Methylene blue removal using modified poly(glycidyl methacrylate) as a low-cost sorbent in batch mode: kinetic and equilibrium studies.

Industrial textile wastewater contains large amounts of cationic dye material. Therefore, a new adsorbent was synthesized as modified poly(glycidyl methacrylate) (mPGMA) with a fluorine group-containing compound 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP). mPGMA was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectrometer (FTIR). The proposed adsorbent has been used to remove methylene blue (MB) from aqueous solutions by the adsorption process. In further experiments, the removal efficiency of adsorbent in both powder (˂600 µm) and granular form was compared from aqueous solutions by adsorption process. Furthermore, the effects of changing parameters such as adsorbent dosage, contact time, pH, temperature, and initial dye concentration on methylene blue adsorption were investigated. Also, Langmuir, Freundlich, and Temkin isotherms have been used to describe the equilibrium characteristics of adsorption. Finally, the experimental data fitted well by Langmuir isotherm with a maximum adsorption capacity of 17.5 mg g-1. The experimental data were applied to pseudo-first- and second-order models. The experimental results were better fitted for the pseudo-second-order model than the other model. Consequently, the experimental results showed that mPGMA is a suitable low-cost adsorbent with great potential benefit in removing methylene blue from aqueous solutions.

One novel calix[4]arene based QCM sensor for sensitive, selective and high performance-sensing of formaldehyde at room temperature.

This work designs the synthesis of a novel amino morpholine schiff base functionalized calix[4]arene cage (SCC), its deposition onto Quartz Crystal Microbalance (QCM) crystal surface, and usage for the selective detecting of formaldehyde (HCHO). The SCC modified QCM sensor has been characterized by contact angle measurements and microscopy images. Initial experiments revealed that the frequency response decreased significantly which means that there was a good interaction between the SCC molecules and HCHO. The proposed sensor exhibited a linear response towards HCHO in different concentrations ranging from 1.85 to 9.25 ppm, having the high sensitivity (S) and low limit of detection (LOD) being 18.324 Hz/ppm and 0.67 ppm, respectively. Furthermore, the adsorption behavior and mechanism of HCHO onto the QCM sensor were investigated for this sensing system and the adsorption data exhibited a good correlation with the Freundlich and Langmuir-Freundlich adsorption models in terms of the regression coefficient. The QCM sensor showed outstanding selective performance to HCHO among %97 RH and some a number of interfering volatile organic compounds (VOCs) such as chloroform, dichloromethane, acetone, n-hexane, methanol, xylene, and ammonia. Thus, real-time, sensitive, selective and effective recognition of HCHO by the sensor can be explained some adsorption mechanisms such as size-fit concept, three-dimensional structures of molecules and interaction between moieties of the sensible film layer and analyte molecules such as hydrogen bonding interactions.

Rapid and real-time detection of arginine enantiomers by QCM sensor having a Calix[4]arene receptor bearing asymmetric centers.

This paper describes the sensing studies of a chiral calix[4]arene receptor (5) having (R)-2-phenylglycinol moiety for arginine enantiomers (D-/L-arginine) by using Quartz Crystal Microbalance (QCM) technique. The initial experiments have revealed that the chiral calix[4]arene 5 coated QCM (CCC-QCM) sensor showed good sensing for arginine enantiomers, such that it has exhibited higher sensing towards D-arginine than that of L-arginine. It has been determined that the sensitivity, limit of detection values of CCC-QCM sensor for the D-/L-arginine solutions as 0.024/0.023 Hz/µM and 0.38/1.29 µM, respectively. On the other hand, the racemic mixture studies were optimized using the response surface methodology with central composite design. Consequently, it has been demonstrated that the QCM sensor modification with a calix[4]arene receptor bearing asymmetric centers provided rapid, real-time, sensitive and effective sensing of arginine enantiomers.

A phenyl glycinol appended calix[4]arene film for chiral detection of ascorbic acid on gold surface.

This paper describes the synthesis of new chiral calix [4]arene derivative having (R)-2-phenylglycinol moiety (compound 6), and its chiral recognition studies for ascorbic acid (AA) enantiomers by using Quartz Crystal Microbalance (QCM). Initial experiments indicated that the outstanding selective chiral recognition (α) was observed as 2.61 for l-enantiomer of AA. The sensitivity (S) and the limit of detection (LOD) values for L-AA were calculated as 0.0226 Hz/µM and 0.63 µM, respectively. Furthermore, the sorption behavior and mechanism of AA onto compound 6 film were evaluated and the sorption data exhibited a good correlation with the Freundlich isotherm models. The maximum uptake of L-AA by the sensor was found as 5895.76 mg/g. In conclusion, chiral recognition of AA enantiomers as real-time, sensitive, selective and effective was performed by a calixarene derivative coated QCM sensor.

Selective chiral recognition of alanine enantiomers by chiral calix[4]arene coated quartz crystal microbalance sensors.

We describe the synthesis of new chiral calix[4]arene derivatives having (R)-1-phenylethylamine, (S)-1-phenylethylamine, (R)-2-phenylglycinol, and (S)-2-phenylglycinol moieties, and chiral recognition studies for enantiomers of some selected α-amino acid derivatives such as alanine, phenylalanine, serine, and tryptophan using a quartz crystal microbalance (QCM). Initial experiments indicated that the highest selective chiral recognition factor was 1.42 for alanine enantiomers. The sensitivity, limit of detection, and time constant for L-alanine were calculated as 0.028 Hz/µM, 60.9 µM, and 36.2 s, respectively. The results indicated that real-time, sensitive, selective, and effective chiral recognition of alanine enantiomers was achieved with a QCM sensor coated with a chiral calix[4]arene derivative having (R)-2-phenylglycinol moieties.

Calix[4]arene coated QCM sensors for detection of VOC emissions: Methylene chloride sensing studies.

This paper describes the sensing studies of QCM sensors with coated some calixarene derivatives bearing different functional groups for some selected Volatile Organic Compounds (VOCs) such as acetone, acetonitrile, carbon tetrachloride, chloroform, methylene chloride (MC), N,N-dimethylformamide, 1,4-dioxane, ethanol, ethyl acetate, xylene, methanol, n-hexane and toluene. The initial experiments have revealed that whole the calix[4]arene modified QCM sensors exhibited strongest sensing ability to MC emissions. Thus, the detailed studies were performed for only MC emissions after the determination of relatively more effective calix-coated QCM sensors for MC emissions in aqueous media. The results demonstrated that QCM sensor coated with calix-7 bearing both amino and imidazole groups was most useful sensor for MC emissions with 54.1ppm of detection limit. Moreover, it was understood that cyclic structures, H-bonding capabilities and also good preorganization properties of calixarene derivatives played an important role in VOC sensing processes.