Meso-scale Oedometer Test System for Volume Change Determination in Problematic Soils

Numerous laboratory swelling tests have been reported for the measurement of swelling pressure and the amount of swell of an expansive soil. These test methods generally involve the use of a conventional one-dimensional oedometer apparatus. Few attempts, however, have been made to formulate a theoretical framework to simulate the testing procedures or to visualize the different stress paths followed when using the various methods. The simulation of the oedometer tests on expansive soils is required to fully understand the prediction of heave. The correct measurement of swelling pressure is required for an accurate prediction of heave. It is further anticipated that some information on unsaturated soils property functions may be approximated from the back-analysis of the data. A theoretical model is proposed to describe the pore-water pressures with time and depth in a specimen as well as the volume changes during various oedometer swell tests. The model is formulated based on equilibrium considerations, constitutive equations for an unsaturated soil, and the continuity requirement for the pore fluid phases. The transient water flow process is coupled with the soil volume change process. The model can be used to describe the volume-change behaviour, pore-water pressure, and vertical total stress development in an unsaturated soil during an oedometer test performed by any one of several test procedures. The model has been put into a finite element formulation using the Galerkin technique. All the parameters required to run the model can be obtained by performing independent, common laboratory tests. The proposed model was used to simulate the results from free-swell, constant-volume, constant water content, and loaded-swell oedometer tests. Computed values of volume change, vertical total stress, and pore-water pressure are in good agreement with measured values.Key words: unsaturated soil, expansive soil, swelling pressure, theoretical simulation, constant-volume oedometer test, free-swell oedometer test, loaded-swell oedometer test.

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Artifacts caused by dehydration and epoxy embedding in TEM

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010008599x ◽

1991 ◽

Vol 49 ◽

pp. 338-339

Author(s):

Hilton H. Mollenhauer

Keyword(s):

Electron Microscopy ◽

Electron Beam ◽

Volume Change ◽

Tissue Damage ◽

Beam Specimen ◽

Chemical Fixation ◽

Resin Impregnation ◽

Storage Vesicles ◽

A Cell ◽

Tissue Shrinkage

Various means have been devised to preserve biological specimens for electron microscopy, the most common being chemical fixation followed by dehydration and resin impregnation. It is intuitive, and has been amply demonstrated, that these manipulations lead to aberrations of many tissue elements. This report deals with three parts of this problem: specimen dehydration, epoxy embedding resins, and electron beam-specimen interactions. However, because of limited space, only a few points can be summarized.Dehydration: Tissue damage, or at least some molecular transitions within the tissue, must occur during passage of a cell or tissue to a nonaqueous state. Most obvious, perhaps, is a loss of lipid, both that which is in the form of storage vesicles and that associated with tissue elements, particularly membranes. Loss of water during dehydration may also lead to tissue shrinkage of 5-70% (volume change) depending on the tissue and dehydrating agent.

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Immunogold labeling of CMP-KDO synthetase produced by recombinant E. Coli cells

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100128900 ◽

1987 ◽

Vol 45 ◽

pp. 924-925

Author(s):

F. A. Durum ◽

R. G. Goldman ◽

T. J. Bolling ◽

M. F. Miller

Keyword(s):

Inclusion Bodies ◽

Large Scale ◽

Recombinant Dna ◽

Test System ◽

Cell Protein ◽

Gram Negative Bacteria ◽

Cytoplasmic Inclusions ◽

Isolation And Purification ◽

E Coli ◽

Low Concentrations

CMP-KDO synthetase (CKS) is an enzyme which plays a key role in the synthesis of LPS, an outer membrane component unique to gram negative bacteria. CKS activates KDO to CMP-KDO for incorporation into LPS. The enzyme is normally present in low concentrations (0.02% of total cell protein) which makes it difficult to perform large scale isolation and purification. Recently, the gene for CKS from E. coli was cloned and various recombinant DNA constructs overproducing CKS several thousandfold (unpublished data) were derived. Interestingly, no cytoplasmic inclusions of overproduced CKS were observed by EM (Fig. 1) which is in contrast to other reports of large proteinaceous inclusion bodies in various overproducing recombinant strains. The present immunocytochemical study was undertaken to localize CKS in these cells.Immune labeling conditions were first optimized using a previously described cell-free test system. Briefly, this involves soaking small blocks of polymerized bovine serum albumin in purified CKS antigen and subjecting them to various fixation, embedding and immunochemical conditions.

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Short-term volume and turgor regulation in yeast

Essays in Biochemistry ◽

10.1042/bse0450147 ◽

2008 ◽

Vol 45 ◽

pp. 147-160 ◽

Cited By ~ 12

Author(s):

Jörg Schaber ◽

Edda Klipp

Keyword(s):

Dynamic Model ◽

Volume Change ◽

Volume Regulation ◽

Time Course ◽

Osmotic Shock ◽

Intracellular Concentration ◽

Short Term ◽

Hydrodynamic Property ◽

Turgor Regulation ◽

Thermodynamic Framework

Volume is a highly regulated property of cells, because it critically affects intracellular concentration. In the present chapter, we focus on the short-term volume regulation in yeast as a consequence of a shift in extracellular osmotic conditions. We review a basic thermodynamic framework to model volume and solute flows. In addition, we try to select a model for turgor, which is an important hydrodynamic property, especially in walled cells. Finally, we demonstrate the validity of the presented approach by fitting the dynamic model to a time course of volume change upon osmotic shock in yeast.

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Real Ear Sound Pressure Levels Developed by Three Portable Stereo System Earphones

American Journal of Audiology ◽

10.1044/1059-0889.0104.52 ◽

1992 ◽

Vol 1 (4) ◽

pp. 52-55 ◽

Cited By ~ 4

Author(s):

Gail L. MacLean ◽

Andrew Stuart ◽

Robert Stenstrom

Keyword(s):

High Frequency ◽

Sound Pressure ◽

Low Frequency ◽

Test System ◽

Output Frequency ◽

Frequency Effects ◽

Adult Men ◽

Frequency Responses ◽

Significant Difference ◽

Sound Pressure Levels

Differences in real ear sound pressure levels (SPLs) with three portable stereo system (PSS) earphones (supraaural [Sony Model MDR-44], semiaural [Sony Model MDR-A15L], and insert [Sony Model MDR-E225]) were investigated. Twelve adult men served as subjects. Frequency response, high frequency average (HFA) output, peak output, peak output frequency, and overall RMS output for each PSS earphone were obtained with a probe tube microphone system (Fonix 6500 Hearing Aid Test System). Results indicated a significant difference in mean RMS outputs with nonsignificant differences in mean HFA outputs, peak outputs, and peak output frequencies among PSS earphones. Differences in mean overall RMS outputs were attributed to differences in low-frequency effects that were observed among the frequency responses of the three PSS earphones. It is suggested that one cannot assume equivalent real ear SPLs, with equivalent inputs, among different styles of PSS earphones.

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