Search Results

You searched for all publications:

with publication states 'Published (Approved)'

Search Again...

These results only include publications that have been reviewed and processed by Diamond Light Source. To also view papers that have not yet been processed click here.

You can use the folder icon under Actions to collate papers as required. You can then click on View Folder in the left-hand navigation to review and/or download your folder.

Exact matches
Related results

3 items found (0 items not approved), displaying all items.1

Instruments / Technical Area	Publication Details	Published
B18-Core EXAFS	Fe(II) interaction with cement phases: Method development, wet chemical studies and X-ray absorption spectroscopy A. Mancini , E. Wieland , G. Geng , B. Lothenbach , B. Wehrli , R. Dähn Journal Of Colloid And Interface Science DOI: 10.1016/j.jcis.2020.11.085 Diamond Proposal Number(s): [21670] Open Access Show Abstract ▼ Abstract: Fe(II) interaction with cement phases was studied by means of co-precipitation and sorption experiments in combination with X-ray absorption fine structure (XAFS) spectroscopy. Oxidation of Fe(II) was fast in alkaline conditions and therefore, a methodology was developed which allowed Fe(II) to be stabilised in the sorption experiments and to prepare samples for spectroscopy. X-ray diffraction (XRD) of the co-precipitation samples showed uptake of a small portion of Fe(II) by calcium-silicate-hydrates (C-S-H) in the interlayer indicated by an increase in the interlayer spacing. Fe(II) incorporation by AFm phases was not indicated. Wet chemical experiments using 55Fe radiotracer revealed linear sorption of Fe(II) irrespective of the Ca/Si ratio of C-S-H and equilibrium pH. The Kd values for Fe(II) sorption on C-S-H are more than three orders of magnitude lower as compared to Fe(III), while they are comparable to those of other bivalent metal cations. XAFS spectroscopy showed Fe(II) binding by C-S-H in an octahedral coordination environment. The large number of neighbouring atoms rules out the formation of a single surface-bound Fe(II) species. Instead the data suggest presence of Fe(II) in a structurally bound entity. The data from XRD and XAFS spectroscopy suggests the presence of both surface- and interlayer-bound Fe(II) species.	Nov 2020
I15-Extreme Conditions	Mechanical behavior and phase change of alkali-silica reaction products under hydrostatic compression Guoqing Geng , Zhenguo Shi , Andreas Leemann , Konstantin Glazyrin , Annette Kleppe , Dominik Daisenberger , Sergey Churakov , Barbara Lothenbach , Erich Wieland , Rainer Daehn Acta Crystallographica Section B Structural Science, Crystal Engineering And Materials 76, 674 - 682 DOI: 10.1107/S205252062000846X Diamond Proposal Number(s): [18643] Show Abstract ▼ Abstract: Alkali-silica reaction (ASR) causes severe degradation of concrete. The mechanical property of the ASR product is fundamental to the multiscale modeling of concrete behavior over the long term. Despite years of study, there is a lack of consensus regarding the structure and elastic modulus of the ASR product. Here, ASR products from both degraded field infrastructures and laboratory synthesis were investigated using high-pressure X-ray diffraction. The results unveiled the multiphase and metastable nature of ASR products from the field. The dominant phase undergoes permanent phase change via collapsing of the interlayer region and in-planar glide of the main layer, under pressure >2 GPa. The bulk moduli of the low- and high-pressure polymorphs are 27±3 and 46±3 GPa, respectively. The laboratory-synthesized sample and the minor phase in the field samples undergo no changes of phase during compression. Their bulk moduli are 35±2 and 76±4 GPa, respectively. The results provide the first atomistic-scale measurement of the mechanical property of crystalline ASR products.	Aug 2020
I15-Extreme Conditions	Influence of decalcification on structural and mechanical properties of synthetic calcium silicate hydrate (C-S-H) Lin Liu , Can Sun , Guoqing Geng , Pan Feng , Jiaqi Li Cement And Concrete Research 123 DOI: 10.1016/j.cemconres.2019.105793 Diamond Proposal Number(s): [18643] Show Abstract ▼ Abstract: Decalcification causes critical degradation of calcium silicate hydrate (C-S-H) – the principal binder in concrete. Contrary to structural change, the decalcification-induced change of C-S-H mechanical properties has not been sufficiently investigated. To fill this gap, here C-S-H was synthesized and decalcified using NH4NO3 solutions. It was then subjected to chemical analysis and high pressure X-ray diffraction study. Our results indicate that C-S-H decalcifies only in the interlayer which reduces its stiffness along the c-axis. The incompressibility and the transverse isotropy remain unchanged for the calcium silicate main layer, despite the vast change of silicate chain linkage. The intralayer Ca does not leach as long as C-S-H maintains the tobermorite-like structure. A ~30% reduction of bulk modulus is estimated for decalcified C-S-H. Our results add fundamental knowledge to the structure-property correlation of C-S-H subjected to decalcification.	Sep 2019

Publications Database

Search Results

You searched for all publications:

Search Again...

Subject Areas (check all that apply) select all

Instruments used to collect data (check all that apply) select all

Collaborations involved (check all that apply) select all

Diamond Offline Facilities used

Relevant Technical Areas (check all that apply) select all

Menu for Anonymous User