GB1465601A - Production of resins - Google Patents
Production of resinsInfo
- Publication number
- GB1465601A GB1465601A GB1400774A GB1400774A GB1465601A GB 1465601 A GB1465601 A GB 1465601A GB 1400774 A GB1400774 A GB 1400774A GB 1400774 A GB1400774 A GB 1400774A GB 1465601 A GB1465601 A GB 1465601A
- Authority
- GB
- United Kingdom
- Prior art keywords
- exs
- resin
- melamine
- acrylic resin
- resins
- 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
- 229920005989 resin Polymers 0.000 title abstract 5
- 239000011347 resin Substances 0.000 title abstract 5
- 229920000877 Melamine resin Polymers 0.000 abstract 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 4
- 239000004925 Acrylic resin Substances 0.000 abstract 3
- 229920000178 Acrylic resin Polymers 0.000 abstract 3
- 239000000975 dye Substances 0.000 abstract 3
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 abstract 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 abstract 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 2
- 229910000831 Steel Inorganic materials 0.000 abstract 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 2
- 229920000728 polyester Polymers 0.000 abstract 2
- 239000010959 steel Substances 0.000 abstract 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 abstract 1
- GFVJWUVFVLFWNG-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;terephthalic acid Chemical compound CCC(CO)(CO)CO.OC(=O)C1=CC=C(C(O)=O)C=C1 GFVJWUVFVLFWNG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 1
- 229930040373 Paraformaldehyde Natural products 0.000 abstract 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 abstract 1
- 125000005442 diisocyanate group Chemical group 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229920002866 paraformaldehyde Polymers 0.000 abstract 1
- ABOYDMHGKWRPFD-UHFFFAOYSA-N phenylmethanesulfonamide Chemical compound NS(=O)(=O)CC1=CC=CC=C1 ABOYDMHGKWRPFD-UHFFFAOYSA-N 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000004033 plastic Substances 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 229920005862 polyol Polymers 0.000 abstract 1
- 150000003077 polyols Chemical class 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
Classifications
-
- 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
- C08G85/00—General processes for preparing compounds provided for in this subclass
-
- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/08—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
- B01J8/10—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by stirrers or by rotary drums or rotary receptacles or endless belts
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
-
- 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
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/18—Details relating to the spatial orientation of the reactor
- B01J2219/182—Details relating to the spatial orientation of the reactor horizontal
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Luminescent Compositions (AREA)
Abstract
1465601 Luminescent compositions BASF AG 29 March 1974 [31 March 1973 5 May 1973] 14007/74 Heading C4S [Also in Division C3] Particulate resins which may be fluorescent are prepared by conducting the polymerization in a rotating or agitated vessel containing inert grinding bodies until a powdered brittle resin is obtained, the mass of reactants (M grams) and the number and size of the grinding bodies (each of S sq. cm. surface and d cm. average diameter) being such that M#0À2#Sd. The vessel may be a vibrating, tube, or tumbling mill, containing spheres, rods or cones of steel, ceramic, non-ferrous metal, or plastics, and is preferably 10-80% full. The starting materials may include dyes, to give pigment powders as products. In Examples 2-6 cm. spheres of alumina or steel are used in a rotating cylindrical mill to prepare powdered resins from: toluene sulphonamide, paraformaldehyde and melamine (Exs. 1-14, 30 and 50), or these with urea, dicyandiamide, benzoguanamine, formoguanamine, acetoguanamine or phenylacetoguanamine instead of melamine (Exs. 28-34), or these plus a polyester or an acrylic resin (Exs. 35-38); toluensulphonamide or a polyol and isophoronic diisocyanate or trimethyl hexamethylene diisocyanate, optionally with melamine or benzoguanamine (Exs. 15-25); a UF, or butylated or methylated MF resin syrup (Exs. 39-41); a trimethylolpropane-terephthalate polyester or hydroxyacrylic resin and trimethyl hexamethylene diisocyanate or phthalic anhydride or an MF resin (Exs. 42- 47); an epoxy acrylic resin and phthalic anhydride (Ex. 48); or an anhydro-acrylic resin and trimethylolpropane (Ex. 49). In every case of fluoresecent dye (or dyes) is also added, examples being specified. Applications are included.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732316300 DE2316300C3 (en) | 1973-03-31 | 1973-03-31 | Process for the production of finely divided ground resins |
| DE2322741A DE2322741A1 (en) | 1973-05-05 | 1973-05-05 | METHOD OF MANUFACTURING RESINS |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1465601A true GB1465601A (en) | 1977-02-23 |
Family
ID=25764902
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1400774A Expired GB1465601A (en) | 1973-03-31 | 1974-03-29 | Production of resins |
Country Status (2)
| Country | Link |
|---|---|
| FR (1) | FR2223421B3 (en) |
| GB (1) | GB1465601A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3037575C2 (en) * | 1980-10-04 | 1982-12-02 | Basf Farben + Fasern Ag, 2000 Hamburg | Process for the preparation of aqueous synthetic resin dispersions |
-
1974
- 1974-03-29 GB GB1400774A patent/GB1465601A/en not_active Expired
- 1974-03-29 FR FR7411269A patent/FR2223421B3/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2223421A1 (en) | 1974-10-25 |
| FR2223421B3 (en) | 1978-02-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |