담양 염장 죽순을 첨가한 요구르트를 개발하기 위해 죽순에 함유되어 있는 일반성분을 분석하였고, 관능검사를 통해 최적 발효조건과 죽순첨가 형태를 결정하였다. 죽순은 수분함량이 82.59 %, 단백질 4.56 %, 지질 0.52 %, 회분 0.50 %, 그리고 식이섬유소가 11.72 %(w/w) 함유되어 있었으며, 무기질은 Ca, P, S, Na, Mg, K 순서로 높은 함량을 보였다. 죽순을 첨가하기 위한 요구르트는 ABT-5 미생물을 0.005 % 접종하여 40 ℃에서 13시간 발효시켰으며, 요구르트 첨가용 죽순은 형태를 달리하여 관능검사를 실시한 결과 5×5×5 mm 크기로 절단한 죽순을 50 % 설탕에 절임하여 15 %(w/w) 비율로 첨가한 시료의 선호도가 가장 높았다. 이와 같이 제조된 죽순 요구르트는 4 ℃ 냉장온도에서 15일 동안 저장 중 pH와 산 생성, 젖산균수, 그리고 비피더스균수의 변화가 나타나지 않아 저장성이 우수였다. 따라서 죽순 첨가 호상요구르트는 기호성과 품질 특성이 우수하고 영양학적으로도 훌륭한 상품적 가치가 있을 것으로 판단된다.

In this study, the effects of the dispersants, i.e., Hypermer KD-2 and poly(l-vinyl-2-pyrrolidone) (PVP), and their concentration on the dispersion stability of Ni nanoparticles () in ethanol were investigated by using a visual inspection, a transmission profile (Turbiscan), and a zeta potential measurement. The transmission profiles measured by Turbiscan showed that the particle size increased over the entire height of the sample for suspensions with both the dispersants without showing any particle coalescence and sedimentation. The visual inspection also confirmed that the Ni suspensions with Hypermer KD-2 and PVP were very stable for more than a year. The zeta potential values varied from positive to negative with increasing the dispersant's concentration. The dispersion stability of the suspensions was not affected by both the dispersant's concentration and the zeta potential values. The observed suspension stability of Ni nanoparticles was attributed to the steric effect for the Hypermer KD-2 and to the bridging effect for the PVP.

Modified polyesters (TTBA-10C, -20C, -30C) that contain phosphorus and chlorine were synthesized by the condensation polymerization of tetramethylene bis(orthophosphate), neohexanediol trichlorobenzoate, 1,4-butanediol and adipic acid, in which tetramethylene bis(orthophosphate) and neohexanediol trichlorobenzoate were prepared previously in our laboratory. In this study, two-component flame-retardant polyurethane coatings (TTBA-10C/HDI-trimer=TTHD-10C, TTBA-20C/ HDI-trimer= TTHD-20C, TTBA-30C/HDI-trimer= TTHD-30C) were obtained by curing at room temperature with the synthesized TTBAs and hexamethylene diisocyanate (HDI)-trimer as a curing agent. The obtained TTHDs were made into coating samples and used as test samples for various physical properties. The physical properties of the flame-retardant coatings containing chlorine and phosphorus groups were generally inferior to those containing only phosphorus group. Flame retardancy was tested by vertical and horizontal combustion method, and 45˚ Meckel burner method. Since the retardancy of flame-retardant coatings containing chlorine and phosphorus groups was better than that containing only phosphorus group, it could be concluded that the retardancy by the synergism effect of chlorine and phosphorus groups exhibited.

In this study, we prepared porous cation exchange membrane using polystyrene such as, EPS (expanded polystyrene), SAN (styrene acrylonitrile copolymer) and HIPS (high impactive polystyrene). These polystyrenes were sulfonated by acetyl sulfate to make porous cation exchange membrane such as, SEPS, SSAN, SHIPS. SEM was employed to confirm porous structure of membrane, and IR spectroscopy was used to confirm sulfonation rate of ion exchange membrane. Water and methanol content were also increased with amount of sulfuric acid in reactants. SSAN-20 showed the highest value in water and methanol content. Fixed ion concentration and conductivity was also increased with an amount of sulfuric acid in reactants. Methanol permeability for SEPS-20, SSAN-20, SHIPS-20 was found to be 1.326 × 10-5 cm2/s, 1.527 × 10-5 cm2/s and 1.096 × 10-5 cm2/s respectively. From the result of electrodialysis experiment in 0.03 M Pb(NO3)2 aqueous solution, anion exclusion and cation selection effects were confirmed.

실리카 입자를 기공 형성제로 사용하여 다공성 키토산 및 키틴 막을 제조하였다. 다공성 막의 제조는 다음의 3단계 절차로서 수행되었다: (1) 키토산 용액에 실리카 입자를 첨가시켜 필름을 형성시킨 후, (2) 이 필름을 알카리 용액에 침지시켜 실리카 입자를 제거하여 다공성의 키토산 막을 제조하였으며, (3) 다공성 키토산 막을 acetic anhydride를 사용하여 아세틸화시킴으로서 다공성 키틴 막을 제조하였다. 물리적 강도가 우수하고, 적절한 순수 투과량을 갖는 다공성 키토산 막과 키틴 막의 최적 제막조건이 제시되었다. 단백질 친화성을 부여하기 위해 다공성 키토산 막에 반응성 염료인 Cibacron Blue 3GA를 고정화시켰으며, BSA 단백질 및 lysozyme 효소의 흡착실험을 수행하여 친화 키토산 막 및 키틴 막의 단백질 결합용량을 측정하였다. 친화 키토산 막의 BSA 단백질 결합용량은 약 22 mg/mL이었으며, 친화 키틴 막의 lysozyme 효소 결합용량은 약 26 mg/mL로서 이는 키토산 또는 키틴을 기반으로 하여 제조된 hydrogel bead의 단백질 결합용량보다 수~수십 배 큰 값으로서, 향후 막여과 크로마토그래피용 친화 막으로의 효과적인 활용이 기대된다.

Solvent-free low foaming scouring agents (LFSC) were prepared by blending of 2-ethylhexylaminoethyl sulfate (2-EHAS), POE(10) octadecylbenzyl- ammonium chloride (POBAC) and Sedlan FF-200 (FF-200). As the results of several tests, 2-EHAS/POBAC/FF-200/water (8g/12g/20g/60g) mixture (LFSC-5) showed good cleaning power, penetrating ability and stability to alkali, and gave less problem in water pollution. The foaming power of LFSC-5 measured by Ross and Miles method was 8mm foam height immediately after foaming, and that measured by Ross and Clark method was less than 300mm foam height at 30℃, and 18mm at 80℃. As a result, LFSC-5 proved a good low foaming scouring agent for fiber.

본 연구는 불소관능기인 perfluorocyclobutane (PFCB)과 fluorene계 방향족 화합물을 동시에 포함하는 술폰화된 고분자 전해질 막의 제조 및 그 특성에 관한 것이다. 이러한 고분자 전해질 막은 세 단계의 합성, 즉 trifluorovinyloxy그룹을 양말단에 포함하는 fluorene계 단량체의 합성, 중부가 반응 형태의 열중합, 그리고 chlorosulfonic acid를 이용한 후술폰화(post-sulfonation)를 통하여 얻어졌다. 후술폰화 반응은 일정한 시간과 온도 조건하에서 술폰화제의 첨가 비율을 달리하여 진행되었으며, 이에 따라 다양한 이온교환 능력(IEC)을 가지는 고분자를 합성할 수 있었다. 제조된 단량체 및 고분자들의 구조와 순도는 각각 FT-IR과 NMR 그리고 질량분석기를 통하여 확인되었다. 사용된 술폰화제의 양이 많아질수록 술폰화도와 이온교환 능력이 증가하는 것을 확인할 수 있었고 그에 따른 함수율도 역시 증가하는 거동을 보였다. 술폰화된 고분자들의 이온전도도를 측정한 결과 술폰화도가 증가할수록 이온 전도도가 증가하는 것을 관찰할 수 있었다. 이렇게 제조된 전해질막 중 IEC 값이 1.86 mmol/g인 고분자(sulfonated polymer 4)의 경우 다양한 온도범위(25~80℃)에서 상용 전해질막인 Nafion-115를 능가하는 우수한 이온전도도를 나타냈다.

To determine the optimum mixing conditions of nopal jelly, samples were prepared with various compounding ratios of gelatin(16, 18, 20, 22 and 24g), sucrose(100, 120, 140, 160 and 180g), Citric acid(2, 3, 4, 5 and 6) using a central composite design. Physical and sensory evaluations were performed and considered using a response surface methodology. The optimum mixing rates which meet sensory items is gelatin 20.19g, sucrose 141.52g and citric acid 4.04g.

This study was conducted to prepare acrylic removable protective coatings by emulsion polymerization. Monomers used were n-butyl acrylate, acrylonitrile, butyl methacrylate. Emulsifiers used were sodium lauryl sulfate and polyoxyethylene lauryl ether, which are an anionic emulsifier and a nonionic emulsifier respectively. Potassium persulfate was used as an initiator and polyvinyl alcohol was used as a stabilizer. Emulsion polymerization was carried out in a semi-batch reactor at 70℃ and agitation speed was 200 rpm. Tensile strength, extension, peel strength, viscosity, and solid contents of the synthesized coatings were examined. The coatings prepared with BA:AN = 60:20 (in weight ratio) satisfied the standard for automobile in terms of extension and peel strength. When the concentration of BMA was in a range of 18~23 wt%, the prepared coatings satisfied the standard for automobile in terms of peel strength and water resistance.

In the present study, silver-doped antibacterial hydroxyapatites were successfully prepared by the sol-gel method. For the starting solution, the molar ratio of was set to 0.075:0.045:20:0.135; was added to a ratio of Ag to total cation concentration of . The prepared sol was dried at for 48h and heat-treated at for 2h to obtain particles in the 200-500nm size range. The product from the synthesis of silver-doped hydroxyapatite was investigated through X-ray diffraction experiments and scanning electron microscopy. The product showed high antibacterial properties, with a disinfection ratio of Staphylococcus aureus (ATCC 6538) and Escherichia coli (ATCC 25922) over as calculated from an antimicrobial effects evaluation by the shake flask method.

Bipolar plates require some specific properties such as electrical conductivity, mechanical strength, chemical stability, and low permeability for the fuel cell application. This study investigated the effects of carbon nanotube (CNT) contents and process conditions of hot press molding on the electrical and physical properties using CNT 3~7 wt% added graphite nano-composites in the curing temperatures range of 140~200℃ and pressure of 200~300 kg/cm2. Bulk density, hardness and flexural strength increased with increasing CNT contents, curing pressure and temperature. With the 7 wt% CNT added noncomposite, the electrical resistance improved by 30% and the flexural strength increased by 25% as compared to that without CNT at the temperature of 160℃ and pressure of 300 kg/cm2. These properties were close to the DOE reference criteria as bulk resistance of 13 mΩcm and tensile strength of 515 kg/cm2.

To maximize a synergy effect in flame-retardancy of flame-retardant coatings, phosphorus and chlorine were introduced in polymer chains. Two-components PU flame-retardant modified polyesters (ABTTC-10C, -20C, -30C) were prepared by curing, at room temperature, of isocyanate (allophanate-trimer) and prepared modified polyesters which contain phosphorus and chlorine. To examine the film properties of the prepared flame-retardant coatings, film specimens were prepared with the prepared coatings. The film properties of ABTTC, ABTTC-10C and ABTTC-20C, which contain 0, 10 and 20wt%, 2,4-dichlorobenzoic acid (2,4-DCBA), respectively, were proved to be good, whereas the film properties of ABTTC-30C, which contains 30wt% 2,4-DCBA, were proved to be a little bit poor. Two kinds of flame retardancy tests, 45˚Meckel burner method and LOI method, were performed. With the 45˚Meckel burner method, three flame-retardant coatings except ABTTC showed less than 3.4 cm of char length, and showed less than 2 seconds of afterflaming and afterglow. From this result, the prepared flame-retardant coatings were proved to have the 1st grade flame retardancy. With the LOI method, the LOI values of the coatings containing more than 10wt% 2,4-DCBA were higher than 30wt%, which means that the coatings possess good flame-retardancy. From these results, it was found that synergistic effect in flame-retardancy was taken place by the introduced phosphorus and chlorine.

키토산 필름은 농업, 식품과 제약 분야에서 응용이 가능하다. 그러나 키토산으로만 만들어진 필름은 기체투과성이 높고 기계적 물성에 약하다. 따라서 본 연구에서는 기체 투과성을 낮추고 기계적 물성을 높이기 위해 층상구조를 갖는 점토광물의 일종인 montorillonite (MMT)와 양이온 생체고분자인 키토산을 이용하여 양이온 교환과 수소결합과정을 통해 Na+-MMT에 키토산을 삽입하여 키토산/Clay 나노복합재료를 제조하였다. 키토산/clay 나노 복합재료의 X-ray 회절패턴에서 2θ=7.5º에서 MMT의 basal reflection이 나타났고, 2θ=3~5º 주위에서의 새로운 약하고 넓은 peak로서 더 낮은 각에서 MMT의 basal reflection의 이동에 의해 삽입된 나노 구조의 형성을 증명하였다. 또한 TGA thermogram를 이용하여 clay의 함유량이 증가할수록 제조된 나노복합재료의 열분해가 일어나는 범위의 질량감소가 줄어드는 것을 확인하므로서 내열성을 관찰하였다. 기계적 물성 성질을 측정하여 clay 함유량의 증가에 따른 인장 강도와 인장 모듈러스의 변화를 관찰하고, 키토산이 층상 실리케이트 내에 삽입하여 제조된 나노복합재료에서 clay의 함유량이 증가할수록 질소 투과경로의 tortuosity를 증가시켜서 기체 투과도를 감소시키는 것도 확인하였다.

In this paper, fly ash was investigated as a basic Si-Al ingredient of geopolymer. Based on compressive and flexural strength, the replacement percentage of fly ash and 3 types of curing regimes were studied to obtain the optimum synthesis condition. The results showed that geopolymer containing 30% fly ash that was prepared at 80˚C for 8 hours, exhibited high mechanical strength. The compressive and flexural strength of the fly ash based geopolymer were 32.2 and 7.15MPa, respectively. In order to investigate the durability behavior of fly ash based geopolymer concrete, CI permeability, freeze-thaw tests were also carried out. The measured results indicated that fly ash based gopolymer concrete had 2.63 times lower coefficient of chloride-ion diffusion and could withdraw 2.2 times more freeze-thaw cycles as compared to Portland concrete with the same compressive strength.