Synthesis,structural elucidation,electro-chemical behaviour and fungitoxic activity of transition metal(II) mixed-ligand complexes with some Schiff bases

The Schiff bases, potassium salt of salicylidene-β-alanine [KHL], bis(benzylidene)ethylenediamine [SB¹] and thiophene-o-carboxaldene-p-toluidine [SB²], and mixed-ligand complexes with Mn(II), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II) have been prepared. They were characterized by elemental analyses, magnetic susceptibility measurements, thermogravimetric analyses (t.g.a.), infrared spectra and electronic spectra. The mixed-ligand complexes were found to have the general composition [M(L)(SB)(H₂O)]. All the mixed-ligand complexes were found to have six-coordinated octahedral geometry. The fungitoxic activity of the ligands, metal salts, control (DMSO), bavistin, emcarb, and mixed-ligand complexes were screened against Aspergillus niger, Fusarium oxysporum and Aspergillus flavus. All the mixed-ligand complexes show higher fungitoxic activity as compared to the Schiff bases, metal nitrate and control (dimethyl sulphoxide, DMSO), and moderate fungitoxic activity as compared to the fungicides (bavistin and emcarb).     

Preparation,characterization and toxic activity of oxovanadium(IV) mixed-ligand complexes

New oxovanadium(IV) mixed-ligand complexes of the general composition [VO(L)(A)], where KHL?=?potassium salt of salicylideneglycine, A¹?=?bis(benzylidene)ethylenediamine, A²?=?bis (acetophenone)ethylenediamine, A³?=?di(2-pyridyl)amine, A⁴?=?bis(benzylidene)-1,8-diaminonaphthalene, A⁵?=?thiophene-o-carboxaldene-aniline, A⁶?=?thiophene-o-carboxaldene-p-anisidine, have been synthesized by the interaction of these ligands with vanadyl sulphate. The mixed-ligand complexes have been characterized on the basis of elemental analysis, magnetic measurements, electronic and infrared spectra. An octahedral structure has tentatively been assigned to all of the mixed-ligand complexes. The mixed-ligand complexes show higher toxic activity against the Salmonella typhi, Escherichia coli and Serratia mercescen as compared to the ligands, vanadyl sulphate and control (dimethyl sulphoxide). The mixed-ligand complexes were also tested against a standard drug (tetracycline).     

Toxic effect of transition metal complexes on Salmonella typhi,Escherichia coli and Serratia marcescens

The present article describes the synthesis, structural features and toxicological studies of the complexes of the type [M(L)(dipy-amine)(H₂O)] or [M(L)(bendan)(H₂O)] where M?=?Mn(II), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II), H₂L?=?salicylidene-o-aminothiophenol, dipy-amine?=di(2-pyridyal)amine, or bendan?=?bis(benzylidene)1,8-diaminonaphthalene. The complexes have been characterized on the basis of elemental analyses, electronic spectra, magnetic measurement and thermogravimetric analyses. The nature of the bonding has been discussed on the basis of infrared spectral data. A thermal study of the complexes has been carried out to ascertain their thermal stability. Magnetic susceptibility measurements and electronic spectral data suggest a six-coordinated octahedral structure for these complexes. The complexes of Mn(II), Co(II), Ni(II), Cu(II) are paramagnetic, while Zn(II) and Cd(II) are diamagnetic in nature. The toxic effects of the investigated complexes were tested against three Gram-negative bacteria, Salmonella typhi, Escherichia coli and Serratia marcescens by the “Disc Diffusion Method”. It is observed that the complexes show higher toxic effects as compared to the ligands, metal salts and control (DMSO), but moderate toxic effects as compared to the standard drug (tetracycline) and the results are discussed.     

Photodegradation of pesticides .1. Photolysis rates and half‐life of acylanilides and their major metabolites in water

The photolysis in water solution of three fungicides (Metalaxyl, Benalaxyl, and Furalaxyl) was studied under artificial light. At λ = 254 Benalaxyl and Furalaxyl underwent fast degradation with rearrangement reactions less complex than those of Metalaxyl. Under A = 254–290 the photolysis was very fast and Benalaxyl and Furalaxyl show a common behaviour. This was found to be a kinetic consecutive process leading, at first, to N‐2,6‐xylyl‐D,L‐alaninate (II), which was degraded to 2,6‐dimethylaniline (IV). This amine gives unknown products. Metalaxyl underwent a parallel/consecutive photodegradtion to give (II) and N‐(methoxyacetyl)‐2,6‐dimethylaniline (VI). While (II) was easily converted to (IV) as earlier, (VI) was more stable to photolysis. Under λ > 290 all the fungicides shown very slow degradation with pseudo first order rate constants. The photoproducts were degraded faster than the parent compounds by factors from 13 to 1800. The presence of photosensitizer in water (humic acids or acetone) resulted in total decomposition of fungicides and of their photoproducts.     

Study on increase in toxicity of Schiff bases on microorganism on chelation with metal

New heterochelates of the type [M(L)(SB)(H₂O)] (where M?=?Mn(II), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II), KHL?=?potassium salt of salicylideneglycine and SB?=?thiophene- O -carboxaldeneaniline) have been synthesized. The heterochelates have been characterized on the basis of elemental analyses, electronic spectra, and magnetic measurement analyses. The structural and geometrical conformation has been discussed on the basis of IR spectral data. A thermal study of the complexes has been carried out to ascertain their thermal stability. Magnetic susceptibility measurements and electronic spectral data suggest a six-coordinated octahedral structure for these complexes. The increase in toxicity of the investigated heterochelate metal compounds was tested against three gram-negative bacteria, S. typhi, E. coli, and Serratia marcescens by the disc diffusion method. It is observed that the heterochelates show higher toxicity when compared to the Schiff bases, metal salts, and control (DMSO) due to chelation. The toxicity is also compared to the standard drug tetracycline.     

Spectroscopic studies and biological evaluation of some transition metal complexes of a novel Schiff base ligands derived from 5-arylazo-salicyladehyde and o-amino phenol

Synthesis and characterization of Cu(II), Ni(II), and Zn(II) Schiff bases complexes resulted from the condensation of salicylaldehyde derivatives with o-amino phenol were discussed using elemental analysis (carbon, hydrogen, and nitrogen), molar conductance, magnetic measurements, mass spectra, and electronic spectra. The essential bands of infrared, ¹HNMR, and UV-Vis spectra as well as thermogravimetric analysis corresponding to the active groups within the three ligands and their complexes were interpreted. The dehydration and decomposition processes of the [Cu(H₂L₁)(H₂O)](OAc)₂, [Ni(H₂L₁)(H₂O)]SO₄ · H₂O, [Zn(H₂L₁)(H₂O)]SO₄ · H₂O, [Cu(H₂L₂)(H₂O)](OAc)₂, [Ni(H₂L₂)(H₂O)]SO₄ · H₂O, [Zn(H₂L₂)(H₂O)]SO₄ · 2H₂O, [Cu(H₂L₃)(H₂O)](OAc)₂ · H₂O, [Ni(H₂L₃)(H₂O)]SO₄ · 2H₂O, [Zn(H₂L₃)(H₂O)]SO₄ complexes were studied thermodynamically using the integral method applying the Coats–Redfern and Horowitz–Metzger equations and the thermodynamic parameters were calculated. It was found from the elemental analysis and the thermal studies, that the ligand behaves as tridentate ligand forming chelates with 1 : 1 (metal : ligand) stoichiometrically. The molar conductance measurements of the complexes in dimethyl sulfoxide solvent indicate that the complexes have an electrolytic nature. The biological activities of the three ligands in comparison with metal(II) complexes were studied against different Gram positive and Gram negative bacteria.     

马拉硫磷及其水解产物对圆瘤浮萍的生长抑制及氧化损伤作用

为了探讨马拉硫磷和主要水解产物对圆瘤浮萍的生长抑制作用及可能的氧化损伤机制,采用静态培养法,研究不同浓度的马拉硫磷及其水解产物二甲基二硫代磷酸酯(DMDTP)、二甲基硫代磷酸酯(DMTP)、二甲基磷酸酯(DMP)对圆瘤浮萍生长、叶绿素含量、叶绿体活性、超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性及丙二醛(MDA)含量的影响。结果表明,暴露7 d后,浓度为100 mg a.i.·L-1处理下的浮萍叶状体生长量与空白对照组无显著性差异;DMDTP、DMTP和DMP对圆瘤浮萍叶状体生长量的半数抑制浓度(7 d-IC50)分别为52.9、45.5和98.0 mg a.i.·L-1。随着试验液中DMDTP、DMTP和DMP浓度的升高,圆瘤浮萍叶绿素含量均明显降低,叶绿体活性则分别表现为诱导-抑制、抑制和抑制效应。在DMDTP、DMTP和DMP胁迫下,脂质过氧化产物丙二醛(MDA)含量明显增加;圆瘤浮萍体内的抗氧化酶系统均受到影响。总体表现为随着DMDTP浓度的增加,SOD活性先降低后升高;DMTP和DMP胁迫下,SOD活性呈现先降后升再降的趋势;POD和CAT活性则随3种水解产物浓度的增加呈现先升后降趋势;这表明抗氧化酶系统对外部胁迫的应答很复杂。马拉硫磷对圆瘤浮萍的毒性较小,其水解产物DMDTP、DMTP和DMP均对圆瘤浮萍的生长产生一定的毒性作用。在实际生产中,应多加关注马拉硫磷水解产物对环境生物的风险评估。     

Design,synthesis, antinociceptive,and anti-inflammatory properties of thiazolopyrimidine derivatives

Ten 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one derivatives were synthesized and evaluated. A series of heterocyclic, 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one were synthesized by reaction of 7-(4-chloro phenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one with appropriately substituted aldehydes in the presence of anhydrous sodium acetate and glacial acetic acid. The antinociceptive activity was evaluated by tail-flick technique, anti-inflammatory activity was evaluated by carrageenan-induced paw edema test and their ulcerogenicity index was determined. The para-substituted methyl, hydroxy, fluoro, chloro, bromo, and nitro derivatives showed significant antinociceptive and anti-inflammatory activities. The detailed synthesis, spectroscopic data, and pharmacological screening of the synthesized compounds were reported.     

Synthesis and biological activities of new azacrown ether Schiff bases and spectrophotometric studies of their complexation with [60]fullerene

A series of novel azacrown ether Schiff bases 1–3 have been synthesized in good yield and in a simple way. Their host–guest interaction with [60]fullerene has been studied in toluene by absorption spectroscopic method. All the complexes are found to be stable with 1:1 stoichiometry. Because of their potential applications in industry, agriculture and medicine, they were investigated for their mutagenic and antimutagenic activities using the spot test and the plate incorporation assay of Ames. Compounds 1, 2 and 3 were found to be nonmutagenic in the Ames test using strains TA 1535, TA100 and TA97a of Salmonella typhimurium. However, using strain TA102 revealed that, although both compounds 1 and 2 were nonmutagenic, compound 2 gave a positive response indicating that it acts as an oxidative mutagen. The structure-activity relationship may throw some light on the biological activity of such series of compounds.     

Toxicity of copper to the marine amphipod Allorchestes compressa in the presence of water-and lipid-soluble ligands

Acute toxicity tests were carried out on the marine amphipod Allorchestes compressa Dana using copper sulphate and some organocopper complexes. For copper sulphate, 96 h LC₅₀ values of 0.11 and 0.5 mg Cu l^-1 were determined for the juveniles and the adults, respectively, juveniles being 4.5 times more sensitive to copper than adults. Organocopper complexes were tested on adults only. The three water-soluble ligands nitrilotriacetic acid, 8-hydroxyquinoline-5-sulphonic acid and tannic acid ameliorated copper toxicity by decreasing the concentration of free ionic copper, while lipid-soluble ligands such as oxine and potassium ethylxanthogenate increased copper toxicity, presumably as a result of the complexes diffusing through the cell membrane and participating in injurious reaction. The copper complex with 2,9-dimethyll, 10-phenanthroline was the most toxic complex tested. It is suggested that the presence of these ligands in the receiving water should be taken into consideration when establishing water-quality criteria.     

水生生物水质基准研究中轮虫、水螅、涡虫类受试生物的筛选

轮虫、水螅、涡虫是水生生态系统的重要生物类群。因其对水体污染较敏感,所以对水生生物基准研究有重要意义。依据我国生物区系资料及毒性数据丰度,筛选出8种代表性本土轮虫、水螅、涡虫类生物。参照美国水生生物基准技术指南,搜集、筛选了这8种代表性生物的急性毒性数据,通过数据分析,筛选出对各物种毒性最大的污染物,主要包括重金属、农药、有机锡化物、表面活性剂、吡啶胺类杀菌剂。分析污染物的物种敏感度分布,依据累积概率对代表性生物的物种敏感性进行分类,结果为:萼花臂尾轮虫(Brachionus calyciflorus)、绿水螅(Hydra viridissima)、普通水螅(Hydra vulgaris)对重金属铜的累积概率为6.5%、8.5%和10.4%,普通水螅(Hydra vulgaris)对重金属汞的累积概率为6.3%;龟甲轮虫(Keratella cochlearis)和四齿腔轮虫(Lecane quadridentata)对五氯酚钠的累积概率为5.1%和7.6%;褐水螅(Hydra oligactis)和绿水螅(Hydra viridissima)对三丁基氧化锡的累积概率为6.9%和13.8%,萼花臂尾轮虫(Brachionus calyciflorus)对氟啶胺的累积概率为6.7%,日本三角涡虫(Dugesia japonica)对四氯化碳、十二烷基苯磺酸钠的累积概率分别为6.7%和7.1%。上述结果表明:萼花臂尾轮虫、绿水螅对重金属铜敏感;普通水螅对重金属铜和汞敏感;龟甲轮虫和四齿腔轮虫对农药敏感;褐水螅和绿水螅对有机锡化物敏感;萼花臂尾轮虫对吡啶胺类杀菌剂敏感;日本三角涡虫对四氯化碳、表面活性剂敏感。这7种代表性生物可作为相关污染物的水生生物基准受试物种。     

Implication of nitric oxide in the heat-stress-induced cell death of the symbiotic alga <Emphasis Type="Italic">Symbiodinium microadriaticum</Emphasis>

One of the major consequences of global warming is a rise in sea surface temperature which may affect the survival of marine organisms including phytoplankton. Here, we provide experimental evidence for heat-induced cell death in a symbiotic microalga. Shifting Symbiodinium microadriaticum from 27 to 32°C resulted in an increase in mortality, an increase in caspase 3-like activity, and an increase in nitric oxide (NO) production. The caspase-like activity was strongly correlated with the production of NO in thermally challenged microalgae. For this experiment, the application of Ac-DEVD-CHO, a mammalian caspase 3-specific inhibitor, partly prevented (by 65%) the increase in caspase-like activity. To verify the relationship between NO and the caspase-like activity, S. microadriaticum were subsequently incubated with 1.0 mM of the following chemical NO donors: sodium nitroprusside (SNP), S-nitrosoglutathione (GSNO), S-nitroso-N-acetylpenicillamine (SNAP) and 3,3bis(Aminoethyl)-1-hydroxy-2-oxo-1-triazene (NOC-18). The supplementation of both SNP and NOC-18 caused a significant increase in caspase-like activity compared to the control treatment. Pre-treatment of the microalgae with the inhibitor Ac-DEVD-CHO before the supplementation of the different NO donors completely prevented the increase in caspase-like activity. These results suggest that NO could play a role in the induction of cell death in heat-stressed S. microadriaticum by mediating an increase in caspase-like activity.     

7种农药对管氏肿腿蜂的毒性及初级风险评价

为评估农药对寄生类自然天敌昆虫的安全性,选择管氏肿腿蜂(Scleroderma guani Xiao et Wu)作为受试生物,采用管测药膜法测定了3种杀虫剂、2种除草剂、2种杀菌剂对其致死效应,并根据田间推荐剂量计算暴露量,采用风险商值HQ对杀虫剂进行风险评估。结果显示,与空白对照比较,3种杀虫剂均具明显毒性作用,其中丁硫克百威、吡虫啉和呋虫胺对管氏肿腿蜂的24 h半致死量(24 h-LR50)分别为5.11、2.92和0.06 g a.i.·ha-1,农田内风险商值分别为60.23、16.64和3 105。除草剂和杀菌剂在3倍最大田间推荐剂量作用下,24 h管氏肿腿蜂死亡率均小于50%。上述结果表明,在田间推荐用量下,3种杀虫剂对管氏肿腿蜂的初级风险评价为存在高风险,建议进一步开展高级阶段风险评估或者采取合理的风险管理措施来降低风险;除草剂和杀菌剂对管氏肿腿蜂的风险可接受。     

Comparative quantitative structure–activity relationship (QSAR) study on acute toxicity of triazole fungicides to zebrafish

We employed two-dimensional quantitative structure–activity relationship (2D-QSAR) and hologram QSAR (HQSAR) methods to quantitatively investigate the mechanism and active site of toxicity for Danio rerio exposed to triazole fungicides. Our results showed that 2D-QSAR models constructed using the energy of the lowest unoccupied molecular orbit, the net C atom charges, the octanol–water partition coefficient and the molecular shape factor had higher predictive abilities. HQSAR models containing the fragment distinctions atoms (As), bonds (Bs), chirality (Ch) and donors and acceptors (D&A) had higher reliability. It was found that 2D-QSAR results explaining the toxicity mechanism were consistent with HQSAR. In summary, the hydrophobicity and shape/size of the molecule were the important factors influencing the toxic effect of these chemicals against D. rerio. In addition, electron exchange may occur between these fungicides and the target. The study provided a method to evaluate the environmental risk of chemicals with a similar structure, based on the QSAR models obtained.     

Cytotoxicity of benalaxyl,metalaxyl, and triadimefon on Chinese hamster ovary cells

The cytotoxicity of the fungicides benalaxyl, metalaxyl, and triadimefon was evaluated in vitro using the Chinese hamster ovary (CHO-K1) cell line. The midpoint cytotoxicity values of neutral red (NR) incorporation (NRI₅₀), total cellular protein content (TCP₅₀), and the methyl tetrazolium assay (MTT₅₀) were estimated. Benalaxyl was the most cytotoxic fungicide, followed by metalaxyl and triadimefon. Fetal calf serum (10%) caused a reduction in benalaxyl, metalaxyl, and triadimefon cytotoxicity by factors of 1.8, 1.3, and 1.3. The effects of sublethal concentrations (NRI₂₅) of the three fungicides on the glutathione redox cycle components glutathione S-transferase, glutathione reductase, glutathione peroxidase, and total glutathione content were studied. The ameliorative effects of extracellular glutathione (1 mmol L^?1), vitamin C (70 µmol L^?1), and vitamin E (30 µmol L^?1) were also investigated. The three antioxidants led to significant effects on the glutathione redox cycle components.     

Synthesis,structural characterization and antimicrobial activity of nickel(II) tetrathiocyanato dicuperate(I) complexes with some acyl hydrazones

Heterobimetallic complexes of the type Ni[Cu(SCN)₂]₂ · L (where L = acetophenone benzoylhydrazone, acetophenone isonicotinoyl hydrazone, acetophenone salicyloylhydrazone (ash), acetophenone anthraniloylhydrazone, p-hydroxy acetophenone benzoylhydrazone, p-hydroxy acetophenone isonicotinoyl hydrazone p-hydroxy acetophenone salicyloylhydrazone (phash), p-hydroxy acetophenone anthraniloyl hydrazone), were synthesized and characterized. The complexes are polymeric, insoluble in common organic solvents and are nonelectrolytes. Magnetic moments and electronic spectral studies suggest a spin-free octahedral geometry for the complexes. IR spectra show the bidentate nature of all the ligands bonding through >C=O and >C=N–groups. The SCN group acts as a bridge between two metal centers. X-ray powder diffraction parameters for Ni[Cu(SCN)₂]₂ · ash and Ni[Cu(SCN)₂]₂ · phash correspond to orthorhombic and tetrahedral crystal lattices, respectively, for these complexes. The complexes show a significant antifungal activity against Rizoctonia, Stemphylium and Aspergillus sp. and antibacterial activity against Clostridium and Pseudomonas sp. The metal complexes are more active than the ligands.     

农药类化合物对大型溞的毒性作用模式:与基线毒性化合物比较研究

农药在控制有害生物的同时,对水生生态系统产生较大的毒性效应。本文通过实验获得了25种基线化合物对大型溞的急性毒性数据,并与57种农药类化合物对大型溞的急性毒性数据进行比较研究,同时根据体外浓度LC_(50)、生物富集因子BCF和体内临界浓度CBR的关系,计算了这些化合物在大型溞体内的临界浓度,研究了农药类化合物对大型溞的毒性作用机理。结果表明,基线化合物在大型溞体内的临界浓度log1/CBR值在一个很窄的范围波动,而农药类化合物在大型溞体内的临界浓度log1/CBR值范围广且较高。这说明多数农药类化合物对大型溞为反应性毒性作用模式。其中,除草剂对大型溞的毒性显著低于杀菌剂和杀虫剂对大型溞的毒性。这可能是因为除草剂主要通过干扰植物光合作用、植物激素或植物分子合成发挥毒性效应,从而导致其对大型溞的生理系统难以发生反应性毒性效应。而杀虫剂和杀菌剂主要通过干扰生物神经系统、生殖系统、呼吸作用或大分子合成发挥毒性效应,因此易与大型溞生理系统发生生物化学反应,从而具有较高的毒性效应。本文分别建立了除草剂、杀菌剂和杀虫剂对大型溞的急性毒性QSAR模型。除草剂对大型溞的急性毒性机理较简单,其毒性与化合物疏水性程度和离子化程度有关;而杀菌剂对大型溞的急性毒性主要与化合物的标准生成热和极性表面积有关;杀虫剂对大型溞的急性毒性作用机理较复杂,它们对大型溞的毒性效应与其和生物分子之间的氢键和范德华力有关。     

Biodegradation of N,N-bis(carboxymethyl)-L-glutamate and its utilization as sole source of carbon,nitrogen, and energy by a Rhizobium radiobacter strain in seawater

Biodegradation of N,N-bis(carboxymethyl)-L-glutamate and its utilization by micro-organisms in marine environments were studied in Organization of Economic Development and Cooperation (OECD) screening tests and with pure bacterial cultures. Biodegradation in excess of 60% was achieved in closed bottle tests in less than 60 days, suggesting complete degradation. The bacterial strain isolated from marine sandy sediment and utilizing N,N-bis(carboxymethyl)-L-glutamate as sole source of carbon, nitrogen, and energy was identified as Rhizobium radiobacter. The strain was capable to mineralize N,N-bis(carboxymethyl)-L-glutamate in seawater and in synthetic media containing 0–60 g L^?1 sea salts. Growth and adaptation studies indicated that N-carboxymethyl-L-glutamate and L-glutamate are main metabolites.     

4种甲氧基丙烯酸酯类杀菌剂不同剂型对斑马鱼急性毒性效应

采用半静态法测定了4种甲氧基丙烯酸酯类杀菌剂原药及制剂对斑马鱼(Brachydonio rerio)急性毒性。结果表明,以实测浓度计,250 g·L~(-1)嘧菌酯悬浮剂对斑马鱼的96 h半数致死浓度(LC50)值为0.539 mg·L~(-1),急性毒性为高毒,95%嘧菌酯原药和50%嘧菌酯水分散粒剂对斑马鱼的LC50(96 h)值分别为1.09和1.21 mg·L~(-1),急性毒性均为中毒;98%啶氧菌酯原药和22.5%的啶氧菌酯悬浮剂对斑马鱼的LC50(96 h)值分别为0.0974和0.0972 mg·L~(-1),急性毒性均为剧毒;95%吡唑醚菌酯原药、15%吡唑醚菌酯悬浮剂和250 g·L~(-1)吡唑醚菌酯乳油对斑马鱼的LC50(96 h)值为0.0613、0.0549和0.0487 mg·L~(-1),急性毒性均为剧毒;95%醚菌酯原药和50%醚菌酯水分散粒剂对斑马鱼的LC50(96 h)值分别为0.468和0.702 mg·L~(-1),急性毒性均为高毒。这4种甲氧基丙烯酸酯类杀菌剂对斑马鱼均有较高风险,会对其他水生生物也存在潜在的风险。     

Removal of selenite using ‘waste’ Fe(III)/Cr(III) hydroxide: Adsorption kinetics and isotherms

Removal of selenite [Se (IV)] from aqueous solution on to industrial solid ‘waste’ Fe(III)/Cr(III) hydroxide as adsorbent was investigated in the present article. Maximum adsorption was found to be at pH 4.0. Pretreated Fe(III)/Cr(III) hydroxide was found to be more efficient for the removal of selenite compared to untreated adsorbent. Langmuir and Freundlich isotherms have been studied. The Langmuir adsorption capacity (Q ₀) of the pretreated and untreated adsorbents was found to be 15.63 and 6.04?mg?g^?1, respectively. The adsorption process fit into the second-order kinetics. Thermodynamic parameters show that the adsorption process is spontaneous and endothermic in the temperature range 32 to 60°C. Coexisting anions vanadate and phosphate significantly affect the adsorption of selenite for both the pretreated and untreated adsorbents. Molybdate, thiocyanate, sulphate, nitrate and chloride do not significantly affect the removal of selenite for pretreated adsorbent.