Lennart Wallström

Strength and adhesion characteristics of elementary flax fibres with different surface treatments

It is known that the best flax fibres can compete in terms of mechanical properties with glass fibres. However, during the manufacturing process flax fibres are often damaged, and hence, the properties can be lowered. Furthermore, these properties change from batch to batch (depending on the time and place of harvest), which means that they are somewhat unpredictable. The most affected fibre property is strength, which can vary in very wide interval due to defects introduced by the manufacturing process. Therefore, there is a need for a simple but reliable testing procedure that allows the estimation of the strength of flax fibres, so called quality control. Regarding the final goal, that is the development of natural fibre composites, another crucial property is the fibre/matrix adhesion. The objective of this study is to investigate the possibility to use the single fibre fragmentation test to characterize strength distribution of flax fibres and to evaluate the adhesion. Untreated flax fibres and fibres coated by a special surface treatment are used. Fragmentation tests are performed on flax fibres embedded in thermoset, vinylester and polyester, resins. Results show that there is a definite improvement in interfacial strength when a fibre surface treatment is applied. Fibre strength distribution is obtained from SFFT and compared with limited results available from single flax fibre tests.

Measurement of cell wall penetration in wood of water-based chemicals using SEM/EDS and STEM/EDS technique

Summary The penetration of bulking chemicals (glycerol, PEG 200, PEG 1500 and pentaerythritol) into the cell wall of wood, Pinus sylvestris, has been studied. A number of different methods for determining the distribution of chemicals in the cell wall were used. Measurements of the increase in cell wall thickness showed that glycerol and PEG 200 resulted in greater cell wall bulking compared to PEG 1500 and pentaerythritol.Examination with SEM/EDS-linescan confirmed these results. However, the better resolution possible with the STEM/EDS-linescan revealed an inhomogenous distribution of the chemical in the cell wall. This is believed to be due to microcracks in the cell wall which are the result of the initial drying of the wood. This general damage to the cell wall could be the reason for the failure to find a stabilizing chemical and method.

Effects of an impregnation procedure for prevention of wood cell wall damage due to drying

Abstract Drying of wood may lead to readily observable macroscale cracks. Recently observations were made indicating that also at the level of cell walls, damage occurs due to drying. A method is presented where green wood is impregnated using a solution of water and a bulking compound such as glycerol. Tensile strength parallel to the grain for wood impregnated in the green state was compared with that for ordinary dried wood and for wood impregnated after drying. Data demonstrate significantly higher strength for wood impregnated in the green state. It is postulated that this is due to damage in the cell walls of non-impregnated wood where the damage is induced by the drying stresses. Support for this hypothesis is also presented in the form of fractography results. For wood impregnated in the green state, damage development during drying is limited. This is because the impregnating chemical (glycerol in the present case) in the cell wall substitutes some of the moisture and therefore limits the drying stresses.

Design and characterization of cellulose fibers with hierarchical structure for polymer reinforcement

This paper describes an approach to manufacture hierarchical composites from environmentally friendly materials by grafting cellulose whiskers onto regenerated cellulose fibers (Cordenka 700). Fourier Transform Infrared spectroscopy, Scanning Electron Microscopy and X-ray diffraction analysis were performed to verify the degree of modification. The mechanical properties of the unmodified and modified fibers were analyzed using fiber bundle tensile static and loading–unloading tests. To show the effect of cellulose whiskers grafting on the Cordenka fibers, epoxy based composites were manufactured and tensile tests done on transverse uni-directional specimens. The mechanical properties were significantly increased by fiber modification and addition of the nano-phase into composite reinforced with micro-sized fibers.

The diffusion, size and location of added silver grains in the cell walls of Swedish pine, Pinus sylvestris

Abstract The size and location of silver particles in K-glycerate/AgNO3 impregnated Swedish pine, green wood as well as high temperature dried, have been studied using TEM micrographs.The diameter of the silver particles was found to be 2–20 nm in the impregnated green wood and as large as 1000 nm (major axis) for the ellipsoid-shaped silver clusters in the impregnated dried wood. Studying the projected area of the silver particles in impregnated green wood indicated that there are a lot of particles (40%) in the compound middle lamella with fewer particles in the S2 (6–8%), S1 (4%) and S3 (2%) layers. The average distance between the silver particles, 50 nm (S2-layer), in impregnated green wood shows that the impregnant is distributed in the cell wall at the microfibrilar level. Experimental results show that the fastest diffusion path into the cell wall is from the lumen over the pit membrane through the compound middle lamella and not from the lumen through the secondary wall layer S3.

Distribution of added chemicals in the cell walls of high temperature dried and green wood of Swedish pine, Pinus sylvestris

Abstract High temperature dried and green wood of Swedish pine was impregnated with glycerate and silver nitrate. TEM and STEM/EDS on ultramicrotomed specimens was used to reveal the location of silver in the cell wall. The silver was precipitated by a new method using silver nitrate impregnated after which the wood had been impregnated with potassium glycerate. A significant difference in the distribution of the silver was observed. In the green wood, there was a homogenous distribution of the impregnant compared to the dried specimens. The inhomogenous distribution in the dried specimens is believed to be the result of damage inside the wood cell walls which in turn will have a negative effect on dimensional stabilizing results. The darker compound middle lamella observed is believed to be an artefact.