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Tensile Strength of Montmorillonite as a Function of Saturating Cation and Water Content
Author(s) -
Dowdy R. H.,
Larson W. E.
Publication year - 1971
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj1971.03615995003500060042x
Subject(s) - montmorillonite , ultimate tensile strength , materials science , clay minerals , strain (injury) , divalent , chemistry , composite material , mineralogy , metallurgy , medicine
The tensile strength, tensile axial strain, and tensile strain energy were determined for Na‐, K‐, Ca‐, Al‐, and Fe‐saturated montmorillonite over the water vapor pressure range ( P / P o ) from 0.02 to 0.92. The procedure used was direct tensile stressing of oriented clay films. Measured tensile strengths ranged from 366 kg cm ‐2 for Fe montmorillonite at 0.02 P / P o to 19 kg cm ‐2 for Ca montmorillonite at 0.92 P / P o . Strength decreased rapidly with added increments of water during initial interlamellar expansion and continued to decrease at a slower rate with further additions of water. In general, strength decreased in the following order: Fe > K ≥ Na > Al > Ca. The tensile strength of Na montmorillonite was of the same order of magnitude as the force required to separate two Na clay platelets as determined from adsorption/desorption water isotherms. Axial strain was independent of P / P o above 0.4 for all systems except the Na‐saturated clay. For Fe montmorillonite, strain was insensitive to water content above 0.15 P / P o . Monovalent clay specimens required the most energy to rupture and divalent samples required the least energy. Aluminum and Fe clays required an intermediate rupture energy. The greater tensile strength and low axial strain of the Fe montmorillonite suggested that a different mechanism controlled the failure characteristics of this clay. Hydroxy iron material may be the major cementing agent in the Fe system. The data show that saturating cation played a dominant role in the strength‐energy properties of the other homoionic clays.

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