• Title/Summary/Keyword: Secondary Gypsum Formation

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Premature Stiffening of Cement Paste Caused by Secondary Gypsum and Syngenite Formation (False Set)

  • Chung, Chul-Woo;Lee, Jae-Yong
    • Architectural research
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    • v.13 no.1
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    • pp.25-32
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    • 2011
  • The purpose of this research is to investigate the effect of specific hydration reaction on the stiffening process of cement paste. The cement compositions are manipulated to cause specific hydration reactions (secondary gypsum and syngenite formation) responsible for false set, and the relationship between specific hydration reactions and the flow and stiffening behavior of cement paste were investigated using modified ASTM C 403 penetration resistance measurement and oscillatory shear rheology. X-ray powder diffraction (XRD) was used for the phase identification associated with premature stiffening of cement paste. Differential thermal analysis (DTA) and thermogravimetric analysis (TGA) were used for verification of syngenite formation. From the results, both secondary gypsum and syngenite formation caused faster stiffening and set. The amount of syngenite produced during 1 hour hydration was approximately 1 % of total mass of the cement paste, but cement paste with syngenite formation showed significantly accelerated stiffening behavior compared to normal cement paste.

Recent Discovery of secondary Mineral Deposit in an Idaho Lava Tube

  • Kesner, D.W.
    • Journal of the speleological society of Korea
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    • no.8
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    • pp.77-84
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    • 1998
  • A large number of lava tubes in southwestern idaho contain some extremely impressive secondary mineral deposits. Gypsum and mirabilite can be found coating entire lava formation and in some cases entire rooms, thenardite and cristobolite can also be found throughout idaho's lava tubes, although in smaller individual concentrations. To a lesser degree iron and copper-based deposits have been found. On rare occasions and in very small quantities calcium carbonate deposits have been found.(omitted)

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Mineralogical Changes Caused by the Weathering of Tailings Deposited on the Riverside of the Nakdong River, Bonghwa, Korea (봉화군 일대 낙동강변에 퇴적된 광미의 풍화에 따른 광물학적 변화)

  • Kim, Min-Jung;Kim, Yeong-Kyoo;Park, Hyoung-Sim;Jeon, Sang-Ho
    • Journal of the Mineralogical Society of Korea
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    • v.21 no.4
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    • pp.331-339
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    • 2008
  • In the upstream of Nakdong river in Bonghwa-gun, Gyeongsangbuk-do, certain areas of riverside were found to be covered by weathered mine tailings which were assumed to be migrated and deposited by flood. This study was conducted to investigate the formation and characteristics of the secondary minerals from tailings and related leaching behavior of heavy metals in the severely weathered tailing deposits by river waters. Quartz, feldspar, micas, chlorite, hornblende, talc, pyroxene (johannsenite), pyrite, and calcite were identified as primary minerals by XRD. Kaolinite can be formed by the weathering of tailings, but considering the short period of weathering time, kaolinite in the deposits is considered to be from unweathered tailings or moved from soils. The secondary minerals such as goethite, gypsum, basanite, and jarosite were also identified. The formation of the secondary minerals was affected by the species of primary minerals and pH conditions. The weathering of pyrite produced sulfate minerals such as gypsum, basanite, jarosite, and also goethite. Mn oxide was also identified by SEM, coated on the primary minerals such as quartz. This Mn oxide was poorly crystalline and thought to be the weathering product of johannsenite (Mn-pyroxene). The Fe and Mn oxides are the main minerals determining the brown/red and black colors of weathered tailings. EDS results showed that those oxides contain high concentrations of Pb, Zn, and As, indicating that, in the river, the formation of Fe and Mn oxides can control the behavior and leaching of heavy metals by co-precipitation or adsorption.

The Synthesis and Hydraulic properties of Calcium Sulfo Aluminate(CSA) derived from Secondary Refining Slag. (제강 2차 정련 슬래그를 재활용한 칼슘설포알루미네이트(CSA) 합성 및 수화 특성)

  • Seo, Chang Woo;Kim, Seon-Hyo;Ko, Sang Jin;Kim, Sang Hyun;Jo, Kyu Young
    • Korean Journal of Metals and Materials
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    • v.46 no.7
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    • pp.437-442
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    • 2008
  • The synthesis and hydration of Calcium Sulfo Aluminate[$3CaO{\cdot}3Al_2O_3{\cdot}CaSO_4(C_4A_3{\overline{S}})$, CSA cement utilizing secondary steelmaking refining slags is studied for recycling the discarded steel plant wastes to meet the environmental requrations imposed on the steel industry. Raw materials of secondary refining slag, lime sludge, gypsum and bauxite were prepared to be sintered at $1,250^{\circ}C$. The sintered samples were hydrated for 1, 3 and 7 days to evaluate the mineralogical and physico-mechanical properties. The hydration products evaluated with the aid of SEM and XRD analyses confirmed the formation and the continuing growth of ettringite phase with the further hydration times, which plays a role in developing the early strength and the expansion properties of cements. The physico-mechanical properties of hydrated CSA products employing the recycled steelmaking refining slags determined in terms of compressive strength and linear expansion of hydrated products are found to be superior to those of the Ordinary Portland Cement(OPC) or the other commercial CSA cements.

Concrete Deterioration Near Coastal Area and Characteristics of Associated Secondary Mineral Formation (해안지역 콘크리트의 성능저하 현상과 이에 수반되는 이차광물의 형성 특징)

  • 이효민;황진연;진치섭
    • Economic and Environmental Geology
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    • v.36 no.5
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    • pp.365-374
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    • 2003
  • Various deleterious chemicals can be introduced to existing concrete structures from various external sources. The deterioration of concrete by seawater attack is involved in complex processes due to various elements contained in seawater. In the present study, attention was paid to the formation of secondary minerals and characteristics of mineralogical and micro-structural changes involved in concrete deterioration caused by the influence of major seawater composition. The characteristics of deterioration occurred in existing concrete structures was carefully observed and samples were collected at many locations of coastal areas in Busan-Kyungnam. The petrographic, XRD, SEM/EDAX analyses were conducted to determine chemical, mineralogical and micro-structural changes in the aggregate and cement paste of samples. The experimental concrete deteriorations were performed using various chloride solutions (NaCl, CaCl, $MgCl_2$ and $Na_2SO_4$ solution. The experimental results were compared with the observation results in order to determine the effect of major elements in seawater on the deterioration. The alkalies in seawater appear to accelerate alkali-silica reaction (ASR). The gel formed by ASR is alkali-calcium-silica gel which known to cause severe expansion and cracking in concrete. Carbonation causes the formation of abundant less-cementitious calcite and weaken the cement paste. Progressive carbonation significantly affects on the composition and stability of some secondary minerals. Abundant gypsum generally occurs in concretes subjected to significant carbonation, but thaumasite ({$Ca_6/[Si(OH)_6]_2{\cdot}24H_2O$}${\cdot}[(SO_4)_2]{\cdot}[(CO_3))2]$) occurs as ettringite-thaumasite solid solution in concretes subjected to less significant carbonation. Experimentally, ettringite can be transformed to trichloroaluminate or decomposed by chloride ingress under controlled pH conditions. Mg ions in seawater cause cement paste deterioration by forming non-cementitious brucite and magnesium silicate hydrate (MSH).

Trends of phosphorus recovery technology from sewage sludge ash by wet chemical method (습식 화학적 방법에 의한 하수 슬러지 소각재에서의 인 회수 기술동향)

  • Lee, Min-Su;Kim, Dong-Jin
    • Journal of Korean Society of Water and Wastewater
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    • v.32 no.2
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    • pp.131-143
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    • 2018
  • Phosphorus (P) is a limited, essential, and irreplaceable nutrient for the biological activity of all the living organisms. Sewage sludge ash (SSA) is one of the most important secondary P resources due to its high P content. The SSA has been intensively investigated to recover P by wet chemicals (acid or alkali). Even though $H_2SO_4$ was mainly used to extract P because of its low cost and accessibility, the formation of $CaSO_4$ (gypsum) hinders its use. Heavy metals in the SSA also cause a significant problem in P recovery since fertilizer needs to meet government standards for human health. Therefore, P recovery process with selective heavy metal removal needs to be developed. In this paper some of the most advanced P recovery processes have been introduced and discussed their technical characteristics. The results showed that further research is needed to identify the chemical mechanisms of P transformation in the recovery process and to increase P recovery efficiency and the yields.