US686949A - Method of making cyanids. - Google Patents
Method of making cyanids. Download PDFInfo
- Publication number
- US686949A US686949A US5141601A US1901051416A US686949A US 686949 A US686949 A US 686949A US 5141601 A US5141601 A US 5141601A US 1901051416 A US1901051416 A US 1901051416A US 686949 A US686949 A US 686949A
- Authority
- US
- United States
- Prior art keywords
- cyanamid
- temperature
- alkali
- carbon
- cyanid
- 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 - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title description 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 12
- 239000003513 alkali Substances 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- 150000001340 alkali metals Chemical class 0.000 description 7
- 229910021529 ammonia Inorganic materials 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000003575 carbonaceous material Substances 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 241001072332 Monia Species 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001722 carbon compounds Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005648 named reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C3/00—Cyanogen; Compounds thereof
- C01C3/08—Simple or complex cyanides of metals
- C01C3/10—Simple alkali metal cyanides
Definitions
- the object of the invention described in the specification of the aforesaid application 4o lfor Letters Patent is to transform immediately into cyanamid the sodiin amid obtained by the combination of sodium and ammonia, so as to protect it from decomposition,
- Y as the said sodium amid is easily decom- 45 posed at the temperature required for the formation of cyanid.
- the same object is attained according to the present invention by4 omitting wholly or in part the addition of cyanid recommended in the specification of 5o the said prior application and keeping the temperature of the Iirst part of -the processen ⁇ low that no cyanid is formed, but the whole of the sodium amid is at the moment of its formation converted into cyanamid by the carbon present. ⁇ While this cyanamid isin the course of formation the temperature must be raised slowly to the higher melting-point ofy this body and brought finally to about 600 centigrade.
- the temperature at which the cyanamid ⁇ is formed according to this invention does not involve any important loss through the decomposition of alkali amid. It is only after the whole of the sodium is converted into cyanamid, and thus protected against losses, that the temperature is so raised as to eect its conversion into cyanid according to Drechsele well-known reaction Name+-022mm.
- solid carbon- such, for example, as charcoal-other carbonaceous substances which contain carbon mechanically or chemically combined and are capable of giving i1 up as required by the above reactions
- liquid or gaseous hydrocarbons may be introduced into the molten sodium through the same inlet as the ammoniaA or through a separate inlet.
- the accompanying drawing shows a melting vessel in sectional elevation, in which m5 process may be carried out.
- a. is the vessel
- b the charging-opening
- c the tube, which may be used for passing ammonia into the vessel.
- alkali cyanide which consists in rst reacting alkali metal with Huid carbon compounds and ammonia while maintaining the temperature of the mass at about 350 to 600 centigrade
- alkali cyauamid is formed, and re- 5 acting the produced cyanamid with a further 4.
- the process herein described of making alkali cyanids which consists in first reacting alkali metal with carbonaceous substances and ammonia while maintaining the temperature at about 350 to 600 centigrade, whereby cyanamid is formed, and then reacting the produced cyanamid with a furtherquantity of carbonaceous substances at a temperature of substantially 750 to 800 centigrade,where by cyanid is formed, as and for the purpose -set forth.
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
No. 686,949. Patented Nov. I9, |901. J. PFLEGER.
METHOD 0F MAKlNG CYANIDS.
(Application filed Mar. l5, 1901.)
(No Model.)
l JWM INITEE STATES PATENT OFFICE.
.OHANNESV'PFLEGER, OF FRANKFORTON-THE-MAIN, GERMANY, ASSIGNOR TO THE FIRM OF DEUTSCHE GOLD 8a SILBER-SCHEIDE AN'STALT, VORM. ROESSLER, OF FRANKFORT-ONgTHElMAlN, GERMANY.
Msi-Honor MAKING oYANlofs.
SPEGIFIGAITI'MW forming part of Letters Patent No. 686,949, dated November 19, 1901.
l Application filed March 145, 1901, Serial Nof 51,416. (N0 specimens.)
To all whom it' may concern:
Be it known that I, JOHANNES'PFLEGER, a subject of the Emperor of Germany, and a resident of 215 Gutleutstrasse,.Frankfort-on- 5 the-Main, Germany, have invented certain new and useful Improvements in the Manufacture of Alkali Oyanids, of which the'following is a specification.
, In the specification of my application for 1o Letters Patent, Serial No. 39,382, dated December 10, 1900, a process is described by which the synthesis of alkali cyanide is effected from an alkali metal, ammonia, and carbon by transforming the alkali amid, 15 which is easily decomposable at a high temperature, into the corresponding remarkably stable cyanamid by adding to it, as it forms a calculated quantity of cyanid, and converting the said L :yanamid into cyanid by 2o combination with a further equivalent of carbon while the temperature is raised. f Further tests made by me have shown that the intermediate formation of the cyanamid and a better utilization of the alkali metal and ain- 25 monia can be eEected in an improved manner. I have discovered that cyanamid can also be formed directly from the amid of the alkali metal and carbon if the temperature of the reacting mixture be maintained at a point 3o not exceeding the temperature at which the amide of the alkali metal decomposes.
The formation of cyanamid from alkali amid and carbon according to the formula:
commences at 350 centigrade and is a vmost powerful one at 400 centigrade.
The object of the invention described in the specification of the aforesaid application 4o lfor Letters Patent is to transform immediately into cyanamid the sodiin amid obtained by the combination of sodium and ammonia, so as to protect it from decomposition,
Y as the said sodium amid is easily decom- 45 posed at the temperature required for the formation of cyanid. The same object is attained according to the present invention by4 omitting wholly or in part the addition of cyanid recommended in the specification of 5o the said prior application and keeping the temperature of the Iirst part of -the processen `low that no cyanid is formed, but the whole of the sodium amid is at the moment of its formation converted into cyanamid by the carbon present. `While this cyanamid isin the course of formation the temperature must be raised slowly to the higher melting-point ofy this body and brought finally to about 600 centigrade. Unlike that which takes place in the direct formation of cyanid, which requires ,a much higher temperature, the temperature at which the cyanamid` is formed according to this invention does not involve any important loss through the decomposition of alkali amid. It is only after the whole of the sodium is converted into cyanamid, and thus protected against losses, that the temperature is so raised as to eect its conversion into cyanid according to Drechsele well-known reaction Name+-022mm.
Instead of solid carbon-such, for example, as charcoal-other carbonaceous substances which contain carbon mechanically or chemically combined and are capable of giving i1 up as required by the above reactions may be used. For instance, liquid or gaseous hydrocarbons may be introduced into the molten sodium through the same inlet as the ammoniaA or through a separate inlet.
The accompanying drawing shows a melting vessel in sectional elevation, in which m5 process may be carried out.
In the drawing, a. is the vessel, b the charging-opening, and c the tube, which may be used for passing ammonia into the vessel..
I claim- 1. The process herein described of making alkali cyanids, lwhich consists in iirst reacting alkali metal with carbon and ammonia in proportions necessary for the formation of alkali cyanamid,while maintaining the temperature of the mass at about 350 to`600 centigrade, and then reacting the 'produced cyanamid with a further. quantity of carbon at a highel temperature, ,whereby cyanid is formed, as
and for the purpose set forth.
, 2. The process herein described of making alkali cyanide, which consists in rst reacting alkali metal with Huid carbon compounds and ammonia while maintaining the temperature of the mass at about 350 to 600 centigrade,
whereby alkali cyauamid is formed, and re- 5 acting the produced cyanamid with a further 4. The process herein described of making alkali cyanids, which consists in first reacting alkali metal with carbonaceous substances and ammonia while maintaining the temperature at about 350 to 600 centigrade, whereby cyanamid is formed, and then reacting the produced cyanamid with a furtherquantity of carbonaceous substances at a temperature of substantially 750 to 800 centigrade,where by cyanid is formed, as and for the purpose -set forth.
' In testimony whereof I have signed my 3 name to this specification in the presence of two subscribing witnesses. JOHANNES PFLEGER. Witnesses:
JEAN GRUND, CARL GRUND.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5141601A US686949A (en) | 1901-03-15 | 1901-03-15 | Method of making cyanids. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5141601A US686949A (en) | 1901-03-15 | 1901-03-15 | Method of making cyanids. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US686949A true US686949A (en) | 1901-11-19 |
Family
ID=2755493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US5141601A Expired - Lifetime US686949A (en) | 1901-03-15 | 1901-03-15 | Method of making cyanids. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US686949A (en) |
-
1901
- 1901-03-15 US US5141601A patent/US686949A/en not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US686949A (en) | Method of making cyanids. | |
| SE438845B (en) | PROCEDURE FOR THE PREPARATION OF CYANVETE OUTLETS FROM CONDENSABLE CARBON AND AMMONIA | |
| US957842A (en) | Production of titanium-nitrogen compounds. | |
| US3028432A (en) | Production of isopropylvinylenedecaborane | |
| US686950A (en) | Method of making cyanamids. | |
| US1083585A (en) | Catalytic production of ammonia. | |
| US1816087A (en) | Fort-on-the-main | |
| US3057808A (en) | Carbon-nitrogen polymers and preparation thereof | |
| US3549684A (en) | Production of o-chlorobenzalmalononitrile | |
| US3028413A (en) | Process for the production of acetonitrile | |
| US682741A (en) | Method of making cyanids. | |
| US1051303A (en) | Process of producing nitrogen compounds. | |
| US2992898A (en) | Preparation of carbonyl sulfide | |
| US3273975A (en) | Production of chlorodifluoramine | |
| US2878249A (en) | Preparation of trimeric hydrogen cyanide | |
| US971501A (en) | Production of ammonia. | |
| US967943A (en) | Process of making hydrocyanic acid. | |
| US553550A (en) | Process of producing illuminating-gas | |
| US1154801A (en) | Volatile aluminum compounds and process of producing same. | |
| US1075085A (en) | Working with hydrogen under pressure. | |
| US649550A (en) | Art of producing illuminating-gas. | |
| US3489528A (en) | Preparation of polyaminoboranes | |
| US671479A (en) | Method of making cyanids. | |
| US954080A (en) | Process of producing hydrocyanic acid. | |
| US698464A (en) | Method of making alkaline cyanids. |