Carbon Production Research Articles

Waste wood tar based porous carbon electrodes for supercapacitors with excellent performances through condensation cross-linking modification

Wood tar is an unavoidable by-product during a slow-pyrolysis process of biomass, which is usually discarded as a waste and results in environment pollution. Recently, wood tar has been used as a starting material for carbon electrodes because of its thermoplasticity and high carbon content. However, wood tar is mainly composed of various light phenolic molecules, which usually leads to a low carbonization yield after carbonization and an inferior electrochemical performance after activation. In this work, in order to improve the carbonization rate and electrochemical performance of these materials, wood tar was first condensed and crosslinked with formaldehyde and urea via a condensation reaction to produce condensed macromolecular resins, which were then carbonized at 550°C and activated with KOH at 800°C to prepare high-performance nitrogen-doped carbon electrodes for supercapacitors. The samples possess high carbonization yield, large specific surface area (3515.1 m2g-1) and moderate nitrogen content (1.11%). The high-performance carbon electrodes fabricated by this method achieves a high capacitance of 437.8Fg-1 (6M KOH electrolyte) at 1A/g-1. The assembled supercapacitor has an energy density of 13.41Whkg-1 at a power density of 124.93Wkg-1. And the capacitance retention was essentially 100% after 10000 cycles at 5Ag-1. The study presents an innovative strategy for the production of porous carbon for supercapacitors using wood tar and improves carbonization yield via condensation cross-linking modification.

The Role of Zooplankton Community Composition in Fecal Pellet Carbon Production in the York River Estuary, Chesapeake Bay

AbstractZooplankton play a key role in the cycling of carbon in aquatic ecosystems, yet their production of carbon-rich fecal pellets, which sink to depth and can fuel benthic community metabolism, is rarely quantified in estuaries. We measured fecal pellet carbon (FPC) production by the whole near-surface mesozooplankton community in the York River sub-estuary of Chesapeake Bay. Zooplankton biomass and taxonomic composition were measured with monthly paired day/night net tows. Live animal experiments were used to quantify FPC production rates of the whole community and dominant individual taxa. Zooplankton biomass increased in surface waters at night (2- to 29-fold) due to diel vertical migration, especially by Acartia spp. copepods. Biomass and diversity were seasonally low in the winter and high in the summer and often dominated by Acartia copepods. Whole community FPC production rates were higher (3- to 65-fold) at night than during the day, with the 0.5–1 mm size class contributing 2–26% to FPC production in the day versus 40–70% at night. An increase in the relative contribution of larger size fractions to total FPC production occurred at night due to diel vertical migration of larger animals into surface waters. Community FPC production was highest in fall due to increased diversity and abundance of larger animals producing larger fecal pellets, and lowest in summer likely due to top-down control of abundant crustacean taxa by gelatinous predators. This study indicates that zooplankton FPC production in estuaries can surpass that in oceanic systems and suggests that fecal pellet export is important in benthic-pelagic coupling in estuaries.

Control of hydrogen concentrations by microbial sulfate reduction in two contrasting anoxic coastal sediments

IntroductionMolecular hydrogen is produced by the fermentation of organic matter and consumed by organisms including hydrogenotrophic methanogens and sulfate reducers in anoxic marine sediment. The thermodynamic feasibility of these metabolisms depends strongly on organic matter reactivity and hydrogen concentrations; low organic matter reactivity and high hydrogen concentrations can inhibit fermentation so when organic matter is poor, fermenters might form syntrophies with methanogens and/or sulfate reducers who alleviate thermodynamic stress by keeping hydrogen concentrations low and tightly controlled. However, it is unclear how these metabolisms effect porewater hydrogen concentrations in natural marine sediments of different organic matter reactivities.MethodsWe measured aqueous concentrations of hydrogen, sulfate, methane, dissolved inorganic carbon, and sulfide with high-depth-resolution and 16S rRNA gene assays in sediment cores with low carbon reactivity in White Oak River (WOR) estuary, North Carolina, and those with high carbon reactivity in Cape Lookout Bight (CLB), North Carolina. We calculated the Gibbs energies of sulfate reduction and hydrogenotrophic methanogenesis.ResultsHydrogen concentrations were significantly higher in the sulfate reduction zone at CLB than WOR (mean: 0.716 vs. 0.437 nM H2) with highly contrasting hydrogen profiles. At WOR, hydrogen was extremely low and invariant (range: 0.41–0.52 nM H2) in the upper 15 cm. Deeper than 15 cm, hydrogen became more variable (range: 0.312–2.56 nM H2) and increased until methane production began at ~30 cm. At CLB, hydrogen was highly variable in the upper 15 cm (range: 0.08–2.18 nM H2). Ratios of inorganic carbon production to sulfate consumption show AOM drives sulfate reduction in WOR while degradation of organics drive sulfate reduction in CLB.DiscussionWe conclude more reactive organic matter increases hydrogen concentrations and their variability in anoxic marine sediments. In our AOM-dominated site, WOR, sulfate reducers have tight control on hydrogen via consortia with fermenters which leads to the lower observed variance due to interspecies hydrogen transfer. After sulfate depletion, hydrogen accumulates and becomes variable, supporting methanogenesis. This suggests that CLB’s more reactive organic matter allows fermentation to occur without tight metabolic coupling of fermenters to sulfate reducers, resulting in high and variable porewater hydrogen concentrations that prevent AOM from occurring through reverse hydrogenotrophic methanogenesis.

Thermodynamic study on the phase assemblage of MPC exposed to natural and accelerated carbonation conditions

AbstractMagnesium phosphate cement (MPC), which belongs to chemically bonded phosphate ceramics, is commonly applied as a repair material and waste stabilization/solidifications. However, studies on the influence of CO2 on the phase assemblages in MPC are limited. A thermodynamic simulation approach is employed to explore the influence of CO2 on the equilibrium phase assemblage of MPC. The mechanisms of natural and enforced carbonation of MPC have been investigated in this work. The results disclose that Mg carbonates are less likely to precipitate in magnesium ammonium phosphate cement (MAPC) cured under CO2, while MgCO3·3H2O is the only carbonation product of magnesium potassium phosphate cement (MKPC). The carbonation resistance of MAPC is better than that of MKPC. The increase of activity of magnesia employed in MPC obviously enhances the formation of brucite and slightly promotes the carbonation of MPC.

Distinct responses of diatom- and flagellate-dominated Antarctic phytoplankton communities to altered iron and light supply

Primary production in the Southern Ocean is strongly influenced by the availability of light and iron (Fe). To examine the response of two distinct natural Antarctic phytoplankton communities (diatom vs. flagellates) to increasing light and Fe availability, we conducted two shipboard incubation experiments during late summer and exposed each community to increasing light intensities (30, 80, and 150 µmol photons m−2 s−1) with or without Fe amendment. Our results show clearly that both communities were Fe-limited since Fe addition resulted in higher particulate organic carbon (POC) production rates. The magnitude of the Fe-dependent increase in POC production, however, varied between the two stations being higher in the diatom-dominated community relative to the flagellate-dominated community. This differential response to increasing Fe supply could be attributed to the higher Fe requirement of the flagellate-dominated assemblage relative to the diatom-dominated assemblage. Irrespective of Fe availability, light also strongly stimulated the POC production of both communities between low and medium light supply (30 versus 80 µmol photons m−2 s−1), indicating that both assemblages were light-limited in situ. However, since POC production of both communities did not increase further at the highest light intensity (150 µmol photons m−2 s−1) even under high Fe supply, this suggests that light supply was saturated or that other conditions must be fulfilled (e.g., availability of trace metals other than Fe) in order for the communities to benefit from the higher light and Fe conditions.

Preparation of aragonite from calcium carbonate via wet carbonation to improve properties of steel slag building materials

Smelting in steel mills emitted large amounts of CO2 and produced the waste product steel slag (SS). Therefore, the use of SS to fix CO2 and produce value-added products could treat waste with waste and promote the effective use of resources. In this study, aragonite-type calcium carbonate was prepared by wet carbonation of SS, and the aragonite-rich SS (ASS) was pressed and moulded in the raw material of SS for semi-dry carbonation to obtain SS products. Through a series of experiments, the optimal conditions for the modulation and the formation mechanism of aragonite whiskers were investigated, and the effects of aragonite as a crystal seed on the properties and the degree of carbonation of SS products were also explored. In this experiment, the carbonation products were characterised microscopically by XRD, TGA, FT-IR and SEM, and the strength was tested by press machine. The results showed that aragonite phase was produced by wet carbonation of SS suspension containing 0.1M/L MgCl2 at 120 °C for 2h. The compressive strength, flexural strength, and secondary carbonation degree of the prepared SS products were increased when 5% ASS was added.

Sugarcane bagasse and iron ore tailings thermochemical conversion towards sustainable iron recovery with biogenic carbon and hydrogen production

The recovery of valuable chemical elements from industrial waste is essential for production processes' economic and environmental sustainability. The interaction between the iron ore tailings and sugarcane bagasse, both wastes, has the potential to provide a secondary iron source for future iron and steelmaking processes. This study evaluated the use of volatiles from sugarcane bagasse (SCB) and iron ore tailings (IOT) to the synergistic promotion of carbon deposition, H2 production and conversion of weak magnetic iron oxides in strong magnetic iron phases. The experiments were carried out at 400, 600, 800, and 1000 ºC with different SCB/IOT ratios under an N2 atmosphere. In all tests, SCB and IOT were heated simultaneously in separate beds to prevent direct contact between the materials. The combination of 600 ºC and higher SCB/IOT ratio resulted in a product with 96.7% magnetite, 98% magnetic fraction recovery, and 3.5% deposited carbon. The use of lower SCB/IOT ratio provided an increase in H2 production. Regardless of the mass ratio, heating the IOT and SCB simultaneously up to 1000 ºC led to significant mineralogical transformations, reaching reduced phases such as wüstite, fayalite and metallic iron, which impaired magnetic separation efficiency. The results indicate an alternative for recovering iron from IOT using biomass waste as a renewable reducing agent for the steel industry.

Machine Learning-Based Prediction of the Adsorption Characteristics of Biochar from Waste Wood by Chemical Activation.

This study employs machine learning models to predict the adsorption characteristics of biochar-activated carbon derived from waste wood. Activated carbon is a high-performance adsorbent utilized in various fields such as air purification, water treatment, energy production, and storage. However, its characteristics vary depending on the activation conditions or raw materials, making explaining or predicting them challenging using physicochemical or mathematical methods. Therefore, using machine learning techniques to determine the adsorption characteristics of activated carbon in advance will provide economic and time benefits for activated carbon production. Datasets, consisting of 108 points, were used to predict the adsorption characteristics of biochar-activated carbon derived from waste wood. The input variables were the activation conditions, and the iodine number of activated carbon was used as the output variable. The datasets were randomly split into 75% for training and 25% for model validation and normalized by the min-max function. Four models, including artificial neural networks, random forests, extreme gradient boosting, and support vector machines, were used to predict the adsorption properties of biochar-activated carbon. After optimization, the artificial neural network model was identified as the best model, with the highest coefficient determination (0.96) and the lowest mean squared error (0.004017). As a result of the SHAP analysis, activation time was the most crucial variable influencing the adsorption properties. The machine learning model precisely predicts the adsorption characteristics of biochar-activated carbon and can optimize the activated carbon production process.

Effect of CO2 curing on mechanical and physical properties of the recycled aggregates containing silica fume

CO2 curing is a promising method for enhancing the properties of the recycled concrete aggregates (RCAs) due to its economic and environmental benefits. However, the knowledge about its effectiveness in improving the properties of aggregates derived from blended supplementary cementitious materials (SCMs) remains limited. This study explores the impact of CO2 curing on the mechanical and physical properties, mineralogical composition, and microstructural changes of recycled aggregates incorporating varying amounts of silica fume (SF). The results showed that upon the incorporation with 5wt% SF, CO2 curing increased the compressive strength of the aggregate samples by 17.9%. The microhardness improved from 50 to 56 HV with the addition of 10wt% SF. Moreover, CO2 curing modified the physical characteristics of the samples regardless of SF content. However, it caused mechanical degradation in samples containing 20wt% SF, at both marco- and micro-scale. X-ray diffraction (XRD) and thermogravimetric analysis (TGA) revealed that higher SF dosages led to the formation of poorly crystallised CaCO3 during CO2 curing. Additionally, Low-field 1H nuclear magnetic resonance (LF-NMR), N2 adsorption/desorption, scanning electron microscopy (SEM), and thermodynamic models showed that the carbonation products enlarged the capillary pores, and reduced the solid volume of the hydration products. Those findings underscore the importance of calcium hydroxide in protecting against mechanical degradation in SF-blended recycled aggregates during CO2 curing. This study provides an insight of the carbonation of SF-blended composites, potentially accelerating the application of CO2 curing on RCAs.

Are Governmental Policies an Effective Way to Reduce Agricultural Carbon Emissions? An Empirical Study of Shandong in Main Grain Producing Areas of China

In the context of global and national carbon reduction targets, agricultural carbon emissions have become a critical focus. As global food demand increases, numerous agricultural policies have been implemented. Faced with limited policy resources, evaluating the impact of these policies on agricultural carbon emissions and production is essential. This study examined the relationship between food production and agricultural carbon emissions during the stage of agricultural development in Shandong Province, one of China’s major grain-producing regions, using the decoupling model. Additionally, the coupled coordination model was employed to assess the specific influence of agricultural policy clusters on this transformation. The results indicate that Shandong is transitioning from high-input, extensive farming to green, low-carbon, modern agriculture, with most cities shifting from strong negative decoupling to strong decoupling. Over time, the role of agricultural policies in driving this shift has grown more significant. Future policymaking should prioritize the overall quality of agricultural producers and maintain a continuous focus on sustainable, green development. Ensuring that policy directions align with evolving stages of agricultural development and adjusting them in real-time will be crucial.

Natural Kapok fiber-derived two-dimensional carbonized sheets as sustainable electrode material

Natural biomass-derived carbon nanostructures have attracted research interest because of their unique surface and electrochemical properties. The present study embodied the carbonized micro-nano sheets derived from the low-cost natural source Kapok silk fiber. The material was obtained via a facile thermal pyrolysis process. Diffraction analysis showed a broad graphene structure-like peak, indicating the formation of graphene-like carbon nanosheets. Field emission scanning electron microscope (FESEM) and transmission electron microscopic (TEM) images confirmed the presence of fragmented carbon sheets, some of which were folded to form a tube-like structure. Raman study showed the presence of D and G band with the Id/Ig ratio of 0.96 which indicated the formation of few-layered carbon nanosheets. Furthermore, the electrochemical performance was evaluated for lithium-ion battery as well as supercapacitor. A specific capacity of 465 mAh.g-1 at 0.1 C rate for Li-ion battery and a specific capacitance of 473.61 F.g-1 for supercapacitor have been obtained with the capacitance retention of 95 %. This study provides insights into a strategy for the sustainable production and utilization of natural fiber-based carbon in energy storage systems.

Design of C2S-CS low-calcium system for synergistic improvement of CO2 sequestration capacity and mechanical properties

Low-calcium minerals exhibit significant potential as energy-efficient binder clinker materials, characterized by reduced emissions and enhanced carbon sequestration through accelerated carbonation curing. However, traditional low-calcium binders typically utilize one or two minerals in a straightforward compound form as clinker, resulting in elevated costs, excessive resource consumption, and suboptimal performance. This study developed a novel C2S-CS low-calcium system that integrated γ-C2S, β-C2S, and CS in specific proportions based on their characteristics, utilizing Simplex-centroid designs. Contour maps achieved to assess relationship between performance and mineral composition, while interaction mechanisms were investigated through carbonation products and reaction heat analysis. Furthermore, optimum proportion range of C2S-CS system can be synthesized efficiently and environmentally from solid waste wollastonite tailings in a single step. The results demonstrated that the designed system achieved synergistic improvements in CO2 sequestration capacity and mechanical properties. After 24 h of carbonation curing, it attained a compressive strength of 129 MPa, sequestered 217 kg/t CO2, and exhibited satisfactory durability. This study provides valuable insights for the practical production of low-calcium binders and reveals opportunities for developing sustainable building materials for eco-friendly construction.

Techno-economic assessment of modified Fischer-Tropsch synthesis process for direct CO2 conversion into jet fuel

Direct use of CO2 through modified Fischer-Tropsch synthesis (FTS) process presents a viable approach for the production of carbon–neutral jet fuel. However, achieving high performance for the CO2-FTS process remains a significant challenge. Current technology can only achieve low CO2 conversion and low jet fuel yield using tailored catalysts, which hinders the commercial deployment of direct CO2-FTS process. This paper presents a techno-economic assessment (TEA) of jet fuel production via CO2-FTS process at commercial-scale. Two ex-situ water removal configurations: (a) multi-stage CO2-FTS process and (b) CO2-FTS with tail gas recycle process were conducted to assess their potential for performance improvement. Process performance was evaluated using a model developed in Aspen Plus® linking with Aspen Custom Modeller® (ACM), while economic evaluation was carried out in Aspen Process Economic Analyzer®. The CO2-FTS model was based on first principles and modified Anderson-Schulz-Flory (ASF) distribution. Results indicated that both ex-situ water removal configurations can significantly improve the process performance. CO2-FTS process with 90% tail gas recycle has the best performance for both technical and economic analysis. The process achieved 85.8% CO2 conversion and 35.6% jet fuel yield with the lowest energy demand of 4.57 MWh per tonne of produced jet fuel. Moreover, it boasts the lowest minimum selling price (MSP) of jet fuel at US$2.6/kg despite incurring the second-highest capital expenditure cost of M$ 451.3. A comparison of the two ex-situ water removal configurations at 61.9% and 76.5% CO2 conversion, suggests that both processes exhibit comparable technical performances, yet the recycling of tail gas holds the potential to reduce economic costs. Consequently, this study will inspire researchers on process improvement and cost reduction of the commercial-scale CO2-FTS jet fuel production.

Air‐Pyrolysis Precision Synthesis of Functional Porous Carbon Materials

AbstractCarbon materials play a pivo tal role across various advanced applications, yet their synthesis traditionally necessitates inert atmospheres to avert oxidation at high temperatures, thus inflating production costs and resource utilization. Achieving precision synthesis of functional porous carbon materials via air‐pyrolysis remains a formidable challenge. Herein, a streamlined, one‐step lava‐like carbonization approach is introduced enabling the fabrication of porous carbons boasting tailored morphologies (0‐3D), elevated specific surface areas (540.7–1047.6 m2g⁻¹), heteroatom doping, and commendable carbon yields (20‐39.1%) through direct pyrolysis within an air environment. Leveraging recyclable boric acid as a reaction medium, a lava‐like flowing protective barrier above 170 °C is engendered that spontaneously creates an oxygen‐free‐like milieu devoid of high pressure or intricate procedures. This boron‐containing lava serves dually as a template and chemical activator, facilitating pore formation and catalyzing porous carbon production. Notably, the method accommodates a spectrum of carbon sources, encompassing sugars, proteins, graphene oxide, and their metal mixtures. The resultant morphologically customizable carbons exhibit excellent performance in areas as diverse as microwave absorption and electrocatalysis. This work pioneers a novel pathway for large‐scale precision synthesis of high‐quality carbon materials via air‐pyrolysis under mild conditions.

Mechanisms of efflorescence of alkali-activated slag

Efflorescence presents not only as a cosmetic concern but also as a structural issue, which impacts the performance of alkali-activated materials (AAMs). In this study, the mechanisms of efflorescence of alkali-activated slag (AAS) pastes are investigated. First, the efflorescence of AAS pastes with different alkali dosages (3 %, 5 % and 7 %), activator types (sodium hydroxide (NH) and sodium silicate (NS)), exposure atmospheres (ambient, N2 and 0.2 vol% CO2), and relative humidities (40 %, 60 % and 80 %) was observed. Subsequently, leaching tests were performed and the impacts of efflorescence on AAS pastes at different heights were studied. It was found that a lower relative humidity facilitated more rapid and severe efflorescence. The positioning of efflorescence products was dependent on the porosity of the matrix. Compared to NH pastes, NS pastes subjected to semi-contact water conditions were more vulnerable to cracking problems, which turned out to be exacerbated by the formation of efflorescence products. A new method to quantify efflorescence was developed and it corresponded well with both efflorescence observations and leaching experiments. Furthermore, a competitive reaction between Ca and Na in the presence of carbonate ions was identified. CaCO3, a representative product of natural carbonation, was rarely found in the regions where efflorescence products (sodium carbonate) formed. Regarding compressive strength, NS pastes were more adversely affected by efflorescence than NH pastes.

Study on properties and CO2 emission of self-pulverizing calcium sulfoaluminate (SPCSA) after carbonization curing

The extensive use of Portland cement (OPC) has resulted in a steady rise in CO2 emissions from the construction industry, posing a significant climate threat. While adopting low-carbon cement enriched with belite minerals holds promise for substantial CO2 emission reduction in the cement industry, the limited early hydration activity of C2S constrains its engineering applications. Carbon capture, storage, and utilization (CCUS) technology, capable of rapidly developing the strength of C2S, opens up a new avenue for utilizing low-carbon cement. This study evaluated the properties of self-powdering calcium sulfoaluminate (SPCSA) cements with different C2S contents, and the carbon emissions during production and application were analyzed. The samples' carbonation area, compressive strength, and capillary water absorption properties were tested. The carbonation products and pore structures were also characterized using XRD, TGA, SEM, and Low-NMR. The results show that when the molar ratio of C4A3S̅ to C2S is 1:12 (S̅12), the compressive strength and CO2 sequestration of SPCSA are 69.78 MPa and 0.15 g/g, respectively. When CCUS technology is adopted, the CO2 emission during the production and application of SPCSA is 585.78 kg/t, much lower than that of OPC of 878.28 kg/t. This is significant as a reference for realizing carbon neutrality in the cement industry.

A Carbon Capture and Utilization Process for the Production of Solid Carbon Materials from Atmospheric CO2 - Part 1: Process Performance.

The successful operation of a process that converts atmospheric CO2 into solid carbon products is presented as an alternative to fossil based solid carbon production. In a first step, CO2 is removed from the atmosphere by a direct air capture (DAC) unit. The gas is then mixed with hydrogen and enters a methanation unit. Depending on the operation conditions, gas mixtures consisting of mainly methane with either H2 or CO2 as side-component are obtained. After precipitating the water formed during the methanation step, the remaining gas mixture is fed into a bubble column reactor filled with liquid tin. During the rise of the gas bubbles, methane is thermally split up into hydrogen and solid carbon. The latter is continuously removed from the liquid metal surface as a fine powder by pneumatic conveying. This article is the first of two articles, focusing on the performance of the methanation and methane pyrolysis steps. The experimental results are complemented by thermodynamic analyses and reaction modelling. A detailed analysis of the solid carbon product of the process is presented in the second part.

From Green to Black Gold: Highly Microporous Carbons from Pistachio Shells by a Controlled Physical Activation Process.

Highly microporous carbons with BET surface areas of up to ca. 3300 m2 g-1 and pore volumes of up to 1.6 cm3 g-1 have been successfully synthesized from pistachio shells, a waste whose generation is growing on account of the nutritive value of pistachios and the resilience of this crop to climate change. Such a high pore development has been achieved by a simple and benign CO2 physical activation process assisted by a custom pre-treatment of the biomass. Herein, different approaches have been explored for the transformation into carbon materials with diverse microstructures, mineral matter content and particle size/morphology, tuning therebytheir reactivities towards CO2 and diffusion kinetics and, in this way,pore development. In particular, the most efficient route for the production of highly microporous carbonsinvolves a hydrothermal carbonization process which increases the degree of aromatization and effectively removes the mineral matter, enhancing thereby the efficiency of both carbon production and porosity generation. By increasing the activation temperature, substantial shortening of the operation time can be achieved without compromising pore development. This work provides new integral strategies towards the production of biomass-based, CO2-activated carbons with a focus on optimizing pore structure, minimizing energy consumption and maximizing product yield.

Wintertime productivity and carbon export potential across the Agulhas Current system

The Agulhas Current plays a major role in heat and salt exchange between the Indian and Atlantic Oceans, yet little is known of its influence on ocean fertility. To investigate carbon production and export potential in the Agulhas Current system, we measured net primary production (NPP), nitrate and ammonium uptake, N2 fixation, and nitrification along a transect of the current and adjacent subtropical subgyre (33.4°S–35.7°S) in winter when nutrient supply, and thus productivity, should be highest. Phytoplankton biomass was lowest in the current core, increasing into the subgyre as surface nitrate declined, and was dominated by nanoplankton (2.7–10 μm; 62 ± 5.1% of total biomass). NPP and nitrate uptake were generally high across the transect and increased from the current core into the subgyre; the rates were dominated by picoplankton (<2.7 μm; 53–93%) in the current core and nanoplankton elsewhere (63–69%). On average, euphotic zone nitrification supplied 7.6 ± 6.4% of the nitrate consumed by phytoplankton and N2 fixation was also low (2.1 ± 1.3% of new production); we thus consider nitrate uptake a reasonable proxy for new production, at least in winter. Nitrate uptake was highest at the southern edge of the current core, consistent with current-associated (sub)mesoscale mixing enhancing the upward nutrient supply. The fraction of NPP available for export (i.e., the f-ratio) was high across the transect, ranging from 0.44 to 0.69. Our data thus indicate that both total and new production are elevated across the Agulhas Current system in winter and suggest that the (sub)mesoscale dynamics associated with the current system may enhance carbon production and export in the otherwise oligotrophic southwest Indian Ocean.

Synergetic effect of iron and tungsten on molybdenum‐doped HZSM‐5 zeolite in catalytic methane dehydroaromatization

AbstractMethane dehydroaromatization is a viable route for production of carbon and valuable petrochemicals. Unlike Fischer–Tropsch and methanol synthesis processes which have been scaled up to commercial level, development of methane dehydroaromatization to commercial level has been hampered by various challenges. In this work, a 5.4 wt. % trimetallic (Fe‐W‐Mo/HZSM‐5) catalyst has been synthesized, characterized, and applied in catalytic methane dehydroaromatization reaction. A gas chromatograph was used to analyze both liquid and gaseous products from the reactor. Based on 0.0013 moles of reacted methane after 240 min time on stream at 750, GHSV 960 mlg‐1cath‐1, and atmospheric pressure, a 5.4% Mo/HZSM‐5 catalyst recorded 7.9% methane conversion, 10.6% C2 hydrocarbon selectivity, 51.8% benzene selectivity, 9.8% toluene selectivity and 27.8% coke selectivity. Doping Mo/HZSM‐5 with Fe reduced methane conversion by 4.0%, increased C2 hydrocarbon selectivity by 1.7%, reduced benzene selectivity by 6.2% and increased toluene and coke selectivity by 1.8% and 2.8% respectively. Doping Mo/HZSM‐5 with W increased methane conversion by 7.3%, reduced C2 hydrocarbon selectivity by 2.1%, reduced benzene selectivity by 7.6% and increased toluene and coke selectivity by 0.3% and 9.4% respectively. When iron and tungsten were loaded onto Mo/HZSM‐5, catalytic activity of the tri‐metallic catalyst in methane conversion reduced by 2.0%, C2 hydrocarbon selectivity increased by 2.7%, benzene selectivity reduced by 3.1%, toluene selectivity reduced by 3.7%, and coke selectivity increased by 4.1%. Therefore, this present work demonstrates that metal synergy in a tri‐metallic catalyst plays a role in methane conversion and selectivity towards useful hydrocarbons.