Evaluating Excavation Support Systems to Protect Adjacent Structures (The 2010 Michael W. O’Neill Lecture)

2010 ◽  
Vol 4 (2) ◽  
pp. 3-19 ◽  
Author(s):  
Richard J. Finno
2022 ◽  
Vol 10 (1) ◽  
pp. 039-057
Author(s):  
Maher T. El-Nimr ◽  
Ali M. Basha ◽  
Mohamed M. Abo-Raya ◽  
Mohamed H. Zakaria

In geotechnical engineering, ground movement caused by excavations is a challenging issue. The excessive differential settlement generated by soil movement induced by wall deflection may cause damage to nearby structures. A detailed literature review on the general deformation behavior of deep excavation support systems is presented in this paper. Many factors, such as normalized horizontal deflection (δh-max/He%), vertical displacement (δv-max/He%), δvmax/δhmax ratio, settlement influence zone (Do), etc., can play significant roles in describing the deflection behavior of the excavation system. A descriptive analysis of the reviewed data was carried out. The concluded δh-max/He% values range between 0.17 to 1.5, with a mean value of 0.58 for soft clay, while in the case of sands and stiff clay soils δh-max/He% value ranges between 0.07 to 0.40, with a mean value of 0.20. δv-max/He% values range between 0.13 to 1.10, with a mean value of 0.49 for soft soil, while its value ranges between 0.02 to 1.10, with a mean value of 0.24 in the case of sands and stiff clay soils. The settlement influence zone (Do) reaches a mean distance of 2.3He, which falls within Do=1.5-3.5He in the case of soft clays, while Do reaches a mean distance of 2.0He and 3.0He in the case of sands and other stiff clay soils, respectively. The relationship between system stiffness and excavation-induced wall and ground movements was discussed. Unfortunately, the literature review offers limited data regarding system stiffness, the 3-D nature of excavation support systems, excavation processes, and time effects.


IFCEE 2021 ◽  
2021 ◽  
Author(s):  
L. Sebastian Bryson ◽  
Jorge Romana-Giraldo ◽  
Sekyi Kobina Intsiful

Author(s):  
Thomas M. Jovin ◽  
Michel Robert-Nicoud ◽  
Donna J. Arndt-Jovin ◽  
Thorsten Schormann

Light microscopic techniques for visualizing biomolecules and biochemical processes in situ have become indispensable in studies concerning the structural organization of supramolecular assemblies in cells and of processes during the cell cycle, transformation, differentiation, and development. Confocal laser scanning microscopy offers a number of advantages for the in situ localization and quantitation of fluorescence labeled targets and probes: (i) rejection of interfering signals emanating from out-of-focus and adjacent structures, allowing the “optical sectioning” of the specimen and 3-D reconstruction without time consuming deconvolution; (ii) increased spatial resolution; (iii) electronic control of contrast and magnification; (iv) simultanous imaging of the specimen by optical phenomena based on incident, scattered, emitted, and transmitted light; and (v) simultanous use of different fluorescent probes and types of detectors.We currently use a confocal laser scanning microscope CLSM (Zeiss, Oberkochen) equipped with 3-laser excitation (u.v - visible) and confocal optics in the fluorescence mode, as well as a computer-controlled X-Y-Z scanning stage with 0.1 μ resolution.


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