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Relevant bibliographies by topics / Cement chemistry

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Academic literature on the topic 'Cement chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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Journal articles on the topic "Cement chemistry"

1

Mason, Patricia. "Chemistry of Cement." Journal of Chemical Education 83, no. 10 (October 2006): 1472A. http://dx.doi.org/10.1021/ed083p1472a.

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Venkatesh, B., D. W. Pigott, A. Fernandez, and S. P. Hendry. "Continuous Measurement of Arterial Blood Gas Status during Total Hip Replacement: A Prospective Study." Anaesthesia and Intensive Care 24, no. 3 (June 1996): 334–41. http://dx.doi.org/10.1177/0310057x9602400306.

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The arterial blood gas chemistry was measured continuously in ten patients during primary cemented total hip replacement in order to define more precisely the patterns of changes in blood gases during various stages of the operation. All ten patients demonstrated significant drops in PaO2 after femoral cement implantation and nine of the ten after acetabular cement implanation. The mean drop in PaO2 following acetabular cement expressed as mean ± SD was 18±8 mmHg (16±6%) (P<0.05) and femoral cement application was 25±11 mmHg (23±9%) (P<0.05). For changes in PaO2 there were corresponding drops in SpO2 in all patients with the femoral cement and in eight patients with the acetabular cement. The mean drop in SpO2 following the application of acetabular and femoral cements respectively were 1.7±1.5% and 3±2.45%. No changes in blood PaO2 were observed during dislocation of the hip joint or reaming of acetabulum and femur. In vitro studies revealed no effect of the liquid monomer or the cured cement on the performance of the Clark electrode of the sensor. We suggest that significant drops in PaO2 occur with both acetabular and femoral cement implantation and that the derangements in blood PaO2 last longer than detected by pulse oximetry following cement implantation.

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Pike, Jack, Andrew Patterson, and Marvin S. Arons. "Chemistry of Cement Burns." Journal of Burn Care & Rehabilitation 9, no. 3 (May 1988): 258–60. http://dx.doi.org/10.1097/00004630-198805000-00004.

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Marangu, Joseph Mwiti, Joseph Karanja Thiong’o, and Jackson Muthengia Wachira. "Review of Carbonation Resistance in Hydrated Cement Based Materials." Journal of Chemistry 2019 (January 1, 2019): 1–6. http://dx.doi.org/10.1155/2019/8489671.

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Blended cements are preferred to Ordinary Portland Cement (OPC) in construction industry due to costs and technological and environmental benefits associated with them. Prevalence of significant quantities of carbon dioxide (CO2) in the atmosphere due to increased industrial emission is deleterious to hydrated cement materials due to carbonation. Recent research has shown that blended cements are more susceptible to degradation due to carbonation than OPC. The ingress of CO2 within the porous mortar matrix is a diffusion controlled process. Subsequent chemical reaction between CO2 and cement hydration products (mostly calcium hydroxide [CH] and calcium silicate hydrate [CSH]) results in degradation of cement based materials. CH offers the buffering capacity against carbonation in hydrated cements. Partial substitution of OPC with pozzolanic materials however decreases the amount of CH in hydrated blended cements. Therefore, low amounts of CH in hydrated blended cements make them more susceptible to degradation as a result of carbonation compared to OPC. The magnitude of carbonation affects the service life of cement based structures significantly. It is therefore apparent that sufficient attention is given to carbonation process in order to ensure resilient cementitious structures. In this paper, an indepth review of the recent advances on carbonation process, factors affecting carbonation resistance, and the effects of carbonation on hardened cement materials have been discussed. In conclusion, carbonation process is influenced by internal and external factors, and it has also been found to have both beneficial and deleterious effects on hardened cement matrix.

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Askar Zhambulovich, Aimenov, Khudyakova Tatyana Mikhailovna, Sarsenbayev Bakytzhan Kudaibergenovich, Dzhakipbekova Nagima Ormanovna, Ali Khalid Abdul Khalim Kheidar, and Alvein Yaser Mukhamed Ali. "Studying the Mineral Additives Effect on a Composition and Properties of a Composite Binding Agent." Oriental Journal of Chemistry 34, no. 4 (August 20, 2018): 1945–55. http://dx.doi.org/10.13005/ojc/3404031.

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A Portland cement is a basic initial component for concrete and reinforced concrete manufacture, which defines their technical-economic and operational properties. One of a perspective ways of increase in the efficiency of cement production without essential change of its technology is inclusion of various mineral additives influencing on a structure and properties of a cement stone. As power inputs make the most part of the costs necessary for cement manufacture, the cement industry is interested in decrease in fuel and electric power expenditures per 1 tonne of cement. To reach the decrease in power inputs and at the same time to raise the environmental safety of cement production the cement industry is recently focused on increase in output of composite cements. Composite cements not only promote optimization of the production in terms of ecology, but also can provide such technical advantages as lower hydration heat, higher chemical resistance and placeability.

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MacLaren, Douglas C., and Mary Anne White. "Cement: Its Chemistry and Properties." Journal of Chemical Education 80, no. 6 (June 2003): 623. http://dx.doi.org/10.1021/ed080p623.

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Viani, A., A. F. Gualtieri, M. Secco, L. Peruzzo, G. Artioli, and G. Cruciani. "Crystal chemistry of cement-asbestos." American Mineralogist 98, no. 7 (July 1, 2013): 1095–105. http://dx.doi.org/10.2138/am.2013.4347.

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van Breugel, K. "Modelling of cement-based systems—the alchemy of cement chemistry." Cement and Concrete Research 34, no. 9 (September 2004): 1661–68. http://dx.doi.org/10.1016/j.cemconres.2004.02.016.

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AGZAMOV, Farit A., Arman KABDUSHEV, Elvira TOKUNOVA, BAUYRZHAN Zh MANAPBAYEV, and Bolat Zh KOZHAGELDI. "MAGNESIA CORROSION OF GROUTING MATERIALS." Periódico Tchê Química 17, no. 34 (March 20, 2020): 951–61. http://dx.doi.org/10.52571/ptq.v17.n34.2020.975_p34_pgs_951_961.pdf.

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The issue of magnesia corrosion of grouting materials in oil and gas wells is very relevant in the construction of oil and gas wells since magnesia salts can lead to the destruction of Portland cement-based cement stone within few months. When fastening powerful intervals of salt deposits represented by magnesium salts, the use of magnesia cements is effective. However, individual layers and interlayers containing dissolved magnesium salts are not individually cemented, but overlap over the entire interval of the open hole with cement Portland cement, which can be destroyed due to magnesia corrosion. The main aim of the paper is to analyze the corrosion of Portland cement stone in aggressive environments of magnesia. As the quantitative indicators characterizing the degree of stone damage, the thickness of the damaged layer and the stone resistance coefficient are taken, characterized by the ratio of the compressive strength or bending strength of stone samples after being in an aggressive environment to the strength of control samples at the same hardening time. The corrosion resistance of cement stone was assessed after 8 weeks in an aggressive magnesia environment. Also, the role of MgCl2 concentration on the mechanism of corrosion damage to cement stone was studied. The use of reducing the water-cement ratio and adding palygorskite clay to reduce the porosity of cement stone and reduce the rate of corrosion damage is proposed. The kinetics and the main factors affecting the corrosion process were considered, an X-ray diffraction analysis of corrosion products and unaffected cement stone was carried out.

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Saito, T. "Cement Chemistry by Dr. Renichi Kondo." Concrete Journal 51, no. 9 (2013): 764–68. http://dx.doi.org/10.3151/coj.51.764.

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Dissertations / Theses on the topic "Cement chemistry"

1

Rodger, S. A. "The chemistry of admixture interaction during cement hydration." Thesis, University of Oxford, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371554.

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Afshar, Ali Behrooz. "The early hydration of cement." Thesis, Heriot-Watt University, 1986. http://hdl.handle.net/10399/1059.

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This thesis details the development and use of an electrical response technique for monitoring the chemical and physical changes occurring within the cement paste during the initial 24 hours after gauging with water. Traditional empirical tests and the more sophisticated laboratory examinations such as X-ray diffraction, scanning and transmission electron microscopy are critically reviewed. The study involves the electrical measurements on realistic sample sizes and constituent proportions. A modified electricalmodel for the response of cement paste to an applied electrical field is proposed. An automated microcomputer data logging system has been developed to facilitate electrical measurements. It has been demonstrated that the electrical response measurements of cement paste can be related to the physio-chemical processes that take place during hydration. Extensive microstructural examination of fracture surfaces of cement pastes using Scanning Electron Microscopy revealed that regions of definite crystallization and the prediction as to the hydrate morphology can be linked to the electrical response. The technique could be offered as an additional tool for investigating the structure building processes and microstructure development within cement paste. The electrical response data can be used to monitor cement hydration and it is shown that assessment of the effect of varying chemical composition; age of cement; addition of admixtures and environmental conditions have a definite influence on hydration processes.

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Bien-Aime, Andre J. "Effect of Cement Chemistry and Properties on Activation Energy." Scholar Commons, 2013. http://scholarcommons.usf.edu/etd/4439.

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The objective of this work is to examine the effect of cement chemistry and physical properties on activation energy. Research efforts indicated that time dependent concrete properties such as strength, heat evolution, and thermal cracking are predictable through the concept of activation energy. Equivalent age concept, which uses the activation energy is key to such predictions. Furthermore, research has shown that Portland cement concrete properties are affected by particles size distribution, Blaine fineness, mineralogy and chemical composition. In this study, four Portland cements were used to evaluate different methods of activation energy determination based on strength and heat of hydration of paste and mortar mixtures. Moreover, equivalency of activation energy determined through strength and heat of hydration is addressed. The findings indicate that activation energy determined through strength measurements cannot be used for heat of hydration prediction. Additionally, models were proposed that are capable of predicting the activation energy for heat of hydration and strength. The proposed models incorporated the effect of cement chemistry, mineralogy, and particle size distribution in predicting activation energy.

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Winbow, Howard David. "The chemistry and properties of magnesia-phosphate cement systems." Thesis, University of Sheffield, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249651.

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Zhang, Xiaozhong. "Some aspects of cement-aggregate interaction." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.330017.

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Hökfors, Bodil. "Phase chemistry in process models for cement clinker and lime production." Doctoral thesis, Umeå universitet, Institutionen för tillämpad fysik och elektronik, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-86004.

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The goal of the thesis is to evaluate if developed phase chemical process models for cement clinker and lime production processes are reliable to use as predictive tools in understanding the changes when introducing sustainability measures. The thesis describes the development of process simulation models in the application of sustainability measures as well as the evaluation of these models. The motivation for developing these types of models arises from the need to predict the chemical and the process changes in the production process, the impact on the product quality and the emissions from the flue gas. The main chemical reactions involving the major elements (calcium, silicon, aluminium and iron) are relatively well known. As for the minor elements, such as sodium and potassium metals, sulphur, chlorine, phosphorus and other trace elements, their influence on the main reactions and the formation of clinker minerals is not entirely known. When the concentrations of minor and trace elements increase due to the use of alternative materials and fuels, a model that can accurately predict their chemistry is invaluable. For example, the shift towards using less carbon intensive fuels and more biomass fuels often leads to an increased phosphorus concentration in the products. One way to commit to sustainable development methods in cement clinker and lime production is to use new combustion technologies, which increase the ability to capture carbon dioxide. Introducing oxy-fuel combustion achieves this, but at the same time, the overall process changes in many other ways. Some of these changes are evaluated by the models in this work. In this thesis, a combination of the software programs Aspen Plus™ and ChemApp™ constitutes the simulation model. Thermodynamic data from FACT are evaluated and adjusted to suit the chemistry of cement clinker and lime. The resulting model has been verified for one lime and two cement industrial processes. Simulated scenarios of co-combustion involving different fuels and different oxy-fuel combustion cases in both cement clinker and lime rotary kiln production are described as well as the influence of greater amounts of phosphorus on the cement clinker quality.

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Mitchell, Lyndon David. "Chemistry of Portland cement as affected by the addition of polyalkanoic acids." Thesis, Keele University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388947.

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8

Andac, Omer. "Calcium sulfoaluminate based cements." Thesis, University of Aberdeen, 1996. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU602277.

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Knowledge of energy requirements, solid solutions and phase compatibilities of high temperature cement phases is essential to the economics and performance of cement clinkers. Both chemical engineering and chemical approaches have been used to determine phase compatibilities and solid solutions of calcium sulfoaluminate, C4A3 S, C3S and C2S as well as to develop a new type of cement based on calcium monosulfoaluminate, C4A3S, tricalcium silicate, C3S, and dicalcium silicate, C2S. Investigation of solid solutions, substitution mechanisms and phase compatibilities of C4A3S, C3S and C2S form the basis of this thesis, and the subject is addressed as follows: (i) Investigation of the structures, solid solutions, phase compatibilities, polymorphism and stabilisation of C4A3S (literature review, theoretical and experimental research). This research discloses the existence of a high temperature polymorph (a) of C4A3S. It can be stabilised to ambient temperature by Fe or Na-Si coupled substitution. Limits of Na, Fe, Si and P solubilities in the C4A3S structure were investigated. When limits of Na2O or NaF in C4A3S solid solutions (~3%) is exceeded, C4A3S becomes unstable as a result of Na2SO4 or Na2Ca(SO4)2 formation. C4A3S is compatible with C2S, with CaO, with C3A, with C12A7, with CA, with CA2, with Al2O3, with C2AS and with Ca3(PO4)2 at 1300 C. (ii) Investigation of the microstructure and microchemistry of commercial calcium sulfoaluminate cement (literature review, theoretical and experimental research). Because of extensive A1 and S substitution, a large Si deficiency can occur in C2S solid solutions. The open structured texture of calcium sulfoaluminate cement explains why it is easily ground. (iii) Investigation of A1 and sulfur substitution into C2S solid solutions (literature review, theoretical and experimental research). A1 and S substitute into C2S by several mechanisms, the most important of which are 2A1+S for 3Si and Ca+S for 2Ca+Si. (iv) Investigation of the NaF-CaO-SiO2 phase equilibria and its resultant effect on C3S formation (literature review, theoretical and experimental research). This investigation revealed that NaF not only acts as flux but mainly it has a mineralising effect on C3S formation and results in extensive solid solutions, NaxCa3.xSiO5.xFx. C3Sss, can be obtained as low as ~1000 C in the presence of NaF. In the course of this study, I phase, structurally similar to that of 9 C3S but consisting of 15 and 24 layer variants, has been characterised. (v) Investigation of the NaF-CaO-Al2O3-SiO2-SO3 system and its resultant effect on both C3S and C4A3S formation. Cement based on C3Sss and C4A3S can be made at ~1300 C if F and SO3 concentrations in the raw materials are controlled. SO3 in excess relative to that required for the formation of C4A3S should be added to inhibit C11A7.CaF2 and C3A formation. In the course of this study, large amount of Si deficiency in the C2S structure, such as that of belite in commercial calcium sulfoaluminate cement (as a result of 2A1+S for 3Si substitution), has been found.

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Worthington, J. C. "A study of the mechanism of chloride attack on concrete." Thesis, University of Hertfordshire, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234365.

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Wongariyakawee, Anchalee. "Novel layered double hydroxide chemistry for application in cement and other building materials." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:3670c777-c860-43a8-9cdc-5a7d2c87b71b.

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The investigation into the syntheses and the intercalations of LDHs is the focus of the work described in this thesis. An introduction to Layered Double Hydroxide (LDH) materials with an emphasis on the possible host lattices and to their applications is given in Chapter 1. The application of LDHs in cement including; history of cement, cement production process, and cement hydration is detailed. The synthesis of the Ga-doped Ca₂Al(OH)₆Cl•nH₂O LDHs (Ca₂Ga_xAl_(1–x)-Cl; where 0 < x < 1) via the co-precipitation method is reported in Chapter 2. The effect of doping Ga³⁺ on a parameter of Ca₂Ga_xAl_(1–x)-Cl was determined by using Vegard’s law and the correlation between a parameter and x value was derived. The intercalation of organic anions including; sodium styrene sulfonate, sodium butene dicarboxylate, sodium fumarate and ammonium poly(styrene sulfonate), in Ca₂Ga-Cl structure is described. The intercalation of lignosulfonate, naphthalene sulfonate and polycarboxylate into Ca₂Al(OH)₆NO₃·6H₂O (Ca₂Al-NO₃) is detailed in Chapter 3. The release behaviour for the LDHs and the kinetic modelling of the release are reported. The effects of these LDHs on cement hydration studied by using the in situ X-ray diffraction and the ultrasound shear-wave reflection are discussed. In Chapter 4, the synthesis of Ca₂Al(OH)₆NO₃·nH₂O via a non-ionic surfactant reverse microemulsion is reported. The effects of the amount and the solubility [Hydrophile-Lipophile Balance (HLB)] of non-ionic surfactant on the morphology and the size distribution of the LDHs are discussed. Two new nitrite intercalated Ca₂Al-LDHs [Ca₂Al(OH)₆NO₂·nH₂O] synthesised via both the co-precipitation and the reverse micro-emulsion method are detailed in Chapter 5. The hydration of Portland cement samples with additive nitrate- and nitrite-intercalated Ca₂Al-LDH made using co-precipitation is discussed. The synthesis of dispersed, uniform nanoplatelet [Ca₂Al(OH)₆DDS]•H₂O LDHs is reported in Chapter 6. The effects of the amount of the surfactant on the morphology and size distribution of the LDHs are described. The experimental procedures and characterising techniques employed in this study are listed in Chapter 7. Additional data are provided in the Appendices.

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Books on the topic "Cement chemistry"

1

Cement chemistry. 2nd ed. London: T. Telford, 1997.

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Kurdowski, Wieslaw. Cement and Concrete Chemistry. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7.

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C, Hewlett P., ed. Lea's chemistry of cement and concrete. 4th ed. London: Arnold, 1998.

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International, Congress on the Chemistry of Cement (10th 1997 Göteborg Sweden). Proceedings of the 10th International Congress on the Chemistry of Cement, Gothenburg, Sweden, June 2-6, 1997. Göteborg, [Sweden]: Amarkai AB and Congrex, 1997.

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International, Congress on the Chemistry of Cement (9th 1992 New Delhi India). 9th international congress on the chemistry of cement,New Delhi, India, 1992: Congress reports. New Delhi: National Council for Cement and Building Materials, 1992.

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International Congress on the Chemistry of Cement (9th 1992 New Delhi, India). 9th international congress on the chemistry of cement,New Delhi, India, 1992: Communication papers. New Delhi: National Council for Cement and Building Materials, 1992.

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International Congress on the Chemistry of Cement (9th 1992 New Delhi, India). 9th International Congress on the Chemistry of Cement, New Delhi, India, 1992. New Delhi: National Council for Cement and Building Materials, 1992.

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International Congress on the Chemistry of Cement (9th 1992 New Delhi, India). 9th international congress on the chemistry of cement,New Delhi, India, 1992: Reports on special panel discussions and poster papers. New Delhi: National Council for Cement and Building Materials, 1992.

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International, Congress on the Chemistry of Cement (11th 2003 Durban South Africa). Cement's contribution to development in the 21st Century: Proceedings of the 11th International Congress on the Chemistry of Cement, 11-16th May, 2003, Durban, South Africa. New Delhi, India: Tech Books International, 2004.

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National Council for Cement and Building Materials (India), ed. Fifth International Conference on Concrete Technology for Developing Countries: Proceedings. New Delhi: The Council, 1999.

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Book chapters on the topic "Cement chemistry"

1

Dai, Caili, and Fulin Zhao. "Cement Slurry Chemistry." In Oilfield Chemistry, 85–113. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-2950-0_3.

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Kurdowski, Wieslaw. "Cement Hydration." In Cement and Concrete Chemistry, 205–77. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_4.

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Roussak, O. V., and H. D. Gesser. "Cement, Ceramics, and Composites." In Applied Chemistry, 291–301. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-4262-2_17.

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Kurdowski, Wieslaw. "Portland Cement Clinker." In Cement and Concrete Chemistry, 21–127. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_2.

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Kühn, Klaus-Dieter. "PMMA Cement Composition and Chemistry." In PMMA Cements, 71–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-41536-4_6.

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Kurdowski, Wieslaw. "Cement Kinds and Principles of their Classification." In Cement and Concrete Chemistry, 1–20. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_1.

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Kurdowski, Wieslaw. "New Concretes." In Cement and Concrete Chemistry, 661–76. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_10.

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Kurdowski, Wieslaw. "Hydration of Clinker Phases." In Cement and Concrete Chemistry, 129–203. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_3.

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Kurdowski, Wieslaw. "The Properties of Cement Paste." In Cement and Concrete Chemistry, 279–368. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_5.

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Kurdowski, Wieslaw. "Concrete Properties." In Cement and Concrete Chemistry, 369–532. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7945-7_6.

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Conference papers on the topic "Cement chemistry"

1

Eoff, L. S., and Buster Doug. "High Temperature Synthetic Cement Retarder." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1995. http://dx.doi.org/10.2118/28957-ms.

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Tyrer, Mark. "Thermodynamic modelling of cement chemistry at high temperature." In Fifth International Conference on Sustainable Construction Materials and Technologies. Coventry University and The University of Wisconsin Milwaukee Centre for By-products Utilization, 2019. http://dx.doi.org/10.18552/2019/idscmt5189.

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Santra, Ashok Kumar, Feng Liang, and Rocky Fitzgerald. "Sorel Cement for HP/HT Downhole Applications." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2009. http://dx.doi.org/10.2118/121102-ms.

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Srivastava, Aman, Ramadan Ahmed, and Subhash Shah. "Carbonic Acid Resistance of Hydroxyapatite Based Cement." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/193585-ms.

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Chatterji, J., R. J. Crook, S. E. Lebo, and S. L. Resch. "Development of a Set Retarder for Foamed Cement Applications." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2003. http://dx.doi.org/10.2118/80244-ms.

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Leko, Leonardus Lewa, Philiph De Rozari, Suwari, and Adrianus Amheka. "Dispersion analysis of SO2 pollutant from cement industry (Case study of Kupang cement plant)." In 3RD INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0062262.

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Miranda, C. R., and J. S. Gold. "Study of Cement Resistance to the Attack of Acid Solutions." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1997. http://dx.doi.org/10.2118/37225-ms.

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Santra, Ashok Kumar, B. R. Reddy, and Mfon Antia. "Designing Cement Slurries for Preventing Formation Fluid Influx After Placement." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2007. http://dx.doi.org/10.2118/106006-ms.

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Stark, J. "Some aspects of cement chemistry regarding self-compacting concrete." In SCC'2005-China - 1st International Symposium on Design, Performance and Use of Self-Consolidating Concrete. RILEM Publications SARL, 2005. http://dx.doi.org/10.1617/2912143624.024.

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Schweitzer, J. S. "Study of cement chemistry with nuclear resonant reaction analysis." In The CAARI 2000: Sixteenth international conference on the application of accelerators in research and industry. AIP, 2001. http://dx.doi.org/10.1063/1.1395492.

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Reports on the topic "Cement chemistry"

1

Kruger, A. A. Pore solution chemistry of simulated low-level liquid waste incorporated in cement grouts. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/198836.

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Weiss, W. Jason, Chunyu Qiao, Burkan Isgor, and Jan Olek. Implementing Rapid Durability Measure for Concrete Using Resistivity and Formation Factor. Purdue University, 2020. http://dx.doi.org/10.5703/1288284317120.

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Abstract:

The durability of in-place concrete is a high priority issue for concrete pavements and bridges. Several studies have been conducted by INDOT to use electrical resistivity as a measure of fluid transport properties. Resistivity is dependent on the chemistry of the cement and supplementary cementitious system used, as such it has been recommended that rather than specifying resistivity it may be more general to specify the formation factor. Samples were tested to establish the current levels of performance for concrete pavements in the state of Indiana. Temperature and moisture corrections are presented and acceptable accelerated aging procedure is presented. A standardized testing procedure was developed (AASHTO TP 119–Option A) resulting in part from this study that provides specific sample conditioning approaches to address pore solution composition, moisture conditioning, and testing procedures. An accelerated aging procedure is discussed to obtain later age properties (91 days) after only 28 days.

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