WO1982004434A1 - Purification of silicon source materials - Google Patents
Purification of silicon source materials Download PDFInfo
- Publication number
- WO1982004434A1 WO1982004434A1 PCT/US1982/000614 US8200614W WO8204434A1 WO 1982004434 A1 WO1982004434 A1 WO 1982004434A1 US 8200614 W US8200614 W US 8200614W WO 8204434 A1 WO8204434 A1 WO 8204434A1
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- WO
- WIPO (PCT)
- Prior art keywords
- trichlorosilane
- impurities
- boron
- silicon
- purification
- Prior art date
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Classifications
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- 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
-
- 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
- C01B33/02—Silicon
- C01B33/021—Preparation
- C01B33/027—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material
- C01B33/035—Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by decomposition or reduction of gaseous or vaporised silicon compounds in the presence of heated filaments of silicon, carbon or a refractory metal, e.g. tantalum or tungsten, or in the presence of heated silicon rods on which the formed silicon is deposited, a silicon rod being obtained, e.g. Siemens process
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Definitions
- This invention relates in general to a process for purifying silicon source materials and more specifically to a process for removing impurities from trichlorosilane or from mixtures of trichlorosilane and silicon tetrachloride.
- Large quantities of polycrystalline silicon are produced by the hydrogen reduction of a silicon bearing reactant gas.
- trichlorosilane or mixtures of trichlorosilane with other silicon bearing reactants such as silicon tetrachloride are reduced to deposit polycrystalline silicon on a heated filament.
- the polycrystalline silicon be of extremely high purity. This in turn requires that the silicon source gas be of high purity and be free from trace impurities.
- BCI3 present as an impurity in HSiCl3 is co plexed by a hydrolysis process in which water vapor is passed over the surface of the trichlorosilane.
- the purified HSiCl3 is then separated from the partially hydrolyzed polysiloxane
- trichlorosilane is purified by reacting trichlorosilane with small quantities of oxygen.
- the complex formed by this oxidation reaction in turn reacts with BCI3 or PCI3 to form a boron or phosphorous complex which can be removed from the purified trichlorosilane by distillation.
- Preferably about 0.01 to 0.2 mole percent of oxygen is used in the reaction and the reaction is carried out at a temperature between about 170 and 300°C. Lower concentrations of oxygen also complex boron and phosphorous compounds, but are less effective. Concentrations of oxygen greater than about 1.0 mole percent consume larger fractions of the HSiCl3 without further enhancing the purification.
- FIG. 1 illustrates the flow and recycling of reactants in a polycrystalline deposition cycle
- FIG. 2 is a flow diagram illustrating apparatus for purification in accordance with the invention.
- FIG. 1 The conventional polycrystalline silicon deposition process is illustrated in FIG. 1. Initially trichloro ⁇ silane 10 and hydrogen 12 are injected into a reactor bell jar 14. Within the bell jar are heated filaments 16. The hydrogen and trichlorosilane react at the surface of the filaments to deposit polycrystalline silicon. By-products and unreacted trichlorosilane and hydrogen are exhausted
- the effluent includes, besides hydrogen and trichlorosilane, hydrogen chloride, silicon tetrachloride, other silicon bearing compounds, and those portions of the impurities which were originally contained in the trichlorosilane and which were not incorporated in the deposited polycrystalline silicon.
- the effluent is processed at 20 to separate out hydrogen 22, silicon bearing reactants 23, and hydrogen chloride 24.
- the hydrogen and silicon bearing reactants are recycled as inputs to the silicon deposition process. Makeup amounts of trichlorosilane are added to the silicon bearing effluent.
- an improved purifi ⁇ cation step specifically for removing boron and phosphorous from either trichlorosilane or other silicon bearing reactants including mixtures of trichlorosilane and silicon tetrachloride is provided.
- boron or phosphorous impurities are complexed by heating the silicon bearing compound and adding a metered amount of oxygen.
- a silicon source material 30 enters the purification system and, for conven ⁇ ience and uniformity, flows into a ballast tank 32.
- the silicon source material is in a gaseous or liquid state and may be, for example, a saturated hydrogen-trichlorosilane gas mixture or the halosilane product stream from a polycrystalline silicon reactor apparatus.
- the latter is comprised mainly of trichlorosilane and silicon tetrachloride.
- From the ballast tank the silicon bearing gas passes through a pump 34 and particulate filters 36 to a gas/gas heat exchanger 38 in which the gas stream is initially warmed.
- the gas After prewarming in the heat exchanger the gas passes through a primary heater 40 where it reaches the desired reaction temperature. After passing through primary heater 40 a carefully controlled amount of oxygen is added at 42. Adding the oxygen to the heated stream of silicon bearing gas results in a chemical reaction (to be described below) which results in the complexing of boron and phosphorous impurites in the gas stream.
- the heated gas stream then passes again through the heat exchanger where the heat is imparted to the incoming gas stream.
- the now cooled gas stream is optionally collected in a holding tank 44, and then continues on to a conventional distilla ⁇ tion apparatus 46 where the boron and phosphorous complexes are separated from the silicon gas stream.
- the purified silicon gas stream is then in condition for injection back into the polycrystalline silicon deposition apparatus.
- GCMS gas chro atography mass spectroscopy
- Competing with the BCI3 reaction is the following side reaction:
- the initital step in this process is the formation of a CI3 Si-OH intermediate.
- the evidence for this type of species is that the final boron reaction product is in the form of B-O-Si species which would originate from a B-Cl species reacting with Si-OH.
- the driving force in this reaction is the thermodynamically favorable formation of the strong B-0 and H-Cl bonds.
- the initial oxidation of the HSiCl3 and the competing side reaction represent trichorosilane which is sacrificed in the purification process. To optimize the process it is desirable that this loss of trichorosilane be minimized. Under laboratory conditions it has been determined that 1.0 moles of O2 reacts to complex about 0.38 moles of boron under the conditions specified above. The amount of oxygen necessary to purify the silicon source
- OMPI material can thus be adjusted depending on known impurity levels. In general about 0.01 to 0.2 mole percent of oxygen will be adequate to remove boron and phosphorous compounds from the source material without resulting in too severe a loss of the source material itself.
- the quantity of HSiCl3 consumed during the purification process is reduced further by diluting the HSiCl3 to be purified with high purity SiCl4.
- the initial oxidative purification step is identical with or without SiCl , namely
- both the HSiCl3 and SiCl ⁇ are found to be greatly reduced in boron and phosphorous contamination.
- Example I Nitrogen at a flow rate of about 0. 2 liters per minute is bubbled through a tank filled with about 3000-3500 grams of HSiCl 3 . As the nitrogen gas bubbles through the HSiCl3, the nitrogen becomes saturated and forms a HSiCl3/ 2 vapor combination. To test the effectiveness of the purification process this vapor is then intentionally contaminated with known quantities of BCI3. High concentrations (about 1.0% in HSiCl3) of BCI3 are used to facilitate analysis of the purification data. The contamination with BCI3 is accomplished by bubbling nitrogen gas through a tank containing about 500 milliliter BCI3 to form a saturated BCI3/N2 vapor combination which is then mixed with HSiCl3/ 2 vapor at a selected rate.
- flow rates and pressures are adjusted to deliver 3.6xl0 ⁇ 2 moles/min. of HSiCl3 and 3.6xl0 ⁇ 4 moles/ min. of BCI3 in the gas stream.
- the gas stream is passed through a furnace tube heated to about 180°C with a residence time of about 20 seconds in the heated tube.
- the effluent stream is sampled approximately every 15 minutes with GCMS equipped for on-line mahual injection.
- Oxygen is added at a flow rate of 2.0x10" ⁇ moles/min. ; the resulting BCI3 in the effluent stream is measured to be reduced to 2.8xl0" 4 moles/min.
- the oxygen flow rate is increased to 4x10" ⁇ moles/min. and the BCI3 in the effluent drops further to 2.1xl0 ⁇ 4 moles/min.
- the oxidative purification is repeated at temperatures of 200, 220, 250, 300, 350, 400, 450 and 500°C. Repro ⁇ ducible results are obtained for temperatures less than or equal to 300°C. Preferably the process is carried out at about 200°C. Above 300°C polysiloxane residue is found to build up in the GCMS transfer lines. Also, slightly less complexing of the BCI3 is found to occur at temperatures over about 300°C.
- the apparatus as depicted in FIG. 2 is used to purify the effluent from a polycrystalline silicon reactor.
- the silicon bearing materials comprise about 25 percent trichlorosilane and balance silicon tetrachloride.
- the boron contaminant level in the mixture of trichlorosilane and silicon tetrachloride is measured to be greater than or equal to about 0.75 ppb (parts per billion).
- the phosphorous contaminant level in the mixture is measured to be greater than or equal to about 0.65 ppb.
- the effluent gas is heated to a temperature of about 180 to 220°C.
- Oxygen at a level of about 0.01 to 0.2 mole O2 per mole HSiCl3 is mixed with the silicon bearing vapor. After the reaction the silicon bearing reactants are distilled to remove higher boiling materials. After the distillation the remaining silicon bearing mixture is analyzed and determined to contain less than 0.10 ppb boron and less than 0.18 ppb phosphorous.
Abstract
A process for the purification of trichlorosilane and other silicon source materials. Trace impurities of boron and phosphorous are removed from trichlorosilane (30) by reacting small amounts of oxygen (42) with the trichlorosilane at a temperature between about 170 and 300 C. The oxygen reacts with the Si-H bond in HSiCl3 to form a 'SiOH' species which in turn complexes impurities such as BCl3 or PCl3 present in the trichlorosilane. Purification of the trichlorosilane is then easily accomplished during a subsequent distillation step (46) which separates the purified trichlorosilane from the less volatile complexed boron or phosphorous compounds.
Description
PURIF1CATION OF SILICON SOURCE MATERIALS
Background of the Invention
This invention relates in general to a process for purifying silicon source materials and more specifically to a process for removing impurities from trichlorosilane or from mixtures of trichlorosilane and silicon tetrachloride. Large quantities of polycrystalline silicon are produced by the hydrogen reduction of a silicon bearing reactant gas. For example, in a commonly used process, trichlorosilane or mixtures of trichlorosilane with other silicon bearing reactants such as silicon tetrachloride are reduced to deposit polycrystalline silicon on a heated filament. In the semiconductor industry it is required that the polycrystalline silicon be of extremely high purity. This in turn requires that the silicon source gas be of high purity and be free from trace impurities. Most impurities can be readily removed from trichlorosilane or silicon tetrachloride by conventional distillation techniques. Trace impurities of boron or phosphorous which are usually present in the form of BCI3 or PCI3, however, are not easily removed by distillation. To reduce such contaminants to an acceptably low level by distillation would require several sequential distillation steps. It is desirable to have a purification process which achieves a still higher level of purification, unobtainable by distillation alone, which does not require the time and expense of multiple distillations.
Other processes have been proposed for purifying trichlorosilane. In one process, for example, BCI3 present as an impurity in HSiCl3 is co plexed by a hydrolysis process in which water vapor is passed over the surface of the trichlorosilane. The purified HSiCl3 is then separated from the partially hydrolyzed polysiloxane
OMPI
residue by distillation. When this type of purification is carried out in an operating system, however, the system can be quickly clogged up by the copious amounts of solid polysiloxane residue which are formed. It has also been suggested that elemental boron (or phosphorous) can be removed from HSiCl3 by the addition of iodine or bromine to the HSiCl3. The boron (or phosphosous) reacts with the iodine or bromine to form iodides or bromides which are readily separated from HSiCl3 by distillation. This purification technique, however, is not effective unless the boron (or phosphorous) is in the elemental state. Thus in most applications this technique is ineffective for the removal of boron and phosphorous compounds. Because of the shortcomings of the prior art processes it has become necessary to deve-lope a novel and improved purification system which will provide the high purity silicon source reactants necessary in the semiconductor industry. It is therefore an object of this invention to provide an improved process for purifying silicon source materials.
It is another object of this invention to provide an improved process for purifying trichlorosilane. It is a further object of this invention to provide an improved process for purifying trichlorosilane admixed with other silicon source gases in the recovery loop of a polycrystalline silicon production process.
It is a still further object of this invention to provide an improved process for purifying mixtures of trichlorosilane and silicon tetrachloride.
It is another object of this invention to provide an improved process for removing boron and phosphorous impurities from silicon source gases and liquids.
IJUREAIT
OMPI
Brief Summary of the Invention
The foregoing and other objects are achieved in the present invention through the use of a novel purification system employing the partial oxidation of the silicon source gas. In one embodiment of the invention trichlorosilane is purified by reacting trichlorosilane with small quantities of oxygen. The complex formed by this oxidation reaction in turn reacts with BCI3 or PCI3 to form a boron or phosphorous complex which can be removed from the purified trichlorosilane by distillation. Preferably about 0.01 to 0.2 mole percent of oxygen is used in the reaction and the reaction is carried out at a temperature between about 170 and 300°C. Lower concentrations of oxygen also complex boron and phosphorous compounds, but are less effective. Concentrations of oxygen greater than about 1.0 mole percent consume larger fractions of the HSiCl3 without further enhancing the purification.
Brief Description of the Drawings
FIG. 1 illustrates the flow and recycling of reactants in a polycrystalline deposition cycle; and FIG. 2 is a flow diagram illustrating apparatus for purification in accordance with the invention.
Detailed Description of Preferred Embodiments
The conventional polycrystalline silicon deposition process is illustrated in FIG. 1. Initially trichloro¬ silane 10 and hydrogen 12 are injected into a reactor bell jar 14. Within the bell jar are heated filaments 16. The hydrogen and trichlorosilane react at the surface of the filaments to deposit polycrystalline silicon. By-products and unreacted trichlorosilane and hydrogen are exhausted
'BU RE U
OMPI
from the bell jar at 18. The effluent includes, besides hydrogen and trichlorosilane, hydrogen chloride, silicon tetrachloride, other silicon bearing compounds, and those portions of the impurities which were originally contained in the trichlorosilane and which were not incorporated in the deposited polycrystalline silicon. The effluent is processed at 20 to separate out hydrogen 22, silicon bearing reactants 23, and hydrogen chloride 24. The hydrogen and silicon bearing reactants are recycled as inputs to the silicon deposition process. Makeup amounts of trichlorosilane are added to the silicon bearing effluent.
Before the silicon bearing effluent is returned to the reactor chamber, it is possible to process the effluent through a purification operation indicated schematically at 26. In the past, this purification has been accomplished by one or more distillation steps. While distillation is effective in removing certain impurities, it is relatively inefficient in removing trace amounts of boron. Trace amounts of boron and phosphorous are typically present in the incoming trichlorosilane. A portion of these impurities is deposited with the polycrystalline silicon as a dopant. The remaining impurities enter the recycling loop and are subsequently returned to the reactor unless removed in some purification step. The amount of impurities in the recycle loop builds up as the process continues. Although the amount of impurities present in the incoming trichlorosilane may be low enough to not have an adverse doping effect of the deposited polycrystalline silicon the amount of impurities resulting from the build up can have such a deleterious effect.
In accordance with the invention, an improved purifi¬ cation step specifically for removing boron and phosphorous from either trichlorosilane or other silicon bearing reactants including mixtures of trichlorosilane and silicon tetrachloride is provided. In the improved process boron
or phosphorous impurities are complexed by heating the silicon bearing compound and adding a metered amount of oxygen.
Apparatus suitable for carrying out the purification process is illustrated in FIG. 2. A silicon source material 30 enters the purification system and, for conven¬ ience and uniformity, flows into a ballast tank 32. The silicon source material is in a gaseous or liquid state and may be, for example, a saturated hydrogen-trichlorosilane gas mixture or the halosilane product stream from a polycrystalline silicon reactor apparatus. The latter is comprised mainly of trichlorosilane and silicon tetrachloride. From the ballast tank the silicon bearing gas passes through a pump 34 and particulate filters 36 to a gas/gas heat exchanger 38 in which the gas stream is initially warmed. After prewarming in the heat exchanger the gas passes through a primary heater 40 where it reaches the desired reaction temperature. After passing through primary heater 40 a carefully controlled amount of oxygen is added at 42. Adding the oxygen to the heated stream of silicon bearing gas results in a chemical reaction (to be described below) which results in the complexing of boron and phosphorous impurites in the gas stream. The heated gas stream then passes again through the heat exchanger where the heat is imparted to the incoming gas stream. The now cooled gas stream is optionally collected in a holding tank 44, and then continues on to a conventional distilla¬ tion apparatus 46 where the boron and phosphorous complexes are separated from the silicon gas stream. The purified silicon gas stream is then in condition for injection back into the polycrystalline silicon deposition apparatus.
The process in the above described apparatus is monitored by standard gas chro atography mass spectroscopy (GCMS) . With the gas heated to a temperature below about 160°C no reaction is observed between the O2 and the
HSiCl3. At higher temperatures the oxidation of HSiCl3
- UREA OMPl_
is rapid and consumption of oxygen is complete. No trace of O2 is detected at these higher temperatures by the GCMS. The major trichlorosilane oxidation products are examined; for reaction temperatures between about 170 and 250°C one small chain species predominants. The resultant oxidation product formed in this temperature range has a molecular weight of m/e = 248 which is consistent with the following structure:
Cl Cl
H - Si - O - Si - Cl
Cl Cl
At higher temperatures, higher molecular weight species result consistent with linear and cyclic compounds containing three and four silicon atoms.
It is believed that the oxidative purification of trichlorosilane can be described by the following equations:
_>170°C
HSiCl + 02 [HOSiCl3] + 0.
The intermediate product indicated by the dagger t then reacts with BCI3 as follows:
BC13 + [HOSiCl3] —> Cl2B-0-SiCl3 + HC1.
Competing with the BCI3 reaction is the following side reaction:
HSiCl3 + [HOSiCl3]f —> Cl3Si-0-SiCl H + HC1.
The initital step in this process is the formation of a CI3 Si-OH intermediate. The evidence for this type of species is that the final boron reaction product is in the form of B-O-Si species which would originate from a B-Cl species reacting with Si-OH. The driving force in this reaction is the thermodynamically favorable formation of the strong B-0 and H-Cl bonds.
It is believed that phosphorous impurities are removed by a similar complexing mechanism. The proposed [H0S Cl3]t intermediate reacts with PC13 as follows:
PCI + [HOSiCl3]+ --> Cl2P-0-SiCl3 + HC1 .
At temperatures greater than about 3t)0°C a more complex reaction occurs and intra and inter species thermally induced polysiloxane rearrangement products are formed. No additional purification is observed at these higher temperatures indicating that the thermal . rearrangement products are not reactive with BCI3 or
The incorporation of boron or phosphorous into the polysiloxane chain raises the boiling point of the boron or phosphorous containing species considerably. During a subsequent distillation process these higher boiling materials are readily separated from the HSiCl3 yielding HSiCl3 essentially free from the original boron and/or phosphorous contamination.
The initial oxidation of the HSiCl3 and the competing side reaction represent trichorosilane which is sacrificed in the purification process. To optimize the process it is desirable that this loss of trichorosilane be minimized. Under laboratory conditions it has been determined that 1.0 moles of O2 reacts to complex about 0.38 moles of boron under the conditions specified above. The amount of oxygen necessary to purify the silicon source
"Bϋ EAtT
OMPI
material can thus be adjusted depending on known impurity levels. In general about 0.01 to 0.2 mole percent of oxygen will be adequate to remove boron and phosphorous compounds from the source material without resulting in too severe a loss of the source material itself.
The quantity of HSiCl3 consumed during the purification process is reduced further by diluting the HSiCl3 to be purified with high purity SiCl4. The initial oxidative purification step is identical with or without SiCl , namely
HSiCl + 0 —> [HOSiCl ] + 0
In addition to reacting with BCI3 and PCI3, the [H0SiCl3]+ reacts with SiCl4 as follows:
SiCl4 + [H0SiCl3]+ > Cl3SiOSiCl3 + HC1
In purifying mixtures of HSiCl3 and SiC^, such as the product mixture recovered from the silicon deposition process, by low level oxidation, both the HSiCl3 and SiCl^ are found to be greatly reduced in boron and phosphorous contamination.
The following non-limiting examples will further serve to illustrate preferred embodiments of the invention.
Example I Nitrogen at a flow rate of about 0. 2 liters per minute is bubbled through a tank filled with about 3000-3500 grams of HSiCl3. As the nitrogen gas bubbles through the HSiCl3, the nitrogen becomes saturated and forms a HSiCl3/ 2 vapor combination. To test the effectiveness of the purification process this vapor is then intentionally contaminated with known quantities of
BCI3. High concentrations (about 1.0% in HSiCl3) of BCI3 are used to facilitate analysis of the purification data. The contamination with BCI3 is accomplished by bubbling nitrogen gas through a tank containing about 500 milliliter BCI3 to form a saturated BCI3/N2 vapor combination which is then mixed with HSiCl3/ 2 vapor at a selected rate.
To test the effectiveness of various oxygen concentra¬ tions and reaction temperatures on the purification process both oxygen concentration and temperature were maintained as variables. Concentration of boron in the HSiCl3 vapor are monitored both before and after the oxidation reaction. Below about 170°C no reaction is observed between the O2 and the HSiCl3. At temperatures greater than about 170°C the oxidation of HSiCl3 is rapid and the consumption of the additive oxygen complete.
Specifically, flow rates and pressures are adjusted to deliver 3.6xl0~2 moles/min. of HSiCl3 and 3.6xl0~4 moles/ min. of BCI3 in the gas stream. The gas stream is passed through a furnace tube heated to about 180°C with a residence time of about 20 seconds in the heated tube. The effluent stream is sampled approximately every 15 minutes with GCMS equipped for on-line mahual injection.
After calibration of the GCMS against various repre- sentative BCI3 flow rates, oxidative purification is initiated. Oxygen is added at a flow rate of 2.0x10"^ moles/min. ; the resulting BCI3 in the effluent stream is measured to be reduced to 2.8xl0"4 moles/min. The oxygen flow rate is increased to 4x10"^ moles/min. and the BCI3 in the effluent drops further to 2.1xl0~4 moles/min.
The oxidative purification is repeated at temperatures of 200, 220, 250, 300, 350, 400, 450 and 500°C. Repro¬ ducible results are obtained for temperatures less than or equal to 300°C. Preferably the process is carried out at about 200°C. Above 300°C polysiloxane residue is found to
build up in the GCMS transfer lines. Also, slightly less complexing of the BCI3 is found to occur at temperatures over about 300°C.
Analysis of the data indicates about 1.0 moles of oxygen reacts with the HSiCl3 to complex about 0.38 moles of BCI3 at temperatures between about 170°C and about 300°C. Increased mechanical and process problems are encountered at temperatures above about 300°C.
Example II
The apparatus as depicted in FIG. 2 is used to purify the effluent from a polycrystalline silicon reactor. The silicon bearing materials comprise about 25 percent trichlorosilane and balance silicon tetrachloride. The boron contaminant level in the mixture of trichlorosilane and silicon tetrachloride is measured to be greater than or equal to about 0.75 ppb (parts per billion). The phosphorous contaminant level in the mixture is measured to be greater than or equal to about 0.65 ppb. The effluent gas is heated to a temperature of about 180 to 220°C. Oxygen at a level of about 0.01 to 0.2 mole O2 per mole HSiCl3 is mixed with the silicon bearing vapor. After the reaction the silicon bearing reactants are distilled to remove higher boiling materials. After the distillation the remaining silicon bearing mixture is analyzed and determined to contain less than 0.10 ppb boron and less than 0.18 ppb phosphorous.
Following each of the above examples the purification apparatus is dismantled and examined. No build-up of oily residues is found, indicating that no long chain molecules are formed during the purification.
Thus it is apparent that there has been provided, in accordance with the invention, a process for purifying silicon source materials which fully meets the objects and advantages set forth above. Boron and phosphorous impurities are effectively removed from silicon source
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-li¬
material by controlled oxidation. While the invention has been described in terms of specific embodiments thereof it is not intended that the invention be so limited. Variations and modifications in the purification apparatus and in the application of the invention will of course be apparent to those skilled in the art. For example, those skilled in the art will recognize that in the production of HSiCl3 from either the reaction of HC1 and metallurgical grade silicon or from -the reaction of SiCl4, metallur- gical grade silicon and hydrogen, oxidative purification in accordance with the invention can be applied to simplify the necessary purification process to yield higher purity silicon source materials at a lower cost. Accordingly, it is intended to embrace all such variations and modifica- tions as fall within the scope of the invention.
Claims
1. A process for removing impurities from silicon source material which comprises the steps of: reacting oxygen with said silicon source material and said impurities to form complexes of said impurities; and separating said complexes from said silicon source material to yield a higher purity source material.
2. The process of claim 1 wherein said step of reacting is accomplished at an elevated temperature.
3. The process of claim 2 wherein said elevated temperature is between about 170 and 300°C.
4. The process of claim 1 wherein said silicon source material comprises trichlorosilane.
5. The process of claim 1 wherein said silicon source material comprises trichlorosilane and silicon tetrachloride.
6. The process of claim 5 wherein said oxygen is present in a ratio with HSiCl3 of about 0.01 to 1.0 mole percent.
7. A process for purifying trichlorosilane which comprises the steps of: heating said trichlorosilane to a temperature between about 170 and 300°C; reacting a portion of said trichlorosilane with oxygen at said temperature to form intermediate trichlorosilane oxidation products; allowing said oxidation products to form a complex incorporating impurities present in said trichlorosilane; and distilling to remove said complex with said impurities from said trichlorosilane.
8. A process for removing boron and phosphorous impurities from trichlorosilane which comprises the steps of: heating trichlorosilane containing boron and phosphorous impurities to a temperature greater than about 170°C; reacting oxygen with said trichlorosilane and said boron and phosphorous impurities to form complexes of boron and complexes of phosphorous; and distilling to remove said complexes from said trichlorosilane.
9. The process of claim 8 wherein said trichlorosilane is admixed with silicon tetrachloride.
10. The process of claim 8 wherein said oxygen is present in a ratio with trichlorosilane of about 0.01 to about 1.0 mole percent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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DE823248813T DE3248813T1 (en) | 1981-06-15 | 1982-05-10 | CLEANING OF SILICON SOURCE MATERIALS |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US273519810615 | 1981-06-15 | ||
US06/273,519 US4374110A (en) | 1981-06-15 | 1981-06-15 | Purification of silicon source materials |
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WO1982004434A1 true WO1982004434A1 (en) | 1982-12-23 |
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US (2) | US4374110A (en) |
JP (1) | JPS58500895A (en) |
DE (1) | DE3248813T1 (en) |
IT (1) | IT1148182B (en) |
WO (1) | WO1982004434A1 (en) |
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DE10048504A1 (en) * | 2000-09-29 | 2002-04-18 | Messer Griesheim Gmbh | Removing impurities such as phosphine and arsine from chlorosilane gas e.g. for semiconductor manufacture, comprises contacting the chlorosilane with a heated surface |
EP2507174B1 (en) | 2009-12-04 | 2013-11-06 | Spawnt Private S.à.r.l. | Method for producing halogenated polysilanes |
EP3168190A4 (en) * | 2014-07-10 | 2018-05-09 | Shin-Etsu Chemical Co., Ltd. | Method for purifying chlorosilane |
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US4529707A (en) * | 1982-09-21 | 1985-07-16 | General Electric Company | Detection of boron impurities in chlorosilanes |
US4585643A (en) * | 1985-05-31 | 1986-04-29 | Union Carbide Corporation | Process for preparing chlorosilanes from silicon and hydrogen chloride using an oxygen promoter |
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DE10048504A1 (en) * | 2000-09-29 | 2002-04-18 | Messer Griesheim Gmbh | Removing impurities such as phosphine and arsine from chlorosilane gas e.g. for semiconductor manufacture, comprises contacting the chlorosilane with a heated surface |
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US9139702B2 (en) | 2009-12-04 | 2015-09-22 | Spawnt Private S.A.R.L. | Method for producing halogenated polysilanes |
US9458294B2 (en) | 2009-12-04 | 2016-10-04 | Spawnt Private S.À.R.L. | Method for removing impurities from silicon |
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Also Published As
Publication number | Publication date |
---|---|
US4374110A (en) | 1983-02-15 |
IT8248535A0 (en) | 1982-05-28 |
DE3248813C2 (en) | 1988-09-22 |
JPS58500895A (en) | 1983-06-02 |
US4409195A (en) | 1983-10-11 |
DE3248813T1 (en) | 1983-06-16 |
JPS641407B2 (en) | 1989-01-11 |
IT1148182B (en) | 1986-11-26 |
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