Development of TiO2-CaCO3 Based Composites as an Affordable Building Material for the Photocatalytic Abatement of Hazardous NOx from the Environment.

This study explores the depollution activity of a photocatalytic cementitious composite comprising various compositions of n-TiO2 and CaCO3. The photocatalytic activity of the CaCO3-TiO2 composite material is assessed for the aqueous photodegradation efficiency of MB dye solution and NOx under UV light exposure. The catalyst CaCO3-TiO2 exhibits the importance of an optimal balance between CaCO3 and n-TiO2 for the highest NOx removal of 60% and MB dye removal of 74.6%. The observed trends in the photodegradation of NOx removal efficiencies suggest a complex interplay between CaCO3 and TiO2 content in the CaCO3-n-TiO2 composite catalysts. This pollutant removal efficiency is attributed to the synergistic effect between CaCO3 and n-TiO2, where a higher percentage of n-TiO2 appeared to enhance the photocatalytic activity. It is recommended that CaCO3-TiO2 photocatalysts are effectiveness in water and air purification, as well as for being cost-effective construction materials.

Facile and Simple Post Treatment Ball Milling Strategy for the Production of Low-Cost TiO2 Composites with Enhanced Photocatalytic Performance and Applicability to Construction Materials.

A facile and cost-effective approach assisted by ball milling (BM) of commercial titanium dioxide (TiO2), has been utilized to develop cheaper and efficient construction materials. At least three of the commercial and cheaper TiO2 samples (BA01-01, BA01-01+ and R996, designated as A1, A4 and R1, respectively) were selected and subjected to BM treatment to enhance their photocatalytic efficiencies, if possible. It was noted, that the samples A1, A4 and R1 were typical composites of TiO2 and calcium carbonate (CaCO3) and contained varying proportions of anatase, and rutile phases of TiO2 and CaCO3. Two of the highly efficient commercial TiO2 samples, Degussa P25 (simply designated as P25) and ST01 (Ishihara Ind.) were selected for making benchmark comparisons of photocatalytic efficiencies. The BM treated TiO2 samples (designated as TiO2-BM with respect to A1, A4 and R1) were evaluated for photocatalytic efficiencies both in both aqueous (methylene blue (MB)) and gaseous (NOx) photodegradation reactions. Based on detailed comparative investigations, it was observed that A1-BM photocatalyst exhibited superior photocatalytic performances over A4-BM and R1-BM, towards both MB and NOx photodegradation reactions. The difference of NOx photodegradation efficiency between the mortar mixed with A1-BM and that mixed with ST01, and P-25 at 15% were 16.6%, and 32.4%, respectively. Even though the mortar mixed with A1-BM at 15% composition exhibited a slightly lower NOx photodegradation efficiency as compared to mortar mixed with the expensive ST01 and P-25 photocatalysts, the present work promises an economic application in the eco-friendly construction materials for air purification considering the far lower cost of A1. The reasons for the superior performance of A1-BM were deduced through characterization of optical properties, surface characteristics, phase composition, morphology, microstructure and particle size distribution between pristine and BM treated A1 using characterization techniques such as diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction analysis, field emission scanning electron microscopy and particle size analysis.

Facile Use of Silver Nanoparticles-Loaded Alumina/Silica in Nanofluid Formulations for Enhanced Catalytic Performance toward 4-Nitrophenol Reduction.

The introduction of toxic chemicals into the environment can result in water pollution leading to the degradation of biodiversity as well as human health. This study presents a new approach of using metal oxides (Al2O3 and SiO2) modified with a plasmonic metal (silver, Ag) nanoparticles (NPs)-based nanofluid (NF) formulation for environmental remediation purposes. Firstly, we prepared the Al2O3 and SiO2 NFs of different concentrations (0.2 to 2.0 weight %) by ultrasonic-assisted dispersion of Al2O3 and SiO2 NPs with water as the base fluid. The thermo-physical (viscosity, activation energy, and thermal conductivity), electrical (AC conductivity and dielectric constant) and physical (ultrasonic velocity, density, refractive index) and stability characteristics were comparatively evaluated. The Al2O3 and SiO2 NPs were then catalytically activated by loading silver NPs to obtain Al2O3/SiO2@Ag composite NPs. The catalytic reduction of 4-nitrophenol (4-NP) with Al2O3/SiO2@Ag based NFs was followed. The catalytic efficiency of Al2O3@Ag NF and SiO2@Ag NF, for the 4-NP catalysis, is compared. Based on the catalytic rate constant evaluation, the catalytic reduction efficiency for 4-NP is found to be superior for 2% weight Al2O3@Ag NF (92.9 × 10-3 s-1) as compared to the SiO2@Ag NF (29.3 × 10-3 s-1). Importantly, the enhanced catalytic efficiency of 2% weight Al2O3@Ag NF for 4-NP removal is much higher than other metal NPs based catalysts reported in the literature, signifying the importance of NF formulation-based catalysis.

Polyethylene Glycol Coated Magnetic Nanoparticles: Hybrid Nanofluid Formulation, Properties and Drug Delivery Prospects.

Magnetic nanoparticles (MNPs) are widely used materials for biomedical applications owing to their intriguing chemical, biological and magnetic properties. The evolution of MNP based biomedical applications (such as hyperthermia treatment and drug delivery) could be advanced using magnetic nanofluids (MNFs) designed with a biocompatible surface coating strategy. This study presents the first report on the drug loading/release capability of MNF formulated with methoxy polyethylene glycol (referred to as PEG) coated MNP in aqueous (phosphate buffer) fluid. We have selected MNPs (NiFe2O4, CoFe2O4 and Fe3O4) coated with PEG for MNF formulation and evaluated the loading/release efficacy of doxorubicin (DOX), an anticancer drug. We have presented in detail the drug loading capacity and the time-dependent cumulative drug release of DOX from PEG-coated MNPs based MNFs. Specifically, we have selected three different MNPs (NiFe2O4, CoFe2O4 and Fe3O4) coated with PEG for the MNFs and compared their variance in the loading/release efficacy of DOX, through experimental results fitting into mathematical models. DOX loading takes the order in the MNFs as CoFe2O4 > NiFe2O4 > Fe3O4. Various drug release models were suggested and evaluated for the individual MNP based NFs. While the non-Fickian diffusion (anomalous) model fits for DOX release from PEG coated CoFe2O4, PEG coated NiFe2O4 NF follows zero-order kinetics with a slow drug release rate of 1.33% of DOX per minute. On the other hand, PEG coated NiFe2O4 follows zero-order DOX release. Besides, several thermophysical properties and magnetic susceptibility of the MNFs of different concentrations have been studied by dispersing the MNPs (NiFe2O4, CoFe2O4 and Fe3O4) in the base fluid at 300 K under ultrasonication. This report on the DOX loading/release capability of MNF will set a new paradigm in view that MNF can resolve problems related to the self-heating of drug carriers during mild laser treatment with its thermal conducting properties.

Cost-Effective Production of TiO2 with 90-Fold Enhanced Photocatalytic Activity Via Facile Sequential Calcination and Ball Milling Post-Treatment Strategy.

Titanium dioxide (TiO2), the golden standard among the photocatalysts, exhibits a varying level of photocatalytic activities (PCA) amongst the synthetically prepared and commercially available products. For commercial applications, superior photoactivity and cost-effectiveness are the two main factors to be reckoned with. This study presents the development of simple, cost-effective post-treatment processes for a less costly TiO2 to significantly enhance the PCA to the level of expensive commercial TiO2 having demonstrated superior photoactivities. We have utilized sequential calcination and ball milling (BM) post-treatment processes on a less-costlier KA100 TiO2 and demonstrated multi-fold (nearly 90 times) enhancement in PCA. The post-treated KA100 samples along with reference commercial samples (P25, NP400, and ST01) were well-characterized by appropriate instrumentation and evaluated for the PCA considering acetaldehyde photodegradation as the model reaction. Lattice parameters, phase composition, crystallite size, surface functionalities, titanium, and oxygen electronic environments were evaluated. Among post-treated KA100, the sample that is subjected to sequential 700 °C calcination and BM (KA7-BM) processes exhibited 90-fold PCA enhancement over pristine KA100 and the PCA-like commercial NP400 (pure anatase-based TiO2). Based on our results, we attribute the superior PCA for KA7-BM due to the smaller crystallite size, the co-existence of mixed anatase-srilankite-rutile phases, and the consequent multiphase heterojunction formation, higher surface area, lattice disorder/strain generation, and surface oxygen environment. The present work demonstrates a feasible potential for the developed post-treatment strategy towards commercial prospects.

Recent Progress in the Abatement of Hazardous Pollutants Using Photocatalytic TiO2-Based Building Materials.

Titanium dioxide (TiO2) has been extensively investigated in interdisciplinary research (such as catalysis, energy, environment, health, etc.) owing to its attractive physico-chemical properties, abundant nature, chemical/environmental stability, low-cost manufacturing, low toxicity, etc. Over time, TiO2-incorporated building/construction materials have been utilized for mitigating potential problems related to the environment and human health issues. However, there are challenges with regards to photocatalytic efficiency improvements, lab to industrial scaling up, and commercial product production. Several innovative approaches/strategies have been evolved towards TiO2 modification with the focus of improving its photocatalytic efficiency. Taking these aspects into consideration, research has focused on the utilization of many of these advanced TiO2 materials towards the development of construction materials such as concrete, mortar, pavements, paints, etc. This topical review focuses explicitly on capturing and highlighting research advancements in the last five years (mainly) (2014-2019) on the utilization of various modified TiO2 materials for the development of practical photocatalytic building materials (PBM). We briefly summarize the prospective applications of TiO2-based building materials (cement, mortar, concretes, paints, coating, etc.) with relevance to the removal of outdoor/indoor NOx and volatile organic compounds, self-cleaning of the surfaces, etc. As a concluding remark, we outline the challenges and make recommendations for the future outlook of further investigations and developments in this prosperous area.

Manganese and Graphene Included Titanium Dioxide Composite Nanowires: Fabrication, Characterization and Enhanced Photocatalytic Activities.

We report the detailed microstructural, morphological, optical and photocatalytic studies of graphene (G) and manganese (Mn) co-doped titanium dioxide nanowires (TiO2(G-Mn) NWs) prepared through facile combined electrospinning-hydrothermal processes. The as-prepared samples were thoroughly characterized using X-ray diffraction (XRD), transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and diffuse reflectance spectroscopy (DRS). XRD studies reveal the formation of mixed anatase-rutile phases or rutile phase depending on the dopant (Mn) precursor concentrations in the electrospinning dope and calcination temperature. The evaluation of lattice parameters revealed that the incorporation of Mn species and carbon atoms in to the lattice of anatase or rutile TiO2 could occur through substituting the sites of oxygen atoms. XPS results confirm the existence of Mn2+/Mn3+ within the TiO2 NW. Raman spectroscopy provides the evidence for structural modification because of the graphene inclusion in TiO2 NW. The optical band gap of G-Mn including TiO2 is much lower than pristine TiO2 as confirmed through UV-vis DRS. The photocatalytic activities were evaluated by nitric oxide (NOx) degradation tests under visible light irradiation. Superior catalytic activity was witnessed for rutile G-Mn-co-doped TiO2 NW over their anatase counterparts. The enhanced photocatalytic property was discussed based on the synergistic effects of doped G and Mn atoms and explained by plausible mechanisms.

Highly selective non-enzymatic electrochemical sensor based on a titanium dioxide nanowire-poly(3-aminophenyl boronic acid)-gold nanoparticle ternary nanocomposite.

A novel three component (titanium dioxide nanowire (TiO2 NW), poly(3-aminophenyl boronic acid) (PAPBA) and gold nanoparticles (Au NPs)) based ternary nanocomposite (TNC) (designated as TiO2 NW/PAPBA-Au TNC) was prepared by a simple two-stage synthetic approach and utilized for the fabrication of a non-enzymatic (enzyme-free) glucose (NEG) sensor. In stage 2, the PAPBA-Au NC was formed by oxidative polymerization of 3-APBA using HAuCl4 as oxidant on the surface of pre-synthesized TiO2 NW via electrospinning (stage 1). The formation of PAPBA-Au NC as the shell on the surface of the TiO2 NW (core) was confirmed by field emission scanning electron microscopy (FE-SEM). Notably, we obtained a good peak to peak separation, and a high peak current for the redox Fe(CN)6 3-/4- process indicating excellent electron transfer capability at the glassy carbon electrode (GCE)/TiO2 NW/PAPBA-Au TNC interface. Also, the fabricated TiO2 NW/PAPBA-Au TNC provides excellent electrocatalytic activity towards glucose detection in neutral (pH = 7.0) phosphate buffer solution. The detection of glucose was monitored using differential pulse voltammetry. The obtained sensitivity and detection limits are superior to many of the TiO2 based enzymatic and non-enzymatic glucose sensors reported in the literature. Furthermore, the TiO2 NW/PAPBA-Au TNC sensor is preferred because of its high selectivity to glucose in the presence of co-existing interfering substances and practical application for monitoring glucose in human blood serum samples.

Functional solid additive modified PEDOT:PSS as an anode buffer layer for enhanced photovoltaic performance and stability in polymer solar cells.

Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is most commonly used as an anode buffer layer in bulk-heterojunction (BHJ) polymer solar cells (PSCs). However, its hygroscopic and acidic nature contributes to the insufficient electrical conductivity, air stability and restricted photovoltaic (PV) performance for the fabricated PSCs. In this study, a new multifunctional additive, 2,3-dihydroxypyridine (DOH), has been used in the PEDOT: PSS buffer layer to obtain modified properties for PEDOT: PSS@DOH and achieve high PV performances. The electrical conductivity of PEDOT:PSS@DOH films was markedly improved compared with that of PEDOT:PSS. The PEDOT:PSS@DOH film exhibited excellent optical characteristics, appropriate work function alignment, and good surface properties in BHJ-PSCs. When a poly(3-hexylthiohpene):[6,6]-phenyl C61-butyric acid methyl ester blend system was applied as the photoactive layer, the power conversion efficiency of the resulting PSCs with PEDOT:PSS@DOH(1.0%) reached 3.49%, outperforming pristine PEDOT:PSS, exhibiting a power conversion enhancement of 20%. The device fabricated using PEDOT:PSS@DOH (1.0 wt%) also exhibited improved thermal and air stability. Our results also confirm that DOH, a basic pyridine derivative, facilitates adequate hydrogen bonding interactions with the sulfonic acid groups of PSS, induces the conformational transformation of PEDOT chains and contributes to the phase separation between PEDOT and PSS chains.

Incorporation of silver nanoparticles on the surface of orthodontic microimplants to achieve antimicrobial properties.

OBJECTIVE: Microbial aggregation around dental implants can lead to loss/loosening of the implants. This study was aimed at surface treating titanium microimplants with silver nanoparticles (AgNPs) to achieve antibacterial properties. METHODS: AgNP-modified titanium microimplants (Ti-nAg) were prepared using two methods. The first method involved coating the microimplants with regular AgNPs (Ti-AgNP) and the second involved coating them with a AgNP-coated biopolymer (Ti-BP-AgNP). The topologies, microstructures, and chemical compositions of the surfaces of the Ti-nAg were characterized by scanning electron microscopy (SEM) equipped with energy-dispersive spectrometer (EDS) and X-ray photoelectron spectroscopy (XPS). Disk diffusion tests using Streptococcus mutans, Streptococcus sanguinis, and Aggregatibacter actinomycetemcomitans were performed to test the antibacterial activity of the Ti-nAg microimplants. RESULTS: SEM revealed that only a meager amount of AgNPs was sparsely deposited on the Ti-AgNP surface with the first method, while a layer of AgNP-coated biopolymer extended along the Ti-BP-AgNP surface in the second method. The diameters of the coated nanoparticles were in the range of 10 to 30 nm. EDS revealed 1.05 atomic % of Ag on the surface of the Ti-AgNP and an astounding 21.2 atomic % on the surface of the Ti-BP-AgNP. XPS confirmed the metallic state of silver on the Ti-BP-AgNP surface. After 24 hours of incubation, clear zones of inhibition were seen around the Ti-BP-AgNP microimplants in all three test bacterial culture plates, whereas no antibacterial effect was observed with the Ti-AgNP microimplants. CONCLUSIONS: Titanium microimplants modified with Ti-BP-AgNP exhibit excellent antibacterial properties, making them a promising implantable biomaterial.

Enantioselective Determination of Polycyclic Musks in River and Wastewater by GC/MS/MS.

The separation of chiral compounds is an interesting and challenging topic in analytical chemistry, especially in environmental fields. Enantioselective degradation or bioaccumulation has been observed for several chiral pollutants. Polycyclic musks are chiral and are widely used as fragrances in a variety of personal care products such as soaps, shampoos, cosmetics and perfumes. In this study, the gas chromatographic separation of chiral polycyclic musks, 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclo-penta-γ-2-benzopyrane (HHCB), 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetra-hydronaphthalene (AHTN), 6-acetyl-1,1,2,3,3,5-hexamethylindane (AHDI), 5-acetyl-1,1,2,6-tetramethyl-3-iso-propylindane (ATII), and 6,7-dihydro-1,1,2,3,3-pentamethyl-4(5H)-indanone (DPMI) was achieved on modified cyclodextrin stationary phase (heptakis (2,3-di-O-methyl-6-O-tert-butyl-dimethylsilyl-ß-CD in DV-1701)). Separation techniques are coupled to tandem mass spectrometry (MS-MS), as it provides the sensitivity and selectivity needed. River and wastewaters (influents and effluents of wastewater treatment plants (WWTPs)) in the Nakdong River were investigated with regard to the concentrations and the enantiomeric ratios of polycyclic musks. HHCB was most frequently detected in river and wastewaters, and an enantiomeric enrichment was observed in the effluents of one of the investigated wastewater treatment plants (WWTPs). We reported the contamination of river and wastewaters in Korea by chiral polycyclic musks. The results of this investigation suggest that enantioselective transformation may occur during wastewater treatment.

Direct electrochemistry of cytochrome c immobilized on titanium nitride/multi-walled carbon nanotube composite for amperometric nitrite biosensor.

In this report, titanium nitride (TiN) nanoparticles decorated multi-walled carbon nanotube (MWCNTs) nanocomposite is fabricated via a two-step process. These two steps involve the decoration of titanium dioxide nanoparticles onto the MWCNTs surface and a subsequent thermal nitridation. Transmission electron microscopy shows that TiN nanoparticles with a mean diameter of ≤ 20 nm are homogeneously dispersed onto the MWCNTs surface. Direct electrochemistry and electrocatalysis of cytochrome c immobilized on the MWCNTs-TiN composite modified on a glassy carbon electrode for nitrite sensing are investigated. Under optimum conditions, the current response is linear to its concentration from 1 µM to 2000 µM with a sensitivity of 121.5 µA µM(-1)cm(-2) and a low detection limit of 0.0014 µM. The proposed electrode shows good reproducibility and long-term stability. The applicability of the as-prepared biosensor is validated by the successful detection of nitrite in tap and sea water samples.

Design of Graphene- and Polyaniline-Containing Functional Polymer Hydrogel as a New Adsorbent for Removal of Chromium (VI) Ions.

Hydrogels find applications in various fields, and the ever-growing spectrum of available monomers, crosslinking, and nanotechnologies widen the application of polymer hydrogels. Herein, we describe the preparation of a new graphene (G)- and polyaniline (PANI)-containing functional polymer gel (G/PANI/FG) through a facile crosslinking copolymerization approach. Several characterization techniques such as field-emission scanning electron microscopy, Fourier-transform infrared, and X-ray photoelectron spectroscopy were employed to understand the physicochemical characteristics of the G/PANI/FG. The new G/PANI/FG was used as an adsorbent for chromium (VI) and exhibited the highest Cr (VI) removal efficiency (~97%). The inclusion of G and PANI in the gel results in high surface area, 3D porous structure, and Cr (VI)-chelating amine sites, which enhanced the Cr (VI) removal efficiency and thermal stability of the gel adsorbent. The results of our study revealed that G/PANI/FG is suited for the removal of Cr (VI) from aqueous solution.

Deposition of Poly(diphenylamine-co-3-aminobenzonitrile)/Palladium Nanocomposite Film and Evaluation of Electrocatalytic Activity Toward Borohydride Oxidation.

New nanocomposites, poly(diphenylamine-co-3-aminobenzonitrile)/palladium (P(DPA-co-3ABN)/Pd) and poly(diphenylamine)/palladium (PDPA/Pd), have been prepared by pulse potentiostatic method and used as electrocatalysts for borohydride oxidation. Linear sweep voltammogram of P(DPA-co-3ABN)/Pd-ME exhibited the oxidation wave between -0.8 V and 0.4 V that corresponds to the direct, potentially four-electron, oxidation of borohydride ions. The peak current for borohydride oxidation is much higher at P(DPA-co-3ABN)/Pd-ME electrode as compared to PDPA/Pd-ME. The incorporation of 3ABN units augments electrocatalytic behavior and thermal stability for the P(DPA-co-3ABN)/Pd catalyst.

Sulfated Titania-Silica Reinforced Nafion Nanocomposite Membranes for Proton Exchange Membrane Fuel Cells.

Sulfated titania-silica (SO4(2-)-/TiO2-SiO2) composites were prepared by a sol-gel method with sulfate reaction and characterized by X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDS). The nanometric diameter and geometry of the sulfated titania-silica (STS) was investigated by transmission electron microscopy (TEM). A small amount of the STS composite in the range of 0.5-3 wt% was then added as reinforcing into the Nafion membrane by water-assisted solution casting method to prepare STS reinforced Nafion nanocomposite membranes (STS-Nafion nanocomposite membranes). The additional functional groups, sulfate groups, of the nanocomposite membrane having more surface oxygenated groups enhanced the fuel cell membrane properties. The STS-Nafion nanocomposite membranes exhibited improved water uptake compared to that of neat Nafion membranes, whereas methanol uptake values were decreased dramatically improved thermal property of the prepared nanocomposite membranes were measured by thermogravimetric analysis (TGA). Furthermore, increased ion exchange capacity values were obtained by thermoacidic pretreatment of the nanocomposite membranes.

Synthesis of Magnetic Nanoparticles Incorporated Smart Gel.

In this work, we prepared new poly(vinyl alcohol) (PVA) based magnetic-pH responsive smart gels comprised of nickel nanoparticles and cross-linked PVA with a pH responsive poly(methyl methacrylic acid) (PMAA) (designated as (PVA-PMAA/Ni-NCGs). We developed a strategy based on the modification of PVA with glycidyl methacrylate (GMA) groups, which has the advantage of being highly efficient in preparing cross-linked PVA with pH responsive polymer chains. The PVA(GMA)-PMAA/Ni-NCGs were characterized by X-ray diffraction, scanning electron microscopy, magnetic measurements and thermogravimetric analysis. We report the relationship between macroscopic properties like the swelling ratio and the network microstructure of PVA(GMA)-PMAA/Ni-NCGs. Swelling in water and drying in air were alternately repeated, in which water was exchanged by new water before each swelling experiment. The PVA(GMA)-PMAA/Ni-NCGs can respond to a magnetic field and the pH changes of an environment. We present an example showing that PVA(GMA)-PMAA/Ni-NCGs can be innovatively exploited as a polymeric material in the application of controlled drug release.

Nanophase Changes in Nickel Doped Titania Composites by Thermal Treatment and Photocatalytic Destruction of NO(x).

This study investigated the influence of Ni doping and thermal treatment (600, 800 degrees and 1000 degrees C) on the physiochemical properties of a commercially available low cost KA100 TiO2. Ni containing KA100 samples were prepared with different loading of Ni (3%, 6% and 9% wt to KA100) and subjected to heat treatement at 600 degrees, 800 degrees and 1000 degrees C. The as-prepared samples were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Diffuse reflection UV-Visible spectroscopy and Raman spectroscopy and nitrogen-adsorption-desorption measurements to observe the nanophase changes in the particle characteristics following Ni modification and thermal treatment. The results show that the Ni atom entered the TiO2 lattice structure upon heat treatment at 800 degrees C and 1000 degrees C influencing the anatase-rutile phase transformation. The TiO2 powders after heat treatment had a bimodal pore-size distribution as the temperature of the heat treatment increased. In addition, the anatase crystallite size and average pore sizes increased. Photodegradation of NO(x) was investigated using the Ni doped KA100 as a photocatalyst. Modification of KA100 with nickel and heat treatment up to 1000 degrees C enhanced the photocatalysis for the degradation of NO(x). Typically, KA100 modified with 6% Ni and heat treated to 1000 degrees C exhibited excellent NO(x) removal activity.

Fabrication of New Thermo-pH Responsive Carbon Nanotube Gels.

Stimuli-responsive gels have widespread attraction due to their potential applications. In this work, we have demonstrated the preparation of new multiwall carbon nanotube (MWNT) incorporate multi-responsive (pH and thermal) gels (MWNT-IPN-MRG) though network formation with functional macromolecules that interact each other via hydrogen bonds, covalent networking and temporary associative forces. A simple strategy has been developed to prepare MWNT-IPN-MRG. Typically, surface of MWNTs was facilitated to form network with pH and thermo responsive polymers and converted into smart MWNT-IPN-MRGs. Fourier transform infrared spectroscopy, thermogravimetric analysis and scanning electron microscopy were employed to examine chemical compositions and microstructures of MWNT-IPN-MRGs. The new MWNT-IPN-MRGs showed thermo-pH responsive swelling-deswelling behaviors. The advantageous approach for the preparation of new multiresponsive gel in this study will potentially pave way for the preparation of nanogels for environmental application.