Industrial Conditions of the Granular Material Manufacturing Process

The article presents industrial conditions of manufacturing multi-component heterogeneous mixtures of granular materials. The study analyzed the production technology and devices used for production such as storage siloes, an impact screen, a cyclone separator, a shaving and dust extractor, a screw mixer, a tensometric weigh, a bucket conveyor. A division and the successive stages of manufacturing process has been presented: unloading, receipt and storage of raw materials, quality control of components, technology cleaning and sorting of raw materials, dosage and mixing of feed material, bagging, storage, extraction processes and evaluation of homogeneity in a fodder mixing plant. Moreover the methods of assessing the homogeneity of the multi-component heterogeneous mixtures has been presented. The research was conducted in industrial conditions.

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Review on Standardization of Ayurvedic Medicine

Journal of Pharmaceutical Research International ◽

10.9734/jpri/2021/v33i57a33986 ◽

2021 ◽

pp. 194-199

Author(s):

Janmejay Pant ◽

. Ripudhaman

Keyword(s):

Quality Control ◽

Raw Materials ◽

Dosage Forms ◽

Classical Literature ◽

Scientific Methods ◽

Ayurvedic Drugs ◽

Drug Manufacturing ◽

And Storage ◽

Current Guidelines

Standardization in Ayurvedic formulations ensures the establishment of standards for the quality and purity of raw materials, quality control during the drug manufacturing process, production of a good quality finished product, storage and distribution to maintain the quality of the final product. It is an essential tool for establishing quality control methods for Ayurvedic drugs. In Ayurveda, standardization has been well defined and documented in the classical and contemporary texts. Still, these have been written with an individualistic intent and not for industrial or commercial purposes. Careful contemplation of the classical literature of Ayurveda was done, the current guidelines of WHO on standardization of herbal drugs, latest researches on the same via the internet were explored and examined in the purview of the newest standardization procedures. In this article, an attempt has been made to bring to light the classical references related to standardization, the milestones in this on-going pursuit have been exhibited, with the use of the latest scientific methods being incorporated for a standardized Ayurvedic drug. It can be concluded from the review that standardization in Ayurveda is an on-going process where one needs to be strictly vigilant about the new scientific methods to study the fine chemical procedures and the intermediate compounds formed, but at the same time be aware of the classical. Ayurvedic methods concepts of the procedure. Asava-arista's medicinal characteristics of Ayurvedic classical dosage forms, liquid dosage forms based on self-generated alcohol with faster absorption, long shelf life, and increased market conformity have led to a continuous rise in demand. New fermentation methods and packaging innovations tend to have been embraced by many Ayurvedic processing units. The importance of standardization of such goods is underlined by these advances in manufacturing, distribution and storage. Therefore, it is of concern to examine the latest manufacturing situation and the standardization of the dosage type regarding the procedure and the consistency and effectiveness of the finished product. In addition to the effort to include criteria of consistency and standardization, the study consists of an overview and deliberates on the importance of improvements made to the conventional preparation processes, ingredients and material used in the process and the potential impact on its efficacy.

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Manufacturing process of high quality phytopreparation on example of herbal sedative

Medicinski pregled ◽

10.2298/mpns1304170d ◽

2013 ◽

Vol 66 (3-4) ◽

pp. 170-176

Author(s):

Sofija Djordjevic ◽

Aleksandra Dickov ◽

Sava Pavkov ◽

Vanja Tadic ◽

Ivana Arsic ◽

...

Keyword(s):

Quality Control ◽

Production Process ◽

Manufacturing Process ◽

Herbal Remedy ◽

Raw Materials ◽

Good Manufacturing Practice ◽

Valeric Acid ◽

Herbal Remedies ◽

Modern Concept ◽

High Quality

Introduction. Rational phytotherapy is a modern concept of using plant-originated drugs which has emerged from the need to improve phytotherapy in order to make the use of herbal remedies more efficient and safer. The aim of this study was to give the health-care workers more information on the manufacturing process of high quality phytopreparation following principles of Good Manufacturing Practice and Good Laboratory Practice on the example of herbal sedative, Odoval S? capsules. Material and Methods. This study was designed to reflect the production process of a high-quality and safe herbal remedy, starting from defining the formulation and the production procedure to the quality control of raw materials, characterization of the final product, and testing stability of active ingredients in the capsules. Results. Formulation of the phytopreparation, validation of the production process, quality control and stability testing, all together have resulted in the production of capsules with defined valeric acid content (1 mg valeric acid per capsule). Discussion. The preparation is recommended to relieve the symptoms caused by chronic stress (anxiety, irritability, fatigue, lack of concentration, heart palpitations) and for mild insomnia. Conclusion. This paper presents the complete cycle of the production of a phytopreparation on the example of a new herbal sedative - Odoval S? capsules.

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Emerging Techniques for the Characterization of Nano-Mechanical Properties of Integrated Circuit Components

ISTFA 2008: Conference Proceedings from the 34th International Symposium for Testing and Failure Analysis ◽

10.31399/asm.cp.istfa2008p0121 ◽

2008 ◽

Author(s):

Nicholas Randall ◽

Rahul Premachandran Nair

Keyword(s):

Mechanical Properties ◽

Quality Control ◽

Integrated Circuits ◽

Integrated Circuit ◽

Manufacturing Process ◽

Solder Bumps ◽

Initial Work ◽

Circuit Components ◽

Materials Used

Abstract With the growing complexity of integrated circuits (IC) comes the issue of quality control during the manufacturing process. In order to avoid late realization of design flaws which could be very expensive, the characterization of the mechanical properties of the IC components needs to be carried out in a more efficient and standardized manner. The effects of changes in the manufacturing process and materials used on the functioning and reliability of the final device also need to be addressed. Initial work on accurately determining several key mechanical properties of bonding pads, solder bumps and coatings using a combination of different methods and equipment has been summarized.

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Analysis of the information management system in the manufacturing process of cigarette enterprises using fuzzy AHP

Journal of Intelligent & Fuzzy Systems ◽

10.3233/jifs-189648 ◽

2021 ◽

pp. 1-11

Author(s):

Song Gang ◽

Wang Xiaoming ◽

Wu Junfeng ◽

Li Shufang ◽

Liu Zhuowen ◽

...

Keyword(s):

Quality Control ◽

Production Process ◽

Information Management ◽

Manufacturing Process ◽

Management System ◽

Fuzzy Ahp ◽

Control Process ◽

Information Management System ◽

Manufacturing Execution System ◽

Quality Control Process

In view of the production quality management of filter rods in the manufacturing and execution process of cigarette enterprises, this paper analyzes the necessity of implementing the manufacturing execution system (MES) in the production process of filter rods. In this paper, the filter rod quality system of cigarette enterprise based on MES is fully studied, and the constructive information management system demand analysis, cigarette quality control process, system function module design, implementation and test effect are given. This paper utilizes the Fuzzy analytic hierarchy process to find the optimal system for processing the manufacturing of cigarette. The implementation of MSE based filter rod quality information management system for a cigarette enterprise ensures the quality control in the cigarette production process. Through visualization, real-time and dynamic way, the information management of cigarette production is completed, which greatly improves the quality of cigarette enterprise manufacturing process.

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The Manufacture of Veterinary Vaccines: Quality Control of the Manufacturing Process

Veterinary Vaccines ◽

10.1002/9781119506287.ch12 ◽

2021 ◽

pp. 147-159

Author(s):

Mehdi El Harrak ◽

Imane Belkourati ◽

Zineb Boumart ◽

Fatima Z. Fakri ◽

Jihane Hamdi

Keyword(s):

Quality Control ◽

Manufacturing Process

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Feasibility of cereal straw for industrial utilization in Minnesota

American Journal of Alternative Agriculture ◽

10.1017/s0889189300008407 ◽

2000 ◽

Vol 15 (1) ◽

pp. 2-8 ◽

Cited By ~ 2

Author(s):

N.C. Wagner ◽

S. Ramaswamy ◽

U. Tschirner

Keyword(s):

Animal Feed ◽

Raw Materials ◽

Low Cost ◽

Economic Feasibility ◽

Raw Material ◽

Cereal Straw ◽

Industrial Utilization ◽

Industrial Use ◽

On Farm ◽

And Storage

AbstractA pre-economic feasibility study was undertaken to determine the potential of cereal straw for industrial utilization in Minnesota. Specifically, utilizing straw for pulp and paper manufacture was of interest. The availability of cereal straw fiber supplies at various locations across the state of Minnesota, along with pre-processing issues such as transportation, harvesting, handling, and storage, are discussed and priced. The greatest economic advantage of straw for industrial use appears to be the low cost of the raw material compared to traditional raw materials. This also provides an excellent opportunity for additional income for farmers. The methodology and information provided here should be helpful in evaluating the feasibility of utilizing straw for other industrial purposes in other parts of the world. However, in some Third World countries, long-standing on-farm, traditional uses of cereal straws for fuel, fiber, and animal feed may limit their availability for industrial utilization.

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Colorants in cosmetic applications

Physical Sciences Reviews ◽

10.1515/psr-2020-0161 ◽

2021 ◽

Vol 0 (0) ◽

Author(s):

Ghita Lanzendörfer-Yu

Keyword(s):

Social Networks ◽

Quality Control ◽

Manufacturing Process ◽

The Ideal

Abstract The color cosmetic market, even though highly dependent on color, is driven by texture. Pigment and color innovation are predominantly taking place in the field of inorganic effect pigments, as colorants are regulated within the different cosmetic directives and toxicological profiles have to be established prior to use. Therefore, the formulation and the packaging are the relevant innovative factors. Nevertheless, color cosmetics are driven by fashion and trends. One of the main drivers for sales is social networks. They are image based and therefore the ideal platform to spread these trends, boosting sales of color cosmetics recently. Even though, color cosmetics seem to be very simple in composition, the development, production and quality control are far from that. In color cosmetics, all cosmetic disciplines cumulate: dispersion strategies, emulsion technologies, molding and extruding of sticks and pencil leads, mixing and compressing of powders, liquid inks and so on. And almost every discipline requires separate production vessels, resulting in a rather complex manufacturing process.

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CERTIFICATION OF VEGETABLE OILS AND QUALITY CONTROL IN THE TECHNOLOGICAL PROCESS OF PRODUCTION

Technical science and innovation ◽

10.51346/tstu-01.19.4.-77-0038 ◽

2019 ◽

Vol 2019 (4) ◽

pp. 119-126

Author(s):

CH Bekmurotov ◽

Keyword(s):

Quality Control ◽

Technological Process ◽

Vegetable Oils ◽

Raw Materials ◽

Cottonseed Oil ◽

Product Classification ◽

Cotton Seeds ◽

The Cost

The article reviewed the certification and quality control of the technological process for the production of vegetable oil. There is a procedure for packaging, quality control of products, determination of quality indicators and quality control of finished products. The procedure for using refined cottonseed oil and its varieties, the requirements for placement and storage of vegetable oils, as specified in the regulatory documents, the quality control of vegetable oils and other solutions for cottonseed oil are provided. The gas analyzer shows a solution for measuring the amount of solution by painting the tubes of a mixture of gas and air in oil. Detailed information on the production of vegetable oils, the cost of raw materials, the level of fat content of cotton seeds and the methods used to produce oil from cotton seeds. Methods for certification of vegetable oils, types of quality control, methods of testing and quality determination are presented. It was shown that the procedure for refined production of cottonseed oils and their types, as well as the state of the product classification of products based on the method of producing vegetable oils for consumer purposes, analysis of the sequence of refined oils and refining processes.

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Development of the technique for quality control of 1,3-bis(3,4-dicyanophenoxy)benzene by HPLC

Тонкие химические технологии ◽

10.32362/2410-6593-2021-16-1-88-98 ◽

2021 ◽

Vol 16 (1) ◽

pp. 88-98

Author(s):

Z. N. Shchekoldina ◽

A. A. Bogolyubov ◽

A. Yu. Zakharov ◽

B. A. Bulgakov ◽

A. V. Babkin ◽

...

Keyword(s):

Quality Control ◽

High Performance ◽

Raw Materials ◽

Reaction Times ◽

Kinetic Studies ◽

Reversed Phase ◽

Quantitative Chemical Analysis ◽

Practical Applications ◽

Good Convergence ◽

Quantitative Hplc Analysis

Objectives. Determination of target products and byproducts is necessary for the quality control of phthalonitrile monomer synthesis as well as production scaling and performing related kinetic studies. High-performance liquid chromatography (HPLC) is a simple and affordable method for quantitative chemical analysis, which also verifies the quality of raw materials. The objective of this study was to develop an HPLC technique for determining the composition of the reaction mixture in the synthesis of 1,3-bis(3,4-dicyanophenoxy)benzene (DPB).Methods. Reversed-phase HPLC was used to quantitatively analyze the reaction mixture.Results. A simple and rapid method for the quantitative HPLC analysis of phthalonitrile monomers and their mixtures with reagents was developed. Reaction times and the accumulation of byproducts were also studied.Conclusions. The successful performance of the developed technique allows us to recommend it for practical applications. The results obtained for reactors of different sizes have good convergence, and DPB synthesis was successfully scaled up to intermediate scale equipment.

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PENERAPAN STATISTICAL QUALITY CONTROL (SQC) PADA PENGENDALIAN MUTU MINYAK TELON (STUDI KASUS DI PT.X)

AGROINTEK ◽

10.21107/agrointek.v13i1.4920 ◽

2019 ◽

Vol 13 (1) ◽

pp. 72

Author(s):

Andan Linggar Rucitra ◽

S Fadiah

Keyword(s):

Quality Control ◽

Raw Materials ◽

Control Process ◽

Statistical Quality Control ◽

Statistical Quality ◽

Quality Control Process ◽

Fishbone Diagram ◽

Potential Factor ◽

Measurement Of Success

Telon oil is one of the traditional medicine in the form of liquid preparations that serves to provide a sense of warmth to the wearer. PT.X is one of the companies that produce telon oil. To maintain the quality of telon oil from PT.X product, required overall quality control that is starting from the quality control of raw materials, quality control process to the quality control of the final product. The purpose of this research is to know the application of Statistical Quality Control (SQC) in controlling the quality of telon oil in PT X. Final product quality become one of the measurement of success of a process, so it needs a good quality control. SQC method used in this research is Pareto Diagram and Cause and Effect Diagram. Pareto diagram is a bar graph that show the problem based on the order of the number of occurrences of the most number of problems until the least happened. A causal diagram is often called a fishbone diagram, a tool for identifying potential causes of an effect or problem. The result of applying the method indicates that 80% defect is caused by unsuitable volume and on the incompatibility of Expired Date (ED) code. The damage is caused by several factors namely the method, labor, and machine while the most potential factor is the volume conformity to reduce the number of defect products.

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