• 한국세라믹학회지
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• 제37권4호
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• pp.388-394
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• 2000

The C4A3S clinker was prepared by the solid-state reaction. The mixture of raw materials; calcite, kaoline and gypsum, was fired at 135$0^{\circ}C$ for 1hr and cooled rapidly in air. C4A3S type expansive was made with C4A3S clinker, CaO and CaSO4. The cement replaced by 10 wt.% C4A3S type expansive was investigated by the measurement of the strength(compressive, tensile, flexural) and length change at various curing conditions. Hydration products were mainly ettringite, monosulfate and Ca(OH)2. The densification and the expansion due to the formation of ettringite during the hydration increased strength and reduced the drying shrinkage of hardened cement.

• 한국세라믹학회지
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• 제19권1호
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• pp.51-57
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• 1982

The clinckers were obtained when a raw mixture consisted of limestone, slags and gypsum was burned at 134$0^{\circ}C$ for 30 minutes, and 128$0^{\circ}C$ for 30 minutes adding $CaF_2$ as a flux. The principal compounds of these clinkers were $C_3S_2$, $\beta-C_2S$, $C_1A_3{\bar{S}}$. To investigate hydration behavior, cements were made and hydrated at constant humidity cabinet (W/C=0.5 20$\pm 1^{\circ}C$). X-ray diffractometer, SEM, and conduction calorimeter were employed to examine the hydration behavior. The hydrates were mainly C-S-H, ettringite, $Ca(OH)_2$. By the hydration of $C_3S$ and $C_4A_3\bar{S}$, the needle-like ettringite filling the inner vacant spaces of the hardened body might contribute to the rapid-hardening and high-strength phenomena. Furthermore, the hardened body became stronger due to the hydration of $C_2S$ at later period. The addition of granulated blastfurnace slags have a potential to be a blended cement.

• 한국세라믹학회지
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• 제26권4호
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• pp.514-520
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• 1989

The early hydration characteristics according to the C3S/C3A ratio and presence of gypsum, in order to establish the hydration mechanism of the system C3S-C3A, have been studied. The rate of C3S dissolution in the system C3S-Gypsum was higher than that in the system C3S. Consequently, the induction period was reduced and the rate of Ca(OH)2 formation in the accleration period was increased. The hydration of C3S in the system C3S-C3A was retarded because Al3+ in the liquid phase originating from the hydration of C3A was incorporated into calcium hydrosilicates formed. The retardation phenomenon of C3S hydration was not appeared in the system C3S-C3A-gypsum because the reaction of monosulfate formation became the rate-determining step.

• 한국양식학회지
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• 제19권2호
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• pp.95-98
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• 2006

This study was performed to determine possibility of compensatory growth of juvenile olive flounder fed a commercial feed during the summer season. Five treatments of fish with triplicates were prepared: C, S1, S2, S3 and S4. Fish in the control group (C) was hand-fed with the commercial feed to apparent satiation twice daily for 6 days a week during 6 weeks. Fish in S1, S2, S3, and S4 experienced 1, 2, 3, and 4 weeks of starvation before fed to satiation twice daily for 5, 4, 3, and 2 weeks, respectively. The feeding trial lasted far 6 weeks. Survival of flounder in C, S1 and S2 was significantly (P<0.05) higher than that offish in S4. Weight gain and specific growth rate (SGR) of flounder in C and S1 were significantly (P<0.05) higher than those of fish in S2, S3 or S4. And weight gain and SGR of flounder in S2 and S3 were significantly (P<0.05) higher than those of fish in S4. Feed consumption of flounder tended to increase with weeks of feeding. Feed efficiency ratio and protein efficiency ratio for flounder in C, S1, S2 and S3 were significantly (P<0.05) higher than those for fish in S4. Moisture content of the whole fish in C was lowest, but highest for fish in S4, respectively. Crude protein content of the whole fish in C was highest, but lowest far fish in S4, respectively. Crude lipid content of the whole fish in C, S1 and S2 was significantly (P<0.05) higher than that of fish in S4. In conclusion, full compensatory growth was obtained in juvenile olive flounder fed for 5 weeks after 1-week feed deprivation during the summer season. Compensatory growth of fish was well supported by improvement in feed efficiency ratio and protein efficiency ratio.

• 대한화학회지
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• 제41권3호
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• pp.150-156
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• 1997

Bulgecinine의 선구물질인 (4S,5R)-1-acetyl-2-formyl-5-benzyloxymethyl-4-pyrrolidinol (15)을 diacetone-D-glucose로부터 합성하였다. Barton 탈산소화 반응, C-5에서의 반전, $-N_3$ 도입과 환원 및 C-2에서의 고리 형성을 통해 bulgecinine의 핵심 중간체인 두 고리 화합물 (6R)-6-Ο-benzyloxymethyl-(3R)-3-methoxy-2-oxa-5-azabicyclo-[2,2,1]heptane (13)을 합성하였다. 화합물 13을 N-아세틸화 후 산가수분해하여 얻은 bulgecinine 선구물질은 토토머화가 수반되어 (2S,4S,5R)-pyrrolidinol 유도체 15와 함께 (2S,4S,5R)-부분 입체 이성질체도 얻어졌다.

• 콘크리트학회논문집
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• 제16권3호
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• pp.369-374
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• 2004

$C_4A_3S$ 합성은 천연원료인 석회석과 산업폐기물 및 부산물인 수산화알루미늄, 이수석고를 일정혼합비로 균일하게 혼합하여 20, 400, 600, $1200^{\circ}C$에서 1시간 소성 후 급냉하여 $C_4A_3S$ 클링커를 합성하였다. 합성한 클링커를 보통 포틀랜드 시멘트에 10 wt%치환하여 수중 양생하에서 수화반응 및 물성특성을 조사하였다. $1200^{\circ}C$에서 $C_4A_3S$ 클링커가 합성됨을 X-Ray diffraction pattern으로 관찰할 수 있었다 $1200^{\circ}C$에서 소성된 시료는 급결성을 띠었으며, 압축강도는 보통 포틀랜드 시멘트보다 20~30% 정도 높게 나타났다. 주요 수화생성물은 ettringite, 수산화 칼슘이며, ettringite의 팽창으로 인하여 모르타르의 건조수축이 보통 포틀랜드 시멘트보다는 낮게 나타났다.

• 한국세라믹학회지
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• 제21권2호
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• pp.143-148
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• 1984

In this study we mainly dealt with the effects of organic retarder(calcium lignosulfate) on the early hydration process of clinker minerals. From a consideration of the hydration process of tricalcium silicate $(C_3S)$ tricalcium silicate $(C_3S)$-tricalcium aluminate $(C_3A)$ tricalcium silicate $(C_3S)$-tetracalcium aluminof-errite $(C_4AF)$ systems with calcium lignosulfate the following results were obtained. 1. when 0.25wt% of CLS was added to $C_3S$ the hydration process was progressed normally but adding of 0.5wt% its hydration was greatly retarded. 2. The hydration of $C_3S$-$C_3A$ system was progressed normally up to 0.5wt% but by adding gypsum its hydration was retarded slightly. 3. The hydration of $C_3S$-$C_4AF$ system was greatly retarded even with 0.25wt% of CLS but by adding gypsum its hydration process was recovered normally.

• 한국세라믹학회지
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• 제27권4호
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• pp.560-566
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• 1990

The early hydration characteristics according to the C3A polymorphism and the presence of gypsum, in order to establish the hydration mechanism of the system C3S-C3A, have been studied. The hydration rate of C3A was changed according to the its crystal structure and influenced the hydration of C3S. That is, the hydration rate of C3S was accelerated in case of orthorhombic-C3A, but that was slightly retarded in case of melt-C3A than that of cubic-C3A. In the system C3S-C3A-gypsum, the retardation phenomenon of the reaction of monosulfate formation was observed in case of both orthorhombic and melt-C3A.

• 한국세라믹학회지
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• 제22권2호
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• pp.33-38
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• 1985

The hydration of supersulphated slag cement which is the mixture of granuloated blast furnace slag anhydrite $C_4A_3$ type clinker and calcined dolomite was studied by X-ray diffraction differential thermal analysis scanning electron microscope observation and measurement of the rate of heat liberation. The main hydrates were ettrigite and C-S-H. This supersulphated slag cement enhanced rapid-hardening and increased in strength at early stage due to the much of ettrigite. Furthermore the hardened cement became stronger due to the C-S-H that was produced from the hydration of the $eta$-$C_2S$ in $C_4A_3$ type clinker and the hydration of the dissolved components from slag at later period.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2010년도 제39회 하계학술대회 초록집
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• pp.36-36
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• 2010

Low-pressure fluorocarbon plasmas are widely used in microelectronics fabrication for a variety of surface modification purposes. In particular, fluorocarbon plasmas are used for the etching of dielectrics such as silicon dioxide and silicon nitride. Among the various fluorocarbons, this study focuses on C4F6 molecules (C4F6s) which are composed of hexafluorocyclobutene (c-C4F6), hexafluoro-1, 3-butadiene (1, 3-C4F6), and hexafluoro-2-butyne (2-C4F6). We have investigated the dissociation reactions of C4F6s, resulting in CF2, CF3, C2F3, and C3F3 fragments, by using the wB97X-D functional with various basis sets. In this presentation, the geometrical properties, energetics, and dissociation mechanisms of C4F6s will be suggested.