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Influence of pH Value on Microstructure and Properties of Strontium Phosphate Chemical Conversion Coatings on Titanium

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07 August 2023

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Abstract
Strontium (Sr) is a trace element in human body that able to promote bone formation and inhibit bone absorption. The conversion coating of strontium phosphate (Sr-P) on the surface of titanium (Ti) can improve its biological properties, and has a wide application prospect in the fields of dentistry and orthopedics. In this present study, Sr-P coatings with SrHPO4 and Sr3(PO4)2 crystals on Ti are prepared by phosphate chemical conversion (PCC) treatment. And the effect of pH on the properties of Sr-P coatings is researched. The results prove that phase composition, morphology and corrosion resistance of coated Ti are different with the pH values in PCC solution. The morphologies of conversion deposition on Ti change from plat-like to cluster-like, and then homogeneous microcrystals, as pH value changed from 2.50 to 3.25. Only discrete SrHPO4 crystals are generating on substrate at lower pH value, while relative stable Sr3(PO4)2 and SrHPO4 crystals are growing and subsequently forming an integrated coating on Ti as pH is higher than 2.50. The corrosion resistance of coated Ti improves comparing with that of bare Ti because of forming Sr-P coatings with Sr3(PO4)2 phase. In addition, it is indicated that the Sr-P coatings can improve the adhesion and differentiation of BMSCs.
Keywords: 
Subject: Chemistry and Materials Science  -   Surfaces, Coatings and Films

1. Introduction

Titanium (Ti) and its alloys have been greatly interested in dentistry and orthopedics surgery owing to their suitable mechanical property, as well as good chemical resistance in vivo with the help of their oxide film [1]. However, the corrosion resistance of Ti implants will be greatly reduced with long-term interaction with body fluids. When it comes to the surgical application, the sustainability of Ti implant is questioned because of toxic ions releasing by corrosion in the harsh condition in vivo, involving chloride ion and proteins. What's more, it is hard for Ti to achieve chemical bonds with bone due to its essential bio-inertness[2]. Therefore, various surface modifications are applied to optimize the properties of Ti and its alloys [3,4]. Chemical conversion treatment is regarded as the simple and effective ways to improve the surface properties of metals [5]. Because of its comparatively low-cost and environment-friendly characteristic, phosphate chemical conversion (PCC) treatment has been widely adopted to augment the corrosion resistance and bioactivity of metal implants [6,7]. In the last decade, the PCC technology has been broadly used in the fields of the surface modification for biomedical metallic materials such as magnesium, titanium and zinc alloys [8-11]. In addition, some biofunctional cations, such as calcium (Ca2+), magnesium (Mg2+), zinc (Zn2+), strontium (Sr4+/Sr2+) were also commonly used as PCC coated materials[12,13].
Strontium (Sr2+) is a bone-seeking trace element which is incorporated in bone in a similar way like Ca2+ . It accounts about 0.035% of mineral component in the skeleton system[14]. It is reported that proper amount of Sr2+ can efficiently stimulate bone formation and be applied partially to enhance the mechanical properties of bone tissues, because it can replace a moderate amount of Ca2+ in the lattice, which leads to making the array of atoms more compact and reduction of lattice defects [15]. Moreover, literature was proved that Sr could improve corrosion resistance and stimulate bone formation by accelerating differentiation of preosteoblast and increasing the number of osteoblasts [16]. Meanwhile, Sr can restrain the activity of osteoclasts and then decrease the number of osteoclasts and inhibits bone resorption [17]. Based on the evidence supplied above, Sr has a promising prospect of application in clinical application. For strontium phosphates (Sr-P), SrHPO4 and Sr3(PO4)2 as main compounds have been taken attention recently. Especially, SrHPO4 can be considered to be an ion exchanger biomaterial for holding both HPO42- and Sr2+ ions [18]. Sr3(PO4)2 also has been researched because it is a precursor of strontium apatite as a great biomaterials [19].
Previous research results indicated that parameters affecting the microstructure and properties of chemical conversion coatings include reaction temperature and time, as well as pH value of solution [20-22]. Among them, the pH value was one of the most effective factors in the formation of coating, which can affect the formation rate and the properties of coatings, such as coating mass, phase, morphology, on metallic substrates [21]. Literatures illustrated that the metal ions phosphate can be deposited easily on metal surface if the pH value of reaction mixture exceeds its solubility limit [23]. Hence, it is important to investigate the effect of pH value in PCC solution on the microstructure and properties of coatings on Ti substrates.
However, few reports have involved in fabrication of Sr-P coatings on Ti substrate, as well as the relationship between its properties and pH value in reaction solution by PCC treatment. Thus, the aim of this study is to explore the feasibility of phosphate chemical conversion coatings dopants with strontium and investigate the effect of pH values on the microstructure and properties, such as wettability, anticorrosion and cytocompatibility, of that coatings on Ti.

2. Materials and experimental methods

2.1. Surface pretreatment

Commercially Ti was processed into Ø10mm×3mm cylinders as substrates. All the Ti samples were polished to obtain homogeneous roughness. Then, the substrates were degreased in 80 g/L sodium hydroxide (NaOH) solution at 50◦C for 15min. Next, the cylinders were etched with 2% hydrofluoric acid (HF) at room temperature for 15s. Finally, the samples were immersed in 3.00 g/L colloidal titanium phosphate to increase the nucleation points on Ti surface. The bare Ti disks was used as control.

2.2. Phosphate chemical conversion

The PCC treatment was similar to that reported previously [24,25]. Briefly, pretreated Ti specimens were put into PCC solution, that contained 0.20mol/L NaH2PO4, 0.40mol/L Sr (NO3)2, 2.00g/L NaNO2 and 5.00g/L Iron powder. After aging for 24h, pH value was adjusted to 2.50-3.25 using H3PO4 or NaOH. Finally, the pretreated Ti samples were incubated in the PCC solution for 30 min at 60◦C.

2.3. Electrochemical measurements

Electrochemical impedance spectroscopy (EIS) of PCC coatings were carried out on an automatic laboratory corrosion measurement system (PARSTAT 2273). And a classical three-electrode cell was set up in the simulated body fluid (SBF), at a scan rate 2 mV/s-1. The saturated calomel electrode (SCE), platinum, and the sample coupon with 1 cm2 exposed area were used as reference, counter, and working electrodes in the three-electrode cell (CHI660E), respectively. The Tafel polarization curve was calculated using a constant voltage scan rate. And then, the equilibrium potential (Ecorr), the corrosion current (Icorr) and the anode/cathode Tafel slope (βa/βc) was deduced. The polarization resistance (Rp) was calculated according to the following equation.
R P = β a ∙ | β c | 2.303 ∙ I c o r r ∙ ( β a + β c )

2.4. Cell cultrue

BMSCs were cultured in fresh Dulbecco’s modified Eagle’s medium (DMEM, Gibco) containing 10% (v/v) fetal bovine serum (FBS, Gibco), 1% penicillin/streptomycin in a humidified atmosphere at 37◦C and 5% CO2. The polished Ti and its coatings were sterilized using ultraviolet for 1h. And then, BMSCs were seeded onto the samples in 24-well plates at a density of 2×104 cell/well. The proliferation rates of BMSCs cells grown on different samples were assessed using a cell counting kit-8 (CCK-8 kit, Dojindo Molecular Technologies). The BMSCs cells with three replicates were seeded into a 24-well plate and pre-incubated for 48h to allow for complete adherence before conducting CCK-8 assay. All the CCK-8 values were normalized to the control, which represents 100% cell viability.

2.5. Characterization of samples

The morphologies of PCC samples and BMSCs on the coated Ti were tested using scanning electron microscope (FE-SEM, HATA-CHI SU-70) equipped with an energy dispersive spectrometer (EDS). All samples were sputtered by nano golden particles before testing. Phase composition of coatings was examined by an X-ray diffractometer (XRD, Rigaku D/max-γB) using a Cu-Kα radiation operated at 40 kV and 100 mA, with a scan rate of 4°/min and a scan step of 0.02° from 10° to 80°.

3. Results

3.1. Phase composition

The XRD patterns of PCC coatings obtained with different pH value at 60°C for 30 min are shown in Figure 1. The result of XRD patterns shows that effective conversion coating is not formed on Ti surface at pH is 2.50. While, SrHPO4 and Sr3(PO4)2 phases are detected on the surface of Ti, as pH exceeds 2.50. Specifically, when pH value is 2.75, SrHPO4 crystals begin to form on the Ti substrate. In addition, some weak peaks of Sr3(PO4)2 appear on the coating with pH=2.75. Meanwhile, the peaks of Ti become weaker, indicating that Ti sample is covered by conversion coating. As the pH value increases to 3.00, the relative intensity of the peaks of SrHPO4 become stronger, which indicates an increase in covered area and coating thickness. Meanwhile, the peaks of Sr3(PO4)2 obviously appear at pH 3.00. As pH up to 3.25, Figure 1 shows that strong diffraction peaks of Sr3(PO4)2 are detected. The peaks at 25.50o, 27.08o and 31.36o are strong and sharp, implying the good crystallinity of SrHPO4 and Sr3(PO4)2 [26].

3.2. Microstructure

Figure 2 shows the surface morphology of conversion coatings on Ti fabricated by PCC treatments at various pH values. The results show that only a few sporadic plate-like conversion crystals are distributed on the Ti surface as pH is 2.50. And the conversion coatings are formed as pH exceeds 2.50. Generally speaking, as pH up to 2.75, almost all the area of Ti substrate is covered by plate-like and cluster-like crystals. And the morphology of conversion crystals on Ti becomes finer and denser when pH value increases to 3.25. Moreover, the cluster-like crystals are distributed between the plate-like crystals, as shown in Figure 2B. The high magnification images (Figure 2 B1-B2) indicate that some microcrystals exist in the long axis direction of plate-like crystal, which proved that the crystals will continuously grow along that way in subsequent steps. In addition, the cluster-like crystals are uncompleted, like numerous flakes being put together. As pH value increased to 3.00 (Figure 2C), almost all plate-like crystals disappear, and are replaced by cluster-like crystals. Different from the cluster-like crystals at pH 2.75, the cluster-like crystals at pH 3.00 are completed and compact. The high magnified images (Figure 2C1-C2) shows that the cluster-like coating consists of compact flaky crystals with a nucleation core. When pH is 3.25, as shown in Figure 2D, the Ti substrate is almost covered by dense and tiny plate-like crystals with directionless growth. These small crystals are not in clusters but distribute evenly on the Ti surface, as shown in Figure 2D1-D2.
Table 1 lists the compositions of conversion crystals detected by EDS analysis. . Table 1 shows that the PCC coatings are mainly composed of C, P, Ti, Sr and O at pH value from 2.50 to 3.25. When pH is 2.50 and 2.75, it is seen that the quality of Sr and P is nearly equality, which suggests that crystals are the SrHPO4 phase. At pH 3.00 and 3.25, the ratios of Sr/P in coating crystals are 1.12 and 1.25, while that ratios are 1.00 and 1.50 in SrHPO4 and Sr3(PO4)2 respectively. That indicates that the coating crystals formed at pH is 3.00 and 3.25 is the mixture of SrHPO4 and Sr3(PO4)2 phase.

3.3. Corrosion Characteristics.

Figure 3 presents the potentiodynamic polarization curves of bare Ti and PCC coated samples treated by different pH values in SBF. The parameters of electrochemical corrosion of different samples are listed in Table 2. Since there are only a few crystals on the surface of Ti at pH=2.50 and no coating is formed at all, its electrochemical data was not presented in this part. The result clearly illustrates that the open circuit potential (Ecorr) value is a function of processing pH values. And Ecorr of samples is improving, and corrosion current density (Icorr) is oppositely decreasing with increasing of pH value of PCC solution. In addition, the bare Ti has the lowest Ecorr and higher Icorr, comparing with other coated Ti substrates. In addition, Table 2 shows that the Rp values of coated Ti are greater than that of bare sample. This proves that the SrHPO4 phosphate coatings can prove the anti-corrosion properties comparing with bare Ti sample. Meanwhile, the coating with pH=3.00 has the highest Rp value and Ecorr compared to other samples, which indicates that it has the best corrosion resistance. These results are closely related to the microstructure of the conversion coatings on Ti surface.

3.4. Cytocompatibility

Figure 4 shows the morphologies and cells number of BMSCs adhering to the surface of Ti substrates after being cultured for 3 days. Due to the incomplete structure of the coatings on Ti obtained at pH is 2.50 and 2.75, only two samples with pH 3.00 and 3.25 are selected for biological tests in this part. The results illustrate that BMMSCs spread well and present elongated pseudopodia on the two kinds of coated Ti implants, while that cells demonstrate approximately spherical shape on the bare Ti samples (Figure 4 (A-C)). Additionally, the cck8 result proves that the adhered cells on the coated Ti surfaces are higher comparing with that on the Bare Ti. And the cells on the Sr-P coatings with pH=3.00 have the most beneficial for differentiation of BMSCs, as shown in Figure 4 (D). These data demonstrate that both the phase composition and microstructure of the conversion coating on Ti can affect the adhesion and differentiation of cells. In addition to the fine crystals structure of the coating, its mixture phases of SrHPO4 and Sr3(PO4)2 phases (as shown in Figure 1) can also promote cells differentiation.

4. Discussion

This present study aims to provide a simple, effective and anticorrosion Sr-P chemical conversion coating by PCC processing to improve the properties of Ti substrates. Electrochemical reactions will proceed during PCC treatment, which includes obtaining electrons around Ti surface and losing electrons at cathode [27]. In PCC processing, all phosphate in solution is mainly treated as H2PO4-, as pH changing from 2.50 to 3.25 . When the discharge of hydrogen ions occurs at a cathode, the regional pH value near the Ti substrate increasing, which will result in forming HPO42- and PO43- according to the reaction of equation(1) [28]. When pH around Ti substrate continues to rise, SrHPO4 will firstly precipitate from PCC solution due to its lower solubility. The reaction of equation (2) will happen and Sr3(PO4)2 formed with increasing of pH value.
H2PO4− ↔ HPO42− + H+ ↔ PO43− + 2H+
Sr2++ HPO42−→SrHPO4↓
3Sr2++2PO43−→Sr3(PO4)2↓
As shown in Figure 2, the number of crystals increases and their size reduces with the augment of pH value, whether the morphology of crystals is mainly plate-like at pH 2.5 and 2.75, or chiefly fine flaky-like at pH 3.00, or small bulk-like at pH 3.25. This result illustrates that the morphology of depositions on Ti substrate is markedly concerned with the H+ ions in chemical solution, which is consistent with the results of some literature. Gashti et al. have shown that morphology of SrHPO4 obtained via 0.8 M Na2HPO4 and 1 M SrCl2 is denser and more compact than that obtained via 0.5 M Na2HPO4 and 0.5 M SrCl2 [29]. A reasonable explanation for these phenomena is that relatively stable and low saturated degree always achieve large-sized single crystals, owing to the fact that low saturated degree could not generate crystal nucleus spontaneously but could only make crystals grow along original nucleus (or crystal) until the completed crystal is formed [30]. In other words, when solution pH is increased, it is easier for H2PO4− to transform to HPO42-, the ingredient of SrHPO4, which leads to the higher saturated degree of SrHPO4. Naturally, accompanied by the increase of crystallization sites is the smaller size. Therefore, the crystals at pH 2.50 are large plate-like, the crystals at pH 3.00 are cluster-like and the crystals at pH 3.25 are denser and smaller. Specifically, the reason why both cluster-like and large plate-like crystals are formed is that the formations of large plate-like crystals augment pH value of the solution which further accelerates the formation of H2PO4− and saturated degree. In addition, those fine flaky crystals that originally clustered at pH 3.00 distribute evenly on the Ti surface. Since SrHPO4 is triclinic crystal and a≠b≠c, α≠β≠γ, SrHPO4 crystals can grow along with any direction and the irregular phases observed in the figure is mainly composed of SrHPO4. Meanwhile, Sr3(PO4)2 matches the characteristic of hexagonal crystal, making its crystals to grow into a more regular shape, and showing a regular structure in the Figure 2D [31].
Icorr and Ecorr derived from the measurements of specimens are used to evaluate the protective property of the coatings. Bare Ti shows good anticorrosion property because of the chemically stable passive film on the surface of Ti, as shown in Figure 3. The higher Ecorr and lower Icorr value in the electrochemical test mean the coating has better anticorrosion property [32]. The coated Ti substrates have better corrosion resistance with the increasing pH values, which because the Sr-P conversion coatings are formed during PCC processing. The sample with pH=2.50 has only the sporadic plate-like SrHPO4 crystals, as a precursor of Sr3(PO4)2 phase [33], is generated, as shown in Figure 1. When this sample is incubated in SBF solution, the passive film TiO2 still plays the anticorrosion major role. But the SrHPO4 crystals on Ti can influence the electrochemical data of Figure 3. As pH value increases, the relative stable Sr3(PO4)2 crystals growing and subsequently forming a coating on Ti substrate, which results in the corrosion resistant property is improving. The further rules and reasons will be researched in the future study.
The biological response of the cells around the implant is the result of the combined effect of the phase composition and microstructure of conversion coatings. So, their optimization should be considered comprehensively when designing the surface modification. As shown in Figure 4, The conversion coatings with pH 3.00 and 3.25 have obvious micr/ nano microstructure, which can provide excellent physical conditions for adhesion and differentiation of BMSC cells. Hulshof's research proved that the fate of cells can be determined through designing the surface microstructure and specific physicochemical properties[34]. The flaky- and bulk-like crystals on the Sr-P coatings allow the cell pseudopods to extend and embed into the gaps between the crystals, thus promote the cell adhesion and differentiation. Apart from the microstructure, the phase composition of the coating also significantly affects the biological behavior of the BMSC cells [16].Under the influence of the culture medium, the two Sr-P conversion coatings can release the functional element Sr, which can significantly improve the differentiation ability of BMSCs, as shown in Figure 4 (D). For the coatings with pH=3.00, there are more SrHPO4 and more Sr2+ ions are released, which leads to the better cell differentiation.

5. Conclusion

The Sr-P conversion coatings are successfully prepared on Ti substrates using a PCC processing in this work. The phase composition, morphology, corrosion resistance and cytocompatibility of coated Ti are different because of various pH values. During the conversion process, SrHPO4 phase is first formed on the Ti surface. As pH is 3.00, the Sr3(PO4)2 phase begins to form on the substrate. And the Sr-P phases content all gradually increases with the increase of pH value. When pH is 2.50, only a few sporadic plate-like SrHPO4 crystals are generated on the substrate. With increasing of pH values, relative stable Sr3(PO4)2 crystals are growing and subsequently forming a continuous coating on Ti substrate. The morphologies of conversion deposition on Ti present the structure from plate-like to flaky-like, and then evenly bulk-like microcrystals, as pH value changed from 2.50 to 3.25. The corrosion resistance of coated Ti improves because of the increase of Sr3(PO4)2 phase in the coatings. In addition, Sr-P coatings also have good cytocompatibility. And the coating with pH=3.00 has the better differentiation due to its microstructure and phase composition.

Acknowledgments

This work was supported by the Shandong Provincial Natural Science Foundation (ZR2021MC176), the Key Research and Development Program of Shandong Province (2021ZLGX01).

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Figure 1. XRD patterns of conversion coatings on Ti with pH value from 2.50-3.25.
Figure 1. XRD patterns of conversion coatings on Ti with pH value from 2.50-3.25.
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Figure 2. Surface morphology of conversion coatings by PCC treatment at various pH values. (A) 2.50, (B) 2.75, (C) 3.00, (D) 3.25.
Figure 2. Surface morphology of conversion coatings by PCC treatment at various pH values. (A) 2.50, (B) 2.75, (C) 3.00, (D) 3.25.
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Figure 3. The electrochemical properties of bare and coated Ti samples fabricated with different pH values. (a) Potentiodynamic polarization, (b) Nyquist plots.
Figure 3. The electrochemical properties of bare and coated Ti samples fabricated with different pH values. (a) Potentiodynamic polarization, (b) Nyquist plots.
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Figure 4. Morphologies and adhering number of BMSCs on bare and coated Ti samples with different pH values after cultured for 48 h. (A) Bare Ti, (B) pH=3.00, (C) pH=3.25 and (D) The number of adhered cells.
Figure 4. Morphologies and adhering number of BMSCs on bare and coated Ti samples with different pH values after cultured for 48 h. (A) Bare Ti, (B) pH=3.00, (C) pH=3.25 and (D) The number of adhered cells.
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Table 1. EDS analysis of conversion crystals by PCC treatment at various pH values.
Table 1. EDS analysis of conversion crystals by PCC treatment at various pH values.
pH value O P Sr Ti C Sr/P
2.50 67.59 9.56 10.10 2.81 9.94 1.06
2.75 62.13 13.52 13.85 ---- 10.50 1.02
3.00 70.17 14.02 15.68 0.13 ---- 1.12
3.25 57.52 13.20 16.52 ---- 12.76 1.25
Note: Data in this table means atom%.
Table 2. Electrochemical corrosion parameters determined by potentiodynamic polarization curves of the bare Ti and coated samples with different pH values. Data are shown as mean ± SD, n = 3.
Table 2. Electrochemical corrosion parameters determined by potentiodynamic polarization curves of the bare Ti and coated samples with different pH values. Data are shown as mean ± SD, n = 3.
Sample Ecorr (V) Icorr (× 10−8 A/cm2) βa (V·dec−1) −βc (V·dec−1) Rp (× 104 Ω·cm2)
Bare Ti −0.426 ± 0.006 12.67 ± 4.35 0.129 ± 0.007 0.107 ± 0.005 11.230 ± 0.675
pH=2.75 −0.212 ± 0.009 28.32 ± 6.24 0.221 ± 0.010 0.179 ± 0.019 15.163 ± 0.022
pH=3.00 −0.325 ± 0.011 30.04 ± 4.54 0.399 ± 0.006 0.088 ± 0.013 24.122 ± 0.286
pH=3.25 −0.072 ± 0.016 53.89 ± 3.46 0.445 ± 0.001 0.215 ± 0.002 16.026 ± 0.954
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