NO843537L - Polymerbetongblanding, samt fremgangsmaate for utfoering av roerledninger - Google Patents

Polymerbetongblanding, samt fremgangsmaate for utfoering av roerledninger

Info

Publication number: NO843537L
Authority: NO; Norway
Prior art keywords: mixture; pipeline; concrete; vinyl ester; weight
Prior art date: 1983-09-06

Application number

NO843537A

Other languages

English (en)

Norwegian (no)

Inventor

Richard Max Robinson

Gordon Svarc

Original Assignee

Dow Chemical Co

Priority date (The priority date 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 date listed.)

1983-09-06

Filing date

1984-09-06

Publication date

1985-03-07

1984-09-06 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1985-03-07 Publication of NO843537L publication Critical patent/NO843537L/no

Links

239000000203 mixture Substances 0.000 title claims description 112
239000002986 polymer concrete Substances 0.000 title claims description 30
238000000034 method Methods 0.000 title claims description 19
229920001567 vinyl ester resin Polymers 0.000 claims description 56
229920005989 resin Polymers 0.000 claims description 55
239000011347 resin Substances 0.000 claims description 55
239000004567 concrete Substances 0.000 claims description 51
239000000945 filler Substances 0.000 claims description 30
239000003999 initiator Substances 0.000 claims description 25
238000011049 filling Methods 0.000 claims description 24
239000004576 sand Substances 0.000 claims description 19
239000000463 material Substances 0.000 claims description 18
150000003254 radicals Chemical class 0.000 claims description 18
239000000178 monomer Substances 0.000 claims description 16
229920006337 unsaturated polyester resin Polymers 0.000 claims description 14
239000002245 particle Substances 0.000 claims description 12
229920006305 unsaturated polyester Polymers 0.000 claims description 10
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 6
235000019400 benzoyl peroxide Nutrition 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
229910052723 transition metal Inorganic materials 0.000 claims description 4
150000003624 transition metals Chemical class 0.000 claims description 4
HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 claims description 2
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims description 2
150000001412 amines Chemical group 0.000 claims description 2
150000003623 transition metal compounds Chemical class 0.000 claims description 2
LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 claims 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 23
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 18
239000004593 Epoxy Substances 0.000 description 15
150000001875 compounds Chemical class 0.000 description 15
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000011248 coating agent Substances 0.000 description 11
238000000576 coating method Methods 0.000 description 11
238000007711 solidification Methods 0.000 description 11
230000008023 solidification Effects 0.000 description 11
229920002959 polymer blend Polymers 0.000 description 10
229920000570 polyether Polymers 0.000 description 9
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 8
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 7
239000004721 Polyphenylene oxide Substances 0.000 description 7
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000004800 polyvinyl chloride Substances 0.000 description 6
230000007797 corrosion Effects 0.000 description 5
238000005260 corrosion Methods 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
JDEJGVSZUIJWBM-UHFFFAOYSA-N n,n,2-trimethylaniline Chemical compound CN(C)C1=CC=CC=C1C JDEJGVSZUIJWBM-UHFFFAOYSA-N 0.000 description 5
239000011236 particulate material Substances 0.000 description 5
229920000915 polyvinyl chloride Polymers 0.000 description 5
150000005846 sugar alcohols Polymers 0.000 description 5
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 4
239000006004 Quartz sand Substances 0.000 description 4
125000002723 alicyclic group Chemical group 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
150000001491 aromatic compounds Chemical class 0.000 description 4
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
239000004568 cement Substances 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
230000002787 reinforcement Effects 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
150000008064 anhydrides Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
230000006378 damage Effects 0.000 description 3
230000001419 dependent effect Effects 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
-1 hydroxyalkyl acrylate Chemical compound 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
238000003466 welding Methods 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
235000011132 calcium sulphate Nutrition 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000012374 esterification agent Substances 0.000 description 2
239000011152 fibreglass Substances 0.000 description 2
239000010881 fly ash Substances 0.000 description 2
239000003365 glass fiber Substances 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000013521 mastic Substances 0.000 description 2
150000002763 monocarboxylic acids Chemical class 0.000 description 2
229920003986 novolac Polymers 0.000 description 2
150000002924 oxiranes Chemical class 0.000 description 2
125000000466 oxiranyl group Chemical group 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000011435 rock Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000010865 sewage Substances 0.000 description 2
239000011343 solid material Substances 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical class CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical class C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
ONPJWQSDZCGSQM-UHFFFAOYSA-N 2-phenylprop-2-enoic acid Chemical compound OC(=O)C(=C)C1=CC=CC=C1 ONPJWQSDZCGSQM-UHFFFAOYSA-N 0.000 description 1
OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
229910001209 Low-carbon steel Inorganic materials 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001334 alicyclic compounds Chemical class 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
239000012753 anti-shrinkage agent Substances 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
BGOJVALFSNMCFD-UHFFFAOYSA-N benzoic acid;1-butylperoxybutane Chemical group OC(=O)C1=CC=CC=C1.CCCCOOCCCC BGOJVALFSNMCFD-UHFFFAOYSA-N 0.000 description 1
ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
FSRYENDEMMDKMT-UHFFFAOYSA-N butoxy ethaneperoxoate Chemical group CCCCOOOC(C)=O FSRYENDEMMDKMT-UHFFFAOYSA-N 0.000 description 1
KBWZTOAYWHAYJX-UHFFFAOYSA-N butylperoxycyclohexane Chemical group CCCCOOC1CCCCC1 KBWZTOAYWHAYJX-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000003518 caustics Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003251 chemically resistant material Substances 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
238000004891 communication Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000007547 defect Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000009415 formwork Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000003944 halohydrins Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000009434 installation Methods 0.000 description 1
230000001788 irregular Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
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 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920000131 polyvinylidene Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000013535 sea water Substances 0.000 description 1
238000007789 sealing Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
230000035939 shock Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000007779 soft material Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
230000007704 transition Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/026—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from the reaction products of polyepoxides and unsaturated monocarboxylic acids, their anhydrides, halogenides or esters with low molecular weight
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/04—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromonomer-Based Addition Polymer (AREA)
Manufacturing Of Tubular Articles Or Embedded Moulded Articles (AREA)
Rigid Pipes And Flexible Pipes (AREA)
Protection Of Pipes Against Damage, Friction, And Corrosion (AREA)

NO843537A 1983-09-06 1984-09-06 Polymerbetongblanding, samt fremgangsmaate for utfoering av roerledninger NO843537L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833332080 DE3332080A1 (de)	1983-09-06	1983-09-06	Verfahren, zusammensetzung und vorrichtung zum fuellen von schweissgurt-zementaussparungen bei mit zement umhuellten rohren

Publications (1)

Publication Number	Publication Date
NO843537L true NO843537L (no)	1985-03-07

Family

ID=6208350

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO843537A NO843537L (no)	1983-09-06	1984-09-06	Polymerbetongblanding, samt fremgangsmaate for utfoering av roerledninger

Country Status (8)

Country	Link
US (1)	US4608280A (de)
EP (1)	EP0143216B1 (de)
AU (1)	AU571261B2 (de)
BR (1)	BR8404533A (de)
DE (2)	DE3332080A1 (de)
DK (1)	DK424284A (de)
ES (1)	ES8608019A1 (de)
NO (1)	NO843537L (de)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5082878A (en) *	1988-04-15	1992-01-21	W.R. Grace & Co.-Conn	Shrink controlled low-temperature-curable polyester resin compositions
US5464886A (en) *	1990-10-19	1995-11-07	Tran; Bang T.	Polymer concrete coating for pipe, tubular shapes, other metal members and metal structures
US5303518A (en) *	1993-02-11	1994-04-19	Strickland Industries, Inc.	Lined manhole assembly and liner
AU7998594A (en) *	1993-10-26	1995-05-22	Balmoral Group Limited	Coated pipes and methods of making them
CA2268859C (en)	1999-04-13	2001-01-23	Steve Lohnes	Polymer concrete structures
US6429242B1 (en)	2000-04-06	2002-08-06	Camie-Campbell, Inc.	Solvent weld cement composition in aerosol form
CA2518167A1 (en) *	2003-03-07	2004-09-23	Polythane Systems, Inc.	Joint fill composition and method
US20070215267A1 (en) *	2004-03-08	2007-09-20	Brown Scott A	Joint fill composition and method
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1983
- 1983-09-06 DE DE19833332080 patent/DE3332080A1/de not_active Withdrawn
1984
- 1984-08-30 US US06/645,584 patent/US4608280A/en not_active Expired - Fee Related
- 1984-09-03 AU AU32670/84A patent/AU571261B2/en not_active Ceased
- 1984-09-04 DE DE8484110488T patent/DE3471645D1/de not_active Expired
- 1984-09-04 EP EP84110488A patent/EP0143216B1/de not_active Expired
- 1984-09-05 DK DK424284A patent/DK424284A/da not_active Application Discontinuation
- 1984-09-05 ES ES535679A patent/ES8608019A1/es not_active Expired
- 1984-09-06 NO NO843537A patent/NO843537L/no unknown
- 1984-09-06 BR BR8404533A patent/BR8404533A/pt unknown

Also Published As

Publication number	Publication date
AU571261B2 (en)	1988-04-14
AU3267084A (en)	1985-03-14
ES8608019A1 (es)	1986-04-01
BR8404533A (pt)	1985-08-06
DE3332080A1 (de)	1985-03-21
DE3471645D1 (en)	1988-07-07
ES535679A0 (es)	1986-04-01
US4608280A (en)	1986-08-26
DK424284D0 (da)	1984-09-05
DK424284A (da)	1985-03-07
EP0143216B1 (de)	1988-06-01
EP0143216A3 (en)	1985-09-04
EP0143216A2 (de)	1985-06-05

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