US1028357A - Illuminant and method of producing the same. - Google Patents
Illuminant and method of producing the same. Download PDFInfo
- Publication number
- US1028357A US1028357A US61517311A US1911615173A US1028357A US 1028357 A US1028357 A US 1028357A US 61517311 A US61517311 A US 61517311A US 1911615173 A US1911615173 A US 1911615173A US 1028357 A US1028357 A US 1028357A
- Authority
- US
- United States
- Prior art keywords
- solvent
- illuminant
- producing
- acetylene
- gas
- 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
- 238000000034 method Methods 0.000 title description 3
- 239000002904 solvent Substances 0.000 description 18
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 13
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 13
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical group CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/50—Carbon dioxide
Definitions
- This invention has reference to a new illu ⁇ minant consisting of a mixture of acetylene gas and the vapor of a highly volatile acetylene solvent, such vapor being luminous when burning and formin an important constituent element of the light producing mixture.
- the carbonyl compounds to which I refer include such liquids as aldehydes, ketones, esters and acids of the fatty series. And I have further found that of the above liquid compounds the one possessing the highest solvent power and at the same time capable of being held in liquid formby placing it under pressure in a closed container is acetaldehyde. This substance is a liquid at temperatures below 21 (1., and evaporates rapidly at temperatures from 5 C. to its boiling point, the amount of evaporation increasing .as the boiling point is approached.
- a tank containing a mixture of acetaldehyde and formaldehyde saturated with acetylene gas comprises a portable packa e from which on release of pressure an il uminant issues consisting of acetylene gas, formalde .hyde gas, and acetaldehyde vapor, all of which are combustible.
- a characteristic of the invention is the employment of a highly volatile solvent, by which I mean a solvent that volatilizes rapidly at ordinary room or laboratory temperatures, and my experience and present knowledge lead me to believe that no solvent boiling above 22 C. will be etficient.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Gas Separation By Absorption (AREA)
Description
Ul FMlE.
JOSEPH .HIDY JAMES, OF PITTSBURGH, PENNSYLVANIA.
ILLUMINANT AND METHOD OF PRODUCING THE SAME,
.No Drawing.
Specification of Letters Patent.
Patented June a, 1912.
Application filed March 17, 1911. Serial No. 615,173.
.ments in Illuminants and Methods of Producing the Same, of which the following is a specification.
This invention has reference to a new illu} minant consisting of a mixture of acetylene gas and the vapor of a highly volatile acetylene solvent, such vapor being luminous when burning and formin an important constituent element of the light producing mixture. Various solvents possess the necessary characteristics, both as to the luminosity of, the solvent vapor, and when in liquid form the capacity for absorbing relatively large volumes of acetylene. I have found that all the best solvents for acetylene are those of organic compounds containing the carbonyl group (=C- 'O), and I have further found that the lower the molecular weight of the compound used the higher is its solvent power for acetylene gas. The carbonyl compounds to which I refer include such liquids as aldehydes, ketones, esters and acids of the fatty series. And I have further found that of the above liquid compounds the one possessing the highest solvent power and at the same time capable of being held in liquid formby placing it under pressure in a closed container is acetaldehyde. This substance is a liquid at temperatures below 21 (1., and evaporates rapidly at temperatures from 5 C. to its boiling point, the amount of evaporation increasing .as the boiling point is approached.
' Further developing the idea of low molecular weight compounds I have discovered that by saturating acetaldehyde with formaldehyde gas the capacity of the solvent for acetylene gas is greatly increased. A tank containing a mixture of acetaldehyde and formaldehyde saturated with acetylene gas comprises a portable packa e from which on release of pressure an il uminant issues consisting of acetylene gas, formalde .hyde gas, and acetaldehyde vapor, all of which are combustible.
, A characteristic of the invention is the employment of a highly volatile solvent, by which I mean a solvent that volatilizes rapidly at ordinary room or laboratory temperatures, and my experience and present knowledge lead me to believe that no solvent boiling above 22 C. will be etficient.
Under the practices-prior to my invention it has not been proposed to have the solvent form a constituent part of the illuminant,
nor has a solvent been proposed heretofore possessing the necessary dual characteristics, viz., capacity in liquid form for absorbing the requisite quantities of acetylene gas, and
sufliciently volatile to emerge as a vapor with the gas. On the contrary, every effort has been directed toward completely separating the acetylene as it emerges from the container, both for producing an unadulterated illuminant and for preserving the solvent so that it may be reused.
I am aware that as incident to the present practice a very small percentage of the solvent escapes with the gas and is burned therewith, but this is not a desired occur rence nor does it to any noticeable or appreciable extent comprise a constituent element of the illuminant. The solvent from which it emanates is not highly volatile, nor volatile in the sense that it may or can const-i tute a vfactor in the composition of the illuminantf With tanks charged as heretofore by the use of non-volatile solvent the delivery pipes leading to the burners are not infrequently flooded, particularlyat the beginning of the discharge, extinguishing the light and wasting the solvent. This inconvenience is obviated herein as the solvent vaporizes as soon as it emerges from the container into the line and cannot reach the burner in liquid form.
The advantages of the composition must be apparent. With the entire gaseous and liquid contents of a container available as an illuminant, far greater lighting hoursservice is provided for a given charge of acetylene than has heretofore been'attained.
I claim: 7
1. An illuminant consisting of a mixture of acetylene gas, acetaldehyde vapor, and In testimony whereof I affix my signature formalldehydele1 gisf d u in presence of two Witnesses.
2. T emet 0 0 r0 ucin ani uminant consisting in saturat ng liqui d acetaldehyde JOSEPH HIDY JAMES 5 with formaldehyde as, charging acetylene Witnesses:
gas into the acetal ehyde thus saturated, J. M. NESBIT, and then vaporizing said liquid. F. E. GAITHER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61517311A US1028357A (en) | 1911-03-17 | 1911-03-17 | Illuminant and method of producing the same. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61517311A US1028357A (en) | 1911-03-17 | 1911-03-17 | Illuminant and method of producing the same. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1028357A true US1028357A (en) | 1912-06-04 |
Family
ID=3096650
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US61517311A Expired - Lifetime US1028357A (en) | 1911-03-17 | 1911-03-17 | Illuminant and method of producing the same. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1028357A (en) |
-
1911
- 1911-03-17 US US61517311A patent/US1028357A/en not_active Expired - Lifetime
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