GB2172305A - Process for the chemical coloration of veneers - Google Patents

Process for the chemical coloration of veneers Download PDF

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Publication number
GB2172305A
GB2172305A GB08605700A GB8605700A GB2172305A GB 2172305 A GB2172305 A GB 2172305A GB 08605700 A GB08605700 A GB 08605700A GB 8605700 A GB8605700 A GB 8605700A GB 2172305 A GB2172305 A GB 2172305A
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GB
United Kingdom
Prior art keywords
veneers
veneer
wood
coloured
tanning substance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB08605700A
Other versions
GB8605700D0 (en
GB2172305B (en
Inventor
Margot Scheithauer
Karsten Aehlig
Rudi Wagenfuhr
Eberhard Kempe
Axel Drossig
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
WTZ HOLZVERARBEITENDE IND
Original Assignee
WTZ HOLZVERARBEITENDE IND
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Filing date
Publication date
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Publication of GB8605700D0 publication Critical patent/GB8605700D0/en
Publication of GB2172305A publication Critical patent/GB2172305A/en
Application granted granted Critical
Publication of GB2172305B publication Critical patent/GB2172305B/en
Expired legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/16Inorganic impregnating agents
    • B27K3/22Compounds of zinc or copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/16Inorganic impregnating agents
    • B27K3/26Compounds of iron, aluminium, or chromium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K5/00Treating of wood not provided for in groups B27K1/00, B27K3/00
    • B27K5/02Staining or dyeing wood; Bleaching wood

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Forests & Forestry (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)

Abstract

In a process for the chemical coloration of veneers, especially of deciduous timbers of low tanning substance content, the aim consists in achievement of a complete colour penetration of the veneer, retaining a positive stained image, under industrial conditions. For this purpose a tanning substance enrichment is achieved in deciduous timbers which guarantees a uniform absorption and distribution of active mordant substance in relatively short treatment times and a chemical colour tone development in the entire veneer cross-section. In accordance with the invention the veneers to be coloured are treated in an iron (II) salt staining bath in common with an auxiliary veneer with a mean tanning substance content of 2 to 7%. As auxiliary veneers there are considered those of the wood of the copper beech, the lime tree and/or the birch. The invention is applied in the improvement of veneers such as ash and poplar.

Description

SPECIFICATION Process for the chemical coloration of veneers The invention concerns a process for the improvement of home-grown veneers, especially from deciduous timbers of low tanning substance content, by uniform coloration throughout while maintaining the natural wood texture.
It is known to impart transparent colorations to veneer timbers. This is effected firstly by physical colour application by means of suitable dyestuff solutions, for which processes have also been developed which render possible the desired great depth of penetration of the dyestuff into the veneer. Apart from problems of colour uniformity, it becomes disturbingly noticeable above all here that, by reason of the greater absorptivity of the porous, naturally light, early wood parts, a negative image of the wood texture is obtained. The "artificial " impression caused by this circumstance even now sets close limits to the use of such coloured veneers for the design of furniture surfaces and internal decoration.
There is also the old craft of mordant treatment which consists in a colour tone development by chemical reaction of the active mordant substances pertaining to the timber predominantly with heavy metal salts. For timbers low in tanning substance there is used, in the form of what is called double staining, a twostage process in which the timber is pretreated with specific mprdant chemicals. For this purpose hydroquinone, pyrogallol, pyrocatechin, resorcin, gailic acid and tannin come under consideration. (For transference of the double-staining process on to the industrial scale mention would have to be made of the technological disadvantage that this, on account of the necessary intermediate water treatment, is a three-bath process. Intermediate drying is also sometimes carried out).
The advantage of mordant treatment is to be seen in that by reason of the higher tanning substance content in the denser parts of the wood (late wood and medullary rays) the image of the wood texture remains positive and even is intensified in desired manner.
However the main drawback consists in that the colour development takes place essentially on the surface of the timber. No adequate colour penetration occurs, so that if surface treatments (sanding) are necessary or even in the case of minor damage the unstained wood becomes visible. The deposit settling on the surface acts as covering colour which is superimposed upon and "blurs" the graining of the wood.
By reason of these disadvantages the mordant process is predominantly of interest for conifer timbers formed from thin walled wide cells, which therefore are better receptive to the chemicals.
In order to arrive at all at an acceptable colour penetration, long storage times of the impregnated wood are necessary. Thus in USSR 390,948 it is proposed to store wood veneer impregnated with pyrocatechin and ferrous sulphate for at least 36 hours in a dense stack in order to obtain a veneer which is coloured throughout.
The aim of the invention consists in achieving a complete colour penetration of veneers in deciduous timbers of low tanning substance content, while retaining a positive stained image, according to the principle of chemical colour tone development in times acceptable for industrial coloration.
The invention is based upon the problem of providing conditions for a tanning substance enrichment in deciduous timbers which guarantees a uniform absortion and distribution of active mordant substance in relatively short treatment times and a chemical colour tone development in the entire veneer cross-section.
It has been found that veneers of timbers of low tanning substance content are completely coloured throughout in a single-bath process by means of iron (II) salt in a short time if, in common with the veneers to be coloured veneers of a timber type with a mean tanning substance content of 2 to 7% are additionally introduced into the stain bath. For this purpose there may be considered veneers of the wood of the copper beech, the birch and/or the lime tree. In this way even deciduous timbers of low tanning substance content which hitherto were not available to such coloration, as for example ash or poplar, are coloured.
As iron salts there come under consideration iron (II) sulphate and Mohr's salt (ammonium ferrous sulphate) which are dissolved in relatively low concentration in the staining bath. Concentrations of 0.5 - 5 g./l. are used. In order to avoid undesired precipitations in the staining bath, the water utilised should be as soft as possible, if necessary deionised water should be used. The pH value of the aqueous is adjusted to between 2.5 and 5 by means of acid, preferably sulphuric acid. Apart from the stabilisation of the bath, the addition of the acid also serves for the control of the desired colour depth. At the higher pH values the achieved coloration becomes stronger and covers any brown tones contained in the timber.
The veneers of the timber type to be treated are set or laid into the path in common with preferably copper beech, birch or lime veneers in a suitable holding device. This can be effected for example by alternate insertion. The mass ratio of the veneer to be treated in each case to the colouring aid veneer here amounts to 1 : 2 to 4 : 1. The colouring is affected preferably in the heated bath at 30 to 80"C. and is terminated after about 2 hours with the complete colour penetration of the veneers. Just as colour depth is controllable by means of the adjustment of the pH valve, so it is also controllable by way of the bath temperature. It is here valid that, with constant pH value, darker colorations are achieved in the higher temperature range. As a result of the coloration, modern grey-brown to grey-green colour tones are obtained.No flakiness or cloudiness of the coloration occurs, the positive graining image (dark wood reflection, light soft wood) is retained.
Surprisingly it has been found that the active mordant contained substances of the wood diffuse in a short time out of the auxiliary veneer functioning as tannning substance dispenser very uniformly into the entire crosssection even of the dense deciduous timber veneers, are drawn onto the wood fibres and here, with the iron salt present from the outset in low concentration in the bath,result in a uniform colour penetration. One special advantage consists in that this action proceeds in the single-bath process, without further intermediate or after-treatments of the veneer being necessary. Obviously the wood content substances taken from the dispenser veneer are available in a form more favourable to utilisation than is the case in treatments with specific artificial chemical additives.
It is especially remarkable that the advantage achievable according to the invention again no longer occurs in the case of timbers very rich in tanning substance with tanning substance contents above 7% (for example oak veneer). In this case a superficial deposition of the formed iron-tanning substance complex occurs and the colour penetration of the veneer is disturbed. The utility of the method is therefore limited to the stated range of auxiliary veneers with tanning substance contents of 2 to 7%. The determination of the tanning substance content here takes place according to the known instruction of SANDERMANN: W. Sandermann, Fundamentals of the Chemistry and Chemical Technology of wood. Akademische Verlagsgesellschaft Geest & Portig KG, Leipzig 1956, pp.
421 - 423.
Example 1 For the coloration of ash veneers a staining bath of 1.5 g./1. FeSO4 in soft water is prepared. The pH value of the bath is adjusted to 4.5 by means of sulphuric acid. An ash veneer and a copper beech veneer (tanning substance content 3.1% determined according to SANDERMANN) are laid in alternation into a veneer insertion device.
After the bath has been heated to 40"C. the veneers are lowered into the staining bath and left therein for 2 hours without circulation of the liquid. After this time the veneers are taken from the bath, aliowed to drip and dried in the drier. The ash veneer has assumed a grey-green colour, the brown core being largely covered. A lighter grey-green tone, retaining the brown core, is obtained under the same conditions if the pH value of the staining bath is adjusted to 3.0.
Example 2 For the coloration of poplar veneers a staining bath is prepared by dissolving 5 g./1.of Mohr's salt in soft water. A pH value of 4.5 is adjusted by addition of sulphuric acid. In alternation a poplar veneer, a copper beech veneer and lime veneer are laid into a veneer insertion device. Further procedure is as in Example 1, but the bath temperature is set to 45"C. and the liquid is pumped around during the two-hour coloration operation.
The coloration of the poplar veneer obtained is brownish-grey with growth-regulated partial blueish zones

Claims (7)

1. Process for the chemical coloration of veneers of deciduous timbers of low tanning substance content by treatment of the veneers in a staining bath consisting of an aqueous solution of an iron (II) salt, characterised in that, in common with the veneers to be coloured, in addition a veneer having a mean tanning substance content of 2 to 7%, determinedby SANDERMANN's method, is put into the staining bath.
2. Process according to Claim 1, characterised in that in common with the veneers to be coloured in addition a veneer of the wood of the copper beech is inserted.
3. Process according to Claim 1, characterised in that in common with the veneers to be coloured in addition a veneer of the wood of the lime tree is inserted.
4. Process according to Claim 1, characterised in that in common with the veneers to be coloured, in addition a veneer of the wood of the birch tree is inserted.
5. Process according to Claim 1, characterised in the mass ratioof the veneer to be coloured to the additionally utilized auxiliary veneer amounts to 1 : 2 to 4: 1.
6. Process according to Claim 1, characterised in that iron (II) sulphate or ammonium ferrous sulphate in a concentration of 0.5 to 5 g./1. is used as iron (II) salt.
7. Process according to Claim 1, characterised in that the staining bath is adjusted to a pH value of 2.5 to 5. Process as claimed in claim 1, substantially as hereinbefore described.
GB08605700A 1985-03-15 1986-03-07 Process for the chemical coloration of veneers Expired GB2172305B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DD85274135A DD235433A1 (en) 1985-03-15 1985-03-15 METHOD FOR THE CHEMICAL FAIRING OF VENEERS

Publications (3)

Publication Number Publication Date
GB8605700D0 GB8605700D0 (en) 1986-04-16
GB2172305A true GB2172305A (en) 1986-09-17
GB2172305B GB2172305B (en) 1988-07-13

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ID=5566048

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08605700A Expired GB2172305B (en) 1985-03-15 1986-03-07 Process for the chemical coloration of veneers

Country Status (5)

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JP (1) JPS61263701A (en)
DD (1) DD235433A1 (en)
DE (1) DE3603865A1 (en)
GB (1) GB2172305B (en)
IT (1) IT1191256B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4570717B2 (en) * 1999-12-22 2010-10-27 中国塗料株式会社 Aqueous stain composition and substrate coloring method using the composition
WO2004018184A1 (en) * 2002-08-16 2004-03-04 Nolte-Möbel Gmbh & Co.Kg Throughput method for the mechanical covering of large, wide furniture components
DE102014100864A1 (en) * 2014-01-27 2015-07-30 Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts Coloring of wood and wood-based materials as well as corresponding wood and wood-based materials

Also Published As

Publication number Publication date
DD235433A1 (en) 1986-05-07
JPS61263701A (en) 1986-11-21
DE3603865A1 (en) 1986-09-25
GB8605700D0 (en) 1986-04-16
IT1191256B (en) 1988-02-24
IT8647739A0 (en) 1986-03-07
GB2172305B (en) 1988-07-13

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PCNP Patent ceased through non-payment of renewal fee