US2698233A - Redwood bark cooking process and resulting products - Google Patents
Redwood bark cooking process and resulting products Download PDFInfo
- Publication number
- US2698233A US2698233A US114459A US11445949A US2698233A US 2698233 A US2698233 A US 2698233A US 114459 A US114459 A US 114459A US 11445949 A US11445949 A US 11445949A US 2698233 A US2698233 A US 2698233A
- Authority
- US
- United States
- Prior art keywords
- bark
- redwood
- cooking
- sulfite
- per cent
- 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.)
- Expired - Lifetime
Links
- 235000003499 redwood Nutrition 0.000 title description 40
- 238000010411 cooking Methods 0.000 title description 38
- 238000000034 method Methods 0.000 title description 10
- 240000005020 Acaciella glauca Species 0.000 title 1
- 239000003513 alkali Substances 0.000 claims description 18
- 238000009413 insulation Methods 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 241001138418 Sequoia sempervirens Species 0.000 description 40
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 32
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 28
- 235000010265 sodium sulphite Nutrition 0.000 description 14
- 239000000428 dust Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000002657 fibrous material Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000000835 fiber Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 238000005553 drilling Methods 0.000 description 3
- 239000002198 insoluble material Substances 0.000 description 3
- 238000011835 investigation Methods 0.000 description 3
- 239000002195 soluble material Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- -1 methoxyl groups Chemical group 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000009048 phenolic acids Nutrition 0.000 description 2
- 150000007965 phenolic acids Chemical class 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical class [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000017343 Quebracho blanco Nutrition 0.000 description 1
- 241000065615 Schinopsis balansae Species 0.000 description 1
- 241001116459 Sequoia Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229940085805 fiberall Drugs 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000020323 palazzo Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21J—FIBREBOARD; MANUFACTURE OF ARTICLES FROM CELLULOSIC FIBROUS SUSPENSIONS OR FROM PAPIER-MACHE
- D21J1/00—Fibreboard
Definitions
- the present invention relates generally to the treatmer t of redwood bark or its components made up of redwood bark fibrous material and redwood bark dust. More specifically, the present invention relates to an improved cookingprocess and includes within its scope the 0 resulting modified redwood bark products.
- the bark contains a relatively high percentage of complex chemicals (as evidenced by the resistance of the redwood tree to decay) and is made up of about equal proportions of redwoodbark'fibrous material and redwood bark dust containing unique high molecular weight phenolic acids characterized bytheir'relatively high con tent of acidic carboxyl groups and negligible content of methoxyl groups. While the disposal of the bark has been a problem in the redwood lumber industry for many years, up until the time of the present invention no proposed solution'providingfor the use of both the bark 9 fibrous material and bark dust hadproven commercially practical.
- the principal object of the present invention is to pro vide the art with novel product's having utility in various fields by a commercially practical process involving the treatment of redwood bark;
- The'prccess comprises the cooking of the redwoodb'ark, preferably in the form of chips or other comminuted form, in an aqueous alkali sulfite (e. g. sodium sulfite or bisulfite) cooking liquor until the bark acids are solubilized and the separation of the resulting insoluble fibrous material from the cooking liquor.
- the fibrous material made up of the insolubles contains along with the bark fiber short cells insoluble in the cooking liquor together with lignin and pectin-like material which has been modified by the sulfite cooking treatment, as well as other insoluble chemicals.
- the cooking liquor made up of the solubles contains the soluble chemicals which have been modified by the sulfite cooking treatment including alkali salts of sulfonated redwood bark organic acids.
- the fibrous material which contains all of the insolubles i. e. the alkali sulfite digested redwood bark pulp
- a board two inches thick may be made from the bark pulp, for example, which will weigh less than two pounds per square foot, i. e. have a density of only about ten pounds per cubic foot.
- a board of this type will have a transverse breaking strength of about 40-80 pounds per square inch and will show a deformation of not more than 5 per cent under a loading of 200 pounds per square foot and will regain, on release of pressure, all but about 1.5 per cent.
- the heat transmission of a board of this type is also of the low value desired in the insulation field, as the coefficient of thermal conductivity or k factor (B. t. u. in./hr. ft. deg. F.) is around 0.285.
- k factor B. t. u. in./hr. ft. deg. F.
- Example About parts by weight of redwood bark chips is first placed in a digester. About 500 parts of cooking liquor made up of Water containing about 15 parts 'of sodium sulfite in solution is then added to the bark. The resulting mixture is then cooked at a temperature of about C. for about 1.5 hours. At the end of the cooking period the digester is discharged into the blow pit where the sodium sulfite digested redwood bark pulp is separated from the cooking liquor. The cooking liquor containing the sodium sulfite digested redwood bark soluble's and made up for the most part of sodium salts of the sulfonated redwood bark acids, is evaporated to a solid content of about 2025 per cent and then spray dried. Before use the fibrous pulp is preferably washed with water and the washings recovered and used to make up the liquor for the next cooking operation.
- the ratio of liquor to solids is about 5:1, that other ratios may be employed. Sufficient water should, of course, be used to bring the cooking liquor containing the sulfite salt into contact with the bark. It will also be understood in the above example where the ratio of bark to the sulfite salt is around 6.6:1 that other ratios may be employed. Invest'igations, however, show that this ratio should not be greater than about 20:1, i. e. that at least about 5 per cent sulfite salt should be used based on the weight of the bark. in most cases the use of 10-20 per cent sodium sulfite based on the weight of the bark is preferred. Larger amounts of sulfite salt, however, may be used if desired, although the use of excessive material over and above about 25 per cent sulfite salt based on the weight of the bark does not result in an improvement in the properties of the reaction products.
- the cooking temperatures and times may be varied with the lower cooking temperatures requiring longer cooking periods and the higher cooking temperatures requiring shorter cooking periods. Investigations in this connection show that for most commercial operations a temperature range of about 90-170" C. is satisfactory for carrying out the cooking operation.
- the use of temperatures below 90 C. requires relatively long cooking periods before the chemicals to be solubilized are solubilized (at which time the bark structure disintegrates upon working), while the use of temperatures above C. tends to deleteriously affect the desired properties of the reaction products.
- alkali sulfite salts such as the alkali metal, e. g. potassium, and ammonium sulfites or bisulfites may be used.
- a bisulfite salt is used as the alkali sulfite salt in place of a salt such as sodium sulfite, more salt is required to sulfonate and solubilize the bark chemicals, i. e. achieve the same degree of cooking.
- the solubility of the alkali sulfite salts in water is an essential characteristic of the sulfite reaction product.
- the alkali sulfite salts may also be used in combination with alkali metal hydroxides, one of the preferred reaction mixtures being made up of per cent sodium hydroxide and per cent sodium sulfite based on the weight of the bark.
- the bark pulp produced by the present invention may be made into insulation board as indicated above or be combined with other materials.
- a satisfactory board may be made by mixing about per cent of bark pulp with 50 per cent of plastic redwood pulp produced in accordance with the process described in U. S. Patent 2,392,162.
- a board made up of this combination has just as good a k factor and compression property as a per cent alkali sulfite digested redwood bark pulp board and will have a somewhat better transverse strength. Sawdust without any added resins, etc. may also be used in place of the plastic pulp.
- a board made up of this combination exhibits a better compression but has a somewhat reduced transverse strength and the k factor goes up to about 0.32.
- a blending agent of loose fill insulation made up of redwood bark fiber separated mechanically from redwood bark slabs may also be used in place of the plastic pulp or sawdust.
- a board made up of this combination (50 per cent alkali sulfite digested redwood bark pulp and 50 per cent uncooked redwood bark fiber) has a. k factor around 0.285, a transverse strength between the sawdust and plastic pulp boards, but a somewhat pooror compression property.
- the remaining bark dust which makes up about 50 Q per cent of the bark may be cooked in the alkali sulfite cooking liquor as described in the above example.
- the preferred cooking conditions C. for about 1.5 hours) are the same except that about 20 per cent sodium sulfite based on the weight of the dust is employed due to the relatively high concentration of chemicals (phenolic acids) in the dust.
- the cooking liquor obtained is substantially the same as the liquor obtained on cooking the whole bark and may be used as indicated above in the drilling mud additive field.
- the cooking liquor is separated from any insoluble material and then preferably evaporated to a solid content of about 20-25 per cent and spray dried.
- the insulation boards produced with the alkali sulfite digested redwood bark pulp of the present invention may be sized with wax emulsions or a variety of petroleum sizes or with rosin sizes. Investigations have shown a sized board after fifteen days immersion in water to pick up less than 25 per cent by volume of water. With a ten per cent rosin size the water pickup on immersion for fifteen days has been found to be not greater than 20 volume per cent.
- the present invention provides a commercially practical process for treating redwood bark. It solves the bark disposal problem and provides the art with novel redwood bark derivatives of value in the insulation and drilling mud additive fields.
- a process which comprises cooking redwood bark in an aqueous alkali sulfite liquor containing at least about 5 per cent sulfite salt based on the weight of the bark, at a temperature of about 90-170 C. until the redwood bark acids are solubilized.
- a process which comprises cooking comminuted redwood bark in an aqueous sodium sulfite liquor containing about 10-20 per cent sulfite salt based on the weight of the bark, at a temperature of about 90l70 C., and separating the sodium sulfite digested redwood bark pulp containing all of the insoluble material from the cooking liquor containing the sodium sulfite digested redwood bark solubles.
- a process of making alkali sulfite digested redwood bark solubles consisting essentially of alkali salts of sulfonated redwood bark acids which comprises cooking redwood bark dust in an aqueous alkali sulfite liquor containing at least about 20 per cent sulfite salt based on the weight of the dust at a temperature of about 90-170" C. until the bark dust acids are solubilized.
- an insulation board comprising consolidated alkali sulfite digested redwood bark pulp.
Landscapes
- Paper (AREA)
Description
REDWOGD BARK COOKING PRQCEEES AND RESULTING PRODUCTS Harry F. Lewis and ltlarion A. Buchanan, Appleton, Wis,
assignors to The Pacific Lumber Company, San-Francisco, Calif., a corporation of Maine No Drawing. Application September 7, 1949, den a N 1. 5
5. Claims. (Cl, 92-.3)
The present invention relates generally to the treatmer t of redwood bark or its components made up of redwood bark fibrous material and redwood bark dust. More specifically, the present inventionrelates to an improved cookingprocess and includes within its scope the 0 resulting modified redwood bark products.
Bark from the California redwood, i. e. a soft wood or conifer known as Sequoia sempervirelis, has 'for the most part been considered a waste material of little economic value. The bark contains a relatively high percentage of complex chemicals (as evidenced by the resistance of the redwood tree to decay) and is made up of about equal proportions of redwoodbark'fibrous material and redwood bark dust containing unique high molecular weight phenolic acids characterized bytheir'relatively high con tent of acidic carboxyl groups and negligible content of methoxyl groups. While the disposal of the bark has been a problem in the redwood lumber industry for many years, up until the time of the present invention no proposed solution'providingfor the use of both the bark 9 fibrous material and bark dust hadproven commercially practical.
The principal object of the present invention is to pro vide the art with novel product's having utility in various fields by a commercially practical process involving the treatment of redwood bark;
Other objects of the present invention will be apparent as the description proceeds hereinafter.
We have discovered a commercially practical process for treating redwood bark in which all of the materials in the bark are converted to products or compositions having utility in various fields. The'prccess comprises the cooking of the redwoodb'ark, preferably in the form of chips or other comminuted form, in an aqueous alkali sulfite (e. g. sodium sulfite or bisulfite) cooking liquor until the bark acids are solubilized and the separation of the resulting insoluble fibrous material from the cooking liquor. The fibrous material made up of the insolubles contains along with the bark fiber short cells insoluble in the cooking liquor together with lignin and pectin-like material which has been modified by the sulfite cooking treatment, as well as other insoluble chemicals. The cooking liquor made up of the solubles contains the soluble chemicals which have been modified by the sulfite cooking treatment including alkali salts of sulfonated redwood bark organic acids.
We have discovered that the fibrous material which contains all of the insolubles, i. e. the alkali sulfite digested redwood bark pulp, can be readily converted by standard means and without the addition of resins, adhesives, etc. into insulation board possessing very desirable strengths and other properties. A board two inches thick may be made from the bark pulp, for example, which will weigh less than two pounds per square foot, i. e. have a density of only about ten pounds per cubic foot. A board of this type will have a transverse breaking strength of about 40-80 pounds per square inch and will show a deformation of not more than 5 per cent under a loading of 200 pounds per square foot and will regain, on release of pressure, all but about 1.5 per cent. The heat transmission of a board of this type is also of the low value desired in the insulation field, as the coefficient of thermal conductivity or k factor (B. t. u. in./hr. ft. deg. F.) is around 0.285. (For a reference to k, see Low Temperature Insulation, Physical Properties-Test Data, published by the Cork Insulation Man- 2,698,233 Patented Dec. 28, 1954 ufacture)s Association, A. I. A. File No. 37-B4, page 8, 1937 We have also discovered that the soluble material in the cooking liquor, i. e. the alkali sulfite digested redwood bark solubles, is particularly adaptable for use as an addi-' tive for oil well drilling muds. Investigations have shown, for example, that the soluble material in the liquor'm'ay be used to control viscosity, water loss and gel strength in ordinary muds as well as in lime-base muds, e. g. muds with a pH around 1l 12. This latter characteristic isunexpected as quebracho is not adaptable for use in limehase muds and redwood bark chemicals which have not been sulfonated, i. e. subjected to the sulfite cooking treatment, are not generally adaptable for use at pH values above 10. While concentrates of the cooking liquor may be used, for most purposes it is preferred to isolate the soluble solid material by evaporating the cooking liquor and then spray drying. Where the free acids are desired in place of the salts, they may be readily obtained by running an aqueous solution of the, salts through an ion exchange column.
The following example of a preferred method of operation will serve to illustrate the present invention.
Example About parts by weight of redwood bark chips is first placed in a digester. About 500 parts of cooking liquor made up of Water containing about 15 parts 'of sodium sulfite in solution is then added to the bark. The resulting mixture is then cooked at a temperature of about C. for about 1.5 hours. At the end of the cooking period the digester is discharged into the blow pit where the sodium sulfite digested redwood bark pulp is separated from the cooking liquor. The cooking liquor containing the sodium sulfite digested redwood bark soluble's and made up for the most part of sodium salts of the sulfonated redwood bark acids, is evaporated to a solid content of about 2025 per cent and then spray dried. Before use the fibrous pulp is preferably washed with water and the washings recovered and used to make up the liquor for the next cooking operation.
It will be understood in the above example, where the ratio of liquor to solids is about 5:1, that other ratios may be employed. Sufficient water should, of course, be used to bring the cooking liquor containing the sulfite salt into contact with the bark. It will also be understood in the above example where the ratio of bark to the sulfite salt is around 6.6:1 that other ratios may be employed. Invest'igations, however, show that this ratio should not be greater than about 20:1, i. e. that at least about 5 per cent sulfite salt should be used based on the weight of the bark. in most cases the use of 10-20 per cent sodium sulfite based on the weight of the bark is preferred. Larger amounts of sulfite salt, however, may be used if desired, although the use of excessive material over and above about 25 per cent sulfite salt based on the weight of the bark does not result in an improvement in the properties of the reaction products.
The cooking temperatures and times may be varied with the lower cooking temperatures requiring longer cooking periods and the higher cooking temperatures requiring shorter cooking periods. Investigations in this connection show that for most commercial operations a temperature range of about 90-170" C. is satisfactory for carrying out the cooking operation. The use of temperatures below 90 C. requires relatively long cooking periods before the chemicals to be solubilized are solubilized (at which time the bark structure disintegrates upon working), while the use of temperatures above C. tends to deleteriously affect the desired properties of the reaction products.
In place of sodium sulfite used in the above example, other alkali sulfite salts such as the alkali metal, e. g. potassium, and ammonium sulfites or bisulfites may be used. When a bisulfite salt is used as the alkali sulfite salt in place of a salt such as sodium sulfite, more salt is required to sulfonate and solubilize the bark chemicals, i. e. achieve the same degree of cooking. The solubility of the alkali sulfite salts in water is an essential characteristic of the sulfite reaction product. The alkali sulfite salts may also be used in combination with alkali metal hydroxides, one of the preferred reaction mixtures being made up of per cent sodium hydroxide and per cent sodium sulfite based on the weight of the bark.
The bark pulp produced by the present invention, and which contains in addition to the fiber all of the materials remaining insoluble after the sulfite cook, may be made into insulation board as indicated above or be combined with other materials. A satisfactory board, for example, may be made by mixing about per cent of bark pulp with 50 per cent of plastic redwood pulp produced in accordance with the process described in U. S. Patent 2,392,162. A board made up of this combination has just as good a k factor and compression property as a per cent alkali sulfite digested redwood bark pulp board and will have a somewhat better transverse strength. Sawdust without any added resins, etc. may also be used in place of the plastic pulp. A board made up of this combination exhibits a better compression but has a somewhat reduced transverse strength and the k factor goes up to about 0.32. A blending agent of loose fill insulation made up of redwood bark fiber separated mechanically from redwood bark slabs may also be used in place of the plastic pulp or sawdust. A board made up of this combination (50 per cent alkali sulfite digested redwood bark pulp and 50 per cent uncooked redwood bark fiber) has a. k factor around 0.285, a transverse strength between the sawdust and plastic pulp boards, but a somewhat pooror compression property. Where the redwood bark fiber is mechanically separated from the bark and used as above, the remaining bark dust which makes up about 50 Q per cent of the bark, may be cooked in the alkali sulfite cooking liquor as described in the above example. The preferred cooking conditions C. for about 1.5 hours) are the same except that about 20 per cent sodium sulfite based on the weight of the dust is employed due to the relatively high concentration of chemicals (phenolic acids) in the dust. The cooking liquor obtained is substantially the same as the liquor obtained on cooking the whole bark and may be used as indicated above in the drilling mud additive field. As in the example, after the bark dust chemicals are solubilized, the cooking liquor is separated from any insoluble material and then preferably evaporated to a solid content of about 20-25 per cent and spray dried.
The insulation boards produced with the alkali sulfite digested redwood bark pulp of the present invention may be sized with wax emulsions or a variety of petroleum sizes or with rosin sizes. Investigations have shown a sized board after fifteen days immersion in water to pick up less than 25 per cent by volume of water. With a ten per cent rosin size the water pickup on immersion for fifteen days has been found to be not greater than 20 volume per cent.
The present invention provides a commercially practical process for treating redwood bark. It solves the bark disposal problem and provides the art with novel redwood bark derivatives of value in the insulation and drilling mud additive fields.
We claim:
1. A process which comprises cooking redwood bark in an aqueous alkali sulfite liquor containing at least about 5 per cent sulfite salt based on the weight of the bark, at a temperature of about 90-170 C. until the redwood bark acids are solubilized.
2. A process which comprises cooking comminuted redwood bark in an aqueous sodium sulfite liquor containing about 10-20 per cent sulfite salt based on the weight of the bark, at a temperature of about 90l70 C., and separating the sodium sulfite digested redwood bark pulp containing all of the insoluble material from the cooking liquor containing the sodium sulfite digested redwood bark solubles.
3. In a process of preparing alkali sulfite digested redwood bark pulp and alkali sulfite digested redwood bark solubles, the steps which comprise cooking redwood bark chips in an aqueous sodium sulfite liquor in which the liquor to solid ratio is about 5:1 and the bark to sodium sulfite ratio is about 6.6:1, for about 1.5 hours at about 160 C., and then separating the bark pulp containing the insoluble material from the cooking liquor containing the soluble material.
4. A process of making alkali sulfite digested redwood bark solubles consisting essentially of alkali salts of sulfonated redwood bark acids, which comprises cooking redwood bark dust in an aqueous alkali sulfite liquor containing at least about 20 per cent sulfite salt based on the weight of the dust at a temperature of about 90-170" C. until the bark dust acids are solubilized.
5. As an article of manufacture, an insulation board comprising consolidated alkali sulfite digested redwood bark pulp.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 49,209 Allen Aug. 8, 1865 51,810 DeGogorza Jan. 2, 1866 1,229,422 Drewsen June 12, 1917 1,244,525 Marusawa Oct. 30, 1917 1,468,036 Shaw Sept. 18, 1923 1,828,243 Darling Oct. 20, 1931 1,959,734 Palazzo et a1. May 22, 1934 2,301,561 MacMullen et a1 Nov. 10, 1942 2,345,339 McClellen et al Mar. 28, 1944 2,476,845 Dawson July 19, 1949 OTHER REFERENCES Lewis et al., Ind. Eng. Chem., vol. 36, No. 8, pp. 759-764 (p. 760 pertinent).
Chem. Abstracts, vol. 39, 1285 1945, Yaichnikova, abstr. of Russ. Pat. 58.592.
Claims (1)
- 5. AS AN ARTICLE OF MANUFACTURE, AN INSULATION BOARD COMPRISING CONSOLIDATED ALKALI SULFATE DIGESTED REDWOOD BARK PULP.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US114459A US2698233A (en) | 1949-09-07 | 1949-09-07 | Redwood bark cooking process and resulting products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US114459A US2698233A (en) | 1949-09-07 | 1949-09-07 | Redwood bark cooking process and resulting products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2698233A true US2698233A (en) | 1954-12-28 |
Family
ID=22355335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US114459A Expired - Lifetime US2698233A (en) | 1949-09-07 | 1949-09-07 | Redwood bark cooking process and resulting products |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2698233A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2831022A (en) * | 1952-08-12 | 1958-04-15 | Rayonier Inc | Aromatic hydroxy sulfonate derivatives and products and processes of making the same |
| US2901429A (en) * | 1956-04-17 | 1959-08-25 | Lignosol Chemicals Ltd | Drilling fluids |
| US2962413A (en) * | 1956-10-19 | 1960-11-29 | Ernest R Hatheway | Method of producing cellulosic pulp |
| US2964469A (en) * | 1957-03-01 | 1960-12-13 | Rayonier Inc | Drilling mud compositions |
| US2999108A (en) * | 1957-10-07 | 1961-09-05 | Rayonier Inc | Bark treatment process and product |
| US3245869A (en) * | 1962-11-30 | 1966-04-12 | Weyerhaeuser Co | Tree bark fiber and process for its preparation |
| US3350261A (en) * | 1966-05-12 | 1967-10-31 | Weyerhaeuser Co | Paper stiffened with bark extractives and method of making the same |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US49209A (en) * | 1865-08-08 | Improvement in the manufacture of paper | ||
| US51810A (en) * | 1866-01-02 | deming | ||
| US1229422A (en) * | 1917-02-27 | 1917-06-12 | Viggo Drewsen | Process of making fiber for paper, &c. |
| US1244525A (en) * | 1917-08-02 | 1917-10-30 | Tsuneya Marusawa | Process of manufacturing paper-pulp. |
| US1468036A (en) * | 1923-09-18 | Redwood-bark wall board | ||
| US1828243A (en) * | 1929-12-16 | 1931-10-20 | Cornstalk Products Company Inc | Pulping farm wastes |
| US1959734A (en) * | 1931-04-22 | 1934-05-22 | Palazzo Francesco Carlo | Process for producing practically pure cellulose (alpha-cellulose) from raw cellulose of any origin |
| US2301561A (en) * | 1941-02-18 | 1942-11-10 | Rohm & Haas | Sulphonated isophorones |
| US2345339A (en) * | 1943-07-05 | 1944-03-28 | Hodaly Emerick | Combined comb and nail file |
| US2476845A (en) * | 1946-06-07 | 1949-07-19 | Shell Dev | Fluid for drilling wells |
-
1949
- 1949-09-07 US US114459A patent/US2698233A/en not_active Expired - Lifetime
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US49209A (en) * | 1865-08-08 | Improvement in the manufacture of paper | ||
| US51810A (en) * | 1866-01-02 | deming | ||
| US1468036A (en) * | 1923-09-18 | Redwood-bark wall board | ||
| US1229422A (en) * | 1917-02-27 | 1917-06-12 | Viggo Drewsen | Process of making fiber for paper, &c. |
| US1244525A (en) * | 1917-08-02 | 1917-10-30 | Tsuneya Marusawa | Process of manufacturing paper-pulp. |
| US1828243A (en) * | 1929-12-16 | 1931-10-20 | Cornstalk Products Company Inc | Pulping farm wastes |
| US1959734A (en) * | 1931-04-22 | 1934-05-22 | Palazzo Francesco Carlo | Process for producing practically pure cellulose (alpha-cellulose) from raw cellulose of any origin |
| US2301561A (en) * | 1941-02-18 | 1942-11-10 | Rohm & Haas | Sulphonated isophorones |
| US2345339A (en) * | 1943-07-05 | 1944-03-28 | Hodaly Emerick | Combined comb and nail file |
| US2476845A (en) * | 1946-06-07 | 1949-07-19 | Shell Dev | Fluid for drilling wells |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2831022A (en) * | 1952-08-12 | 1958-04-15 | Rayonier Inc | Aromatic hydroxy sulfonate derivatives and products and processes of making the same |
| US2901429A (en) * | 1956-04-17 | 1959-08-25 | Lignosol Chemicals Ltd | Drilling fluids |
| US2962413A (en) * | 1956-10-19 | 1960-11-29 | Ernest R Hatheway | Method of producing cellulosic pulp |
| US2964469A (en) * | 1957-03-01 | 1960-12-13 | Rayonier Inc | Drilling mud compositions |
| US2999108A (en) * | 1957-10-07 | 1961-09-05 | Rayonier Inc | Bark treatment process and product |
| US3245869A (en) * | 1962-11-30 | 1966-04-12 | Weyerhaeuser Co | Tree bark fiber and process for its preparation |
| US3350261A (en) * | 1966-05-12 | 1967-10-31 | Weyerhaeuser Co | Paper stiffened with bark extractives and method of making the same |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4186242A (en) | Preparation of a lignocellulosic composite | |
| US2698233A (en) | Redwood bark cooking process and resulting products | |
| US4193814A (en) | Binding lignocellulosic materials | |
| US2379889A (en) | Etherification of lignins and ligninlike material | |
| US2674575A (en) | Well drilling composition | |
| US1873056A (en) | Manufacture of fibrous articles | |
| US3062783A (en) | Reaction products of polymethylol phenol and sulfited tannins | |
| Blankenhorn et al. | Compressive strength of hardwood-cement composites | |
| US2528350A (en) | Two-step digestion of hardwoods | |
| US2674594A (en) | Alkali-metal sulfite-digested redwood bark solubles | |
| US3931070A (en) | Plywood adhesive | |
| US2381205A (en) | Molding powder and method of making same | |
| US2247204A (en) | Method of producing moldable lignocellulose and product thereof | |
| US2664377A (en) | Method of impregnating and laminating fibrous materials with lignin | |
| US4127544A (en) | Process for the partial substitution of ammonium lignosulfonate for phenol in phenolic-aldehyde resin adhesives | |
| Schwerin | The chemistry of reaction wood. Part II. The polysaccharides of Eucalyptus goniocalyx and Pinus radiata | |
| DE1569945A1 (en) | Phenolic resin adhesives containing extenders | |
| US2303345A (en) | Process of making predominantly plastic material and tough products thereof from lignocellulose | |
| US2528351A (en) | Alkaline sulfite digestion of hardwood | |
| US2319951A (en) | Thermoplastic lignocellulosic product and method of making the same | |
| US2292390A (en) | Method of treating lignocellulosic material to produce moldable products | |
| US2773847A (en) | Bark components as resin ingredients | |
| US2698307A (en) | Adhesive or molding composition comprising brown rotted wood and phenolformaldehye resin | |
| US3758377A (en) | Treated paper sheet | |
| US1859846A (en) | Wood pulp and process of making the same |