The Effect of Alginate Concentration on Crystallinity, Morphology, and Thermal Stability Properties of Hydroxyapatite/Alginate Composite

Hydroxyapatite (HAp) has been used for various applications such as orthopedics, drug delivery material, and bone tissue engineering. It is well known that HAp has a good biocompatibility and osteoconductivity, so HAp can be used in biomedical applications. Hydroxyapatite can be combined with other materials, in particular polymer, to expand its range of applications. In this study, the polymer that will be used as a support for the HAp composite is alginate (Alg). The HAp/Alg composite has been synthesized by the precipitation method. The XRD results show that the crystal system of HAp was hexagonal. The spheric-like shaped particles can be observed from SEM images, and particle size distribution spread from 400 to 1100 nm. The EDS spectrum exhibited the peak of Ca, C, P, and O elements, indicating that alginate had interacted with hydroxyapatite in the synthesized composite. The as-fabricated composite showed not only good crystallinity but also high thermal resistance. Thermogravimetric-differential thermal analysis (TGA-DTA) revealed that the HAp/Alg composites have a constant weight at 750 °C, so it might be applied in advanced applications such as bioimaging, drug carrier, and other cancer treatments.


Introduction
Hydroxyapatite (HAp), Ca 10 (PO 4 ) 6 (OH) 2 is a bioceramic-based calcium phosphate compound that is stable under body fluids [1]. The crystal structure of HAp is hexagonal, having a molar ratio of a Ca/P of 1.67 [2], which is currently widely applied in biomedical fields such as orthopedics and dentistry, bone tissue engineering, drug delivery materials, and cell imaging [3]. Various methods, such as the hydrothermal method [4], precipitation method [5], sol-gel method [6], electrodeposition techniques [7], double diffusion technique [8], biomimetics [9], emulsion [10] and template method [11] have reported for the fabrication of HAp. It can grow spheric-like, needle-like, fibrous, rod-shaped, irregularly spherical, and flake-shaped, depending on the different growth conditions of crystal faces of each method.
However, to widen the application of HAp, it is mainly composited with other materials, one of them being a polymer. Polymers are large molecules formed by small and simple chemical units in the form of monomers. Therefore, polymers are often used, such as alginate [12], chitosan [13], cellulose [14], silk fibroin [1], PVA [15], and others. In this study, the polymer is alginate. Alginate is a polymer of great interest because it is an unbranched polysaccharide containing various compositions of beta-D-mannuronate (M) and alpha-L-guluronate (G) residues [12][13][14][15][16]. Hence the high cross-linking will reduce the hydrogel's swelling and create a trapped drug. In addition, alginate (Alg) is not only cheap but also has good biocompatibility and biodegradability, so it supports drug delivery systems [2,17]. Recently, biopolymer matrix composites and inorganic reinforcement have been investigated for use in biomedical applications, including drug delivery, tissue engineering, enzyme immobilization, bioadsorption, and dentistry. In addition, these new inorganicreinforced composites have demonstrated improved mechanical properties. Various biopolymer composite materials have been prepared in many drug delivery applications to enhance drug encapsulation/loading. They provide sustained release capabilities due to the synergistic action of inorganic materials and biopolymers in the composite matrix. Therefore, the enhanced characteristics of these biopolymer matrix-based composites can be further modified by varying the reinforcement type and ratio. Recently, various inorganic materials, such as carbon nanotubes (CNT), montmorillonite (MMT), calcium silicate (CS), β-tricalcium phosphate (β-TCP), and hydroxyapatite (HAp), have been used as reinforcement to alginate-based composites for use in drug delivery as shown in Table 1 [18]. The table shows that alginate composites with CNT, MMT, CS, β-TCP, and HAp can be applied as materials drug carriers, such as metronidazole, theophylline, bovine serum albumin, ofloxacin, irinotecan, venlafaxine HCl, diclofenac sodium, and vancomycin.
Meanwhile, research on composites using alginate not as a matrix but as a reinforcement has also been carried out. Sekar et al. (2022) reported the preparation of HAp/SA by coprecipitation method with maximum fluoride adsorption capacity of HAp, HAp/SA1, and HAp/SA4 was 10 mg/g, 35 mg/g, and 50 mg/g, respectively [19]. Sukhodub et al. (2018) presented the synthesizing HAp/Alg nanocomposites with swelling(%) and porosity values in HAp/Alg composites calcined at 1100 • C higher than pure Hap [20]. So, adding alginate to HAp is expected to increase the adsorption ability of composite when it is applied for drug delivery in the following research. β-TCP-ALG Vancomycin [28] In this study, we aim to perform the following: synthesize hydroxyapatite-alginate (HAp/Alg) composites by precipitation method and study the alginate concentration role in the properties of HAp/Alg composite. The composites prepared were analyzed by a series of characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM with EDAX), Fourier infra-red spectroscopy (FTIR), and thermogravimetricdifferential thermal analysis (TG-DTA).

Fabrication of HAp/Alg Composites
The method of synthesizing HAp/Alg composites is the precipitation method. The diammonium hydrogen phosphate and calcium oxide powder were weighted in a molar ratio of 1.67, and five samples of alginate powder of 9.1, 16.7, 23.1, 28.6, 33.3 w/w% were taken. The alginate sample was dispersed in diammonium hydrogen phosphate of 50 mL at 80 • C in a magnetic stirrer at 250 rpm for two hours. Subsequently, the calcium oxide solution in nitric acid was mixed into the solution containing diammonium hydrogen phosphate and alginate at 300 rpm for two hours. The pH of the mixture was adjusted by adding ammonia until the pH was 10. Next, the precipitate was rinsed a few times to obtain an ammonia-free solution. At last, the sample was dried at 110 • C for about five hours to obtain HAp/Alg composites.

Characterizations
Calcium in bamboo shell powder was analyzed using X-ray fluorescence (PAN analytical). Then, the structural phase of the prepared composite was evaluated by X-ray diffraction (XRD) (PAN analytical, Malvern Panalytical, Malvern, UK) at 10-60 • using radiation of Cu-Ka (k = 1.54 Å.) with a step size is 0.02 • . The absorbance bands were revealed by Fourier Transform of Infra-Red spectroscopy (PerkinElmer Spectrum IR Version 10.6.1, Waltham, MA, USA) in the range of 4000-400 cm −1 using the ATR technique. The morphology and composition characterizations of the product were observed by SEM scanning electron microscope (Thermo Scientific Quatro S, Thermo Fisher Scientific, Waltham, MA, USA). The sample is sprinkled on carbon tape and then coated with gold. The coating method is ion sputerring. Then, the size particle distribution was measured using ImageJ software. The product's thermal characteristic (10 mg) was evaluated by TG-DTA (Perkin Elmer) from 0 • C to 800 • C at a rate of 10 • C min -1 .

The XRF Analysis
Hydroxyapatite was synthesized using bamboo shell Sollen spp. as a biosource of calcium ions. The XRF analysis showed that the highest content of the shell is calcium (Figure 1), so it can be used as a precursor of calcium for the synthesis of the hydroxyapatite.

Fabrication of HAp/Alg Composites
The method of synthesizing HAp/Alg composites is the precipitation method. The diammonium hydrogen phosphate and calcium oxide powder were weighted in a molar ratio of 1.67, and five samples of alginate powder of 9.1, 16.7, 23.1, 28.6, 33.3 w/w% were taken. The alginate sample was dispersed in diammonium hydrogen phosphate of 50 mL at 80 °C in a magnetic stirrer at 250 rpm for two hours. Subsequently, the calcium oxide solution in nitric acid was mixed into the solution containing diammonium hydrogen phosphate and alginate at 300 rpm for two hours. The pH of the mixture was adjusted by adding ammonia until the pH was 10. Next, the precipitate was rinsed a few times to obtain an ammonia-free solution. At last, the sample was dried at 110 °C for about five hours to obtain HAp/Alg composites.

Characterizations
Calcium in bamboo shell powder was analyzed using X-ray fluorescence (PAN analytical). Then, the structural phase of the prepared composite was evaluated by X-ray diffraction (XRD) (PAN analytical, Malvern Panalytical, Malvern, UK) at 10-60° using radiation of Cu-Ka (k = 1.54 Å.) with a step size is 0.02°. The absorbance bands were revealed by Fourier Transform of Infra-Red spectroscopy (PerkinElmer Spectrum IR Version 10.6.1, Waltham, MA, USA) in the range of 4000-400 cm −1 using the ATR technique.
The morphology and composition characterizations of the product were observed by SEM scanning electron microscope (Thermo Scientific Quatro S, Thermo Fisher Scientific, Waltham, MA, USA). The sample is sprinkled on carbon tape and then coated with gold. The coating method is ion sputerring. Then, the size particle distribution was measured using ImageJ software. The product's thermal characteristic (10 mg) was evaluated by TG-DTA (Perkin Elmer) from 0 °C to 800 °C at a rate of 10 °C min -1 .

The XRF Analysis
Hydroxyapatite was synthesized using bamboo shell Sollen spp. as a biosource of calcium ions. The XRF analysis showed that the highest content of the shell is calcium (Figure 1), so it can be used as a precursor of calcium for the synthesis of the hydroxyapatite.
where λ is the wavelength of X-rays (1.5406 Å), β is full width at half maximum (FWHM) value, and θ is the diffraction angle [32]. The crystallite sizes of HAp and all of the composite are displayed in Table 2  The Scherrer equation (Equation (1)) was used to determine the particles crystallite size.
where λ is the wavelength of X-rays (1.5406 Å), β is full width at half maximum (FWHM) value, and θ is the diffraction angle [32]. The crystallite sizes of HAp and all of the composite are displayed in Table 2

The FTIR Analysis
The spectra of FTIR of the pure alginate, the hydroxyapatite, and the hydroxyapatitealginate 9.1%, 16.7%, 23.1%, 28.6%, and 33.3% composite are displayed in Figure 3. The absorption bands are observed at 963; 438.56; 1023 and 560.64 cm −1 for symmetric stretching v 1 , bending v 2 , asymmetric stretching v 3 , and bending v 4 of PO 3− 4 group, respectively [13,33,34]. A broad band at 3359 cm −1 was marked to the O-H stretching vibration of hydroxyapatite and alginate in composite [35]. Meanwhile, the main characteristic bands of alginate involve two carboxylic group bands at 1613 cm −1 and 1421 cm −1 as (-COOasymmetric) and (-COO-symmetric) bands [2,33]. Moreover, the vibration mode of C-O stretching appeared at 1421 cm −1 [36]. Mostly the absorption band is shifted toward the lower and higher region due to some interaction between hydroxyapatite and alginate in composite fabrication, as displayed in Table 3. However, these results correspond to the XRD result, as shown in Figure 2. alginate 9.1%, 16.7%, 23.1%, 28.6%, and 33.3% composite are displayed in Figure 3. The absorption bands are observed at 963; 438,56; 1023 and 560,64 cm −1 for symmetric stretching v1, bending v2, asymmetric stretching v3, and bending v4 of PO 4 3− group, respectively [33,13,34]. A broad band at 3359 cm −1 was marked to the O-H stretching vibration of hydroxyapatite and alginate in composite [35]. Meanwhile, the main characteristic bands of alginate involve two carboxylic group bands at 1613 cm −1 and 1421 cm −1 as (-COO-asymmetric) and (-COO-symmetric) bands [2,33]. Moreover, the vibration mode of C-O stretching appeared at 1421 cm −1 [36]. Mostly the absorption band is shifted toward the lower and higher region due to some interaction between hydroxyapatite and alginate in composite fabrication, as displayed in Table 3. However, these results correspond to the XRD result, as shown in Figure 2.   Figure 4. Figure 4a is the SEM image of HAp, which shows that HAp has irregular flake-like shapes [37]; meanwhile, in Figure 4b, the alginate particles are well dispersed and distributed over the HAp particles [20]. However, due to the concentration of alginate increases the SEM images of HAp/Alg 28.6% and HAp/Alg 33.3% show spheric-like particles only with no flake-like particles. Among all variations in alginate concentration, the HAp/Alg 33.3% sample was more homogeneous in shape with a smaller particle size, which spread from 400 to 1100 nm, as shown in Figure 5. The EDS spectrum of HAp and HAp/Alg 33.3% are displayed in Figure 6, which exhibited the peak of Ca, P, and O elements for HAp and the peak of Ca, C, P, and O elements for HAp/Alg composite. The Ca/P molar ratio of HAp and HAp/Alg 33.3% composite are 1.67 and 1.43, respectively. The HAp/Alg 33.3% composite has a lower molar ratio because of the appearance of the C element from alginate. The attendance of the C element indicated that alginate had interacted with hydroxyapatite in the synthesized composite.

Thermal Stability
Thermal property is important for approximating the thermal performance and relative strength of the prepared sample. The TGA curve of HAp, alginate, and HAp/Alg composites was examined, as displayed in Figure 7. It shows a slow weight loss system between 30 and 750 °C. The TGA curve shows that the sample had a slight weight loss in Figure 6. EDX spectrum of (a) the pure HAp, (b) HAp/Alg 33.3% composite.

Thermal Stability
Thermal property is important for approximating the thermal performance and relative strength of the prepared sample. The TGA curve of HAp, alginate, and HAp/Alg composites was examined, as displayed in Figure 7. It shows a slow weight loss system between 30 and 750 • C. The TGA curve shows that the sample had a slight weight loss in the range of 30-150 • C could be due to water molecules vaporization in the prepared samples. The subsequent weight loss at the temperature between 200 and 350 • C is identified as the degradation of composite alginate reinforcement [33]. The last weight loss seems to be at 350-500 • C, which might be attributed to the advanced degradation of the composite. Furthermore, at a temperature of about 600 • C, weight loss can be observed because of carbonation decomposition. As a result, there was no more weight loss up to 750 • C, which confirms the high thermal stability of the prepared composite [38].
Corresponding to the weight losses of the TGA analysis, the DTA curve presented sharp endothermic peaks at a minimum temperature of 58. might be attributed to a strong interaction between alginate and HAp in the fabrication of the composite.
The total percentage of weight losses during the whole process was about 4.61% for pure HAp, whereas 6.50% for the HAp/Alg 9.1%, 10.09% for the HAp/Alg 16.7%, 9.12% for the HAp/Alg 23.1%, 10.81% for the HAp/Alg 28.6% and 9.63% for the HAp/Alg 33.3%. These results imply that alginate plays a role in thermal stability improvement.

Conclusions
In this study, the HAp-Alg composites were successfully synthesized, and their structural phase, functional group, morphology, elemental composition, and thermal stability were explored. The XRD results show that the crystal system of HAp was hexagonal, and the crystallite size of HAp, HAp/Alg 33.3% was 4.80 nm; 5.60 nm, respectively. Moreover, the functional group, such as PO 4 3− , OH − , COO, and C-H, were revealed by FTIR analysis. The porous spherical-shaped particles can be observed, and the distribution particle range of HAp/Alg 33.3% was spread from 400 to 1100 nm. Furthermore, the EDS spectrum of the synthesized composite is shown, which exhibited the peak of Ca, C, P, and O elements. The attendance of the C element indicated that alginate had interacted with hydroxyapatite in the synthesized composite. At last, the TGA-DTA thermogram shows no more weight loss up to 750 °C. It can be concluded that the prepared composite HAp/Alg has high thermal resistance, so it might be applied in many advanced applications such as bioimaging and drug carrying.

Conclusions
In this study, the HAp-Alg composites were successfully synthesized, and their structural phase, functional group, morphology, elemental composition, and thermal stability were explored. The XRD results show that the crystal system of HAp was hexagonal, and the crystallite size of HAp, HAp/Alg 33.3% was 4.80 nm; 5.60 nm, respectively. Moreover, the functional group, such as PO 3− 4 , OH − , COO, and C-H, were revealed by FTIR analysis. The porous spherical-shaped particles can be observed, and the distribution particle range of HAp/Alg 33.3% was spread from 400 to 1100 nm. Furthermore, the EDS spectrum of the synthesized composite is shown, which exhibited the peak of Ca, C, P, and O elements. The attendance of the C element indicated that alginate had interacted with hydroxyapatite in the synthesized composite. At last, the TGA-DTA thermogram shows no more weight loss up to 750 • C. It can be concluded that the prepared composite HAp/Alg has high thermal resistance, so it might be applied in many advanced applications such as bioimaging and drug carrying.