Occurrence, distribution, and ecological risk assessment of heavy metals in Chao Phraya River, Thailand.

Understanding heavy metals in rivers is crucial, as their presence and distribution impact water quality, ecosystem health, and human well-being. This study examined the presence and levels of nine heavy metals (Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, and Zn) in 16 surface water samples along the Chao Phraya River, identifying Fe, Mn, Zn, and Cr as predominant metals. Although average concentrations in both rainy and dry seasons generally adhered to WHO guidelines, Mn exceeded these limits yet remained within Thailand's acceptable standards. Seasonal variations were observed in the Chao Phraya River, and Spearman's correlation coefficient analysis established significant associations between season and concentrations of heavy metals. The water quality index (WQI) demonstrated varied water quality statuses at each sampling point along the Chao Phraya River, indicating poor conditions during the rainy season, further deteriorating to very poor conditions in the dry season. The hazard potential index (HPI) was employed to assess heavy metal contamination, revealing that during the dry season in the estuary area, the HPI value exceeded the critical threshold index, indicating the presence of heavy metal pollution in the water and unsuitable for consumption. Using the species sensitivity distribution model, an ecological risk assessment ranked the heavy metals' HC5 values as Pb > Zn > Cr > Cu > Hg > Cd > Ni, identifying nickel as the most detrimental and lead as the least toxic. Despite Cr and Zn showing a moderate risk, and Cu and Ni posing a high risk to aquatic organisms, the main contributors to ecological risk were identified as Cu, Ni, and Zn, suggesting a significant potential ecological risk in the Chao Phraya River's surface water. The results of this study provide fundamental insights that can direct future actions in preventing and managing heavy metal pollution in the river ecosystem.

Phytoextraction Potential of Sunn Hemp, Sunflower, and Marigold for Carbaryl Contamination: Hydroponic Experiment.

The phytoextraction ability and responses of sunn hemp, sunflower, and marigold plants were investigated toward carbaryl insecticide at 10 mg L-1 and its degradative product (1-naphthol). All test plants exhibited significant carbaryl removal capability (65-93%) with different mechanisms. Marigold had the highest translocation factor, with carbaryl taken up, translocated and accumulated in the shoots, where it was biotransformed into 1-naphthol. Consequently, marigold had the least observable toxicity symptoms caused by carbaryl and the highest bioconcentration factor (1848), indicating its hyperaccumulating capability. Sunflower responded to carbaryl exposure differently, with the highest carbaryl accumulation (8.7 mg kg-1) in roots within 4 days of cultivation, leading to a partial toxicity effect. Sunn hemp exhibited severe toxicity, having the highest carbaryl accumulation (91.7 mg kg-1) that was biotransformed to 1-naphthol in the sunn hemp shoots. In addition, the different models were discussed on plant hormone formation in response to carbaryl exposure.

Recycling rice husk for removal of phosphate and nitrate from synthetic and swine wastewater: Adsorption study and nutrient analysis of modified rice husk.

The objective of this study was to determine the adsorbent potential of rice husk and its modified form for phosphate and nitrate removal from synthetic and swine-farm wastewater. The mechanism of adsorption as well as the potential of phosphate-/nitrate- adsorbed rice husk as nutrient rich residue was also investigated. Two-step modification of RH (using base-washing (BW) and chemical modification (CM) was conducted to compare the phosphate and nitrate removal. The effects of several factors (pH, sorbent dosage, contact time, initial concentration, and coexistence of both ions) were investigated to gain insight into the adsorption rate, behavior, and mechanism of the modified RH regarding phosphate and nitrate removal. The results of Fourier-transform infrared spectroscopy showed that the modification was successful by crosslinking with the amine group of the chemical agent. Fitting the adsorption kinetic data of phosphate showed physical adsorption, intraparticle diffusion, and chemisorption, whereas for nitrate, the data indicated mainly chemisorption. Fitting the adsorption isotherm data of phosphate and nitrate together showed adsorption on a monolayer coating of anions on the homogeneous sorbent's surface. The maximum phosphate and nitrate adsorption capacities were 6.94 and 2.46 mg/g, respectively, for a single adsorbate and 11.14 and 1.76 mg/g, respectively, for the binary solution. In real swine wastewater, removal efficiencies of phosphate, nitrite, nitrate, sulfate, and ammonia were 83.8%, 65.0%, >45.0%, 36.6%, and 2.6%, respectively, indicating that the modified RH would be effective for phosphate and nitrate removal from real wastewater. Finally, nutrient analysis of the phosphate- and nitrate-sorbed RH showed increases in nitrogen and phosphorus, which would be beneficial for further use of the RH as nutrient or fertilizer after adsorption.

Biotransformation of struvite by Aspergillus niger: phosphate release and magnesium biomineralization as glushinskite.

Struvite (magnesium ammonium phosphate-MgNH4 PO4 ·6H2 O), which can extensively crystallize in wastewater treatments, is a potential source of N and P as fertilizer, as well as a means of P conservation. However, little is known of microbial interactions with struvite which would result in element release. In this work, the geoactive fungus Aspergillus niger was investigated for struvite transformation on solid and in liquid media. Aspergillus niger was capable of solubilizing natural (fragments and powder) and synthetic struvite when incorporated into solid medium, with accompanying acidification of the media, and extensive precipitation of magnesium oxalate dihydrate (glushinskite, Mg(C2 O4 ).2H2 O) occurring under growing colonies. In liquid media, A. niger was able to solubilize natural and synthetic struvite releasing mobile phosphate (PO4 3- ) and magnesium (Mg2+ ), the latter reacting with excreted oxalate resulting in precipitation of magnesium oxalate dihydrate which also accumulated within the mycelial pellets. Struvite was also found to influence the morphology of A. niger mycelial pellets. These findings contribute further understanding of struvite solubilization, element release and secondary oxalate formation, relevant to the biogeochemical cycling of phosphate minerals, and further directions utilizing these mechanisms in environmental biotechnologies such as element biorecovery and biofertilizer applications.

Bisphenol A removal from a plastic industry wastewater by Dracaena sanderiana endophytic bacteria and Bacillus cereus NI.

Understanding the significance of plant-endophytic bacteria for bisphenol A (BPA) removal is of importance for any application of organic pollutant phytoremediation. In this research, Dracaena sanderiana with endophytic Pantoea dispersa showed higher BPA removal than uninoculated plants at 89.54 ± 0.88% and 79.08 ± 1.20%, respectively. Quantitative Real-Time PCR (qPCR) showed that P. dispersa increased from 3.93 × 107 to 8.80 × 107 16S rRNA gene copy number in root tissues from day 0 to day 5 which indicated that it could assist the plant in removing BPA during the treatment period. pH, chemical oxygen demand (COD), biochemical oxygen demand (BOD), total dissolved solids (TDS), conductivity, and salinity were reduced after 5 days of the experimental period. Particularly, BOD significantly decreased due to activities of the plants and microorganisms. Furthermore, an indigenous bacterial strain, Bacillus cereus NI, from the wastewater could remove BPA in high TDS and alkalinity condition of the wastewater. This work suggests that D. sanderiana plants could be used as a tertiary process in a wastewater treatment system and should be combined with its endophytic bacteria. In addition, B. cereus NI could also be applied for BPA removal from wastewaters with high TDS and salinity.

Performance of packed bed column using Chara aculeolata biomass for removal of Pb and Cd ions from wastewater.

Biosorption of Pb and Cd from aqueous solution by biomass of Chara aculeolata was studied in a continuous packed bed column. C. aculeolata in the fixed bed column is capable of decreasing Pb and Cd concentrations from 10 mg/L to a value below the detection limit of 0.02 mg/L. Selective uptake of Pb and Cd in a binary solution resulted in Pb having much higher relative affinity than Cd. The experiments were conducted to study the effects of column design parameters, bed depth, and flow rate on the metal biosorption. Pb uptake capacity of C. aculeolata increased with increased bed depth and decreased flow rate, while Cd uptake capacity increased with increased bed depth but remained constant at any flow rate. The Thomas model was found in a suitable fitness with the experiment data for Pb and Cd (R2 > 0.90). The efficiency of biosorbent regeneration achieved by 0.1 M HCl was very high, that was, 98% for Pb and 100% for Cd in the third reused cycle. It can be concluded that C. aculeolata is a good biosorbent for treating wastewater having low concentrations of Pb and Cd contamination.

Adsorption of Antimony by Bagasse Fly Ash: Chemical Modification and Adsorption Mechanism.

Modification of bagasse fly ash (BFA) and the adsorption mechanism of antimony (Sb) by modified BFA were studied. It was found that BFA grafted with acrylic acid (BFAG) and BFA treated with hydrochloric acid (BFA/HCl) led to a decrease in the pH of the zero point of charge (pHzpc) of the adsorbents. The pHzpc of BFA, BFAG, BFA/HCl and activated carbon (AC) were 8.3, 6.4, 6.2 and 8.2, respectively. The maximum adsorption capacities (Qmax) of Sb by BFA, BFAG, BFA/HCl and AC were 0.14, 0.34, 0.38 and 0.29 mg Sb/g adsorbent, respectively. Modified BFA had Qmax higher than AC although the BET surface area of AC was the highest. This was due to the system pH of BFAG and BFA/HCl was 5.20-6.00 and the pHzpc of BFAG and BFA/HCl accounted for 6.4 and 6.2, respectively. Therefore, the adsorbent surface had a positive charge, resulting in increasing adsorption of Sb.

Color removal from textile wastewater by using treated flute reed in a fixed bed column.

This study investigated the ability of acid treated flute reed to adsorb color (dye) from synthetic reactive dye solutions, and actual dyeing and printing textile wastewaters in a laboratory scale fixed bed column. The effects of particle size, initial reactive dye concentration, bed depth and flow rate on adsorption performances were examined. The results from experiments with synthetic reactive dye solutions showed that the volume treated (until the breakthrough occurred) increased with decreasing particle size, influent reactive dye concentration and flow rate, and increasing bed depth. The bed depth service time model was suitable for describing the experimental data. The treated flute reed was able to reduce color efficiently, 99% for dyeing textile wastewater with ten adsorption columns in series and 78% for printing textile wastewater with a single adsorption column. The difference in the numbers of columns used for the two types of actual textile wastewater led to a substantial discrepancy in suspended solids removal, 99% for dyeing wastewater and 12% for printing wastewater. Similar pH and chemical oxygen demand (COD) results were obtained for the two types of textile wastewater. The acid pretreatment of flute reed resulted in dramatic decreases in pH after the adsorption and very acidic effluents (pH 3). Increases of COD after the adsorption due to organic leaching from the treated flute reed were observed. A different pretreatment method to solve these pH and COD problems is needed before flute reed can be used in practice.

Removal of lead (Pb(2+)) by the cyanobacterium Gloeocapsa sp.

Pb(2+) removal ability of the viable-freshwater cyanobacterium Gloeocapsa sp. was studied in batch experiments. Gloeocapsa sp. was cultured in the Medium 18 with pH adjusted to 3, 4, 5, 6 and 7. Growth was subsequently determined based on the increase of chlorophyll-a content. Gloeocapsa sp. was able to grow at all pH levels tested, except at pH 3. Removal of Pb(2+) was then further studied under pH 4. The results showed that Pb(2+) concentration in the range of 0-20 mg L(-1) was not inhibitory to Gloeocapsa sp. growth but reduced its Pb(2+) removal efficiency (by 4.5% when Pb(2+) concentration increased from 2.5 to 20 mg L(-1)). Pb(2+) removal characteristics followed the Langmuir adsorption isotherm with the maximum removal capacity (q(max)) of 232.56 mg g(-1). Adsorption of Pb(2+) by this cyanobacterium followed the second order rate reaction and intraparticle diffusion was likely the rate-determining step. The initial rate of Pb(2+)adsorption during intraparticle diffusion was slower under light than under dark conditions, indicating that light probably slowed down the initial rate of intraparticle diffusion through the repulsion effects on cell membrane.

Production, composition and Pb2+ adsorption characteristics of capsular polysaccharides extracted from a cyanobacterium Gloeocapsa gelatinosa.

Pb2+ adsorption by the living cells of the cyanobacterium Gloeocapsa gelatinosa was studied. Cyanobacterial cells with intact capsular polysaccharide (CPS) showed 5.7 times higher Pb adsorption capacity than that of cells without CPS. The adsorbed Pb was desorbed by EDTA, indicating that Pb2+ adsorption occurred mainly on cell surface. Production, sugar content and ability of CPS to remove Pb2+ were then studied in details. CPS production by G. gelatinosa increased when culture time was prolonged. The maximum CPS production was 35.43 mg g(-1) dry weight after 30-day cultivation. Xylose, arabinose, ribose, rhamnose, galactose, glucose, mannose and fructose were the neutral sugars presented in CPS of G. gelatinosa. Acidic sugars including galacturonic and glucuronic acids were also found in CPS. The amount and composition of G. gelatinosa's CPS varied according to its growth phase and culture conditions. The highest amount of acidic sugars was produced when cultured under low light intensity. The extracted CPS rapidly removed Pb2+ from the solution (82.22+/-4.82 mg Pb2+ per g CPS), directly demonstrating its roles in binding Pb2+ ions. Its ability to remove Pb2+ rapidly and efficiently, to grow under sub-optimal conditions (such as low pH and low light intensity), and to produce high amount of CPS with acidic sugars, leads us to conclude that G. gelatinosa is a potential viable bioadsorber for mildly acidic water contaminated with Pb2+.

Improvement of selective removal of heavy metals in cyanobacteria by NaOH treatment.

In the freshwater cyanobacterium, Tolypothrix tenuis, treatment with 0.1 M NaOH increased its Cd-selective adsorption ability in the presence of Ca(2+) or Mg(2+). The selective adsorption was also achieved by other alkaline treatments. Energy-distributed spectroscopy analysis revealed that Cd(2+) was found mainly on the surface of non-treated cells, whereas it was distributed throughout the cell after NaOH treatment. The alkaline treatment was effective in increasing the selective adsorption ability of the cyanobacterium for other bivalent heavy metals such as Cu(2+), Pb(2+) and Zn(2+). The treatment was also applicable to Anabaena variabilis and Microcystis aeruginosa, which are typical cyanobacteria causing algal blooms. The main binding site of Cd(2+) in NaOH-treated cells is assumed to be the carboxyl groups because the binding ability of the cells was diminished by the esterification of carboxyl groups. These results suggest that alkaline treatment of cyanobacteria is a useful technique for producing biosorbents having highly specific binding abilities for heavy metals.

Decolorization of basic, direct and reactive dyes by pre-treated narrow-leaved cattail (Typha angustifolia Linn.).

The efficiency of basic, direct and reactive dye removal from water by narrow-leaved cattail (NLC) powder treated with distilled water (DW-NLC), 37% formaldehyde+0.2 N sulfuric acid (FH-NLC), or 0.1 N sodium hydroxide (NaOH-NLC) at various pH levels (3, 5, 7, and 9) was tested. Desorption of the adsorbed dyes was also investigated. The type of NLC treatment and pH of the dye solution had little effect on removal of basic dyes, and efficiencies ranged from 97% to 99% over the range of pH used. Over a wide range of pH levels, all types of treated cattail powder had negative charges and probably attracted the basic dyes possessing positive charges. Efficiency of removal by the three NLC treatments ranged from 37% to 42% for direct dyes and from 22% to 54% for direct dyes at pH 7. The pH of the dye solution had substantial effects on the efficiency of removal in direct and reactive dyes. Dye removal was highest at pH 3, with 99% for a direct dye (Sirius Red Violet RL) and 96% for a reactive dye (Basilen Red M-5B). There was mutual attraction between negatively charged direct dye molecules and positively charged molecules on the surface of the FH-treated cattail. In tests of desorption of dyes from cattail in distilled water, the desorption percentage for FH-NLC after adsorbing basic, direct and reactive dyes was 6%, 10% and 35%, respectively, which indicated a chemisorption mechanism for basic and direct dyes and some physiosorption for reactive dyes.