Method of optical bleaching quenching on fibrous cellulose material in paper production

专利摘要:
1490077 Imidazoline derivative SANDOZ Ltd 17 Oct 1974 [19 Oct 1973] 45025/74 Heading C2C [Also in Divisions C3 D1-D2 and B1-B2] The compound of Formula IV in which n is 1, Y is -CO-NH-, X is a group of formula and the benzene rings are attached at their ppositions is prepared by reacting terephthalic acid dimethyl ester with diethylene triamine in a molar ratio of ester to amine of 1 : 8À5 or 1 : 10 with cyclization by heating. [Examples 1 and 2].
公开号:SU878203A3
申请号:SU742071223
申请日:1974-10-18
公开日:1981-10-30
发明作者:Распанти Джузеппе
申请人:Сандос Аг (Фирма)；
IPC主号:

专利说明:

(54) METHOD FOR DETERMINING OPTICAL OTBEJMBAHHH ON BOJLBKHICTOM PURPOSE MATERIAL IN PAPER PRODUCTION
one
This invention relates to optical bleaching quenching methods. fibrous cellulosic materials and may find use in papermaking.6
When using optical brighteners, such as stilbene, in paper production on a paper machine there is a large amount of bleach-10 residues, which requires periodic, time-consuming cleaning of the machine from them. Such cleaning is quite expensive and leads to a decrease in the productivity of the paper machine. It is especially undesirable to have such an appearance in cases when, after making paper with optical bleach, papermaking machine 20 switches to the production of paper that does not require the introduction of optical brighteners.
The most rational is to add to unbleached paper 25.
the mass before the ebb or after it of chemical compounds that extinguish the effect of optical brighteners. A known method of quenching the effect of optical bleaching on fibrous cellulosic material in the manufacture of paper by treating the material with acidic or ammonium salts of compounds containing a group of the formula
The compounds used according to a known method by acylation of 1 mole of triethylene tetraamine with 1 mole of phthalic, terephthalic acid or their functional derivatives are anhydrides, halides or esters. The acylation products are then cyclized to the compounds containing the imidazoline group and converted to their acid addition or quaternary ammonium salts 1. However, this method is not sufficiently intensive due to the significant residual fluorescence of the compounds used. The purpose of the invention is to intensify the quenching. The delivered chain is achieved by using salts of compounds obtained by acylation of more than 1.5 mo of polyethylene polyamine of the formula H (HN — CH — CH, j) —NHj, nz (2-S. Per 1 Mole terephthalic acid) of isophthalic acid or their functional derivatives, cyclization of the compounds containing imidazoline groups and
eng), - n
I in
X -c Ng-ZN2-H-e- /
Where
.
y-CO-NH when
or
. dn FdHg-dHgj
at
..,.,, -, RS is hydrogen or nonR,. R R.
R.
H 2 i Y is alkyl substituted by phenyl or naphthyl, R may also be a bond, if Rjj is a bond, then R5 is a group
ir if4ciH2) e
eleven
0 o
about
where
The compounds of formula 1 provide the highest maximum quenching of the bleaching effect in comparison with the known compounds for this purpose.
. To obtain a group of monomeric salts of the formulas 1 1 1, in which R means H, an excess of bo is acylated. {Hg-eHg-Wf S warheads
 ;
(I) i
Nv
uh
more than 1.5 mole of poly (polyethylene polyamine) of formula
H (nm-sn - s) -NH
2. 1
Where
for example, dystilenetriamine or triethylentetraamine on an I-mole of terephthalic acid or isophthalic acid or their functional derivatives, such as their acid halides or ester. In this case, 3 mol of polyethylene polyamine with 2 mol of phthalic acid is stoichiometrically. The resulting acylation products of cyclic residues into compounds of formula 1 containing imidazole groups. In this case, it is likely that mainly monomeric compounds of formula 34 are formed by subsequent acylation with 0.31.0 mol of aliphatic dicarboxylic acid with an alkylene group with 1-6 carbon atoms or a functional carbon dioxide derivative, and these salts are introduced in an amount of 0.05-5 weight, 7, by weight of absolutely fibrous cellulosic material. In this case, dystilene triamine is used as a polystyrene polyamine. In addition, as the aliphatic dicarboxylic acid is used. adipic acid, and as a functional derivative of carbon dioxide - phosgene or urea. The removal of material is carried out by salts of a compound of the formula n- (ny-en-c; nO „- Y-J
in which X, n
u have the indicated value.
The possibility of obtaining the compounds used according to the invention is that the compounds of formula II are converted by a known method, such as described in the prototype method, directly into acid addition salts. The compounds used according to the invention are prepared in such a way that the compounds of formula II, before they are converted to water-soluble acid addition salts, are acylated by bi-functional acylating agents. The acylation can be carried out by a bifunctional carbon-acid derivative, such as a carbon dioxide halide, for example phosgene or a carbonic ester, such as ethyl chlorocarbonate, or urea or aliphatic dicarboxylic acid with 1-6 carbon atoms, or bifunctional derivatives, such as their halides, acids, anhydrides or ester. The method of acylation by these agents is known to itself.
As an acylating agent, preference is given to adipic acid, in particular bifunctional (eHt), R - alkylene group with 1-6 carbon atoms is preferable to NH- (eHf), - 5r-o-nn-binging: Substituents in phenol nuclei Formulas III and IV are predominantly para-positioned. After intermolecular binding of the compound of formula I, acid addition occurs. To prepare a compound of formula 1, wherein at least one of the residues R, in this case substituted, is alkyl.
production, for example, adipic acid dimethyl ester. Another acylating agent is phosgene or urea.
It is known that the acylation of 1 mol of the compound of formula II with 0.62, 0, preferably 0.8-1.4, in particular about 1 mol of the acylating agent, as urea dimethyl adipic acid dimethyl ester, condenses in a solvent, for example propylene glycol , at high temperature, mainly at 150180 ° С.
In the preparation, the compounds used according to the invention are preferred with the starting product of the formula nil, where, and for which diethylenetriamine is used, since it is simple and cheap. When condensed with a bifunctional binder together with diethylenetriamine, a large amount of pure compounds are also formed, characterized by unambiguous structural formulas.
Preferred for use in the proposed method are compounds containing a returnable unit of the formula
-en, en-1g- O - - - °
 TO
Actually by the butylene group, go to the repeating unit of the formula (; n, - "n)" - n, f ".n-sheygNe-Iy-CO O) After alkylation, conversion into acid-additive salt can be performed. For quaternary, an excess of the amount of alkylcourse needed is taken. As an alkylating and / or quaternizing agent, use is made of a compound that in this case introduces alkyl groups with 1-2 carbon atoms substituted by phenyl or naphthyl, for example dimethyl sulfate, diethyl sulfate, benzyl chloride, methyl ester or ethyl ester benzene or toluene sulfonic acid, 1-chloro methylnaphthalene or -chloroethylbenzene. The salts used according to the invention contain predominantly tionic groups, which are formed as a result of acid addition or quaternization of nitrogen atoms with an alkyl group containing predominantly 1-2 carbon atoms. The anions of these salts are predominantly salts of a strong inorganic acid, for example, CJ Br, or a strong displaced organic-inorganic acid, for example, CHjSOv, and anions of benzene or toluenesulfonic acid. It, which is preferred, is C1. Used in the invention are water-soluble acid addition salts and quaternary ammonium salts used in half to a maximum of 50 times the weight of optical brighteners. In examples 1-3, possible options for obtaining the compounds used in the proposed method are described. Example 1. 194 g (1 mol) of complex dimethyl terephthalic acid zerphine are transferred to 877 h of diethylenetriamine (8.5 mol.). The mixture is heated for 1.5 h to 187 C. During this time, the distillate is collected 64 h with temperature boiling at 60-148 ° C. The distillate consists mainly of methanol. Within 30 minutes the temperature rises to 200 C. At the same time, the reaction water and excess diethylenetriamine start to be distilled off at a temperature of 160 C. As the distillation rate decreases, the temperature of the reaction mixture in for 3.5 hours rises to 225 C. After that A vacuum of 12–13 torr is created and a further distillation is carried out within one hour. In total, 758 hours of secondary distant are obtained. With nitrogen, unloading and ethylene glycol are added to the residue at 220–190 ° C. ; up to 130 ° C and 27 hours (0.45 mol) of urea are added. The ammonia formed is trapped in dilute hydrochloric acid. When gas is stopped, the reaction is heated to and the reaction mass is stirred at this temperature for 3 hours. Then it is cooled to 90-95 ° and 167 hours of 33% hydrochloric acid are added in such a way that the temperature without cooling always remains 90-100 ° C. After the addition is completed, further mixing is carried out for half an hour. Thereafter, the pH of the product is about 5.3, and it contains a solution of the hydrochloride salt of the compound in which the group of formula II is the return unit. Example 2. 194.2 h of terephthalic acid dimethyl ester at 25 C with stirring is added to 1031 h of diethylenetriamine (molar ratio 1:10). The mixture is heated under nitrogen for 3 hours to 180 ° C. During this time, 52 hours of distillate is collected with a boiling point of 80-162 ° C. The distillate consists mainly of methanol. At 187-199 C, the mixture is further stirred for 7.5 h, the reaction water being distilled off with diethylenetriamine. Excess diethylenetriamine is then removed under vacuum. 255.5 hours of product are obtained as a residue. This product is dissolved in 115 hours of propylene glycol, 26.3 urinals are added (molar ratio terephthalic acid; urea 1: 0.5) and the reaction mixture is stirred at 155-170 ° C for 2 hours. Then the exchange product is cooled to 80 ° With and during cooling it is neutralized with 211 h, 26.6% hydrochloric acid. After cooling, a 50%, slightly viscous, brown-colored solution of the hydrochloride salt of the compound is obtained, the group of the formula IV being the return unit. Example 3. Proceed according to example 1 only with the difference that to 255.5 hours of the residue, dissolved in 115 hours of propylene glycol, 74 hours of dimethyl adipate ester are added and the reaction mixture is stirred at 155-175 ° C. for 2 hours. During this time, the methanol produced by the exchange is distilled. Then the reaction product is cooled to 80 ° C and when cooled, 296 hydrochloric acid (} 9.8%) is neutralized. A 50% slightly viscous solution of the hydrochloride salt of the compound is obtained, in which the group of formula III together with the butylene group, as K. is returnable. The following is a specific implementation of the proposed method of quenching the effect of optical bleaching using compounds according to formulas 1-1 and III and IV, as well as compounds according to the prototype method. Example 4-6. A 2.5% suspension of cellulose, in which the pulp consists of 50% of bleached beech pulp and 50% of bleached sulfite pulp, is bleached with 0.1% of an optical bleach of the formula
The absorption time of the optical bleach is 10 minutes. The suspension is glued with .2% resin glue and 3% aluminum sulphate (HjO). The bleached cellulose suspension, divided into 18 separate parts, is mixed with an 18 h cellulose suspension, which contains 5 g of 1utro cellulose per 200 MP. Amounts of resin glue and aluminum sulphate are not related to the weight of the suspension bbnbg-Ing
(/ Vc-n
( her.
While stirring, 3 different pipette solutions are added to the 3 groups of 6 each.
The additive is in% of the quencher: 0.05, 0.1, 0.2, 1, 2, and the quench solid is a solid lutro-cellulose.
Consumption of the coins extinguisher to be increased to 5%.
After 5 min after the addition of the solutions, the quencher forms sheets of suppression using the Rapid-Ketten high-speed apparatus.
After pressing and drying with EO-CQ. From these sheets, the fluorescence coefficients are determined. A glued unbleached pulp sheet and a glued bleached pulp sheet are made for zero samples. In both cases, there is no additive quencher. A fluorescent photometer calibrates cellulose, and dry weight is 1utro-cellulose. When mixing 18 separate mixed parts of cellulose, they are divided into three groups of 6 hours each. To each group, solutions are added that contain a specific quencher. The three different quenchers are the hydrochloride compound of formula III, the hydrochloride compound of formula IV and the compound of the returning unit
2СНз00ч
with zero samples. The zeroing of the galvanometer is carried out with the help of a glued unbleached sheet of cellulose. After that, the bleached pulp sheet is measured and the galvanometer is calibrated to 100.
All sheets tested are measured on the front and back side. The final measured value is the calculated average value. Average values are plotted on semi-log paper depending on the amount of extinguisher used.

权利要求:
Claims (4)
[1]
The graph shows the effectiveness of quenching in all three options. Curve I - compound according to the prototype curve 2 - compound of formula III as hydrochloride, curve 3 - compound of formula IV as hydrochloride. It can be seen from the graph that the hydrochloride of the compound of formula 1I and especially the hydrochloride of the compound of formula IV has a lower residual fluorescence value than the known compounds: This indicates that the proposed quench method is more intense. Claim 1. Method of optical optical whitening on fibrous cellulosic material in papermaking with those surface treatment of an acidic additive material 1 or ammonium salts of compounds containing the formula of formula II, characterized in that the purpose of intensifying the quenching is using salts compounds obtained Kg () th U. where X- (JHj (JH | -N e, V-CO-NH with n-1 .i94te "-eH8- f.4. g) hydrogen substituted, or substituted by phenyloacylation of more than 1.5 mol of the polyethylenepolyamine of the formula: per mole terephthalic or isophthalic acid or functional derivatives, cyclization to the compounds containing imidaioline groups and subsequent acylation with 0.31, 0 mol of aliphatic dicarboxylic acid with alkylene group with 1-6 carbon atoms or functional carbon dioxide derivative, and these salts are introduced in the amount of 0 , 05-5.0 wt.% From the mass of absolutely dry fibrous center lyuloznogo material.
[2]
2. A method according to claim 1, characterized in that diethylenetriamine is used as the poly (ethylene polyamine).
[3]
3. The method according to claim 1, characterized by the fact that adipic acid is used as an aliphatic dicarboxylic acid, and phosgene or urea is used as a functional carbon dioxide derivative.
[4]
4. A method according to claim 1, characterized in that the processing of the material is carried out with compounds of the formula, Bz or naphthyl alkyl, in addition, it can be an H bond, if R is a bond, then j. is a group-d or 4 "iH,) - e where. Sources of information taken into account during the examination 1. Patent of Germany No. 1912647, cl. D 06 L 3/12, publ. 1970.
-
SOS ti g. f
Laval and go,

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IT1127312B|1979-12-21|1986-05-21|Apital Prod Ind|PROCEDURE FOR THE ELIMINATION OF THE FLUORESCENCE OF OPTICAL BANDS|

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JP4728646B2|2005-01-06|2011-07-20|大王製紙株式会社|Non-fluorescent board|

法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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CH1480873A|CH572128A5|1973-10-19|1973-10-19|

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