본 연구에서는 PVA(Poly Vinyl Alcohol)섬유와 GO(Graphene Oxide)를 혼입한 섬유보강 콘크리트(FRC)의 역학적 특성 을 평가하고자 하였다. GO와 PVA 섬유를 동시에 혼입한 FRC 각각의 재료를 단일로 사용하였을 때보다 기대효과가 다소 미흡 하였지만, 각 재료의 하이브리드화로 인장강도가 개선되면서 PVA 섬유 혼입률 0.1∼0.3%과 GO 혼입률 0.025%에서 우수한 효 과를 얻을 수 있었다. 특히 PVA 섬유는 0.3%로 혼합하였을 때 부작용을 최소화하면서 최대의 효과를 보였지만, 적절한 GO 배 합비를 조절할 필요가 있으며 FRC내 GO와 PVA 섬유의 최적배합을 구하기 위한 추가적인 연구가 필요할 것으로 사료된다.

2ZrO2·P2O5 powder, which is not synthesized by solid reaction method, was successfully synthesized through PVA solution method. In this process, the firing temperature and the PVA content strongly affected the crystallization behavior and final particle size. A stable α-phase 2ZrO2·P2O5 was synthesized at a firing temperature of 1200 oC and holding time of 4 h. β-phase 2ZrO2·P2O5 was observed, with un-reacted ZrO2 phases, for firing temperatures lower than 1200 oC. In terms of the PVA content effect, the powder prepared with a PVA mixing ratio of 12:1 showed stable α-phase 2ZrO2·P2O5; however, the β-phase was found to co-exist at relatively higher PVA content. The synthesized α-phase 2ZrO2·P2O5 powder showed an average particle size of 100~250 nm and an average thermal expansion coefficient of −2.5 × 10−6/oC in the range of room temp. ~800 oC.

As a renewable nanomaterial, cellulose nanocrystal (CNC) isolated from wood grants excellent mechanical properties in developing high performance nanocomposites. This study was undertaken to compare the reinforcing efficiency of two different CNCs, i.e., cellulose nanowhiskers (CNWs) and cellulose nanofibrils (CNFs) from hardwood bleached kraft pulp (HW-BKP) as reinforcing agent in polyvinyl alcohol (PVA)-based nanocomposite. The CNWs were isolated by sulfuric acid hydrolysis while the CNFs were isolated by 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated oxidation. Based on measurements using transmission electron microscopy, the individual CNWs were about 6.96±0.87 nm wide and 178±55 nm long, while CNFs were 7.07±0.99 nm wide. The incorporation of CNWs and CNFs into the PVA matrix at 5% and 1% levels, respectively, resulted in the maximum tensile strength, indicating different efficiencies of these CNCs in the nanocomposites. Therefore, these results suggest a relationship between the reinforcing potential of CNCs and their physical characteristics, such as their morphology, dimensions, and aspect ratio.

수증기 투과는 용이하게 하면서 Dimethyl methylphosphonate (DMMP)에 대한 방호성능을 부여하는 선택투과성 능을 가지도록 고안된 몇가지 복합막을 제조하였다. 선택투과막 재료는 폴리비닐알코올 고분자를 기반으로 염기성 작용기를 가지는 기능성 고분자를 포함하도록 하였다. 이들 재료를 사용하여 화생방호성능을 보유한 차세대 소재로서의 가능성을 확인 하기 위하여 선택투과능을 평가하였다. 시험한 결과, 폴리비닐알코올/폴리에틸렌이민 소재가 우수한 수증기 투과성능(2,200 ~ 2,900 g/m 2 /day) 및 DMMP 증기 방호성능(47 g/m 2 /day)을 가지는 것을 확인하였다.

PVA와 PAA블랜드의 용액주조법을 통하여 겔 고분자 전해질막이 제조되었다. 블랜드 내의 PAA함량은 30에서 80 wt% 사이 범위에서 조절되었다. 겔 고분자 전해질을 이용하여 아연공기전지를 제작하였다. 제조된 겔 고분자 전해질의 기계적, 전기적 특성을 인장실험과 임피던스 실험을 통하여 측정하였다. 아연공기전지의 성능은 current interrupt method와 정전류 방전실험을 통하여 측정하였다. 겔 고분자 전해질 내의 PAA함량이 증가함에 따라 인장강도 및 인장탄성계수가 감소하였다. 반면, PAA함량의 증가에 따라 겔 고분자 전해질막의 이온전도도는 증가하였다. 이와 같은 이온전도도의 증가의 아연공기전지 내에서의 효과는 current interrupt method와 정전류 방전실험에서 확인되었다. PAA함량이 높은 겔 전해질막으로 제조된 전지는 낮은 IR손실과 높은 방전용량을 보였다.

LAS-system ceramic powder, spodumene (), was successfully synthesized by a chemical solution technique employing PVA(polyvinyl alcohol) as an organic carrier. The PVA content affected the microstructure of porous precursor gels and the crystalline development. The optimum PVA content contributed to homogeneous distribution of metal ions in the precursor gel and it resulted in the synthesis of glass free -spodumene powder having a specific surface area of . The agglomerated -spodumene powders were also enough soft to grind to fine powders by a simple ball milling process. The microstructures of the densified powder compacts were strongly dependant on the minor phases of spodumene solid solution and amount of liquid phase, which were formed from the inhomogeneous precursors.

Cellulose nanofibers from microfibril cellulose (MFC) was prepared by hydrobromic acid (HBr) treatment at different concentrations. Polyvinyl alcohol (PVA) composite films at various loading level of nanofibers were manufactured by a film casting method. The analysis of degree of polymerization (DP), crystallinity (Xc) and molecular weight (Mw) of cellulose after acid treatment was conducted. The mechanical and thermal properties of the cellulose nanofibers reinforced PVA films were characterized using tensile tests and thermogravimetric analysis (TGA). The DP and Mw of MFC by HBr hydrolysis considerably decreased, but Xc showed no significant change. After acid hydrolysis, the diameter of cellulose nanofibers was in the range of 100 to 200 nm. The thermal stability of the films was steadily improved with the increase of nanofiber loading. There was a significant increase in the tensile strength of PVA composite films with the increase in MFC loading. Finally, 5 wt.% nanofiber loading exhibited the highest tensile strength and thermal stability of PVA composite films.

In this study, the fiber blending ratio and strain rate effect on the tensile behavior of hybrid fiber reinforced cement composite was evaluated. Hooked steel fiber and polyvinyl alcohol fiber were used for reinforcing fiber. The fiber blending ratio of HSF+PVA were 1.5+0.5, 1.0+1.0 and 0.5+1.5vol.%. As a results, the tensile strength, strain capacity and fracture toughness of the hooked steel fiber reinforced cement composites were improved by the increase of the bond strength of the fiber and the matrix according to increase of strain rate. However, the tensile stress sharply decreased after the peak stress because of the decrease in the number of straightened pull-out fibers by micro cracks in the matrix around hooked steel fiber. On the other hand, PVA fiber showed cut-off fracture at strain rate 10-6/s with multiple cracks. However, at the strain rate 101/s, the multiple cracks and strain capacity were decreased because of the pull-out fracture of PVA fiber. The HSF1.5PVA0.5 shown the highest tensile strength because the PVA fiber suppressed the micro cracks in the matrix around the hooked steel fiber and improved the pull-out resistance of hooked steel fiber. Thus, DIF of strain capacity and fracture toughness of HSF1.5PVA were greatly improved. In addition, the synergistic response of fracture toughness was positive because the tensile stress was slowly decreased after the peak stress by improvement of the pull-out resistance of hooked steel fiber at strain rate 101/s

Immobilized nitrifier bead in airlift bioreactor were used to remove high levels of ammonia nitrogen from synthetic wastewater. Polyvinylalcohol (PVA) bead for immmobilization of nitrifier consortium were prepared by PVA-boric acid method by varying concentration of PVA and nitrifier consortium. By determining viscosity, sphercity and tailing, the characteristics of prepared beads were investigated and the continous immobilization process was developed. Synthetic wastewater containg 25g/㎥ of ammonia nitrogen could be treated within 0.5 hour and the highest removal rate of ammonia nitrogen was 934.2g/㎥ ·day.

Nitrifier consortium immobilized in polyvinyl alcohol was used for the removal of ammonia nitrogen from synthetic aquaculture water in the airlift bioreactor. At the aeration rate of 0.15 vvm and bead packing volume fraction of 20%, airlift bioreactor was operated effectively for a removal of ammonia nitrogen and for a stability of operation. Ammonia nitrogen removal rate by airlift bioreactor was continuously increased with decreasing hydraulic residence time. At the HRT(hydraulic residence time) of 0.3 hour, ammonia nitrogen removal rate was 84.3 g/㎥·d and the highest ammonia nitrogen removal rate was 130.8 g/㎥·d when HRT was 0.1 hour.