GB931335A - Improvements in or relating to boron phosphide - Google Patents

Improvements in or relating to boron phosphide

Info

Publication number
GB931335A
GB931335A GB3496559A GB3496559A GB931335A GB 931335 A GB931335 A GB 931335A GB 3496559 A GB3496559 A GB 3496559A GB 3496559 A GB3496559 A GB 3496559A GB 931335 A GB931335 A GB 931335A
Authority
GB
United Kingdom
Prior art keywords
boron
coating
boron phosphide
metal
phosphide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3496559A
Inventor
Robert Arthur Ruehrwein
Forrest Vaughan Williams
Therald Moeller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Priority to GB3496559A priority Critical patent/GB931335A/en
Publication of GB931335A publication Critical patent/GB931335A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/06Hydrogen phosphides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Coating By Spraying Or Casting (AREA)
  • Catalysts (AREA)
  • Turbine Rotor Nozzle Sealing (AREA)

Abstract

Cubic crystalline boron phosphide may be prepared by reacting together a boron halide, hydride or alkyl compound with a phosphorus halide or hydride in the gas phase at a temperature above 1100 DEG F. Suitable boron compounds are:- BCl3, B Br3, BI3, mixed halides, Me3B, Et3B, tri normal propyl boron, tri iso propyl boron, tri tert butyl boron, ethylated decaborane, diborane, pentaborane, decaborane. In a modification phosphorus and hydrogen may be used with one of the above boron compounds. The proportions are preferably 1-1,5 mols. of phosphorus (calculated as the monatomic form) and from 1,5-5 mols. of hydrogen per each mol. of boron compound. In both cases the process is carried out in a high temperature furnace and the compounds introduced into two separate gas streams to undergo turbulent mining, the temperature being in the range 1600 DEG -2700 DEG F. and the boron phosphide being deposited on the walls of the collecting vessel or as a coating on a metal or graphite surface or on a prototype of molybdenum. The crystalline boron phosphide may be shaped by hot pressing, e.g. at 500-20,000 psig and 1000 DEG -6000 DEG F., or cold pressing, may be diffused into metal or ceramic shapes by packing round the shape and heating to 1500 DEG -6000 DEG F., may be applied as a coating of particles by flame spraying, electrophoresis, or from a slurry, or may be slip cast and subsequently fired. In all cases fluxes and bonding agents may be added, e.g. Cr, Fe, Ni, Co, Nb, Ta, Ti, Zr, W, Mo, Hf, Al2O3, ZrO2, HfO2, SiO2, BeO2, TiO2, ThO2, alkali metal borates or phosphates, boron phosphate or sodium silicate. Porosity may be produced by adding naphthalene, cork or asbestos. The shape or coating may be densified and sintered, and may be subsequently subjected to reduction with H2, where metal oxides are also present, or oxidation. For slurry coating the boron phosphide is dispersed in water with carbonymethyl cellulose. Examples of applications for the resulting temperature and chemical resistant boron phosphide or composition as an article or coating are:-crucibles, missile nose cones, rocket fuel tanks and pump impellers, jet nozzles, Venturi throats, exhaust deflectors, grinding wheels, shaping tools, turbine blades and nozzles, observation windows for furnaces, nuclear reactors, or space ships, burners, agitators, nuclear reactor shields, semi conductors, strengthened metal wear plates, or radiation meters. Porous material may be used as filters or to provide cooling by passage of liquids. Specification 923,860 also is referred to.ALSO:Cubic crystalline boron phosphide may be prepared by reacting together a boron halide, hydride or alkyl compound with a phosphorus halide or hydride (see Group III) at above 1100 DEG F. The crystalline boron phosphide may be shaped by hot pressing, e.g. at 500-20,000 p.s.i. g. and 1000-6000 DEG F., or cold pressing, may be diffused into metal or ceramic shapes by packing round the shape and heating to 1500-6000 DEG F., may be applied as a coating of particles by flame spraying, electrophoresis, or from a slurry, or may be slip cast and subsequently fired. In all cases fluxes and bonding agents may be added e.g. Cr, Fe, Ni, Co, Nb, Ta, Ti, Zr, W, Mo, Hf, Al2O3, ZrO2, HfO2, SiO2, BeO2, TiO2, ThO2, alkali metal borates or phosphates, boron phosphate or sodium silicate. Porosity may be produced by adding naphthalene, cork, or asbestos. The shape or coating may be densified and sintered, and may be subsequently subjected to reduction with H2, where metal oxides are also present, or oxidation. For slurry coating the boron phosphide is dispensed in water with carboxymethylcellulose. Examples of application for the resulting temperature and chemical resistant boron phosphide or composition as an article or coating are:- crucibles, missile nose cones, rocket fuel tanks and pump impellers, jet nozzles, venturi throats, exhaust deflectors, grinding wheels, shaping tools, turbine blades and nozzles, observation windows for furnaces, nuclear reactors or space ships, burners, agitators, nuclear reactor shields, semiconductors, strengthened metal wear plates, or radiation meters. Porous material may be used as filters or to provide cooling by passage of liquids. Specification 923,860 also is referred to.
GB3496559A 1959-08-06 1959-08-06 Improvements in or relating to boron phosphide Expired GB931335A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3496559A GB931335A (en) 1959-08-06 1959-08-06 Improvements in or relating to boron phosphide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3496559A GB931335A (en) 1959-08-06 1959-08-06 Improvements in or relating to boron phosphide

Publications (1)

Publication Number Publication Date
GB931335A true GB931335A (en) 1963-07-17

Family

ID=10372196

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3496559A Expired GB931335A (en) 1959-08-06 1959-08-06 Improvements in or relating to boron phosphide

Country Status (1)

Country Link
GB (1) GB931335A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106029563A (en) * 2013-12-23 2016-10-12 皮埃尔和玛利居里大学(巴黎第六大学) Production of boron phosphide by reduction of boron phosphate with an alkaline metal

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106029563A (en) * 2013-12-23 2016-10-12 皮埃尔和玛利居里大学(巴黎第六大学) Production of boron phosphide by reduction of boron phosphate with an alkaline metal
CN106029563B (en) * 2013-12-23 2018-06-22 皮埃尔和玛利居里大学(巴黎第六大学) It is prepared by using the boron phosphide of alkali metal reduction boron phosphate

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