ACS Sustainable Chemistry & Engineering
·
2023
·
IF 8.4
Xuejian Liu,Yan Li,Guang-Jin Chen,Dao-Yi Chen,Bo Sun,Zhenyuan Yin
CO2 capture and sequestration are broadly recognized as the most effective technology for reducing CO2 emissions and mitigating global climate change. In this regard, hydrate-based CO2 sequestration (HBCS) has been proposed as an effective method for long-term safe and stable CO2 sequestration. It is a promising technology for reducing the concentration of CO2 in the atmosphere and achieving carbon neutrality. However, one major challenge related to HBCS technology is the lack of understanding of how to improve the formation kinetics of CO2 hydrate effectively. Herein, in this study, we identified the synergistic promotion effect on CO2 hydrate formation when a low-dose thermodynamic promoter (tetrahydrofuran, THF) is coupled with an environment-friendly kinetic promoter (l-methionine, l-Met). Based on the kinetic experiments and the morphological observation, 0.6 mol % THF coupled with 0.1 wt %l-Met yields the optimal CO2 gas uptake. In situ Raman spectra reveal the mechanism of the observed two-step growth behavior at the molecular level, where low-dose THF promotes the initial CO2-THF sII hydrate nucleation and growth in the solution and l-Met promotes the subsequent CO2 sI hydrate growth along the surface of the reactor. Our study unveils the underlying synergistic mechanism when thermodynamic and kinetic promoters are coupled for CO2 hydrate formation. The results provide guidance for the identification and use of novel bio-friendly thermodynamic and kinetic promoters and are beneficial to a series of sustainable hydrate-based technologies when fast CO2 formation is required.
研究领域:
化学工程
·
环境科学
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材料科学
·
可持续能源
✓ 已验证
产品关联
DOI
高影响因子
APPLIED ENERGY
·
2024
·
IF 10.1
Yaning Kong,Honglin Yu,Mengqi Liu,Guodong Zhang,Fei Wang
Hydrate was considered to be the next generation hydrogen storage material , and hydrate-based hydrogen storage (HBHS) would play an important role in future hydrogen economy, but sluggish hydrate formation kinetics presents huge technological challenge for its application. Herein, a nano promoter of -SO 3 − @PSNS was prepared by soap-free emulsion polymerization , and a dual kinetic promoter system (L-methionine/-SO 3 − @PSNS) was applied to enhance the formation kinetics of mixed H 2 /DIOX hydrate. At a moderate condition (12 MPa and 274.15 K), hydration efficiency under a driving force of 2.1 MPa is significantly enhanced by the synergy of the dual kinetic promoters, hydrate induction time reduces from 443.2 ± 209.73 min to 24.7 ± 17.16 min, while hydrate growth rate increases by 43.75%, and hydrogen storage capacity is up to 0.473 ± 0.041 wt% that increases by 62.8%. At a more moderate condition (10 MPa and 274.15 K) with an extremely low driving force of 0.1 MPa, enhanced hydrate formation was obtained in a composite promotion system of the dual kinetic promoters and dual thermodynamic promoters (THF/DIOX), which also performs exceptionally in term of recycling. The presence of a small amount (0.35 mol%) of THF reduces the induction time by 93.5%, and hydrate growth rate increases by 130.18%, while satisfactory hydrogen storage capacity (0.346 ± 0.017 g/g) is still remained in mixed H 2 /DIOX/THF hydrate, the structure of which was confirmed by Raman spectrum . This work presents an effect approach on enhancing the formation kinetics of H 2 -contained hydrate under low driving force, and this finding provides important insight for HBHS.
研究领域:
物理化学
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能源材料
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气体储存
·
化学工程
·
纳米材料科学
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分子模拟
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可持续能源
✓ 已验证
DOI
高影响因子
Catalysis Science & Technology
·
2025
·
IF 4.2
Zhongtao Sun,Jielang Huang,Ling Zhou,Yi Zhang
The reverse water gas shift (RWGS) reaction is a critical and essential step in the CO2 hydrogenation of iron-based catalysts to produce high-value chemicals such as olefins and higher alcohols. Modification iron-based catalysts by promoter is a popular way in design efficient catalysts which not only can regulate the iron active species but also alter the CO2 adsorption and hydrogenation performance of the catalyst. Herein, a series of Na and Pd promoted 10Fe/SiO2 were prepared. 1Pd/2Na10Fe/SiO2 catalyst exhibited the highest CO2 conversion (13.2 %), the highest CO selectivity (99.7 %) and good catalyst stability. Combination of various characterization results, such as XPS, HRTEM, Mössbauer spectroscopy, CO/CO2-TPD, H2-TPD and in situ DRIFTS, it was found that the addition of Na promoter altered the reaction pathway from redox and associated pathway to only following an associative pathway, contributing to the high CO selectivity. Besides, when the content of Fe2+ species was similar, the associated pathway would be advantageous to high CO formation rate during RWGS reaction over iron-based catalysts. On the other hand, in the same reaction pathway, the content of Fe2+ species would determine the CO formation rate over iron-based catalysts during RWGS reaction.
研究领域:
催化化学
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材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
ENERGY & FUELS
·
2025
·
IF 5.3
Jingyu Lv,Kang Tan,Fei Wang,Chuanyu Dang,Mengting Sun
Slow CO2 hydrate formation kinetics restricts the development and industrial application of hydrate-based carbon capture and sequestration (CCS) technology. Here, sodium p-styrenesulfonate (SSS) was employed as a novel promoter for CO2 hydrate formation, and its efficiency, promotion mechanism, and recyclability were systematically studied. Results indicated that SSS improved the hydrate formation kinetics remarkably and yielded the highest CO2 uptake of 8.033 ± 0.348 mmol mL–1 as well as the rapidest hydrate growth rate (HGR) of 0.437 ± 0.075 mmol mL–1 min–1 at concentrations of 50 and 100 mmol L–1. SSS under a moderate concentration also presented high efficacy; 6 mmol L–1 SSS led to a short induction time of 36.37 ± 32.14 min, a rapid HGR of 0.307 ± 0.029 mmol mL–1 min–1, and a high CO2 uptake of 7.036 ± 0.472 mmol mL–1. Morphological observation revealed that the promotion effects were mainly attributed to the climbing hydrate growth caused by capillary effect, which was markedly influenced by the sidewall hydrophilicity and the SSS concentration. Stronger hydrophilicity of the sidewall and a higher SSS concentration both favored the liquid movement, boosted the climbing hydrate growth, and improved the formation kinetics. Additionally, SSS did not produce foam when hydrates dissociated and kept admirable promotion performance in at least six repeated cycles, indicating its excellent recyclability.
研究领域:
化学工程
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环境科学
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能源技术
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
Microorganisms
·
2022
·Vol. 10
·期 3
·575
·
IF 4.926
Ge Gao,Yan Zhang,Shaofang Niu,Yu Chen,Shaojing Wang,Nusratgul Anwar,Shuai Chen,Guoqiang Li,Ting Ma
Precise classification of bacteria facilitates prediction of their ecological niche. The genusEnterobacterincludes pathogens of plants and animals but also beneficial bacteria that may require reclassification. Here, we propose reclassification ofEnterobacterFY-07 (FY-07), a strain that has many plant-growth-promoting traits and produces bacterial cellulose (BC), to theKosakoniagenera. To re-examine the taxonomic position of FY-07, a polyphasic approach including 16S rRNA gene sequence analysis, ATP synthase β subunit (atpD) gene sequence analysis, DNA gyrase (gyrB) gene sequence analysis, initiation translation factor 2 (infB) gene sequence analysis, RNA polymerase β subunit (rpoB) gene sequence analysis, determination of DNA G + C content, average nucleotide identity based on BLAST, in silico DNA–DNA hybridization and analysis of phenotypic features was applied. This polyphasic analysis suggested thatEnterobactersp. FY-07 should be reclassified asKosakonia oryzendophyticaFY-07. In addition, the potential of FY-07 to promote plant growth was also investigated by detecting related traits and the colonization of FY-07 in rice roots.Keywords:Enterobacter;Kosakonia;reclassification;FY-07;promote plant growth
研究领域:
微生物学
·
植物科学
✓ 已验证
DOI
PubMed
高影响因子
KINETICS AND CATALYSIS
·
2024
·Vol. 65
·期 3
·251-260
·
IF 1.3
Yang Zhi,Luo Mingsheng,Liu Qinglong,Li Chenmeng,Wang Yatao,Li Hongjuan,Yao Lifei
Abstract The direct production of higher alcohols from syngas in a single step remains a great challenge. In this work, a series of K and Ni promoted Mo 2 C/Al 2 O 3 catalysts were prepared by impregnation method to enhance the selectivity of Mo 2 C-based catalysts for the one-step conversion of syngas to higher alcohols. The catalysts were continuously tested under the following conditions: 300°C, 3.0 MPa, velocity—11.50 \({\text{Lg}}_{{{\text{Mo}}}}^{{ - 1}}\) h –1 , H 2 /CO ratio of 2. The catalysts promoted with K and Ni demonstrated the highest total alcohol selectivity of 67.7%. Moreover, the selectivity for total C 2+ alcohols reached as high as 56%, with 37% being ethanol. X-ray diffraction (XRD), hydrogen temperature-programmed reduction (H 2 -TPR) and X-ray photoelectron spectroscopy (XPS) characterization data reveal that K can promote the crystallinity of β-Mo 2 C, lower the catalyst reduction temperature and increase the proportion of high-valent Mo on the catalyst surface. In addition, adding Ni as a promoter to the KMo 2 C/Al 2 O 3 catalyst can generate a synergistic effect to further enhance the catalytic activity and the selectivity of higher alcohols.
研究领域:
化学工程
·
催化
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
ENERGY & FUELS
·
2017
·
IF 3.091
Hongxia Gao,Zeyang Wu,Helei Liu,Xiao Luo,Zhiwu Liang
The absorption/desorption performance of carbon dioxide (CO2) in aqueous 5 M monoethanolamine (MEA) solutions in the presence of various solution regeneration promoters was comprehensively investigated using a multiple rapid screening method. The promoters considered were N-methyldiethanolamine (MDEA), N,N-dimethylethanolamine (DMEA), N,N-diethylethanolamine (DEEA), 1-dimethylamino-2-propanol (1DMA2P), 1-diethylamino-2-propanol (1DEA2P), 3-dimethylamino-1-propanol (3DMA1P), 2-(dimethylamino)-2-methyl-1-propanol (2DMA2M1P), triethanolamine (TEA), 3-(dimethylamino)-1,2-propanediol (3DMA-1,2-PD), and 3-(diethylamino)-1,2-propanediol (3DEA-1,2-PD). The molar concentration of these promoters added into 5 M MEA was set to 1 mol/L. At the atmospheric pressure, the absorption and stripping experiments were carried out at 313.15 and 353.15 K, respectively. Especially, the CO2 partial pressure was controlled at constant 15 kPa for absorption experiments. In addition, the equilibrium solubility of CO2 was also determined in order to evaluate the driving force of each amine system. The results showed that the highest CO2 equilibrium solubility of 0.5548 mol CO2/mol amine was obtained by MEA/1DEA2P, whereas both the fastest absorption and regeneration rates were achieved for aqueous blended MEA/1DMA2P solution which made MEA/1DMA2P to exhibit the highest CO2 cyclic capacity of 1.6710 mol CO2/L.
研究领域:
化学工程
·
环境科学
·
能源技术
·
物理化学
✓ 已验证
DOI
高影响因子
ENERGY & FUELS
·
2022
·
IF 4.654
Fei Wang,Fu-Peng Song,Chang Li,Meng-Ting Sun
The natural gas hydrate (NGH) technology has aroused more attention due to its great promise in natural gas (mainly containing methane) storage and transportation. Micronized swollen hydrogel poly(styrenesulfonate-co-acrylamide) (PSS-co-AAm), which included ample −SO3– groups, could remarkably promote methane hydrate formation kinetics. To further improve the promotion efficiency of this hydrogel-based promoter, we optimized the monomer ratio, that is, the molar ratio of styrenesulfonate to acrylamide (MRSA), during hydrogel preparation and investigated the effects of −SO3– density on the promotion efficiency of the hydrogel. Results indicated that the hydrogel at an appropriate MRSA performed better at promoting methane hydrate formation kinetics. Hydrate formation processes within hydrogels at MRSAs of 1:2 and 1:3 reached the highest hydrate formation rates of 0.0741 ± 0.0132 mmol mL–1 min–1 and the highest storage capacities of 126.5 ± 9.35 v/v, respectively. At MRSAs of 1:1 and 1:2, hydrate formation processes occurred with short induction durations of 24.33 ± 25.73 min and 34.33 ± 59.47 min, respectively. This revealed that high −SO3– density could be in favor of accelerating methane hydrate formation. Additionally, −SO3– density could also influence absorption capacity and water distribution of the hydrogel, which further affected promotion efficiency in methane hydrate formation kinetics. This work might be beneficial to large-scale applications of the PSS-co-AAm hydrogel promoter and be significant for the industrialization of the NGH technology.
研究领域:
化学工程
·
能源技术
✓ 已验证
DOI
高影响因子
FUEL PROCESSING TECHNOLOGY
·
2022
·
IF 8.129
Hao Bi,Zhiwei Wang,Hao Zhan,Lijian Leng,Zhiyong Zeng,Xinming Wang,Huacai Liu,Xiuli Yin,Chuangzhi Wu
Chinese herbal residue (CHR) is an association of renewable resource and hazardous waste , and high nitrogen content and low energy density are two primary obstacles to its efficient and clean thermal utilization. In this paper, acid-promoted hydrothermal was employed to probe the feasibility on CHR toward enhanced solid biofuel concerning upgradation and denitrogenation. A more excellent hydrothermal promoter (H 2 SO 4 ) was demonstrated to upgrade and denitrogenate CHR with better energy (1.125) and nitrogen densities (0.586) at optimal conditions (160 °C, 0.5 N H 2 SO 4 ), which could be attributed to the improved removal of oxygen, amino and ash during acid-promoted hydrothermal. Compared to raw feedstock or the conventional hydrochar , the acid-promoted hydrochar had enhanced compositional characteristics with higher heating value (21.00 kJ·mol −1 ), lower nitrogen (1.44 wt%) and ash (11.03 wt%) contents, thus showing more stable combustion flame with a higher comprehensive combustion index of 4.861 × 10 −8 , a higher combustion stability index of 4979.342, lower combustion alkali index of 0.026, and less nitrogen gaseous pollutant emission. Thus, acid-promoted hydrothermal would be a promising way to convert CHR into much cleaner and higher-grade solid biofuel.
研究领域:
能源与环境科学
·
生物质能工程
✓ 已验证
产品关联
DOI
高影响因子
FUEL
·
2024
·
IF 6.7
Guojun Liu,Shaoshuai Wang,Caiming Zhou,Qiang Zhao,Jiaxue Hu,Zhenzheng Gui,Yuhui Chen,Yong Huang,Peng Zhang,Fenfen Wang
Formic acid is a versatile and promising value-added chemical derived from the chemoselective transformation of renewable biomass resources. However, achieving a high production rate of formic acid remains a pivotal and enormous challenge. Herein, we synthesized a sequence of BiVO x catalysts based on vanadium-promotion by a facile and cost-effective strategy for selective oxidation of biomass-derived xylose in water under O 2 atmosphere. Particularly, the resultant Bi 1 V 2 O x exhibited a remarkably enhanced catalytic activity, higher selectivity toward formic acid, and excellent recyclability, giving a yield of 75.8 % and a production rate of formic acid (9.22 mol FA mol V −1 h −1 ) at 170 °C within only 20 min. Such pronounced improved performance was largely attributed to the synergistic effect between V and Bi species, with higher surface area, abundant surface acidity, as well as stronger adsorption energy, meanwhile efficiently suppressing the formation of undesired by-products. This study demonstrates that the promotion of V in BiVO x leads to more efficient catalytic oxidation of xylose to formic acid, and with further driven research that proved great potential for generating formic acid from renewable biomass resources for future industrial application.
研究领域:
化学工程
·
可再生资源转化
·
催化材料科学
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2016
·Vol. 24
·期 1
·676-684
·
IF 2.76
Tu Baosheng,Shi Nian,Sun Wei,Cao Limei,Yang Ji
In this paper, Pt supports on carbon black powder (Vulcan XC-72) were synthesized via a hydrothermal method for selective catalytic reduction (SCR) of NO with H 2 in the presence of 2 vol% O 2 over a wide temperature of 20–300 °C. The results showed that the 3 and 5 wt% Pt/C catalysts resulted in high NO conversion (>90 %) over a temperature range of 120 to 300 °C, and the maximum NO conversion of 98.6 % was achieved over 5 wt% Pt/C at 120 °C. Meanwhile, the influence of SO 2 and H 2 O on the catalyst performance of 3 wt% Pt/C was investigated. The catalysts exhibited good SO 2 poisoning resistance when the SO 2 concentration was lower than 260 ppm. Moreover, a positive effect on NO conversion was detected with the addition of 3 and 5 vol% H 2 O in the feed gas stream.
TEM image and good NO conversion performance of the Pt/C catalysts
研究领域:
催化化学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Drug Delivery and Translational Research
·
2023
·
IF 5.4
Nan Longyi,Song Haoyuan,Wang Haijun,Mi Ru,Wang Xiaoxu,Fang Liang
The aim of this study was to design a tulobuterol (TUL) patch with good penetration behavior and mechanical properties. Particular attention was paid to the effect of transdermal permeation enhancers on the release process of metal ligand-based acrylic pressure-sensitive adhesive (AA-NAT/Fe 3+ ). The type and dosage of the enhancers were screened by in vitro transdermal penetration in rat skin. The optimized formulation was evaluated in a pharmacokinetic study in rats. Furthermore, the molecular mechanism by which Azone (AZ) improves the release rate of TUL from AA-NAT/Fe 3+ was investigated by FT-IR, shear strength test, rheological study, and molecular simulation. As a result, the optimized formula using AA-NAT/Fe 3+ showed better mechanical properties compared to commercial products. Meanwhile, the AUC 0-t and C max of the optimized patch were 1045 ± 89 ng/mL·h and 106.8 ± 28.5 ng/mL, respectively, which were not significantly different from those of the commercial product. In addition, AZ increased the mobility of the pressure-sensitive adhesive (PSA) rather than decreasing the drug-PSA interaction, which was the main factor in enhancing TUL release from the patch. In conclusion, a TUL transdermal drug delivery patch was successfully developed using metal-coordinated PSA, and a reference was provided for the design of metal-coordinated acrylic PSA for transdermal patch delivery applications. Graphical Abstract
研究领域:
药学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）