Flocculation performance of epichlorohydrin-dimethylamine polyamine in treating dyeing wastewater

Epichlorohydrin-dimethylamine polymers with different intrinsic viscosity (η) and cationicity (τ) were synthesized. The flocculation performance and mechanism of these polymers in the removal of the reactive and disperse dyes from synthetic wastewater was investigated in terms of flocculation dynamics and color removal efficiency. The polymer flocculation efficiency was compared with that of polyaluminum chloride (PAC) and a composite flocculant based on polyaluminum chloride-epichlorohydrin-dimethylamine polyamine. The results showed that epichlorohydrin-dimethylamine polymer was effective over a pH range of 2–10 for the reactive and disperse dye removal (Reactive Brilliant Red and Disperse Yellow dyes). Epichlorohydrin-dimethylamine polymer with the highest η and τ gave the best reactive dye removal efficiency, and its adsorption-bridging and electric neutralization ability played important roles in the flocculation process. The higher the η viscosity of the epichlorohydrin-dimethylamine polymer, the better the flocculation performance of epichlorohydrin-dimethylamine polyamine, and stronger adsorption-bridging ability was obtained for removing the disperse dye from dyeing wastewaters. Epichlorohydrin-dimethylamine polymer achieved better decolorization performance when used together with PAC.     

Thermochemical esterifying citric acid onto lignocellulose for enhancing methylene blue sorption capacity of rice straw

In this paper, rice straw was esterified thermochemically with citric acid (CA) to produce potentially biodegradable cationic sorbent. The modified rice straw (MRS) and crude rice straw (CRS) were evaluated for their methylene blue (MB) removal capacity from aqueous solution. The effects of various experimental parameters (e.g., initial pH, sorbent dose, dye concentration, ion strength, and contact time) were examined. The ratio of MB sorbed on CRS increased as the initial pH was increased from pH 2 to 10. For MRS, the MB removal ratio came up to the maximum value beyond pH 3. The 1.5g/l or up of MRS could almost completely remove the dye from 250mg/l of MB solution. The ratio of MB sorbed kept above 98% over a range from 50 to 450mg/l of MB concentration when 2.0g/l of MRS was used. Increase in ion strength of solution induced decline of MB sorption. The isothermal data fitted the Langmuir model. The sorption processes followed the pseudo-first-order rate kinetics. The intraparticle diffusion rate constant (k(id)) was greatly increased due to modification.     

CMF微生物菌剂修复河流污水的动力学分析

本文利用甲壳素包裹的复合微生物菌剂CMF，对河流污水进行生物治理，CX3Dcr去除率达87．75％，BOD5去除率为86％以上。建立了河水中有机物降解的动力学模型，并通过工程实验数据，推算出了污水中有机物降解的动力学参数。     

Investigation on solar photocatalytic degradation of various dyes in the presence of Er3+:YAlO3/ZnO–TiO2 composite

In this work, Er³⁺:YAlO₃/ZnO–TiO₂ and ZnO–TiO₂ composites were prepared by the ultrasonic dispersion and liquid boiling method. In succession, they were then characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Acid red B as a model dye compound was degraded under solar light irradiation to evaluate the photocatalytic activities of the Er³⁺:YAlO₃/ZnO–TiO₂ and ZnO–TiO₂ composites. We found that the photocatalytic activity of ZnO–TiO₂ composite can be enhanced by adding an appropriate amount of Er³⁺:YAlO₃. We reviewed influencing factors, such as Er³⁺:YAlO₃ content, heat-treated temperature and heat-treated time on the photocatalytic activity of the Er³⁺:YAlO₃/ZnO–TiO₂ composites. In addition, the effects of solar light irradiation time, dye initial concentration, Er³⁺:YAlO₃/ZnO–TiO₂ amount and solution acidity on the photocatalytic degradation of acid red B dye in aqueous solution were investigated in detail. Simultaneously, the degradation and comparison of other dyes such as methyl orange (MO), rhodamine B (RM-B), azo fuchsine (AF), congo red (CG-R) and methyl blue (MB) were also reviewed. In addition, we attempted to explore both the principle of possible excitation of Er³⁺:YAlO₃/ZnO–TiO₂ under solar light irradiation and the mechanism of photocatalytic degradation.     

染料废水脱色的物理化学处理技术

染料废水目前主要的脱色方法有吸附、混凝、氧化还原和生化法.活性炭吸附适用于低浓度的染料废水处理.聚硅硫酸铁混凝效果与Fe/SiO4摩尔比和pH值相关.氢氧化镁可有效去除印染废水中的直接红染料.有机絮凝剂往往需要和其它药剂复配.氧化法脱色率大,但成本高昂,且受染料废水的组成、氧化性及pH值影响.还原法药剂价格低廉,但还原降解产物具有毒性,必须经过二次处理.生物法成本较低,又受制于染料的生物降解性.因此发展多种手段联合应用已是当前染料废水处理的研究方向.     

咪唑银配位聚合物吸附偶氮染料研究

以咪唑银配位聚合物{Ag（im）}n作吸附剂,对偶氮染料刚果红和甲基橙的吸附进行了研究,结果表明：刚果红的最佳吸附条件是吸附剂加入量为31．5mg,温度为30℃,pH值为3,吸附时间为70min,最高染料脱除率为90。7％;甲基橙的最佳吸附条件是吸附剂加入量为36．7mg,温度为30℃,pH值为2,吸附时间为50min,最高染料脱除率为58．3％。     

间接电化学降解亚甲基蓝废水的可行性研究

研究以ClO^-／Cl^-作媒介，间接电化学降解亚甲基蓝模拟废水的可行性。结果表明，亚甲基蓝的电化学降解与电极材料、电流密度以及添加剂种类等因素有关。以石墨为阳极，不锈钢为阴极，在无隔膜的烧杯中放置50ml浓度为1000mg/L的亚甲基蓝模拟废水，在室温25℃，pH6．0－8．0，槽电压10V，电流密度30．0mA/cm^2，Cl^-加入量2g/L的条件下，电解60min后，亚甲基蓝溶液的平均消色率达到98．0％，CODcr降解率为97．0％，BOD5降解率为99．0％；用浸涂过MnO2薄膜的石墨棒作阳极可显著加快其消解速率，而用浸涂过CeO2薄膜的石墨棒作阳极对其消解速率无明显的影响。并初步讨论了其降解机理。     

Environmental issues for polymer matrix composites and structural adhesives

The U.S. Department of Defense (DoD) has been utilizing polymer matrix composite (PMC) and structural adhesive materials in military equipment for over 20 years. However, the volume of PMCs in fielded systems has remained relatively low. Currently, however, the DoD has established strategic goals that will necessitate the use of lightweight composites in order to meet performance requirements. Therefore, the volume of composites used in DoD systems is expected to see an unprecedented 100-fold increase over the next 30 years. As production volumes increase, the need to address environmental impact increases. The major contributions to environmental degradation from composites are generation of hazardous air pollutants (HAPs) and generation of hazardous (HW) and solid wastes. HAPs result primarily during the curing of the composite. HWs arise from expiration of stockpiled resin materials and from soiled support media used during manufacturing and clean up. Due to the wide range of applications and materials systems, as well as manufacturing and repair requirements, a family of environmentally benign solutions is needed to reduce and eliminate environmental impacts from PMC manufacturing. Solutions are proposed involving use of new technologies and materials to reduce pollutants from composite manufacturing. The technologies proposed include alternative curing of thermoset composites using electron beam (E-beam) irradiation and materials substitution employing thermoplastics processed using electromagnetic irradiation.     

Photocatalytic degradation of organic wastes by electrochemically assisted TiO2 photocatalytic system

Photocatalytic degradation of organic wastes with nanosized titanium dioxide particles has been studied for a long time in order to offer an appropriate method for wastewater treatment, but its practical application is greatly limited by the slow process. In this work, an electrochemically assisted TiO2 photocatalytic system was set-up by combining a TiO2 photocatalytic cell with a three-electrode potentiostatic unit. The composite system revealed high photocatalytic activity towards organic wastes mineralization. After continuous treatment for 0.5 h, the maximum absorption of rhodamine 6G (R-6G) was reduced by more than 90%; chemical oxygen demand (COD) and biochemical oxygen demand (BOD5) of textile dye wastewater (TDW) were decreased by 93.9 and 88.7%, respectively. The biodegradability of TDW was also improved because the COD/BOD5 ratio decreased from 2.1 to 1.2. All these results indicated that the composite system could be used for effective organic wastes mineralization or as a feasible detoxification and color removal pretreatment stage for biological post treatment.     

Intensification of degradation of aqueous solutions of rhodamine B using sonochemical reactors at operating capacity of 7 L

In the present work, degradation of rhodamine B, a typical dye effluent commonly observed in chemical processing wastewaters has been investigated using a sonochemical reactor with capacity of 7 L. The reactor consists of an ultrasonic bath equipped with a single large transducer having longitudinal vibrations with operating frequency of 25 kHz and rated power output of 1 kW. The effect of operational conditions such as the rhodamine B initial concentration, operating pH and use of additives such as H(2)O(2), CCl(4) and TiO(2) has been investigated initially. A mathematical model has also been fitted to estimate the rate constant for rhodamine B removal under different operating conditions. Intensification studies have been carried by combining sonochemical oxidation with photocatalytic oxidation under optimized conditions. In all the investigated systems, complete removal of rhodamine B (10 ppm initial concentration) was obtained using a combination of sonochemical reactor and CCl(4). Sonocatalysis (in the presence of TiO(2)) of rhodamine B showed 92% degradation, while sonophotocatalysis gave degradation of 93%. TOC analysis at various optimum conditions was also performed to quantify the extent of mineralization and it was observed that the extent of mineralization is always lower than the extent of removal of parent compound.     

DIQUAT DISTRIBUTION IN WATER AFTER APPLICATION TO SUBMERSED WEEDS1

ABSTRACT: Diquat herbicide and rhodamine WT dye were applied in a lake to three 1.6 ha plots either with a polymer, which reportedly aids in sinking and confinement of aquatic herbicides, or without a polymer. Diquat and dye concentrations were measured at three different depths in the water column within the plots during the first three hours after application to determine vertical distribution of diquat and dye, and in composite samples at fixed distances from the plot up to 168 hours after application to determine movement out of the treated plots. Diquat and dye were homogeneous in the water column when no polymer was used, but were concentrated near the surface when polymer was used. This distribution may have resulted from temperature stratification. Polymer did not affect movement of diquat or dye out of the plots. The half-lives of diquat within the plots were 25 (SE=6.2) hr, 39 (SE=4.3) hr, and 25 (SE=2.0) hr. Forty-six percent of samples collected at the edges of the plots did not contain detectable diquat residues and only 66 percent of those samples with detectable diquat contained greater than the potable water tolerance (10 ppb). Diquat was not found in any samples 168 hours after application 61 m or farther from the edge of the plots. Dye and diquat concentrations were weakly correlated within and outside the plots. Dye half-lives were consistently higher than diquat, which suggests that the herbicide was removed from the water by plants and sediments more rapidly than dye.     

Degradation of polycyclic aromatic hydrocarbons by combined chemical pre-oxidation and bioremediation in creosote contaminated soil

The ability of pre-oxidation to overcome polycyclic aromatic hydrocarbons (PAH) recalcitrance to biodegradation was investigated in creosote contaminated soil. Sand and peat artificially spiked with creosote (quality WEI C) were used as model systems. Ozonation and Fenton-like treatment were proved to be feasible technologies for PAH degradation in soil. The efficiency of ozonation was strongly dependent on the water content of treated soil samples. The removal of PAH by Fenton-like treatment depended on the applied H2O2/soil weight ratio and ferrous ions addition. It was determined that the application of chemical oxidation in sand resulted in a higher PAH removal and required lower oxidant (ozone, hydrogen peroxide) doses. The enhancement of PAH biodegradability by different pre-treatment technologies also depended on the soil matrix. It was ascertained that combined chemical and biological treatment was more efficient in PAH elimination in creosote contaminated soil than either one alone. Thus, the combination of Fenton-like and the subsequent biological treatment resulted in the highest removal of PAH in creosote contaminated sand, and biodegradation with pre-ozonation was found to be the most effective technology for PAH elimination in peat.     

Visible light driven instantaneous photocatalytic degradation of aniline blue (AB) and methyl violet (MV) by strontium ferrite nanoparticles

Toxic organic dyes released into aquatic sources as a result of industrial activities pose a significant threat to the environment. The removal of such dyes from water sources is a challenging task in the context of environmental emergencies. In this present effort, the strontium ferrite nanoparticles were synthesized by coprecipitation followed by a calcination method and is applied for photocatalytic degradation of such organic dyes. The ferrite nanoparticles were characterized by FTIR, XRD, VSM, SEM-EDX, TEM, and HR-TEM studies. In the existence of H₂O₂ under visible light, the catalyst performs efficient degradation of aniline blue (AB) and methyl violet (MV) dyes in a remarkably short interval of time. The superparamagnetic performance of the catalyst was confirmed by VSM, and thus it can be easily recovered from the degraded dye by applying an external magnet. The Fenton mechanism justifies the elevated rate of photo degradation, which generates hydroxyl and perhydroxyl radicals in the progress of the reaction.     

A comparative study on the properties,mechanisms and process designs for the adsorption of non-ionic or anionic dyes onto cationic-polymer/bentonite

The adsorption properties and mechanisms of a cationic-polymer/bentonite complex (EPI-DMA/bentonite), prepared from polyepicholorohydrin-dimethylamine and bentonite, for non-ionic dyes (Disperse Blue SBL and Vat Scarlet R) and anionic dyes (Reactive Violet K-3R and Acid Dark Blue 2G) were investigated in this study. The solution pH, presence of salt and surfactant can significantly affect the dye removal efficiency. The equilibrium data were analyzed using the Langmuir and Freundlich models. The Langmuir model is the most suitable to describe non-ionic dye adsorption, but for anionic dyes the Freundlich model is best. The kinetic data for the adsorption of different dyes were analyzed using pseudo first- and second-order equations, and the experimental data conformed to the pseudo second-order kinetic model better. The possibility of intraparticle diffusion was also examined by using the intraparticle diffusion equation. The single-stage batch adsorber design for the adsorption of both types of dyes onto EPI-DMA/bentonite was studied based on the Langmuir isotherm model for non-ionic dyes and the Freundlich isotherm model for anionic dyes. The results showed that the required amount of EPI-DMA/bentonite for 95% dye removal in 5 L dye solution with a concentration of 50 mg/L is 378.0 g for DB SBL, 126.5 g for VS R, 9.7 g for RV K-3R and 15.5 g for ADB 2G.     

KH-550对废PCBs非金属粉/PP复合材料性能的影响

对回收的纸基印刷线路板非金属粉表面硅烷化处理,研究了硅烷偶联剂KH-550最佳用量和对非金属粉/PP复合材料的力学性能以及耐热性能的影响,并通过扫描电镜对复合材料的界面进行研究。结果表明,硅烷偶联剂的最佳用量为非金属粉质量的1.5%;经偶联剂表面处理非金属粉与PP基体树脂能够形成有效的界面粘结,与未处理非金属粉的PP复合体系相比,其力学性能和热性能得到明显提高。硅烷偶联剂KH-550在一定程度上能够改善复合材料的性能。     

Response surface optimization of acid red 119 dye from simulated wastewater using Al based waterworks sludge and polyaluminium chloride as coagulant

In this research, the performance of Polyaluminium Chloride (PAC) and Polyaluminium Chloride sludge (PACS) as coagulants for acid red 119 (AR119) dye removal from aqueous solutions were compared. The sample of PACS was collected from "Baba Sheikh Ali" water treatment plant (Isfahan, Iran) where PAC is used as a coagulant in the coagulation/flocculation process. A response surface methodology was applied to evaluate the simple and combined effects of the operating variables including initial pH, coagulant dosage and initial dye concentration and to optimize the operating conditions of the treatment process. Results reveal that the optimal conditions for dye removal were initial pH 3.42, coagulant dosage of 4.55 g dried PACS/L and initial dye concentration of 140 mg/L for PACS, while the optimal initial pH, coagulant dosage and initial dye concentration for PAC were 3.8, 57 mg/L and 140 mg/L, respectively. Under these optimal values of process parameters, the dye removal efficiency of 94.1% and 95.25% was observed for PACS and PAC, respectively. Although lower amount of PAC in comparison with PACS was needed for specific dye removal, the reuse of PACS as a low-cost material can offer some advantages such as high efficiency for AR119 dye removal and economic savings on overall water and wastewater treatment plant operation costs.     

Recycle of bio-waste banana and sisal fiber filled harmlessness epoxy hybrid composite for automotive roof application

Insists of polymer matrix composite is prepared by using natural fiber facilitates high tensile, flexural, and impact toughness properties. The natural fiber utilization in the polymer matrix can overcome the synthetic fiber demerits of poor compatibility, high moisture absorption, and high cost. The present research investigates developing a low-cost, environmentally eco-friendly epoxy hybrid composite using different volume percentages of chopped natural waste banana (0Vol%, 5Vol%, 10Vol%, and 15Vol%) and sisal fiber (0Vol%, 15Vol%, 10Vol%, and 5Vol%) through hand mould hot compression technique. The presence of natural waste banana and sisal fiber on tensile strength, flexural strength, and thermal adsorption properties of the epoxy hybrid composite are evaluated by ASTM test standards. The ASTM standard measured test results of epoxy hybrid composite with and without natural waste banana and sisal fiber were compared and sample three was identified by good tensile strength, flexural strength, and better thermal adsorption properties compared to all others. The sample three epoxy hybrid sample is recommended for automotive roof application.     

Removal of an anionic dye (Acid Blue 92) by coagulation–flocculation using chitosan

Chitosan (a biopolymer) is an aminopolysaccharide that can be used for the treatment of colored solutions by coagulation–flocculation (as an alternative to more conventional processes such as sorption). Acid Blue 92 (a sulfonic dye) was selected as a model dye for verifying chitosan's ability to treat textile wastewater. A preliminary experiment demonstrated that chitosan was more efficient at color removal in tap water than in demineralized water, and that a substantially lower concentration of chitosan could be used with tap water. Dye removal reached up to 99% under optimum concentration; i.e., in terms of the acidic solutions and the stoichiometric ratio between the amine groups of the biopolymer and the sulfonic groups in the dye. The flocs were recovered and the dye was efficiently removed using alkaline solutions (0.001–1 M NaOH solutions) and the biopolymer, re-dissolved in acetic acid solution, was reused in a further treatment cycle.     

Mechanisms and chemistry of dye adsorption on manganese oxides-modified diatomite

The investigations into structural changes which occur during adsorbent modification and the adsorption mechanisms are essential for an effective design of adsorption systems. Manganese oxides were impregnated onto diatomite to form the type known as δ-birnessite. Initial investigations established the effectiveness of manganese oxides-modified diatomite (MOMD) to remove basic and reactive dyes from aqueous solution. The adsorption capacity of MOMD for methylene blue (MB), hydrolysed reactive black (RB) and hydrolysed reactive yellow (RY) was 320, 419, and 204 mg/g, respectively. Various analytical techniques were used to characterise the structure and the mechanisms of the dye adsorption process onto MOMD such as Fourier transform infrared (FTIR), X-ray diffraction (XRD) and atomic absorption spectrometry (A.A.). A small shift to higher values of the d-spacing of dye/MOMD was observed indicating that a small amount of the dye molecules were intercalated in the MOMD structure and other molecules were adsorbed on the external surface of MOMD. Two mechanisms of dye adsorption onto MOMD were proposed; intercalation of the dye in the octahedral layers and adsorption of the dye on the MOMD external surface. Moreover, the results demonstrated that the MOMD structure was changed upon insertion of MB and RY with an obvious decrease in the intensity of the second main peak of the MOMD X-ray pattern.     

Mechanical performance of woodfibre–waste plastic composite materials

Plastic products used for packaging are often discarded after a single use resulting in an inexhaustible supply of waste polymeric materials. The stiffness and strength of polymeric materials have been known to improve with the addition of lignocellulosic fibres available in abundance in nature. Hence, composite materials containing natural fibres and waste plastics would result in the reduction of solid wastes and the use of cheap, renewable resources. Composite specimens, consisting of waste plastics obtained from a Kerbside collection (high density polyethylene (HDPE) waste, Janitorial waste, Kerbside waste I and Kerbside waste II) and Pinus radiata woodfibres (medium density fibres (MDF)), have been produced through melt blending and injection moulding. The effects of fibre content, matrix type and interfacial bonding on the tensile and flexural properties of these composite materials have been determined through extensive testing at various conditions. The mechanical properties of these composites at room temperature and humidity depend on the amount of woodfibres, the mechanical properties of the waste plastics used and the presence of a suitable coupling agent. The tensile strengths of MDF/waste plastic composites do not generally change with fibre content except for 40% MDF/HDPE waste and 40% MDF/Kerbside waste II (plus 1% Epolene™) composites, where the tensile strengths increase by about 25% compared to those of the corresponding waste plastics. Flexural strengths of MDF/waste plastic composites increase with the addition of medium density fibres with the exception of MDF/Kerbside waste I composites. The tensile and flexural moduli of MDF/waste plastic composites mostly increase with increasing fibre content.