Abstract
Biogas has been widely regarded as a promising source of renewable energy. Recently, the direct conversion of biogas over heterogeneous catalysts for the simultaneous production of syngas and carbon nanotubes exhibits a high potential for full utilization of biogas with great benefits. Involving the combined dry reforming of methane and catalytic decomposition of methane, the efficiency of process is strongly depended on the catalyst activity/stability, mainly caused by carbon deposition. In this study, Ni–Mo catalyst is engineered to provide a life-long performance and perform high activity in the combined process. The surface modification of catalysts by a controlled carburization pretreatment is proposed for the first time to produce a carbide catalyst along with improving the catalyst stability as well as the reactivity for direct conversion of biogas. The performance of as-prepared carbide catalysts is investigated with comparison to the oxide and metallic ones. As a result, the Ni–Mo2C catalyst exhibited superior activity and stability over its counterparts, even though the condensed nanocarbon was largely grown and covered on the surface. In addition, up to 82% of CH4 conversion and 93% of CO2 conversion could remain almost constant at 800 °C throughout the entire test period of 3 h under a high flowrate inlet stream of pure biogas at 48,000 cm3 g−1 h−1. The XPS spectra of catalysts confirmed that the presence of Mo2C species on the catalyst surface could promote the stability and reactivity of the catalyst, resulting in higher productivity of carbon nanotubes over a longer time.
Similar content being viewed by others
Explore related subjects
Find the latest articles, discoveries, and news in related topics.Introduction
The drastic increase in the world’s population and the radical industrial transformation are considered the major reason for exponential growth in total energy demand. Indeed, a gigantic portion of global energy supplies is dominated by fossil fuel combustion, which is expected to be one of the crucial sources of CO2 emissions and leads to environmental issues. In the meantime, hydrogen is getting further recognition around the globe as an energy carrier and as a potential fuel that promises to reduce the consumption of these conventional fossil fuels. Moreover, it offers pollution-free solutions for the sustainable development of fuel cell technology1,2,3. At present, there are numerous feasible pathways that have been proposed for hydrogen production such as steam reforming, partial oxidation, coal gasification, hydrocarbon pyrolysis, and so on4,5,6,7. Apart from the traditional renewable energy productions, dry reforming of methane (DRM) in Eq. (1) is being increasingly studied and stands as the most attractive way for utilizing biogas and producing syngas mixtures (H2 + CO). This is because it can provide syngas with H2/CO ratio close to 1.0, particularly on account of the abatement of two of the primary substantial greenhouse gases8,9.
Active metals from groups like Ru, Rh, Ir, Pd, and Pt, have been found to perform superior reactivity and stable performances with high resistance to coke formation in DRM. On the one hand, the uneconomical cost of these precious metal catalysts and their restricted availability make them unsuitable for commercial upscaling applications10. Supported Ni-based catalysts, on the other, are much preferably suggested due to their affordable price and comparable activity to those of noble metals11,12,13,14. Nevertheless, the deactivating of the active phase affected by carbon poisoning taking place mainly in the reforming process is the primary intensive drawback for such reforming catalysts15. In this regard, most studies have been conducted with a focus on the way to prevent these unwanted carbonaceous deposits on the catalyst surface16,17,18,19. In our previous work20, we successfully proposed an effective approach to overcome this momentous concern by transforming the deposited carbon into valuable nanomaterials such as carbon nanotubes (CNTs), which can be simultaneously promoted alongside the catalytic decomposition of methane (CDM) reaction, as shown in Eq. (2). The results demonstrated that the use of bimetallic Ni–Mo/MgO catalysts showed catalytically outstanding performance at 800 °C in the conversion of biogas into H2-rich syngas and multi-walled carbon nanotubes (MWCNTs) via the integrative processes between dry reforming of methane and catalytic decomposition of methane. Even so, in the long-term practical point of view, a great drop in CH4 and CO2 reaction rates seemed to become clear. This degradation behavior can be explained by catalyst deactivation while performing in a 20 h run. Hence, there is a desire to further develop a catalyst that is low-cost, well-qualified, and allowed to withstand for an extended duration.
A short while ago, the arisen temptation in the interstitial compounds displayed in transition metal carbides (TMCs) has promisingly driven research as an alternative material for this purpose because they can act similarly or even greatly better than that of platinum in a variety of reactions including the reforming of hydrocarbon species, hydrogenation, desulfurization, isomerization, and biomass conversion21,22,23,24,25. These early classes of catalysts can also possess non or less amount of coking compared with traditional reduced Ni catalysts, which suffered from these serious problems26. As pointed out in the aforementioned existing literature reviews, the carbides of molybdenum and tungsten (Mo2C and WC) are the popular choices among all the available TMC materials applied for DRM reaction. Claridge et al.27 illustrated that the highly stable activity of more than 72 h operation could be achieved over β-Mo2C at elevated pressures (8 bar). However, carbides were found to deactivate immediately corresponding to the transformation of Mo2C to an inactive MoO2 phase via its bulk oxidation with CO2 (Eq. 3) at atmospheric pressure, as observed by York et al.28. The physicochemical properties of carbide and oxide phases may change alternatively based on whether it is in the presence of CO2 or CH4. This redox mechanism is so-called the “oxidation-carburization” cycle29,30. As a result, it is worth noting that at ambient pressure the reaction of CO2 with monometallic carbides was considerably preferred and resulted in losing their activity by the oxidation of carbide catalysts. Such kind of issue can be solved by introducing nickel (Ni) to carbides because it is widespread to facilitate the dissociation of CH4 (Eq. 4) in the carbide-cycled system. Thus, it is possible to promote the regenerated form of Mo2C, which is responsible for maintaining the catalyst stability29,31,32,33,34,35,36.
In this study, Ni–Mo/MgO catalyst is engineered to provide a lifelong performance in dry reforming of methane and catalytic decomposition of methane reactions, as well as yielding syngas with high purity and well-structured carbon nanotubes by emphasizing studying on catalyst pretreatment process. The impact of surface modification of catalysts controlled under different gas environments of O2, H2, and CH4 (denoted as oxide, metallic, and carbide) was examined, and the long-term stability of the as-prepared catalysts was tested. The catalysts acquired before and after the reaction with all the gases and solid products were analyzed thoroughly to better understand the relationship between the characteristics of catalysts and their catalytic performance.
Experimental
Synthesis of catalyst
The Ni–Mo catalyst supported on magnesium oxide (MgO) was synthesized by impregnating 7 g of dried MgO nano-powder (Merck, 98%) with a proper matching amount of Ni(NO3)2·6H2O and (NH4)6Mo7·4H2O blended aqueous solution (Sigma-Aldrich, 99.99% trace metals basis) using wetness impregnation method. This procedure gives the nominal Ni and Mo metal loadings of 30wt% (Ni/Mo ratio = 1/1 w/w)20. Then, the impregnated solvent was evaporated by a hotplate at 80 °C, attempting to remove excess de-ionized water (DI) from the sample. Lastly, the obtained material was calcined in the exposure of air in a muffle furnace at 500 °C for 3 h with a ramp rate of 10 °C/min.
Pretreatment of catalyst
All the catalytic tests were carried out in a customary fixed-bed reactor at ambient pressure. In the beginning, 0.5 g of as-prepared catalysts filled on a 100 mm long quartz boat were slid into the center of a horizontal 26 mm i.d. tubular quartz reactor (see Fig. 1). A detailed description of the reactor has been previously stated in several works in the literatures20,37. For the subsequent proceeding, the oxide precursor (NiMoOx) was treated under a variant of activating agents (O2, H2, and CH4) at a feed flow rate of 100 ml/min to achieve the target catalysts. In the meantime, the system was heated from room temperature to 700 °C at a rate of 5 °C/min and then kept at this temperature for 1 h. The resultant Ni–Mo/MgO bimetallic catalysts with a series of various active phases (oxide, metallic, and carbide) were understandably marked hereinafter as NM-O, NM-R, and NM-C, respectively.
Production process of syngas and CNTs
Prior to the evaluation, the catalyst was pretreated and subsequently heated to 800 °C in a flowing of 60% CH4 and 40% CO2, which was allowed to continuously pass through along the reactor at a feed rate of 400 ml/min (GHSV = 48,000 cm3 g−1 h−1). The outlet gas steam was sampled regularly at 10 min intervals and analyzed by gas chromatography (TCD, Shimadzu, GC-2014). Finally, after completing a run, the reactor was cooled down in the atmosphere with an inert He flow of 50 ml/min, and in cases where solid carbon produced on the catalyst surface was later collected and preserved for characterization. The reaction time for the activity test was set for 3 h, while the stability was extended to 24 h.
Evaluation of catalyst activity and stability
The catalytic evaluation of catalysts for the combined reaction of dry reforming of methane and catalytic decomposition of methane, along with the quantitative numerical product analysis was calculated according to the following equation:
where mproduct, mcatalyst, and mcarbon, feed represent a mass of solid product, initial weight of the fresh catalyst, and total carbon in the feed stream (based on methane), respectively.
Characterization
The N2 adsorption–desorption isotherms were used to measure the specific surface area and pore size distribution of catalysts, using the BET and BJH methods in a Micromeritics TriStar II 3020 analyzer. The chemical composition in the prepared catalysts was confirmed by inductively coupled plasma optical emission spectroscopy (ICP-OES, PerkinElmer) equipment using a Avio™ 550 Max spectrometer. Prior to that, each material was completely mineralized using mixed acids of HNO3 and HCl (1:1 v/v). The surface chemistry of the catalyst samples was studied via Mo 3d spectrum measured by X-ray photoelectron spectroscopy (XPS) investigations using a Kratos Axis ultra (DLD) equipped with an Al Kα X-ray source. To determine the crystalline phases within the catalyst structure, the X-ray diffraction (XRD) analysis was carried out on a Bruker D2 Phaser X-ray powder diffractometer, from 10° to 80° (2θ). Moreover, the SEM and TEM micrographs recorded in the field-emission scanning (FE-SEM, JEOL, JSM-7610F) and high-resolution transmission electron microscope (HR-TEM, JEOL, JEM-2100 Plus, Japan) analyses allow the identification of morphology and internal structure on the surface of materials. In the case of carbon products generated during the reaction, the purity and quality of CNTs were further characterized. The purity of synthesized CNTs was calculated from TGA curves. The experiment was done with a Mettler Toledo TGA/DSC 3 + LF instrument. Approximately 3 mg of each sample was heated from room temperature to 900 °C with a heating rate of 10 °C/min under O2 flow of 50 ml/min. Lastly, Raman spectrophotometer (PerkinElmer® Spectrum™ GX) was used to quantify the crystallinity and graphitization degree of structure of nanomaterials.
Results and discussion
Physicochemical properties of the catalysts
The textural properties and chemical compositions of the catalysts were characterized by BET and ICP analyses. The N2 adsorption–desorption isotherms of the catalysts under pretreated conditions are reported in Fig. 2a. It is shown that the isotherms of all samples are presented in type IV with a large portion of N2 gas adsorbed at high relative pressure (P/P0), ascribed to the existence of mesopores accompanied by macroporous structure. These hysteresis characteristics are also classified as a H3-type hysteresis loop, which is often ascribed to porous materials made up of slit-shaped with non-rigid aggregates of plate-like pores, according to IUPAC classification38. It is suggested that materials that give rise to pore diameters less than 2.0 nm are referred to the micro-structured pores, while the occurrence of pores having a size in the range of 2.0–50.0 nm is associated with mesopore structure. Figure 2b displays the pore size distribution of various catalyst samples obtained by the BJH method. This is confirmed by the curves that all catalysts show two main distribution regions with the predominant and highly strong peak at the average pore diameter ranging between 18.9 and 34.4 nm, which is implied that the majority of porosity in the catalysts is in the characteristic range of mesoporous materials. Textural properties of each catalyst, i.e., the specific surface area (SBET), the volume of mesopores (Vmeso), total pore volume (Vtotal), and mean pore diameter (Dpore) are given in Table 1. In comparison with a catalyst in the reduced form (NM-R), the oxide of Ni–Mo/MgO catalyst (NM-O) provides a higher BET specific surface area of 54.6 m2/g. When those oxides were reduced into metallic Ni phases with H2 flow, their surface area and pore volume declined to 47.9 m2/g and 0.537 cm3/g. This indicated that there was a blockage of some pores in the NM-R sample. On the contrary, a significant improvement in BET surface area and pore volume was observed for the NM-C catalyst (49.8 m2/g and 0.644 cm3/g), which consequently may give a positive effect on the catalyst performance by improving the catalytic activity of the catalysts39,40. Corresponding to the ICP results, it is certified that the actual weight percentages of Ni and Mo metal are almost equivalent to the nominal value ones.
The XRD diffractograms of the catalysts prepared after calcination and pretreatment under varied conditions are shown in Fig. 3. As for all the catalyst samples, it can be found that several diffraction peaks at 2θ = 37.2°, 43.2°, 62.3°, 74.6°, and 78.6°, are predominantly ascribable to (111), (200), (220), (311), and (222) reflection planes of magnesium oxide support (JCPDS 45-0946) with high crystalline, which is proved by a sharp peak of XRD results. In case of treating catalyst in a flow of O2, the XRD signal exhibits noticeably similar to that obtained from the fresh calcined catalyst at 500 °C for 3 h. On the other hand, it was noticed that two reflection peaks assigned to metallic phases of Ni (JCPDS 03-1051) were clearly detected at 2θ values of 44.4° and 51.5° as to NM-C and NM-R. No other obvious characteristic peaks of their metal oxides were observed in both cases. These results evidence that the conversion of Ni2+ into active Ni0 metals could be properly reduced by use of H2 and CH4 activating gases. The low intensity of the diffraction features might be contributed to a high dispersion ability of Ni in the support41. In addition, through the carbothermal treatment of MoOx in a 20 vol% CH4/H2 gas mixture, the formation of Mo2C would appear. However, as elucidated in Fig. 3b, the diffraction peaks of Mo2C species cannot be identified in the carbide catalyst, perhaps owing to the small loading of molybdenum and/or a highly dispersed state of carbide phase42.
X-ray photoelectron spectroscopy (XPS) measurement was employed in essence to study the chemical states and elemental compositions within a material or covering its surface. The Mo 3d spectrums of as-prepared catalysts analyzed by XPS are exemplified in Fig. 4. The curve-fitting of Mo 3d profiles was performed to observe the distribution of molybdenum oxidation states and some information on these peaks was estimated and summarized in Table 2. With respect to the observation of collected results in all catalysts, the doublet peaks should split into 3d5/2 and 3d3/2 of Mo core levels with a spin energy separation of roughly around 3.0–3.2 eV, which corresponds to the coupling effect of spin-orbital43. Over the sample of NM-O, it is found that only the characteristic peaks of molybdenum oxide phases appeared at the surface region of Mo4+ (229.1 eV), Mo5+ (230.5 eV), and Mo6+ (232.6 eV) 3d5/2 transitions involved in Mo–O bonding44,45,46. The result reveals that the surface oxidation of a catalyst can be completely achieved in a flow of O2-containing gas stream. In Fig. 4b, the peaks assigned to MoO2, Mo2O5, and MoO3 notably decreased, while fabricating a new peak with Mo 3d5/2 binding energy (B.E.) of 227.7 eV, which contributes to the reduced metallic Mo0 phase47. The main Mo species detected in NM-C is dominated by the molybdenum atoms in the carbidic phase arranged at lower oxidation states ranging from 228.4 to 228.7 eV, involving the Mo–C bond48. Considering in Fig. 4c and Table 2, a much smaller concentration of Mo5+ and Mo6+ at 230.6 and 232.5 eV, as well as the almost absence of Mo4+ species were evidenced on the surface of the carbide catalyst. As previously reported elsewhere, the presence of these oxides could be explained by surface oxidation during the passivation process36,49,50,51. However, none of these catalysts was passivated in the exposure to air prior to the XPS analysis. In this circumstance, it is possible to conclude that some of the oxides remaining in the catalyst should be owing to the incomplete carburization35,52. As demonstrated in Table 2, the value of molybdenum carbide to total molybdenum species also affirmed that although there were Mo oxides presented during the process, the overall portion of molybdenum species is in the form of carbide.
The existence of Mo2C species
To further investigate the phenomena involved in the Mo2C formation, an in-situ study of gas evolution during the carburization process was conducted. The catalyst was exposed to a CH4/H2 constant flow of 100 ml/min at an elevated temperature of 700 °C. The outlet concentration of evolved gases was analyzed by GC-TCD detector at intervals of 10 min and the results are illustrated in Fig. 5a. It can be observed that CO and H2 were being increasingly produced from the outlet stream after 110 min time (around 600 °C). It is known that carbides of molybdenum (Mo2C) commonly form at temperatures above 500 °C53. According to Eq. (4) and Fig. 5a, the production of CO and H2 at higher temperatures could be attributed to the oxide-carbide transformation. During the carburization, the reduction of nickel oxide can simultaneously occur, (Eq. 12), as evidenced by the presence of Ni in the XRD pattern of fresh NM-C catalyst. In addition, the experimental results surprisingly showed a small amount of CO2 generated in the outflow at the initial carburizing time. This may be related to the water–gas shift reaction (WGS), represented in Eq. (13). The reaction consumes all the H2O that was produced by the reduction of NiO. Since WGS is an exothermic reaction, thus low temperatures are more favorable54, resulting in a slightly detectable CO2 at 0–110 min. After the in-situ observations, the NM-C catalyst sample was characterized by using Raman analysis. From the spectra in Fig. 5b, the peak at 143 cm−1 also confirms the existence of Mo2C species on the surface of the NM-C catalyst and no other characteristic band of pyrolytic carbons was observed.
Catalytic performances
The performance variation of NM-O, NM-R, and NM-C catalysts demonstrated in terms of activity, selectivity, and stability as a function of time on stream (TOS) during a 3 h reaction is shown in Fig. 6. From Fig. 6a, it was obvious that NM-R and NM-C showed a similar trend in the rate of CO2, with approximately 90% conversion which remained constant throughout the reaction time. However, a rapid decrease in CH4 conversion was observed over the reduced Ni–Mo/MgO (see Fig. 6b). Meanwhile, Ni–Mo2C/MgO exhibits stable performance with a slightly higher CH4 conversion than that of NM-R over the entire test period. This could be implied that the presence of Mo2C species may have a significant improvement in the catalyst activity and durability. In contrast, the CO2 was relatively converted through the dry reforming of methane reaction for the oxide form of the catalyst. Also, an almost undetectable conversion of CH4 and no carbon deposition indicates that the catalyst was unable to activate the decomposition of methane for producing H2 and CNTs. Thus, it implies that the NM-O catalyst would favor DRM more than CDM, complying with DRM theoretically producing an equal rate of H2 and CO as in Fig. 6c. Table 3 shows the analysis of total moles of carbon in feed and products (gas and solid) together with carbon balance for the 3 h reaction time. It was found that there was only a slow rate of DRM over NM-O (CO = 0.14 mol), and no CDM occurred. Considering carbon products from DRM and CDM (CO, C), it was found that the rate of DRM over NM-R catalyst was 3 times higher than CDM (DRM: CH4 + CO2 → 2CO + 2H2 ; CO = 2.02 mol, CDM: CH4 → C + 2H2 ; C = 0.37 mol). Compared to NM-R counterpart, NM-C catalyst enhanced the rate of CDM more than DRM as CH4 consumed more than CO2. The mole of CH4 reduced from 0.40 to 0.32 mol, while CO2 was slightly reduced from 0.10 to 0.08. It confirms that the existence of Mo2C can improve the catalytic activities of both DRM and CDM, but it pronounces the enhancement of CDM than DRM. The exact product output data of gas and solid phases derived using different catalysts after a constant reaction time of 3 h are summarized in Table 4. Compared to NM-O, it was discovered that the yield of H2 greatly increased when the NM-R and NM-C were used, attributed to the presence of Ni0 enhancing CH4 dissociation. Theoretically, there are two possible pathways for generating hydrogen. One can produce from DRM, while the other is CDM55. However, as observed from rates of H2 (Fig. 6d,e) thus, it could be said that most of H2 produced in this system comes primarily through DRM reaction. As a result, the syngas H2/CO ratio of 1.42–1.45 was higher than 1.0. This value is suitable for producing a broad range of clean fuels and valuable hydrocarbon products, including olefins, diesel, gasoline, and so on, via the well-known catalytic chemical process, namely Fischer–Tropsch (FT) synthesis56. In the case of solid carbon shown in Fig. 6f, the production yield of carbon nanotubes shows a similar trend as the same as H2 yield, relating to CDM reaction. Furthermore, it is apparent that the largest amount of CNT was synthesized over NM-C. This could be explained by the large pore volume of the catalyst (see Table 1). It has demonstrated that the pore volume of the catalyst may have an important effect on the CNT yield. The high capacity of pore volume promotes the reduction of the barriers to diffusion and transport, which enable biogas molecules to distribute deep into the inner surface of the catalyst and result in a higher CNTs yield57. Besides, it has been reported that the Mo2C phase enhances the diffusivity of carbon atoms into neighboring Ni nanoparticles, avoiding the encapsulation of carbon deposition and leading to CNT growth42,58. As described so far, it is reasonable to deduce that the carbide catalyst not only shows comparable reactivity and durability but is also capable of producing CNTs with the highest yield.
Chemical, structural, and morphological analyses of CNTs
To investigate the quality and purity of CNTs formed over these catalysts, several techniques have been employed. Figure 7a illustrates the TGA data curves for as-obtained CNTs over the spent catalysts. Obviously, a similar oxidation pattern with one dominant slope at the high-temperature region above 600 °C was observed for the NM-R and NM-C samples. It is known that a pronounced peak of weight loss is referred to the amount of deposited carbon burned in oxygen, which can be attributed to the yield of carbonaceous nanomaterials generated on the catalyst surface during the reaction59. On top of that, the remaining mass in the TGA of CNTs could be explainable to unreacted catalysts retained in the sample after completing a run of 3 h. It has been reported that such impurities can be removed by various chemical-treated techniques to achieve better-purified CNTs, such as the acid leaching method60,61. The CNTs yield calculated from TGA data curves are also attached in the figure. It is observed that NM-C has the highest carbon content compared to the other catalysts. On the contrary, there is no evident weight loss curve due to the oxidation of carbon was presented for the NM-O, showing that CNTs cannot be formed over the NM-O catalyst sample. Additionally, the prominent weight loss curves detected in the TGA profiles of NM-R and NM-C, which reflected at the elevated temperatures show the high thermal stability and graphitization structure of CNTs produced over these catalysts. This is due to the amorphous carbon is typically oxidized at temperatures less than 400 °C62.
In Fig. 7b, the Raman spectroscopy measurement has been carried out to further shed light on the crystallinity and quality of the as-produced MWCNTs received over spent NM-O, NM-R, and NM-C catalysts. It is evident that there are three distinct peaks appeared for all samples. The one with the signal detection at the wavelength ranges of 2600–2700 cm−1 can be attributed to the G′ peak, which is used to assure the typical characteristics of multiwall carbon nanotubes63. The other two absorption bands appearing at around 1345 cm−1 and 1586 cm−1 were identified as the D peak and G peak, respectively. In general, the D-band is assigned to the structural defects or disordered-structured carbons such as amorphous carbon presented on the extrinsic surface of CNTs walls. Whereas the G-band is related to the tangential stretching vibration of C=C bonded atoms in the aromatic layers of graphene crystalline64,65. The relative integral areas of the G and D bands demonstrated in terms of Ig/Id ratio have been widely applied for quantifying the graphitization degree of MWCNTs20,37,59. As can be seen from the spectra, the respective Ig/Id ratios of the synthesized CNTs were found to be in the range of 0.86–1.29, while the poorest value of 0.73 was given by the commercial CNTs. The result indicates that all catalysts possess better-graphitized MWCNTs as compared to the commercial one. In addition, three absorption peaks attributed to MoO3 were also found at 273, 389, and 450 cm−1 for the NM-O catalyst66. It is implied that the metal oxide was unable to reduce into a metallic form during the catalytic test, decreasing the catalyst activity. Figure 7c displays the XRD pattern of reacted catalysts. Clearly, the characteristic diffraction peaks of MgO phases were diminished in the patterns of the NM-R and NM-C. As opposed to the XRD profiles of the fresh catalysts, two dominant peaks were observed at 2θ reflections of 26.1° and 42.6° in the spent catalysts, which can be attributed to the characteristic of graphitic carbon and therefore to the formation of carbon nanomaterials (CNTs)67. In addition, the peaks attributed to metallic Ni0 at 2θ = 43.8° and 51.2° were detected in both samples and there is no peak assigned to their metal oxide was observed. This indicates the complete reduction of Ni oxide into active Ni during the reaction. As for the diffractogram of the NM-O sample, it was found that most of the peaks in the diffraction pattern are in the form of oxide phases, which are in accordance with the previous results provided by Raman spectra.
To further investigate a deep insight into the surface morphological and internal structured differences of carbon deposition after a run of 3 h, the reacted catalysts were characterized by TEM analysis. The recorded micrograph and its magnified version are presented in Fig. 8. The diameter size distribution of nanotubes on the catalysts was estimated based on the TEM images and the results are given in Table 5. As shown in Fig. 8, it was evident that the highly dense CNTs were produced in all catalyst configurations. Only the catalyst sample that was not very active presented a negligible amount of such filamentary nanocarbon. For the NM-R and NM-C, the general nanostructure of deposited carbon is quite similar, consisting of jointed compartments resembling the formation of bamboo plant with hollow stem cavities separated by diaphragms, which represents a morphology typical of filamentous carbon with bamboo-like structure68,69,70,71. A few segments are assembled with encapsulated catalyst particles, while the others are empty. The number of the graphitic layer in tube walls is varied from 8 to 27 layers and it correlates well with the thickness of the tubes (Table 5). As can be seen, it was shown that the presence of CNTs synthesized over NM-R exhibits mainly those bamboo-like nanostructures with larger particles and irregular morphology. This could be attributed to the sintering effects of catalysts during the reaction, which might be responsible for the deactivation problems. On the opposite hand, small particles with uniform diameters were detected in the micrographs of Ni–Mo2C/MgO. The results suggested that the catalytic particles were somehow confined or controlled by carbon layers of carbide species covering the catalyst surface, which was hypothesized to be a possible reason for the reduction in particle agglomeration. Therefore, it is interesting to note that NM-C has a better resistance to particle sintering compared to the conventional reduced form, which can be also responsible for the stabilization of its catalytic performance.
Stability test
The long-term performance of NM-O, NM-R, and NM-C catalysts for the combined process of DRM and CDM was evaluated at a low biogas feeding rate (decreased from 400 ml/min to 160 ml/min) over a 24 h run. The GHSV was fixed at 48,000 ml/g-h (using 0.2 g of catalysts). Figure 9 presents all the possible gases detected in the outlet stream during the stability test at 800 °C. In Fig. 9a, it is obvious that the rate of biogas consumption has not changed much compared to the inlet gas compositions. Meanwhile, the rate of H2 generation slowly increased and after 800 min of TOS, the effluent gases of H2 show a constant trend at a low concentration of around 10–11%. A possible reason for this phenomenon might be that NM-O could not act promptly as the catalytic role at an early stage of reaction. This is because the active state of these catalysts should be in a metallic form (Ni0), which can be achieved under H2 flow. When there was enough hydrogen generated out from the stream to complete the reduction of catalysts, the conversion would be improved. For the NM-R and NM-C catalysts, the compositions of effluent gases exhibited similar trends, with approximately 95% of the CO2 being completely converted. In addition, a high fraction of CO concentration was produced from the outlet stream and progressively retain constant over 24 h of TOS in both cases, whereas a higher concentration of H2 was observed for the NM-C catalyst. Considerably, the carbide catalyst can promote an improved selectivity toward high-purity hydrogen production. It is also demonstrated that the NM-C shows a prolonged catalytic stability, while NM-R could be active in a short period for only 1 h. Then, the production rate of H2 decreased rapidly. The main mechanism is due to the presence of individual phases of Ni and Mo2C. It is worth noting that the contact between Ni and Mo2C phases could exhibit dual-active sites, creating the redox cycle of the carbide phase35,36. According to this cycle, CO2 in biogas is activated by Mo2C, then, the formation of adsorbed O2 replaces the carbon of Mo2C to MoO2. On the other hand, Ni is responsible for the dissociation of CH4, and carbon species formed on Ni sites allow MoO2 to be reduced back into Mo2C, thus, slow down the easy deactivation of active phases from the sintering as well as coke formation caused by catalytic decomposition of methane, which is responsible for maintaining the catalytic activity and stability of the system during the reaction.
The productivity and properties of the as-grown CNTs on these catalysts were investigated. After completing the 24 h reaction, a solid post-reaction catalyst was collected and calculated in terms of yield, while the purity of CNTs was estimated by TGA measurement. And the relative intensity ratio of Ig/Id acquired from Raman spectroscopy analysis, was applied to evaluate the crystallinity and the graphitization degree of carbon deposition. Table 6 summarizes the yields, purity, and Ig/Id value of synthesized CNTs as well as those corresponding commercial CNTs for comparison. Evidently, there is no carbon nanofilaments are detected on the NM-O catalyst, suggesting that the oxide catalyst could not be functionalized sufficiently to catalyze the CDM under the employed reaction conditions. On the other hand, the highest CNTs yields was achieved over the NM-C catalyst within a 24 h run. So, it is interesting pointing out that the Ni–Mo2C catalyst exhibited superior performance over its counterparts, even though the condensed nanocarbon was largely generated and covered on the catalyst surface.
The TGA profiles, Raman spectra, and X-ray diffraction pattern of CNTs synthesized over spent catalysts after a reaction of 24 h are provided in Fig. 10. As determined from the TGA plots comparing 3 h results, a gigantic portion corresponding to the oxidation with oxygen appeared in the weight loss behavior of NM-C and NM-R samples, suggesting that there was a large number of carbonaceous materials deposited on the catalyst surface, which hence verifies the high purity of as-produced CNTs. This is confirmed by the obtained purity of nearly close to 95.0% over these catalysts, which is also much higher than the features of the 3 h reaction test (around up to 85.0%) and is in line with the results evident in many reports, quoting that the purity of CNTs can be improved by conducting a longer reaction time20,37,59. Moreover, the slope of mass disappearance reflected at temperatures of over 550 °C certifies that the CNTs showed excellent properties in terms of thermal stabilization and degree of graphitization structure. In particular, when compared with the commercial CNTs, being thermally stable below 450 °C with lower CNTs purity. On the other hand, the percentage of weight loss due to the burning of CNTs does not change for the thermogravimetric curve of the NM-O catalyst, indicating the absence of such carbon species in the sample. This is in good agreement with the arising of MoO3 phases at the Raman shift of 273, 382, and 453 cm−1 as shown in Fig. 10b, which present prominently and dominantly amongst the remaining peaks that would assign to the characteristic bands of CNTs. Meanwhile, the data illustrates that the carbon deposited on the NM-C and NM-R catalysts have a more crystalline and well-graphitized structure of CNTs than that on the typical ones since the relative ratios are 0.98 and 1.24, respectively.
In Fig. 11, a similar XRD pattern was noticed over the catalysts prepared under a flow of H2 and CH4 with the main reflection peaks at 2θ = 25.9° and 42.9°, which relates to the appearance of as-synthesized CNTs. On the contrary, the overall proportion of phases derived over the spent NM-O catalyst is in the form of metal oxides and there is no peak attributed to carbonaceous species was observed as virtually elucidated in the SEM and TEM images (see Fig. 12a). This is also in line with the results acquired from TGA and Raman shift. In addition, it should be noted that the molybdenum oxide phase (MoO2) is arisen as a consequence of the reduction of Mo6+ into Mo4+ by hydrogen produced during the reaction. More interestingly, according to the data in Table 7, it was found that the crystallite size of Ni particle of the used NM-C catalyst significantly decreased in comparison with the fresh carbide sample, having 4.7 nm, whereas an increase in particle size from 5.5 to 11.2 nm was observed over NM-R sample. This proves that the carbide catalyst had a greater ability to keep control of the crystal structure. Furthermore, the existence of Ni and Mo2C found in the XRD postreaction of the NM-C configuration supports the presumption that there was an oxidation-carburization cycle occurred during the reaction, which is the reason why the system can be maintained for a long time.
Figure 12 illustrates the results of SEM and TEM analyses of the post-reaction catalysts in the long-term (24 h) catalytic stability test. All the analyzed morphological parameters calculated based on SEM and TEM characterization are also listed in Table 8. It is clear that there is no sign of carbonaceous nanofilament appearing on the segment of NM-O. In the magnification images, it is understandably seen that most of the active particles were embedded inside some spherical layer, showing the smaller reacting area available, resulting in losing its activity. Also, the CNTs sample generated over NM-O exhibits broad diameters with a large mean particle size of around 44.4 nm. As for the micrographs of Ni–Mo/MgO and Ni–Mo2C/MgO catalysts, it is revealed that the white spots in SEM images were barely found in both samples with some of them nucleated at the end of elongated compartments. The most brightness area should be corresponded to the metal particles of the catalyst. Therefore, it can be said that NM-R and NM-C catalysts provided CNTs products with less impurity, which later reduces the cost of related purification processes. Moreover, the CNTs grown over these samples considerably have lower average diameters when compared to those of the 3 h reaction test. Especially on the carbide catalyst, giving the smallest and narrowest number in terms of tube diameter and CNTs wall, which is in accordance with the crystallite data results of XRD, as clearly shown in Table 7.
Conclusion
The catalytic performance of bimetallic Ni–Mo catalysts supported on MgO prepared under different treatment gases (O2, H2, and CH4) was investigated in the process of direct biogas conversion for the simultaneous production of H2-rich syngas and CNTs. The experimental results demonstrated that carbide Ni–Mo catalyst prepared by controlled carburization exhibits high reactivity and excellent stability over the long-term test period (24 h). The highest yield CNTs with purity up to 95% can be achieved. In addition, more than 80% of H2 yield and 90% syngas purity with H2/CO = 1.45 were obtained. By correlating the XPS and Raman results with in-situ study, it is suggested that the layer of carbide species of Ni–Mo2C formed on the catalyst surface was primarily responsible for controlling the crystal structure of Ni–Mo and therefore leading to the improved catalytic performance with resultants of the smaller nanotubes of filamentous carbon. On the other hand, a significant decrease in CH4 conversion was observed over the conventional reduced Ni–Mo catalyst. As a result, the as-grown CNTs have a much larger size of nanotubes than other catalyst samples due to the sintering. In summary, the presence of Mo2C species on the catalyst surface can promote the stability and reactivity of the catalyst for direct biogas conversion. The new findings in this study would accelerate the research and development of direct conversion process of biogas into a stage of commercialization.
Data availability
All data related to the finding of this study are accessible upon request from the corresponding author Sakhon Ratchahat.
References
Zhang, X. & Dincer, I. Energy Solutions to Combat Global Warming Vol. 33 (Springer, 2017). https://doi.org/10.1007/978-3-319-26950-4.
Ishaq, H. & Dincer, I. in Accelerating the Transition to a 100% Renewable Energy Era (ed Uyar, T. S.) 275–307 (Springer, 2020).
Ishaq, H. & Dincer, I. Comparative assessment of renewable energy-based hydrogen production methods. Renew. Sustain. Energy Rev. 135, 110192. https://doi.org/10.1016/j.rser.2020.110192 (2021).
Agrafiotis, C., von Storch, H., Roeb, M. & Sattler, C. Solar thermal reforming of methane feedstocks for hydrogen and syngas production—A review. Renew. Sustain. Energy Rev. 29, 656–682. https://doi.org/10.1016/j.rser.2013.08.050 (2014).
Nikolaidis, P. & Poullikkas, A. A comparative overview of hydrogen production processes. Renew. Sustain. Energy Rev. 67, 597–611. https://doi.org/10.1016/j.rser.2016.09.044 (2017).
Abdin, Z. et al. Hydrogen as an energy vector. Renew. Sustain. Energy Rev. 120, 109620. https://doi.org/10.1016/j.rser.2019.109620 (2020).
Msheik, M., Rodat, S. & Abanades, S. Methane cracking for hydrogen production: A review of catalytic and molten media pyrolysis. Energies 14, 3107 (2021).
Xu, J., Zhou, W., Li, Z., Wang, J. & Ma, J. Biogas reforming for hydrogen production over a Ni–Co bimetallic catalyst: Effect of operating conditions. Int. J. Hydrogen Energy 35, 13013–13020. https://doi.org/10.1016/j.ijhydene.2010.04.075 (2010).
Lucrédio, A. F., Assaf, J. M. & Assaf, E. M. Reforming of a model biogas on Ni and Rh–Ni catalysts: Effect of adding La. Fuel Process. Technol. 102, 124–131. https://doi.org/10.1016/j.fuproc.2012.04.020 (2012).
Baharudin, L., Rahmat, N., Othman, N. H., Shah, N. & Syed-Hassan, S. S. A. Formation, control, and elimination of carbon on Ni-based catalyst during CO2 and CH4 conversion via dry reforming process: A review. J. CO2 Util. 61, 102050. https://doi.org/10.1016/j.jcou.2022.102050 (2022).
Fidalgo, B., Arenillas, A. & Menéndez, J. A. Mixtures of carbon and Ni/Al2O3 as catalysts for the microwave-assisted CO2 reforming of CH4. Fuel Process. Technol. 92, 1531–1536. https://doi.org/10.1016/j.fuproc.2011.03.015 (2011).
Castro Luna, A. E. & Iriarte, M. E. Carbon dioxide reforming of methane over a metal modified Ni–Al2O3 catalyst. Appl. Catal. A Gen. 343, 10–15. https://doi.org/10.1016/j.apcata.2007.11.041 (2008).
Hao, Z., Zhu, Q., Jiang, Z., Hou, B. & Li, H. Characterization of aerogel Ni/Al2O3 catalysts and investigation on their stability for CH4–CO2 reforming in a fluidized bed. Fuel Process. Technol. 90, 113–121. https://doi.org/10.1016/j.fuproc.2008.08.004 (2009).
Zhang, G., Su, A., Du, Y., Qu, J. & Xu, Y. Catalytic performance of activated carbon supported cobalt catalyst for CO2 reforming of CH4. J. Colloid Interface Sci. 433, 149–155. https://doi.org/10.1016/j.jcis.2014.06.038 (2014).
Nikoo, M. K. & Amin, N. A. S. Thermodynamic analysis of carbon dioxide reforming of methane in view of solid carbon formation. Fuel Process. Technol. 92, 678–691. https://doi.org/10.1016/j.fuproc.2010.11.027 (2011).
le Saché, E., Pastor-Pérez, L., Watson, D., Sepúlveda-Escribano, A. & Reina, T. R. Ni stabilised on inorganic complex structures: Superior catalysts for chemical CO2 recycling via dry reforming of methane. Appl. Catal. B 236, 458–465. https://doi.org/10.1016/j.apcatb.2018.05.051 (2018).
Littlewood, P., Xie, X., Bernicke, M., Thomas, A. & Schomäcker, R. Ni0.05Mn0.95O catalysts for the dry reforming of methane. Catal. Today 242, 111–118. https://doi.org/10.1016/j.cattod.2014.07.054 (2015).
Al-Fatesh, A. S. et al. CO2-reforming of methane to produce syngas over Co–Ni/SBA-15 catalyst: Effect of support modifiers (Mg, La and Sc) on catalytic stability. J. CO2 Util. 21, 395–404. https://doi.org/10.1016/j.jcou.2017.08.001 (2017).
Tsoukalou, A. et al. Dry-reforming of methane over bimetallic Ni–M/La2O3 (M=Co, Fe): The effect of the rate of La2O2CO3 formation and phase stability on the catalytic activity and stability. J. Catal. 343, 208–214. https://doi.org/10.1016/j.jcat.2016.03.018 (2016).
Saconsint, S. et al. Development of high-performance nickel-based catalysts for production of hydrogen and carbon nanotubes from biogas. Sci. Rep. 12, 15195. https://doi.org/10.1038/s41598-022-19638-y (2022).
Xu, W., Ramirez, P. J., Stacchiola, D. & Rodriguez, J. A. Synthesis of α-MoC1-x and β-MoCy catalysts for CO2 hydrogenation by thermal carburization of Mo-oxide in hydrocarbon and hydrogen mixtures. Catal. Lett. 144, 1418–1424. https://doi.org/10.1007/s10562-014-1278-5 (2014).
Rodriguez, J. et al. Desulfurization reactions on surfaces of metal carbides: Photoemission and density-functional studies. Top. Catal. 53, 393–402. https://doi.org/10.1007/s11244-010-9452-5 (2010).
Han, J. et al. Nanostructured molybdenum carbides supported on carbon nanotubes as efficient catalysts for one-step hydrodeoxygenation and isomerization of vegetable oils. Green Chem. 13, 2561–2568. https://doi.org/10.1039/C1GC15421D (2011).
Li, R. et al. Nanostructured molybdenum carbide on biochar for CO2 reforming of CH4. Fuel 225, 403–410. https://doi.org/10.1016/j.fuel.2018.03.179 (2018).
Chan-Thaw, C. E. & Villa, A. Metal carbides for biomass valorization. Appl. Sci. 8, 259 (2018).
Zhang, Q., Pérez, L., Gu, S. & Ramirez Reina, T. Transition metal carbides (TMCs) catalysts for gas phase CO2 upgrading reactions: A comprehensive overview. Catalysts 10, 955. https://doi.org/10.3390/catal10090955 (2020).
Claridge, J. B. et al. New catalysts for the conversion of methane to synthesis gas: Molybdenum and tungsten carbide. J. Catal. 180, 85–100. https://doi.org/10.1006/jcat.1998.2260 (1998).
York, A. P. E., Claridge, J. B., Brungs, A. J., Tsang, S. C. E. & Green, M. L. H. Molybdenum and tungsten carbides as catalysts for the conversion of methane to synthesis gas using stoichiometric feedstocks. Chem. Commun. 1, 39–40 (1997).
Guo, J. et al. A carbide catalyst effective for the dry reforming of methane at atmospheric pressure. Adv. CO2 Convers. Util. 12, 181–196 (2010).
Czaplicka, N., Rogala, A. & Wysocka, I. Metal (Mo, W, Ti) carbide catalysts: Synthesis and application as alternative catalysts for dry reforming of hydrocarbons—A review. Int. J. Mol. Sci. 22, 12337 (2021).
Yao, Z. et al. Insights into the deactivation mechanism of metal carbide catalysts for dry reforming of methane via comparison of nickel-modified molybdenum and tungsten carbides. RSC Adv. https://doi.org/10.1039/C5RA24815A (2016).
Zhang, A. et al. In-situ synthesis of nickel modified molybdenum carbide catalyst for dry reforming of methane. Catal. Commun. 12, 803–807. https://doi.org/10.1016/j.catcom.2011.01.019 (2011).
Zhang, L., Yang, Y., Yao, Z., Shi, Y. & Kang, X. Finding of a new cycle route in Ni/Mo2C catalyzed CH4–CO2 reforming. Catal. Sci. Technol. https://doi.org/10.1039/D0CY02428G (2021).
Silva, C. G., Passos, F. B. & Teixeira da Silva, V. Effect of carburization conditions on the activity of molybdenum carbide-supported catalysts promoted by nickel for the dry reforming of methane. Energy Fuels 35, 17833–17847. https://doi.org/10.1021/acs.energyfuels.1c02110 (2021).
Shi, C. et al. Ni-modified Mo2C catalysts for methane dry reforming. Appl. Catal. A 431–432, 164–170. https://doi.org/10.1016/j.apcata.2012.04.035 (2012).
Han, B. et al. The promotional role of β-cyclodextrin on Ni–Mo2C/MgO catalyst for biogas reforming. Mol. Catal. 515, 111897. https://doi.org/10.1016/j.mcat.2021.111897 (2021).
Rattanaamonkulchai, R. et al. Simultaneous production of hydrogen and carbon nanotubes from biogas over mono- and bimetallic catalyst. J. Environ. Chem. Eng. 10, 107910. https://doi.org/10.1016/j.jece.2022.107910 (2022).
Alothman, Z. A review: Fundamental aspects of silicate mesoporous materials. Materials 5, 2874–2902. https://doi.org/10.3390/ma5122874 (2012).
Tüysüz, H. & Schüth, F. in Advances in Catalysis Vol. 55 (eds Gates, B. C. & Jentoft, F. C.) 127–239 (Academic Press, 2012).
Saikia, P., Miah, A. & Malakar, B. Superior activity of Au/CeO2/SiO2 catalyst for CO oxidation reaction. Bull. Catal. Soc. India 13, 1–12 (2015).
Awadallah, A. E., Aboul-Enein, A. A. & Aboul-Gheit, A. K. Impact of group VI metals addition to Co/MgO catalyst for non-oxidative decomposition of methane into COx-free hydrogen and carbon nanotubes. Fuel 129, 27–36. https://doi.org/10.1016/j.fuel.2014.03.038 (2014).
Yao, L., Wang, Y., Galvez, M. E., Hu, C. & Da Costa, P. Ni–Mo2C supported on alumina as a substitute for Ni–Mo reduced catalysts supported on alumina material for dry reforming of methane. C. R. Chim. 21, 247–252. https://doi.org/10.1016/j.crci.2017.06.002 (2018).
Wan, C., Regmi, Y. & Leonard, B. Multiple phases of molybdenum carbide as electrocatalysts for the hydrogen evolution reaction. Angewandte Chemie Int. Ed. https://doi.org/10.1002/anie.201402998 (2014).
Oshikawa, K., Nagai, M. & Omi, S. Characterization of molybdenum carbides for methane reforming by TPR, XRD, and XPS. J. Phys. Chem. B 105, 9124–9131 (2001).
Cheekatamarla, P. K. & Thomson, W. J. Poisoning effect of thiophene on the catalytic activity of molybdenum carbide during tri-methyl pentane reforming for hydrogen generation. Appl. Catal. A 287, 176–182. https://doi.org/10.1016/j.apcata.2005.03.043 (2005).
Choi, J. G. & Thompson, L. T. XPS study of as-prepared and reduced molybdenum oxides. Appl. Surf. Sci. 93, 143–149. https://doi.org/10.1016/0169-4332(95)00317-7 (1996).
Huo, X., Wang, Z., Huang, J., Zhang, R. & Fang, Y. Bulk Mo and Co–Mo carbides as catalysts for methanation. Catal. Commun. 79, 39–44. https://doi.org/10.1016/j.catcom.2016.03.001 (2016).
Shi, C. et al. Synergism in NiMoOx precursors essential for CH4/CO2 dry reforming. Catal. Today 233, 46–52. https://doi.org/10.1016/j.cattod.2013.10.076 (2014).
Zhang, X. et al. A stable low-temperature H2-production catalyst by crowding Pt on α-MoC. Nature 589, 396–401. https://doi.org/10.1038/s41586-020-03130-6 (2021).
Xiang, M. & Zou, J. CO hydrogenation over transition metals (Fe Co, or Ni) modified K/Mo2C catalysts. J. Catal. 2013, 195920. https://doi.org/10.1155/2013/195920 (2013).
Clair, T. P. S. et al. Surface characterization of α-Mo2C (0001). Surf. Sci. 426, 187–198 (1999).
Patt, J., Moon, D. J., Phillips, C. & Thompson, L. Molybdenum carbide catalysts for water–gas shift. Catal. Lett. 65, 193–195. https://doi.org/10.1023/A:1019098112056 (2000).
Jourdain, V. & Bichara, C. Current understanding of the growth of carbon nanotubes in catalytic chemical vapour deposition. Carbon 58, 2–39. https://doi.org/10.1016/j.carbon.2013.02.046 (2013).
Schmider, D., Maier, L. & Deutschmann, O. Reaction kinetics of CO and CO2 methanation over nickel. Ind. Eng. Chem. Res. 60, 5792–5805. https://doi.org/10.1021/acs.iecr.1c00389 (2021).
Aieamsam-Aung, P. et al. Effect of CoMo metal loading on H2 and CNTs production from biogas by integrative process. Int. J. Hydrogen Energy 47, 41444–41460. https://doi.org/10.1016/j.ijhydene.2022.05.216 (2022).
van de Loosdrecht, J. et al. Fischer–Tropsch synthesis: Catalysts and chemistry. Surf. Inorg. Chem. Heterog. Catal. 7, 525–557 (2013).
Setyopratomo, P., Wulan, P. & Sudibandriyo, M. The effect of metal loading on the performance of tri-metallic supported catalyst for carbon nanotubes synthesis from liquefied petroleum gas. Int. J. Technol. 9, 120. https://doi.org/10.14716/ijtech.v9i1.1165 (2018).
Park, S. J. et al. Effect of reduction conditions of Mo–Fe/MgO on the formation of carbon nanotube in catalytic methane decomposition. J. Ind. Eng. Chem. 109, 384–396. https://doi.org/10.1016/j.jiec.2022.02.023 (2022).
Kludpantanapan, T. et al. Development of CoMo-X catalysts for production of H2 and CNTs from biogas by integrative process. J. Environ. Chem. Eng. 10, 107901. https://doi.org/10.1016/j.jece.2022.107901 (2022).
Ko, F.-H., Lee, C.-Y., Ko, C.-J. & Chu, T.-C. Purification of multi-walled carbon nanotubes through microwave heating of nitric acid in a closed vessel. Carbon 43, 727–733 (2005).
Abdulrazzak, F. H., Esmail, S. K., Dawod, H. A., Abbas, A. M. & Almaliki, M. K. X-ray analysis for purification process of synthesized multi-walled carbon nanotubes by chemical vapor deposition. Int. J. Theor. Appl. Sci. 8, 37 (2016).
Yoshida, A., Kaburagi, Y. & Hishiyama, Y. Full width at half maximum intensity of the G band in the first order Raman spectrum of carbon material as a parameter for graphitization. Carbon 44, 2333–2335 (2006).
Singh, B. P. et al. The production of a multi-walled carbon nanotube/hexamethylene diisocyanate nanocomposite coating on copper by electrophoretic deposition. Surf. Coat. Technol. 206, 1319–1326. https://doi.org/10.1016/j.surfcoat.2011.08.054 (2011).
Paniago, R. et al. Surface properties of oxidized and aminated multi-walled carbon nanotubes. J. Braz. Chem. Soc. 23, 1078. https://doi.org/10.1590/S0103-50532012000600012 (2012).
Wang, W., Wang, H., Yang, Y. & Jiang, S. Ni–SiO2 and Ni–Fe–SiO2 catalysts for methane decomposition to prepare hydrogen and carbon filaments. Int. J. Hydrogen Energy 37, 9058–9066. https://doi.org/10.1016/j.ijhydene.2012.03.003 (2012).
Pinilla, J. L. et al. Ni- and Fe-based catalysts for hydrogen and carbon nanofilament production by catalytic decomposition of methane in a rotary bed reactor. Fuel Process. Technol. 92, 1480–1488. https://doi.org/10.1016/j.fuproc.2011.03.009 (2011).
Pudukudy, M. & Yaakob, Z. Methane decomposition over Ni, Co and Fe based monometallic catalysts supported on sol gel derived SiO2 microflakes. Chem. Eng. J. 262, 1009–1021. https://doi.org/10.1016/j.cej.2014.10.077 (2015).
Giannakopoulou, T. et al. Effect of processing temperature on growing bamboo-like carbon nanotubes by chemical vapor deposition. Mater. Today Chem. 19, 100388. https://doi.org/10.1016/j.mtchem.2020.100388 (2021).
Li, W. Z., Wen, J. G. & Ren, Z. F. Effect of temperature on growth and structure of carbon nanotubes by chemical vapor deposition. Appl. Phys. A 74, 397–402. https://doi.org/10.1007/s003390201284 (2002).
Jia, Z. et al. Controllable and large-scale synthesis of carbon nanostructures: A review on bamboo-like nanotubes. Catalysts 7, 256 (2017).
Nxumalo, E. & Coville, N. Nitrogen doped carbon nanotubes from organometallic compounds: A review. Materials https://doi.org/10.3390/ma3032141 (2010).
Acknowledgements
This research project is supported by Mahidol University (Fundamental Fund: fiscal year 2023 by National Science Research and Innovation Fund (NSRF)). Also, authors would like to thank Nawapol Udpuay, Chawalit Takoon, Suwilai Chaveanghong, and Bancha Panyacharoen scientists at Mahidol University-Frontier Research Facility (MU-FRF) for their kind assistance in instrumental operation of XRD and Raman spectroscopy.
Author information
Authors and Affiliations
Contributions
S.S.: Conceptualization, investigation, methodology, data curation, validation, and writing—original draft preparation. A.S.: Resources, visualization, and validation. W.K.-A.: Resources. S.A.: Resources, visualization, and validation. N.S.: Visualization. C.F.: Resources. S.R.: Conceptualization, methodology, validation, visualization, data curation, supervision, funding acquisition, and writing—reviewing and editing.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Saconsint, S., Srifa, A., Koo-Amornpattana, W. et al. Development of Ni–Mo carbide catalyst for production of syngas and CNTs by dry reforming of biogas. Sci Rep 13, 12928 (2023). https://doi.org/10.1038/s41598-023-38436-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-023-38436-8
- Springer Nature Limited
This article is cited by
-
Simultaneous production of syngas and carbon nanotubes from CO2/CH4 mixture over high-performance NiMo/MgO catalyst
Scientific Reports (2024)
-
Synthesis and Characterization of AlPO4-18 Supported Mesoporous and Crystalline β-Mo2C, Ni3C, and WC Nanoparticles
Catalysis Letters (2024)
-
Role of support bio-templating in Ni/Al2O3 catalysts for hydrogen production via dry reforming of methane
Scientific Reports (2023)