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DESIGNED MONOMERS AND POLYMERS · 2018 · IF 1.37

Synthesis of soluble oligsiloxane-end-capped hyperbranched polyazomethine and their application to CO2/N2 separation membranes

Liang Xu,Tianyang Lei,Boyu Jing,Yu Zang,Fengjuan Miao,Toshiki Aoki,Masahiro Teraguchi,Takashi Kaneko

Three soluble hyperbranched polyazomethines containing oligosiloxane end group HBP-PAZ-SiOn were successfully synthesized. HBP-PAZ-SiOns were used as modifiers of ethyl cellulose (EC) and polysulfone (PS) membranes. Blend membranes, HBP-PAZ-SiOn/EC and HBP-PAZ-SiOn/PS were prepared by blending the THF solution of HBP-PAZ-SiOn with ethanol solution of EC and dichloromethane solution of PS, respectively. Surprisingly, the permeabilities for CO2 of the blend membranes were more than 15–16 times higher than those of pure EC and PS membranes without any drop of pemselectivity to N2. This unusual improvement has been achieved by both enhancement of diffusivity for carbon dioxide and nitrogen by the oligosiloxane groups and enhancement of affinity of the amino groups with carbon dioxide at the end groups of HBP-PAZ-SiOn.

CAS / MDL: 626-19-7 108-78-1
研究领域: 材料科学 · 化学工程
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JOURNAL OF MEMBRANE SCIENCE · 2023 · IF 9.5

PEO-based mixed matrix membranes containing N-doped microporous carbon microparticles for enhanced CO2/N2 separation

Run Li,Ying Yang,Zezhou Zhang,Shaohan Lian,Quan Zhao,Chunfeng Song

As a promising strategy to reduce greenhouse gas emissions, carbon dioxide capture from industrial and power plants has been proposed. Due to its advantages of low consumption and a modest environmental impact, membrane technology has been widely used in the gas separation process. Advanced porous fillers can be successfully added into the polymer matrix to create mixed matrix membranes (MMMs) with simple processing and applicable gas separation performance. The high porosity and stability of microporous carbon materials make them desirable for use in the gas separation process. Herein, N-doped microporous carbon microparticles (NMCP) were successfully synthesized and incorporated into UV crosslinked polyethylene oxide (XLPEO) matrix membranes. Fast CO 2 transport channels are created in MMMs by rationally constructing NMCP fillers with ultra-micropores (∼0.53 nm), high-content heteroatoms (N, 13.94%), and two-dimensional morphology. The relationship between the structure of the NMCP samples and the gas separation performance of MMMs was discussed. Additionally, tests were conducted on the effects of NMCP loading, operating conditions, and long-term stability of NMCP/XLPEO membranes. NMCP/XLPEO membranes with a 2.5 wt% NMCP loading displayed a CO 2 permeability of 606 Barrer and a CO 2 /N 2 selectivity of 56.4, approaching the 2019 upper bound. This work offers a novel perspective to build fast gas transport channels in porous carbon-based MMMs for carbon capture.

CAS / MDL: 26570-48-9
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Boosting the CO2/N2 selectivity of MMMs by vesicle shaped ZIF-8 with high amino content

Rui Ding,Ziheng Li,Yan Dai,Xiangcun Li,Xuehua Ruan,Jiaming Gao,Wenji Zheng,Gaohong He

The amino functionalization of MOFs has been verified to be effective in improving the selective permeation of CO 2 . However, the introduction of amino groups into ZIF-8 by mixed ligands strategy is hard to achieve due to the high steric hindrance of benzene ring in 2-aminobenzimidazole ligand, resulting in insufficient content of amino groups. Therefore, in this work, polystyrene-acrylate (PSA) template is proposed to provide abundant adsorption and reaction sites for the rapid synthesis of NH 2 -ZIF-8 with high content of 2-aminobenzimidazole. Furthermore, the incomplete etching strategy is used to construct PSA modified hollow NH 2 -ZIF-8 nanospheres (PHNZ). Importantly, the thickness of PSA layer and the hollow size are adjusted by the etching time, as revealed by the SEM and TEM images. In this PHNZ, the modified PSA can provide good interface compatibility between PHNZ and Pebax matrix to enhance the CO 2 selectivity, while the hollow structure can reduce the mass transfer resistance and improve the gas permeability. Moreover, the introduced amino groups can enhance the CO 2 affinity of PHNZ and further improve the CO 2 /N 2 selectivity of the PHNZ-based mixed matrix membranes (MMMs). Benefiting from the synergy of good interface compatibility and enhanced CO 2 affinity from the amino groups, the PHNZ/Pebax MMMs present greatly improved CO 2 /N 2 selectivity in contrast with pure Pebax and NH 2 -ZIF-8 based membranes. Besides, as the etching time increases, the PHNZ-2 and PHNZ-3 based MMMs present a higher CO 2 permeability than that of NH 2 -ZIF-8 based MMM, revealing the significance of the hollow structure. The PHNZ-2/Pebax MMM with filler loading of 10 wt% expresses the best gas separation performance with the CO 2 permeability of 121.9 Barrer and CO 2 /N 2 selectivity of 96.6, respectively, showing an increase of 54.7 % and 98.0 % in contrast with pure Pebax membrane. Meanwhile, this CO 2 separation performance is far beyond the Robeson upper bound in 2008 and close to the McKeown upper bound in 2019, demonstrating that the proposed PHNZ displays a promising and competitive potential in MMM based CO 2 capture.

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Membranes · 2021 ·Vol. 11 ·期 9 ·693 · IF 4.106

A Novel Composite Material UiO-66@HNT/Pebax Mixed Matrix Membranes for Enhanced CO2/N2 Separation

Fei Guo,Bingzhang Li,Rui Ding,Dongsheng Li,Xiaobin Jiang,Gaohong He,Wu Xiao

Mixing a polymer matrix and nanofiller to prepare a mixed matrix membrane (MMM) is an effective method for enhancing gas separation performance. In this work, a unique UiO-66-decorated halloysite nanotubes composite material (UiO-66@HNT) was successfully synthesized via a solvothermal method and dispersed into the Pebax-1657 matrix to prepare MMMs for CO2/N2separation. A remarkable characteristic of this MMM was that the HNT lumen provided the highway for CO2diffusion due to the unique affinity of UiO-66 for CO2. Simultaneously, the close connection of the UiO-66 layer on the external surface of HNTs created relatively continuous pathways for gas permeation. A suite of microscopy, diffraction, and thermal techniques was used to characterize the morphology and structure of UiO-66@HNT and the membranes. As expected, the embedding UiO-66@HNT composite materials significantly improved the separation performances of the membranes. Impressively, the as-obtained membrane acquired a high CO2permeability of 119.08 Barrer and CO2/N2selectivity of 76.26. Additionally, the presence of UiO-66@HNT conferred good long-term stability and excellent interfacial compatibility on the MMMs. The results demonstrated that the composite filler with fast transport pathways designed in this study was an effective strategy to enhance gas separation performance of MMMs, verifying its application potential in the gas purification industry.Keywords:composite material;UiO-66;HNT;mixed matrix membrane;CO2/N2separation

CAS / MDL: 62-31-7 10026-11-6
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JOURNAL OF POROUS MATERIALS · 2025 · IF 3.2

Sustainable waste Biomass-Derived porous carbons with superior hierarchical porosity for High-Performance CO2 capture

Shen Fumin,Yao Shunyang,Pei Yuanchao,Sun Rubin

The increasing levels of carbon dioxide (CO 2 ) emissions driven by industrial activities highlight the urgent need for the development of efficient and sustainable CO 2 capture technologies. Biomass-derived porous carbons have emerged as promising candidates for CO 2 adsorption due to their low cost, high surface area, and adjustable pore structure. In this study, hierarchically porous carbons (HPCs) were synthesized from waste acer truncatum wood through pre-carbonization and subsequent KOH activation. The synthesis conditions, including activation temperature and activating agent concentration, were optimized to precisely tailor the pore architecture. The resulting HPC exhibited excellent CO 2 adsorption capacities of 7.56 mmol·g⁻ 1 at 0 °C and 4.29 mmol·g⁻ 1 at 25 °C under ambient pressure. Notably, ultramicropores (< 0.7 nm) exhibited a dominant role in CO 2 capture at low pressures, while narrow micropores (< 1.0 nm) contributed significantly across a range of low-pressure conditions. The hierarchical pore structure enhanced CO 2 uptake at higher pressures. Furthermore, the material demonstrated exceptional CO 2 /N 2 selectivity, reaching up to 112 at 0.15 bar and 0 °C, along with good cyclic stability, highlighting its potential in post-combustion CO 2 capture. This work provides a sustainable strategy for converting waste biomass into high-value adsorbents, offering a solution that addresses both environmental concerns and economic feasibility.

研究领域: 环境科学 · 材料科学 · 碳材料 · 气候变化缓解 · 吸附技术
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JOURNAL OF MEMBRANE SCIENCE · 2026 · IF 9

Stepwise growth for preparing highly loaded ZIF-8 ultrathin mixed matrix membranes towards efficient CO2/N2 separation

Peng Li,De Ao,Zhenjie Gu,Zhihua Qiao,Chongli Zhong

Metal-organic framework (MOF)-based membranes show promising potential for gas separation. However, it remains challenging to fully exploit the synergistic advantages of MOF crystals and polymers for fabricating highly loaded mixed matrix membranes (MMMs). Herein, a highly loaded ZIF-8 ultrathin MMM was prepared in situ via a stepwise growth strategy. Driven by the diffusion rate difference between the ligand and polyethyleneimine (PEI-600), preferentially formed ZIF-8 crystals served as the dominant phase, while the subsequently developed PEI-Zn 2+ crosslinked network acted as an intergranular densification phase. Owing to the reduction in ZIF-8 crystal size induced by PEI, the MMMs exhibited an ultrathin thickness of only 160 nm. Furthermore, PEI enhanced the molecular sieving ability of crystals and membrane's CO 2 /N 2 solubility selectivity by regulating the pore structure and membrane composition. With a high ZIF-8 loading of 84.3 %, the resulting MMMs demonstrated an excellent CO 2 permeance of 3177.4 GPU, accompanied by a CO 2 /N 2 selectivity of 36.9. Notably, it maintained stable separation performance after bending and during long-term operation, showing good processability and industrial application potential. This strategy not only reinforces the advantages of MOF-based gas separation membranes but also provides a new paradigm for fabricating highly loaded MMMs.

CAS / MDL: 10196-18-6
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2017 · IF 2.726

Absorption performance of (CO2 + N2) gas mixtures in amino acid ionic liquids promoted N-methyldiethanolamine aqueous solutions

Dong Fu,Xue Feng,Pan Zhang

Amino acid ionic liquids (AAILs) including 1-butyl-3-methylimidazolium glycinate ([Bmim][Gly]), 1-butyl-3-methylimidazolium L -lysinate ([Bmim][Lys]) and tetramethylammonium glycinate ([N 1111 ][Gly]) were used to enhance the absorption of CO 2 in N -methyldiethanolamine (MDEA) aqueous solutions. The mole fractions of CO 2 in N 2   +   CO 2 gas mixtures ranged from 0.2 to 1.0. The mass fractions of MDEA and AAILs respectively ranged from 0.300 to 0.400 and 0.050 to 0.100. The absorption capacity and absorption rate under series of conditions were presented and the influences of CO 2 partial pressure and the types of AAILs on the absorption performance were demonstrated.

研究领域: 化学工程 · 环境科学
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ACS Applied Polymer Materials · 2026 · IF 5.2

Thermally Tailored Amidoxime-Functionalized PIM-1 Membranes with CO2-Imprinted UiO-66-NH2 for CO2/N2 Separation

Ziyi Yuan,Zhihong Lin,Kejing Li,Jian Li,Viatcheslav Freger,Xuezhong He

Polymers of intrinsic microporosity (PIMs) are promising membrane materials for CO2 separation due to their high permeability; however, their limited CO2/N2 selectivity restricts practical application. Herein, mixed-matrix membranes (MMMs) were fabricated by incorporating a CO2-molecularly imprinted UiO-66-NH2 filler (MIP@U) into amidoxime-functionalized PIM-1 (AOPIM-1), followed by thermal treatment at 160 or 250 °C under vacuum to regulate the membrane microstructure. Spectroscopic and porosity analyses (FTIR, XRD, and N2 physisorption) show that thermal treatment at 160 °C promoted oxadiazole-ring formation, leading to enhanced subnanometer microporosity and improved CO2/N2 selectivity. In contrast, treatment at 250 °C partially regenerates nitrile groups and generates larger micropores, resulting in higher CO2 permeability but reduced selectivity. The MIP@U filler introduces CO2-recognition cavities and improves interfacial compatibility, enabling synergistic control of polymer microporosity and interfacial transport pathways. The optimized 3 wt % MIP@U/AOPIM-1-TR160 membrane achieves a CO2 permeability of ∼1600 Barrer and a CO2/N2 selectivity of 50.8. The membrane also demonstrates stable performance under pressures up to 12 bar and during 30 h of continuous operation at 2 bar. This study highlights a dual-approach strategy combining thermally tailored PIM chemistry with molecularly imprinted MOF fillers for designing high-performance MMMs for CO2 capture.

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INORGANIC CHEMISTRY · 2026 ·Vol. 65 ·期 35 ·20723-20730 · IF 4.6

Zr6–Cluster-Embedded ZIF-8 Membranes Fabricated by Electrochemical Deposition for CO2/N2 and CO2/CH4 Separation

Cong Shenzhen,Sun Si,Wang Ming,Zhang Yijing,Shen Qin,Zhang Yatao,Pang Huan

Membrane-based separation technology holds great promise for CO 2 capture, yet conventional membranes are often constrained by the permeability-selectivity trade-off. In this study, we developed a zirconium-cluster (Zr 6 )-incorporated ZIF-8 membrane via an electrochemical synthesis strategy to address this limitation. The resulting Zr 6 @ZIF-8 composite membrane exhibits high crystallinity, a dense microstructure, and homogeneous dispersion of Zr 6 clusters within the ZIF-8 framework. The optimized Zr 6 @ZIF-8–2 membrane demonstrates outstanding CO 2 separation performance with a CO 2 permeance of up to 300.0 gas permeation unit and CO 2 /N 2 and CO 2 /CH 4 selectivities of 27.0 and 14.8, respectively. The Zr 6 clusters enable effective structural regulation of ZIF-8 membranes, resulting in enhanced CO 2 separation performance and leading to improved diffusion selectivity. Furthermore, the membrane shows a stable separation performance under varying feed pressures and temperatures, along with excellent long-term operational stability. This work provides an effective electrochemical approach for fabricating high-performance MOF-based membranes, offering a promising candidate for industrial CO 2 capture and natural-gas purification.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2026 · IF 9.1

Regulating polymer transport resistance to enhance ZIF-8 contribution in mixed-matrix membranes for CO2/N2 separation

Jia Wang,Yizhen Situ,Wenyu Zheng,Weidong Zhang,Qingyuan Yang

Polymer transport resistance was tuned by controlling the solvent evaporation rate. • Reduced polymer transport resistance promoted a more effective contribution of ZIF-8 transport pathways to CO 2 /N 2 separation. • The 7.8 wt% in situ-grown MMM achieved a CO 2 permeability of 510 Barrer and a CO 2 /N 2 selectivity of 33.0. Beyond filler modification, regulating the polymer structure is also crucial for optimizing gas transport in mixed-matrix membranes (MMMs), yet this aspect remains insufficiently explored. Herein, the solvent evaporation rate was controlled to regulate the transport resistance of Pebax 2533 and elucidate its influence on the transport contribution of ZIF-8 in ZIF-8/Pebax MMMs for CO 2 /N 2 separation. For Pebax 2533 membranes, increasing the evaporation rate reduced both crystallinity and relative fractional free volume, resulting in a non-monotonic variation in CO 2 permeability and a decrease in CO 2 /N 2 selectivity. At a moderate evaporation rate of 2.5 × 10 −5  kg·m −2 ·s −1 , the balance between reduced crystallinity and preserved free volume resulted in lower polymer transport resistance, enabling the contribution of ZIF-8 to be more effectively translated into membrane separation performance. As a result, the in situ-grown MMM containing 7.8 wt% ZIF-8 achieved a CO 2 permeability of 510.0 Barrer and a CO 2 /N 2 selectivity of 33.0, with its CO 2 permeability exceeding that of most reported Pebax-based MMMs. This work demonstrates that controlling solvent evaporation is an effective strategy to regulate polymer transport resistance and enhance the contribution of ZIF-8 in MMMs. Download: Download high-res image (207KB) Download: Download full-size image

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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

In-situ synthesis of ZIF-8 gel network in mixed matrix membranes for enhanced CO2/N2 separations

Xiaoting Feng,Chenlu Liu,Kunkun Ren,Xinglei Zhao,Longjie Liu,Keming Zhang,Xiaohe Tian,Qingnan Wang,Xiangyu Liu,Yueyangchao Yu,Tianhe Gu,Shaofei Wang

The urgent need for efficient CO 2 capture technologies to mitigate climate change has driven the advancement of membrane-based separation systems. We report a mixed matrix membrane design through the in-situ growth of a ZIF-8 gel network within a Pebax-1657 matrix. By tuning the solvent ratio and concentration of modulator, ZIF-8 gel rather than particles are formed within the polymer, establishing a three-dimensional interconnected MOF network that ensures homogeneous filler dispersion and creates continuous gas transport nanochannels. The optimized membrane achieves a remarkable CO 2 permeability of 183.9 Barrer and a CO 2 /N 2 selectivity of 73.3, surpassing the 2008 Robeson upper bound. These values represent 190.4 % and 34.9 % enhancements in permeability and selectivity, compared to the pristine polymer. The membrane also demonstrates robust operational stability and maintains > 95 % of its initial performance over 60 days. This work offers a promising solution to creating continuous channels in CO 2 separation membranes.

CAS / MDL: 121-44-8
研究领域: 材料科学 · 化学工程 · 环境技术 · 膜分离 · 碳捕集
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

CO2 capture from CO2/N2 mixed gas using synthesized binder-free zeolite X pellets by adsorption technology

Nan Li,Penny Xiao,Weijie Liu,Liying Liu,Zijian Wang,Jian Wang,Peng Gao,Qi Wu,Xinchao Ma,Gang Kevin Li

Compared with traditional commercial adsorbent zeolite pellets, binder-free molecular sieves can provide better adsorption performance. In this paper, we reported a novel method to synthesize binder-free zeolite X pellets (BF-Z), that is, zeolite X powder was intricately combined with halloysite nanotubes (HNTs) using hydroxypropyl methylcellulose (HPMC), and then the sample was calcinated to form crystals, where HPMC was decomposed and HNTs was also completely converted into binder-free X zeolite. The synthesized BF-Z showed the highest CO 2 adsorption capacity of 4.98 mmol/g at 303 K and 1 bar, compared with commercial NaX zeolites produced by Jianlong, Sigma and UOP companies. Calculated by IAST model, the separation coefficient of CO 2 to N 2 (CO 2 /N 2  = 25/75) on BF-Z is 74 at 303 K and 1 bar. The great separation performance of CO 2 from N 2 (CO 2 /N 2  = 25/75) was also exhibited in breakthrough experiments and a designed VSA process. Compared with commercial NaX (UOP), in breakthrough experiment, BF-Z presented high CO 2 adsorption capacity and rapid adsorption rate; and in designed thirty six-step vacuum swing adsorption process (VSA), the six-bed VSA system using BF-Z as adsorbents demonstrated excellent separation performance such as high CO 2 purity and recovery, low energy consumption and enhanced CO 2 production capacity. The notable efficacy of BF-Z in CO 2 adsorption and separation underscores its promising utility in both commercial and industrial settings.

CAS / MDL: 9004-65-3
研究领域: 材料科学 · 环境科学 · 化学工程
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