is the OIM sustained release, when the release rate is controlled by the initiate threshold concentration of water for the un-swollen gel and the inhibitor pathway in the swollen gel.
(3) The corrosion protection performance of the OIM@PAM solid inhibitor in 3.5 wt.% NaCl solutions with a wide range of pH values is checked through weight loss measurement. The corrosion rate of L80 steel in the NaCl solution can be reduced to below 0.076 mm/y, and the IE% for the OIM@PAM in all conditions are higher than 80%. The Raman and SEM results further confirmed the corrosion protection effect of OIM@PAM.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28031314/s1, Figure S1: The pores area distribution of OIM@PAM, (a) the surface of OIM@PAM, (b) the interface of OIM@PAM; Figure S2: The macro images of as-prepared OIM@PAM immersed in different time in 3.5% (wt) NaCl with virous pH conditions; Table S1: Average corrosion rate and inhibition efficiency of L80 steel in different pH solutions of 3.5% (wt) NaCl without and with OIM@PAM at 25 °C.

Author Contributions

Q.Y.: Conceptualization, Methodology, Data curation and Writing—original draft. B.L.: Methodology, Formal analysis, Data curation, Writing—original draft and Writing—review and editing. J.T.: Conceptualization, Methodology, Resources and Writing—review and editing. Y.W.: Writing—review and editing. H.Z. (Hongpeng Zheng): Writing—review and editing. H.Z. (Hailong Zhang): Formal analysis. Z.N.: Funding Acquisition. Y.Z.: Funding Acquisition. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Natural Science Foundation of China (Grant No. 52201088), Project Funding to the Key R&D Program of Science and Technology Department of Sichuan Province (Grant No. 2021ZYD0099 and 2021ZDZX0002), PetroChina Key Technical Research on Marine Oil and Gas Development and Engineering (Grant No. 2021DJ2503), and the 2020 Post-Doctor Scientific Research Special Foundation of Department of Human Resources and Social Security of Sichuan Province, China.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The synthesized OIM@PAM samples and all raw/processed data necessary for reproducing the results in this study can be accessed upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. The surface (a) and interior (b) SEM micrographs of the as-prepared PAM after vacuum-drying; The surface (c) and interior (d) SEM micrographs of the as-prepared OIM@PAM after vacuum-drying.
Figure 1. The surface (a) and interior (b) SEM micrographs of the as-prepared PAM after vacuum-drying; The surface (c) and interior (d) SEM micrographs of the as-prepared OIM@PAM after vacuum-drying.
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Figure 2. FTIR spectra of pure OIM, PAM and OIM@PAM.
Figure 2. FTIR spectra of pure OIM, PAM and OIM@PAM.
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Figure 3. TGA curves of pure OIM, PAM and OIM@PAM.
Figure 3. TGA curves of pure OIM, PAM and OIM@PAM.
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Figure 4. (a) Tensile stress–strain curve of PAM and OIM@PAM after vacuum-drying for 24 h at 45 °C; (b) the values of the tensile strength and the elongation at break of OIM and OIM@PAM.
Figure 4. (a) Tensile stress–strain curve of PAM and OIM@PAM after vacuum-drying for 24 h at 45 °C; (b) the values of the tensile strength and the elongation at break of OIM and OIM@PAM.
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Figure 5. The three-times-tested average concentration (a) and the cumulative release (b) of OIM from OIM@PAM in different pH solutions at 25 °C.
Figure 5. The three-times-tested average concentration (a) and the cumulative release (b) of OIM from OIM@PAM in different pH solutions at 25 °C.
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Figure 6. Plots of the two kinetic models: (a) Korsmeyer–Peppas model and (b) Parabolic model for the release of OIM from OIM@PAM in the two stages.
Figure 6. Plots of the two kinetic models: (a) Korsmeyer–Peppas model and (b) Parabolic model for the release of OIM from OIM@PAM in the two stages.
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Figure 7. Schematic of two releasing stages of the inhibitor from OIM@PAM.
Figure 7. Schematic of two releasing stages of the inhibitor from OIM@PAM.
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Figure 8. The change in volume of OIM@PAM immersed in various pH test solutions for 7 days.
Figure 8. The change in volume of OIM@PAM immersed in various pH test solutions for 7 days.
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Figure 9. The internal SEM images of OIM@PAM after releasing for 168 h in different pH solutions. (a) pH 3, (b) pH 5, (c) pH 7, (d) pH 9 and (e) pH 11.
Figure 9. The internal SEM images of OIM@PAM after releasing for 168 h in different pH solutions. (a) pH 3, (b) pH 5, (c) pH 7, (d) pH 9 and (e) pH 11.
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Figure 10. Corrosion rate and inhibition efficiency of L80 in different pH solution of 3.5 wt.% NaCl at 25 °C with and without OIM@PAM, (a) without OIM@PAM and (b) with OIM@PAM.
Figure 10. Corrosion rate and inhibition efficiency of L80 in different pH solution of 3.5 wt.% NaCl at 25 °C with and without OIM@PAM, (a) without OIM@PAM and (b) with OIM@PAM.
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Figure 11. Raman spectrum of pure OIM and L80 immersed in 3.5 wt.%NaCl with and without OIM@PAM after 72 h.
Figure 11. Raman spectrum of pure OIM and L80 immersed in 3.5 wt.%NaCl with and without OIM@PAM after 72 h.
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Molecules 28 01314 g012 550
Figure 12. SEM micrographs of the L80 steel surface immersed in test solutions for 168 h: (a) pH 3 uninhibited solution, (b) pH 7 uninhibited solution, (c) pH 11 uninhibited solution, (d) pH 3 solution with OIM@PAM, (e) pH 7 solution with OIM@PAM and (f) pH 11 solution with OIM@PAM.
Figure 12. SEM micrographs of the L80 steel surface immersed in test solutions for 168 h: (a) pH 3 uninhibited solution, (b) pH 7 uninhibited solution, (c) pH 11 uninhibited solution, (d) pH 3 solution with OIM@PAM, (e) pH 7 solution with OIM@PAM and (f) pH 11 solution with OIM@PAM.
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Molecules 28 01314 g013 550
Figure 13. Schematic diagram of the synthesis of OIM@PAM solid corrosion inhibitors.
Figure 13. Schematic diagram of the synthesis of OIM@PAM solid corrosion inhibitors.
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Figure 14. (a) UV–Vis spectra for different OIM solutions of known concentrations, and (b) the fitted standard curve of OIM.
Figure 14. (a) UV–Vis spectra for different OIM solutions of known concentrations, and (b) the fitted standard curve of OIM.
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Table
Table 1. The fitting parameter and mechanisms of OIM from OIM@PAM in different pH solutions.
Table 1. The fitting parameter and mechanisms of OIM from OIM@PAM in different pH solutions.
pH ValueStage 1 (0~24 h)Stage 2 (24~168 h)
Korsmeyer–Peppas ModelParabolic Model
nkR2Release MechanismkaR2Release Mechanism
30.53400.003510.9952Anomalous transport0.070340.000440.9978Sustainable release
50.74350.00280.9962Anomalous transport0.1304−0.004130.9998Sustainable release
70.65140.00330.9949Anomalous transport0.1156−0.003070.9988Sustainable release
90.55260.06120.9960Anomalous transport0.1106−0.002880.9918Sustainable release
110.61140.00330.9939Anomalous transport0.1010−0.001850.9984Sustainable release
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MDPI and ACS Style

Yang, Q.; Lin, B.; Tang, J.; Wang, Y.; Zheng, H.; Zhang, H.; Nie, Z.; Zhang, Y. A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium. Molecules 2023, 28, 1314. https://doi.org/10.3390/molecules28031314

AMA Style

Yang Q, Lin B, Tang J, Wang Y, Zheng H, Zhang H, Nie Z, Zhang Y. A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium. Molecules. 2023; 28(3):1314. https://doi.org/10.3390/molecules28031314

Chicago/Turabian Style

Yang, Qing, Bing Lin, Junlei Tang, Yingying Wang, Hongpeng Zheng, Hailong Zhang, Zhen Nie, and Yanna Zhang. 2023. "A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium" Molecules 28, no. 3: 1314. https://doi.org/10.3390/molecules28031314

APA Style

Yang, Q., Lin, B., Tang, J., Wang, Y., Zheng, H., Zhang, H., Nie, Z., & Zhang, Y. (2023). A pH-Controlled Solid Inhibitor Based on PAM Hydrogel for Steel Corrosion Protection in Wide Range pH NaCl Medium. Molecules, 28(3), 1314. https://doi.org/10.3390/molecules28031314

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