Natural Biomass Research Articles

The Role of Low-Carbon Fuels and Carbon Capture in Decarbonizing the U.S. Clinker Manufacturing for Cement Production: CO2 Emissions Reduction Potentials

Low-carbon fuels, feedstocks, and energy sources can play a vital role in the decarbonization of clinker production in cement manufacturing. Fuel switching with renewable natural gas, green hydrogen, and biomass can provide a low-carbon energy source for the high-temperature process heat during the pyroprocessing steps of clinker production. However, up to 60% of CO2 emissions from clinker production are attributable to process-related CO2 emissions, which will need the simultaneous implementation of other decarbonization technologies, such as carbon capture. To evaluate the potential of fuel switching and carbon capture technologies in decarbonizing the cement industry, a study of the facility-level CO2 emissions is necessary. This study evaluates the potential for using a single low-carbon fuel as an energy source in clinker production for cement manufacturing compared to conventional clinker production (which uses a range of fuel mixes). In addition, conventional carbon capture (operated with natural gas-based steam for solvent regeneration) and electrified carbon capture configurations were designed and assessed for net-zero emission targets. Carbon emissions reductions with and without biogenic emissions credits were analyzed to ascertain their impact on the overall carbon accounting. Results show that carbon emissions intensity of cement can vary from 571 to 784 kgCO2eq/metric ton of cement without carbon capture and from 166.33 to 438.66 kgCO2eq/metric ton of cement with carbon capture. We find that when biogenic carbon credits are considered, cement production with a sustainably grown biomass as fuel source coupled with conventional carbon capture can lead to a net-negative emission cement (−271 kgCO2eq/metric ton of cement), outperforming an electrified capture design (35 kgCO2eq/metric ton of cement). The carbon accounting for the Scope 1, 2, and biogenic emissions conducted in this study is aimed at helping researchers and industry partners in the cement and concrete sector make an informed decision on the choice of fuel and decarbonization strategy to adopt.

Efficient conversion of syngas to linear α-olefins by phase-pure χ-Fe5C2.

Oil has long been the dominant feedstock for producing fuels and chemicals, but coal, natural gas and biomass are increasingly explored alternatives1-3. Their conversion first generates syngas, a mixture of CO and H2, which is then processed further using Fischer-Tropsch (FT) chemistry. However, although commercial FT technology for fuel production is established, using it to access valuable chemicals remains challenging. A case in point is linear α-olefins (LAOs), which are important chemical intermediates obtained by ethylene oligomerization at present4-8. The commercial high-temperature FT process and the FT-to-olefin process under development at present both convert syngas directly to LAOs, but also generate much CO2 waste that leads to a low carbon utilization efficiency9-14. The efficiency is further compromised by substantially fewer of the converted carbon atoms ending up as valuable C5-C10 LAOs than are found in the C2-C4 olefins that dominate the product mixtures9-14. Here we show that the use of the original phase-pure χ-iron carbide can minimize these syngas conversion problems: tailored and optimized for the process of FT to LAOs, this catalyst exhibits an activity at 290 °C that is 1-2 orders higher than dedicated FT-to-olefin catalysts can achieve above 320 °C (refs. 12-15), is stable for 200 h, and produces desired C2-C10 LAOs and unwanted CO2 with carbon-based selectivities of 51% and 9% under industrially relevant conditions. This higher catalytic performance, persisting over a wide temperature range (250-320 °C), demonstrates the potential of the system for developing a practically relevant technology.

Application of natural biomass of prickly pear peel in methyl violet 2b removal: Adsorptive multivariable optimization and mechanistic approach

Application of natural biomass of prickly pear peel in methyl violet 2b removal: Adsorptive multivariable optimization and mechanistic approach

Sustainable ammonia and amines from chitin

Efforts are underway to explore alternative methods to the Haber-Bosch process for sustainable ammonia production, while the potential for ammonia extraction from natural nitrogenous biomass is under-exploited. Here, a synergistic catalytic strategy involving acid and modified Ru-based catalysts is communicated for the direct production of amines and ammonia from chitin. Phosphoric acid promotes the cleavage of ether bonds in biomass polymers and also serves to protect amino groups from being removed. Selective hydrogenation, deoxygenation, and amination can be achieved by controllably adjusting the ratio of Ru0/Run+. The utilization of nitrogen atoms in chitin can reach up to 95 % (21 % amines, 74 % ammonium), and the catalytic process is applicable to waste shrimp shells. This study demonstrates the possibility of efficient production of nitrogen-containing compounds from abundant biopolymers.

Porosity Regulation of Surfactant‐Assisted Glycerol Organosolv Lignin Modified Hyper‐Cross‐Linked Polymers and Their Efficient Adsorption for Dyes From Water

ABSTRACTHere, we tried to use the natural biomass resources (lignin) to modify porous organic polymers (POPs) and expected to reduce the preparation cost and enhance the adsorption performance. Specifically, the surfactant‐assisted glycerol organosolv lignin (saGO lignin) was used as the modified agents to prepare lignin modified hyper‐cross‐linked polymers (LHCPs) by the copolymerization and Friedel‐Crafts reaction. We investigated the effect of synthesis conditions (the types and dosages of crosslinkers, the feeding amount of lignin, and so on) on the structure and adsorption performance of LHCPs. The results showed that divinyl benzene (DVB) crosslinked LHCP‐D (1041.3 m2/g) showed higher specific areas (SBET) than N,N′‐methylene diacrylamide (MBA) crosslinked LHCP‐M (183.1 m2/g), and the SBET had a certain increase with increasing the amount of DVB. Intriguingly, the SBET and micropore volume (Vmicro) of LHCPs appeared a linear decrease with the increase of lignin dosage, meanwhile, their morphology had a change from irregular block to agglomerated spherical particles, indicated their porosity and morphology can be well controlled. The Rhodamine B (RhB) adsorption experiments indicated that these LHCPs possessed fast adsorption rate (equilibrium time < 240 min) and good recycling performance, especially, LHCP‐D (lignin of 0.5 g, DVB of 1.0 g, catalyst of 3.0 g, reaction time of 10 h) showed the ultrahigh adsorption capacity, up to 743.7 mg/g. The adsorption mechanism was preliminarily investigated by X‐ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and adsorption models analysis, we found that the physical adsorption played the dominated roles by the π–π interaction, hydrogen bonding, and electrostatic interaction. This work not only offered an important reference for the high‐value utilization of lignin, but also provided an effective sustainable adsorbent for environmental remediation.

Evaluating the Efficacy of an Extract for UV Defense and Mitigation of Oxidative Stress, Transitioning from Biomass to Bioprotection

This study evaluated natural extracts from plant biomass for UV protection and oxidative stress reduction. Conducted in Bucharest, Romania, it focused on medicinal mushrooms and pomegranate bark. The biotechnological process involved a two-phase extraction: hot water processing of Ganoderma lucidum, Hericium erinaceus, Inonotus obliquus, and Tremella mushrooms, followed by ethanol extraction with pomegranate bark and green tea. The spectrophotometric analysis identified phenolics and flavonoids. The ethanol extract showed higher phenolic content and antioxidant activity, particularly in DPPH radical scavenging. UVB exposure tests demonstrated its protective effect, comparable to vitamin B3, delaying oxidative stress onset by 30 min. This research underscores the potential of using natural biomass extracts in skincare, promoting environmental sustainability and economic viability by converting agricultural waste into valuable bioactive compounds.

Bacterial cellulose nanofiber reinforced self-healing hydrogel to construct a theranostic platform of antibacterial and enhanced wound healing

In order to promote wound healing, self-healing hydrogels with moisturizing property are employed as wound dressing. In this study, bacterial cellulose nanofibers (BCN) with high mechanical strength are used as reinforcement to improve the mechanical properties of self-healing hydrogels. A multifunctional self-healing hydrogel has been constructed by incorporating natural biomass, including Ag hybrid bacterial cellulose nanofiber (Ag-BCN), resveratrol (Res), and carbon nanodots (CNDs). The results of in vitro experiments demonstrate that the mechanical strength of the hybrid hydrogel was increased by 6 times with the addition of Ag-BCN, which also offers excellent antibacterial efficiency (S. aureus 99.99 % and E. coli 99.68 %). The hydrogel with CNDs can observe the healing process of the crack in real time and realize the controlled release of Res through photothermal effect. Moreover, the results of animal model experiments indicate that the prepared hydrogel could reduce the infection of the wound, effectively shorten the progress of wound healing (from 21d to 14 d). All the results imply that the prepared hydrogel has great promise in the application of skin wound healing.

Facile fabrication of sulfur-doped porous carbon from waste sugarcane bagasse for high performance supercapacitors

Our research has led to a significant breakthrough in the field of energy storage. For the first time, we have prepared a series of highly porous sulfur-doped activated carbon derived from natural biomass sugarcane bagasse. The sulfur-doped waste sugarcane bagasse-derived activated carbon (WSC/S) possess a unique properties of large specific surface area (SSA) with high mesoporosity, better wettability, and numerous redox active dopant sites. These unique properties of WSC/S significantly enhance supercapacitor functionality. There are a large number of mesopores on the WSC/S, which shorten the ion diffusion path length and make their ion transport efficient. As the results of that the WSC/S achieved a high specific capacitance of 282.25 Fg−1 with a current density of 0.1 Ag−1 and excellent cycling stability with >96 % capacitance retention after 10,000 cycles in 6 M KOH electrolyte. We explored WSC/S as an anode material to fabricate an asymmetric supercapacitor (ASC) device, where activated carbon cloth was used as a cathode. The ASC device showed an energy density of 43.26 Wh kg−1 with a power density of 0.1 kW kg−1 at a current density of 0.1 Ag−1, which is superior to that obtained for symmetric WSC/S//WSC/S supercapacitor. These performances indicate the potential of the WSC/S for high-performance energy storage systems.

A biomass-based protective layer with rigid structure and ion conductivity for high-performance lithium metal batteries

Lithium (Li) metal has been considered as an effective anode material because of its high theoretical capacity, but the uncontrolled dendrite growth and the unstable electrode/electrolyte interface limit its practical application. In this work, proanthocyanidin (PA), a natural extracted biomass, was designed and developed as a coating material to guide homogeneous deposition and restrain side reaction for lithium metal batteries. The rigid benzene ring structure of PA can increase the mechanical strength to restrain dendrite growth on Li surface. Moreover, the spontaneous formation of organolithium (PA-Li) structure from the reaction of phenolic hydroxyl group with Li metal increase the ion transportation ability of PA layer and induce the uniform deposition of Li+ ions to hinder the growth of Li dendrites, as well as prevent the direct contact of organic electrolyte with Li metal to suppress the interface side reaction. As a result, Li metal anode with PA-Li exhibits stable cycling properties for 2800 h at 2 mA cm-2 and 2 mAh cm-2, better that of bare Li (200 h). Li-sulfur full battery with PA-Li can still achieve a capacity of 570 mAh g-1 after 300 cycles. This work provides an effective strategy for the construction a natural functional layer on Li surface to enhance the electrochemical performance, as well as the implementation of high-value utilization for natural biomass.

Stock status and spawning potential ratio of orange mud crab (Scylla olivacea, Herbst 1796) in the southwestern coastal waters of Bangladesh

Scylla olivacea (Orange mud crab) is a second commercial invertebrate species exported from Bangladesh. Though a significant portion of exports are supported by aquaculture, their farming ultimately depends on their wild stocks. Unfortunately, unregulated exploitation has led to a significant decline in the natural biomass of this species, raising concerns about the sustainability of crab production in Bangladesh. The study aimed to assess the stock status of S. olivacea (Orange mud crab) from the Southwestern coastal water of Bangladesh. One-year length frequency (width frequency-WF for crustacean fishery) data were collected and analyzed using the LBB (Length-based Bayesian Biomass) and LB-SPR (Length-based spawning potential ratio) methods. The assessed width parameter depicted the exploitation of small-size individuals (Wc=< Wc_opt) of S. olivacea. The estimated B/B0 (0.25) suggests that 75 % of the wild stock had already been harvested, and biomass cannot produce MSY. The mean estimates for SW50 % and SW95 % were 8.29 cm and 12.76 cm respectively, revealing the use of a small mesh-size net for crab harvesting. The assessed Spawning Potential Ratio (SPR) was 12 % which is below the SPR limit reference point (SRP) of 20 %. This research confirmed the overfished (F/M = 1.4) and overexploited (E = 0.58) status of S. olivacea in Bangladesh. To ensure the sustainability of coastal fisheries in Bangladesh, the authorities must take immediate management measures to control the overexploitation of this species.

Scalable and Sustainable Zinc (II) Ions‐Glue‐Assisted Conversion of Biomass Waste Bits into Carbon Aerogels for Efficient Uranium Extraction

AbstractCarbon aerogels (CAs) have garnered significant attention due to their multifunctional applications. Biomass waste, abundantly generated by agriculture and industry, serves as a primary carbon source. However, developing a facile, sustainable, and efficient method to produce CAs from biomass waste remains challenging. In this study, a one‐step Zn2+ ion‐glue‐assisted carbonization technique was developed to produce large‐scale, high‐performance CAs. Various biomass materials (wood bits, peanut shells, bamboo bits, and straw waste) were treated in a molten salt system (ZnCl2/KCl) at 300 °C for 2 h to obtain large‐block CAs derived from biomass bits. Zn2+ ions cleave cellulose hydrogen bonds in natural biomass, facilitating the dehydration crosslinking reaction among cellulose, hemicellulose, and lignin, thus reconstructing the entire block structure. The resulting CAs exhibited high porosity (95 %) and low density (0.078 g/cm3). Numerous hydroxyl and carbonyl groups were preserved during the low‐temperature treatment, facilitating chemical modification for diverse applications. For instance, amidoxime functionalized CAs were utilized as filters for selective and highly efficient extraction of U(VI) from wastewater. The adsorption capacity and extraction efficiency reached 801.2 mg/g and 95 % with a flux rate of 6.1×103 L/m2 ⋅ h.

Scalable and Sustainable Zinc (II) Ions-Glue-Assisted Conversion of Biomass Waste Bits into Carbon Aerogels for Efficient Uranium Extraction.

Carbon aerogels (CAs) have garnered significant attention due to their multifunctional applications. Biomass waste, abundantly generated by agriculture and industry, serves as a primary carbon source. However, developing a facile, sustainable, and efficient method to produce CAs from biomass waste remains challenging. In this study, a one-step Zn2+ ion-glue-assisted carbonization technique was developed to produce large-scale, high-performance CAs. Various biomass materials (wood bits, peanut shells, bamboo bits, and straw waste) were treated in a molten salt system (ZnCl2/KCl) at 300 °C for 2 h to obtain large-block CAs derived from biomass bits. Zn2+ ions cleave cellulose hydrogen bonds in natural biomass, facilitating the dehydration crosslinking reaction among cellulose, hemicellulose, and lignin, thus reconstructing the entire block structure. The resulting CAs exhibited high porosity (95 %) and low density (0.078 g/cm3). Numerous hydroxyl and carbonyl groups were preserved during the low-temperature treatment, facilitating chemical modification for diverse applications. For instance, amidoxime functionalized CAs were utilized as filters for selective and highly efficient extraction of U(VI) from wastewater. The adsorption capacity and extraction efficiency reached 801.2 mg/g and 95 % with a flux rate of 6.1×103 L/m2 ⋅ h.

Antimicrobial Functionalization of Surfaces by a Chimeric Adhesive Protein.

The main aim of this work is to account for the prevention and control of microbial growth on surfaces of interest in medical technology. Surface modification is often achieved by physiotherapy or chemical treatments that can involve time-consuming steps, hazardous reagents, and harsh conditions. One of the ways to overcome these drawbacks is the use of surface-active proteins such as hydrophobins. They can form stable protein layers on different surfaces, serving as anchoring points for other molecules of interest. The fungal hydrophobin Vmh2, already exploited for its adhesive ability, has been fused with the antimicrobial peptide GKY20, forming the chimeric protein used herein for functionalizing polystyrene (PS) and bacterial cellulose (BC). As a natural biomass, BC has multiple advantages, including biodegradability, low cost, renewability, high purity, and excellent mechanical properties. The chimeric protein has been proven to successfully adhere to both surfaces. A strong decrease in biofilm formation on PS and a good bactericidal effect of BC have been demonstrated. These findings provide evidence of an alternative strategy to obtain functional composites using a green, easy process.

Optimization of a novel hydrogen production process integrating biomass and sorption-enhanced reforming for reduced CO2 emissions

Recently, there has been a growing demand for clean and sustainable energy sources to bridge the energy gap. Hydrogen has emerged as an attractive and environmentally friendly energy carrier due to its potential for high energy efficiency and minimal pollution generation, making it a promising alternative to fossil fuels. This study proposes and investigates a novel coupled process that utilizes chemical looping technologies for hydrogen production, simultaneously utilizing natural gas and biomass as feedstocks. The primary objective of this research is to develop a process model that maximizes hydrogen production while minimizing carbon dioxide emissions. Aspen Plus version 10 was employed to simulate and analyze the proposed process configuration to achieve this. One of the proposed process's key advantages is its competitiveness compared to conventional steam methane reforming (SMR) processes, which are widely used in industry. The novel process offers significant benefits, such as enhanced hydrogen purity and reduced CO2 content in the product gas. The simulation results obtained from Aspen Plus reveal the successful production of highly pure hydrogen with a molar ratio of H2/CO equal to 268 and syngas with a molar ratio of H2/CO approximately equal to 1. Additionally, the process demonstrates the capability to produce highly high-purity hydrogen with a molar ratio of H2/CO equal to 155,000 in three-section reactors.

Bioconversion of agriculture by-products with functionally enhanced Streptomyces sp. SCUT-3: Fish skin as a model

With the global population continuously rising, efficient bioconversion of inedible agricultural by-products is crucial for human food and energy sustainability. We here propose solid-state fermentation approaches to efficiently convert biopolymers into oligomers/monomers by accelerating the natural degradation process of the versatile Streptomyces sp. strain SCUT-3. Using fish skin as a representative by-product, 54.3 g amino acids and 14.7 g peptides (91 % < 2500 Da) were recovered from 89.0 g protein in 100 g tilapia skin sample by collagenase-overexpressed SCUT-3 for seven days at a 1:4 substrate:liquid ratio. Fish skin collagen hydrolysates exhibited excellent anti-oxidation, anti-hypertension, scratch-repairing, anti-aging, anti-ultraviolet radiation, and anti-inflammation effects on human skin fibroblasts In vitro and zebrafish larvae in vivo, indicating their potential applications in healthcare/skincare and anti-atopic dermatitis. As Laozi said, the divine law follows nature. This study underscores the efficacy of genetically engineered SCUT-3 according to its natural biomass utilization laws in large-scale biopolymer conversion.

Flexible and synergistic methanol production via biomass gasification and natural gas reforming

Sustainable liquid fuels are essential for decarbonization of various means of transportation which are challenging to address through electrification or hydrogen use. A possible method for producing low-carbon liquid fuel is through the thermochemical biomass to liquid (BTL) process. In this study, we conduct a technoeconomic-environmental analysis of two processes which take advantage of integration of natural gas reforming and biomass gasification, with the objective of improving the economics. By integrating H2-rich syngas (a mixture of H2/CO) obtained from natural gas reforming with carbon-rich syngas from biomass gasification, we harness synergistic effects. This combination allows us to achieve the optimal H2/CO ratio required for methanol synthesis, while also ensuring efficient carbon utilization. In the first design, natural gas is reformed in an autothermal reformer (ATR) to produce syngas. A Solid Oxide Electrolysis Cell (SOEC) is utilized to supply the O2 for both gasification and reforming processes. The H2 produced by the SOEC adjusts the H2 content in the syngas before the methanol synthesis reactor. In the second design, natural gas is reformed in a gas-heated-reformer (GHR) before an ATR, while an Air Separation Unit (ASU) produces the O2 for the process. As a benchmark, the economics and flexible operation of both processes are compared to a conventional BTL process. In addition, the techno-economic impact of operating in biomass-only or natural gas-only modes are investigated. For a 134 MWth plant with 50 % of entering carbon from biomass, the levelized cost of methanol (LCOMeOH) of ATR+SOEC case is 34 % higher than the BTL reference case, while that of ATR+GHR case is 24 % lower than the BTL reference case. A lifecycle analysis (LCA) is conducted for these designs. Utilizing renewable electricity and 50 % biogenic carbon, the ATR+SOEC case emits 908 kgCO2e /tonne MeOH for a 100-year Global Warming Potential (GWP), while the ATR+GHR case emits 721 kgCO2e /tonne MeOH. For a 20-year GWP, these emissions are 1055 and 915 kgCO2e /tonne MeOH, respectively. These emissions correspond to more than 50 % reduction in LCA emissions when compared to natural gas based LCA emissions.

NiFe-Prussian blue analogs catalyst for glucose electrolytic hydrogen production and biomass valorization

Making green hydrogen from natural biomass glucose electrolysis represents a successful win-win scenario which not only achieves energy-efficient hydrogen production but also yields high-value-added chemicals. Herein, we report a NiFe-PBA catalyst synthesized by a facile co-precipitation method for glucose electrooxidation reaction (GOR). Benefiting from the unique ligand structure and the optimal electron, the Ni1·6Fe-PBA achieves a current density of 50 mA cm⁻2 at a potential of only 1.42 V versus Reversible Hydrogen Electrode (RHE), and it maintains potential stability for 50 h. Through an intermittent multipotential-step method it was known that NiOOH is the active site of GOR. Based on the superior GOR activity of this catalyst, we constructed a two-electrode glucose electrolysis hydrogen making system. At a current density of 50 mA cm⁻2, this system reduced the voltage of 230 mV compared to traditional water electrolysis. This improvement significantly reduces energy consumption, requiring only 43.4 kWh to produce 1 kg of H2, saving 6.1 kWh of energy power. To our excitement, we analyzed the electrolyte after stability measurement and found the production of GRA, an important platform molecule for chemical industry and medical treatment. This research provides a promising and sustainable approach for efficient hydrogen production and the value-up of biomass feed-stock.

Thermodynamic analysis of trigeneration system with controlled thermal-electric ratio by coupling liquefied natural gas cold energy and biomass partial gasification

Efficient utilization of biomass energy is crucial for addressing environmental challenges. However, the low calorific value of syngas from biomass gasification poses subsequent utilization issues. This study proposes a trigeneration system integrating biomass partial gasification and LNG cold energy to address surge problems using syngas combined cycle systems. The design includes air separation units, combined cycle, and biomass gasifier, achieving an adjustable thermal-electric ratio. An air separation unit and two-stage Organic Rankine Cycle fully utilize LNG cold energy. A thermodynamic model was established in Aspen Plus, and energy, exergy, and economic analyses were conducted to assess feasibility, followed by a sensitivity analysis. Results show that with a mix burning ratio and carbon conversion rate of 0.6 and 0.7, the system's exergy, energy, and electrical efficiencies are 36.94 %, 60.14 %, and 33.32 % in cooling mode. The unit exergy cost and CO2 emissions are 0.0748$ and 95.29 kg/s, respectively. Analysis reveals variations in efficiency and outputs with changes in mix burning ratio and carbon conversion rate. Adjusting operational parameters enhances the system's ability to regulate the thermal-electric ratio, demonstrating its potential for efficient biomass energy utilization and environmental sustainability.

Multi-interface engineering design of nitrogen-doped bamboo-based carbon/Fe/Fe3C composite electromagnetic wave absorber based on honeycomb-ant nest-like structure

The integration and development of artificial intelligence (AI) and 5G communication technology have brought tremendous changes to human society. How to create a green electromagnetic environment has attracted people's attention. Rich heterostructure design based on interface engineering is considered an effective means of obtaining efficient electromagnetic wave absorbers. In this work, we have achieved innovative design of nitrogen doped carbon/Fe/Fe3C multi-interface heterostructures. The delignification modification of bamboo enriches the cellular pore channels, effectively regulates the loading of Fe3+and the diffusion binding of pyrrole molecules and promotes the deep construction of multi-layer heterogeneous interfaces. Further in-situ pyrolysis resulted in the formation of abundant honeycomb ant nest like structural pores and nitrogen doped multiphase heterostructure interfaces. Provided the best multi-component loss mechanism and impedance matching for the material, improving the overall dielectric and interface polarization effects of the material. Therefore, the obtained absorbent exhibits satisfactory electromagnetic wave absorption performance at a low load of 20 %, with an effective absorption bandwidth of 6.5 GHz (1.85 mm). This work provides new ideas for the high-value utilization of biomass in nature, optimization and innovative design of multi-level pore structures for microwave absorbers.

Endowing Three-Dimensional Porous Wood with Hydrophobicity/Superhydrophobicity Based on Binary Silanization.

Wood, as a natural biomass material, has long been a research focus. Superhydrophobic modified wood, in particular, has shown great promise in a myriad of engineering applications such as architecture, landscape, and shipbuilding. However, commercial development has encountered significant resistance due to preparation difficulties and sometimes unsatisfactory performance. In this study, hydrophobic/superhydrophobic wood comodified with methyltrimethoxysilane (MTMS) and 1H,1H,2H,2H-perfluorodecyltrimethoxysilane (PFDTMS) was fabricated by a one-step sol-gel method that uses an in situ growth process. Low-molecular-weight MTMS was allowed to permeate the three-dimensional porous wood interior. Then, acid-base catalysts were used to regulate the hydrolytic condensation process of MTMS and PFDTMS composite silanes to generate micro/nano hierarchical structures with low surface energy on the wood surface. The physicochemical characteristics of modified wood were investigated and the reaction mechanism established. The modified wood displayed excellent internal hydrophobicity/surface superhydrophobicity, water-moisture resistance, and dimensional stability at low fluorine concentrations. The resulting superhydrophobic surface provided stain resistance, self-cleaning ability, and loading capacity in water while exhibiting good mechanochemical stability; wood mechanical strength was also enhanced. This methodology created a superhydrophobic surface and bulk hydrophobization of wood in one step. Beyond wood, this approach is expected to provide a promising approach for functional modification of other porous composite materials.