scholarly journals Degradation of hydroxypropyl guar gum at wide pH range by a heterogeneous Fenton-like process using bentonite-supported Cu(0)

2020 ◽  
Vol 82 (8) ◽  
pp. 1635-1642
Author(s):  
Ling Zhou ◽  
Zhongying Xu ◽  
Jie Zhang ◽  
Zhifang Zhang ◽  
Ying Tang

Abstract To seek for efficient Fenton-like oxidation processing for treatment of waste fracturing fluid containing hydroxypropyl guar gum (HPGG), in heterogeneous reaction, five bentonite-supported zero-valent metal catalysts were prepared by liquid-phase reduction. The results showed that the bentonite-supported zero-valent copper exhibited best catalytic performance, attributed to the high dispersion of active sites of zero-valent copper. The effects of the most relevant operating factors (H2O2 concentration, catalyst dosage, temperature and pH) were evaluated in detail. Moreover, the chemical oxygen demand removal rate of HPGG can achieve 76% when the reaction time was selected at 45 min under optimal experimental conditions. The stability evaluation showed that the catalytic performance was almost unaffected after the catalyst was recycled and used once more showing the good stability of the bentonite-supported zero-valent copper in the application process.

2019 ◽  
Vol 79 (9) ◽  
pp. 1667-1674 ◽  
Author(s):  
Ying Tang ◽  
Huan Liu ◽  
Ling Zhou ◽  
Haomiao Ren ◽  
Hong Li ◽  
...  

Abstract A series of EDTA-metal complexes was prepared for the Fenton oxidation catalysts and Fe(II)L exhibits high catalytic performance for degradation of hydroxypropyl guar gum in a wide pH range 7.0–13.0. The viscosity of hydroxypropyl guar gum can be reduced with the 10.0% H2O2 and 5.0% Fe(II)L. The viscosity average molecular weight of hydroxypropyl guar gum was decreased from almost 2 million to 3,199. Most important of all, the chemical oxygen demand (COD) value can be decreased to 104 mg/L from 8,080 mg/L with enough H2O2, and Fe(II)L also shows great catalytic ability in the degradation of various polymers by H2O2. The proposed mechanism of the activation of H2O2 by the complex was studied.


2017 ◽  
Vol 77 (3) ◽  
pp. 565-575 ◽  
Author(s):  
Zhenchao Zhang

Abstract Hydroxypropyl guar gum is considered to be a main component of oilfield fracturing wastewater (OFW). This work is intended to optimize the experimental conditions for the maximum oxidative degradation of hydroxypropyl guar gum by the coagulation and UV/H2O2/ferrioxalate complexes process. Optimal reaction conditions were proposed based on the chemical oxygen demand (COD) removal efficiency and UV_vis spectra analysis. The overall removal efficiency of COD reached 83.8% for a dilution ratio of raw wastewater of 1:2, pH of 4 and FeCl3 loading of 1,000 mg/L in the coagulation process; the dosage of H2O2 (30%,v/v) was 0.6% (v/v) and added in three steps, the n(H2O2)/n(Fe2+) was 2:1, n(Fe2+)/n(C2O42−) was 3:1 and pH was 4 in the UV/H2O2/ferrioxalate complexes process; pH was adjusted to 8.5–9 by NaOH and then cationic polyacrylamide (CPAM) of 2 mg/L was added in the neutralization and flocculation process. The decrease in COD during the coagulation process reduced the required H2O2 dosage and improved efficiency in the subsequent UV/H2O2/ferrioxalate complexes process. Furthermore, COD removal efficiency significantly increased by more than 13.4% with the introduction of oxalate compared with UV/Fenton. The UV_vis spectra analysis results indicated that the coagulation and UV/H2O2/ferrioxalate complexes process could efficiently remove the hydroxypropyl guar gum dissolved in OFW. An optimal combination of these parameters produced treated wastewater that met the GB8978-1996 Integrated Wastewater Discharge Standard level III emission standard.


2015 ◽  
Vol 117 ◽  
pp. 636-643 ◽  
Author(s):  
Hiroyuki Kono ◽  
Hideyuki Hara ◽  
Hisaho Hashimoto ◽  
Yuuichi Shimizu

2021 ◽  
Author(s):  
Chaofei Song ◽  
Yue Lv ◽  
Xia Qin ◽  
Jiaxin Cui ◽  
Chengrui Guo ◽  
...  

Abstract In this paper, the active component zero-valent copper (ZVC) supported by chitosan activated carbon ball (CTS-ACB) (i.e. ZVC/CTS-ACS catalyst) was successfully prepared. The characterization results showed obvious characteristics of activated carbon and zero-valent copper. The catalyst was used to degrade fulvic acid (FA) in catalytic wet oxidation(CWO) system. The two significant factors acidity and temperature were found with the statistical tool Plackett-Buimanhe(PB) in CWO for FA removal. Then the response surface methodology(RSM) model was used to optimize the experimental conditions in order to obtain the optimal FA removal rate. With the optimal experimental parameters, that is, a temperature of 94°C and an acidity of 3.8, the average maximum removal rate of FA was 93.02%, which was in agreement with the expected result of the model 93.86%, indicating that the model is well established. The comparison of catalytic performance showed that the addition of catalyst ZVC / CTS-ACS could increase the removal rate of FA, colour number(CN) and TOC by 93.6%, 83.5% and 81.9% respectively. The utilization of ZVC can greatly increase the mineralization rate of FA , which indicates the high catalytic activity and minerazation of the catalyst.


Author(s):  
Xiaobing Huang ◽  
Gang Chang ◽  
Xiaoyi Wei ◽  
Fei Wang ◽  
Lihong Cui ◽  
...  

2020 ◽  
pp. 174751982092599
Author(s):  
Heng Zhang ◽  
Chunhao Yang ◽  
Shengying Zhao ◽  
Tingting Wang ◽  
Wancheng Zhu

Ordered mesoporous silica, SBA-15 and MCM-41, and three-dimensionally ordered macroporous SiO2 were used as the supports of H4PMo11VO40 heteropolyacid for methacrolein oxidation. The dispersion and structural evolutions of the heteropolyacid along with thermal treatment were investigated. It was found that the heteropolyacid entered the one-dimensional mesoporous channels of SBA-15 and MCM-41, and the crystallization and growth were limited, leading to high dispersion of the heteropolyacid. However, the thermal stability was decreased under high dispersion. The migration of the heteropolyacid was observed to the end of the one-dimensional channels of SBA-15 and the outer surface of MCM-41 with calcination, accompanied by the decomposition of the heteropolyacid and the formation of MoO3. In comparison, the crystallization and growth of heteropolyacid were not limited in the open macropores of three-dimensionally ordered macroporous SiO2. Dispersed particles on the surface of the macropores with size of about 5 nm exhibited a higher thermal stability. The decomposition of the heteropolyacid in the SBA-15 and MCM-41 supported catalysts resulted in the loss of strong acid sites, causing low selectivity to methacrylic acid in methacrolein oxidation. High thermal stability with high exposure of the active sites in the three-dimensionally ordered macroporous SiO2 supported catalyst contributed to the enhancement in the catalytic performance.


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