Synthesis of biocomposite alginate-chitosan-magnetite nanoparticle beads for removal of organic persistent contaminants from water systems

Abstract

The invention provides biocomposites alginate/chitosan beads integrated with magnetite nanoparticles and modified-surface magnetite derivate created and designed to remove from environmental waters and aquatic systems different types of organic persistent compounds such as benzophenone-3 (oxybenzone).

Claims

1. A method of synthesizing a biodegradable adsorbent bead comprising: blending magnetite nanoparticles with sodium alginate in their solid-state phases to form a mixture; adding said mixture to a solution of chitosan and mechanically stir the mixture; diluting the stirred mixture to form a homogeneous solution; mechanically stirring the homogeneous solution while heating said homogeneous solution until a predefined temperature is reached; transferring said heated homogeneous solution to a basic solution to form solid beads; magnetically stirring said solid beads, and removing said solid beads from the basic solution to obtain a composite biodegradable adsorbent bead.

2. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said mixture and said solution of chitosan are mechanically stirred at 330 rpm for 50 minutes.

3. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said stirred mixture is diluted on Acetic Acid.

4. The method of synthesizing a biodegradable adsorbent bead according to claim 3, wherein said Acetic Acid is made from glacial acid diluted by deionization water.

5. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein the homogeneous solution is stirred at 330 rpm while heated at 35 C.

6. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said heated homogeneous solution is transferred to said basic solution dropwise.

7. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said heated homogeneous solution is maintained at said predefined temperature while being transferred to said basic solution.

8. The method of synthesizing a biodegradable adsorbent bead according to claim 6, wherein said heated homogeneous solution is transferred at a constant flow rate.

9. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said heated homogeneous solution is transferred to a closed container enclosing said basic solution.

10. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said basic solution comprises potassium hydroxide.

11. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said solid beads are magnetically stirred at 60 rpm for 24 hours.

12. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein a magnetic bar is provided inside said closed container to maintain the solution moving during transfer avoiding particle aggregation.

13. The method of synthesizing a biodegradable adsorbent bead according to claim 1, wherein said solid beads are removed from the basic solution after 24 hours and washed using a sieve.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Further features and advantages of the invention will become apparent from the following detailed description taken in conjunction with the accompanying figures showing illustrative embodiments of the invention, in which:

(2) FIG. 1 shows a schematic diagram for the synthesis of chitosan/alginate magnetic beads according to the present invention.

(3) FIG. 2 shows a schematic diagram for continuation of the synthesis of chitosan/alginate magnetic beads shown in FIG. 1, according to the present invention.

(4) FIG. 3 shows a schematic diagram for continuation of the synthesis of chitosan/alginate magnetic beads shown in FIG. 2, according to the present invention.

(5) FIG. 4A shows a schematic diagram for continuation of the synthesis of chitosan/alginate magnetic beads shown in FIG. 3, according to the present invention.

(6) FIG. 4B shows a photo of the final prepared beads according to the present invention.

(7) FIG. 5 shows ATR-FTIR spectrum of magnetic Fe.sub.3O.sub.4-CABs wherein significant functional groups are identified and wavenumber located by arrow.

(8) FIG. 6 shows the points of zero charge 8.3 pH for absorbent magnetic Fe.sub.3O.sub.4-CABs in different ionic strengths solutions ranging between 0.5 and 1.0 M NaCl for 24 hour contacted time.

(9) FIG. 7 shows the effect of solution-pH on absorptive removal percentage onto magnetic Fe.sub.3O.sub.4-CABs, according to the present invention.

(10) FIG. 8 shows the effects of initial concentration on the removal percentages of BP3 when using 0.15 g/100 of magnetic Fe.sub.3O.sub.4-CABs as absorbent.

(11) FIG. 9 shows Freundlich isotherms for different adsorbent weight ranging 0.15, 0.10, and 0.05 g effects adsorbed amount of BP3 under experimental parameters and solution-pH 8 with an Equilibrium time of 15 hours.

(12) FIG. 10 shows a Langmuir plot of BP3 adsorption onto Fe.sub.3O.sub.4-CABs with different adsorbent dosage ranges from 0.15 g (square), 0.10 g (triangle) and 0.05 g (cross) with experimental; solution-pH of 8 and equilibrium time of 15 hours.

DETAILED DESCRIPTION OF THE INVENTION

Materials and Methods

Chemicals, Reagents and Equipment

(13) The reagents were acquired with ACS-grade analytical purity, FeCl.sub.3.6H.sub.2O (>98%, ACROS Organics) , FeCl.sub.2.4H.sub.2O (>97%, ACROS Organics) and potassium hydroxide (85%), as-received by Fischer Chemical. Sodium oleate (>98%), and chitosan medium molecular weight contained degree of deacetylation (75-85%) were acquired from Sigma-Aldrich Co. The alginic acid sodium salt was procured by MP Biomedicals, LLC, whereas calcium chloride dihydrate (99%, ACS purity) and glacial acetic acid (99%, ACS-grade) were purchased from Fisher Chemical. The selected emerging contaminant benzophenone-3 (BP3) was provided as a fine grain powder, as-received from Sigma-Aldrich Co., (98%, Alfa Aesar). Some organic solvents such as acetone HPLC-grade (99% purity certified ACS) and ethanol (95%) were procured from Fischer Chemical. All dilution for standard concentrations and individual sorption solutions were made by using deionized water of 18.2 M.Math.cm at DOC<0.3 mg/L (Millipore Corp, USA).

Synthesis of Biodegradable Adsorbent Beads

(14) The method of synthesizing the biodegradable adsorbent beads according to an embodiment of the present invention will be discussed in conjunction with FIGS. 1-4.

(15) As illustrated in FIG.1, magnetite nanoparticles, chitosan, and sodium-alginate were used to prepare the beads of the present invention. Specifically, a combination of magnetite nanoparticles and surface-modified magnetite derivate 1 were first blended with sodium-alginate 2 in their solid-state phases (Step 1). This mixture was then added to a solution of 2% (w/v) chitosan 3 and mechanical overhead stirred at 330 rpm for 50 minutes. Accordingly, Na-Alginate (gr)+Magnetite nanoparticles (gr)+Chitosan (gr) were mixed and diluted on 5% Acetic Acid (Total Dilution Volume=60 mL), wherein the solution of 5% Acetic Acid were made from 5 mL Glacial Acid [concentrated acid] diluted by 95 mL DI-H2O. A resultant homogeneous solution 4 of magnetite nanoparticles, alginate, and chitosan is formed (Step 2) as shown in FIG. 1. The solution is maintained in constant agitation at 330 rpm by a mechanical overhead stirrer 5 while being heated to 35 C. by a hotplate 6 and monitored by a thermometer 7.

(16) Once the solution reaches 35 C., it is transferred to a basic solution using a peristaltic pump (Step 3) as shown in FIG. 2. Heat pads 8 are used to heat or maintain the solution at a temperature while it is transferred. Specifically, heat pads 8 are provided at the input and output of the peristaltic pump 9 to maintain warm temperatures closed to 35 C. The mean temperature of the heat pads 8 of 35 C. was provided by the manufacturer. No temperature measurements were taken after the solution was pumped transferred dropwise to a basic solution. The solution is pumped dropwise at a constant flow rate of 7 ml per minute.

(17) As shown in FIG. 3, the aqueous solution of magnetite, alginate and chitosan 4 was transferred dropwise to a closed container 14 enclosing a 400 mL solution of 0.5 M of potassium hydroxide (KOH) diluted with deionization (DI) water (Step 4) creating the bio-composites solid beads of the present invention. Variations in concentrations between 0.05 to 0.5, and 1 Mole/L of KOH were prepared in 400 mL DI-water. Specifically, the concentrations are selected to optimize the process. In a preferred embodiment according to the present invention, a concentration of 0.5 Mole/L (M) KOH was used.

(18) Once the composite solution is completed transferred to the potassium hydroxide solution the spherical beads were stirred at 60 rpm for 24 hours by a magnetic stirrer 12, as shown in FIG. 3. A magnetic bar 11 is provided to maintain the solution (magnetite+alginate+chitosan) moving during transfer. Once a volume portion of this solution contacts the KOH solution a solid phase is formed creating the beads. The magnetic bar creates a whirlpool effect that reduces aggregation of the transferred phase preventing the volume transferred from becoming aggregated at a single location.

(19) Finally, the resulting synthesized sphere-shape beads were removed from the KOH solution after 24 hours and washed using a sieve 14 during several cycles to rinse out the synthesized beads as shown in FIG. 4A. FIG. 4B is a photo showing the final prepared beads according to the present invention.

Characterization of Biodegradable Adsorbent Beads

Infrared Spectroscopy

(20) An attenuated transmittance-reflectance Fourier Transform Infrared Perkin Elmer Spectrum Two (ATR-FTIR) was used to collect and identify functional groups on the surface covering the magnetic nanoparticle. The accumulation-scanning amount of 100 was subjected to a 4 cm.sup.1 resolution. An ATR mode parameter for the spectra wavenumber ranging between 4000 cm.sup.1 and 550 cm.sup.1 was applied on all sample studies.

(21) The spectrum seen on FIG. 5 shows evidence of the magnetic nanocomposite composed of Fe.sub.3O.sub.4 and chitosan and alginate biopolymers beads (CAB). The functional groups present in the alginate and chitosan matrix are clearly visible in the spectrum shown in FIG. 5. The presence of the carbon oxygen double bonds and the carboxylic acid functional groups are characteristic of the alginate biopolymer. The presence of the NH and CN bands are characteristic of the chitosan biopolymer. The above spectrum represents a mixture of both alginate and chitosan biopolymers.

Raman Spectroscopy

(22) Raman spectra were observed from a Horiba Raman microscope Olympus, BX41, equipped with a laser source at wavelengths of 514 nm and 633 nm. The resolution of the spectrum was adjusted to 4 cm1 and the power of the laser was adjusted to 15 mW for each of the specimens tested with an acquisition time of approximately 360 second.

Particle Size Distribution

(23) The average particle size and its distribution was determined by a Zeta Potential/Particle Sizer NICOMPTM 380 ZLS, (Santa Barbara, Calif., USA). The parameters for the acquisition of data were optimized to 646 nm laser, counting mode every 50 seconds for 3 minutes, with 90 degrees between the incident beam and the diffracted diffraction angle.

Point of Zero Charge

(24) The point of zero charge (pH.sub.pzc) was used to relate the pH and the net charge of the magnetic particle in aqueous medium. Enclosing volume of 100 mL solution concentrations of 0.01 M NaCl were prepared on amber screw-cap bottles for each solutions-pH, wherein a consistent adsorbent dosage of 0.05 grams of Fe.sub.3O.sub.4-CABs was added.

(25) This adsorbent material was introduced, after the initial solution-pH (pH.sub.0) range was adjusted from 4, 6, 8, and 10 pH-scale. These specific acid-base aqueous solution-pH where acquired by adding certain amount of 0.01M NaOH and 0.01M HCl. Specifically, the amount depends on the inital desired pH of the solution. For example, for pH 4, 1500 uL of 0.01 M HCL was added and for pH 6, 700 uL was added. For solutions with basic pH (pH 8), 1300 uL of 0.01M NaOH was added and 2700 uL de 0.01M NaOH was added to reach a pH 10.

(26) Each sample solutions were kept in mechanical agitation at 250 rpm at average mean room temperatures of 27 C. After 48 hours the final solutions-pH (pH.sub.F) per sample are measured. The difference between (pH.sub.0ph.sub.F) and pH.sub.0 was plotted to determine the pH.sub.pzc. The pH value where neutrality at adsorbent surface is most probable was observed on the intersection between the plotted curve and the x-axis. This experiment was prepared and tested in triplicate for each sample of solutions-pH.

(27) The Point of Zero Charge (PH.sub.pzc) is the pH in which the surface of the material becomes neutral. PH.sub.pzc is related to an equilibrium balance charges between positive and negative charge on the surface and above this point the surface becomes negative and below it becomes positive. It's a very important parameter to understand surface absorption. FIG. 6 shows the determinations of the PH.sub.pzc for different ionic strength solutions. The amount of 3 gr of magnetic Fe.sub.3O.sub.4-CABs was used on each solution-pH which ranged from 3, 5, 7, 9, and 11 pH.

pH Dependence Experiments and % BP3 Removal

(28) FIG. 7 shows the effect of solution-pH on absorptive removal percentage onto magnetic Fe.sub.3O.sub.4-CABs from solution volume 100 mL at different BP3 initial concentrations as depicted on the top legend. For each concentration of BP3 that was tested, various pH solutions were adjusted ranging from 4, 6, 8 and 10 pH, and triplicate samples were prepared per initial concentrations of BP3 that was used for statistical assays. As can be appreciated from FIG. 7, the maximum % BP3 removal was observed between pH 6 and 9, which is compatible with real scenarios found for natural or most wastewaters. These results evidence the applicability of the developed magnetic composite for real applications.

Adsorption Experiments

(29) The experimental data of the isotherms was evaluated to determine the adsorption of acetone from aqueous solutions onto synthesized Fe.sub.3O.sub.4-CABs. A series of batch experiments were performed on different selected experimental parameters such as initial concentration of acetone (3, 5, 10, 15, 20, 30 mg/L), adjusted initial solution-pH (4, 6, 8, 10), and initial adsorbent amounts (0.05, 0.10, 0.15 g). Fixed experimental parameters were used on temperature at 25 C. and solutions volume of 100 mL were hold on an amber screw tap vessel of 125 mL. Preparation of concentration samples for adsorption experiments required a stock solution of 500 mg/L acetone. The standard concentration for the solutions was selected within a range between 3, 5, 10, 15, 20, 30 mg/L and were made from stock aliquot transfer volumes.

(30) FIG. 8 shows absorption experiments of 3, 5, 10, 15, 20 and 30 ppm of BP3 when 0.15 g/100 ml of the magnetic Fe.sub.3O.sub.4-CABs absorbent was used at pH 8.03. The results show that equilibrium was reach after approximately 15 hours at 250 rpm shaker. Also FIG. 8 shows a similar absorption trend for all BP3 concentrations except for 3 ppm. The maximum % BP3 removal varies between 80 and 90% at equilibrium. Each sorption tests were carried-out under similar batch experimental parameters, solution-pH 8.030.01 as well as absorbent dosage of 0.15 g in a volume of 100 mL under controlled temperature of 26 C. The initial concentrations of BP3 ranging from 3 to 30 ppm are depicted on the top legend of the Figure at pH 8.0.

Absorption Isotherms: the Freundlich and Langmuir Models

(31) Table 1 below and FIG. 9 show the results for the Freundlich isotherms models and Table 2 below summarizes the results for the Langmuir isotherm model. The R.sup.2 results in Table 1 shows values of 0.94, 0.99 and 0.98 at pH 6 and 8 for absorbent loads of 150 g, 0.100 and 0.050 g respectively; for pH 6 these R.sup.2 values are 0.96, 0.98 and 0.98. The R.sup.2 values for the Langmuir model presented in Table 2 show more consistent values at the same pH 6 and 8, which ranged between 0.98 and 0.99, which indicate that this model fits better the results for absorption process. The data from these tables indicate that the Langmuir isotherm model fits better the results obtained in this absorption experiments.

(32) TABLE-US-00001 TABLE 1 Freundlich isotherms parameters evaluated on different adsorbent dosages Solution-pH Absorbent 4 6 8 10 0.150 g n 1.05 1.98 1.30 0.90 K.sub.f 0.81 1.73 3.81 0.76 R.sup.2 0.99 0.96 0.94 0.99 0.100 g n 1.08 1.30 1.65 0.95 K.sub.f 0.44 2.17 4.80 0.60 R.sup.2 0.99 0.98 0.99 0.99 0.050 g n 1.81 1.14 1.23 1.50 K.sub.f 1.77 1.43 4.94 1.22 R.sup.2 0.93 0.98 0.98 0.90

(33) TABLE-US-00002 TABLE 2 Langmuir isotherms parameters evaluated on different adsorbent dosages. Solution-pH Adsorbent 4 6 8 10 0.150 g Q.sub.m (mg/g) 52.91 64.10 68.03 37.88 K.sub.L (L/mg) 0.011 0.076 0.147 0.018 R.sup.2 0.99 0.98 0.98 0.99 0.100 g Q.sub.m (mg/g) 42.04 76.34 158.73 48.31 K.sub.L (L/mg) 0.004 0.079 0.053 0.016 R.sup.2 0.99 0.99 0.99 0.97 0.050 g Q.sub.m (mg/g) 83.33 109.89 204.08 44.64 K.sub.L (L/mg) 0.01 0.053 0.026 0.014 R.sup.2 0.99 0.99 0.98 0.98

(34) From the Langmuir and Freundlich models the absorption capacity of the absorbent can be calculated. The Freundlich constant (Kf) and Langmuir maximum absorbed capacity (Qm) a good estimate of the absorption capacity of the absorbed can be calculated. In our case the Langmuir models fits better the absorption data. From the Freundlich model the highest value of Kf of 4.94 (mg BP3 per g absorbent) was achieved for pH 8 and a 0.050 g of absorbent load. From the Langmuir model Q.sub.m, which represents the maximum amount absorbed (Table 2) shows that the highest Qm (204.08 mg/g was also for pH 8 and 0.050 g of absorbent (FIG. 10). The high K.sub.f and Q.sub.m values suggest for the magnetic nanocomposite absorbent composed of Fe.sub.2O.sub.3alginate-chitosan beads has a good affinity for BP3 and has a great potential to be used in the cleaning of organic pollutants present in water such as BP3 among others.

(35) Although the invention has been described in conjunction with specific embodiments, it is evident that many alternatives and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, the invention is intended to embrace all of the alternatives and variations that fall within the spirit and scope of the invention.