• Carbon letters
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• 제10권2호
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• pp.114-122
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• 2009

Crushed, depitted peach stones were impregnated activated with 50% $H_3PO_4$ followed by pyrolysis at $500^{\circ}C$. Two activated carbons were produced, one under its own evolved gases during pyrolysis, and the second conducted with air flow throughout the carbonization stage. Physicochemical properties were investigated by several procedures; carbon yield, ash content, elemental chemical analysis, TG/DTG and FTIR spectra. Porosity characteristics were determined by the conventional $N_2$ adsorption at 77 K, and data analyzed to get the major texture parameters of surface area and pore volume. Highly developed activated carbons were obtained, essentially microporous, with slight effect of air on the porous structure. Oxygen was observed to be markedly incorporated in the carbon matrix during the air treatment process. Cation exchange capacity towards Cu (II) and Cd (II) was tested in batch single ion experimental mode, which proved to be slow and a function of carbon dose, time and initial ion concentration. Copper was up taken more favorably than cadmium, under same conditions, and adsorption of both cations was remarkably enhanced as a consequence of the air treatment procedure. Sequestration of the metal ions was explained on basis of the combined effect of the oxygen functional groups and the phosphorous-containing compounds; both contributing to the total surface acidity character.

• Asian Journal of Atmospheric Environment
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• 제10권2호
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• pp.99-113
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• 2016

In order to improve the portability of basic absorbents monoethanolamine (MEA) and glycine (Gly), both were supported on microporous activated carbon (AC). Chemical modification by alkali-metal ion exchange (of Li, Na, K) was carried out on Gly-based absorbents. All supported absorbents were subjected to $CO_2$ absorption capacity (pure $CO_2$) and selectivity (indoor level) tests. Textural and chemical characterizations were carried out on test sorbents. All impregnation brought about significant reduction of specific surface area and microporosity of the adsorbent Depreciation in the textural properties was found to result to reduction in pure $CO_2$ sorption. Contrarily, low-level $CO_2$ removal capacity was enhanced as the absorbent dosage increases, resulting in supported 5 molar MEA in methanol solution. Adsorption capacities were improved from 0.016 and 0.8 in raw ACs to 1.065 mmol/g for MEA's. Surface chemistry via X-ray photoelectron spectroscopy (XPS) of the supported sorbents showed the presence of amine, pyrrole and quaternary-N. In reducing sequence of potency, pyridine, amine and pyrrolic-N were noticed to contribute significantly to $CO_2$ selective adsorption. Furthermore, the adsorption isotherm study confirms the presence of various SNGs heterogeneously distributed on AC. The adsorption mechanism of the present AC adsorbents favored Freundlich and Langmuir isotherm at lower and higher $CO_2$ concentrations respectively.

• 멤브레인
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• 제18권1호
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• pp.75-83
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• 2008

본 연구에서는 Polyethylene (PE, Asahi) 이차전지용 막의 표면불소화를 통해 기계적 강도 및 열적 안정성과 고출력에서의 안정성을 높이기 위한 연구를 실시하였다. 전자주사현미경(scanning electron microscope, SEM), 접촉각(contact angle)을 통하여 불소가스 노출시간에 따른 막의 표면과 구조의 변화를 관찰하고, 인장강도와 표면 친수성 실험을 통하여 막의 기계적 물성을 확인하였다. 제조된 막의 전기화학적 특성을 확인하기 위하여 충/방전 실험, 수명특성. 고율방전시험을 실시하여 고출력에서 온도에 대한 안정성이 향상되었음을 확인하였다.

• 공업화학
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• 제35권4호
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• pp.352-359
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• 2024

Environmental pollution from heavy metal ions (HMIs) is a global concern. Recently, biosorption methods using cellulose sorbents have gained popularity. The objective of this study was to assess the removal efficiency of Cu(II), Pb(II), and Hg(II) ions at low concentration levels (100-700 ppb) from aqueous solutions using three different cellulose fiber-based filter media. Sample A was pure cellulose fiber, Sample B was 10% activated carbon-cellulose fiber, and Sample C was cellulose fiber-glass fiber-30% activated carbon-20% amorphous titanium silicate (ATS). The samples were characterized by several physicochemical techniques. The porosity measurements using N₂ sorption isotherms revealed that Samples A and B are nonporous or macroporous materials, whereas the addition of 50% filler materials into the cellulose resulted in a microporous material. The Brunauer-Emmett-Teller (BET) surface area and pore volume of Sample C were found to be 320.34 m²/g and 0.162 cm³/g, respectively. The single ion batch adsorption experiments reveal that at 700 ppb initial metal ion concentration, Sample A had removal efficiencies of 7.5, 11.5, and 13.7% for Cu(II), Pb(II), and Hg(II) ions, respectively. Sample B effectively eliminated 99.6% of Cu(II) ions compared to Pb(II) (14.2%) and Hg(II) (31.9%) ions. Cu(II) (99.37%) and Pb(II) (96.3%) ions are more efficiently removed by Sample C than Hg(II) (68.2%) ions. The X-ray photoelectron spectroscopy (XPS) wild survey spectrum revealed the presence of Cu(II), Pb(II), and Hg(II) ions in HMI-adsorbed filter media. The high-resolution C1s spectra of Samples A and B reveal the presence of -C-OH and -COOH groups on their surface, which are essential for HMIs adsorption via complexation reactions. Additionally, the ATS in Sample C facilitates the adsorption of Pb(II) and Hg(II) ions through ion exchange.

• 한국막학회:학술대회논문집
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• 한국막학회 1996년도 춘계 총회 및 학술발표회
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• pp.16-19
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• 1996

Separation with synthetic membrane have become increasingly important processes in many fields. In the most application of membrane process, polymer membrane is used. the main advantage of polymers as a material for membrane preparation is the relative simplicity of this film formation which enables one to obtain rather high permeability rates. However, polymeric membranes have several limitations, such as high temperature instability, swelling and decomposition in organic solvent, et. al.. These limitations can be overcome by inorganic membrane. At the present time, commercially available inorganic membranes have pore diameters ranging 5nm to 50mm, and the predominant flow regime in such membrane is Knudsen diffusion. Since the Knudsen permeability is directly proportional to the molecular velocity, gases can be separated due to their molecular masses. However, this separation mechanism is only of important for light gases such as H2 and He. Other separation mechanisms like surface diffusion, active diffusion can play an important role only with very small pore diameters(2nm) and give rise to large permselectivities. Therefore, preparation of inorganic membrane with nano-sized pore have been attracting more and more attention.

• 폴리머
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• 제27권4호
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• pp.307-312
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• 2003

고밀도 폴리에틸렌 (HDPE)과 초고분자량 폴리에틸렌 (UHMWPE)을 혼합하여 중공사막을 제조하고, 이의 형태구조와 물성 변화를 조사하였다. 분자량 측정과 FT-IR을 이용한 분석 결과, 상품화된 중공사막(Sterapore)은 고분자량의 HDPE로 제조되었으며, 표면은 친수성 고분자인 비닐 알코올/비닐 아세테이트 공중합체로 코팅되어 높은 수투과도를 갖는 이유를 규명하였다. HDPE/UHMWPE 블렌드에서 UHMWPE의 혼합 한계 조성비는 10 wt% 이하이며, UHMWPE의 분산성을 높이기 위하여 혼합과정에서 광유를 도입하여야 할 것으로 판단되었다. 제조된 HDPE/UHMWPE 블렌드 중공사의 기계적 물성과 막 구조는 Sterapore와 유사하였다.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2009년도 추계학술발표대회
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• pp.46.1-46.1
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• 2009

산업이 점차 발달함에 따라 발생하는 환경오염으로 인해 인간의 삶에 있어 불가분의 관계에 있는 물에 대한 관심이 지속적으로 높아지고 있는 추세이다. 각종 질병의 요인이 되는 박테리아는 주로 물을 운송 매개체로 하기 때문에 이로 인한 물의 오염으로 인도의 경우 모든 질병 발생의 80%를 차지하는 것으로 세계보건기구(WHO)에 의해 보고되었다. 현재까지물 또는 공기의 항균 및 살균 정화를 위해 화학적, 생물학적 방식 등 다양한 기술이 개발되었으나 박테리아와같은 세균제거에는 무리가 있는 실정이다. 따라서 본 연구에서는 여러 물질 중에서도 특히 항균작용(Antibacterial activity)이 탁월한 은(Ag)을 나노입자화하여 in-situ 코팅을 통한 다공성 알루미늄 하이드록사이드 나노복합재의 제조함으로써 생물학, 생체의용공학, 약학 등에 응용될 수 있는 새로운 형태의 항균재료제조방법을 제안하였다. 우선, 다공성 알루미늄 하이드록사이드기판은 알루미늄 기판에 알칼리 표면개질을 실시함으로서 표면에 마이크로포어가 형성된 알루미늄 하이드록사이드 기판을 제조하였다. 이렇게 제조된 다공성 기판에 Polyol 공정으로 은나노입자를 합성 및 분산시킴으로서 in-situ로 은나노입자가 분산된 알루미늄 하이드록사이드 나노복합재 기판을 만들수 있었다. 본 연구를 통하여 제조된 은나노입자가 분산된 알루미늄 하이드록사이드 나노복합재 기판은 주사전자현미경(SEM) 및 투과전자현미경(TEM)을 통하여 미세구조와 상분석을 실시하였으며 X선 광전자분석(XPS)를 이용하여 기판 표면의 화학적 상태를 분석하였다.

• Carbon letters
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• 제11권3호
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• pp.192-200
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• 2010

Common reed (Fragmites australis), a local invasive grass, was investigated as a possible feedstock for the production of activated carbon. Dried crushed stems were subjected to impregnation with phosphoric acid (30, 40 and 50%) followed by pyrolysis at $400{\sim}500^{\circ}C$ with final washing and drying. Obtained carbons were characterized by determining: carbon yield, ash content, slurry pH, textural properties and capacity to remove color bodies from factory-grade sugar liquor. Produced carbons possessed surface area up to 700 $m^2/g$, total pore volumes up to 0.37 $cm^3/g$, and proved to be microporous in nature. Decolorization of hot sugar liquor at $80^{\circ}C$ showed degrees of color removal of 60 up to 77% from initial color of 1100~1300 ICU, at a carbon dose of 1.0 g/100 ml liquor. No correlation seems to hold between synthesis conditions and % R but depends on the degree of microporosity. A commercial activated carbon N showed a comparative better color removal capacity of 91%. Common reed proved to be a viable carbon precursor for production of good adsorbing carbon suitable for decolorization in the sugar industry, as well as in other environmental remediation processes.

• 한국염색가공학회지
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• 제17권4호
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• pp.27-34
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• 2005

In order to prepare acetate nano filter for the adsorption of nicotine/tar in tobbaco, acetate nano fiber was fabricated by elecrospining from acetate solution dissolved in acetone/DMAc(2/1). Above a critical polymer concentration($15\%$), the nano fiber was formed. The average diameter of nano fiber was decreased with the applied voltage and increased with the feeding rate. Appropriate spinning condition was considered to be $15wt\%$ polymer concentration, 11.25kV applied voltage, 0.6ml/h feeding rate, and 13-15cm TCD. Using the nano fiber, acetate nano filter was fabricated. It showed good nicotine/tar adsorption ability compared with general tobbaco filter. It was considered that the increase of surface area and the development of microporous structure in filter was much affected to the adsorption of nicotine/tar.

• 멤브레인
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• 제23권2호
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• pp.136-143
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• 2013

최근 큰 각광을 받고 있는 표면개질소재 중 하나인 도파민은 알칼리 수용액상에서 자발적으로 반응이 진행되어 금속, 고분자 등 거의 모든 소재에 강하게 흡착되는 물질로 흡착 메커니즘 및 반응 후 최종구조에 관해 많은 논란이 있다. 기존의 도파민의 최종구조는 aryl-aryl 결합에 의한 고분자 구조가 제안되었지만, 본 연구에서는 구조분석을 통해 기존에 제안된 aryl-aryl 결합이 형성되지 않는 결과와 열적거동을 통해 고분자의 특징이 나타나지 않는 것을 확인하였으며, 기체투과거동을 통해 고분자와 같이 비다공성 코팅층을 형성하지 못하는 결과를 토대로, 도파민의 최종구조는 2차 결합에 의한 초분자 구조로 서로 응집되어 있는 것으로 판단된다.