scispace - formally typeset
Search or ask a question
Author

Paripurnanda Loganathan

Bio: Paripurnanda Loganathan is an academic researcher from University of Technology, Sydney. The author has contributed to research in topics: Adsorption & Langmuir. The author has an hindex of 39, co-authored 144 publications receiving 5248 citations. Previous affiliations of Paripurnanda Loganathan include Information Technology University & University of California, Davis.
Topics: Adsorption, Langmuir, Soil water, Soil pH, Phosphate


Papers
More filters
Journal ArticleDOI
TL;DR: A comprehensive and critical review of the literature on the effectiveness of a number of sorbents, especially some novel ones that have recently emerged, in removing and recovering phosphate can be found in this article.
Abstract: Sorption is an effective, reliable, and environmentally friendly treatment process for the removal of phosphorus from wastewater sources which otherwise can cause eutrophication of receiving waters. Phosphorus in wastewater, if economically recovered, can partly overcome the future scarcity of phosphorus resulting from exhaustion of natural phosphate rock reserves. The authors present a comprehensive and critical review of the literature on the effectiveness of a number of sorbents, especially some novel ones that have recently emerged, in removing and recovering phosphate. Mechanisms and thermodynamics of sorption, as well as regeneration of sorbents for reuse using acids, bases, and salts, are critically examined.

461 citations

Journal ArticleDOI
TL;DR: Future research needs to explore highly efficient, low cost adsorbents that can be easily regenerated for reuse over several cycles of operations without significant loss of adsorptive capacity and which have good hydraulic conductivity to prevent filter clogging during the fixed-bed treatment process.

287 citations

Journal ArticleDOI
TL;DR: In this article, the capacity of Co, Zn, Ca, Na, and Na at pH 4 was investigated at 24.0 ± 0.5°C and pH 4.

277 citations

Journal ArticleDOI
TL;DR: In this paper, the authors present the present knowledge on the mechanisms and hysteresis of Cadmium sorption and desorption in soils and factors such as pH, ionic strength, index cation, other heavy metal cations, inorganic anions, organic ligands, Cd loading rate, and the type and amounts of organic matter and inorganic colloids influencing these processes.
Abstract: Cadmium (Cd) is an environmental pollutant that can be readily taken up by plants and may enter the food chain, causing risk to human health. It can also affect soil quality and, if easily leached, has the potential to pollute surface and ground waters. Sorption and desorption are critical processes controlling the phytoavailability and mobility of Cd in soils. The authors present the present knowledge on the mechanisms and hysteresis of Cd sorption and desorption in soils and factors such as pH, ionic strength, index cation, other heavy metal cations, inorganic anions, organic ligands, Cd loading rate, and the type and amounts of organic matter and inorganic colloids influencing these processes. The methods used to determine the nature and magnitude of Cd sorption and desorption are also critically reviewed.

236 citations

Journal ArticleDOI
TL;DR: Current information on surface modifications of adsorbents is reviewed, the enhanced nitrate adsorption capacities achieved by the modifications, and the mechanisms of Adsorption are compared, and advantages and drawbacks of the techniques are presented.

235 citations


Cited by
More filters
Journal ArticleDOI
TL;DR: In this paper, an analytical procedure involving sequential chemicai extractions was developed for the partitioning of particulate trace metals (Cd, Co, Cu, Ni, Pb, Zn, Fe, and Mn) into five fractions: exchangeable, bound to carbonates, binding to Fe-Mn oxides and bound to organic matter.
Abstract: An analytical procedure involving sequential chemicai extractions has been developed for the partitioning of particulate trace metals (Cd, Co, Cu, Ni, Pb, Zn, Fe, and Mn) into five fractions: exchangeable, bound to carbonates, bound to Fe-Mn oxides, bound to organic matter, and residual. Experimental results obtained on replicate samples of fluvial bottom sediments demonstrate that the relative standard deviation of the sequential extraction procedure Is generally better than =10%. The accuracy, evaluated by comparing total trace metal concentrations with the sum of the five Individual fractions, proved to be satisfactory. Complementary measurements were performed on the Individual leachates, and on the residual sediments following each extraction, to evaluate the selectivity of the various reagents toward specific geochemical phases. An application of the proposed method to river sediments is described, and the resulting trace metal speciation is discussed.

10,518 citations

Journal ArticleDOI

7,335 citations

01 Jan 2007
TL;DR: The Third edition of the Kirk-Othmer encyclopedia of chemical technology as mentioned in this paper was published in 1989, with the title "Kirk's Encyclopedia of Chemical Technology: Chemical Technology".
Abstract: 介绍了Kirk—Othmer Encyclopedia of Chemical Technology(化工技术百科全书)(第五版)电子图书网络版数据库,并对该数据库使用方法和检索途径作出了说明,且结合实例简单地介绍了该数据库的检索方法。

2,666 citations

Journal ArticleDOI
TL;DR: In this paper, the authors give an overview of those chemical processes that are directly induced by plant roots and which can affect the concentration of P in the soil solution and, ultimately, the bioavailability of soil inorganic P to plants.
Abstract: In most soils, inorganic phosphorus occurs at fairly low concentrations in the soil solution whilst a large proportion of it is more or less strongly held by diverse soil minerals. Phosphate ions can indeed be adsorbed onto positively charged minerals such as Fe and Al oxides. Phosphate (P) ions can also form a range of minerals in combination with metals such as Ca, Fe and Al. These adsorption/desorption and precipitation/dissolution equilibria control the concentration of P in the soil solution and, thereby, both its chemical mobility and bioavailability. Apart from the concentration of P ions, the major factors that determine those equilibria as well as the speciation of soil P are (i) the pH, (ii) the concentrations of anions that compete with P ions for ligand exchange reactions and (iii) the concentrations of metals (Ca, Fe and Al) that can coprecipitate with P ions. The chemical conditions of the rhizosphere are known to considerably differ from those of the bulk soil, as a consequence of a range of processes that are induced either directly by the activity of plant roots or by the activity of rhizosphere microflora. The aim of this paper is to give an overview of those chemical processes that are directly induced by plant roots and which can affect the concentration of P in the soil solution and, ultimately, the bioavailability of soil inorganic P to plants. Amongst these, the uptake activity of plant roots should be taken into account in the first place. A second group of activities which is of major concern with respect to P bioavailability are those processes that can affect soil pH, such as proton/bicarbonate release (anion/cation balance) and gaseous (O2/CO2) exchanges. Thirdly, the release of root exudates such as organic ligands is another activity of the root that can alter the concentration of P in the soil solution. These various processes and their relative contributions to the changes in the bioavailability of soil inorganic P that can occur in the rhizosphere can considerably vary with (i) plant species, (ii) plant nutritional status and (iii) ambient soil conditions, as will be stressed in this paper. Their possible implications for the understanding and management of P nutrition of plants will be briefly addressed and discussed.

2,120 citations

Journal ArticleDOI
TL;DR: The remediation of heavy metal(loid) contaminated soils through manipulating their bioavailability using a range of soil amendments will be presented.

1,507 citations