Influence of pyrolytic carbon coatings on complex permittivity and microwave absorbing properties of Al_2O_3 fiber woven fabrics

The pyrolytic carbon （PyC） coatings were fabricated on A1203 fiber fabrics by the method of chemical vapor deposition （CVD）. The microstructures of A1203 fibers with and without PyC coatings were characterized by SEM and Raman spectroscopy. The influence of deposition time of PyC on the DC conductivity （ad） of A1203 filaments and complex permittivity of fabrics at X band （8.2-12.4 GHz） were investigated. The values of Crd and complex permittivity increase with increasing deposition time of PyC. The electron relaxation polarization and conductance loss were supposed to be contributed to the increase of ε＇ and ε＂, respectively. In addition, the reflection loss （RL） of fabrics was calculated. The results show that the microwave absorbing properties of Al2O3 fiber fabrics can be improved by PyC coatings. The best RL results are for 60 min-deposition sample, of which the minimum value is about -40.4 dB at about 9.5 GHz and the absorbing frequency band （AFB） is about 4 GHz.

Effect of Catalyst Properties on Hydrocracking of Pyrolytic Lignin to Liquid Fuel in Supercritical Ethanol

The metal-acid bifunctional catalysts have been used for bio-oil upgrading and pyrolytic lignin hydrocracking. In this work, the effects of the metal-acid bifunctional catalyst prop- erties, including acidity, pore size and supported metal on hydrocracking of pyrolytic lignin in supercritical ethanol and hydrogen were investigated at 260 ℃. A series of catalysts were prepared and characterized by BET, XRD, and NHa-TPD techniques. The results showed that enhancing the acidity of the catalyst without metal can promote pyrolytic lignin poly- merization to form more solid and condensation to produce more water. The pore size of microporous catalyst was smaller than mesoporous catalyst. Together with strong acid- ity, it caused pyrolytic lignin further hydrocrack to numerous gas. Introducing Ru into acidic catalysts promoted pyrolytic lignin hydrocracking and inhibited the polymerization and condensation, which caused the yield of pyrolytic lignin liquefaction product to increase significantly. Therefore, bifunctional catalyst with high hydrocracking activity metal Ru supported on materials with acidic sites and mesopores was imperative to get satisfactory results for the conversion of pyrolytic lignin to liquid products under supercritical conditions and hydrogen atmosphere.

Effects of Preform and Pyrolytic Carbon Structure on Thermophysical Properties of 2D Carbon／Carbon Composites

Four kinds of carbon/carbon (C/C) composites, including the needled carbon fiber felt/the pyrolytic carbon (two different pyrolytic carbon microstructures), the chopped carbon fiber/the resin + pyrolytic carbon (PyrC), and the carbon cloth/PyrC, named as the composites 1#, 4#, 2#, and 3#, are prepared respectively. Effects of the preform and pyrolytic carbon structure on the thermophysical properties of 2D C/C composites are studied. The C/C composites possess low coefficient of thermal expansion (CTE). In a range of some temperatures, the negative expansion emerges in x-y direction for four C/C composites. From 0 to 900℃, the CTE is small and almost linear with the temperatures. The C/C composites have high thermal conductivities (TCs). As a function of temperature, TCs of the C/C composites are varied with the structures of preform and pyrc as well as the direction of heat transfer. In x-y and z direction, TCs differ greatly and that in x-y direction (25.6-174 W/m·K) is several times larger than that in z direction(3.5-50 W/m·K).

Intensification of adsorption process by using the pyrolytic char from waste tires to remove chromium(Ⅵ) from wastewater

Pyrolysis has the potential of transforming waste into valuable recyclable products. Pyrolytic char(PC) is one of the most important products from the pyrolysis of used tires. One of the most significant applications for pyrolytic char recovered is used for the removal of Cr(Ⅵ) in the wastewater effluent to control waste by waste. The surface chemistry properties of surface element distribution / concentration and chemical structure were examined for the pyrolytic char and the commercial activated carbon(CAC) respectively. The results showed that surfaces of PC possesses a large amount of ester and hydrocarbon graft, whereas there are mainly carbon functional components of C—OH, C O and COOH on the surface of CAC. Therefore the surface electronegativity of PC is lower than that of CAC in the water. The repulsive interactions between the surfaces of PC and the negatively charged Cr(Ⅵ) ion are weaker than that of CAC, which results in an intensification of the adsorption process by the utilization of PC. The adsorption isotherms of Cr(Ⅵ) ion on the two kinds of carbons were determined experimentally. The larger adsorption amount on the PC in the case of Cr(Ⅵ) may be attributed mainly to its special surface micro-chemical environment. The mechanism of the removal Cr(Ⅵ) from aqueous solution was assumed to be the integration of adsorption and redox reaction. The adsorption was the rate-controlled step for Cr(Ⅵ) removal. The adsorption of Cr(Ⅵ) was identified as pseudo-second-order kinetics. The rate constants of adsorption were evaluated.

Characterization of Pyrolytic Lignin Extracted from Bio-oil

Bio-oil is a new liquid fuel produced by fast pyrolysis,which is a promising technology to convert bio-mass into liquid. Pyrolytic lignin extracted from bio-oil,a fine powder,contributes to the instability of bio-oil. The paper presents the structural features of three kinds of pyrolytic lignin extracted from bio-oil with different methods(WIF,HMM,and LMM) . The pyrolytic lignin samples are characterized by Fourier transform infrared spectrometer(FTIR) and X-ray photoelectron spectroscopy(XPS) . FTIR data indicate that the three pyrolytic lignin samples have similar functional groups,while the absorption intensity is different,and show characteristic vibra-tions of typical lignocellulosic material groups O H(3340-3380 cm-1) ,C H(2912-2929 cm-1) and C O(1652-1725 cm-1) . Comparison in the region(3340-3380 cm-1) indicates that WIF has more O H stretch groups than HMM and LMM. The carbon spectra are fitted to four peaks:C1,C C or C H,BE 283.5 eV;C2,C OR or C OH,BE 284.5-285.8 eV;C3,C O or HO C OR,BE 286.10-287.10 eV;C4,O C O,BE 287.5-287.7 eV. The absence of C1,C C or C H indicates the dominant polymerization structure of aro-matic carbon in pyrolytic lignin samples. For HMM and WIF,C2a and C2b can not be separated,so there is no free hydroxyl group in the samples. The oxygen peaks are also fitted to four peaks:O1,OH,BE = 530.3 eV;O2,RC O,BE 531.45-531.72 eV;O3,O C O,BE = 532.73-533.74 eV;O4,H2O,BE 535 eV. The absence of O1 and O4 indicates that little hydroxyl groups and adsorbed water are present in the samples.

Electrochemical preparation and characterization of gold-polyaniline core-shell nanocomposites on highly oriented pyrolytic graphite

A simple electrochemical method for the in situ preparation of homogeneously dispersed gold-polyaniline core/shell nanocomposite particles with controlled size on the highly oriented pyrolytic graphite(HOPG)was demonstrated.The HOPG surface was modified preferentially by covalent bonding of a two-dimensional 4-aminophenyl monolayer employing diazonium chemistry.AuCl4 -ions were attached to the Ar-NH2 termination and reduced electrochemically.This results in the formation of Au nuclei that could be further grown into gold nanoparticles.The formation of polyaniline as the shell wrap of Au nanoparticle was established by localized electro-polymerization.These core-shell nanocomposites prepared were characterized by AFM and cyclic voltammetry.The results show that the gold-polyaniline core-shell composites on HOPG have a mean particle size of 100 nm in diameter and the polyaniline shell thickness is about 15 nm.

Characterization of pyrolytic lignins with different activities obtained from bio-oil

Pyrolytic lignin, the water-insoluble fraction in bio-oil, often shows a high content and has strong intermolecular interactions with other compounds in bio-oil. In order to obtain pure pyrolytic lignin and facilitate the utilization of aqueous phase obtained from water extraction of bio-oil, methanol–water extraction method was employed to further separate the bio-oil water-insoluble phase in this paper. Different technologies, including Fourier transform infrared spectroscopy, gel permeation chromatography, and nuclear magnetic resonance, were adopted to characterize the structures of pyrolytic lignins with different activities obtained through this method. Both the heating value and the polymerization degree of high-molecular-weight pyrolytic lignin were higher than those of low-molecular-weight pyrolytic lignin. The molecular weight distribution of high-molecular-weight pyrolytic lignin was relatively wider, among which the contents of dimers to pentamers all accounted for 12% –18%,while the low-molecular-weight pyrolytic lignin mainly consisted of trimers(75.38%). The pyrolytic lignins had similar basic structures, both of which contained syringyl and guaiacyl units, whereas the low-molecular-weight pyrolytic lignin had more abundant syringyl units, reactive carbonyl groups and hydroxyl groups. Meanwhile,thermogravimetric study revealed that the final char residue yield of low-molecular-weight pyrolytic lignin was lower than that of high-molecular-weight pyrolytic lignin.

Microwave dielectric properties of Nextel-440 fiber fabrics with pyrolytic carbon coatings in the temperature range from room temperature to 700℃

Pyrolytic carbon(PyC) coatings are deposited on the Nextel-440 fiber fabrics by chemical vapor deposition(CVD).The dielectric properties of the Nextel-440 fiber fabrics with PyC coatings(Nextel-440/PyC) are investigated in a temperature range from room temperature to 700℃ in X-band. Compared with the permittivity of the original Nextel-440 received,the complex permittivity of the Nextel-440/PyC(the real part εand the imaginary part ε), is significantly improved: εof the Nextel-440/PyC has a positive temperature coefficient, in contrast, εof the Nextel-440/PyC exhibits a negative temperature coefficient. Moreover, the reflection loss in units of d B is calculated. The results indicate that the microwave absorbing properties of the Nextel-440/PyC coatings is enhanced at 700℃ compared with that at lower temperatures.

The Electrocatalytic Activity of Bare Pyrolytic Graphite and Single Wall Carbon Nanotube Modified Glassy Carbon Sensors Is Same for the Quantification of Bisoprolol Fumarate

A comparison of voltammetric behavior of bisoprolol fumarate (BF) at edge and basal plane pyrolytic graphite electrodes (EPPGE/BPPGE) has been made with single wall carbon nanotube modified glassy carbon. The electrochemical properties are investigated exercising the cyclic voltammetry and square wave voltammetry (SWV). Enhanced peak current associated with bisoprolol fumarate oxidation at EPPGE is due to its better electron transfer property. Quantification of bisoprolol fumarate was carried out at pH 7.2 at both the pyrolytic graphite electrodes. Well-defined peak has been observed at ~ 792 and 954 mV at EPPGE and BPPGE respectively for bisoprolol fumarate oxidation. The detection limit is found to be 2.8 × 10–7 M and 7.3 × 10–7 M for EPPGE and BPPGE respectively. A comparison of common quantification parameters for bisoprolol at carbon nanotube modified glassy carbon electrode and bare BPPGE and EPPGE has been made and it is observed that carbon naotube modified glassy carbon exhibits sensitivity and detection limit close to that observed at bare basal plane pyrolytic graphite electrode. The method developed is applicable for determination of bisoprolol fumarate in pharmaceutical preparations and real samples.

Study on the Pyrolytic Carbon Generated by the Electric Heating CVD Method

A new method of fabricating C/C composite materials, namely electric heating CVD method, was used, which electrified the carbon fiber directly by using the conductivity of itself. Acetylene was used as the carbon source with nitrogen as dilution gas, and the pyrolytic carbon started to deposit on the carbon fiber surface when the deposition temperature was reached. The morphology of pyrolytic carbon was characterized by SEM, and the surface properties of carbon fibers before and after CVD were characterized by Raman spectroscopy. The experimental results show that the electric heating method is a novel method to fabricate C/C composite materials, which can form a dense C/C composite material in a short time. The order degree and the average crystallite size of the carbon fiber surface were decreased after the experiment.

Observations on Durability of a Pyrolytic Carbon Bileaflet Mechanical Heart Valve

This study aims to observe the durability of a pyrolytic carbon bileaflet mechanical valve prosthesis. The mechanical valves prosthesis was tested in vitro by the durability test instrument of valve prosthesis. Then in vivo, the durability of the implanted valves was observed with animal experiments and elinieal application. In the impact test for 5 min and durability test of 380 million eyeles in vitro, there was no the phenomenon of flyer, perforation and fracture observed, as well as no wear or pit found on the surface of valve leaflets. The valve leaflets could normally be turned on or off. The weight of the valve was（1.0031 ± 0.0004） g for 23 mm and（1.6003 ± 0.0002） g for 27 mm. The hydrodynamies test demonstrated that the valve prosthesis had still exeellent hemodynamic performance after the durability test. The animal autopsy showed that the valve leaflets could normally be turned on or off, and no wear was found. By follow-up of 62 patients implanted the valves, all patients had long-terms survival, no complication caused by valve was found. The age of the longest survival was more than 10 years. This study demonstrates that the new meehanieal valve prosthesis have excellent durable performance.

Electrochemical Determination of Epinephrine with a Pyrolytic Graphite Electrode in the Presence of Ascorbic Acid and Dopamine

A method for determination of epinephrine（EP） in the presence of ascorbic acid （AA） and dopamine （DA） with bare pyrolytic graphite electrodes has been described for the first time. In pH 7.0 phosphate buffer solution, the linear relationship was observed between the reduction peak current of EP and its concentration over the range from 1×10^-4 to 5×10^-7 mol/L, the related coefficient is 0.9992 （N=8）.

KINETICS OF LASER INDUCED PYROLYTIC DEPOSITION FROM Mn_2(CO)_1.

An optical transmission method was used in-situ to measure the rate of pyrolytic deposition from Mn_2(CO)_(10) induced by a CW CO_2 laser. The effect of the laser intensity, Mn_2(CO)_(10) vapor pressure and added gases (CO, O_2 and Ar) on the deposition rate has been examined.

GROWTH CHARACTERSAND MODEL OF PYROLYTIC CARBON IN CHEMICAL VAPOR INFILTRATION PROCESS

Chemical Vapor Infiltration (CVI) processes are the essential techniques for fabrication of high performance carbon carbon composites. Based on the polarized light and scanning electron analysis, the authors study the micro morphology and texture characteristics of pyrolytic carbon deposited in CVI process, as well as the growth behavior of pyrolytic carbon. The research shows that Rough Laminar (RL) texture has the hierarchical and self similar structural features, which reflects the stage growth and self similar behavior during the growth course of pyrolytic carbon. According to the two growth features, a laminated growth model of pyrolytic carbon is proposed with the concept of Cone Growth Units (CGU). The laminated growth model can provide a fine description for the growth course of RL pyrolytic carbon. The model indicates that formation, developing and combination of local high order structures (such as CGU structures) are the essential factors for the growth of RL texture. Smooth Laminar (SL) texture and ISO carbon come into being with long range orderliness and isotropy structure respectively, which no local high orderliness intermediate involves in.

Some Unusual Features of Highly Oriented Pyrolytic Graphite Observed by Electrochemical Scanning Tunneling Microscopy

Highly oriented pyrolytic graphite (HOPG) is the substrate often used in scanningtunneling Ancroscopy (STM). It is well known that STM images of the basal plane of HOPG showsome unusual structUral patterns. In this letter, we present in situ STM images of some unusualfeatures on HOPG in solutions, including normal or abnormal chain-like featUres and hexagonal oroblique superPeriodic structures. These features emerge both next to and apart from the step ofHOPG.

A Study on the Pyrolytic Characteristics of Xanthoceras Sorbifolia Husk and Its Crude Cellulose Extract

Huge amounts of Xanthoceras sorbifolia husks(XSH)are typically discarded after oil extraction.Since pyrolysis represents a promising solution to harness the bio-energy of XSH,in the present work the pyrolytic and kinetic characteristics of XSH and related crude cellulose extract(CCE)were studied considering different rates of heating(10,30 and 50℃ min^(-1)).The pyrolysis activation energy,pre-exponential factors and mechanism function were computed using different models namely Popescu,FWO(Flynn-Wall-Ozawa)and KAS(Kissinger-Akahira-Sunose).The pyrolysis process was articulated into three stages:dehydration(Stage I),primary devolatilization(Stage II),residual decomposition(Stage III).Marked variations in the average activation energy,thermal stability,final residuals and rate of reaction were noted.Stage II of XSH and CCE could be described by the Avramic-Erofeev equations.The average activation energies of XSH and CCE were found to be 269 and 296 kJ mol^(-1),respectively.

Recovery Method of Pyrolytic Carbon Surface after Exposure to Chlorine Trifluoride Gas

An annealing process was developed for the practical recover of a purified py-rolytic carbon (PPyC) surface from damage, such as color change and peeling, due to fluorination during exposure to chlorine trifluoride gas at high tempera-tures for the cleaning of a silicon carbide chemical vapor deposition reactor. The PPyC surface was annealed at 900°C for 10 min in ambient nitrogen con-taining oxygen at the concentrations of 0.01% - 20%. The rainbow-like colored surface returned to the dark gray color of the original PPyC. Simultaneously, the thin peeled films disappeared. The Raman spectra showed that the PPyC surface chemical bonding returned to that of the original one. The oxygen concentration as low as 0.01% could recover the PPyC surface along with re-ducing the surface pit formation, when the combination of the exposure to chlorine trifluoride gas and the recovery was repeated.

An innovative wood derived carbon-carbon nanotubes-pyrolytic carbon composites with excellent electrical conductivity and thermal stability

The functionality of wood has evolved with time to adapt to the emerging needs of society.Carbonized wood-based composites have attracted tremendous interest in the fields of aerospace,military power,electric power,and system electronic devices,especially at high temperatures.Nevertheless,their electrical conductivity and thermal stability characteristics are still far from satisfactory.Herein,an innova-tive wood-derived carbon-carbon nanotubes-pyrolytic carbon composites(WDC-CNTs-PyCs)is successfully fabricated by chemical vapor deposition and chemical vapor infiltration.The combination of wood-derived carbon(WDC),carbon nanotubes(CNTs),and pyrolytic carbon(PyC)has never been reported in any previous work.We have innovatively introduced PyC into the WDC by chemical vapor infiltration.CNTs promote the continuous deposition of PyC to form dense structures.WDC-CNTs-PyC demonstrates significant compressive strength(85.4 MPa)and excellent electrical conductivity(632 S cm^(-1)).The weight loss rate of WDC-CNTs-PyC is 6%after heating at 500℃ for 10 min in the air atmosphere.Furthermore,WDC-CNTs-PyC could resist oxyacetylene ablation above 2300℃ for 15 s.With excellent electrical conductivity,outstanding thermal stability,and mechanical properties,WDC-CNTs-PyC opens up a surprising strategy for efficiently fabricating various high-performance electronic device composites that could be used in high-temperature fields.

Effect of pyrolytic carbon interphase on mechanical properties of mini T800-C/SiC composites

The effect of pyrolytic carbon(PyC) thickness on the tensile property of mini T800 carbon fiber reinforced SiC matrix composites(C/SiC) was studied. PyC interphase was prepared by chemical vapor infiltration(CVI) process using C3H6–Ar as gas source, the PyC thickness was adjusted from 0 to 400 nm, and then the SiC matrix was prepared by CVI process using methyltrichlorosilane(MTS)–H2–Ar as precursor and gas source. The results showed that the tensile strength of mini T800-C/SiC increased first and then decreased with the increase of the PyC thickness. When the thickness of PyC was 100 nm, the average strength reached the maximum value of 393 ± 70 MPa. The Weibull modulus increased from 2.0 to 8.06 with the increase of PyC thickness, and the larger the Weibull modulus, the smaller the dispersion, which indicated that the regulation of PyC thickness was conducive to improve tensile properties.

Effect of Temperature on the Synthesis of SiC Coating on Carbon Fibers by the Reaction of SiO with the Deposited Pyrolytic Carbon Layer

The influence of reaction temperature on the preparation of SiC coating on carbon fibers by the reaction of silicon monoxide with the deposited pyrolytic carbon （PyC） layer has been discussed.With rising reaction temperature,the thickness of SiC layer increases and the SiC grain is coarsening.The apparent activation energy for the synthesis of SiC layer is about 103.3 kJ/mol.The oxidation resistance of carbon fiber can be improved by the SiC/PyC layers significantly.The initial oxidation temperature of the SiC/PyC coated carbon fiber is about 300℃ higher than that of the uncoated carbon fiber.The oxidation of the SiC/PyC coated carbon fiber is owing to the diffusion of oxygen through the cracks generated by the mismatch of thermal expansion.