The pultruded fiber reinforced polymer plastic (PFRP) is one of the most actively studied composite materials for the structural member in construction industries. In domestic design process, the PFRP member is designed as an isotropic material having only longitudinal material properties for simplicity, because it is too complex to consider orthotrophy of PFRP perfectly. In this study, three cases of buckling analysis of PFRP plate is conducted theoretically and numerically. First, the PFRP plate is considered as an orthotropic material. Second, the PFRP plate is considered as an isotropic plate having only longitudinal material properties. Third, the PFRP plate is considered as an isotropic plate having geometric mean of longitudinal and transverse material properties. As a result of buckling analysis, a buckling strength of PFRP plate as an isotropic plate having only longitudinal material properties is about 2.21 times larger than that of PFRP plate analyzed as an orthotropic plate. On the other hand, a buckling strength of PFRP plate as an isotropic plate having geometric mean material properties is about 1.19 times larger than that of PFRP plate analyzed as an orthotropic plate. In conclusion, the safety factor of 3 used in domestic design process of PFRP member is no longer applicable due to overestimation of buckling strength of PFRP member which leads to nonconservative design.

노즐시험기로 측정되는 직물의 당김 힘은 직물이 갖는 포괄적인 촉감을 나타낸다. 노즐시험기는 기존 KES 시스템보다 저가이며, 측정에 있어서 절차가 간단하고 빠르다. 본 연구에서는 노즐시험기로 측정되는 직물의 촉감을 정량적으로 평가하기 위해 마찰법칙을 기초로 하여 반 실험적 촉감 방정식을 개발하였다. 모델 식에서 고려된 변수들은 직물의 마찰계수, 그리고 직물의 굽힘 길이와 전단 신도에 의해 결정되는 직물의 3차원적 변형 특성을 나타내는 드레이프 계수이다. 12 종류의 서로 다른 물성의 면과 폴리에스터 직물들을 사용하여 실험 측정한 촉감 값과 모델 방정식으로부터 예측한 촉감 값들을 비교 분석하였다. 높은 마찰계수, 높은 굽힘 길이, 그리고 낮은 전단 신도를 갖는 직물일수록 높은 촉감 마찰력, 즉 낮은 촉감 성능을 보여주었다. 실험 측정한 촉감 값과 모델 식으로부터 계산한 값들 사이 잘 일치하였으며, 이와 같은 결과는 모델 식을 사용하여 직물의 고유 물성들로써 촉감의 객관적인 예측이 가능함과 더불어 촉감 성능의 향상을 위한 직물설계에 있어서도 유용한 정보를 제공할 수 있음을 보여준다.

막 구조는 자유로운 형태, 경량성, 내구성, 햇빛 투광성 및 균질성 때문에 전 세계적으로 현대 건축물에 다양하게 사용되어 왔다. 새로운 막 재료의 개발로 새로운 건축 구조설계에 대한 가능성을 열어가고 있다. 최근 주로 사용되는 막 구조의 지붕 재료에는 PVC, PVF, PVDF, PTFE 코팅 막재 및 ETFE 막재가 수로 사용되고 있다. 건축용 막은 내화성, 강도 부족, 인열강도, 내구성 및 탄성 등에 대한 몇가지 문제점들을 가지고 있다. 이러한 문제점들을 평가하기 위해서 본 연구에서는 PVDF 코팅 폴리에스터 막재에 대한 인장강도, 인열 강도 및 반복하중거동 시험을 실시하여 건축용 막재의 기초적인 역학적 특성을 분석하고자 한다. 막재의 탄성계수는 337.30~1257.63N/㎟, 신율은 17.90~26.91%로 주어졌다.

In this study DMT(Dimethylterephthalate), NDC(Dimethyl-2, 6-Naphthalene Dicarboxylate) were used to synthesize polyester polyol which shows enhanced storage stability, improved flame retardancy, and good compressive strength. If DMT and NDC react respectively with DEG(Diethylene Glycol) which is kind of linear diol, the obtained polyester polyols tend to crystallize easily after the reaction. In case of DMT, PA(Phthalic Anhydride) which has asymmetric structure was introduced to retard the crystallization. In case of NDC, DPG(Dipropylene Glycol) which has an methyl side chain was introduced to prevent the crystallization. It was found that to introduce DPG was much more effective method to prevent the crystallization than PA. NDC and DMT were reacted together with DPG for various compositions of NDC:DMT(8:2, 6:4, 4:6 mol ratio). The obtained NDC-DMT-DPG based polyester polyol showed improved flame retardancy, and good compressive strength with increasing the content of NDC.

The aim of this study is to enhance the flame retardancy by the synergism effect of phosphorus and bromine groups. The flame-retardant polyurethane coatings containing phosphorus and bromine compounds were synthesized. After synthesizing the intermediate products of tetramethylene bis(orthophosphate) (TBOP) and trimethylolpropane/2,3-dibromopropionic acid (2,3-DBP) [2,3-DBP-adduct], the condensation polymerization was performed with four different monomers of two intermediate products, 1,4-butanediol, and adipic acid to obtain four-components copolymer. In the condensation polymerization, the content of phosphorus was fixed to be 2wt%, and the content of 2,3-DBP that provides bromine component was varied to be 10, 20, and 30wt%, and we designated the prepared modified polyesters containing phosphorus and bromine as DTBA-10C, -20C, -30C. Average molecular weight and polydispersity index of the preparation of DTBAs were decreased with increasing 2,3-DBP content because of increase of hydroxyl group that retards reaction. We found that the thermal stability of the prepared DTBAs increased with bromine content at high temperature.

In order to obtain the maximum flame retardancy with the minimal deterioration of physical properties of PU flame-retardant coatings, chlorine and phosphorous functional groups were introduced into the pre-polymer of modified polyesters. In the first step, the tetramethylene bis(orthophosphate) (TBOP) and neohexanediol dichloroacetate (DCA-adduct) intermediates were synthesized. In the second step, 1,4-butanediol and adipic acid monomers were polymerized with the two kind of intermediates to obtain copolymer. The modified polyesters containing chlorine and phosphorous (ATBA-10C, -20C, and -30C) were synthesized by adjusting the contents of chlorine compound (dichloroacetic acid, 10, 20, 30 wt%) with fixed the content of phosphorous compound (2 wt%). The PU flame-retardant coatings (TTBAH -10C, -20C, and -30C) were prepared using the synthesized ATBAs and HDI-trimer as curing agent at room temperature. The physical properties of PU flame-retardant coatings with chlorine and phosphorous were inferior to those with phosphorous only and the properties were getting worse with increasing chlorine content. Flame retardancy was tested with three methods. With the vertical method, Complete combustion time of ATBAHs were 259~347 seconds, which means that the prepared coatings are good flame-retardant. With the 45˚ Meckel burner method, char lengths of the three prepared coatings were less than 2.9 cm, which indicates that the prepared coatings are 1st grade flame retardancy. With the limiting oxygen index (LOI) method, the LOI values of the three prepared coatings were in the range of 30~35%, which proves good flame retardancy of the prepared coatings. From the results of flame retardancy tests of the specimens that contain the same amounts of flame retarding compounds, it was found that the coatings containing both phosphorous and chlorine show higher flame retardancy than the coatings containing phosphorous alone. This indicates that some synergy effect of flame retardancy exists between phosphorous and chlorine.

The PU flame-retardant coatings (TTBAH, ATBAH-10C, -20C, and -30C) were prepared using the synthesized ATBAs and HDI-trimer as curing agent at room temperature. The physical properties of PU flame-retardant coatings with chlorine and phosphorus were inferior to those with phosphorus only and the properties were getting worse with increasing chlorine content. Flame retardancy was tested with three methods. With the vertical method, complete combustion time of ATBAHs were 259~347 seconds, which means that the prepared coatings are good flame-retardant. With the 45˚ Meckel burner method, char lengths of the three prepared coatings were less than 2.9 cm, which indicates that the prepared coatings are first grade. With the limiting oxygen index (LOI) method, the LOI values of the three prepared coatings were in the range of 30~35%, which proves good flame retardancy of the prepared coatings. from the result of flame retardancy tests of the specimens that contain the same amounts of flame retarding compounds. it was found that the coatings containing both phosphorus and chlorine show higher flame retardancy than the coatings containing only phosphorus. This indicates that there exists, some synergy effect between coexisting phosphorus and chlorine.

In order to obtain the maximum flame retardancy as well as the minimum deterioration of physical properties of PU flame-retardant coatings, chlorine and phosphorus functional groups were introduced into the pre-polymer of modified polyesters. In the first step, the tetramethylene bis(orthophosphate) (TBOP) and neohexanediol dichloroacetate (DCA-adduct) intermediates were synthesized. In the second step, 1,4-butanediol and adipic acid monomers were polymerized with the two kinds of intermediates to obtain copolymers. The modified polyesters containing chlorine and phosphorus (ATBA-10C, -20C, and -30C) were synthesized by adjusting that the content of phosphorus compound was fixed as 2wt% and the contents of chlorine compound (dichloroacetic acid) were varied as 10, 20, and 30wt%. Average molecular weight and polydispersity index of the preparation of ATBAs were decreased with increasing DCA content because of the increase in hydroxyl group that retards reaction.

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.

The aim of this study is to synthesis basic resins for the preparation of PU flame-retardant coatings that contain phosphorus and chlorine. After synthesizing intermediates of tetramethylene bis(orthophophate) (TMBO) and neohexanediol trichlorobenzoate (TBA-adduct), the condensation polymerization was performed with the intermediates, 1,4-butanediol, and adipic acid to obtain four-component copolymers. In the condensation polymerization, the content of phosphorus was fixed to be 2%, and the content of trichlorobenzoic acid (TBA) that provides chlorine component was varied to be 10, 20, and 30wt%, and we designated the prepared modified polyesters containing chlorine and phosphorus as TTBA-10C, TTBA-20C and TTBA-30C. Average molecular weight and polydispersity index of the prepared TTBAs decreased with increasing TBA content because of the increase in the number of hydroxyl groups that retards reaction. We found that the thermal stability of the prepared TTBAs increased with chlorine content at high temperatures.