Selective Removal of the Emerging Dye Basic Blue 3 via Molecularly Imprinting Technique.

A molecularly imprinting polymer (MIP) was synthesized for Basic Blue 3 dye and applied to wastewater for the adsorption of a target template. The MIPs were synthesized by bulk polymerization using methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA). Basic Blue 3 dye (BB-3), 2,2'-azobisisobutyronitrile (AIBN) and methanol were used as a functional monomer, cross linker, template, initiator and porogenic solvent, respectively, while non-imprinting polymers (NIP) were synthesized by the same procedure but without template molecules. The contact time was 25 min for the adsorption of BB-3 dye from 10 mL of spiked solution using 25 mg polymer. The adsorption of dye (BB-3) on the MIP followed the pseudo-second order kinetic (k2 = 0.0079 mg·g-1·min-1), and it was according to the Langmuir isotherm, with maximum adsorption capacities of 78.13, 85.4 and 99.0 mg·g-1 of the MIP at 283 K, 298 K and 313 K, respectively and 7 mg·g-1 for the NIP. The negative values of ΔG° indicate that the removal of dye by the molecularly imprinting polymer and non-imprinting polymer is spontaneous, and the positive values of ΔH° and ΔS° indicate that the process is endothermic and occurred with the increase of randomness. The selectivity of the MIP for BB-3 dye was investigated in the presence of structurally similar as well as different dyes, but the MIP showed higher selectivity than the NIP. The imprinted polymer showed 96% rebinding capacity at 313 K towards the template, and the calculated imprinted factor and Kd value were 10.73 and 2.62, respectively. In this work, the MIP showed a greater potential of selectivity for the template from wastewater relative to the closely similar compounds.

2,6-bis(E)-4-methylbenzylidine)-cyclohexan-1-one as a Fluorescent-on Sensor for Ultra Selective Detection of Chromium Ion in Aqueous Media.

The ligand 2,6-bis(E)-4-methylbenzylidine)-cyclohexan-1-one sensor has been synthesized as a fluorescence-on sensor/probe for the trace level detection of chromium III ion. The synthesized ligand was characterized by FTIR, 1H-NMR spectroscopy, and fluorimetery. The sensor exhibited an ultra-selective response to chromium among the tested heavy metal ions. Different parameters were optimized like pH, effect of concentration of sensor C, metal ion and contact time. The binding stoichiometry of C:Cr3+ was calculated to be 2:1 (Job's plot) with a significantly low detection limit of 2.3 × 10- 9 M. Sensor C were practically employed for detection of chromium in spiked water samples.

Mixed-mode open tubular column for peptide separations by capillary electrochromatography.

Mixed-mode chromatography open tubular column has been developed for peptide separation in electrochromatography. A column with 92 cm effective length and 50 µm internal diameter is fabricated internally with a copolymer sheet of restricted thickness. Catalyst facilitated binding of the coupling agent 3,5-bis (trifluoromethyl) phenyl isocyanate has been carried out at the interior surface of the column. The initiator sodium diethyldithiocarbamate was bound to the coupling agent. A small amount of N-[2-(acryloylamino) phenyl] acrylamide was used along with methacrylic acid and styrene in the monomer mixture to induce a little polar character in the stationary phase fabricated inside the column. Twenty-three peptides have been separated from a chemically digested protein mixture present in cytochrome C in capillary electrochromatography, in addition to the separation of six commercial peptides. We achieved an average plate count of over 1.5 million/m with the column of current study both for the digested protein components and commercial peptides using 70/30% v/v (acetonitrile/20 mM ammonium formate) at pH 6.5. In addition, the column resulted in baseline separation of all the peptides with very good resolution, enhanced peak capacity, and better retention time span.

Particle packed mixed-mode chromatographic stationary phase for the separation of peptide in liquid chromatography.

A particle-based stationary phase has been prepared for the separation of five synthetic peptides and a mixture containing tryptic digest of cytochrome C in liquid chromatography. Particles originating from silica monolith were differentially sedimented to obtain 1-2 µm particles. A stationary phase was achieved by the coating of poly(styrene-methacrylic acid-N-phenylacrylamide) copolymer onto the particles via reversible addition-fragmentation chain transfer polymerization reaction. Stainless steel column (30 cm long and 1 mm internal diameter) was packed with stationary phase. Very high separation efficiency (ca. 351 000 plates/m) was achieved for five commercial peptides with a percent relative standard deviation of less than 1%. Protocol for the synthesis and modification of silica monolith particles has been well optimized with a good reproducibility both in particle and pore size. The column resolved about 21 peptide components from a mixture containing tryptic digest of cytochrome C, under the elution conditions of acetonitrile/15 mM ammonium format (65/35 v/v%) with a flow rate of 28 µL/min.

Open tubular capillary column for the separation of cytochrome C tryptic digest in capillary electrochromatography.

A silica capillary of 50 µm internal diameter and 500 mm length (416 mm effective length) was chemically modified with 4-(trifluoromethoxy) phenyl isocyanate in the presence of dibutyl tin dichloride as catalyst. Sodium diethyl dithiocarbamate was reacted with the terminal halogen of the bound ligand to incorporate the initiator moiety, and in situ polymerization was performed using a monomer mixture of styrene, N-phenylacrylamide, and methacrylic acid. The resultant open tubular capillary column immobilized with the copolymer layer was used for the separation of tryptic digest of cytochrome C in capillary electrochromatography. The sample was well eluted and separated into many components. The elution patterns of tryptic digest of cytochrome C were studied with respect to pH and water content in the mobile phase. This preliminary study demonstrates that open tubular capillary electrochromatography columns with a modified copolymer layer composed of proper nonpolar and polar units fabricated by reversible addition-fragmentation transfer polymerization can be useful as separation media for proteomic analysis.

Open tubular capillary electrochromatography with an N-phenylacrylamide-styrene copolymer-based stationary phase for the separation of anomers of glucose and structural isomers of maltotriose.

A ligand with a terminal halogen (4-chloromethylphenyl isocyanate) was chemically bound on the inner surface of pretreated silica capillary with 50 µm internal diameter and 58 cm total and 50 cm effective length in the presence of dibutyl tin dichloride as a catalyst through isocyanate-hydroxyl reaction. Attachment of initiator (sodium diethyl dithiocarbamate) to the bound ligand was carried out and followed by in situ polymerization. Reversible addition-fragmentation chain transfer polymerization was used for the immobilization of N-phenylacrylamide-styrene copolymer on the inner surface of capillary column. The resultant open tubular column showed excellent separation performance for derivatized saccharide isomers in capillary electrochromatography. D-Glucose was separated into α- and ß-anomers while five structural isomers were separated for derivatized maltotriose with separation efficiency above one million theoretical plates per meter. The effects of pH and acetonitrile composition on the electrochromatographic performance of the derivatized saccharides were studied and the optimized elution condition was found to be 90:10 v/v% acetonitrile/30 mM sodium acetate at pH 6.6. UV absorption at 214 nm was used as detection mode in open tubular capillary electrochromatography separations.

C18-bound porous silica monolith particles as a low-cost high-performance liquid chromatography stationary phase with an excellent chromatographic performance.

Ground porous silica monolith particles with an average particle size of 2.34 µm and large pores (363 Å) exhibiting excellent chromatographic performance have been synthesized on a relatively large scale by a sophisticated sol-gel procedure. The particle size distribution was rather broad, and the d(0.1)/d(0.9) ratio was 0.14. The resultant silica monolith particles were chemically modified with chlorodimethyloctadecylsilane and end-capped with a mixture of hexamethyldisilazane and chlorotrimethylsilane. Very good separation efficiency (185,000/m) and chromatographic resolution were achieved when the C18 -bound phase was evaluated for a test mixture of five benzene derivatives after packing in a stainless-steel column (1.0 mm × 150 mm). The optimized elution conditions were found to be 70:30 v/v acetonitrile/water with 0.1% trifluoroacetic acid at a flow rate of 25 µL/min. The column was also evaluated for fast analysis at a flow rate of 100 µL/min, and all the five analytes were eluted within 3.5 min with reasonable efficiency (ca. 60,000/m) and resolution. The strategy of using particles with reduced particle size and large pores (363 Å) combined with C18 modification in addition to partial-monolithic architecture has resulted in a useful stationary phase (C18 -bound silica monolith particles) of low production cost showing excellent chromatographic performance.

A simple and cost-effective hybrid stationary phase for the separation of peptides, proteins and benzene derivatives through liquid chromatography.

A very simple and cost-effective silica-based hybrid stationary phase was synthesized for the separation of five synthetic peptides, five proteins, and benzene derivatives. Silica monolith was synthesized via sol-gel process. Particles obtained through the grinding of silica monolith were suspended in methanol and sedimented under gravity to obtain sub-2 µm particles. A hybrid LC stationary phase was obtained by coating an ethylene glycol dimethacrylate co-polymer onto the particles via RAFT polymerization. The resultant stationary phase was characterized using SEM, FTIR, BET, and EDX analysis. A stainless steel column (200 mm long × 0.2 mm ID) was packed with the resultant stationary phase via pressure tapering protocol using a slurry packing machine. The column resulted in the average number of theoretical plates/meter (287 500 for synthetic peptides, 276 800 for proteins, and 226 100 for benzene derivatives) under the elution conditions of acetonitrile/50 mM ammonium format (68/32 v/v%) with a flow rate of 0.785 µL min-1. Since the column resulted in the separation of synthetic peptides, proteins, and benzene derivatives with very good chromatographic performance, it could possibly separate any complex mixture of peptides and proteins with better chromatographic performance.

Molecular imprinted polymers for separation science: a review of reviews.

Molecular imprinted polymer is an artificial receptor made by imprinting molecules of a template in a polymer matrix followed by removing the template molecules via thorough washing to give the permanent template grooves. They show favored affinity to the template molecule compared to other molecules, and this property is the basic driving force for such diverse application of this techniques. Such techniques have been increasingly employed in a wide scope of applications such as chromatography, sample pretreatment, purification, catalysts, sensors, and drug delivery, etc., mostly in bioanalytical areas. A major part of them is related to development of new stationary phases and their application in chromatography and sample pretreatment. Embodiments of molecular imprinted polymer materials have been carried out in a variety of forms such as irregularly ground particles, regular spherical particles, nanoparticles, monoliths in a stainless steel or capillary column, open tubular layers in capillaries, surface attached thin layers, membranes, and composites, etc. There have been numerous review articles on molecular imprinted polymer issues. In this special review, the reviews in recent ca. 10 years will be categorized into several subgroups according to specified topics in separation science, and each review in each subgroup will be introduced in the order of date with brief summaries and comments on new developments and different scopes of prospects. Brief summaries of each categories and conclusive future perspectives are also given.

N-Phenyl acrylamide-incorporated porous silica-bound graphene oxide sheets with excellent removal capacity for Cr(iii) and Cr(vi) from wastewater.

The sophisticatedly altered Hummer's and sol-gel procedures were applied for the synthesis of graphene oxides and porous silica monolith particles respectively. The Fischer esterification protocol was used for coupling silica monoliths with graphene oxides. A N-phenyl acrylamide-incorporated porous polymer was synthesized at the surface of composites via reversible addition fragmentation chain transfer polymerization. The composition was confirmed by Fourier transform infra-red spectroscopy, FE-SEM, X-ray diffraction, zeta potential (zeta pH), Brunauer-Emmett-Teller (BET/BJH) analysis, and EDAX analysis. The resulting polymer-bound composite efficiently removed Cr(vi) and Cr(iii) from waste water. Adsorption parameters such as contact time, pH effect, temperature, and adsorbent and adsorbate concentration were optimized for the optimal output of the composite. The kinetic and equilibrium models were applied to the adsorption of Cr(vi) and Cr(iii) at the adsorbent surface. The maximum adsorption capacity (qe) of Cr(vi) and Cr(iii) was found to be 298.507 mg g-1 and 401.874 mg g-1, respectively, using the same initial concentration of Cr(vi) and Cr(iii) [10-60 ppm]. The adsorption data of both states of the Cr-metal followed the pseudo 2nd-order kinetic model with regression values of 0.996 ∼ Cr(vi) and 0.999 ∼ Cr(iii) at ambient temperature. Similarly, the adsorption data of Cr(vi) best fit into the Langmuir adsorption isotherm (R2 = 0.972) while that of Cr(iii) followed the Freundlich model (R2 = 0.983).

Synthesis of fructose bound Fe(iii) integrated carbon dots as a robust turn-off detection sensor for chlortoluron.

A simple, sensitive, and robust fluorescent sensor for chlortoluron detection has been developed. Fluorescent carbon dots were synthesized using ethylene diamine and fructose via a hydrothermal protocol. The molecular interaction between fructose carbon dots and Fe(iii) resulted in a fluorescent metastable state exhibiting remarkable fluorescence quenching at λem of 454 nm and interestingly, further quenching occurred upon the addition of chlortoluron. The quenching in the fluorescence intensity of CDF-Fe(iii) towards chlortoluron occurred in the concentration range of 0.2-5.0 µg mL-1 where the limit of detection was found to be 0.0467 µg mL-1, the limit of quantification was 0.14 µg mL-1, and the relative standard deviation was 0.568%. The selective and specific recognitive nature of the Fe(iii) integrated fructose bound carbon dots towards the chlortoluron make it a suitable sensor for real sample applications. The proposed strategy was applied for the determination of chlortoluron in soil, water, and wheat samples with recoveries in the range of 95% to 104.3%.

Development of Fluorescent Co (II)-Integrated Carbon Dots and Their Application as a Off-On Mesotrione Detection Sensor.

A very simple mesotrione-sensing medium with enhanced sensitivity detection limits has been proposed. A renovated hydrothermal method was adopted for synthesizing fluorescent carbon dots from ethylenediamine and glucose using a Teflon-lined simple autoclave in a GC oven. The resultant carbon dots were characterized via TEM, FTIR, UV-vis, particle size distribution, and EDX and evaluated in a fluorimeter as the sensing medium for mesotrione detection. The binding approach of the Co (II)-integrated glucose-bound carbon dots toward mesotrione is selective, making them an effective sensor for the real sample applications, where majority of the coexisting substances showed insignificant interference effect. Formation of the metastable state due to the molecular interaction between carbon dots and Co (II) resulted in fluorescence quenching at 456 nm. Enhancement in the fluorescence intensity occurred when mesotrione was added in the concentration range of 0.2-5.0 µg mL-1, with a limit of detection, limit of quantification, standard deviation, and relative standard deviation of 0.054, 0.164, 0.00082 µg mL-1, and 0.682%, respectively. Mesotrione determination was demonstrated in soil, water, and tomato samples with recoveries in the range of 95.38-104.7%. The selectivity of the sensor was found to be good enough when checked for the complex tomato sample spiked with different pesticides of the triketone family having structural similarities to mesotrione.

Regulation of futile ligation during early steps of BER in M. tuberculosis is carried out by a ß-clamp-XthA-LigA tri-component complex.

The Class-II AP-endonuclease (XthA) is a mycobacterial DNA base excision repair (BER) pathway enzyme that functions in the initial steps. It acts on DNA substrates that contain abasic sites to create nicks with 3'-hydroxyl (OH) and 5'-deoxyribose phosphate (5'-dRP) moieties. The NAD+-dependent DNA ligase (LigA) is the terminal player in mycobacterial BER and seals such nicks efficiently. Here, we demonstrate that the Mtbß-clamp-MtbXthA complex that exists in the initial steps of BER engages with MtbLigA to form a novel tri-component BER complex. Size exclusion chromatography (SEC) experiments analysis show that the three proteins interact with equimolar stoichiometry. Small angle X-ray scattering (SAXS) analysis and associated studies reveal that the apo tri-component BER-complex adopts an extended conformation where MtbXthA is sandwiched between the Mtbß-clamp and MtbLigA. The studies support that in the apo-complex MtbXthA binds subsite-I of Mtbß-clamp through 239QLRFPKK245 motif and to MtbLigA by 104DGQPSWSGKP113 motif simultaneously. However, the complex adopts a less-extended conformation in the presence of substrate DNA, where MtbXthA interactions switch from predominantly subsite-I to subsite-II of the Mtbß-clamp. Overall, the novel tri-component complex prevents futile ligation activity of MtbLigA on the product of MtbXthA and ensures forward progression of the pathway and productive mycobacterial BER interactions.

Electrochromic Displays via the Room-Temperature Electrochemical Oxidation of Nickel.

Electrochromism refers to the persistent and reversible change in color by applying an electric field. The phenomenon involves the insertion and extraction of electrons and ions within the active material. There is a keen interest in electrochromic (EC) materials, since they exhibit a wide range of potential applications. In recent years, transition-metal oxides have been widely investigated as EC materials due to their low power requirement, high coloration efficiency, and memory effect under an open-circuit condition. Nickel oxide (NiO), a p-type wide band gap semiconductor, exhibits attractive features such as a high color contrast ratio, good chemical stability, cost-effectiveness, and good compatibility with the cathodically coloring tungsten oxide. NiO thin films have been fabricated by various methods, but these are not cost-effective, scalable, or suitable for flexible applications. With the increasing demand for flexible and soft EC devices, it is essential to find routes to fabricate NiO thin films at lower temperatures. In this work, a NiO/Ni(OH)2-based thin EC layer on fluorine-doped tin oxide-coated glass is developed via an electroless nickel (EN) deposition route, followed by room-temperature electrochemical oxidation. The deposition time is optimized to control the film thickness. The EC performance is investigated in an aqueous alkaline electrolyte (1 M KOH) by means of cyclic voltammetry, chronoamperometry, and transmittance measurements. Both the as-deposited and annealed films, after electrochemical oxidation, exhibit excellent EC properties with an optical modulation of approximately 64% (at 550 nm) and good response times of approximately 3 s (coloration) and 14 s (bleaching). A 2 × 2 display obtained by patterning the EN deposition is also demonstrated as part of this work.

Synthesis of monolith silica anchored graphene oxide composite with enhanced adsorption capacities for carbofuran and imidacloprid.

Highly efficient adsorbent was prepared for the removal of carbofuran and imidacloprid pesticides from wastewater. The silica monolith anchored graphene oxide composite was synthesized by the modified Fischer esterification protocol. The composite showed improved adsorption capacity for the removal of pesticides from wastewater. Graphene oxide was synthesized using the modified Hummer's method, while the silica monolith was prepared via sol-gel method. The composite was characterized via X-ray diffraction, Fourier transform infra-red, Brunauer Emmett and Teller (BET/BJH) analysis, zeta potential, and FESEM imaging. Different adsorption parameters such as pH, contact time, adsorbate and adsorbent concentration, and temperature were optimized for the adsorption of pesticides. The equilibrium and kinetic models were applied to the adsorption process of the pesticides. Qe of the composite as found to be 342.46 mg g-1 for imidacloprid and 37.15 mg g-1 for carbofuran. The adsorption process followed the pseudo 2nd order kinetic model for carbofuran (R2~0.9971) and imidacloprid (R2~0.9967). The Freundlich isotherm best fitted to the adsorption data of the pesticides with R2 value of 0.9956 for carbofuran and 0.95 for imidacloprid. The resultant adsorbent/composite material came out with very good results for the removal of pesticides.

Synthesis, column packing and liquid chromatography of molecularly imprinted polymers for the acid black 1, acid black 210, and acid Brown 703 dyes.

Molecularly imprinted polymers have been synthesized for the acid black 1, acid black 210, and acid brown 703 dyes using methacrylic acid, ethylene glycol, and azobisisobutyronitrile as the monomer, cross-linker, and initiator, respectively, in the ratio of 1 : 10 : 44 (template:monomer:cross-linker). The MIPs were used for the selective removal of their corresponding dyes. The selective nature of the MIPs towards their respective dyes was confirmed by a homemade liquid chromatography system. The resultant polymer materials were packed in a stainless steel column and checked for the separation of mixtures of dyes in liquid chromatography. The dyes complementary in structure to the imprinted cavities in the MIPs had long retention times, showing the highly selective nature of the MIPs. The pH, quantity of the MIPs, time, and concentration of the dyes were optimized for the highly efficient removal of the newly synthesized MIP adsorbents in batch adsorption studies. First-order, second-order, and intra-particle diffusion models were applied to all the three MIP-based adsorbents for their kinetic investigations towards the dyes. All the three MIPs selectively absorbed their target template molecule in the presence of four other template dyes having closely related structures with % RSD < 4% for the three batch experiments. The synthesized MIPs were characterized by FTIR, SEM imaging and liquid chromatography. FTIR results strongly confirmed the presence of hydrogen bonding interactions (600-900) between the template and the individual monomers present in the unwashed MIPs. Liquid chromatography revealed the highly selective nature of the MIPs towards their template molecules. The synthesized polymeric substances possess excellent thermal, chemical, and mechanical stability and can be reused several hundred times. The MIPs were applied in the removal of dyes from spiked water samples (river water, tap water and distilled water) where the % removal of the dyes by their corresponding MIPs was greater than 90%.

Sedimentation assisted preparation of ground particles of silica monolith and their C18 modification resulting in a chromatographic phase of improved separation efficiency.

The sedimentation procedure has been adopted in production of ground silica monolith particles to improve chromatographic separation efficiency of the resultant phase. First, silica monolith particles have been successfully prepared in a large scale by a sol-gel process followed by grinding. The particles after calcination were separated by sedimentation into three zones using an Imhoff sedimentation cone. The particles of the bottom zone were derivatized with a C18 ligand and end-capped. The sedimentation process was found to not only eliminate troublesome minute particles but also narrow down the particle size distribution. The resultant phase was packed in glass lined stainless steel micro-columns. The average number of theoretical plates (N) of the columns for a test mixture was 47,000 and 29,300 for the 300 and 150mm columns (1mm internal diameter), corresponding to 157,000/m and 195,000/m, respectively.

Catalyst assisted synthesis of initiator attached silica monolith particles via isocyanate-hydroxyl reaction for production of polystyrene bound chromatographic stationary phase of excellent separation efficiency.

Dibutyltin dichloride (DBTDC) was used as a catalyst to chemically bind 4-chloromehtylphenylisocynate (4-CPI) to porous monolithic silica particles via isocyanate-hydroxyl reaction, and the reaction product was reacted with sodium diethyldithiocarbamate (SDDC) to yield initiator attached silica monolith particles. Reversible addition-fragmentation transfer (RAFT) polymerization was taken place on them to result in polystyrene attached silica particles that showed excellent separation efficiency when packed in a chromatographic column (1.0 mm × 300 mm). The numbers of theoretical plates (N) of 56,500 is better than those of any commercially available HPLC or UHPLC column yet.

Comprehensive overview of recent preparation and application trends of various open tubular capillary columns in separation science.

Open tubular (OT) capillary columns have been increasingly used in a variety of fields of separation science such as CEC, LC, and SPE. Especially their application in CEC has attracted a lot of attention for their outstanding separation performance. Various forms of OT stationary phase materials have been employed such as in-situ prepared polymers, molecular imprinted polymers (MIPs), brush ligands, host ligands, block copolymers, aptamers, carbon nanotubes, polysaccharides, proteins, tentacles, nanoparticles, monoliths, and polyelectrolyte multi-layers. They have been prepared either in the chemically bound format or physically adsorbed format. Sol-gel technologies and nanoparticles have been sometimes involved in their preparation. There have been also some unique miscellaneous studies, for example, adopting preferentially adsorbed mobile phase components as stationary phases. In this review, recent progresses since mostly 2007 will be critically discussed in detail with some summarized descriptions for the work before the date.

Recent applications of molecular imprinted polymers for enantio-selective recognition.

Molecular imprinted polymer (MIP) techniques have been increasingly used in a variety of fields including chromatography, sample pretreatment, purification, sensors, drug delivery, and catalysts, etc. MIP is a specific artificial receptor that shows favored affinity to the template molecule. The cavities of the template are produced by carrying out polymerization of a reaction mixture followed by eliminating the template molecules by washing. Various forms of MIP materials have been prepared for diverse applications including irregularly ground particles, regular spherical particles, nanoparticles, monoliths in a stainless steel or capillary column, open tubular layers in capillaries, membranes, surface attached thin layers, and composites, etc. When an enantiomer is used as the template, then the resulting MIP can show capability of enantiomeric recognition between the pair of enantiomers. In this review, progresses in applications of enantio-selective recognition by MIPs will be critically reviewed for the recent period since 2007.