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Infrared Spectrometry (infrared + spectrometry)
Kinds of Infrared Spectrometry Selected AbstractsGraphene-Based Nanoporous Materials Assembled by Mediation of Polyoxometalate NanoparticlesADVANCED FUNCTIONAL MATERIALS, Issue 16 2010Ding Zhou Abstract A kind of graphene-based nanoporous material is prepared through assembling graphene sheets mediated through polyoxometalate nanoparticles. Owing to the strong interaction between graphene and polyoxometalate, 2D graphene sheets with honeycomb-latticed carbon atoms could assemble into a porous structure, in which 3D polyoxometalate nanoparticles serve as the crosslinkers. Nitrogen and hydrogen sorption analysis reveal that the as-prepared graphene-based hybrid material possesses a specific surface area of 680 m2 g,1 and a hydrogen uptake volume of 0.8,1.3 wt%. Infrared spectrometry is used to probe the electron density changes of polyoxometalate particle in the redox-cycle and to verify the interaction between graphene and polyoxometalate. The as-prepared graphene-based materials are further characterized by Raman spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. [source] Accelerated ageing of polypropylene stabilized by phenolic antioxidants under high oxygen pressureJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Emmanuel Richaud Abstract Polypropylene (PP) samples stabilized by a hindered phenol (Irganox 1010) were submitted to thermal ageing at 80°C in air at atmospheric pressure or in pure oxygen at 5.0 MPa pressure. Both the polymer oxidation and the stabilizer consumption were monitored by Infrared spectrometry and thermal analysis. The stabilizer efficiency, as assessed by the ratio induction time/stabilizer concentration is almost constant at atmospheric pressure even when the stabilizer concentration is higher than its solubility limit in PP (0.4% or 24 × 10,3 mol L,1). In contrast, at high pressure, the efficiency decreases almost hyperbolically with the stabilizer concentration when this latter is higher than 6.0 × 10,3 mol L,1. The results indicate the existence of a direct phenol-oxygen reaction negligible at low oxygen pressure but significant at 5.0 MPa pressure. The reality of this reaction has been proved on the basis of a study of the thermal oxidation of a phenol solution in a nonoxidizable solvent. A kinetic model of PP oxidation in which stabilization involves three reactions has been proposed. It simulates correctly the effect of oxygen pressure and stabilizer concentration on carbonyl build-up and stabilizer consumption. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Infrared spectrometry based 13C-octanoic acid breath test in measuring human solid gastric emptyingJOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, Issue 1 2003CHIH-PING CHEN Abstract Background and Aims: Because of the convenience of non-dispersive infrared spectrometry (NDIRS), we attempted to validate the usefulness of NDIRS compared with scintigraphy in human solid gastric emptying (GE) measurement, and tried to establish the normal range of solid GE based on NDIRS. Methods: Twelve healthy volunteers (three men, nine women) were recruited for simultaneous scintigraphy and 13C-octanoic acid breath test (13C-OABT) studies. Stomach half-emptying time (t1/2) and lag phase (tlag) were the two main GE parameters measured and correlated. The breath samples were analyzed using NDIRS every 10,15 min for a total of 6 h, while scintigraphy was taken minute by minute for the first 30 min, then hourly for 4 h. Another 32 healthy volunteers (19 men, 13 women) received only the 13C-OABT to measure their solid GE. Results: A significant correlation for t1/2 was found between the breath test and scintigraphy (r = 0.85, P = 0.001), while tlag was also positively correlated (r = 0.73, P = 0.007). The reference range of t1/2B based on all 44 subjects was 89.4,185.1 min (135.9 ± 21.1 min (mean ± SD)), while the range for tlagB was 37.1,117.8 min (81.9 ± 17.4 min). No demographic characteristics were found to influence the GE parameters. Conclusions:13C-octanoic acid breath test determined by NDIRS is a simple, non-invasive and reliable measurement, which may provide an ,office-based' tool to detect solid GE. © 2003 Blackwell Publishing Asia Pty Ltd [source] Curing kinetics of boron-containing phenol,formaldehyde resin formed from paraformaldehydeINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 11 2002Yanfang Liu A boron-containing phenol,formaldehyde resin (BPFR) was synthesized from boric acid, phenol, and paraformaldehyde. The curing reaction of BPFR was studied by Fourier-transform infrared spectrometry and differential scanning calorimetry. According to the heat evolution behavior during the curing process, several influencing factors on isothermal curing reaction were evaluated. The results show that the isothermal kinetic reaction of BPFR follows autocatalytic kinetics mechanism, and kinetic parameters m, n, k1, and k2, were derived, respectively. In the latter reaction stage, the curing reaction becomes controlled mainly by diffusion. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 638,644, 2002 [source] Les fards rouges cosmétiques et rituels a base de cinabre et d'ocre de l'époque punique en Tunisie: analyse, identification et caractérisationINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 5 2001A. Alatrache Synopsis Natural antique colorants include mainly red pigments such as cinnabar and ochre. These archeological pigments were used especially as funeral and cosmetic makeup and are a material proof of handicraft activities and exchanges. The identification and characterization of a group of punic colorants, corresponding to samples discovered during excavations at several Tunisian archeological sites (Cartage, Ksour Essef, Kerkouane, Bekalta, Makthar, Bou Arada), were conducted using the least destructive analysis techniques such us scanning electron microscopy coupled to X-ray fluorescence microprobe, direct current plasma emission spectroscopy, atomic absorption spectrometry, Fourier transform infrared spectrometry and X-ray diffraction. Eleven natural red colorants from punic period were subject to this investigation and were compared to contemporary substances. Five colorants were cinnabar and the other six were ochre. Résumé Les colorants antiques naturels comportent principalement les pigments rouges tels que le cinabre et l'ocre. Ces pigments archéologiques ont été utilisés spécialement comme fards funéraires et cosmétiques, qui sont des témoins matériels d'activités artisanales et d'échanges. La caractérisation et l'identification d'un ensemble de colorants puniques correspondant à des échantillons découverts lors des fouilles sur divers sites de Tunisie (Carthage, Ksour Essef, Kerkouane, Bekalta, Makthar, Bou Arada) ont été conduites en employant des techniques d'analyse les moins destructives possibles telles que la microscopie électronique à balayage (MEB) couplée à une microsonde de fluorescence X (XRF), les spectrométries d'émission plasma à courant direct (DCP), d'absorption atomique (SAA) et infrarouge à transformée de Fourier (FTIR) et la diffraction aux rayons X (RX). Onze colorants naturels rouges puniques ont été soumis à l'étude et comparés avec des matières contemporaines. Cinq d'entre eux sont des composés de cinabre, les six autres des ocres. [source] In situ generated hydroxyl-terminated polybutadiene nanoparticles in polyimide filmsADVANCES IN POLYMER TECHNOLOGY, Issue 1 2009Anand Kumar Gupta Abstract Polyimide (PI) has been extensively investigated as matrices for blends in the search for novel materials for microelectronics and engineering application. The processing of the PI with hydroxyl-terminated polybutadiene (HTPB) offers a considerable advantage to develop a material having good mechanical and thermal stability. Taking this into account, the HTPB was blended with polyamic acid, which is precursor to PI to form PI + HTPB films. A number of properties were evaluated for PI + HTPB films with ultra low concentrations of HTPB. The films prepared with ultra low concentration (10,3,1 wt%) showed unusual synergism, which is attributed to the presence of in situ generated micro/nanostructures derived from HTPB. The microhardness study was used to elucidate the actual mechanical performance due to structure formation of HTPB in a nanometer regime within PI matrix. Atomic force microscopy analysis confirmed the dispersion of HTPB at nano regime within PI matrix. The enhanced thermal stability as determined by thermogravimetric analyzer and Fourier transform infrared spectrometry was attributed to the presence of micro/nanoparticle of HTPB within the PI matrix. The water absorption isotherms were measured and their abnormal behavior was correlated with micro-/nano-sized particles in the PI/HTPB film. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:48,59, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20144 [source] Ceric ammonium sulfate/sodium disulfite initiated grafting of acrylamide on to Cassia reticulata seed gumJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Vandana Singh Abstract Ceric ammonium sulfate/sodium disulfite redox system was evaluated for the poly(acrylamide) (PAM) grafting on to Cassia reticulata (CR) seed gum. Grafting conditions were optimized and the maximum %Grafting (%G) and %Efficiency (%E) achieved were 152 and 97.2%, respectively, using [disulfite] 0.005M; [ceric ammonium sulfate] 0.026M; [acrylamide] 0.11M; [gum] 0.125 g/25mL at 40 ± 0.2°C. Representative CR-grafted gum (CRPAM) was characterized by Fourier transform infrared spectrometry (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Under identical conditions, the redox initiator could result 142.6 %G and 91.2 %E on to guar gum (GG). Various physical properties of the CR gum/grafted CR gum, such as viscosity, water retention, and saline retention, were studied and compared with GG/grafted GG to find out the potential industrial use of CR gum and PAM- grafted -CR gum. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] CHRACTERIZATION AND 1,1-DIPHENYL-2-PICRYLHYDRAZYL RADICAL SCAVENGING ACTIVITY OF METHANOL AND SUPERCRITICAL CARBON DIOXIDE EXTRACTS FROM LEAVES OF ADINANDRA NITIDAJOURNAL OF FOOD BIOCHEMISTRY, Issue 4 2008BENGUO LIU ABSTRACT Leaves of Adinandra nitida are consumed in southern China as health tea (Shiyacha) and as herbal medicine. In this study, the methanol and supercritical fluid extracts from leaves of A. nitida were obtained by traditional solvent extraction and supercritical carbon dioxide extraction, respectively. Both the extracts showed high 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity. By using ultraviolet-visible spectrometry (UV), infrared spectrometry (IR), nuclear magnetic resonance, electrospray ionization mass spectrometry (ESI-MS), high-performance liquid chromatography-ESI/MS, the main bioactive constituents in the methanol extract (ME) were identified as camellianin A, camellianin B, apigenin. By analysis of gas chromatography-mass spectrometry, a total of 16 compounds accounting for 98.79% of the supercritical fluid extract (SFE) were identified as ,-sitosterol, vitamin E, ,-tocopherol and so on. These compounds found in ME and SFE could contribute to the DPPH radical scavenging performance of the extracts in this study. PRACTICAL APPLICATION Adinandra nitida is a kind of particular wild plant in South China. Few reports have been published about it in the world. In this study, the methanol and supercritical fluid extracts from leaves of A. nitida were respectively obtained by two kinds of industrially significant methods, traditional solvent extraction and supercritical carbon dioxide extraction. By using ultraviolet-visible spectrometry (UV), infrared spectrometry (IR), nuclear magnetic resonance, electrospray ionization mass spectrometry (ESI-MS), high-performance liquid chromatography-ESI/MS, gas chromatography-MS, the main bioactive constituents in the two extracts were identified as flavonoids and plant sterols. Both the extracts showed high 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity and this activity of the flavonoid-rich methanol extract was 10 times more than that of butylated hydroxytoluene. These results showed that leaves of A. nitida is a new kind of natural antioxidant-rich, flavonoid-rich plant source with great commercial interest in the food and phytopharmaceutical market. [source] Infrared spectrometry based 13C-octanoic acid breath test in measuring human solid gastric emptyingJOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, Issue 1 2003CHIH-PING CHEN Abstract Background and Aims: Because of the convenience of non-dispersive infrared spectrometry (NDIRS), we attempted to validate the usefulness of NDIRS compared with scintigraphy in human solid gastric emptying (GE) measurement, and tried to establish the normal range of solid GE based on NDIRS. Methods: Twelve healthy volunteers (three men, nine women) were recruited for simultaneous scintigraphy and 13C-octanoic acid breath test (13C-OABT) studies. Stomach half-emptying time (t1/2) and lag phase (tlag) were the two main GE parameters measured and correlated. The breath samples were analyzed using NDIRS every 10,15 min for a total of 6 h, while scintigraphy was taken minute by minute for the first 30 min, then hourly for 4 h. Another 32 healthy volunteers (19 men, 13 women) received only the 13C-OABT to measure their solid GE. Results: A significant correlation for t1/2 was found between the breath test and scintigraphy (r = 0.85, P = 0.001), while tlag was also positively correlated (r = 0.73, P = 0.007). The reference range of t1/2B based on all 44 subjects was 89.4,185.1 min (135.9 ± 21.1 min (mean ± SD)), while the range for tlagB was 37.1,117.8 min (81.9 ± 17.4 min). No demographic characteristics were found to influence the GE parameters. Conclusions:13C-octanoic acid breath test determined by NDIRS is a simple, non-invasive and reliable measurement, which may provide an ,office-based' tool to detect solid GE. © 2003 Blackwell Publishing Asia Pty Ltd [source] Characterization and use of acid-activated montmorillonite-illite type of clay for lead(II) removalAICHE JOURNAL, Issue 9 2010John U. Kennedy Oubagaranadin Abstract The natural local deposits of montmorillonite-illite type of clay (MIC) were susceptible for acid activation. Raw clay was taken for experimentation, disintegrated on acid activation with sulfuric acid, which showed a particle size distribution. The montmorillonite and illite phases in the raw clay disappeared on acid activation and the activated clay, MIC(AA), showed with sodium-aluminum-silicate and beidellite phases apart from quartz (low) phase. The raw and acid-activated clays were characterized using X-ray powder diffractometry, X-ray fluorescence, Fourier transform infrared spectrometry, and energy dispersive X-ray, and their adsorption capacities were compared. When tested for adsorption of Pb(II) in aqueous solutions, the acid-activated clay showed about 50% increased adsorption than raw clay. Sips adsorption isotherm and pseudo-second-order kinetic models were found to be best for the batch adsorption data. Kinetic studies showed the existence of film diffusion and intraparticle diffusion. A two-stage batch adsorber was designed for the removal of Pb(II) from aqueous solutions. © 2010 American Institute of Chemical Engineers AIChE J, 2010 [source] Cefuroxime axetil solid dispersions prepared using solution enhanced dispersion by supercritical fluidsJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 12 2005Seoung Wook Jun Cefuroxime axetil (CA) solid dispersions with HPMC 2910/PVP K-30 were prepared using solution enhanced dispersion by supercritical fluids (SEDS) in an effort to increase the dissolution rate of poorly water-soluble drugs. Their physicochemical properties in solid state were characterized by differential scanning calorimeter (DSC), powder X-ray diffraction (PXRD), Fourier transform infrared spectrometry (FT-IR) and scanning electron microscopy. No endothermic and characteristic diffraction peaks corresponding to CA were observed for the solid dispersions in DSC and PXRD. FTIR analysis demonstrated the presence of intermolecular hydrogen bonds between CA and HPMC 2910/PVP K-30 in solid dispersions, resulting in the formation of amorphous or non-crystalline CA. Dissolution studies indicated that the dissolution rates were remarkably increased in solid dispersions compared with those in the physical mixture and drug alone. In conclusion, an amorphous or non-crystalline CA solid dispersion prepared using SEDS could be very useful for the formulation of solid dosage forms. [source] The Role of Oxidation in the Migration Mechanism of Layered Silicate in Poly(propylene) NanocompositesMACROMOLECULAR RAPID COMMUNICATIONS, Issue 9 2006Mauro Zammarano Abstract Summary: Evidence of clay migration from the core to the surface of poly(propylene)/montmorillonite nanocomposites is provided. A three- to fivefold increase in the clay concentration of the surface is obtained during isothermal heating in oxidative atmosphere. The mechanism of migration is investigated by means of attenuated total reflectance Fourier transform infrared spectrometry. It is shown that oxygen plays a fundamental role in the migration mechanism. ,Si versus c for the annealed samples. [source] The effect of nitrogen incorporation on surface properties of silicon oxynitride filmsPHYSICA STATUS SOLIDI - RAPID RESEARCH LETTERS, Issue 1 2009Jongin Hong Abstract In order to investigate the surface heterogeneity of silicon oxynitride films, we observed the nanoscale variation of the surface potential by Kelvin probe force microscopy (KFM), the molecular bonding characteristics by Fourier transform infrared spectrometry (FTIR), and the wetting behavior by contact angle measurement. Nitrogen incorporation into silicon oxynitride films influenced the decrease in the surface potential and the polar component of the surface free energy. We present the first correlation between the nanoscale measurement of the surface potential and the macroscopic measurement of the surface free energy in silicon oxynitride films grown by a standard plasma-enhanced chemical vapor deposition (PECVD) technique. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Calcium oxalate and sulphate-containing structures on the thallial surface of the lichen Ramalina lacera: response to polluted air and simulated acid rainPLANT CELL & ENVIRONMENT, Issue 12 2002J. GARTY Abstract The formation of calcium-containing structures on the thallial surface of the lichen Ramalina lacera (With.) J.R. Laund. in response to air pollution and to simulated acid rain, was studied in in situ and transplanted thalli. In situ thalli were collected from an unpolluted site and transplanted to heavily polluted and less polluted sites for a 10 month period. Additional thalli were treated either with double distilled water or with simulated acid rain. Scanning electron microscopy and infrared spectrometry revealed that thallial surfaces of in situ R. lacera samples collected in unpolluted sites were covered with two kinds of calcium oxalate crystals: whewellite and weddellite. These aggregates of calcium oxalate crystals appear to disintegrate and provide a crystal layer on the thallial surface. Infrared spectroscopy of powder scraped from thallial surfaces of transplants, retrieved from non-polluted sites, showed the presence of whewellite and weddellite, whereas powders obtained from thalli retrieved from polluted sites contained whewellite, weddellite and gypsum. It is suggested that a certain fraction of the gypsum detected in crater-like structures in transplants from polluted sites and in thalli treated with simulated acid rain is endogenous and should be considered a biomineral. [source] Interfacial interactions and performance of polyamide 6/modified attapulgite clay nanocompositesPOLYMER COMPOSITES, Issue 2 2009Bingli Pan Attapulgite (AT) clay was firstly treated with sodium polyacrylate (PAS), then polyamide 6 (PA6)/AT nanocomposites were prepared by simple melt compounding. Transmission electron microscope (TEM) and Fourier transform infrared spectrometry (FT-IR) of treated AT confirm the success of purifying and surface modification of the original AT by PAS. X-ray diffraction spectra for the nanocomposites show that the microstructure of AT in PA6 matrix is almost unchanged. It indicates that a strong interfacial adhesion exists between AT and PA6 matrix through analyzing fracture surfaces of the nanocomposites, the variation of glass transition temperature (Tg) obtained by dynamic mechanical analysis, and interfacial interaction factors; field emission scanning electron microscopy on the fracture surfaces of the nanocomposites shows that a uniform dispersion of AT is obtained. The above two aspects conform to the improvement of mechanical and thermal properties of the nanocomposites. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Synthesis and thermal properties of ester-type crosslinked epoxy resins derived from lignosulfonate and glycerolPOLYMER INTERNATIONAL, Issue 2 2010Tuan Noor Maznee Tuan Ismail Abstract Among various biomass-based components, both lignin and glycerol are important, since they are abundantly produced as by-products in industrial processes. Accordingly, in the present study, new types of crosslinked epoxy resins were synthesized from lignin and glycerol. Polymers derived from two types of lignin-based crosslinked epoxy resins were prepared through two-step reactions, ester-carboxylic acid derivative preparation followed by crosslinked epoxy resin preparation, in order to establish a crosslinked epoxy resin system in which glycerol units were included. The resins obtained were labeled as follows: series 1, lignosulfonate-glycerol polyacid (Ser1LSGLYPA); and series 2, glycerol diglycidyl ether (Ser2GLYDGE). The functional groups of the resins were analyzed using Fourier transform infrared spectrometry. The thermal properties of the resins were analyzed using differential scanning calorimetry and thermogravimetry. The glass transition temperature of the crosslinked epoxy resins increased with increasing LSGLYPA and GLYDGE contents for Ser1LSGLYPA and Ser2GLYDGE, respectively. The thermal degradation temperature for Ser1LSGLYPA and Ser2GLYDGE did not show significant change, suggesting that the crosslinked epoxy resins were thermally stable. The mass residue at 500 °C was not affected by the changes of LSGLYPA and GLYDGE contents. Copyright © 2009 Society of Chemical Industry [source] Interfacial polymerization of morphologically modified polyaniline: from hollow microspheres to nanowiresPOLYMER INTERNATIONAL, Issue 2 2008Jinbo Li Abstract BACKGROUND: Polyaniline (PANI) has attracted much attention in many fields due to its chemical and physical properties, and different nanostructures of PANI changing from one-dimensional to three-dimensional have been obtained. By changing the concentration of cetyltrimethylammonium bromide (CTAB), the morphology of hydrochloric acid-doped polyaniline could be changed from one-dimensional nanoneedles or nanowires with a network structure (50,100 nm in diameter) to three-dimensional hollow microspheres (ca 400 nm in outer diameter) via combining interfacial polymerization and self-assembly process. RESULTS These different nanostructures of PANI were proved using scanning electron and transmission electron microscopies. A plausible mechanism of the formation of the changeable nanostructures of PANI may be different from that of interfacial polymerization without surfactant or a traditional homogenous reaction system using CTAB as surfactant. CONCLUSION The results obtained from Fourier transform infrared spectrometry, X-ray diffraction and the four-probe method showed that the molecular structure of PANI does not change with increasing CTAB concentration, but crystallinity and conductivity of PANI increase with surfactant concentration. Copyright © 2007 Society of Chemical Industry [source] Synthesis and characterization of polyurethane/polybenzoxazine-based interpenetrating polymer networks (IPNs)POLYMER INTERNATIONAL, Issue 8 2003Yanjun Cui Abstract Sequential interpenetrating polymer networks (IPNs), based on polyurethane and polybenzoxazine, were synthesized. Fourier Transform infrared spectrometry was employed to monitor the formation kinetics, which indicated that only physical bonding existed in the resulting IPNs. Morphological investigations revealed a lightly phase separation behaviour in all of the IPNs studied. © 2003 Society of Chemical Industry [source] Effect of conjugated linoleic acid grafting on the hemocompatibility of polyacrylonitrile membranePOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 6 2006Fu-Chen Kung Abstract Polyacrylonitrile (PAN) membrane was hydrolyzed with NaOH(aq) and grafted with conjugated linoleic acid (CLA) via esterification with 1,3-propanediol. The resulting CLA grafted PAN membranes were characterized using Fourier transform infrared spectrometry (FT-IR) and X-ray photoelectronic spectroscopy (XPS). The effects of CLA grafting on the blood coagulation, platelet aggregation, and oxidative stress were evaluated using human blood. The complete blood count (CBC) and coagulation time (CT) was evaluated in vitro for hemocompatibility. After CLA grafting, the proliferation of human umbilical vein endothelial cells (HUVECs) on the membranes were improved. In addition, the production of reactive oxygen species (ROS) was measured by the chemiluminescence (CL) method to evaluate the oxidative stress. The results showed that the CLA-grafted PAN membrane could keep the CBC values more stable than unmodified PAN membrane. The CLA-grafted PAN membranes also showed longer CT. CLA-grafted PAN membrane could keep the CL counts of hydrogen peroxide and superoxide values more stable than unmodified PAN membrane. These results suggest that a CLA-grafted PAN membrane could offer protection for patients against oxidative stress and would be helpful for reducing the dosage of anticoagulant during hemodialysis. Copyright © 2006 John Wiley & Sons, Ltd. [source] UV curing kinetics and mechanism of a highly branched polycarbosilaneAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 1 2009Houbu Li Abstract The UV curing process in both air and nitrogen atmosphere for the highly branched polycarbosilane system was investigated by differential scanning photo calorimeter. The UV cured products were characterized by Fourier-transform infrared spectrometry (FTIR). By comparison with the FTIR results of the uncured liquid mixture and the cured samples, the possible cross-linking reactions were determined. The kinetics of the curing systems was studied. The rate constant k was calculated based on the experimental results. The activation energies in different curing conditions were obtained. According to these results, it was learned that the mechanism for the UV curing in nitrogen was controlled by the photolysis of photoinitiator. Comparably, the UV curing process in air was complicated. It was affected by not only the photolysis of photoinitiator, but also oxygen and tripropane glycol diacrylate. Copyright © 2008 John Wiley & Sons, Ltd. [source] Fungal biodegradation of hard coal by a newly reported isolate, Neosartorya fischeriBIOTECHNOLOGY JOURNAL, Issue 11 2008Eric E. Igbinigie Abstract Cynodon dactylon (Bermuda grass) has been observed to grow sporadically on the surface of coal dumps in the Witbank coal mining area of South Africa. Root zone investigation indicated that a number of fungal species may be actively involved in the biodegradation of hard coal, thus enabling the survival of the plant, through mutualistic interaction, in this extreme environment. In an extensive screening program of over two thousand samples, the Deuteromycete, Neosartorya fischeri, was isolated and identified. The biodegradation of coal by N. fischeri was tested in flask studies and in a perfusion fixed-bed bioreactor used to simulate the coal dump environment. The performance of N. fischeri was compared to Phanaerochaete chrysosporium and Trametes (Polyporus) versicolor, previously described in coal biodegradation studies. Fourier transform infrared spectrometry and pyrolysis gas chromatography mass spectrometry of the biodegradation product indicated oxidation of the coal surface and nitration of the condensed aromatic structures of the coal macromolecule as possible reaction mechanisms in N. fischeri coal biodegradation. This is a first report of N. fischeri -mediated coal biodegradation and, in addition to possible applications in coal biotechnology, the findings may enable development of sustainable technologies in coal mine rehabilitation. [source] Morphology Investigation of Electrolessly Deposited Ag Film on Ag-Activated p-Type Silicon(111) WaferCHINESE JOURNAL OF CHEMISTRY, Issue 4 2006Hao Tong Abstract A method of electroless silver deposition on silver activated p-type silicon(111) wafer was proposed. The silver seed layer was deposited firstly on the wafer in the solution of 0.005 mol/L AgNO3+0.06 mol/L HF. Then the silver film was electrolessly deposited on the seed layer in the electroless bath of AgNO3+NH3+acetic acid+NH2NH2 (pH 10.2). The morphology of the seed layer and the silver films prepared under the condition of the different bath composition was compared by atomic force microscopy. The reflectance of the silver films with different thickness was characterized by Fourier transform infrared spectrometry. The experimental results indicate that the seed layer possesses excellent catalytic activity toward electroless silver deposition and rotating of the silicon wafer during the electroless silver deposition could lead to formation of the smoother silver film. [source] Novel anti-bacterial acid dyes derived from naphthalimide: synthesis, characterisation and evaluation of their technical properties on nylon 6COLORATION TECHNOLOGY, Issue 2 2010Zinat Mohammadkhodaei As an attempt to combine the dyeing and functional finishing steps into one process, two novel anti-bacterial monoazo acid dyes based on N -ester-1,8-naphthalimide were synthesised. To do this, 4-amino- N -ethyl glycinate-1,8-naphthalimide was prepared, diazotised and then coupled to thiosalicylic acid or salicylic acid to produce anti-bacterial dyes. The synthesised dyes were purified and then fully characterised using Fourier Transform,infrared spectrometry, proton nuclear magnetic resonance spectroscopy and melting point analysis. Dispersion of the dyes was prepared in water and applied to nylon 6 fabrics. The novel dyes offered good build-up properties on the substrate. The anti-bacterial efficacy of the synthesised dyes was assessed, with the dyes showing activity against both Gram-positive and Gram-negative bacteria. [source] | |||||||||||||||||||