• 제목/요약/키워드: post-synthetic modification

검색결과 6건 처리시간 0.017초

Enhanced Electrochemical Detection of Heavy Metal Ions via Post-synthetic Schiff Base Modification of MWCNT-MOF Composites

  • Yeon-Joo Kim;Seung-Ho Choi;Seon-Jin Choi
    • 센서학회지
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    • 제33권5호
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    • pp.366-372
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    • 2024
  • In this study, we present a novel approach to improve electrochemical heavy metal ion (HMI) sensing responses via post-synthetic modification of carbon nanotube-based metal-organic framework (MOF) nanocomposites with a Schiff base. UiO66-NH2 was employed as the MOF and incorporated with multi-walled carbon nanotubes (MWCNT) through in-situ growth, enhancing the electrical conductivity of the MWCNT-UiO66-NH2 composite. Subsequently, the Schiff base, which has been proven to be an excellent ligand for metal ion detection, was functionalized onto MWCNT-UiO66-NH2 via post-synthetic modification to improve its HMI absorption capacity. To evaluate the effect of the Schiff base on HMI detection capacity, electrochemical sensing of Cd2+, Pb2+, Cu2+, and Hg2+ was performed in an aqueous solution utilizing the MWCNT-UiO66-Schiff modified electrode as well as the bare electrode. Individual differential pulse anodic stripping voltammetry results revealed that the modified electrode with MWCNT-UiO66-Schiff exhibited increased HMI sensing properties, especially with 1.82-fold improvement in average oxidation currents toward 10 µM of Cu2+ compared to that for a bare glassy carbon electrode. The selective Cu2+-sensing properties of MWCNT-UiO66-Schiff were reflected in the highly selective Cu2-binding affinity of the Schiff base-containing model molecules compared to those of Cd2+, Hg2+, and Pb2+. Our work provides a new strategy for improving the sensing properties of electrochemical HMI sensors by the post-synthetic modification of MWCNT-UiO66 with a Schiff base.

Recent Progress on Adsorptive Removal of Cd(II), Hg(II), and Pb(II) Ions by Post-synthetically Modified Metal-organic Frameworks and Chemically Modified Activated Carbons

  • Rallapalli, Phani Brahma Somayajulu;Choi, Suk Soon;Ha, Jeong Hyub
    • 공업화학
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    • 제33권2호
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    • pp.133-144
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    • 2022
  • Fast-paced industrial and agricultural development generates large quantities of hazardous heavy metals (HMs), which are extremely damaging to individuals and the environment. Research in both academia and industry has been spurred by the need for HMs to be removed from water bodies. Advanced materials are being developed to replace existing water purification technologies or to introduce cutting-edge solutions that solve challenges such as cost efficacy, easy production, diverse metal removal, and regenerability. Water treatment industries are increasingly interested in activated carbon because of its high adsorption capacity for HMs adsorption. Furthermore, because of its huge surface area, abundant functional groups on surface, and optimal pore diameter, the modified activated carbon has the potential to be used as an efficient adsorbent. Metal-organic frameworks (MOFs), a novel organic-inorganic hybrid porous materials, sparked an interest in the elimination of HMs via adsorption. This is due to the their highly porous nature, large surface area, abundance of exposed adsorptive sites, and post-synthetic modification (PSM) ability. This review introduces PSM methods for MOFs, chemical modification of activated carbons (ACs), and current advancements in the elimination of Pb2+, Hg2+, and Cd2+ ions from water using modified MOFs and ACs via adsorption.

Stability of Proteasomes Extracted from Pressurized, Aged Skeletal Muscles

  • Yamamoto, Shuhei;Suzuki, Atsushi;Nishiumi, Tadayuki
    • Asian-Australasian Journal of Animal Sciences
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    • 제22권2호
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    • pp.282-288
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    • 2009
  • The present paper describes the effects of pressure and post-mortem aging treatments on in situ proteasome activity in rabbit and bovine skeletal muscles. Synthetic peptide hydrolyzing activity of rabbit proteasomes remained in the muscle after exposure to pressures up to 100 MPa. However, when a pressure of 400 MPa or more was applied, proteasomes were markedly inactivated. The extraction of proteasomes from excessively pressurized muscle appeared to be difficult. Proteasomes in aged muscle remained relatively stable throughout the aging process, with activity after 168 h (7 days) being 35%, 48%, 53% and 31% of the 0 h post-mortem LLVY, LSTR, AAF and LLE total hydrolyzing activities, respectively. The synthetic peptide hydrolyzing activities of bovine muscle proteasomes were similar to those of rabbit skeletal muscle proteasomes. The results suggest that synthetic peptide hydrolyzing activity remains in muscle exposed to relatively low pressures. Furthermore, it is known that high-pressure treatment induces fragmentation of myofibrils, modification of actin-myosin interaction and activation of intramuscular proteinases, cathepsins and calpains. Thus, proteasomes are probably involved in the tenderization process in combination with other intramuscular proteinases under high-pressure conditions. Our findings confirmed that proteasomes play a role in meat tenderization induced by high-pressure treatment or aging.

Enhanced Carbon Dioxide Adsorption on Post-Synthetically Modified Metal-Organic Frameworks

  • Ko, Na-Keun;Kim, Ja-Heon
    • Bulletin of the Korean Chemical Society
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    • 제32권8호
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    • pp.2705-2710
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    • 2011
  • Four MOFs functionalized with 1-Me, 1-Pr, 1-Ph, and 1-$PhCF_3$ were prepared through post-synthetic modifications of a metal-organic framework (MOF), UMCM-1-$NH_2$ (1) with acetic, butyric, benzoic, and 4-(trifluoromethyl)benzoic anhydrides, respectively. Methane adsorption measurements between 253 and 298 K at pressures up to 1 bar indicated that both 1-Ph and 1-$PhCF_3$ adsorbed more $CH_4$ than the parent MOF, 1. All the functionalized MOFs adsorbed more $CO_2$ than 1 under conditions similar to the $CH_4$ test. The introduction of functional groups promoted adsorption of both $CH_4$ and $CO_2$ despite significantly reducing Brunauer-Emmet-Teller (BET) surface area: 4170 (1), 3550 (1-Me), 2900 (1-Pr), 3680 (1-Ph), and 3520 $m^2/g$ (1-$PhCF_3$). Electron-withdrawing aromatic groups (1-Ph, 1-$PhCF_3$) more effectively enhanced $CO_2$ adsorption than electron-donating alkyl groups (1-Me, 1-Pr). In particular, 1-Ph adsorbed 23% more $CO_2$ at 298 K and 50% more at 253 K than 1.

Glutamic Acid-Grafted Metal-Organic Framework: Preparation, Characterization, and Heavy Metal Ion Removal Studies

  • Phani Brahma Somayajulu Rallapalli;Jeong Hyub Ha
    • 공업화학
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    • 제34권5호
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    • pp.556-565
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    • 2023
  • Fast industrial and agricultural expansion result in the production of heavy metal ions (HMIs). These are exceedingly hazardous to both humans and the environment, and the necessity to eliminate them from aqueous systems prompts the development of novel materials. In the present study, a UIO-66 (COOH)2 metal-organic framework (MOF) containing free carboxylic acid groups was post-synthetically modified with L-glutamic acid via the solid-solid reaction route. Pristine and glutamic acid-treated MOF materials were characterized in detail using several physicochemical techniques. Single-ion batch adsorption studies of Pb(II) and Hg(II) ions were carried out using pristine as well as amino acid-modified MOFs. We further examined parameters that influence removal efficiency, such as the initial concentration and contact time. The bare MOF had a higher ion adsorption capacity for Pb(II) (261.87 mg/g) than for Hg(II) ions (10.54 mg/g) at an initial concentration of 150 ppm. In contrast, an increased Hg(II) ion adsorption capacity was observed for the glutamic acid-modified MOF (80.6 mg/g) as compared to the bare MOF. The Hg(II) ion adsorption capacity increased by almost 87% after modification with glutamic acid. Fitting results of isotherm and kinetic data models indicated that the adsorption of Pb(II) on both pristine and glutamic acid-modified MOFs was due to surface complexation of Pb(II) ions with available -COOH groups (pyromellitic acid). Adsorption of Hg(II) on the glutamic acid-modified MOF was attributed to chelation, in which glutamic acid grafted onto the surface of the MOF formed chelates with Hg(II) ions.

다결정 금속 유기 골격체 분리막의 후처리 성능 제어기술 개발 동향 (Reviews on Post-synthetic Modification of Metal-Organic Frameworks Membranes)

  • 권혁택;엄기원
    • 멤브레인
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    • 제32권6호
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    • pp.367-382
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    • 2022
  • 유기 전구체와 금속 이온, 또는 금속-옥소 클로스터 간의 규칙적 배열을 통한 종의 다양성을 장점으로 하는 금속-유기 골격체(Metal-Organic Frameworks, MOFs)는 에너지 사용량이 높은 상변화 기반 분리공정을 대체할 수 있는 에너지 효율적인 막 기반 분리 기술의 개발 가능성을 열어주었다. 이에 최근 10년 동안 다결정 MOFs 분리막 합성 기술에서 상당한 진전이 있었지만, 매우 제한된 종류의 MOFs만이 활용되고 있다. 이러한 기술 개발의 정체는 다결정 분리막의 비 선택적인 확산 경로인 결정 사이 결함(intercrystalline defects)에 대한 명확한 해결법이 없기 때문이다. 후처리 성능 제어기술(postsynthetic modifications, PSMs)은 기존 분리막을 플랫폼으로 활용하고 이를 물리적 그리고/혹은 화학적으로 처리함을 통해 분리 특성을 개선 혹은 변경하는 기술을 말한다. PSMs 기술은 특정 분리막을 개발하는 데 있어서 새로운 MOFs를 설계하거나 막 합성 기술을 개발하지 않아도 된다는 장점이 있어서 다결정 MOF 분리막의 다양성을 제공하기 위한 새로 부상하는 전략으로 평가 된다. 본 총설에서는 PSMs 기술을 7개의 세부기술((1) 공유결합법, (2) 결정간 결함 플러깅법, (3) 결정 내부 결함 치유법, (4) 기공내 기능성 소재 함침법, (5) 기공 경화법, (6) 전구체 치환법 및 (7) 비정질화법)로 분류하고, 각 세부기술의 연구 동향 및 도전과제 그리고 향후 연구 방향에 대해 논의하고자 한다.