Active clays, Diatomite, bentonite and zeolite were used as porous materials for fabricating hygroscopic gypsum boards. Pohang active clay and Cheolwon diatomite showed excellent characteristics of moisture adsorption and desorption. These characteristics were caused by higher surface area and pore volume of porous materials. Moisture adsorption content of gypsum board with 10% active clay(P1) was 62.0 g/m2, and moisture desorption content was 50.2 g/m2. Moisture adsorption content of gypsum board with 10% diatomite(P) was 59.5 g/m2, and moisture desorption content was 49.0 g/m2. Moisture adsorption contents of gypsum boards with porous materials were higher than that moisture desorption contents of gypsum board without porous materials. Correlation coefficient between surface area and moisture adsorption content of gypsum boards was 0.98. Also, correlation coefficient between surface area and moisture desorption content of gypsum boards was 0.97. Moisture adsorption and desorption contents were influenced by surface area and pore volume of the gypsum boards, and surface area had a larger effect on moisture adsorption and desorption.

In this study, porous electrospun carbon fibers were prepared by electrospinning with PAN and MgCl2, as a MgO precursor. MgO was selected as a substrate because of its chemical and thermal stability, no reaction with carbon, and ease of removal after carbonization by dissolving out in acidic solutions. MgCl2 was mixed with polyacrylonitrile (PAN) solution as a precursor of MgO with various weight ratios of MgCl2/PAN. The average diameter of porous electrospun carbon fibers increased from 1.3 to 3 μm, as the MgCl2 to PAN weight ratio increased. During the stabilization step, MgCl2 was hydrolyzed to MgOHCl by heat treatment. At elevated temperature of 823 K for carbonization step, MgOHCl was decomposed to MgO. Specific surface area and pore structure of prepared electrospun carbon fibers were decided by weight ratio of MgCl2/PAN. The amount of hydrogen storage increased with increase of specific surface area and micropore volume of prepared electrospun carbon fibers.

높은 포장온도는 아스팔트포장 소성변형의 주요인이나 소성변형을 줄이기 위한 방안으로서 포장온도를 줄이는 측면에서는 아직 많은 연구가 이루어지지 않은 실정이다. 본 연구에서는 소성변형결함을 줄이기 위한 하나의 대안으로, 온도저감 효과가 있는 것으로 알려져 있는 보수성 포장을 배수성 포장의 하부층에 설치한 포장의 공용특성을 연구하였다. 본 연구의 목적은 보수형 배수성 포장의 온도저감효과를 정량화하고, 포장가속시험(Accelerated Pavement Testing)을 이용하여 온도 저감에 따른 소성변형 감소효과를 확인하고, 정량화하는데 있다. 또한 추가적으로 보수성 포장의 상대강도계수를 분석하고, 일반 포장과 비교하여 설계법 적용시 포장두께를 줄일 수 있는지 여부를 알아보고자 하였다. 본 연구를 위해 보수형 배수성포장 2개 단면 및 일반 배수성 포장 1개 단면 등 총 3개 시험구간이 시공되었다. 히팅 및 살수를 일정주기로 실시하였으며 하중조건은 윤하중 8.2ton, 타이어 공기압 7.03kgf/cm2 타이어 접지면적 610cm2이었다. 이 연구에서 포장체 온도저감효과는 중간층의 경우 6.6~7.9℃(평균7.4℃), 표층의 경우 7.9~9.8℃(평균 8.8℃)였으며, 이를 통해 포장표면의 소성변형 발생을 26% 감소시킬 수 있었다. 또한 탄성계수로부터 추정된 보수성 포장의 상대강도계수는 0.173으로 일반 밀입도 포장의 1.2배 정도였으며, 일반배수성 포장 구간에서는 표층, 중간층, 기층 모두 소성변형이 발생한데 반해 보수형 배수성 포장 구간에서는 표층에서 대부분의 소성변형이 발생된 것으로 나타났다.

Disk type porous nickel membrane was fabricated by in-situ reduction/sintering process using compacted NiO/PMMA (PMMA; Polymethyl methacrylate) mixture at 800℃ in hydrogen atmosphere. The porosity (4958%) of these membrane was investigated as an amount of PMMA additive. The thermal decomposition and reduction behavior of NiO/PMMA were analyzed by TG/DTA in hydrogen atmosphere and the activation energy for the hydrogen reduction of NiO and thermal degradation of PMMA was calculated as 61.1 kJ/mol, evaluated by Kissinger method. Finally, the filtering performance and pressure drop were measured by particle counting system.

Ti scaffolds with a three-dimensional porous structure were successfully fabricated using powder metallurgy and modified rapid prototyping (RP) process. The fabricated Ti scaffolds showed a highly porous structure with interconnected pores. The porosity and pore size of the scaffolds were in the range of 66~72% and 300~400 μm, respectively. The sintering of the fabricated scaffolds under the vacuum caused the Ti particles to bond to each other. The strength of the scaffolds depended on the layering patterns. The compressive strength of the scaffolds ranged from 15 MPa to 52 MPa according to the scaffolds' architecture. The alkali treatment of the fabricated scaffolds in an aqueous NaOH solution was shown to be effective in improving the bioactivity. The surface of the alkali-treated Ti scaffolds had a nano-sized fibre-like structure. The modified surface showed a good apatite forming ability. The apatite was formed on the surface of the alkali treated Ti scaffolds within 1 day. The thickness of the apatite increased when the soaking time in a simulated body fluid (SBF) solution increased. It is expected that the surface modification of Ti scaffolds by alkali treatment could be effective in forming apatites in vivo and can subsequently enhance bone formation.

본 연구는 배수성 아스팔트 포장의 표면을 아크릴 수지로 코팅 처리할 경우 내구성 측면 및 기능적 측면에서 어떠한 효과가 있는가를 실내시험을 통해 평가하는 기초적인 연구이다. 포장의 내구성 측면에서는 칸타브로 및 휠트래킹, 수분손상 간접 인장 피로 시험 등을 실시하였다. 시험결과 시편을 수지로 코팅을 한 경우 칸타브로 손실률이 3배 정도 감소되었고 균열에 대한 저항성도 대폭 향상되었으나 수분손상 및 소성변형의 저항성은 큰 차이가 없는 것으로 나타났다. 기능적인 측면에서는 코팅 전 후의 투수계수 및 공극률 BPT(British Pendulum Tester)를 사용한 미끄럼 저항성의 변화를 측정하였다. 시험결과 공극률 및 투수계수는 약간 저하되나 기능상의 문제는 없을 것으로 판단되며, 미끄럼 저항성은 규사를 살포하지 않을 경우 미끄럼 저항성이 감소되나 규사를 살포할 경우 코팅 전 수준 이상의 미끄럼 저항성을 확보하는 것으로 나타났다.

To improve the filtration efficiency of porous materials used in filters, an extensive specific surface area is required to serve as a site for adsorption of impurities. In this paper, a method for creating a hybridized porous alloy using a powder metallurgical technique to build macropores in an Al-4 wt.% Cu alloy and subsequent surface modification for a microporous surface with a considerably increased specific surface area is suggested. The macropore structure was controlled by granulation, compacting pressure, and sintering; the micropore structure was obtained by a surface modification using a dilute NaOH solution. The specific surface area of surface-modified specimen increased about 10 times compare to as-sintered specimen that comprised of the macropore structure. Also, the surface-modified specimens showed a remarkable increase in micropores larger than 10 nm. Such a hybridized porous structure has potential for application in water and air purification filters, as well as membrane pre-treatment and catalysis.

Porous carbon materials synthesized from various plant derived precursors i.e. seeds of [Castor (Ricinus communis), Soap nut (Sapindus sp.), Cashew-nut (Semecarpus anacardium), Jack fruit (Artocarpus heterophyllus), Safflower (Carthamus tinctorius), Ambadi (Crotolaria juncea), Neem (Azadirachta indica), Bitter Almond (Prunus amygdalus), Sesamum (Sisamum indicum), Date-palm (Phoenix dactylifera),Canola (Brassica napus), Sunflower (Helianthus annulus)] and fibrous materials from [Corn stem- (Zea mays), Rice straw (Oryza sativa), Bamboo (Bombax bambusa) and Coconut fibers (Cocos nucifera)] were screened to make supercapacitor in 5M KOH solution. Carbon material obtained from Jack fruit seeds (92.0 F/g), Rice straw (83.0 F/g), Soap nut seeds (54.0 F/g), Castor seeds (44.34 F/g) and Bamboo (40.0 F/g) gave high capacitance value as compared to others. The magnitude of capacitance value was found to be inversely proportional to the scan rate of measurement. It is suggested that carbon material should possess large surface area and small pore size to get better value of capacitor. Moreover, the structure of carbon materials should be such that majority of pores are in the plane parallel to the plane of electrode and surface is fluffy like cotton ball.

Porous HAp with three-dimensional network channels was prepared in a polymer foam process using a in-situ formation. HAp/polyol with various HAp solid contents was formed with an addition of isocyanate. Under all conditions, the obtained porous HAp had pore sizes ranging 50 μm to 250 μm. The influence of the HAp content on the physical and mechanical properties of porous HAp scaffolds was investigated. As the solid content increased, the porosity of the porous HAp decreased from 79.3% to 77.9%. On the other hand, the compressive strength of the porous HAp increased from 0.7 MPa to 3.7 MPa. With a HAp solid content of 15 g, the obtained porous HAp had physical properties that were more suitable for scaffolds compared to other conditions.

지하수나 폐수 등에 포함된 독성을 가진 음이온류나 양이온류 등의 유독물질을 경제적으로 처리하는데 탁월한 분리기능을 가진 것으로 알려진 전기투석공정에 사용하기 위해 음이온 교환 복합막을 제조하여 그 전기화학적인 특성을 조사하였다. 다양한 조성의 vinylbenzylchloride (VBC)와 divinylbenzene (DVB) 그리고 α,α-azobis(isobutyronitrile) (AIBN)으로 이루어진 단량체 용액에 다공성 지지체인 poly(ethylene) (PE)을 함침한 후 열중합 가교시켜 poly(VBC-DVB)/PE 복합막을 생성한 다음 trimethylamine(TMA)과 acetone을 이용해 음이온 교환기(-N + (CH3)3)를 함유하는 복합막을 제조하였다. 음이온 교환막 제조시 VBC/DVB의 비율과 TMA/Acetone의 비율에 따른 막의 함수율, 이온교환용량(IEC) 및 전기저항을 조사하였다. 그 결과 제조된 막들은 사용된 PE지지체의 얇은 막두께에 기인하여 아스톰사의 상용화 음이온 교환막(AMX)보다 높은 IEC와 낮은 전기저항 및 낮은 함수율 등을 나타내는 것을 확인할 수 있었다. 본 실험에서 제조된 복합막은 저렴한 제조비용과 우수한 전기화학적 특성으로 정수 및 폐수처리를 위한 전기투석공정에 충분히 적용될 수 있음을 알 수 있었다.

Al-Cu alloy nano powders have been produced by the electrical explosion of Cu-plated Al wire. The porous nano particles were prepared by leaching for Al-Cu alloy nano powders in 40wt% NaOH aqueous solution. The surface area of leached powder for 5 hours was 4 times larger than that of original alloy nano powder. It is demonstrated that porous nano particles could be obtained by selective leaching of alloy nano powder. It is expected that porous Cu nano powders can be applied for catalyst of SRM (steam reforming methanol).

Porous Ti implant samples were fabricated by the sintering of spherical Ti powders in a high vacuum furnace. To increase their surface area and biocompatibility, anodic oxidation and a hydrothermal treatment were then applied. Electrolytes in a mixture of glycerophosphate and calcium acetate were used for the anodizing treatment. The resulting oxide layer was found to have precipitated in the phase form of anatase TiO2 and nano-scaled hydroxyapatite on the porous Ti implant surface. The porous Ti implant can be modified via an anodic oxidation method and a hydrothermal treatment for the enhancement of the bioactivity, and current multi-surface treatments can be applied for use in a dental implant system.

이산화황 흡수 수용액이 다공성 분리막 접촉기를 연속적으로 순환하는 시스템에서 다양한 운전변수에 따른 이산화황의 분리 효율을 고찰하였다. 공급 기체로는 이산화황/공기 혼합 기체를 사용하였으며 흡수제로는 Na2SO3 수용액을 사용하였다. 운전 변수들인 흡수제 농도와 공급 기체 내의 이산화황 농도, 분리막 재질, 흡수제 유속 변화에 따른 분리 효율에 대한 영향을 확인하고자 하였다. 흡수제의 농도 0.05 M에서 0.2 M로 증가할수록 이산화황 제거 효율은 74%에서 100%로 증가하였다. 이산화황 농도가 700 ppm에서 2,500 ppm으로 증가할수록 제거 효율은 100%에서 75%로 감소하였다. 또한 흡수제의 유속이 2.5 mL/min에서 15 mL/min으로 증가할수록 제거 효율은 85%에서 100%로 증가하였고, 분리막은 기공률이 클수록 제거 효율이 증가함을 확인할 수 있었다.

본 연구는 포장재로서 투수콘크리트의 실질적인 현장적용을 위한 자료제시와 성능향상 방안을 도출하기 위하여 슬래그골재와 플라이애시의 혼입률에 따른 포장용 투수콘크리트의 역학적 특성을 평가하였다. 시험결과, 포장용 투수콘크리트의 공극률 및 투수계수는 슬래그골재의 혼합비율이 증가함에 따라 증가하고 플라이애시 혼입률 증가에 의하여 감소하는 경향을 나타내었으며 국내 포장용 투수콘크리트에 관한 규정(8% 및 0.01cm/sec)을 만족하였다. 압축강도 및 휨강도는 슬래그골재의 혼입률이 증가함에 따라 감소하였으나, 플라이애시의 혼입률이 증가함에 따라 크게 증가하는 경향을 나타내어 플라이애시를 5% 이상 혼입하면 슬래그골재를 50% 사용한 경우에도 국내 포장콘크리트에 관한 규정(18MPa 및 4.5MPa 이상)을 만족하였다. 또한 강섬유를 0.75vol.% 혼입한 경우 사용하지 않은 경우에 비하여 휨강도가 22.8% 증가 하였다. 미끄럼저항성은 슬래그골재의 혼입률이 증가에 따라 BPN값은 증가하였고, 플라이애시의 혼입률 증가에 의해 BPN값은 감소하는 경향을 나타내었으며, 내마모성 및 동결융해저항성은 부순골재만을 사용한 경우에 비해 슬래그골재의 혼합비율이 증가함에 따라 감소하였고, 플라이애시를 10% 혼입한 경우에는 현저히 개선되어 혼입하지 않은 경우에 비하여 내마모성 및 내동해성이 각각 약 5.6% 및 14.3% 정도 개선되는 것으로 확인되었다.

Aluminum was anodized in a H2SO4 solution, and titanium (IV) oxide (TiO2) was electrodeposited into nanopores of anodic porous alumina in a mixed solution of TiOSO4 and (COOH)2. The photocatalytic activity of the prepared film was analyzed for photodegradation of methylene blue aqueous solution. Consequently, we found it was possible to electrodeposit TiO2 onto anodic porous alumina, and synthesized it into the nanopores by hydrolysis of a titanium complex ion under AC 8-9 V when film thickness was about 15-20μm. The photocatalytic activity of TiO2-loaded anodic porous alumina (TiO2/Al2O3) at an impressed voltage of 9 V was the highest in every condition, being about 12 times as high as sol-gel TiO2 on anodic porous alumina. The results revealed that anodic porous alumina is effective as a substrate for photocatalytic film and that high-activity TiO2 film can be prepared at low cost.

Porous poly(e-caprolactone) (PCL) scaffolds were fabricated by salt leaching method. The PCL scaffolds were treated with aqueous NaOH for 0h, 2h, 4h, 8h, and 12h at 40˚C. The NaOH-treated PCL scaffolds were dipped in CaCl2 and K2HPO4·3H2O solution alternately three times to induce apatite nuclei onto the surface of the scaffolds. The NaOH-treated PCL scaffolds were immersed into SBF solution for 1day to grow the apatite. The apatite formation were investigated as a fuction of NaOH treatment time. The hydrophilicty and surface area of the PCL scaffolds were increased with NaOH-treatment time. The NaOH-treated PCL scaffolds were successfully formed a dense and uniform bone-like apatite layer after immersion for 1 day in SBF solution.

1'0 develop an effi cient scaffold fo1' t issue-engineered bone 1'egene1'ation, we evaluated fully in terconnected globular porous bisphasic calcium-phosphate ceramics. Materials and Methods: Biphasic HA/TCP cera mic scaffolds having f띠 l y interconnected globular structure with small fenestrations adopting foaming method were p1'epared. They were evaluated by cytotoxici ty‘ cellular attachment. and theil‘ differentiation in vitro and the hi s tocompatibili ty, osteoconductivity. and ectopic os teoinductive capacity in 띠 vo ， respectively. They have average 400um s ized spherical pores and ave1'age 100um s ized inter connecting interpores with average 85% porosity. They r evealed comparable compression strength with cancellous bone. They were nontoxic and revealed no noxious effect on cellular proliferation and osteoblastic diffe re ntiation. The cul tured cells on scaffolds were well attacbed and proliferated in multi-layers. The increased surface in fully interconnected globular porous scaffold facilitated osteogenic repair by favored cell ular attachment and osteogenic differentia tion with good osteoconductivity. 1n addition. the scaffold-cell constructs induced favorable ectopic bone formati on These findings suggest that the fully interconnected globular porous biphas ic HA/ß -TCP ceramic scaffold formed by foaming method can be a promising bone substitute and a scaffold fo 1' tissue-engineered bone 1'egeneration

We evaluated the influence of internal macro- porous structure on tissue-engineered bone regeneration by cOll1paring the effi cien cy of scaffold-cell construct forll1ation and its bone induction activity. T매o types of macro-porous CMP cera rnic blocks having 400 um average pore s ize in an interconnected trabecular framework and interconnected globular structu1'e with small fenestrations were prepa1'ed, adopting sponge method and foaming method. respectively. They ware evaluated by cytotoxicity. cell ular attachment. and t heir differenti ation in vitro and the histocompatibility, osteoconductivity, and ectopic osteoinductive potenetial in vivo, respecti vely. Both scaffolds having either interconnected trabecu lar pOI‘es formed by sponge ll1ethod 0 1' fully interconnected globu lar pores formed by foam-based technology were no cyt otoxic and induced neither an immune nor an infl ammatory response regardless 0 1' geometry and manufacturing methods. The fu lly interconnected globul 81 porous scaffold showed more favora ble compression strength compared to the interconnected trabecualr porous scaffold (8.7 :tO. 5 MPa va 5. 5:t0. 5 MPa) . The increased surface in fully interconnected globular po1'ous scaffold facilitated osteogenic repall‘ by favored cellular attachment and osteogenic differentiation with good osteoconductivity. These results suggest that the fully interconnected globular porous structure be more sui table for both bone s ubstit ute and scaffold for t issue-engineered bone regeneration‘