GB549234A - Method of polymerizing unsaturated methylene compounds - Google Patents
Method of polymerizing unsaturated methylene compoundsInfo
- Publication number
- GB549234A GB549234A GB14972/40A GB1497240A GB549234A GB 549234 A GB549234 A GB 549234A GB 14972/40 A GB14972/40 A GB 14972/40A GB 1497240 A GB1497240 A GB 1497240A GB 549234 A GB549234 A GB 549234A
- Authority
- GB
- United Kingdom
- Prior art keywords
- peroxide
- acrylic
- esters
- colour
- methacrylic
- 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
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 title 1
- 230000000379 polymerizing effect Effects 0.000 title 1
- 150000002978 peroxides Chemical class 0.000 abstract 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 3
- 229910052740 iodine Inorganic materials 0.000 abstract 3
- 239000011630 iodine Substances 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 abstract 3
- 239000000243 solution Substances 0.000 abstract 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical compound C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 abstract 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000013098 chemical test method Methods 0.000 abstract 1
- 238000004737 colorimetric analysis Methods 0.000 abstract 1
- 238000007865 diluting Methods 0.000 abstract 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- WJHVRRJYTNYNIW-UHFFFAOYSA-N formyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=O WJHVRRJYTNYNIW-UHFFFAOYSA-N 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- -1 isopropene Chemical group 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- 125000005394 methallyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/123—Ultraviolet light
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/02—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
- B29C41/04—Rotational or centrifugal casting, i.e. coating the inside of a mould by rotating the mould
Landscapes
- Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymerization Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
549,234. Chemical testing. NORTON GRINDING WHEEL CO., Ltd. Oct. 7, 1940, No. 14972. Convention date, Oct. 6, 1939. Drawings to Specification. [Class 1 (i)] [Also in Group IV] The unsaturated monomeric methylene compounds specified below are exposed to air or oxygen to form therein a small proportion of the peroxide of the compound to act as a catalyst in the subsequent polymerization of the monomer. The concentration of the peroxide in the monomer may be determined by a colorimetric test, the yellow colour of iodine liberated from a freshly prepared solution of potassium iodide in water being compared either with the colour of iodine liberated from a similar solution by the addition of a known amount of peroxide, or with standards prepared by diluting aqueous solutions of potassium dichromate to match the colour of iodine liberated by a solution of peroxide of known concentration. The unsaturated monomeric compounds specified are (1) vinyl esters of lower aliphatic acids, (2) acrylic and methyl acrylic acids and their lower alkyl esters, (3) substituted ethylenes, (4) ketones containing the unsaturated methylene group, (5) aldehydes, (6) mixed anhydrides such as acrylic and methacrylic formic anhydride, (7) vinyl, isopropene, allyl and methallyl esters of methacrylic acid, (8) polyhydric alcohol (including the hypothetical ethylidine glycol) esters of acrylic and methacrylic acids, (9) divinyl ketone and alpha substituted divinyl ketones, and (10) interpolymers of mixtures of the monomers specified above.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US549234XA | 1939-10-06 | 1939-10-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB549234A true GB549234A (en) | 1942-11-12 |
Family
ID=21994407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14972/40A Expired GB549234A (en) | 1939-10-06 | 1940-10-07 | Method of polymerizing unsaturated methylene compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB549234A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2493343A (en) * | 1944-09-21 | 1950-01-03 | Pittsburgh Plate Glass Co | Stabilization of polymerizable mixtures |
US2525628A (en) * | 1946-08-02 | 1950-10-10 | Du Pont | Preparation of organic peroxide polymerization catalysts |
US2619452A (en) * | 1945-12-22 | 1952-11-25 | Gen Aniline & Film Corp | Purification of vinyl sulfonic acids |
US2628178A (en) * | 1950-07-29 | 1953-02-10 | Gen Electric | Oxygenated polymerizable acrylic acid type esters and methods of preparing and polymerizing the same |
US2628210A (en) * | 1950-07-29 | 1953-02-10 | Gen Electric | Oxygenated polymerizable esters as cure accelerators and as copolymerizable materials |
US2683704A (en) * | 1950-12-30 | 1954-07-13 | Gen Aniline & Film Corp | Preparation of colorless, colorstable mass polymers of methyl alpha-chloroacrylate |
DE950031C (en) * | 1943-10-15 | 1956-10-04 | Hoechst Ag | Process for the production of polymers of unsaturated organic compounds |
US2911436A (en) * | 1953-09-08 | 1959-11-03 | Gen Electric | Method of preparing polymeric peroxides |
-
1940
- 1940-10-07 GB GB14972/40A patent/GB549234A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE950031C (en) * | 1943-10-15 | 1956-10-04 | Hoechst Ag | Process for the production of polymers of unsaturated organic compounds |
US2493343A (en) * | 1944-09-21 | 1950-01-03 | Pittsburgh Plate Glass Co | Stabilization of polymerizable mixtures |
US2619452A (en) * | 1945-12-22 | 1952-11-25 | Gen Aniline & Film Corp | Purification of vinyl sulfonic acids |
US2525628A (en) * | 1946-08-02 | 1950-10-10 | Du Pont | Preparation of organic peroxide polymerization catalysts |
US2628178A (en) * | 1950-07-29 | 1953-02-10 | Gen Electric | Oxygenated polymerizable acrylic acid type esters and methods of preparing and polymerizing the same |
US2628210A (en) * | 1950-07-29 | 1953-02-10 | Gen Electric | Oxygenated polymerizable esters as cure accelerators and as copolymerizable materials |
US2683704A (en) * | 1950-12-30 | 1954-07-13 | Gen Aniline & Film Corp | Preparation of colorless, colorstable mass polymers of methyl alpha-chloroacrylate |
US2911436A (en) * | 1953-09-08 | 1959-11-03 | Gen Electric | Method of preparing polymeric peroxides |
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