Balsa (Ochroma bicolor) and pulai (Alstonia scholaris) wood around 7 years old, sourced from a community forest area near Dramaga subdistrict in Bogor, West Java, were taken from defect-free middle trunks, with a diameter of approximately 18 cm and a length of ±100 cm. The logs were cross-cut into box-shaped specimens measuring of 2 cm × 2 cm × 1 cm³ (length × width × thickness, based on cross-section area), with 10 samples per treatment. The wood samples were oven-dried at 103 ± 2°C for 24 h before chemical treatment. For dual-stages delignification, sodium sulfite (Na₂SO₃, >98%) and sodium hydroxide (NaOH, >98%) were used, followed by treatment with hydrogen peroxide (H₂O₂, 30%). These chemicals were procured from Sigma-Aldrich and verified suppliers via e-commerce platforms. For adsorption performance analysis, isopropyl alcohol (C₃H₇OH) and commercial engine oil (AHM Oil MPX2) were selected as model liquid pollutants. The experimental setup included standard laboratory equipment such as beakers, containers, magnetic stirrers with hot plates, thermometer, ovens, refrigeration units, freeze-dry machines, digital calipers, and analytical balances.

This research focused on the differences in wood species and treatment durations, specifically during dual-stages delignification treatment utilizing Na₂SO₃ + NaOH and H₂O₂. Analysis of variance (ANOVA) was conducted as the main method to determine the statistical significance of the differences among treatments. If the ANOVA result shows a significant difference at the 95% confidence level (p < 0.05), Duncan multiple range test was performed as a post-hoc analysis to compare pairwise differences of each treatment. All statistical analyses were performed using IBM SPSS Statistics 23.0 (SPSS Inc., Chicago, IL, USA).

Wood density is defined as the ratio of wood mass to its volume at the same conditions. A higher density is generally associated with greater mechanical strength [35]. In general, it is highly dependent on the intrinsic characteristics of the species. Fig. 2 illustrates the density variation of balsa and pulai wood before and after the dual-stages delignification treatment. The comparison shows that both species experienced a decrease in density with increasing treatment duration [38]. This trend suggests that prolonged delignification reduces the structural components such as lignin, hemicellulose, and cellulose, leading to a decrease in density and potentially compromising the strength and stiffness of the resulting wood sponge [39]. This finding is supported by the ANOVA results (Table 3). The density of balsa wood sponge decreased significantly, with the reductions ranging from 22.4% to 47.2% (average decrease is 29.6%) (Fig. 2). In contrast, pulai wood sponge showed a slightly smaller reduction in density, ranging from 4.1% to 14.7% with an average of around 17.9%. Specifically, the density of balsa wood dropped from 0.13 to 0.7 g/cm³, while pulai wood decreased from 0.21 to 0.17 g/cm³. These two values are in accordance with previous studies [26].

A previous study also reported similar findings on delignified wood, where dual-stages delignification applied to poplar and Eurasian aspen resulted in a density reduction of approximately 10%–20% [40]. This reduction is primarily attributed to the effective removal of lignin during the process, which leads to a loosening of the wood’s structural matrix and a corresponding increase in porosity [41]. Although the removal of lignin softens the structure, it does not necessarily compromise its performance. According to Zhu et al. [42], the decrease in density can actually contribute to improved mechanical properties, as the delignification process facilitates the expansion and realignment of cellulose fibers. This expansion forms a more flexible and interconnected network, which enhances certain mechanical characteristics, particularly in low-density wood sponge applications.

Additional insights confirm the correlation between the reduction in wood density and lignin loss due to the dual-stages delignification process [42,43]. The application of NaOH and Na₂SO₃ in the alkaline phase of delignification significantly removes lignin and hemicellulose. Alkaline delignification enhances structural fragmentation by cleaving lignin–carbohydrate complexes and β-O-4 ether bonds [18], resulting in greater exposure of hydroxyl groups on the cellulose surface. In order to facilitate complete delignification, bleaching stage using hydrogen peroxide was applied. This phase promotes lignin degradation through a series of oxidative chain reactions involving peroxide ions (HOO⁻), superoxide (O₂⁻) radicals, and hydroxyl (HO^•) radicals. Among these, HOO⁻ is the principal bond responsible for breaking the linkages between aromatic rings in lignin [44]. Specifically, HOO⁻ ions cleave bonds between aromatic rings and side chains, disrupt unsaturated bonds in lignin side chains, and generate intermediates that are further oxidized into carbonyl and carboxyl compounds. Other reactive sites, such as HO ions and O₂ radicals, also contribute to oxidation and degradation of lignin [29]. Therefore, H₂O₂ treatment is crucial for residual lignin collapse and achieving complete delignification of the wood cell wall structure [24]. Delignification using H₂O₂ leads to total collapse of residual lignin on the cell walls and complete delignification of wood; therefore, determining the concentration of H₂O₂ is an important process [45]. H₂O₂ delignification mainly operates through oxidative cleavage of lignin, generating reactive oxygen and attacking the lignin aromatic rings and side chains, leading to breaking of ether and carbon bonds, converting lignin into smaller water-soluble fragments [44]. Usually, acidic delignification itself could create density around 0.24–0.12 g/cm³, indicating a removal of lignin and hemicellulose, thus substantially reduces the wood density when no further processing is applied [46]. During dual-stages delignification, wood itself would react to the chemical, leading to covalent bond formation [47], crosslinking [44], or surface modification [24]. However, the efficiency of this process is highly dependent on parameters such as concentration, time, and temperature. Previous studies have shown that insufficient temperature results in high lignin residue [48], whereas optimal delignification efficiency is achieved by increasing temperature [49].

Another important indicator is specific gravity (SG), which reflects wood quality. A higher SG value often indicates a stronger and more durable wood material [50,51]. SG is defined as the ratio of wood density to water density and can also distinguish between hardwoods and softwoods in terms of mechanical performance [52]. Fig. 3 illustrates the changes in SG values for balsa and pulai wood in each treatment applied. A clear declining trend is observed, with balsa wood showing a decrease ranging from 0.07 to 0.12 (average: 0.09), while pulai wood declined from approximately 0.15 to 0.21 (average: 0.17). ANOVA results confirmed significant differences between all treatment groups and the control sample, with specific gravity decreasing as delignification time increased (Table 3). These findings align with previous results by Lin et al. [53] who observed the delignification process combined with freeze-drying can reduce both the moisture content and specific gravity of the wood sponge. Nonetheless, pulai wood exhibited a relatively lower reduction in SG compared to balsa wood, which may be attributed to its high extractive content [54]. These extractives can hinder the penetration of delignification chemicals, necessitating longer exposure durations or higher chemical concentrations to achieve comparable effects [55].

Weight loss refers to the percentage reduction in mass after the delignification process relative to the original dry weight of the wood. This parameter serves as an indirect indicator of the extent of lignin and hemicellulose removal. A significant difference in weight loss was observed between balsa and pulai wood (Fig. 4). Balsa wood exhibited a higher weight loss, ranging from 15.30% to 36.47%, with an average of 24.64%. In contrast, pulai wood showed a more moderate reduction, ranging from 13.06% to 20.98%, with an average of 15.57%. Weight loss of balsa and pulai woods showed fluctuating results, because of the extreme impact of dual-stages delignification and freeze-dry process. Delignification process can significantly reduce partly hemicellulose and lignin content within the wood structure, thus subsequently increasing the weight loss of the wood sponge samples. Moreover, freeze-dry process can effectively remove the water and decrease the weight content of samples through sublimation, however, this reduction occurs only due to water loss, as freeze drying does not cause significant volume reduction or shrinkage of wood, unlike conventional drying methods [23]. These findings suggest that balsa wood is more susceptible to weight loss during the delignification process, potentially due to its lower density and looser fiber structure, which allows easier chemical penetration. Among the treatment combinations, the highest weight loss for balsa and pulai woods was recorded under the 10N3H treatment condition (Fig. 4).

Since both balsa and pulai woods are classified as hardwood, their structural composition are dominated by fibers (ranging from 0.2–1.2 mm in length) with relatively small lumina, which primarily provide mechanical support [18]. Differences in fiber morphology and anatomical characteristics may contribute to the varying delignification responses between the two species. The lower weight loss observed in pulai wood suggests that it is more resistant to chemical degradation during the delignification process. The fibers in pulai wood may possess a unique arrangement or composition that enhances compactness and provides greater protection to lignin, particularly within the middle lamella and cell corners. These regions contain densely packed lignin that are less accessible to delignifying agents such as alkali or acid treatments, thereby limiting chemical penetration and resulting in lower weight loss [54]. Moreover, compared to balsa wood, pulai wood has greater density, higher resistance to brittleness, and a higher proportion of cellulose and hemicellulose relative to lignin, resulting in a less rigid structure with hollow lumina that enhances overall flexibility [55,56]. These factors collectively contribute to pulai wood’s increased resistance to chemical degradation during delignification [29,56].

This finding aligns with the results reported by Owoyemi et al. [57], who noted that higher-density wood species tend to exhibit lower weight loss following chemical treatments due to their denser and more compact structure. Supporting this conclusion, the anatomical structure of balsa wood is characterized by wider pore diameters and lower pore distribution, which facilitates deeper chemical penetration and, consequently, greater component loss. In contrast, pulai wood has narrower pores but with higher pore distribution, which contributes to greater stiffness and structural integrity [58,59]. These anatomical differences likely affect not only the degree of chemical accessibility but also the extent of lignin and hemicellulose removal during dual-stages delignification.

Wood treated through a dual-stages delignification process tends to retain its naturally porous structure while forming a hierarchical pore system (Fig. 5). This treatment significantly reduces lignin content and increases pore distribution by generating nanopores within the cell walls. The morphological differences between balsa and pulai wood after delignification can be identified through light microscopy, which allows observation of anatomical changes such as vessel expansion, wall thinning, and pore structure [60]. The removal of major structural compounds such as lignin and hemicellulose results in an increase in both the number and size of voids within the wood matrix. As lignin is removed, the overall void volume increases, which in turn leads to a rise in through-pore porosity and an observable widening of gaps between adjacent cell walls as these walls become thinner and more fragile [61]. Moreover, fibers and vessels often experience collapse due to the loss of intracellular support components, leading to reduced pore size uniformity and microstructural instability. In the preparation of wood sponges, the use of hydrogen peroxide not only promotes complete lignin degradation but also causes noticeable color changes in the wood structure, which is typically associated with the breakdown of chromophore lignin units [62]. Similar result by Li et al. [27] who reported that delignified wood cell structures exhibit a disordered and hollow morphology, particularly in the parenchyma tissues.

According to Figs. 5 and 6, the comparison of balsa and pulai wood morphologies highlights several distinctive anatomical features, and reassures the location on the cell wall. Balsa wood is characterized by its solitary pores, a mixed vessel arrangement, and a clearly visible wood ray structure, despite the parenchyma cells being less observable [58]. It also exhibits simple perforation plates. In contrast, pulai wood displays a more complex pore structure, including vessel fusion, a clearer visibility of both rays and parenchyma, and the presence of diffuse apotracheal and ribbon-like parenchyma, with regularly aligned intercellular spacing [59]. These observations support the idea that dual-stages delignification not only removes lignin but also significantly alters the microstructure, leading to the formation of nano- and mesopores. According to previous findings, the removal of lignin facilitates the formation of nano-sized voids, which in turn contribute to the development of mesoporous networks within the wood matrix [61]. Consistent with this, Li et al. [27] reported that both microscale and nanoscale voids emerge within the cell walls after lignin removal, further enhancing the porous architecture of delignified wood.

Based on the results presented in Table 4, all treatments applied to both balsa and pulai wood led to an increase in pore diameter. The most significant increase was observed in the 10N3H treatment, with balsa wood reaching a pore diameter of approximately 374.3 μm and pulai wood around 351.8 μm. This observation is consistent with previous findings which reported that fully delignified wood sponges treated for six hours exhibited a highly mesoporous structure, as evidenced by the resulting pore size distribution. Furthermore, Li et al. [27] state that the increase in pore size and porosity distribution is primarily attributed to the expansion of void volume following lignin removal. The delignification process significantly increases the internal porosity; while simultaneously improving accessibility by widening the pore diameter through the removal of extractives. This phenomenon results in the observed enhancement of adsorption capabilities.

Pore distribution in wood is typically categorized into macropores, mesopores, and micropores. The results indicate a clear enhancement in pore distribution, as illustrated in Fig. 7. A progressive increase in pore distribution was observed from the UTFD samples to those of treated samples with the longest delignification duration. The ANOVA results confirmed a significant difference among treatments, with longer delignification times resulting in increased pore diameter and distribution (Table 3). Specifically, in balsa wood, pore distribution increased from 55% to 88%, with an average improvement of approximately 79%. Meanwhile, pulai wood exhibited a more pronounced increase, ranging from 48% to 82%, with an average of around 68%. The best treatment outcomes in terms of pore distribution were recorded at 88% for balsa wood and 82% for pulai wood. This increase in pore distribution is attributed to the effective removal of lignin during the dual-stages delignification process. These findings align with prior research by Fu et al. [63], which reported that enhanced pore distribution results from dual-stages delignification, accompanied by an increase in specific surface area from 9 to 41 m²/g. Interestingly, despite the structural changes at the microscopic level, the overall morphology of the wood remained relatively unchanged. Li et al. [64], suggested that such processes primarily remove chromophore components of lignin while preserving bulk lignin, maintaining the general morphology of the wood structure.

After delignification, the wood cell wall exhibited increased porosity and an expanded cell lumen area. This structural transformation effectively opened the native cellular network, enhancing internal passageways within the wood [18]. The significant changes in pore diameter observed after dual-stages delignification also correspond with previous findings on wood sponges, which emphasize that their hierarchical pore structures arise from a combination of nanoscale cross-linked chemical networks and micrometer-scale intercellular channels [28].

Based on the results, the dual-stages delignification process effectively enhances the brightness and whiteness of the wood, as indicated by a significant increase in the L (lightness) values and ∆E (total color difference) values according to the CIE Lab color system. In this system, a parameter represents the red-green axis, while b indicates the yellow-blue axis. As shown in Fig. 8, both balsa and pulai woods exhibit fluctuating color changes throughout the treatments. Balsa wood tends to be more easily delignified, resulting in more pronounced changes in brightness and color, whereas pulai wood shows a more resistant behavior toward delignification, likely due to its intrinsic anatomical and chemical characteristics. This resistance influences the extent of color change after treatment. These findings are supported by Bradai et al. [65], who reported that wood with lower lignin content could enhance light penetration. Lignin contributes to the natural brownish coloration of wood due to its phenolic structure. Upon delignification, the removal of lignin leads to a cellulose-rich matrix that becomes more translucent, although the structural shape of the wood remains intact. The degree of color change varied significantly between treatments. In pulai wood, distinct total color changes occurred in the first treatment applied, the ∆E value increased from 6.15 (UTFD) to 41.85 (8N1H), whereas for balsa wood, the ∆E value increased from 10.15 (UTFD) to 33.68 (10N3H).

The lightness (L) values in each wood species and treatment applied were presented in Fig. 9. For pulai wood, the highest increase in lightness was observed in the 8N3H treatment, where the L value increased significantly from 54.64 (UTFD) to 81.50. Meanwhile, for balsa wood, the 9N1H treatment showed the greatest escalation, from 63.67 (UTFD) to 87.71. This considerable improvement in brightness is primarily attributed to the delignification process, which removes lignin and extractives from the wood. Lignin and certain extractive compounds are known to cause significant light absorption and scattering within the visible spectrum due to their complex phenolic structures. Their removal enhances the wood’s ability to reflect light, resulting in a brighter and whiter appearance [66]. As delignification progresses, the reduction in these chromophore compounds contributes to the increased lightness observed, reinforcing the role of chemical composition, particularly lignin content, in determining wood color response to treatment [67].

According to Table 5, the results of converting the CIELAB color values into the RGB spectrum indicate that brightness escalation occurred in all treatments, with balsa wood exhibiting a higher degree of translucency compared to pulai wood (Fig. 10). Although pulai wood is more resistant to delignification, it still showed a consistent increase in brightness across the treatments (Fig. 10). This finding shows similarity with previous research that underlines the effect of delignification. The impact of lignin removal could result in a white, cellulose-rich scaffold of the wood skeleton [67]. Furthermore, the delignification process led to a noticeable discoloration in both wood types. Based on the classification of color variation, all treatments demonstrated ΔE values greater than 12.0, indicating a “very distinct” or “clearly noticeable” color change [68]. This significant change is strongly associated with lignin removal, particularly during longer delignification durations, which contributes to enhanced visibility and the translucent appearance of the resulting wood sponges.

Fourier Transform Infrared Spectroscopy (FTIR) analysis was conducted to examine the chemical component changes in wood sponges from each treatment, focusing on the effectiveness of lignin removal while preserving cellulose integrity. As shown in Fig. 11A, significant spectral differences were observed in the range of 1940–3420 cm⁻¹. These variations indicate a decrease in C–O bond intensity, which is commonly associated with the presence of lignin and hemicellulose. Notably, balsa wood exhibited a distinct peak at 1055 cm⁻¹ and a noticeable shift at 1252 cm⁻¹, suggesting C–O bond stretching. These spectral shifts imply that the delignification process primarily targeted lignin and hemicellulose, while cellulose remained largely unaffected. This observation aligns with previous findings that the C–O stretching vibration absorption peak at around 1232 cm⁻¹ originates mainly from lignin and hemicellulose components. Moreover, the gradual weakening of the C=O carbonyl stretching peak at 1733 cm⁻¹ further confirms the partial removal of hemicellulose through hydrogen peroxide treatment. Declining slope in the region of 1780–2290 cm⁻¹ indicates the presence of carboxyl group stretching, while a distinct signal at 2335 cm⁻¹ suggests degradation of lignin and hemicellulose. Additionally, a broad absorption band between 3051–3589 cm⁻¹, especially around 3340 cm⁻¹, corresponds to O–H stretching vibrations, highlighting further breakdown of hydroxyl-containing compounds such as hemicellulose and lignin. These spectral changes clearly demonstrate that the hydrogen peroxide-assisted delignification effectively reduces lignin and hemicellulose content while preserving the cellulose framework.

The results shown in Fig. 11B illustrate the FTIR spectral analysis of pulai wood before and after the delignification process. Stretching vibrations were observed across the range of 866–3645 cm⁻¹, with a notable broad peak at 3339 cm⁻¹ corresponding to O–H stretching. This indicates that the delignification process was effective in disrupting hydroxyl-containing components, particularly lignin. These findings are in line with previous research, which stated that untreated wood typically exhibits a distinct peak around 1734 cm⁻¹—commonly associated with carbonyl groups in hemicellulose and lignin—and that the reduction or disappearance of this peak reflects successful removal of these components. Further confirmation is provided by the appearance of stretching at 2355 cm⁻¹, which corresponds to C–H stretching, a marker of residual lignin presence. The persistence of this peak suggests that pulai wood is more resistant to delignification compared to other wood types, likely due to its anatomical and chemical characteristics. Pulai wood is classified as a hardwood species, yet it is lightweight and possesses relatively fine fibers, typically ranging from 0.2 to 1.22 mm in length, and smaller fiber pits, making chemical penetration more difficult. These hardwood fibers contribute significantly to pulai wood’s mechanical strength, thereby complicating the delignification process [18]. Nonetheless, Table 6 FTIR data clearly show that even in pulai wood, the delignification process induces considerable chemical changes, particularly in lignin and hemicellulose removal, although to a lesser extent than in balsa wood. In addition, pulai wood is one of the hardwoods that have a low density with a special characteristic, having the length of fibers about 0.2–1.22 mm with smaller pits, and the extractive content (flavonoid and alkaloid), as well as a packed lignin composition that is more resistant to chemical degradation by alkali or acid treatment [29,69].

Based on the data presented in Table 6, the delignification process affected absorption within the wavenumber ranging from 1125–1736 cm⁻¹, particularly at the C–O stretching bands, which are indicative of hemicellulose and lignin structures. The observed spectral changes confirm the progressive dissolution of these components. In balsa wood, a distinct peak at 1055 cm⁻¹ and a shift observed at 1252 cm⁻¹ suggest the reduction of lignin and hemicellulose content, along with a weakening band at 1433 cm⁻¹, which further supports the removal of hemicellulose. In addition, balsa wood showed a flatter pattern around wavenumbers of 3555 cm⁻¹ (hydroxyl group/–OH), 1650–1750 cm⁻¹ (carboxyl (–COOH) and C=O groups stretching) as a prolonged delignification process (10N3H) due to lignin and hemicellulose bound breaking with wood structure [23,42,75,76]. On the other hand, pulai wood exhibited a comparable pattern, with a notable peak at 1734 cm⁻¹—characteristic of lignin—and stretching around 2355 cm⁻¹ (C–H group), which reflects the partial degradation of lignin and hemicellulose. reduced accessibility to chemical agents, ultimately impacting the efficiency of lignin degradation [40]. Even though, pulai wood showed a similar/comparable pattern, however, it remains more difficult to delignify in the same condition with balsa wood. From these findings, it can be concluded that the most effective treatment for both balsa and pulai wood, in terms of lignin and hemicellulose removal as identified through FTIR analysis, was the 10N3H treatment.

The lignin extraction method applied in this study followed a modified TAPPI protocol 1990 [36], which involves sequential extraction steps from finely ground mesh samples. The obtained data support the conclusion that extended durations in the dual-stages delignification process significantly enhance lignin removal. During delignification, the complex structure of lignin is chemically degraded and becomes soluble in the applied solution. This approach, which aims to remove lignin and hemicellulose while preserving the cellulose framework, is a key strategy in developing advanced wood-based sponge materials with improved functional properties. As shown in Table 7, balsa wood exhibited the lowest lignin content after 10N3H treatment, at approximately 10.5%, whereas the highest lignin content was observed in the untreated (UTFD) samples, reaching 18.8%. In contrast, pulai wood demonstrated more variation, with the lowest lignin content also observed in the 10N3H treatment at 21.9%, while the highest was found in the 8N3H treatment at 29.5%. These findings are consistent with prior studies, which reported significant reductions in lignin content following similar delignification. Further supporting evidence from literature confirms that lignin can be effectively removed by sequential cooking in NaOH and Na₂SO₃ solutions, followed by hydrogen peroxide (H₂O₂) treatment, which enhances the breakdown and solubilization of lignin compounds [63].

Adsorption capability was evaluated using isopropyl alcohol and engine oil by submerging the delignified wood sponge samples in both liquids and measuring their adsorption capability. Adsorption plays a crucial role, especially considering that contaminants such as oils and alcohols—which tend to adsorb strongly onto soil and water are often recalcitrant to biodegradation [77]. As shown in Table 8, there is a significant difference between balsa and pulai wood in terms of their adsorption performance. Pulai wood exhibited fluctuating adsorption values, with the optimal performance at treatment 8N3H, reaching 3.5 g/g for isopropyl alcohol and 2.5 g/g for engine oil. In contrast, balsa wood demonstrated higher adsorption values overall, with the best results observed at 10N3H—5.7 g/g for isopropyl alcohol and 4.5 g/g for engine oil. This indicates that balsa wood, due to its lower density and more open pore structure, is more suitable as an adsorbent material compared to pulai wood. These findings also confirm the effectiveness of the dual-stages delignification using H₂O₂ which appears to enhance the porous structure and increase surface area available for adsorption. The use of an alkaline solution (NaOH + Na₂SO₃) in the first stage helps break down lignin, and the subsequent peroxide treatment likely removes remaining matrix components, further opening up the wood structure for fluid absorption.

The primary factor influencing the adsorption capability of balsa and pulai wood lies in their cell wall structure and resulting porosity. The collapse of porous structures during drying has been well documented, yet several studies have reported that delignification significantly enhances wood porosity, leading to the formation of an open, interconnected porous system in fully delignified wood. Structurally, the wood cell wall is composed of multiple layers built from oriented cellulose microfibrils, which are closely associated with hemicellulose and embedded within a matrix formed by lignin. Lignin primarily acts as an adhesive, contributing to the rigidity and cohesion of the cell wall, especially within the middle lamella that binds adjacent wood cells together [70]. During the dual-stages delignification process—initially using NaOH + Na₂SO₃ followed by hydrogen peroxide treatment—the lignin and a portion of hemicellulose are removed, leaving behind a more exposed and accessible cellulose framework. This transformation results in a layered, sponge-like architecture with increased surface area and porosity. As reflected in the adsorption data, balsa wood demonstrated a superior capability for adsorbing oil and organic solvents compared to pulai wood. This difference is attributed to the more open and layered microstructure developed in balsa wood after delignification, which facilitates greater fluid uptake [78]. These findings align with previous reports indicating that dual-stages chemical delignification enhances the adsorption behavior of lignocellulosic materials by improving pore accessibility and interconnectivity [43].

It can be concluded that the higher porosity tends to give more storage space for adsorbing more liquid spills and enhancing capillary action, wood sponges with higher porosity (often >80%) and exhibit a significantly larger adsorption performance [23], directly boosting the capability of wood sponges, and creating a more larger and more interconnected pores [37].

Wood porosity refers to the amount and distribution of void spaces or pores within the wood structure. The formation of a mesoporous structure, particularly through delignification, significantly enhances the specific surface area, which is a key factor in determining the adsorption behavior and overall performance of wood-based materials such as aerogels. As shown in Table 9, the porosity values of balsa and pulai wood after being submerged in isopropyl alcohol exhibit a similar trend to their adsorption capability. Balsa wood demonstrated the highest porosity value of 84% with the 10N3H treatment when tested with isopropyl alcohol, while pulai wood reached a porosity of 61.1% under the same treatment. These findings confirm that the dual-stages delignification process substantially increases the porosity compared to the untreated/control samples. This increase is attributed to the removal of lignin and hemicellulose, which creates additional voids and enlarges existing lumens within the wood structure. A study by Vitas et al. [30] supports this observation, stating that delignification can increase the number and size of ray cell voids, typically ranging from 20 to 50 μm. Furthermore, literature indicates that ideal porosity levels for highly functional absorbent materials range from 90% to 98% [79]. However, even porosity levels above 80%—as observed in balsa wood—are sufficient to produce a dense network of micropores and mesopores, which provide storage capacity for liquids and enhance the capillary-driven adsorption behavior of wood sponges.

Based on Fig. 12, wood sponges with higher porosity (often >80%) and larger pore diameter exhibit a significant adsorption performance [23]. A positive trend was observed between pore diameter and adsorption capability on balsa wood (y = 0.0194x − 2.4619; R² = 0.3038) and pulai wood (y = 0.0183x − 3.187; R² = 0.331). However, pulai wood has a lower R² than balsa wood due to a smaller pore diameter, which could reflect its lower adsorption capability. On the other hand, the characteristics of the liquid play a major role. The absorption capability during engine oil immersion is lower than isopropyl alcohol due to differences in their characteristics. After treatment, wood sponge exhibits enhanced hydrophilic and could offer an eco-friendly, sustainable, efficient solution for oil-separation and absorption for non-polar substances such as alcohol [80]. Another factor is the formation of mesopores during the dual-stages delignification process, as noted by Liang et al. [79]. This contributes to the high adsorption of isopropyl solution, since delignification enhances the capillary action and pore structure of wood, favoring the uptake of less viscous liquids like isopropyl alcohol [23,37]. This process directly boosts the capability of wood sponges, and creates larger and interconnected pores.