Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity

Both producers and users of divided solids regularly face the problem of caking after periods of storage and/or transport. Particle agglomeration depends not only on powder water content, temperature and applied pressure, but also on the inter...

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Main Authors: Marina Langlet, Frederic Nadaud, Mohammed Benali, Isabelle Pezron, Khashayar Saleh, Pierre Guigon, Léa Metlas-Komunjer
Format: Article
Language:English
Published: Hosokawa Powder Technology Foundation 2014-03-01
Series:KONA Powder and Particle Journal
Subjects:
Online Access:https://www.jstage.jst.go.jp/article/kona/29/0/29_2011019/_pdf/-char/en
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author Marina Langlet
Frederic Nadaud
Mohammed Benali
Isabelle Pezron
Khashayar Saleh
Pierre Guigon
Léa Metlas-Komunjer
author_facet Marina Langlet
Frederic Nadaud
Mohammed Benali
Isabelle Pezron
Khashayar Saleh
Pierre Guigon
Léa Metlas-Komunjer
author_sort Marina Langlet
collection DOAJ
description Both producers and users of divided solids regularly face the problem of caking after periods of storage and/or transport. Particle agglomeration depends not only on powder water content, temperature and applied pressure, but also on the interactions between the solid substance and water molecules present in the atmosphere, i.e. on relative humidity (RH) at which the product is stored. Ambient humidity plays an important role in most events leading to caking: capillary condensation of water at contact points between particles, subsequent dissolution of a solid and formation of a saturated solution eventually followed by precipitation of the solid during the evaporation of water. Here, we focus on the kinetics of dissolution followed by evapo-recrystallization of a hygroscopic sodium chloride powder under controlled temperature and RH, with the aim of anticipating caking by predicting rates of water uptake and loss under industrial conditions. Precise measurements of water uptake show that the rate of dissolution is proportional to the difference between the imposed RH and deliquescence RH, and follows a model based on the kinetic theory of gases. Evaporation seems to be governed by more complex phenomena related to the mechanism of crystal growth from a supersaturated salt solution.
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spelling doaj.art-2dbdcaa19b444897837a9a359add61cb2022-12-21T22:21:57ZengHosokawa Powder Technology FoundationKONA Powder and Particle Journal0288-45342187-55372014-03-0129016817910.14356/kona.2011019konaKinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative HumidityMarina Langlet0Frederic Nadaud1Mohammed Benali2Isabelle Pezron3Khashayar Saleh4Pierre Guigon5Léa Metlas-Komunjer6UTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)UTC/ESCOM, Service d’Analyses Physico-ChimiqueUTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)UTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)UTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)UTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)UTC/ESCOM, Équipe d’Accueil “Transformations Intégrées de la Matière Renouvelable” (EA 4297)Both producers and users of divided solids regularly face the problem of caking after periods of storage and/or transport. Particle agglomeration depends not only on powder water content, temperature and applied pressure, but also on the interactions between the solid substance and water molecules present in the atmosphere, i.e. on relative humidity (RH) at which the product is stored. Ambient humidity plays an important role in most events leading to caking: capillary condensation of water at contact points between particles, subsequent dissolution of a solid and formation of a saturated solution eventually followed by precipitation of the solid during the evaporation of water. Here, we focus on the kinetics of dissolution followed by evapo-recrystallization of a hygroscopic sodium chloride powder under controlled temperature and RH, with the aim of anticipating caking by predicting rates of water uptake and loss under industrial conditions. Precise measurements of water uptake show that the rate of dissolution is proportional to the difference between the imposed RH and deliquescence RH, and follows a model based on the kinetic theory of gases. Evaporation seems to be governed by more complex phenomena related to the mechanism of crystal growth from a supersaturated salt solution.https://www.jstage.jst.go.jp/article/kona/29/0/29_2011019/_pdf/-char/ensodium chloridehygroscopyknudsen lawvapor sorptioncaking
spellingShingle Marina Langlet
Frederic Nadaud
Mohammed Benali
Isabelle Pezron
Khashayar Saleh
Pierre Guigon
Léa Metlas-Komunjer
Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
KONA Powder and Particle Journal
sodium chloride
hygroscopy
knudsen law
vapor sorption
caking
title Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
title_full Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
title_fullStr Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
title_full_unstemmed Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
title_short Kinetics of Dissolution and Recrystallization of Sodium Chloride at Controlled Relative Humidity
title_sort kinetics of dissolution and recrystallization of sodium chloride at controlled relative humidity
topic sodium chloride
hygroscopy
knudsen law
vapor sorption
caking
url https://www.jstage.jst.go.jp/article/kona/29/0/29_2011019/_pdf/-char/en
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