Disclosure of Invention
The invention aims to provide a pulping process using gramineae as a raw material, which uses cheap gramineae as the raw material and adopts a mode of combining chemical liquid medicine and biological enzyme liquid medicine to carry out pulping so as to solve the problems of large pollution and difficult recovery of pulping residual liquid.
A pulping process using gramineous plants as raw materials comprises a secondary cooking step,
the cooking liquor used for the first cooking consists of the following components in percentage by mass: 5-8% of sodium hydroxide, 0.5-1.0% of sodium sulfite, 1-2.5% of sodium sulfide, 0.3-0.5% of anthraquinone, 0.02-0.1% of sodium dodecyl sulfate and the balance of water;
the cooking liquor used for the second cooking comprises enzyme liquor I and enzyme liquor II according to the mass ratio of 1-3: 1, wherein the enzyme solution I is raka lactuca (a)Irpex lacteus) After fermentation of CGMCC3.275, obtaining clarified crude enzyme liquid by separating thalli; the enzyme solution II is Inonotus crassipes (A), (B)Coriolopsis gallica) After fermentation of CICC2689, the clarified crude enzyme solution is obtained by separating thalli.
The gramineous plants of the present invention are preferably reed, wheat straw, triarrhena indica, etc.
Preferably, the cooking liquor used for the second cooking further comprises an enzyme stabilizer, and the concentration of the enzyme stabilizer is 0.5-2 mmol/L.
Preferably, the cooking liquor used for the second cooking also comprises water, and the using amount of the water is 60-300 times of that of the mixed enzyme liquor.
Preferably, the first cooking process is as follows: and (3) performing primary cooking according to the liquor ratio of 1: 3-1: 6, wherein the cooking temperature is 70-100 ℃, and the cooking time is 10-30 min.
Preferably, the second cooking process is: and (3) performing secondary cooking according to the liquid ratio of 1: 4-1: 8, wherein the cooking temperature is 55-70 ℃, and the cooking time is 10-30 min.
Preferably, the cooking liquor used in the second cooking is prepared from enzyme liquor I and enzyme liquor II according to the mass ratio of 1.3-2.5: 1, an enzyme stabilizer and water, wherein the concentration of the enzyme stabilizer in the cooking liquor is 0.5-2 mmol/L, and the using amount of the water is 100-200 times of that of the mixed enzyme solution.
Preferably, the method comprises the following process steps:
s1 preparing materials, namely cutting the gramineous plant raw materials into pieces and removing impurities;
s2, primary cooking: carrying out primary cooking according to the liquid ratio of 1: 3-1: 6, wherein the cooking temperature is 70-100 ℃, the cooking time is 10-30 min, and washing with water;
s3 secondary cooking: and (3) performing secondary cooking according to the liquid ratio of 1: 4-1: 8, wherein the cooking temperature is 55-70 ℃, the cooking time is 10-30 min, and washing with water.
The invention has the beneficial effects that: the method comprises two cooking steps, wherein the first cooking step adopts the sword-process pulping cooking liquor, the cooking liquor is used for realizing the internal permeation of the raw material, so that the raw material is swelled, and partial components such as hybrid cells, hemicellulose and the like are dissolved. And then, performing secondary cooking by using the mixed enzyme liquid, and decomposing lignin by using biological enzyme to disperse the fibers into single fibers. The process has the advantages that the alkali consumption and the enzyme consumption are both small, the waste discharge amount is reduced, the mixed enzyme cooking liquor can be repeatedly utilized, and the environment is protected; meanwhile, the process has short cooking time and good cooking effect.
Detailed Description
Enzyme solutions I described in the examples: culture medium: wort 1.0L, agar 15.0g, natural pH 12 Brix. Raking bacteria of milk white (Irpex lacteus) Inoculating CGMCC3.275 strain on slant culture medium, culturing in constant temperature incubator at 26 deg.C for 4 days, transferring to culture medium, and culturing at 26 deg.C for 3 days to obtain fermentation liquid; filtering the fermentation liquor with 0.22 micron filter membrane for sterilization to obtain the final product.
Enzyme solution II described in the examples: culture medium: 1.0L of potato extract, 20.0g of glucose and 15.0g of agar, and the pH is natural. Potato extract: removing peel of potato 200g, cutting into small pieces, adding water 1.0L, boiling for 30min, filtering to remove potato pieces, and adding filtrate to 1.0L. Prepared from Inonotus scaber (Koch.), (Coriolopsis gallica) Inoculating the CICC2689 strain on a slant culture medium, culturing for 4 days in a constant-temperature incubator at 28 ℃, then transferring to the culture medium, and culturing for 3 days at 28 ℃ to obtain a fermentation liquid; filtering the fermentation liquor with 0.22 micron filter membrane for sterilization to obtain the final product.
In the embodiment, the cooking liquor used for the second cooking is prepared from an enzyme liquor I and an enzyme liquor II according to the mass ratio of 1.3-2.5: 1, an enzyme stabilizer and water, wherein the concentration of the enzyme stabilizer in the cooking liquor is 0-2 mmol/L, and the using amount of the water is 100-200 times of that of the mixed enzyme solution.
Example 1
S1, preparing materials, namely cutting the reed raw material into pieces and removing impurities;
s2, primary cooking: carrying out primary cooking according to a liquor ratio of 1:4, wherein the cooking temperature is 80 ℃, the cooking time is 15min, and washing with water, wherein the cooking liquor comprises the following components in percentage by mass: 6% of sodium hydroxide, 0.5% of sodium sulfite, 1.6% of sodium sulfide, 0.5% of anthraquinone, 0.03% of sodium dodecyl sulfate and the balance of water;
s3 secondary cooking: and (2) carrying out secondary cooking according to a liquid ratio of 1:5, wherein the cooking temperature is 60 ℃, the cooking time is 15min, and washing is carried out, and the used cooking liquid is prepared from enzyme liquid I and enzyme liquid II according to a mass ratio of 1.3: 1 and water, wherein the amount of the water is 150 times of that of the mixed enzyme solution.
Example 2
S1, preparing materials, namely cutting the reed raw material into pieces and removing impurities;
s2, primary cooking: carrying out primary cooking according to a liquid ratio of 1:4, wherein the cooking temperature is 75 ℃, the cooking time is 20min, and washing with water, wherein the cooking liquid comprises the following components in percentage by mass: 6% of sodium hydroxide, 0.5% of sodium sulfite, 1.6% of sodium sulfide, 0.5% of anthraquinone, 0.03% of sodium dodecyl sulfate and the balance of water;
s3 secondary cooking: and (2) carrying out secondary cooking according to a liquor ratio of 1:5, wherein the cooking temperature is 55 ℃, the cooking time is 15min, and washing with water, wherein the used cooking liquor is prepared from enzyme liquor I and enzyme liquor II according to a mass ratio of 2.1: 1 and water, wherein the amount of the water is 150 times of that of the mixed enzyme solution.
Example 3
S1, preparing materials, namely cutting the reed raw material into pieces and removing impurities;
s2, primary cooking: carrying out primary cooking according to a liquid ratio of 1:5, wherein the cooking temperature is 85 ℃, the cooking time is 10min, and washing with water, wherein the cooking liquid comprises the following components in percentage by mass: 8% of sodium hydroxide, 0.6% of sodium sulfite, 2% of sodium sulfide, 0.5% of anthraquinone, 0.07% of sodium dodecyl sulfate and the balance of water;
s3 secondary cooking: and (2) carrying out secondary cooking according to the liquid ratio of 1:6, wherein the cooking temperature is 65 ℃, the cooking time is 15min, and washing with water, wherein the used cooking liquid is prepared from enzyme liquid I and enzyme liquid II according to the mass ratio of 1.5: 1, an enzyme stabilizer and water, wherein the concentration of the enzyme stabilizer (glycerol) in the cooking liquor is 1mmol/L, and the using amount of the water is 200 times of that of the mixed enzyme liquid.
Example 4
S1, preparing materials, namely cutting the reed raw material into pieces and removing impurities;
s2, primary cooking: carrying out primary cooking according to a liquid ratio of 1:5, wherein the cooking temperature is 85 ℃, the cooking time is 10min, and washing with water, wherein the cooking liquid comprises the following components in percentage by mass: 8% of sodium hydroxide, 0.6% of sodium sulfite, 2% of sodium sulfide, 0.5% of anthraquinone, 0.07% of sodium dodecyl sulfate and the balance of water;
s3 secondary cooking: and (2) carrying out secondary cooking according to a liquid ratio of 1:8, wherein the cooking temperature is 65 ℃, the cooking time is 15min, and washing with water, wherein the used cooking liquid is prepared from enzyme liquid I and enzyme liquid II according to a mass ratio of 2.3: 1, an enzyme stabilizer and water, wherein the concentration of the enzyme stabilizer (glycerol) in the cooking liquor is 1.5mmol/L, and the using amount of the water is 200 times of that of the mixed enzyme solution.
Example 5
S1 preparing materials, namely cutting the wheat straw raw material and removing impurities;
s2, primary cooking: carrying out primary cooking according to a liquid ratio of 1:3, wherein the cooking temperature is 70 ℃, the cooking time is 15min, and washing with water, wherein the cooking liquid comprises the following components in percentage by mass: 8% of sodium hydroxide, 0.6% of sodium sulfite, 2% of sodium sulfide, 0.5% of anthraquinone, 0.07% of sodium dodecyl sulfate and the balance of water;
s3 secondary cooking: performing secondary cooking according to a liquid ratio of 1:6, wherein the cooking temperature is 55 ℃, the cooking time is 20min, and washing with water, wherein the used cooking liquid is prepared from enzyme liquid I and enzyme liquid II according to a mass ratio of 1.5: 1, an enzyme stabilizer and water, wherein the concentration of the enzyme stabilizer (glycerol) in the cooking liquor is 1.5mmol/L, and the using amount of the water is 100 times of that of the mixed enzyme solution.
Comparative example 1
The procedure of example 1 was repeated, except that all of the enzyme solutions used were enzyme solution I.
Comparative example 2
The procedure of example 1 was repeated, except that all of the enzyme solutions used were enzyme solution II.
TABLE 1