A breakthrough column study for removal of malachite green using coco-peat

Abstract

A continuous adsorption study in a fixed bed column using coco-peat (CP) as an adsorbent was carried out for the removal of toxic malachite green (MG) from contaminated water. Fixed bed column studies were carried out to check field application viability. Various parameters like particle size, pH, concentration, dose and interference were exercised to optimize dye removal. Data obtained from breakthrough column studies were evaluated using Thomas and BDST model. Thomas rate constants K_t (0.22?ml min^?1 mg^?1) and adsorption capacity q_o (181.04?mg g^?1) were estimated and found to favor efficiency of CP. Thomas model was tested with several parameters like flow rate, concentration, and bed depth. Upon increase in input dye concentration, flow rate and bed height, adsorption coefficients increased. According to BDST model, maximum dye uptake of 468.26?mg/l was obtained with an input dye concentration of 5?mg/l. HYBRID and MPSD error functions were tested and found that Thomas model fits best. Dilute hydrochloric acid was found best for desorption. Real wastewater from textile industry was analyzed and confirmed the prospect of large-scale industrial application. In conclusion, coco-peat can be used as a promising bio-sorbent in column bed for scavenging of MG from contaminated water.     

Lipid metabolism of monosodium glutamate obese rats after partial removal of adipose tissue

We analyzed the effects of partial fat pad removal on retroperitoneal and epididymal fat depots and carcass metabolism of control (C) and MSG-obese (M) rats. Three-month-old C and M male Wistar rats were submitted to either partial surgical excision of epididymal and retroperitoneal fat tissue (lipectomy, L) or sham surgery (S) and studied after 7 or 30 days. Retroperitoneal and epididymal tissue re-growth after lipectomy was not observed, as indicated by the low pads weight of the L groups. The lipolysis rate was stimulated in LC7 and LM7, probably due to surgical stress and low insulin levels. In LM7, but not in LC7, in vivo lipogenesis rate increased in retroperitoneal and epididymal fat tissue, as did the diet-derived lipid accumulation in epididymal fat tissue. Although these local increases were no longer present in LM30, this group showed a large increase in the percentage of small area adipocytes in both pads as well as increased carcass lipogenesis rate. The present data showed that the partial removal of fat depots affected the metabolism of control and MSG-obese rats differently. In the obese animals only, it stimulated both local and carcass lipogenesis rate as well as adipocyte differentiation, i.e. responses likely to favor excised tissue re-growth and/or compensatory growth of non-excised depots.     

分布式模型在流域蒸散模拟中的应用与验证

根据四川杂谷脑河流域上游地区1989～2000年气象站常规观测数据,应用分布式模型方法,考虑流域的空间异质性及时空变异性,选择离散单元格尺度为500 m,时间步长为1 d,采用Penman-Monteith公式的改进形式,估算流域多年平均潜在蒸散量的时空分布;结合流域下垫面特点,估算逐日实际蒸散量的时空分布;并将模型模拟的多年平均值与研究区同期水量平衡法计算结果相比,相对误差为+3.47%且时空分布合理.为流域分布式降雨-径流模型提供了可靠的实际蒸散量模拟方法.     

Simultaneous determination of malachite green and its metabolite leucomalachite green in eel plasma using post-column oxidation

A rapid HPLC method with solid-phase extraction (SPE) clean-up for malachite green (MG) and leucomalachite green (LMG) in eel plasma was developed. MG and LMG were extracted with a buffered methanolic solution. The extract was subjected to aromatic sulphonic acid SPE. MG and LMG were eluted from the SPE column with methanol after a treatment with ammonia gas. The reconstituted eluate was analyzed on a Chromspher B column with acetonitrile-ion-pair buffer (ph 4.0) (6:4, v/v) as the mobile phase and detection at 610 nm after post column oxidation with PbO₂. The average recoveries for MG and LMG over the linear range of applicability (20–2500 ng/ml) were 82±1% and 83±1%, respectively. The limits of quantification were 5.0 μg/1 for MG and 0.9 μ/1 for LMG.     

Observations on malachite green in relation to its application to fish diseases

Summary Experiments were carried out to evaluate several properties determining the mutual influence of the system: fish-bath-malachite green-pathogen.The toxicity of malachite green solutions in concentrations varying between 1 : 80,000 and 1 : 2,560,000 was tested on immature sand whiting. As regards the toxicity of 1 : 80,000 solutions, for practical purposes no distinction between fish of different size, between equal concentrations of chloride and oxalate salts of the dye, or between fresh and decolourized solutions appears necessary.The survival time increased appreciably with decreasing temperature for the range 13.5–28.0°C.The dye solutions always showed significant decolourization when the pH was higher than 5.Several body tissues of the fish, notably the central nervous system and the lateral red muscles, were stained by fresh as well as decolourized malachite green solutions.The dye proved bacteriostatic but not bactericidal, to pseudomonad and coccus cultures when 1 : 80,000 solutions were used. Once decolourized, the dye became a less effective bacteriostatic.The addition of the dye, or formaldehyde, to the bath induced hyperventilation in the fish.A triple dye mixture, consisting of malachite green, brilliant green and crystal violet, was found to be a valuable therapeutic agent.

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Zusammenfassung Einige Versuche werden durchgeführt zur Erklärung verschiedener Eigenschaften, die die gegenseitige Einwirkung in dem System: Fisch - Bad - Malachitgrün - Pathogen bestimmen.Die Toxizität von Malachitgrün-Lösungen in Konzentrationen welche variierten zwischen 1 : 80,000 and 1 : 2,560,000 wurde geprüft an jungen Sand Whiting. Was die Toxizität der 1 : 80,000 Lösungen betrifft, scheint, für praktischen Zwecke, kein Unterschied zu sein zwischen Fischen verschiedener Länge, zwischen gleichen Konzentrationen von Chlorid und Oxalat-Salzen des Farbstoffes, oder zwischen frischen und entfärbten Lösungen. Die Überlebungszeit nahm merklich zu, wenn die Temperatur erniedrigt war, im Gebiet von 13.5°–28.0°C. Die Farbstoff-Lösungen zeigten erhebliche Entfärbung, wenn der pH - Wert grösser war als 5. Verschiedene Körpergewebe des Fisches, insbesondere das Zentralnervensystem und die lateralen roten Muskeln, werden von frischen sowie entfärbten Lösungen grün gefärbt. Der Farbstoff zeigte in 1 : 80,000 Lösungen bakteriostatische, aber keine bakterizide Wirkung, wenn geprüft an Pseudomonas und Kokkus Kulturen. Zusatz des Farbstoffes, oder Formaldehyde, zum Bade veranlasste in dem Fisch Hyperventilation. Ein Tripelfarbstoff-Gemisch, das bestand aus Malachitgrün, Brilliantgrün und Kristallviolett, zeigte sich ein wertvolles Therapeutikum.

     

A malachite green procedure for orthophosphate determination and its use in alkaline phosphatase-based enzyme immunoassay

An improved procedure for phosphate determination based on a highly colored complex of phosphomolybdate and malachite green is described. All necessary reagents are combined in one concentrated solution, making the assay sensitive and convenient. The procedure is based on the finding that the dye is easily soluble and stable in the presence of 6 N acid. The addition of Tween 20 is required to stabilize the dye-phosphomolybdate complex at phosphate concentrations above 10 microM. The time of color development at 25 degrees C is about 3 min. The procedure was adopted to measure alkaline phosphate activity in heterogeneous enzyme immunoassay with rho-nitrophenyl phosphate and pyrophosphate as substrates. In both cases, a 4-fold increase in sensitivity in terms of absorbance readings was obtained compared to the standard method based on rho-nitrophenol measurement. In visual analysis, the gain in sensitivity was as high as 20-fold, due to contrast color change (yellow to greenish blue).     

Potentiation of vasopressin analgesia in rats treated neonatally with monosodium glutamate

The analgesic response elicited by central administration of arginine vasopressin (AVP) appears to be dependent upon the integrity of the hypothalamic paraventricular nucleus (PVN), since lesions placed in the PVN eliminate AVP analgesia. A projection to the zona externa of the median eminence constitutes one of the VP-containing efferents of the PVN. Neonatal treatment with monosodium glutamate (MSG) destroys perikarya of the arcuate nucleus and median eminence. The present study examined whether AVP analgesia was affected in the MSG-treated rat and whether these alterations were accompanied by specific changes in VP immunoreactivity in the zona externa of the median eminence. Female rats, neonatally treated with either MSG or a saline control, were tested as adults on the tail-flick test following intracerebroventricular injections of 0, 75, 150 and 500 ng doses of AVP. After testing, selected animals were prepared for AVP and oxytocin immunocytochemistry of the median eminence. Significant potentiations in the magnitude of AVP analgesia were observed in MSG-treated rats. AVP and oxytocin immunoreactivity in the zona interna and oxytocin immunoreactivity in the zona externa of the median eminence were similar in MSG-treated and control rats. In contrast, AVP immunoreactivity in the zona externa of the median eminence was markedly reduced in the MSG-treated rat. These data suggest that VP analgesia may normally be inhibited by those medial-basal hypothalamic neurons affected by neonatal MSG treatment.     

Alkali process for enhancing susceptibility of autohydrolysed beech sawdust to enzymatic hydrolysis

Autohydrolysed beech sawdust has been treated with aqueous NaOH solution in a three-stage process to increase the susceptibility of cellulose to cellulolytic enzymes. This process consisted of neutralization of autohydrolysed wood, extraction of lignin and alkali treatment of residual solids with 1.5% aqueous NaOH solution at 135°C for 1 h. The cellulose in the residues was then hydrolysed with Novo (SP 122) and Fusarium sp. 27 cellulases [see 1,4-(1,3;1,4)-β-d-glucan 4-glucanohydrolase, EC 3.2.1.4]. The susceptibility of cellulose to cellulases was increased 2.3 to 2.7-fold.     

Reduction of malachite green to leucomalachite green by intestinal bacteria.

Intestinal microfloras from human, rat, mouse, and monkey fecal samples and 14 pure cultures of anaerobic bacteria representative of those found in the human gastrointestinal tract metabolized the triphenylmethane dye malachite green to leucomalachite green. The reduction of malachite green to the leuco derivative suggests that intestinal microflora could play an important role in the metabolic activation of the triphenylmethane dye to a potential carcinogen.     

A malachite green colorimetric assay for protein phosphatase activity.

A simple and sensitive colorimetric assay for protein phosphatase activity based on the determination of released Pi by an improved malachite green procedure (A. A. Baykov, O. A. Evtushenko, and S.M. Avaeva, 1988, Anal. Biochem. 171, 266-270) is described. Proteins must be removed or stabilized prior to Pi determination with 0.25 N sulfuric acid or 3% (w/w) perchloric acid. Alternatively, to avoid possible acid hydrolysis of phosphate groups from organic compounds during deproteinization, the protein present in the phosphatase assay mixture can be stabilized with sodium dodecyl sulfate. In this case, the excess detergent is subsequently removed by precipitation with KCl because it colors with the malachite green reagent. The above procedure was applied to the determination of phosphorylase phosphatase activity in bovine brain extracts and the results are comparable to those obtained with the radioisotopic phosphatase assay.     

Biodegradation of malachite green by Ochrobactrum sp.

This study presents the biodegradation of malachite green (MG), a triphenylmethane dye, using a novel microorganism isolated from textile effluent contaminated environment. The organism responsible for degradation was identified as Ochrobactrum sp JN214485 by 16S rRNA analysis. The effect of operating parameters such as temperature, pH, immobilized bead loading, and initial dye concentration on % degradation was studied, and their optimal values were found to be 30 °C, 6, 20 g/L and 100 mg/L, respectively. The analysis showed that the extracellular enzymes were responsible for the degradation. The biodegradation of MG was confirmed by UV–visible spectroscopic and FTIR analysis. The phytotoxicity test concluded that the degradation products were less toxic compared to MG. The kinetics of biodegradation was studied and the activation energy was found to be 10.65 kcal/mol.     

Inorganic phosphate assay with malachite green: An improvement and evaluation

An improvement over existing procedures for the determination of nanomole quantities of inorganic phosphate (P_i) is described. The protocol is simplified, and the effective concentration range of P_i in which the assay may be used is increased to 60 nmol/ml. Many of the substances commonly used in association with P_i assays (i.e. phosphohydrolase studies) are shown not to interface with the measurement of P_i by this method. The effects of detergents and protein on the assay also were investigated, and methods for avoiding interferences by them are described.     

Treatment with polyamines can prevent monosodium glutamate neurotoxicity in the rat retina

It has been previously shown that treatment of newborn rats with the polyamines putrescine, spermidine and spermine can rescue sympathetic neurons from naturally occurring cell death and from induced death after axotomy or immunosympathectomy. The present study demonstrates that polyamine treatment can also prevent the neurodegenerative effects in the retina and the loss of body weight caused by monosodium glutamate. The findings indicate that polyamine treatment may have a rather general beneficial effect on neuron survival.     

Synthesize of β‐cyclodextrin functionalized dendritic fibrous nanosilica and its application for the removal of organic dye (malachite green)

Dye removal from industrial waste water has become an important issue. The highvisibility, undesirability and recalcitrance are the significant environmental problemfor the dyes. In the present work,β‐cyclodextrin functionalized KCC‐1 (KCC‐1‐NH‐β‐CD)was synthesized and utilized to the removal of hazardous malachite green. In order to study the morphology of the synthesized nano adsorbent, Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) were obtained from the surface of the sample. Additionally, the functionalization of KCC‐1 with β‐cyclodextrin was confirmed with Furrier Transform Infrared spectroscopy (FTIR). The textural property of KCC‐1 was verified using nitrogen adsorption/ desorption analysis (BET equation). UV‐Vis spectroscopy utilized for the investigation of malachite green by KCC‐1‐NH‐β‐CD. Specific surface area of the adsorbent was calculated to be 140 m²/g and it can be stated that the synthesized nano adsorbent has high removal efficiency. It should be noted that the adsorption capacity of the employed nano adsorbent was more than 95%, which could be attributed to high porosity of β‐cyclodextrin functionalized KCC‐1.     

Determination of residues of malachite green in aquatic animals

Residues of malachite green (MG) were extracted from homogenized animal tissues with a mixture of McIlvaine buffer (pH 3.0)-acetonitrile, and purified over an aromatic sulfonic acid solid-phase extraction column followed by HPLC or LC-ESI-MS-MS analysis. Ascorbic acid and N,N,N',N'-tetramethyl-1,4-phenylenediamine dihydrochloride were added to reduce de-methylation of the dye. Responses were recorded at 620 nm (HPLC) or by multiple-reaction-monitoring (LC-MS-MS) after post-column oxidation using PbO(2). MG and its primary metabolite leuco-malachite green (LMG) were successfully determined at 2.5-2000 microg/kg in catfish, eel, rainbow trout, salmon, tropical prawns and turbot, with a limit of detection at 1 microg/kg (HPLC) and 0.2 microg/kg (LC-MS-MS) for both MG and LMG. Recoveries for LMG were between 86+/-15% (prawn) and 105+/-14% (eel). Freeze-thawing cycles, and storage at 4 degrees C and -20 degrees C affected the recovery of both MG and LMG. Analyses of eel, trout and (processed) salmon field samples collected at local retailers, fish-market and -shops demonstrated trace levels of MG-residues.