Formation of uniform colloidal spheres from lignin, a renewable resource recovered from pulping spent liquor
Literature Information
Yong Qian, Yonghong Deng, Xueqing Qiu, Hao Li, Dongjie Yang
Alkali lignin, recovered from the pulping black liquor, was chemically modified by acetylating, and then used as a biomass resource to prepare uniform colloidal spheres via self-assembly. The self-assembled structure and colloid formation mechanism of the acetylated lignin (ACL) were investigated by DLS, SLS, TEM, AFM, XPS, FTIR, elemental analysis and contact angle measurements. Results show that ACL colloidal spheres are obtained from gradual hydrophobic aggregation of ACL molecules, induced by continuously adding water into the ACL–THF solution. ACL molecules start to form colloidal spheres at a critical water content of 44 vol% when the initial concentration of ACL in THF is 1.0 mg mL−1, and the colloidization process is completed at a water content of 67 vol%. An excessive amount of water is added into the dispersions to “quench” the structures formed and then the ACL dispersion is treated by rotary evaporation for recycling THF and acquiring colloidal spheres. The ACL colloidal spheres have an
Related Literature
Electrical impedance spectroscopy of a PET chip sandwiched between two disk electrodes: understanding the contribution of the polymer/electrode interface
L. Chaal, V. Vivier, B. Tribollet, J. Gamby
DOI: 10.1039/C6CP03042D
π-Ring currents in doped coronenes with nitrogen and boron: diatropic–paratropic duality
Inmaculada García Cuesta, Barnaby Pownall, Stefano Pelloni, Alfredo M. Sánchez de Merás
DOI: 10.1039/C5CP03732H
Semitransparent polymer solar cells with simultaneously improved efficiency and color rendering index
Wenjuan Yu, Xu Jia, Mengnan Yao, Linghui Zhu, Yongbing Long, Liang Shen
DOI: 10.1039/C5CP03467A
Flexible Ag–C60 nano-biosensors based on surface plasmon coupled emission for clinical and forensic applications
Pradyumna Mulpur, Sairam Yadavilli, Praharsha Mulpur, Neeharika Kondiparthi, Venkataramaniah Kamisetti
DOI: 10.1039/C5CP04268B
Unravelling the optical responses of nanoplasmonic mirror-on-mirror metamaterials
Debabrata Sikdar, Shakeeb B. Hasan, Michael Urbakh, Joshua B. Edel, Alexei A. Kornyshev
DOI: 10.1039/C6CP04551K
Synthesis of barbituric acid containing nucleotides and their implications for the origin of primitive informational polymers
Chaitanya V. Mungi, Sachin Kumar Singh, Sudha Rajamani
DOI: 10.1039/C6CP00686H
Predicting suitable optoelectronic properties of monoclinic VON semiconductor crystals for photovoltaics using accurate first-principles computations
DOI: 10.1039/C5CP03924J
Low polarity water, a novel transition species at the polyethylene–water interface
Edward M. Kosower, Galina Borz
DOI: 10.1039/C5CP04439A
Reaction rate of a composite core–shell nanoreactor with multiple nanocatalysts
Duccio Fanelli, Stefano Angioletti-Uberti
DOI: 10.1039/C6CP01179A
Troponin structure: its modulation by Ca2+ and phosphorylation studied by molecular dynamics simulations
Juan Eiros Zamora, Maria Papadaki, Andrew E. Messer, Steven B. Marston, Ian R. Gould
DOI: 10.1039/C6CP02610A
You might also like
What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?
When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...
What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?
4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...
How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?
5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...
What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?
The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?
3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...
What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?
N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...
What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?
This compound is primarily used in the pharmaceutical industry for the synthesis...
How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?
2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...
What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?
Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...
Source Journal
Green Chemistry

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.












![6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure](https://static.chemtradehub.com/structs/136/1369160-12-2-6524.webp)

