Wood chemistry,
from trunk to atom

A hard university course made clear. Dive into wood with Russian textbooks and world research as your guide.

Move the lens: this is a stained cross-section of a pine log

Seven zoom levels

Trunk10 cm

A tree grows from the outside, not the inside. A thin layer under the bark, the cambium, adds a new layer of wood every year. That is where annual rings come from.

The cambium is a lateral meristem between phloem and xylem. Outer rings form the sapwood that conducts water. In many species the inner rings become heartwood: the living parenchyma cells die and extractives accumulate there.

Annual ring1 mm

In spring the tree builds wide cells with thin walls to move water fast. In summer the walls get thicker and the openings narrower. That gives the light and dark bands of a ring.

In softwoods, earlywood tracheids are thin walled with wide lumina and mostly conduct water. Latewood tracheids are thick walled, flattened radially and carry most of the mechanical load, so latewood is markedly denser.

Tracheids50 µm

Pine and spruce wood is built almost entirely from long hollow cells called tracheids. They are dead: only the walls remain, like a honeycomb made of tubes.

Tracheids make up more than 90% of softwood volume and are typically 2-4 mm long. Neighbouring cells connect through bordered pits. In hardwoods, vessels conduct water while libriform fibres give strength.

Cell wall5 µm

The wall is layered like plywood. In each layer the cellulose threads run at their own angle. The thickest layer, S2, runs almost along the cell, and that is what makes wood strong in tension.

The middle lamella (ML) glues cells together and is rich in lignin. Then come the primary wall P and the secondary wall: S1 with microfibrils at roughly 50-70° to the cell axis, S2 at 10-30° forming the bulk of the wall, and S3 at 60-90°.

Microfibril20 nm

Zoom further and the wall looks like reinforced concrete. The rebar is thin cellulose threads, the concrete is lignin, and hemicelluloses bind the two together.

A cellulose microfibril about 3 nm thick holds roughly 18-24 parallel chains with more and less ordered regions. Hemicelluloses adsorb onto its surface; lignin fills the space between and is covalently linked to hemicelluloses in lignin-carbohydrate complexes.

Cellulose chain2 nm

Cellulose is a chain of thousands of glucose units. Each unit is flipped relative to the previous one, so the chain is straight and flat, and neighbouring chains stick together with hydrogen bonds.

Cellulose is a β-(1→4)-D-glucan with cellobiose as the 1.03 nm repeating unit. The degree of polymerisation of native wood cellulose is around 10 000. Hydrogen bonds, together with hydrophobic stacking of the chains, account for its crystallinity and insolubility in water.

Atoms0.3 nm

Underneath it all there are just three elements. About half the mass of wood is carbon, over 40% is oxygen and about 6% is hydrogen. Nitrogen and minerals are fractions of a percent.

The elemental composition of temperate woods barely depends on species: about 50% C, 6% H and 44% O; nitrogen usually 0.1% or less, ash usually below 0.5% (rarely up to 1%) of dry mass.

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What wood is made of

Two thirds of dry wood are carbohydrates, a quarter is lignin. Softwoods carry more lignin and mannans, hardwoods more xylan.

Sjöström's data for Scots pine and silver birch, % of dry wood. Softwood lignin is almost pure guaiacyl type; hardwood lignin mixes guaiacyl and syringyl units.

  • Cellulose40.0
  • Glucomannan16.0
  • Glucuronoxylan8.9
  • Other polysaccharides3.6
  • Lignin27.7
  • Extractives3.5
  • Unaccounted0.3

One square equals 1% of dry wood mass. Sjöström 1993.

Three polymers hold a tree together

Cellulose

Long straight chains of glucose packed side by side. They form the strong threads of the cell wall. Cotton is almost pure cellulose, and most paper is made mainly of it.

Linear homopolysaccharide of β-D-glucopyranose units joined by (1→4) glycosidic bonds. Chains aggregate into microfibrils of cellulose I; in wood the Iβ form dominates. Degree of polymerisation around 10 000.

monomer
D-glucose
bond
β-(1→4)
DP
~10 000
share
40-45%
Schematic, not to scale
Schematic: wall swelling exaggerated for clarity.

Water inside the wall

Freshly cut wood is full of water. First the free water leaves the cell cavities and nothing changes in size. Only when the walls start to dry does the wood shrink and crack.

Below the fibre saturation point (about 30% moisture content) water is bound to hydroxyl groups of the cell wall polymers, and losing it causes shrinkage. Tangential shrinkage is roughly twice the radial one, which is why logs check radially.

0%fibre saturation point ~30%120%
bound water
30%
free water
30%

From monomers to resins

Synthetic polymers are built the same way as natural ones: small molecules join into long chains. Plywood and particleboard are held together by such resins.

Chain (addition) polymerisation joins monomers without by-products, for example in polyvinyl acetate glue. Polycondensation releases a small molecule, usually water, as the chains grow: phenol-formaldehyde and urea-formaldehyde resins cure this way.

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What this atlas stands on

Every number on the site has a source. Russian textbooks give the course structure; international monographs and papers give the details.

Russian textbooks

  1. Азаров В.И., Буров А.В., Оболенская А.В. Химия древесины и синтетических полимеров: учебник. 2-е изд. СПб.: Лань, 2010.
  2. Лукаш А.А. Химия древесины: учебное пособие для вузов. СПб.: Лань, 2025. 129 с.
  3. Евстигнеев Э.И. и др. Химия древесины и синтетических полимеров. Ч. 1. Строение, свойства, химические реакции и производные целлюлозы: учебно-методическое пособие. СПб.: СПбГТУРП, 2010.

International monographs and research

  1. Sjöström E. Wood Chemistry: Fundamentals and Applications. 2nd ed. San Diego: Academic Press, 1993.
  2. Fengel D., Wegener G. Wood: Chemistry, Ultrastructure, Reactions. Berlin; New York: De Gruyter, 1984.
  3. Ek M., Gellerstedt G., Henriksson G. (eds.) Wood Chemistry and Wood Biotechnology. Pulp and Paper Chemistry and Technology, vol. 1. Berlin: De Gruyter, 2009.
  4. Rowell R.M. (ed.) Handbook of Wood Chemistry and Wood Composites. 2nd ed. Boca Raton: CRC Press, 2013.
  5. Ralph J. et al. Lignins: natural polymers from oxidative coupling of 4-hydroxyphenyl-propanoids. Phytochemistry Reviews 3, 29-60 (2004).
  6. Ross R.J. (ed.) Wood Handbook: Wood as an Engineering Material. General Technical Report FPL-GTR-282. Madison, WI: USDA Forest Service, Forest Products Laboratory, 2021.