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Nitriding, allowance

It has been claimed that boron nitride allows much faster production rates with metallocene LLDPEs than fluoropolymer process aids. American Ceramics is one supplier. [Pg.133]

Much more so than the carbides, the interstitial nitrides are susceptible to the presence of even minute amounts of impurities particularly oxygen, vdiich tend to distort the structure. Like the carbides, the interstitial nitrides allow norunetal vacancies (i.e., nitrogen) in the lattice, but unlike the carbides, they also tolerate metal-atom vacancies. This means that, if the metal-atom vacancies are more numerous than the nitrcgen-atom vacancies, the nitrogen-to-metal ratio will be >1. As a result, the structure of interstitial nitrides is sometimes difficult to identify with certainty. [Pg.164]

The use of nitride allows the possibility of pure plutonium fuel without uranium diluent. The thermal rating of such fuel would be very high, which means either that some other diluent material must be found, or the design of the fuel elements must be altered radically. Whichever direction is chosen the design will be different from the familiar pins... [Pg.538]

Electronic structure calculations of 3d- and 4d-metal impurities in cubic carbides and nitrides allow some general rules for the formation of local DOS of metallic impurities in refractory phases to be proposed (Fig. 7.5). [Pg.181]

Boron nitride can be prepared by allowing ammonia to react with boron trichloride. The first product is boron amide which decomposes on heating to give the nitride ... [Pg.156]

Plasmas can be used in CVD reactors to activate and partially decompose the precursor species and perhaps form new chemical species. This allows deposition at a temperature lower than thermal CVD. The process is called plasma-enhanced CVD (PECVD) (12). The plasmas are generated by direct-current, radio-frequency (r-f), or electron-cyclotron-resonance (ECR) techniques. Eigure 15 shows a parallel-plate CVD reactor that uses r-f power to generate the plasma. This type of PECVD reactor is in common use in the semiconductor industry to deposit siUcon nitride, Si N and glass (PSG) encapsulating layers a few micrometers-thick at deposition rates of 5—100 nm /min. [Pg.524]

The binary borides (p. 145), carbides (p. 299), and nitrides (p. 418) have already been discussed. Suffice it to note here that the chromium atom is too small to allow the ready insertion of carbon into its lattice, and its carbide is consequently more reactive than those of its predecessors. As for the hydrides, only CrH is known which is consistent with the general trend in this part of the periodic table that hydrides become less stable across the d block and down each group. [Pg.1007]

Diamond is an electrical insulator with the highest thermal conductivity at room temperature of any material and compares favorably with beryllia and aluminum nitride. P3]-P5] jg undoubtedly the optimum heat-sink material and should allow clock speeds greater than 100 GHz compared to the current speed of less than 40 GHz. [Pg.375]

Nitridoborates of lanthanum and the lanthanides were obtained from reactions of lanthanide metal or lanthanide metal nitride with layer-like (a-)BN at elevated temperatures (3>1200°C). These reactions require elaborated techniques in the inert gas sample-handling and the use of efficient heating sources, such as induction heating. Only some compounds remain stable in this high-temperature segment, and the yields of such reactions are often limited due to the competing stability of binary phases, allowing only the most (thermodynamically) stable compounds to exist. [Pg.131]

For the generation of more nitrogen-rich compounds, a nitride is included in the reaction. This synthesis allows the formation of different nitridoborate (8) ions as well as nitridoborate nitrides (9) [26] ... [Pg.131]

Re-use of the catalyst The high activity of the solid catalysts also allows one to re-use high surface area titanium nitride several times. By centrifugation, the solid can be separated and used in a new reaction. The catalyst was used up to four times. Figure 19.10 shows the conversion of DPE with time. [Pg.290]

Electrochemical experiments have been carried out on materials deposited by PVD on silicon microfabricated arrays of Au pad electrodes [Guerin et al., 2006a]. The substrate is made up of a square silicon wafer capped with silicon nitride (31.8 mm x 31.8 mm), which has an array of 100 individually addressable Au pad electrodes. These electrodes make up a square matrix on the wafer, which can be masked when placed in a PVD chamber, allowing deposition of thin films on the Au electrodes. Figure 16.3 is a schematic drawing of the configuration. Small electrical contact pads in Au for the individual addressing of electrodes (0.8 mm x 0.8 mm) are placed on the boundaries. [Pg.574]

The preparation of similar precursors suitable for the deposition of metal nitrides is analogous to the preparations of phosphorus and arsenic compounds. The initial reaction of metal trialkyls MR3 (M = A1, Ga, In) with amines (NHR 2) results in the formation of oligomeric amido compounds [R2MNR 2] (n = 2 or 3) which eliminate alkanes on thermolysis. The incorporation of a proton as a substituent on the pnictide bridging ligand has been examined, and many compounds of the type [R2MNHR ]2 have been synthesized. The presence of this proton may facilitate /3-elimination, allowing lower deposition temperatures to be used. [Pg.1038]

Hydrides of variable composition are not only formed with pure metals as solvents. A large number of the binary metal hydrides are non-stoichiometric compounds. Non-stoichiometric compounds are in general common for d,f and some p block metals in combination with soft anions such as sulfur, selenium and hydrogen, and also for somewhat harder anions like oxygen. Hard anions such as the halides, sulfates and nitrides form few non-stoichiometric compounds. Two factors are important the crystal structures must allow changes in composition, and the transition metal must have accessible oxidation states. These factors are partly related. FeO,... [Pg.221]

The main goal of another microhotplate design was the replacement of all CMOS-metal elements within the heated area by materials featuring a better temperature stability. This was accomplished by introducing a novel polysilicon heater layout and a Pt temperature sensor (Sect. 4.3). The Pt-elements had to be passivated for protection and electrical insulation, so that a local deposition of a silicon-nitride passivation through a mask was performed. This silicon-nitride layer also can be varied in its thickness and with regard to its stress characteristics (compressive or tensile). This hotplate allowed for reaching operation temperatures up to 500 °C and it showed a thermal resistance of 7.6 °C/mW. [Pg.108]

This approach allows the deposition of thin films at low temperatures. By comparison, polymer deposition generally requires very high temperatures. For instance, the chemical vapor deposition of silicon nitride requires a temperature of about 900°C, whereas the plasma chemical deposition requires a temperature of only 350°C. [Pg.202]

Fullerenes can also be produced by direct inductive heating of a carbon sample held in a boron nitride support [43]. Evaporation at 2700 °C in a helium atmosphere affords fullerene-containing soot that is collected on the cold Pyrex glass of the reaction tube. This method allows a continuous operation by keeping the graphite... [Pg.10]


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