JP2002253150A - Inorganic particle dispersion for noodle and method for producing the same, and mineral-enriched noodle incorporated with the dispersion - Google Patents
Inorganic particle dispersion for noodle and method for producing the same, and mineral-enriched noodle incorporated with the dispersionInfo
- Publication number
- JP2002253150A JP2002253150A JP2001053731A JP2001053731A JP2002253150A JP 2002253150 A JP2002253150 A JP 2002253150A JP 2001053731 A JP2001053731 A JP 2001053731A JP 2001053731 A JP2001053731 A JP 2001053731A JP 2002253150 A JP2002253150 A JP 2002253150A
- Authority
- JP
- Japan
- Prior art keywords
- noodles
- inorganic particle
- particle dispersion
- dispersion
- calcium carbonate
- 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.)
- Withdrawn
Links
- 235000012149 noodles Nutrition 0.000 title claims abstract description 112
- 239000010954 inorganic particle Substances 0.000 title claims abstract description 96
- 239000006185 dispersion Substances 0.000 title claims abstract description 93
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims abstract description 10
- 239000011707 mineral Substances 0.000 title claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 239000002245 particle Substances 0.000 claims abstract description 55
- 239000007900 aqueous suspension Substances 0.000 claims abstract description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
- 150000002681 magnesium compounds Chemical class 0.000 claims abstract description 7
- 229940043430 calcium compound Drugs 0.000 claims abstract description 6
- 150000001674 calcium compounds Chemical class 0.000 claims abstract description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 158
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 79
- 238000000034 method Methods 0.000 claims description 45
- 239000001506 calcium phosphate Substances 0.000 claims description 22
- 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 claims description 22
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 18
- 229910000389 calcium phosphate Inorganic materials 0.000 claims description 16
- 235000011010 calcium phosphates Nutrition 0.000 claims description 16
- 238000009826 distribution Methods 0.000 claims description 16
- 239000001095 magnesium carbonate Substances 0.000 claims description 15
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 15
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 claims description 13
- 239000003381 stabilizer Substances 0.000 claims description 13
- 239000000839 emulsion Substances 0.000 claims description 12
- 229910019142 PO4 Inorganic materials 0.000 claims description 11
- 239000010452 phosphate Substances 0.000 claims description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 11
- 239000004137 magnesium phosphate Substances 0.000 claims description 8
- 229910000157 magnesium phosphate Inorganic materials 0.000 claims description 8
- 229960002261 magnesium phosphate Drugs 0.000 claims description 8
- 235000010994 magnesium phosphates Nutrition 0.000 claims description 8
- 235000010216 calcium carbonate Nutrition 0.000 claims description 3
- 235000014380 magnesium carbonate Nutrition 0.000 claims description 3
- 230000001804 emulsifying effect Effects 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 58
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 24
- 239000007789 gas Substances 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000001569 carbon dioxide Substances 0.000 description 16
- 229910002092 carbon dioxide Inorganic materials 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 16
- 235000008446 instant noodles Nutrition 0.000 description 16
- 230000000704 physical effect Effects 0.000 description 16
- 239000000725 suspension Substances 0.000 description 15
- 235000013312 flour Nutrition 0.000 description 14
- 239000007787 solid Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- 238000001179 sorption measurement Methods 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 11
- 241000519695 Ilex integra Species 0.000 description 11
- 235000011941 Tilia x europaea Nutrition 0.000 description 11
- 239000004571 lime Substances 0.000 description 11
- 235000013336 milk Nutrition 0.000 description 11
- 239000008267 milk Substances 0.000 description 11
- 210000004080 milk Anatomy 0.000 description 11
- 239000002994 raw material Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 10
- 238000010298 pulverizing process Methods 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 9
- -1 sodium phosphate Chemical compound 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 238000009835 boiling Methods 0.000 description 8
- 238000007796 conventional method Methods 0.000 description 8
- 230000018044 dehydration Effects 0.000 description 8
- 238000006297 dehydration reaction Methods 0.000 description 8
- 230000001953 sensory effect Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 229920002472 Starch Polymers 0.000 description 7
- 230000005484 gravity Effects 0.000 description 7
- 235000010755 mineral Nutrition 0.000 description 7
- 229920001592 potato starch Polymers 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 235000019698 starch Nutrition 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 229920000591 gum Polymers 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 239000008107 starch Substances 0.000 description 6
- 229940078499 tricalcium phosphate Drugs 0.000 description 6
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 6
- 235000019731 tricalcium phosphate Nutrition 0.000 description 6
- 238000001238 wet grinding Methods 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229910000400 magnesium phosphate tribasic Inorganic materials 0.000 description 5
- 238000004438 BET method Methods 0.000 description 4
- 240000008620 Fagopyrum esculentum Species 0.000 description 4
- 235000009419 Fagopyrum esculentum Nutrition 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 235000015927 pasta Nutrition 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 229920001615 Tragacanth Polymers 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000000305 astragalus gummifer gum Substances 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 239000008120 corn starch Substances 0.000 description 2
- MHJAJDCZWVHCPF-UHFFFAOYSA-L dimagnesium phosphate Chemical compound [Mg+2].OP([O-])([O-])=O MHJAJDCZWVHCPF-UHFFFAOYSA-L 0.000 description 2
- 229910000395 dimagnesium phosphate Inorganic materials 0.000 description 2
- 235000011180 diphosphates Nutrition 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 2
- HDFXRQJQZBPDLF-UHFFFAOYSA-L disodium hydrogen carbonate Chemical compound [Na+].[Na+].OC([O-])=O.OC([O-])=O HDFXRQJQZBPDLF-UHFFFAOYSA-L 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 235000013373 food additive Nutrition 0.000 description 2
- 239000002778 food additive Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000002085 persistent effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000015067 sauces Nutrition 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000014347 soups Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- 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 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- SATHPVQTSSUFFW-UHFFFAOYSA-N 4-[6-[(3,5-dihydroxy-4-methoxyoxan-2-yl)oxymethyl]-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy-2-(hydroxymethyl)-6-methyloxane-3,5-diol Chemical compound OC1C(OC)C(O)COC1OCC1C(O)C(OC)C(O)C(OC2C(C(CO)OC(C)C2O)O)O1 SATHPVQTSSUFFW-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000001904 Arabinogalactan Substances 0.000 description 1
- 229920000189 Arabinogalactan Polymers 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000001879 Curdlan Substances 0.000 description 1
- 229920002558 Curdlan Polymers 0.000 description 1
- 229920002148 Gellan gum Polymers 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- HDSBZMRLPLPFLQ-UHFFFAOYSA-N Propylene glycol alginate Chemical compound OC1C(O)C(OC)OC(C(O)=O)C1OC1C(O)C(O)C(C)C(C(=O)OCC(C)O)O1 HDSBZMRLPLPFLQ-UHFFFAOYSA-N 0.000 description 1
- 241000934878 Sterculia Species 0.000 description 1
- 240000004584 Tamarindus indica Species 0.000 description 1
- 235000004298 Tamarindus indica Nutrition 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 235000019312 arabinogalactan Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 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
- 235000013339 cereals Nutrition 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 235000019316 curdlan Nutrition 0.000 description 1
- 229940078035 curdlan Drugs 0.000 description 1
- AZSFNUJOCKMOGB-UHFFFAOYSA-K cyclotriphosphate(3-) Chemical compound [O-]P1(=O)OP([O-])(=O)OP([O-])(=O)O1 AZSFNUJOCKMOGB-UHFFFAOYSA-K 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000001177 diphosphate Substances 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 235000010492 gellan gum Nutrition 0.000 description 1
- 239000000216 gellan gum Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
- 239000000231 karaya gum Substances 0.000 description 1
- 229940039371 karaya gum Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 150000004712 monophosphates Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000010409 propane-1,2-diol alginate Nutrition 0.000 description 1
- 239000000770 propane-1,2-diol alginate Substances 0.000 description 1
- 229940048084 pyrophosphate Drugs 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 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
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Noodles (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、麺類用無機粒子分
散体及びその製造方法、並びに該分散体を添加してなる
ミネラル強化麺類に関し、より詳しくは、特に、麺類を
茹でた後の食感、特に麺類にモチモチ感を付与並びに維
持することが可能な麺類用無機粒子分散体及びその製造
方法、並びに該分散体を添加してなるミネラル強化麺類
に関する。The present invention relates to an inorganic particle dispersion for noodles, a method for producing the same, and a mineral-enriched noodle to which the dispersion is added, and more particularly to a texture after boiling the noodles. In particular, the present invention relates to an inorganic particle dispersion for noodles capable of imparting and maintaining a moist feeling to noodles, a method for producing the same, and a mineral-enriched noodle to which the dispersion is added.
【0002】[0002]
【従来の技術】麺類は、茹で麺が一般的で、従来は、茹
でた後、弾力に富んだコシのある歯ごたえのある麺が求
められ、即席麺、中華麺、うどん、パスタ類では、やや
タンパク含有量の高い中力ないしは準強力小麦粉が主原
料として用いられ、更には澱粉などの混合により、コシ
のある食感が発現されている。しかしながら、近年、消
費者の嗜好性の変化・多様化により、日本人の主食であ
る米飯食と同様の食感、即ち、モチモチ感が各種食品に
おいて支持される傾向が出てきている。従って、モチモ
チ感を発現するために、小麦粉にタカピオ加工澱粉を加
えて調整した麺等が作製されているが、茹でた状態で放
置しておくと短時間で食感が柔らかくなりすぎる等の茹
で伸び現象が発生し易く、満足する物性の麺を得ること
が困難である。また、釜揚げうどん等を食する際には、
長期間茹で汁などの湯またはタレなどの麺つゆに漬けら
れるために、麺が柔らかくなり食感が低下し易いという
欠点がある。2. Description of the Related Art Noodles are generally boiled noodles. Conventionally, boiled noodles with a firm and chewy texture are required after boiled. Instant noodles, Chinese noodles, udon, pasta, etc. Medium- or medium-strength wheat flour having a high protein content is used as a main raw material, and further, by mixing with starch and the like, a firm texture is exhibited. However, in recent years, due to changes and diversification of consumer preferences, various foods tend to support a texture similar to that of cooked rice, which is a Japanese staple food, that is, a mochi feeling. Therefore, noodles and the like prepared by adding Takapio-processed starch to flour have been produced in order to express the mochi feeling, but if left in a boiled state, the texture will become too soft in a short time and so on. The elongation phenomenon easily occurs, and it is difficult to obtain noodles having satisfactory physical properties. Also, when eating kamaage udon etc.
Since it is soaked in hot water such as boiling juice or noodle soup such as sauce for a long period of time, there is a drawback that the noodles are softened and the texture is easily deteriorated.
【0003】更に、近年、家庭や外食産業のレストラン
等で電子レンジや熱湯等により加熱するだけで、或い
は、加熱の前後で別添ソースやスープと合わせるだけで
簡単に食することの出来るレトルト食品や即席麺が広く
普及しているが、中でも茹でスパゲティがその製造時に
レトルト殺菌により柔らかくなり過ぎたりする傾向があ
り、即席麺においても作成後、短時間のうちに上記と同
様の現象が確認されることが多い。Further, in recent years, retort foods that can be easily eaten simply by heating in a microwave oven or hot water in a home or restaurant of the restaurant industry, or by combining with an additional sauce or soup before and after heating. And instant noodles are widespread, but among them, boiled spaghetti tends to be too soft due to retort sterilization during its manufacture, and the same phenomenon as above is confirmed in a short time after making instant noodles. Often.
【0004】従って、茹で麺の食感を改良するために各
種の検討が行われているが、従来の方法では、茹で上げ
や蒸し上げ等の熱処理後に優れた食感を維持した麺を製
造することは容易なことではなく、モチモチ感のある食
感の付与並びに維持した麺類を得る方法は困難とされて
いる。Accordingly, various studies have been made to improve the texture of the boiled noodles. However, in the conventional method, noodles having an excellent texture are produced after heat treatment such as boiling or steaming. This is not easy, and it has been considered difficult to provide a chewy texture and obtain a maintained noodle.
【0005】また、従来より、麺生地を調製する際に炭
酸カルシウム等の無機粒子を配合することは行われてい
るが、その製造方法として、ドライブレンド、即ち、小
麦粉等の諸原料と無機粒子の乾粉とを混合する方法が採
られている。しかしながら、無機の微粉粒子は、乾燥時
にその凝集性が極めて強くなるため、ドライブレンドで
はシェアが掛かり難く、そのため生地中に十分に均一分
散されているとは言い難く、その後の小麦粉等と無機粒
子粉体との混合粉体に水を加えて練る工程においても凝
集した無機粒子を完全分散させることは困難であり、そ
の結果、モチモチ感を十分に付与した麺は得られていな
い。また、無機粒子と小麦粉等の諸原料をドライブレン
ドで調製した場合、その比重が異なるため、麺中に無機
粒子を均一に配合・分散させることが難しく、カルシウ
ム等のミネラル成分を麺中に均一に配合・分散させるた
めには、強撹拌を行う等の操作も必要である。[0005] In addition, conventionally, inorganic particles such as calcium carbonate have been blended in preparing noodle dough. The method of producing the same is dry blending, that is, various raw materials such as flour and inorganic particles. And a method of mixing the same with a dry powder. However, the inorganic fine powder particles have a very strong cohesiveness when dried, so it is difficult to apply a share in the dry blend, and therefore it is difficult to say that the inorganic fine particles are sufficiently uniformly dispersed in the dough. It is difficult to completely disperse the aggregated inorganic particles even in the step of adding water to the mixed powder with the powder and kneading, and as a result, noodles sufficiently imparting a moist feeling have not been obtained. In addition, when various ingredients such as inorganic particles and flour are prepared by dry blending, the specific gravities are different, so that it is difficult to uniformly mix and disperse the inorganic particles in the noodles, and to uniformly disperse mineral components such as calcium in the noodles. In order to mix and disperse the mixture into the mixture, operations such as strong stirring are required.
【0006】[0006]
【発明が解決しようとする課題】本発明の目的は、上記
の欠点を克服すべく、麺にモチモチ感を付与並びに維持
することが可能な無機粒子分散体、及びその製造方法、
並びに該分散体を含有してなる、優れた食感を有すると
同時にカルシウム、マグネシウム等のミネラルを強化し
た即席麺、中華麺類、そば・うどん類、パスタ類等の麺
類を提供することにある。DISCLOSURE OF THE INVENTION An object of the present invention is to overcome the above-mentioned drawbacks, to provide an inorganic particle dispersion capable of imparting and maintaining a moist feeling to noodles, and a method for producing the same.
Another object of the present invention is to provide instant noodles, Chinese noodles, buckwheat noodles, pasta, and other noodles containing the dispersion, which have an excellent texture and are reinforced with minerals such as calcium and magnesium.
【0007】[0007]
【課題を解決するための手段】本発明者らは、上記実状
に鑑み、麺類にモチモチ感を付与並びに維持することが
可能な、即席麺、中華麺類、そば・うどん類、パスタ類
等の麺類を得るべく、鋭意検討を重ねた結果、特定の条
件を満たしたカルシウム化合物、マグネシウム化合物よ
り選ばれた少なくとも1種の無機粒子を含む水懸濁液か
らなり、特定の粒度特性を具備してなる無機粒子分散体
が、麺類にモチモチ感を付与並びに維持することが可能
であることを見出し、本発明を完成した。DISCLOSURE OF THE INVENTION In view of the above-mentioned circumstances, the present inventors have developed instant noodles such as instant noodles, Chinese noodles, buckwheat noodles, and pasta, which can impart and maintain a moist feeling to the noodles. As a result of intensive studies, a calcium suspension satisfying a specific condition and an aqueous suspension containing at least one inorganic particle selected from a magnesium compound and having a specific particle size characteristic are obtained. The present inventors have found that an inorganic particle dispersion can impart and maintain a moist feeling to noodles, and completed the present invention.
【0008】即ち、本発明の第1(請求項1)は、20
℃の水に対する溶解度が0.1(g/100g−水)以
下のカルシウム化合物及びマグネシウム化合物より選ば
れた少なくとも1種の無機粒子を含む水懸濁液からな
り、下記(a)及び(b)の要件を具備してなることを
特徴とする麺類用無機粒子分散体を内容とする。 (a)0.2≦M≦15 (b)0≦N≦3 但し 分散係数N=(d90−d1
0)/M M :マイクロトラックFRAレーザー式粒度分布計
により測定した粒子の50%平均粒子径(μm) d90:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計90%粒子径
(μm) d10:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計10%粒子径
(μm)That is, the first (claim 1) of the present invention is the following.
A water suspension containing at least one inorganic particle selected from a calcium compound and a magnesium compound having a solubility in water at 0.1 ° C. of 0.1 (g / 100 g-water) or less, the following (a) and (b): The composition comprises an inorganic particle dispersion for noodles, characterized by satisfying the following conditions. (A) 0.2 ≦ M ≦ 15 (b) 0 ≦ N ≦ 3 where the dispersion coefficient N = (d90−d1
0) / M M: 50% average particle diameter (μm) of the particles measured by a Microtrac FRA laser type particle size distribution analyzer d90: 90% total particle diameter of particles passing through a sieve measured by a Microtrac FRA laser type particle size distribution analyzer (Μm) d10: Total 10% particle diameter (μm) of particles passing through the sieve measured by a Microtrac FRA laser type particle size distribution analyzer (μm)
【0009】好ましい態様としての請求項2は、下記
(c)の要件を具備してなる請求項1記載の麺類用無機
粒子分散体である。 (c)0≦N≦2In a preferred embodiment, the inorganic particle dispersion for noodles according to the first aspect has the following requirement (c). (C) 0 ≦ N ≦ 2
【0010】好ましい態様としての請求項3は、下記
(c)及び(d)の要件を具備してなる請求項1記載の
麺類用無機粒子分散体である。 (c)0≦N≦2 (d)0.2≦M≦5Claim 3 as a preferred embodiment is the inorganic particle dispersion for noodles according to claim 1, which satisfies the following requirements (c) and (d). (C) 0 ≦ N ≦ 2 (d) 0.2 ≦ M ≦ 5
【0011】好ましい態様としての請求項4は、下記
(e)及び(f)の要件を具備してなる請求項1記載の
麺類用無機粒子分散体である。 (e)0.2≦M≦1.5 (f)0≦N≦1.5[0011] Claim 4 as a preferred embodiment is the inorganic particle dispersion for noodles according to claim 1, which satisfies the following requirements (e) and (f). (E) 0.2 ≦ M ≦ 1.5 (f) 0 ≦ N ≦ 1.5
【0012】好ましい態様としての請求項5は、無機粒
子が、炭酸カルシウム、リン酸カルシウム、炭酸マグネ
シウム、リン酸マグネシウムより選ばれた少なくとも1
種である請求項1〜4の何れか1項に記載の麺類用無機
粒子分散体である。In a preferred embodiment, the inorganic particles are at least one selected from the group consisting of calcium carbonate, calcium phosphate, magnesium carbonate and magnesium phosphate.
The inorganic particle dispersion for noodles according to any one of claims 1 to 4, which is a seed.
【0013】好ましい態様としての請求項6は、乳化安
定剤、縮合リン酸塩から選ばれた少なくとも1種を添加
してなる請求項1〜5の何れか1項に記載の麺類用無機
粒子分散体である。In a preferred embodiment, the dispersion of inorganic particles for noodles according to any one of claims 1 to 5, wherein at least one selected from an emulsion stabilizer and a condensed phosphate is added. Body.
【0014】本発明の第2(請求項7)は、20℃の水
に対する溶解度が0.1(g/100g−水)以下のカ
ルシウム化合物及びマグネシウム化合物より選ばれた少
なくとも1種の無機粒子を含む水懸濁液を粉砕及び/又
は分散させることを特徴とする請求項1〜5の何れか1
項に記載の麺類用無機粒子分散体の製造方法を内容とす
る。A second (claim 7) of the present invention is that at least one type of inorganic particles selected from calcium compounds and magnesium compounds having a solubility in water at 20 ° C. of 0.1 (g / 100 g-water) or less. The water suspension containing is pulverized and / or dispersed.
The method for producing an inorganic particle dispersion for noodles described in the section is described.
【0015】好ましい態様としての請求項8は、水懸濁
液に乳化安定剤、縮合リン酸塩から選ばれた少なくとも
1種を添加する請求項6記載の麺類用無機粒子分散体の
製造方法である。In a preferred embodiment, the method for producing an inorganic particle dispersion for noodles according to claim 6, wherein at least one selected from an emulsion stabilizer and a condensed phosphate is added to the aqueous suspension. is there.
【0016】好ましい態様としての請求項9は、水懸濁
液を湿式粉砕機、高圧乳化分散装置、超音波分散機から
選ばれた少なくとも1種を用いて粉砕及び/又は分散さ
せる請求項7又は8記載の製造方法である。In a preferred embodiment, the water suspension is pulverized and / or dispersed using at least one selected from a wet pulverizer, a high-pressure emulsifying and dispersing apparatus, and an ultrasonic disperser. 8. The method according to item 8.
【0017】本発明の第3(請求項10)は、請求項1
〜6のいずれか1項に記載の麺類用無機粒子分散体を添
加してなることを特徴とするミネラル強化麺類を内容と
する。A third (claim 10) of the present invention is claim 1
7. A mineral-enriched noodle, comprising the inorganic particle dispersion for noodles according to any one of Nos. To 6 described above.
【0018】以下、本発明を詳述する。本発明に用いる
粒子は、20℃の水に対する溶解度が0.1(g/10
0g−水)以下のカルシウム化合物及び/又はマグネシ
ウム化合物であり、具体的には、炭酸カルシウム、リン
酸カルシウム、水酸化マグネシウム、炭酸マグネシウ
ム、リン酸水素マグネシウム、リン酸マグネシウム等が
例示出来る。特に、麺類にモチモチ感を付与させるため
には、炭酸カルシウム、リン酸カルシウム、炭酸マグネ
シウム、リン酸マグネシウムがより好ましい。20℃の
水に対する溶解度が0.1(g/100g−水)より大
きい場合は、麺類の食感改善効果が十分でないばかりで
なく、風味が悪化する傾向にある。Hereinafter, the present invention will be described in detail. The particles used in the present invention have a solubility in water at 20 ° C. of 0.1 (g / 10
0 g-water) The following calcium compounds and / or magnesium compounds, and specific examples thereof include calcium carbonate, calcium phosphate, magnesium hydroxide, magnesium carbonate, magnesium hydrogen phosphate, and magnesium phosphate. In particular, calcium carbonate, calcium phosphate, magnesium carbonate, and magnesium phosphate are more preferable for giving the noodles a mochi feeling. If the solubility in water at 20 ° C. is greater than 0.1 (g / 100 g-water), the effect of improving the texture of the noodles is not sufficient, and the flavor tends to deteriorate.
【0019】本発明に用いる炭酸カルシウムは、例えば
炭酸カルシウムを50重量%以上含有するコーラル炭酸
カルシウム、重質炭酸カルシウム、合成炭酸カルシウム
が挙げられるが、水酸化カルシウムの水懸濁液である石
灰乳と炭酸ガスを反応させる炭酸ガス法に代表される化
学的合成方法により調製される合成炭酸カルシウムが、
微細な分散体を得易い点で好ましい。炭酸ガス法におい
て合成炭酸カルシウムを調製する際の好ましい方法とし
て、以下に示す方法を例示できる。The calcium carbonate used in the present invention includes, for example, coral calcium carbonate, heavy calcium carbonate and synthetic calcium carbonate containing 50% by weight or more of calcium carbonate, and lime milk which is an aqueous suspension of calcium hydroxide. And synthetic calcium carbonate prepared by a chemical synthesis method typified by a carbon dioxide method of reacting carbon dioxide,
This is preferable because a fine dispersion can be easily obtained. As a preferable method for preparing synthetic calcium carbonate in the carbon dioxide method, the following method can be exemplified.
【0020】石灰乳を炭酸ガスを用いて炭酸化反応し、
得られる炭酸カルシウムの水懸濁液の調製工程におい
て、炭酸化反応終了して調製されたpHの値がQの炭酸
カルシウムの水懸濁液を撹拌、及び/又は湿式粉砕、及
び/又は静置し、該炭酸カルシウムの水懸濁液のpHを
以下に示す式(x)及び(y)を満たすpH値Rに上昇
せしめた後、水懸濁液中に存在するアルカリ物質を除去
及び/又はアルカリ物質の単位体積当たりの濃度を低下
せしめ、炭酸カルシウムの水懸濁液のpHを、以下に示
す式(z)を満たすpH値Sに調整し、炭酸カルシウム
を調製する。 R≧8.6・・・・・・・・・・・・(x) 10(R+2) /10Q ≧125・・・・(y) 10(S+2) /10R ≦80・・・・・(z) 但し、Q,Rは同一温度条件下のpHである。また、p
H値Sは、Sが8.6未満の場合、Sは8.6として計
算。The lime milk undergoes a carbonation reaction using carbon dioxide gas,
In the step of preparing the obtained aqueous suspension of calcium carbonate, the aqueous suspension of calcium carbonate having a pH value of Q prepared after the completion of the carbonation reaction is stirred and / or wet-pulverized and / or allowed to stand. After raising the pH of the aqueous suspension of calcium carbonate to a pH value R satisfying the following formulas (x) and (y), the alkaline substance present in the aqueous suspension is removed and / or The concentration of the alkaline substance per unit volume is reduced, and the pH of the aqueous suspension of calcium carbonate is adjusted to a pH value S that satisfies the following equation (z) to prepare calcium carbonate. R ≧ 8.6 (x) 10 (R + 2) / 10 Q ≧ 125 (y) 10 (S + 2) / 10 R ≦ 80 ... (Z) where Q and R are pH values under the same temperature condition. Also, p
When the S value is less than 8.6, the S value is calculated as 8.6.
【0021】また、本発明の原料として用いる上記記載
の炭酸カルシウムの窒素吸着法(BET法)による比表
面積は、2m2 /g〜50m2 /gの範囲が好ましく、
より好ましくは、7m2 /g〜40m2 /gの範囲、更
に好ましくは、10m2 /g〜25m2 /gである。比
表面積が2m2 /g未満の場合、粒子径が大きいため、
麺類に練り込んだ際の食感がざらつく傾向にあるだけで
なく、モチモチ感も得られにくい傾向にあるため好まし
くなく、一方、50m2 /gを越える場合、粒子の凝集
力が極めて強くなるため麺類がパサパサする傾向にあ
り、極端な場合、麺類が切れる場合があり好ましくな
い。[0021] In addition, the specific surface area by the nitrogen adsorption method of calcium carbonate described above is used as a raw material (BET method) of the present invention is preferably in the range of 2m 2 / g~50m 2 / g,
More preferably, the range of 7m 2 / g~40m 2 / g, more preferably 10m 2 / g~25m 2 / g. When the specific surface area is less than 2 m 2 / g, the particle size is large.
Not only does the texture tend to be rough when kneaded into the noodles, but also it tends to be difficult to obtain a mochi feeling. On the other hand, if it exceeds 50 m 2 / g, the cohesive force of the particles becomes extremely strong. The noodles tend to dry, and in extreme cases, the noodles may be cut off, which is not preferable.
【0022】本発明に用いる燐酸カルシウムとは、燐酸
のカルシウム塩からなる無機物を指称し、燐酸カルシウ
ムとしては、燐酸カルシウムを50重量%以上含有する
天然燐酸カルシウム、牛骨、合成燐酸カルシウムが挙げ
られるが、水酸化カルシウム、炭酸カルシウム、塩化カ
ルシウム等のカルシウム塩と燐酸、燐酸ソーダ等の燐酸
塩を反応させる化学的合成方法により調製される合成燐
酸カルシウムが、微細な分散体を得易い点で好ましく、
中でも燐酸三カルシウムがより好ましい。The calcium phosphate used in the present invention refers to an inorganic substance consisting of a calcium salt of phosphoric acid. Examples of the calcium phosphate include natural calcium phosphate containing 50% by weight or more of calcium phosphate, bovine bone, and synthetic calcium phosphate. However, calcium hydroxide, calcium carbonate, synthetic calcium phosphate prepared by a chemical synthesis method of reacting a calcium salt such as calcium chloride and a phosphoric acid, a phosphate such as sodium phosphate, is preferable because a fine dispersion can be easily obtained. ,
Among them, tricalcium phosphate is more preferred.
【0023】また、本発明の原料として用いる上記記載
のリン酸カルシウムの窒素吸着法(BET法)による比
表面積は2m2 /g〜90m2 /gの範囲が好ましく、
より好ましくは、6m2 /g〜60m2 /gの範囲、更
に好ましくは、10m2 /g〜30m2 /gの範囲であ
る。比表面積が2m2 /g未満の場合、粒子の粒子径が
大きいため、麺類に練り込んだ際の食感がざらつく傾向
にあるだけでなく、モチモチ感も得られにくい傾向にあ
るため好ましくなく、一方、90m2 /gを越える場
合、粒子の凝集力が極めて強くなるため麺類がパサパサ
する傾向にあり、極端な場合、麺類が切れる場合があり
好ましくない。[0023] In addition, the specific surface area by using as a raw material of the present invention the nitrogen adsorption method of calcium phosphate described above (BET method) is preferably in the range of 2m 2 / g~90m 2 / g,
More preferably, the range of 6m 2 / g~60m 2 / g, more preferably in the range of 10m 2 / g~30m 2 / g. When the specific surface area is less than 2 m 2 / g, the particle size of the particles is large, so that not only the texture when kneaded into noodles tends to be rough, but also the mochi feeling tends to be hardly obtained, which is not preferable. On the other hand, if it exceeds 90 m 2 / g, the cohesive force of the particles becomes extremely strong, so that the noodles tend to fluff. In extreme cases, the noodles may be cut off, which is not preferable.
【0024】本発明に用いられる炭酸マグネシウムは、
例えば炭酸マグネシウムを40重量%以上含有するプロ
トドロマイト、化学的に合成させて得られる重質炭酸マ
グネシウム及び軽質炭酸マグネシウムが挙げられるが、
より細かな分散体を得易い点で、軽質炭酸マグネシウム
を用いることがより好ましい。The magnesium carbonate used in the present invention is:
For example, protodolomite containing 40% by weight or more of magnesium carbonate, heavy magnesium carbonate and light magnesium carbonate obtained by chemically synthesizing,
It is more preferable to use light magnesium carbonate because a finer dispersion can be easily obtained.
【0025】また、本発明の原料として用いる上記記載
の炭酸マグネシウムの窒素吸着法(BET法)による比
表面積は2m2 /g〜60m2 /gの範囲が好ましく、
より好ましくは、6m2 /g〜40m2 /gの範囲、更
に好ましくは、10m2 /g〜30m2 /gの範囲であ
る。比表面積が2m2 /g未満の場合、粒子の粒子径が
大きいため、麺類に練り込んだ際の食感がざらつく傾向
にあるだけでなく、モチモチ感も得られにくい傾向にあ
るため好ましくなく、一方、60m2 /gを越える場
合、粒子の凝集力が極めて強くなるため麺類がパサパサ
する傾向にあり、極端な場合、麺類が切れる場合があり
好ましくない。[0025] In addition, the specific surface area by the nitrogen adsorption method of magnesium carbonate of the described used as a raw material of the present invention (BET method) is preferably in the range of 2m 2 / g~60m 2 / g,
More preferably, the range of 6m 2 / g~40m 2 / g, more preferably in the range of 10m 2 / g~30m 2 / g. When the specific surface area is less than 2 m 2 / g, the particle size of the particles is large, so that not only the texture when kneaded into noodles tends to be rough, but also the mochi feeling tends to be hardly obtained, which is not preferable. On the other hand, if it exceeds 60 m 2 / g, the cohesive force of the particles becomes extremely strong, so that the noodles tend to fluff. In an extreme case, the noodles may be cut off, which is not preferable.
【0026】本発明に用いる燐酸マグネシウムとは、酸
化マグネシウムとリン酸溶液とを反応させて得る燐酸水
素マグネシウム塩や硫酸マグネシウムとリン酸水素二ナ
トリウムの水溶液に炭酸水素二ナトリウムを加え、弱ア
ルカリで反応させて得るリン酸三マグネシウムが例示出
来るが、より微細な分散体を得易い点で、リン酸三マグ
ネシウムを用いることがより好ましい。The magnesium phosphate used in the present invention refers to a magnesium hydrogen phosphate obtained by reacting a magnesium oxide and a phosphoric acid solution or an aqueous solution of magnesium sulfate and disodium hydrogen phosphate to which disodium hydrogen carbonate is added. Trimagnesium phosphate obtained by the reaction can be exemplified, but it is more preferable to use trimagnesium phosphate in that a finer dispersion can be easily obtained.
【0027】また、本発明の原料として用いる上記記載
のリン酸マグネシウムの窒素吸着法(BET法)による
比表面積は、2m2 /g〜90m2 /gの範囲が好まし
く、より好ましくは、6m2 /g〜60m2 /gの範
囲、更に好ましくは、10m2/g〜30m2 /gの範
囲である。比表面積が2m2 /g未満の場合、粒子の粒
子径が大きいため、麺類に練り込んだ際の食感がざらつ
く傾向にあるだけでなく、モチモチ感も得られにくい傾
向にあるため好ましくなく、一方、90m2 /gを越え
る場合、粒子の凝集力が極めて強くなるため麺類がパサ
パサする傾向にあり、極端な場合、麺類が切れる場合が
あり好ましくない。[0027] In addition, the specific surface area by the nitrogen adsorption method of magnesium phosphate (BET method) of the described used as a raw material of the present invention is preferably in the range of 2m 2 / g~90m 2 / g, more preferably, 6 m 2 / g~60m 2 / g range, more preferably in the range of 10m 2 / g~30m 2 / g. When the specific surface area is less than 2 m 2 / g, the particle size of the particles is large, so that not only the texture when kneaded into noodles tends to be rough, but also the mochi feeling tends to be hardly obtained, which is not preferable. On the other hand, if it exceeds 90 m 2 / g, the cohesive force of the particles becomes extremely strong, so that the noodles tend to fluff. In extreme cases, the noodles may be cut off, which is not preferable.
【0028】本発明の原料として用いる無機粒子の形態
に関しては、通常の方法で調製される無機粒子の水懸濁
液(水スラリー)でもよく、また該水懸濁液を常法に従
い脱水、乾燥、粉砕を経て調製される無機粒子の粉体
に、再度水を添加して得られた水懸濁液でもよいが、食
品添加物規格厳守及び衛生管理面の観点から、後者の形
態を採用するのが好ましい。The form of the inorganic particles used as a raw material of the present invention may be an aqueous suspension (water slurry) of inorganic particles prepared by a usual method, and the aqueous suspension may be dehydrated and dried according to a conventional method. An aqueous suspension obtained by adding water again to the powder of inorganic particles prepared through pulverization may be used, but from the viewpoint of strict adherence to food additive standards and hygiene management, the latter form is adopted. Is preferred.
【0029】次に、前述の無機粒子の水懸濁液を粉砕及
び/又は分散させ、無機粒子分散体を調製する。この際
に不可欠な要件として、無機粒子分散体を下記(a)及
び(b)の要件を共に具備することであり、好ましく
は、下記(a)及び(c)の要件を共に具備することが
好ましく、より好ましくは、下記(c)及び(d)の要
件を共に具備することが好ましく、最も好ましくは、下
記(e)及び(f)の要件を共に具備することが好まし
い。Next, the above-mentioned aqueous suspension of inorganic particles is pulverized and / or dispersed to prepare an inorganic particle dispersion. In this case, it is indispensable that the inorganic particle dispersion satisfies both of the following requirements (a) and (b), and preferably that it satisfies both of the following requirements (a) and (c). It is preferable, more preferably, to satisfy both of the following requirements (c) and (d), and most preferably, to satisfy both of the following requirements (e) and (f).
【0030】(a)0.2≦M≦15 (b)0≦N≦3 但し 分散係数N=(d90−d1
0)/M(A) 0.2 ≦ M ≦ 15 (b) 0 ≦ N ≦ 3 where the dispersion coefficient N = (d90−d1
0) / M
【0031】(c)0≦N≦2 (d)0.2≦M≦5(C) 0 ≦ N ≦ 2 (d) 0.2 ≦ M ≦ 5
【0032】(e)0.2≦M≦1.5 (f)0≦N≦1.5(E) 0.2 ≦ M ≦ 1.5 (f) 0 ≦ N ≦ 1.5
【0033】M :マイクロトラックFRAレーザー
式粒度分布計により測定した粒子の50%平均粒子径
(μm) d90:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計90%粒子径
(μm) d10:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計10%粒子径
(μm)M: 50% average particle diameter (μm) of the particles measured by a Microtrack FRA laser type particle size distribution analyzer d90: 90% particle diameter of the particles passing through a sieve measured by a Microtrack FRA laser type particle size distribution analyzer ( μm) d10: Total 10% particle diameter (μm) of particles passing through a sieve measured by a Microtrac FRA laser type particle size distribution analyzer (μm)
【0034】粒子の50%平均粒子径Mは0.2≦M≦
15である必要があり、好ましくは0.2≦M≦5、よ
り好ましくは0.2≦M≦1.5である。Mが0.2μ
m未満では、粒子径が小さい過ぎるため、麺類に練り込
んだ場合、麺類の粘り気が強くなり過ぎるため、しつこ
い食感となる傾向にある。一方、Mが15μmを越えた
場合、粒子径が大きい過ぎるため、麺類に練り込んだ場
合、食感がざらつく傾向にあるだけでなく、モチモチ感
も得られにくい傾向にある。The 50% average particle diameter M of the particles is 0.2 ≦ M ≦
It must be 15, preferably 0.2 ≦ M ≦ 5, more preferably 0.2 ≦ M ≦ 1.5. M is 0.2μ
If it is less than m, the particle size is too small, and when kneaded into noodles, the noodles tend to be too sticky and tend to have a persistent texture. On the other hand, when M exceeds 15 μm, the particle size is too large, so that when kneaded into noodles, not only the texture tends to be rough, but also the mochi feeling tends to be hardly obtained.
【0035】分散係数Nは0≦N≦3である必要があ
り、好ましくは、0≦N≦2、より好ましくは、0≦N
≦1.5である。Nが3を越えた場合、粒度分布がブロ
ードとなり、粗大粒子と微細粒子が共に多量に存在する
ため、麺類に配合した際に麺類の部分によりムラが発生
し食感が不均一になる。The dispersion coefficient N must be 0 ≦ N ≦ 3, preferably 0 ≦ N ≦ 2, and more preferably 0 ≦ N ≦ 3.
≦ 1.5. When N exceeds 3, the particle size distribution becomes broad, and both coarse and fine particles are present in large amounts, so that when blended into noodles, unevenness occurs in the noodles and the texture becomes uneven.
【0036】水懸濁液の粉砕及び/又は分散方法として
は特に制限されないが、例えばダイノーミル、サンドミ
ル、コボールミル等の湿式粉砕機、ナノマイザー、マイ
クロフルイタイザー、アルティマイザー、ホモゲナイザ
ー等の高圧乳化分散装置、超音波分散機等が好ましく使
用できる。The method for pulverizing and / or dispersing the aqueous suspension is not particularly limited, and examples thereof include a wet pulverizer such as a dyno mill, a sand mill, and a coball mill; An ultrasonic disperser or the like can be preferably used.
【0037】また、本発明の麺類用無機粒子分散体に分
散性や食感改良の目的で、乳化安定剤、縮合リン酸塩か
ら選ばれる1種を添加処理しても構わない。本発明で用
いられる乳化安定剤としては、(ポリ)グリセリン脂肪
酸エステル、有機酸モノグリセリド、HLBが8以上の
ショ糖脂肪酸エステル、レシチン、大豆多糖類、カロボ
キシメチルセルロース、アルギン酸ソーダ、アルギン酸
プロピレングリコールエステル、加工澱粉、グアーガ
ム、ローストビーンガム、キサンタンガム、ペクチン、
カラギーナン、ガティガム、カードラン、タマリンドシ
ードガム、カラヤガム、タラガム、ジェランガム、トラ
ガントガム、アラビアガム、アラビーノガラクタン等が
例示されるが、好ましくは、酵素分解タイプ等のレシチ
ン類、パルミチン酸、ステアリン酸等のポリグリセリン
脂肪酸エステル、HLBが8以上のショ糖脂肪酸エステ
ル、ガディガム、トラガントガムが、麺類の食感を長時
間維持する観点より好ましい。Further, for the purpose of improving dispersibility and texture, the inorganic particle dispersion for noodles of the present invention may be added with one selected from an emulsion stabilizer and a condensed phosphate. Examples of the emulsion stabilizer used in the present invention include (poly) glycerin fatty acid ester, organic acid monoglyceride, sucrose fatty acid ester having HLB of 8 or more, lecithin, soybean polysaccharide, carboxoxymethylcellulose, sodium alginate, and propylene glycol alginate. , Modified starch, guar gum, roasted bean gum, xanthan gum, pectin,
Examples include carrageenan, gati gum, curdlan, tamarind seed gum, karaya gum, cod gum, gellan gum, tragacanth gum, gum arabic, arabinogalactan, and the like. Polyglycerin fatty acid esters, sucrose fatty acid esters having an HLB of 8 or more, gaddy gum, and tragacanth gum are preferred from the viewpoint of maintaining the texture of noodles for a long time.
【0038】本発明で用いられる縮合リン酸塩として
は、リン酸一、リン酸二、リン酸三、ピロリン酸、トリ
ポリリン酸、テトラポリリン酸、ペンタポリリン酸、ト
リメタリン酸、ヘキサメタリン酸のNa、K、アンモニ
ウム等のアルカリ金属塩等が例示されるが、弾力性とモ
チモチ感のある食感を得るためには、ピロリン酸以上の
長鎖長の縮合リン酸塩を用いることが好ましい。The condensed phosphate used in the present invention includes monophosphate, diphosphate, triphosphate, pyrophosphate, tripolyphosphate, tetrapolyphosphate, pentapolyphosphate, trimetaphosphate, and Na, K of hexametaphosphate. And alkali metal salts such as ammonium, etc., and the like. In order to obtain elasticity and a chewy texture, it is preferable to use a condensed phosphate having a longer chain length than pyrophosphoric acid.
【0039】前述の乳化安定剤、縮合リン酸塩をそれぞ
れ単独で又は併用する場合の配合量としては、無機粒子
100重量部に対して、0.01〜50重量部の範囲が
好ましいが、より好ましくは、0.03〜20重量部、
更に好ましくは、0.05〜10重量部である。乳化安
定剤、縮合リン酸塩の配合量が、0.01重量部未満の
場合は、分散性、食感の改善効果が十分とは言えず、一
方、50重量部を越えた場合は、麺類が硬くなり過ぎた
り、風味が低下する傾向にあるため好ましくない。When the above-mentioned emulsion stabilizer and condensed phosphate are used alone or in combination, the mixing amount is preferably in the range of 0.01 to 50 parts by weight with respect to 100 parts by weight of the inorganic particles. Preferably, 0.03 to 20 parts by weight,
More preferably, it is 0.05 to 10 parts by weight. When the amount of the emulsion stabilizer and the condensed phosphate is less than 0.01 part by weight, the dispersibility and the effect of improving the texture cannot be said to be sufficient. On the other hand, when the amount exceeds 50 parts by weight, the noodles Is too hard or the flavor tends to decrease.
【0040】本発明の無機分散体に乳化安定剤及び/又
は縮合リン酸塩を無機粒子に添加処理する方法として
は、通常の方法で調製される無機粒子の水懸濁液に乳化
安定剤等を添加処理する方法でもよく、また該水懸濁液
を常法に従い脱水、乾燥、粉砕を経て調製される無機粒
子の粉体に、再度水を添加して得られた水懸濁液に乳化
安定剤等を添加処理する方法の何れの方法でも構わない
が、食品添加物規格厳守及び衛生管理面の観点から、後
者の形態を採用するのが好ましい。As a method for adding an emulsion stabilizer and / or a condensed phosphate to the inorganic particles of the inorganic dispersion of the present invention, an emulsion stabilizer or the like may be added to an aqueous suspension of inorganic particles prepared by a conventional method. May be added, and the aqueous suspension may be emulsified into an aqueous suspension obtained by adding water again to powder of inorganic particles prepared through dehydration, drying, and pulverization according to a conventional method. Any method of adding a stabilizer or the like may be used, but the latter form is preferably adopted from the viewpoint of strict adherence to food additive standards and hygiene management.
【0041】また、前述の方法で得られた乳化安定剤を
含む無機粒子分散体スラリーを長期間保存したり、また
輸送や貯蔵の効率化を図るために、該無機粒子分散体ス
ラリーを乾燥粉末化することにより、無機粒子分散体パ
ウダーを調製することが出来る。無機粒子分散体スラリ
ーの乾燥方法に関しては特別の制限はないが、乳化安定
剤等の変質防止の観点より極めて短時間に乾燥を行うこ
とが好ましく、スプレードライヤー、スラリードライヤ
ー等の液滴噴霧型乾燥機を用いることが望ましい。In order to preserve the inorganic particle dispersion slurry containing the emulsion stabilizer obtained by the above-mentioned method for a long period of time and to improve the efficiency of transportation and storage, the inorganic particle dispersion slurry is dried powder. Thus, an inorganic particle dispersion powder can be prepared. There is no particular limitation on the method for drying the inorganic particle dispersion slurry, but it is preferable to perform drying in a very short time from the viewpoint of preventing deterioration of the emulsion stabilizer and the like, and droplet spray drying such as a spray drier or a slurry drier. It is desirable to use a machine.
【0042】上記の如くして得られる麺類用無機粒子分
散体は、麺類に添加され、麺類のミネラルを強化すると
ともに、モチモチ感を付与又は維持することができる。The inorganic particle dispersion for noodles obtained as described above can be added to the noodles to strengthen the minerals of the noodles and to impart or maintain a sticky feeling.
【0043】麺類の原料には、通常、麺類に使用可能な
原料が全て使用出来る。即ち、原料粉として、小麦粉、
米粉、そば粉、トウモロコシ澱粉、ジャガイモ澱粉、コ
ーンスターチ、馬鈴薯澱粉、タピオカ澱粉、片栗粉等の
各種澱粉を単独又は混合して使用出来る。澱粉として
は、生澱粉、α化澱粉、エーテル化澱粉等が使用可能で
ある。As raw materials for noodles, all raw materials that can be used for noodles can generally be used. That is, as a raw material flour,
Various starches such as rice flour, buckwheat flour, corn starch, potato starch, corn starch, potato starch, tapioca starch, and potato starch can be used alone or in combination. Raw starch, pregelatinized starch, etherified starch and the like can be used as the starch.
【0044】麺類の製造方法としては、小麦粉等の諸原
料に水を加えて混練し麺生地を調製する際に、本発明の
麺類用無機粒子分散体を混合し、他は定法により麺生地
を調製すればよい。また、調整した麺生地を必要に応じ
て熟成してもよい。As a method for producing noodles, the inorganic particle dispersion for noodles of the present invention is mixed when water is added to various raw materials such as flour and kneaded to prepare the noodle dough. It may be prepared. Further, the adjusted noodle dough may be aged as needed.
【0045】麺類における麺類用無機粒子分散体の配合
量としては、麺類100重量部に対して、0.03重量
部以上3重量部以下が好ましく、より好ましくは、0.
05重量部以上2重量部以下、更に好ましくは、0.1
重量部以上1重量部以下である。配合量が0.03重量
部未満の場合は、麺類にモチモチ感を十分に発現させる
ことが困難であり、一方、3重量部を越えた場合は、麺
類の粘り気が強くなり過ぎるため、食感がしつこい食感
となる傾向にあり、好ましくない。The amount of the inorganic particle dispersion for noodles in the noodles is preferably from 0.03 to 3 parts by weight, more preferably from 0.03 to 3 parts by weight, per 100 parts by weight of the noodles.
05 parts by weight or more and 2 parts by weight or less, more preferably 0.1 part by weight or less.
It is not less than 1 part by weight and not more than 1 part by weight. When the amount is less than 0.03 parts by weight, it is difficult to sufficiently express the mochi feeling in the noodles. On the other hand, when the amount exceeds 3 parts by weight, the noodles become too sticky, so It tends to have a persistent texture, which is not preferable.
【0046】本発明の麺類用無機粒子分散体は全ての麺
類に適用され、具体的には、中華そば、ワンタン、シュ
ーマイ、春巻及びぎょうざの皮を含む麺類、中華麺、き
しめん、ひらめん、うどん、ひやむぎ、そうめん、そば
等の日本麺、マカロニ、グラタン、スパゲティ等のパス
タ類、インスタントラーメン、インスタント焼きそば等
の即席麺、更には、小麦粉の一部または全部をその他の
雑穀類で置き換えた大麦麺、米粉麺、ハトムギ麺などの
各種麺類が例示される。本発明の麺類には、必要に応じ
て、ビタミン、香料等を添加しても何ら差し支えない。The inorganic particle dispersion for noodles of the present invention can be applied to all noodles, and specifically, noodles including Chinese noodles, wonton, shomai, spring roll and gyoza rind, Chinese noodles, kishimen, hiramen, Japanese noodles such as udon, hiyamugi, somen, and soba, pasta such as macaroni, gratin, and spaghetti, instant noodles such as instant noodles and instant fried noodles, and barley in which part or all of flour is replaced with other cereals Various noodles such as noodles, rice flour noodles, barley noodles and the like are exemplified. The noodles of the present invention may be added with vitamins, flavors, and the like, if necessary.
【0047】[0047]
【実施例】以下に実施例、比較例を示し本発明をより詳
細に説明するが、本発明はこれら実施例のみに限定され
るものではない。実施例及び比較例で使用する無機粒子
粉体の製造方法を以下に示す。The present invention will be described in more detail with reference to examples and comparative examples, but the present invention is not limited to these examples. The method for producing the inorganic particle powder used in the examples and comparative examples is shown below.
【0048】炭酸カルシウム粉体I 比重1.055で温度が15℃の石灰乳10000リッ
ターに、炭酸ガス濃度27重量%の炉ガス(以下、炭酸
ガスと略記する)を25m3 /minの流速で導通し炭
酸化反応を行い、25℃におけるpHがpH9.0の炭
酸カルシウムの水懸濁液を得た。次にpH9.0の炭酸
カルシウム水懸濁液を、50℃で12時間撹拌し、炭酸
カルシウム水懸濁液の25℃におけるpHが11.7に
達した時点でフィルタープレスを用いて脱水し、炭酸カ
ルシウム固形分濃度が48重量%の脱水ケーキを得た。
次に、得られた脱水ケーキに再度水を加え撹拌し、脱水
前の炭酸カルシウム水懸濁液と同一濃度の炭酸カルシウ
ム水懸濁液を得た。該炭酸カルシウム水懸濁液のpHは
11.5であった。次に、該炭酸カルシウム水懸濁液
を、50℃で再度6時間撹拌し、炭酸カルシウム水懸濁
液の25℃におけるpHが11.3に達した時点でフィ
ルタープレスを用いて脱水し、炭酸カルシウム固形分濃
度が48重量%の脱水ケーキを得た。次に、得られた脱
水ケーキに再度水を加え撹拌し、脱水前の炭酸カルシウ
ム水懸濁液と同一濃度の炭酸カルシウム水懸濁液を得
た。該炭酸カルシウム水懸濁液のpHは11.0であっ
た。該炭酸カルシウム水懸濁液に再度炭酸ガスを導通
し、炭酸カルシウム水懸濁液のpHを7.0に低下せし
めた後、該炭酸カルシウム水懸濁液をフィルタープレス
を用い脱水し、そのプレスケーキをパドルドライヤーを
用いて乾燥し、乾式粉砕機を用いて炭酸カルシウム粉体
を得た。該炭酸カルシウムの窒素吸着法による比表面積
を、QUANTA、CHROME製表面積測定装置NO
VA2000を用いて測定した結果28m2 /gであっ
た。Calcium carbonate powder I A furnace gas having a carbon dioxide gas concentration of 27% by weight (hereinafter abbreviated as carbon dioxide gas) was supplied to 10,000 liters of lime milk having a specific gravity of 1.055 and a temperature of 15 ° C. at a flow rate of 25 m 3 / min. By conducting the reaction, a carbonation reaction was carried out to obtain an aqueous suspension of calcium carbonate having a pH of 9.0 at 25 ° C. Next, an aqueous calcium carbonate suspension having a pH of 9.0 was stirred at 50 ° C. for 12 hours. When the pH of the aqueous calcium carbonate suspension at 25 ° C. reached 11.7, dehydration was performed using a filter press. A dehydrated cake having a calcium carbonate solid content of 48% by weight was obtained.
Next, water was added again to the obtained dehydrated cake and stirred to obtain a calcium carbonate aqueous suspension having the same concentration as the calcium carbonate aqueous suspension before dehydration. The pH of the aqueous calcium carbonate suspension was 11.5. Next, the aqueous calcium carbonate suspension was stirred again at 50 ° C. for 6 hours. When the pH of the aqueous calcium carbonate suspension at 25 ° C. reached 11.3, dehydration was performed using a filter press. A dehydrated cake having a calcium solid content of 48% by weight was obtained. Next, water was added again to the obtained dehydrated cake and stirred to obtain a calcium carbonate aqueous suspension having the same concentration as the calcium carbonate aqueous suspension before dehydration. The pH of the aqueous calcium carbonate suspension was 11.0. Carbon dioxide gas was again passed through the aqueous calcium carbonate suspension to lower the pH of the aqueous calcium carbonate suspension to 7.0, and then the aqueous calcium carbonate suspension was dehydrated using a filter press. The cake was dried using a paddle dryer and a calcium carbonate powder was obtained using a dry mill. The specific surface area of the calcium carbonate by a nitrogen adsorption method was measured using a surface area measuring device NO.
The result of measurement using VA2000 was 28 m 2 / g.
【0049】炭酸カルシウム粉体II 比重1.055で温度が15℃の石灰乳10000リッ
ターに、炭酸ガス濃度27重量%の炉ガスを25m3 /
minの流速で導通し炭酸化反応を行い、25℃におけ
るpHがpH9.0の炭酸カルシウムの水懸濁液を得
た。その後、撹拌を行い、炭酸カルシウムの水懸濁液の
pHが11.0に達した時点で炭酸ガスを導通し、炭酸
カルシウムの水懸濁液のpHを9.5に低下せしめ、そ
の後、50℃で50時間撹拌を行い、再度炭酸ガスを導
通し、炭酸カルシウム水懸濁液に炭酸ガスを導通し、炭
酸カルシウム水懸濁液のpHを7.0に低下せしめた
後、該炭酸カルシウム水懸濁液をフィルタープレスを用
い脱水し、そのプレスケーキをパドルドライヤーを用い
て乾燥し、乾式粉砕機を用いて炭酸カルシウム粉体を得
た。該炭酸カルシウムの窒素吸着法による比表面積を、
QUANTA、CHROME製表面積測定装置NOVA
2000を用いて測定した結果15m2 /gであった。Calcium carbonate powder II A furnace gas having a carbon dioxide gas concentration of 27% by weight was added to 10,000 liters of lime milk having a specific gravity of 1.055 and a temperature of 15 ° C. at a rate of 25 m 3 /
The reaction was conducted at a flow rate of min to carry out a carbonation reaction to obtain an aqueous suspension of calcium carbonate having a pH of 9.0 at 25 ° C. Thereafter, stirring was performed, and when the pH of the aqueous suspension of calcium carbonate reached 11.0, carbon dioxide gas was passed, and the pH of the aqueous suspension of calcium carbonate was lowered to 9.5. After stirring at 50 ° C. for 50 hours, carbon dioxide gas was passed again, and carbon dioxide gas was passed through the aqueous calcium carbonate suspension to lower the pH of the calcium carbonate aqueous suspension to 7.0. The suspension was dehydrated using a filter press, and the press cake was dried using a paddle dryer, and a calcium carbonate powder was obtained using a dry pulverizer. Specific surface area of the calcium carbonate by a nitrogen adsorption method,
QUANTA, CHROME surface area measuring device NOVA
As a result of measurement using 2000, it was 15 m 2 / g.
【0050】炭酸カルシウム粉体III 比重1.055で温度が15℃の石灰乳10000リッ
ターに、炭酸ガス濃度27重量%の炉ガスを25m3 /
minの流速で導通し炭酸化反応を行い、25℃におけ
るpHがpH9.0の炭酸カルシウムの水懸濁液を得
た。次に該水懸濁液に15℃の石灰乳4000リッター
を加え、炭酸ガス濃度27重量%の炉ガスを5m3 /m
inの流速で導通し炭酸化反応を行い、25℃における
pHが7.0の炭酸カルシウムの水懸濁液を得た。該炭
酸カルシウム水懸濁液をフィルタープレスを用い脱水
し、そのプレスケーキをパドルドライヤーを用いて乾燥
し、乾式粉砕機を用いて炭酸カルシウム粉体を得た。該
炭酸カルシウムの窒素吸着法による比表面積を、QUA
NTA、CHROME製表面積測定装置NOVA200
0を用いて測定した結果5.5m2 /gであった。Calcium carbonate powder III To 10,000 liters of lime milk having a specific gravity of 1.055 and a temperature of 15 ° C., a furnace gas having a carbon dioxide gas concentration of 27% by weight was added at 25 m 3 /
The reaction was conducted at a flow rate of min to carry out a carbonation reaction to obtain an aqueous suspension of calcium carbonate having a pH of 9.0 at 25 ° C. Next, 4000 liters of lime milk at 15 ° C. was added to the water suspension, and a furnace gas having a carbon dioxide gas concentration of 27% by weight was supplied with 5 m 3 / m 3.
The reaction was conducted at a flow rate of in to carry out a carbonation reaction to obtain an aqueous suspension of calcium carbonate having a pH of 7.0 at 25 ° C. The aqueous calcium carbonate suspension was dehydrated using a filter press, and the press cake was dried using a paddle dryer, and a calcium carbonate powder was obtained using a dry pulverizer. The specific surface area of the calcium carbonate by the nitrogen adsorption method
NTA, CHROME surface area measuring device NOVA200
As a result of measurement using 0, the value was 5.5 m 2 / g.
【0051】炭酸カルシウム粉体IV 比重1.055で温度が15℃の石灰乳10000リッ
ターに、石灰乳中の水酸化カルシウムに対して、2.5
重量%の硫酸を加え、炭酸ガス濃度27重量%の炉ガス
を25m3 /minの流速で導通し炭酸化反応を行い、
pHがpH7.0で炭酸化反応を完結させ、炭酸カルシ
ウムの水懸濁液を得た。該炭酸カルシウム水懸濁液をフ
ィルタープレスを用い脱水し、そのプレスケーキをパド
ルドライヤーを用いて乾燥し、乾式粉砕機を用いて炭酸
カルシウム粉体を得た。該炭酸カルシウムの窒素吸着法
による比表面積を、QUANTA、CHROME製表面
積測定装置NOVA2000を用いて測定した結果65
m2 /gであった。Calcium carbonate powder IV A specific gravity of 1.055, a temperature of 15 ° C. and 10,000 liters of lime milk, and a calcium hydroxide in lime milk of 2.5 liters
Wt% sulfuric acid was added, and a furnace gas having a carbon dioxide gas concentration of 27 wt% was passed at a flow rate of 25 m 3 / min to perform a carbonation reaction.
When the pH was 7.0, the carbonation reaction was completed to obtain an aqueous suspension of calcium carbonate. The aqueous calcium carbonate suspension was dehydrated using a filter press, and the press cake was dried using a paddle dryer, and a calcium carbonate powder was obtained using a dry pulverizer. The specific surface area of the calcium carbonate by a nitrogen adsorption method was measured using a surface area measuring device NOVA2000 manufactured by QUANTA and CHROME.
m 2 / g.
【0052】炭酸カルシウム粉体V 比重1.100で温度が35℃の石灰乳10000リッ
ターに、炭酸ガス濃度27重量%の炉ガスを4.5m3
/minの流速で導通し炭酸化反応を行い、pHがpH
7.0で炭酸化反応を完結させ、炭酸カルシウムの水懸
濁液を得た。次に該水懸濁液に15℃の石灰乳5000
リッターを加え、炭酸ガス濃度27重量%の炉ガスを5
m3 /minの流速で導通し炭酸化反応を行い、25℃
におけるpHがpH7.0の炭酸カルシウムの水懸濁液
を得た。該炭酸カルシウム水懸濁液をフィルタープレス
を用い脱水し、そのプレスケーキをパドルドライヤーを
用いて乾燥し、乾式粉砕機を用いて炭酸カルシウム粉体
を得た。該炭酸カルシウムの窒素吸着法による比表面積
を、QUANTA、CHROME製表面積測定装置NO
VA2000を用いて測定した結果1m2 /gであっ
た。Calcium carbonate powder V To 10,000 liters of lime milk having a specific gravity of 1.100 and a temperature of 35 ° C., 4.5 m 3 of furnace gas having a carbon dioxide gas concentration of 27% by weight.
/ Min to conduct carbonation reaction at a flow rate of
At 7.0, the carbonation reaction was completed to obtain an aqueous suspension of calcium carbonate. Next, lime milk 5000 at 15 ° C. was added to the aqueous suspension.
Liter and 5% of furnace gas with carbon dioxide concentration of 27% by weight.
The reaction was conducted at a flow rate of m 3 / min to carry out a carbonation reaction.
, A water suspension of calcium carbonate having a pH of 7.0 was obtained. The aqueous calcium carbonate suspension was dehydrated using a filter press, and the press cake was dried using a paddle dryer, and a calcium carbonate powder was obtained using a dry pulverizer. The specific surface area of the calcium carbonate by a nitrogen adsorption method was measured using a surface area measuring device NO.
As a result of measurement using VA2000, it was 1 m 2 / g.
【0053】燐酸三カルシウム粉体 比重1.055で温度が50℃の石灰乳10000リッ
ターに、75%リン酸を添加撹拌後、脱水を行い、得ら
れたプレスケーキをパドルドライヤーを用いて、乾燥、
乾式粉砕を行い白色粉体を得た。X線回折測定により該
白色粉体が燐酸三カルシウムであることを確認した。該
燐酸三カルシウム水懸濁液をフィルタープレスを用い脱
水し、そのプレスケーキをパドルドライヤーを用いて乾
燥し、乾式粉砕機を用いて白色粉体を得た。また、該粉
体の窒素吸着法による比表面積を、QUANTA、CH
ROME製表面積測定装置NOVA2000を用いて測
定した結果50m2 /gであった。Tricalcium phosphate powder 75% phosphoric acid was added to 10,000 liters of lime milk having a specific gravity of 1.055 and a temperature of 50 ° C., followed by stirring and dehydration. The obtained press cake was dried using a paddle dryer. ,
Dry pulverization was performed to obtain a white powder. X-ray diffraction measurement confirmed that the white powder was tricalcium phosphate. The tricalcium phosphate aqueous suspension was dehydrated using a filter press, and the press cake was dried using a paddle dryer, and a white powder was obtained using a dry mill. Further, the specific surface area of the powder by the nitrogen adsorption method is defined as QUANTA, CH.
As a result of measurement using a ROME surface area measuring device NOVA2000, it was 50 m 2 / g.
【0054】炭酸マグネシウム粉体 塩化マグネシウム溶液に炭酸カリウムを80℃に加熱し
ながら混合撹拌を行い、沈殿物を得た。該沈殿物を、脱
水し、更に温水を加え、再び、脱水する作業を数回繰り
返し、その後、乾燥、乾式粉砕を行い、白色粉体を得
た。該白色粉体をX線回折測定により炭酸マグネシウム
であることを確認した。該粉体の窒素吸着法による比表
面積を、QUANTA、CHROME製表面積測定装置
NOVA2000を用いて測定した結果20m2 /gで
あった。Magnesium Carbonate Powder Mixing and stirring the magnesium carbonate solution while heating potassium carbonate to 80 ° C. gave a precipitate. The precipitate was dehydrated, hot water was added thereto, and the operation of dehydration was repeated several times. Thereafter, drying and dry pulverization were performed to obtain a white powder. The white powder was confirmed to be magnesium carbonate by X-ray diffraction measurement. The specific surface area of the powder by a nitrogen adsorption method was measured using a surface area measuring device NOVA2000 manufactured by QUANTA and CHROME. As a result, it was 20 m 2 / g.
【0055】リン酸三マグネシウム粉体 硫酸マグネシウム水溶液とリン酸水素二ナトリウムの水
溶液に炭酸水素二ナトリウムを加え、pH9で放置し、
沈殿物を得た。該沈殿物を、脱水し、更に温水を加え、
再び、脱水する作業を数回繰り返し、その後、乾燥、乾
式粉砕を行い、白色粉体を得た。該白色粉体をX線回折
測定によりリン酸三マグネシウムであることを確認し
た。該粉体の窒素吸着法による比表面積を、QUANT
A、CHROME製表面積測定装置NOVA2000を
用いて測定した結果40m2 /gであった。Trimagnesium phosphate powder Disodium bicarbonate was added to an aqueous solution of magnesium sulfate and an aqueous solution of disodium hydrogen phosphate, and the mixture was allowed to stand at pH 9;
A precipitate was obtained. The precipitate is dehydrated and hot water is added,
The operation of dehydration was repeated several times, and thereafter, drying and dry pulverization were performed to obtain a white powder. The white powder was confirmed to be trimagnesium phosphate by X-ray diffraction measurement. The specific surface area of the powder by the nitrogen adsorption method was determined as QUANT.
A, It was 40 m 2 / g as a result of measurement using a surface area measuring device NOVA2000 made by CHROME.
【0056】実施例1 前述の方法で得た炭酸カルシウム粉体Iに固形分濃度が
20重量%となるように水を添加し攪拌混合を行い、湿
式粉砕機ダイノーミルKD−パイロットを用い湿式粉砕
を行い、無機粒子分散体を得た。該無機粒子分散体の物
性を表1に示す。Example 1 Water was added to the calcium carbonate powder I obtained by the above-described method so that the solid content concentration became 20% by weight, and the mixture was stirred and mixed, and wet pulverization was performed using a wet pulverizer Dynomill KD-Pilot. Then, an inorganic particle dispersion was obtained. Table 1 shows the physical properties of the inorganic particle dispersion.
【0057】実施例2 前述の方法で得た炭酸カルシウム粉体IIを用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性を表1に示す。Example 2 An inorganic particle dispersion was obtained by wet grinding under the same conditions as in Example 1 except that the calcium carbonate powder II obtained by the above-mentioned method was used. Table 1 shows the physical properties of the inorganic particle dispersion.
【0058】実施例3 前述の方法で得た炭酸カルシウム粉体III を用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性を表1に示す。Example 3 An inorganic particle dispersion was obtained by performing wet pulverization under the same conditions as in Example 1 except that the calcium carbonate powder III obtained by the above-mentioned method was used. Table 1 shows the physical properties of the inorganic particle dispersion.
【0059】実施例4 前述の方法で得たリン酸三カルシウム粉体を用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性を表1に示す。Example 4 An inorganic particle dispersion was obtained by wet grinding under the same conditions as in Example 1 except that the tricalcium phosphate powder obtained by the above method was used. Table 1 shows the physical properties of the inorganic particle dispersion.
【0060】実施例5 前述の方法で得た炭酸マグネシウム粉体を用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性を表1に示す。Example 5 An inorganic particle dispersion was obtained by performing wet grinding under the same conditions as in Example 1 except that the magnesium carbonate powder obtained by the above-mentioned method was used. Table 1 shows the physical properties of the inorganic particle dispersion.
【0061】実施例6 前述の方法で得たリン酸三マグネシウム粉体を用いる以
外は、実施例1と同条件で湿式粉砕を行い、無機粒子分
散体を得た。該無機粒子分散体の物性を表1に示す。Example 6 An inorganic particle dispersion was obtained by wet grinding under the same conditions as in Example 1 except that the trimagnesium phosphate powder obtained by the above-mentioned method was used. Table 1 shows the physical properties of the inorganic particle dispersion.
【0062】実施例7 前述の方法で得たリン酸三カルシウム粉体を用い、リン
酸三酸カルシウム固形分100重量部に対し、ペンタポ
リリン酸Na(太平化学産業製)5重量部及び水を固形
分濃度が20重量%となるように添加し攪拌混合を行う
以外は、実施例1と同条件で湿式粉砕を行い、無機粒子
分散体を得た。該無機粒子分散体の物性を表1に示す。Example 7 Using the tricalcium phosphate powder obtained by the above-described method, 5 parts by weight of sodium pentapolyphosphate (manufactured by Taihei Chemical Industry) and water were added to 100 parts by weight of the solid content of calcium phosphate. Wet pulverization was carried out under the same conditions as in Example 1 except that the solid content concentration was 20% by weight and stirring and mixing were carried out to obtain an inorganic particle dispersion. Table 1 shows the physical properties of the inorganic particle dispersion.
【0063】実施例8 前述の方法で得た炭酸カルシウム粉体IIを用い、炭酸カ
ルシウム固形分100重量部に対し、ガディガム(三栄
薬品工業製)3重量部及び水を固形分濃度が20重量%
となるように添加し攪拌混合を行い、高圧式ホモジナイ
ザーを用い、500kg/cm2 の圧力で分散を行い、
無機粒子分散体を得た。該無機粒子分散体の物性を表1
に示す。Example 8 Using calcium carbonate powder II obtained by the above-described method, 3 parts by weight of gaddy gum (manufactured by Sanei Pharmaceutical Co., Ltd.) and water were added to 100 parts by weight of calcium carbonate solids at a solids concentration of 20% by weight.
The mixture was stirred and mixed, and dispersed using a high-pressure homogenizer at a pressure of 500 kg / cm 2 .
An inorganic particle dispersion was obtained. Table 1 shows the physical properties of the inorganic particle dispersion.
Shown in
【0064】実施例9 前述の方法で得た炭酸カルシウム粉体Iを用い、炭酸カ
ルシウム固形分100重量部に対し、HLBが15のシ
ョ糖脂肪酸エステル(第一工業製薬製)を18重量部及
び水を固形分濃度が20重量%となるように添加し攪拌
混合を行い、湿式粉砕機ダイノーミルKD−パイロット
を用い湿式粉砕を行い、無機粒子分散体スラリーを得
た。該無機粒子分散体スラリーをスプレードライヤーを
用いて乾燥を行い、無機粒子分散体パウダーを得た。得
られた無機粒子分散体パウダーに水を加えて高速ディス
パーで15分間撹拌し、20重量%の無機分散体パウダ
ーの再分散液を得た。該無機粒子分散体の再分散液の物
性を表1に示す。尚、ショ糖脂肪酸エステルは、65℃
の温水で溶解後、20℃に冷却して使用した。Example 9 Using calcium carbonate powder I obtained by the above method, 18 parts by weight of sucrose fatty acid ester having an HLB of 15 (manufactured by Daiichi Kogyo Seiyaku) and 100 parts by weight of calcium carbonate solids were used. Water was added so that the solid content concentration became 20% by weight, followed by stirring and mixing, and wet pulverization was performed using a wet pulverizer Dynomill KD-Pilot to obtain an inorganic particle dispersion slurry. The inorganic particle dispersion slurry was dried using a spray drier to obtain an inorganic particle dispersion powder. Water was added to the obtained inorganic particle dispersion powder, and the mixture was stirred with a high-speed disper for 15 minutes to obtain a 20% by weight redispersion of the inorganic dispersion powder. Table 1 shows the physical properties of the redispersion liquid of the inorganic particle dispersion. In addition, sucrose fatty acid ester is 65 ° C.
, And cooled to 20 ° C before use.
【0065】実施例10 前述の方法で得た炭酸カルシウム粉体II及び炭酸マグネ
シウム粉体を用い、炭酸カルシウムと炭酸マグネシウム
を1:1の比率で混合後、該混合粉体固形分100重量
部に対し、トラガントガム(五協産業製)7重量部及び
水を固形分濃度が20重量%となるように添加し攪拌混
合を行い、超音波ホモジナイザー(1200W、15k
Hz)を用い、1分間超音波分散を行い、無機粒子分散
体を得た。該無機粒子分散体の物性を表1に示す。Example 10 Calcium carbonate and magnesium carbonate were mixed at a ratio of 1: 1 using the calcium carbonate powder II and the magnesium carbonate powder obtained by the above-mentioned method, and then mixed with 100 parts by weight of the solid content of the mixed powder. On the other hand, 7 parts by weight of tragacanth gum (manufactured by Gokyo Sangyo) and water were added so that the solid content concentration became 20% by weight, followed by stirring and mixing, and an ultrasonic homogenizer (1200 W, 15 k).
Hz) for 1 minute to obtain an inorganic particle dispersion. Table 1 shows the physical properties of the inorganic particle dispersion.
【0066】実施例11 前述の方法で得た炭酸カルシウム粉体III を用い、炭酸
カルシウム固形分濃度が20重量%となるように水を添
加し、高速ディスパーを用い1時間強攪拌を行い、無機
粒子分散体を得た。該無機粒子分散体の物性を表1に示
す。Example 11 Using the calcium carbonate powder III obtained by the above-mentioned method, water was added so that the calcium carbonate solid content concentration became 20% by weight, and the mixture was vigorously stirred for 1 hour using a high-speed disperser. A particle dispersion was obtained. Table 1 shows the physical properties of the inorganic particle dispersion.
【0067】比較例1 前述の方法で得た炭酸カルシウム粉体IVを用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性は、表1に示す如
く、分散係数Nの大きい粒度分布がブロードで、分散状
態の良くないものしか得ることが出来なかった。Comparative Example 1 An inorganic particle dispersion was obtained by performing wet grinding under the same conditions as in Example 1 except that the calcium carbonate powder IV obtained by the above-mentioned method was used. As shown in Table 1, the physical properties of the inorganic particle dispersion were such that only those having a large particle size distribution with a large dispersion coefficient N and a poor dispersion state could be obtained.
【0068】比較例2 前述の方法で得た炭酸カルシウム粉体Vを用いる以外
は、実施例1と同条件で湿式粉砕を行い、無機粒子分散
体を得た。該無機粒子分散体の物性は、表1に示す如
く、粒度分布における平均粒子径Mが極めて大きなもの
しか得ることが出来なかった。Comparative Example 2 An inorganic particle dispersion was obtained by performing wet grinding under the same conditions as in Example 1 except that the calcium carbonate powder V obtained by the above-mentioned method was used. As shown in Table 1, the physical properties of the inorganic particle dispersion were such that only an average particle diameter M in the particle size distribution was extremely large.
【0069】比較例3 前述の方法で得たリン酸マグネシウム粉体を用い、リン
酸マグネシウム固形分濃度が20重量%となるように水
を添加し、高速ディスパーを用い1時間強攪拌を行い、
無機粒子分散体を得た。該無機粒子分散体の物性は、表
1に示す如く、分散係数Nが大きい粒度分布のブロード
なものしか得られなかった。従って、更に1時間強撹拌
を続け、再度、粒度分布の測定を行ったが、再撹拌前の
結果と大差はなかった。Comparative Example 3 Using the magnesium phosphate powder obtained by the above method, water was added so that the magnesium phosphate solid content concentration was 20% by weight, and the mixture was vigorously stirred for 1 hour using a high-speed disperser.
An inorganic particle dispersion was obtained. As shown in Table 1, only a broad particle size distribution having a large dispersion coefficient N was obtained as physical properties of the inorganic particle dispersion. Therefore, strong stirring was continued for another hour and the particle size distribution was measured again, but there was no great difference from the result before the re-stirring.
【0070】比較例4 前述の方法で得たリン酸カルシウム粉体を用い、リン酸
カルシウム固形分濃度が20重量%となるように水を添
加し、高速ディスパーを用い1時間強攪拌を行い、無機
粒子分散体を得た。該無機粒子分散体の物性は、表1に
示す如く、分散係数Nが大きい粒度分布のブロードなも
のしか得られなかった。従って、更に1時間強撹拌を続
け、再度、粒度分布の測定を行ったが、再撹拌前の結果
と大差はなかった。Comparative Example 4 Using the calcium phosphate powder obtained by the above-mentioned method, water was added so that the calcium phosphate solid concentration became 20% by weight, and the mixture was vigorously stirred for 1 hour using a high-speed disper to obtain an inorganic particle dispersion. I got As shown in Table 1, only a broad particle size distribution having a large dispersion coefficient N was obtained as physical properties of the inorganic particle dispersion. Therefore, strong stirring was continued for another hour and the particle size distribution was measured again, but there was no great difference from the result before the re-stirring.
【0071】[0071]
【表1】 [Table 1]
【0072】実施例12 小麦粉8800g、馬鈴薯澱粉2200gに実施例1で
調製した無機粒子分散体3750g及びかん水、食塩等
を加え混合した。混合した生地を常法に従い、ロール等
で延伸、裁断し生麺を生成した後、所定時間蒸し、油で
揚げ、即席麺を得た。得られた即席麺に熱湯を投入後、
ふたをし3分間放置後開封し、更に1分間放置し、男女
10名による官能試験により、食感に関して下記の5段
階評価を行った。その評価結果を表2に示す。Example 12 To 8800 g of wheat flour and 2200 g of potato starch, 3750 g of the inorganic particle dispersion prepared in Example 1 and brine, salt and the like were added and mixed. The mixed dough was stretched and cut with a roll or the like according to a conventional method to produce raw noodles, steamed for a predetermined time and fried in oil to obtain instant noodles. After adding boiling water to the obtained instant noodles,
The lid was left after leaving for 3 minutes, opened, and further left for 1 minute, and the following five-grade evaluation was performed on the texture by a sensory test by 10 men and women. Table 2 shows the evaluation results.
【0073】「モチモチ感」 モチモチ感が十分ある・・・5 ややある・・・・・・・・・4 普通・・・・・・・・・・・3 あまりない・・・・・・・・2 全くない・・・・・・・・・1"Mochi mochi feeling" There is sufficient mochi mochi feeling ... 5 Somewhat motivating ... 4 ... Normal ... 3 Not much ...・ 2 Not at all ・ ・ ・ ・ ・ ・ ・ ・ ・ 1
【0074】「弾力性」 弾力性が十分ある・・・・・5 ややある・・・・・・・・・4 普通・・・・・・・・・・・3 あまりない・・・・・・・・2 全くない・・・・・・・・・1[Elasticity] Elasticity is sufficient ... 5 Somewhat ... 4 ... Normal ... 3 Not so much ...・ ・ ・ 2 Not at all ・ ・ ・ ・ ・ ・ ・ ・ ・ 1
【0075】「食感の維持性(茹で延び性)」 全く問題がない・・・・・・5 やや延びた感がある・・・・4 少し延びた感がある・・・・3 かなり延びた感がある・・・2 極めて延びた感がある・・・1"Maintenance of texture (boilability and elongation)" No problem at all ... 5 Somewhat extended feeling ... 4 Somewhat extended feeling ... There is a feeling ... 2 There is a feeling of being extremely extended ... 1
【0076】「総合」 とてもおいしく感じる・・・5 ややおいしく感じる・・・・4 普通・・・・・・・・・・・3 あまりおいしくない・・・・2 全くおいしくない・・・・・1[Overall] Feel very delicious ... 5 Feel slightly delicious ... 4 Normal ... 3 Not very delicious ... 2 Not quite delicious ... 1
【0077】実施例13〜22、比較例5〜8 前述の実施例2〜11、比較例1〜4で調製した無機粒
子分散体を用いること除き、他は実施例12と同様の方
法で即席麺を得た。また、これらの即席麺の食感に関す
る官能試験を、実施例12に示す同様の方法で行った。
その評価結果を表2に示す。Examples 13 to 22 and Comparative Examples 5 to 8 Except that the inorganic particle dispersions prepared in the above Examples 2 to 11 and Comparative Examples 1 to 4 were used, the procedure was the same as in Example 12, except that the inorganic particle dispersions were used. I got the noodles. A sensory test on the texture of these instant noodles was performed in the same manner as in Example 12.
Table 2 shows the evaluation results.
【0078】比較例9 小麦粉8800g、馬鈴薯澱粉2200gに前述の炭酸
カルシウム粉体III をミキサーでドライブレンドを行
い、その後、かん水、食塩及び水等を加え混練した。混
合した生地を常法に従い、ロール等で延伸、裁断し生麺
を生成した後、所定時間蒸し、油で揚げ、即席麺を得
た。得られた即席麺に熱湯を投入後、ふたをし3分間放
置後開封し、更に1分間放置し、男女10名よりなる官
能試験を、実施例12に示す同様の方法で行った。その
評価結果を表2に示す。Comparative Example 9 The above-mentioned calcium carbonate powder III was dry-blended with 8,800 g of wheat flour and 2,200 g of potato starch using a mixer, and then, water, brine, water and the like were added and kneaded. The mixed dough was stretched and cut with a roll or the like according to a conventional method to produce raw noodles, steamed for a predetermined time and fried in oil to obtain instant noodles. After boiling water was poured into the obtained instant noodles, the lid was closed, left for 3 minutes, opened, and further left for 1 minute, and a sensory test of 10 men and women was performed in the same manner as described in Example 12. Table 2 shows the evaluation results.
【0079】比較例10〜11 前述の炭酸カルシウム粉体III の代わりに炭酸マグネシ
ウム粉体、リン酸カルシウム粉体を用いること除き、他
は比較例9と同様の方法で即席麺を得た。また、これら
の即席麺の食感に関する官能試験を、実施例12に示す
同様の方法で行った。その評価結果を表2に示す。Comparative Examples 10 to 11 Instant noodles were obtained in the same manner as in Comparative Example 9 except that magnesium carbonate powder and calcium phosphate powder were used instead of the calcium carbonate powder III. A sensory test on the texture of these instant noodles was performed in the same manner as in Example 12. Table 2 shows the evaluation results.
【0080】[0080]
【表2】 [Table 2]
【0081】実施例23 小麦粉6600g、馬鈴薯澱粉4400gに実施例1で
調製した無機粒子分散体3750g及び食塩等を加え混
合・混練した。該生地を30分間熟成した後、生地を常
法に従い、延伸、裁断し、生うどんを得た。該生うどん
を10分間茹で完全茹で直前でレトルト包材に充填後、
121℃で5分のレトルト処理を行い、更に2分間放置
後、該うどんの男女10名よりなる官能試験を、実施例
12に示す同様の方法で行った。その評価結果を表3に
示す。Example 23 3750 g of the inorganic particle dispersion prepared in Example 1 and salt and the like were added to 6600 g of wheat flour and 4400 g of potato starch, followed by mixing and kneading. After the dough was aged for 30 minutes, the dough was stretched and cut according to a conventional method to obtain raw udon. After boiling the raw udon for 10 minutes and filling the retort packaging just before boiling completely,
After performing a retort treatment at 121 ° C. for 5 minutes and leaving the mixture to stand for 2 minutes, a sensory test of 10 men and women of the udon was performed in the same manner as in Example 12. Table 3 shows the evaluation results.
【0082】実施例24〜33、比較例12〜15 前述の実施例2〜11、比較例1〜4で調製した無機粒
子分散体を用いること除き、他は実施例23と同様の方
法でうどんを得た。また、これらのうどんの食感に関す
る官能試験を、実施例11に示す同様の方法で行った。
その評価結果を表3に示す。Examples 24 to 33, Comparative Examples 12 to 15 Udon noodles were prepared in the same manner as in Example 23 except that the inorganic particle dispersions prepared in Examples 2 to 11 and Comparative Examples 1 to 4 were used. I got A sensory test on the texture of these udon noodles was performed in the same manner as in Example 11.
Table 3 shows the evaluation results.
【0083】比較例16 小麦粉6600g、馬鈴薯澱粉4400gに前述の炭酸
カルシウム粉体III 750gをミキサーでドライブレン
ドを強力に行い、その後、かん水、食塩及び水等を加え
混練した。該生地を30分間熟成した後、生地を常法に
従い、延伸、裁断し、生うどんを得た。該生うどんを1
0分間茹で完全茹で直前でレトルト包材に充填後、12
1℃で5分のレトルト処理を行い、更に1分間放置後、
該うどんの男女10名よりなる官能試験を、実施例12
に示す同様の方法で行った。その評価結果を表3に示
す。Comparative Example 16 750 g of the above-mentioned calcium carbonate powder III was intensively dry-blended with 6600 g of wheat flour and 4400 g of potato starch using a mixer, and then kneaded with brine, salt and water. After the dough was aged for 30 minutes, the dough was stretched and cut according to a conventional method to obtain raw udon. One of the raw udon
Boil for 0 minutes, fill the retort packaging just before boiling completely, and add 12
Perform a retort treatment at 1 ° C for 5 minutes and leave it for another 1 minute.
A sensory test consisting of 10 men and women of the udon was carried out in Example 12.
Was performed in the same manner as described above. Table 3 shows the evaluation results.
【0084】比較例17〜18 前述の炭酸カルシウム粉体III の代わりに炭酸マグネシ
ウム粉体、リン酸カルシウム粉体を用いること除き、他
は他は比較例16と同様の方法で生うどんを得た。ま
た、これらの即席麺の食感に関する官能試験を、実施例
11に示す同様の方法で行った。その評価結果を表3に
示す。Comparative Examples 17 to 18 Raw udon was obtained in the same manner as in Comparative Example 16 except that magnesium carbonate powder and calcium phosphate powder were used instead of the calcium carbonate powder III. A sensory test on the texture of these instant noodles was performed in the same manner as in Example 11. Table 3 shows the evaluation results.
【0085】[0085]
【表3】 [Table 3]
【0086】[0086]
【発明の効果】以上のように、本発明の麺類用無機粒子
分散体は、麺類に添加され、麺類にモチモチ感を付与
し、優れた食感を実現又は維持することが可能となると
同時に、カルシウム、マグネシウム等のミネラルを強化
した麺類を提供することができる。As described above, the inorganic particle dispersion for noodles of the present invention is added to noodles to impart a moist feeling to the noodles, thereby realizing or maintaining an excellent texture, and Noodles reinforced with minerals such as calcium and magnesium can be provided.
Claims (10)
/100g−水)以下のカルシウム化合物及びマグネシ
ウム化合物より選ばれた少なくとも1種の無機粒子を含
む水懸濁液からなり、下記(a)及び(b)の要件を具
備してなることを特徴とする麺類用無機粒子分散体。 (a)0.2≦M≦15 (b)0≦N≦3 但し 分散係数N=(d90−d1
0)/M M :マイクロトラックFRAレーザー式粒度分布計
により測定した粒子の50%平均粒子径(μm) d90:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計90%粒子径
(μm) d10:マイクロトラックFRAレーザー式粒度分布計
により測定した粒子のふるい通過側累計10%粒子径
(μm)1. The solubility in water at 20 ° C. is 0.1 (g).
/ 100g-water) The aqueous suspension contains at least one inorganic particle selected from the group consisting of the following calcium compounds and magnesium compounds, and satisfies the following requirements (a) and (b): An inorganic particle dispersion for noodles. (A) 0.2 ≦ M ≦ 15 (b) 0 ≦ N ≦ 3 where the dispersion coefficient N = (d90−d1
0) / M M: 50% average particle diameter (μm) of the particles measured by a Microtrac FRA laser type particle size distribution analyzer d90: 90% total particle diameter of particles passing through a sieve measured by a Microtrac FRA laser type particle size distribution analyzer (Μm) d10: Total 10% particle diameter (μm) of particles passing through the sieve measured by a Microtrac FRA laser type particle size distribution analyzer (μm)
1記載の麺類用無機粒子分散体。 (c)0≦N≦22. The dispersion of inorganic particles for noodles according to claim 1, which satisfies the following requirement (c). (C) 0 ≦ N ≦ 2
なる請求項1記載の麺類用無機粒子分散体。 (c)0≦N≦2 (d)0.2≦M≦53. The inorganic particle dispersion for noodles according to claim 1, which satisfies the following requirements (c) and (d). (C) 0 ≦ N ≦ 2 (d) 0.2 ≦ M ≦ 5
なる請求項1記載の麺類用無機粒子分散体。 (e)0.2≦M≦1.5 (f)0≦N≦1.54. The inorganic particle dispersion for noodles according to claim 1, which satisfies the following requirements (e) and (f). (E) 0.2 ≦ M ≦ 1.5 (f) 0 ≦ N ≦ 1.5
ルシウム、炭酸マグネシウム、リン酸マグネシウムより
選ばれた少なくとも1種である請求項1〜4の何れか1
項に記載の麺類用無機粒子分散体。5. The method according to claim 1, wherein the inorganic particles are at least one selected from calcium carbonate, calcium phosphate, magnesium carbonate, and magnesium phosphate.
Item 10. The inorganic particle dispersion for noodles according to item 8.
少なくとも1種を添加してなる請求項1〜5の何れか1
項に記載の麺類用無機粒子分散体。6. The method according to claim 1, wherein at least one selected from an emulsion stabilizer and a condensed phosphate is added.
Item 10. The inorganic particle dispersion for noodles according to item 8.
/100g−水)以下のカルシウム化合物及びマグネシ
ウム化合物より選ばれた少なくとも1種の無機粒子を含
む水懸濁液を粉砕及び/又は分散させることを特徴とす
る請求項1〜5の何れか1項に記載の麺類用無機粒子分
散体の製造方法。7. The solubility in water at 20 ° C. is 0.1 (g).
/ 100 g-water) An aqueous suspension containing at least one inorganic particle selected from the following calcium compounds and magnesium compounds is pulverized and / or dispersed. The method for producing an inorganic particle dispersion for noodles according to the above.
ら選ばれた少なくとも1種を添加する請求項6記載の麺
類用無機粒子分散体の製造方法。8. The method for producing an inorganic particle dispersion for noodles according to claim 6, wherein at least one selected from an emulsion stabilizer and a condensed phosphate is added to the aqueous suspension.
置、超音波分散機から選ばれた少なくとも1種を用いて
粉砕及び/又は分散させる請求項7又は8記載の製造方
法。9. The production method according to claim 7, wherein the aqueous suspension is pulverized and / or dispersed using at least one selected from a wet pulverizer, a high-pressure emulsifying and dispersing apparatus, and an ultrasonic disperser.
麺類用無機粒子分散体を添加してなることを特徴とする
ミネラル強化麺類。10. A mineral-enriched noodle comprising the inorganic particle dispersion for noodles according to any one of claims 1 to 6.
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Cited By (2)
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WO2015141394A1 (en) * | 2014-03-17 | 2015-09-24 | 白石工業株式会社 | Conditioning agent for fish paste product, and method for manufacturing fish paste product |
JP2019013199A (en) * | 2017-07-10 | 2019-01-31 | 吉原食糧株式会社 | Manufacturing method of powder composition for noodle-making |
-
2001
- 2001-02-28 JP JP2001053731A patent/JP2002253150A/en not_active Withdrawn
Cited By (4)
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WO2015141394A1 (en) * | 2014-03-17 | 2015-09-24 | 白石工業株式会社 | Conditioning agent for fish paste product, and method for manufacturing fish paste product |
JP2015173646A (en) * | 2014-03-17 | 2015-10-05 | 白石工業株式会社 | Quality improver for marine products and method for producing marine products |
JP2019013199A (en) * | 2017-07-10 | 2019-01-31 | 吉原食糧株式会社 | Manufacturing method of powder composition for noodle-making |
JP6994752B2 (en) | 2017-07-10 | 2022-01-14 | 吉原食糧株式会社 | Method for manufacturing powder composition for noodle making |
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