PL20040B1 - Method to prevent salt baking. - Google Patents
Method to prevent salt baking. Download PDFInfo
- Publication number
- PL20040B1 PL20040B1 PL20040A PL2004032A PL20040B1 PL 20040 B1 PL20040 B1 PL 20040B1 PL 20040 A PL20040 A PL 20040A PL 2004032 A PL2004032 A PL 2004032A PL 20040 B1 PL20040 B1 PL 20040B1
- Authority
- PL
- Poland
- Prior art keywords
- salts
- salt
- sintering
- prevent salt
- solution
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims description 21
- 238000000034 method Methods 0.000 title claims description 3
- 238000001035 drying Methods 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- 150000004679 hydroxides Chemical class 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 150000002739 metals Chemical class 0.000 claims 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000001103 potassium chloride Substances 0.000 description 4
- 235000011164 potassium chloride Nutrition 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 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 3
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229960004887 ferric hydroxide Drugs 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 235000014413 iron hydroxide Nutrition 0.000 description 2
- IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 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
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Inorganic materials [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
Description
Wiele soli, wytwarzanych w przemysle, posiada sklonnosc do spiekania sie przy przechowywaniu, tworzac mniej lub wiecej twarde masy, które trudno jest rozbic, czy to lopata czy tez zapomoca urzadzen me¬ chanicznych. Rozbijanie takie pociaga za soba znaczne koszta.Spiekanie sie soli moze miec miejsce równiez w czasie transportu, np. w wago¬ nach lub lodziach, powodujac niedogodno¬ sci przy wyladowywaniu. Przy stosowaniu takich spieczonych soli wystepuja dalsze niekorzystne objawy, jak zle wysiewanie sie spieczonych nawozów, powolne rozpu¬ szczanie sie spieczonych soli, zatykanie i uszkadzanie przez nie urzadzen transpor¬ towych.Spiekanie sie nastepuje nietylko przy solach, które podlegaja podczas przecho¬ wywania dalszym chemicznym przemia¬ nom, jak np. superfosfat i inne, lecz rów¬ niez przy solach, którym przy przechowy¬ waniu nie towarzysza chemiczne zmiany.W przypadku, gdy spiekanie sie so¬ li powodowane jest wykrystalizowaniem drobniutkich krysztalków soli z resztek roztworu solnego, przylegajacego do kry¬ sztalków lub z roztworu wytworzonego na skutek pochlaniania wilgoci przez sól, uda¬ je sie przewaznie przez dobre wysuszenie i nastepne zabezpieczenie soli od wilgoci zmniejszyc jej sklonnosc do spiekania s^e.Liczne sole spiekaja sie jednakowoz w znacznym stopniu takze bez dostepu wil-gaci,' przyczem solc drobnoziarniste silniej niz sole, w wiekszych agregatach. Obecnie stwierdzono, ze powyzsze zjawisko, spieka¬ nia sie mozna w zupelnosci usunac, wzgled¬ nie znacznie zmniejszyc, jesli do soli do¬ dac nieorganicznych sub&tancyj koloidal¬ nych, posiadajacych zdolnosc wytworzenia warstwy ochronnej na poszczególnych zia¬ renkach soli. Jako taki srodek nadaje sie np. wodorotlenek zelazawy, otrzymany dzialaniem lugu sodowego na siarczan ze¬ lazawy. Wodorotlenek zelazawy utlenia sie na powietrzu do wodorotlenku zelazowego, który tworzy warstewke ochronna na zia¬ renkach soli. Jak dalece delikatna jest te¬ ka powloka ochronna, wynika z ilosci Fe, potrzebnego do wytworzenia powyzszej powloki. Wystarcza ilosc Fe, wynoszaca jedna lub kilka setnych procentu.Wynalazek niniejszy nie ogranicza sie tylko do zwiazków zelaza, które maja tyl¬ ko te przewage, ze sa najtansze i dlatego nadaja sie do stosowania na duza skale.Mozna równiez stosowac inne koloidalne substancje nieorganiczne, zwlaszcza wte¬ dy, gdy niepozadana jest obecnosc zelaza.Nadaja sie tu swiezo stracone wodoro¬ tlenki magnezu, glinu, manganu i tern po¬ dobne, które w formie zawiesiny dodaje I*sie do soli przed ich ostatecznem wysusze¬ niem. Dodatki mozna w ten sposób dobie¬ rac, aby same wykazywaly korzystne wla¬ snosci, jak np. mangan przy nawozach sztucznych.Przyklad I. 100 ton 80%-ego chlorku potasu, wytworzonego do celów nawozo¬ wych, miesza sie dokladnie przed susze¬ niem, z zawiesina wodorotlenku zelazawe¬ go, która otrzymuje sie przez dodanie 12 kg lugu sodowego do roztworu 115 kg krysta¬ licznego siarczanu zelazawego (Fe S04. . 7H2OJ w 430 kg wody. Po wysuszeniu o- lrzymuje sie chlorek potasu, wykazujacy nadzwyczaj duza trwalosc przy przecho¬ wywaniu.Przyklad II. 1 tone saletry chilijskiej miesza sie z zawiesina wodorotlenku ma¬ gnezu, wytworzona przez dodanie 1,3 kg lugu sodowego do roztworu 1,5 kg chlorku magnezu w 10 kg wody. Saletra z powyz¬ szym dodatkiem jest bardzo trwala przy przechowywaniu.Przyklad III. 10 ton wysokoprocento¬ wego (okolo 99%) chlorku potasu, stoso¬ wanego do elektrolizy, traktuje sie zawie¬ sina wodorotlenku glinu, wytworzona przez dodanie 95 kg lugu potasowego do roz¬ tworu 75 kg krystalicznego siarczanu glinu (Al2(SOJ3.18H20) w 450 kg wody. Po wysuszeniu otrzymuje sie chlorek potasu calkowicie pozbawiony sklonnosci do spie¬ kania sie. PLMany commercially manufactured salts tend to cake when stored, forming more or less hard masses that are difficult to break, be it with a shovel or with the aid of mechanical devices. Such breaking up entails considerable costs. Baking of the salt can also take place during transport, for example in wagons or boats, causing inconvenience for unloading. When using such parched salts, there are further disadvantages, such as bad sowing of parched fertilizers, slow dissolution of parched salts, clogging and damage to transport equipment. changes, such as, for example, superphosphate and others, but also in the case of salts, which are not accompanied by chemical changes during storage. In the case when salt sintering is caused by the crystallization of tiny salt crystals from the remnants of the salt solution adhering to crystals or a solution produced by the absorption of moisture by salt, are usually successful by drying well and then protecting the salt from moisture, reducing its tendency to sinter. Many salts, however, sinter to a large extent also without the access of moisture. pants, 'because I salt the fine grains more strongly than the salts, in larger aggregates. It has now been found that the above-mentioned sintering phenomenon can be completely removed, or significantly reduced, by adding inorganic colloidal substances to the salt, which have the ability to form a protective layer on individual salt grains. As such a medium, for example, iron hydroxide obtained by treatment with sodium lye on iron sulfate is suitable. The iron hydroxide is oxidized in air to ferric hydroxide, which forms a protective film on the salt grains. How delicate this protective coating is is due to the amount of Fe needed to form the above coating. A quantity of Fe of one or a few hundredths of a percent is sufficient. The present invention is not limited only to iron compounds, which have the only advantage of being the cheapest and therefore suitable for large-scale use. Other colloidal inorganic substances may also be used, especially when the presence of iron is undesirable. Freshly lost magnesium, aluminum, manganese and the like hydroxides, which are suspended in the form of a slurry and added to the salt before their final drying, are suitable. this method was chosen so that they themselves exhibit favorable properties, such as, for example, manganese in artificial fertilizers. Example I. 100 tons of 80% potassium chloride, produced for fertilizing purposes, are mixed thoroughly before drying, with a ferric hydroxide suspension, which is obtained by adding 12 kg of sodium liquor to a solution of 115 kg of crystalline ferrous sulfate (FeSO4. 7H2OJ in 430 kg of water. After drying, potassium chloride is obtained, showing an abundance of salt). usually have a long shelf life. Example II. 1 ton of Chilean nitrate is mixed with a suspension of magnesium hydroxide, prepared by adding 1.3 kg of sodium lug to a solution of 1.5 kg of magnesium chloride in 10 kg of water. Saltpeter with the above-mentioned additive is very stable for storage. Example III. 10 tons of high-percentage (about 99%) potassium chloride used in the electrolysis are treated with an aluminum hydroxide suspension prepared by adding 95 kg of potassium liquor to a solution of 75 kg of crystalline aluminum sulfate (Al2 (SOJ3.18H2O) in 450 kg of water After drying, potassium chloride is obtained completely free of sintering. PL
Claims (1)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL20040B1 true PL20040B1 (en) | 1934-05-30 |
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