Increasing Softwood Pulp Yield by Minimizing Primary Peeling of Wood Carbohydrates Using Sodium Methyl Mercaptide Before and During Kraft Pulping

The objective of this work was to determine the effect of sodium methyl mercaptide (SMM) on the minimization of peeling reactions of southern pine chips in the kraft pulping process. Two methods were evaluated for SMM addition to the pulping process: 1) pre-treatment before pulping or 2) co-addition with white liquor. The effect of SMM charge, pre-treatment temperature and time, and pH of pre-treatment liquor was studied. The experimental results showed about 1.5 to 2.5 % (on O.D. (oven dry) wood basis) increase in the pulp yield after pre-treatment with or co-addition of 4.38% SMM (on O.D. wood basis). The use of 4.38% SMM allowed a decrease of the white liquor effective alkali charge (EA, on O.D. wood basis) by 3%. 4.38% SMM charge seemed to be optimum for the pre-treatment. Pre-treatment at lower pH resulted in a significant decrease in yield and an increase in rejects. The increase in pulp yield was mostly due to the increased retention of cellulose and xylan. The retention of galactoglucomannan was negligible. About 80% of the cellulose yield increase is due to the suppression of primary peeling. The remainder (0.3–0.4% of the yield increase (on O.D. wood basis) is due to reduced alkaline hydrolysis and subsequent secondary peeling.

Effect on Silt Capillary Water Absorption upon Addition of Sodium Methyl Silicate (SMS) and Microscopic Mechanism Analysis

Silt has the characteristics of developed capillary pores and strong water sensitivity, and capillary water is an important factor inducing the erosion and slumping of silt sites. Therefore, in order to suppress the effect of capillary water, this article discusses the improvement effect of sodium methyl silicate (SMS) on silt. The effect was investigated by capillary water rise testing and contact angle measurement, and the inhibition mechanism is discussed from the microscopic view by X-ray diffraction (XRD) testing, X-ray fluorescence (XRF) testing, scanning electron microscope (SEM) testing and mercury intrusion porosimetry (MIP) testing. The results show that SMS can effectively inhibit the rise of capillary water in silt, the maximum height of capillary rise can be reduced to 0 cm when the ratio of SMS (g) to silt (g) increases to 0.5%, and its contact angle is 120.2°. In addition, considering also the XRD, XRF, SEM and MIP test results, it is considered that SMS forms a water-repellent membrane by reacting with water and carbon dioxide, which evenly distribute on the surface of silt particles. The membrane reduces the surface energy and enhances the water repellence of silt, and combines with small particles in the soil, reduces the number of 2.5 μm pores and inhibits the rise of capillary water.

Importance of sulfate radical anion formation and chemistry in heterogeneous OH oxidation of sodium methyl sulfate, the smallest organosulfate

Organosulfates are important organosulfur compounds present in atmospheric particles. While the abundance, composition, and formation mechanisms of organosulfates have been extensively investigated, it remains unclear how they transform and evolve throughout their atmospheric lifetime. To acquire a fundamental understanding of how organosulfates chemically transform in the atmosphere, this work investigates the heterogeneous OH radical-initiated oxidation of sodium methyl sulfate (CH3SO4Na) droplets, the smallest organosulfate detected in atmospheric particles, using an aerosol flow tube reactor at a high relative humidity (RH) of 85 %. Aerosol mass spectra measured by a soft atmospheric pressure ionization source (direct analysis in real time, DART) coupled with a high-resolution mass spectrometer showed that neither functionalization nor fragmentation products are detected. Instead, the ion signal intensity of the bisulfate ion (HSO4−) has been found to increase significantly after OH oxidation. We postulate that sodium methyl sulfate tends to fragment into a formaldehyde (CH2O) and a sulfate radical anion (SO4 ⋅ −) upon OH oxidation. The formaldehyde is likely partitioned back to the gas phase due to its high volatility. The sulfate radical anion, similar to OH radical, can abstract a hydrogen atom from neighboring sodium methyl sulfate to form the bisulfate ion, contributing to the secondary chemistry. Kinetic measurements show that the heterogeneous OH reaction rate constant, k, is (3.79 ± 0.19) × 10−13 cm3 molecule−1 s−1 with an effective OH uptake coefficient, γeff, of 0.17 ± 0.03. While about 40 % of sodium methyl sulfate is being oxidized at the maximum OH exposure (1.27 × 1012 molecule cm−3 s), only a 3 % decrease in particle diameter is observed. This can be attributed to a small fraction of particle mass lost via the formation and volatilization of formaldehyde. Overall, we firstly demonstrate that the heterogeneous OH oxidation of an organosulfate can lead to the formation of sulfate radical anion and produce inorganic sulfate. Fragmentation processes and sulfate radical anion chemistry play a key role in determining the compositional evolution of sodium methyl sulfate during heterogeneous OH oxidation.