前苏联专利SU1429945A3 Paper, method of its production and method of production of articles from this paper

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专利摘要:
A paper material has been invented that contains cellulose substituted by means of N-methylol compounds. As N-methylol compounds may be used, e.g., reaction products of urea, glyoxal, and formaldehyde, methylolated melamines, and N-methylol-acrylamide copolymers. The paper is manufactured best by impregnating paper with an aqueous solution or dispersion of a N-methylol compound and by drying it at 130 to 200<o>C in order to produce condensation. Papers in accordance with the invention have good properties of strength against decomposition and wet strength, which properties can be adjusted readily by varying the degree of substitution or cross-linking of the cellulose. The papers are particularly well suitable, e.g., for the manufacture of plant-growing pots and corrugated fibreboard.
公开号:SU1429945A3
申请号:SU853843341
申请日:1985-01-18
公开日:1988-10-07
发明作者:Экслунд Дан；Эрккиля Юкка；Ингман Матти；Лассус Андерс；Пелтонен Кауко；Сааринен Кари
申请人:Ляннен Техтаат Ой (Фирма)；
IPC主号:

专利说明:

42)
IS5
WITH
with
4 SL
CM
i The invention relates to the pulping industry, in particular to the manufacture of paper which contains chemically substituted pulp and Can be used to make pots for plants.
The purpose of the invention is to increase the resistance of paper to rot and its moisture resistance ..
The essence of the invention is (that the paper is made from {coniferous wood pulp, replaced by an N-methylol compound JB in an amount of 1-3% by weight of the paper.; Dimethylol-dioxy-ethylene urea is used as the N-methylol compound: (DVDOEM), or mono; methylol-dioxy-ztilenemourea
(MMDOEM) or dioxyethyl urea
(DOEM), j or methylol melamine, or,
N-methylol-acetylenediamine.
The above compounds are formulated: strong bonds with cellulose.
: When cyclic N-methylol compounds are used, it is advantageous that a carbon atom placed as a neighboring atom from a nitrogen atom has an adjacent nitrogen or oxygen atom. This is the case, for example, in dimethylol dioxyethyl urea and methyl tin melamine.
The paper according to the invention is preferably made by surface treatment of ordinary paper. At high temperatures, or especially when using a long reaction time, it is recommended to apply the surface treatment in a separate block from the paper machine. In principle, it is also possible to add agents in the sizing press of a paper machine and carry out simple condensation in a separate installation.
To carry out the reaction, it is necessary to increase the temperature and evaporation of the water absorbed during the reaction. N-methylol compounds additionally require a catalyst to react with cellulose. The usual catalyst is MgCl; a suitable concentration of the catalyst is, for example, 20% by weight when calculated from the reactive compound. The temperature may be, for example, in the range of 130-200 0, preferably 140-180 s. The required condensation time depends on
Q

0
five
five
0
0
perature. If an acidic catalyst is used and the temperature is too high, then a very short condensation time is required.
By varying the concentration of the reactive agent in the solution or dispersion, it is possible to regulate the amount of the reactive agent absorbed by the paper and thereby influence the degree of resistance of the paper to decomposition. Depending on the desired degradation resistance, 1-3% of the M-methylol compound is calculated based on the dry solids content of the paper, depending on the desired dosage.
The use of difunctional or polyfunctional reagents can create cross-links, which, in addition to resistance to decomposition, also give the paper excellent moisture resistance,
The raw paper materials offered have relatively little durability, the paper can be made under quite mild conditions, and since only water-soluble or dispersible reagents are used in the manufacture, production is also convenient from the point of view of occupational health.
. The proposed paper has good resistance to decomposition and good water resistance and the degree of these properties can be easily adjusted by changing the degree of substitution of the cross-links of cellulose. N-methyl compounds also increase the dimensional stability and rigidity of paper products, which is an important advantage, for example, in the manufacture and use of corrugated fibreboard.
Paper can be used everywhere where good resistance to degradation and moisture resistance is needed, namely, in the production of packaging materials - bags, corrugated fibreboard, boxes and barrels, paper rope and, in particular, pots for plants and bases for plant digestion.
In the manufacture of paper bags, ropes, barrels and other products, it is possible either to process the paper from which the product will be made, or to give the product the necessary ready-made shape and to process the finished product. Processing is always the same
and the same: the paper is impregnated with a solution or dispersion, containing the N-methylol compound, after which suction / condensation and condensation take place, requiring the supply of heat. As an intermediate production mode, production can be considered in which the paper is soaked, dried, shaped, and then the finished product is heat treated.
In the production of all these products, it is essential that the paper sizing degree is low, which can avoid the use of rosin glues, and that the paper is made from softwood pulp. Thus, no high concentration of N-methylolol compounds is required to provide substantial resistance to decomposition. On the other hand, paper breakage and deterioration of other technical properties of the paper are avoided.
Paper that decomposes by forming holes can also be made by applying a substance containing carboxyl groups to certain areas of the paper. In these areas, the N-methylol compound reacts only with this protective substance and the cellulose will remain unsubstituted. A suitable substance is, for example, carboxyte. In this way, it also achieves a d-, sharpened projection for a medium layer of corrugated fiberboard. Corrugated glue must be water resistant. That glue, for example, is starch ns paste, to which is added a synthetic resin — urea-fiber
10 maldehyde or resorcin-formal hydna. The condensation of the N-methyl tin compound is carried out after the polishing.
As initial materials
15 corrugated cardboard it is possible to use the available facing cardboard and corrugated cardboard. It is important, however, that the degree of cardboard yarn is as far as possible.
20 lower, which makes it easier to sleep. The modern middle layer of rifled cardboard is often made from semi-chemical mass of hardwood. She, however,
25 holds an excess of carboxyl gr, which is why it is preferable that, for example, the middle layer is made from softwood (or waste paper).
30 The strength of the proposed paper is tested by fermenting it for three days in a ra- ter containing 2.5 liters of buffer thief, 25 g of Meicelase powder (e-cellulose), 0.7 g of Triton (foams
40
simethyl cellulose (CMC). Convenient to-,
use a whole solution of low in the bulk), 31 g of citric acid, bone to obtain sufficient 40 g. substance absorption. A suitable concentration of the substance is, for example, 7%.
A substance containing carboxyl groups may be added to the paper, for example, using a net cylinder. After the addition of the aqueous solution, the water is evaporated by drying. In this way, the substance adheres to the fibers and the penetration of the substance into certain places is avoided.
Using a mesh cylinder, the size and number of spots can be more easily adjusted.
In the manufacture of corrugated fibreboard that is resistant to rotting, it is preferable that both the corrugating medium (paper for corrugation) and the outer layer are treated with H-metric compound before corrugation and merging of layers with paper impregnated with DVEDA. The decomposition was also tested. Samples were taken in boxes that were ground with a pH of 4.8, conductivity 4 was the concentration of nutrients mg / l: Ca 830; K 117; F 20; Mg 2 and N 10. The boxes were kept in Potma with a relative humidity of 75%. Tensile strength was determined in accordance with the standards of the society according to the standard with the help of the Alwetron apparatus.
Example 1. Paper, prop on moehem.
The paper is impregnated with monomethyl-dioxy-55 flaxurea (urea: glyoxal aldehyde 1: 1: 1) for various concentrations of solutions, used as a lysator, by weight of resin. Then paper with
50
those. In this way, a d-, shredded sheet for the middle layer of corrugated fibreboard is also achieved. Corrugated cardboard adhesive must be waterproof. Such an adhesive, for example, is a starch paste, to which a synthetic resin is added - a urea-formaldehyde or resorcin-formaldehyde. The condensation of the N-methylol compound takes place after the corrugation.
As raw materials
5 corrugated paperboard, it is possible to use available facing paperboard and corrugated paperboard. It is important, however, that the sizing of the cardboard is as far as possible.
0 lower, which facilitates soaking. A modern middle layer of corrugated cardboard is often made from semi-chemical mass of hardwood. It, however, contains an excess of carboxyl groups, which is why, for example, the middle layer is preferably made of softwood (or possibly waste paper).
0 The strength of the proposed paper is tested by fermenting it for three days in a solution containing 2.5 l of a buffer solution, 25 g of Meicelase powder (cellulose enzyme), 0.7 g of Triton (foam,
40
cider), 31 g of citric acid, 40 g. With paper impregnated with DVDOEM, tests were also carried out for long-term decomposition. Samples were placed in boxes that were filled with earth with a pH of 4.8, conductivity 4.7, nutrient concentration, mg / l: Ca 830; K 117; F 20; Mg 283 and N 10. The boxes were kept in a Potma incubator at a relative humidity of 75%. The tensile strength was determined in accordance with the standards of the society by standards using the Alwetron apparatus.
Example 1. Paper impregnated with mosques.
The paper is impregnated for 10 with solutions of various concentrations containing monomethylol-dioxyethy- 55 lentaurea (urea: glyoxal: formaldehyde 1: 1: 1), as a catalyst is used (20% by weight of resin). Then the paper is dried
50
at 10 minutes The paper measures the increase in the weight of the gf apr. And, also, the tensile strength of both raw and dry paper before and after fermentation. The data are given in table. one.
Example 2. Paper impregnated on DNOCOEM.
i The paper is impregnated with solutions, containing: 2-8% dimethylol dioxye and lentourene (catalyst - MgCl x SH / j IB amount of 20% by weight of resin) in; for 10 s at 25 ° C and dried with j 1Q chern at. Then she is tested. For this, I paper is placed in crates full; Zempei with pH 4.8, conductivity 4.7, I nutrient concentration, mg / l: Ca 830; K 117; F 20 Mg 283 and N 10. Then the boxes are placed in a Potma incubator and kept at 1 and a relative humidity of 75%. Tensile strength is determined according to a standard using an Alwetrou apparatus. The results are shown in Table. 2 and 3 ..
Example 3. Paper impregnated with a urea-glyoxin resin (DOEM).
The paper is passed through for 10 seconds with a urea-resin resin (1: 1), and dried for 10 minutes at 150 ° C. MgCl2 6H O is used as a catalyst in the amount of 20% by weight of resin. The results are shown in table 4.
Example 4. Paper soaked in N-methylol-acrylamide.
The paper is impregnated for 10 with a solution containing water and latex in a 1: 1 ratio, the latex containing 5% methylol-acrylamide and 95% vinyl acetate, and then dried at 9 minutes.
The results are presented in table.5.
Example 5. Methylol melanin impregnated paper.
The paper is impregnated for 20 seconds with a solution that contains 80 g / l of methyl tin melamine (Kaurit M-70 Basf) and 8 r / ji MgCl; in6H, 20, and then condensation takes about 10 minutes
with leo-uo c.
The results are presented in table. 6
Example 6: Belen Pine sulphate paper, mono impregnated
1429945
5 0 5
g
g
five
0
dk-j three - or tetrameti a goal r -. n - - urea.
The resin is prepared as follows: a mixture of urea, glyoxal and formaldehyde (2: 1: 1-4) is dissolved in water to obtain a solution of 0, 5 M, the pH of which is adjusted from 8 to 9, and the mixture is kept for 5 hours
The paper is passed through for 10 seconds with a solution and dried at 10 minutes. The catalyst used in an amount of 20% by weight of the resin. The results are presented in table. 7
Example 7. Paper SR-25, dimethylol-dioxy-ethylene-urea impregnated.
Bleached sulphate pine cellulose paper SR-25 is impregnated (impregnated) with aqueous solutions containing dimethylol-dioxy-ethylene-urea and as a catalyst. The mass ratio between the reactant and the catalyst is 4i1. After drinking, the paper is dried at 160 ° C for 10 minutes.
The results are shown in Table. eight.

权利要求:
Claims (6)
[1]
1.Paper made from cellulosic fiber substituted by an N-methylol compound, a reaction product of urea, glyoxal
and formaldehyde, characterized in that, in order to increase the resistance of the paper to rotting and its moisture resistance, it contains, as cellulose fiber, softwood pulp, replaced by an N-methylol compound, in an amount of 1-3% by weight of paper.
[2]
2.Paper 1, characterized in that it contains dimethylol-dioxyethyl ethylene monogamine or monomethylol dioxyethylene urea, or dioxyethylene urea, or methylylene melamine, or N-methylol as the N-methanol compound. -atsetil e-n-dimoch yu.
[3]
3.Paper 1, characterized in that it contains areas with unsubstituted cellulose.
[4]
4. The paper making method, which includes the impregnation of a paper web made of cellulose fiber, with a solution containing the N-methyl compound, is the product of the reaction of urea, glyoxal and formaldehyde, and the catalyst is magnesium chloride, and subsequent drying at 130-1 UO C characterized in that cellulose softwood pulp is used as cell fiber.
[5]
5. The method according to claim 4, characterized by the fact that, in order to obtain paper with partially substituted fibers, before impregnation onto the paper web using a mesh cylinder

28.65
11.80
4.92
34.48
14.85
6.15
111.4
106.5
97.6
79.7 86.9 77.9
causes a 7% aqueous solution of carboxymethylcellulose.
[6]
6. A method of making paper products that involves using paper containing cellulosic fiber substituted by M-methyl tin and a compound that is a reaction product of urea, glyoxal and formaldehyde, characterized in that it uses cellulose as a fiber for paper. from coniferous wood.
Table 1
52.7 77.3 39.8
60.3 44.8 30.1
58.2 63.2 55.2
43.5
21.9
9.0
Bleached Pine Sulphate Pulp
SR 25 Same
Unbleached pine sulphate pulp
SR 25 Same
From bleached birch sulphate pulp
SR 25 Same
Unbleached birch sulphate pulp
SR 25
Also
Unbleached spruce sulphite pulp
SR 30
Also
-
T a f l to
From bleached pine sulphate cellulose SR 25
Unbleached pine sulphate pulp SR 25
Made from bleached birch sulphate pulp SR 25
From unbleached birch sulphate cellulose ss 25
From unbleached spruce sulphite pulp- SR 30
From bleached pine sulphite pulp SR 30
Bleached Pine Sulphate Pulp
SR 25 Same
Unbleached birch sulphate pulp
SR 25
59
48
51
64
25
13
13
ABOUT
78
27
18
66
50
32
Table 4
103
12
37
Bleached Middle Sulfate (No Cellulose)
ISR 25
From unbleached birch sulphate-Pus cellulose SR 25
6.95
6, 75
6, 87
8.26
96
94
72
95
Table 5
67
66
27
28
74
58
28
nineteen
Table 6
56
58
13
58
76
42
72
17
49
4.0
48
71
14
Monomethyl-Acetilen-di.) U
Table .8

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同族专利:

公开号 | 公开日

WO1984004553A1|1984-11-22|

GB8430283D0|1985-01-09|

FR2546197A1|1984-11-23|

DE3490237T1|1985-05-30|

FR2546197B1|1987-11-13|

CA1247307A|1988-12-28|

NL8420130A|1985-04-01|

SE8500195D0|1985-01-16|

IT1179667B|1987-09-16|

AU571235B2|1988-04-14|

FI831767A0|1983-05-19|

BR8406599A|1985-03-12|

ES532545A0|1986-06-01|

GB2149826A|1985-06-19|

GB2149826B|1986-10-01|

AU2960584A|1984-12-04|

US4610761A|1986-09-09|

IT8467489D0|1984-05-16|

SE8500195L|1985-01-16|

FI831767L|1984-11-20|

ES8607452A1|1986-06-01|

JPS60501317A|1985-08-15|

引用文献:

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

GB502724A|1936-07-22|1939-03-21|Scott Paper Co|Improvements in the manufacture of papers having a high wet strength|

US2407376A|1942-10-31|1946-09-10|American Cyanamid Co|Colloidally dispersed dimethylol urea resins|

DE916048C|1943-01-28|1954-08-02|Basf Ag|Process for improving the water resistance of structures which contain fibrous materials and considerable amounts of high molecular weight organic strengthening or binding agents|

US2624686A|1948-11-04|1953-01-06|Olin Mathieson|High wet-strength paper and process of making|

US3102364A|1961-07-03|1963-09-03|Pullen Molded Products Inc|Cellulosic molded transplanter pot or other products containing bagasse components|

GB1156792A|1965-07-02|1969-07-02|Courtaulds Ltd|Treatment of Fibres for Paper Making.|

GB1200683A|1967-06-28|1970-07-29|Nippon Beet Sugar Mfg|A seed tray for transplating seedlings|

FR1600269A|1968-12-31|1970-07-20|

US3858273A|1971-05-11|1975-01-07|Sun Chemical Corp|Corrugated paperboard compositions|

US3798120A|1972-04-11|1974-03-19|Kimberly Clark Co|Disposable tissue with controlled wet break-up|

CA982420A|1972-05-22|1976-01-27|Harry M. Andersen|Ethylene/vinyl chloride/n-methylolacrylamide/n-acrylamide|

US3773612A|1973-01-17|1973-11-20|Scott Paper Co|Glyoxal-acrylamide-formaldehyde-urea wet strength resin|

JPS59100793A|1982-11-24|1984-06-11|Nippon Beet Sugar Mfg|Production of pot shaped paper for growing seedling|US4731162A|1984-08-17|1988-03-15|National Starch And Chemical Corporation|Polysaccharide derivatives containing aldehyde groups for use as paper additives|

US4788280A|1987-03-19|1988-11-29|National Starch And Chemical Corporation|Polysaccharide derivatives containing aldehyde groups on an aromatic ring, their preparation from the corresponding acetals and use in paper|

FI80741C|1987-10-29|1990-07-10|Laennen Tehtaat Oy|PAPER MODIFICATION.|

FI90716C|1989-02-01|2000-01-21|Kalottinvest Oy|Wall material for the nursery comb|

JP2769656B2|1992-03-27|1998-06-25|日本甜菜製糖株式会社|Agricultural paper and its manufacturing method|

GB9216847D0|1992-08-07|1992-09-23|Vernon Packaging Ltd|Plant pot|

US5435841A|1994-05-25|1995-07-25|Henkel Corporation|Insolubilizers for binders in paper coating compositions|

JP3865506B2|1997-09-08|2007-01-10|ユニ・チャーム株式会社|Water-decomposable fiber sheet containing fibers with different fiber lengths|

JP3566044B2|1997-09-24|2004-09-15|ユニ・チャーム株式会社|Water-disintegrable fiber sheet and wiping sheet on which it is stacked|

US8076113B2|2001-04-02|2011-12-13|Danisco Us Inc.|Method for producing granules with reduced dust potential comprising an antifoam agent|

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TW202124809A|2019-09-06|2021-07-01|日商日本甜菜製糖股份有限公司|Decay-resistant paper|

法律状态:

优先权:

申请号 | 申请日 | 专利标题

FI831767A|FI831767L|1983-05-19|1983-05-19|CHEMISTRY OF PAPPER INNEHAOLLANDE SUBSTITUTES CELLULOSA.|

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