Production Of Chemicals Research Articles

Strategy-based optimization and life cycle environmental impact assessment of a stable photovoltaic power-to-hydrogen system

With the growing global emphasis on reducing greenhouse gas emissions and transitioning to a low-carbon economy, renewable hydrogen is expected to play a vital role in the chemical industry. However, there is a contradiction between the continuous and stable hydrogen demand of chemical process systems and the intermittent and fluctuating nature of renewable energy systems when coupling them together in the industrial chemical production. There are currently few studies addressing year-round stable hydrogen load systems while considering renewable energy intermittency and capacity optimization. Moreover, the comprehensive life cycle environmental impact study of such stable renewable-hydrogen production system is extremely limited. Therefore, this study focuses on a photovoltaic power-to-hydrogen system that can operate stably for 8,760 h per year, specifically targeting its application in the chemical industry. Two operating strategies of the hydrogen system were considered: fully off-grid and ultra-light grid-connected scenarios. The capacity configuration under each scenario was optimized using gird search algorithm, with the objective of minimizing the levelized cost of hydrogen. Based on the optimization results, the energy flow network, cost-effectiveness, and comprehensive life cycle environmental impacts of such system were analyzed. The results show that the ultra-light grid-connected hydrogen production system, due to the support of the power grid, has improved the reliability of the hydrogen production system and significantly reduced the capacity configuration of system components, thereby demonstrating better performance in terms of economics and overall lifecycle environmental impact compared to a completely off-grid hydrogen production system. Its global warming potential (GWP) and levelized cost of hydrogen under electricity sales scenario are 12% and 31% lower, respectively, compared to fully off-grid hydrogen production. Considering China’s future demand for large-scale renewable hydrogen, ultra-light grid-connected hydrogen production may become the primary transitional pathway in the near to medium term.

Interplay between photosynthetic electron flux and organic carbon sinks in sucrose-excreting Synechocystis sp. PCC 6803 revealed by omics approaches

BackgroundAdvancing the engineering of photosynthesis-based prokaryotic cell factories is important for sustainable chemical production and requires a deep understanding of the interplay between bioenergetic and metabolic pathways. Rearrangements in photosynthetic electron flow to increase the efficient use of the light energy for carbon fixation must be balanced with a strong carbon sink to avoid photoinhibition. In the cyanobacterium Synechocystis sp. PCC 6803, the flavodiiron protein Flv3 functions as an alternative electron acceptor of photosystem I and represents an interesting engineering target for reorganizing electron flow in attempts to enhance photosynthetic CO2 fixation and increase production yield.ResultsWe have shown that inactivation of Flv3 in engineered sucrose-excreting Synechocystis (S02:Δflv3) induces a transition from photoautotrophic sucrose production to mixotrophic growth sustained by sucrose re-uptake and the formation of intracellular carbon sinks such as glycogen and polyhydroxybutyrate. The growth of S02:Δflv3 exceeds that of the sucrose-producing strain (S02) and demonstrates unforeseen proteomic and metabolomic changes over the course of the nine-day cultivation. In the absence of Flv3, a down-regulation of proteins related to photosynthetic light reactions and CO2 assimilation occurred concomitantly with up-regulation of those related to glycolytic pathways, before any differences in sucrose production between S02 and S02:Δflv3 strains were observed. Over time, increased sucrose degradation in S02:Δflv3 led to the upregulation of respiratory pathway components, such as the plastoquinone reductase complexes NDH-11 and NDH-2 and the terminal respiratory oxidases Cyd and Cox, which transfer electrons to O2. While glycolytic metabolism is significantly up-regulated in S02:Δflv3 to provide energy for the cell, the accumulation of intracellular storage compounds and the increase in respiration serve as indirect sinks for photosynthetic electrons.ConclusionsOur results show that the presence of strong carbon sink in the engineered sucrose-producing Synechocystis S02 strain, operating under high light, high CO2 and salt stress, cannot compensate for the lack of Flv3 by directly balancing the light transducing source and carbon fixing sink reactions. Instead, the cells immediately sense the imbalance, leading to extensive reprogramming of cellular bioenergetic, metabolic and ion transport pathways that favor mixotrophic growth rather than enhancing photoautotrophic sucrose production.

On application of molecular dynamics simulation for studying the effect of temperature and heating rate on HTL of biomass

Abstract Hydrothermal liquefaction (HTL) of biomass has garnered increasing attention as a promising pathway for converting solid biomass to liquid biofuels and valuable chemical products. HTL involves processing of biomass in water at high-temperature and high-pressure conditions. The heating rate during this process plays a critical role in determining the yield and composition of the liquefied products. To probe the impact of heating rate, we develop a detailed atomistic model biomass by using cellulose as model compound and place it in a simulated HTL reactor. Our Reactive molecular dynamics simulations are capable of capturing the dynamic chemical reactions and structural changes during HTL. The effect of reaction temperature and heating rates on reaction pathways, product distributions, and reaction kinetics is rigorously analyzed. Our findings reveal that the reaction temperature and heating rate significantly influences the extent of cellulose degradation and the composition of bio-oil product.

Edible Gelatin and Cosmetic Activated Carbon Powder as Biodegradable and Replaceable Materials in the Production of Supercapacitors

Environmental pollution is currently one of the most worrying factors that endangers human health. Therefore, attempts are being made to reduce it by various means. One of the most important sources of pollution in terms of the current RoHS and REACH directives is the pollution caused by the use of chemical products for the production of sources for the storage and generation of electricity. The aim of this article is therefore to develop supercapacitors made of biodegradable materials and to investigate their electrical performance. Among the materials used to make these electrodes, activated carbon was identified as the main material and different combinations of gelatin, calligraphy ink and glycerol were used as the binders. The electrolyte consists of a hydrogel based on gelatin, NaCl 20 wt% solution and glycerol. In the context of this research, the electrolyte, which has the consistency of a gel, fulfills the dual function of the separator in the structure of the manufactured cells. Due to its structure, the electrolyte has good mechanical properties and can easily block the contact between the two electrodes. Most of the materials used for the production of supercapacitor cells are interchangeable materials, which are mainly used in other application fields such as the food or cosmetics industries, but were also successfully used for the investigations carried out in this research. Thus, remarkable results were recorded regarding a specific capacitance between 101.46 F/g and 233.26 F/g and an energy density between 3.52 Wh/kg and 8.09 Wh/kg, with a slightly lower power density between 66.66 W/kg and 85.76 W/kg for the manufactured supercapacitors.

An Autonomous Unmanned Ground Vehicle: A Technology Driven Approach for Spraying Agrochemicals in Agricultural Crops

The application of chemicals through spraying is an essential component of agricultural management systems. However, the use of these chemical products results in the accumulation of residues in the soil, leading to a decline in soil fertility and plant diversity. Additionally, farmers who manually spray pesticides onto their crop fields are at risk of developing health issues such as tumors, hypersensitivity, allergies, and skin diseases. As the global population continues to grow and climate change impacts farmland ecosystems, the occurrence of pest epidemics in crops is becoming more frequent. Consequently, there is a greater demand for enhanced tools and methods to improve crop production. Unmanned ground vehicles (UGVs) have the potential to revolutionize agricultural spraying by offering efficient and effective applications of crop protection agrochemicals. This article provides an overview and consolidation of the present research and advancements in UGV application technologies and different sensors that are specifically designed for spray applications of agrichemicals. It examines the features of both hardware and software architecture for implementing control strategies, obstacle detection, and avoidance systems with real-time integrated systems, and the ability to perform variable-rate agrochemical applications.

Three‐Dimensional Venus Cloud Structure Simulated by a General Circulation Model

AbstractThe clouds have a great impact on Venus's energy budget and climate evolution, but its three‐dimensional structure is still not well understood. Here we incorporate a simple Venus cloud physics scheme into a flexible GCM to investigate the three‐dimensional cloud spatial variability. Our simulations show good agreement with observations in terms of the vertical profiles of clouds and H2SO4 vapor. H2O vapor is overestimated above the clouds due to efficient transport in the cloud region. The cloud top decreases as latitude increases, qualitatively consistent with Venus Express observations. The underlying mechanism is the combination of H2SO4 chemical production and meridional circulation. The mixing ratios of H2SO4 at 50–60 km and H2O vapors in the main cloud deck basically exhibit maxima around the equator, due to the effect of temperature's control on the saturation vapor mixing ratios of the two species. The cloud mass distribution is subject to both H2SO4 chemical production and dynamical transport and shows a pattern that peaks around the equator in the upper cloud while peaks at mid‐high latitudes in the middle cloud. At low latitudes, H2SO4 and H2O vapors, cloud mass loading and acidity show semidiurnal variations at different altitude ranges, which can be validated against future missions. Our model emphasizes the complexity of the Venus climate system and the great need for more observations and simulations to unravel its spatial variability and underlying atmospheric and/or geological processes.

Cooperative dual single atom Ni/Cu catalyst for highly selective CO2-to-ethanol reduction

The electrochemical CO2-to-ethanol conversion bargains a promising approach to lowering CO2 emission while yielding valuable chemical products. Here, we report the NiCu-SACs/N-C catalysts with cooperative dual heteroactive sites that achieve by far the highest catalytic activity for yielding ethanol with the unprecedented Faradaic efficiency of 92.2 % at the potential of −0.6 V versus RHE. The catalyst exhibits the lowest onset potential of −0.4 V versus RHE to catalyze CO2-to-ethanol conversion. In-operando X-ray absorption spectroscopy provides an interesting observation of restructuring behavior of dynamically generated Cu clusters from atomically distributed Cu single-atoms and reversible structural changes or oxidation states of Cu sites while Ni sites remain unchanged during the catalytic reactions. Our experimental analysis and DFT computation suggest that CO produced on Cu-N4/Ni-N3 cooperative single atom sites undergoes C-C coupling, which is further reduced into ethanol. This strategy provides a new route to design selective and efficient catalysts for CO2-to-ethanol conversion.

AB-INITIO CALCULATIONS OF THE RHODIUM-DOPED (001) SURFACE OF THE RHOMBOHEDRAL PHASE BaTiO<sub>3</sub>

The advancement of effective, durable, and economically viable photocatalytic systems aimed at solar-driven water splitting into hydrogen and oxygen represents a strategically vital pathway for future fuel and chemical production from renewable sources. Water splitting is a promising strategy for the sustainable production of renewable hydrogen and for addressing the global energy and environmental crisis. However, the large-scale application of this method is limited by the low efficiency and high cost of solar water splitting systems. The search for economical, efficient, and stable photocatalysts is crucial in the development of solar water splitting technologies. Perovskite-based photocatalysts have recently attracted considerable attention for use in solar water splitting processes due to their simple structure and flexible composition. BaTiO3 is a promising photocatalyst because of its adjustable electronic structure. Initially considered a poor photocatalyst due to its wide band gap, this material has become the focus of various strategies aimed at reducing the band gap. In this paper, we study the effect of Rh doping on the electronic structure of the (001) BaTiO3 perovskite surface. Theoretical results show that Rh atoms can occupy both sites simultaneously, or only Ti sites, or Ba sites. The electronic structure was modeled for two conditions. When Rh atoms occupy one Ba position and one Ti position, the electronic structure shows the presence of an acceptor level within the band gap above the Fermi level, effectively reducing the band gap of the material.

Highly Selective Photocatalytic Synthesis of Acetic Acid at 0‐25oC

Abstract Acetic acid (AA), a vital compound in chemical production and materials manufacturing, is conventionally synthesized by starting with coal or methane through multiple steps including high‐temperature transformations. Here we present a new synthesis of AA from ethane through photocatalytic selective oxidation of ethane by H2O2 at 0‐25°C. The catalyst designed for this process comprises g‐C3N4 with anchored Pd1 single‐atom sites. In‐situ studies and computational simulation suggest the immobilized Pd1 atom becomes positively charged under photocatalytic condition. Under photoirradiation, the holes on the Pd1 single‐atom of OH‐Pd1Å/g‐C3N4 serves as a catalytic site for activating a C‐H instead of C‐C of C2H6 with a low activation barrier of 0.14 eV, through a concerted mechanism. Remarkably, the selectivity for synthesizing AA reaches 98.7%, achieved under atmospheric pressure of ethane at 0°C. By integrating photocatalysis with thermal catalysis, we introduce a highly selective, environmentally friendly, energy‐efficient synthetic route for AA, starting from ethane, presenting a promising alternative for AA synthesis. This integration of photocatalysis in low‐temperature oxidation demonstrates a new route of selective oxidation of light alkanes.

Highly Selective Photocatalytic Synthesis of Acetic Acid at 0‐25oC

Abstract Acetic acid (AA), a vital compound in chemical production and materials manufacturing, is conventionally synthesized by starting with coal or methane through multiple steps including high‐temperature transformations. Here we present a new synthesis of AA from ethane through photocatalytic selective oxidation of ethane by H2O2 at 0‐25°C. The catalyst designed for this process comprises g‐C3N4 with anchored Pd1 single‐atom sites. In‐situ studies and computational simulation suggest the immobilized Pd1 atom becomes positively charged under photocatalytic condition. Under photoirradiation, the holes on the Pd1 single‐atom of OH‐Pd1Å/g‐C3N4 serves as a catalytic site for activating a C‐H instead of C‐C of C2H6 with a low activation barrier of 0.14 eV, through a concerted mechanism. Remarkably, the selectivity for synthesizing AA reaches 98.7%, achieved under atmospheric pressure of ethane at 0°C. By integrating photocatalysis with thermal catalysis, we introduce a highly selective, environmentally friendly, energy‐efficient synthetic route for AA, starting from ethane, presenting a promising alternative for AA synthesis. This integration of photocatalysis in low‐temperature oxidation demonstrates a new route of selective oxidation of light alkanes.

Investigation on the steam gasification mechanism of different chars using isotopic tracing method

Gasification can provide syn-gas for consequent chemical production from carbon resources. The control of CO2 emission produced from gasification calls for the lower temperature and the more biomass char for the feed compared with traditional gasification, and the mechanism for steam gasification of different chars is more important. The gasification behaviors of four biomass chars and four coal chars are studied. The mechanism is probed using H216O/H218O period step tracing method coupled with various solid-state analyses on char structures. The increment of intermediates with increasing conversion demonstrate other slow step exists during gasification, and the solid state spectra of chars after and before gasification demonstrates that the condensation of poly-aromatic clusters in chars occurs accompanied with gasification. The addition reactions of radicals generated from gasifying agents and unsaturated carbon bonds C = C in chars is the slower step during gasification and enhancing the addition of radicals to unsaturated C = C bonds may be helpful for the higher gasification rate.

Chemical upcycling of polyolefins into liquid refinery feedstock from the circularity and chemical engineering aspects

Three quarters of all plastics produced each year are discarded to landfill after a single use without proper waste management practices, causing a global environmental crisis: waste plastics suffocating our world at enormously large volumes. Discarding plastics into landfill, inefficiently processing them to lower value materials, or incinerating them cause an irreversible loss of the stored energy in plastics. These plastics, however, represent a tremendous resource for the production of chemicals and can be upcycled into high-quality value-added refinery feedstock that could be used to produce virgin polyolefins. In this article, we review pyrolysis and hydrogenolysis based chemical transformations to convert waste polyolefins into liquid hydrocarbons with a special emphasis on life cycle assessment (LCA), reactor technologies, and integration to existing refineries. Several patented technologies are described in detail to shed a light on engineering aspects of the chemical recycling. Liquid products obtained from chemical recycling are examined from the circularity point of view. Feedstock and stream locations in existing refineries and around steam crackers are recommended to feed and/or blend the products obtained from chemical recycling of polyolefins. Challenges, perspectives, and emerging areas of research and engineering are mentioned.

High-efficient microwave-assisted conversion of fructose to 5-hydroxymethylfurfural over rice straw-derived sulfonated porous carbonaceous catalyst

5-Hydroxymethylfurfural (HMF) has emerged as a pivotal platform chemical derived from biomass, attracting considerable attention for its renewable applications. In this study, sulfonated rice straw biochar (RSBC-SA) catalysts were developed and employed for microwave-assisted catalytic conversion of fructose to HMF. The RSBC-SA catalysts, synthesized by pyrolyzing rice straw biomass at different temperatures and subsequent functionalization with sulfonic acid groups, were characterized using X-ray photoelectron spectroscopy (XPS), elemental analysis, temperature programmed desorption (TPD) and Fourier-transform infrared spectroscopy (FT-IR). A comparative analysis of catalytic performance between microwave irradiation and conventional oil bath heating revealed a substantial enhancement in efficiency with the former. Notably, the 700 ℃ pyrolyzed RSBC-SA catalyst demonstrated the highest HMF yield of 92.6 % within just 5 min of reaction time under a microwavehydrothermal condition, surpassing the conventional oil bath heating method. In addition, moderate to high yields of HMF were achieved from different carbohydrates in our developed microwave reaction system, demonstrating significant catalytic activity. This superior catalytic effect under microwave irradiation can be attributed to the responsive dipole polarization of sulfonic acid groups, selective heating of the RSBC carrier via microwave absorption, and synergistic interactions among these factors. Overall, this study highlights the innovative use of agricultural waste and introduces a new method for creating microwave-responsive catalysts with biochar. This strategy enables efficient fructose conversion to HMF, promotes sustainable biomass transformation, and offers value-added uses for agricultural residues in chemical production.

PRELIMINARY CHARACTERIZATION OF THE PHYTOEXTRACTS FROM ACMELLA OLERACEA WITH THERAPEUTIC

The use of plant extracts in dermatocosmetic preparations, instead of chemical synthesis products, is a trend that is becoming more prominent in an effort to meet customer needs and guarantee product quality. In this context, the aim of the work is to present the obtaining and characterization of the extract of Acmella oleracea, by classical or combined liquid-solid extraction methods. Their physical-chemical characterization was based on the determination of the content of polyphenols and flavonoids and their antioxidant activity. The emulsion based on Acmella oleracea extract was preliminarily characterized in terms of stability and homogeneity.

Catalytic Dehydration of Biomass-Derived Feedstocks to Obtain 5-Hydroxymethylfurfural and Furfural

Biomass-produced furanics, furfural and 5-hydroxymethylfurfural (5-HMF), are considered as vital platform chemicals used in the production of active pharmaceutical ingredients (APIs), commodity goods, and fuels. The primary challenge associated with their production pertains to the high cost involved in scaling up to industrial levels. Consequently, it is essential to explore more cost-effective options that yield efficient end products. In this study, the use of Lewis and Brønsted acids such as HCl and AlCl3 enhances the isomerization of glucose through catalytic dehydration into 5-HMF. It was observed that employing moderate reaction conditions increased the yield of 5-HMF to 44.94 % and 50.60 % respectively, with changes in HCl concentration and AlCl3 mass loading. The suitable conditions to achieve the highest yield of 5-HMF were 100 μL of HCl, 0.75 g of AlCl3, reaction temperature 150 °C, and reaction time 4 h. In the second experiment, corncob was converted into furfural in the presence of 20 % H2SO4, in combination with NaCl as a promoter. The optimal conditions under which a yield of 44.77 % was achieved were as follows: 50 mL of 20 % H2SO4, reaction temperature 140 °C, 0.5 g of NaCl, 5 g of corncob, and reaction time 160 min. Furthermore, a proposed reaction mechanism was outlined to elucidate the pathway for the production of the aforementioned platform chemicals.

Exploiting the Thermotolerance of Clostridium Strain M1NH for Efficient Caproic Acid Fermentation from Ethanol and Acetic Acid.

A novel thermotolerant caproic acid-producing bacterial strain, Clostridium M1NH, was successfully isolated from sewage sludge. Ethanol and acetic acid at a molar ratio of 4:1 proved to be the optimal substrates, yielding a maximum caproic acid production of 3.5g/L. Clostridium M1NH exhibited remarkable tolerance to high concentrations of ethanol (up to 5% v/v), acetic acid (up to 5% w/v), and caproic acid (up to 2% w/v). The strain also demonstrated a wide pH tolerance range (pH 5.5-7.5) and an elevated temperature optimum between 35 and 40°C. Phylogenetic analysis based on 16S rRNA gene sequences revealed that Clostridium M1NH shares a 98% similarity with Clostridium luticellarii DSM 29923T. The robustness of strain M1NH and its efficient caproic acid production from low-cost substrates highlight its potential for sustainable bio-based chemical production. The maximum caproic acid yield achieved by Clostridium M1NH was 1.6-fold higher than that reported for C. kluyveri under similar fermentation conditions. This study opens new avenues for valorizing waste streams and advancing a circular economy model in the chemical industry.

Improved Glowworm Swarm Optimization for Parkinson’s Disease Prediction Based on Radial Basis Functions Networks

Parkinson’s disease is caused by a disruption in the chemical products that enables the communication between brain cells. The brain’s dopamine cells are responsible for movement control, adaptability, and fluidity. Parkinson’s motor symptoms manifest when 60–80% of these cells are damaged due to insufficient dopamine. Researchers are working to find a way to identify the non-motor symptoms that manifest early detection in the disease to stop the disease’s progression because it is believed that the disease starts many years before the motor symptoms. This research presents Parkinson’s disease diagnosis based on deep learning. Processes for feature selection and classification encompass the suggested diagnosis technique. The proposed model searches for the best subset of characteristics using the Improved Glowworm Swarm Optimization (IGSO) algorithm. Radial Basis Functions Networks (RBFN) classifiers evaluate the chosen features. The suggested model is tested using datasets from Parkinson’s Handwriting samples and Parkinson’s Speech and voice with various sound recordings. With an accuracy of about 95.78%, the suggested algorithm forecasts Parkinson’s disease using the VoicePD dataset more precisely.

Reinforced Electrons Transfer and Capture in S‐Scheme TiO2@Co(OH)F‐Pt Heterojunction for Excellent Solar Hydrogen Evolution

AbstractTiO2 with the merits of non‐toxicity, high stability, strong redox capability, and low cost, has garnered considerable attention in the fields of renewable energy. However, the practical application is limited by the rapid recombination of photogenerated electron–hole pairs, posing a challenge to enhance electron utilization without compromising catalytic activity. Herein, S‐scheme TiO2@Co(OH)F‐Pt heterojunction through a simple hydrothermal and photo‐deposition method is constructed. The experimental tests and theoretical computation indicate that Co(OH)F possesses a smaller work function and a more negative conduction band (CB) position, significantly accelerating the separation of photogenerated charge carriers. Furthermore, the built‐in electric field, band bending between TiO2 and Co(OH)F, and the electron sink of Pt nanoparticles, facilitate the reduction of protons to hydrogen. The as‐prepared TiO2@Co(OH)F‐Pt exhibits high‐performance solar hydrogen evolution with an evolution rate of 1401 µmol h−1. The apparent quantum yield (AQY) is determined to be 22.8% at a single wavelength of 365 nm. After reacting 12 h for three cycles, no noticeable performance degradation occurs, showing good stability of the catalyst. This work provides a rational strategy for the design of heterojunction photocatalysts for driving the production of new energy and useful chemicals.

Energy‐Efficient Co‐production of Benzoquinone and H2 Using Waste Phenol in a Hybrid Alkali/Acid Flow Cell

AbstractIn both the manufacturing and chemical industries, benzoquinone is a crucial chemical product. A perfect and economical method for making benzoquinone is the electrochemical oxidation of phenol, thanks to the traditional thermal catalytic oxidation of phenol process requires high cost, serious pollution and harsh reaction conditions. Here, a unique heterostructure electrocatalyst on nickel foam (NF) consisting of nickel sulfide and nickel oxide (Ni9S8‐Ni15O16/NF) was produced, and this catalyst exhibited a low overpotential (1.35 V vs. RHE) and prominent selectivity (99 %) for electrochemical phenol oxidation reaction (EOP). Ni9S8‐Ni15O16/NF is beneficial for lowering the reaction energy barrier and boosting reactivity in the EOP process according to density functional theory (DFT) calculations. Additionally, an alkali/acid hybrid flow cell was successfully established by connecting Ni9S8‐Ni15O16/NF and commercial RuIr/Ti in series to catalyze phenol oxidation in an alkaline medium and hydrogen evolution in an acid medium, respectively. A cell voltage of only 0.60 V was applied to produce a current density of 10 mA cm−2. Meanwhile, the system continued to operate at 0.90 V for 12 days, showing remarkable long‐term stability. The unique configuration of the acid‐base hybrid flow cell electrolyzer provides valuable guidance for the efficient and environmentally friendly electrooxidation of phenol to benzoquinone.

Energy-Efficient Co-production of Benzoquinone and H2 Using Waste Phenol in a Hybrid Alkali/Acid Flow Cell.

In both the manufacturing and chemical industries, benzoquinone is a crucial chemical product. A perfect and economical method for making benzoquinone is the electrochemical oxidation of phenol, thanks to the traditional thermal catalytic oxidation of phenol process requires high cost, serious pollution and harsh reaction conditions. Here, a unique heterostructure electrocatalyst on nickel foam (NF) consisting of nickel sulfide and nickel oxide (Ni9S8-Ni15O16/NF) was produced, and this catalyst exhibited a low overpotential (1.35 V vs. RHE) and prominent selectivity (99 %) for electrochemical phenol oxidation reaction (EOP). Ni9S8-Ni15O16/NF is beneficial for lowering the reaction energy barrier and boosting reactivity in the EOP process according to density functional theory (DFT) calculations. Additionally, an alkali/acid hybrid flow cell was successfully established by connecting Ni9S8-Ni15O16/NF and commercial RuIr/Ti in series to catalyze phenol oxidation in an alkaline medium and hydrogen evolution in an acid medium, respectively. A cell voltage of only 0.60 V was applied to produce a current density of 10 mA cm-2. Meanwhile, the system continued to operate at 0.90 V for 12 days, showing remarkable long-term stability. The unique configuration of the acid-base hybrid flow cell electrolyzer provides valuable guidance for the efficient and environmentally friendly electrooxidation of phenol to benzoquinone.