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Fabrication of coconut shell-derived porous carbons for CO adsorption application

《化学科学与工程前沿（英文）》 2023年 第17卷 第8期   页码 1122-1130 doi: 10.1007/s11705-022-2292-6

摘要： Biomass-derived porous carbons have been considered as the most potential candidate for effective CO2 adsorbent thanks to being widely-available precursor and having highly porous structure and stable chemical/physical features. However, the biomass-derived porous carbons still suffer from the poor optimization process in terms of the synthesis conditions. Herein, we have successfully fabricated coconut shell-derived porous carbon by a simple one-step synthesis process. The as-prepared carbon exhibits advanced textual activity together with well-designed micropore morphology and possesses oxygen-containing functional groups (reached 18.81 wt %) within the carbon matrix. Depending on the different activating temperatures (from 700 to 800 °C) and KOH/biomass mass ratios (from 0.3 to 1), the 750 °C and 0.5 mass ratio were found to be enabling the highest CO2 capture performance. The optimal adsorbent was achieved a high CO2 uptake capacity of 5.92 and 4.15 mmol·g−1 at 0 and 25 °C (1 bar), respectively. More importantly, as-prepared carbon adsorbent exhibited moderate isosteric heat of adsorption and high CO2/N2 selectivity. The results were revealed not only the textural feature but also the surface functional groups critically determine the CO2 capture performance, indicating coconut shell-derived porous carbon has a considerable potential as a solid-state adsorbent for the CO2 capture.

关键词： porous carbons     CO2 adsorption     KOH activation     single step reaction     biomass    

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S-enriched porous polymer derived N-doped porous carbons for electrochemical energy storage and conversion

Chao Zhang, Chenbao Lu, Shuai Bi, Yang Hou, Fan Zhang, Ming Cai, Yafei He, Silvia Paasch, Xinliang Feng, Eike Brunner, Xiaodong Zhuang

《化学科学与工程前沿（英文）》 2018年 第12卷 第3期   页码 346-357 doi: 10.1007/s11705-018-1727-6

摘要：

Porous polymers have been recently recognized as one of the most important precursors for fabrication of heteroatom-doped porous carbons due to the intrinsic porous structure, easy available heteroatom-containing monomers and versatile polymerization methods. However, the heteroatom elements in as-produced porous carbons are quite relied on monomers. So far, the manipulating of heteroatom in porous polymer derived porous carbons are still very rare and challenge. In this work, a sulfur-enriched porous polymer, which was prepared from a diacetylene-linked porous polymer, was used as precursor to prepare S-doped and/or N-doped porous carbons under nitrogen and/or ammonia atmospheres. Remarkably, S content can sharply decrease from 36.3% to 0.05% after ammonia treatment. The N content and specific surface area of as-fabricated porous carbons can reach up to 1.32% and 1508 m2·g−1, respectively. As the electrode materials for electrical double-layer capacitors, as-fabricated porous carbons exhibit high specific capacitance of up to 431.6 F·g−1 at 5 mV·s−1 and excellent cycling stability of 99.74% capacitance retention after 3000 cycles at 100 mV·s−1. Furthermore, as the electrochemical catalysts for oxygen reduction reaction, as-fabricated porous carbons presented ultralow half-wave-potential of 0.78 V versus RHE. This work not only offers a new strategy for manipulating S and N doping features for the porous carbons derived from S-containing porous polymers, but also paves the way for the structure-performance interrelationship study of heteroatoms co-doped porous carbon for energy applications.

关键词： porous polymers     porous carbons     sulfur and nitrogen doping     supercapacitor    

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Tuning porosity of coal-derived activated carbons for CO2 adsorption

《化学科学与工程前沿（英文）》 2022年 第16卷 第9期   页码 1345-1354 doi: 10.1007/s11705-022-2155-1

摘要： A simple method was developed to tune the porosity of coal-derived activated carbons, which provided a model adsorbent system to investigate the volumetric CO2 adsorption performance. Specifically, the method involved the variation of the activation temperature in a K2CO3 induced chemical activation process which could yield activated carbons with defined microporous (< 2 nm, including ultra-microporous < 1 nm) and meso-micro-porous structures. CO2 adsorption isotherms revealed that the microporous activated carbon has the highest measured CO2 adsorption capacity (6.0 mmol∙g–1 at 0 °C and 4.1 mmol∙g–1 at 25 °C), whilst ultra-microporous activated carbon with a high packing density exhibited the highest normalized capacity with respect to packing volume (1.8 mmol∙cm−3 at 0 °C and 1.3 mmol∙cm–3 at 25 °C), which is significant. Both experimental correlation analysis and molecular dynamics simulation demonstrated that (i) volumetric CO2 adsorption capacity is directly proportional to the ultra-micropore volume, and (ii) an increase in micropore sizes is beneficial to improve the volumetric capacity, but may lead a low CO2 adsorption density and thus low pore space utilization efficiency. The adsorption experiments on the activated carbons established the criterion for designing CO2 adsorbents with high volumetric adsorption capacity.

关键词： coal-derived activated carbons     porosity     CO2 adsorption     molecular dynamics    

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Cobalt nanoparticle decorated N-doped carbons derived from a cobalt covalent organic framework for oxygen

《化学科学与工程前沿（英文）》 2021年 第15卷 第6期   页码 1550-1560 doi: 10.1007/s11705-021-2104-4

摘要： The low cost and highly efficient construction of electrocatalysts has attracted significant attention owing to the use of clean and sustainable energy technologies. In this work, cobalt nanoparticle decorated N-doped carbons (Co@NC) are synthesized by the pyrolysis of a cobalt covalent organic framework under an inert atmosphere. The Co@NC demonstrates improved electrocatalytic capabilities compared to N-doped carbon without the addition of Co nanoparticles, indicating the important role of cobalt. The well-dispersed active sites (Co-Nx) and the synergistic effect between the carbon matrix and Co nanoparticles greatly enhance the electrocatalytic activity for the oxygen reduction reaction. In addition, the Co content has a significant effect on the catalytic activity. The resulting Co@NC-0.86 exhibits a superb electrocatalytic activity for the oxygen reduction reaction in an alkaline electrolyte in terms of the onset potential (0.90 V), half-wave potential (0.80 V) and the limiting current density (4.84 mA·cm–2), and a high selectivity, as well as a strong methanol tolerance and superior durability, these results are comparable to those of the Pt/C catalyst. Furthermore, the superior bifunctional activity of Co@NC-0.86 was also confirmed in a home-built Zn-air battery, signifying the possibility for application in electrode materials and in current energy conversion and storage devices.

关键词： cobalt embedment     N-doped carbons     covalent organic framework     oxygen reduction     Zn-air battery    

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实现“不可行”的共聚反应以构筑氮掺杂多孔碳的理想聚合物前驱体 Article

亓士超, 陆筱杰, 楼寅聪, 周睿, 薛丁铭, 刘晓勤, 孙林兵

《工程（英文）》 2022年 第16卷 第9期   页码 154-161 doi: 10.1016/j.eng.2021.07.031

摘要：

某些预想的概念验证反应虽可能产生具有新功能或新应用潜力的材料，但最终常被证明是不可实现的或从商业角度上是不可行的。为了在溶剂环境中探索未知反应的反应条件，科研人员已付出了大量的努力，也浪费了大量的精力。因为人们普遍相信通过将反应物溶解在溶剂中，可以提高反应物的活性，从而促进反应。本研究发现了一个反常现象：在不同溶剂环境下，1,3,5-三（氯甲基）-2,4,6-三甲基苯与三聚氰胺的共聚反应都是无法实现的，然而利用无溶剂法却可成功地实现该反应。通过第一性原理计算和分子动力学模拟，证明了溶剂反应不具备的两个决定性因素，即由副产物的及时释放所推动的反应平衡和活化单体分子在固相中的受限热运动却可基于无溶剂法实现。由于具有较高的芳香性和氮杂环含量，由无溶剂法得到的共聚物表现出良好的应用潜力，可作为制备氮掺杂多孔碳的前驱体，使氮掺杂多孔碳具有令人满意的碳产率、理想的残氮含量、理想的结构特性，与最近报道的其他代表性同类吸附剂相比，在二氧化碳捕获能力方面展现出竞争潜力。

关键词： 无溶剂法     溶剂效应     共聚反应     氮掺杂多孔碳    

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Activated carbons and amine-modified materials for carbon dioxide capture –– a review

Zhenhe CHEN, Shubo DENG, Haoran WEI, Bin WANG, Jun HUANG, Gang YU

《环境科学与工程前沿（英文）》 2013年 第7卷 第3期   页码 326-340 doi: 10.1007/s11783-013-0510-7

摘要： Rapidly increasing concentration of CO in the atmosphere has drawn more and more attention in recent years, and adsorption has been considered as an effective technology for CO capture from the anthropogenic sources. In this paper, the attractive adsorbents including activated carbons and amine-modified materials were mainly reviewed and discussed with particular attention on progress in the adsorbent preparation and CO adsorption capacity. Carbon materials can be prepared from different precursors including fossil fuels, biomass and resins using the carbonization-activation or only activation process, and activated carbons prepared by KOH activation with high CO adsorbed amount were reviewed in the preparation, adsorption capacity as well as the relationship between the pore characteristics and CO adsorption. For the amine-modified materials, the physical impregnation and chemical graft of polyethylenimine (PEI) on the different porous materials were introduced in terms of preparation method and adsorption performance as well as their advantages and disadvantages for CO adsorption. In the last section, the issues and prospect of solid adsorbents for CO adsorption were summarized, and it is expected that this review will be helpful for the fundamental studies and industrial applications of activated carbons and amine-modified adsorbents for CO capture.

关键词： adsorption capacity     CO2 capture     activated carbon     amine-impregnated adsorbents    

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Characteristics of typical dissolved black carbons and their influence on the formation of disinfection

《环境科学与工程前沿（英文）》 2022年 第16卷 第12期 doi: 10.1007/s11783-022-1585-9

摘要：

● The physicochemical and structural properties of DBC were characterized.

关键词： Dissolved black carbon (DBC)     Chlorine     Chloramine     Disinfection by-products (DBPs)     Disinfection by-products formation potential (DBPFP)    

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Fabrication, characterization and evaluation of mesoporous activated carbons from agricultural waste:

Lei YU,Chen TU,Yongming LUO

《环境科学与工程前沿（英文）》 2015年 第9卷 第2期   页码 206-215 doi: 10.1007/s11783-014-0631-7

摘要： This work explores the feasibility of Jerusalem artichoke stem (JAS), an agricultural waste, as an alternative precursor for fabrication of mesoporous activated carbon (MAC) via conventional ZnCl activation. The as-prepared JAS-MACs were characterized by thermogravimetric, nitrogen gas adsorption isotherm and high resolution scanning electron microscopy analysis. The interacting effects of chemical dosage, activation temperature and time on the mesoporosity, mesopore volume and carbon yield were investigated, and further optimized by response surface methodology (RSM). The Brunauer-Emmett-Teller surface area, mesoporosity and mesopore volume of the JAS-MAC prepared under optimum condition were identified to be 1631 m ·g , 90.16% and 1.11 cm ·g , respectively. Compared with commercial activated carbons, this carbon exhibited a comparable monolayer adsorption capacity of 374.5 mg·g for Methylene Blue dye. The findings suggest that RSM could be an effective approach for optimizing the pore structure of fabricated activated carbons.

关键词： mesoporous activated carbon     response surface methodology     adsorption isotherm     agricultural wastes    

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Chitosan/polyethylene glycol impregnated activated carbons: Synthesis, characterization and adsorption

Ehsan Salehi, Fereshteh Soroush, Maryam Momeni, Aboulfazl Barati, Ali Khakpour

《化学科学与工程前沿（英文）》 2017年 第11卷 第4期   页码 575-585 doi: 10.1007/s11705-017-1650-2

摘要： Novel modified activated carbons (ACs) with enhanced adsorptive properties were obtained coating by chitosan (CS), polyethylene glycol (PEG) and blends of the two polymers (0:1, 1:0, 1:1, 1:2 and 2:1 wt/wt) on ACs by an impregnation technique. The adsorption performances of the pristine, acidified and polymer-impregnated ACs were studied using methylene blue as a model adsorbate. The adsorbents were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy and abrasion hardness tests. The average coating thicknesses were between 10 to 23 microns. The pore sizes, pore densities and pore capacities of the activated carbons increased as the wt-% PEG in the coating increased. The highest adsorption capacity (424.7 mg/g) was obtained for the chitosan-coated ACs and this adsorption was well described by the Langmuir isotherm model. The kinetic results were best described by the pseudo-second-order kinetic model. The highest rate constant was obtained with the ACs modified with the CS:PEG (2:1) coating and this result was almost 2.6 times greater than that of the unmodified ACs. The CS/PEG impregnated ACs also displayed superior hardness (~90%), compared to unmodified ACs (~85%). Overall the chitosan had a greater effect on improving adsorption capacity whereas the polyethylene glycol enhanced the adsorption rate.

关键词： carbon biocomposites     impregnation     chitosan     polyethylene glycol     image processing    

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Fabricating sustainable lignin-derived porous carbon as electrode for high-performance supercapacitors

《化学科学与工程前沿（英文）》 2023年 第17卷 第8期   页码 1065-1074 doi: 10.1007/s11705-023-2313-0

摘要： Lignocellulosic biomass such as plants and agricultural waste are ideal to tackle the current energy crisis and energy-related environmental issues. Carbon-rich lignin is abundant in lignocellulosic biomass, whose high-value transformation and utilization has been the most urgent problem to be solved. Herein, we propose a method for the preparation of porous carbon from lignin employing an H3PO4-assisted hydrothermal method. We characterize the as-prepared lignin-derived porous carbon and investigate its potential for energy storage. After assisted hydrothermal treatment followed by carbonization at 800 °C, the lignin-derived porous carbon displays a high specific capacitance (223.6 F·g–1 at 0.1 A·g–1) and excellent cycling ability with good capacitance retention. In this present study, the resultant lignin-derived porous carbon was used as the electrode of a supercapacitor, illustrating yet another potential high-value use for lignin, namely as a candidate for the sustainable fabrication of main supercapacitor components.

关键词： lignin     porous carbon     electrode     supercapacitor    

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Optimized porous clay heterostructure for removal of acetaldehyde and toluene from indoor air

Pu ZHAO,Lizhong ZHU

《环境科学与工程前沿（英文）》 2016年 第10卷 第2期   页码 219-228 doi: 10.1007/s11783-014-0760-z

摘要： Adsorption is the most widely used technology for the removal of indoor volatile organic compounds (VOCs). However, existing adsorbent-based technologies are inadequate to meet the regulatory requirement, due to their limited adsorption capacity and efficiency, especially under high relative humidity (RH) conditions. In this study, a series of new porous clay heterostructure (PCH) adsorbents with various ratios of micropores to mesopores were synthesized, characterized and tested for the adsorption of acetaldehyde and toluene. Two of them, PCH25 and PCH50, exhibited markedly improved adsorption capability, especially for hydrophilic acetaldehyde. The improved adsorption was attributed to their large micropore areas and high micropore-to-mesopore volume ratios. The amount of acetaldehyde adsorbed onto PCH25 at equilibrium reached 62.7 mg·g , eight times as much as the amount adsorbed onto conventional activated carbon (AC). Even at a high RH of 80%, PCH25 removed seven and four times more of the acetaldehyde than AC and the unmodified raw PCHs did, respectively. This new PCH optimized for their high adsorption and resistance to humidity has promising applications as a cost-effective adsorbent for indoor air purification.

关键词： porous clay heterostructure     volatile organic compounds     adsorption     adsorbent     indoor air    

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Maximum entropy based finite element analysis of porous media

Emad NOROUZI, Hesam MOSLEMZADEH, Soheil MOHAMMADI

《结构与土木工程前沿（英文）》 2019年 第13卷 第2期   页码 364-379 doi: 10.1007/s11709-018-0470-x

摘要： The maximum entropy theory has been used in a wide variety of physical, mathematical and engineering applications in the past few years. However, its application in numerical methods, especially in developing new shape functions, has attracted much interest in recent years. These shape functions possess the potential for performing better than the conventional basis functions in problems with randomly generated coarse meshes. In this paper, the maximum entropy theory is adopted to spatially discretize the deformation variable of the governing coupled equations of porous media. This is in line with the well-known fact that higher-order shape functions can provide more stable solutions in porous problems. Some of the benchmark problems in deformable porous media are solved with the developed approach and the results are compared with available references.

关键词： maximum entropy FEM     fully coupled multi-phase system     porous media    

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Hierarchically porous materials: Synthesis strategies and emerging applications

Minghui Sun, Chen Chen, Lihua Chen, Baolian Su

《化学科学与工程前沿（英文）》 2016年 第10卷 第3期   页码 301-347 doi: 10.1007/s11705-016-1578-y

摘要： Great interests have arisen over the last decade in the development of hierarchically porous materials. The hierarchical structure enables materials to have maximum structural functions owing to enhanced accessibility and mass transport properties, leading to improved performances in various applications. Hierarchical porous materials are in high demand for applications in catalysis, adsorption, separation, energy and biochemistry. In the present review, recent advances in synthesis routes to hierarchically porous materials are reviewed together with their catalytic contributions.

关键词： hierarchically porous materials     synthesis     application    

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Boron and nitrogen co-doped porous carbon derived from sodium alginate enhanced capacitive deionization

《化学科学与工程前沿（英文）》 2023年 第17卷 第12期   页码 2014-2024 doi: 10.1007/s11705-023-2346-4

摘要： Capacitive deionization can alleviate water shortage and water environmental pollution, but performances are greatly determined by the electrochemical and desalination properties of its electrode materials. In this work, B and N co-doped porous carbon with micro-mesoporous structures is derived from sodium alginate by a carbonization, activation, and hydrothermal doping process, which exhibits large specific surface area (2587 m2·g‒1) and high specific capacitance (190.7 F·g‒1) for adsorption of salt ions and heavy metal ions. Furthermore, the materials provide a desalination capacity of 26.9 mg·g−1 at 1.2 V in 500 mg·L‒1 NaCl solution as well as a high removal capacity (239.6 mg·g‒1) and adsorption rate (7.99 mg·g‒1·min‒1) for Pb2+ with an excellent cycle stability. This work can pave the way to design low-cost porous carbon with high-performances for removal of salt ions and heavy metal ions.

关键词： capacitance deionization     porous carbon     B/N co-doping     heavy metal ions     water purification    

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The role of single deformed bubble on porous foam tray with submerged orifices on the mass transfer enhancement

《化学科学与工程前沿（英文）》 2023年 第17卷 第12期   页码 2127-2143 doi: 10.1007/s11705-023-2363-3

摘要： Foam trays with porous submerged orifices endow bubbles uniformly distributed, which are considered attractive column internals to enhance the gas-liquid mass transfer process. However, its irregular orifice and complex gas-liquid flow make it lack pore-scale investigations concerning the transfer mechanism of dynamic bubbling. In this work, the actual porous structure of the foam tray is obtained based on micro computed tomography technology. The shape, dynamic, and mass transfer of rising bubbles at porous orifices are investigated using the volume of fluid and continue surface force model. The results demonstrate that the liquid encroaching on the gas channels causes the increasing orifices velocity, which makes the trailing bubble easily detach from the midst of the leading bubble and causes pairing coalescence. Additionally, we found that the central breakup regimes significantly improve the gas-liquid interface area and mass transfer efficiency. This discovery exemplifies the mechanism of mass transfer intensification for foam trays and serves to promote its further development.

关键词： bubble formation     porous submerged orifices     process intensification     foam tray    

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标题 作者 时间 类型 操作

Fabrication of coconut shell-derived porous carbons for CO adsorption application

期刊论文

S-enriched porous polymer derived N-doped porous carbons for electrochemical energy storage and conversion

Chao Zhang, Chenbao Lu, Shuai Bi, Yang Hou, Fan Zhang, Ming Cai, Yafei He, Silvia Paasch, Xinliang Feng, Eike Brunner, Xiaodong Zhuang

期刊论文

Tuning porosity of coal-derived activated carbons for CO2 adsorption

期刊论文

Cobalt nanoparticle decorated N-doped carbons derived from a cobalt covalent organic framework for oxygen

期刊论文

实现“不可行”的共聚反应以构筑氮掺杂多孔碳的理想聚合物前驱体

亓士超, 陆筱杰, 楼寅聪, 周睿, 薛丁铭, 刘晓勤, 孙林兵

期刊论文

Activated carbons and amine-modified materials for carbon dioxide capture –– a review

Zhenhe CHEN, Shubo DENG, Haoran WEI, Bin WANG, Jun HUANG, Gang YU

期刊论文

Characteristics of typical dissolved black carbons and their influence on the formation of disinfection

期刊论文

Fabrication, characterization and evaluation of mesoporous activated carbons from agricultural waste:

Lei YU,Chen TU,Yongming LUO

期刊论文

Chitosan/polyethylene glycol impregnated activated carbons: Synthesis, characterization and adsorption

Ehsan Salehi, Fereshteh Soroush, Maryam Momeni, Aboulfazl Barati, Ali Khakpour

期刊论文

Fabricating sustainable lignin-derived porous carbon as electrode for high-performance supercapacitors

期刊论文

Optimized porous clay heterostructure for removal of acetaldehyde and toluene from indoor air

Pu ZHAO,Lizhong ZHU

期刊论文

Maximum entropy based finite element analysis of porous media

Emad NOROUZI, Hesam MOSLEMZADEH, Soheil MOHAMMADI

期刊论文

Hierarchically porous materials: Synthesis strategies and emerging applications

Minghui Sun, Chen Chen, Lihua Chen, Baolian Su

期刊论文

Boron and nitrogen co-doped porous carbon derived from sodium alginate enhanced capacitive deionization

期刊论文

The role of single deformed bubble on porous foam tray with submerged orifices on the mass transfer enhancement

期刊论文