In this study, waste corrugated paper was used as carbon precursor with KOH-NaOH mixture (mole ratio was 51:49 and the melting point is 170 °C) as activator to prepare porous carbon at different reaction temperature and different mass ratio of KOH-NaOH mixture/waste corrugate paper fiber. The micro-morphology, pore structure information and composition of porous carbon were analyzed, and the formation mechanism of pores was investigated. The effect of activator amount and pyrolysis temperature on the morphology and structure of porous carbon were studied. The adsorption capacity of porous carbon was evaluated with the methylene blue as model pollutant. The effect of adsorbent amount, adsorption time and temperature on the adsorption performance of the porous carbon were analyzed. The maximum specific surface area is 1493.30 m2 ·g−1 and the maximum adsorption capacity of methylene blue is 518 mg·g−1. This study provides a new idea for efficient conversion and utilization of waste paper.
Core–shell ZIFs wrapped CuO hybrid materials (CuO@ZIF-67(Co)) were designed, synthesized, characterized, and employed as peroxymonosulfate (PMS) activators to degrade methylene blue (MB). It demonstrated outstanding catalytic activity on account of the unique structure and the synergistic effect between CuO cores and ZIF-67(Co) shells, resulting in complete degradation of MB (10 mg/L) in 1 min. Reactive oxygen species (ROSs) research showed that both SO4 − and OH were responsible for the removal of MB. The synergistic activation mechanisms in the CuO@ZIF-67(Co)/PMS system were investigated, which mainly involved the effective electron transfer of CuO and ZIF-67(Co) for accelerating the cycle of CuII/ CuI and CoIII/ CoII. This study broadens the application of MOF-derived materials for wastewater treatment.
Background and Purpose: Antimicrobial photodynamic therapy using Methylene blue (MB-PDT) has been proposed as an adjunctive to scaling and root planing (SRP) to provide preferable results for the treatment of periodontitis. The multi-factor mechanism of aPDT action correlates with various influencing components such as the photosensitizer and the light delivery system. The paper aims to review the recorded parameters of MB-PDT from clinical trials of periodontitis which may serve to improve the treatment of periodontal diseases. Materials and Methods: PubMed search engine was used to identify human clinical trials of PDT in dentistry. After applying specific keywords, additional filters, exclusion criteria, the initial number of 17378 was reduced to 12. Results: More than half of the articles of SRP + MB-PDT presented better results [pocket depth (PD) reduction, clinical attachment level (CAL) gain, etc.] compared to SRP alone in the treatment of periodontitis. Conclusions: While more clinical evidence is needed, recent studies demonstrate that MB-PDT combined with SRP show a greater potential as a treatment of periodontal diseases in comparison to SRP alone.
일상적인 화학제품들의 사용량이 증가함에 따라 사용되었던 염료 폐기물 처리 또한 중요한 환경 적인 문제로 대두되었다. 이러한 염료폐기물은 광촉매를 이용하여 분해시킬 수 있는데, 졸-겔 기술을 활용 하면 매우 비용 효율적으로 광촉매를 합성할 수 있다. 졸-겔 기술은 나노스케일의 막 형성에도 상당히 유 용하며 간단하게 다층구조를 형성할 수도 있다. 본 연구에서는 다양한 염료 분해에 효과가 있는 산화아연 (ZnO) 이용하여 다중 회전도포 방법으로 다층구조(3층, 5층)를 가진 ZnO 막을 형성하였다. 성능비교를 위해 단일 회전도포 방법에 의한 단층구조를 가진 ZnO 막을 대조군으로 준비하였다. X선 회절분석기 및 에너지 분산 X선 분광계를 이용하여 ZnO의 구조 및 원소분석을 수행하였고, 주사전자현미경을 통해 나노 선같은 표면형상을 관찰할 수 있었다. 추가적으로 UV-Vis 분광광도계를 활용하여 자외선의 흡수도를 측정 하였다. 5층구조를 가진 ZnO 막이 단층 구조를 가진 ZnO 막에 비해 모의 메틸렌 블루를 49% 더 많이 분해하였다. 결론적으로, 다층구조를 가진 ZnO 는 메틸렌블루 염료를 더욱 효과적으로 분해하는 광촉매로 써 유용하다는 알 수 있었다.
단순 침전법으로 제조한 CdZnS/ZnO 광촉매를 이용하여 가시광선하에서 메틸렌블루의 광분해 반응에 대한 연구를 수행하였다. X선 회절분석법과 UV-vis 확산반사 분광법 등을 이용하여 제조된 촉매들의 물리화학적 특성을 분석하였다. 그리고 CdZnS/ZnO 광촉매의 활성을 조사하고 CdS 및 TiO2와 비교 검토하였다. CdZnS/ZnO 광촉매는 자외선뿐만 아니라 400nm에서 600nm 범위의 가시광선 영역에 있어서도 우수한 광흡수 특성을 나타내었다. 가시광선하에서 메틸렌 블루의 광분해 반응에 대해서 CdZnS/ZnO 광촉매는 CdS 와 TiO2 보다 우수한 광촉매 활성을 나타내는 것을 알 수 있었다. 그리고 가시광선하에서의 메틸렌블루의 광분해 반응에는 광촉매 반응뿐만 아니라 감광반응도 관여하고 있음을 확인할 수 있었다.
The discharge of dye-containing industrial effluents such as methylene blue (MB) in water bodies has resulted in severe aquatic and human life problems. In addition to this factor, there is the accumulation of banana peel wastes, which can generate ecological damage. Thus, this research purpose a different method from the literature using the banana peel waste (BP) to produce activated carbon (ACBP) by NaOH activation followed by pyrolysis at 400 °C to remove methylene blue (MB). The material was characterized by TGA, XRD, SEM, BET, and FTIR. The influence of dye concentration (10, 25, 50, 100, 250, and 500 mg L−1) was investigated. ACBP presented a well-developed pore structure with a predominance of mesopores and macropores. This morphological structure directly influences the MB removal capacity. The highest efficiency for dye removal was in the MB initial concentration of 25 mg L−1, sorbent of 0.03 g, and contact time of 60 min, which were 99.8%. The adsorption isotherms were well defined by Langmuir, Freundlich, and Temkin isotherm models. The Langmuir model represented the best fit of experimental data for ACBP with a maximum adsorption capacity of 232.5 mg g−1. This adsorbent showed a comparatively high performance to some previous works. So, the banana peel waste is an efficient resource for producing activated carbon and the adsorption of methylene blue.
Spent Calgon Filtrasorb activated carbon (SAC) from glycerine deodorization unit was evaluated for the removal of methylene blue (MB). The SAC was used without further modification. The SAC was characterized for BET surface area, pH, pHpzc and FTIR to determine the textural and chemical properties of SAC. The batch adsorption study of MB was carried out under different initial concentrations (5–500 mg/L), pH (2–11) and contact time (0–200 h). The SAC was found to have high BET surface area, pore volume and average pore diameter of 735 m2/g, 0.292 cm3/g and 2.56 nm, respectively. The properties of SAC contributed to high MB adsorption capacity of 283 mg/g. The equilibrium data fitted well with Langmuir model, indicating monolayer adsorption; while the activation energy (Ea) of Dubinin–Radushkevitch (D–R) model is lower than 8 kJ/mol, signifying physisorption. The adsorption kinetics was best illustrated by pseudo-second-order model, while the intraparticle diffusion and Boyd models suggested that film diffusion is the rate-controlling step. These findings showed that Calgon Filtrasorb SAC from glycerine deodorization unit can be potentially reused an adsorbent for the removal of dyes.
The oxygen-rich activated carbon (AC) was facilely developed using petroleum coke as a raw material by KOH activation under the rapid heating rate. The porosity and surface chemistry of ACs prepared under different heating rates were characterized and their adsorption properties for methylene blue (MB) were investigated. The results showed that the AC5 prepared under the heating rate of 5 °C min−1 had the highest surface area compared with the AC10, AC15 or AC20, while the AC20 prepared under the heating rate of 20 °C min−1 consisted of the highest oxygen content and most –OH functional group compares with the other ACs. These indicated that rapid heating rate was against the formation of more developed porosity, however, it was beneficial to producing more oxygen functional groups. As to MB adsorption, AC15 exhibited the maximum adsorption capacity for MB of 884 mg g−1 due to high surface area of 2803 m2 g−1 and high oxygen content of 23.27%. Moreover, despite the fact that AC20 had much lower surface area than the AC5, the AC20 showed higher MB adsorption capacity than the AC5. This was because the AC20 has the highest content of –OH, which was a positive impetus for MB adsorption. Therefore, rapid heating rate was an effective and simple approach to preparing the oxygen-rich ACs for improving the adsorption capacity of MB.
The present work is aimed at evaluating the kinetics and dynamic adsorption of methylene blue by CO2- activated carbon gels. The carbon gels were characterized by textural properties, thermal degradation and surface chemistry. The result shows that the carbon gels are highly microporous with surface area of 514 m2/g and 745 m2/g for resorcinol-to-catalyst ratios of 1000 (AC1) and 2000 (AC2), respectively. The kinetics data could be described by pseudo-first-order model, with a longer duration to attain equilibrium due to restricted pore diffusion as concentration increases. Also, AC1 exhibits insignificant kinetics with fluctuating adsorption with time at concentrations of 20 and 25 mg/L. However, AC1 reveals a better performance than AC2 in dynamic adsorption due to concentration gradient for molecules diffusion to active sites. The applicability of Yoon–Nelson and Thomas models indicates that the dynamic adsorption is controlled by external and internal diffusion.
Trametes versicolor showed the ability of degrading synthetic dyes such as congo red (CR) and methylene blue (MB) in solid and liquid culture conditions. The T. versicolor strains isolated in Korea degraded MB more efficiently than CR, differently most of other white mushrooms known to have difficulties in degrading MB than other dyes. Thus the Koren strains of T. versicolor showed the commercial potential to be used for cleaning dye-contaminated region without any patent-related problem. The main enzyme responsible for dye deradation was laccase. The manganese peroxidase (MnP) was also detected and supposed to be involved in the degradation process of synthetic dyes. However, no lignin peroxidase (LiP) was detected from degradation process, indicating LiP is not the enzyme T. versicolor use to degrade CR and MB.
Wastewater from textile industries is a major cause of water pollution in most developing countries. In order to address the issues of water pollution and high cost for treatment processes, the use of an inexpensive and environmentally benign adsorbents has been studied. The objective was to find a better alternative to the conventional methods. Lemon grass waste (ash) collected from a lemon grass stream distillation subunit in Bhutan was tested for dye removal from aqueous solutions. The study investigated the removal of methylene blue using the following operational parameters: initial concentration (100-600 mg/L), contact time, adsorbent dose (0.1-0.55 gm/100 mL), and pH (3-10). It was found that the percentage removal of dye increased with a decrease of the initial concentration and increased contact time and dose of adsorbent. The basic pH solution of dye showed better adsorption capacity as compared to the acidic dye solution. Langmuir and Freundlich adsorption isotherms were fitted to the data well. Data fitted better to Lagergren pseudo 2nd order kinetics than a 1st order kinetic model. Surface morphology was also examined via scanning electron microscopy. An elemental analysis was also carried out and the chemical composition and functional groups were analyzed using energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy techniques, respectively. The obtained results indicate that lemon grass ash could be employed as a low cost alternative to commercial activated carbon in wastewater treatment for the removal of dyes.
An increase in population initiating rapid industrialization was found to consequently in-crease the effluentsand domestic wastewater into the aquatic ecosystem. In this research the potentialities of Sambucus nigra L. (SNL) plant in the remediation of water, contaminated with methylene blue (MB), a basic dye were investigated. SNL was chemically impregnated with KHCO3. Operating variables studied were pH, amount of adsorbent and contact time. In general, pH did not have any significanteffect on colour removal and the highest adsorp-tion capacity was obtained in 0.035 g MB/g-activated carbon. The Langmuir, Freundlich, Temkin and Dubinin-Radushkevich adsorption models were applied to describe the equi-librium isotherms. The adsorption isotherm data were fittedto the Temkin isotherm. The mass transfer property of the sorption process was studied using Lagergren pseudo-firstorder and chemisorption pseudo-second-order kinetic models. The sorption process obeyed the pseudo-second-order kinetic model. The surface area, pores volume and diameter were assessed by the Brunauer-Emmett-Teller and Barrett-Joyner-Halenda methods. The results were compared to those from activated carbon (Merck) and an actual sample. The results indicate that SNL can be employed as a natural and eco-friendly adsorbent material for the removal of dye MB from aqueous solutions.
Coloured wastewater is released as a direct result of the production of dyes as well as from various other chemical industries. Many dyes and their breakdown products may be toxic for living organisms. Activated carbon is one of the best materials for removal of dyes from aqueous solutions. The present study describes the adsorption behaviour of methylene blue dye on three microporous activated carbons, where two samples (AC-1 and AC-2) were prepared by a polymer blend technique and the other is a microporous activated carbon (ARY-3) sample from viscose rayon yarn prepared by chemical-physical activation. The effects of contact time and activated carbon dosage on decolourisation capacity have been studied. The results show that activated carbon having mixed microporosity and mesoporosity show tremendous decolourisation capacity for methylene blue. In addition, the activated carbon in the powder form prepared by the polymer blend technique shows better decolourisation capacity for methylene blue than the activated rayon yarn sample.
For the present paper, we prepared MgO/MWCNT/TiO2 photocatalyst by using multi-walled carbon nanotubes(MWCNTs) pre-oxidized by m-chlorperbenzoic acid (MCPBA) with magnesium acetate tetrahydrate (Mg(CH2COO)2·4H2O)and titanium n-butoxide (TiOC(CH3)34) as magnesium and titanium precursors. The prepared photocatalyst was analyzed byX-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) analysis. The decompositionof methylene blue (MB) solution was determined under irradiation of ultraviolet (UV) light. The XRD results show that theMgO/MWCNT/TiO2 photocatalyst have cubic MgO structure and anatase TiO2 structure. The porous structure and the TiO2agglomerate coated on the MgO/MWCNT composite can be observed in SEM images. The Mg, O, Ti and C elements can bealso observed in MgO/MWCNT/TiO2 photocatalyst from EDX results. The results of photodegradation of MB solution under UVlight show that the concentration of MB solution decreased with an increase of UV irradiation time for all of the samples. Also,the MgO/MWCNT/TiO2 photocatalyst has the best photocatalytic activity among these samples. It can be considered that theMgO/MWCNT/TiO2 photocatalyst had a combined effect, the effect of MWCNT, which could absorb UV light to create photo-induced electrons (e−), and the electron trapping effect of MgO, which resulted in an increase of the photocatalytic activity of TiO2.
Purpose: The interaction of methylene blue (MB) with Na-saturated clay from Maghnia deposit in aqueous suspension was investigated using visible absorption spectroscopy. Methods: The effect of the optical properties of dyes in aqueous solutions and adsorbed onto Na-saturated clay was assessed in terms of the absorption bands maxima and the removal rate as a function of pH. Results: The adsorption of MB dye onto Na-saturated clay surface leads to the methacromatic effect in the absorption spectrum of the dye. Formation of MB dimers and higher agglomerates depended sensitively on the potential of the layer charge density. MB agglomerates occurred predominantly in the Na-saturated clay with high charge density, even with low charge density. The redistribution of MB molecules over the surface of Na-saturated clay of lower charge density (high acidic medium) leads to a reduction of the dye aggregation, accompanied by a bathochromic shift of the band maximum of MB dye to the longer wavelengths. Conclusion: The methachromatic effect was analyzed by the R=A(MB+)/A(MB+)n parameter, which decreases with the charge density, owing to the increase in the pH solution. To explain the relationship between the layer charge density and the adsorption, so- colled model 2-pKa of surface complexation (SCM) was developed.
Methylene blue (MB) was degraded by TiO2 and ZnO deposited on an activated carbon fiber (ACF) surface under UV light. The ACF/TiO2 and ACF/ZnO composites were characterized by BET, SEM, XRD, and EDX. The BET surface area was related to the adsorption capacity for composites. The SEM results showed that titanium dioxide and zinc oxide are distributed on the ACF surface. The XRD results showed that the ACF/TiO2 and ACF/ZnO composites contained a unique anatase structure for TiO2 and a typical hexagonal phase for ZnO respectively. These EDX spectra showed the presence of peaks of Ti element on ACF/TiO2 composite and peaks of Zn element on the ACF/ZnO composite. The blank experiments for either illuminating the MB solution or the suspension containing ACF/TiO2 or ACF/ZnO in the dark showed that both illumination and the catalyst were necessary for the mineralization of organic dye. Additionally, the ACF/TiO2 composites proved to be efficient photocatalysts due to degradation of MB at higher reaction rates. The addition of an oxidant ([NH4]2S2O8) led to an increase of the degradation rate of MB for ACF/TiO2 and ACF/ZnO composites.