• 폴리머
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• 제31권6호
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• pp.532-537
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• 2007

본 연구에서는 poly(vinyl alcohol)(PVA)를 dimethyl sulfoxide(DMSO)에 녹여 이 용액의 유변학적 특성에 미치는 PVA의 분자량분포의 영향에 관하여 고찰하였다. 동일 평균분자량인 경우에도 수지 혼합(resin blending)에 의해 분자량분포가 넓어지면 점도와 손실탄성률이 더 낮아짐을 알 수 있었다. 이것은 동일 평균 분자량의 경우 분자량분포가 넓은 PVA/DMSO 용액계의 자유체적이 증가되기 때문이라고 생각된다. 분자량 분포가 저장탄성률에 미치는 영향은, 14 wt%용액의 경우에는, 1.3 rad/sec보다 낮은 진동수 영역에서는 동일 평균분자량의 경우 분자량분포가 넓은 PVA/DMSO 용액계가 탄성이 더 크고, 1.3 rad/sec보다 높은 진동수 영역에서는 분자량분포가 좁은 PVA/DMSO 용액계가 탄성이 더 크게 측정되었다. 14 wt% 용액의 경우에 Modified Cole-Cole plot에서의 기울기는 분자량분포가 넓어지면 진동수에 따른 상전이 현상이 더 뚜렷해졌다.

• 방사선산업학회지
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• 제10권1호
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• pp.21-27
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• 2016

Periodontitis is disease of damaged gum tissue that is not removed the plaque onto teeth. In case that the symptoms of disease get pain worse, it will have to extract tooth because of tumefy or bleeding at gums so treatment of drug was required to periodontitis. In this study, the hydrogel was prepared by including superior viscous, excellent elastic, and biocompatibility of Poly(vinyl alcohol, PVA) and antimicrobial drug of Metronidazole (MD). The 15 wt% PVA was dissolved in deionized water and then prepared PVA solution was irradiated using gamma-ray at 25 kGy ($10kGy\;hr^{-1}$). In addition, PVA hydrogel was immersed in each 0.1, 0.25 and 0.5 wt% MD solution using stirrer for 24 hr. The result of the gelation, 0.5 wt% MD loaded PVA hydrogel(76%) was lower than PVA hydrogel (88.2%). The swelling ration of 0.5 wt% MD loaded PVA hydrogel (294.8%) was higher than PVA hydrogel (105.2%). The compressive strength and thermal properties of MD loaded PVA hydrogel was gradually lower. The drug release test of 0.5 wt% MD loaded PVA hydrogel (61%) was higher than 0.1 wt% MD loaded PVA hydrogel (12%). Therefore, MD loaded PVA hygrogel may be a promising tool for periodontitis medicine by gamma-ray.

• Fibers and Polymers
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• 제3권2호
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• pp.73-79
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• 2002

Nanoscaled PVA fibers were prepared by electrospinning. This paper described the electrospinning process, the processing conditions fiber morphology, and some potential applications of the PVA nato-fibers. PVA fibers with various diameters (50-250 nm) were obtained by changing solution concentration, voltage and tip to collector distance (TCD). The major factor was the concentration of PVA solution which affected the fiber diameter evidently. Increasing the concentration, the fiber diameter was increased, and the amount of beads was reduced even to 0%. The fibers were found be efficiently crosslinked by glyoxal during the curing process. Phosphoric acid was used as a catalyst activator to reduce strength losses during crosslinking. Scanning electron micrograph (SEM) and differential scanning calorimetric (DSC) techniques were employed to characterize the morphology and crosslinking of PVA fibers. It was fecund that the primary factor which affected the crosslinking density was the content of chemical crosslinking agent.

• 멤브레인
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• 제12권4호
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• pp.255-261
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• 2002

폴리비닐알콜을 고분자계 가교제인 폴리아크릴산-말레산 공중합체를 이용하여 가교제의 농도를 변화시키면서 가교하여 막을 제조하였다. 제조한 막은 FT-IR과 수팽윤도 측정을 통하여 가교반응을 확인하였으며, 가교제 농도 증가에 따라서 수팽윤도가 감소하는 경향을 나타내었다. 고분자가교제인 폴리아크릴산-말레산 공중합체로 가교된 폴리비닐알콜 막은 글루탈알데히드로 가교된 폴리비닐알콜이나 변성 폴리비닐알콜 막에 비해서 수팽윤도가 감소하였다. 이는 고분자가교제에 의한 화학적가교와 더불어 물리적인 가교효과가 증가하여 막의 팽윤을 억제하기 때문으로 사료된다. 에탄올수용액에 대한 투과증발실험 결과 가교제의 농도가 증가할수록 선택도는 증가하며, 투과유량은 감소하는 경향을 나타내었으며, 공급액 중의 물의 농도가 증가할수록 선택도는 약간 감소하나 투과유량은 급격히 증가하고, 공급액 중의 물의 농도가 증가하여도 가소화현상이 나타나지 않는 것을 관찰하였다. 이는 고분자가교제에 의한 팽윤억제 메카니즘이 작용하기 때문으로 사료된다.

• 청정기술
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• 제20권3호
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• pp.251-255
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• 2014

테노일트리플루오로아세톤(thenoyltrifluoroacetone, HTTA)과 트리옥틸포스핀옥사이드(trioctylphoshineoxide, TOPO)를 폴리비닐알콜(poly vinyl alcohol, PVA)로 고정화한 PVA 겔 비드를 제조하고, 이를 사용하여 수중의 $Cu^{2+}$를 제거하였다. 제조한 PVA 겔 비드의 $Cu^{2+}$ 제거특성은 유사 2차 속도식에 잘 적용되었으며, 랑미어 등온식에서 구한 $Cu^{2+}$의 최대 제거량은 9.59 mg/g이었다. $Cu^{2+}$ 제거의 최적 pH 범위는 pH 3.5~6이었다. PVA겔 비드를 5차례 재사용한 경우에도 추출제의 손실이나 PVA겔 비드의 손상은 관찰되지 않았다.

• 한국유변학회:학술대회논문집
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• 한국유변학회 2002년도 추계학술발표회 논문집
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• pp.11-14
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• 2002

• Journal of Microbiology and Biotechnology
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• 제16권3호
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• pp.414-422
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• 2006

Before applying PVA bio-beads to practical biological treatment of nitrate-containing wastewater, their characteristics were examined. PVA bio-beads could steadily produce nitrogen gas from nitrate for 28 batches with 0.04 ml/l/h of the maximum gas production rate; however, the maximum gas production rate dropped remarkably thereafter with apparent deformation of beads. Addition of 2.2% solution containing 1% casamino acid, 1% yeast extract, 0.1% mineral solution, and 0.1% vitamin solution to the culture medium resulted in not only recovery of activity of deactivated beads, but also a higher rate of gas production. Calculation of economic benefit for the use of bio-beads in a long-run operation indicated that reactivation of bio-beads by chemicals had economical advantages over packing new bio-beads in the system. The continuously stirred bioreactor exhibited a satisfactory performance at HRT of 20.0 h. With a 9.5 mg $NO_{3}^{-}N/l/h$ nitrate removal rate, nitrate could completely be removed without nitrite accumulation. The use of PVA bio-beads in nitrate removal appears very promising.

• 한국의류학회지
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• 제38권3호
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• pp.372-385
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• 2014

Lignin is an abundant natural polymer in the biosphere and second only to cellulose; however, it is under-utilized and considered a waste. In this study, lignin was fabricated into nanofibers via electrospinning. The critical parameters that affected the electrospinnability and morphology of the resulting fibers were examined with the aim to utilize lignin as a resource for a new textile material. Poly(vinyl alcohol) (PVA) was added as a carrier polymer to facilitate the fiber formation of lignin, and the electrospun fibers were deposited on polyester (PET) nonwoven substrate. Eleven lignin/PVA hybrid solutions with a different lignin to PVA mass ratio were prepared and then electrospun to find an optimum concentration. Lignin nano-fibers were electrospun under a variety of conditions such as various feed rates, needle gauges, electric voltage, and tip-to-collector distances in order to find an optimum spinning condition. We found that the optimum concentration for electrospinning was a 5wt% PVA precursor solution upon the addition of lignin with the mass ratio of PVA:lignin=1:5.6. The viscosity of the lignin/PVA hybrid solution was determined as an important parameter that affected the electrospinning process; in addition, the interrelation between the viscosity of hybrid solution and the electrospinnability was examined. The solution viscosity increased with lignin loading, but exhibited a shear thinning behavior beyond a certain concentration that resulted in needle clogging. A steep increase in viscosity was also noted when the electrospun system started to form fibers. Consequently, the viscosity range to produce bead-free lignin nanofibers was revealed. The energy dispersive X-ray analysis confirmed that lignin remained after being transformed into nanofibers. The results indicate the possibility of developing a new fiber material that utilizes biomass with resulting fibers that can be applied to various applications such as filtration to wound dressing.

• 한국분말재료학회지
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• 제20권1호
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• pp.37-42
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• 2013

$YAG:Ce^{3+}$ phosphor powders were synthesized using a $Al_2O_3$ seed (average particle size: 5 ${\mu}m$) by the polymer solution route. PVA solution was added to the sol precursors consisting of the seed powder and metal nitrate salts for homogeneous mixing in atomic scale. All dried precursor gels were calcined at $500^{\circ}C$ and then heated at $1400^{\circ}C{\sim}1500^{\circ}C$ in $N_2/H_2$ atmosphere. The final powders were characterized by using XRD, SEM, PSA, PL and PKG test. All synthesized powders were crystallized to YAG phase without intermediate phases of YAM or YAP. The phosphor properties and morphologies of the synthesized powders were strongly dependent on the PVA content. Finally, the synthesized $YAG:Ce^{3+}$ phosphor powder heated at $1500^{\circ}C$, which is prepared from 12:1 PVA content and has an average particle size of 15 ${\mu}m$, showed similar phosphor properties to a commercial phosphor powder.

• 폴리머
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• 제25권5호
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• pp.728-735
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• 2001

본 연구에서는, $^{60}cO$ 방사선 (${\gamma}$-rays) 가교를 이용하여 PVA/키토산과 PVP/키토산의 혼합물로부터 하이드로겔을 제조하였다. 하이드로겔이 상처 치료용 드레싱으로 사용될 수 있는지 예측하기 위해 겔화율, 팽윤도, 겔강도같은 기계적 성질을 측정하였다. PVA와 키토산 및 PVP와 키토산의 비는 97 : 3 ~ 90 : 10이고, PVA/키토산 및 PVP/키토산 용액의 고형분의 농도는 15wt% 이었다. 하이드로겔의 기계적 성질에 조사선량이 미치는 영향을 예측하기 위해 PVA/키토산 및 PVP/키토산 혼합물에 25~70kGy의 감마선을 조사하였다. 겔화율과 겔강도는 키토산 조성비가 작을수록, 조사선량이 커질수록 증가하였다 팽윤도는 키토산 조성비가 클수록, 조사선량이 작을수록 증가하였다.