• Journal of Korean Society on Water Environment
• /
• v.26 no.1
• /
• pp.19-27
• /
• 2010

Submerged plants whose most of vegetative mass are below the water surface can have great effects on wetland biogeochemistry and water purification through their photosynthesis and nutrient uptake processes. In this study, change of dissolved oxygen concentration and pH as well as nutrient removal capacity of the submerged plant dominant wetland were investigated using wetland mesocosm experiments. Obvious periodic DO and pH fluctuation was observed due to photosynthetic activities of the submerged plants. It implies that the submerged plants can provide periodic or sequential changes of oxic and anoxic conditions that affect nitrification and denitrification processes and contribute permanent nitrogen removal in the wetland system. The pH changes in the wetland mesocosm suggested that submerged plant could also play an important role as a temporary $CO_2$ storage. Higher nutrient removal efficiency was observed in the submerged plant dominant wetland mesocosm. The removal efficiencies under experimental conditions were 38.89, 84.70, 91.21, 70.76, 75.30% of TN, DIN, $NH_4-N$, TP, $PO_4-P$ in the wetland mesocosm, while those were 26.11, 57.34, 63.87, 28.19, 55.15% in the control treatment, respectively.

• Applied Chemistry for Engineering
• /
• v.19 no.2
• /
• pp.205-208
• /
• 2008

Sulfonated polySEBS and sulfonated PS were synthesized by sulfonation at the aromatic group of polySEBS and PS. Novel sulfonated polySEBS/sulfonated PS blending films for the ion exchange membrane of polymer electrolyte fuel cell were prepared from these sulfonated polymers. The proton conductivities of these blending films were varied in $10^{-2}{\sim}10^{-3}S/cm$ with the blending ratio of sulfonated polySEBS/sulfonated PS. Especially, the film prepared from the addition of the sulfonated PS (0.5 g) in the sulfonated polySEBS (10.0 g) has the best proton conductivity (0.07 S/cm) with ion exchange capacity (0.75 meq/g) and water uptake (25%).

• Environmental Engineering Research
• /
• v.11 no.6
• /
• pp.303-310
• /
• 2006

The aim of this study is to assess the applicability of sericite in wastewater treatment particularly the removal of two important heavy metal toxic ions viz., Cu(II) and Pb(II) from aqueous solutions. The batch type experiments showed that sericite is found to be one of useful natural sorbent for the removal of these two cations from aqueous solutions and it is also to be observed that with the increase in sorptive concentration amount of metal uptake increases and the concentration dependence data obtained are fitted well for the Langmuir adsorption isotherm rather than Freundlich adsorption model. Further, the Langmuir monolayer adsorption capacity is found to be $1.674\;mg\;g^{-1}$ for Cu(II) and $4.697\;mg\;g^{-1}$ for Pb(II). Kinetic studies enabled, an apparent equilibria can be achieved between soild/solution interface within ca 10 mins for Cu(II) and ca 90 mins for Pb(II). Moreover, the removal behavior of sericite for these two metal ions is greatly influenced by solution pH.

• Journal of Hydrogen and New Energy
• /
• v.29 no.5
• /
• pp.458-465
• /
• 2018

This study reports the fabrication of anion exchange membranes (AEMs) containing two kinds of functional groups: i) trimethylphosphite (TMP) and ii) trimethylamine (TMA). We carried out the synthesis of polymers to enhance thermal stability and ion conductivity. The alternative polymer was prepared using 2,2-bis(4-hydroxy-3-methylphenyl)propane and decafluorobiphenyl. The membrane was fabricated by solution casting method. The thermal stability of membranes was examined by TGA. The physiochemical properties of membranes were also investigated in terms of water uptake, swelling ratio, ion exchange capacity, and ion conductivity. The hydroxide ion conductivity of the membranes reached about 20.2 mS/cm for quaternary ammonium poly(arylene ether) (QA-PAE) containing TMA moiety and 5.1 mS/cm for quaternary phosphonium PAE (QP-PAE) containing TMP moiety at $90^{\circ}C$.

• KSBB Journal
• /
• v.8 no.4
• /
• pp.336-340
• /
• 1993

Zoogloea ramigera 115, well known type of bacteria to produce slime in sewage plants, was selected for biopolymer production. The extracted biopolymer showed high uptake capacity of metals such as cadmium and zinc. Especially the fermentor broth itself showed high adsorption of metal and could be used a biosorbent without an additional separation process. Biopolymer was immobilized into beads of calcium alginate and used in a packed bed reactor for the purpose of valued metals recovery. The biopolymer showed high removal efficiencies of 80% or greater for Cu, Cd, Mn and Zn, and high stability in sorption-desorption-resorption experiments. The immobilized biopolymer systems were found to be comparable to other metal removal systems such as ion exchange resins and to be of potential industrial application value.

• International Journal of Industrial Entomology and Biomaterials
• /
• v.23 no.2
• /
• pp.207-213
• /
• 2011

The diapause of $Telegryllus$ $emma$, the Emma field cricket, was investigated to study the ecological characteristics of the species. Changes in the volume, oxygen consumption, and water content of T. emma eggs were followed from oviposition. An increase in volume, oxygen consumption and water uptake occurred from 7 to 8 days following oviposition. The oxygen consumption of the eggs increased slowly for 7 days following oviposition, but then decreased until 15 days following oviposition. These results showed that a physiological change at diapause initiation affected the volume, water content, and oxygen consumption of the $T.$ $emma$ eggs. An experimental investigation of egg hatching showed that the eggs could be stocked at $10^{\circ}C$ for 40 days with a 14 day pre-period after laying and yield, 62.1% hatchability under these conditions. Maintaining the temperature at approximately $10^{\circ}C$ was favorable for hatching. Another experiment on egg hatching showed that the storage of eggs at $10^{\circ}C$ from 40 to 180 days would ensure satisfactory, hatching capacity.

• Proceedings of the Membrane Society of Korea Conference
• /
• 1999.07a
• /
• pp.115-115
• /
• 1999

In this work a new process was developed for the sulfonation of the chemicallly stable engineering polymer polyethersulfone as membrane materials for electrodialysis or a flow battery applications. Commercially available polyethersulfone polymer was partially sulfonated using a CSA sulfonating agent in a dichloromethane solvent, which sulfonated polyethersulfone with various sulfonation levels have been prepared. Sulfonated polyethersulfone (SPES) membranes with different ion capacities were prepared for the purpose of identifying cation exchange membrane properties, in an attempt to find a low cost replacement for Nafion, which most of the perfluorinated membranes, known to exhibit a prolonged service life, are expensive and difficult to process. The following features were determined: the degree of sulfonation, water uptake, thermal analysis, and electrochemical properties such as ion exchange capacities, resistivity, selectivity of ion permeation. The surface of the cation exchange membranes, decomposed with the H202-treatment, were observed by using scanning electron microscope. The area resistivities of SPES mebranes in 5N-NaOH decreased from $2,150{\;}{\Omega}-cm2$ to less than $15{\Omega}-cm2$ as the ion exchange capacity (IEC) increased from 0.62 to 1.73 millieequivlants per dry gram(meq/dg).eq/dg).

• Carbon letters
• /
• v.8 no.3
• /
• pp.199-206
• /
• 2007

The activated carbon produced from rubber wood sawdust by chemical activation using phosphoric acid have been utilized as an adsorbent for the removal of Cu(II) from aqueous solution in the concentration range 5-40 mg/l. Adsorption experiments were carried out in a batch process and various experimental parameters such as effect of contact time, initial copper ion concentration, carbon dosage, and pH on percentage removal have been studied. Adsorption results obtained for activated carbon from rubber wood sawdust were compared with the results of commercial activated carbon (CAC). The adsorption on activated carbon samples increased with contact time and attained maximum value at 3 h for CAC and 4 h for PAC. The adsorption results show that the copper uptake increased with increasing pH, the optimum efficiency being attained at pH 6. The precipitation of copper hydroxide occurred when pH of the adsorbate solution was greater than 6. The equilibrium data were fitted using Langmuir and Freundlich adsorption isotherm equation. The kinetics of sorption of the copper ion has been analyzed by two kinetic models, namely, the pseudo first order and pseudo second order kinetic model. The adsorption constants and rate constants for the models have been determined. The process follows pseudo second order kinetics and the results indicated that the Langmuir model gave a better fit to the experimental data than the Freundlich model. It was concluded that activated carbon produced using phosphoric acid has higher adsorption capacity when compared to CAC.

• Korean Membrane Journal
• /
• v.11 no.1
• /
• pp.8-14
• /
• 2009

The sulfonated poly(styrene-divinylbenzene-acrylonitrile) (ST-DVB-AN) composite polymer electrolyte membrane based on the original PVC film was successfully synthesized to improve oxidative stability using semi-interpenetrated polymer network (semi-IPN). Weight gain ratio after copolymerization was enhanced by the DVB and AN contents, and the sulfonated membranes were characterized in terms of proton conductivity (k), ion exchange capacity (IEC), and water uptake ($W_U$). The effect of DVB content and AN addition were thoroughly investigated by comparing the resulted properties including oxidative stability. The obtained ST-DVB-AN composited semi-IPN membranes showed relatively high proton conductivity and IEC compared with Nafion117, and greatly improved oxidative stability of the synthesized membrane was obtained. This study demonstrated that a semi-interpenetrated sulfonated ST-DVB-AN composited membrane reinforced by PVC polymer network is a promising candidate as an inexpensive polymer electrolyte membrane for fuel cell applications.

• Korean Membrane Journal
• /
• v.11 no.1
• /
• pp.1-7
• /
• 2009

This work reports the preparation of proton conductive crosslinked polymer electrolyte membranes by blending poly(vinyl chloride)-g-poly(hydroxyl ethyl acrylate) (PVC-g-PHEA) and poly(vinyl alcohol) (PVA). The PHEA chains of the graft copolymer were crosslinked with PVA using sulfosuccinic acid (SA) via the esterification reaction between -OH of polymer matrix and -COOH of SA. The PVC-g-PHEA graft copolymer was synthesized via atom transfer radical polymerization (ATRP) using direct initiation of the secondary chlorines of PVC backbones. Ion exchange capacity (IEC) continuously increased with increasing concentrations of SA, due to the increasing portion of charged groups in the membrane. However, the water uptake increased up to 20.0 wt% of SA concentration above which it decreased monotonically. The membrane exhibited a maximum proton conductivity of 0.026 S/cm at 20.0 wt% of SA concentration, which is presumably due to competitive effect between the increase of ionic sites and the crosslinking reaction.