CH126586A - Process for improving the combustibility of liquid fuels and fuel obtained by this process. - Google Patents
Process for improving the combustibility of liquid fuels and fuel obtained by this process.Info
- Publication number
- CH126586A CH126586A CH126586DA CH126586A CH 126586 A CH126586 A CH 126586A CH 126586D A CH126586D A CH 126586DA CH 126586 A CH126586 A CH 126586A
- Authority
- CH
- Switzerland
- Prior art keywords
- organic body
- incorporated
- combustibility
- liquid
- improving
- Prior art date
Links
- 239000000446 fuel Substances 0.000 title claims description 21
- 239000007788 liquid Substances 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 18
- 239000000686 essence Substances 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 6
- -1 polycyclic terpene compound Chemical class 0.000 claims description 5
- 239000000341 volatile oil Substances 0.000 claims description 5
- 235000007586 terpenes Nutrition 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 150000001923 cyclic compounds Chemical class 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- JMFRWRFFLBVWSI-NSCUHMNNSA-N coniferol Chemical compound COC1=CC(\C=C\CO)=CC=C1O JMFRWRFFLBVWSI-NSCUHMNNSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- XOKSLPVRUOBDEW-UHFFFAOYSA-N pinane Chemical compound CC1CCC2C(C)(C)C1C2 XOKSLPVRUOBDEW-UHFFFAOYSA-N 0.000 description 3
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- 239000004857 Balsam Substances 0.000 description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 244000004281 Eucalyptus maculata Species 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- 244000018716 Impatiens biflora Species 0.000 description 2
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
- 241000779819 Syncarpia glomulifera Species 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- BEWYHVAWEKZDPP-UHFFFAOYSA-N bornane Chemical compound C1CC2(C)CCC1C2(C)C BEWYHVAWEKZDPP-UHFFFAOYSA-N 0.000 description 2
- 239000010630 cinnamon oil Substances 0.000 description 2
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 2
- 229940119526 coniferyl alcohol Drugs 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229930007927 cymene Natural products 0.000 description 2
- 229960002217 eugenol Drugs 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000001739 pinus spp. Substances 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 2
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 2
- 229940036248 turpentine Drugs 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 244000068485 Convallaria majalis Species 0.000 description 1
- 235000009046 Convallaria majalis Nutrition 0.000 description 1
- 244000304337 Cuminum cyminum Species 0.000 description 1
- 235000007129 Cuminum cyminum Nutrition 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- 235000016622 Filipendula ulmaria Nutrition 0.000 description 1
- 244000061544 Filipendula vulgaris Species 0.000 description 1
- XETQTCAMTVHYPO-UHFFFAOYSA-N Isocamphan von ungewisser Konfiguration Natural products C1CC2C(C)(C)C(C)C1C2 XETQTCAMTVHYPO-UHFFFAOYSA-N 0.000 description 1
- 244000304222 Melaleuca cajuputi Species 0.000 description 1
- 235000001167 Melaleuca cajuputi Nutrition 0.000 description 1
- 235000017710 Melaleuca viridiflora Nutrition 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 244000302151 Myroxylon pereirae Species 0.000 description 1
- 235000014150 Myroxylon pereirae Nutrition 0.000 description 1
- 240000009023 Myrrhis odorata Species 0.000 description 1
- 235000007265 Myrrhis odorata Nutrition 0.000 description 1
- 235000012550 Pimpinella anisum Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 240000002657 Thymus vulgaris Species 0.000 description 1
- 235000007303 Thymus vulgaris Nutrition 0.000 description 1
- 244000007731 Tolu balsam tree Species 0.000 description 1
- 235000007423 Tolu balsam tree Nutrition 0.000 description 1
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 229940011037 anethole Drugs 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229930006742 bornane Natural products 0.000 description 1
- 239000001877 cajuput oil Substances 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- 239000010634 clove oil Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000010656 jasmine oil Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000001673 myroxylon balsanum l. absolute Substances 0.000 description 1
- 239000001157 myroxylon pereirae klotzsch resin Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 229930006728 pinane Natural products 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- 229940088660 tolu balsam Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Landscapes
- Liquid Carbonaceous Fuels (AREA)
Description
Procédé pour améliorer la combustibilité de combustibles liquides et combustible obtenu selon ce procédé. La présente invrntion a pour objet un pro cédé pour améliorer la combustibilité de com bustibles liquides, tels que: huiles minérales, végétales et animales, goudrons (goudron de houille), benzols, alcools et en particulier les pétroles lampants ou autres hydrocarbures li quides ou huiles lourdes. L'invention com- hrcnd,aussi un combustible liquide à combus tibilité améliorée obtenu selon ledit procédé.
Dans les moteurs utilisant comme com- bu=tible ries hydrocarbures, la dissociation des molécules d'hydrocarbure est généralement d'autant plus brutale, que ceux-ci sont plus lourds. Il en résulte que l'hydrogène brûle avant le carbone et que celui-ci s'allumant en retard, sa combustion n'est que partielle et donne lieu à. un @harbonneme@nt, c'est-à-dire à une mise en liberté de carbone qui se dé pose dans le cylindre en provoquant des en crassements, ou s'en échappe sous forme de fumée noire.
Pour éviter cet inconvénient, on a proposé d'ajouter aux combustibles hydro carbures liquides, des composés organo-mé- talliqurs tels que le plomb tétraéthylé. Mais si l'usage de ces composés peut améliorer la combustion des hydrocarbures lourds, il pré sente non seulement l'inconvénient de l'en crassement des cylindres moteurs par les composés métalliques solides formés lors de la combustion, mais également celui de répan dre dans l'atmosphère avec les produits de la combustion, des vapeurs métalliques toxiques qui ont donné lieu à des accidents.
Le procédé, objet de la présente invention, permet d'améliorer la combustibilité des com bustibles liquides sans toutefois présenter les inconvénients ci-dessus. Il est caractérisé en ce que l'on incorpore aux liquides combusti bles une quantité extrêmement faible d'au moins un corps organique de ceux contenus dans les huiles essentielles. De préférence la quantité dudit corps est comprise entre<B>0,001</B> et 1 % du liquide combustible. .
En effet, dès que l'un de ces corps au moins est présent ans une proportion très mi nime dans le combustible, l'encrassement des moteurs, par exemple, est notablement dimi nué, la quantité de carbone non brûlée est bien plus faible et il n'apparaît pas de com posés métalliques nuisibles comme cela a lieu par l'usage d'autres composés et procédés. Lors de la combustion des combustibles li quides ainsi obtenus, on peut fournir plus d'air de combustion ou ce qui revient au même, on peut réduire le débit du combus tible, ce qui produit une augmentation du rendement, une économie de combustible.
Lors de la. vaporisation de ces combustibles, par exemple dans un carburateur, il est utile également de fournir un peu plus de chaleur à ces combustibles liquides améliorés qu'aux combustibles ordinaires.
Les corps additionnés, suivant l'invention, peuvent être constitués soit de carbone et d'hydrogène, soit de carbone, d'hydrogène et d'oxygène et ne contiennent pas de métaux swsceptibles de produire .des composés nuisi bles. On peut employer soit .des huiles essen tielles qui sont des mélanges complexes, soit une ou un mélange de substances que con tiennent ces essences, et qu'on peut aussi ob tenir artificiellement.
Parmi les corps susceptibles d'être incor porés, on citera @ I. Certains hydrocarbures cycliques (sa turés et non saturés) contenus dans les hui les essentielles, par exemple: a) le menthane (hydrocarbure saturé).
b) les constituants des essences végétales telle que l'essence de citron, l'essence de cumin, l'essence d'eucalyptus (hydrocarbures cycliques non saturés). Tels sont par exemple: le limonène, qui est un hydrocarbure terpé- nique et le, cymène qui est un hydrocarbure benzénique.
II. Des composés terpéniques polycycli ques, notamment ceux contenus. dans les es sences végétales, par exemple des, groupes du pinane et du camphane. Parmi les repré sentants les plus importants du groupe du pinane, on citera les pinènes.
III. Des composés cycliques oxygénés, en particulier ceux contenus dans les essences végétales: par exemple le menthol dans l'es- sence de menthe, le terpinéol dans l'essence -de muguet (composés terpéniques).
IV. Des composés de la série aromatique, tels que: L'alcool benzylique (essence de jasmin), l'acide benzoïque ou l'acide cinnamique, con tenus dans le baume du Pérou, le baume de tolu, le baume de copahu, le baume de ben join; L'aldéhyde cinnamique, constituant prin cipal de l'essence -de cannelle; Le thymol (essence de thym); L'alhéhyde orthoxybenzylique (essence de reine des prés); L'eugénol, l'isoeugénol, la. vanilline (es sences de girofle, de cajeput, d'eucalyptus).
Des substances odorantes contenues dans les essences naturelles et obtenues aussi arti ficiellement: L'alcool coniférylique, l'essence de mou tarde, l'essence d'anis, l'anéthol, l'eucalyptol. Voici, à titre d'exemple, comment on peut préparer divers combustibles liquides, selon le procédé de l'invention: Exemple <I>1:</I> Du pétrole lampant. d'un poids spécifique compris entre 0,780 et. 0,820 est additionné de @0,4 à 0,5 %, en poids, d'essence de t6ré- benthine et de 0,002 à 0,003 % en poids de cymène. Le mélange est utilisable dans des moteurs à explosion.
<I>Exemple 2:</I> Du pétrole lampant d'un poids spécifique compris entre 0,780 et 0,820 est a,d-d.itionné de 0,3 à 0,4 %, en poids, d'essence de t6ré- benthine et d'environ 0,004 % d'essence de canelle, 0,002 % d'essence de cajeput et 0,001 % d'essence de girofle. Le produit est utilisable dans des moteurs à explosion.
Selon d'autres exemples, on peut addition ner au pétrole lampant., du limonène, de l'eu- génol ou isoeugénol, de l'alcool coniférylique, seuls ou en mélange dans des proportions également minimes.
<I>Exemple 3:</I> 50 parties en poids de pétrole traité sui vant les exemples précédents sont addition- .fées à. 50 parties, en poids, d'essence miné rale légère d'une densité de 0,710.
lie produit obtenu peut remplacer prati quement l'essence légère dans des moteurs à explosion.
Les combustibles de densité supérieure additionnés du corps organique selon l'inven tion, peuvent être utilisés comme succédanés des essences légères ou éthers de pétrole uti lisés jusqu'à présent dans certains moteurs (aviation).
L'invention n'est pas limitée aux produits obtenus suivant l'un ou l'autre des exemples qui ont été donnés et l'on peut prévoir d'au tres proportions des substances qui entrent dans la composition des produits sans que l'on s'écarte de la présente invention. Du reste, l'expérience a, montré que les corps mentionnés agissent plutôt par leur présence que par les proportions de leur dosage.
Process for improving the combustibility of liquid fuels and fuel obtained by this process. The present invention relates to a process for improving the combustibility of liquid fuels, such as: mineral, vegetable and animal oils, tars (coal tar), benzols, alcohols and in particular lamp oils or other liquid or liquid hydrocarbons. heavy oils. The invention also comprises a liquid fuel with improved combustibility obtained by said process.
In engines using hydrocarbon fuels as fuel, the dissociation of the hydrocarbon molecules is generally all the more brutal the heavier they are. As a result, hydrogen burns before carbon and the latter ignites late, its combustion is only partial and gives rise to. a @ harbonneme @ nt, that is to say a release of carbon which settles in the cylinder causing fouling, or escapes in the form of black smoke.
To avoid this drawback, it has been proposed to add to liquid hydrocarbon fuels, organometallic compounds such as tetraethylated lead. But if the use of these compounds can improve the combustion of heavy hydrocarbons, it presents not only the drawback of the fouling of the engine cylinders by the solid metal compounds formed during combustion, but also that of spreading in the atmosphere with the products of combustion, toxic metal fumes which have resulted in accidents.
The process which is the subject of the present invention makes it possible to improve the combustibility of liquid fuels without, however, exhibiting the above drawbacks. It is characterized in that an extremely small amount of at least one organic body of those contained in essential oils is incorporated into the combustible liquids. Preferably, the amount of said body is between <B> 0.001 </B> and 1% of the combustible liquid. .
Indeed, as soon as at least one of these bodies is present in a very small proportion in the fuel, the fouling of the engines, for example, is notably reduced, the quantity of unburned carbon is much lower and no harmful metal compounds occur as occurs through the use of other compounds and processes. During the combustion of the liquid fuels thus obtained, more combustion air can be supplied, or what amounts to the same thing, the fuel flow rate can be reduced, which produces an increase in efficiency, fuel economy.
When. vaporizing these fuels, for example in a carburetor, it is also useful to provide a little more heat to these improved liquid fuels than to ordinary fuels.
The additives according to the invention can consist of either carbon and hydrogen or carbon, hydrogen and oxygen and do not contain metals which are suspected of producing harmful compounds. Either essential oils which are complex mixtures can be used, or one or a mixture of substances which these essences contain, and which can also be obtained artificially.
Among the bodies liable to be incorporated, we can cite @ I. Certain cyclic hydrocarbons (unsaturated and unsaturated) contained in the essential oils, for example: a) menthane (saturated hydrocarbon).
b) the constituents of vegetable essences such as lemon essence, cumin essence, eucalyptus essence (unsaturated cyclic hydrocarbons). Such are, for example: limonene, which is a terpene hydrocarbon and cymene which is a benzene hydrocarbon.
II. Polycyclic terpene compounds, in particular those contained. in plant species, for example groups of pinane and camphane. Among the most important representatives of the pinane group, we can mention the pinenes.
III. Oxygenated cyclic compounds, in particular those contained in plant essences: for example menthol in mint oil, terpineol in lily of the valley oil (terpene compounds).
IV. Compounds of the aromatic series, such as: Benzyl alcohol (jasmine oil), benzoic acid or cinnamic acid, contained in Peru balsam, tolu balsam, copahu balsam, balsam from ben join; Cinnamic aldehyde, the main constituent of cinnamon oil; Thymol (essence of thyme); Orthoxybenzyl alhyde (essence of meadowsweet); Eugenol, isoeugenol, la. vanillin (essences of cloves, cajeput, eucalyptus).
Odorous substances contained in natural essences and also obtained artificially: Coniferyl alcohol, essence of soft tarde, essence of anise, anethole, eucalyptol. Here is, by way of example, how various liquid fuels can be prepared, according to the process of the invention: Example <I> 1: </I> Lamp oil. with a specific weight of between 0.780 and. 0.820 is added from 0.4 to 0.5%, by weight, of turpentine and from 0.002 to 0.003% by weight of cymene. The mixture can be used in internal combustion engines.
<I> Example 2: </I> Lamp oil with a specific gravity between 0.780 and 0.820 is added to 0.3 to 0.4%, by weight, of turpentine and about 0.004% cinnamon oil, 0.002% cajuput oil and 0.001% clove oil. The product can be used in internal combustion engines.
According to other examples, it is possible to add to the kerosene, limonene, eugenol or isoeugenol, coniferyl alcohol, alone or as a mixture in likewise minimal proportions.
<I> Example 3: </I> 50 parts by weight of petroleum treated according to the preceding examples are added to. 50 parts by weight of light mineral spirits with a specific gravity of 0.710.
the product obtained can practically replace light gasoline in internal combustion engines.
The higher density fuels added with the organic body according to the invention can be used as substitutes for light gasolines or petroleum ethers hitherto used in certain engines (aviation).
The invention is not limited to the products obtained according to one or the other of the examples which have been given and it is possible to provide other very proportions of the substances which enter into the composition of the products without the need for departs from the present invention. Moreover, experience has shown that the substances mentioned act rather by their presence than by the proportions of their dosage.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE126586X | 1925-11-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH126586A true CH126586A (en) | 1928-06-16 |
Family
ID=3863479
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH126586D CH126586A (en) | 1925-11-21 | 1926-11-15 | Process for improving the combustibility of liquid fuels and fuel obtained by this process. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH126586A (en) |
-
1926
- 1926-11-15 CH CH126586D patent/CH126586A/en unknown
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