Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B33/00—Silicon; Compounds thereof
  • C01B33/08—Compounds containing halogen
  • C01B33/107—Halogenated silanes
  • C01B33/10778—Purification
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B33/00—Silicon; Compounds thereof
  • C01B33/08—Compounds containing halogen
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B33/00—Silicon; Compounds thereof
  • C01B33/08—Compounds containing halogen
  • C01B33/107—Halogenated silanes
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B33/00—Silicon; Compounds thereof
  • C01B33/08—Compounds containing halogen
  • C01B33/107—Halogenated silanes
  • C01B33/1071—Tetrachloride, trichlorosilane or silicochloroform, dichlorosilane, monochlorosilane or mixtures thereof
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B33/00—Silicon; Compounds thereof
  • C01B33/08—Compounds containing halogen
  • C01B33/107—Halogenated silanes
  • C01B33/10778—Purification
  • C01B33/10794—Purification by forming addition compounds or complexes, the reactant being possibly contained in an adsorbent

Definitions

• the invention relates to a process for reducing the content of elements of the third main group of the periodic table, preferably of boron and aluminum, in technical grade halosilanes for the production of ultrahigh-purity halosilanes, in particular ultrahigh-purity chlorosilanes. Furthermore, the invention relates to a system for carrying out this method.
• boron-containing impurities (BCI 3 ) are transferred in a first step by addition of diphenylthiocarbazone and triphenylchloromethane in high-boiling complexes and removed by column distillation in the second step, in the third step, phosphorus chlorides (PCI3) and Phosphorus-containing impurities and arsenic and aluminum-containing impurities and other metallic Impurities separated as distillation residues in a second column distillation.
• PCI3 phosphorus chlorides
• PCI3 Phosphorus-containing impurities and arsenic and aluminum-containing impurities and other metallic Impurities
• the object of the present invention is to develop a simpler and thus more economical process and a plant for the production of ultrahigh-purity halosilanes, in particular chlorosilanes, which are suitable for the production of solar silicon or in particular also for the production of semiconductor silicon.
• a process is provided which allows the production of ultrahigh-purity halosilanes from technical grade halogensilanes in which the elements of the third main group of the Periodic Table (III PSE), in particular boron and / or aluminum, are removed quantitatively, in particular starting from a hydrohalogenation of metallurgical silicon ,
• the invention relates to a process for reducing the content of elements of the third main group of the periodic table, in particular the boron and / or aluminum content, in technical grade halosilanes for the production of ultrahigh-purity halosilanes, consisting of the following steps: a) addition of the halosilanes to be purified with triphenylmethyl chloride to form complexes with compounds of these elements, in particular with boron and / or aluminum-containing compounds, and b) obtaining ultrahigh-purity halosilanes by distillative separation of the complexes, in particular by a single distillation.
• the separation of the complexes formed takes place according to the invention by means of a one-time distillation of the reaction mixture from step a) via a distillation column, for example-but not exclusively-via a rectification column having from one to 100 theoretical plates.
• the complexes formed thereby remain advantageously in the distillation residue.
• High-purity halosilanes according to the invention have an impurity content of boron and aluminum of ⁇ 50 ⁇ g / kg in each case in relation to the element per kilogram of halosilane.
• the technical grade of halosilanes have not previously been subjected to any separation of compounds containing phosphorus or phosphorus and / or the ultrahigh-purity halosilanes are not subjected to any subsequent separation of phosphorus and / or phosphorus-containing compounds.
• the phosphorus content in the technical grade halogen silanes is already below 4 ⁇ g / kg, preferably ⁇ 2 ⁇ g / kg, in particular
• the content of phosphorus is determined by means of a method familiar to the competent expert for analysis. For example, by IPC-MS, wherein the content of phosphorus in the sample is previously enriched by conventional methods.
• the content of boron in the obtained ultrahigh-purity halosilanes is preferred
• halosilanes silicon tetrachloride and / or trichlorosilane are usually carried out at head temperatures of about 31, 8 0 C and 56.7 0 C and a pressure of about 1013.25 hPa or 1013.25 mbar a bs- At higher or lower pressures, the head temperature changes accordingly , In the case of volatile halogenosilanes, it may be expedient to distill under excess pressure.
• step (a) the displacement of the halosilanes to be purified with triphenylmethyl chloride to form the complexes, takes place in a complexing device (2) from which the halosilanes and the complexes are at least partly preferably completely, in a distillation column (3) for the separation of the complexes in step (b) are transferred.
• step (a) is carried out separately from step (b), in particular spatially separated. About the distillation column (3), the quantitative separation of boron and aluminum-containing complexes.
• the steps (a) and (b) are incorporated in a continuous process for the preparation of ultrahigh-purity halosilanes, preferably starting from a reaction of metallurgical silicon, in particular starting from a hydrohalogenation of metallurgical silicon.
• the advantage of this procedure lies in the fact that the complexation is separated from the separation and in this way the separation of boron and / or aluminum-containing compounds can be integrated into a continuous overall process.
• This can be done, for example, such that at least one device for complexing (2), preferably a plurality of devices (2) connected in parallel, are assigned to a distillation column (3).
• devices connected in series for complexing are each assigned to a distillation column (3).
• the device or devices for complexation (2) can, for example, batchwise or continuously - set reactor or tubular reactor - filled with halosilanes or be flowed through, the content of boron and optionally further impurities can be determined analytically.
• the halosilanes to be purified are treated with Thphenylmethylchlohd, preferably with a slight excess of ⁇ 20 mol .-%, ⁇ 10 mol .-%, preferably of ⁇ 5 mol .-% or less.
• the resulting reaction mixture can be homogenized in order to ensure complete complexing of the boron and / or aluminum-containing compounds.
• the homogenization can be carried out by stirring or in the tubular reactor by turbulence. Subsequently, the halosilanes and optionally the complexes are transferred to the distillation column (3) or into the associated distillation flask. There, according to the invention, the distillative separation of the halosilanes and the complexes follows in order to obtain ultrahigh-purity halosilanes.
• the process of the invention can be integrated into a continuous overall process for the production of ultrahigh halosilanes starting from a hydrohalogenation of metallurgical silicon.
• boron and / or aluminum and process-related compounds containing boron and / or aluminum may be mentioned.
• the thphenylmethylchlohd can form complexes with all typical Lewis acids.
• these may also be tin, titanium, vanadium and / or antimony or compounds containing these foreign metals.
• Halogensilanes are preferably chlorosilanes and / or bromosilanes, silicon tetrachloride, trichlorosilane and / or mixtures thereof Silanes optionally with further halogenated silanes, such as dichlorosilane and / or monochlorosilane, are particularly preferred. Therefore, the method is generally well suited for reducing the content of elements of the third main group of the periodic table in halosilanes, if these compounds would have a comparable boiling point as the halosilanes or would proceed as an azeotrope with the halosilanes and / or in which the solubility the complexes formed is correspondingly low.
• the method can also be used for the purification of tetrabromosilane, tribromosilane and / or mixtures of halosilanes.
• each halogen can be selected independently of other halogen atoms from the group fluorine, chlorine, bromine or iodine, so that, for example, mixed halosilanes such as SiBrCl 2 F or SiBr 2 CIF can be included.
• Halogen silanes of industrial purity are understood as meaning, in particular, halosilanes whose content of halosilanes is> 97% by weight and whose content of elements of the third main group of the periodic system is in each case ⁇ 0.1% by weight. preferably between ⁇ 0.1% by weight and> 100 ⁇ g / kg, more preferably between ⁇ 0.1% by weight and> 30 ⁇ g / kg. They preferably have at least a content of 99.00% by weight, in particular a content of at least 99.9% by weight, of the desired halosilane (s).
• the composition may have a content of 97.5% by weight of silicon tetrachloride (SiCl 4 ) and 2.2% by weight of trichlorosilane (HSiCl 3 ), or approx. 85 wt .-% SiCI 4 and 15 wt .-% HSiCI 3 , or even to 99.0 wt .-% silicon tetrachloride. It is preferred if the phosphorus content in the technical grade halosilanes is already below 4 ⁇ g / kg, particularly preferably ⁇ 2 ⁇ g / kg, in particular ⁇ 1 ⁇ g / kg, in particular without the phosphorus content being removed by the formation of precipitates ,
• the highest-purity halosilanes are halosilanes having a content of halosilanes of> 99.99% by weight and having a maximum impurity with one element each of the third main group of the PSE, in particular of boron and of aluminum-containing compounds, of ⁇ 30 ⁇ g / kg with respect to the element per kilogram of halosilane, in particular of ⁇ 25 ⁇ g / kg, preferably from
• ⁇ 2 ⁇ g / kg or ⁇ 1 ⁇ g / kg per element in the halosilane is particularly preferred according to the invention each of boron and aluminum.
• the halosilanes of industrial purity are, in particular, halosilanes, which also comprise halosilane mixtures containing> 97% by weight of halosilanes and ⁇ 0.1% by weight of elements of the third main group of the periodic table, preferably with a content of elements between ⁇ 0.1 wt .-% and> 6 micrograms / kg, more preferably between ⁇ 0.1 wt .-% and> 5 micrograms / kg, then apply as ultrahigh halogensilanes the halosilanes, the a content of halosilanes of ⁇ 99.99 wt .-% and maximum contamination with, respectively a member of the third main group of the PSE, in particular of boron and in particular of aluminum-containing compounds, of ⁇ 5 ⁇ g / kg with respect to the element per kilogram of halosilane.
• halosilanes which also comprise halosilane mixtures containing> 97% by weight of halosilanes and ⁇ 0.1% by weight of elements of the third main
• Boron-containing compounds are, for example, boron trichloride or boron esters.
• all boron-containing compounds produced in the synthesis of halosilanes or entrained in the processes can be up to a residual content of in particular ⁇ 20 ⁇ g / kg, preferably ⁇ 5 ⁇ g / kg, ⁇ 2 ⁇ g / kg, more preferably ⁇ 1 ⁇ g / kg of boron per kilogram of halosilane are reduced.
• boron and / or a boron-containing compound can be reduced by 50 to 99.9% by weight, depending on the starting concentration thereof.
• a typical aluminum-containing compound is AICI 3 .
• the complex-forming compound triphenylmethyl chloride is preferably added in an amount such that the solubility product of the formed complexes of an element of the third main group of the periodic table (purple PSE) is exceeded with triphenylmethyl chloride, in particular of the compounds containing this element preferably the boron and / or aluminum-containing compounds, and forms a sparingly soluble complexes.
• the amount of added triphenylmethyl chloride is such that this compound only in a slight excess of about ⁇ 20 mol .-%, in particular ⁇ 10 mol .-%, particularly preferably ⁇ 5 mol .-% in Is added to the contamination with elements of the third main group of the periodic table.
• the content of impurities should be determined in the technical grade halosilanes which form low-volatility and / or sparingly soluble complexes with triphenylmethyl chloride.
• These are in particular the above-mentioned boron and / or aluminum-containing compounds.
• the content determination can be done for example by means of ICP-MS.
• the required amount of triphenylmethyl chloride can then be determined.
• triphenylmethyl chloride was added in significant excess to the boron compounds contained.
• the required amount of triphenylmethyl chloride can be adapted to the degree of contamination.
• the added amount of triphenylmethyl chloride can, for example, be adapted more precisely to the solubility product of the sparingly soluble boron and / or aluminum complexes in an environmentally friendly manner.
• triphenylmethyl chloride in process step a) can be carried out by a single metered addition or else stepwise. It can vary depending on
• Plant type or process management the addition as a solid or dissolved in a solvent.
• solvents inert, high-boiling
• Solvent or preferably ultrahigh halosilane, such as silicon tetrachloride and / or trichlorosilane can be used. In this way, the addition of the triphenylmethyl chloride can be metered very accurately and a thorough mixing in a short time
• the halosilanes of technical purity are usually with
• Triphenylmethyl chloride under an inert gas atmosphere, optionally stirred.
• stirring follows for several hours.
• the reaction mixture is stirred for 5 minutes to 10 hours, usually up to one hour.
• the mixture is then worked up by distillation. The process can be carried out batchwise or continuously as needed.
• Examples 1 a to 1 d show that to reduce the content of boron, the distillative workup can be carried out directly after the addition of the triphenylmethyl chloride to separate the sparingly soluble complexes. A certain service life of the reaction mixture leads to no further reduction of the content of boron in the ultrahigh-purity halosilanes. Similarly, thermal treatment of the reaction mixture in terms of heating to complete the reaction is not essential.
• halosilanes prepared in this way in particular the ultrahigh-purity silicon tetrachloride and / or trichlorosilane, can be used to produce epitaxial
• the invention further relates to a plant (1), as well as their use to reduce the content of elements of the third main group of the periodic table (purple PSE), in particular the boron and / or aluminum content, in halosilanes technical grade for the production of ultrahigh-purity halosilanes comprising a device for complexing (2) compounds of these elements, which is associated in particular with a metering device, and a distillation column (3) assigned to the device for complexing.
• purple PSE the third main group of the periodic table
• halosilanes technical grade for the production of ultrahigh-purity halosilanes comprising a device for complexing (2) compounds of these elements, which is associated in particular with a metering device, and a distillation column (3) assigned to the device for complexing.
• purple PSE the third main group of the periodic table
• halosilanes of technical purity for the production of ultrahigh-purity halosilanes from a device for complexation (2) in particular associated with a metering device, and from a distillation column (3) associated with the device (2).
• the distillation column (3) is connected downstream of at least one apparatus for complexation (2), in particular the distillation column (3) is separated from the apparatus for complexing (2).
• the apparatus for complexing (2) parallel and / or in series reactors, such as set and / or tubular reactors, for semi- or continuous complexation and homogenization of the reaction mixture, downstream of which at least one distillation column (3) for the separation of the halosilanes is assigned by the complexes.
• the reactors connected in series are each assigned a distillation column (3).
• the distillation column (3) are associated with a distillation bubble and at least one distillation template for receiving the ultrahigh-purity halosilanes.
• the distillation column (3) in particular a rectification column, has between 1 and 100 theoretical plates.
• the distillatively purified product fractions of ultrahigh-purity halosilanes such as silicon tetrachloride and / or trichlorosilane, are recovered, while the soluble and / or nonvolatile complexes remain in the distillation still.
• the system can be operated in batch mode or continuously.
• the plant (1) may be part of a larger plant, the production of ultrahigh-grade halosilanes starting from metallurgical Silicon is used, in particular the plant (1) is associated with a complete plant comprising a reactor for the conversion of metallurgical silicon.
• the weighing of silicon tetrachloride and triphenylmethyl chloride was carried out as quickly as possible in a beaker on a balance with the respective accuracy.
• the added amount of triphenylmethyl chloride was determined by weighing back the weighing dish. As a rule, a yellow, flaky precipitate formed directly upon addition of the complexing agent.
• the temperature of the reaction mixture did not change.
• the reaction mixture was then transferred to a 500 ml four-necked flask. In the following, a batch was refluxed for an additional hour before the distillative purification of the silicon tetrachloride was carried out. All further batches were processed directly by distillation.
• the distillation was carried out via a distillation column with Keramiksattel analyses (6 mm, 20 cm) and a column head without removal control, with stirring with a Magnetic stir bar under a nitrogen atmosphere.
• the temperature was supplied via an oil bath with temperature control. The bath temperature was during distillation about 80 0 C and the temperature in the distillation bubble towards the end of a distillation up to 60 0 C.
• the boiling point of silicon tetrachloride was at about 57 0 C at atmospheric pressure.
• Triphenylmethyl chloride formed a yellow, fluffy precipitate. There were obtained 186.8 g of a colorless, clear distillate and 9.7 g of a distillation residue.
• the boron content before the addition of the triphenylmethyl chloride was 880 ⁇ g / kg and after the distillation ⁇ 5 ⁇ g / kg.
• FIG. 1 Schematic representation of a plant with a distillation column.
• the plant (1) shown in Figure 1 for reducing the content of elements of the third main group of the Periodic Table in halosilanes is made of a material resistant to the reaction conditions, for example, a stainless steel alloy.
• the plant (1) comprises a device for complexing (2) compounds containing these elements and a distillation column (3) associated with the device.
• the apparatus for complexing (2) is usually a reactor, this may be a boiler reactor or a tubular reactor, which is assigned to the distillation column (3).
• the complexing device (2) has one or two feeders (2.1) and (2.2). About the feed (2.1), the triphenylmethyl chloride and the feed (2.2) can be fed to the technical grade of halosilanes.
• the distillation column with one to 100 theoretical plates is assigned a distillation bubble for the removal of higher-boiling impurities and complexes with triphenylmethyl chloride (3.2) and at least one distillation template (3.1) for receiving in each case one ultrahigh-purity halosilane.
• the distillation column (3) is arranged downstream of the device for complexing (2).
• the complexing device (2) may be assigned a metering device (not shown).

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Inorganic Chemistry (AREA)
• Silicon Compounds (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=40758535

Family Applications (1)

Country Status (11)

Families Citing this family (13)

Family Cites Families (40)

• 2008
  • 2008-01-14 DE DE102008004396A patent/DE102008004396A1/de not_active Withdrawn
  • 2008-11-20 EP EP08871093A patent/EP2252549A2/de not_active Ceased
  • 2008-11-20 US US12/812,857 patent/US20110052474A1/en not_active Abandoned
  • 2008-11-20 UA UAA201010055A patent/UA101175C2/ru unknown
  • 2008-11-20 JP JP2010542547A patent/JP5579078B2/ja not_active Expired - Fee Related
  • 2008-11-20 CA CA2710796A patent/CA2710796A1/en not_active Abandoned
  • 2008-11-20 KR KR1020107015483A patent/KR20100112576A/ko not_active Application Discontinuation
  • 2008-11-20 BR BRPI0822003-4A patent/BRPI0822003A2/pt not_active IP Right Cessation
  • 2008-11-20 WO PCT/EP2008/065902 patent/WO2009089951A2/de active Application Filing
  • 2008-11-20 RU RU2010133877/05A patent/RU2502669C2/ru not_active IP Right Cessation
• 2009
  • 2009-01-13 CN CNA2009100022353A patent/CN101486464A/zh active Pending

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events