Maria C.G. Juenger

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Name: Juenger, Maria G.
Organization: University of Texas at Austin , USA
Department: Department of Civil
Title: Associate(PhD)

TOPICS

Co-reporter:Susan A. Bernal;Maria C. G. Juenger;Xinyuan Ke
Materials and Structures 2017 Volume 50( Issue 1) pp:26
Publication Date(Web):10 August 2016
DOI:10.1617/s11527-016-0909-2
Working Group 1 of RILEM TC 238-SCM ‘Hydration and microstructure of concrete with supplementary cementitious materials (SCMs)’ is defining best practices for the physical and chemical characterization of SCMs, and this paper focusses on their thermal analysis. Thermogravimetric analysis (TGA) can provide valuable data on the chemical and mineralogical composition of SCMs. Loss-on-ignition (LOI) testing is a commonly used, standardized, but less sophisticated version of TGA that measures mass at endpoints only, with heating generally in air. In this paper we describe the use of TGA and LOI to characterize Portland cement with limestone additions, coal combustion fly ashes, ground-granulated blast furnace slag, calcined clays, and natural pozzolans. This paper outlines the value and limitations of TGA and LOI (in the formats defined in different standards regimes) for material characterization, and describes testing methods and analysis. TGA testing parameters affect the mass loss recorded at temperatures relevant for LOI measurements (700–1000 °C) of slags and fly ashes, mainly associated with oxidation reactions taking place upon heating. TGA of clays and natural pozzolans is utilized to identify optimal calcination conditions leading to dehydroxylation and consequent structural amorphization, particularly for kaolinite. However, dehydroxylation and amorphization do not occur at similar temperatures for all clays, limiting the applicability of TGA for this purpose. Although TGA is widely utilized for characterization of SCMs, the testing parameters significantly affect the results obtained, and TGA results require careful interpretation. Therefore, standardization of TGA testing conditions, particularly for LOI determination of slags and fly ashes, is required.
Co-reporter:Saamiya Seraj, Rachel Cano, Raissa D. Ferron, Maria C.G. Juenger
Cement and Concrete Composites 2017 Volume 80(Volume 80) pp:
Publication Date(Web):1 July 2017
DOI:10.1016/j.cemconcomp.2017.03.009
A critical area overlooked in previous research on pumice is understanding how its physical characteristics influence its behavior as a supplementary cementitious material (SCM). This study investigated three pumices with different particle size distributions to observe whether these porous materials exhibit enhanced nucleation and growth of hydration products, in the same way as non-porous materials, and whether the rate of pozzolanic reaction can be changed through particle size. The effect of particle size on compressive strength, rheology and resistance to alkali silica reaction (ASR) was also evaluated. Results showed that reducing particle size increased the rates of cement hydration, pozzolanic reaction, and compressive strength gain, while also increasing mixture viscosity. Interestingly, particle size did not impact the yield stress of the mixture or the resistance to ASR. These new findings give insight about how the particle size of pumice can be used to overcome drawbacks reported in previous literature.
Co-reporter:Saamiya Seraj, Raissa D. Ferron, Maria C.G. Juenger
Cement and Concrete Research 2016 Volume 85() pp:102-110
Publication Date(Web):July 2016
DOI:10.1016/j.cemconres.2016.04.002

Abstract

Despite the benefits to long-term concrete durability, the use of natural zeolites as supplementary cementitious materials (SCMs) is uncommon due to their high water demand. The motivation of the research presented here was to better understand how the physical and chemical characteristics of natural zeolites influenced the workability of cementitious mixtures and whether those properties could be modified through calcination to mitigate the high water demand of natural zeolites. In this research, three different natural zeolites were characterized in their original and calcined states using x-ray diffraction (XRD) and Brunauer–Emmett–Teller (BET) surface area measurements. Rheology experiments were then conducted on cementitious pastes containing these natural zeolites, in their original and calcined states, to assess mixture viscosity and yield stress. Results showed that calcination destabilized the structure of the natural zeolites and reduced their surface area, which led to an improvement in mixture viscosity and yield stress.

Co-reporter:Lisa E. Burris, Maria C.G. Juenger
Cement and Concrete Composites 2016 Volume 65() pp:163-170
Publication Date(Web):January 2016
DOI:10.1016/j.cemconcomp.2015.09.008
This work examined the effects of milling using a gravity ball mill on the reactivity of natural zeolites used as supplementary cementitious materials (SCMs). Six different particle size distributions of zeolites, created by milling the as-received zeolite in a ball mill for a specified amount of time, were characterized using x-ray fluorescence, quantitative x-ray diffraction, particle size analysis, pore size distribution and surface area analysis. Following material characterization, the pozzolanic reactivity of the zeolites was determined by measuring the quantity of calcium hydroxide in paste after 28 or 90 days and by tracking the compressive strength of zeolite-cement mortars. Results showed that a critical milling time exists, corresponding to a d50 of 7–9 μm, after which reductions in particle size can no longer be achieved and zeolite performance can no longer be improved through ball milling.
Co-reporter:Feraidon F. Ataie, Maria C.G. Juenger, Sarah C. Taylor-Lange, Kyle A. Riding
Cement and Concrete Research 2015 Volume 72() pp:128-136
Publication Date(Web):June 2015
DOI:10.1016/j.cemconres.2015.02.023

Abstract

Sucrose and zinc oxide (ZnO) are effective cement hydration retarders. The goal of this study was to provide a new look into the ZnO cement hydration mechanism and to investigate impacts of various supplementary cementitious materials (SCMs) on retardation behavior of ZnO and sucrose. Changes in the pore solution composition and reaction kinetics were measured for cementitious systems with ZnO or sucrose that contained rice straw ash (RSA), wheat straw ash, silica fume, metakaolin, and fly ash. Among the SCMs used, RSA dramatically suppressed ZnO and sucrose retardation. Experimental results indicated that the mechanism by which ZnO retards hydration reaction could be nucleation and/or growth poisoning of C-S-H. Reduced retardation of paste samples containing RSA was attributed to the ability of RSA to provide nucleation sites for C-S-H precipitation. This study provides a better understanding of the interaction between SCMs and cement hydration retarders essential in predicting retarder–dose effects.

Co-reporter:Maria C.G. Juenger, Rafat Siddique
Cement and Concrete Research 2015 Volume 78(Part A) pp:71-80
Publication Date(Web):December 2015
DOI:10.1016/j.cemconres.2015.03.018

Abstract

Supplementary cementitious materials (SCMs) are commonly used in concrete mixtures as a replacement of a portion of clinker in cement or as a replacement of a portion of cement in concrete. This practice is favorable to the industry, generally resulting in concrete with lower cost, lower environmental impact, higher long-term strength, and improved long-term durability. SCMs have been used in Portland cement concrete for decades and many of their effects are well-understood. Most recent research on SCMs has focused on a few areas: exploring new materials, increasing replacement amounts, developing better test methods, treating or modifying materials, and using additives (e.g. limestone or nanosilica) to improve performance. The advances in knowledge provided by research in these areas are reviewed in this paper, emphasizing the impact of the research on the field.

Co-reporter:Clement J. Cros;Alexandra L. Terpeluk;Lisa E. Burris
Materials and Structures 2015 Volume 48( Issue 10) pp:3159-3171
Publication Date(Web):2015 October
DOI:10.1617/s11527-014-0388-2
Oxides of nitrogen (NOx) are ubiquitous pollutants in large urban areas of the world. Photocatalytic materials have been studied, primarily in the laboratory, for their ability to remove oxides of nitrogen. The study described herein compared NOx removal efficacies of three commercially-available photocatalytic coatings (a stucco, a white paint and a clear paint) applied to roadside concrete. The study aimed to elucidate how environmental parameters and exposure to real roadside conditions impact NOx removal. This was achieved through periodic laboratory chamber testing and material characterization of concrete slabs stored by busy roadways for a 20-month period. It was observed that roadside exposure led to physical degradation of the clear paint coating, while the other two remained intact. The stucco coating was the most effective at NOx removal, but the efficacy nonetheless diminished over time.
Co-reporter:Irvin A. Chen, Craig W. Hargis, Maria C.G. Juenger
Cement and Concrete Research 2012 Volume 42(Issue 11) pp:1560-1562
Publication Date(Web):November 2012
DOI:10.1016/j.cemconres.2012.08.001
Reply to the discussion of the paper “Understanding expansion in calcium sulfoaluminatebelite cements” by G.L. Valenti, M. Marroccoli, M.L. Pace, A. Telesca.
Co-reporter:Irvin A. Chen, Craig W. Hargis, Maria C.G. Juenger
Cement and Concrete Research 2012 Volume 42(Issue 1) pp:51-60
Publication Date(Web):January 2012
DOI:10.1016/j.cemconres.2011.07.010
Calcium sulfoaluminate–belite (CSAB) cements are promoted as sustainable alternatives to portland cement because of their lower energy and CO2 emissions during production and comparable performance. However, the formation of ettringite, the main hydration product in CSAB cements, can be expansive, sometimes resulting in cracking. The factors controlling expansive behavior in CSAB cements have not been completely elucidated. In this study, three CSAB cements synthesized from reagent-grade chemicals with varied phase compositions were examined for dimensional stability in water and sulfate solutions. The interdependent effects of C4A3Ŝ (Ye'elimite) content, calcium sulfate content, water-to-cement ratio, and particle fineness on CSAB cement expansion were evaluated. The results show that the expansive behavior can be controlled by altering chemical and physical factors in CSAB clinker, cement, and paste.
Co-reporter:Irvin A. Chen, Maria C.G. Juenger
Cement and Concrete Composites 2012 Volume 34(Issue 8) pp:893-902
Publication Date(Web):September 2012
DOI:10.1016/j.cemconcomp.2012.04.006
In recent years, calcium sulfoaluminate-belite (CSAB) cement has been promoted as a sustainable alternative to Portland cement due to lower energy used and less CO2 emitted during production, while providing comparable performance. However, a potential problem facing the widespread adoption and production of CSAB cement is the cost and availability of raw materials and it is therefore desirable to find alternative raw materials to keep costs competitive. In this study, two CSAB cement clinkers with a similar target phase composition were synthesized from combinations of natural and waste materials (coal combustion residuals). The two CSAB cement clinkers were compared against a CSAB clinker made from reagent-grade chemicals, enabling examination of the effects of impurities on performance. Cements made from the clinkers were examined for hydration rate, hydration product formation, dimensional stability, and compressive strength.
Co-reporter:M.C.G. Juenger, F. Winnefeld, J.L. Provis, J.H. Ideker
Cement and Concrete Research 2011 Volume 41(Issue 12) pp:1232-1243
Publication Date(Web):December 2011
DOI:10.1016/j.cemconres.2010.11.012
There is a burgeoning interest in the development, characterization, and implementation of alternatives to Portland cement as a binder in concrete. The construction materials industry is under increasing pressure to reduce the energy used in production of Portland cement clinker and the associated greenhouse gas emissions. Further, Portland cement is not the ideal binder for all construction applications, as it suffers from durability problems in particularly aggressive environments. Several alternative binders have been available for almost as long as Portland cement, yet have not been extensively used, and new ones are being developed. In this paper, four promising binders available as alternatives to Portland cement are discussed, namely calcium aluminate cement, calcium sulfoaluminate cement, alkali-activated binders, and supersulfated cements. The history of the binders, their compositions and reaction mechanisms, benefits and drawbacks, unanswered questions, and primary challenges are described.
Co-reporter:Andrew J. Maas, Jason H. Ideker, Maria C.G. Juenger
Cement and Concrete Research 2007 Volume 37(Issue 2) pp:166-174
Publication Date(Web):February 2007
DOI:10.1016/j.cemconres.2006.10.011

Abstract

It is commonly accepted that replacement of a portion of cement in mortar or concrete with well-dispersed silica fume reduces expansion caused by alkali silica reaction. Recently there has been much discussion that large, agglomerated particles of silica fume may actually act as alkali silica reactive aggregates, thereby increasing expansion rather than reducing it. The data in the literature, from both field and laboratory studies, are inconsistent. This prompted an extensive laboratory investigation into the alkali silica reactivity of silica fume. Results from accelerated expansion testing and microscopic investigations are presented. It was seen that some agglomerated silica fumes participate in ASR while others do not. Factors determining the reactivity of silica fume agglomerates are suggested.

Co-reporter:M.C.G. Juenger, P.J.M. Monteiro, E.M. Gartner, G.P. Denbeaux
Cement and Concrete Research 2005 Volume 35(Issue 1) pp:19-25
Publication Date(Web):January 2005
DOI:10.1016/j.cemconres.2004.05.016

Abstract

Calcium chloride (CaCl2) is one of the most recognized and effective accelerators of hydration, setting, and early strength development in portland cement and tricalcium silicate (C3S) pastes. The mechanisms responsible for this acceleration, as well as the microstructural consequences, are poorly understood. Soft X-ray transmission microscopy has recently been applied to the study of cementitious materials and allows the observation of hydration in situ over time. This technique was applied to the examination of tricalcium silicates hydrating in a solution containing CaCl2. It appears that CaCl2 accelerates the formation of “inner product” calcium silicate hydrate (C-S-H) with a low-density microstructure.

Co-reporter:M.C.G Juenger, C.P Ostertag
Cement and Concrete Research 2004 Volume 34(Issue 8) pp:1389-1402
Publication Date(Web):August 2004
DOI:10.1016/j.cemconres.2004.01.001

Abstract

Pozzolanic materials, including silica fume, are commonly added to concrete to reduce expansion due to alkali–silica reaction (ASR). It has been noted, however, that commercial silica fume is not always adequately dispersed, and large agglomerates may be present. These large particles have been hypothesized to act as amorphous silica aggregates, thereby participating in an expansive reaction with the alkalis present in cement paste pore solution. If such were the case, some silica fume particles would actually aggravate expansion due to ASR rather than suppress it. The present investigation characterizes the microstructure and morphology of agglomerated and sintered silica fume particles and compares their effects on alkali–silica-related expansion. While a 5% replacement of moderately reactive sand with sintered silica fume aggregates caused significant expansion under accelerated testing conditions (modified ASTM C1260), the replacement with large agglomerates of densified silica fume decreased expansion compared with control mortar bars containing only sand. Both the sintered aggregates and the agglomerates reacted with the pore solution; one reaction was expansive, while the other was not.

Co-reporter:David J. Corr, Maria C.G. Juenger, Paulo J.M. Monteiro, Jacob Bastacky
Cement and Concrete Composites 2004 Volume 26(Issue 8) pp:1007-1012
Publication Date(Web):November 2004
DOI:10.1016/j.cemconcomp.2004.02.035
This paper describes the application of low temperature scanning electron microscopy to the materials science of Portland cement. The details of low-temperature scanning electron microscopy are described, along with a number of specimen preparation techniques. There are three main research topics presented in this paper: (1) ice morphology in entrained air voids, (2) development of air voids during early hydration and (3) progression of hydration in Portland cement. The first research focus examines ice in air voids at freezing temperatures, and various cement paste ages. The second research focus tracks the development of the air voids during the first hour of hydration. In the third research focus, the progression of hydration with and without accelerating and retarding admixtures is described. Each of these research programs demonstrates how low-temperature scanning electron microscopy can be an effective tool in Portland cement research.
Radon, isotope of mass222
hexacalcium hexaoxotris[sulphato(2-)]dialuminate(12-)
dicalcium silicate