본 연구는 젖소에 있어서 다량의 수정란을 생산하여, 고능력의 유전인자를 조기에 확산할 수 있도록, 젖소에 있어서 PEG를 이용하여 과배란 처리기법 확립을 위해 실시하였으며, 그 결과는 다음과 같다. 1. 성선자극호르몬의 처리 방법에 따른 황체반응은 Folltropin 단독처리시 , Folltropin+EB는 , Folltropin+PEG는 로 나타났으며, 유의적인 차이를 보였다(p<0.01). 2. 성선자극호르몬의 처리 방법에 따른 이식 가능 수정란 수

계면활성제(SF316+FB0800)가 처리된 폴리에틸렌 필름 시설에서 직경 9cm 원안의 필름 표면에 부착된 수적량은 무처리구에서 1.21 mL, 1% 처리구에서 0.15mL, 2% 처리구에서 0.07 mL가 측정되었다. 그러나 육안으로는 1%와 2% 처리구 사이에 차이를 관찰하기가 어려웠다. 수적량은 하루 중 오전 10시에 가장 많았고, 기온의 상승된 오후 2시에 적었다. 무처리구에 비하여 계면활성제 1%와 2% 처리구 사이에 차이를 관찰하기가 어려웠다. 수적량은 하루 중 오전 10시에 가장 많았고, 기온이 상승된 오후 2시에 적었다. 무처리구에 비하여 계면활성제 1%와 2% 처리구에서 투광율은 각각 9.3%, 12.9% 높았다. 기온과 습도는 계면활성제가 처리된 비닐하우스와 머처리 비닐하우스 사이에 뚜렸한 차이를 나타내지 않았다. 오전의 기온은 계면활성제 처리 비닐하우스에서 1~2℃ 정도 높았으며, 지온의 경우는 계면활성제 처리시설에서 3~4℃ 정도 높은 경향을 나타냈다. 겨울철 상추의 생육은 계면활성제가 처리된 필름으로 피복된 비닐하우스에서 빨랐다. 그러나 계면활성제농도 1%와 2% 처리구 사이에는 뚜렸한 차이를 보이지 않았다.

Many of researches regarding mechanical properties of composite materials are associated with humid environment and temperature. Especially the temperature is a very important factor influencing the design of thermoplastic composites. However, the effect of temperature on impact behavior of reinforced composites have not yet been fully explored. An approach which predicts critical fracture toughness GIC was performed by the impact test in this work. The main goal of this work is to study the effect of temperature and span of specimen supports on the results of Charpy impact test for GF/PE composite. The critical fracture energy and failure mechanism of GF/PE composites were investigated in the temperature range of 60℃;to;-50℃ by the Charpy impact test. The critical fracture energy showed the maximum at the ambient temperature, and it tended to decrease as the temperature increased or decreased from the ambient temperature. The major failure mechanisms are the fiber matrix debonding, the fiber pull-out and/or delamination and the matrix deformation.n.

Oxidized polyethylene wax is obtained by oxidation of polyethylene wax and it is composed of various chemicals, e.g., fatty acid, alcohol, ketone and ester. The application of oxidized polyethylene wax is determined by the composition of these chemical substances. In this basic study we observed the basic reaction parameters of time, temperature, oxygen concentration and catalysts on the oxidation reaction of low molecular weight polyethylene(PE wax) by analyzing the acid value, physical and chemical properties of oxidized PE wax to develop a new oxidation process. Acid values are increased with temperature increase in the rage of 150℃~180℃ but decreased beyond 190℃. Acid values are also increased with oxygen concentration. As the oxidation reaction proceeds the molecular weight and softening points of oxidation products are decreased by cracking reaction, but the viscosities are increased. To observe the crystallinity of oxidation products SEM experiment was performed. To obtain a high acid-value product in a mild condition, we adopted free radical catalysts and the acid value of the product using catalyst was higher than the product obtained without catalyst in the same reaction condition. The effective initiators were dicumyl peroxide(DCPO), t-butylperoxy-2-ethyl hexanoate(HOPO) and benzoyl peroxide(BPO) having long half-life.

Thermosetting matrix composites have disadvantages in terms of moulding time, repairability and manufacturing cost. Thus the high-performance thermoplastic composites to eliminate such disadvantages have been developed so far. As a result of environmental and economical concerns, there is a growing interest in the use of thermoplastic composites. However, since their mechanical properties are very sensitive to the environment such as moisture, temperature etc., those behaviors need to be studied. Particularly the temperature is a very important factor influencing the mechanical behavior of thermoplastic composites. The effect of temperature have not yet been fully quantified. Since engineering applications of reinforced composites necessitate their fracture mechanic characterization, work is in progress to investigate the fracture and related failure behavior. An approach which predicts the tensile strength was perpormed in the tensile test. The main goal of this work is to study the effect of temperature on the result of tensile test with respect to GF/PE composite. The tensile strength and failure mechanisms of GF/PE composites were investigated in the temperature range 60℃ to -50℃. The tensile strength increased as the fiber volume fraction ratio increased. The tensile strength showed the maximum at -50℃, and it tended to decrease as the temperature increased from -50℃. The major failure mechanism was classified into the fiber matrix debonding, the fiber pull-out, the delamination and the matrix deformation.

본 실험에서는 한우에 있어서 PEG를 이용한 FSH의 투여 방법에 따른 과배란 유기 방법 및 수정란 이식의 효율을 조사하였다. 과배란 처리는 대조구를 포함하여 네 그룹으로 나누어 비교 실험하였으며, 대조구는 12시간 간격으로 1일 2회, 4일간 50 mg의 FSH를 근육주사, 처리구 1은 30% PEG에 용해시킨 400 mg의 FSH를 1회 피하주사, 처리구 2는 30% PEG에 용해시킨 200 mg의 FSH를 1회 피하주사, 그리고 처리구 3은 30%

본 연구는 폐폴리에틸렌필름(폐비닐)을 아스팔트 혼합물에 첨가하여 아스팔트 포장재료의 품질특성을 향상시키고 환경적으로 문제가 되고 있는 폐비닐을 재활용하기 위한 연구의 일환으로 수행되었다. 폐비닐 사용시 나타날 수 있는 포장체의 특성을 파악하기 위하여 국내에서 가장 많이 수거되는 LDPE 폐비닐을 사용하여 현장에서의 실용성을 고려한 건식혼합법으로 아스팔트 혼합물을 제조하였다. 제조한 혼합물에 대하여 마샬안정도 시험, 간접인장강도 시험, 반복주행시험 및 피로시험을 수행한 결과 폐비닐을 혼합한 혼합물이 일반혼합물에 비하여 인장강도가 향상되고 윤하중에 의한 소성변형 저항성 및 피로균열 저항에 크게 효과적인 것으로 나타났다.

본 연구는 폐폴리에틸렌필름(폐비닐)을 아스팔트 혼합물에 첨가하여 아스팔트 포장재료의 품질특성을 향상시키고 환경적으로 문제가 되고 있는 폐비닐을 재활용하기 위한 연구의 일환으로 수행되었다. 폐비닐 사용시 나타날 수 있는 포장체의 특성을 파악하기 위하여 국내에서 가장 많이 수거되는 LDPE 폐비닐을 사용하여 현장에서의 실용성을 고려한 건식혼합법으로 아스팔트 혼합물을 제조하였다. 제조한 혼합물에 대하여 마샬안정도 시험, 간접인장강도 시험, 반복주행시험 및 피로시험을 수행한 결과 폐비닐을 혼합한 혼합물이 일반혼합물에 비하여 인장강도가 향상되고 윤하중에 의한 소성변형 저항성 및 피로균열 저항에 크게 효과적인 것으로 나타났다.

본 연구는 붕소이온 분리를 위하여 4-Vinylpyridine-divinylbenzene(이하 4-VP-DVB라 칭함) 음이온 교환수지를 합성하고, polyethylene(이하 PE라 칭함)을 지지체로 사용하여 불균질계 음이온교환막을 제조하였다. 또한 그들의 구조와 기계적 성질 및 전기화학적 특성ㅇ르 FT-IR, conductometer와 pH meter 등의 기기로 측정하였으며, 유속과 전압의 변화에 따른 막의 성능을 평가하였다. 막의 분리성능은 PE 지지체 내에 4VP-DVB 이온교환 수지의 함량이 50wt%인 불균질막이 가장 우수하였으며, 산처리한 막이 수처리한 막의 그것보다 우수하였다. 막을 이용한 전기투석 실험에서 붕소이온 분리시 최적유속, 전압 및 시간은 각각 10mol/min, 18volt, 4시간이었다.

α-sulfonated fatty acid polyethylene glycol esters with polyethylene oxide(addition, 3, 5, 10mol) were synthesized through esterification of α-sulfonated fatty acid methyl esters with alkyl chain length C12~C18. Their compounds were separated with column chromatography, and confirmed by TLC. Quantitative analysis of all the sulfonates were performed according to JIS K-3362 method, and ethylene oxide unit number were determined by ISO 2270 method. Structural properties of α-sulfonated fatty acid methyl esters and their derivatives were also identified from IR, and 1H NMR spectra.

All the surface activities including surface tension, foaming power, foam stability, emulsifying power, dispersion effect, and detergency were measured and critical micelle concentration(cmc) was evaluated in dilute aqueous solution. The cmc evaluated by the Ring method was 10-3~10-4mol/L in case of monoesters, and 10-3~5.0×10-5mol/L in case of diesters, respectively. Surface tension of the aqueous solution was decreased to 45~50dyne/cm, showing the tendency that the ability of lowering the surface tension was dependent on increasing of carbon atom number in alkyl chain. Foaming power of all the monoesters was better than that of diesters. while foam stability of diesters was to the contrary. Emulsifying power of soybean oil or benzene was specially expected to be good for emulsifiers in industrial application fields. HLB values of monoesters and diesters evaluated by Griffin's method were in the range of 8 to 12. Dispersion property of ferric oxide was stable in the range of 4.5×10-5~5.0×-4mol/L in case of monoesters, and 10-5~10-4mol/L in case of diesters.

본 논문은 용액법으로 성장시킨 저밀도 폴리에틸렌 박막의 냉각 조건에 따른 결정화도의 관계와 냉각 조건에 따른 전기전도현상, 유전특성 및 절연파괴에 관하 연구로서 박막은 140[˚C]에서 2시간 유지후 냉각 조건을 달리하여 제작하였다. 결정화도는 XRD를 이용하여 측정하였으며 냉각 속도가 빠를수록 결정화도가 감소함을 볼 수 있었다. 전기전도현상은 냉각 조건에 무관하게 저전계에서는 이온전도특성이 나타나고 고전계에서는 공간전하제한전류이론이 지배적이다. 절연파괴전계는 냉각속도가 증가할수록 증가하고 self-healing절연파괴 방법에서는 시험회수가 증가할수록 증가하였다.

The procedure to prepare an acrylic emulsion water repellents by blending of arcylic copolymer, activated polyethylene, wax, and emulsifiers was published in the previous paper. After the treatment of the prepared water repellents on a cotton fabrics with and without textile finishing resin, washability, contact angle, tearing strength, and crease recovery were tested. As the result, there were remarkable improvements in physical properties. Proper curing temperature of the synthesized water repellents impellents was 150℃ : proper using concentration was 5wt% : sodium acetate was the best catalyst for water repellents among the used, and proper concentration was 1.0wt%.

Durable softening water repellents such as PODCWs were prepared by blending cationized compound of poly(octadecyl methacrylate-co-2-diethylaminoethyl methacrylate), of which synthetic methods were reported in the previous paper, activated polythylene, waxes, and emulsifiers. Water repellency of prepared PODCWs was measured by performing water repellent finish to various fabrics, PODCWs showed a good water repellency for P/C blended fabrics and their repelling tendency was in the order of P/C blended fabrics〉cotton fabrics〉nylon taffeta. The initial water repellencies of PODCW-1 and PODCW-2 were 100 and 100- points, respectively, for P/C blended fabrics. And also, PODCW-1 and PODCW-2 were confirmed as durable water repellents with the results of making little difference of water repellency as ±5 point after and before washing.

It is well known that the membrane permeation in pervaporation is governed by both the chemical nature of the membrane material and the physical structure of the membrane and also the separation can be achieved by differences in either solubility, size or shape. The solubility of the penerrant in the polymeric membrane can be described qualitively by applying the Hildebrand relation [1] which relates the energy of mixing of the penerrant and the polymer material. Froehling et al. have tried to predict the swelling behavior of polymers for the systems of polyvinylchloride(PVC)-toluene-methanol, PVC-trichloroethylene-nitromethane and PVC-n-butylacetate-nitromethane[2]. The former two systems which do not show the donor/acceptor interactions upon mixing showed the successful results[2]. In addition to this technique, there are several other possible approaches to predict the swelling behaviors of polymers, such as the surface thermodynamic approach[3, 4], the comparison of the membrane polarity with the solvent polarity in terms of Dimroth's solvent polarity value[5].