Performance evaluation and upgrade options for existing sequencing batch reactor for nutrient removal

Assessment and upgrade of existing sewage treatment plants (STPs) are necessary due to the revision of the existing effluent regulations which now monitors nutrients including ammonia, nitrate and phosphates. The aim of this study is the performance evaluation of four sequencing batch reactor (SBR) type of STP based on the following parameters: biological oxygen demand (BOD), chemical oxygen demand (COD), total suspended solids (TSS), nitrates, ammonia, phosphates and pH; and their potential upgrade based on the revised regulations stated in DAO 2016-08. Four sequencing batch reactor (SBR) type of STP were assessed for 12 weeks for this study. Results showed noncompliance with nutrient levels, thus upgrade is necessary. Analytical Hierarchy Process (AHP), a Multi-Criteria-Analysis (MCA) tool, was used to select the best option for upgrade among options that include (1) additional SBR tank, (2) diverting wastewater to another treatment facility, and (3) converting the SBR into membrane bioreactor (MBR). Considering the criterion for upgrade, option 2 was the most preferred decision followed by option 1 then option 3

Acetylation of Nata de coco (bacterial cellulose) and membrane formation

Nata de coco (NDC), a bacterial cellulose formed by Acetobacter xylinum, was utilized to fabricate a membrane via acetylation and phase inversion methods. The NDC was activated and dissolved in N,N-Dimethylacetamide (DMAc) with lithium chloride (LiCl) at varying amounts of NDC, LiCl/DMAc ratio, activation temperature, and dissolution temperature. Acetylation was done by adding acetic anhydride (in a mass ratio of 1:12 NDC-anhydride) to NDC-DMAc/LiCl solution at a dissolution temperature of 110 °C for 3 hours. The modified-NDC was recovered via precipitation in methanol. The modified-NDC was washed with deionized water then freeze-dried. Modification was verified by determining the degree of substitution (DS) using titration and FTIR analysis. It was observed that the modification could be carried out at an NDC/DMAc (w/v) ratio of 1:75 at 120 °C for 1 hour, and addition of 8% (w/v) LiCl catalyst at 110 °C for 20 minutes. The DS of the modified-NDC was observed in the range of 2.84 – 3.69, which indicates a successful modification. This was further verified by the FTIR results. Membrane fabrication was carried out using the modified-NDC via immersion-precipitation and solvent evaporation methods. A successful membrane formation was observed using solvent evaporation

Phosphorus recovery from wastewater and sludge

Wastewater and sludge are potential resource of phosphorus (P) for fertilizer production. One method of recovering phosphorus is via chemical precipitation. In the study, phosphorus was recovered from wastewater and sludge. First, hydrolysis was carried out to release the phosphorus in the sludge by the addition of 1.0M acid (sulfuric acid) or base (sodium hydroxide) solution mixed for three hours at 200 rpm. The hydrolyzed sludge was filtered, and the pH of the solution was adjusted to 9.0. Precipitation for both wastewater and hydrolyzed sludge solution was carried out using magnesium chloride hexahydrate (MgCl2•6H2O) and ammonium chloride (NH4Cl). The mixture was stirred for an hour for crystallization. Precipitates were allowed to settle for 24 hours before it was filtered and dried in an oven at 55-58oC for 24 hours. The dried sample was grinded and characterized using Fourier transform infrared spectroscopy (FTIR), x-ray fluorenscence (XRF), and scanning electron microscope with energy-dispersive x-ray spectroscopy(SEM-EDX)

Adsorption of hydrogen in scandium/titanium decorated nitrogen doped carbon nanotube

Nitrogen doped Carbon Nanotube with divacancy (4ND-CNxNT) that is decorated with Scandium and Titanium as potential hydrogen storage medium using the pseudo potential density functional method was investigated. Highly localized states near the Fermi level, which are derived from the nitrogen defects, contribute to strong Sc and Ti bindings, which prevent metal aggregation and improve the material stability. A detailed Comparison of the Hydrogen adsorption capability with promising system-weight efficiency of Sc over Ti was elucidated when functionalized with 4ND-CNxNT. Finally, the (Sc/4ND)10-CNxCNT composite material has a thermodynamically favorable adsorption and consecutive adsorption energy for ideal reversible adsorption and desorption of hydrogen at room temperature such that it can hold at least 5.8 wt% hydrogen molecules at the LDA and GGA level. © 2016 Elsevier B.V

Sulfur copolymers (SDIB) from inverse vulcanization of elemental sulfur (S8) for polymer blend

Elemental sulfur (S8) is largely available resource as by-product from petroleum refining process which is causing excess sulfur problem\u27 due to its limited usage. The utilization of sulfur as valuable material will not only address environmental concerns but provide cost-effective ways of consuming this huge amount of waste to develop new high-value, high-volume products. One facile synthetic method of utilizing sulfur directly as feedstock to produce polymeric material is inverse vulcanization. In this study, sulfur copolymers (SDIB) was synthesized via inverse vulcanization from S8 and processed into polymer blend with component polymers, polybenzoxazine (PBz) and poly(methyl methacrylate) (PMMA) to show its potential processability into polymer blend. Initially, synthesis of SDIB with varying feed ratios of sulfur to comonomer 1, 3-diisopropenylbenzene (DIB) was evaluated for its resulting properties. Spectroscopy showed copolymerization reactions occurred based on the change in characteristic absorption peaks (C=C-H, C=C, C-H) present in the spectra. Thermogravimetric analysis (TGA) indicated that SDIB is more thermally stable with the increase in onset temperature of degradation. Differential scanning calorimetry (DSC) profile exhibited new single glass transition temperature (Tg) that slightly increased with higher DIB ratio indicating evolution of microstructures of copolymers produced. The processability of SDIB into polymer blend was investigated by using SDIB (50 wt% S) with PBz and PMMA. Blending process using simple mixing technique with solvents was carried out for SDIB/PBz (10/10 wt%) and SDIB/PMMA (7.65/7.65 wt%) blend compositions. The results of this study demonstrated that polymercopolymers interactions influenced the phase structure and behaviour with polymer blend of SDIB/PBz showing higher degree of miscibility with more homogeneous and transparent blend as compared to SDIB/PMMA blend. The suitability of polymer blend in electrospinning of nanofibers could provide variety of new applications for SDIB. © 2020 IOP Publishing Ltd

A Sulfur Copolymers (SDIB)/Polybenzoxazines (PBz) Polymer Blend for Electrospinning of Nanofibers

This study demonstrated the processability of sulfur copolymers (SDIB) into polymer blend with polybenzoxazines (PBz) and their compatibility with the electrospinning process. Synthesis of SDIB was conducted via inverse vulcanization using elemental sulfur (S8). Polymer blends produced by simply mixing with varying concentration of SDIB (5 and 10 wt%) and fixed concentration of PBz (10 wt%) exhibited homogeneity and a single-phase structure capable of forming nanofibers. Nanofiber mats were characterized to determine the blending effect on the microstructure and final properties. Fiber diameter increased and exhibited non-uniform, broader fiber diameter distribution with increased SDIB. Microstructures of mats based on SEM images showed the occurrence of partial aggregation and conglutination with each fiber. Incorporation of SDIB were confirmed from EDX which was in agreement with the amount of SDIB relative to the sulfur peak in the spectra. Spectroscopy further confirmed that SDIB did not affect the chemistry of PBz but the presence of special interaction benefited miscibility. Two distinct glass transition temperatures of 97 °C and 280 °C indicated that new material was produced from the blend while the water contact angle of the fibers was reduced from 130° to 82° which became quite hydrophilic. Blending of SDIB with component polymer proved that its processability can be further explored for optimal spinnability of nanofibers for desired applications

A sulfur copolymers (Sdib)/polybenzoxazines (pbz) polymer blend for electrospinning of nanofibers

© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This study demonstrated the processability of sulfur copolymers (SDIB) into polymer blend with polybenzoxazines (PBz) and their compatibility with the electrospinning process. Synthesis of SDIB was conducted via inverse vulcanization using elemental sulfur (S8). Polymer blends produced by simply mixing with varying concentration of SDIB (5 and 10 wt%) and fixed concentration of PBz (10 wt%) exhibited homogeneity and a single-phase structure capable of forming nanofibers. Nanofiber mats were characterized to determine the blending effect on the microstructure and final properties. Fiber diameter increased and exhibited non-uniform, broader fiber diameter distribution with increased SDIB. Microstructures of mats based on SEM images showed the occurrence of partial aggregation and conglutination with each fiber. Incorporation of SDIB were confirmed from EDX which was in agreement with the amount of SDIB relative to the sulfur peak in the spectra. Spectroscopy further confirmed that SDIB did not affect the chemistry of PBz but the presence of special interaction benefited miscibility. Two distinct glass transition temperatures of 97 °C and 280 °C indicated that new material was produced from the blend while the water contact angle of the fibers was reduced from 130° to 82° which became quite hydrophilic. Blending of SDIB with component polymer proved that its processability can be further explored for optimal spinnability of nanofibers for desired applications

Characteristics and Performance of PTU-Cu Composite Membrane Fabricated through Simultaneous Complexation and Non-Solvent Induced Phase Separation

This study aims to integrate copper (Cu) during membrane formation by a facile simultaneous phase separation process to alleviate biofouling and improve membrane performance. Polythiourea (PTU) polymer synthesized through condensation polymerization of 4,4-oxydianiline and p-phenylene diisothiocyanate in dimethyl sulfoxide was used in the preparation of dope solution. By incorporating different concentrations of cupric acetate in the non-solvent bath, both non-solvent induced phase separation and complexation induced phase separation occur instantaneously. Scanning electron microscopy—energy dispersive X-ray, fourier-transform infrared spectroscopy and time-of-flight secondary ion mass spectroscopy analysis accompanied by color change of the membrane surfaces—confirms the interaction of the polymer with Cu. Interaction of Cu at the interface during membrane formation results in a decrease in contact angle from 2 to 10° and a decrease in surface roughness from 30% to 52% as measured by atomic force microscope analysis. Pure water flux of PTU-Cu membrane increased by a factor of 3 to 17 relative to pristine PTU membrane. Both the pristine PTU and PTU-Cu membrane showed antibacterial characteristics against E. coli

Plasma-enhanced chemical vapor deposition of indene for gas separation membrane

Polyindene (PIn) Philippines membrane was fabricated onto a zeolite 5A substrate by using plasma-enhanced chemical vapor deposition (PECVD) at low temperature. Membrane characterization was done by taking Scanning Electron Microscopy (SEM) and FT-IR measurements and the new peak was found in the plasma-derived PIn film. Membrane performance was analyzed by checking permeability of pure gases (H2, N2, and CO2) through the membrane. PECVD-derived PIn membrane showed high gas barrier properties and selectivities of 8.2 and 4.0 for H2/CO2 and H2/N2, respectively, at room temperature. © 2019, Gadjah Mada University. All rights reserved

Effect of a direct sulfonation reaction on the functional properties of thermally-crosslinked electrospun polybenzoxazine (PBz) nanofibers

Electrospun nanofibers of polybenzoxazines (PBzs) were fabricated using an electrospinning process and crosslinked by a sequential thermal treatment. Functionalization by the direct sulfonation process followed after the post-electrospinning modification treatment. The first stage of experiment determined the effects of varying the concentration of sulfuric acid as the sulfonating agent in the sulfonation reaction under ordinary conditions. The second stage examined the mechanism and kinetics of the sulfonation reaction using only concentrated H2SO4 at different reaction time periods of 3 h, 6 h, and 24 h. The mechanism of the sulfonation reaction with PBz nanofibers was proposed with only one sulfonic acid (-SO3H) group attached to each of the repeating units since only first type substitution in the aromatic structure occurs under this condition. The kinetics of the reaction exhibited a logarithmic correlation where the rate of change in the ion exchange capacity (IEC) with the reaction time increased rapidly and then reached a plateau at the reaction time between 18 h and 24 h. Effective sulfonation was confirmed by electron spectroscopy with a characteristic peak associated with the C-S bond owing to the sulfonate group introduced onto the surface of the nanofibers. ATR-FTIR spectroscopy also confirmed these results for varying reaction times. The SEM images showed that sulfonation has no drastic effects on the morphology and microstructure of the nanofibers but a rougher surface was evident due to the wetted fibers with sulfonate groups attached to the surface. EDX spectra exhibited sulfur peaks where the concentration of sulfonate groups present in the nanofibers is directly proportional to the reaction time. From surface wettability studies, it was found that the nanofibers retained the hydrophobicity after sulfonation but the inherent surface property of PBz nanofibers was observed by changing the pH level of water to basic, which switches its surface properties to hydrophilic. The thermal stability of the sulfonated nanofibers showed almost the same behavior compared to non-sulfonated nanofibers except for the 24 h sulfonation case, which has slightly lower onset temperature of degradation. This journal is © The Royal Society of Chemistry