GB845363A - Polymers of hydrolysis products of hydrocyanic acid and compositions containing the same - Google Patents
Polymers of hydrolysis products of hydrocyanic acid and compositions containing the sameInfo
- Publication number
- GB845363A GB845363A GB32542/56A GB3254256A GB845363A GB 845363 A GB845363 A GB 845363A GB 32542/56 A GB32542/56 A GB 32542/56A GB 3254256 A GB3254256 A GB 3254256A GB 845363 A GB845363 A GB 845363A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide
- hydrolysed
- polymer
- lead
- salt
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/14—Clay-containing compositions
- C09K8/18—Clay-containing compositions characterised by the organic compounds
- C09K8/22—Synthetic organic compounds
- C09K8/24—Polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Water-insoluble polymerized hydrocyanic acid is partially or completely hydrolysed with an aqueous solution of a non-oxidising acid or of an alkali at 25-200 DEG C. The hydrolysis may be represented: - <FORM:0845363/III/1> where X is H or a salt forming cation, preferably alkali metal or ammonium. The hydrolysis product is a mixture of the two substances with the second predominating. Liquid HCN at least 95%, preferably anhydrous, is polymerized at 20-30 DEG C. at atmospheric pressure under reflux in the presence of an alkaline reacting catalyst, say 0.1-10%, of e.g. methylamine, trimethylamine, ethylamine, triethylamine, tri-n-butylamine, n-propylamine, aniline, toluidine, benzylamine, naphthylamine, hydrazine, potassium or sodium hydroxide or carbonate, or ammonium hydroxide. Excess HCN evaporates and the solid polymer is dried. The polymer is hydrolysed by refluxing at 25-200 DEG C. with sulphuric or hydrochloric acid, or alkali metal or ammonium hydroxide. The hydrolysed polymer is recovered as an aqueous solution from which solid is recovered by evaporation. A minor amount of the hydrolysed polymer or the metal or ammonium salt thereof may be used as a dispersing or deflocculating agent for dispersions of finely divided solid e.g. pigments, clays, adhesives, or cement, in aqueous media. 0.5-5% of the hydrolysed polymer or salt may be added to pigment dispersions in paint processing and may be incorporated as an aqueous solution or solid and may be added during milling or simultaneous mixing and dispersion. Pigments referred to are :- ferric oxide, iron blues, red lead, basic lead carbonate or sulphate, lead chromate, zinc oxide, chromate, or sulphide, lithopone, chromium oxide, titanium oxide (anatase and rutile), antimony oxide, cadmium sulphide, lead titanate, titania coated barium sulphate or calcium carbonate, zinc sulphide coated magnesium carbonate, or mixtures of lead chromate and oxide (chrome orange), or of iron blue and lead chromate (chrome green). Examples III, IV, V and VIII refer to aqueous dispersions of titanium dioxide, zinc oxide, kaolin, and soot respectively. 1-4 lbs. of the hydrolysed polymer may be added to a 42 gal. barrel of drilling mud consisting of a dispersion of clay, e.g. bentonite or mediumyield clays, in fresh or salt water, or in an oil in water emulsion, which may also contain weighting materials, e.g. barytes, iron oxide, calcium carbonate, or silica, and other additions, e.g. caustic alkali, quebracho, lime, cement, or gypsum. Examples VI and VII refer to drilling muds containing Tennessee Ball clay, bentonite, and Dixie Bond clay dispersed in fresh and salt water respectively. Specification 456,151 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US845363XA | 1955-10-25 | 1955-10-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB845363A true GB845363A (en) | 1960-08-24 |
Family
ID=22185575
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32542/56A Expired GB845363A (en) | 1955-10-25 | 1956-10-25 | Polymers of hydrolysis products of hydrocyanic acid and compositions containing the same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB845363A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0003571A2 (en) * | 1978-02-14 | 1979-08-22 | Bayer Ag | Solid modified azulmic acids with intact polycyclic structure, process for their preparation and their use |
EP0003585A2 (en) * | 1978-02-14 | 1979-08-22 | Bayer Ag | Stabilised azulmic acids, process for their preparation and their use |
EP0008420A1 (en) * | 1978-08-18 | 1980-03-05 | Bayer Ag | Chemically stabilised azulmic acids, process for their preparation and their use |
-
1956
- 1956-10-25 GB GB32542/56A patent/GB845363A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0003571A2 (en) * | 1978-02-14 | 1979-08-22 | Bayer Ag | Solid modified azulmic acids with intact polycyclic structure, process for their preparation and their use |
EP0003585A2 (en) * | 1978-02-14 | 1979-08-22 | Bayer Ag | Stabilised azulmic acids, process for their preparation and their use |
EP0003571A3 (en) * | 1978-02-14 | 1979-09-05 | Bayer Aktiengesellschaft | Modified azulmic acids, process for their preparation and their use |
EP0003585A3 (en) * | 1978-02-14 | 1979-09-05 | Bayer Aktiengesellschaft | Stabilised azulmic acids, process for their preparation and their use |
US4396733A (en) | 1978-02-14 | 1983-08-02 | Bayer Aktiengesellschaft | Stabilized azulmic acids, processes for their preparation and their use |
EP0008420A1 (en) * | 1978-08-18 | 1980-03-05 | Bayer Ag | Chemically stabilised azulmic acids, process for their preparation and their use |
US4263181A (en) | 1978-08-18 | 1981-04-21 | Bayer Aktiengesellschaft | Chemically stabilized azulmic acids, processes for their preparation and their use |
US4341650A (en) | 1978-08-18 | 1982-07-27 | Bayer Aktiengesellschaft | Chemically stabilized azulmic acids, processes for their preparation and their use |
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