US2128368A - Method of making waterproof igniting compositions - Google Patents
Method of making waterproof igniting compositions Download PDFInfo
- Publication number
- US2128368A US2128368A US80022A US8002236A US2128368A US 2128368 A US2128368 A US 2128368A US 80022 A US80022 A US 80022A US 8002236 A US8002236 A US 8002236A US 2128368 A US2128368 A US 2128368A
- Authority
- US
- United States
- Prior art keywords
- igniting
- chlorate
- resol
- mass
- per cent
- 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
- 239000000203 mixture Substances 0.000 title description 20
- 238000004519 manufacturing process Methods 0.000 title description 6
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 26
- 229920003987 resole Polymers 0.000 description 14
- 239000003513 alkali Substances 0.000 description 9
- 238000002485 combustion reaction Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 235000011837 pasties Nutrition 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000011049 filling Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 229960004011 methenamine Drugs 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229940079938 nitrocellulose Drugs 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06F—MATCHES; MANUFACTURE OF MATCHES
- C06F3/00—Chemical features in the manufacture of matches
Definitions
- the usual safety match has proved insufliciently resistive to the influence of the moist air, and the reasons for this fact are among other things the following.
- the heads of the matches are porous, the moist air can easily penetrate even into the interior parts of the heads, thereby subjecting the whole igniting mass to the influence of the humidity.
- the greater part of the head consists of salts soluble in water, these salts will disappear partially due to the influence oi the humidity, and-as the binding l agent is capable of absorbing considerable amounts of water, it will lose its rigidity and be loosened from the match splint, when the latter is rubbed against an igniting surface.
- Another proposal involves the employment of a product of condensation, in which case the igniting composition has been prepared by mixing the requisite chemicals with water, phenol, aldehyde, and a catalyst.
- This method sufiers from considerable inconveniences due to the fact that the igniting mass, even after drying, still contains large amounts of water which cannot be removed.
- the product of condensation produced is by itself incombustible and cannot, as a result, aid in the development of power during the combustion, but on the other hand 10 large amounts of heat are required to vaporize the water included.
- the sensibility of the mass to ignition will still be sufiiciently high, even when such a large amount of binding agent as 20-30 per cent is used, which still, in turn, affords a reliable protection of the imbedded chlorate grains against moisture.
- the binding agent may by itself burn at a very low speed of combustion, a reduction of the speed of combustion of the igniting mass will consequently result, so that the combustible substance of the match splint (as wood, cardboard, stearin and so on) may have sufilcient time to be ignited.
- the artificial resin most suitable as binding agent is an intermediate product in the preparation of resite known as resol.
- a product especially fit for the purpose may be prepared, for instance, as follows: 100 parts phenol, 100 parts formaline, and 5 parts ammonia are heated to about 100 C., until a heavy muddiness appears as result of the precipitated resol, which is al lowed to settle to the bottom and then can be easily separated.
- This product is insoluble in water but easily soluble in alcohol, acetone and other usual solvents.
- the preparation of the igniting mass can either be effected by first dissolving the resol in alcohol and then admixing the other substances to be included in the mass, or by grinding the resol together with one or more of the substances not developing oxygen, and then moistening the mixture with alcohol and admixing the remaining chemicals.
- Such an igniting mass' may be of the following composition:
- the igniting mass of the above stated composition is fit for use as paste in the heading of matches which may be dried in the usual way after the heads have been put on. If it is desired toimpart to the match heads an especially high degree of hardness this may be effected by hardening at a temperature of 100-150 C. Ac cording to the time and temperature of the hardening process the resol will then be converted, less or more, into the final product, resite, which is non-burning. Moreover, the hardening process may be accelerated or carried out at lower temperature if a small quantity of, for instance, hexamethylene tetramine is added.
- Artificial resins may also be employed for the igniting composition of igniting rods, and the desired speed of combustion may be obtained by accordingly regulating the degree of hardening.
- a method of manufacturing a moistureproof initial igniting body which consists in mixing in an organic solvent, to form a pasty mixture, resol, a chlorate of alkali, and combustible and filling materials, said resol amounting to between 15 and 30 per cent and said chlorate of alkali amounting'to at least per cent by weight of the dry ingredients, forming such mixture into an igniting body, and evaporating the solvent.
- a method of manufacturing a moistureproof initial igniting body which consists in mixing in an organic solvent, to form a pasty mixture, resol and a chlorate of alkali, and combustible and filling materials, said resol amounting to between 15 and 30 per cent and said chlorate of alkali amounting to at least 50 per cent by weight of the dry ingredients, forming such mixture into an igniting body, evaporating the solvent, and converting the resol into resite by heat treatment.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
- Dental Preparations (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Air Bags (AREA)
Description
Patented Aug. 30, 1938 UNITED STATES PATENT OFFiCE METHOD OF MAKING WATERPROOF IGNITING COMPOSITIONS Sweden No Drawing. Original application November 20,
1933, Serial No. 698,94 plication May 15, 193
2. Divided and this ap- 6. Serial No. 80,022. In
Sweden November 28, 1932 3 Claims.
This application is-a division of Serial No. 693,942, filed November 20, 1933.
In countries with a very humid climate the usual safety match has proved insufliciently resistive to the influence of the moist air, and the reasons for this fact are among other things the following. As the heads of the matches, as a rule, are porous, the moist air can easily penetrate even into the interior parts of the heads, thereby subjecting the whole igniting mass to the influence of the humidity. As the greater part of the head consists of salts soluble in water, these salts will disappear partially due to the influence oi the humidity, and-as the binding l agent is capable of absorbing considerable amounts of water, it will lose its rigidity and be loosened from the match splint, when the latter is rubbed against an igniting surface.
Because of the absence of an oxidizing agent which is insoluble in water as substitution for the chlorate usually employed, experiments with moisture-proof igniting composition, have only had for their object, as a rule, to flnd an insoluble binding agent. Many proposals with this object in view have also been made, but they have always proved to suiler from drawbacks, which have rendered them less flt for commercial use.
Thus, for instance, an admixture of linseed oil or latex to the composition has been made. These substances, however, render the igniting mass less ignitable so that only up to 6-7 per cent could be used with advantage, whereas considerably larger amounts are required in order to reliably imbed the chlorate in the binding agent to afford protection against moisture. It is thus evident that in this way there will be obtained no essential improvement, but on the contrary an impairment, in as much as the moisture that enters can only be caused to disappear with great diiliculty, whereas igniting compositions containing a water soluble binding agent may, as a rule, again be fit for use after having been dried for a little while.
Furthermore, proposals have also been made to use some easily combustible substances dlssolved in organic solvents, as nitro-cellulose in amyl acetate and resin in spirits, but in case of the admixture of a suflicient quantity of chlorate to permit ignition of the composition against a striking surface, there will occur a very violent combustion of very short duration, rendering the transfer of the flame to the splint diflicult.
Another proposal involves the employment of a product of condensation, in which case the igniting composition has been prepared by mixing the requisite chemicals with water, phenol, aldehyde, and a catalyst. This method, however, sufiers from considerable inconveniences due to the fact that the igniting mass, even after drying, still contains large amounts of water which cannot be removed. The product of condensation produced is by itself incombustible and cannot, as a result, aid in the development of power during the combustion, but on the other hand 10 large amounts of heat are required to vaporize the water included. The combustion will, consequently, take place at a low temperature, and this circumstance together with the smothering eifect of the water vapors results, as a rule, in a suppression of the flame so that the igniting mass may only glow. From manufacturing point of view still another drawback arises, namely, that the binding agent under consideration may only for a very short while maintain a consistency suitable for the dipping action.
It is an object of this invention to overcome all these drawbacks by a new method of producing a moisture-proof initial igniting body which consists in mixing in an organic solvent, to form a pasty mixture, an artificial resin, as a binding agent a chlorate of alkali, and combustible and filling materials, said artificial resin amounting to at least 15 per cent by weight and said chlorate of alkali amounting to at least 50 per cent by weight of the dry ingredients, and forming such mixture into an igniting body, whereupon the solvent is caused to evaporate.
By the use of such a high amount of chlorate of alkali the sensibility of the mass to ignition will still be sufiiciently high, even when such a large amount of binding agent as 20-30 per cent is used, which still, in turn, affords a reliable protection of the imbedded chlorate grains against moisture. As, on the other hand, the binding agent may by itself burn at a very low speed of combustion, a reduction of the speed of combustion of the igniting mass will consequently result, so that the combustible substance of the match splint (as wood, cardboard, stearin and so on) may have sufilcient time to be ignited.
The artificial resin most suitable as binding agent is an intermediate product in the preparation of resite known as resol. A product especially fit for the purpose may be prepared, for instance, as follows: 100 parts phenol, 100 parts formaline, and 5 parts ammonia are heated to about 100 C., until a heavy muddiness appears as result of the precipitated resol, which is al lowed to settle to the bottom and then can be easily separated. This product is insoluble in water but easily soluble in alcohol, acetone and other usual solvents. The preparation of the igniting mass can either be effected by first dissolving the resol in alcohol and then admixing the other substances to be included in the mass, or by grinding the resol together with one or more of the substances not developing oxygen, and then moistening the mixture with alcohol and admixing the remaining chemicals. Such an igniting mass'may be of the following composition:
Potassium chlorate 59 parts Potassium bichromate 1 part Manganese dioxide 3 parts Sulphur 6 parts Powdered glass 6 parts Resol 25 parts-i-alcohol 17.5 P rts 100 parts The igniting mass thus produced will not solidify so rapidly as the well-known product of condensation above referred to, but can be maintained at a pasty consistency for a long while.
The igniting mass of the above stated composition is fit for use as paste in the heading of matches which may be dried in the usual way after the heads have been put on. If it is desired toimpart to the match heads an especially high degree of hardness this may be effected by hardening at a temperature of 100-150 C. Ac cording to the time and temperature of the hardening process the resol will then be converted, less or more, into the final product, resite, which is non-burning. Moreover, the hardening process may be accelerated or carried out at lower temperature if a small quantity of, for instance, hexamethylene tetramine is added. Because of the heat required for the hardening process it is advisable, to parafiine the matches after the hardening instead of before the dipping, as is amasce otherwise usual, as in other case the paramne will melt and flow away. Since the hardening process has the efiect of reducing the speed of combustion of the igniting composition, it is possible, by moderating the degree of hardening, to regulate the speed of combustion within wide limits.
Artificial resins may also be employed for the igniting composition of igniting rods, and the desired speed of combustion may be obtained by accordingly regulating the degree of hardening.
What I claim is:-
1. A method of manufacturing a moistureproof initial igniting body which consists in mixing in an organic solvent, to form a pasty mixture, resol, a chlorate of alkali, and combustible and filling materials, said resol amounting to between 15 and 30 per cent and said chlorate of alkali amounting'to at least per cent by weight of the dry ingredients, forming such mixture into an igniting body, and evaporating the solvent.
2. A method of manufacturing a moistureproof initial igniting body which consists in mixing in an organic solvent, to form a pasty mixture, resol and a chlorate of alkali, and combustible and filling materials, said resol amounting to between 15 and 30 per cent and said chlorate of alkali amounting to at least 50 per cent by weight of the dry ingredients, forming such mixture into an igniting body, evaporating the solvent, and converting the resol into resite by heat treatment.
3. A method of manufacturing a moistureproof initial igniting body which consists in mixing in an organic solvent, to form a pasty mix ture, a resol, a chlorate of alkali, and combustible and filling materials, said resole amounting to between 15 and 30 per cent and said chlorate of alkali amounting to at least 50 per cent by weight of the dry ingredients, applying such mixture to match splints, evaporating the solvent, converting the resol into resite by heat treatment, and afterwards paraifining the matches.
LARS ERIK LARSSON.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE399864D BE399864A (en) | 1932-11-28 | ||
| NL38522D NL38522C (en) | 1932-11-28 | ||
| DEL84807D DE640903C (en) | 1932-11-28 | 1933-11-16 | Process for the production of Zuendholzern with water-insensitive ignition compound |
| GB32514/33A GB414938A (en) | 1932-11-28 | 1933-11-21 | Improved method of making water-proof matches |
| FR764397D FR764397A (en) | 1932-11-28 | 1933-11-27 | Process for manufacturing matches with a moisture-insensitive ignition paste |
| US80022A US2128368A (en) | 1932-11-28 | 1936-05-15 | Method of making waterproof igniting compositions |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE414938X | 1932-11-28 | ||
| US69894233A | 1933-11-20 | 1933-11-20 | |
| US80022A US2128368A (en) | 1932-11-28 | 1936-05-15 | Method of making waterproof igniting compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2128368A true US2128368A (en) | 1938-08-30 |
Family
ID=32045758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US80022A Expired - Lifetime US2128368A (en) | 1932-11-28 | 1936-05-15 | Method of making waterproof igniting compositions |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2128368A (en) |
| BE (1) | BE399864A (en) |
| DE (1) | DE640903C (en) |
| FR (1) | FR764397A (en) |
| GB (1) | GB414938A (en) |
| NL (1) | NL38522C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2635954A (en) * | 1948-09-21 | 1953-04-21 | Monsanto Chemicals | Moisture resistant friction elements and process of producting same |
| US2863751A (en) * | 1954-08-18 | 1958-12-09 | Bjorn Tore | Ignition compositions for matches, striking surfaces and the like |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2421778A (en) * | 1943-12-24 | 1947-06-10 | Olin Ind Inc | Initiating explosives |
| FR2682375B1 (en) * | 1991-10-10 | 1993-11-26 | Exploitation Indle Tabacs Allume | COMPOSITION FOR MATCH BUTTONS CONTAINING IRON PHOSPHIDES. |
-
0
- BE BE399864D patent/BE399864A/xx unknown
- NL NL38522D patent/NL38522C/xx active
-
1933
- 1933-11-16 DE DEL84807D patent/DE640903C/en not_active Expired
- 1933-11-21 GB GB32514/33A patent/GB414938A/en not_active Expired
- 1933-11-27 FR FR764397D patent/FR764397A/en not_active Expired
-
1936
- 1936-05-15 US US80022A patent/US2128368A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2635954A (en) * | 1948-09-21 | 1953-04-21 | Monsanto Chemicals | Moisture resistant friction elements and process of producting same |
| US2863751A (en) * | 1954-08-18 | 1958-12-09 | Bjorn Tore | Ignition compositions for matches, striking surfaces and the like |
Also Published As
| Publication number | Publication date |
|---|---|
| DE640903C (en) | 1937-01-15 |
| FR764397A (en) | 1934-05-19 |
| BE399864A (en) | |
| NL38522C (en) | |
| GB414938A (en) | 1934-08-16 |
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