US1595052A - Process of deflocculating solids - Google Patents
Process of deflocculating solids Download PDFInfo
- Publication number
- US1595052A US1595052A US93328A US9332826A US1595052A US 1595052 A US1595052 A US 1595052A US 93328 A US93328 A US 93328A US 9332826 A US9332826 A US 9332826A US 1595052 A US1595052 A US 1595052A
- Authority
- US
- United States
- Prior art keywords
- deflocculating
- agent
- solids
- solid
- colloidal
- 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
- 239000007787 solid Substances 0.000 title description 13
- 238000000034 method Methods 0.000 title description 8
- 239000003795 chemical substances by application Substances 0.000 description 18
- 239000002245 particle Substances 0.000 description 6
- 238000005189 flocculation Methods 0.000 description 5
- 239000000084 colloidal system Substances 0.000 description 4
- 238000001935 peptisation Methods 0.000 description 4
- 235000018553 tannin Nutrition 0.000 description 4
- 229920001864 tannin Polymers 0.000 description 4
- 239000001648 tannin Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 238000001802 infusion Methods 0.000 description 3
- 241000209504 Poaceae Species 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000381592 Senegalia polyacantha Species 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- -1 lead ars'enate Chemical compound 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0004—Preparation of sols
- B01J13/0021—Preparation of sols containing a solid organic phase
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0004—Preparation of sols
- B01J13/0034—Additives, e.g. in view of promoting stabilisation or peptisation
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/901—Substantially pure carbon, e.g. graphite, lamp black, carbon black, fullerenes
Definitions
- This invention relates to the art of deflocculating solid bodies, and comprises a process whereby the defiocculation can be accomplished more readily, more rapidly and with greater yields than heretofore.
- deflocculation is used herein in its commonly accepted sense, as indicating the subdivision of solid bodies, such for instance as graphite, carbon black, clay, pigments, insecticides such as lead ars'enate, sulfur,
- deflocculating agents which ag nt has the general properties of tannin a tannin-like bodies.
- deflocculating agents as heretofore used in this art, I may mention tannin, cutch, and extracts from roasted cereals or starchy "bodies, usually employed in conjunction with ammonia. While all of these substances possess in common the property of deflocculating such solids as are mentioned above, they differ considerably among themselves, particularly with respect to rapidity of action and the stability of the resulting colloid.
- the deflocculating agent disappears, wholly or substantially, from the aqueousor ammoniacal solution, being absorbed by the particles of the solid. It is observed however that if an excess of deflocculating agent be used, or if the process of attrition be too prolonged, re-flocculation sets in, the previously deflocculated or colloidal particles're-uniting into aggregates which are-no longer of colloidal dimensions and subside when suspended in-water.
- I first add to the solid to be deflocculated, for example graphits in the form of a heavy paste, a relatively smallproportlon, say six ercent by weight,
- tannin referably together with a small amount 0 aqueous ammonia; and I sub ect the paste to attrition under the usual conditions until the deflocculating agent has been substantially adsorbed. I then repeat this operation, adding new por tions of'the deflocculating agent, a number of times, depending on the results sought; but always ultimately introducing suflicient deflocculatlng agent so that a thorough mixing operation, following the final addition of agent, will bring about the re-flocculation of most or all of the initially deflocculated solid.
- the material to be deflocculated was electric furnace graphlte
- the deflocculating agent used was tannin
- the total amount of agent added amounted to about eighteen percent of the dry weight of the graphite.
- these re-' flocculated aggregates may be resolved again into their component particles of colloid dimensions by treating them with certain deflocculating or peptizing agents other than those used in Among such a ti'zing agents in order to distinguish them from the deflocculating agents used in the use infusions of grasses (Gramineae) such as hay, straw and the like; although .I may use other vege table infusions capable of the same peptizing efiect; or inorganic peptizing agents such as sodium silicate may be used. This peptization may be carried out in the same or other mill, and under essentially'the same conditions as the initial deflocculating treatment.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Description
' relatively Patented Aug. 3, I926.
UNITED STATES GEORGE W. Ao'nEson, or GALDWEEE, NEW JERSEY.
PROCESS OF DEFLOCCULATING SOLIDS.
No Drawing.
This invention relates to the art of deflocculating solid bodies, and comprises a process whereby the defiocculation can be accomplished more readily, more rapidly and with greater yields than heretofore. The term deflocculation is used herein in its commonly accepted sense, as indicating the subdivision of solid bodies, such for instance as graphite, carbon black, clay, pigments, insecticides such as lead ars'enate, sulfur,
etc., etc. into particles of colloidal dimensions,
by a process of prolonged attrition in presence of moisture and of an organic deflocculating, agent, which ag nt has the general properties of tannin a tannin-like bodies. Among such deflocculating agents, as heretofore used in this art, I may mention tannin, cutch, and extracts from roasted cereals or starchy "bodies, usually employed in conjunction with ammonia. While all of these substances possess in common the property of deflocculating such solids as are mentioned above, they differ considerably among themselves, particularly with respect to rapidity of action and the stability of the resulting colloid. I
In the operation of deflocculating as ordinarily practiced, the deflocculating agent disappears, wholly or substantially, from the aqueousor ammoniacal solution, being absorbed by the particles of the solid. It is observed however that if an excess of deflocculating agent be used, or if the process of attrition be too prolonged, re-flocculation sets in, the previously deflocculated or colloidal particles're-uniting into aggregates which are-no longer of colloidal dimensions and subside when suspended in-water. Heretofore it has been universal practice to avoid carefully such conditions as lead toreflocculation in the mill such re-flocculation involving a limitation upon or even a reduction of the obtainable yield of particlesof colloid dimensions;- the result being, in the case of graphite for example, that only a small proportion [of the total charge can be defioccula'ted in a single operation. In a typical case the proportion of aphite' defiocculated or converted into the colloidal state in course of a single through the 'mill is of the order 0 six oreight percent. This percentage difiers of course. with difierent materials subjected to the operation, and also with the particular deflocculating agent used. ,1
&..
first stage, I prefer to assag'e' Application filed. March 8, 1926. Serial No. 93,323.
According to my improved process in its preferred embodiment, I first add to the solid to be deflocculated, for example graphits in the form of a heavy paste, a relatively smallproportlon, say six ercent by weight,
of one of the known de occulating agents,
for example tannin, referably together with a small amount 0 aqueous ammonia; and I sub ect the paste to attrition under the usual conditions until the deflocculating agent has been substantially adsorbed. I then repeat this operation, adding new por tions of'the deflocculating agent, a number of times, depending on the results sought; but always ultimately introducing suflicient deflocculatlng agent so that a thorough mixing operation, following the final addition of agent, will bring about the re-flocculation of most or all of the initially deflocculated solid. In a typical instance, where the material to be deflocculated was electric furnace graphlte, and the deflocculating agent used was tannin, the total amount of agent added amounted to about eighteen percent of the dry weight of the graphite.
At this stage a substantial proportion, in some cases upward of 80%, of the initial charge has passed through the deflocculated stage but had undergone re-flocculation. ThlS however does not mean that the original physical-condition of the solid has been restored; for the re-flocculated aggregates, being assemblies of particles which have once passed through the colloidal state, are extremely fragile, although. not capable of belng resolved again into their colloidal components by simple stirring.
I have discovered however that these re-' flocculated aggregates may be resolved again into their component particles of colloid dimensions by treating them with certain deflocculating or peptizing agents other than those used in Among such a ti'zing agents in order to distinguish them from the deflocculating agents used in the use infusions of grasses (Gramineae) such as hay, straw and the like; although .I may use other vege table infusions capable of the same peptizing efiect; or inorganic peptizing agents such as sodium silicate may be used. This peptization may be carried out in the same or other mill, and under essentially'the same conditions as the initial deflocculating treatment. The result of this treatment, involvfiocculating-agent; and thereafter peptizing ing an initial deflocculation carrried through the re-flocculated' aggregates. 1 to partial or complete re-flocculation, and 2. Process of treating solid bodies to prefollowed by peptization of the re-fiocculated pare particles of colloidal dimensions, comaggregates, is greatly to increase the ultimate prising deflocculating and re-fiocculating the yield of'colloid, as Well as to increase the said solid by attrition with an organic dcrate at which it is prepared from the iniflocculating agent; and thereafter peptiz- 20 tial raw material. I ing the re-flocculated aggregates by means I claim; I of an infusion of a grass.
1. Process of treating solid bodies to pre- In testimony whereof, I affix my signapare particlesof colloidal dimensions, comll prising deflocculating and re-flocculating the said solid by attrition with an organic de-' GEORGE W. ACHESON.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93328A US1595052A (en) | 1926-03-08 | 1926-03-08 | Process of deflocculating solids |
| FR619718D FR619718A (en) | 1926-03-08 | 1926-07-31 | Process for breaking up solid bodies |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93328A US1595052A (en) | 1926-03-08 | 1926-03-08 | Process of deflocculating solids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1595052A true US1595052A (en) | 1926-08-03 |
Family
ID=22238331
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US93328A Expired - Lifetime US1595052A (en) | 1926-03-08 | 1926-03-08 | Process of deflocculating solids |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US1595052A (en) |
| FR (1) | FR619718A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5849219A (en) * | 1994-04-13 | 1998-12-15 | U.S. Philips Corporation | Aqueous dispersion of particles |
| US20040234852A1 (en) * | 2002-12-24 | 2004-11-25 | Penox Gmbh | Additive for producing the positive active material for lead-acid storage batteries, a method for its production, and its use |
-
1926
- 1926-03-08 US US93328A patent/US1595052A/en not_active Expired - Lifetime
- 1926-07-31 FR FR619718D patent/FR619718A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5849219A (en) * | 1994-04-13 | 1998-12-15 | U.S. Philips Corporation | Aqueous dispersion of particles |
| US20040234852A1 (en) * | 2002-12-24 | 2004-11-25 | Penox Gmbh | Additive for producing the positive active material for lead-acid storage batteries, a method for its production, and its use |
| US7435758B2 (en) * | 2002-12-24 | 2008-10-14 | Penarroya Oxide Gmbh | Additive for producing the positive active material for lead-acid storage batteries, a method for its production, and its use |
Also Published As
| Publication number | Publication date |
|---|---|
| FR619718A (en) | 1927-04-07 |
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