Modified Silica Nanoparticles from Rice Husk Supported on Polylactic Acid as Adsorptive Membranes for Dye Removal

Industrial effluents and wastewater treatment have been a mainstay of environmental preservation and remediation for the last decade. Silica nanoparticles (SiO2) obtained from rice husk (RH) are an alternative to producing low-cost adsorbent and agriculture waste recovery. One adsorption challenge is facilitating the adsorbate separation and reuse cycle from aqueous medium. Thus, the present work employs SiO2 supported on polylactic acid (PLA) nanofibers obtained by the electrospinning method for Rhodamine B (RhB) dye adsorption. The silica surface was modified with trimethylsilyl chloride (TMCS) to increase affinity towards organic compounds. As a result, the silanized surface of the silica from rice husk (RHSil) promoted an increase in dye adsorption attributed to the hydrophobic properties. The PLA fibers containing 40% SiO2 (w w−1) showed about 85–95% capacity adsorption. The pseudo-first-order kinetic model was demonstrated to be the best model for PLA:SiO2 RHSil nanocomposites, exhibiting a 1.2956 mg g−1 adsorption capacity and 0.01404 min−1 kinetic constant (k1) value. In the reuse assay, PLA:SiO2 membranes preserved their adsorption activity after three consecutive adsorption cycles, with a value superior to 60%. Therefore, PLA:SiO2 nanocomposites from agricultural waste are an alternative to “low-cost/low-end” treatments and can be used in traditional treatment systems to improve dye removal from contaminated waters.


Introduction
Environmental remediation processes have been applied in waste treatment to minimize the ecological impacts occasioned by human actions [1,2]. The adsorption of pollutants with low-cost adsorbents is controlled mainly by physical interactions, making this process more attractive for wastewater treatment since this characteristic allows the adsorbent to be reused in many cycles [3,4]. Among the desirable features of adsorbents are the high specific surface area (SSA), easy regeneration, and low-cost production [5]. In this context, activated carbon is the most used material due to its efficient adsorption capacity [6][7][8]. On the other hand, nanomaterials are a promising alternative due to the improvement of properties through surface and structural modifications [9][10][11][12]. Therefore, many researchers have studied alternative adsorbents that can efficiently substitute for activated carbon, including agricultural residues (sugar cane bagasse, coconut husk, corn cob) [13], zeolites [14,15], and silica [16][17][18], among others [19,20].
Silica (SiO 2 ) has a tetrahedral structure in which the silicon atom occupies the central position coordinated with four oxygen atoms [21]. As a result, crystalline forms, such as quartz, tridymite, and cristobalite, could be formed. On the other hand, the random arrangement of tetrahedra characterizes silica in the amorphous (non-crystalline) form [22]. SiO 2 after the surface modification. The authors attributed the high adsorption efficiency to the attractive forces between the adsorbent amine group and the dye molecules. In this context, silica with a hydrophobic nature and highly efficient adsorption of organic contaminants can be produced from functionalization reactions with suitable silane reagents. However, removing particulate solids from aqueous solutions, especially in nanometer scales, induce a challenge due to the complex, large-scale application of these materials [37].
The use of supports in heterogeneous adsorption methods promotes an adsorbentaccessible recovery and simple separation from the aqueous medium [38][39][40][41]. Additionally, nanocomposites combine individual characteristics to increase desirable properties [42][43][44][45]. Fibrous membranes are one alternative to immobilizing the nanoparticles due to the porosity and diameter characteristics improving the surface area [46,47]. Specifically for adsorption process applications, using nanoparticles immobilized on fibers aims to facilitate the adsorbent material's removal from the aqueous medium and promote its reuse for many cycles [48]. One technique to produce fibrous membranes is electrospinning, a simple and practical way to introduce nanoparticles into a polymer matrix [32,37,49]. Xu et al. [50] obtained polyacrylic acid (PAA) fibers with SiO 2 functionalized with mercapto silane groups with a maximum indigo carmine dye adsorption of 523 mg g −1 . In further work [47], this group used the PAA:SiO 2 membrane to adsorb malachite green dye. In the results, the membranes demonstrate stability after multiple cycles without significant loss of their adsorption capacity. Among the different polymers, polylactic acid (PLA) has gained special attention attributed to its non-toxicity, biodegradability, and flexibility [51,52]. Therefore, PLA has been used in applications such as biomedical [53], active packaging [54], and remediation supports [14,55]. From this perspective, a system based on PLA:SiO 2 fibers shows desirable characteristics for a membrane to be applied in adsorption processes.
The great potential stemming from joining SiO 2 nanoparticles has been investigated recently. For instance, PLA/silica composites have been successfully applied to packaging [56] and oil removal [57]. Nevertheless, studies concerning PLA:SiO 2 membranes for water remediation (i.e., dye elimination) are scarce. Furthermore, research has focused on high-cost, synthetic silica-based solutions for removing water contaminants. On the other hand, plenty of waste sources are available to synthesize silica nanoparticles. Therefore, the present study developed adsorbing membranes predicated on low-cost silica nanoparticles incorporated into silica particles. Specifically, mesoporous silica was attained from rice husk agri-waste by simple acid leaching and thermal annealing. Then, this material was supported on PLA fibers measuring up to both commercial and sol-gel synthesized silica nanoparticles for Rhodamine B removal. In addition, the SiO 2 external surface was modified with the trimethylsilyl chloride silane (TMSCl) to promote interaction with Rhodamine B (RhB). Thus, the proposed nanocomposite material can be regarded as a "low-end" platform for the adsorption of pollutants from aqueous solutions. In fact, rice-husk-derived PLA:SiO 2 membranes are suitable for recovery and multiple reuses.

SiO 2 from Rice Husk Synthesis (RH)
Rice husk residues (RHs) were used to prepare the RH SiO 2 sample, as reported in the literature [31,58,59]. First, pristine RHs were washed with deionized water and dried overnight in an oven at 100 • C. Then, in sequence, 10 g of dried RHs were soaked into a 3M HCl solution (200 mL) and maintained under stirring and reflux at 80 • C. After 3 h, the RHs were removed from the leaching solution, washed to neutral pH with distilled water, and dried in an oven at 80 • C. Finally, the material was annealed in a muffle furnace at 600 • C for 3 h. The characterization results and RhB adsorption performances of the prepared silica nanoparticles were compared and contrasted to commercially available nanostructured Sigma-Aldrich silica (AC) and synthetic silica obtained by the sol-gel method (SG).

SiO 2 by Sol-Gel Synthesis (SG)
SG SiO 2 nanoparticles were synthesized by the sol-gel method according to the procedure reported by Stöber [60]. Briefly, 8 mL of NH 4 OH and 7.5 mL of tetraethyl orthosilicate were added to an aqueous ethanol solution (1:1.5 V V −1 ) in a round bottom flask. The mixture was maintained under vigorous stirring for 1 h at room temperature. After that, solvents were evaporated to attain a solid residue. Next, this material was thermally treated for 3 h at 350 • C and subsequently at 400 • C for 2 h.

SiO 2 Surface Modification with Trimethylsilyl Chloride (TMSCl)
The TMSCl was used to functionalize SiO 2 surface nanoparticles in a procedure adapted from Kulkarni et al. [33,61]. At room temperature, 1.0 g of dry SiO 2 was dispersed in 15 mL of toluene by constant stirring for 1 h. Then, 2 mL of TMSCl was added, and the mixture was kept under reflux for 48 h. The obtained material was washed with toluene and dried in an oven at 80 • C. Silanized samples were labeled XSil, where X is AC, SG, or RH.

PLA:SiO 2 Silanized Fibers
Silanized SiO 2 nanoparticles (Sil) were immobilized on PLA fibers by electrospinning. According to the methodology described above, PLA was initially solubilized in a mixture of chloroform and dimethylsulfoxide in a 3:1 (V V −1 ) ratio. After complete PLA solubilization, modified SiO 2 was added, and the solution was continuously stirred at room temperature for 2 h. After homogenizing, the mixture was transferred to a glass syringe to electrospin the PLA:SiO 2 fibers. A 40 wt% silica load (concerning PLA mass) was chosen for the composite fabrication. Electrospinning parameters were set as follows: applied voltage at 20 kV, needle tip-to-collector distance equal to 5 cm, and flow rate at 3 mL h −1 .

Characterizations
Silica particles and PLA:SiO 2 Sil composite fibers were fully characterized (i.e., by structure, composition, morphology). Specifically, the crystallographic phase composition of SiO 2 particles was investigated by X-ray diffraction (XRD). A Lab-XRD-6000 Shimadzu ® (Kyoto, Japan) diffractometer equipped with a Cu-Kα radiation source (λ = 1.5406 Å), 2θ angular range from 5 • to 80 • , and a scanning step of 1 • min −1 was used. Chemical and structural features were obtained by 29 Si solid-state nuclear magnetic resonance (NMR) spectroscopy performed with a Bruker (Billerica, MA, USA) Avance III HD 400 MHz spectrometer operating at 10 kHz. Thermogravimetric analysis (TGA) was exploited to verify the complete removal of organic residues in the RH SiO 2 sample and quantify the composite fibers' silica amount. TGA was carried out using a Netzsch (Selb, Germany) model STA 409 ® equipment in an alumina pan, from room temperature to 900 • C under nitrogen flux and with a 10 • C min −1 scan rate. The morphology of SiO 2 particles and fibers was investigated by scanning electron microscopy (SEM) using a JEOL (Tokyo, Japan) JSM-6510 field emission electron microscope equipped with an EDS (electron dispersion spectroscopy) detector for compositional analysis. Finally, particle size was measured by transmission electron microscopy (TEM). Therefore, the samples were dispersed in acetone through ultrasonication and analyzed with a FEI ® (Hillsboro, OR, USA) TECNAI G2 F20 microscope. The specific surface area (SAA), micropore area (A Pore ), external area (A Ext ), and pore diameter of the powder samples were determined by nitrogen adsorption/desorption through the Brunauer-Emmett-Teller (BET) method. Zeta potential and contact angle measurements were performed on pristine and TMSCl-functionalized SiO 2 particles (SG and RH) using a Malvern Instruments ® (Malvern, UK), Zetasizer Nano ZS90 and an Optical contact angle and surface tension meter model CAM100 by KSV, respectively.

SiO 2 Nanoparticles
SiO 2 -free unmodified and TMSCl-modified particles were evaluated to verify the efficiency of the different samples: SiO 2 extracted from rice husk, sol-gel synthesis, and commercial SiO 2 . Thus, 40 mg of each adsorbent was added to an aqueous solution (40 mL) containing 5 mg L −1 of RhB dye and continuously stirred for 24 h at a neutral pH. At the end of the tests, powder adsorbents were removed by centrifugation. Finally, the residual RhB concentration was evaluated by UV-Vis absorption spectroscopy (with a Shimadzu model UV-1601PC).

PLA:SiO 2 Sil Membranes
The RhB dye adsorption was initially carried out with different adsorbent concentrations (1, 2, and 4 g L −1 ) to determine the ideal amount to achieve high adsorption efficiencies. First, the test was performed in RhB solution (5 mg L −1 , 20 mL) under continuous stirring for 24 h at 25 • C. Then, the adsorbents were removed manually, and the RhB residual solution concentration was determined by UV-Vis spectroscopy.
Subsequently, the time required to reach equilibrium to remove the maximum percentage of the dye was evaluated. A kinetic study was performed for 2 and 4 g L −1 of PLA:SiO 2 SGSil and PLA:SiO 2 RHSil, respectively. The dye removal was monitored at different time points (30,60,120,180,240, and 1440 min). The kinetic study for the RhB dye adsorption with the membranes was performed by applying the pseudo-first-order (Equation (1)) and pseudo-second-order (Equation (2)) models according to the following equations: Pseudo-first order: Pseudo-second order: where q e (mg g −1 ) is the RhB amount adsorbed at equilibrium, q t (mg g −1 ) is the amount adsorbed at time t (min), and k 1 (min −1 ) and k 2 (g mg −1 min −1 ) are the rate constants for the pseudo-first-order and pseudo-second-order reactions, respectively. According to the literature [62][63][64], these kinetic models are the ones most commonly applied for RhB adsorption systems, presenting the best fit for the experimental results. A reuse assay was performed to verify the stability of the adsorbent membranes for RhB dye removal. The evaluation up to three reuse cycles was realized using the best response conditions for the adsorption process. In this stage, the reused fibers were subjected to the RhB adsorption/desorption process. After the recovery, the membranes were washed using ethanol and dried to undergo a new cycle. All the experiments were replicated thrice under agitation at 25 • C for 180 min.

Results and Discussion
The XRD patterns concerning SG and RH are reported in Figure 1. The commercial silica (AC) diffractogram is also inserted for comparison in Figure 1. All samples presented a broad diffraction peak at 2θ = 22.5 • , a distinctive feature of amorphous (i.e., poorly crystalline) silica [25]. There is significant evidence that the RH sample showed no crystalline reflections of impurities from the original raw material. The AC nanoparticles were found to be made out of pure, mainly amorphous, silica. Furthermore, TMSCl functionalization did not affect the materials' crystal structure or composition (see Figure 1).
where qe (mg g −1 ) is the RhB amount adsorbed at equilibrium, qt (mg g −1 ) is t adsorbed at time t (min), and k1 (min −1 ) and k2 (g mg −1 min −1 ) are the rate const pseudo-first-order and pseudo-second-order reactions, respectively. Accordin erature [62][63][64], these kinetic models are the ones most commonly applied for R tion systems, presenting the best fit for the experimental results.
A reuse assay was performed to verify the stability of the adsorbent mem RhB dye removal. The evaluation up to three reuse cycles was realized using sponse conditions for the adsorption process. In this stage, the reused fibers wer to the RhB adsorption/desorption process. After the recovery, the membr washed using ethanol and dried to undergo a new cycle. All the experiments cated thrice under agitation at 25 °C for 180 min.

Results and Discussion
The XRD patterns concerning SG and RH are reported in Figure 1. The c silica (AC) diffractogram is also inserted for comparison in Figure 1. All sa sented a broad diffraction peak at 2θ = 22.5°, a distinctive feature of amor poorly crystalline) silica [25]. There is significant evidence that the RH sample crystalline reflections of impurities from the original raw material. The AC na were found to be made out of pure, mainly amorphous, silica. Furthermore, TM tionalization did not affect the materials' crystal structure or composition (see Thermal analysis was performed on pristine and acid-treated rice husks (F confirm the RH purity. Moreover, TGA curves were also acquired for acid-t husks before and after calcination at 600 °C. Thermal analysis was performed on pristine and acid-treated rice husks ( Figure 2) to confirm the RH purity. Moreover, TGA curves were also acquired for acid-treated rice husks before and after calcination at 600 • C.
Regardless of the specific treatment, the sample without heat treatment presented a mass loss of 2% at about 70 • C, corresponding to the release of physisorbed water. Additionally, a considerable mass loss of 6%, beginning at about 250 • C (inflection point at 330 • C), was attributed to the rapid cracking of cellulose, hemicellulose, and lignin [65]. An additional loss of 82% after 490 • C was attributed to the complete removal of cellulose, hemicellulose, and lignin degradation products [66]. As expected, the acid-treated rice husk's total mass loss was more significant than the pristine material. Indeed, acid leaching could remove rice husk's inorganic components (mainly potassium and calcium). In addition, the thermal treatment causes the crystallization of potassium and calcium oxides, acting as trapping centers for carbon residues [67]. Thus, HCl leaching can be considered instrumental in attaining high-purity SiO 2 . Moreover, the acid-treated silica calcined at 600 • C presented a negligible mass loss indicating the complete elimination of any organic impurities, as was suggested by the visual inspection of the sample (white color). This fact was supported by the XRD results ( Figure 1). terials 2023, 14, x FOR PEER REVIEW

Figure 2. Thermogravimetric analysis of SiO2 before and after rice husk (RH) treatme
Regardless of the specific treatment, the sample without heat treatment mass loss of 2% at about 70 °C , corresponding to the release of physisorbed tionally, a considerable mass loss of 6%, beginning at about 250 °C (inflec 330 °C), was attributed to the rapid cracking of cellulose, hemicellulose, and An additional loss of 82% after 490 °C was attributed to the complete removal hemicellulose, and lignin degradation products [66]. As expected, the acid husk's total mass loss was more significant than the pristine material. Indeed ing could remove rice husk's inorganic components (mainly potassium and addition, the thermal treatment causes the crystallization of potassium and ca acting as trapping centers for carbon residues [67]. Thus, HCl leaching can b instrumental in attaining high-purity SiO2. Moreover, the acid-treated silic 600 °C presented a negligible mass loss indicating the complete elimination of impurities, as was suggested by the visual inspection of the sample (white col was supported by the XRD results ( Figure 1).
TEM images of commercial and synthetic SiO2 are illustrated in Figure 3 comprises well-separated, quasi-spherical nanoparticles with an average around 15-16 nm. On the other hand, small particle sizes (5-10 nm) compared observed concerning SG and RH. As for SG, the formation of tiny particles wa favored by the large H2O/NH3 ratio used during the synthesis. In addition, w TEOS hydrolysis, generating plenty of nuclei in the initial reaction stages. Co limited amount of ammonia keeps the nuclei from growing. Concerning RH, is mainly determined by the annealing temperature. Usually, 600 °C is cons ficient trade-off between high reactivity assured by small particle (i.e., large face area) size and the complete removal of organic matter [30,31,58,66]. TEM images of commercial and synthetic SiO 2 are illustrated in Figure 3. The former comprises well-separated, quasi-spherical nanoparticles with an average diameter of around 15-16 nm. On the other hand, small particle sizes (5-10 nm) compared to AC were observed concerning SG and RH. As for SG, the formation of tiny particles was most likely favored by the large H 2 O/NH 3 ratio used during the synthesis. In addition, water triggers TEOS hydrolysis, generating plenty of nuclei in the initial reaction stages. Conversely, the limited amount of ammonia keeps the nuclei from growing. Concerning RH, particle size is mainly determined by the annealing temperature. Usually, 600 • C is considered an efficient trade-off between high reactivity assured by small particle (i.e., large specific surface area) size and the complete removal of organic matter [30,31,58,66]. Regardless of the specific treatment, the sample without heat treatment presente mass loss of 2% at about 70 °C , corresponding to the release of physisorbed water. Ad tionally, a considerable mass loss of 6%, beginning at about 250 °C (inflection poin 330 °C ), was attributed to the rapid cracking of cellulose, hemicellulose, and lignin [6 An additional loss of 82% after 490 °C was attributed to the complete removal of cellulo hemicellulose, and lignin degradation products [66]. As expected, the acid-treated r husk's total mass loss was more significant than the pristine material. Indeed, acid lea ing could remove rice husk's inorganic components (mainly potassium and calcium) addition, the thermal treatment causes the crystallization of potassium and calcium oxi acting as trapping centers for carbon residues [67]. Thus, HCl leaching can be conside instrumental in attaining high-purity SiO2. Moreover, the acid-treated silica calcined 600 °C presented a negligible mass loss indicating the complete elimination of any orga impurities, as was suggested by the visual inspection of the sample (white color). This f was supported by the XRD results ( Figure 1).
TEM images of commercial and synthetic SiO2 are illustrated in Figure 3. The form comprises well-separated, quasi-spherical nanoparticles with an average diameter around 15-16 nm. On the other hand, small particle sizes (5-10 nm) compared to AC w observed concerning SG and RH. As for SG, the formation of tiny particles was most lik favored by the large H2O/NH3 ratio used during the synthesis. In addition, water trigg TEOS hydrolysis, generating plenty of nuclei in the initial reaction stages. Conversely, limited amount of ammonia keeps the nuclei from growing. Concerning RH, particle s is mainly determined by the annealing temperature. Usually, 600 °C is considered an ficient trade-off between high reactivity assured by small particle (i.e., large specific s face area) size and the complete removal of organic matter [30,31,58,66].  Specific surface area (SSA) data and pore size salient parameters for the silica samples (before and after TMSCl treatment) are reported in Table 1. In particular, the average particle size (estimated by TEM), micropore area (A Pore ), external area (A Ext ), total surface area (A Pore + A Ext = SSA BET ), and pore diameter are reported. SSA values partially reflected the particle size and the agglomeration degree of the samples. Therefore, RH had the lowest SSA BET (246 m 2 g −1 ) because of particle clustering brought about by the thermal treatment required to burn off the organics. On the other hand, SG SSA BET (537 m 2 g −1 ) benefited from the small particle size deriving from the excess water utilized in the material preparation. Despite larger particle sizes, AC SSA BET (527 m 2 g −1 ) proved to be similar to SG due to the low level of particle clustering. In addition, AC SSA BET was almost equally shared between external and pore surface area.
On the contrary, the external surface area can be regarded as the only contribution to SSA BET for RH and SG. The lack of porous structure for the two prepared samples is expected from the nature of the synthetic procedure. Indeed, the RH and SG preparation routes employed no templating agents (e.g., surfactants) to promote pore formation. Thus, their limited amount of mesopores probably resulted only from interparticle porosity. Interestingly, silanization affected each sample differently in terms of surface area. Although introducing organic groups from TMSCl decreased the SSA BET of all samples, the synthetic nanoparticles retained most of the SSA. Hence, commercial silica (CA) SSA BET dropped dramatically (from 526 to 278 m 2 g −1 ). In contrast, surface area reduction was reasonably contained for RH and SG (17.6% and 28.4%) compared to the initial SSA BET value. It is worth noting that AC wider pore size and significant surface accessibility might have allowed a higher amount of silyl groups to be anchored on the commercial silica, hindering nitrogen physisorption.
Besides influencing the SSA, silanization also altered the silica surface hydrophilic character by replacing Si-OH groups on the SiO 2 with Si-O-Si-(CH 3 ) 3 moieties. Since Cl − is a good leaving group for nucleophilic substitution reactions, silica surface hydrophobization using TMSCl was strongly favored [33]. Figure 4 shows the contact angle measurements performed on pristine and TMSCl-functionalized silica powders. The surface properties of each silica sample changed dramatically, switching from a very hydrophilic to a remarkably hydrophobic behavior. Such a feature is supposed to improve silica affinity for RhB, enhancing the adsorption rate and promoting the incorporation of silica nanoparticles into the PLA fibers.
Since XRD could not detect any structural changes brought about by silanization, 29 Si NMR spectra were collected on the SiO 2 surface-modified nanoparticles. In both nanoparticles, we detected the silica surface species referred to as Q 2 -Q 4 according to the number of siloxane bonds ( Figure 5). Specifically, the non-functionalized AC (i.e., pure silica) showed three signals corresponding to chemical shift values of −110, −101, and −92 ppm and representing the Q 2 , Q 3, and Q 4 units, respectively. On the other hand, functionalized silica presented a 13 ppm shift associated with the Si-O-Si-(CH 3 ) 3 unit, aside from the pure silica signals. In addition, an intensity decrease of the signals corresponding to Q 2 and Q 3 was observed in the silanized silica.  Since XRD could not detect any structural changes brought about by silanization, 29 Si NMR spectra were collected on the SiO2 surface-modified nanoparticles. In both nanoparticles, we detected the silica surface species referred to as Q 2 -Q 4 according to the number of siloxane bonds ( Figure 5). Specifically, the non-functionalized AC (i.e., pure silica) showed three signals corresponding to chemical shift values of −110, −101, and −92 ppm and representing the Q 2 , Q 3, and Q 4 units, respectively. On the other hand, functionalized silica presented a 13 ppm shift associated with the Si-O-Si-(CH3)3 unit, aside from the pure silica signals. In addition, an intensity decrease of the signals corresponding to Q 2 and Q 3 was observed in the silanized silica.  Since XRD could not detect any structural changes brought about by silanization, 29 S NMR spectra were collected on the SiO2 surface-modified nanoparticles. In both nanopa ticles, we detected the silica surface species referred to as Q 2 -Q 4 according to the numbe of siloxane bonds ( Figure 5). Specifically, the non-functionalized AC (i.e., pure silica showed three signals corresponding to chemical shift values of −110, −101, and −92 ppm and representing the Q 2 , Q 3, and Q 4 units, respectively. On the other hand, functionalize silica presented a 13 ppm shift associated with the Si-O-Si-(CH3)3 unit, aside from the pur silica signals. In addition, an intensity decrease of the signals corresponding to Q 2 and Q was observed in the silanized silica. After being characterized, all silica nanoparticles were tested for RhB adsorption. Figure 6 illustrates the UV-Vis absorption spectra of RhB solutions (5 ppm) depending on different adsorbents used for the dye removal. In addition, optical absorbance (i.e., color) attenuation was calculated from the 550 nm absorption peak of the initial RhB solution (blank). After being characterized, all silica nanoparticles were tested for RhB ad ure 6 illustrates the UV-Vis absorption spectra of RhB solutions (5 ppm) d different adsorbents used for the dye removal. In addition, optical absorban attenuation was calculated from the 550 nm absorption peak of the initial (blank). The TMSCl-functionalized silica performed better than their unmodi parts in terms of RhB removal, confirming the crucial role played by surface zation. In particular, SGSil proved to be the most effective adsorbent, ach color removal rate. The RHSil reached a dye removal rate (83%) similar to the Not surprisingly, adsorption results for the silanized samples were perfectl the SSA data (SGSil > ACSil > RHSil). Despite mesopores being large enough date the RhB molecule (length 1.8 nm, width 0.7 nm [68]), most adsorption the external surface of RHS, with the dye removal percentage similar to the addition, steric hindrance due to rhodamine aromatic groups reasonably h access to CS mesopores lowering the adsorption rate. Apart from the surfa phenomena such as electrostatic, hydrogen bond, and hydrophobic interac considered for RhB adsorption on silica [69,70]. Regarding electrostatic inte removal can exploit the opposite charges on RhB molecules and SiO2 surface is a cationic dye, while the latter possesses a negatively charged surface as ve potential measurements (−35, −32, and −31 mV, for ACSil, SGSil, and RHSil, Consequently, even the non-functionalized samples demonstrated the abi RhB. Nonetheless, electrostatic interactions are insufficient to ensure a hig sorption. Therefore, effects brought about by surface silanization, like van teractions mediated by the TMSCl methyl group, should be considered [69]. already been reported how the existence of hydrogen bonds between the hyd on the silica surface and the carboxyl groups on RhB [70,71] may further en sorbent-adsorbate interaction. RH and SG SiO2-modified nanoparticles showed significant efficiency removal. Thus, both SiO2 samples were deposited onto a PLA membrane u The TMSCl-functionalized silica performed better than their unmodified counterparts in terms of RhB removal, confirming the crucial role played by surface hydrophobization. In particular, SGSil proved to be the most effective adsorbent, achieving a 99% color removal rate. The RHSil reached a dye removal rate (83%) similar to the CS one (85%). Not surprisingly, adsorption results for the silanized samples were perfectly in line with the SSA data (SGSil > ACSil > RHSil). Despite mesopores being large enough to accommodate the RhB molecule (length 1.8 nm, width 0.7 nm [68]), most adsorption took place on the external surface of RHS, with the dye removal percentage similar to the CS value. In addition, steric hindrance due to rhodamine aromatic groups reasonably hampered dye access to CS mesopores lowering the adsorption rate. Apart from the surface area, other phenomena such as electrostatic, hydrogen bond, and hydrophobic interactions must be considered for RhB adsorption on silica [69,70]. Regarding electrostatic interactions, dye removal can exploit the opposite charges on RhB molecules and SiO 2 surfaces. The former is a cationic dye, while the latter possesses a negatively charged surface as verified by zeta potential measurements (−35, −32, and −31 mV, for ACSil, SGSil, and RHSil, respectively). Consequently, even the non-functionalized samples demonstrated the ability to adsorb RhB. Nonetheless, electrostatic interactions are insufficient to ensure a high level of adsorption. Therefore, effects brought about by surface silanization, like van der Waals interactions mediated by the TMSCl methyl group, should be considered [69]. Finally, it has already been reported how the existence of hydrogen bonds between the hydroxyl groups on the silica surface and the carboxyl groups on RhB [70,71] may further enhance the adsorbent-adsorbate interaction.
RH and SG SiO 2 -modified nanoparticles showed significant efficiency for RhB dye removal. Thus, both SiO 2 samples were deposited onto a PLA membrane using the electrospinning method. Figure 7 exhibits the SEM images for the pure PLA fibers and the PLA:SiO 2 nanocomposites. Initially, it can be seen that the SiO 2 insertion preserved the fiber shape with a rough appearance and diameter between 0.4 and 1.2 µm. However, regardless of the size distribution of the fiber diameters, it was verified from the histograms that the addition of SiO 2 nanoparticles promoted a decrease in the size and greater homogeneity of the fibers compared with the pure PLA (0.6-2 µm). This result may have been caused due to the intercalation of the nanoparticles between the PLA polymer chains, causing a decrease in polymer entanglement. Consequently, the electrospinning process favored the stretching of the polymer, resulting in more homogeneous fibers with smaller diameters [72]. Thus, the PLA:SiO 2 nanocomposite membranes in both cases allowed a gain of morphological properties of the fibers, indicating a good interaction between particle and polymer. homogeneity of the fibers compared with the pure PLA (0.6-2 µm). This result may have been caused due to the intercalation of the nanoparticles between the PLA polymer chains, causing a decrease in polymer entanglement. Consequently, the electrospinning process favored the stretching of the polymer, resulting in more homogeneous fibers with smaller diameters [72]. Thus, the PLA:SiO2 nanocomposite membranes in both cases allowed a gain of morphological properties of the fibers, indicating a good interaction between particle and polymer. The presence of SiO2 nanoparticles and their distribution in the PLA fibers were verified in the composites by energy dispersive X-ray spectroscopy (EDS), as shown in Figure  8. In the fibers of PLA:SiO2 SGSil and PLA:SiO2 RHSil, the detection of the element silicon (Si) in superposition with oxygen (O) demonstrated the presence of SiO2 in the PLA fibers. In addition, the mappings obtained suggest a distribution in the membrane situated in separate regions, which indicates a certain degree of accumulation of the particulates. Such a result may be due to the high SiO2 Sil concentration, 40% (w w −1 ), favoring the interaction of particles with each other in the polymer solution. In this sense, both fibers showed a behavior, regardless of the SiO2 agglomeration, of being more elucidated for the SiO2 extracted from rice husks (Figure 8b). The presence of SiO 2 nanoparticles and their distribution in the PLA fibers were verified in the composites by energy dispersive X-ray spectroscopy (EDS), as shown in Figure 8. In the fibers of PLA:SiO 2 SGSil and PLA:SiO 2 RHSil, the detection of the element silicon (Si) in superposition with oxygen (O) demonstrated the presence of SiO 2 in the PLA fibers. In addition, the mappings obtained suggest a distribution in the membrane situated in separate regions, which indicates a certain degree of accumulation of the particulates. Such a result may be due to the high SiO 2 Sil concentration, 40% (w w −1 ), favoring the interaction of particles with each other in the polymer solution. In this sense, both fibers showed a behavior, regardless of the SiO 2 agglomeration, of being more elucidated for the SiO 2 extracted from rice husks (Figure 8b).
After confirming the presence of the particulate materials in the PLA fibers, thermogravimetric analyses were performed (Figure 8) to quantify the silica mass present in the composites. The determination of particulates in the PLA:SiO 2 (SGSil and RHSil) fibers was obtained by comparing the PLA and the silica pure nanoparticles' loss events. The TGA curves show that the non-functionalized samples (SG and RH) had a slight loss in mass due to the adsorbed water loss. On the other hand, in the functionalized samples (SGSil and RHSil), a greater mass loss was observed (9% and 8%, respectively). These values were associated with the additional contribution related to the loss of organic material from surface modification (TMSCl). Concerning pure PLA, a considerable mass loss was observed at 350 • C due to the PLA thermal decomposition [51,55]. The remaining PLA mass probably corresponds to ash formation with increasing temperature. The composite materials of PLA:SiO 2 SGSil and PLA:SiO 2 RHSil showed a remaining group of about 27%. This percentage refers to the silica mass present in the fibers. Considering the polymeric solution added 40% (w w −1 ) silica and the functionalized material nanoparticles lost about 9% (Figure 9), the silica mass is expected to be 31%. Thus, the value found in both TGA curves is within the desired values, demonstrating the complete incorporation of the 40% SiO 2 into the PLA fibers. After confirming the presence of the particulate materials in the PLA fibers, thermogravimetric analyses were performed (Figure 8) to quantify the silica mass present in the composites. The determination of particulates in the PLA:SiO2 (SGSil and RHSil) fibers was obtained by comparing the PLA and the silica pure nanoparticles' loss events. The TGA curves show that the non-functionalized samples (SG and RH) had a slight loss in mass due to the adsorbed water loss. On the other hand, in the functionalized samples (SGSil and RHSil), a greater mass loss was observed (9% and 8%, respectively). These values were associated with the additional contribution related to the loss of organic material from surface modification (TMSCl). Concerning pure PLA, a considerable mass loss was observed at 350 °C due to the PLA thermal decomposition [51,55]. The remaining PLA mass probably corresponds to ash formation with increasing temperature. The composite materials of PLA:SiO2 SGSil and PLA:SiO2 RHSil showed a remaining group of about 27%. This percentage refers to the silica mass present in the fibers. Considering the polymeric solution added 40% (w w −1 ) silica and the functionalized material nanoparticles lost about 9% (Figure 9), the silica mass is expected to be 31%. Thus, the value found in both TGA curves is within the desired values, demonstrating the complete incorporation of the 40% SiO2 into the PLA fibers. After characterization, PLA:SiO 2 SGSil and PLA:SiO 2 RHSil composite membranes were evaluated for RhB adsorption (5 mg L −1 ). Preliminary experiments were conducted to establish the maximum capacity adsorption, as shown in Figure 10. Initially, PLA:SiO 2 RHSil fibers were shown to be effective in removing RhB over the entire range of adsorbent concentrations (1-4 g L −1 ). A maximum adsorption capacity of 93% was achieved for 2 g L −1 . Conversely, the increase in RhB adsorption of PLA:SiO 2 RHSil was more sensitive to the adsorbent concentration. The highest capacity adsorption (83%) was reached with the maximum concentration evaluated (4 g L −1 ). The difference in RhB dye adsorption by the membranes can be correlated to the characteristics of the SiO 2 -modified nanoparticles. The result observed in Figure 10 corroborates with the free adsorbent particles in Figure 6. In that case, SGSil (99%) showed superior adsorption compared to RHSil (83%). This behavior is attributed to the RHSil's lower surface area (202 m 2 g −1 ) after surface modification (Table 1). Thus, as expected, PLA:SiO 2 RHSil showed less effectiveness compared to PLA:SiO 2 SGSil in similar conditions. Moreover, silica immobilized in polymer fibers can reduce the number of SiO 2 active sites available for dye adsorption. Additionally, the distinct interaction of nanoparticles with the polymeric matrix influences the distribution of particles on the membrane surface, as demonstrated in Figure 8. Consequently, the surface area decreases, affecting RHSil adsorption performance in the filter membrane.
RhB adsorption kinetic curves are reported in Figure 11. In the observed results, the dye removal percentage increased steadily to 93% by 180 min for PLA:SiO 2 SGSil. On the other hand, the maximum capacity was slowly reached for PLA:SiO 2 RHSil up to 240 min. The longer time required for the PLA:SiO 2 RHSil membranes to achieve equilibrium may be related to its smaller surface area of nanoparticles and agglomeration effect in the fibers, resulting in fewer sites for adsorption. Thus, RhB dye removal for PLA:SiO 2 RHSil likely needs more diffusion through the fiber membranes resulting in a more extended time exposition for adsorption. After characterization, PLA:SiO2 SGSil and PLA:SiO2 RHSil composite membranes were evaluated for RhB adsorption (5 mg L −1 ). Preliminary experiments were conducted to establish the maximum capacity adsorption, as shown in Figure 10. Initially, PLA:SiO2 RHSil fibers were shown to be effective in removing RhB over the entire range of adsorbent concentrations (1-4 g L −1 ). A maximum adsorption capacity of 93% was achieved for 2 g L −1 . Conversely, the increase in RhB adsorption of PLA:SiO2 RHSil was more sensitive to the adsorbent concentration. The highest capacity adsorption (83%) was reached with the maximum concentration evaluated (4 g L −1 ). The difference in RhB dye adsorption by the membranes can be correlated to the characteristics of the SiO2-modified nanoparticles. The result observed in Figure 10 corroborates with the free adsorbent particles in Figure  6. In that case, SGSil (99%) showed superior adsorption compared to RHSil (83%). This behavior is attributed to the RHSil's lower surface area (202 m 2 g −1 ) after surface modification (Table 1). Thus, as expected, PLA:SiO2 RHSil showed less effectiveness compared to PLA:SiO2 SGSil in similar conditions. Moreover, silica immobilized in polymer fibers can reduce the number of SiO2 active sites available for dye adsorption. Additionally, the distinct interaction of nanoparticles with the polymeric matrix influences the distribution of particles on the membrane surface, as demonstrated in Figure 8. Consequently, the surface area decreases, affecting RHSil adsorption performance in the filter membrane. RhB adsorption kinetic curves are reported in Figure 11. In the observed results, the dye removal percentage increased steadily to 93% by 180 min for PLA:SiO2 SGSil. On the other hand, the maximum capacity was slowly reached for PLA:SiO2 RHSil up to 240 min. other hand, the maximum capacity was slowly reached for PLA:SiO2 RHSil up to 240 min. The longer time required for the PLA:SiO2 RHSil membranes to achieve equilibrium may be related to its smaller surface area of nanoparticles and agglomeration effect in the fibers, resulting in fewer sites for adsorption. Thus, RhB dye removal for PLA:SiO2 RHSil likely needs more diffusion through the fiber membranes resulting in a more extended time exposition for adsorption. The kinetic parameters were determined from linear regression ( Figure 12) and are presented in Table 2. According to the correlation coefficient (R 2 ) analyses, the pseudofirst-order model best fits the experimental data, showing R 2 values of 0.9865 and 0.9842 for PLA:SiO2 SGSil and PLA:SiO2 RHSil, respectively. Based on this model, the calculated qe values (2.7158 and 1.2956 mg g −1 ) were close to the experimental qe values (2.3012 and 1.0648 mg g −1 ) established for dye adsorption using PLA:SiO2 SGSil and PLA:SiO2 RHSil, respectively. This result resembles those in the literature [73,74], which employed SiO2supported nanocomposites as adsorbents for RhB removal. In addition, PLA:SiO2 SGSil The kinetic parameters were determined from linear regression ( Figure 12) and are presented in Table 2. According to the correlation coefficient (R 2 ) analyses, the pseudofirst-order model best fits the experimental data, showing R 2 values of 0.9865 and 0.9842 for PLA:SiO 2 SGSil and PLA:SiO 2 RHSil, respectively. Based on this model, the calculated q e values (2.7158 and 1.2956 mg g −1 ) were close to the experimental q e values (2.3012 and 1.0648 mg g −1 ) established for dye adsorption using PLA:SiO 2 SGSil and PLA:SiO 2 RHSil, respectively. This result resembles those in the literature [73,74], which employed SiO 2 -supported nanocomposites as adsorbents for RhB removal. In addition, PLA:SiO 2 SGSil fibers showed a speed constant (k 1 ) that was almost twice (0.02602 min −1 ) as high as that of PLA:SiO 2 RHSil (0.01404 min −1 ), confirming the more difficult diffusion access to adsorption sites. fibers showed a speed constant (k1) that was almost twice (0.02602 min −1 ) as high as that of PLA:SiO2 RHSil (0.01404 min −1 ), confirming the more difficult diffusion access to adsorption sites.    RhB adsorption/desorption cycles were executed on PLA:SiO 2 SGSil and PLA:SiO 2 RHSil to evaluate nanocomposite regeneration/reuse capabilities. Figure 13 shows the RhB dye adsorption during three reuse cycles. PLA pure fibers as an adsorbent achieved a less than 20% removal rate in the 1 • cycle. On the other hand, both filter membranes showed adsorptions greater than 80% (1 • cycle). Hence, RhB removal was nearly entirely due to the SiO 2 nanoparticles supported on PLA fibers. In the reuse cycles, all materials demonstrated a decreased capacity for adsorption. In this way, both nanocomposites (PLA:SiO 2 SGSil and PLA:SiO 2 RHSil) maintained affinity interactions with RhB dye after desorption, promoting adsorption saturation. As a result, PLA:SiO 2 SGSil and PLA:SiO 2 RHSil had decreased adsorption capacities from 93% to 86% and 83% to 68%, respectively, after three reuse cycles.  The current results are consistent with similar works involving dye ad silica-polymer composite fibers. Wu et al. [75] investigated RhB dye adsorp nanoparticles supported on polystyrene electrospun fibers. In this study, a 33% dye adsorption was reported. Xu et al. [47] evaluated PAA:SiO2 composite nan branes in the removal of malachite green dye. As a result, the membrane reach removal after 240 min in the 1° cycle, maintaining about 70% dye removal af sorption/desorption cycles. Therefore, the system absorbent based on PLA TMSCl surface modification showed significant results in adsorption remov the present adsorptive membrane exhibited comparable results to the "low-co The current results are consistent with similar works involving dye adsorption on silica-polymer composite fibers. Wu et al. [75] investigated RhB dye adsorption on SiO 2 nanoparticles supported on polystyrene electrospun fibers. In this study, a 33% maximum dye adsorption was reported. Xu et al. [47] evaluated PAA:SiO 2 composite nanofiber membranes in the removal of malachite green dye. As a result, the membrane reached 98% dye removal after 240 min in the 1 • cycle, maintaining about 70% dye removal after three adsorption/desorption cycles. Therefore, the system absorbent based on PLA:SiO 2 with TMSCl surface modification showed significant results in adsorption removal. Further, the present adsorptive membrane exhibited comparable results to the "low-cost/low-end" rice husk-based nanocomposite for wastewater treatment.

Conclusions
Mesoporous SiO 2 nanoparticles with diameters less than 20 nm, with high purity, and a surface area of 245 m 2 g −1 were obtained by extraction from rice husks (RH). The surface modification of SiO 2 nanoparticles with TMCS contributed to an increase in RhB dye adsorption from 49% to 83%. This result was comparable with that found for commercial and sol-gel synthesized silica. Furthermore, the modified SiO 2 nanoparticles [40% (w w −1 )] were impregnated efficiently into PLA fibers using the electrospinning method. The PLA:SiO 2 nanocomposite membranes from rice husk showed more than 80% dye removal, maintaining 60% activity after three cycles. In this context, this paper offers a system with high RhB affinity, proving that the silica nanoparticles supported on PLA nanofibers promote easy removal and reuse cycles without significantly impairing adsorption. Silica (e.g., quartz) surface functionalization is already exploited on an industrial scale in direct and reverse minerals flotation. Furthermore, TMSCl is used mainly in organic synthesis as a trimethylsilyl group or anhydrous chloride source. The production fibers have been quickly improved to minimize economic costs for large-scale applications by solution blowing spinning from electrospinning knowledge. Finally, the development of adsorptive membranes from agri-wastes such as rice husks can minimize costs and enable their use in real applications involving the adsorption of organic pollutants in water to favor environmental remediation.