scholarly journals Clarification of sugarcane juice by ultrafiltration membrane: Toward the direct production of refined cane sugar

2020 ◽  
Vol 264 ◽  
pp. 109682 ◽  
Author(s):  
Thevu Vu ◽  
Jeffrey LeBlanc ◽  
Chung Chi Chou
2020 ◽  
Vol 13 (2) ◽  
pp. 188-194
Author(s):  
Eresh Kumar Kuruba ◽  
P.V.K. Jagannadha Rao ◽  
D. Khokhar ◽  
S. Patel

Jaggery is a solid unrefined, non- centrifugal cane sugar (NCS) with unique colour, flavor and aroma obtained from crushing of cane and evaporating of sugarcane juice. In this paper vacuum pan evaporation method were used sugarcane juice boiling at vacuum pressure (Vp : 500-700 mm of Hg), time (t:60-90 min) and temperature (T:100-1200 C). The quality attributes of jaggery developed from vacuum pan evaporator were investigated at different process variables. The developed jaggery were analyzed for physiochemical. Results showed that TSS (0 Brix) and Hardness (Hd) increased with increase in vacuum pressure and time, whereas moisture content percentage (%) and water activity (aw) decreased with increase in vacuum pressure and time at variable temperature of 1100 C. Fuzzy logic method was used to evaluate the sensory characteristic of prepared jaggery.


Desalination ◽  
2002 ◽  
Vol 147 (1-3) ◽  
pp. 157-160 ◽  
Author(s):  
Sanjay Nene ◽  
Suhkvinder Kaur ◽  
K. Sumod ◽  
Bhagyashree Joshi ◽  
K.S.M.S. Raghavarao

2020 ◽  
pp. 728-734
Author(s):  
Narendranath Mullapudi

With the selection of available process equipment and practicing best operating conditions, sugar of less than 50 IU can be produced at a cane mill without back-end refinery. Cane diffusers are being used which are energy efficient and produce cane juice with low suspended solids. The double sulphitation process is followed using the ejector system to obtain a better colour and turbidity removal. High efficiency, low residence time and low turbulence settling clarifier is being used for juice clarification. Syrup clarification is also used to polish the syrup further without using any colour precipitants. A 3½ stage crystallization scheme is employed. For A massecuite a seed magma of B2 sugar is used. B2 sugar is produced from B sugar as seed and syrup and dissolved B and C sugar is used. Purity of A massecuite is maintained around 90% producing a sugar of below 50 IU with 70% of the crystallizate having a size of 1200–1700 μm with low residual SO2 content.


Desalination ◽  
2004 ◽  
Vol 161 (3) ◽  
pp. 305 ◽  
Author(s):  
Sanjay Nene ◽  
Sukhvinder Kaur ◽  
K. Sumod ◽  
Bhagyashree Joshi ◽  
K.S.M.S. Raghavarao

1880 ◽  
Vol 9 (219supp) ◽  
pp. 3491-3491
Author(s):  
E. Demole
Keyword(s):  

2015 ◽  
Vol 30 (2) ◽  
pp. 171 ◽  
Author(s):  
CHEN Tao-Tao ◽  
LI Dan ◽  
JING Wen-Heng ◽  
FAN Yi-Qun ◽  
XING Wei-Hong

2019 ◽  
Author(s):  
Huifang Xu ◽  
Weinan Liang ◽  
Linlin Ning ◽  
Yuanyuan Jiang ◽  
Wenxia Yang ◽  
...  

P450 fatty acid decarboxylases (FADCs) have recently been attracting considerable attention owing to their one-step direct production of industrially important 1-alkenes from biologically abundant feedstock free fatty acids under mild conditions. However, attempts to improve the catalytic activity of FADCs have met with little success. Protein engineering has been limited to selected residues and small mutant libraries due to lack of an effective high-throughput screening (HTS) method. Here, we devise a catalase-deficient <i>Escherichia coli</i> host strain and report an HTS approach based on colorimetric detection of H<sub>2</sub>O<sub>2</sub>-consumption activity of FADCs. Directed evolution enabled by this method has led to effective identification for the first time of improved FADC variants for medium-chain 1-alkene production from both DNA shuffling and random mutagenesis libraries. Advantageously, this screening method can be extended to other enzymes that stoichiometrically utilize H<sub>2</sub>O<sub>2</sub> as co-substrate.


2018 ◽  
Vol 84 (12) ◽  
pp. 5-19
Author(s):  
D. N. Bock ◽  
V. A. Labusov

A review of publications regarding detection of non-metallic inclusions in metal alloys using optical emission spectrometry with single-spark spectrum registration is presented. The main advantage of the method - an extremely short time of measurement (~1 min) – makes it useful for the purposes of direct production control. A spark-induced impact on a non-metallic inclusion results in a sharp increase (flashes) in the intensities of spectral lines of the elements that comprise the inclusion because their content in the metal matrix is usually rather small. The intensity distribution of the spectral line of the element obtained from several thousand of single-spark spectra consists of two parts: i) the Gaussian function corresponding to the content of the element in a dissolved form, and ii) an asymmetric additive in the region of high intensity values ??attributed to inclusions. Their quantitative determination is based on the assumption that the intensity of the spectral line in the single-spark spectrum is proportional to the content of the element in the matter ablated by the spark. Thus, according to the calibration dependence constructed using samples with a certified total element content, it is possible not only to determine the proportions of the dissolved and undissolved element, but also the dimensions of the individual inclusions. However, determination of the sizes is limited to a range of 1 – 20 µm. Moreover, only Al-containing inclusions can be determined quantitatively nowadays. Difficulties occur both with elements hardly dissolved in steels (O, Ca, Mg, S), and with the elements which exhibit rather high content in the dissolved form (Si, Mn). It is also still impossible to determine carbides and nitrides in steels using C and N lines. The use of time-resolved spectrometry can reduce the detection limits for inclusions containing Si and, possibly, Mn. The use of the internal standard in determination of the inclusions can also lower the detection limits, but may distort the results. Substitution of photomultipliers by solid-state linear radiation detectors provided development of more reliable internal standard, based on the background value in the vicinity of the spectral line. Verification of the results is difficult in the lack of standard samples of composition of the inclusions. Future studies can expand the range of inclusions to be determined by this method.


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