• Title/Summary/Keyword: $C_3$S

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과량의 $SO_3$가 존재할 때 $3CaO.SiO_2$의 생성 저하 메카니즘 (Mechanism of $3CaO.SiO_2$ Prevention in Presence of Excess $SO_3$)

  • 정해문;한기성;최상흘
    • 한국세라믹학회지
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    • 제30권7호
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    • pp.527-534
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    • 1993
  • The phenomena that excess sulfate hindred the C3S formation in the presence of clinker liquid phase were investigated. In the case of (NH4)2SO4, assuming SO3 atmospheric condition, sulfate stabilized C2S and was enriched at the surface of C2S grains, so C2S was prevented from being dissolved into clinker melt. CaSO4 showed the similar aspect with (NH4)2SO4, however, the prevention of C3S formation by CaSO4 took more influence that C2AS and C4A3 were formed below 100$0^{\circ}C$, and remained upto clinkering temperature, 145$0^{\circ}C$, thus these intermediate phases caught CaO which would participate the C3S formation.

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시멘트 초기 수화과정에 대한 유기혼화제의 영향(I) (Effect of Organic Admixture(Calcium Lignosulfonate) (I) on the Early Hydration Process of Protland Cement)

  • 문정연;최상홀
    • 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.

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PFOS 대체물질의 환경유해성에 관한 연구 (Study on Environmental Hazards of Alternatives for PFOS)

  • 최봉인;정선용;나숙현;신동수;유병택
    • 대한환경공학회지
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    • 제38권6호
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    • pp.317-322
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    • 2016
  • PFOS sodium salt ($C_8F_{17}SO_3Na$)는 28일 동안 미생물에 의한 분해가 이루어지지 않은 반면 4종의 대체물질($C_{25}F_{17}H_{32}S_3O_{13}Na_3$, $C_{15}F_9H_{21}S_2O_8Na_2$, $C_{23}F_{18}H_{28}S_2O_8Na_2$, $C_{17}F_9H_{25}S_2O_8Na_2$)은 각각 21.6%, 20.5%, 15.8% 그리고 6.4% 분해가 이루어졌다. Daphnia magna를 이용하여 48시간 동안 수행한 물벼룩급성독성시험에서 sodium salt ($C_8F_{17}SO_3Na$)의 반수영향농도($EC_{50}$)는 54.5 mg/L 인 것으로 확인된 반면 4종의 대체물질은 500.0 mg/L에서 아무런 영향이 나타나지 않았다. 500.0 mg/L에서 PFOS sodium salt($C_8F_{17}SO_3Na$)의 표면장력은 46.2 mN/m이었으며 대체물질 4종의 표면장력은 모두 PFOS sodium salt 보다 우수한 것으로 확인되었다. $C_{23}F_{18}H_{28}S_2O_8Na_2$ (20.9 mN/m)는 가장 낮은 표면장력을 갖고 있었다. 그 다음은 $C_{15}F_9H_{21}S_2O_8Na_2$ (23.4 mN/m), $C_{17}F_9H_{25}S_2O_8Na_2$ (27.3 mN/m) 그리고 $C_{25}F_{17}H_{32}S_3O_{13}Na_3$ (28.2 mN/m) 순인 것으로 확인되었다. 미생물분해시험, 물벼룩급성독성시험 그리고 표면장력측정 결과를 종합해 보면 4종의 PFOS 대체물질($C_{25}F_{17}H_{32}S_3O_{13}Na_3$, $C_{15}F_9H_{21}S_2O_8Na_2$, $C_{23}F_{18}H_{28}S_2O_8Na_2$, $C_{17}F_9H_{25}S_2O_8Na_2$)은 모두 PFOS sodium salt ($C_8F_{17}SO_3Na$) 보다 우수한 것으로 확인되었으며 특히 3종의 대체물질($C_{15}F_9H_{21}S_2O_8Na_2$, $C_{23}F_{18}H_{28}S_2O_8Na_2$, $C_{25}F_{17}H_{32}S_3O_{13}Na_3$)은 미생물분해율이 15.8~21.6%로 상대적으로 높고, 물벼룩급성독성과 표면장력측정이 PFOS sodium salt 보다 상당히 우수하다. 그러므로 이들 4종의 대체물질은 PFOS 대체물질로 활용이 가능할 것으로 판단된다.

중금속(Zn, Cu, Cr)이 시멘트 수화반응이 미치는 영향 (Effects of Heavy Metals(Zn, Cu, Cr) on Hydration Reaction of Cement)

  • 이동건;오희갑
    • 한국세라믹학회지
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    • 제38권8호
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    • pp.732-739
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    • 2001
  • 산업부산자원으로부터 유입되는 중금속이 시멘트 수화반응에 미치는 영향에 대하여 연구하였다. 출발물질은 순수시약을 사용하여 $C_3$S와 $C_2$S 조성으로 배합하고 여기에 Zn, Cu, Cr의 중금속 산화물을 1000ppm, 2000ppm, 3000ppm 첨가하여 150$0^{\circ}C$에서 1시간 소결하여 중금속의 고용분배, 결정구조, 용출상태 그리고 수화열을 관찰하였다. 중금속중 Zn는 $C_3$S와 간극질에 집중 고용되고 Cu는 간극물질에 집중 고용되며 Cr은 $C_3$S와 $C_2$S에 집중 고용되었다. 광학현미경 및 XRD 관찰결과 중금속 함량별로 $C_3$S와 $C_2$S의 결정상에는 큰 영향이 없는 것으로 나타났다. 그리고 7일간 수화시 Zn는 40~50%, Cu와 Cr은 전량 용출되었다. Conduction calorimeter 분석결과 중금속 함량별 변화에도 $C_3$S와 $C_2$S 수화열에는 차이가 없었다.

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Fe-Scale과의 반응에 의한 $Cr_3C_2$계 복합체의 산화손상 (Oxidation of $Cr_3C_2$ Composites with Fe-Scale)

  • 한동빈;홍기곤;박병학
    • 한국세라믹학회지
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    • 제31권7호
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    • pp.767-771
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    • 1994
  • In a salb-preheating furnace of steel-making industry, the oxidation/degradation behavior of Cr3C2 ceramic composited dkid button reaction with scale in Fe-oxide system occurs and was thermodynamically examined. The reaction of scale with Cr3C2 skid button produces Cr3C2(s) and C(s), and Co gas is then evolved from the reaction of C(s) with Fe-scale. Cr3C2(s) from oxidation of Cr3C2(s) reacted with Fe-oxide(s) becomes high-melting chromite. The chromite acts as protection layer against further oxidation and improves resistance of the reaction of Cr3C2 skid button with Fe-scale.

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$3CaO.SiO_2$ 생성반응과 미세조직에 있어서 Alkali Oxide와 $SO_3$의 상호작용 (Interaction of Alkali Oxide and $SO_3$ on $3CaO.SiO_2$ Formation and Microstructure)

  • 정해문;최상흘
    • 한국세라믹학회지
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    • 제30권12호
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    • pp.1071-1079
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    • 1993
  • Interaction of alkali oxides and SO3 and C3S formation and microstructure was studied using K2CO3 and Na2CO3 as alkali sources and (NH4)2SO4 for SO3. When SO3/K2O=1.43 as mole ratio, K2O and SO3 react to form K2SO4, this phase is immiscible with other oxide melt and thus could not affect C3S formation as well as its microstructure. In a condition of SO3/K2O 1, C3S crystals were round and grown in a much larger size. With addition of Na2O and SO3 by only 1wt% each, C3S formation was strongly hindered. Since C2S was stabilized by Na+ and SO4-2, it could not react to give C3S formation. However in the condition of SO3/Na2O=1.43, a little amount of C3S was formed. It is considered that small amount of Na2SO4 was formed, this phase was immiscible with clinker liquid, and the C3S crystals were formed locally in the liquid part of relatively low Na2O and SO3 compositions. These crystals had irregular and rough surfaces and contained more inclusions than those grown from K2O.SO3 system.

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$C_4A_3\bar{S}$-Calciumsicate계 크링커의 수화반응 (Hydration of $C_4A_3\bar{S}$-Calciumsicate Clinker)

  • 이승주;최상흘
    • 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.

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클링커 광물 함량 변화시 Modified belite Cement의 특성 (Properties of Modified Belite Cement with the Content of Clinker Minerals)

  • 최연묵;이양수;김남호;최상홀
    • 한국세라믹학회지
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    • 제35권5호
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    • pp.479-485
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    • 1998
  • 천연 원료인 석회석, 규석, bauxite, 무수석고를 이용하여 belite계 시멘트의 한 종류인 고기능성의 modified belite cement를 제조하고자 $C_4A_3{\={S}}$에 비해 $C_2S$의 함량이 상대적으로 많은 두가지 클링커를 합성하였다. 주광물 $C_2S$는, 고온형의 ${\alpha}'-C_2S$를 상온까지 안정화시켜서 수화시 활성을 높이기 위해 붕사($Na_2O\;2B_2O_3{\cdot}10H_2O$)를 첨가하였다. 붕사의 첨가량을 변화시켜 각 클링커의 소성과 수화특성을 비교하고, 이들을 시멘트로 제조할 때 무수석고의 함량을 변화시켜 강도 증진에 기여하는 적정 석고 혼합량을 구하고자 하였다. 그 결과, $C_2S$의 함량을 60 wt.%로 목적할 때, ${\alpha}'-C_2S$로 안정화시키기 위한 붕사의 첨가량은 5 wt.%가 효과적이었으며, 시멘트 제조시 $SO_3/Al_3O_3$ 비가 1.3이 되도록 무수석고를 첨가한는 것이 적절하였다. 붕사가 없는 경우 수화 초기에 ettringite만이 강도에 기여하는 반면 봉사를 첨가하면 수화 초기에 ettringite와 함게 C-S-H 수화물이 생성되었음을 알 수 있었다.

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Modified Belite Cement 구성광물의 생성에 미치는 붕상의 영향 (The Effects of Borax on Formation of Modified Belite Cement Minerals)

  • 채우형;최상홀
    • 한국세라믹학회지
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    • 제33권10호
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    • pp.1163-1169
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    • 1996
  • The effects of borax on the phase formation of C2S, C4A3 and $\alpha$'-C2S phases. It has negative effects on formation of C4A3 And it lowers the forming temperature of C4AF. It also has been found that borax improves the clinkerization of MBC. In the MBC clinker with borax 3% C2S have larger and more irregular shapes, larger C/S mole ratio and C4A3 have smaller size larger C/ molr ratio than in the clinker without borax.

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A Novel Complement Fixation Pathway Initiated by SIGN-R1 Interacting with C1q in Innate Immunity

  • Kang, Young-Sun
    • 한국미생물학회:학술대회논문집
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    • 한국미생물학회 2008년도 International Meeting of the Microbiological Society of Korea
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    • pp.23-25
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    • 2008
  • Serum complement proteins comprise an important system that is responsible for several innate and adaptive immune defence mechanisms. There were three well described pathways known to lead to the generation of a C3 convertase, which catalyses the proteolysis of complement component C3, and leads to the formation of C3 opsonins (C3b, iC3b and C3d) that fix to bacteria. A pivotal step in the complement pathway is the assembly of a C3 convertase, which digests the C3 complement component to form microbial-binding C3 fragments recognized by leukocytes. The spleen clears microorganisms from the blood. Individuals lacking this organ are more susceptible to Streptococcus pneumoniae. Innate resistance to S. pneumoniae has previously been shown to involve complement components C3 and C4, however this resistance has only a partial requirement for mediators of these three pathways, such as immunoglobulin, factor B and mannose-binding lectin. Therefore it was likely that spleen and complement system provide resistance against blood-borne S. pneumoniae infection through unknown mechanism. To better understand the mechanisms involved, we studied Specific intracellular adhesion molecule-grabbing nonintegrin (SIGN)-R1. SIGN-R1, is a C-type lectin that is expressed at high levels by spleen marginal-zone macrophages and lymph-node macrophages. SIGN-R1 has previously been shown to be the main receptor for bacterial dextrans, as well as for the capsular pneumococcal polysaccharide (CPS) of S. pneumoniae. We examined the specific role of this receptor in the activation of complement. Using a monoclonal antibody that selectively downregulates SIGN-R1 expression in vivo, we show that in response to S. pneumoniae or CPS, SIGN-R1 mediates the immediate proteolysis of C3 and fixation of C3 opsonins to S. pneumoniae or to marginal-zone macrophages that had taken up CPS. These data indicate that SIGN-R1 is largely responsible for the rapid C3 convertase formation induced by S. pneumoniae in the spleen of mice. Also, we found that SIGN-R1 directly binds C1q and that C3 fixation by SIGN-R1 requires C1q and C4 but not factor B or immunoglobulin. Traditionally C3 convertase can be formed by the classical C1q- and immunoglobulin-dependent pathway, the alternative factor-B-dependent pathway and the soluble mannose-binding lectin pathway. Furthermore Conditional SIGN-R1 knockout mice developed deficits in C3 catabolism when given S. pneumoniae or its capsular polysaccharide intravenously. There were marked reductions in proteolysis of serum C3, deposition of C3 on organisms within SIGN-$R1^+$ spleen macrophages, and formation of C3 ligands. The transmembrane lectin SIGN-R1 therefore contributes to innate resistance by an unusual C3 activation pathway. We propose that in the SIGN-R1 mediated complement activation pathway, after binding to polysaccharide, SIGN-R1 captures C1q. SIGN-R1 can then, in association with several other complement proteins including C4, lead to the formation of a C3 convertase and fixation of C3. Therefore, this new pathway for C3 fixation by SIGN-R1, which is unusual as it is a classical C1q-dependent pathway that does not require immuno globulin, contributes to innate immune resistance to certain encapsulated microorganisms.

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