Surface Treatment of Biochar—Methods, Surface Analysis and Potential Applications: A Comprehensive Review

: In recent years, biochar has emerged as a remarkable biosourced material for addressing global environmental, agricultural, biomedical, and energy challenges. However, the performances of biochar rest in part on ﬁnely tuning its surface chemical properties, intended to obtain speciﬁc functionalities. In this review, we tackle the surface treatment of biochar with silane and other coupling agents such as diazonium salts, titanates, ionic/non-ionic surfactants, as well as nitrogen-containing (macro)molecules. We summarize the recent progress achieved mostly in the last ﬁve years and correlate the nature and extent of functionalization to eye-catchy end applications of the surface-engineered biochar.


Introduction and Scope of the Review
It is without any doubt that biochar is a very hot topic due to its central position at the crossroads of materials science, materials and surface chemistry, surface science, catalysis, and organic reactions. Biochar is at the heart of sustainable development and concerns biomass and waste valorization and utilization for de-pollution and soil amendment. Such an infatuation for biochar is motivated by the availability of numerous varieties of biomasses and wastes worldwide and the need for valorization and/or transformation into functional materials. This resulted in skyrocketing number of publications, exceeding 5500 since 2021.
The most important applications of biochar concern soil amendment and agriculture [1][2][3], but recently much has been achieved in the design of biochar-supported nanocatalysts for water treatment consisting of total mineralization of organic pollutants such as dyes and drugs [4,5], or for the reductive process [6], or for catalyzing organic chemistry reactions [7,8]. Other applications concern the use of biochar as fillers in composite materials [9][10][11], electrode materials [12,13], and the development of novel engineered biochar for the treatment of neglected tropical diseases (NTDs) [14,15], to name just these applications.
Whilst biochar can be employed as freshly obtained by thermochemical conversion of the biomass, it nevertheless requires particular surface treatment in order to impart it with new functionalities. In this mini-review, the focus is on the functionalization of biochar with molecular/macromolecular surface modifiers or coupling agents and catalytic The review discusses activation, surface amination or carboxylation, and doping of various carbon allotropes, including biochar, for extensive capture of CO 2 .
2021 [18] Biochar as a support for nanocatalysts and other reagents The review paper summarizes the knowledge on the use of biochar-supported nanocatalyst, and discusses the mode of coordination of the catalyst nanoparticles by the biochar.
2021 [19] Phosphorus adsorption by functionalized biochar Inefficient crop fertilization induces water pollution by phosphorus. The review discusses biomass pretreatment as well as post-modification of biochar to obtain efficient phosphorus porous adsorbents 2022 [20] Surface modification of biochar for dye removal The review discusses several strategies of obtaining functional biochar for the removal of dyes from water. 2022 [21] Biochar for the removal of contaminants from industrial wastewaters The paper reviews methods for obtaining pristine and engineered biochar for the efficient removal of numerous contaminants from industrial wastewaters.
This article is focused on the key properties of highly reinforcing fillers, such as particle size, structure, and surface activity. The review essentially covers silane modification of biochar.
2023 [10] These reviews concerned various carbon allotrope surface modifications [18], classical activation methods [17] that rest on acid or alkali treatment of biochar, activation with metal chlorides, and post-pyrolysis under steam, to name but a few. However, despite the numerous advances in biochar production, post-modification, and applications, only a few reviews covered surface modification, for example, the surface treatment of biochar particles with silanes for the design of high performance composites (see Table 1). Coverage of the chemical modification of biochar surface with a large series of well-known coupling agents such as silanes, diazonium salts, aminated compounds, surfactants and macromolecules is lacking despite its interest in several domains, i.e., organic chemistry, polymer science and technology, environmental remediation, and sustainable energy. This is what has motivated this review article.

Biomass Conversion to Biochar
Biochar and other related porous carbon materials can be obtained by conversion of biomass using pyrolysis under an inert or reducing atmosphere. Figure 1 displays the impact of pyrolysis parameters on the types of products obtained [23][24][25][26]. Slow pyrolysis is the recommended technique for obtaining biochar.
Surfaces 2023, 6, FOR PEER REVIEW 3 Figure 1. Pyrolysis techniques and the effect of process parameters on product distribution (rt: residence time). Adapted from [26].
The biochar-making method governs its textural and structural properties and chemical composition. These characteristics decide the potential application of the carbonaceous matter. For example, microwave pyrolysis is recommended for applications such as adsorption and heterogeneous catalysis; indeed, the latter requires a pronounced porous Figure 1. Pyrolysis techniques and the effect of process parameters on product distribution (rt: residence time). Adapted from [26].
The biochar-making method governs its textural and structural properties and chemical composition. These characteristics decide the potential application of the carbonaceous matter. For example, microwave pyrolysis is recommended for applications such as adsorption and heterogeneous catalysis; indeed, the latter requires a pronounced porous structure and a high specific surface area. Moreover, an increased yield of high-quality biochar could be obtained by microwave pyrolysis compared to the conventional pathways [32]. Gasification based on partial oxidation of the bio-feedstock using carbon dioxide, oxygen, air, steam, or a mixture of these gases, promotes the production of syngas/producer gas, resulting in a relatively low biochar yield in the 5-10 percentage range [33]. The pyrolysis conditions (temperature, residence time) of biomass are known to be the key factor controlling the polycyclic aromatic hydrocarbons (PAHs) and volatile organic compounds (VOCs) content in biochar; their control is crucial to monitor the release of PAHs and VOCs from the carbonized biomass in soil amendment application [34,35].
Besides the conversion method, the initial biomass could be mixed with ZnCl 2 or KOH, or H 3 PO 4 (used before or after pyrolysis) in order to control the biochar yield and textural properties [23]. As noted above, the gas used during pyrolysis has a major effect on the chemical structure. For example, the mixture N 2 /H 2 induces less oxygen in the final biochar and a higher isoelectric point (IEP) compared to the same biochar obtained using pure N 2 [16]. Textural properties could be controlled via green approaches consisting of mechanical grinding [36] or maceration of the initial biomass in a water/alcohol mixture [15]. We have recently noted that the preparation of biochar@nickel composite by pyrolysis of biomass impregnated with nickel salt-induced an unusual fishnet-like structure of biochar [37]. Actually, nickel catalyzes the carbonization of biomass and leads to a more porous biochar structure [38]. Figure 2 schematically illustrates shortlisted pathways for chemical modification of biochar surface. The literature survey using Google Scholar and the Web of Science indicated that the most employed compounds are silane coupling agents, ionic or non-ionic surfactants, and aryl diazonium salts. For catalytic purposes, titanates have also been proposed. Silanes require hydroxylated surfaces and thus are applicable to biochar as most biochar materials are prepared by thermochemical conversion at 300-500 • C, a range of temperature that ensures the presence of reactive functional groups such as OH and C=O [21]. Such groups can also be obtained by post-acidic treatment [21,39]. Concerning diazonium salts, most carbon allotropes react with these modern surface modifiers to provide C-C bonds and ester linkages [40]. As far as surfactants are concerned, anionic and cationic surfactants interact with biochar via completely different mechanisms (biocharhydrophobic tail, or biochar-hydrophilic head) [41]. Non-ionic surfactants have completely different behavior and rather interact with biochar via oxygen atoms or OH groups (see Section 3.4). Titanates are able to form TiO 2 nanoparticles, in situ, at the surface of biochar and are thus important for providing photocatalytic composites [42]. Another emerging coupling agent is polyethyleneimine (PEI) [43].

General Aspects
In this review, we concentrate on coupling agents that react/interact chemically with biochar, via covalent linkages or through strong electrostatic interactions, hydrogen bonds, or hydrophobic interactions. Other strategies consisting of direct immobilization of nanocatalysts on biochar obtained by pyrolysis of biomass impregnated with metal salt precursor will be briefly summarized at the end of the review. C-C bonds and ester linkages [40]. As far as surfactants are concerned, anionic and cationic surfactants interact with biochar via completely different mechanisms (biochar-hydrophobic tail, or biochar-hydrophilic head) [41]. Non-ionic surfactants have completely different behavior and rather interact with biochar via oxygen atoms or OH groups (see Section 3.4). Titanates are able to form TiO2 nanoparticles, in situ, at the surface of biochar and are thus important for providing photocatalytic composites [42]. Another emerging coupling agent is polyethyleneimine (PEI) [43]. In this review, we concentrate on coupling agents that react/interact chemically with biochar, via covalent linkages or through strong electrostatic interactions, hydrogen bonds, or hydrophobic interactions. Other strategies consisting of direct immobilization of nanocatalysts on biochar obtained by pyrolysis of biomass impregnated with metal salt precursor will be briefly summarized at the end of the review.

Surface Functionalization with Silane Coupling Agents
Silanization is the process of modification of surfaces by incorporating organofunctional alkoxysilane [44]. The reaction is usually conducted in aqueous or hydro-alcoholic media. The important steps in silanization are [45]: (i) silane hydrolysis, which leads to R-Si(OH)3, (ii) hydrogen bonding between the hydrolyzed silane and the surface, (iii) condensation with the surface resulting in surface-O-Si linkage, (iv) possible polymerization of the silane in solution, and (v) reaction with pending R group with other species as is briefly discussed below.
In the case of biochar, the abundance of -OH functional groups is crucial for its functionalization with silane coupling agents. Such a modification permits the fabrication of

Surface Functionalization with Silane Coupling Agents
Silanization is the process of modification of surfaces by incorporating organofunctional alkoxysilane [44]. The reaction is usually conducted in aqueous or hydro-alcoholic media. The important steps in silanization are [45]: (i) silane hydrolysis, which leads to R-Si(OH) 3 , (ii) hydrogen bonding between the hydrolyzed silane and the surface, (iii) condensation with the surface resulting in surface-O-Si linkage, (iv) possible polymerization of the silane in solution, and (v) reaction with pending R group with other species as is briefly discussed below.
In the case of biochar, the abundance of -OH functional groups is crucial for its functionalization with silane coupling agents. Such a modification permits the fabrication of high-performance biochar-filled polymer composites, immobilized catalysts, and metal complexes, materials for electromagnetic shielding and road engineering, among numerous applications. We will select a few case studies of distinct types of applications in order to show the possibilities offered by silanes to impart new functionalities and performances to biochar. Figure 3a depicts a general pathway of functionalization of biochar that bears surface hydroxyl groups. The group R borne by the silane is chosen in a way it imparts a specific functionality to biochar: post-functionalization, hydrophilic/hydrophobic interactions, metal complexation/chelation, in situ polymerization, and dispersion in the polymer matrix. Indeed, modified biochar can be used to make composite membranes for pervaporation, a process that uses a poly(dimethyl siloxane) (PDMS) for the separation of ethanol/water mixture [46]. Figure 3b shows the steps involved in biochar silanization. Firstly, silanes go through hydrolysis, followed by condensation, to produce oligomers. Finally, oligomers react with -OH groups on the biochar surface, thus leading to biochar-O-Si covalent bonds [47]. Pending methoxy groups react with PDMS, which results in a biochar/PDMS composite membrane. Vinyl-silanized biochar imparts superior hydrophobic properties to the PDMA membrane compared to aminosilane, as the latter interacts favorably with water due to its free amine group [46]. nol/water mixture [46]. Figure 3b shows the steps involved in biochar silanization. Firstly, silanes go through hydrolysis, followed by condensation, to produce oligomers. Finally, oligomers react with -OH groups on the biochar surface, thus leading to biochar-O-Si covalent bonds [47]. Pending methoxy groups react with PDMS, which results in a biochar/PDMS composite membrane. Vinyl-silanized biochar imparts superior hydrophobic properties to the PDMA membrane compared to aminosilane, as the latter interacts favorably with water due to its free amine group [46]. Silanization of the surface with monosilane ( Figure 4), followed by condensation, led to a removal capacity of CO2 3.7 mmol/g (specific surface area SSA = 394 m 2 /g), higher than 3.4 mmol/g, obtained with Norit, a commercial product of which SSA = 3.4 mmol/g [48]. Silanization of the surface with monosilane ( Figure 4), followed by condensation, led to a removal capacity of CO 2 3.7 mmol/g (specific surface area SSA = 394 m 2 /g), higher than 3.4 mmol/g, obtained with Norit, a commercial product of which SSA = 3.4 mmol/g [48].  Silanization could be an important step to enable the post-functionalization of biochar with complex structures such as metal chelators. Figure 5 depicts a strategy for anchoring ruthenium (Figure 5a), iron, and nickel-containing moieties (Figure 5b). They have exhibited enhanced catalytic activity with high turnover frequency for organic reactions. Silanization could be an important step to enable the post-functionalization of biochar with complex structures such as metal chelators. Figure 5 depicts a strategy for anchoring ruthenium (Figure 5a), iron, and nickel-containing moieties (Figure 5b). They have exhibited enhanced catalytic activity with high turnover frequency for organic reactions. If silanization permits to impart of new functionality to biochar, the spatial distribution of the surface-bound reactive groups is an issue. For example, Huang et al. [51] have brought strong supporting evidence for the effect of pyrolysis temperature on the silanization extent of pine sawdust biochar; they have shown that mercapto-silanization was more efficient with the decreasing order of temperature 300 > 500 > 700 °C. Indeed, biochar has much more OH, C=O, and COOH groups at low pyrolysis temperatures, therefore, enabling even distribution of SH groups at the surface, resulting in larger removal of Hg(II) and 3HCHg + ions ( Figure 6). Interestingly, the high-resolution S2p region from 3BS biochar (prepared at 300 °C and silanized) exhibited peak broadening due to the formation of mercury sulfide. Although 3B and 3BS samples exhibited the lowest specific surface area (1.7 and 4.2 m 2 /g, respectively), substantial mercury compounds could be removed (see Figure 6b,c). This is a clear indication that an even and densely packed distribution of mercapto groups overcame the textural properties imparted by high pyrolysis temperature (335 and 235 m 2 /g for 7B and 7BS, respectively). If silanization permits to impart of new functionality to biochar, the spatial distribution of the surface-bound reactive groups is an issue. For example, Huang et al. [51] have brought strong supporting evidence for the effect of pyrolysis temperature on the silanization extent of pine sawdust biochar; they have shown that mercapto-silanization was more efficient with the decreasing order of temperature 300 > 500 > 700 • C. Indeed, biochar has much more OH, C=O, and COOH groups at low pyrolysis temperatures, therefore, enabling even distribution of SH groups at the surface, resulting in larger removal of Hg(II) and 3 HCHg + ions ( Figure 6). Interestingly, the high-resolution S2p region from 3BS biochar (prepared at 300 • C and silanized) exhibited peak broadening due to the formation of mercury sulfide. Although 3B and 3BS samples exhibited the lowest specific surface area (1.7 and 4.2 m 2 /g, respectively), substantial mercury compounds could be removed (see Figure 6b,c). This is a clear indication that an even and densely packed distribution of mercapto groups overcame the textural properties imparted by high pyrolysis temperature (335 and 235 m 2 /g for 7B and 7BS, respectively).  Figure 6. Fabrication of mercapto-silanized biochar for the removal of Hg compounds. Schematic illustration of the pyrolysis temperature effect on silanization extent, textural and adsorption capacity of biochar (a); effect of pyrolysis temperature and silanization on the removal of Hg 2+ (b), and CH3Hg + (c). Reproduced from [51] with permission of Elsevier. Table 2 reports different silane coupling agents employed to modify biochar surfaces and their potential applications. It shows that either silane-modified biochar or their further modification has been used for different purposes, including water treatment, nanoparticles capture, polymer reinforcement, membranes, road engineering, landfill cover, etc. Figure 6. Fabrication of mercapto-silanized biochar for the removal of Hg compounds. Schematic illustration of the pyrolysis temperature effect on silanization extent, textural and adsorption capacity of biochar (a); effect of pyrolysis temperature and silanization on the removal of Hg 2+ (b), and CH 3 Hg + (c). Reproduced from [51] with permission of Elsevier. Table 2 reports different silane coupling agents employed to modify biochar surfaces and their potential applications. It shows that either silane-modified biochar or their further modification has been used for different purposes, including water treatment, nanoparticles capture, polymer reinforcement, membranes, road engineering, landfill cover, etc.

Titanate Surface Modifiers
Titanates are well-known coupling agents in composite science and technology [58,59], generally speaking, and more specifically, in the domain of dental materials [60,61]. They are proposed for the fabrication of robust dental composite materials.
They have been explored in surface modification of rice bran biochar, but without mention of potentially occurring surface reaction [42]. For this purpose, magnetic biochar was prepared by post-modification with Fe(II) and Fe(III) iron chlorides via pyrolysis, followed by sol-gel process synthesis of TiO 2 from titanate in the presence of the magnetic biochar@Fe. The final material was applied for the photocatalyzed removal of tetracycline antibiotics and for antibacterial application. Of particular interest to surface and interface phenomena, Ti-O-C interfacial functional group was probed by FTIR, which accounts for the covalent attachment of TiO 2 to the underlying biochar.
In another study, titanates were used in order to modify preformed biochar in a sol-gel process. The titanate-modified biochar was pyrolyzed in order to obtain biochar@TiO 2 . Further, wetting impregnation with silver nitrate followed by pyrolysis resulted in biochar@TiO 2 -Ag with antibacterial activity against E. coli (99% of sterilization ratio in 5 min, under daylight) [62].
XPS analysis was used to probe titanate interaction with carbon allotropes, but only rare examples have been found. For example, activated carbon was treated with titanate in order to design supercapacitors (specific capacitance: 376.2 F.g −1 , internal resistance: 0.91 Ω) [63].
Although not strictly on biochar, but of relevance to this review and the scope of the journal Surfaces, recently, titanates were proposed for the covalent attachment of graphene oxide ( Figure 7) in order to provide surface-bound alkyl groups that ensure dispersion of GO in hydraulic oils [64]. Interestingly, C1s spectra show a drastic decrease in the C-O component due to the covalent attachment of the long alkyl chains to the GO via titanium. Such surface-bound groups permitted excellent dispersion of titanate-modified GO in hydraulic oil with remarkably improved tribological properties.

Modification of Biochar by Ionic and Nonionic Surfactants
Biochar surface properties could be changed through modification with the surfactant layers. The ionic and non-ionic surfactant adsorbed on the solid surface influence the specific surface area, the content of acidic-basic functional groups, and the hydrophobic properties of these materials. Various mechanisms of surfactant molecule binding can be involved in such kinds of systems. The electrostatic interactions, hydrogen bonds, inter-

Modification of Biochar by Ionic and Nonionic Surfactants
Biochar surface properties could be changed through modification with the surfactant layers. The ionic and non-ionic surfactant adsorbed on the solid surface influence the specific surface area, the content of acidic-basic functional groups, and the hydrophobic properties of these materials. Various mechanisms of surfactant molecule binding can be involved in such kinds of systems. The electrostatic interactions, hydrogen bonds, interactions between the π-π electrons, bilayer formation, and hydrophobic interactions are associated with the adsorption of the surfactant, schematically presented in Figure 8. These modifications with the surface active agents can both increase and decrease the biochar adsorption capacity, depending on the adsorbate and surfactant chemical character. The adsorption phenomenon could take place due to all the above-mentioned mechanisms. Moreover, the surfactant-adsorbate multilayer creation and the formation of the micelles have a positive effect on the adsorbed amounts of inorganic and organic substances ( Figure 9). These modifications with the surface active agents can both increase and decrease the biochar adsorption capacity, depending on the adsorbate and surfactant chemical character. The adsorption phenomenon could take place due to all the above-mentioned mechanisms. Moreover, the surfactant-adsorbate multilayer creation and the formation of the micelles have a positive effect on the adsorbed amounts of inorganic and organic substances ( Figure 9).
Biochar obtained from the Populus alba tree was modified with the cationic surfactant cetyltrimethyl ammonium bromide (CTAB) and used for Cr(VI) adsorption. The obtained results proved that the surfactant modification affects the Cr(VI) adsorption favorably. The adsorbed amount increases on the modified biochar surface in comparison with the non-modified one, independently of the adsorbent dose [65]. CTAB was also used for the biochar derived from the rice husk. The obtained results showed that due to the modification of the adsorbent, its surface charge changed to be positive. The modified biochar was used for inorganic nitrogen fertilizers removal from the aqueous solution. The Surfaces 2023, 6 190 removal percentage increased by 13% in the case of the modified adsorbent application in comparison to the non-modified material [66]. Biochar obtained from the Populus alba tree was modified with the cationic surfactant cetyltrimethyl ammonium bromide (CTAB) and used for Cr(VI) adsorption. The obtained results proved that the surfactant modification affects the Cr(VI) adsorption favorably. The adsorbed amount increases on the modified biochar surface in comparison with the non-modified one, independently of the adsorbent dose [65]. CTAB was also used for the biochar derived from the rice husk. The obtained results showed that due to the modification of the adsorbent, its surface charge changed to be positive. The modified biochar was used for inorganic nitrogen fertilizers removal from the aqueous solution. The removal percentage increased by 13% in the case of the modified adsorbent application in comparison to the non-modified material [66].
The cationic CTAB modification was also performed in the case of the activated biochars obtained from the peanut shells and corncobs used for the anionic polymerpoly(acrylic acid) (PAA) adsorption. The surfactant modification favored the increase in the polymer adsorption amount on both examined adsorbents. The poly(acrylic acid) removal from the aqueous solution is strongly related to its pH value; however, at all examined pH values (3,6,9), the anionic polymer is better adsorbed on the surface of the CTABmodified activated biochar. In such a case, the maximum PAA adsorbed amount was 68 mg/g [67].
The CTAB-modified biochar obtained from the peanut shells and corncobs was likewise used for the Bisphenol A adsorption. The pyrolysis was performed at 300, 500, and 700 °C. It was found that the CTAB modification inhibits the Bisphenol A adsorption, and this effect becomes stronger with an increasing pyrolysis temperature. It was also proved that when the surfactant concentration applied was higher, a smaller adsorbed amount of Bisphenol was found [68].
The CTAB-modified coffee husk-activated biochar was used for the reactive dye removal from the aqueous solution. The reactive yellow 145 (RDY145) dye adsorbed amount was the largest on the surface of the CTAB-modified activated biochar in comparison to two commercially available different non-modified activated carbons. The pH value has no significant effect on the RDY145 adsorbed amount. The Reactive Red 195 and Reactive Blue 222 dyes were also effectively separated from the aqueous system [69]. The other studies deal with the adsorption of Orange II (OII) and Methylene Blue (MB) dyes on the CTAB-modified biochar obtained from the cornstalk. Due to the adsorbent charge changing to positive (the non-modified biochar has a negative surface charge), the adsorbed amount of positively charged methylene blue decreases. In turn, the adsorbed amount of negatively charged OII increases compared to that observed for non-modified biochar. The cationic CTAB modification was also performed in the case of the activated biochars obtained from the peanut shells and corncobs used for the anionic polymerpoly(acrylic acid) (PAA) adsorption. The surfactant modification favored the increase in the polymer adsorption amount on both examined adsorbents. The poly(acrylic acid) removal from the aqueous solution is strongly related to its pH value; however, at all examined pH values (3,6,9), the anionic polymer is better adsorbed on the surface of the CTAB-modified activated biochar. In such a case, the maximum PAA adsorbed amount was 68 mg/g [67].
The CTAB-modified biochar obtained from the peanut shells and corncobs was likewise used for the Bisphenol A adsorption. The pyrolysis was performed at 300, 500, and 700 • C. It was found that the CTAB modification inhibits the Bisphenol A adsorption, and this effect becomes stronger with an increasing pyrolysis temperature. It was also proved that when the surfactant concentration applied was higher, a smaller adsorbed amount of Bisphenol was found [68].
The CTAB-modified coffee husk-activated biochar was used for the reactive dye removal from the aqueous solution. The reactive yellow 145 (RDY145) dye adsorbed amount was the largest on the surface of the CTAB-modified activated biochar in comparison to two commercially available different non-modified activated carbons. The pH value has no significant effect on the RDY145 adsorbed amount. The Reactive Red 195 and Reactive Blue 222 dyes were also effectively separated from the aqueous system [69]. The other studies deal with the adsorption of Orange II (OII) and Methylene Blue (MB) dyes on the CTAB-modified biochar obtained from the cornstalk. Due to the adsorbent charge changing to positive (the non-modified biochar has a negative surface charge), the adsorbed amount of positively charged methylene blue decreases. In turn, the adsorbed amount of negatively charged OII increases compared to that observed for non-modified biochar. These effects are related to the electrostatic adsorption mechanism. The obtained maximum removal using the modified biochar was 40% for methylene blue and 100% for OII [70].
The anionic surfactant, sodium dodecyl benzene sulfonate (SDBS), was used for the surface modification of the biochar obtained from the rice husk. The modified adsorbent was used for the inorganic nitrogen fertilizers removal from the aqueous solution. It was proved that the surfactant modification increases the removal efficiency by 2% compared to the non-modified biochar [66].
Sodium dodecyl sulfate (SDS) is an anionic surfactant that was used for the modification of activated biochars obtained from peanut shells, corncobs, and peat. All the above-mentioned adsorbents were used for the poly(acrylic acid) adsorption. The experiments indicated that the SDS modification effect on the PAA adsorbed amount depends largely on the adsorbent type and the solution pH value. On the surface of the activated biochars obtained from the peanut shells and corncobs, poly(acrylic acid) adsorption was inhibited at pH 9; however, at pH 3 and 6, the surfactant modification affected the polymer adsorbed amount favorably. This is probably related to the PAA conformation change at different pH values. The maximum removal was 60% [67]. Moreover, the SDS modification largely reduced the PAA adsorbed amount at pH 4.5, 6, and 9 on the surface of activated biochar derived from the peat compared to the non-modified one. However, at pH 3, the modification did not significantly affect the polymer removal, which remained in the amount of over 90% [71].
The anionic SDBS surfactant was used for the modification of the biochar derived from the peanut shells. The obtained biochar was used for the Bisphenol A adsorption. It was proved that the SDBS modification affects the Bisphenol A adsorbed amount negatively. The inhibition became stronger and stronger with the increasing surfactant concentration. The Bisphenol A amount adsorbed on the surface of the non-modified biochar was 100 mg/g, and on the surface of SDBD-modified biochar was 10 mg/g [68].
The biochar obtained from the cassava peels was modified with the SDBS and SDS surfactants and used for Methylene Blue adsorption. It was proved that the SDBS-modified sample resulted in a larger number of surface active sites and increased the dye adsorbed amount. In the case of SDS, due to the changes of the adsorbent surface charge to negative, it had a favorable impact on the dye adsorbed amount increase [72,73]. MB was also adsorbed on the surface of the SDS-modified biochar obtained from the peanut shells. The adsorbent was modified with SDS of different concentrations. The obtained results showed that with the increasing surfactant concentration, the surface area accessible to adsorption increases. As a result, the Methylene Blue adsorbed amounts were considerably larger. The maximum adsorption capacity of the SDS-modified biochar as regards MB was 503 mg/g [74].
The SDBS and SDS anionic surfactants were applied for the magnetic biochars derived from the corncobs and furfural residue modification. The obtained adsorbents were used for norfloxacin (an antibiotic with bactericidal action) adsorption. It was proved that the surfactant modification increased the norfloxacin adsorbed amount. The SBDS with a small concentration showed a larger impact on antibiotic adsorption, whereas SDS with higher concentrations was more effective [41].
Magnetic biochars modified with the amphoteric surfactant-dodecyl dimethyl betaine (BS-12) were used for the phenanthrene adsorption. The adsorbed amount of phenanthrene BS-MC (a substance from the group of polycyclic aromatic hydrocarbons) decreased with the increasing BS-12 surface coating ratio. The change in the solution pH values caused no significant effects on the phenanthrene adsorption [75].
Triton X-100 (2-{4-(2,4,4-trimethylpentan-2-yl)phenoxy}ethanol) belongs to the group of non-ionic surfactants. It was used for the activated biochar derived from the horsetail herb modification. The obtained adsorbent was successfully applied for the poly(acrylic acid) polymer and toxic Pb(II) heavy metal adsorption from the aqueous solutions. It was shown that the PAA adsorbed amounts decrease on the surface of the modified biochar compared to the non-modified one, whereas the Pb(II) adsorption is more effective on the surface of the Triton X-100-modified adsorbent [76]. Poly(acrylic acid) was also adsorbed on the surface of the activated biochars obtained from the peanut shells and corncobs, modified with Triton X-100. The surfactant modification had a small impact on the PAA adsorbed amount. Moreover, the changes in the solution pH values (3,6,9) influenced the poly(acrylic acid) adsorbed amount more significantly compared with any adsorbent modifications with the surface active agent. The obtained maximum adsorbed amount of PAA on the Triton X-100-modified activated biochar was 55 mg/g [67].
The biochars obtained from the peanut shells used for the Bisphenol A removal were modified with the non-ionic surfactant Tween 20 (polyoxyethylene (20) sorbitan monolaurate). Its effect on Bisphenol A adsorbed amount was similar to that caused by the ionic surfactants (CTAB, SDBS). The adsorbed amount decreased by 10 times on the surface of the Tween 20-modified biochar in comparison to the non-modified one. The adsorption efficiency decreased with the increasing concentration of Tween 20 [68].
After the chemical activation, the biochars obtained from the eucalyptus sawdust were modified with three different non-ionic surfactants: PEG 2000 (polyethylene glycol), Pluronic P-123 (poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol)), and Pluronic F-127 (2-{2-(2-hydroxyethoxy)propoxy}ethanol)) and used for the adsorption of metronidazole (an antibiotic used to treat infections with anaerobic microorganisms and mixed flora with anaerobes). All of the examined surfactants (dissolved in ethanol) affected the solid porous structure. PEG 2000 and Pluronic P-123 increased the pore volume and its mean diameter, whereas Pluronic F-127 enhanced only the pore size. All the above surfactants had an impact on metronidazole adsorption. The antibiotic exhibited the greatest affinity for the surface of the adsorbent modified with PEG 2000 (removal 100%), whereas its adsorbed amount was the smallest on the surface of the Pluronic F-127-modified biochar (removal 80%) [77]. Table 3 summarizes the experimental conditions for the design and salient features of surfactant-modified biochar specimens, whereas Figure 10 presents the possible applications of surfactant-modified biochars.

Surface Arylation with Diazonium Salts
The chemistry of aryl diazonium salts dates back to the mid-1800s [78] and was at the origin of the industrial production of azo dyes [79]. It is also explored in numerous organic synthesis reactions [80]. Only since 1992 has it been applied worldwide to modify materials surfaces, particularly carbon allotropes [40,81]. This approach is alluring because of its commercially abundant comprising aromatic amines with various functional groups as diazonium precursors.
A general pathway for the modification of carbon materials is depicted in Figure 11. Mostly, the ex situ or in situ generated diazonium salt reacts in aqueous or organic solvents in order to provide radicals that attack the surface, or the diazonium forms a diazoether interfacial bond, followed by the release of dinitrogen and formation of C-O-C interface. An example is given for carbon surface-bearing surface functional groups.
Biochar is among these functionalized carbons and is thus prone to arylation with diazonium salts. The grafted aryl groups display scaffolds to link moieties through specific reactions as they possess suitable functional groups. They comprise amide coupling, coordination bonding, and click chemistry [55]. The surface-aryl bond is usually strong owing to its covalent nature, therefore ensuring remarkable mechanical properties of polymers reinforced with arylated fillers or strong adhesive bonding of polymers to arylated surfaces. One can also take advantage of the strong arylation of carbonaceous supports to anchor bimetallic nanocatalysts with excellent dispersion and narrow size distribution for nitrate electroreduction application [82].    Metronidazole adsorption [77] pore volume and its mean diameter, whereas Pluronic F-127 enhanced only the pore size. All the above surfactants had an impact on metronidazole adsorption. The antibiotic exhibited the greatest affinity for the surface of the adsorbent modified with PEG 2000 (removal 100%), whereas its adsorbed amount was the smallest on the surface of the Pluronic F-127-modified biochar (removal 80%) [77]. Table 3 summarizes the experimental conditions for the design and salient features of surfactant-modified biochar specimens, whereas Figure 10 presents the possible applications of surfactant-modified biochars.

Surface Arylation with Diazonium Salts
The chemistry of aryl diazonium salts dates back to the mid-1800s [78] and was at the origin of the industrial production of azo dyes [79]. It is also explored in numerous organic synthesis reactions [80]. Only since 1992 has it been applied worldwide to modify materials surfaces, particularly carbon allotropes [40,81]. This approach is alluring because of its commercially abundant comprising aromatic amines with various functional groups as diazonium precursors.
A general pathway for the modification of carbon materials is depicted in Figure 11. Mostly, the ex situ or in situ generated diazonium salt reacts in aqueous or organic solvents in order to provide radicals that attack the surface, or the diazonium forms a diazoether interfacial bond, followed by the release of dinitrogen and formation of C-O-C interface. An example is given for carbon surface-bearing surface functional groups. Biochar is among these functionalized carbons and is thus prone to arylation with diazonium salts. The grafted aryl groups display scaffolds to link moieties through specific reactions as they possess suitable functional groups. They comprise amide coupling, coordination bonding, and click chemistry [55]. The surface-aryl bond is usually strong owing to its covalent nature, therefore ensuring remarkable mechanical properties of polymers reinforced with arylated fillers or strong adhesive bonding of polymers to arylated surfaces. One can also take advantage of the strong arylation of carbonaceous supports to anchor bimetallic nanocatalysts with excellent dispersion and narrow size distribution for nitrate electroreduction application [82].
The arylation of carbon allotropes, including fullerene, graphene, and carbon nanotubes with diazonium salts, showed enhanced properties and performances in several do-R COO N Δ Figure 11. Schematic illustration of the modification of a graphitic surface with aryl diazonium salts.
The arylation of carbon allotropes, including fullerene, graphene, and carbon nanotubes with diazonium salts, showed enhanced properties and performances in several domains such as electrocatalysis, sensing, and optics [55]. However, these precursors are expensive with limited large-scale applications. Alternatively, the obtained biochar from agrowaste pyrolysis can provide a highly porous matrix compared to the initial lignocellulosic materials [83]. Biochar can be treated with acids or alkalis to provide a higher surface area with an enhanced porous structure. Apple leave-derived char was activated through various processes. This work study was concerned with investigating the impact of acid and thermal treatments on the physico-chemical properties of the resulting biochar. The latter was capable of abstracting the organic pollutants from water [84]. Several Raman spectra for carbonaceous matter seem to be complex. It may be referred to as the complicated structure they possess. The simplest spectrum is for graphite because of the uniformity of its formation showing planar and stratified laminates. Relative deformations may arise in this structure, expressing a weak D band with a directly proportional intensity to the extent of disorders in this structure. Khalil et al. [85] investigated fundamental variations in the D/G peak intensity ratio on going from the pristine biochar derived from pomegranate peels when compared to different arylated biochar samples, namely Biochar-COOH, biochar-SO 3 H, and biochar-Azure A. The results expressed that the D/G peak ratio grows with arylation without depending on the kind of diazonium compound. The intensity of Raman D/G peaks was correlated to the elementary concentration of the employed diazonium salts. Figure 12a depicts the general route for the arylation of pomegranate biochar with in situ generated three diazonium salts. Figure 12b compares the Raman bands of pristine and arylated biochar; the D/G intensity ratio increases upon treatment of diazonium salts, which is a sign of true covalent modification resulting from arylation. Figure 12c plots the D/G ratio as a function of the grafting extent determined by TGA. Interestingly, for similar high initial concentrations, Azure A induces marginal change in D/G intensity ratio due to steric hindrance. Figure 12d schematically illustrates the gradual change in the grafting density of aryl groups at the surface. High initial concentration is likely to result in oligomerization of the aryl groups [56,86], hence the tendency of the D/G intensity ratio to reach a plateau value. Indeed, chemical grafting reactions no longer affect the carbon allotrope support but the organic layer, previously attached [87]. Snoussi et al. [88] prepared biochar from the pyrolysis of the pulp of sugarcane pulp bagasse (PSCB) at 500 °C and modified it with sulfanilic acid-based, in situ generated diazonium salts. AgCu bimetallic nanocatalyst was loaded by in situ reduction of the silver and copper nitrate-impregnated arylated biochar (SO3H-Biochar) using phytochemicals extracted from the biomass. Sulfonation and deposition of the bimetallic AgCu nanocatalysts were probed by XPS ( Figure 13A). Raman spectra ( Figure 13B) curve fitting permitted to determine D and G band area and height. This curve-fitting showed deformations in the carbon lattice resulting from the arylation process with some disorders when compared to the pristine biochar ( Figure 13B(a,b)). A noticeable increase in biochar defects can be referred to the surface arylation ( Figure 13B(b)), whereas a minor effect results in a Snoussi et al. [88] prepared biochar from the pyrolysis of the pulp of sugarcane pulp bagasse (PSCB) at 500 • C and modified it with sulfanilic acid-based, in situ generated diazonium salts. AgCu bimetallic nanocatalyst was loaded by in situ reduction of the silver and copper nitrate-impregnated arylated biochar (SO 3 H-Biochar) using phytochemicals extracted from the biomass. Sulfonation and deposition of the bimetallic AgCu nanocatalysts were probed by XPS ( Figure 13A). Raman spectra ( Figure 13B) curve fitting permitted to determine D and G band area and height. This curve-fitting showed deformations in the carbon lattice resulting from the arylation process with some disorders when compared to the pristine biochar ( Figure 13B(a,b)). A noticeable increase in biochar defects can be referred to the surface arylation ( Figure 13B(b)), whereas a minor effect results in a slightly higher D/G band intensity ratio. However, upon metal deposition, a significant relative increase in the G band area or height and, thus, a decrease in the D/G band area or peak height intensity ratio suggested an increase in the graphitization, resulting in boosting the catalytic efficiency.
Surfaces 2023, 6, FOR PEER REVIEW 23 or peak height intensity ratio suggested an increase in the graphitization, resulting in boosting the catalytic efficiency.  Arylation of the activated carbon with 4-sulfobenzene diazonium chloride was carried out for synthesizing 4-sulfophenyl activated carbon to act as an efficient catalyst. Changing the conditions of the reaction provided an arylated activated carbon with sulfanilic acid possessing numerous acid sites. The used catalyst was recovered easily upon utilizing it in esterification reactions of some fatty acids [89]. Bamboo-activated carbon was arylated by sulfanilic acid to produce heterogeneous catalysts. The prepared arylated catalysts showed high activity in esterifying oleic acid with alcohol. The microstructure shrinkage may lead to the deactivation of the heterogeneous acid catalyst. Meanwhile, the regenerated catalyst can be used, providing an efficiency of over 90% [90]. Sulfonated sucrose-based and N-doped activated carbon were prepared using N-source, pore-forming, and sulfonating agents to act as catalysts. They were then employed in producing furfural from wheat straw ( Figure 14). One of these modified catalysts showed acceptable recyclability. The aromatic sulfanilic acid groups were successfully grafted onto the activated carbons via a simple sulfonation procedure [91].
Surfaces 2023, 6, FOR PEER REVIEW 24 Arylation of the activated carbon with 4-sulfobenzene diazonium chloride was carried out for synthesizing 4-sulfophenyl activated carbon to act as an efficient catalyst. Changing the conditions of the reaction provided an arylated activated carbon with sulfanilic acid possessing numerous acid sites. The used catalyst was recovered easily upon utilizing it in esterification reactions of some fatty acids [89]. Bamboo-activated carbon was arylated by sulfanilic acid to produce heterogeneous catalysts. The prepared arylated catalysts showed high activity in esterifying oleic acid with alcohol. The microstructure shrinkage may lead to the deactivation of the heterogeneous acid catalyst. Meanwhile, the regenerated catalyst can be used, providing an efficiency of over 90% [90]. Sulfonated sucrose-based and N-doped activated carbon were prepared using N-source, pore-forming, and sulfonating agents to act as catalysts. They were then employed in producing furfural from wheat straw (Figure 14). One of these modified catalysts showed acceptable recyclability. The aromatic sulfanilic acid groups were successfully grafted onto the activated carbons via a simple sulfonation procedure [91]. In another study, sulfonated bio-carbon samples were prepared via partial carbonization of biomass-based substrates with sulfuric acid or diazonium salt. The performance of the catalysts relied upon the concentration of sulfonic acid groups [92]. Sulfonated carbon materials are covalently functionalized with sulfonic acid groups. They show promising efficiency and selectivity, surpassing traditional acid catalysts. The eminent performance of sulfonated carbonaceous substrates may be correlated to their distinctive topographical features, enhancing catalysis and selective adsorption [93]. Amino-arene-sulfonic acid was used to sulfonate biochar for producing a hydrophobic sulfonic acid functional biochar in a one-pot diazo-reduction process. The length of the arene chain and the grafting magnitude of arenesulfonic acid are substantial factors in monitoring the hydrophobicity of the functionalized biochar catalysts. The latter has a large surface area with an appropriate pore size distribution. This modified biochar supplies an active catalyst in many transformation reactions. These catalysts showed catalytic efficiencies in alkylating 2-methylfuran with cyclopentanone in biofuel production [94]. Table 4 gathers the salient features of some biochar samples arylated under diverse conditions and for various applications such as the catalyzed transformation of furfural or esterification reaction. Arylation is certainly of interest, but if it is conducted with a high initial diazonium concentration, it will lead to a sharp decrease in the specific surface area and the porous volume. Arylation with in situ generated diazonium salts requires a strong acidic medium, i.e., 25-37% HCl. This could favor the formation of a porous structure. In another study, sulfonated bio-carbon samples were prepared via partial carbonization of biomass-based substrates with sulfuric acid or diazonium salt. The performance of the catalysts relied upon the concentration of sulfonic acid groups [92]. Sulfonated carbon materials are covalently functionalized with sulfonic acid groups. They show promising efficiency and selectivity, surpassing traditional acid catalysts. The eminent performance of sulfonated carbonaceous substrates may be correlated to their distinctive topographical features, enhancing catalysis and selective adsorption [93]. Amino-arene-sulfonic acid was used to sulfonate biochar for producing a hydrophobic sulfonic acid functional biochar in a one-pot diazo-reduction process. The length of the arene chain and the grafting magnitude of arenesulfonic acid are substantial factors in monitoring the hydrophobicity of the functionalized biochar catalysts. The latter has a large surface area with an appropriate pore size distribution. This modified biochar supplies an active catalyst in many transformation reactions. These catalysts showed catalytic efficiencies in alkylating 2-methylfuran with cyclopentanone in biofuel production [94]. Table 4 gathers the salient features of some biochar samples arylated under diverse conditions and for various applications such as the catalyzed transformation of furfural or esterification reaction. Arylation is certainly of interest, but if it is conducted with a high initial diazonium concentration, it will lead to a sharp decrease in the specific surface area and the porous volume. Arylation with in situ generated diazonium salts requires a strong acidic medium, i.e., 25-37% HCl. This could favor the formation of a porous structure.  Table 4. Surface treatment of biochar with aryl diazonium salts.
Drastic reduction of SSA from 1422 to 190 m 2 /g for biochar prepared at 800 °C, and from 1658 to 30 m 2 for biochar-urea and sulfonated biocharurea. Sulfur content: 0.08 to 2.29 mmol/g. With urea, very high arylationD/G increased with arylation.
In situ deposition of Ag(I) and Cu(II) ions, followed by reduction using sugarcane bagasse extract.
Drastic reduction of SSA from 1422 to 190 m 2 /g for biochar prepared at 800 °C, and from 1658 to 30 m 2 for biochar-urea and sulfonated biocharurea. Sulfur content: 0.08 to 2.29 mmol/g. With urea, very high arylationD/G increased with arylation.
Acid catalyst. Up to 96% catalyzed esterification of oleic acid with ethanol. [90] Biochar prepared at 600-800 • C without urea, and at 750 • C in the presence of urea. 1 g biochar mixed with 4 g sulfanilic acid and 2 g isoamyl nitrite, in 150 mL DIW. Arylation at 80 • C overnight.
Drastic reduction of SSA from 1422 to 190 m 2 /g for biochar prepared at 800 • C, and from 1658 to 30 m 2 for biochar-urea and sulfonated biochar-urea. Sulfur content: 0.08 to 2.29 mmol/g. With urea, very high arylationD/G increased with arylation.
Catalytic furfural production from wheat straw.
Drastic reduction of SSA from 1422 to 190 m 2 /g for biochar prepared at 800 °C, and from 1658 to 30 m 2 for biochar-urea and sulfonated biocharurea. Sulfur content: 0.08 to 2.29 mmol/g. With urea, very high arylationD/G increased with arylation.

Surface-Modified Biochar with Nitrogen-Based Compounds
Owing to the versatility of sp 2 carbon surface and the availability of highly interacting functional groups, biochar is prone to molecular and macromolecular post-functionalization with aminated compounds. Doping biochar with nitrogen-containing compounds during pyrolysis or hydrothermal treatment of the biomass is out of the scope of this review, and the reader is referred to selected articles on the topic [95][96][97]. Similarly, strong activation with nitric acid to provide surface amino groups is covered but not with a dedicated section; for example, see the work of Bamdad et al. [98].
Modification can proceed with a molecular coupling agent or with the adsorption of a monomer that is subjected to polymerization.
Two major nitrogen-containing compounds have been employed to modify the surface of biochar: aniline and 2-aminothiophenol-related compounds and polyethyleneimine (PEI). The aniline derivatives are usually subjected to in situ oxidative polymerization in the presence of biochar. Surface-confined polymerization proceeds with the adsorption of the aniline derivative, most probably driven by biochar-COOH . . . H 2 N-C 6 H 4 -R hydrogen bonding. For example, 2-aminothiophenol can be adsorbed on the surface of biochar and subjected to oxidative polymerization using ammonium persulfate to yield poly(2-aminothiophenol)-coated biochar particles ( Figure 15) [99]. Note that, in Figure 15, hydrogen bonds are shown for N . . . N interactions; in our fair opinion, hydrogen bonds occur between NH 2 from the monomer and the COOH and/or OH from the biochar surface. Indeed, Lewis acid-base interactions, or more particularly, hydrogen bonds, are maximized for COOH-NH 2 rather than NH 2 -NH 2 interactions [100]. The biochar composite was tested for the uptake of Hg and As from wastewater and was found to remove over twice as many contaminants, at pH 9, compared to the untreated biochar. Adsorption leveled off at~32 and 119 mg/g As(III) and Pb(II), respectively. These values are much higher than those recorded with unmodified biochar (14 and 47 mg/g for AS(III) and Pb(II), respectively. At this stage, it is essential to note that despite a drastic two-fold decrease in the specific surface area of the engineered biochar owing to the polymer coating (118 and 59 m 2 /g for engineered and pristine biochar, respectively), the removal of As(III) and Pb(II) remained high.

Surface-Modified Biochar with Nitrogen-Based Compounds
Owing to the versatility of sp 2 carbon surface and the availability of highly interacting functional groups, biochar is prone to molecular and macromolecular post-functionalization with aminated compounds. Doping biochar with nitrogen-containing compounds during pyrolysis or hydrothermal treatment of the biomass is out of the scope of this review, and the reader is referred to selected articles on the topic [95][96][97]. Similarly, strong activation with nitric acid to provide surface amino groups is covered but not with a dedicated section; for example, see the work of Bamdad et al. [98].
Modification can proceed with a molecular coupling agent or with the adsorption of a monomer that is subjected to polymerization.
Two major nitrogen-containing compounds have been employed to modify the surface of biochar: aniline and 2-aminothiophenol-related compounds and polyethyleneimine (PEI). The aniline derivatives are usually subjected to in situ oxidative polymerization in the presence of biochar. Surface-confined polymerization proceeds with the adsorption of the aniline derivative, most probably driven by biochar-COOH…H2N-C6H4-R hydrogen bonding. For example, 2-aminothiophenol can be adsorbed on the surface of biochar and subjected to oxidative polymerization using ammonium persulfate to yield poly(2-aminothiophenol)-coated biochar particles ( Figure 15) [99]. Note that, in Figure 15, hydrogen bonds are shown for N…N interactions; in our fair opinion, hydrogen bonds occur between NH2 from the monomer and the COOH and/or OH from the biochar surface. Indeed, Lewis acid-base interactions, or more particularly, hydrogen bonds, are maximized for COOH-NH2 rather than NH2-NH2 interactions [100]. The biochar composite was tested for the uptake of Hg and As from wastewater and was found to remove over twice as many contaminants, at pH 9, compared to the untreated biochar. Adsorption leveled off at ~32 and 119 mg/g As(III) and Pb(II), respectively. These values are much higher than those recorded with unmodified biochar (14 and 47 mg/g for AS(III) and Pb(II), respectively. At this stage, it is essential to note that despite a drastic two-fold decrease in the specific surface area of the engineered biochar owing to the polymer coating (118 and 59 m 2 /g for engineered and pristine biochar, respectively), the removal of As(III) and Pb(II) remained high.  Aniline is a much more investigated monomer to provide composites of biochar and polyaniline (PANI). It can be synthesized in the presence of biochar and remains glued to the latter via hydrogen bonds ( Figure 16).
Surfaces 2023, 6, FOR PEER REVIEW 27 Aniline is a much more investigated monomer to provide composites of biochar and polyaniline (PANI). It can be synthesized in the presence of biochar and remains glued to the latter via hydrogen bonds ( Figure 16). Douglas fir biochar was prepared by fast pyrolysis at 900-1000 °C and served for the in situ deposition of PANI by oxidative polymerization [101]. 1 g biochar-PANI composite removed 150 mg Cr(VI) and 72 mg nitrates, at pH 2 and 6, respectively, much more than the pristine biochar. PANI provides nitrogen-based anchoring sites for Cr(VI) and hydrogen bonding acceptors from biochar OH and COOH groups.
Magnetic biochar-PANI composites were prepared by wet impregnation of durian rind powder with three iron precursors, followed by pyrolysis at 800 °C. The resulting magnetic biochars were further coated with PANI via in situ oxidative polymerization of aniline using ammonium persulfate, in an acidic medium (1 M HCl), at 0-5 °C. The highest specific surface was 855 m 2 /g. The magnetic biochar prepared using FeCl3·6H2O precursor and topped with PANI was used as a supercapacitor; it exhibited a specific capacitance of 615 F/g at 10 mV/s and an energy density of 76.9 Wh/kg [102].
Magnetic banana stem biochar was prepared in situ deposition of magnetite after the carbonization process of the biomass at 500 °C. PANI was prepared by in situ polymerization to yield a supercapacitor composite material that has a specific capacitance Cs = 315.7 Fg −1 , higher than that of the magnetic biochar without any PANI (Cs = 234.8 Fg −1 ) [103].
Tobacco biochar was fabricated, treated with phosphoric acid, and mixed with PANI, then Ag3PO4 was synthesized in situ. The final Biochar/PANI/Ag3PO4 was employed as a photocatalyst to degrade triclosan [104]. The rationale for making this ternary composite lies in the synergy between (i) the excellent photocatalytic properties of Ag3PO4, (ii) the electronic conductivity of biochar that favors the rapid transfer of photogenerated electron (e − ) of Ag3PO4, and (iii) PANI, a promoter of the transfer and separation of photogenerated hole-electron pairs (h + -e − ), as well as an inhibitor of the photo-corrosion and oxidation of Ag3PO4. The composite catalyzed the degradation of triclosan at a rate of 85% within 10 min.
Another type of biochar/polymer composites can be prepared by mixing biochar with PEI, using methanol or ethanol [105][106][107][108][109]. Electrostatic interaction between the protonated amino groups from the biochar and the carboxylate groups from biochar can take place. Further, strong hydrogen bonds are expected. Covalent grafting of PEI could be achieved using glutaraldehyde [43,110] or EDTA dianhydride [106]. For example, the frequently Douglas fir biochar was prepared by fast pyrolysis at 900-1000 • C and served for the in situ deposition of PANI by oxidative polymerization [101]. 1 g biochar-PANI composite removed 150 mg Cr(VI) and 72 mg nitrates, at pH 2 and 6, respectively, much more than the pristine biochar. PANI provides nitrogen-based anchoring sites for Cr(VI) and hydrogen bonding acceptors from biochar OH and COOH groups.
Magnetic biochar-PANI composites were prepared by wet impregnation of durian rind powder with three iron precursors, followed by pyrolysis at 800 • C. The resulting magnetic biochars were further coated with PANI via in situ oxidative polymerization of aniline using ammonium persulfate, in an acidic medium (1 M HCl), at 0-5 • C. The highest specific surface was 855 m 2 /g. The magnetic biochar prepared using FeCl 3 ·6H 2 O precursor and topped with PANI was used as a supercapacitor; it exhibited a specific capacitance of 615 F/g at 10 mV/s and an energy density of 76.9 Wh/kg [102].
Magnetic banana stem biochar was prepared in situ deposition of magnetite after the carbonization process of the biomass at 500 • C. PANI was prepared by in situ polymerization to yield a supercapacitor composite material that has a specific capacitance Cs = 315.7 Fg −1 , higher than that of the magnetic biochar without any PANI (Cs = 234.8 Fg −1 ) [103].
Tobacco biochar was fabricated, treated with phosphoric acid, and mixed with PANI, then Ag 3 PO 4 was synthesized in situ. The final Biochar/PANI/Ag 3 PO 4 was employed as a photocatalyst to degrade triclosan [104]. The rationale for making this ternary composite lies in the synergy between (i) the excellent photocatalytic properties of Ag 3 PO 4 , (ii) the electronic conductivity of biochar that favors the rapid transfer of photogenerated electron (e − ) of Ag 3 PO 4 , and (iii) PANI, a promoter of the transfer and separation of photogenerated hole-electron pairs (h + -e − ), as well as an inhibitor of the photo-corrosion and oxidation of Ag 3 PO 4 . The composite catalyzed the degradation of triclosan at a rate of 85% within 10 min.
Another type of biochar/polymer composites can be prepared by mixing biochar with PEI, using methanol or ethanol [105][106][107][108][109]. Electrostatic interaction between the protonated amino groups from the biochar and the carboxylate groups from biochar can take place. Further, strong hydrogen bonds are expected. Covalent grafting of PEI could be achieved using glutaraldehyde [43,110] or EDTA dianhydride [106]. For example, the frequently em-ployed glutaraldehyde is a good coupling agent as it reacts with OH functional groups [111] from biochar surface and the NH/NH 2 groups from PEI. An example of a composite is illustrated in Figure 17, showing the fabrication of magnetic biochar-PEI nanocomposite employed for the removal of Cr(VI).
Surfaces 2023, 6, FOR PEER REVIEW 28 employed glutaraldehyde is a good coupling agent as it reacts with OH functional groups [111] from biochar surface and the NH/NH2 groups from PEI. An example of a composite is illustrated in Figure 17, showing the fabrication of magnetic biochar-PEI nanocomposite employed for the removal of Cr(VI). As a few examples of the performance of PEI-modified biochar materials, PEI-modified pine needles biochar enabled the ability to adsorb 294 mg/g Congo Red, almost 10fold the adsorption capacity of the pristine biochar (30.8 mg/g) [112].
PEI-modified biochar was employed for the detoxification of Cr(VI); it was found to remove 435.7 mg per g of biochar, nearly 20 times higher than 23.1 mg/g for pristine biochar [105]. Table 5 reports experimental conditions, properties, and applications of shortlisted biochars modified with nitrogen-containing molecules and macromolecules. As a few examples of the performance of PEI-modified biochar materials, PEI-modified pine needles biochar enabled the ability to adsorb 294 mg/g Congo Red, almost 10-fold the adsorption capacity of the pristine biochar (30.8 mg/g) [112].
PEI-modified biochar was employed for the detoxification of Cr(VI); it was found to remove 435.7 mg per g of biochar, nearly 20 times higher than 23.1 mg/g for pristine biochar [105]. Table 5 reports experimental conditions, properties, and applications of shortlisted biochars modified with nitrogen-containing molecules and macromolecules.   Catalytic degradation of dimethomorph [116] Forestry waste Co-polymerization of polypyrrole/polyaniline on ferrate-modified biochar. pyrrole/aniline (Volume ratios = 0:1 (0, 1 mL) − 1:0 (1, 0 mL) and 1 g CTAB were added into the above solution with HCl of 1 mol/L. SSA 56.97 m 2 /g Pore-size distributions 17.98 nm Adsorption of hexavalent chromium in water [113] pyrrolic-and pyridine-like N  Catalytic degradation of dimethomorph [116] Surfaces 2023, 6, FOR PEER REVIEW 30 Pistachio shells 10 g of pistachio shell as the carbon source, 2 g of melamine as the nitrogen source, and 5 g of Na-HCO3/K2CO3 as the activator.
SSA increased by about 1000 m 2 g −1 after N-doping, the surface N content increased by more than 3%, and hydrophilicity and polarity declined.
Selective adsorption of toluene under humid conditions [117] the formation of abundant N-containing functionalities in the form of C-N, C=N and N-H in C-N polymer structures.

Melon seed shell
Melon seed shell/melamine Weight ratio = 1:1, in solvent (water and CH3CH2OH with a mass ratio of 1: 1), Dried and pyrolyzed at 400 °C. D/G = 0.71 (peak area ratio), formation of mesopores structure, average pore size of 12.6 nm, melamine or its derivatives reacted with the C=O functionality on the biochar, forming the C-N, C=N, and N-H bond on the biochar. Biochar became hydrophilic after introducing nitrogen species Photocatalytic production of hydrogen [118] Pretreating biomass with (NH4)2S2O8 50 g of the Camellia oleifera shells powder was SSA increased from 134.9 m 2 g −1 to 739.9 m 2 g −1 , and the pore volume also increased from 0.301 cm 3 g −1 to 0.588

Pomelo peel
Reaction with one-pot pyrolysis, Pomelo peel powder, NaHCO 3 and melamine at a mass ratio of 1 Catalytic degradation of dimethomorph [116] Pistachio shells 10 g of pistachio shell as the carbon source, 2 g of melamine as the nitrogen source, and 5 g of NaHCO 3 /K 2 CO 3 as the activator.
SSA increased by about 1000 m 2 g −1 after N-doping, the surface N content increased by more than 3%, and hydrophilicity and polarity declined.
Selective adsorption of toluene under humid conditions [117]  Photocatalytic production of hydrogen [118] C-N, amino groups Camellia oleifera shells Pretreating biomass with (NH 4 ) 2 S 2 O 8 50 g of the Camellia oleifera shells powder was added to 100 mL of ammonium persulfate (1 mol L−1) until dry, and then placed into a N 2 atmosphere for pyrolysis at 700 • C.
SSA increased from 134.9 m 2 g −1 to 739.9 m 2 g −1 , and the pore volume also increased from 0.301 cm 3 g −1 to 0.588 cm 3 g −1 after introduce N-containing groups, pretreatment with (NH 4 ) 2 S 2 O 8 introduces various polar nitrogen-containing and sulfur-containing functional groups into biochar.
The adsorption capacity for Cu(II) and tetracycline. [119] pyridinic-N (N-6), pyrrole/pyridine-N (N-5), and quaternary-N (N-Q) The N groups on nitrogen-containing biochar were mainly Pyridine nitrogen and pyrrole nitrogen groups, the N atom was fixed in the carbon lattice.
Donor performance and conductivity of carbon materials. [122] SSA: specific surface area.
The N groups on nitrogen-containing biochar were mainly Pyridine nitrogen and pyrrole nitrogen groups, the N atom was fixed in the carbon lattice.
Donor performance and conductivity of carbon materials. [122] SSA: specific surface area.

Modification of Biochar with Catalyst Nanoparticles
Biochar is a very versatile platform for nanocatalyst immobilization. This is a hot topic of interest for environmental and other applications such as organic synthesis. Our primary goal was to focus on biochar with molecular and macromolecular compounds. However, as most of the nanocatalysts immobilized on biochar were obtained from metal ion compounds, this section closes the review with a logical sequence when one considers the size: molecules, macromolecules, and nano-or macroparticles. Figure 18 summarizes the main methods of preparation of biochar loaded with catalytic particles: -Method (i) consists in impregnating the initial biomass with catalyst precursor prior to pyrolysis. This process yields biochar powder impregnated with nanoparticles [37,[123][124][125]. -Method (ii) concerns the deposition of catalyst precursor onto prefabricated biochar, followed by in situ reductive process to obtain biochar-immobilized nanocatalysts [8, 88,126]. -Method (iii) is based on a simple mixture of prefabricated biochar and catalysts [7,127].

Modification of Biochar with Catalyst Nanoparticles
Biochar is a very versatile platform for nanocatalyst immobilization. This is a hot topic of interest for environmental and other applications such as organic synthesis. Our primary goal was to focus on biochar with molecular and macromolecular compounds. However, as most of the nanocatalysts immobilized on biochar were obtained from metal ion compounds, this section closes the review with a logical sequence when one considers the size: molecules, macromolecules, and nano-or macroparticles. Figure 18 summarizes the main methods of preparation of biochar loaded with catalytic particles: -Method (i) consists in impregnating the initial biomass with catalyst precursor prior to pyrolysis. This process yields biochar powder impregnated with nanoparticles [37,[123][124][125]. -Method (ii) concerns the deposition of catalyst precursor onto prefabricated biochar, followed by in situ reductive process to obtain biochar-immobilized nanocatalysts [8, 88,126]. -Method (iii) is based on a simple mixture of prefabricated biochar and catalysts [7,127]. From the own experience of the authors, Method (i) yields no loss and evenly dispersed nanoparticles in the nanoscale regime. It requires simple wet impregnation prior to pyrolysis. Method (ii) usually combines two processes: pyrolysis in dry conditions, followed by adsorption of metal ions and their in situ reduction by "beaker chemistry". Method (iii) is perhaps the one that is amenable to pilot or higher scale process as it requires mixing two preformed components of the final composites. However, agglomerated catalyst nanoparticles might be difficult to disperse, with small size, over the biochar surface. Table 6 provides the summarized experimental work for the preparation of catalyst-modified biochar and potential applications of the shortlisted systems. From the own experience of the authors, Method (i) yields no loss and evenly dispersed nanoparticles in the nanoscale regime. It requires simple wet impregnation prior to pyrolysis. Method (ii) usually combines two processes: pyrolysis in dry conditions, followed by adsorption of metal ions and their in situ reduction by "beaker chemistry". Method (iii) is perhaps the one that is amenable to pilot or higher scale process as it requires mixing two preformed components of the final composites. However, agglomerated catalyst nanoparticles might be difficult to disperse, with small size, over the biochar surface. Table 6 provides the summarized experimental work for the preparation of catalyst-modified biochar and potential applications of the shortlisted systems. Biochar was prepared in two steps: hydrothermal treatment at 180 • C/24 h followed by pyrolysis of the resulting hydrochar at 500 • C (1 h). CuNi bimetallic catalyst was prepared from equimolar mixture of copper and nickel chlorides. 0.5 g CuNi and 1 g biochar were mixed in 30 mL water under sonication for 30 min. The mixture was treated in autoclave at 140 • C for 12 h. The biochar@CuNi was dried at 80 • C for 4 h.

Conclusions
In this review, we have summarized the essential findings on the (macro)molecular and nanoparticulate levels of biochar surface treatment. We have covered the modifications of numerous biochar types with silane and titanate coupling agents, aryl diazonium salts, ionic and non-ionic surfactants, nitrogen-containing compounds, and nanocatalysts. Nitrogen species could be a polymerizable monomer (aniline derivatives) or a preformed polymer such as polyethyleneimine (PEI) adsorbed from an alcoholic solution.
One could draw numerous conclusions: -In general, surface modification reduces the specific surface area and porous volume, but it is worth it because it imparts functionalities that unmodified biochar samples do not possess. -Silanization requires rich oxygen functionalities at the surface, which could be obtained at moderate pyrolysis temperature or after oxidization of the biochar. -Titanate could be envisaged to create new biochar-polymer composites if the primary intention is not to design biochar-titania photocatalysts. -Aryl diazonium salts could be regarded as new coupling agents in materials surface chemistry as witnessed over the last three decades; their use to modify biochar particles is recent and very encouraging. Some of us have demonstrated that surface modification is limited by steric hindrance effects of the aryl group, and change in the carbon structure of the biochar is significant at low initial diazonium concentration. -Modification with non-ionic and ionic surfactant adsorbed layers influences the textural characteristics of biochar, as well as acid-basic and hydrophilic-hydrophobic properties of its surface, changing the affinity for other substances present in the aqueous phase. The electrostatic, hydrogen bonds, π-π electrons, and hydrophobic interactions are responsible for the surfactant molecules binding and can result in the formation of more complex surface structures, such as surfactant-adsorbate multilayers and micelles. - The preparation of biochar-polyaniline composites is investigated by several researchers, particularly for the fabrication of supercapacitors, whereas poly(2-aminothiophenol) could be a remarkable alternative to provide surface-immobilized NH and SH groups able to chelate metal ions for environmental remediation issues. -Polyethyleneimine is a nitrogen-rich polymer and could be coated on biochar particles by adsorption from methanol or ethanol solution. Tight, covalent immobilization and crosslinking require using organic coupling agents such as glutaraldehyde. -Other attractive nitrogen-modification of biochar rest on the doping with ammonium persulfate or urea prior to pyrolysis, with a result of enhancing pyridinic, pyrrolic, and graphitic nitrogen in the biochar structure. -Finally, there are numerous routes for catalytic nanoparticle modification of biochar groups in three major methods. They provide surface-immobilized nanoparticles, but pyrolysis of catalyst precursor-impregnated biomass seems to provide narrow-size distribution nanoparticles that are immobilized both at the surface and into the large pores of the biochar. -These are the most investigated surface modifiers, but others are worth deeper insight, e.g., mercaptoethanol [129] and vitamin B6 [130]. Nevertheless, all in one, there is much to anticipate from a surface chemical modification of biochar in the coming years. Surface modification imparts remarkable new functionalities such as pollutant adsorption, immobilization of catalysts, and improved energy storage properties, to name but a few.
Concerning bulk, surface, and textural properties, we witnessed recurrent utilization of XPS, Raman and FTIR, XRD, nitrogen adsorption (for BET and porous volume), and TGA. Other techniques are also applied in the case of specific applications such as energy storage, namely DC voltage-current measurements and cyclic voltammetry. Ironically, we have noted that the biochar topic tackles the valorization of wastes with zero value but requires a high number of analytical techniques, which is excessively costly for academic laboratories.
From the above, the conversion of agro-and other organic wastes into biochar is a very hot topic, with over 5500 publications per year. This will continue to grow in this era of economic crisis, on the one hand, and address some of the 17 sustainable development goals, on the other hand. We thus expect even more publications on the topic and the valorization of numerous other wastes. There are already, and there will be new regional niches from north to south to valorize biomasses such as Douglas fir, [101] brewer spent grain [124], sugarcane bagasse [88], olive [128,131] and date [132] stones, durian [102], etc. However, more rationality is needed to select which agrowaste is worth the thermochemical transformation into biochar by determining the initial cellulose-hemicellulose-lignin composition as their thermochemical transformation yields biochars with completely different properties and thus different potential applications, for example, as electrode materials [13]. Pyrolysis is interesting and offers advantages, but for other applications, hydrochars could be a solution because the treatment is faster, and the process might provide extraction of phytochemicals useful for reductive reaction processes [15] and also carbon dots [133]. Recently, microwave heating has emerged as an alternative for the fabrication of carbonaceous chars, with low energy cost of preparation, and remarkable properties [132]. Yet, when it comes to surface modification, this review has indicated numerous opportunities, but also challenges to overcome, such as the balance between surface chemistry and textural properties in order to achieve the desired end properties and performances.