US917706A - Formic-aldehyde-containing composition and process of making the same. - Google Patents
Formic-aldehyde-containing composition and process of making the same. Download PDFInfo
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- US917706A US917706A US368855A US1907368855A US917706A US 917706 A US917706 A US 917706A US 368855 A US368855 A US 368855A US 1907368855 A US1907368855 A US 1907368855A US 917706 A US917706 A US 917706A
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- aldehyde
- formic
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title description 28
- 239000000203 mixture Substances 0.000 title description 21
- 238000000034 method Methods 0.000 title description 12
- 230000008569 process Effects 0.000 title description 11
- 150000001299 aldehydes Chemical class 0.000 description 23
- 239000003921 oil Substances 0.000 description 17
- 235000019198 oils Nutrition 0.000 description 15
- 235000015112 vegetable and seed oil Nutrition 0.000 description 10
- 235000005687 corn oil Nutrition 0.000 description 9
- 239000005871 repellent Substances 0.000 description 9
- 239000008158 vegetable oil Substances 0.000 description 9
- 239000003981 vehicle Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 235000013311 vegetables Nutrition 0.000 description 7
- 230000009471 action Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 230000002421 anti-septic effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000346 nonvolatile oil Substances 0.000 description 3
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229960005233 cineole Drugs 0.000 description 2
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000002070 germicidal effect Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000019871 vegetable fat 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
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical group C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- HHBOUFYYHJJTNU-UHFFFAOYSA-N 1,3,6-thiadiazepane-2,7-dithione Chemical compound S=C1NCCNC(=S)S1 HHBOUFYYHJJTNU-UHFFFAOYSA-N 0.000 description 1
- 241001527902 Aratus Species 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 229960003920 cocaine Drugs 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 239000013003 healing agent Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
Definitions
- This invention relates to a new composiion 'of matter for disinfecting, germicide, an-
- tiseptic and medicinal purposes and process of making the same and it consists of a mixture, compound, or solution of formic .aides hyde or its polymerides'in a iixed Water-repellent, such as fixed vegetable oils or fatty vehicles, which compounds, or compositions, may or may not be associated with other medica-ting agents, the object being to produce ai'ixed fatty composition of Water-repellent nature containing forniic aldehyde which macde, antiseptic, and medicinal properties,
- Fig. 2 is a sectional View of an axial stuffing ⁇ box through which passes the inlet and outlety pipes for the purpose of heating the contents of the apparatus by means pf steam;
- ⁇ Fig. 3 is a View of a perforated pipe through Which the formic aldehyde is introduced into the apparatus.
- l As soon as the oil has become heated to about l0() degrees C., l introduce into the oLthrough the perforated pipe X foi-mic aldehyde gas, under a pressure of about twenty pounds, by opening ⁇ the valve l.
- This foi-mic aldehyde gas passes' first through the check-valvell Which prcventsthe oil or other substances in the receptacleV A from being forced back in to the formic aldehyde -reservoir or generating apparatus.
- the a aratus is maintained in a rotary condltion for about two hours, whereby the formic aldehyde becomes thoroughly dissolved in or assimilated. with the oil by the agitative action ot' the revolving drum and the fixed steam heating coil o and perforated coil .r through which the formic aidehyde is introduced.
- the revolution of the apparatus is then stopped and the oil, charged With ormic aldehyde, is Withdrawn through the nine-K by opening the valve lc.
- the pipe K is provided at its outer end With-a flange .e for the purpose of coupling lup or clamping to conduits leading to a reservoir for the fixed oil charged with forinic aldehyde.
- the Whole apparatus is axially supported by the stands L'through which the ends of the hollow trunnions of the receptacle A are supported.
- l l L lt can be seen that the oil and formic aldehyde are thus thoroughly mixed and assimilated by the action ol" heat and pressure, together ⁇ With the agitation caused by..
- eucalyptol I can employ any other ymedicinal agent, as desired, such as menthol, cocaine, morphine, etc., with the fixed oily formic aldehyde vehicle, or l can employ other vegetable fats, oils, or aliliatic esters as the base for the forinic alde iyde vehicle without departing Vfrom the spirit of my invention, and I intend to in c ude the dense vegetable oils or other vegetable aliphatic or similar Oxy-acid esters which, may be of solid, semi-solid, or uid consistencg;d at ordinary atmosphericpressure and temperature, the said fatty Water-repellent formic aldeliyde compositions of which may be employed as a vehicle for other medicating or medicinal agents.
- v the dense vegetable oils or other vegetable aliphatic or similar Oxy-acid esters which, may be of solid, semi-solid, or uid consistencg;d at ordinary atmosphericpressure and temperature, the said fatty Water-repellent formic aldeli
- 4Hinert employed throughout this speciiication and claims has particular reference to the character ol' the' solvent for the forrnic aldehyde and its character in relation to the fermic aldehyde content; and the. terni "fixed vegetable oil to the crude vor conuuercial inert, fixed, water-repellent,
- l"lhe fixed vegetable oils cr tats are .more stable than animal cils or fats, such as lard,
- a new composition of matter comprising a AIixed vegetable ester, formic aldehyde and' encalyptol.
- y 10 AThe process of making the new composition o matter herein set forth, which consists in mixing la fixed vegetable oil with formic aide-hyde and exposing the sameito intimate associationuntil theV formic aldehyde had become associated therewith or occluded therein,
- the process :of making the new comi position of matter herein set forth which consists of mixing vmaize oil with formic aldehyde and'exposing the 'same to intimate association, until the forlnic aldehyde has become associated therewith or 4occluded therein.
- the process of making'the new composition of Vmatter herein set fortlnwhic'h consists ofmixing maize oil with vgaseous .formic -aldehyde and exposing the same to intimate association until the formic aidehyde has become associated therewith or.
- the process of making consists in mixing maize oil with formic alldehyde under super-atmospheric pressure and exposing the same to Intimate association until theformic aldehyde -has become.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
POBMIC ALDEHYDE GONTAINI APPLIOATION r H. S. BLAGKMORE.
NG COMPOSITION AND PROCESS-0F MAKING THE SAME. ILBD APR. 1s, 1907. RENEW/BD JAN. 12, 190s.
Patented Apl". 6, 1909.
[NVE/WOR .Mms rum ummm: ummm a c lBLAoKMonn, a citizen'of the United States, residing at Mount Vernon, in the county ot UNITED STATES PATENT onirica- HENRY SPENCER BLAGKMORE, OFMOUNT VERNON, NEW YORK.`
lOmnALDEE'YI-CONTAINING CMPOSETINAND PRGGESS MAKING THE Specification of Letters Patent.
Patented April .6, 1909.
Original application led August 7, 1903, Serial No. l'.A Divided and this application filed April 18, 1907, Serial No. 368,855. Renewed January 12, 190s, Serial No. 471,911.
To allwhom it muyhonoriert;V A
Be it known that l, HENRY SPENCER Vlestchester and Stateof New York, have invented certain. new ,and useful Improvements in Formia-Aldehyde-Containing Compositions and Processes of Makin the Same,
'of which the following is a speci cation, be-
ing a division of application Serial No. 168,673, iiled AugustV 7, 1903.
This invention relates to a new composiion 'of matter for disinfecting, germicide, an-
tiseptic and medicinal purposes and process of making the same, and it consists of a mixture, compound, or solution of formic .aides hyde or its polymerides'in a iixed Water-repellent, such as fixed vegetable oils or fatty vehicles, which compounds, or compositions, may or may not be associated with other medica-ting agents, the object being to produce ai'ixed fatty composition of Water-repellent nature containing forniic aldehyde which micide, antiseptic, and medicinal properties,
may be employed per sc or as a vehicle for other medicating or medicinal agents.
As a speciic illustration of my new composition and the manner in which the same 1s produced, I will take, for example,the production ofja solution of formic aldehyde in maize oil '(corn oil) which oil consists largely of glycerol-oleic ester. The manner in which 1 prefer to produce this iixed Water-repellent or oily formic aldehyde solution or compound, is to place the desired fixed oil, such as maize oil, in a proper container and associate it with forinic aldehyde under increased pressure, at the same time agitating it,'whereby .the formic aldehyde becomes absorbed, occluded, or retained therein. When the fixed oil has become saturated With formic aldehyde it is removed, the formic aldehyde content ascertained by test, and the composition diluted with more oil to obtain the percentage content of formic aldehyde desired. The polymerides of formic aldehyde, such as paraformaldehyde or trioxymethylene may be dissolved in the oil, preferably by the action of heat, producing compounds not departing from the spirit of my invention, as, upon heating in the formation of the composition, formic aldehyde is generated and the composition-is found to have like disinfectant, gerand to all intents andpurposes ma e considered, and is herein included, as an equivalent'composition in accordance with my invention.
The apparatus, in which the solution ot' vformic aldehyde in inert and ixed Water-repellent vehicles in accordance with my process is made, is illustrated in the accompanying drawing, in which,
'Figure l is a longitudinal vertical section;
Fig. 2 is a sectional View of an axial stuffing` box through which passes the inlet and outlety pipes for the purpose of heating the contents of the apparatus by means pf steam; `Fig. 3 is a View of a perforated pipe through Which the formic aldehyde is introduced into the apparatus.
In carrying out my invention for making a solution of lormic aldehyde in maize oil, l.
the valves d in the pipes D and pass therethrough and through'the coil O a current of steam, whereby the maize or corn oil in the drum A. becomes heated. l As soon as the oil has become heated to about l0() degrees C., l introduce into the oLthrough the perforated pipe X foi-mic aldehyde gas, under a pressure of about twenty pounds, by opening` the valve l. This foi-mic aldehyde gas passes' first through the check-valvell Which prcventsthe oil or other substances in the receptacleV A from being forced back in to the formic aldehyde -reservoir or generating apparatus. Connected with pipe F, through W ich the forniic aldehyde gas under -p'res-4 sure passes toV the coil X from which the lorxnic aldehyde gas is discharged through the perfor-ations J1, is a pressure gage GlWhic-h becomes operative on opening the valve g. As soon as the formic` aldehyde begin to passinto the oil in receptacleA through the small perforations 1v, 'the drum A is revolved by means of 'the cog-Wheel M actuated 4bv the movement of the revolving Wheel ln the axial ends of the drum A are the stufling boxes E and P, the steam pipes D .passing through the fixed section e of the stufling-box E, While Athe pipe F through passing flowing the oil against the fixed -coils which the foi-mic aldehyde is introduced into the apparatus passes through the stuflingbox P. As the apparatus revolves, the con tents are simultaneously heated by the steam through the pipesD and the formic aldehyde is introduced throu 7h the pipe F,
-the pressure being maintaine preferably at.
about twenty pounds. After `a sufiicient amount of formic aldehyde has been introduced into the` oil in the apparatus to produce theI desired percentage content, the a aratus is maintained in a rotary condltion for about two hours, whereby the formic aldehyde becomes thoroughly dissolved in or assimilated. with the oil by the agitative action ot' the revolving drum and the fixed steam heating coil o and perforated coil .r through which the formic aidehyde is introduced. The revolution of the apparatus is then stopped and the oil, charged With ormic aldehyde, is Withdrawn through the nine-K by opening the valve lc. The pipe K is provided at its outer end With-a flange .e for the purpose of coupling lup or clamping to conduits leading to a reservoir for the fixed oil charged with forinic aldehyde.
The Whole apparatus is axially supported by the stands L'through which the ends of the hollow trunnions of the receptacle A are supported. l l L lt can be seen that the oil and formic aldehyde are thus thoroughly mixed and assimilated by the action ol" heat and pressure, together` With the agitation caused by..
the revolution of the drum, thus continually and O.
l have found it of advantage to employ this fixed Water-re `)ellent con'iposition containing formic al ehyde or its described equivalent as a vehic e for other medicinal agents, such, for instance, as eucalyptol, in.
Which case it is found to act with satisfaction as an antiseptic and healing` agent for application to suppur'ating surfaces, bringing about the destruction and removal of' the cause of the iniiammatory or suppurating condition and lat the same time apparently acting as a local anesthetic and thereby relieving the pain withwhich such inilammations are usually accompanied. lt is preferable that the formic aldehyde content of the fixed oily vehicle, in cases of this kind, should not exceed one-tenth of one per cent., but it can be varied at theoption of the prescriber to meet the exigencies and idiosyncrasies of the case.
Instead of. eucalyptol I can employ any other ymedicinal agent, as desired, such as menthol, cocaine, morphine, etc., with the fixed oily formic aldehyde vehicle, or l can employ other vegetable fats, oils, or aliliatic esters as the base for the forinic alde iyde vehicle without departing Vfrom the spirit of my invention, and I intend to in c ude the dense vegetable oils or other vegetable aliphatic or similar Oxy-acid esters which, may be of solid, semi-solid, or uid consistencg;d at ordinary atmosphericpressure and temperature, the said fatty Water-repellent formic aldeliyde compositions of which may be employed as a vehicle for other medicating or medicinal agents. v
lt is found that, aside from the advantages derived from the employment of the fixed oily formic aldehyde compositions as a velcle for other medicating or medicinal agents, that, the formc aldehyde 'content prevents the oily base from becoming oxidizedor rancid and the composition is found to be of itself of great advantage as ahemostatic and when applied to cuts or Wounds is ia rapid healing agent by reason of its antiseptic and coagulating action upon the albuminous con- 'tent of the blood or exposed raw surfaces.
it may be noted that dry formic aldehyde,z
which is a gas, unites or combines very readily with the ixed oils or aliphatic esters and becomes more readily assimilated With or retained. or occluded therein in a more permanent manner and to a larger percentage Without danger of polymerization than is the case with aqueous solutions.
'.ihe term 4Hinert employed throughout this speciiication and claims has particular reference to the character ol' the' solvent for the forrnic aldehyde and its character in relation to the fermic aldehyde content; and the. terni "fixed vegetable oil to the crude vor conuuercial inert, fixed, water-repellent,
vegetable fat or oil, as Well as purified productsor esters and is intended to include in-V ert, fixed, Water-repellent compositions of fixed oily nature which are derived from vegetable substances or artificially or synthetically prepared, it being understood that the term iixer implies that the substance is of non-volatile and permanent character under ordinary atmospheric pressure and temperature and the term water-repellent designates a composition ordinarily insoluble or incompatible with, water.
l"lhe fixed vegetable oils cr tats are .more stable than animal cils or fats, such as lard,
and are not so prone to be dec-rmip'osed by hydrolysis into fatty acids and glycerin, because they are associated in nature largely with Water-repellent vegetable substances which protect the. esters present, and, furthermore, they are f'ree from such decomposition products as acrolein and other. disintegrating aldehydes .which are present in ani- Y mal fats, by reason of' the method by which they are obtained such as heat; v'while-vegetable oils are largely obtained by cold compression or through the medium or solventaction of some volatile vehicle or nienstruum.
The decomposition products, or products of destructive distillation, present in animal oils or fats, act to enhance the decomposition or hydrolytic disruption of the fixed esters into fatty acids and glycerin. Maize oil rel sents an admirable vehicle for formic a dehyde, in that it is practically a waste prod-v uct, being a vby-pfroduct in the manufacture of corn products. is hardly saponiiiable 4 'fenoughjtobe em loyed for making soap, and does not possess ryingqualities enough to be used as ayehicle for paints, but contains more or less. vegetable -albuminoids which 1p ge'vent -or retard hydrolyti'c action onA theA 4 ed .fester contents, and will absorb, 'occlude,v or retain, Alarge quantities of. formic aldehyde gas and allow it to gradually be discharged in thepresence of the atmosphere and moisture,` while its non-drying and unsaponifiable' properties tend to prevent decomposi- 20.' tion and the drying of the oil."
. One ofv the particularapplications of themaize `oil formic aldehydecomposition, for .'h gienic pu oses, vis to. apply it to, or em p oy it in, te ephone transmitters', where, by 2.5 the action v-of` the moisture of the breath,
formic 'aldehyde is discharged gradually, thus rendering the device perfectly antiseptic in an automatic manner.
i Another valuable a plication ofthe comvopositionis foroilingl oors oi' schools, halls,
public buildings, etc. for the purpose of re taining dust, thereby 'preventing its circulation in the air and thus producing a sanitary and germicidal condition, and also inv conjunctionwith absorbent substances,` such as saw-dust, etcg'for collecting dust during the process of sweeping.
Having'now described my invention,.what
Iclaim as new and desire to secure by Let- 1. A new comosition of matter comprising a fixed vegeta le oil andformic aldehyde.
.1 2. new composition of matter compris-- ing a'xed vegetable oil, formic aldehyde,
comprisl tol. A new composltlon of. matter comprisoccluded therein.
in presence oftwo witnesses.
ing a fixed vegetable ester and formi@l aldehyde.
8'.' A new composition of matter compris-` mg a iix'ed vegetable ester, formlc aldehyde, v
and a medicating agent. v
9. A new composition of matter comprisinga AIixed vegetable ester, formic aldehyde and' encalyptol. y 10. AThe process of making the new composition o matter herein set forth, which consists in mixing la fixed vegetable oil with formic aide-hyde and exposing the sameito intimate associationuntil theV formic aldehyde had become associated therewith or occluded therein,
V11'. The process of making the new compositionlof matter herein set forth, which consists in mixinfl a'fixed .vegetable oil with gaseous formic a dehyde and exposing the same to intimate yassociation until the formic aldehyde has becomeas'sociated therewith or occluded therein. j
' 12. The process of making the new composition of matter herein set forth, which conslsts ofl mixing a iixed vegetable oil vwith formic aldehyde under super-atmospheric pressure and ex osing the-same to intimate association unti the formic aldehyde `has become associatedv therewith or occluded therein.
13. The process :of making the new comi position of matter herein set forth, which consists of mixing vmaize oil with formic aldehyde and'exposing the 'same to intimate association, until the forlnic aldehyde has become associated therewith or 4occluded therein. 14. The process of making'the new composition of Vmatter herein set fortlnwhic'h .consists ofmixing maize oil with vgaseous .formic -aldehyde and exposing the same to intimate association until the formic aidehyde has become associated therewith or.
15. The process of making consists in mixing maize oil with formic alldehyde under super-atmospheric pressure and exposing the same to Intimate association until theformic aldehyde -has become.
associated therewith or occludedthereln.
In testimony whereof l aflix my signature HENRY SPENCER'BLACKMORE. Witnesses:
E. M. HOLMES, J. R. NOTTINGHAM.
the new .com-vv yposition of matter hereln setforth,"w hich Y
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US368855A US917706A (en) | 1903-08-07 | 1907-04-18 | Formic-aldehyde-containing composition and process of making the same. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16867303A US909527A (en) | 1903-08-07 | 1903-08-07 | Composition for antiseptic and other purposes. |
US368855A US917706A (en) | 1903-08-07 | 1907-04-18 | Formic-aldehyde-containing composition and process of making the same. |
Publications (1)
Publication Number | Publication Date |
---|---|
US917706A true US917706A (en) | 1909-04-06 |
Family
ID=2986141
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US368855A Expired - Lifetime US917706A (en) | 1903-08-07 | 1907-04-18 | Formic-aldehyde-containing composition and process of making the same. |
Country Status (1)
Country | Link |
---|---|
US (1) | US917706A (en) |
-
1907
- 1907-04-18 US US368855A patent/US917706A/en not_active Expired - Lifetime
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