Comparative Studies of Hemicelluloses Solubilized during the Treatments of Maize Stems with Peroxymonosulfuric Acid, Peroxyformic Acid, Peracetic Acid, and Hydrogen Peroxide. Part 1. Yield and Chemical Characterization

Holzforschung ◽  
2000 ◽  
Vol 54 (4) ◽  
pp. 349-356 ◽  
Author(s):  
RunCang Sun ◽  
J. Tomkinson ◽  
Z. C. Geng ◽  
N. J. Wang

Summary Treatment of the water-extracted maize stems with peroxymonosulfuric acid at 20 °C for 144 h, peroxyformic acid at 80°C for 6 h, peracetic acid at 50°C for 6 h, and 2% hydrogen peroxide at 45°C for 12 h at pH 1.5, 4.4, 9.5, 11.5, 12.0, and 12.6, respectively, solubilized 47.1%, 91.3%, 33.3%, 16.6%, 15.9%, 17.4%, 86.2%, 87.7%, and 91.3% of the original lignin, and hydrolysed or dissolved 12.1%, 99.1%, 4.5%, 2.7%, 3.1%, 3.1%, 63.3%, 64.7%, and 83.0% of the original hemicelluloses, respectively. Substantial lignins and hemicelluloses were degraded or released during the treatment with peroxyformic acid and alkaline peroxide at pH ≥ 11.5, while an insignificant effect on delignification and hemicellulose solubilization was observed by using peroxymonosulfuric acid, peracetic acid, and hydrogen peroxide in acidic, natural, and weak alkaline media. The optimum condition for extraction of hemicelluloses was found to use 2% H2O2 at 45°C for 12 h at pH 11.5–12.0, which yielded 63.3–64.7% of the original hemicelluloses having much lighter color than those obtained by peroxymonosulfuric acid and peracetic acid under conditions used and 2% H2O2 at pH 1.5, 4.4, 9.5, and 12.6. Xylose and arabinose were the major sugar constituents in these hemicellulose preparations, whereas glucose, galactose, mannose, rhamnose, and fucose were present as minor components. The α-ether linkages between lignin and hemicelluloses in the cell wall of maize stems were substantially cleaved during the treatment with 2% H2O2 at pH ≥11.5 as shown by a minimal amount of associated lignin (2.9–3.9%), rich in syringyl units, in the solubilized hemicelluloses.

Holzforschung ◽  
2000 ◽  
Vol 54 (5) ◽  
pp. 492-496 ◽  
Author(s):  
Runcang Sun ◽  
J. Tomkinson ◽  
Z. C. Geng ◽  
N. J. Wang

Summary Ten hemicellulosic preparations, obtained by treatments of the water-extracted maize stems with peroxymonosulfuric acid, peroxyformic acid, peracetic acid, and 2% hydrogen peroxide under the conditions given, respectively, were investigated by gel permeation chromatography and spectroscopic techniques such as Fourier transform infrared and carbon-13 nuclear magnetic resonance. Under an optimum extracting condition (2% H2O2, 45°C, 12 h, pH 11.5–12.0), the hemicelluloses obtained represented 63.3–64.7 % of the original hemicelluloses and had high weight-average molar mass between 69060 and 54740 g mol−1. The most obvious feature was found that the alkaline peroxide treatment of the stems under the conditions used did not affect the overall structure of the hemicelluloses. The thermal stability of the hemicelluloses was found to increase slightly with increasing molar mass. All the hemicellulosic preparations were, however, to varying degree thermally unstable at temperature above 180°C.


1997 ◽  
Vol 35 (2-3) ◽  
pp. 7-14 ◽  
Author(s):  
A. Schnell ◽  
M. J. Sabourin ◽  
S. Skog ◽  
M. Garvie

As part of an extensive audit of the Alkaline-Peroxide Mechanical Pulping (APMPTM) plant at the Malette Quebec Inc. mill in St. Raymond, Que., effluents were sampled from various stages of the process for comprehensive chemical characterizations, aquatic toxicity testing and anaerobic biotreatability assessments. In addition, untreated and secondary treated combined effluent from the integrated paper mill were sampled to determine the effectiveness of a conventional activated sludge process at the mill site. During the one-day sampling period, the APMP plant processed a mixed wood furnish consisting of 50% spruce/balsam fir and 50% aspen, with a chemical charge of 3.5% sodium hydroxide and 3.8% hydrogen peroxide on oven-dry fibre, while the Machine Finish Coated (MFC) paper production rate was 100 odt/d (oven dry metric tonnes per day). Measured production-specific contaminant discharge loadings from the novel APMP process were 56 kg BOD5/odt and 155 kg COD/odt in a combined effluent flow of 28 m3/odt. Sources of process effluent were chip washing, three stages of wood chip pretreatment and chemical impregnation (i.e., Impressafiner stages), interstate washing and pulp cleaning. The three Impressafiner pressates were found to be the most concentrated (i.e., 12-26 g COD/L) and toxic streams. Microtox testing of the pressates revealed EC50 concentrations of 0.07-0.34% v/v. The warm and concentrated effluents generated by the non-sulphur APMP process were found to be highly amenable to anaerobic degradation as determined by batch bioassay testing. Filterable BOD5 and COD(f) of the process effluents were reduced by 87-95% and 70-77%, respectively, with corresponding theoretical methane yields being attained. Acid-soluble dissolved lignin compounds exhibited biorecalcitrance, as revealed by limited removals of 34-55%, and were the main constituents contributing to residual COD(f), while resin and fatty acids (RFA) were reduced by 80-94%. The conservatively operated full scale activated sludge treatment process achieved a similar high 74% COD(f) removal from the whole mill effluent, while BOD5 and RFA reductions were virtually complete and the treated effluent was non-toxic, as measured by Microtox.


ACS Omega ◽  
2021 ◽  
Author(s):  
Shu-shu Zhong ◽  
Jun Zhang ◽  
Ze-hua Liu ◽  
Zhi Dang ◽  
Yu Liu

Pathogens ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 24
Author(s):  
Akikazu Sakudo ◽  
Daiki Anraku ◽  
Tomomasa Itarashiki

Prion diseases are proteopathies that cause neurodegenerative disorders in humans and animals. Prion is highly resistant to both chemical and physical inactivation. Here, vaporized gas derived from a hydrogen peroxide–peracetic acid mixture (VHPPA) was evaluated for its ability to inactivate prion using a STERIACE 100 instrument (Saraya Co., Ltd.). Brain homogenates of scrapie (Chandler strain) prion-infected mice were placed on a cover glass, air-dried, sealed in a Tyvek package, and subjected to VHPPA treatment at 50–55 °C using 8% hydrogen peroxide and <10% peracetic acid for 47 min (standard mode, SD) or 30 min (quick mode, QC). Untreated control samples were prepared in the same way but without VHPPA. The resulting samples were treated with proteinase K (PK) to separate PK-resistant prion protein (PrPres), as a marker of the abnormal isoform (PrPSc). Immunoblotting showed that PrPres was reduced by both SD and QC VHPPA treatments. PrPres bands were detected after protein misfolding cyclic amplification of control but not VHPPA-treated samples. In mice injected with prion samples, VHPPA treatment of prion significantly prolonged survival relative to untreated samples, suggesting that it decreases prion infectivity. Taken together, the results show that VHPPA inactivates prions and might be applied to the sterilization of contaminated heat-sensitive medical devices.


TAPPI Journal ◽  
2020 ◽  
Vol 19 (10) ◽  
pp. 511-524
Author(s):  
TASLIMA FERDOUS ◽  
M.A. QUAIYYUM ◽  
KAZI M. YASIN ARAFAT ◽  
M. SARWAR JAHAN

In this paper, chia plant was characterized in terms of chemical, morphological, and anatomical properties. Chia plant was characterized with low α-cellulose (30.5%); moderate lignin (23.2%) with syringyl to guaiacyl ratio of 1.41; and shorter fiber length (0.67 mm) with thinner cell wall (1.91 μm) and good flexibility coefficient (71.44). Anatomical features showed that chia plant consists of vessels, fibers, parenchyma cells, and collenchyma cells. Chia plant pulping was evaluated in soda-anthraquinone (soda-AQ) and formic acid/peroxyformic acid (FA/PFA) processes. Chia plant was difficult to delignify in the alkaline process. The FA/PFA process produced higher pulp yield at the same kappa number than the soda-AQ process. Unbleached soda-AQ chia pulp exhibited good proper-ties in terms of tensile, bursting, and tearing strengths, even at the unrefined stage, due to high drainability of the pulps. Alkaline peroxide bleached FA/PFA pulp exhibited better papermaking properties and 2% higher brightness than the D0(EP)D1 bleached soda-AQ pulp.


Endoscopy ◽  
2008 ◽  
Vol 40 (03) ◽  
pp. 231-231 ◽  
Author(s):  
R. Coriat ◽  
U. Chaput ◽  
Z. Ismaili ◽  
S. Chaussade

2003 ◽  
Vol 2 (5) ◽  
pp. 1018-1024 ◽  
Author(s):  
Neeraj Chauhan ◽  
Diane Inglis ◽  
Elvira Roman ◽  
Jesus Pla ◽  
Dongmei Li ◽  
...  

ABSTRACT Ssk1p of Candida albicans is a putative response regulator protein of the Hog1 two-component signal transduction system. In Saccharomyces cerevisiae, the phosphorylation state of Ssk1p determines whether genes that promote the adaptation of cells to osmotic stress are activated. We have previously shown that C. albicans SSK1 does not complement the ssk1 mutant of S. cerevisiae and that the ssk1 mutant of C. albicans is not sensitive to sorbitol. In this study, we show that the C. albicans ssk1 mutant is sensitive to several oxidants, including hydrogen peroxide, t-butyl hydroperoxide, menadione, and potassium superoxide when each is incorporated in yeast extract-peptone-dextrose (YPD) agar medium. We used DNA microarrays to identify genes whose regulation is affected by the ssk1 mutation. RNA from mutant cells (strain CSSK21) grown in YPD medium for 3 h at 30°C was reverse transcribed and then compared with similarly prepared RNA from wild-type cells (CAF2). We observed seven genes from mutant cells that were consistently up regulated (three-fold or greater compared to CAF2). In S. cerevisiae, three (AHP1, HSP12, and PYC2) of the seven genes that were up regulated provide cells with an adaptation function in response to oxidative stress; another gene (GPH1) is regulated under stress conditions by Hog1p. Three other genes that are up regulated encode a cell surface protein (FLO1), a mannosyl transferase (MNN4-4), and a putative two-component histidine kinase (CHK1) that regulates cell wall biosynthesis in C. albicans. Of the down-regulated genes, ALS1 is a known cell adhesin in C. albicans. Verification of the microarray data was obtained by reverse transcription-PCR for HSP12, AHP1, CHK1, PYC2, GPH1, ALS1, MNN4-4, and FLO1. To further determine the function of Ssk1p in the Hog1p signal transduction pathway in C. albicans, we used Western blot analysis to measure phosphorylation of Hog1p in the ssk1 mutant of C. albicans when grown under either osmotic or oxidative stress. We observed that Hog1p was phosphorylated in the ssk1 mutant of C. albicans when grown in a hyperosmotic medium but was not phosphorylated in the ssk1 mutant when the latter was grown in the presence of hydrogen peroxide. These data indicate that C. albicans utilizes the Ssk1p response regulator protein to adapt cells to oxidative stress, while its role in the adaptation to osmotic stress is less certain. Further, SSK1 appears to have a regulatory function in some aspects of cell wall biosynthesis. Thus, the functions of C. albicans SSK1 differ from those of S. cerevisiae SSK1.


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