2003
DOI: 10.1007/s00107-003-0430-5
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Determination of surface area and pore volume of holocellulose and chemically modified wood flour using the nitrogen adsorption technique

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Cited by 52 publications
(29 citation statements)
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“…Another reason is due to the smaller size and the polarity of water molecules, which enables them to penetrate into micropores or capillaries that are usually not accessible to the larger nitrogen molecules. Similar studies by Papadopoulos et al [14] and Bismarck et al [35] showed that the dried natural fibers exhibit very small specific surface area of approximately 0.5 m 2 /g and also very small pore volumes [36]. The fibers dried by water evaporation consist of only single lamellae, which cause internal fiber structure to collapse resulting in the lower surface areas.…”
Section: Surface Characterizationmentioning
confidence: 65%
See 1 more Smart Citation
“…Another reason is due to the smaller size and the polarity of water molecules, which enables them to penetrate into micropores or capillaries that are usually not accessible to the larger nitrogen molecules. Similar studies by Papadopoulos et al [14] and Bismarck et al [35] showed that the dried natural fibers exhibit very small specific surface area of approximately 0.5 m 2 /g and also very small pore volumes [36]. The fibers dried by water evaporation consist of only single lamellae, which cause internal fiber structure to collapse resulting in the lower surface areas.…”
Section: Surface Characterizationmentioning
confidence: 65%
“…Coating and filler materials reduce the pore size and pore volume to some extent as a result of blocking the pores between the fibers on the paper surface. There are a variety of physical techniques to measure geometry of pores on the material surface that include: gas adsorption isotherms, mercury intrusion porosimetry, solute exclusion, thermoporosimetry, nuclear magnetic resonance and microscopic techniques [12,14]. In this study, nitrogen and water vapor adsorption isotherms were used for the analysis of the specific surface area, pore sizes and pore size distribution for both unmodified and modified paper samples.…”
Section: Introductionmentioning
confidence: 99%
“…Some criticisms to the use of BET gas adsorption for measuring surface area and mesoporosity of biomass and pretreated materials have been reported. The sample preparation and oven drying required for BET ana lysis may result in decreased surface area and pore volume due to collapse of pore structures during cell wall drying [19,42], thereby reducing the overall nitrogen accessible porosity [41]. For some Ammonia Fiber Expansion (AFEX™) pretreatment conditions, BET ana lysis has been shown to underestimate surface Figure 10.…”
Section: Gas Adsorption Studiesmentioning
confidence: 99%
“…Microfibrillar bands are composed with crystalline and non-crystalline regions of varying dimension. That morphological structure of cellulose was extensively studied by XRD for many years; it controls not only the access of solvents within the fibers, but also the chemical reactivity of that polymer (Papadopoulos et al, 2003;Aimin et al, 2005). However, the supramolecular structure of cellulose showed susceptibility to chemical treatments such as alkalization which modified the crystallinity of cellulose treated with sodium hydroxide (Mwaikambo and Ansell, 2002).…”
Section: Introductionmentioning
confidence: 99%