JPH0637574B2 - Heat resistant gel manufacturing method - Google Patents
Heat resistant gel manufacturing methodInfo
- Publication number
- JPH0637574B2 JPH0637574B2 JP62027074A JP2707487A JPH0637574B2 JP H0637574 B2 JPH0637574 B2 JP H0637574B2 JP 62027074 A JP62027074 A JP 62027074A JP 2707487 A JP2707487 A JP 2707487A JP H0637574 B2 JPH0637574 B2 JP H0637574B2
- Authority
- JP
- Japan
- Prior art keywords
- sodium
- potassium
- calcium
- heat
- salt
- 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 - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000000499 gel Substances 0.000 claims description 57
- 235000010443 alginic acid Nutrition 0.000 claims description 25
- 229920000615 alginic acid Polymers 0.000 claims description 25
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 20
- 238000010438 heat treatment Methods 0.000 claims description 17
- 239000000783 alginic acid Substances 0.000 claims description 16
- 229960001126 alginic acid Drugs 0.000 claims description 16
- 150000004781 alginic acids Chemical class 0.000 claims description 16
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 14
- 239000011575 calcium Substances 0.000 claims description 14
- 229910052791 calcium Inorganic materials 0.000 claims description 14
- 239000003349 gelling agent Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 229910052708 sodium Inorganic materials 0.000 claims description 13
- 229920001817 Agar Polymers 0.000 claims description 12
- 239000008272 agar Substances 0.000 claims description 12
- 235000010419 agar Nutrition 0.000 claims description 12
- 159000000007 calcium salts Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 108010010803 Gelatin Proteins 0.000 claims description 10
- 239000008273 gelatin Substances 0.000 claims description 10
- 229920000159 gelatin Polymers 0.000 claims description 10
- 235000019322 gelatine Nutrition 0.000 claims description 10
- 235000011852 gelatine desserts Nutrition 0.000 claims description 10
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 6
- 239000001814 pectin Substances 0.000 claims description 6
- 235000010987 pectin Nutrition 0.000 claims description 6
- 229920001277 pectin Polymers 0.000 claims description 6
- 235000015424 sodium Nutrition 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 5
- 239000001509 sodium citrate Substances 0.000 claims description 5
- 235000004298 Tamarindus indica Nutrition 0.000 claims description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 4
- 238000001879 gelation Methods 0.000 claims description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 229910000160 potassium phosphate Inorganic materials 0.000 claims description 4
- 235000011009 potassium phosphates Nutrition 0.000 claims description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- FNAQSUUGMSOBHW-UHFFFAOYSA-H calcium citrate Chemical group [Ca+2].[Ca+2].[Ca+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FNAQSUUGMSOBHW-UHFFFAOYSA-H 0.000 claims description 3
- 239000001354 calcium citrate Substances 0.000 claims description 3
- 229940061607 dibasic sodium phosphate Drugs 0.000 claims description 3
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- 150000004804 polysaccharides Chemical class 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 3
- 235000013337 tricalcium citrate Nutrition 0.000 claims description 3
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 claims description 2
- 235000010216 calcium carbonate Nutrition 0.000 claims description 2
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 claims description 2
- 235000019700 dicalcium phosphate Nutrition 0.000 claims description 2
- 229940095079 dicalcium phosphate anhydrous Drugs 0.000 claims description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 claims description 2
- CVOQYKPWIVSMDC-UHFFFAOYSA-L dipotassium;butanedioate Chemical compound [K+].[K+].[O-]C(=O)CCC([O-])=O CVOQYKPWIVSMDC-UHFFFAOYSA-L 0.000 claims description 2
- AVTYONGGKAJVTE-OLXYHTOASA-L potassium L-tartrate Chemical compound [K+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O AVTYONGGKAJVTE-OLXYHTOASA-L 0.000 claims description 2
- 235000011056 potassium acetate Nutrition 0.000 claims description 2
- 239000011736 potassium bicarbonate Substances 0.000 claims description 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 2
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 235000011181 potassium carbonates Nutrition 0.000 claims description 2
- 239000001508 potassium citrate Substances 0.000 claims description 2
- 229960002635 potassium citrate Drugs 0.000 claims description 2
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 claims description 2
- 235000011082 potassium citrates Nutrition 0.000 claims description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 2
- 229940086066 potassium hydrogencarbonate Drugs 0.000 claims description 2
- 235000011118 potassium hydroxide Nutrition 0.000 claims description 2
- 239000001415 potassium malate Substances 0.000 claims description 2
- SVICABYXKQIXBM-UHFFFAOYSA-L potassium malate Chemical compound [K+].[K+].[O-]C(=O)C(O)CC([O-])=O SVICABYXKQIXBM-UHFFFAOYSA-L 0.000 claims description 2
- 235000011033 potassium malate Nutrition 0.000 claims description 2
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 claims description 2
- 235000019828 potassium polyphosphate Nutrition 0.000 claims description 2
- 239000001472 potassium tartrate Substances 0.000 claims description 2
- 229940111695 potassium tartrate Drugs 0.000 claims description 2
- 235000011005 potassium tartrates Nutrition 0.000 claims description 2
- 229940005657 pyrophosphoric acid Drugs 0.000 claims description 2
- 235000019265 sodium DL-malate Nutrition 0.000 claims description 2
- 239000001632 sodium acetate Substances 0.000 claims description 2
- 235000017281 sodium acetate Nutrition 0.000 claims description 2
- 239000001394 sodium malate Substances 0.000 claims description 2
- 235000019830 sodium polyphosphate Nutrition 0.000 claims description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 claims description 2
- 239000001433 sodium tartrate Substances 0.000 claims description 2
- 229960002167 sodium tartrate Drugs 0.000 claims description 2
- 235000011004 sodium tartrates Nutrition 0.000 claims description 2
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 claims description 2
- 235000019731 tricalcium phosphate Nutrition 0.000 claims description 2
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 claims description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 2
- 159000000000 sodium salts Chemical class 0.000 claims 2
- 240000004584 Tamarindus indica Species 0.000 claims 1
- 235000011132 calcium sulphate Nutrition 0.000 claims 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 claims 1
- 229940001593 sodium carbonate Drugs 0.000 claims 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 235000015110 jellies Nutrition 0.000 description 8
- 239000008274 jelly Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 235000013305 food Nutrition 0.000 description 7
- 230000001954 sterilising effect Effects 0.000 description 7
- 238000004659 sterilization and disinfection Methods 0.000 description 7
- -1 alkali metal alginate Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000006188 syrup Substances 0.000 description 5
- 235000020357 syrup Nutrition 0.000 description 5
- 229930006000 Sucrose Natural products 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 3
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 241000596504 Tamarindus Species 0.000 description 3
- 229940072056 alginate Drugs 0.000 description 3
- 235000021552 granulated sugar Nutrition 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000010413 sodium alginate Nutrition 0.000 description 3
- 239000000661 sodium alginate Substances 0.000 description 3
- 229940005550 sodium alginate Drugs 0.000 description 3
- 235000019983 sodium metaphosphate Nutrition 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- 235000013605 boiled eggs Nutrition 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 229960005069 calcium Drugs 0.000 description 1
- 235000010410 calcium alginate Nutrition 0.000 description 1
- 239000000648 calcium alginate Substances 0.000 description 1
- 229960002681 calcium alginate Drugs 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- 108010033929 calcium caseinate Proteins 0.000 description 1
- 229960004256 calcium citrate Drugs 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000005341 metaphosphate group Chemical group 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000002683 reaction inhibitor Substances 0.000 description 1
- 235000019515 salmon Nutrition 0.000 description 1
- 235000014102 seafood Nutrition 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Jellies, Jams, And Syrups (AREA)
Description
【発明の詳細な説明】 〔発明の背景〕 技術分野 本発明は、一般に使用される熱可逆性ゲル化剤、すなわ
ち寒天、ゼラチン、ペクチン、カラーギナン、ファーセ
ルラン、タマリンド種子多糖類(以下熱可逆ゲル化剤と
記載する)に、アルギン酸、アルカリ剤およびカルシウ
ム塩をゲル化抑制剤と併用混合し、耐熱性ゲルを製造す
るのであり、本発明の方法によって得た耐熱性ゲルは加
熱によって形くずれせず、十分加熱殺菌に耐え、しかも
熱可逆性ゲル本来の食感、透明感等を維持することがで
き、保存期間の長いゲル食品やゼリー入りパウンドゲー
キ等新しいゲル状食品を提供するものである。Description: BACKGROUND OF THE INVENTION Technical Field The present invention relates to commonly used thermoreversible gelling agents, namely agar, gelatin, pectin, carrageenan, furcellulan, tamarind seed polysaccharide (hereinafter thermoreversible). Alginic acid, an alkaline agent and a calcium salt are mixed together with a gelation inhibitor to produce a heat resistant gel, and the heat resistant gel obtained by the method of the present invention is deformed by heating. Without providing sufficient heat sterilization, it is possible to maintain the original texture, transparency, etc. of the thermoreversible gel, and to provide a new gel-like food such as a gel food with a long shelf life and a pound jake containing jelly. .
先行技術 アルギン酸アルカリ金属塩とカルシウムとの反応により
生成するアルギン酸カルシウムゲル(以下、アルギンゲ
ルと略記する)は熱不可逆性であり、熱に強いためこの
性質を熱に弱い熱可逆性ゲル化剤に付与する試みとし
て、たとえば寒天等にアルギン酸アルカリ金属塩を併用
する方法が提案されている(特公昭44-780、特公昭49-3
5150、特開昭60-110252、特開昭60-192556)。Prior art Calcium alginate gel (hereinafter abbreviated as algin gel) produced by the reaction between alkali metal alginate and calcium is thermo-irreversible and is resistant to heat, so this property is imparted to a thermo-reversible gelling agent that is weak to heat. As an attempt to do so, for example, a method of using agar together with an alkali metal alginate has been proposed (Japanese Patent Publication No. 44-780, Japanese Patent Publication No. 49-3).
5150, JP-A-60-110252, JP-A-60-192556).
これらの方法は、寒天等にアルギン酸ナトリウムを配合
したものを加熱溶解し、冷却して作製したゲルを、適当
な形状にカットした後、カルシウム塩溶液に浸漬する
か、又は加熱溶解の状態でノズルからカルシウム塩溶液
中に押し出す方法のいずれかである。These methods involve heating and dissolving a mixture of agar and sodium alginate, cooling the gel, cutting it into an appropriate shape, and then immersing it in a calcium salt solution, or by heating and dissolving it with a nozzle. From the calcium salt solution.
これらの方法によっても耐熱性は改善されるが、これら
公知の方法には以下の問題点がある。Although heat resistance is also improved by these methods, these known methods have the following problems.
1)アルギン酸ナトリウムとカルシウムとの反応がゲルの
表面から進行するので、表面と内部が不均一となり、ゲ
ルの堅さに差異が出る。また、反応の進展によりゲルの
収縮、変形が起る。1) Since the reaction between sodium alginate and calcium proceeds from the surface of the gel, the surface and the inside become non-uniform and the hardness of the gel becomes different. In addition, the gel contracts and deforms as the reaction progresses.
2)カルシウムイオンのゲル内部浸透に時間を要するた
め、大形ゲルでは適用し難い。2) Since it takes time for the calcium ions to penetrate into the gel, it is difficult to apply it to large gels.
3)ゲル形成とカルシウム反応との2つの工程が必要であ
る。3) Two steps, gel formation and calcium reaction, are required.
4)たとえば、みつまめ寒天の場合、シロップ中にカルシ
ウムの塩を共存させてゲルの安定化を図ることもある
が、カルシウム塩によるシブ味が問題となる。4) For example, in the case of Mitsume agar, the calcium salt may coexist in the syrup to stabilize the gel, but the shibu taste due to the calcium salt poses a problem.
又、アルギン酸ナトリウムとカゼインカルシウムとの反
応により、耐熱性ゲルを作製する方法(特公昭58-5660
8、特公昭60-29461、特開昭61-1358、特開昭61-19457)
も提案されるが、製造されたゲルは透明感がなく、透明
なゲルを求める場合に適した方法ではない。Further, a method for producing a heat-resistant gel by reacting sodium alginate and calcium caseinate (Japanese Patent Publication No. 58-5660).
8, JP-B-60-29461, JP-A-61-1358, JP-A-61-19457)
However, the produced gel does not have transparency and is not a suitable method for obtaining a transparent gel.
要旨 本発明は上記の問題点を解決することを目的とし、熱可
逆性ゲル化剤と熱不可逆性のアルギンゲルとの相乗効果
について種々検討の結果、反応抑制剤の併用によって冷
水中ではアルギンゲルの生成が極めておそく、加温し、
冷却することによって反応が促進して均一な耐熱性ゲル
が形成されることを見出し、本発明を完成するに至っ
た。SUMMARY OF THE INVENTION The present invention aims to solve the above problems, and as a result of various studies on the synergistic effect of a thermoreversible gelling agent and a thermo-irreversible algin gel, the formation of algin gel in cold water by the combined use of a reaction inhibitor. Is extremely slow, warms,
It was found that the reaction is accelerated by cooling to form a uniform heat resistant gel, and the present invention has been completed.
即ち、本発明は、寒天、ゼラチン、ペクチン、カラーギ
ナン、ファーセルラン、タマリンド種子多糖類等の熱可
逆性ゲル化剤の粉体の1種、又は2種以上の混合物に、
アルギン酸、アルカリ剤、カルシウム塩及びゲル化抑制
剤、更に必要に応じて分散剤を混合したものを水中に分
散後加温し、冷却することを特徴とする耐熱性ゲルの製
造法である。That is, the present invention provides one type of a powder of a thermoreversible gelling agent such as agar, gelatin, pectin, color ginnan, furcellan, tamarind seed polysaccharide, or a mixture of two or more types,
A method for producing a heat-resistant gel, which comprises heating a mixture of alginic acid, an alkali agent, a calcium salt, a gelation inhibitor, and optionally a dispersant, which is dispersed in water, followed by heating and cooling.
本発明によるゲルの製造は、一般に使用されている熱可
逆性ゲル化剤と全く同様な方法で、水中に分散後加温
し、冷却するだけてよく、形成されたゲルは耐熱性に富
み、透明感も良好で、ゲルの収縮、変形もなく、すぐれ
た耐熱性ゲルである。The preparation of the gel according to the present invention may be carried out in the same manner as a commonly used thermoreversible gelling agent, by dispersing in water, then heating and cooling, and the gel formed is highly heat resistant, It is a heat-resistant gel with excellent transparency and no shrinkage or deformation of the gel.
耐熱性ゲル化製剤の組成 1)熱可逆性ゲル化剤に添加するアルギン酸の添加量は熱
可逆性ゲル化剤の種類と目的とする耐熱性ゲルの性状に
よって相違するが、ゼラチンに対しては5.0〜20.0重量
%、寒天、カラーギナン、タマリンド等に対しては10.0
〜50.0重量%、ペクチンに対しては70.0〜120.0重量%
が好ましい範囲である。Composition of heat-resistant gelling agent 1) The amount of alginic acid added to the thermoreversible gelling agent varies depending on the type of thermoreversible gelling agent and the properties of the desired heat-resistant gel. 5.0-20.0% by weight, 10.0 for agar, color ginnan, tamarind, etc.
~ 50.0% by weight, 70.0-120.0% by weight for pectin
Is a preferable range.
2)アルカリ剤としては炭酸水素ナトリウム又はカリウ
ム、炭酸ナトリウム又はカリウム、水酸化ナトリウム又
はカリウム、第2リン酸ナトリウム又はカリウム、第3
リン酸ナトリウム又はカリウム、ピロリン酸ナトリウム
又はカリウム、ポリリン酸ナトリウム又はカリウム、ク
エン酸ナトリウム又はカリウム、コハク酸二ナトリウム
又はカリウム、酒石酸ナトリウム又はカリウム、リンゴ
酸ナトリウム又はカリウム、酢酸ナトリウム又はカリウ
ム等の1種以上が使用できる。添加量はアルギン酸の0.
2〜5当量に相当する量、好ましくはゲル化製剤の熱溶
解後の液pHを5〜8とする量が良い。pHがこれより低い
とゲルが不均質となりやすく、透明性も損なわれる。逆
に高いと耐熱性が不充分であったり、味覚が変化したり
する。2) As the alkaline agent, sodium or potassium hydrogen carbonate, sodium or potassium carbonate, sodium or potassium hydroxide, dibasic sodium or potassium phosphate, third
One of sodium or potassium phosphate, sodium or potassium pyrophosphate, sodium or potassium polyphosphate, sodium or potassium citrate, disodium or potassium succinate, sodium or potassium tartrate, sodium or potassium malate, sodium or potassium acetate, etc. The above can be used. The addition amount is 0. of alginic acid.
An amount corresponding to 2 to 5 equivalents, preferably an amount such that the pH of the solution after heat dissolution of the gelled preparation is 5 to 8 is good. If the pH is lower than this, the gel tends to be inhomogeneous and the transparency is impaired. On the other hand, if it is too high, the heat resistance will be insufficient or the taste will change.
3)カルシウム塩としては水に難溶性のクエン酸カルシウ
ム、第二燐酸カルシウム、炭酸カルシウム、第三燐酸カ
ルシウムなどが使用できるが、最も大切なのはアルギン
酸に対するカルシウムの比率で、カルシウムとしてアル
ギン酸の0.3〜1.2当量に相当する量、好ましくは0.5〜
1.0当量に相当する量がよい。カルシウムの添加量が0.3
当量以下ではゲルの耐熱性が不充分であるばかりでな
く、ゲルに糊状感が残り、1.2当量以上では未反応のカ
ルシウム塩が混在して不透明ゲルとなり、味覚も変化す
る。3) As the calcium salt, it is possible to use poorly water-soluble calcium citrate, dibasic calcium phosphate, calcium carbonate, tricalcium phosphate, etc., but the most important is the ratio of calcium to alginic acid, which is 0.3 to 1.2 of alginic acid as calcium. Equivalent amount, preferably 0.5-
An amount equivalent to 1.0 equivalent is preferable. The amount of calcium added is 0.3
If the amount is less than the equivalent, not only the heat resistance of the gel is insufficient, but also a pasty feeling remains on the gel, and if it is more than 1.2 equivalent, unreacted calcium salts are mixed to form an opaque gel, and the taste also changes.
4)中和されたアルギン酸とカルシウムとを均一に反応さ
せるためのゲル化抑制剤としてはピロリン酸、トリポリ
リン酸、メタリン酸等の重合燐酸のナトリウム又はカリ
ウム塩、EDTA.,炭酸ナトリウム、クエン酸ナトリウムな
どが使用できる。これらの中でも重合燐酸塩、とくにメ
タリン酸塩が有効である。配合量はカルシウムに対して
1〜10倍量好ましくは3〜7倍量である。1倍量以下で
はアルギンゲルの生成が不均一となり、10倍以上ではア
ルギンゲルが形成困難となる。4) As gelation inhibitors for uniformly reacting neutralized alginic acid and calcium, pyrophosphoric acid, tripolyphosphoric acid, sodium or potassium salts of polymerized phosphoric acid such as metaphosphoric acid, EDTA., Sodium carbonate, sodium citrate. Etc. can be used. Of these, polymerized phosphates, especially metaphosphates are effective. The blending amount is 1 to 10 times, preferably 3 to 7 times the amount of calcium. If the amount is less than 1 time, the formation of algin gel becomes non-uniform, and if the amount is more than 10 times, the formation of algin gel becomes difficult.
5)必要に応じて添加される分散剤は耐熱性ゲル化剤の水
中への分散を促進するために添加するもので、グラニュ
ー糖、ブドー糖、果糖などが使用されるが、量、種類と
もとくに制限されるものではない。5) The dispersant that is added as needed is added to accelerate the dispersion of the heat-resistant gelling agent in water.Granulated sugar, budo sugar, fructose, etc. are used, but the amount and type are both It is not particularly limited.
耐熱性ゲルの生成 本発明による耐熱性ゲルは適切に配合された耐熱性ゲル
化製剤を水中に分散させた後加温し冷却することによっ
て形成される。Generation of Heat-Resistant Gel The heat-resistant gel according to the present invention is formed by dispersing an appropriately blended heat-resistant gel preparation in water, followed by heating and cooling.
ゲル化製剤を水中に分散した段階でアルギン酸はアルカ
リ剤により、アルギン酸アルカリ金属塩となり溶解す
る。When the gelled preparation is dispersed in water, alginic acid becomes an alkali metal salt of alginic acid with an alkaline agent and dissolves.
加温温度はアルギン酸の含有量および、カルシウム含有
比率により、又主剤である熱可逆性ゲル化剤の種類によ
っても相違するが、一般的に用いられているゼラチンの
溶解温度すなわち60℃以上が必要である。加温すること
によって熱可逆性ゲル化剤とアルギン酸アルカリ金属塩
が均一に混合し、次で冷却することによって徐々にカル
シウムと反応してアルギンゲルが形成されるのである
が、包含するカルシウム塩が炭酸カルシウムのような極
めて難容性塩の場合は冷却直前にクエン酸、酒石酸等に
よりpHを4.0〜6.0に調整することが望ましい。The heating temperature differs depending on the content of alginic acid, the calcium content ratio, and the type of thermoreversible gelling agent, which is the main ingredient, but the melting temperature of commonly used gelatin, that is, 60 ° C or higher is required. Is. By heating, the thermoreversible gelling agent and the alkali metal alginate are uniformly mixed, and then by cooling, they gradually react with calcium to form an algin gel. In the case of an extremely refractory salt such as calcium, it is desirable to adjust the pH to 4.0 to 6.0 with citric acid, tartaric acid or the like immediately before cooling.
冷却したゲルは充分反応を進行させるため少なくとも6
0分、好ましくは90分以上室温に放置することによっ
て耐熱性を付加したゲルが得られる。The cooled gel should be at least 6% to allow the reaction to proceed sufficiently.
By leaving it at room temperature for 0 minutes, preferably 90 minutes or more, a gel having heat resistance is obtained.
発明の効果 耐熱性ゲルの適性用途として、加熱殺菌により賞味期間
の延長できるゲル状食品があげられる。EFFECTS OF THE INVENTION Suitable applications of heat-resistant gels include gel foods that can be extended in shelf life by heat sterilization.
また、細菌抑制の方法としては防腐剤の添加、塩分、糖
分等による水分活性の調整などもあるが、消費者の健康
意識からみて好ましい方法と言えず、食品の種類でも制
約されるので加熱による殺菌処理が最も安全かつ確実と
みなされている。In addition, as a method for controlling bacteria, there are addition of antiseptics, adjustment of water activity by salt content, sugar content, etc., but it is not a preferable method from the viewpoint of consumers' health consciousness, and it is limited by the type of food, so heating Sterilization is considered the safest and most reliable.
ところが一般に使用されている熱可逆性ゲルでは、比較
的高融点である寒天でさえ80〜85℃で融解し、ゼラチン
ゲルでは20〜30℃の低温で保形困難となる。そこでみつ
まめ寒天の加熱殺菌ではせいぜい80℃程度が限界で、シ
ロップ中に酸を加えてpH調整することで菌の抑制が考慮
されているが加熱温度の調節を失敗すると形くずれによ
る不良品の発生となる。However, in the commonly used thermoreversible gel, even agar, which has a relatively high melting point, melts at 80 to 85 ° C, and gelatin gel becomes difficult to retain its shape at a low temperature of 20 to 30 ° C. Therefore, heat sterilization of Mitsumame agar is limited to about 80 ° C at most, and it is considered that bacteria can be suppressed by adjusting the pH by adding acid to the syrup. It will occur.
また、魚介類をゼリーで囲んだ「にこごり」食品、卵、
ハム、サーモンなどを具材とした「アスピック」(洋風
にこごり)等にゼラチンが使用されるが、これらは加温
によりゼラチンゲルが融解し、具材が移動して「にこご
り」あるいは「アスピック」本来の美観を損ない商品価
値を消失する。すなわち、現在市場にあるこの種ゼリー
食品は加熱殺菌処理を経ず、日配商品として販売される
ため賞味期間は非常に短い。Also, "Nikogori" foods, eggs, which are seafood surrounded by jelly,
Gelatin is used in "Aspic" (Western-style nigorigo) made from ham, salmon, etc., but the gelatin gel is melted by heating and the ingredients move to cause "nicotine" or "aspic". The original aesthetics are lost and the commercial value is lost. That is, since this type of jelly food currently on the market is not heat-sterilized and is sold as a daily product, the shelf life is very short.
しかし、本発明の方法において、寒天製剤によって作製
したゲルは、95℃30分の加熱殺菌に耐え、ゲルの均質
度、食感に優れ、収縮、変形もなく、シロップに添酸不
要のみつまめ寒天、杏仁豆腐などが製造できる。However, in the method of the present invention, the gel produced by the agar formulation withstands heat sterilization at 95 ° C. for 30 minutes, the homogeneity of the gel, the texture is excellent, there is no shrinkage or deformation, and the syrup does not require any additional acid. , Apricot tofu, etc. can be manufactured.
また、本発明において、ゼラチン製剤を使用すれば、レ
トルト条件である120℃20分間の加熱殺菌処理を経て
も、具材の移動はなく、透明感に優れた「にこごり」、
「アスピック」などの食品が製造できる。Further, in the present invention, if a gelatin preparation is used, even after heat sterilization treatment at 120 ° C. for 20 minutes, which is a retort condition, there is no migration of ingredients, and “nikogori” excellent in transparency,
Food such as "Aspic" can be manufactured.
さらに、本発明において、ペクチン製剤の利用により、
ゼリーのだれ、変形のないゼリー入りパウンドケーキ、
フルーツケーキなどが製造できる。Further, in the present invention, the use of a pectin formulation,
Jelly pound cake with no deformation,
Can produce fruit cakes.
以上の応用例の外、本発明の方法によれば、広い領域で
ゲルに耐熱性を付加できるので、熱可逆性ゲル化剤の利
用範囲が拡大する。In addition to the above application examples, according to the method of the present invention, heat resistance can be added to the gel in a wide range, so that the application range of the thermoreversible gelling agent is expanded.
次に本発明の実施例を示すが、ここにおける部は重量部
を示している。Next, examples of the present invention will be shown, where parts are parts by weight.
実施例1 寒天33部、アルギン酸14部、炭酸水素ナトリウム7部、
クエン酸カルシウム5部、メタリン酸ナトリウム5部、
グラニュー糖36部を混合したゲル化製剤3部を冷水中に
分散する。次で98℃40分間加温溶解後パット中に流し込
み、12時間室温に放置してゲルを形成させ、1cm角に裁
断する。Example 1 33 parts of agar, 14 parts of alginic acid, 7 parts of sodium hydrogen carbonate,
5 parts calcium citrate, 5 parts sodium metaphosphate,
3 parts of a gelled preparation in which 36 parts of granulated sugar are mixed is dispersed in cold water. Next, after melting by heating at 98 ° C for 40 minutes, it is poured into a pad, left to stand at room temperature for 12 hours to form a gel, and cut into 1 cm squares.
別に上白糖64部、水36部を85℃30分加熱してシロップを
つくる。Separately, heat 64 parts of white sucrose and 36 parts of water at 85 ° C for 30 minutes to make a syrup.
裁断した耐熱性角寒天220部とシロップ140部を耐熱性ナ
イロンポリ袋につめ、密封後90℃30分間加熱殺菌し、次
で冷水中で冷却した。ゲルの形状は加熱によって全く変
化なく、食感は極めて良好であった。220 parts of cut heat-resistant kaku agar and 140 parts of syrup were packed in a heat-resistant nylon polybag, sealed, heat-sterilized at 90 ° C for 30 minutes, and then cooled in cold water. The shape of the gel did not change at all by heating, and the texture was extremely good.
実施例2 ゼラチン79部、アルギン酸10部、第二リン酸ナトリウム
6部、炭酸カルシウム2部、メタリン酸ナトリウム3部
を混合したゲル化製剤4部を濃縮調味液2部、食塩0.2
部、カラメル1部とともに水92.8部に分散させ、80℃5
分間加熱溶解し、10%クエン酸溶液小量を加えて、pH5.
0〜6.0に調整する。この溶液を内径10cm、高さ3cmのポ
リプロピレン容器に流し込み、固まらない内に具材とし
て半割うずらのゆで卵とえびを飾り並べ、シールして密
閉する。冷蔵庫中にて60分間冷却してゲル化させたもの
を90℃40分間加熱殺菌した後冷水中で冷却した。Example 2 4 parts of a gelled preparation prepared by mixing 79 parts of gelatin, 10 parts of alginic acid, 6 parts of dibasic sodium phosphate, 2 parts of calcium carbonate and 3 parts of sodium metaphosphate with 2 parts of concentrated seasoning solution and 0.2 parts of salt.
And 9 parts of water together with 1 part of caramel and 80 ℃ 5
Dissolve by heating for 1 minute, add a small amount of 10% citric acid solution, and adjust to pH 5.
Adjust from 0 to 6.0. This solution is poured into a polypropylene container having an inner diameter of 10 cm and a height of 3 cm, and half-boiled quail boiled eggs and shrimp are placed as ingredients in a container that does not solidify, and then sealed and sealed. The gel that was cooled in the refrigerator for 60 minutes and gelled was sterilized by heating at 90 ° C. for 40 minutes and then cooled in cold water.
加熱殺菌による具材の移動は全くなく、透明感に優れ、
ゼラチン本来の食感を維持したアスピックを得た。本品
を25℃3週間保存した結果、細菌数0であった。There is no movement of ingredients due to heat sterilization, excellent transparency,
An aspic having the original texture of gelatin was obtained. As a result of storing this product at 25 ° C. for 3 weeks, the number of bacteria was 0.
実施例3 H.M.ペクチン9部、アルギン酸9部、クエン酸ナトリウ
ム10部、炭酸カルシウム1部、メタリン酸ナトリウム1
部、上白糖70部を混合したゲル化製剤10部を70部の冷水
中に分散させ、30秒間加熱煮沸する。さらに上白糖100
部を加え加熱して溶解させた後、10%クエン酸溶液5部
を添加したものをパットに流し込み冷却させる。2時間
放置して生成したゲルを1cm角に裁断して角型ゼリーを
作る。Example 3 HM pectin 9 parts, alginic acid 9 parts, sodium citrate 10 parts, calcium carbonate 1 part, sodium metaphosphate 1
10 parts of a gelled preparation obtained by mixing 70 parts of sucrose and 70 parts of white sucrose is dispersed in 70 parts of cold water and heated and boiled for 30 seconds. Furthermore, white sugar 100
After adding 5 parts by weight of the solution to dissolve it, 5 parts of a 10% citric acid solution was added to the pad to cool it. The gel produced by leaving it for 2 hours is cut into 1 cm squares to make square jelly.
別にバター25部、グラニュー糖25部、卵25部、小麦粉25
部、ペーキングパウダー0.3部を常法により混ぜ込み、
パウンドケーキ用生地とする。この生地に角型ゼリーを
分散して封入し180℃85分間オーブンで焼成した。出来
上ったパウンドケーキの内部は、ゼリーが原形のまま保
持されゼリー入りパウンドケーキが作製できた。Separately, butter 25 parts, granulated sugar 25 parts, egg 25 parts, flour 25
Part, 0.3 parts of paking powder are mixed by a conventional method,
Use as dough for pound cake. Square jelly was dispersed and enclosed in this dough, and baked in an oven at 180 ° C for 85 minutes. Inside the finished pound cake, the jelly was kept in its original shape, and a pound cake containing jelly could be prepared.
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Claims (6)
ン、ファーセルラン、タマリンド種子多糖類等の熱可逆
性ゲル化剤の粉体の1種、又は2種以上の混合物にアル
ギン酸、アルカリ剤、カルシウム塩、及び、重合燐酸の
ナトリウム塩またはカリウム塩、EDTA、炭酸ナトリウ
ム、クエン酸ナトリウムなどのゲル化抑制剤の一種以上
で、カルシウム塩のカルシウム量に対して1〜10倍量
のゲル化抑制剤を、更に必要に応じて分散剤を、混合し
たものを水中に分散後、加温し、冷却することを特徴と
する耐熱性ゲルの製造法。1. An alginic acid, an alkaline agent, and a calcium salt in one or a mixture of two or more powders of a thermoreversible gelling agent such as agar, gelatin, pectin, color ginnan, furcellulan, and tamarind seed polysaccharide. , And one or more gelling inhibitors such as sodium salt or potassium salt of polymerized phosphoric acid, EDTA, sodium carbonate, sodium citrate, etc., and 1 to 10 times the gelling inhibitor with respect to the calcium amount of the calcium salt. A method for producing a heat-resistant gel, further comprising dispersing a mixture of a dispersant, if necessary, in water, heating, and cooling.
0〜120.0重量%に相当する量添加されるものである特許
請求の範囲第1項記載の耐熱性ゲルの製造法。2. Alginic acid is used as a thermoreversible gelling agent.
The method for producing a heat-resistant gel according to claim 1, which is added in an amount corresponding to 0 to 120.0% by weight.
リウム、炭酸ナトリウム又はカリウム、水酸化ナトリウ
ム又はカリウム、第2リン酸ナトリウム又はカリウム、
第3リン酸ナトリウム又はカリウム、ピロリン酸ナトリ
ウム又はカリウム、ポリリン酸ナトリウム又はカリウ
ム、クエン酸ナトリウム又はカリウム、コハク酸二ナト
リウム又はカリウム、酒石酸ナトリウム又はカリウム、
リンゴ酸ナトリウム又はカリウム、酢酸ナトリウム又は
カリウムからなる群から選択された1種以上である特許
請求の範囲第1項記載の耐熱ゲルの製造法。3. The alkaline agent is sodium or potassium hydrogencarbonate, sodium or potassium carbonate, sodium or potassium hydroxide, dibasic sodium or potassium phosphate,
Tertiary sodium or potassium phosphate, sodium or potassium pyrophosphate, sodium or potassium polyphosphate, sodium or potassium citrate, disodium or potassium succinate, sodium or potassium tartrate,
The method for producing a heat-resistant gel according to claim 1, which is one or more selected from the group consisting of sodium or potassium malate and sodium or potassium acetate.
燐酸カルシウム、第三燐酸カルシウム、炭酸カルシウ
ム、硫酸カルシウムの単独又は併用で、カルシウムとし
てアルギン酸の0.3〜1.2当量に相当する量添加されるも
のである特許請求の範囲第1項記載の耐熱性ゲルの製造
法。4. The calcium salt is calcium citrate, dibasic calcium phosphate, tribasic calcium phosphate, calcium carbonate or calcium sulfate alone or in combination, which is added in an amount corresponding to 0.3 to 1.2 equivalents of alginic acid as calcium. A method for producing a heat-resistant gel according to claim 1.
酸、メタリン酸等の重合燐酸のナトリウム塩またはカリ
ウム塩の単独または併用で、カルシウム塩のカルシウム
量に対して1〜10倍量添加されるものである特許請求の
範囲第1項記載の耐熱性ゲルの製造法。5. A gelation inhibitor is added alone or in combination with a sodium salt or potassium salt of polymerized phosphoric acid such as pyrophosphoric acid, tripolyphosphoric acid, metaphosphoric acid, etc., and is added in an amount of 1 to 10 times the calcium amount of the calcium salt. The method for producing a heat-resistant gel according to claim 1, wherein the method is for producing a heat-resistant gel.
範囲第1項記載の耐熱性ゲルの製造法。6. The method for producing a heat-resistant gel according to claim 1, wherein heating is performed at 60 ° C. or higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62027074A JPH0637574B2 (en) | 1987-02-10 | 1987-02-10 | Heat resistant gel manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62027074A JPH0637574B2 (en) | 1987-02-10 | 1987-02-10 | Heat resistant gel manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63196633A JPS63196633A (en) | 1988-08-15 |
| JPH0637574B2 true JPH0637574B2 (en) | 1994-05-18 |
Family
ID=12210922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62027074A Expired - Lifetime JPH0637574B2 (en) | 1987-02-10 | 1987-02-10 | Heat resistant gel manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0637574B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014063358A1 (en) * | 2012-10-26 | 2014-05-01 | Dow Global Technologies Llc | Aqueous fragrance release gels |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185172A (en) * | 1989-07-10 | 1993-02-09 | Kfc Corporation | Method for simulating open flame broiled meat products |
| DE102004063612B4 (en) * | 2004-01-02 | 2017-01-12 | Manfred Helms | Gel-like base preparation and use of a gelling agent for its preparation |
| WO2020067548A1 (en) * | 2018-09-28 | 2020-04-02 | Spiber株式会社 | Fire-retardant protein molded body and production method for same |
| JP7084086B1 (en) * | 2022-03-25 | 2022-06-14 | 伊那食品工業株式会社 | Heat-resistant gel formulations and heat-resistant gels |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61185155A (en) * | 1985-02-14 | 1986-08-18 | Toyo Jozo Co Ltd | Composition for highly foamy food |
-
1987
- 1987-02-10 JP JP62027074A patent/JPH0637574B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014063358A1 (en) * | 2012-10-26 | 2014-05-01 | Dow Global Technologies Llc | Aqueous fragrance release gels |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63196633A (en) | 1988-08-15 |
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