SE415768B - Sett att framstella en polymer berare som innehaller aromatiskt bundna kvicksilver(ii)joner - Google Patents
Sett att framstella en polymer berare som innehaller aromatiskt bundna kvicksilver(ii)jonerInfo
- Publication number
- SE415768B SE415768B SE7310883A SE7310883A SE415768B SE 415768 B SE415768 B SE 415768B SE 7310883 A SE7310883 A SE 7310883A SE 7310883 A SE7310883 A SE 7310883A SE 415768 B SE415768 B SE 415768B
- Authority
- SE
- Sweden
- Prior art keywords
- parts
- mercury
- weight
- ions
- water
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims description 14
- -1 MERCURY SILVER (II) IONS Chemical class 0.000 title claims description 9
- 229910052753 mercury Inorganic materials 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 9
- IJSVVICYGLOZHA-UHFFFAOYSA-N 2-methyl-n-phenylprop-2-enamide Chemical compound CC(=C)C(=O)NC1=CC=CC=C1 IJSVVICYGLOZHA-UHFFFAOYSA-N 0.000 claims description 8
- BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 8
- 239000000725 suspension Substances 0.000 claims description 7
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- YLKADOPTDHJSSC-UHFFFAOYSA-N (2-acetamido-2-phenoxyethyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(NC(=O)C)OC1=CC=CC=C1 YLKADOPTDHJSSC-UHFFFAOYSA-N 0.000 claims description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000002730 mercury Chemical class 0.000 claims description 2
- VAYDQPPHPFGABZ-UHFFFAOYSA-N ethene prop-2-enoic acid Chemical compound C=C.C=C.OC(=O)C=C.OC(=O)C=C VAYDQPPHPFGABZ-UHFFFAOYSA-N 0.000 claims 1
- OUGJKAQEYOUGKG-UHFFFAOYSA-N ethyl 2-methylidenebutanoate Chemical compound CCOC(=O)C(=C)CC OUGJKAQEYOUGKG-UHFFFAOYSA-N 0.000 claims 1
- 230000000977 initiatory effect Effects 0.000 claims 1
- BPCNEKWROYSOLT-UHFFFAOYSA-N n-phenylprop-2-enamide Chemical compound C=CC(=O)NC1=CC=CC=C1 BPCNEKWROYSOLT-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical group [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 9
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 229920001222 biopolymer Polymers 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
-
- 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
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS574272A CS171847B1 (en, 2012) | 1972-08-18 | 1972-08-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE415768B true SE415768B (sv) | 1980-10-27 |
Family
ID=5402884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7310883A SE415768B (sv) | 1972-08-18 | 1973-08-08 | Sett att framstella en polymer berare som innehaller aromatiskt bundna kvicksilver(ii)joner |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS578802B2 (en, 2012) |
| AT (1) | AT336270B (en, 2012) |
| AU (1) | AU476521B2 (en, 2012) |
| BE (1) | BE803717A (en, 2012) |
| CA (1) | CA1002241A (en, 2012) |
| CH (1) | CH593998A5 (en, 2012) |
| CS (1) | CS171847B1 (en, 2012) |
| DE (1) | DE2340520C2 (en, 2012) |
| FR (1) | FR2196350B1 (en, 2012) |
| GB (1) | GB1426374A (en, 2012) |
| NL (1) | NL7310962A (en, 2012) |
| SE (1) | SE415768B (en, 2012) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60190821U (ja) * | 1984-05-24 | 1985-12-18 | 三笠産業株式会社 | 輾圧機の特殊作業用ハンドル |
| JPS6289309U (en, 2012) * | 1985-11-26 | 1987-06-08 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2137236A (en) * | 1934-09-13 | 1938-11-22 | Squibb & Sons Inc | Mercuri alkyl phenol derivatives |
-
1972
- 1972-08-18 CS CS574272A patent/CS171847B1/cs unknown
-
1973
- 1973-08-01 AT AT676573A patent/AT336270B/de not_active IP Right Cessation
- 1973-08-07 CA CA178,195A patent/CA1002241A/en not_active Expired
- 1973-08-07 GB GB3742873A patent/GB1426374A/en not_active Expired
- 1973-08-08 SE SE7310883A patent/SE415768B/sv unknown
- 1973-08-08 NL NL7310962A patent/NL7310962A/xx not_active Application Discontinuation
- 1973-08-09 AU AU59104/73A patent/AU476521B2/en not_active Expired
- 1973-08-10 DE DE19732340520 patent/DE2340520C2/de not_active Expired
- 1973-08-14 JP JP9063373A patent/JPS578802B2/ja not_active Expired
- 1973-08-15 CH CH1177673A patent/CH593998A5/xx not_active IP Right Cessation
- 1973-08-17 BE BE134674A patent/BE803717A/xx unknown
- 1973-08-17 FR FR7330016A patent/FR2196350B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE803717A (fr) | 1973-12-17 |
| JPS578802B2 (en, 2012) | 1982-02-18 |
| ATA676573A (de) | 1976-08-15 |
| AU476521B2 (en) | 1976-09-23 |
| AT336270B (de) | 1977-04-25 |
| CS171847B1 (en, 2012) | 1976-11-29 |
| FR2196350B1 (en, 2012) | 1977-05-13 |
| DE2340520C2 (de) | 1983-04-21 |
| NL7310962A (en, 2012) | 1974-02-20 |
| GB1426374A (en) | 1976-02-25 |
| DE2340520A1 (de) | 1974-02-28 |
| CA1002241A (en) | 1976-12-21 |
| FR2196350A1 (en, 2012) | 1974-03-15 |
| JPS4986493A (en, 2012) | 1974-08-19 |
| AU5910473A (en) | 1975-02-13 |
| CH593998A5 (en, 2012) | 1977-12-30 |
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