NO161295B - OPERATING DEVICE WITH SWINGING BOTTOMS. - Google Patents
OPERATING DEVICE WITH SWINGING BOTTOMS. Download PDFInfo
- Publication number
- NO161295B NO161295B NO841363A NO841363A NO161295B NO 161295 B NO161295 B NO 161295B NO 841363 A NO841363 A NO 841363A NO 841363 A NO841363 A NO 841363A NO 161295 B NO161295 B NO 161295B
- Authority
- NO
- Norway
- Prior art keywords
- weight
- parts
- operating device
- hydroperoxides
- masses
- Prior art date
Links
- -1 aralkyl hydroperoxides Chemical class 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229920006305 unsaturated polyester Polymers 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- YWBMNCRJFZGXJY-UHFFFAOYSA-N 1-hydroperoxy-1,2,3,4-tetrahydronaphthalene Chemical compound C1=CC=C2C(OO)CCCC2=C1 YWBMNCRJFZGXJY-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical class [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- JQRRFDWXQOQICD-UHFFFAOYSA-N biphenylen-1-ylboronic acid Chemical compound C12=CC=CC=C2C2=C1C=CC=C2B(O)O JQRRFDWXQOQICD-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- FGGJBCRKSVGDPO-UHFFFAOYSA-N hydroperoxycyclohexane Chemical compound OOC1CCCCC1 FGGJBCRKSVGDPO-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical class [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
- G05D19/00—Control of mechanical oscillations, e.g. of amplitude, of frequency, of phase
- G05D19/02—Control of mechanical oscillations, e.g. of amplitude, of frequency, of phase characterised by the use of electric means
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Automation & Control Theory (AREA)
- Apparatuses For Generation Of Mechanical Vibrations (AREA)
- Vibration Prevention Devices (AREA)
- Catching Or Destruction (AREA)
- Percussion Or Vibration Massage (AREA)
Description
Lagringsdyktige, herdbare masser på basis av innettede polyestere. Storable, hardenable compounds based on cross-linked polyesters.
Gjenstand for hovedpatentet, patent Subject of the main patent, patent
nr. 110 019, er lagringsdyktige, herdbare no. 110 019, are storable, hardenable
masser av blandinger av umettede polyestere og på-polymeriserbare monomerer masses of mixtures of unsaturated polyesters and on-polymerizable monomers
av umettede forbindelser og/eller ikke of unsaturated compounds and/or not
polymeriserbare oppløsningsmidler og polymerizable solvents and
ketonhydroperoxyder, som kjennetegnes ketone hydroperoxides, which are characterized
ved et innhold av sekundære aromatiske by a content of secondary aromatics
aminer av den generelle formel: amines of the general formula:
hvor Ar er en eventuelt substituert aromatisk rest og R er en alifatisk, cycloalifa-tisk eller aromatisk rest, eventuelt med et where Ar is an optionally substituted aromatic residue and R is an aliphatic, cycloaliphatic or aromatic residue, optionally with a
ytterligere innhold av andre aminer og/ additional content of other amines and/
eller fosfiner og/eller arsiner og/eller sti-biner. or phosphines and/or arsines and/or stibines.
Det har nu vist seg at slike masser i It has now been shown that such masses in
steden for ketonhydroperoxydene også kan the place of the ketone hydroperoxides can also
inneholde andre hydroperoxyder, som contain other hydroperoxides, such as
alkyl-, cycloalkyl- og aralkylhydroperoxy-der, f. eks. cumolhydroperoxyd, tert. bu-tylhydroperoxyd, tetralinhydroperoxyd, alkyl, cycloalkyl and aralkyl hydroperoxides, e.g. cumene hydroperoxide, tert. butyl hydroperoxide, tetralin hydroperoxide,
cyclohexylhydroperoxyd og diisopropyl-benzen-monohydroperoxyd. cyclohexyl hydroperoxide and diisopropylbenzene monohydroperoxide.
Eksempel 1. Example 1.
En polyester fremstilt ved kondenser-ing av 152 vektdeler maleinsyreanhydrid, 141 vektdeler fthalsyreanhydrid og 195 vektdeler propandiol-1,2, og med syretall 47, tilsettes 0,045 vektdeler hydrokinon og oppløses til en herdbar masse i 65 pst.ig konsentrasjon i styren. 50 g's porsjoner av denne masse tilsettes de i tabellen angitte peroxyder, tilsetninger ifølge oppfinnelsen og dessuten i hvert tilfelle 10 g styren. Holdbarhetsprøvningen skjer ved 30° C i en termostat. A polyester produced by condensing 152 parts by weight of maleic anhydride, 141 parts by weight of phthalic anhydride and 195 parts by weight of propanediol-1,2, and with an acid number of 47, 0.045 parts by weight of hydroquinone is added and dissolved into a curable mass in a 65% concentration in styrene. 50 g portions of this mass are added to the peroxides indicated in the table, additives according to the invention and also in each case 10 g of styrene. The durability test takes place at 30° C in a thermostat.
De i tabellen også angitte reaktiviteter ble enten bestemt ved oppvarming av mas-sen i hvert tilfelle til 80° C mellom glass-plater eller ved tilsetning av 0,016 vektpst. kobolt som koboltnafthenat ved 20° C i termostat. The reactivities also indicated in the table were either determined by heating the mass in each case to 80° C between glass plates or by adding 0.016 wt. cobalt as cobalt naphthenate at 20° C in a thermostat.
Eksempel 2. Example 2.
En umettet polyester fremstilt ved kon-densering av 882 vektdeler maleinsyreanhydrid, 1332 vektdeler fthalsyreanhydrid, An unsaturated polyester produced by condensation of 882 parts by weight maleic anhydride, 1332 parts by weight phthalic anhydride,
1098 vektdeler ethylenglycol og 963 vektdeler trimethylolpropan-diallylether i nær-vær av 0,43 vektdeler hydrokinon, og med 1098 parts by weight of ethylene glycol and 963 parts by weight of trimethylolpropane diallyl ether in the presence of 0.43 parts by weight of hydroquinone, and with
syretall 23, oppløses til 65 pst.ig konsentrasjon i styren til en formrespektive over-trekksmasse. Prøver av denne masse tilsettes, som angitt i nedenstående tabell, med tilsetninger ifølge oppfinnelsen. Efter ytterligere tilsetning av 4 pst. cumolhydro-peroxydoppløsning (70 pst.ig) måles hold-barheten ved 30° C i termostat. acid number 23, is dissolved to a concentration of 65 percent in styrene to form a coating compound of the respective shape. Samples of this mass are added, as indicated in the table below, with additives according to the invention. After further addition of 4 percent cumene hydroperoxide solution (70 percent), the durability is measured at 30° C in a thermostat.
De i tabellen også angitte reaktiviteter ble bestemt efter en ytterligere tilsetning av 0,016 vekt-% kobolt (som koboltnafthenat) ved 80° C i termostat. The reactivities also stated in the table were determined after a further addition of 0.016% by weight of cobalt (as cobalt naphthenate) at 80° C in a thermostat.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS832524A CS241379B1 (en) | 1983-04-08 | 1983-04-08 | Driving unit for extractors with vibrating levels |
Publications (3)
Publication Number | Publication Date |
---|---|
NO841363L NO841363L (en) | 1984-10-09 |
NO161295B true NO161295B (en) | 1989-04-24 |
NO161295C NO161295C (en) | 1989-08-02 |
Family
ID=5362629
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO841363A NO161295C (en) | 1983-04-08 | 1984-04-06 | OPERATING DEVICE WITH SWINGING BOTTOMS. |
Country Status (5)
Country | Link |
---|---|
CS (1) | CS241379B1 (en) |
DK (1) | DK160984A (en) |
FI (1) | FI73888C (en) |
NO (1) | NO161295C (en) |
SE (1) | SE462065B (en) |
-
1983
- 1983-04-08 CS CS832524A patent/CS241379B1/en unknown
-
1984
- 1984-03-21 DK DK160984A patent/DK160984A/en not_active Application Discontinuation
- 1984-03-27 SE SE8401693A patent/SE462065B/en not_active IP Right Cessation
- 1984-04-05 FI FI841355A patent/FI73888C/en not_active IP Right Cessation
- 1984-04-06 NO NO841363A patent/NO161295C/en unknown
Also Published As
Publication number | Publication date |
---|---|
SE8401693D0 (en) | 1984-03-27 |
NO161295C (en) | 1989-08-02 |
SE8401693L (en) | 1984-10-09 |
FI841355A0 (en) | 1984-04-05 |
FI841355A (en) | 1984-10-09 |
FI73888B (en) | 1987-08-31 |
NO841363L (en) | 1984-10-09 |
SE462065B (en) | 1990-04-30 |
CS241379B1 (en) | 1986-03-13 |
CS252483A1 (en) | 1985-08-15 |
FI73888C (en) | 1987-12-10 |
DK160984A (en) | 1984-10-09 |
DK160984D0 (en) | 1984-03-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3432478A (en) | Polyhydroxy-containing unsaturated polyesters and their preparation | |
US2691007A (en) | Unsaturated acidic polyester ethoxyline resinous compositions | |
EP0250351A3 (en) | A process for the preparation of polymer dispersions in hydroxylated polyesters | |
GB913861A (en) | Flame-resistant polyester resinous compositions | |
NO157786B (en) | STABILIZED, THERMOROUS ETHYLENIC UNSATATED EPOXYESTER RESIN MIXTURES, AND PROCEDURES FOR THE MANUFACTURE OF THESE. | |
FI81108C (en) | Process for the preparation of vinyl ester resins containing trazine or triazine and oxazoline groups | |
NO161295B (en) | OPERATING DEVICE WITH SWINGING BOTTOMS. | |
US3507933A (en) | Self-extinguishing polyester compositions of 2,2-bis(bromomethyl)-1,3-propanediol and method of making the same | |
EP0084227B1 (en) | Acryloyl and alkylarcryloyl polyalkoxy carbamate compositions and their use in radiation curable coatings | |
US4684706A (en) | Compositions containing maleimide-amide compounds as well as the preparation and application thereof | |
US3151182A (en) | Nu-allyloxymethyl maleimide, and homopolymers and copolymers thereof | |
US3357964A (en) | Process for the polymerization of vinyl aromatic compounds | |
US4680337A (en) | Transparent impact polymers | |
US3067179A (en) | Unsaturated polyester resin from certain benzene tricarboxylic acids, alkenedioic acids and glycols | |
EP0264948A2 (en) | Aromatic dicarboxylic acid diallyl ester derivative, prepolymer derived from the derivative and curable resin composition containing the derivative | |
US3327019A (en) | Diethers and copolymerizates therefrom | |
EP0214370B1 (en) | Low styrene emission vinyl ester resin employing polyacrylates for fiber-reinforced applications | |
EP0055585B1 (en) | Stabilizer system for thermosetting polyesters | |
US3687860A (en) | Polymerizable mixtures comprising a halogenated bivalent metal salt of an acrylate- or methacrylate-phthalate ester of an alkylene glycol | |
US3390116A (en) | Process for the manufacture of solutions of prepolymers of a diallylphthalate | |
DE1544903A1 (en) | Storage-stable hardenable masses based on unsaturated polyester | |
US5292841A (en) | Laminating resins having low organic emissions | |
US3225002A (en) | Diesters of terminally unsaturated monocarboxylic acids and halophenoxymethyl, alkane diols | |
AT267187B (en) | In-stock hardenable compound based on unsaturated polyester | |
US3020256A (en) | Unsaturated polyester composition containing phenyl chlorophosphonates to reduce color |