Effect of coagulation on palm oil mill effluent and subsequent treatment of coagulated sludge by anaerobic digestion

A new effluent treatment scheme is proposed for treating palm oil mill effluent based on coagulation and anaerobic digestion of coagulated sludge. The effectiveness of anionic (N9901) and cationic (N9907) polyelectrolytes manufactured by NALCO (Malaysia) was evaluated both as coagulant and coagulant aid. The results showed that the anionic and cationic polyelectrolytes were best suited as a coagulant aid, and the cationic polyelectrolyte showed better performance than the anionic polyelectrolyte. For an influent chemical oxygen demand (COD) concentration of 59 700 mg L^?1 at an alum dosage of 1700 mg L^?1, the residual COD, suspended solid removal, sludge volume and pH were found to be 39 665 mg L^?1, 87%, 260 mL L^?1 and 6.3, respectively. For the above influent COD and alum dosage with the addition of 2 mg L^?1 of cationic polyelectrolyte as coagulant aid, the results were 30 870 mg L^?1, 90%, 240 mL L^?1 and 6.2, respectively. The sludge resulting from the coagulation process using alum as coagulant and cationic polyelectrolyte as coagulant aid was tested for its digestibility in an anaerobic digester. The quantity of biogas generated per gram of volatile solids (VS) destroyed at a loading rate of 26.7 ± 0.5 and 35.2 ± 0.4 g VS L^?1 d^?1 was found to be 0.68 and 0.72 L g^?1 VS destroyed. The anaerobic biomass when subjected to varying alum dosage in the coagulated palm oil sludge did not exhibit inhibition as the digester performance was in conformity with the regular treatment process Copyright © 2006 Society of Chemical Industry     

Interfacial properties of polyelectrolyte-cellulose systems. IV. Electrokinetic properties of carboxymethylcellulose fibers with adsorbed multilayers of cationic polyelectrolyte

Zeta potential measurements by the streaming current method were performed on carboxymethylcellulose (CMC) with and without irreversibly adsorbed multilayers of cationic polyelectrolyte. Factors affecting the electrokinetic properties such as the amount of adsorbed polymer, polymer molecular weights (M_n 50,000 and 200,000), ionic strength (10^?5 ～ 10^?2M KCl), and pH of the streaming medium (KCl solutions) were examined. The negative zeta potential of CMC decreased to the point of monolayer formation and increased from that point to the saturated multilayer formation. The polarity of the zeta potential was negative throughout every adsorption stage. The negative zeta potential increase was attributed to: (a) binding of anions (Cl^? and OH^?) to the outermost layer of the multilayer from KCl solutions and (b) change in chemical potentials of counterions in a diffuse double layer due to expansion of the double layer in the presence of the adsorbed multilayer on CMC. The results suggest that the carboxyl groups under the monolayer are undetectable electrokinetically; however, the negative charge, due to unneutralized carboxyl groups under the monolayer, appears to cause further adsorption forming a saturated multilayer. When the effect of unneutralized carboxyls of CMC are shielded at higher levels of adsorption, the outermost layer of the multilayer becomes a potential-determining layer.     

Polysulfobetaines and corresponding cationic polymers. VI. Synthesis and aqueous solution properties of cationic poly(methyl iodide quaternized acrylamide–N,N-dimethylaminopropylmaleimide copolymer) [poly(MIQADMAPM)]

The copolymer prepared by copolymerizing with acrylamide and maleic anhydride was imidized with N,N-dimethylaminopropylamine. The obtained acrylamide–N,N-dimethylaminopropylmaleimide (ADMAPM) copolymer was then reacted with methyl iodide to yield a poly(methyl iodide quaternized acrylamide–N,N-dimethylaminopropylmaleimide) copolymer [poly(MIQADMAPM)]. Its aqueous solution properties were studied by measurements of reduced viscosity, intrinsic viscosity, and flocculation test in this study. The reduced viscosity and intrinsic viscosity of this cationic polyelectrolyte were related to the types and concentration of the added salt. “Soft” salt anions were more easily bound to the quaternary ammonium cation (R₄N⁺) of poly(MIQADMAPM) than were “hard” salt anions. Halide anions are hard anions; consequently, hard cations were more easily attracted to halide anions and reduced the binding degree of halide anion on the quaternary ammonium group (R₄N⁺). The intrinsic viscosity behavior for cationic polyelectrolyte resulting from the electrostatic repulsive force of the polymer chain was contrasted with polyampholyte. The effect of various flocculants on flocculation in different pH values was accessed in this study. © 1996 John Wiley & Sons, Inc.     

An ab initio study on properties of cationic chalcogen bonds in XF2Y+⋯NCZ (X═H,CN, F; Y═S,Se; Z═H,Cl, Br) complexes

The geometries, interaction energies, and bonding properties of cationic chalcogen bonds are studied in binary complexes XF₂Y⁺?NCZ (X═H, CN, F; Y═S, Se; Z═H, Cl, Br). The nature of these interactions is studied by a vast number of methods, including molecular electrostatic potential (MEP), Noncovalent Interaction Index (NCI), quantum theory of atoms in molecules (QTAIM), and natural bond orbital (NBO) analyses. The interaction energies of these complexes vary between ?20.94?kcal/mol in HF₂S⁺?NCH and ?33.72?kcal/mol in F₃Se⁺?NCBr. According to the QTAIM analysis, all these cationic chalcogen bonds are classified as a closed-shell interaction with a partial covalent character. Moreover, cooperative effects between cationic chalcogen bond and hydrogen or halogen bond interactions are studied in ternary XF₂Y⁺?NCZ?NH₃ complexes. These cooperative effects are analyzed in terms of the parameters derived from the QTAIM and NBO analyses, and electron density difference plots.     

Determination of Rate Constants for Ozonation of Ofloxacin in Aqueous Solution

The ozonation of the quinolone antibiotic ofloxacin in water has been investigated with focus on kinetic parameters determination. The apparent stoichiometric factor and the second-order rate constants of the reactions of ozone and hydroxyl radical with ofloxacin were determined at 20 °C in the pH range of 4–9. The apparent stoichiometric factor was found to be about 2.5 mol O₃/mol ofloxacin regardless of the pH. The rate constant of the reaction between ozone and ofloxacin was determined by a competitive method (pH = 6–9) and a direct ozonation method (pH = 4). It was found that this rate constant increases with pH due to the dissociation of ofloxacin in water. The direct rate constants of ofloxacin species were determined to be 1.0?×?10², 4.3?×?10⁴ and 3.7?×?10⁷ for cationic, neutral-zwitterion and anionic species, respectively. Accordingly, the attack of ozone to ofloxacin mainly takes place at the tertiary amine group of the piperazine ring, though some reactivity is also due to the quinolone structure and oxazine substituent. The rate constant of the reaction between ofloxacin and hydroxyl radical was obtained from UV/H₂O₂ photodegradation experiments. It was found that this rate constant varies with pH from 3.2?×?10⁹ at pH 4 to 5.1?×?10⁹ at pH 9.     

Removal of Dichromate Anions with Nanofiltration‐Complexation by using Amino Calix[4]arene Derivative

Abstract

Herein the removal and recovery of chromium anions from aqueous solutions by using nanofiltration pilot‐scale equipment (Osmonics Sepa CF Membrane Cell) with a water‐soluble amino calix[4]arene derivative was studied. To understand the selectivity, the authors also examined the retention of chromium anions in the presence of Cl^?, NO₃ ^?, SO₄ ^2?, HSO₄ ^?, CO₃ ^2?, PO₄ ^3?, H₂PO₄ ^? anions in nanofiltration‐complexation. From the results water‐soluble amino calix[4]arene was effective and selective ligand for dichromate anions over nitrate anions, in a nanofiltration‐complexation system at pH 2.5. Moreover, the recovery and reusability studies of dichromate and nitrate anions and also ligand were performed.     

Aqueous solution properties of poly(trimethyl acrylamido propyl ammonium iodide) [poly(TMAAI)]

The aqueous solution properties of a cationic poly(trimethyl acrylamido propyl ammonium iodide) [poly(TMAAI)] were studied by measurements of reduced viscosity, intrinsic viscosity, and flocculation test. The reduced viscosity and intrinsic viscosity of this cationic polyelectrolyte were related to the types and concentration of added salt. “Soft” salt anions were more easily bound on the quaternary ammonium (R₄N⁺) of poly(TMAAI) than those of “hard” salt anions. Halide anions are hard anions; consequently, hard cations were more easily attracted to halide anions for reducing the binding degree of halide anion on the quaternary ammonium group (R₄N⁺). Some salt ions were observed to strongly attract the quaternary ammonium of the cationic polymeric side chain for coagulation of the polymers. This effect would make the polymeric aqueous solution become turbid. The intrinsic viscosity behavior for cationic polyelectrolyte resulting from the electrostatic repulsive force of the polymer chain is contrasted with polyampholyte. A comparison of various flocculants as to the effect of flocculation was also studied. © 1994 John Wiley & Sons, Inc.     

Potentiels biioniques de membranes liquides fortement dissociees

The liquid membranes are solutions in nitrobenzene of alkyl-trimethyl-ammonium salts which, in the concentration range studied, have a dissociation coefficient higher than 0·9. Biionic potentials obtained when opposing Cl^??Br^?, Br^??I^? and Br^??Pi^? are studied. The values of the parameters appearing in the mathematical expression of biionic potentials (ion mobility, standard chemical affinity of transfer from water to nitrobenzene) are determined.     

Synthesis,solution properties and scale‐inhibiting behaviour of a diallylammonium/sulfur dioxide cyclocopolymer bearing phospho‐ and sulfopropyl pendents

Zwitterion (Z) monomer 3‐[diallyl{3‐(diethoxyphosphoryl)propyl}ammonio]propane‐1‐sulfonate underwent cyclocopolymerization with sulfur dioxide to give a new alternating copolymer poly(Z‐alt‐SO₂) in excellent yield (ca 90%). The polyzwitterion (±) (PZ) (i.e. poly(Z‐alt‐SO₂), bearing a diethylphosphonate as well as a sulfonate functionality in each repeat unit, upon ester hydrolysis gave its corresponding pH‐responsive polyzwitterionic acid (±) (PZA). The pH‐induced equilibrations (+) cationic polyelectrolyte ? (±) PZA ? polyzwitterion/anion (± ?) (PZAN) ? polyzwitterion/dianion (± =) (PZDAN) permitted us to examine the effects of charge types and their densities on the interesting solubility and viscosity behaviours. The apparent protonation constants of the basic functionalities &tbond;N^±PO₃^2? in (± =) PZDAN and &tbond;N^±PO₃H^1? in (± ?) PZAN in salt‐free water and 0.1 mol L^?1 NaCl were determined using potentiometric titrations. (±) PZA at a meagre concentration of 20 ppm was found to be an effective antiscalant to inhibit the precipitation of CaSO₄ from its supersaturated solution: after 500 and 800 min, the respective scale inhibitions of 86 and 98% indicated its potential use as an effective antiscalant in reverse osmosis plant. © 2014 Society of Chemical Industry     

Flotation of perrhenates with cationic surfactants: Effect of surfactant's structure

An experimental investigation is presented on the flotation of perrhenate anions from diluted aqueous solutions (5.10^?5 M ) with numerous cationic surfactants of systematically varying molecular structure. Alkyltrimethyl-ammonium bromides, alkoxycarbonylmethyl-trimethylammonium chlorides, alkoxycarbonylmethyl-dimethylbenzylammonium chlorides, ethoxycarbonylmethyl-dimethylalkylammonium chlorides, N-substituted dodecylamines, and diquaternary ammonium bromides were investigated at their initial concentrations in the feed solution, 1.10^?4 M or 2.10^?4 M . It was found that both the length of the main hydrocarbon chain and of the short hydrocarbon groups govern the affinity of a cationic surfactant towards perrhenate anions. In order to achieve the effective flotation of perrhenate or similar anions the value of C:N atomic ratio for a tertiary or a quaternary ammonium surfactant should be in the range 15 to about 26. This value can be used as a primary criterion for the sufficient flotation capability of an alkylammonium surfactant.     

Interactions of a smart cationic polyelectrolyte based on hydroxypropylcellulose with an anionic surfactant

Novel thermosensitive, cationic polyelectrolyte was obtained by grafting N‐vinylformamide onto hydroxypropylcellulose followed by the hydrolysis of the formamide groups to the amine groups. The effect of the ionic strength on the lower critical solution temperature of the polymers was studied. The interactions of the polymers with sodium dodecyl sulfate (SDS) as a model anionic surfactant were studied. It was found by the measurements of the light scattering and fluorescence spectroscopy that the graft copolymers obtained strongly interact with SDS with the formation of polymer‐surfactant complexes. The values of critical association concentration (cac) of these polymer‐surfactant systems were found to be of the order of 10^?5 mol/dm³ at pH = 6.5 and of the order of 10^?6 mol/dm³ at pH = 2.5. The polymer was shown to be potentially useful for the purification of water from anionic surfactants. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Interfacial properties of polyelectrolyte–cellulose systems. II. Electrokinetic properties of cellulose fibers with adsorbed monolayers of cationic polyelectrolyte

Zeta potential measurements by the streaming current method were performed on pulp (DP) fibers with or without irreversibly adsorbed monolayers of cationic polyelectrolyte. Factors affecting the electrokinetic properties of these fibers, such as the amount of adsorbed polymer, the polymer molecular weight (M_n 50,000 and 200,000), ionic strength (10^?5 ～ 10^?2M KCl), and the pH of the streaming medium (KCl solution), were examined. As the amount of adsorbed polymer increased, the negative zeta potential of the fibers decreased until the polarity of the zeta potential was reversed to the positive side. A marked change in the value of zeta potential was not observed when the formation of the saturated monolayer was completed. The zeta potential also varied in proportion to an increase in the amount of polymer adsorbed. Experimental results are interpreted with reference to the origin of the surface charge, the amphoteric nature of the surface, the modes of adsorption, and the adsorbed polymer chain configuration. Possible effects of the adsorbed monolayer formation on the structural change of the electric double layer at the fiber surface are discussed. It is concluded that the formation of a monolayer of cationic polyelectrolytes on the negatively charged cellulose fibers under the condition of k₁ > k₂ (part I) provides a means to arbitrarily control the charge of the fibers until formation of a saturated monolayer.     

Novel real-time method using the stopped-flow for evaluating bisphenol A degradation kinetics by molecular ozone and radical mechanisms

A novel real-time method was developed to evaluate the bisphenol A degradation kinetics by molecular ozone and radical pathway using the stopped-flow technique. The second-order kinetics was determined under pseudo-first-order conditions for the molecular pathway by the absolute rate constant method and for the radical pathway by the R_ct concept involving the hydroxyl radical and ozone ratio. Bisphenol A degradation by ozone was performed and evaluated at a pH ranging from 2 to 10. At pH?4?M^?1?s^?1 and for the radical pathway at pH?>?10, the constant was 3.43?×?10⁹?M^?1?s^?1. To validate the method, ciprofloxacin degradation kinetics was determined at pH 8 by radical pathway, in 4.55?×?10⁹?M^?1?s^?1. The method permits the determination of kinetic parameters for the design of chemical reactors; avoiding the generation of undesirable reactions and by-products in the degradation of emerging compounds.     

Poly(sulfobetaine)s and corresponding cationic polymers. XI. Synthesis and aqueous solution properties of a cationic poly(methyl iodide quaternized ethyl vinyl ether/N,N‐dimethylaminopropyl maleamidic acid) copolymer

A copolymer prepared by the copolymerization of ethyl vinyl ether and maleic anhydride underwent amidoacidation with N,N‐dimethylaminopropylamine. The obtained ethyl vinyl ether/dimethylaminopropyl maleamidic acid copolymer was then reacted with methyl iodide to yield poly(methyl iodide quaternized ethyl vinyl ether/N,N′‐dimethylaminopropyl maleamidic acid) (MIQEDMAPMA). The greatest difference from other polyelectrolytes was the carboxylic group on the polymer chain unit of MIQEDMAPMA. Its aqueous solution properties in various salts and at various pH values were studied by measurements of the reduced viscosity and intrinsic viscosity. The reduced viscosity and intrinsic viscosity of this cationic polyelectrolyte were related to the types and concentrations of the added salts. The tendency of the salt effect was similar to that of other polyelectrolytes; that is, soft salt anions were more easily bound to the quaternary ammonium (R₄N⁺) of MIQEDMAPMA than hard salt anions. Some salt ions strongly attracted the quaternary ammonium of the cationic polymeric side chain for the agglomeration of the polymers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2261–2269, 2003     

Application of the Bifunctional Switch-Type Cryptand Ion Chromatographic Stationary Phase for Ion Separation

ABSTRACT

Poly(styrene/divinylbenzene) resin with cryptand 22 as an anchoring group was synthesized and applied in ion chromatography as a packing material for separations of organic anions as well as cations. The cryptand can not only form strong complexes with metal cations, but it has also shown a remarkable complexing ability with organic anions after protonation at pH < 7. The protonated cryptand resin has been applied as an anion exchanger to successfully separate some organic carboxylate anions including HCOO^?, CH₃COO^?, CH₃CH₂COO^?, and some geometric isomers, e.g., fumarate and maleate ions, with water as the eluent. Alternatively, after deprotonated at pH > 7, the cryptand resin can be switched as a cation exchanger to separate inorganic cations. The effects of solvents, temperature, pH values, and flow rates of eluents on the separation of organic anions were also investigated.     

Interaction of functional groups of gelatin and montmorillonite in nanocomposite

As an amphoteric polyelectrolyte, gelatin could intercalate into the galleries of montmorillonite (MMT). In this paper, sodium laurate/MMT composites and sodium laurate/dehydroxylated MMT composites were introduced as low molecular simulation to investigate the interaction functional groups of gelatin and MMT. The composites were characterized by X‐ray diffraction (XRD), Fourier transform infrared spectra (FTIR), thermogravimetric analysis (TGA) and ¹³C nuclear magnetic resonance (¹³C NMR). Furthermore, the effect of interaction between gelatin and MMT on the mechanical properties of the composites was investigated. The results indicated that ? COO^?, not ? COOH, in gelatin chains could interact strongly with the MMT sheets. The reactive sites on MMT were hydroxyl groups, which could interact with ? COO^? in gelatin chains by forming hydrogen bonds. The gelatin/MMT composites prepared in alkalic media have better mechanical properties due to stronger interaction. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1556–1561, 2006     

Electrokinetic Properties of Vermiculite and Expanded Vermiculite: Effects of pH,Clay Concentration and Mono- and Multivalent Electrolytes

Abstract

In this study, the zeta potential values of vermiculite and expanded vermiculite were measured to determine the effect of pH, clay concentration, and various mono- and multivalent electrolytes including NaCl, KCl, NH₄Cl, NaNO₃, NaClO₄, Na₂SO₄, Na₂CO₃, Na₃PO₄·12H₂O, MgCl₂·6H₂O, CaCl₂·2H₂O, BaCl₂, SrCl₂·6H₂O, CuCl₂·2H₂O, CoCl₂·6H₂O, NiCl₂, AlCl₃, and CrCl₃·6H₂O on the electrokinetic properties of vermiculite samples. It was found that generally the measured zeta potential values of expanded vermiculite for the studied systems were slightly more negative than that of vermiculite. The pH profiles of vermiculite and expanded vermiculite at acidic, natural, and basic pH values were obtained to determine the effect of time on the pH values of clay suspensions. The zeta potential measurements showed that the surface charge of clay particles was negative in water. The isoelectric point of vermiculite and expanded vermiculite were determined as pH 2.30 and 2.57, respectively. Divalent cations (Mg²⁺, Ca²⁺, Sr²⁺, and Ba²⁺), heavy metal ions (Cu²⁺, Ni²⁺, and Co²⁺) and trivalent cations (Al³⁺ and Cr³⁺) were potential determining ions for vermiculite and expanded vermiculite particles. Moreover, divalent and trivalent cations caused the change of surface charge from negative to positive. On the other hand, monovalent cations (Na⁺, K⁺ and NH₄ ⁺), monovalent anions (Cl^?, NO₃ ^?, and ClO₄ ^?) and multivalent anions (SO₄ ^2?, CO₃ ^2?, and PO₄ ^3?) acted as indifferent ions for these clay particles.     

Dilute solution properties of cationic poly(dimethyl sulfate quaternized dimethylaminoethyl methacrylate)

The dilute solution properties of a cationic polyelectrolyte, poly(dimethyl sulfate quaternized dimethylaminoethyl methacrylate) [poly(DMAEM · C₂H₆SO₄)], are studied by measurements of intrinsic viscosity, degree of binding, and flocculation application. The intrinsic viscosity of this polyelectrolyte is related to the type and concentration of added salt. The intrinsic viscosity behavior for cationic polyelectrolyte resulting from the electrostatic repulsive force of the polymer chain is contrasted with polyampholyte. The polyelectrolyte in the presence of KCl has a lower degree of binding, indicating that the proton ion (H⁺) is relatively difficult to bind to the CH₃SO₄^? at the polymer end. The polymerization of DMAEM · C₂H₆SO₄ in 0.5M KCl aqueous solution proceeded more easily than that of DMAEM · C₂H₆SO₄ in pure water. The polymerization rate of DMAEM · C₂H₆SO₄ is found to pass through an extreme value as a function of pH. Optimum flocculation, corresponding to the complete removal of turbidity in the supernatant, is achieved. Beyond the optimum flocculation, high polymer dosages redisperse the bentonite suspensions.     

Polysulfobetaines and corresponding cationic polymers. IV. Synthesis and aqueous solution properties of cationic poly(MIQSDMAPM)

A cationic poly(methyl iodide quaternized styrene-dimethylaminopropylmaleimide) copolymer [poly(MIQSDMAPM)] was synthesized by imidizing styrene-maleic anhydride (SMA) copolymer. Its aqueous solution properties were studied by measurements of reduced viscosity, intrinsic viscosity, and a flocculation test. The reduced viscosity and intrinsic viscosity of this cationic polyelectrolyte were related to the types and concentration of the added salt. “Soft” salt anions were more easily bound to the quaternary ammonium cation (R₄N⁺) of poly(MIQSDMAPM) than “hard” salt anions. Halide anions are hard anions; consequently, hard cations were more easily atracted to halide anions, and reduced binding degree of halide anion on the quaternary ammonium group (R₄N⁺). Some salt ions were observed to strongly attract the quaternary ammonium group of the cationic polymeric side chain and resulted in agglomeration of the polymers. A comparison of various flocculants as to the effect of flocculation was made in this study. © 1996 John Wiley & Sons, Inc.     

Photocatalytic removal of methyl orange in an aqueous solution by a WO3/TiO2 composite film

WO₃/TiO₂ composite film was prepared by microarc oxidation technique and characterized by SEM, XRD, UV-vis spectra and Zeta-potential. The photocatalytic activity of WO₃/TiO₂ composite film was evaluated by examining the degradation of methyl orange. The influence of solution pH and inorganic anions on removal ratio of methyl orange was investigated. Removal ratio of methyl orange decreased with an increase of pH value in acidic solution, while it increased with the pH value in alkaline solution. The influence of added anions on the removal ratio is divided into two aspects. Addition of Cl^? and SO ₄ ^2? resulted in a decrease in photocatalytic removal ratio of methyl orange, while it was facilitated by PO ₄ ^3? , HCO ₃ ^? and NO ₃ ^? .