US2919181A - Process for the manufacture of globular nitrocellulose - Google Patents

Process for the manufacture of globular nitrocellulose Download PDF

Info

Publication number
US2919181A
US2919181A US481486A US48148655A US2919181A US 2919181 A US2919181 A US 2919181A US 481486 A US481486 A US 481486A US 48148655 A US48148655 A US 48148655A US 2919181 A US2919181 A US 2919181A
Authority
US
United States
Prior art keywords
lacquer
water
globules
nitrocellulose
manufacture
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
Application number
US481486A
Inventor
Charles M Reinhardt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olin Corp
Original Assignee
Olin Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Olin Corp filed Critical Olin Corp
Priority to US481486A priority Critical patent/US2919181A/en
Application granted granted Critical
Publication of US2919181A publication Critical patent/US2919181A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0033Shaping the mixture
    • C06B21/0066Shaping the mixture by granulation, e.g. flaking
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S149/00Explosive and thermic compositions or charges
    • Y10S149/11Particle size of a component
    • Y10S149/111Nitrated organic compound

Definitions

  • This invention relates to plastics and particularly to the manufacture of minute spheres, or near-spheres, of
  • nitrocellulose, -orv the like is' formed and dispersed in; water irrraccc'irdan'ce.with the'te'achingsfof the aforesaid patents,'and the 'sizeof the dispersedglobules is-reducedv process disclosed in tth'e copending application of 1 Eugene? A.:.Andrew, Serial.No. 470,412. While the aforesaid patents proclaim that the grain: size may" be'controll'ed byzvaryingrthervigor: of the: agitation (the more vigorous thezagitation, the.
  • a lacquer-of to the;greatesflpractical extent by both decreasing the viscosity (-i.e., increasing the solvent content) of the" lacquer. ;and-"by increasing the rate of agitation.
  • the globules shrink to a volume-of about one-fortieth of their original size. .Consequently, if care be taken to reduce. the globules to the smallest size feasibleby the techniquesjof viscosity reduction nadvigorous agitation; the smallest size can be further reduced by upwards of ethyl acetate or a methyleth'yl ketone-toluene mixture, be-made into-a homogeneous lacquer o'fhigh-fluidity containing sayt 1.0 parts by weight of solvent to-each part of nitrocellulose; With this thin lacquer,*alarge quart-f tity of water, at least equal to,':and' preferably in excess of, the.
  • the weight' ofthe lacquer, but containing an hydrophobic surface-active agent is mixed; The mixture is then vigorously agitated for a time"-suiiicient to thoroughlyemulsify the water. within the lacquer. .Ther e after, the water-in-lacquer emulsion is. dispersedin the; unemulsified excess of water .towhich 'is'iadded sufiicient of an hydrophilic surface-active agent.
  • the globules accordance with the present invention is many times the water content of the globules envisionedbythe aforesaidpatents, thedewatering phase (as taught specifically by PatentNo. 2,160,626)[is'neces sarily more prolonged than inthe, practice describedin saidpatents.
  • thedewatering phase as taught specifically by PatentNo. 2,160,626)[is'neces sarily more prolonged than inthe, practice describedin saidpatents.
  • th'e process one partby weight of nitrocellulose is formed into -a lacquer with. parts by 'weiglit ofethyl acetate.
  • the lacquer may, if desired, contain asmall amount of a suitable stabilizer, such as 2-nitrodiphenylamine.
  • a suitable stabilizer such as 2-nitrodiphenylamine.
  • the mixture of solvent and nitrocellulose with or without stabilizer is agitated and mixed for aboutthirty minutes, or until a homogeneous lacquer is produced. 25 parts of water containing.0.0l25 part of an hydrophobic surface-active agent, such as diethyleneglycol monolaurate, is then vigorously agitated.
  • the temperature of the batch is elevated to about40 C., at which time there is added to the mixture a solu tion consisting of: I
  • sodium dihexylsulfosuccinate, or sodium'tetral decyl sulfate may be utilized.
  • the globules are dewatered in. accordance with the practice taught in Pat ent Np. 2,160,626by the introduction of sodium sulfate,; or other-appropriate salt, into the aqueous external phase of thewater-imlacquer-in-water emulsion;
  • sodium sulfate or other-appropriate salt
  • the rate of heat input to the mixture is increased over a period of two hours to bring the quer is emulsified into said lacquer as the internal phase thereof, subdividing said emulsion into fine globules and suspending said globules in an aqueous bath by vigorous, agitation, andwhile so suspended: adding a water-soluble solute immiscible with the lacquer to the bath, maintaining the globules in suspension until substantially all of the, water is removed therefrom so as to shrink said glob:
  • a manufacture prepared by the process of claim 1 comprising solidifiedglobules of nitrocellulose lacquer having a diameter of 0.001 inch or less. r
  • dewatering the suspended lacquer globules by maintaining the suspension of the globules in the bath containing thesolute and removing the solvent from the dewatered lacquer globules.

Description

United States Patent PROCESS FOR THE MANUFACTURE OF GLOBULAR NITROCELLULOSE Charles M. Reinhardt, St. Louis, Mo., assignor to Olin Mathiesou Chemical Corporation, East Alton, IlL, a corporation of Virginia No Drawing. Application January 12, 1955 Serial No. 481,486
'4 Claims. (Cl. 5222) g This invention relates to plastics and particularly to the manufacture of minute spheres, or near-spheres, of
the majority of the grains ina given-production batch will fall within fairly close limits (within the normal size range), such controls have definite limitations. It has notheretoforebeen possible to produce on a mass scale smaller sizes of well-formed globular grains} except to the extent that about 1%, or less, of a batch of,
normal size grains might approach a diameter of 0.002- inch. Y I Forsome years; it has been thought that the manufacture of globular powder grainshaving a diameteron the-order'of' 0.001 inch, or less, would be desirable for certain purposes, and vwhile manyeiforts have been made in: that 1 direction, they have been uniformly unsuccessful with thesole exception, so far as I- am informed, of the ently inconquerable tendency to coalescgand conse quentlyt'i'ieii-"yield' or well-formed grains of the size ap-.-
nitrocellulose, -orv the like, is' formed and dispersed in; water irrraccc'irdan'ce.with the'te'achingsfof the aforesaid patents,'and the 'sizeof the dispersedglobules is-reducedv process disclosed in tth'e copending application of 1 Eugene? A.:.Andrew, Serial.No. 470,412. While the aforesaid patents proclaim that the grain: size may" be'controll'ed byzvaryingrthervigor: of the: agitation (the more vigorous thezagitation, the. smaller theglobules) of the liquor in which the-.lacqueris suspended,- on by varyingzthViscositynofr'thedac quer (the-zhigher the. viscosity,'.the'" larger I the-figlobules'y, the :first: mentioned-mode of control "exhibits-very definitezlimitsyof opera'bility while the last mentionechmodez-of controlisierraticand uncertain; For example; using: .ar -typical' lacquer consisting. of: 3 spar-ts byzwei'ghtr of. ethyl: acetate to each part of nitrocellulose,- n i 'fll filz t-in'gi :the -agitator in a commercial production f still\-:a,t-.-.-1.6.0 r:p.m'..-.during: the grainingrstageof the procz-f; @SS, results in the production of a batchiofghardened grains, 60% of which will fall within the diameter limits of 0.016 to.0,025. inch and,;be.,near-perfect. spheres. If, other conditions remaining the same, the agitator speed is increased to-i2'30r.p:-m. idur ing theligraiiiiiig stage, 70% ofthe finishedgrains will be between 0.009. and 0.016 inch andqtbejnearertectspheres.It Tthe'f agitator speed; ,be furtherii'ncreased'to 3001;111:111; about 90% of the grains will; :be Ehetween 0:006 and 0:012 inchijn diametn'but thefincidence. of'matformatiomis greater. Further crease in agitator "speedhasno"appreciable infilll'lQQfi grain. size;
Despit f .orable"indic'ati'onswhi hj'have perenniaa no hTet'o' tinre"with"lab story. scaleibatcli'e's, theuncertainty which"attends "eifot'ts "of control grain size by varying the viscosity of the lacquer is well-known 98% by dewatering and desolventization.
.More; specifically, the invention "contemplates that iii-- trocelluloseglor the like, and a suitable solvent, such as to those who have had the experience with the manufacturef'-,of. globular-powder in commercial production stills?" The erratic and uncertain nature of. the results obtained from merely varying the viscosity of the la q er, at thesame. speed of agitation, is 'illustrated by the folld ng table which gives the; screen analysis; of the end-"product from four runs of the. same commercial still agitated at r.p.m., but at progressively increas-. ing solvent ratio (ethyl acetatemitrocellulose);- I I Solv. Ratio v on on on {on on. through 0. 3 18. 1 30; 2 17,2 21. l 12. 0.2 1.3 38.2 i 30.3 20.8 9. 0. 0 2. 9 46. 8' 23.8 16,2 10. 0.1 v 0.2 34 2 35.1 21.7 8.
Efforts to 'lc'ombine high agitation spee ds with low viscosity ia'eqfiersmv been; repeatedly made, bu t the trial batches made for this purpose have exhibited an apparproaching- 0.002 inch'in diametefhas been even lessthan the accidental yield of such grains from normal size grain .p'roduction.- I
It:.'is .-.an-1object of the present-"invention; to provide a process: forthe .mass production of near-spheres. of nitrocelliiloseandthe like, having a diameteron the order; of;.0.f00.-1 inch: or less. v
In accordance with the present'invention, a lacquer-of to the;greatesflpractical extent byboth decreasing the viscosity (-i.e., increasing the solvent content) of the" lacquer. ;and-"by increasing the rate of agitation. In
addition,'.the-invention is predicated upon the' discovery; thatfurtherureduction ini'thezultimate grain sizemay be accomplishedby emulsifying withineachlacquer globule a substantial quantity, ontheforderof 50% by volume,- of water. After the high water content lacquer globules aredispersed in the aqueous medium, they may'be'dewatered by'the techniques disclosed-inthe aforesaid patent, No. 2,160,626, and :then" solid ifie'd by removal of solvent; Upon such dewatering and desolventization,
the globules shrink to a volume-of about one-fortieth of their original size. .Consequently, if care be taken to reduce. the globules to the smallest size feasibleby the techniquesjof viscosity reduction nadvigorous agitation; the smallest size can be further reduced by upwards of ethyl acetate or a methyleth'yl ketone-toluene mixture, be-made into-a homogeneous lacquer o'fhigh-fluidity containing sayt 1.0 parts by weight of solvent to-each part of nitrocellulose; With this thin lacquer,*alarge quart-f tity of water, at least equal to,':and' preferably in excess of, the. weight' ofthe lacquer, but containing an hydrophobic surface-active agent, is mixed; The mixture is then vigorously agitated for a time"-suiiicient to thoroughlyemulsify the water. within the lacquer. .Ther e after, the water-in-lacquer emulsion is. dispersedin the; unemulsified excess of water .towhich 'is'iadded sufiicient of an hydrophilic surface-active agent. to emulsify the' water-in-lacquer emulsionvwithinthe excess oflwater so i as to produce a water in lacquer'in water-"emulsionin vvhiQhr heZ'dis ersed globuleseof'lacquercoritain pn the order of 50% by volume of water. Thereafter, the
graining, dewatering, desolventization and hardening techniques taught by the aforesaid patents may be prof2,9'19,1s11 Pat te pe 2 3 .1959
ceeded with. In view of the fact that the water content at atmospheric pressure,
of the globules accordance with the present invention is many times the water content of the globules envisionedbythe aforesaidpatents, thedewatering phase (as taught specifically by PatentNo. 2,160,626)[is'neces sarily more prolonged than inthe, practice describedin saidpatents. As a specific example of th'e process, one partby weight of nitrocellulose is formed into -a lacquer with. parts by 'weiglit ofethyl acetate. The lacquer may, if desired, contain asmall amount of a suitable stabilizer, such as 2-nitrodiphenylamine.The mixture of solvent and nitrocellulose with or without stabilizer is agitated and mixed for aboutthirty minutes, or until a homogeneous lacquer is produced. 25 parts of water containing.0.0l25 part of an hydrophobic surface-active agent, such as diethyleneglycol monolaurate, is then vigorously agitated.
with the lacquer for about an hour, emulsifying at least Up to this stage;
When the emulsification of'water intothelacquer has about half'the water into the lacquer. the process is carried out at room temperature.
been accomplished, the temperature of the batch is elevated to about40 C., at which time there is added to the mixture a solu tion consisting of: I
r I Parts: Water 1.25 Gum arabic 0.125 Sodium"dioctylsulfosuccinate ;.005
In lieu of the gum arabic, other protective colloids, .such as Belgian; gum, animal plues, or collagenous. vegetable protein, may;be utilized. In lieuof the sodium dioctylsulfosuccinate, other hydrophilic surfaceeactive agents,
such as sodium dihexylsulfosuccinate, or sodium'tetral decyl sulfate, may be utilized.
is around 70-' l2 During thistwo-hour period of temperature elevation, the water in lacquer globules are dewatered and shrunk to about 50% of their previous volume. Desolventization proceeds after the temperatureof solvent vaporization is achieved, .and in view of the high content of solvent within the globules, it is desirable that the removal thereof proceed slowly so that about six hours is allowed for its completion. Upon removal of thesolvent from the globules, they will have shrunk to less than 10% of their dewatercd volume so that when the solvent .removal is completed, and the grains are hardened, the size of the globules i-sabout 5%, or less, of their original size. The
greater the amount? of water emulsified within each individual globule, ,the smaller, will be the ultimate size of that globule. In carrying out the process as just indicated, the final product consisted of well-rounded grains having a diameter under 7.5 microns. I j
Having thus described the invention, what is claimed and desired to be secured by Letters Patent is: ,1 1. In the manufacture of solidified globules having a diameter of 0.001 inch or less from a lacquer whose base g material is nitrocellulose,-the process comprising preparing a lacquer consisting essentially of 1 partpf nitrd cellulose and approximately 10 parts of a water-immiscible solventktherefor, agitating said lacquer with water containing a hydrophobic surface active agent until an amount of water at least equal to the weight ofthe lacquer reverses phase so. asto become the external phaseof, a watenih-lacquerein-water emulsion wherein wateriii-lacquer globules are dispersed in an aqueous external phasen Agitation iscontinued at: a rate such as to reduce th e globules of lacquer, (containing water) to the desired size, 1 Agitation speeds. of the character employed in ;a particular still for the production of normal sized globular powder, grain'slwill sufiice, but where it -is desired to produce the smallest possible sizes, the agitation,spedshould be furtherjncreased to just short of the .speed whereat malformation (due to coalescence 'of globules) becomes appreciable, it being noted in this connectionthatthe maximum tolerable speed of agitation depends upon .the idiosyncrasies ofthe particular still employed. ;-In order to-produce globular grains approach ing colloidal size,.khow.ever, care must be exercised that the globules-"of water-in-lacquercontain on the order of 50%, water after-such globules are emulsified as the internal phase of the emulsion.
Having 1 produced the water-in-lacquer-in-water emul sion with globules. of thersmallest practicable size, but
containing ontheuorder of"50% water, the globules are dewatered in. accordance with the practice taught in Pat ent Np. 2,160,626by the introduction of sodium sulfate,; or other-appropriate salt, into the aqueous external phase of thewater-imlacquer-in-water emulsion; For th1Spl11'pQS6,0.75 part of sodium sulfate dissolved in" 1.5133115. of water. may be gradually added over ape riod of:,about1thirty minutes: while the temperatureof the mixture is maintained' at 50-52 C. Atthe endof the, salt addition, the rate of heat input to the mixture is increased over a period of two hours to bring the quer is emulsified into said lacquer as the internal phase thereof, subdividing said emulsion into fine globules and suspending said globules in an aqueous bath by vigorous, agitation, andwhile so suspended: adding a water-soluble solute immiscible with the lacquer to the bath, maintaining the globules in suspension until substantially all of the, water is removed therefrom so as to shrink said glob:
ulesyand then further shrinking the globules by remova ing solvent therefrom.
2. A manufacture prepared by the process of claim 1:,comprising solidifiedglobules of nitrocellulose lacquer having a diameter of 0.001 inch or less. r
3. The process of claim lwherein the water content.
3 tate and a methyl ethyl ketone-toluene mixture, agitating said lacquer with water containing a hydrophobic surface: active agent until an amount of water at least equal to the' weight of the lacquer is emulsifiedinto said lacquer *as the internal phase thereof, subdividing the lacquer into globules and suspending them in an aqueous bath by vigorous agitation of thebath, dissolving a water soluble solute immiscible with the lacquerin the bath,
dewatering the suspended lacquer globules by maintaining the suspension of the globules in the bath containing thesolute and removing the solvent from the dewatered lacquer globules.
"ReterencesCited inthe fileiof this patent v UNITED STATES PATENTS 1,965,577 Cochran July 10, 1934 1,972,891 f Ingraham Sept. 11, 1934 2,027,114 r Olsen Jail 7, 1936 2,16 O,'626- Scha e fer- May 30, 1939 2,176,678 ,Neuroth Oct. 17, 1939 2,179,314 Allison NOV. 7, 1939 2,201,640 Weldin May 21, 1940 2,213.255 5 Olsen Sept. 3 1940

Claims (1)

1. IN THE MANUFACTURE OF SOLIDIFIED GLOBULES HAVING A DIAMETER OF 0.001 INCH OR LESS FROM A LACQUER WHOSE BASE MATERIAL IS NITROCELLULOSE, THE PROCESS COMPRISING PREPARING A LACQUER CONSISTING ESSENTIALLY OF 1 PART OF NITROCELLULOSE AND APPROCIMATELY 10 PARTSD OF A WATER-IMMISCIBLE SOLVENT THEREFOR, AGITATING SAID LACQUER WITH WATER CONTAINING A HYDROPHOBIC SURFACE ACTIVE AGENT UNTIL ANAMOUNT OF WATER AT LEAST EQUAL TO THE WEIGHT OF THE LACQUER IS EMULSIFIED INTO SAID LAQUER AS THE INTERNAL PHASE THEREOD SUBDIVING SAID EMULSION INTO FINE GLOBLUBLES AND SUSPENDING SAID GLOBLUES IN AN AQUEOUS BATH BY VIGOROUS AGITATION AND WHILE SO SUSPENDED: ADDING A WATER-SOLUBLE SOLUTE IMMISCIBLE WITH THE LACQUER TO THE BATH, MAINTAINING THE GLOBLUSE IN SUSPENSION UNTIL SUBSTANTIUALLY ALL OF THE WATER IS REMOVED THEREFROM SO AS TO SHRINK SAID GLOBULES, AND THEN FURTHER SHRINKING THE GLOBLUES BY REMOVING SOLVENT THEREFROM.
US481486A 1955-01-12 1955-01-12 Process for the manufacture of globular nitrocellulose Expired - Lifetime US2919181A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US481486A US2919181A (en) 1955-01-12 1955-01-12 Process for the manufacture of globular nitrocellulose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US481486A US2919181A (en) 1955-01-12 1955-01-12 Process for the manufacture of globular nitrocellulose

Publications (1)

Publication Number Publication Date
US2919181A true US2919181A (en) 1959-12-29

Family

ID=23912116

Family Applications (1)

Application Number Title Priority Date Filing Date
US481486A Expired - Lifetime US2919181A (en) 1955-01-12 1955-01-12 Process for the manufacture of globular nitrocellulose

Country Status (1)

Country Link
US (1) US2919181A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4783484A (en) * 1984-10-05 1988-11-08 University Of Rochester Particulate composition and use thereof as antimicrobial agent
US4826689A (en) * 1984-05-21 1989-05-02 University Of Rochester Method for making uniformly sized particles from water-insoluble organic compounds

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1965577A (en) * 1933-06-21 1934-07-10 Du Pont Manufacture of nitrocellulose
US1972891A (en) * 1933-06-07 1934-09-11 William T Ingraham Method of extracting diphenylamine
US2027114A (en) * 1932-03-12 1936-01-07 Western Cartridge Co Manufacture of smokeless powders
US2160626A (en) * 1936-01-02 1939-05-30 Western Cartridge Co Explosive
US2176678A (en) * 1937-04-17 1939-10-17 Kalle & Co Ag Method of treating cellulose ethers
US2179314A (en) * 1938-10-06 1939-11-07 Hercules Powder Co Ltd Progressive-burning smokeless powder
US2201640A (en) * 1937-12-14 1940-05-21 Hercules Powder Co Ltd Progressive burning smokeless powder
US2213255A (en) * 1936-01-06 1940-09-03 Western Cartridge Co Explosive
US2722528A (en) * 1951-05-08 1955-11-01 Hercules Powder Co Ltd Preparation of finely divided cellulose plastics

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2027114A (en) * 1932-03-12 1936-01-07 Western Cartridge Co Manufacture of smokeless powders
US1972891A (en) * 1933-06-07 1934-09-11 William T Ingraham Method of extracting diphenylamine
US1965577A (en) * 1933-06-21 1934-07-10 Du Pont Manufacture of nitrocellulose
US2160626A (en) * 1936-01-02 1939-05-30 Western Cartridge Co Explosive
US2213255A (en) * 1936-01-06 1940-09-03 Western Cartridge Co Explosive
US2176678A (en) * 1937-04-17 1939-10-17 Kalle & Co Ag Method of treating cellulose ethers
US2201640A (en) * 1937-12-14 1940-05-21 Hercules Powder Co Ltd Progressive burning smokeless powder
US2179314A (en) * 1938-10-06 1939-11-07 Hercules Powder Co Ltd Progressive-burning smokeless powder
US2722528A (en) * 1951-05-08 1955-11-01 Hercules Powder Co Ltd Preparation of finely divided cellulose plastics

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4826689A (en) * 1984-05-21 1989-05-02 University Of Rochester Method for making uniformly sized particles from water-insoluble organic compounds
US4997454A (en) * 1984-05-21 1991-03-05 The University Of Rochester Method for making uniformly-sized particles from insoluble compounds
US4783484A (en) * 1984-10-05 1988-11-08 University Of Rochester Particulate composition and use thereof as antimicrobial agent

Similar Documents

Publication Publication Date Title
US2183053A (en) Vitamin preparation and method of making same
US5342644A (en) Production of tempered confectionery
US2375175A (en) Smokeless powder process
US4217372A (en) Method for improving the structural properties of fats
US2919181A (en) Process for the manufacture of globular nitrocellulose
US5045243A (en) Method for dry fractionation of fats and oils
US2800493A (en) Separation of high molecular organic compound mixtures
US2740705A (en) Process of manufacturing globular propellent powder
US2853390A (en) Process for shortening manufacture
US3679782A (en) Manufacture of globular powder
US2183084A (en) Method of making activated gelatin
US3232971A (en) Process for the production of glycerides having melting points differing from the starting glyceride material
US2885736A (en) Nitrocellulose particles
US2691619A (en) Fat-soluble vitamin-containing products and process therefor
US2892732A (en) Aerated solid wax composition and process of making it
EP2314170B1 (en) Method for producing storage stable seed crystals made of cocoa butter or chocolate masses
US1949434A (en) Derivative of cellulose composition and method of preparing the same
US2625485A (en) Lard crystal modification process
US2974135A (en) Method of making plastic pellets
Ehlers Controlled crystallization of complex confectionery fats
US2325393A (en) Manufacture of margarine and cooking fats
US2018781A (en) Method for the production of storable mixtures of lecithin and oil
CN108774328A (en) A kind of preparation method of Azide graft modification nitrocellulose microballoon
DE844150C (en) Process for the continuous sulfonation of organic compounds using chlorosulfonic acid
EP0953555A1 (en) Process for preparing particles of meltable propellants and explosives