{"title":"在175°c氢氧化钙和二氧化硅悬浮液中形成化合物","authors":"T. Dambrauskas, K. Baltakys","doi":"10.5755/J01.CT.64.2.6100","DOIUrl":null,"url":null,"abstract":"Compound formation peculiarities in the Ca(OH) 2 –SiO 2 ∙nH 2 O–H 2 O system with the molar ratio of CaO/SiO 2 equal to 1.5 have been examined. The hydrothermal synthesis of the compounds has been carried out in unmixed suspensions at a temperature of 175 °C. The duration of isothermal curing was 4, 8, 16, 24, 48, and 72 hours. In unstirred Ca(OH) 2 and SiO 2 ∙nH 2 O suspensions with CaO/SiO 2 = 1.5, within 4 hours of isothermal curing at 175 °C, dicalcium silicate hydrates – a-C 2 S hydrate, C-S-H(II) and a low base semi-crystalline C-S-H(I) type calcium silicate hydrate – were formed. Within 48 h of hydrothermal synthesis, Ca(OH) 2 was fully reacted, and semi-crystalline C-S-H(II) became metastable and recrystallized into stable compounds – a-C 2 S hydrate and C-S-H(I). The typical destruction temperatures of a-C 2 S hydrate and Ca(OH) 2 were possible to determine by using differential thermogravimetric analysis data: the destruction of Ca(OH) 2 intensively proceeded at a temperature of ~456 oC when a sample lost 1.85 % of its mass. Meanwhile, a-C 2 S hydrate destruction occurred at a higher temperature (~478 oC), and weight loss was equal to 0.58 %. After 72 h of synthesis, a-C 2 S hydrate prevailed in the products. DOI: http://dx.doi.org/10.5755/j01.ct.64.2.6100","PeriodicalId":22505,"journal":{"name":"the Chemical Technology","volume":"11 1","pages":"45-50"},"PeriodicalIF":0.0000,"publicationDate":"2014-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"COMPOUND FORMATION AT 175 °C IN CALCIUM HYDROXIDE AND SILICA DIOXIDE SUSPENSION\",\"authors\":\"T. Dambrauskas, K. Baltakys\",\"doi\":\"10.5755/J01.CT.64.2.6100\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Compound formation peculiarities in the Ca(OH) 2 –SiO 2 ∙nH 2 O–H 2 O system with the molar ratio of CaO/SiO 2 equal to 1.5 have been examined. The hydrothermal synthesis of the compounds has been carried out in unmixed suspensions at a temperature of 175 °C. The duration of isothermal curing was 4, 8, 16, 24, 48, and 72 hours. In unstirred Ca(OH) 2 and SiO 2 ∙nH 2 O suspensions with CaO/SiO 2 = 1.5, within 4 hours of isothermal curing at 175 °C, dicalcium silicate hydrates – a-C 2 S hydrate, C-S-H(II) and a low base semi-crystalline C-S-H(I) type calcium silicate hydrate – were formed. Within 48 h of hydrothermal synthesis, Ca(OH) 2 was fully reacted, and semi-crystalline C-S-H(II) became metastable and recrystallized into stable compounds – a-C 2 S hydrate and C-S-H(I). The typical destruction temperatures of a-C 2 S hydrate and Ca(OH) 2 were possible to determine by using differential thermogravimetric analysis data: the destruction of Ca(OH) 2 intensively proceeded at a temperature of ~456 oC when a sample lost 1.85 % of its mass. Meanwhile, a-C 2 S hydrate destruction occurred at a higher temperature (~478 oC), and weight loss was equal to 0.58 %. After 72 h of synthesis, a-C 2 S hydrate prevailed in the products. DOI: http://dx.doi.org/10.5755/j01.ct.64.2.6100\",\"PeriodicalId\":22505,\"journal\":{\"name\":\"the Chemical Technology\",\"volume\":\"11 1\",\"pages\":\"45-50\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"the Chemical Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5755/J01.CT.64.2.6100\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"the Chemical Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5755/J01.CT.64.2.6100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
COMPOUND FORMATION AT 175 °C IN CALCIUM HYDROXIDE AND SILICA DIOXIDE SUSPENSION
Compound formation peculiarities in the Ca(OH) 2 –SiO 2 ∙nH 2 O–H 2 O system with the molar ratio of CaO/SiO 2 equal to 1.5 have been examined. The hydrothermal synthesis of the compounds has been carried out in unmixed suspensions at a temperature of 175 °C. The duration of isothermal curing was 4, 8, 16, 24, 48, and 72 hours. In unstirred Ca(OH) 2 and SiO 2 ∙nH 2 O suspensions with CaO/SiO 2 = 1.5, within 4 hours of isothermal curing at 175 °C, dicalcium silicate hydrates – a-C 2 S hydrate, C-S-H(II) and a low base semi-crystalline C-S-H(I) type calcium silicate hydrate – were formed. Within 48 h of hydrothermal synthesis, Ca(OH) 2 was fully reacted, and semi-crystalline C-S-H(II) became metastable and recrystallized into stable compounds – a-C 2 S hydrate and C-S-H(I). The typical destruction temperatures of a-C 2 S hydrate and Ca(OH) 2 were possible to determine by using differential thermogravimetric analysis data: the destruction of Ca(OH) 2 intensively proceeded at a temperature of ~456 oC when a sample lost 1.85 % of its mass. Meanwhile, a-C 2 S hydrate destruction occurred at a higher temperature (~478 oC), and weight loss was equal to 0.58 %. After 72 h of synthesis, a-C 2 S hydrate prevailed in the products. DOI: http://dx.doi.org/10.5755/j01.ct.64.2.6100