Hydrothermal Solubilization–Hydrolysis–Dehydration of Cellulose to Glucose and 5-Hydroxymethylfurfural Over Solid Acid Carbon Catalysts

Solid acid catalysts based on graphite-like mesoporous carbon material Sibunit were developed for the one-pot solubilization–hydrolysis–dehydration of cellulose into glucose and 5-hydroxymethylfurfural (5-HMF). The catalysts were produced by treating Sibunit surface with three different procedures to form acidic and sulfo groups on the catalyst surface. The techniques used were: (1) sulfonation by H₂SO₄ at 80–250 °C, (2) oxidation by wet air or 32 v/v% solution of HNO₃, and (3) oxidation-sulfonation what meant additional sulfonating all the oxidized carbons at 200 °C. All the catalysts were characterized by low-temperature N₂ adsorption, titration with NaOH, TEM, XPS. Sulfonation of Sibunit was shown to be accompanied by surface oxidation (formation of acidic groups) and the high amount of acidic groups prevented additional sulfonation of the surface. All the Sibunit treatment methods increased the surface acidity in 3–15 times up to 0.14–0.62 mmol g^?1 compared to pure carbon (0.042 mmol g^?1). The catalysts were tested in the depolymerization of mechanically activated microcrystalline cellulose at 180 °C in pure water. The main products 5-HMF and glucose were produced with the yields in the range of 8–22 wt% and 12–46 wt%, respectively. The maximal yield were achieved over Sibunit sulfonated at 200 °C. An essential difference in the composition of main products obtained with solid acid Sibunit carbon catalysts (glucose, 5-HMF) and soluble in water H₂SO₄ catalysts (formic and levulinic acids) as well as strong dependence of the reaction kinetics on the morphology of carbon catalysts argue for heterogenious mechanism of cellulose depolymerization over Sibunit.     

A method to assess downward flame spread and dripping characteristics of fire‐retardant polymer composites

A method is described to assess the flame retardancy of polyethylene composites by measuring both their downward flame spread rates as well as their combined melting and dripping rates on rectangular rods, ignited at their top. The composite materials were produced by mixing pulverized polymer with organic additives of differing particle sizes, shapes, and mass fractions. The resulting mix was melted in a mold, and then it was solidified into rods. The additives were carbonaceous solids with particle sizes spanning from tens of nanometers to tens of micrometers. The mass fraction of the additives in the polymer matrix varied from 1 to 5 wt%. Upon ignition of the upper tips of the polymer composite rods, the downward flame spread rate and the melting and dripping rate were separately assessed by measuring their mass loss and their heights. The addition to polyethylene of finely sized carbonaceous additives at mass fractions of 4 to 5 wt% proved effective at significantly slowing down its downward flame spread by drastically hindering its dripping tendency. The effectiveness of the additives increased with increasing their mass fraction and decreasing their particle size. High mass fractions of carbon additives resulted in wicking, which can enhance radiatively the heat transfer.     

Synthesis of monohydric alcohols from CO and H<Subscript>2</Subscript> on Fe/Sibunit catalysts

It was demonstrated that R ₂–R ₄ saturated monohydric alcohols can be synthesized from CO and H₂ in the presence of Fe catalysts containing a carbon support of the Sibunit type with granule sizes of 3–5, 1–2, and 0.05–0.1 mm in a fixed-bed reactor at 3 MPa and 240–300°C. It was found that the activity of Fe/Sibunit catalysts and their selectivity for the formation of liquid synthetic products increased with the size of granules and the amount of iron. The catalysts make it possible to obtain fatty alcohols, in which the fraction of R ₂–R ₄ alcohols is as high as 75%, in yields to 56 g/m³.     

High-performance B4C–TiB2–SiC composites with tuneable properties fabricated by reactive hot pressing

In this work, we systematically studied the effects of powder characteristics (B₄C, TiC and Si powders) on the existential form of toughening phases (SiC and TiB₂) as well as the overall microstructure and properties of B₄C–TiB₂–SiC composites fabricated by reactive hot pressing. The particle size of the TiC powder plays a largely determining role in the development of novel toughening phases, the TiB₂–SiC composite structure, that are formed in the B₄C matrix, while the Si particle size affects the agglomerate level of the SiC phase. The TiB₂–SiC composite structure and SiC agglomerates enhance the fracture toughness, but decrease the flexural strength. Both the microstructure and mechanical properties of B₄C–TiB₂–SiC composites can be effectively tuned by regulating the combinations of the particle sizes of the starting powders. The B₄C–TiB₂–SiC composites demonstrate flexural strength, fracture toughness and Vickers hardness in the respective range of 567–632 MPa, 5.11–6.38 MPa m^1/2, and 34.8–35.6 GPa.     

Taguchi method to optimize the micron and submicron size cenosphere particulates filled E‐glass fiber‐reinforced vinylester composites

In this work, the mechanical and tribological characteristics of E‐glass fiber‐reinforced vinylester composites have been investigated experimentally under dry sliding conditions. The E‐glass fiber‐reinforced vinylester composites with uniform micron and submicron size cenosphere particulates of three different sizes (2 µm, 900 nm, and 400 nm) had been prepared in the laboratory. In this work the effect of parameters such as applied normal load, particulate size, sliding speed, sliding distance and roughness on friction and wear behavior have been carried. A plan of experiments, based on the Taguchi design, was performed to acquire data in a controlled way. An orthogonal array L₂₇ (3¹³) and Analysis of variance (ANOVA) have been applied to investigate the influence of process parameters on the coefficient of friction (COF) and sliding wear behavior of these composites. It was found that the submicron size particulates 400 nm as filler contributed significantly to improve the mechanical properties and wear resistance of the composites. The experimental results indicate that the specific wear rate is greatly influenced by applied normal load and particle size. ANOVA results showed that the applied normal load significantly influence the specific wear rate of cenosphere filled glass fiber‐reinforced vinylester composites. Regression analysis is carried to check the suitability of the prediction equation and modeling of the wear parameters and the typical R² values for COF and specific wear rate are 86.7 and 94.3%, respectively. The scanning electron microscopy are used clarify the experimental in the frictional and wear testing. POLYM. COMPOS., 35:775–787, 2014. © 2013 Society of Plastics Engineers     

Influence of carbon support on the performance of platinum based oxygen reduction catalysts in a polymer electrolyte fuel cell

Novel carbons from the Sibunit family prepared via pyrolysis of hydrocarbons [Yermakov YI, Surovikin VF, Plaksin GV, Semikolenov VA, Likholobov VA, Chuvilin AL, Bogdanov SV (1987) React Kinet Catal Lett 33:435] possess a number of attractive properties for fuel cell applications. In this work Sibunit carbons with BET surface areas ranging from ca. 20 to 420 m² g⁻¹ were used as supports for platinum and the obtained catalysts were tested as cathodes in a polymer electrolyte fuel cell. The metal loading per unit surface area of carbon support was kept constant in order to maintain similar metal dispersions (∼0.3). Full cell tests revealed a strong influence of the carbon support texture on cell performance. The highest mass specific activities at 0.85 V were achieved for the 40 and 30 wt.% Pt catalysts prepared on the basis of Sibunit carbons with BET surface areas of 415 and 292 m² g⁻¹. These exceeded the mass specific activities of conventional 20 wt.% Pt/Vulcan XC-72 catalyst by a factor of ca. 4 in oxygen and 6 in air feed. Analysis of the I–U curves revealed that the improved cell performance was related to the improved mass transport in the cathode layers. The mass transport overvoltages were found to depend strongly on the specific surface area and the texture of the support.     

Effect of particle size on the properties of Mg(OH)2‐filled rubber composites

A novel nanomagnesium hydroxide powder and three kinds of micro‐Mg(OH)₂, with different particle sizes, were chosen as fillers and mixed with ethylene–propylene–diene monomer rubber (EPDM) to form a series of composites by a traditional rubber‐processing technique. The results showed that the mechanical properties of composites improved with decreasing particle size. The nanocomposites were far stronger than the microcomposites, which also supported the view that rubber reinforcement requires nanoreinforcement. The effect of particle size on the fire resistance of composites was investigated by cone calorimetry and limiting oxygen index analysis, which showed that the particle size of powder had an impact on the fire resistance of composites. For the composites filled with untreated powder, the peak value of heat release rate decreased and T_ign increased with decreasing particle size. In conclusion, the fire resistance of nanocomposites was better than that of microcomposites. Surface modification of particles sometimes substantially improved the mechanical properties of nanocomposites, but had no effect on either the mechanical properties of microcomposites or the fire resistance of nanocomposites and flame retardance. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2341–2346, 2004     

Strength retention of self-reinforced,absorbable polyglycolide rods in hydrolytic environment

Absorbable polyglycolide suture fibers were sintered with the compression molding techniques to cylindrical rods at temperatures between 205°C and 232°C for 3–5 min with final pressures of 50–80 N/mm². The cylindrical rods had nominal diameters between 1.5–4.5 mm and a length of 50 mm. The initial bending moduli and the initial bending strengths of the rods were between 9–15 GPa and 220–430 MPa, respectively. The shear strengths of the rods were between 165–255 MPa. The hydrolytic loss of mechanical strength of the above self-reinforced, absorabable polyglycolide rods were studied in phosphate buffer at 37°C and 77°C. It was found that the rate of strength loss decreases with the increasing diameter of the rods. On the other hand, the rate of strength loss increases when the temperature of the buffer solution is raised. The strength, retention time at 37°C was between 7–10 weeks showing that the loss of mechanical strength of self-reinforced polyglycolide rods occurs more rapidly in vivo than in vitro.     

Water sorption on composites “LiBr in a porous carbon”

Water sorption equilibrium of LiBr confined to pores of a mesoporous synthetic carbon Sibunit and a macroporous expanded graphite (samples SWS-2C and SWS-2EG, respectively) was studied. Isobars of water sorption on these composites are measured at vapor pressure 6–81 mbar and temperature 30–145 °C. The type of sorption equilibrium for the two composites appears to be quite different. The isobars for SWS-2EG have a plateau corresponding to one molecule of H₂O adsorbed by one molecule of LiBr, which indicates the formation of crystalline hydrate LiBr·H₂O inside pores with a monovariant type of equilibrium. At lower temperatures, the equilibrium becomes divariant that is typical for LiBr–water solutions. On the contrary, the water sorption equilibrium for SWS-2C is divariant over the whole temperature and pressure range which means that no crystalline hydrates are formed inside Sibunit pores. In our opinion, this distinction results from differences in a pore structure of the host carbons. The composite sorption capacity can reach 0.6–1.1 g H₂O per 1 g of the dry sorbent at relative humidity 70%. The advanced sorption capacity makes the sorbents promising for gas drying, thermal storage of energy and other applications.     

A study of localized curing of glass‐filled composites using microhardness measurements

Extent of cure of hybrid composite systems is examined by conducting hardness measurements at different stages of the photopolymerization reaction and obtaining kinetic parameters that matched the experimental data. The materials are commercial dental composites based on bis[4‐(2‐hydroxy‐3‐methacryloyloxypropoxy)phenyl]propane resins with different photoinitiator concentrations as well as filler particle sizes and combinations. Samples (five per group) were made using nylon molds (2.5 × 5 mm) of the tested composites. The samples were light cured with a constant‐power light source for durations up to 20 s. After curing, all samples underwent Vicker's hardness testing of top and bottom surfaces. While there are significant differences in the polymerization behavior between the top and bottom locations for the tested composites, the corresponding growth exponent n, a kinetic parameter in the kinetic theory, is very close in all cases. For the tested materials the coefficient factor k is much lower for the bottom surfaces compared with the top surfaces. This reduction in the value of k is more severe for the material with a higher concentration of the photoinitiator as well as a higher percentage of glass filler particles in the wavelength range affecting the photopolymerization. It is argued that a relationship between k and the irradiation intensity can be used to quantify the decay of irradiated light with its penetration into the composites. The comparisons can be used to draw preliminary conclusions on the parameters controlling the effective depth of cure in a hybrid composite. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 426–431, 2005     

Large-scale and ultra-low thermal conductivity of ZrO2 fibrofelt/ZrO2-SiO2 aerogels composites for thermal insulation

The large-scale fibrous/aerogels composites are prepared by using zirconia fibrofelt (ZFF) as skeleton to give high strength and ZrO₂-SiO₂ aerogels (ZSA) as filler to give excellent thermal insulation through vacuum impregnation. The ZFF/ZSA with a low density of 0.302?g/cm³ and a high porosity (89%) exhibits large size of 180?mm in length, 180?mm in width and 25?mm in height which is larger than other fibrous aerogels. Meanwhile, the ZFF/ZSA exhibits high compressive strength of up to 0.17?MPa which is approximately six times higher than that of ZFF (0.028?MPa). The ZFF/ZSA shows a much lower thermal conductivity of 0.0341?W?m^?1 K^?1 at room temperature and 0.0460–0.096?m^?1 K^?1 during 500?°C and 1100?°C which are lower than that of conventional fibrous materials, indicating its excellent thermal insulation property in a wide temperature range, and the thermal insulation mechanism is analyzed. Thus, the large-scale, low density, high strength, and low thermal conductivity of ZFF/ZSA composites show enormous potential application in the fields of architecture, engineering pipes and aerospace for thermal insulation and protection.     

Specific features in the transformation of liquid drops during their motion in a gas medium

Using high-speed video cameras (up to 10⁵ frames per second), a cross-correlation measuring system, and panoramic optical tracer visualization methods, some specific features have been revealed in the transformation of drops of liquids widely used in chemical technologies (kerosene, ethanol, water, acetone). The studies were performed for individual drops with characteristic sizes (radii) of 1–3 mm during their motion through a gas medium (air at a temperature of nearly 300 K) at velocities of 0.5–5 m/s. The ranges of change in the aerodynamic resistance coefficients c _d were determined for the studied liquid drops under the considered conditions. The effect of the sizes and velocities of drops on this parameter have been established. Real values of c _d for typical applications were shown to be much greater than for the corresponding droplike shapes.     

Critical effect and enhanced thermal conductivity of Cu-diamond composites reinforced with various diamond prepared by composite electroplating

Despite the great potential value as heat sink materials, their practical application of high thermal conductivity (TC) Cu-diamond composites is limited since high temperature and high pressure (above 1000 K and 60 MPa) were requisite in the conventional process. In this study, high TC void-free Cu-diamond composites reinforced with various diamond particles were prepared via composite electroplating. The impacts of diamond particle sizes (ranged from 10 to 400 μm) on microstructure, interface and TC of the composites were investigated. The TC of Cu-diamond composites was improved with the increase of diamond particle sizes and well-combined interface. Interestingly, a critical size for improved the TC of Cu-diamond composites was clearly observed and the critical value (22 μm) was derived from Kipitza theory. Based on the TC results and critical analysis, the Cu-diamond composite reinforced with large diamond particles (400 μm) was synthesized, which possessed the TC of 846.52 W m⁻¹ K⁻¹ and the thermal expansion coefficient of 7.2 × 10⁻⁶ K⁻¹. Such attractive thermal properties suggested that electroplating Cu-diamond composites showed the promising application as heat sink materials in microelectronic industry.     

Fragmentation of wood char in a laboratory scale fluidized bed combustor

Casuarina equisetifolia, a hard wood, and a popular energy crop in many tropical countries, was investigated experimentally for its char fragmentation in a laboratory scale atmospheric bubbling fluidized bed combustor. The effect of fuel shape and size on wood char fragmentation was studied. Wood particles of spherical, cylindrical (aspect ratio of 1), and cubical shapes of different sizes ranging from 10 to 25 mm were used in the experiments. Fragmentation of wood char was quantified in terms of various parameters, such as Number of Fragments (NF), Percentage of Fragmentation Events, Frequency of Fragmentation, Timing interval of Fragmentation, Size distribution of char and Fragmentation Index (FI). Also, qualitative observations on the evolution of char in terms of deformation, cracks and surface texture are discussed. It was observed that Casuarinaequisetifolia wood of sizes greater than 15 mm, of all shapes undergoes primary fragmentation during the devolatilization phase. Furthermore, chars fragment at the early stages (1st or 2nd quarter) of the char combustion phase, underscoring the significance of the phenomenon in fluidized bed combustion. For all the shapes of wood considered, there appears to be a cut-off size of the initial wood, below which its char certainly undergoes fragmentation. It was observed that the average char particle size at any instance during its combustion falls in a narrow range of 3.7–6.9 mm, 3–6.6 mm and 3–9.5 mm for spherical, cylindrical and cubical wood particles, respectively. Wood of initially cylindrical shape undergoes extensive fragmentation when compared with spherical and cubical shapes.     

Generating Particle Beams of Controlled Dimensions and Divergence: II. Experimental Evaluation of Particle Motion in Aerodynamic Lenses and Nozzle Expansions

A particle-beam-forming apparatus for producing narrow particle beams was developed based on the theory discussed in paper I of this series. It consists of a variable number of aerodynamic lenses (short capillaries and/or thin-plate orifices with diameters ranging from 3.5 to 7.0 mm) followed by an accelerating nozzle (3 mm). It was evaluated using monodisperse DOS and NaCl particles (0.02–0.24 μm) at upstream pressures on the order of 1 torr. The particle beams produced by the lens-nozzle system were focused through a skimmer (1 mm) into a high vacuum chamber (10^?4–10^?5 torr) where the beam widths, velocities and transport efficiencies were measured. The experiments showed that as more lenses were added the particle beam widths were reduced asymptotically to the minimum values. For spherical particles (DOS) these minimum values are in good agreement with the Brownian limit derived in paper I. For nonspherical particles (NaCl) these minimum widths are much larger than the Brownian limit, indicating that beam broadening is dominated by lift forces (see paper I). The particle transport efficiencies through the lens-nozzle-skimmer system exceed 90% for particle sizes from 0.03 to 0.24 μm. The measured beam velocities are also in good agreement with the calculated values.     

Effect of particle size on thermal decomposition and devolatilization kinetics of melon seed shell

Thermogravimetric analysis (TGA) and devolatilization kinetics of melon seed shell (MSS) at different particle sizes (150?µm and 500?µm) and at different heating rates (10, 15, 20, and 25?°C/min) were investigated with the aid of TGA. The results of the TGA analysis show that the TGA curves corresponding to the first and third stages for 150?µm particle sizes exhibited some bumps that developed at the first and third stages of pyrolysis. It was also observed that at constant heating rate, the maximum peak temperature increases as the particle sizes increase from 150 to 500?µm, whereas 500?µm particle sizes exhibited higher peak temperatures compared to 150?µm particle sizes. The resulting TGA data were applied to the Kissinger (K), Kissinger–Akahira–Sunose (KAS) and Flynn–Wall–Ozawa (FWO) methods and kinetic parameters (activation energy, E and frequency factor, A) were determined. The E and A obtained using K method were 74.27?kJ mol^?1 and 3.84?×?10⁵?min^?1 for 150?µm particle size, whereas for 500?µm particle size were 97.12?kJ mol^?1 and 3.74?×?10⁷?min^?1, respectively. However, the average E and A obtained using KAS and FWO methods were 82.35?kJ mol^?1, 1.29?×?10⁷?min^?1, and 88.50?kJ mol^?1, 1.32?×?10⁷?min^?1 for 150?µm particle sizes. While for 500?µm particle sizes, the E and A were 108.46?kJ mol^?1, 3.14?×?10⁹?min^?1, and 113.05?kJ mol^?1, 7.56?×?10⁹?min^?1, respectively. It was observed that E and A calculated from FWO and KAS methods were very close and higher than that obtained by K method. It was observed that the minimum heat required for the cracking of MSS particles into products is reached later at higher peak temperatures since the heat transfer is less effective as they are at lower peak temperatures.     

Effect of filler content and size on the properties of ethylene vinyl acetate copolymer–wood fiber composites

In this study, the main focus was on the effect of wood fiber (WF) content and particle size on the morphology and mechanical, thermal, and water‐absorption properties of uncompatibilized and ethylene glycidyl methacrylate copolymer (EGMA) compatibilized ethylene vinyl acetate copolymer–WF composites. For uncompatibilized composites, the tensile strength decreased with increasing WF content, whereas for compatibilized composites, the tensile strength initially decreased, but it increased for composites containing more than 5% WF. Small‐WF‐particle‐containing composites had higher tensile strengths than composites containing larger WF particles, both in the presence and absence of EGMA. WF particle size did not seem to have much influence on the degradation behavior of the composites, whereas water absorption by the composites seemed to be higher in composites with smaller particle sizes for both compatibilized and uncompatibilized composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3645–3654, 2007     

Exploring the self-cleaning and antimicrobial efficiency of the magnesium oxychloride cement composites

Composites of magnesium oxychloride cement (MOC) functionalized with TiO₂ nanoparticles are proposed here as an alternative technology to maintain clean building surfaces from airborne pollutants and microorganisms. The MOC composites were characterized by different techniques such as XRD, FTIR, SEM, EDS, UV–Vis, compressive strength, and nanoindentation tests. According to the results, phase 3 (3 Mg(OH)₂^.MgCl₂^.8H₂O) with needle-like morphology was the primary crystallized hydration product for the MOC composites. Also, the samples exhibited good mechanical properties and good light absorption, allowing them to activate under solar light irradiation. The self-cleaning efficiency of the MOC composites was evaluated by measuring the removal of three types of pollutants: methylene blue (MB), rhodamine B (RhB), and reactive black 5 (RB5), under two scenarios: natural sunlight and accelerated weathering conditions. The self-cleaning tests revealed outstanding efficiencies of the composites to remove MB (82%), RhB (88%), and RB5 (91%) under solar light and accelerated weathering tests. On the other hand, the antimicrobial activity was evaluated against E. coli (gram-negative) and S. aureus (gram-positive) under irradiation. The zone of inhibition (ZOI) showed diameters higher than 21 mm to E. coli for samples with 5% of TiO₂ or superior, revealing a high microbial inhibition of the gram-negative bacteria. Also, the structural and morphological stability of the MOC composites was confirmed after several cycles for the accelerating weathering tests, demonstrating their potential to be used outdoors to reduce environmental pollution.     

Significance of hot pressing parameters and reinforcement size on sinterability and mechanical properties of ZrB2–25 vol% SiC UHTCs

The influences of hot pressing parameters and SiC particle size on the bulk density, the average ZrB₂ grain size and Vickers hardness of ZrB₂–25 vol% SiC ultrahigh temperature ceramic composites were investigated. In this paper, the Taguchi methodology (An L9 orthogonal array) was used to specify the contributions of four parameters: the hot pressing temperature, holding time, applied pressure and SiC particle size. The experimental procedure included nine tests for four parameters with three levels which were employed to optimize the process parameters. The statistical analyses recognized the hot pressing pressure and temperature as the most consequential parameters affecting the density and hardness of ZrB₂–SiC composites. The SiC particle size and holding time were specified as the most effective parameters on the average ZrB₂ grain size. The bulk density, average ZrB₂ grain size, Vickers hardness and fracture toughness of the sample, hot pressed at optimal conditions (1850 °C, 90 min, 16 MPa and 200 nm), reached about 5.36 g/cm³, 10.03 µm, ~17.1 GPa and 5.9 MPa m^1/2, respectively. The confirmation test, carried out under optimum conditions, showed that the experimental results were relatively equal to the predicted values from the Taguchi prediction model. Finally, the mechanisms of enhanced fracture toughness of the hot pressed ZrB₂–SiC ceramic composites were discussed.     

The effect of carbon source and molar ratio in Fe–Ti–C system on the microstructure and mechanical properties of in situ TiC/Fe composites

The size, distribution, and morphology of TiC particle in Fe–Ti–C system have a great influence on the mechanical properties of TiC/Fe composites. In this work, TiC/Fe composites were fabricated in the Fe–Ti–C system with different carbon source and molar ratio by combustion synthesis and hot-pressing method. Morphology and size of ceramic particles, as well as microstructure, interface bonding and mechanical properties of composites were compared. The results showed that the size of TiC particles decreased with increase of Fe content of Fe–Ti–C systems fabricated by the same carbon source, while the particles change from spherical shapes to cubic shapes which can reduce stress concentration between ceramic particles and matrix. Furthermore, TiC/Fe composites fabricated by 5Fe–Ti-carbon blacks (CBs) system exhibited superior yield strength (1523 MPa) compressive strength (2203 MPa) and microhardness (691.5 HV), caused by the high interface bonding strength and lamellar pearlite matrix which can commendably limit the dislocation slip. By comparison, TiC/Fe composites fabricated by 21Fe–Ti-carbon nanotubes (CNTs) system showed higher fracture strain (25.85%) on account of the ferrite matrix with favorable plastic. This work reveals the influence of carbon source and molar ratio of Fe–Ti–C system on TiC/Fe composites, which is helpful to further improve the properties of TiC/Fe composites.