Vs and Vp cross hole measurements by automatic generators

Bulletin of Engineering Geology and the Environment - The large extension, in the last few years, of propagation velocity measurements of shear and compression waves for the determination of...     

Dynamic analysis and optimal feedback control synthesis applied to biological waste treatment

The dynamics and optimal feedback control of biological waste treatment processes are examined. Modern feedback control theory is applied and results are obtained for both proportional and proportional plus integral control. A dynamic mathematical model of the system is developed by employing a Monod kinetic model, which is modified to account for endogenous metabolism, and a complete mixing flow model in the growth chamber. The feedback control is implemented via the flow rate so as to maintain desired effluent concentrations. External disturbances which cause changes in substrate concentration and/or cell concentration are considered and optimal control effort is applied. Results are also presented for impulse and step changes in the influent substrate concentration. It is found that by changing the values of the weighting factors in the objective function, it is possible to obtain good control of either the effluent substrate concentration or cell concentration.     

The development of macrolayer thickness of water in the pool boiling regime

ABSTRACT

The main purpose of this study is to analyse the phenomenon of pool boiling in water over a horizontally placed copper tube heater of 28?mm diameter. The experiment has been carried out to observe the bubble growth and departure characteristics for the heat flux range up to 40,000?W/m². The entire process is being recorded by a digital camera at different time intervals. The measured parameters have been used to determine the initial layer thickness, macro layer thickness and critical heat flux and validated with models proposed in the literature.     

Particles and vegetation: implications for the transfer of particle-bound organic contaminants to vegetation

This paper presents a comprehensive review of the mechanisms responsible for the transfer of atmospheric particulate deposition and soil particulate re-suspension onto vegetation. The nature of atmospheric aerosols and dry/wet particulate deposition are reviewed, together with information from the literature on radionuclides as tracers of the air particle/soil particle to vegetation transfer processes. Information from these fields is used to make inferences about the potential significance of these pathways in supplying particle-bound semi-volatile organic chemicals (e.g. polycyclic aromatic hydrocarbons, polychlorinated dibenzo-p-dioxins and dibenzofurans, polychlorinated biphenyls) to vegetation. Retention of compounds on particles brought to the above-ground plant surfaces is discussed. In the absence of definitive field/experimental studies, calculations are made drawing on the literature data to estimate the contributions of atmospheric and soil particle-bound organic contaminants to the plant concentration. These show that depending on the site-specific, species-specific and compound-specific scenarios considered, particulate-bound inputs may be negligible or may dominate the supply of organic contaminants to the above-ground portion of plants. However, field/experimental studies and direct measurements are needed to provide reliable quantitative data on this topic.     

A semiautomated procedure for the determination of phosphorus in water, waste waters and particulates

Improved procedures for the determination of total dissolved phosphorus (TDP), particulate phosphorus (PP) and dissolved inorganic orthophosphate (DP) are described. Organic particulate material is solubilized in 5 n NaOH, and phosphorus compounds are oxidized and mineralized to orthophosphate by persulfate digestion. DP is determined by an improved automated molybdenum blue procedure that does not require sample pH adjustment or a correction for silicate interference in the 0–50 mg Si 1^?1 range. The use of 36-position digestion racks allows 32 TDP or PP samples to be digested in ca. 1 and 4 h respectively. Detection limits in μg of phosphorus 1^?1 are DP, 2; TDP, 5; and PP. 1. Waste water samples were analyzed for TDP and PP by the nitric acid-sulfuric acid procedure and by the proposed method. There was no significant difference between the two sets of data (P > 0.45).     

Results of evaluation of the strength of concrete placed in the shafts of cast-in-place piles

Conclusions 1. Application of the method of underwater concreting with the use of a container is inexpedient in connection with the presence of a large number of flaws detected in the shafts of cast-in-place piles formed by this method; concreting of holes by the VAT method is preferable.2. The strength of concrete in the shafts of cast-in-place piles increases, reaching a maximum at a depth of 0.4–0.5 the length of the shaft. Variation in strength along the shaft is explained primarily by the percentage of coarse aggregate contained in the concrete.3. The quality of pile concrete should be monitored during all stages of pile installation, and, primarily during the stage of concreting, i.e., when there is a chance of correcting an observed defect.All-Union Institute for the Design and Planning of Health Resorts. Scientific-Research Institute of Foundations and Underground Structures. Translated from Osnovaniya, Fundamenty i Mekhanika Gruntov, No. 5, pp. 14–17, September–October, 1976.     

A colorimetric method for ammonia in natural waters

An improved phenol-hypochlorite method for determining ammonia in water using nitroprusside as catalyst has been investigated. Unlike other recently published methods, the method is simple (and sufficiently sensitive for low-level analyses) and does not require accurate time intervals between reagents, not expensive equipment. The method is well suited for routine use.

Beer's Law was obeyed over the whole ammonia range investigated. Reproducibility was 1·3 per cent with 10 μg N, and 5·7 per cent with 1 μg N.     

Partitioning of polycyclic aromatic hydrocarbons between dissolved and particulate phases in natural waters

Quantities of polycyclic aromatic hydrocarbons (PAH), some of which are carcinogens, enter natural waters in effuents of coke production and other high-temperature industrial pyrolysis processes. Because of their low water solubilities. PAH compounds are generally considered to occur in particulate form in lakes and rivers. However, present studies of ¹⁴C-anthracene adsorption by autoclaved yeast cells indicated that significant fractions of both dissolved and particulate forms of PAH may exist in natural waters. Quantities of anthracene adsorbed exceeded values for PAH adsorption onto mineral surfaces by more than an order of magnitude: suspended organic material may thus be more important than mineral particles in adsorption of PAH compounds. Adsorption was highly dependent upon the yeast cell concentration, and varied widely through the range of suspended organic solids normally encountered in natural waters. The heat of adsorption (5.2 kcal/mole) was characteristic of a physical adsorptive process. Because ecological effects and pathways of dissolved and particulate PAH may differ, adsorptive partitioning may be important in determining PAH hazards to higher organisms in aquatic food chains, and ultimately to man.